NZ619159B2 - Combustible heat source for a smoking article - Google Patents
Combustible heat source for a smoking article Download PDFInfo
- Publication number
- NZ619159B2 NZ619159B2 NZ619159A NZ61915912A NZ619159B2 NZ 619159 B2 NZ619159 B2 NZ 619159B2 NZ 619159 A NZ619159 A NZ 619159A NZ 61915912 A NZ61915912 A NZ 61915912A NZ 619159 B2 NZ619159 B2 NZ 619159B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- combustible heat
- heat source
- temperature
- heat sources
- smoking article
- Prior art date
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- 230000000391 smoking effect Effects 0.000 title claims abstract description 244
- 238000002485 combustion reaction Methods 0.000 claims abstract description 117
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 52
- 229910001960 metal nitrate Inorganic materials 0.000 claims abstract description 51
- 150000002823 nitrates Chemical class 0.000 claims abstract description 49
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000001301 oxygen Substances 0.000 claims abstract description 37
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 37
- 238000005979 thermal decomposition reaction Methods 0.000 claims abstract description 10
- 239000000758 substrate Substances 0.000 claims description 91
- 238000011144 upstream manufacturing Methods 0.000 claims description 68
- 239000000463 material Substances 0.000 claims description 57
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- 239000011777 magnesium Substances 0.000 claims description 29
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- 150000001875 compounds Chemical class 0.000 claims description 22
- 239000011230 binding agent Substances 0.000 claims description 19
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- 239000000654 additive Substances 0.000 description 15
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- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000002459 porosimetry Methods 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 238000001812 pycnometry Methods 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000007569 slipcasting Methods 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910000018 strontium carbonate Inorganic materials 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910000166 zirconium phosphate Inorganic materials 0.000 description 1
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/10—Chemical features of tobacco products or tobacco substitutes
- A24B15/16—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes
- A24B15/165—Chemical features of tobacco products or tobacco substitutes of tobacco substitutes comprising as heat source a carbon fuel or an oxidized or thermally degraded carbonaceous fuel, e.g. carbohydrates, cellulosic material
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
- A24D1/00—Cigars; Cigarettes
- A24D1/22—Cigarettes with integrated combustible heat sources, e.g. with carbonaceous heat sources
-
- A24F47/006—
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23Q—IGNITION; EXTINGUISHING-DEVICES
- F23Q2/00—Lighters containing fuel, e.g. for cigarettes
- F23Q2/18—Lighters with solid fuel
Abstract
combustible heat source (4) for a smoking article (2) comprises carbon and at least one ignition aid selected from the group consisting of metal nitrate salts having a thermal decomposition temperature of less than about 600°. The ignition aid is present in an amount of at least 20 percent by dry weight of the combustible heat source. The combustible heat source (4) has a first portion and an opposed second portion. At least part (4b) of the combustible heat source (4) between the first portion and the second portion is wrapped in a combustion resistant wrapper (22) that is one or both of heat conducting and substantially oxygen impermeable. Upon ignition of the first portion of the combustible heat source (4), the second portion of the combustible heat source increases in temperature to a first temperature. During subsequent combustion of the combustible heat source (4), the second portion of the combustible heat source (4) maintains a second temperature lower than the first temperature. weight of the combustible heat source. The combustible heat source (4) has a first portion and an opposed second portion. At least part (4b) of the combustible heat source (4) between the first portion and the second portion is wrapped in a combustion resistant wrapper (22) that is one or both of heat conducting and substantially oxygen impermeable. Upon ignition of the first portion of the combustible heat source (4), the second portion of the combustible heat source increases in temperature to a first temperature. During subsequent combustion of the combustible heat source (4), the second portion of the combustible heat source (4) maintains a second temperature lower than the first temperature.
Description
COMBUSTIBLE HEAT SOURCE FOR A SMOKING ARTICLE
The present invention relates to a combustible heat source for use in a smoking article and
to a smoking article comprising a combustible heat source according to the invention.
A number of smoking articles in which tobacco is heated rather than combusted have been
proposed in the art. One aim of such heated smoking articles is to reduce known harmful smoke
constituents produced by the combustion and pyrolytic degradation of tobacco in conventional
cigarettes. Typically in heated smoking articles, an aerosol is generated by the transfer of heat from
a combustible fuel element or heat source to a physically separate aerosol-generating material,
which may be located within, around or downstream of the heat source. In use the combustible heat
source of the heated smoking article is lit and volatile compounds released from the aerosol-
generating material by heat transfer from the combustible heat source are entrained in air drawn
through the heated smoking article. As the released compounds cool they condense to form an
aerosol that is inhaled by the consumer.
For example, US-A-4,714,082 discloses smoking articles comprising a high density
combustible fuel element, a physically separate aerosol-generating means and a heat-conducting
member. The heat-conducting member contacts the fuel element and the aerosol-generating
means around at least a portion of their peripheral surfaces and conducts heat from the burning fuel
element to the aerosol-generating means. In the smoking articles of US-A-4,714,082, the heat-
conducting member preferably is recessed from the lighting end of the fuel element and forms a
conductive container that encloses the aerosol-generating means along its entire length.
WO-A2-2009/022232 discloses a smoking article comprising a combustible heat source, an
aerosol-generating substrate downstream of the combustible heat source and a heat-conducting
element around and in contact with a rear portion of the combustible heat source and an adjacent
front portion of the aerosol-generating substrate. In the smoking article of WO-A2-2009/022232,
aerosol-generating substrate extends at least about 3 mm downstream beyond the heat-conducting
element.
Advantageously, the combustion temperature of a combustible heat source for use in a
heated smoking article should not be so high as to result in combustion or thermal degradation of
the aerosol forming material during use of the heated smoking article. However, the combustion
temperature of the combustible heat source should also advantageously be sufficiently high to
generate enough heat to release sufficient volatile compounds from the aerosol forming material to
produce an acceptable aerosol, especially during early puffs. To avoid a delay between a consumer
igniting the combustible heat source and an acceptable aerosol being produced, the combustible
heat source should rapidly reach an appropriate combustion temperature after ignition thereof.
A variety of combustible carbon-based and non-carbon-based heat sources for use in
heated smoking articles have previously been proposed in the art. Combustible carbon-based and
non-carbon-based heat sources and methods for producing such heat sources are described in, for
example, US-A-5,076,297 and US-A-5,146,934.
Although many combustible carbon-based heat sources are known in the art, such heat
sources are often difficult to ignite with a conventional yellow flame cigarette lighter. Additionally,
when used in a heated smoking article, known combustible carbon-based heat sources often do not
generate enough heat after ignition thereof to produce an acceptable aerosol during early puffs.
It has been proposed in the art to include oxidizing agents and other additives in combustible
carbon-based heat sources in order to improve the ignition and combustion properties thereof.
However, generally such additives have only been included in small amounts relative to the total
weight of the combustible carbon-based heat source. For example, EP–A1-0 627 174 discloses
that oxidants such as perchlorates, chlorates, nitrates and permanganates may be included in the
carbonaceous heat sources disclosed therein in an amount of between about 0.05% and 10% by
weight of the heat source and preferably between about 0.2% and 4%.
There remains a need for a combustible heat source that generates enough heat to produce
an acceptable aerosol during early puffs of a heated smoking article, but not so much heat as to
result in combustion or thermal degradation of the aerosol-generating material. Moreover, there is a
need for such a combustible heat source that is mechanically and chemically stable at ambient
temperatures and humidity and can be ignited easily and rapidly with a conventional yellow flame
cigarette lighter.
According to the invention there is provided a combustible heat source for a smoking article
comprising carbon and at least one ignition aid selected from the group consisting of metal nitrate
salts having a thermal decomposition temperature of less than about 600°C, chlorates, peroxides,
thermitic materials, intermetallic materials, magnesium, zirconium, and combinations thereof,
wherein the at least one ignition aid is present in an amount of at least about 20 percent by dry
weight of the combustible heat source. The combustible heat source has a first portion and an
opposed second portion, wherein at least part of the combustible heat source between the first
portion and the second portion is wrapped in a combustion resistant wrapper that is one or both of
heat conducting and substantially oxygen impermeable. Upon ignition of the first portion of the
combustible heat source the second portion of the combustible heat source increases in
temperature to a first temperature and during subsequent combustion of the combustible heat
source the second portion of the combustible heat source maintains a second temperature lower
than the first temperature.
As used herein, the term ‘ignition aid’ is used to denote a material that releases one or both
of energy and oxygen during ignition of the combustible heat source.
As used herein, the terms ’first portion’ and ‘second portion’ are used to denote two spaced-
apart regions of the combustible heat source.
As used herein, the term ‘combustion resistant wrapper’ is used to denote a wrapper that
remains substantially intact throughout combustion of the combustible heat source.
As used herein, the term ‘wrapped’ is used to denote that the combustion resistant wrapper
is around and in direct contact with the periphery of the combustible heat source.
According to the invention there is also provided a smoking article comprising a combustible
heat source according to the invention.
In particular, according to the invention there is provided a smoking article comprising a
combustible heat source according to the invention; and an aerosol-generating substrate.
According to the invention there is further provided a smoking article comprising a
combustible heat source according to the invention; and an aerosol-generating substrate
downstream of the combustible heat source, wherein the first portion of the combustible heat source
is an upstream end of the combustible heat source and the second portion of the combustible heat
source is a downstream end of the combustible heat source.
As used herein, the terms ‘upstream’ and ‘front’, and ‘downstream’ and ‘rear’, are used to
describe the relative positions of components, or portions of components, of smoking articles
according to the invention in relation to the direction of air drawn through the smoking articles during
use thereof.
Preferably, at least a rear part of the combustible heat source is wrapped in the combustion
resistant wrapper.
Preferably, at least a rear part of the combustible heat source and at least a front part of the
aerosol-generating substrate are wrapped in the combustion resistant wrapper. In such
embodiments, the combustion resistant wrapper is around and in direct contact with the periphery of
at least a rear part of the combustible heat source and the periphery of at least a front part of the
aerosol-generating substrate.
Preferably, a rear part of the aerosol-generating substrate is not wrapped in the combustion
resistant wrapper.
Preferably, a front part of the combustible heat source is not wrapped in the combustion
resistant wrapper.
Upon ignition of the first portion thereof, combustible heat sources according to the invention
undergo a two-stage combustion process. In an initial first stage combustible heat sources
according to the invention exhibit a ‘boost’ in temperature and in a subsequent second stage the
combustible heat sources undergo sustained combustion at a lower temperature. This two-stage
combustion process is reflected in the temperature profile of the second portion of combustible heat
sources according to the invention. The second portion of combustible heat sources according to
the invention initially increases in temperature to a first ‘boost’ temperature and then subsequently
decreases in temperature to a second ‘cruising’ temperature lower than the first temperature. The
difference between the first temperature and the second temperature of the second portion of
combustible heat sources according to the invention establishes the magnitude of the ‘boost’ in
temperature of the second portion of the combustible heat sources during the first stage of
combustion of the combustible heat sources.
It will be appreciated that the second portion of combustible heat sources according to the
invention may or may not itself combust during the first and second stages of combustion of the
combustible heat sources.
The initial ‘boost’ in temperature of the second portion of combustible heat sources
according to the invention arises due to very rapid propagation of heat throughout the entirety of the
combustible heat sources upon ignition of the first portion thereof. The very rapid propagation of
heat may be the result of a chain reaction in which a part of the combustible heat sources that is
ignited triggers the ignition of an adjacent unignited part of the combustible heat sources.
In use in smoking articles according to the invention, the rapid increase in temperature of the
second portion of combustible heat sources according to the invention to the first ‘boost’
temperature quickly raises the temperature of the aerosol-generating substrate of the smoking
articles to a level at which volatile organic aroma and flavour compounds are generated from the
aerosol-generating substrate. This ensures that smoking articles according to the invention produce
a sensorially acceptable aerosol as of the first puff. The subsequent decrease in temperature of the
second portion of combustible heat sources according to the invention to the second ‘cruising’
temperature ensures that the temperature of the aerosol-generating substrate of the smoking
articles does not reach a level at which combustion or thermal degradation of the aerosol-generating
substrate occurs.
Controlling the temperature of the second portion of combustible heat sources according to
the invention in the manner described above advantageously enables smoking articles according to
the invention to be provided that not only produce a sensorially acceptable aerosol during early
puffs, but in which combustion or thermal degradation of the aerosol-generating substrate is also
substantially avoided.
Combustible heat sources according to the invention comprise at least one ignition aid,
wherein the at least one ignition aid is present in an amount of at least about 20 percent by dry
weight of the combustible heat source.
The quantity of one or both of energy and oxygen released by the at least one ignition aid
during ignition of the combustible heat source must be sufficient to result in the combustible heat
source undergoing the two-stage combustion process described above.
It will be appreciated that the amount of at least one ignition aid that must be included in a
combustible heat source according to the invention in order to achieve the two-stage process
described above will vary depending on the specific at least one ignition aid included in the
combustible heat source.
In general, the greater the quantity of one or both of energy and oxygen released by the at
least one ignition aid per unit mass thereof, the lower the amount of the at least one ignition aid that
must be included in a combustible heat source according to the invention in order to achieve the
two-stage combustion process described above.
In some embodiments, the at least one ignition aid is preferably present in an amount of at
least about 25 percent, more preferably at least about 30 percent, most preferably at least about 40
percent by dry weight of the combustible heat source.
Preferably, the at least on ignition aid is present in an amount of less than about 65 percent
by dry weight of the combustible heat source.
In some embodiments, the at least one ignition aid is preferably present in an amount of at
less than about 60 percent, more preferably less than about 55 by dry weight of the combustible
heat source, most preferably less than about 50 by dry weight of the combustible heat source.
Unless otherwise stated, the temperatures of combustible heat sources according to the
invention given in the following description of the invention are temperatures of the combustible heat
sources as measured in isolation. As used herein, the terms ‘in isolation’ and ‘isolated’ are used to
describe a combustible heat source according to the invention when separate from the remainder of
a smoking article according to the invention.
The temperatures of isolated combustible heat sources according to the invention given in
the following description are measured using a thermocouple inserted a short distance of between
about 1 mm and about 2 mm into a distal region of the second portion of the combustible heat
source.
As used herein, the term ‘distal region’ is used to denote a region of the second portion of
the combustible heat source situated furthest from the first portion of the combustible heat source
that is ignited.
Preferably, the first temperature of the second portion of combustible heat sources according
to the invention is at least about 400°C.
Preferably, the first temperature of the second portion of combustible heat sources according
to the invention is less than or equal to about 1200°C.
Preferably, the first temperature of the second portion of combustible heat sources according
to the invention is between about 400°C and about 1200°C.
The second temperature of the second portion of combustible heat sources according to the
invention is lower than the first temperature of the second portion of combustible heat sources
according to the invention.
Preferably, the second temperature of the second portion of combustible heat sources
according to the invention is at least about 200°C.
Preferably, the second temperature of the second portion of combustible heat sources
according to the invention is less than or equal to about 1000°C.
Preferably, the second temperature of the second portion of combustible heat sources
according to the invention is between about 200°C and about 1000°C.
Preferably, the first temperature of the second portion of combustible heat sources according
to the invention is at least about 400°C and the second temperature of the second portion of
combustible heat sources according to the invention is at least about 200°C.
Preferably, the first temperature of the second portion of combustible heat sources according
to the invention is less than or equal to about 1200°C and the second temperature of the second
portion of combustible heat sources according to the invention is less than or equal to about
1000°C.
Preferably, the second temperature of the second portion of combustible heat sources
according to the invention is between about 200°C and about 1000°C lower than the first
temperature of the second portion of the combustible heat sources. More preferably the second
temperature of the second portion of combustible heat sources according to the invention is
between about 200°C and about 500°C lower than the first temperature of the second portion of the
combustible heat sources.
The initial ‘boost’ in temperature of the second portion of combustible heat sources according
to the invention is preferably initiated at low temperature by igniting the first portion of the
combustible heat sources using a low energy lighter or other ignition means.
Preferably, the ignition temperature of the first portion of combustible heat sources according
to the invention is between about 200°C and about 1000°C, more preferably between about 300°C
and about 800°C, most preferably between about 300°C and about 500°C.
In particularly preferred embodiments of the invention, the first portion of combustible heat
sources according to the invention can be ignited with a conventional yellow flame cigarette lighter in
seconds or less, more preferably in 10 seconds or less, most preferably in 5 seconds or less.
As used herein, the term ‘ignited’ is used to mean that at least part of the first portion of the
combustible heat source is sustainably combusting and that the combustion is propagating to other
parts of the combustible heat source.
The temperature of the second portion of combustible heat sources according to the
invention is not directly influenced by the temperature of the lighter or other ignition means used to
ignite the first portion thereof.
Upon ignition of the first portion of combustible heat sources according to the invention, the
second portion of the combustible heat sources preferably increases in temperature to the first
temperature at a rate of between about 100°C/second and about 1000°C/second, more preferably
at a rate of between about 400°C/second and about 800°C/second.
Upon ignition of the first portion of combustible heat sources according to the invention, the
second portion of the combustible heat sources preferably increases in temperature to the first
temperature within between about L/20 seconds and about 2L seconds, more preferably within
between about L/10 seconds and about L seconds, most preferably within between about
L/10 seconds and about L/2 seconds. As used herein, ‘L’ is used to denote the distance in mm
between the first portion of combustible heat sources according to the invention that is ignited and
the opposed second portion of the combustible heat sources.
For example, where the distance in mm between the first portion and the second portion of a
combustible heat source according to the invention is about 10 mm, upon ignition of the first portion
of the combustible heat source the second portion of the combustible heat source preferably
increases in temperature to the first temperature within between about 0.5 seconds and about
seconds, more preferably within between about 1 second and about 10 seconds, most preferably
within between about 1 second and about 5 seconds.
As described above, having rapidly increased to the first ‘boost’ temperature, the
temperature of the second portion of combustible heat sources according to the invention then
subsequently decreases to the second ‘cruising’ temperature. Preferably, the second portion of
combustible heat sources according to the invention decreases in temperature from the first
temperature to the second temperature within between about 1 second and about 30 seconds, more
preferably between about 1 second and about 20 seconds, most preferably between about 1 second
and about 15 seconds. In particularly preferred embodiments of the invention, the second portion of
combustible heat sources according to the invention decreases in temperature from the first
temperature to the second temperature within between about 1 second and about 10 seconds, more
preferably within between about 1 second and about 5 seconds.
Preferably, the temperature of the second portion of combustible heat sources according to
the invention remains substantially stable at the second temperature for at least about 3 minutes,
more preferably for at least 4 minutes, most preferably for at least 5 minutes.
As used herein, the term ‘substantially stable’ is used to describe a temperature variation of
less than or equal to about 50°C.
The first and second temperatures of the second portion of combustible heat sources
according to the invention as measured within smoking articles according to the invention may be
the same as the first and second temperatures of the second portion of combustible heat sources
according to the invention as measured in isolation.
However, it will be appreciated that in use in smoking articles according to the invention, the
temperature of the second portion of combustible heat sources according to the invention may be
affected by, for example, the composition, quantity, shape, dimensions and location of the aerosol-
generating substrate and other components of the smoking articles. Consequently, the first and
second temperatures of the second portion of combustible heat sources according to the invention
as measured within smoking articles according to the invention may differ from the first and second
temperatures of the second portion of combustible heat sources according to the invention as
measured in isolation.
Combustible heat sources according to the invention may be produced having different
shapes and dimensions depending upon their intended use.
Preferably, combustible heat sources according to the invention are elongate combustible
heat sources. The first portion of elongate combustible heat sources according to the invention is a
first end of the elongate combustible heat sources and the second portion of elongate combustible
heat sources according to the invention is an opposed second end of the elongate combustible heat
sources.
According to a preferred embodiment of the invention there is provided an elongate
combustible heat source for a smoking article comprising carbon and at least one ignition aid
selected from the group consisting of metal nitrate salts having a thermal decomposition
temperature of less than about 600°C, chlorates, peroxides, thermitic materials, intermetallic
materials, magnesium, zirconium, and combinations thereof, wherein the at least one ignition aid is
present in an amount of at least about 20 percent by dry weight of the combustible heat source, the
elongate combustible heat source having an upstream end and an opposed downstream end,
wherein at least part of the elongate combustible heat source between the upstream end and the
downstream end is wrapped in a combustion resistant wrapper that is one or both of heat
conducting and substantially oxygen impermeable and wherein upon ignition of the upstream end of
the elongate combustible heat source the downstream end of the elongate combustible heat source
increases in temperature to a first temperature and wherein during subsequent combustion of the
elongate combustible heat source the downstream end of the elongate combustible heat source
maintains a second temperature lower than the first temperature.
Preferably, elongate combustible heat sources according to the invention are substantially
rod-shaped.
More preferably, elongate combustible heat sources according to the invention are
substantially cylindrical. The first portion of cylindrical combustible heat sources according to the
invention is a first end face of the cylindrical combustible heat sources and the second portion of
cylindrical combustible heat sources according to the invention is an opposed second end face of
the cylindrical combustible heat sources.
According to a particularly preferred embodiment of the invention there is provided a
cylindrical combustible heat source for a smoking article comprising carbon and at least one ignition
aid selected from the group consisting of metal nitrate salts having a thermal decomposition
temperature of less than about 600°C, chlorates, peroxides, thermitic materials, intermetallic
materials, magnesium, zirconium, and combinations thereof, wherein the at least one ignition aid is
present in an amount of at least about 20 percent by dry weight of the combustible heat source, the
cylindrical combustible heat source having an upstream end face and an opposed downstream end
face, wherein at least part of the cylindrical combustible heat source between the upstream end face
and the downstream end face is wrapped in a combustion resistant wrapper that is one or both of
heat conducting and substantially oxygen impermeable and wherein upon ignition of the upstream
end face of the cylindrical combustible heat source the downstream end face of the cylindrical
combustible heat source increases in temperature to a first temperature and wherein during
subsequent combustion of the cylindrical combustible heat source the downstream end face of the
cylindrical combustible heat source maintains a second temperature lower than the first
temperature.
Preferably, elongate combustible heat sources according to the invention are of substantially
circular, oval or elliptical transverse cross-section.
Preferably, elongate combustible heat sources according to the invention have a diameter of
between about 5 mm and about 9 mm, more preferably of between about 7 mm and about 8 mm.
As used herein, the term ‘diameter’ denotes the maximum transverse dimension of elongate
combustible heat sources according to the invention.
Preferably, elongate combustible heat sources according to the invention are of substantially
uniform diameter. However, elongate combustible heat sources according to the invention may
alternatively be tapered so that the diameter of the downstream end of the elongate combustible
heat sources is greater than the diameter of the upstream end of the elongate combustible heat
sources.
Preferably, elongate combustible heat sources according to the invention have a length of
between about 7 mm and about 17 mm, more preferably of between about 11 mm and about
mm, most preferably of between about 11 mm and about 13mm. As used herein, the term
‘length’ denotes the maximum longitudinal dimension of elongate combustible heat sources
according to the invention between the upstream end and the downstream end thereof.
Elongate combustible heat sources according to the invention may be wrapped in a
combustion resistant wrapper along substantially their entire length. Alternatively, elongate
combustible heat sources according to the invention may be wrapped in a combustion resistant
wrapper along only a portion of their length.
Preferably, at least a downstream part of elongate combustible heat sources according to
the invention is wrapped in the combustion resistant wrapper.
Preferably, an upstream part of elongate combustible heat sources according to the
invention is not wrapped in the combustion resistant wrapper.
Combustible heat sources according to the invention may be wrapped in a combustion
resistant wrapper that is heat-conducting.
In use in smoking articles according to the invention, heat generated during combustion of
combustible heat sources according to the invention wrapped in a heat-conducting combustion
resistant wrapper may be transferred by conduction to the aerosol-generating substrate of the
smoking articles via the heat-conducting combustion resistant wrapper. This may significantly
impact the temperature of the second portion of the combustible heat sources. Heat drain exerted
by the conductive heat transfer may significantly lower the temperature of the second portion of the
combustible heat sources. This increases the difference between the first temperature and the
second temperature of the second portion of the combustible heat sources and thus the magnitude
of the ‘boost’ in temperature of the second portion of the combustible heat sources.
In use, in such embodiments the heat drain exerted by conductive heat transfer through the
heat-conducting combustion resistant wrapper may keep the second temperature of the second
portion of the combustible heat sources significantly below the self-ignition temperature of the
second portion of the combustible heat sources.
Alternatively or in addition, combustible heat sources according to the invention may be
wrapped in an oxygen-restricting combustion resistant wrapper that restricts or prevents oxygen
access to the at least part of the combustible heat sources wrapped in the oxygen-restricting
combustion resistant wrapper. For example, combustible heat sources according to the invention
may be wrapped in a substantially oxygen impermeable combustion resistant wrapper.
In such embodiments, the at least part of the combustible heat sources wrapped in the
oxygen-restricting combustion resistant wrapper substantially lacks access to oxygen. Therefore, in
such embodiments, the at least part of the combustible heat sources wrapped in the oxygen-
restricting combustion resistant wrapper does not itself combust during the second stage of
combustion of the combustible heat sources.
Preferably, combustible heat sources according to the invention are wrapped in a
combustion resistant wrapper that is both heat-conducting and oxygen restricting.
Suitable combustion resistant wrappers for use in the invention include, but are not limited
to: metal foil wrappers such as, for example, aluminium foil wrappers, steel foil wrappers, iron foil
wrappers and copper foil wrappers; metal alloy foil wrappers; graphite foil wrappers; glass fibre
wrappers; ceramic fibre wrappers; and certain paper wrappers.
Preferably, combustible heat sources according to the invention are substantially
homogeneous in composition.
However, combustible heat sources according to the invention may alternatively be
composite combustible heat sources.
Preferably, combustible heat sources according to the invention have a carbon content of at
least about 35 percent, more preferably of at least about 40 percent, most preferably of at least
about 45 percent by dry weight of the combustible heat source.
In some embodiments, combustible heat sources according to the invention may be
combustible carbon-based heat sources.
As used herein, the term ‘carbon-based heat source’ is used to describe a heat source
comprised primarily of carbon.
Combustible carbon-based heat sources according to the invention preferably have a carbon
content of at least about 50 percent, more preferably of at least about 60 percent, most preferably of
at least about 80 percent by dry weight of the combustible carbon-based heat source.
Preferably, combustible heat sources according to the invention have a porosity of between
about 20% and about 80%, more preferably of between about 40% and 60%.
Combustible heat sources according to the invention preferably comprise at least one
ignition aid that releases energy during ignition of the first portion of the combustible heat sources.
In such embodiments, the release of energy by the at least one ignition aid upon ignition of
the first portion of the combustible heat sources directly causes a ‘boost’ in temperature during the
first stage of combustion of the combustible heat sources. This is reflected in the temperature
profile of the second portion of the combustible heat sources.
As used herein the term ‘ignition aid’ does not include alkali metal salts of carboxylic acids
(such as alkali metal citrate salts, alkali metal acetate salts and alkali metal succinate salts), alkali
metal halide salts (such as alkali metal chloride salts), alkali metal carbonate salts or alkali metal
phosphate salts. As illustrated in Figure 9, even when present in a large amount relative to the total
weight of the combustible heat source, such alkali metal burn salts do not release enough energy
during ignition of a combustible heat source to cause a ‘boost’ in temperature during the first stage
of combustion of the combustible heat source.
Combustible heat sources according to the invention may comprise one or more ignition aids
consisting of a single element or compound that release energy upon ignition of the first portion of
the combustible heat sources. For example, in certain embodiments combustible heat sources
according to the invention may comprise one or more energetic materials consisting of a single
element or compound that reacts exothermically with oxygen upon ignition of the first portion of the
combustible heat sources. Examples of suitable energetic materials include magnesium and
zirconium.
Alternatively or in addition, combustible heat sources according to the invention may
comprise one or more ignition aids comprising two or more elements or compounds that react with
one another to release energy upon ignition of the first portion of the combustible heat sources. For
example, in certain embodiments combustible heat sources according to the invention may
comprise one or more thermites or thermite composites comprising a reducing agent such as, for
example, a metal, and an oxidizing agent such as, for example, a metal oxide, that react with one
another to release energy upon ignition of the first portion of the combustible heat sources.
Examples of suitable metals include, but are not limited to, magnesium, and examples of suitable
metal oxides include, but are not limited to, iron oxide (Fe O ) and aluminium oxide (Al O )
2 3 2 3
In other embodiments, combustible heat sources according to the invention may comprise
one or more ignition aids comprising other materials that undergo exothermic reactions upon ignition
of the first portion of the combustible heat sources. Examples of suitable metals include
intermetallic materials.
Combustible heat sources according to the invention preferably comprise at least one
ignition aid that releases oxygen during ignition of the first portion of the combustible heat sources.
In such embodiments, the release of oxygen by the at least one ignition aid upon ignition of
the first portion of the combustible heat sources indirectly results in a ‘boost’ in temperature during
the first stage of combustion of the combustible heat sources by increasing the rate of combustion
of the combustible heat sources. This is reflected in the temperature profile of the second portion of
the combustible heat sources.
For example, combustible heat sources according to the invention may comprise one or
more oxidizing agents that decompose to release oxygen upon ignition of the first portion of the
combustible heat sources. Combustible heat sources according to the invention may comprise
organic oxidizing agents, inorganic oxidizing agents or a combination thereof. Examples of suitable
oxidizing agents include: nitrates such as, for example, potassium nitrate, calcium nitrate, strontium
nitrate, sodium nitrate, barium nitrate, lithium nitrate, aluminium nitrate and iron nitrate; chlorates
such as, for example, sodium chlorate and potassium chlorate; organic peroxides such as, for
example, benzoyl peroxide and acetone peroxide; and inorganic peroxides such as, for example,
hydrogen peroxide, strontium peroxide, magnesium peroxide, calcium peroxide, barium peroxide,
zinc peroxide and lithium peroxide;.
Combustible heat sources according to the invention may comprise one or more ignition aids
consisting of a single element or compound that release oxygen upon ignition of the first portion of
the combustible heat sources. Alternatively or in addition, combustible heat sources according to
the invention may comprise one or more ignition aids comprising two or more elements or
compounds that react with one another to release oxygen upon ignition of the first portions of the
combustible heat source.
Combustible heat sources according to the invention may comprise one or more ignition aids
that release both energy and oxygen upon ignition of the first portion of the combustible heat
sources. For example, combustible heat sources according to the invention may comprise one or
more oxidizing agents that decompose exothermically to release oxygen upon ignition of the first
portion of the combustible heat sources.
Alternatively, or in addition, combustible heat sources according to the invention may
comprise one or more first ignition aids that release energy upon ignition of the first portion of the
combustible heat sources and one or more second ignition aids, which are different to the one or
more first ignition aids, that release oxygen upon ignition of the first portion of the combustible heat
sources.
In one embodiment, combustible heat sources according to the invention comprise at least
one metal nitrate salt having a thermal decomposition temperature of less than about 600°C, more
preferably of less than about 400°C.
Preferably, the at least one metal nitrate salt has a decomposition temperature of between
about 150°C and about 600°C, more preferably of between about 200°C and about 400°C.
In such embodiments, when the first portion of the combustible heat sources is exposed to a
conventional yellow flame lighter or other ignition means, the at least one metal nitrate salt
decomposes to release oxygen and energy. This causes an initial boost in the temperature of the
combustible heat sources and also aids in the ignition of the combustible heat sources. Following
total decomposition of the at least one metal nitrate salt, the combustible heat sources continue to
combust at a lower temperature.
The inclusion of at least one metal nitrate salt advantageously results in ignition of the
combustible heat sources being initiated internally, and not only at a point on the surface thereof.
Preferably, the at least one metal nitrate salt is distributed substantially homogeneously throughout
the combustible heat sources.
As previously explained above, in use the boost in temperature of the combustible heat
sources upon ignition of the first portion thereof resulting from the decomposition of the at least one
metal nitrate salt is reflected in the increase in temperature of the second portion of the combustible
heat sources to the first ‘boost’ temperature. In use in smoking articles according to the invention,
this advantageously ensures that sufficient heat is transferred from the combustible heat sources to
the aerosol forming material of the smoking articles to produce an acceptable aerosol during early
puffs thereof.
As also previously explained above, the subsequent decrease in temperature of the
combustible heat sources following the decomposition of the at least one metal nitrate salt is also
reflected in the subsequent decrease in temperature of the second portion of the combustible heat
sources to the second ‘cruising’ temperature. In use in smoking articles according to the invention,
this advantageously ensures that the aerosol-generating substrate of the smoking articles is not
thermally degraded or combusted.
The magnitude and duration of the boost in temperature resulting from the decomposition of
the at least one metal nitrate salt may be advantageously controlled through the nature and amount
of the at least one metal nitrate salt in the combustible heat sources.
Preferably, the at least one metal nitrate salt is present in the combustible heat sources in an
amount of between about 20 percent and about 50 percent by dry weight of the combustible heat
sources.
Preferably, the at least one metal nitrate salt is selected from the group consisting of
potassium nitrate, sodium nitrate, calcium nitrate, strontium nitrate, barium nitrate, lithium nitrate,
aluminium nitrate and iron nitrate.
Preferably, combustible heat sources according to the invention comprise at least two
different metal nitrate salts.
In one embodiment, combustible heat sources according to the invention comprise
potassium nitrate, calcium nitrate and strontium nitrate. Preferably, the potassium nitrate is present
in an amount of between about 5 percent and about 15 percent by dry weight of the combustible
heat sources, the calcium nitrate is present in an amount of between about 2 percent and about 10
percent by dry weight of the combustible heat sources and the strontium nitrate is present in an
amount of between about 15 percent by weight and about 25 percent by dry weight of the
combustible heat sources.
In another embodiment, combustible heat sources according to the invention comprise at
least one peroxide that actively evolves oxygen at a temperature of less than about 600°C, more
preferably at a temperature of less than about 400°C.
Preferably, the at least one peroxide or superoxide actively evolves oxygen at a temperature
of between about 150°C and about 600°C, more preferably of between about 200°C and about
400°C, most preferably at a temperature of about 350°C.
In use, when the first portion of the combustible heat sources is exposed to a conventional
yellow flame lighter or other ignition means, the at least one peroxide decomposes to release
oxygen. This causes an initial boost in the temperature of the combustible heat sources and also
aids in the ignition of the combustible heat sources. Following total decomposition of the at least
one peroxide, the combustible heat sources continue to combust at a lower temperature.
The inclusion of at least one peroxide advantageously results in ignition of the combustible
heat sources being initiated internally, and not only at a point on the surface thereof. Preferably, the
at least one peroxide is distributed substantially homogeneously throughout the combustible heat
sources.
As previously explained above, in use the boost in temperature of the combustible heat
sources upon ignition of the first portion thereof resulting from the decomposition of the at least one
peroxide is reflected in the increase in temperature of the second portion of the combustible heat
sources to the first ‘boost’ temperature. In use in smoking articles according to the invention, this
advantageously ensures that sufficient heat is transferred from the combustible heat sources to the
aerosol forming material of the smoking articles according to the invention to produce an acceptable
aerosol during early puffs thereof.
As also previously explained above, the subsequent decrease in temperature of the
combustible heat sources following the decomposition of the at least one peroxide is also reflected
in the subsequent decrease in temperature of the second portion of the combustible heat sources to
the second ‘cruising’ temperature. In use in smoking articles according to the invention, this
advantageously ensures that the aerosol-generating substrate of the smoking articles is not
thermally degraded or combusted.
The magnitude and duration of the boost in temperature resulting from the decomposition of
the at least one peroxide may be advantageously controlled through the nature and amount of the at
least one peroxide in the combustible heat sources.
The at least one peroxide is preferably present in the combustible heat sources in an amount
of between about 20 percent and about 50 percent by dry weight of the combustible heat sources,
more preferably in an amount of between about 30 percent and about 50 percent by dry weight of
the combustible heat sources.
Suitable peroxides for inclusion in combustible heat sources according to the invention
include, but are not limited to, calcium peroxide, strontium peroxide, magnesium peroxide, barium
peroxide, lithium peroxide, and zinc peroxide.
Preferably, the at least one peroxide is selected from the group consisting of calcium
peroxide, strontium peroxide, magnesium peroxide, barium peroxide and combinations thereof. The
inclusion of at least one peroxide is particularly preferred where combustible heat sources according
to the invention are combustible carbon-based heat sources.
Combustible heat sources according to the invention may be formed from one or more
suitable carbon-containing materials. Suitable carbon-containing materials are well known in the art
and include, but are not limited to, carbon powder.
If desired, one or more binders may be combined with the one or more carbon containing
materials. The one or more binders may be organic binders, inorganic binders or a combination
thereof. Suitable known organic binders include but are not limited to: gums such as, for example,
guar gum; modified celluloses and cellulose derivatives such as, for example, methyl cellulose,
carboxymethyl cellulose, hydroxypropyl cellulose and hydroxypropyl methylcellulose; wheat flour;
starches; sugars; vegetable oils; and combinations thereof.
Suitable known inorganic binders include, but are not limited to: clays such as, for example,
bentonite and kaolinite; alumino-silicate derivatives such, for example, as cement, alkali activated
alumino-silicates; alkali silicates such as, for example, sodium silicates and potassium silicates;
limestone derivatives such as, for example, lime and hydrated lime; alkaline earth compounds and
derivatives such as, for example, magnesia cement, magnesium sulfate, calcium sulfate, calcium
phosphate and dicalcium phosphate; and aluminium compounds and derivatives such as, for
example, aluminium sulphate.
In one embodiment, combustible heat sources according to the invention are formed from a
mixture of: carbon powder; modified cellulose, such as, for example, carboxymethyl cellulose; flour
such as, for example, wheat flour; and sugar such as, for example, white crystalline sugar derived
from beet.
In another embodiment, combustible heat sources according to the invention are formed
from a mixture of carbon powder, modified cellulose, such as, for example, carboxymethyl cellulose;
and optionally bentonite.
Instead of, or in addition to one or more binders, other additives may also be combined with
the one or more carbon containing materials in order to improve the properties of the combustible
heat sources. Suitable additives include, but are not limited to, additives to promote consolidation of
the combustible heat sources (for example, sintering aids, such as calcium carbonate), additives to
promote combustion of the combustible heat sources (for example, potassium and, alkali metal burn
salts, for example potassium salts, such as potassium chloride and potassium citrate) and additives
to promote decomposition of one or more gases produced by combustion of the combustible heat
sources, for example catalysts, such as copper oxide (CuO), iron oxide (Fe O ), iron oxide silicate
powder and aluminium oxide (Al O ).
The one or more carbon containing materials are preferably mixed with the one or more
binders and other additives, where included, and pre-formed into a desired shape. The mixture of
one or more carbon containing materials, one or more binders and other additives may be pre-
formed into a desired shape using any suitable known ceramic forming methods such as, for
example, slip casting, extrusion, injection moulding and die compaction or pressing. Preferably, the
mixture is pre-formed into a desired shape by pressing or extrusion.
Preferably, the mixture of one or more carbon containing materials, one or more binders and
other additives is pre-formed into a cylindrical rod. However, it will be appreciated that the mixture of
one or more carbon containing materials, one or more binders and other additives may be pre-
formed into other desired shapes.
After formation, the cylindrical rod or other desired shape is preferably dried to reduce its
moisture content.
In a first embodiment of the heat source production process, the dried cylindrical rod is
pyrolysed in a non-oxidizing atmosphere at a temperature sufficient to carbonise the one or more
binders, where present, and substantially eliminate any volatiles in the cylindrical rod or other shape.
Preferably, the cylindrical rod or other desired shape is pyrolysed in a nitrogen atmosphere at a
temperature of between about 700°C and about 900°C. At least one metal nitrate salt may be
incorporated in combustible heat sources according to the invention by including at least one metal
nitrate precursor in the mixture of one or more carbon containing materials, one or more binders and
other additives and then subsequently converting the at least one metal nitrate precursor into at
least one metal nitrate salt in-situ, by treating the pyrolysed pre-formed cylindrical rod or other shape
with an aqueous solution of nitric acid.
The at least one metal nitrate precursor may be any metal or metal-containing compound
such as, for example, metal oxide or metal carbonate, that reacts with nitric acid to form a metal
nitrate salt. Suitable metal nitrate salt precursors include, but are not limited to calcium carbonate,
potassium carbonate, calcium oxide, strontium carbonate, lithium carbonate and dolomite (calcium
magnesium carbonate).
Preferably, the concentration of the aqueous solution of nitric acid is between about 20
percent and about 50 percent by weight, more preferably of between about 30 percent and about 40
percent by weight. As well as converting the at least one metal nitrate precursor to at least one
metal nitrate salt, treatment of combustible heat sources according to the invention with nitric acid
advantageously enhances the porosity of the combustible heat sources, activates the carbon
structure by increasing the surface area thereof and results in a substantially homogeneous
distribution of the at least one metal nitrate salt throughout the combustible heat sources.
The aqueous solution of nitric acid may further comprise one or more water-soluble metal
nitrate salts having a thermal decomposition temperature of less than about 400°C. For example,
the aqueous solution of nitric acid may further comprise potassium nitrate. As well as converting the
at least one metal nitrate precursor to at least one metal nitrate salt, treatment of combustible heat
sources according to the invention with nitric acid comprising one or more substantially water-
soluble metal nitrate salts advantageously infiltrates the combustible heat sources with the one or
more substantially water-soluble nitrates.
Alternatively or in addition, at least one metal nitrate salt may be incorporated in combustible
heat sources according to the invention by directly infiltrating the pyrolysed pre-formed shape with a
solution comprising the at least one metal nitrate salt.
Preferably, combustible heat sources according to the invention are infiltrated with an
aqueous solution of the at least one metal nitrate salt. In a particularly preferred embodiment of the
invention, combustible heat sources according to the invention are infiltrated with an aqueous
solution comprising potassium nitrate, calcium nitrate and strontium nitrate.
Combustible heat sources according to the invention are preferably infiltrated with aqueous
solutions comprising at least one metal nitrate salt. Preferably, the at least one metal nitrate salt has
a solubility in water of at least about 30 g/100 mL at 25°C.
However, it will be appreciated that combustible heat sources according to the invention may
alternatively be infiltrated with non-aqueous solutions comprising at least one metal nitrate salt.
In a second embodiment of the heat source production process, the one or more carbon
containing materials, one or more binders, other additives and at least one ignition aid are mixed
and formed into a desired shape by, for example, pressing or extrusion, without a pyrolisation step.
This method is preferably used where the at least one ignition aid comprises one or materials
selected from the group consisting of peroxides, thermites, intermetallics, magnesium and
zirconium.
Preferably, combustible heat sources according to the invention have a mass of between
about 300 mg and about 500 mg, more preferably of between about 400 mg and about 450 mg prior
to infiltration with a solution comprising the at least one metal nitrate salt.
The porosity of combustible heat sources has a substantial impact on their ignition and
combustion properties. Combustible heat sources according to the invention preferably have a
porosity of between about 20 percent and about 80 percent, more preferably of between about 20
percent and 60 percent. Where the combustible heat source comprises at least one metal nitrate
salt, this advantageously allows oxygen to diffuse into the mass of the combustible heat source at a
rate sufficient to sustain combustion as the at least one metal nitrate salt decomposes and
combustion proceeds.
The required porosity may be readily achieved during production of combustible heat
sources according to the invention using conventional methods and technology, and may be
measured by Hg-porosimetry and He-pycnometry in a known manner.
For example, combustible heat sources according to the invention having a porosity of
between about 20 percent and about 80 percent may be prepared by pyrolysis of a mixture
comprising a carbon-containing material and one or more suitable known pore formers. Suitable
known pore formers include, but are not limited to, corn, cellulose flakes, stearate, carbonates,
polyethylene and polypropylene beads, wood pellets and cork.
Alternatively or in addition, combustible heat sources according to the invention may be
treated with an acid in order to achieve a desired porosity.
Advantageously, combustible heat sources according to the invention have an apparent
density of between about 0.6 g/cm and about 1.0 g/cm .
Combustible heat sources according to the invention may be ‘blind’ combustible heat
sources. As used herein, the term ‘blind combustible heat source’ is used to denote a combustible
heat source that does not contain any longitudinal airflow channels. As used herein, the term
‘longitudinal airflow channel’ is used to denote a hole passing through an inner portion of the
combustible heat source and extending along the entire length of the combustible heat source.
Alternatively, combustible heat sources according to the invention may comprise at least one
longitudinal airflow channel. For example, combustible heat sources according to the invention
comprise one, two or three longitudinal airflow channels. In such embodiments, combustible heat
sources according to the invention preferably comprise a single longitudinal airflow channel, more
preferably a single substantially central longitudinal airflow channel. The diameter of the single
longitudinal airflow channel is preferably between about 1.5 mm and about 3 mm.
The inner surface of the at least one longitudinal airflow channel of combustible heat sources
according to the invention may be partially or entirely coated. Preferably, the coating covers the
inner surface of all longitudinal airflow channels.
Preferably, the coating comprises a layer of solid particulate matter and is substantially air
impermeable. Advantageously, the substantially air impermeable coating is of low thermal
conductivity. The coating may be formed from one or more suitable materials that are substantially
thermally stable and non-combustible at the combustion temperature of the combustible heat
sources. Suitable materials are known in the art and include, for example, clays, metal oxides, such
as iron oxide, alumina, titania, silica, silica-alumina, zirconia and ceria, zeolites, zirconium
phosphate and other ceramic materials or combinations thereof. Preferred coating materials include
clays, glasses and iron oxide. If desired, catalytic ingredients, such as ingredients that promote the
oxidation of carbon monoxide to carbon dioxide, may be incorporated in the coating material.
Suitable catalytic ingredients include, for example, platinum, palladium, transition metals and their
oxides.
Preferably, the coating has a thickness of between about 30 microns and about 200 microns,
more preferably of between about 50 microns and about 150 microns.
The coating may be applied to the inner surface of the at least one longitudinal airflow
channel of the combustible heat sources by any suitable method, such as the methods described in
US-A-5,040,551. For example, the inner surface of each longitudinal airflow channel may be
sprayed, wetted or painted with a solution or a suspension of the coating. Alternatively, the coating
may be provided by insertion of a liner into one or more longitudinal airflow channels. For example,
a substantially air impermeable hollow tube may be inserted into each longitudinal airflow channel.
In one embodiment, the coating is applied to the inner surface of the at least one longitudinal
airflow channel of the combustible heat sources by the process described in WO-A2-2009/074870
as the combustible heat sources are extruded.
Optionally, combustible heat sources according to the invention may comprise one or more,
preferably up to and including six, longitudinal grooves that extend along part of or the entire
periphery of the combustible heat sources. If desired, combustible heat sources according to the
invention may comprise one or more longitudinal grooves and at least one longitudinal airflow
channel. Alternatively, combustible heat sources according to the invention may be blind
combustible heat sources comprising one or more longitudinal grooves.
Combustible heat sources according to the invention are particularly suited for use in
smoking articles of the type disclosed in WO-A-2009/022232. However, it will be appreciated that
combustible heat sources according to the invention may also be used in smoking articles having
different constructions.
Smoking articles according to the invention may comprise a combustible heat source
according to the invention and an aerosol-generating substrate located immediately downstream of
the combustible heat source. In such embodiments, the aerosol-generating substrate may abut the
second portion of the combustible heat source.
Alternatively, smoking articles according to the invention may comprise a combustible heat
source according to the invention and an aerosol-generating substrate located downstream of the
combustible heat source, wherein the aerosol-generating substrate is spaced apart from the
combustible heat source.
Preferably, smoking articles according to the invention comprise a combustible heat source
according to the invention wrapped in a heat-conducting and oxygen-restricting combustion resistant
wrapper.
Preferably, at least a rear part of the combustible heat source of smoking articles according
to the invention is wrapped in the combustion resistant wrapper.
Smoking articles according to the invention may comprise a combustible heat source
according to the invention that is wrapped in a combustion resistant wrapper along substantially its
entire length.
However, preferably only a rear part of the combustible heat source of smoking articles
according to the invention is wrapped in the combustion resistant wrapper, such that a front part of
the combustible heat source is not wrapped in the combustion resistant wrapper.
Preferably, the front part of the combustible heat source not wrapped in the combustion
resistant wrapper is between about 4 mm and about 15 mm in length, more preferably between
about 4 mm and about 8 mm in length.
Preferably, the rear part of the combustible heat source wrapped in the combustion resistant
wrapper is between about 2 mm and about 8 mm in length, more preferably between about 3 mm
and about 5 mm in length.
Preferably, at least a rear part of the combustible heat source and at least a front part of the
aerosol-generating substrate of smoking articles according to the invention are wrapped in the
combustion resistant wrapper. In such embodiments, the combustion resistant wrapper is around
and in direct contact with the periphery of at least a rear part of the combustible heat source and the
periphery of at least a front part of the aerosol-generating substrate of the smoking articles. As
previously described above, where the combustion resistant wrapper is heat-conducting, the
combustion resistant wrapper thus provides a thermal link between these two components of the
smoking articles.
At least a rear part of the combustible heat source and the entire aerosol-generating
substrate of smoking articles according to the invention may be wrapped in the combustion resistant
wrapper.
However, preferably only a front part of the aerosol-generating substrate of smoking articles
according to the invention is wrapped in the combustion resistant wrapper, such that a rear part of
the aerosol-generating substrate is not wrapped in the combustion resistant wrapper.
Preferably, the rear part of the aerosol-generating substrate not wrapped in the combustion
resistant wrapper is at least about 3 mm in length. In other words, the aerosol-generating substrate
preferably extends at least about 3 mm downstream beyond the combustion resistant wrapper.
Preferably, the aerosol-generating substrate has a length of between about 5 mm and about
mm, more preferably of between about 8 mm and about 12 mm. Preferably, the front part of the
aerosol-generating substrate wrapped in the combustion resistant wrapper is between about 2 mm
and about 10 mm in length, more preferably between about 3 mm and about 8 mm in length, most
preferably between about 4 mm and about 6 mm in length. Preferably, the rear part of the aerosol-
generating substrate not wrapped in the combustion resistant wrapper is between about 3 mm and
about 10 mm in length. In other words, the aerosol-generating substrate preferably extends
between about 3 mm and about 10 mm downstream beyond the combustion resistant wrapper.
More preferably, the aerosol-generating substrate extends at least about 4 mm downstream beyond
the combustion resistant wrapper.
Preferably, the aerosol-generating substrate of smoking articles according to the invention
comprises at least one aerosol former and a material capable of emitting volatile compounds in
response to heating. The aerosol may be visible or invisible and includes vapours as well as gases
and liquid droplets of condensed vapours.
The at least one aerosol former may be any suitable known compound or mixture of
compounds that, in use, facilitates formation of a dense and stable aerosol and that is substantially
resistant to thermal degradation at the operating temperature. Suitable aerosol formers are well
known in the art and include, for example, polyhydric alcohols, esters of polyhydric alcohols, such as
glycerol mono-, di- or triacetate, and aliphatic esters of mono-, di- or polycarboxylic acids, such as
dimethyl dodecanedioate and dimethyl tetradecanedioate. Preferred aerosol formers for use in
smoking articles according to the invention are polyhydric alcohols or mixtures thereof, such as
triethylene glycol, 1,3-butanediol and, most preferred, glycerine.
Preferably, the material capable of emitting volatile compounds in response to heating is a
charge of plant-based material, more preferably a charge of homogenised plant-based material. For
example, the aerosol-generating substrate may comprise one or more materials derived from plants
including, but not limited to, tobacco, tea, for example green tea, peppermint, laurel, eucalyptus,
basil, sage, verbena and tarragon. The plant based-material may comprise additives including, but
not limited to, humectants, flavourants, binders and mixtures thereof. Preferably, the plant-based
material consists essentially of tobacco material, most preferably homogenised tobacco material.
Smoking articles according to the invention preferably further comprise an expansion
chamber downstream of the aerosol-generating substrate. The inclusion of an expansion chamber
advantageously allows further cooling of the aerosol generated by heat transfer from the
combustible heat source to the aerosol-generating substrate. The expansion chamber also
advantageously allows the overall length of smoking articles according to the invention to be
adjusted to a desired value, for example to a length similar to that of conventional cigarettes,
through an appropriate choice of the length of the expansion chamber. Preferably, the expansion
chamber is an elongate hollow tube.
Smoking articles according to the invention may also further comprise a mouthpiece
downstream of the aerosol-generating substrate and, where present, downstream of the expansion
chamber. The mouthpiece may, for example, comprise a filter having one or more segments. The
filter may comprise one or more segments of cellulose acetate, paper or other suitable known
filtration materials. Preferably, the integral mouthpiece is of low filtration efficiency, more preferably
of very low filtration efficiency. Alternatively or in addition, the filter may comprise one or more
segments comprising absorbents, adsorbents, flavourants, and other aerosol modifiers and
additives used in filters for conventional cigarettes, or combinations thereof.
If desired, ventilation may be provided at a location downstream of the combustible heat
source of smoking articles according to the invention. For example, where present, ventilation may
be provided at a location along the integral mouthpiece of smoking articles according to the
invention.
Smoking articles according to the invention may be assembled using known methods and
machinery.
The invention will be further described, by way of example only, with reference to the
accompanying drawings in which:
Figure 1 shows a schematic longitudinal cross-section of a smoking article according to the
invention;
Figure 2a shows a graph of the temperature of the downstream end of the combustible heat
source of a smoking article according to a first embodiment of the invention upon ignition of the
upstream end thereof.
Figure 2b shows a graph of the temperature of the downstream end of the combustible heat
source of the smoking article according to the first embodiment of the invention during subsequent
combustion of the combustible heat source;
Figure 3a shows a graph of the temperature of the aerosol-generating substrate of the
smoking article according to the first embodiment of the invention during combustion of the
combustible heat source thereof;
Figure 3b shows a graph of the absorbance at 320nm of the aerosol generated by the
smoking article according to the first embodiment of the invention as a function of puff number;
Figure 4a shows a graph of the temperature of the downstream end of the combustible heat
source of a smoking article according to a second embodiment of the invention upon ignition of the
upstream end thereof;
Figure 4b shows a graph of the temperature of the downstream end of the combustible heat
source of the smoking article according to the second embodiment of the invention during
subsequent combustion of the combustible heat source;
Figure 5a shows a graph of the temperature of the aerosol-generating substrate of the
smoking article according to the second embodiment of the invention;
Figure 5b shows a graph of the absorbance at 320nm of the aerosol generated by the
smoking article according to the second embodiment of the invention as a function of puff number;
Figure 6a shows a plan view of the upstream end of the combustible heat source of a
smoking article according to a third embodiment of the invention; and
Figure 6b shows a longitudinal cross-section of the combustible heat source of a smoking
article according to a third embodiment of the invention;
Figure 7 shows a graph of the temperature of the downstream end of the combustible heat
source of a smoking article according to a fourth embodiment of the invention upon ignition of the
upstream end thereof;
Figure 8 shows a graph of the temperature of the downstream end of the combustible heat
sources of: (i) a smoking article according to a fifth embodiment of the invention; (ii) a smoking
article according to a sixth embodiment of the invention; (iii) a first comparative smoking article; and
(iv) a second comparative smoking article upon ignition of the upstream ends thereof;
Figure 9a shows a graph of the temperature of the downstream end of the combustible heat
source of a smoking article according to a seventh embodiment of the invention upon ignition of the
upstream end thereof;
Figure 9b shows a graph of the temperature of the downstream end of the combustible heat
source of the smoking article according to the seventh embodiment of the invention during
subsequent combustion of the combustible heat source;
Figure 10 shows a graph of the temperature of the downstream end of the combustible heat
source of a smoking article according to an eighth embodiment of the invention upon ignition of the
upstream end thereof;
Figure 11 shows a graph of the temperature of the downstream end of the combustible heat
source of a smoking article according to a ninth embodiment of the invention upon ignition of the
upstream end thereof; and
Figure 12 shows a graph of the combustible heat sources of: (i) a smoking article according
to the ninth embodiment of the invention; (ii) a third comparative smoking article; and (iii) a fourth
comparative smoking article upon ignition of the upstream ends thereof; and
Figure 13 shows a graph of the combustible heat sources of: (i) a smoking article according
to the fourth embodiment of the invention; (ii) a fifth comparative smoking article; and (iii) a sixth
comparative smoking article upon ignition of the upstream ends thereof.
In the graphs of Figures 2a, 2b, 3a, 4a, 4b, 5a, 7, 8, 9a, 9b, 10, 11, 12 and 13 time zero
indicates the time of the first puff.
The smoking article 2 shown in Figure 1 has an overall length of 70 mm, a diameter of
7.9 mm and comprises a combustible heat source 4 according to the invention, an aerosol-
generating substrate 6, an elongate expansion chamber 8 and a mouthpiece 10. As shown in
Figure 1, the combustible heat source 4, aerosol-generating substrate 6, elongate expansion
chamber 8 and mouthpiece are in abutting coaxial alignment and are overwrapped in an outer
wrapper of cigarette paper 12 of low air permeability.
The combustible heat-source 4 is 11 mm in length and 7.8 mm in diameter and comprises a
central airflow channel 16 of circular cross-section that extends longitudinally through the
combustible heat source 4. A substantially air impermeable, heat resistant, partially sintered glass
coating 14 having a thickness of 80 microns is provided on the inner surface of the central airflow
channel 16, which is 2 mm in diameter.
The aerosol-generating substrate 6, which is 10 mm in length and 7.8 mm in diameter and
has density of 0.8 g/cm , is located immediately downstream of the combustible heat source 4. The
aerosol-generating substrate 6 comprises a cylindrical plug of homogenised tobacco material 18
comprising glycerine as an aerosol former and circumscribed by filter plug wrap 20. The
homogenised tobacco material 18 consists of longitudinally aligned filaments of extruded tobacco
material.
A combustion resistant wrapper 22 consisting of a tube of aluminium foil having a thickness
of 20 microns, a length of 9 mm and a diameter of 7.8 mm surrounds and is in contact with a rear
part 4b of the combustible heat source 4 of 4 mm in length and an abutting front part 6a of the
aerosol-generating substrate 6 of 5 mm in length. As shown in Figure 1, a front part 4a of the
combustible heat source 4 of 7 mm in length and a rear part 6b of the aerosol-generating substrate
6 of 5 mm in length are not surrounded by the combustion resistant wrapper 22.
The elongate expansion chamber 8, which is 42 mm in length and 7.8 mm in diameter, is
located downstream of the aerosol-generating substrate 6 and comprises a cylindrical open-ended
tube of cardboard 24. The mouthpiece 10 of the smoking article 2, which is 7 mm in length and
7.8 mm in diameter, is located downstream of the expansion chamber 8 and comprises a cylindrical
plug of cellulose acetate tow 26 of very low filtration efficiency circumscribed by filter plug wrap 28.
The mouthpiece 10 may be circumscribed by tipping paper (not shown).
In use, the consumer ignites the combustible heat source 4 and then draws air through the
central airflow channel 16 downstream towards the mouthpiece 10. The front part 6a of the aerosol-
generating substrate 6 is heated primarily by conduction through the abutting non-combusting rear
part 4b of the combustible heat source 4 and the combustion resistant wrapper 22. The drawn air is
heated as it passes through the central airflow channel 16 and then heats the aerosol-generating
substrate 6 by convection. The heating of the aerosol-generating substrate 6 releases volatile and
semi-volatile compounds including the aerosol former from the aerosol-generating substrate 18,
which are entrained in the heated drawn air as it flows through the aerosol-generating substrate.
The heated air and entrained compounds pass downstream through the expansion chamber 8, cool
and condense to form an aerosol that passes through the mouthpiece into the mouth of the
consumer at about ambient temperature.
To make the smoking article 2, a rectangular piece of the combustion resistant wrapper 22 is
glued to cigarette paper 12. The combustible heat source 4, the plug of the aerosol-generating
substrate 6 and the expansion chamber 8 are suitably aligned and positioned on the cigarette paper
12 with the attached combustion resistant wrapper 22. The cigarette paper 12 with the attached
combustion resistant wrapper 22 is wrapped around the rear part 4b of the combustible heat source
4, the aerosol-generating substrate 6 and the expansion chamber 8 and glued. The mouthpiece 10
is attached to the open end of the expansion chamber using known filter combining technology.
Smoking articles according to a first embodiment of the invention having the structure shown
in Figure 1 and described above were assembled using combustible heat sources according to a
first embodiment of the invention produced in accordance with Example 1.
Smoking articles according to a second embodiment of the invention having the structure
shown in Figure 1 and described above were assembled using combustible heat sources according
to a second embodiment of the invention produced in accordance with Example 2.
Smoking articles according to a third embodiment of the invention having the structure
shown in Figure 1 and described above were assembled using combustible heat sources according
to a third embodiment of the invention produced in accordance with Example 3.
Smoking articles according to a fourth embodiment of the invention having the structure
shown in Figure 1 and described above were assembled using combustible heat sources according
to a fourth embodiment of the invention produced in accordance with Example 4.
Smoking articles according to a fifth embodiment of the invention having the structure shown
in Figure 1 and described above were assembled using combustible heat sources according to a
fifth embodiment of the invention produced in accordance with Example 5.
Smoking articles according to a sixth embodiment of the invention having the structure
shown in Figure 1 and described above were assembled using combustible heat sources according
to a fifth embodiment of the invention produced in accordance with Example 5.
First comparative smoking articles having the structure shown in Figure 1 and described
above were assembled using first comparative combustible heat sources produced in accordance
with Example 5.
Second comparative smoking articles having the structure shown in Figure 1 and described
above were assembled using second comparative combustible heat sources produced in
accordance with Example 5.
Smoking articles according to a seventh embodiment of the invention having the structure
shown in Figure 1 and described above were assembled using combustible heat sources according
to a seventh embodiment of the invention produced in accordance with Example 6.
Smoking articles according to an eighth embodiment of the invention having the structure
shown in Figure 1 and described above were assembled using combustible heat sources according
to an eighth embodiment of the invention produced in accordance with Example 7.
Smoking articles according to a ninth embodiment of the invention having the structure
shown in Figure 1 and described above were assembled using combustible heat sources according
to a ninth embodiment of the invention produced in accordance with Example 8.
Third comparative smoking articles having the structure shown in Figure 1 and described
above were assembled using third comparative combustible heat sources produced in accordance
with Example 9.
Fourth comparative smoking articles having the structure shown in Figure 1 and described
above were assembled using fourth comparative combustible heat sources produced in accordance
with Example 9.
Fifth comparative smoking articles having the structure shown in Figure 1 and described
above were assembled using fifth comparative combustible heat sources produced in accordance
with Example 10.
Sixth comparative smoking articles having the structure shown in Figure 1 and described
above were assembled using sixth comparative combustible heat sources produced in accordance
with Example 10.
EXAMPLE 1
Combustible heat sources according to a first embodiment of the invention were prepared by
mixing 525 g of carbon powder, 225 g of calcium carbonate (CaCO ), 51.75 g of potassium citrate,
84 g of modified cellulose, 276 g of flour, 141.75 g of sugar and 21 g of corn oil with 579 g of
deionised water to form an aqueous slurry.
The aqueous slurry was then extruded through a die having a central die orifice of circular
cross-section with a diameter of 8.7 mm to form cylindrical rods having a length of about 20-22 cm
and a diameter of about 9.1-9.2 mm. A single longitudinal air flow passageway was formed in the
cylindrical rods by a mandrel of circular cross-section with an outer diameter of approximately 2 mm
mounted centrally in the die orifice. During extrusion of the cylindrical rods, a glass coating slurry
was pumped through a feed passageway extending through the centre of the mandrel to form a thin
coating of about 150-300 microns on the inner surface of the single longitudinal air flow
passageway.
The cylindrical rods were dried at about 20-25°C, 40-50 percent relative humidity, for
between about 12 hours and about 72 hours and then pyrolysed in a nitrogen atmosphere at 750°C
for about 240 minutes.
After pyrolysis, the cylindrical rods were cut and shaped to a defined diameter using a
grinding machine to form individual combustible heat sources having a length of about 11 mm, a
diameter of about 7.8 mm and a dry mass of about 400 mg.
The individual combustible heat sources were dried at 130°C for approximately 1 hour and
then placed in an aqueous solution of nitric acid having a concentration of 38 percent by weight,
which was saturated with potassium nitrate (KNO ).
After approximately 5 minutes, the individual combustible heat sources were removed from
the solution and dried at 130°C for approximately 1 hour.
After drying the individual combustible heat sources were placed once again in an aqueous
solution of nitric acid having a concentration of 38 percent by weight, which was saturated with
potassium nitrate (KNO ).
After approximately 5 minutes, the individual combustible heat sources were removed from
the solution and dried at 130°C for approximately 1 hour, then at 160°C for approximately 1 hour
and finally at 200°C for approximately 1 hour.
The dried individual combustible heat sources had an ignition aid (potassium nitrate) content
of about 39 percent by dry weight of the combustible heat source.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the first embodiment of the invention upon ignition of the upstream end of the
combustible heat source was measured in the smoking article using a thermocouple attached to the
surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the
aerosol-generating substrate thereof. The results are shown in Figure 2a.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the first embodiment of the invention during subsequent combustion of the combustible
heat source was also measured in the smoking article using a thermocouple attached to the surface
of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the aerosol-
generating substrate thereof. The results are shown in Figure 2b.
The temperature of the aerosol-generating substrate of the smoking article according to the
first embodiment of the invention during combustion of the combustible heat source was measured
using a thermocouple attached to the surface of the smoking article at a position (illustrated by line
P in Figure 1) 2 mm downstream of the combustible heat source. The results are shown in Figure
The absorbance of the aerosol generated during each puff of the smoking article according
to the first embodiment of the invention was measured using a UV-Visible optical spectrometer with
an optical cell set up to record data in the Near UV region at 320 nm. The results, which are
indicative of the density of the aerosol generated, are shown in Figure 3b.
To generate the profiles shown in Figures 2a-3b, the combustible heat sources of smoking
articles according to the first embodiment of the invention were ignited using a conventional yellow
flame lighter. Puffs of 55 ml (puff volume) were then taken in 2 seconds (puff duration) every 30
seconds (puff frequency) using a smoking machine.
EXAMPLE 2
Combustible heat sources according to a second embodiment of the invention were
prepared by mixing 639 g of carbon powder, 51.75 g of potassium citrate, 195.5 g of copper oxide
(CuO), 111 g of corn, 84 g of modified cellulose, 276 g of flour, 21 g of corn oil and 141.75 g of
sugar with 579 g of deionised water to form an aqueous slurry.
The aqueous slurry was then extruded through a die having a central die orifice of circular
cross-section with a diameter of 8.7 mm to form cylindrical rods having a length of about 20-22 cm
and a diameter of about 9.1-9.2 mm. A single longitudinal air flow passageway was formed in the
cylindrical rods by a mandrel of circular cross-section with an outer diameter of approximately 2 mm
mounted centrally in the die orifice. During extrusion of the cylindrical rods, a glass coating slurry
was pumped through a feed passageway extending through the centre of the mandrel to form a thin
coating of about 150-300 microns on the inner surface of the single longitudinal air flow
passageway.
The cylindrical rods were dried at about 20-25°C, 40-50 percent relative humidity, for
between about 12 hours and about 72 hours and then pyrolysed in a nitrogen atmosphere at 750°C
for about 240 minutes.
After pyrolysis, the cylindrical rods were cut and rectified down to a defined diameter using a
grinding machine to form individual combustible heat sources having a length of about 11 mm, a
diameter of about 7.8 mm and a dry mass of about 425 mg. The results of an elemental analysis of
the combustible heat sources are given in Table 1 below:
Element Amount (weight percent)
Calcium 1
Potassium 1.9
Copper 16.6
Carbon 80
Table 1
X-ray diffraction analysis of the combustible heat sources indicated that the majority of the
CuO is reduced to Cu metal during pyrolysis, with minor phases of Cu O and CuO present.
The individual combustible heat sources were dried at 130°C for approximately 1 hour and
then placed in an aqueous solution comprising 34 percent by weight of strontium nitrate (Sr(NO ) ),
16 percent by weight of potassium nitrate (KNO ) and 11 percent by weight of calcium nitrate
(Ca(NO ) *4H O), which was pre-heated to a temperature of between about 80°C to about 85°C.
3 2 2
After approximately 15 minutes, the individual combustible heat sources were removed from
the solution and placed in deionised water for approximately 5 to 30 seconds. The individual
combustible heat sources were then removed from the deionised water and dried, first at ambient
temperature for approximately 1 hour and then at 130°C for approximately 1 hour.
The dried individual combustible heat sources had an ignition aid (strontium nitrate,
potassium nitrate and calcium nitrate) content of about 33 percent by dry weight of the combustible
heat source.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the second embodiment of the invention upon ignition of the upstream end of the
combustible heat source was measured in the smoking article using thermocouples attached to the
surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the
aerosol-generating substrate thereof. The results are shown in Figure 4a.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the second embodiment of the invention during subsequent combustion of the
combustible heat source was also measured in the smoking article using a thermocouple attached
to the surface of the smoking article at a position (illustrated by line T1 in Figure 1) 1 mm upstream
of the aerosol-generating substrate thereof. The results are shown in Figure 4b.
The temperature of the aerosol-generating substrate of the smoking article according to the
second embodiment of the invention during combustion of the combustible heat source was
measured using a thermocouple attached to the surface of the smoking article at a position
(illustrated by line P in Figure 1) 2 mm downstream of the combustible heat source. The results are
shown in Figure 5a.
The absorbance of the aerosol generated during each puff of the smoking article according
to the second embodiment of the invention was measured using a UV-Visible optical spectrometer
with an optical cell set up to record data in the Near UV region at 320 nm. The results, which are
indicative of the density of the aerosol generated, are shown in Figure 5b.
To generate the profiles shown in Figures 4a-5b, the upstream ends of the combustible heat
sources of the smoking articles according to the second embodiment of the invention were ignited
using a conventional yellow flame lighter. Puffs of 55 ml (puff volume) were then taken in 2 seconds
(puff duration) every 30 seconds (puff frequency) using a smoking machine.
Figures 2a and 4a show that upon ignition, the temperature of the downstream ends of the
combustible heat sources of the smoking articles according to the first and second embodiments of
the invention, respectively, rapidly rises to between about 650°C and about 750°C as a result of the
decomposition of the metal nitrate salts therein.
In both embodiments, the combustion of the carbon in the combustible heat sources
propagates at the same time as the decomposition of the metal nitrate salts therein, from the
upstream end of the combustible heat sources, where the yellow flame lighter is placed, throughout
the entire length of the combustible heat sources. This is clearly shown by a change in colour at the
surface of the combustible heat sources due to downstream movement of a deflagration front from
the upstream end to the downstream end of the combustible heat sources.
After the initial boost in temperature resulting from decomposition of the metal nitrate salts,
the temperature of the downstream ends of the combustible heat sources of the smoking articles
according to the first and second embodiments of the invention advantageously falls to a
temperature of between about 200°C and about 350°C, as shown in Figure 2b and Figure 4b,
respectively.
As shown in Figures 3a and 3b and Figures 6a and 6b, the initial boost in temperature and
rapid ignition of the combustible heat sources of the smoking articles according to the first and
second embodiments of the invention resulting from the decomposition of the metal nitrate salts
therein, advantageously quickly raises the temperature of the aerosol-generating substrates of the
smoking articles to a level at which volatile organic aroma and flavour compounds are generated
from the aerosol-generating substrates in sufficient quantities to produce a sensorially acceptable
aerosol as of the first puff.
Furthermore, the decrease in temperature of the combustible heat sources of the smoking
articles according to the first and second embodiments of the invention following decomposition of
the metal nitrates salts therein advantageously ensures that the temperature of the aerosol-
generating substrates of the smoking articles does not reach a level at which combustion or thermal
degradation of the aerosol-generating substrates occurs.
EXAMPLE 3
Combustible heat sources according to a third embodiment of the invention were prepared
by mixing 750 g of carbon powder, 51.75 g of potassium citrate, 84 g of modified cellulose, 276 g of
flour, 141.75 g of sugar and 21 g of corn oil with 579 g of deionised water to form an aqueous slurry.
The aqueous slurry was then extruded through a die having a central die orifice of circular
cross-section with a diameter of 8.7 mm to form cylindrical rods having a length of about 20-22 cm
and a diameter of about 9.1-9.2 mm. A single longitudinal air flow passageway was formed in the
cylindrical rods by a mandrel of circular cross-section with an outer diameter of approximately 2 mm
mounted centrally in the die orifice. During extrusion of the cylindrical rods, a glass coating slurry
was pumped through a feed passageway extending through the centre of the mandrel to form a thin
coating of about 150-300 microns on the inner surface of the single longitudinal air flow
passageway.
The cylindrical rods were dried at about 20-25°C, 40-50 percent relative humidity, for
between about 12 hours and about 72 hours and then pyrolysed in a nitrogen atmosphere at 750°C
for about 240 minutes.
After pyrolysis, the cylindrical rods were cut and shaped to a defined diameter using a
grinding machine to form individual combustible heat sources having a length of about 11 mm, a
diameter of about 7.8 mm and a dry mass of about 425 mg and then dried at 130°C for
approximately 1 hour.
As shown in Figures 6a and 6b, four equally spaced apart longitudinal grooves having a
length of 9 mm as measured from the upstream end of the combustible heat source and a diameter
of between and 1.5 mm and about 1.8 mm were formed along the circumferential outer surface of
each individual combustible heat source using an electric drill. A suspension of 1 percent
nitrocellulose binder and 66 percent zirconium by weight in acetone was applied within each of the
longitudinal grooves along the circumferential outer surface of the individual combustible- heat
sources using a syringe.
The individual combustible heat sources were then dried at 130°C for approximately 1 hour.
The dried individual combustible heat sources had an ignition aid (zirconium) content of
about 20 percent by dry weight of the combustible heat source.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the third embodiment of the invention upon ignition of the upstream end of the
combustible heat source was measured in the smoking article using thermocouples attached to the
surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the
aerosol-generating substrate thereof.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the third embodiment of the invention during subsequent combustion of the
combustible heat source was also measured in the smoking article using a thermocouple attached
to the surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream
of the aerosol-generating substrate thereof.
In both cases, the combustible heat sources of the smoking articles according to the third
embodiment of the invention were ignited using a conventional yellow flame lighter. Puffs of 55 ml
(puff volume) were then taken in 2 seconds (puff duration) every 30 seconds (puff frequency) using
a smoking machine.
Upon ignition, the temperature of the downstream end of the combustible heat source of the
smoking article according to the third embodiment of the invention rises to about 500°C as a result
of the reaction with oxygen of the zirconium in the four longitudinal grooves disposed about the
circumference of the combustible heat source. As illustrated by the reaction scheme below, this
reaction is highly exothermic and produces inert zirconium oxide particles:
Zr + O → ZrO + ΔE (-1081 kJ/mol)
While as shown in Figure 6b, the four longitudinal grooves do not extend from the upstream
end to the downstream end of the combustible heat source, they do extend beneath the combustion
resistant wrapper of the smoking article according to the third embodiment of the invention. In this
embodiment heat generated upon ignition of the upstream end of the combustible heat source as a
result of the reaction of the zirconium with oxygen is, therefore, transferred directly by conduction to
the aerosol-generating substrate via the combustion resistant wrapper. This advantageously quickly
raises the temperature of the aerosol-generating substrate of the smoking article according to the
third embodiment of the invention to a level at which volatile organic aroma and flavour compounds
are generated from the aerosol-generating substrates in sufficient quantities to produce a sensorially
acceptable aerosol as of the first puff.
The exothermic reaction with oxygen of the zirconium in the four longitudinal grooves of the
combustible heat source is sufficiently energetic that, as well as heat being transferred to the
aerosol-generating substrate of the smoking article via the combustion resistant wrapper, energy is
radiated radially throughout the entire combustible heat source. This initiates combustion of the
carbon in the combustible heat source.
After the initial boost in temperature resulting from the reaction with oxygen of the zirconium
to form zirconium oxide, the temperature of the downstream end of the combustible heat source of
the smoking article according to the third embodiment of the invention advantageously also falls to a
temperature of between about 200°C and about 400°C during subsequent combustion of the
combustible heat source. The decrease in temperature of the combustible heat source according to
the third embodiment of the invention following the reaction with oxygen of the zirconium therein
advantageously ensures that the temperature of the aerosol-generating substrate of the smoking
article according to the third embodiment of the invention does not reach a level at which
combustion or thermal degradation of the aerosol-generating substrate occurs.
In the third embodiment of the invention described above, zirconium is deposited in four
equally spaced apart longitudinal grooves disposed about the circumference of the combustible heat
source. However, it will be appreciated that zirconium and other materials that release energy upon
ignition of the upstream end of the combustible heat sources may be deposited or otherwise
provided in more than four or fewer than four grooves disposed about the circumference of
combustible heat sources according to invention.
It will also be appreciated that combustible heat sources according to the invention may
comprise one or materials that release energy upon ignition of the upstream end of the combustible
heat sources in other locations.
EXAMPLE 4
Combustible heat sources according to a fourth embodiment of the invention were prepared
by mixing 135 g of carbon powder, 150 g of calcium peroxide (75 percent purity) and 15 g of
carboxymethyl cellulose with 180 g of deionised water to form a granulated mixture.
The granulated mixture was then extruded through a die having a central die orifice of
circular cross-section with a diameter of 7.6 mm to form cylindrical rods having a length of about 20-
cm and a diameter of about 7.8 mm. A single longitudinal air flow passageway was formed in the
cylindrical rods by a mandrel of circular cross-section with an outer diameter of approximately 2 mm
mounted centrally in the die orifice. A clay coating slurry was applied to the inner surface of the
single longitudinal air flow passageway to form a thin coating of about 150-300 microns on the inner
surface of the single longitudinal air flow passageway.
The cylindrical rods were dried at about 20-25°C, 40-50 percent relative humidity, for
between about 12 hours and about 48 hours. After drying, the cylindrical rods were cut to form
individual combustible heat sources having a length of about 13 mm and a diameter of about 7.8
mm. The individual combustible heat sources were then dried at 130°C for approximately 1 hour.
The dried individual combustible heat sources had a mass of about 500 mg.
The dried individual combustible heat sources had an ignition aid (calcium peroxide) content
of about 38 percent by dry weight of the combustible heat source.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the fourth embodiment of the invention upon ignition of the upstream end of the
combustible heat source was measured in the smoking article using a thermocouple attached to the
surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the
aerosol-generating substrate thereof. The results are shown in Figure 7.
To generate the profile shown in Figure 7, the upstream end of the combustible heat source
of the smoking article according to the fourth embodiment of the invention was ignited using a
conventional yellow flame lighter. Puffs of 55 ml (puff volume) were then taken in 2 seconds (puff
duration) every 30 seconds (puff frequency) using a smoking machine.
Figure 7 shows that upon ignition, the temperature of the downstream end of the
combustible heat source of the smoking article according to the fourth embodiment of the invention
rapidly rises to between about 500°C and about 600°C as a result of the decomposition of the
calcium peroxide therein.
The combustion of the carbon in the combustible heat source propagates at the same time
as the decomposition of the calcium peroxide therein, from the upstream end of the combustible
heat source, where the yellow flame lighter is placed, throughout the entire length of the combustible
heat source. This is clearly shown by a change in colour at the surface of the combustible heat
source due to downstream movement of a deflagration front from the upstream end to the
downstream end of the combustible heat source.
After the initial boost in temperature resulting from the decomposition of the calcium
peroxide, the temperature of the downstream end of the combustible heat source of the smoking
article according to the fourth embodiment of the invention advantageously falls to a temperature of
below about 375°C.
The initial boost in temperature and rapid ignition of the combustible heat source of the
smoking article according to the fourth embodiment of the invention resulting from the
decomposition of the calcium peroxide therein, advantageously quickly raises the temperature of the
aerosol-generating substrate of the smoking article to a level at which volatile organic aroma and
flavour compounds are generated from the aerosol-generating substrate in sufficient quantities to
produce a sensorially acceptable aerosol as of the first puff.
Furthermore, the decrease in temperature of the combustible heat source of the smoking
article according to the fourth embodiment of the invention following decomposition of the calcium
peroxide therein advantageously ensures that the temperature of the aerosol-generating substrate
of the smoking article does not reach a level at which combustion or thermal degradation of the
aerosol-generating substrate occurs.
EXAMPLE 5
Combustible heat sources according to a fifth embodiment of the invention and a sixth
embodiment of the invention having the ignition aid (calcium peroxide) contents shown in Table 2
were prepared as in Example 4 by the mixing the components shown in Table 2 to form a
granulated mixture.
First comparative combustible heat sources and second comparative combustible heat
sources having the ignition aid (calcium peroxide) contents shown in Table 2 were also prepared as
in Example 4 by the mixing components shown in Table 2 to form a granulated mixture.
The temperature of the downstream end of the combustible heat sources of: (i) a smoking
article according to a fifth embodiment of the invention; (ii) a smoking article according to a sixth
embodiment of the invention; (iii) a first comparative smoking article; and (iv) a second comparative
smoking article upon ignition of the upstream end of the combustible heat sources was measured in
the smoking article using a thermocouple attached to the surface of the smoking article at a position
(illustrated by line P in Figure 1) 1 mm upstream of the aerosol-generating substrate thereof. The
results are shown in Figure 8.
Combustible Heat Source
Fifth Sixth First Second
Embodiment Embodiment comparative Comparative
Carbon powder (g) 45 55 60 65
Calcium peroxide (75 percent
50 40 35 30
purity) (g)
Carboxymethyl cellulose (g) 5 5 5 5
Deionised water (g)
60 61 61 62
Ignition aid (calcium peroxide)
content (percent by dry weight 38 30 26 23
of the combustible heat source)
Table 2
To generate the profiles shown in Figure 8, the upstream ends of the combustible heat
sources of the: (i) smoking article according to a fifth embodiment of the invention; (ii) smoking
article according to the sixth embodiment of the invention; (iii) first comparative smoking article; and
(iv) second comparative smoking article were ignited using a conventional yellow flame lighter.
Puffs of 55 ml (puff volume) were then taken in 2 seconds (puff duration) every 30 seconds (puff
frequency) using a smoking machine.
Figure 8 shows that upon ignition, the temperature of the downstream end of the
combustible heat source of the smoking article according to the fifth embodiment of the invention,
which has a calcium peroxide content of about 38 percent by dry weight of the combustible heat
source, rapidly rises to between about 650°C and about 750°C as a result of the decomposition of
the calcium peroxide therein.
Figure 8 also shows that upon ignition, the temperature of the downstream end of the
combustible heat source of the smoking article according to the sixth embodiment of the invention,
which has a calcium peroxide content of about 30 percent by dry weight of the combustible heat
source, rapidly rises to between about 450°C and about 500°C as a result of the decomposition of
the calcium peroxide therein.
However, upon ignition, the temperature of the downstream end of the combustible heat
source of the first comparative smoking article, which has a calcium peroxide content of about
26 percent by dry weight of the combustible heat source, and the temperature of the downstream
end of the combustible heat source of the second comparative smoking article, which has a calcium
peroxide content of about 23 percent by dry weight of the combustible heat source, do not exhibit a
‘boost’ in temperature.
As shown in Figure 8, reducing the amount of calcium peroxide in the combustible heat
source reduces the magnitude of the ‘boost’ in temperature of the downstream end of the
combustible heat source obtained upon ignition of the upstream end of the combustible heat source.
As also shown in Figure 8, reducing the amount of calcium peroxide in the combustible heat source
increases the time taken for the downstream end of the combustible heat source to reach the ‘boost’
temperature upon ignition of the upstream end of the combustible heat source.
Combustible heat sources according to the invention must comprise at least one ignition aid
selected from the group consisting of metal nitrate salts having a thermal decomposition
temperature of less than about 600°C, chlorates, peroxides, thermitic materials, intermetallic
materials, magnesium, zirconium, and combinations thereof in an amount of at least about 20
percent by dry weight of the combustible heat source. However, Figure 8 illustrates that the amount
of at least one ignition aid that must be included in order for the second portion of a combustible
heat source according to the invention to exhibit the required ‘boost’ in temperature upon ignition of
the first portion thereof may be greater than about 20 percent by dry weight of the combustible heat
source depending on the specific at least one ignition aid included in the combustible heat source.
EXAMPLE 6
Combustible heat sources according to a seventh embodiment of the invention were
prepared by mixing 180 g of carbon powder, 90 g of calcium peroxide (75 percent purity), 15g of
magnesium and 15 g of carboxymethyl cellulose with 180 g of deionised water to form a granulated
mixture.
The granulated mixture was then extruded through a die having a central die orifice of
circular cross-section with a diameter of 7.6 mm to form cylindrical rods having a length of about 20-
cm and a diameter of about 7.8 mm. A single longitudinal air flow passageway was formed in the
cylindrical rods by a mandrel of circular cross-section with an outer diameter of approximately 2 mm
mounted centrally in the die orifice. A clay coating slurry was applied to the inner surface of the
single longitudinal air flow passageway to form a thin coating of about 150-300 microns on the inner
surface of the single longitudinal air flow passageway.
The cylindrical rods were dried at about 20-25°C, 40-50 percent relative humidity, for
between about 12 hours and about 48 hours. After drying, the cylindrical rods were cut to form
individual combustible heat sources having a length of about 13 mm and a diameter of about 7.8
mm. The individual combustible heat sources were then dried at 130°C for approximately 1 hour.
The dried individual combustible heat sources had a mass of about 500 mg.
The dried individual combustible heat sources had an ignition aid (calcium peroxide and
magnesium) content of about 28 percent by dry weight of the combustible heat source.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the seventh embodiment of the invention upon ignition of the upstream end of the
combustible heat source was measured in the smoking article using a thermocouple attached to the
surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the
aerosol-generating substrate thereof. The results are shown in Figure 9a.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the seventh embodiment of the invention during subsequent combustion of the
combustible heat source was also measured in the smoking article using a thermocouple attached
to the surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream
of the aerosol-generating substrate thereof. The results are shown in Figure 9b.
To generate the profiles shown in Figures 9a and 9b, the upstream end of the combustible
heat source of the smoking article according to the seventh embodiment of the invention was ignited
using a conventional yellow flame lighter. Puffs of 55 ml (puff volume) were then taken in 2 seconds
(puff duration) every 30 seconds (puff frequency) using a smoking machine.
Figure 9a shows that upon ignition, the temperature of the downstream end of the
combustible heat source of the smoking article according to the seventh embodiment of the
invention rapidly rises to between about 600°C and about 700°C as a result of the decomposition of
the calcium peroxide therein and the exothermic reaction with oxygen of the magnesium therein.
The combustion of the carbon in the combustible heat source propagates at the same time
as the decomposition of the calcium peroxide therein and the reaction with oxygen of the
magnesium therein, from the upstream end of the combustible heat source, where the yellow flame
lighter is placed, throughout the entire length of the combustible heat source. This is clearly shown
by a change in colour at the surface of the combustible heat source due to downstream movement
of a deflagration front from the upstream end to the downstream end of the combustible heat
source.
After the initial boost in temperature resulting from the decomposition of the calcium peroxide
and the reaction with oxygen of the magnesium, the temperature of the downstream end of the
combustible heat source of the smoking article according to the seventh embodiment of the
invention advantageously falls to a temperature of between about 250°C and about 400°C as shown
in Figure 9b.
The initial boost in temperature and rapid ignition of the combustible heat source of the
smoking article according to the seventh embodiment of the invention resulting from the
decomposition of the calcium peroxide therein and the reaction with oxygen of the magnesium
therein, advantageously quickly raises the temperature of the aerosol-generating substrate of the
smoking article to a level at which volatile organic aroma and flavour compounds are generated
from the aerosol-generating substrate in sufficient quantities to produce a sensorially acceptable
aerosol as of the first puff.
Furthermore, the decrease in temperature of the combustible heat source of the smoking
article according to the seventh embodiment of the invention following decomposition of the calcium
peroxide therein and the reaction with oxygen of the magnesium therein advantageously ensures
that the temperature of the aerosol-generating substrate of the smoking article does not reach a
level at which combustion or thermal degradation of the aerosol-generating substrate occurs.
EXAMPLE 7
Combustible heat sources according to an eighth embodiment of the invention were
prepared by mixing 525 g of carbon powder, 225 g of calcium carbonate (CaCO ), 51.75 g of
potassium citrate, 84 g of modified cellulose, 276 g of flour, 141.75 g of sugar and 21 g of corn oil
with 579 g of deionised water to form an aqueous slurry.
The aqueous slurry was then extruded through a die having a central die orifice of circular
cross-section with a diameter of 8.7 mm to form cylindrical rods having a length of about 20-22 cm
and a diameter of about 9.1-9.2 mm. A single longitudinal air flow passageway was formed in the
cylindrical rods by a mandrel of circular cross-section with an outer diameter of approximately 2 mm
mounted centrally in the die orifice. During extrusion of the cylindrical rods, a glass coating slurry
was pumped through a feed passageway extending through the centre of the mandrel to form a thin
coating of about 150-300 microns on the inner surface of the single longitudinal air flow
passageway.
The cylindrical rods were dried at about 20-25°C, 40-50 percent relative humidity, for
between about 12 hours and about 72 hours and then pyrolysed in a nitrogen atmosphere at 750°C
for about 240 minutes.
After pyrolysis, the cylindrical rods were cut and shaped to a defined diameter using a
grinding machine to form individual combustible heat sources having a length of about 11 mm, a
diameter of about 7.8 mm and a dry mass of about 400 mg.
The individual combustible heat sources were dried at 130°C for approximately 1 hour and
then placed in an aqueous solution of nitric acid having a concentration of 38 percent by weight,
which was saturated with potassium nitrate (KNO ).
After approximately 5 minutes, the individual combustible heat sources were removed from
the solution and dried at 130°C for approximately 1 hour.
After drying the individual combustible heat sources were placed in an aqueous solution of
sodium chlorate (NaClO ) having a concentration of 0.98 mol/L.
After approximately 30 seconds, the individual combustible heat sources were removed from
the solution and dried for 10 minutes at room temperature, then at 120°C for approximately 1 hour.
The dried individual combustible heat sources had an ignition aid (calcium nitrate, potassium
nitrate and sodium chlorate) content of between about 30 percent and about 40 percent by dry
weight of the combustible heat source.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the eighth embodiment of the invention upon ignition of the upstream end of the
combustible heat source was measured in the smoking article using a thermocouple attached to the
surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the
aerosol-generating substrate thereof. The results are shown in Figure 10.
To generate the profile shown in Figure 10, the upstream end of the combustible heat source
of the smoking article according to the eighth embodiment of the invention was ignited using a
conventional yellow flame lighter. Puffs of 55 ml (puff volume) were then taken in 2 seconds (puff
duration) every 30 seconds (puff frequency) using a smoking machine.
Figure 10 shows that upon ignition, the temperature of the downstream end of the
combustible heat source of the smoking article according to the eighth embodiment of the invention
rapidly rises to between about 650°C and about 700°C as a result of the decomposition of the metal
nitrate salts and metal chlorate salt therein therein.
After the initial boost in temperature resulting from decomposition of the metal nitrate salts
and metal chlorate salt, the temperature of the downstream end of the combustible heat source of
the smoking article according to the eighth embodiment of the invention falls to a temperature of
below about 500°C.
EXAMPLE 8
Combustible heat sources according to a ninth embodiment of the invention were prepared
by mixing 35 g of carbon powder, 35.9 g of iron oxide (Fe O ), 16.4 g of magnesium, 6 g of
bentonite and 6.7 g of carboxymethyl cellulose with 73.3 g of deionised water to form a granulated
mixture.
The granulated mixture was then extruded through a die having a central die orifice of
circular cross-section with a diameter of 7.6 mm to form cylindrical rods having a length of about
-25 cm and a diameter of about 7.8 mm.
The cylindrical rods were dried at about 20-25°C, 40-50 percent relative humidity, for
between about 12 hours and about 48 hours. After drying, the cylindrical rods were cut to form
individual combustible heat sources having a length of about 11 mm and a diameter of about
7.8 mm. The individual combustible heat sources were then dried at 130°C for approximately
1 hour. The dried individual combustible heat sources had a mass of about 400 mg.
The dried individual combustible heat sources had an ignition aid (iron oxide (Fe O ) and
magnesium) content of about 52 percent by dry weight of the combustible heat source.
The temperature of the downstream end of the combustible heat source of a smoking article
according to the ninth embodiment of the invention upon ignition of the upstream end of the
combustible heat source was measured in the smoking article using a thermocouple attached to the
surface of the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the
aerosol-generating substrate thereof. The results are shown in Figure 11.
To generate the profile shown in Figure 11, the upstream end of the combustible heat source
of the smoking article according to the ninth embodiment of the invention was ignited using a
conventional yellow flame lighter. Puffs of 55 ml (puff volume) were then taken in 2 seconds (puff
duration) every 30 seconds (puff frequency) using a smoking machine.
Figure 11 shows that upon ignition, the temperature of the downstream end of the
combustible heat source of the smoking article according to the ninth embodiment of the invention
rapidly rises to between about 1000°C and about 1100°C as a result of the exothermic reaction
between the iron oxide (Fe O ) and the magnesium therein.
After the initial boost in temperature resulting from the exothermic reaction between the iron
oxide (Fe O ) and the magnesium, the temperature of the downstream end of the combustible heat
source of the smoking article according to the ninth embodiment of the invention falls to a
temperature of below about 500°C.
EXAMPLE 9
Third comparative combustible heat sources and fourth comparative combustible heat
sources having the ignition aid (iron oxide (Fe O ) and magnesium) contents shown in Table 2 were
prepared as in Example 8 by mixing the components shown in Table 3 to form a granulated mixture.
The temperature of the downstream end of the combustible heat sources of: (i) a smoking
article according to the ninth embodiment of the invention; (ii) a third comparative smoking article;
and (iii) a fourth comparative smoking article upon ignition of the upstream end of the combustible
heat sources was measured in the smoking article using a thermocouple attached to the surface of
the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the aerosol-
generating substrate thereof. The results are shown in Figure 12.
To generate the profiles shown in Figure 12, the upstream ends of the combustible heat
sources of the (i) smoking article according to the ninth embodiment of the invention; (ii) third
comparative smoking article; and (iii) fourth comparative smoking article were ignited using a
conventional yellow flame lighter. Puffs of 55 ml (puff volume) were then taken in 2 seconds (puff
duration) every 30 seconds (puff frequency) using a smoking machine.
Combustible Heat Source
Third Fourth
comparative Comparative
Carbon powder (g) 40 45
Iron oxide (Fe O ) (g) 32.6 29.3
Magnesium (g) 14.9 13.4
Bentonite (g) 6 6
Carboxymethyl cellulose (g)
6.5 6.3
Deionised water (g) 73.3 73.3
Ignition aid (Iron oxide (Fe O ) and
magnesium) content (percent by dry weight of 48 43
the combustible heat source)
Table 3
Figure 12 shows that upon ignition, the temperature of the downstream end of the
combustible heat source of the smoking article according to the ninth embodiment of the invention,
which has an iron oxide (Fe O ) and magnesium content of about 52 percent by dry weight of the
combustible heat source, rapidly rises to between about 1000°C and about 1100°C as a result of the
exothermic reaction between the iron oxide (Fe O ) and the magnesium therein.
However, upon ignition, the temperature of the downstream end of the combustible heat
source of the third comparative smoking article, which has an iron oxide (Fe O ) and magnesium
content of about 48 percent by dry weight of the combustible heat source, and the temperature of
the downstream end of the combustible heat source of the fourth comparative smoking article, which
has an iron oxide (Fe O ) and magnesium content of about 43 percent by dry weight of the
combustible heat source, do not exhibit a ‘boost’ in temperature.
As shown in Figure 12, reducing the iron oxide (Fe O ) and magnesium content of the
combustible heat source reduces the magnitude of the ‘boost’ in temperature of the downstream
end of the combustible heat source obtained upon ignition of the upstream end of the combustible
heat source.
Combustible heat sources according to the invention must comprise at least one ignition aid
selected from the group consisting of metal nitrate salts having a thermal decomposition
temperature of less than about 600°C, chlorates, peroxides, thermitic materials, intermetallic
materials, magnesium, zirconium, and combinations thereof in an amount of at least about 20
percent by dry weight of the combustible heat source. However, Figure 12 illustrates that the
amount of at least one ignition aid that must be included in order for the second portion of a
combustible heat source according to the invention to exhibit the required ‘boost’ in temperature
upon ignition of the first portion thereof may be greater than about 20 percent by dry weight of the
combustible heat source depending on the specific at least one ignition aid included in the
combustible heat source.
EXAMPLE 10
Fifth comparative combustible heat sources and sixth comparative combustible heat sources
were prepared as in Example 4 by mixing the components shown in Table 4 to form a granulated
mixture.
Combustible Heat Source
Fifth Sixth
comparative Comparative
Carbon powder (g) 285 135
Carboxymethyl cellulose (g) 15 15
Potassium citrate (g) - 150
Deionised water (g) 180 75
Alkali metal burn salt (potassium citrate)
content (percent by dry weight of the - 50
combustible heat source)
The temperature of the downstream end of the combustible heat sources of: (i) a smoking
article according to the fourth embodiment of the invention; (ii) a fifth comparative smoking article;
and (iii) a sixth comparative smoking article upon ignition of the upstream end of the combustible
heat sources was measured in the smoking article using a thermocouple attached to the surface of
the smoking article at a position (illustrated by line P in Figure 1) 1 mm upstream of the aerosol-
generating substrate thereof. The results are shown in Figure 13.
To generate the profiles shown in Figure 13, the upstream ends of the combustible heat
sources of the (i) smoking article according to the fourth embodiment of the invention; (ii) fifth
comparative smoking article; and (iii) sixth comparative smoking article were ignited using a
conventional yellow flame lighter. Puffs of 55 ml (puff volume) were then taken in 2 seconds (puff
duration) every 30 seconds (puff frequency) using a smoking machine.
Figure 13 shows that upon ignition, the temperature of the downstream end of the
combustible heat source of the smoking article according to the fourth embodiment of the invention,
which has a calcium peroxide content of about 38 percent by dry weight of the combustible heat
source, rapidly rises to between about 750°C and about 800°C as a result of the decomposition of
the calcium peroxide therein,
However, upon ignition, the temperature of the downstream end of the combustible heat
source of the fifth comparative smoking article, which contains no ignition aid, and the temperature
of the downstream end of the combustible heat source of the sixth comparative smoking article,
which has an alkali metal burn salt (potassium citrate) content of about 50 percent by dry weight of
the combustible heat source, do not exhibit a ‘boost’ in temperature.
As shown in Figure 13, in the absence of at least one ignition aid selected from the group
consisting of metal nitrate salts having a thermal decomposition temperature of less than about
600°C, chlorates, peroxides, thermitic materials, intermetallic materials, magnesium, zirconium, and
combinations thereof in an amount of at least about 20 percent by dry weight of the combustible
heat source, the second portion of a combustible heat source does not exhibit a ‘boost’ in
temperature upon ignition of the first portion thereof.
As also shown in Figure 13, even when included in an amount much greater than at least
about 20 percent by dry weight of the combustible heat source, alkali metal citrate burn salts do not
release enough energy upon ignition of the first portion of a combustible heat source to produce a
‘boost’ in temperature of the second portion thereof.
The term ‘comprising’ as used in this specification and claims means ‘consisting at least in
part of’. When interpreting statements in this specification and claims which include the term
‘comprising’, other features besides the features prefaced by this term in each statement can also
be present. Related terms such as ‘comprise’ and ‘comprised’ are to be interpreted in a similar
manner.
Claims (24)
1. A combustible heat source for a smoking article comprising carbon and at least one ignition aid selected from the group consisting of metal nitrate salts having a thermal decomposition 5 temperature of less than about 600°C, chlorates, peroxides, thermitic materials, intermetallic materials, magnesium, zirconium, and combinations thereof, wherein the at least one ignition aid is present in an amount of at least about 20 percent by dry weight of the combustible heat source, the combustible heat source having a first portion and an opposed second portion, wherein at least part of the combustible heat source between the first portion and the second portion is 10 wrapped in a combustion resistant wrapper that is one or both of heat conducting and substantially oxygen impermeable, and wherein upon ignition of the first portion of the combustible heat source the second portion of the combustible heat source increases in temperature to a first temperature and wherein during subsequent combustion of the combustible heat source (4) the second portion of the combustible 15 heat source maintains a second temperature lower than the first temperature.
2. A combustible heat source according to claim 1 wherein the at least one ignition aid is present in an amount of less than 65 percent by dry weight of the combustible heat source. 20
3. A combustible heat source according to claim 1 or 2 wherein the at least one ignition aid comprises a peroxide.
4. A combustible heat source according to claim 1, 2, or 3 further comprising one or more binders.
5. A combustible heat source according to claim 4 comprising: one or more organic binders selected from the group consisting of gums, modified celluloses and cellulose derivatives, wheat flour, starches, sugars, vegetable oils, and combinations thereof; one or more inorganic binders selected from the group consisting of clays, alumino-silicate 30 derivatives, alkali activated alumino-silicates, alkali silicates, limestone derivatives, alkaline earth compounds and derivatives, and aluminium compounds and derivatives; or a combination thereof.
6. A combustible heat source according to any of claims 1 to 5 wherein the combustible heat 35 source is substantially cylindrical and the first portion of the combustible heat source is a first end face of the combustible heat source and the second portion of the combustible heat source is an opposed second end face of the combustible heat source.
7. A combustible heat source according to any of claims 1 to 6 wherein the temperature of the second portion of the combustible heat source remains substantially stable at the second temperature for at least 3 minutes.
8. A combustible heat source according to any of claims 1 to 7 wherein the first temperature is between 400°C and 1200°C.
9. A combustible heat source according to any of claims 1 to 8 wherein the second temperature 10 is between 200°C and 1000°C.
10. A combustible heat source according to any of claims 1 to 9 wherein the second temperature is between 200°C and 1000°C. 15
11. A combustible heat source according to any of claims to 10 wherein the ignition temperature is between 200°C and 1000°C lower than the first temperature.
12. A combustible heat source according to any of claims 1 to 11 wherein upon ignition of the first portion of the combustible heat source the second portion of the combustible heat source 20 increases in temperature to the first temperature at a rate of between 100°C/second and 1000°C/second.
13. A smoking article comprising a combustible heat source according to any of claims 1 to 12. 25
14. A smoking article comprising: a combustible heat source according to any of claims 1 to 12; and an aerosol-generating substrate downstream of the combustible heat source, wherein the first portion of the combustible heat source is an upstream end of the combustible heat source and the second portion of the combustible heat source is a downstream 30 end of the combustible heat source.
15. A smoking article according to claim 14 wherein at least a rear part of the combustible heat source is wrapped in the combustion resistant wrapper.
16. A smoking article according to claim 15 wherein at least a rear part of the combustible heat source and at least a front part of the aerosol-generating substrate are wrapped in the combustion resistant wrapper.
17. A smoking article according to claim 16 wherein a rear part of the aerosol-generating substrate is not wrapped in the combustion resistant wrapper.
18. A smoking article according to any of claims 14 to 17 wherein a front part of the combustible 10 heat source is not wrapped in the combustion resistant wrapper.
19. A smoking article according to any of claims 14 to 17 wherein the combustible heat source is wrapped in the combustion resistant wrapper along substantially its entire length. 15
20. A smoking article according to any of claims 14 to 19 wherein the combustible heat source is substantially cylindrical.
21. A combustible heat source for a smoking article, the combustible heat source substantially as herein described with reference to any embodiment shown in the accompanying drawings.
22. A combustible heat source substantially as herein described with reference to any embodiment disclosed.
23. A smoking article substantially as herein described with reference to any embodiment shown 25 in the accompanying drawings.
24. A smoking article according to claim 13 or 14 substantially as herein described with reference to any embodiment disclosed.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11250578.9 | 2011-06-02 | ||
| EP11250578 | 2011-06-02 | ||
| PCT/EP2012/060411 WO2012164077A1 (en) | 2011-06-02 | 2012-06-01 | Combustible heat source for a smoking article |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ619159A NZ619159A (en) | 2015-09-25 |
| NZ619159B2 true NZ619159B2 (en) | 2016-01-06 |
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ID=
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