US3561451A - Process of manufacturing reconstituted tobacco of light color - Google Patents
Process of manufacturing reconstituted tobacco of light color Download PDFInfo
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- US3561451A US3561451A US639032A US3561451DA US3561451A US 3561451 A US3561451 A US 3561451A US 639032 A US639032 A US 639032A US 3561451D A US3561451D A US 3561451DA US 3561451 A US3561451 A US 3561451A
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- tobacco
- water
- plus
- polyphenols
- extract
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- 241000208125 Nicotiana Species 0.000 title abstract description 90
- 235000002637 Nicotiana tabacum Nutrition 0.000 title abstract description 90
- 238000000034 method Methods 0.000 title abstract description 25
- 238000004519 manufacturing process Methods 0.000 title abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 35
- 150000008442 polyphenolic compounds Chemical class 0.000 abstract description 23
- 235000013824 polyphenols Nutrition 0.000 abstract description 23
- 239000000284 extract Substances 0.000 abstract description 17
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 14
- 238000005406 washing Methods 0.000 abstract description 11
- 239000006286 aqueous extract Substances 0.000 abstract description 5
- 239000002250 absorbent Substances 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 17
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 16
- 238000010438 heat treatment Methods 0.000 description 13
- 239000003463 adsorbent Substances 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 9
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 8
- 235000019253 formic acid Nutrition 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 239000002002 slurry Substances 0.000 description 6
- 150000001720 carbohydrates Chemical class 0.000 description 5
- 235000014633 carbohydrates Nutrition 0.000 description 5
- 239000013642 negative control Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000012137 tryptone Substances 0.000 description 5
- 229930091371 Fructose Natural products 0.000 description 4
- 239000005715 Fructose Substances 0.000 description 4
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 229930006000 Sucrose Natural products 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 239000000428 dust Substances 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- 229940046892 lead acetate Drugs 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000005720 sucrose Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 238000010411 cooking Methods 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000013641 positive control Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 235000019505 tobacco product Nutrition 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000002023 wood Substances 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
- A24B15/12—Chemical features of tobacco products or tobacco substitutes of reconstituted tobacco
Definitions
- Price and Murray Schaffer ABSTRACT A process of treating tobacco in the manufacture of reconstituted tobacco is disclosed wherein the color of the finished reconstituted product is lightened by the removal of basic polyphenols present in the starting batch. The process involves washing the tobacco with water to form an aqueous extract thereof, separating the extract and treating it with absorbent agents such as activated alumina or polyamids to remove the basic polyphenols and finally reincorporating the extract minus the removed polyphenols into the fibrous tobacco mass.
- absorbent agents such as activated alumina or polyamids
- the present invention relates to a method for the preparation of reconstituted tobacco sheet and more particularly to an improved process for preparing light colored reconstitutet. tobacco sheet, despite the use of heat as a processing aid at any step of the process.
- the commercial method for the manufacture of reconstituted tobacco sheet requires the application of heat at some stage in the processing e.g. either in the preparative stages and/or in the drying. It is known that the color of the finished tobacco product darkens because of the heating; the level of darkening being a function of temperature and heating time. As a rule, it is desirable to produce a light colored tobacco sheet and various steps are taken to achieve this goal, for example, the addition of dyes or coloring chemicals, the addition a of color masking agents (whiteners”) such as titanium dioxcially if excessive amounts are needed to produce the desired results. Excessive use of dyes can produce leaching" problems while excessive use of whiteners" can result in sheets which are greyish in appearance or lack proper physical structure.
- the invention herein revealed makes it possible to produce a light colored, reconstituted tobacco sheet without the resort to dyes for color preservation and without any undue limitations on the temperature and heating time used in the process. This is achieved by selectively removing from the tobacco the agents responsible for the darkening of the tobacco on heating.
- tobacco such as stems, field scrap, cuttings, whole leaf and the like
- tobacco is usually uniformly comminuted and formed into tobacco sheet suitable for later machine processing.
- the tobacco is usually ground to colloid-forming size particles by a wet process or refining.
- the large amount of energy and time required for the preparation of these colloid-forming size' tobacco particles has limited its use for the preparation of reconstituted sheets.
- a further object of the present invention is to provide a method for producing a light colored reconstituted tobacco sheet despite the use of heat as a processing aid.
- a still further object of the present invention is to remove Still another object of the present invention is to provide a.
- Tobacco as defined for this invention includes any type of tobacco suitable for the manufacture: of reconstituted tobacco sheet, such as stern, veins, scrap and waste tobacco, cuttings and the like, as well as whole leaf or portions thereof.
- the method of the present invention discloses a method of removing from the tobacco washings the agents responsible for the darkening of the tobacco when it is exposed to heat.
- the treated washings are then returned to the tobacco being processed, and the product prepared in a conventional manner to provide a reconstituted tobacco sheet of good physical properties without detriment to the sheet color.
- the agents responsible for the darkening of the tobacco on cooking were the carbohydrates and the amino acids, which react during the heating to form dark colored compounds, the process being called the Mai1lard" reaction.
- a series of tests were run to isolate and determine the agents which caused tobacco darkening upon heating. The following procedure illustrates how the polyphenols were identified as the agents which cause tobacco darkening during heating.
- a sample of Bright stern dust weighing 10 g. was mixed with ml. of distilled water.
- the slurry was filtered on a Buchner funnel using Whatrnan No. l filter paper.
- the filter cake and filtrate were retained.
- the filter cake was subsequently mixed with 90 ml. of a predleterrnined liquid and the slurry transferred to a vessel, such as a mason jar, which was sealed and placed in a pressure cooker, where it washeated at 250 F. at 15 psi. for 2 hours.
- test results in table l were obtained with various add i tives in the predetermined liquid and serve to illustrate that polyphenols are the agents causing the darkening of the tobacco on exposure to heat.
- Water-washed Bright stern dust was used in all cases, unless otherwise indicated.
- the weight of the washed tobacco in each sample was 7 g. dry weight and this was suspended in 90 ml. of liquid prior to heating.
- the polyphenol fractions shown in table I were obtained as follows: 90 ml. of a tobacco-water extract, prepared as described above, was mixed with ml. ofa 10 percent lead acetate solution, and the formed precipitate was removed by centrifugation. This precipitate comprised the acidic polyphenol fraction.
- the tobacco water washings can be treated with adsorbent material, which adds nothing to the extract, but selectively removes the darkening agent or agents by adsorption.
- tobacco water washings are passed through a column containing a selected adsorbent material, such as activated alumina. The adsorbent removes the darkening material, but leaves the other valuable tobacco constituents unchanged in the extract.
- the treated extract is then recombined with the original washed tobacco and the combination is processed into reconstituted tobacco sheet, which retains its commercially acceptable light color with no additives.
- untreated tobacco such as broken leaves, cuttings, stemmings, various fragments or waste, field scrap
- a water extraction operation so as to separate the water-soluble constituents.
- the water-soluble constituents of the tobacco or extract are separated from the insoluble portion by any convenient process, such as draining, pressing, or centrifuging.
- the aqueous extract contains various water-soluble materials, including polyphenols.
- This aqueous extract can then be passed through a column containing an adsorbent material, such as activated alumina. Continuous operation in a column can be effected by placing the adsorbent material and passing the aqueous extract continuously through a column.
- the adsorbent material removes the color-forming bodies, but leaves the other valuable tobacco constituents unchanged in the column effluent.
- the effluent is then recombined with the original washed tobacco and the combination is processed in a conventional form and a light colored reconstituted tobacco sheet is produced.
- the extracted coloring materials can be eluted from the adsorbent so that it can be reused as desired.
- a glass column (25 cm. x 3 cm.) was filled with a slurry of 100 gm. of activated alumina (8l4 mesh) in water. The water was allowed to drain and the column was washed repeatedly with about 500l000 ml. fresh water. A water extract of tobacco dust obtained by the method described previously was passed over the column at a flow rate such that effluent was collected at 0.5 ml. per minute. The column was then washed with water until the washings were colorless. The combined water washings and collected effluent were then concentrated to 100 ml. under vacuum in a flash evaporator using a temperature range of 36-38 C. The solids content in the concentrate, as well as in the original water tobacco extract were determincd and the recovery of material from the column calculated from these values. The test results are presented in table 2.
- the material not removed from the column by water washing was eluted off by passing 2 normal formic acid through the column. Fractions were collected at a rate of 0.5 ml. per minute. The eluted samples were very dark in color. The 2 normal formic acid removed all the adsorbed material leaving the activated alumina free of color. The alumina was washed with water until free of acid, dried in the oven l30-l40 C.) overnight and used again.
- the formic acid was removed from the eluate (i.e., the eluate
- the material. which could not be removed from the column by water could be eluted off by other suitable solvents, such as 50 percent ethanol containing 2 normal HCl or by 2 normal HCl solution.
- suitable solvents such as 50 percent ethanol containing 2 normal HCl or by 2 normal HCl solution.
- formic acid is preferred, since it is easily removed by evaporation under vacuum. This makes it possible to recover the solids from the formic acid eluate and their subsequent utilization in the color experiments. In an operation where these solids are of no consequence, their removal from the alumina would be carried out more economically with a 2 normal HCI solution.
- these materials are fine meshed and pack easily in the columns, so as to reduce flow through the columns.
- a pressure source would be necessary to obtain satisfactory flow through columns using these adsorbent materials.
- the preferred adsorbents need not be used in a column. They can also be employed effectively in slurry-type removal polyphenols.
- Adsorbents other than activated alumina, were examined. Regenerated alumina worked as well as unused alumina.
- adsorbent materials such as magnesol, silicic acid or adsorption alumina, and the like.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacture Of Tobacco Products (AREA)
- Jellies, Jams, And Syrups (AREA)
Abstract
A process of treating tobacco in the manufacture of reconstituted tobacco is disclosed wherein the color of the finished reconstituted product is lightened by the removal of basic polyphenols present in the starting batch. The process involves washing the tobacco with water to form an aqueous extract thereof, separating the extract and treating it with absorbent agents such as activated alumina or polyamids to remove the basic polyphenols and finally reincorporating the extract minus the removed polyphenols into the fibrous tobacco mass.
Description
United States Patent [72] Inventors Harry Jacin Norwalk; Joseph V. Fiore, Fairfield, Conn. [21] Appl. No. 639,032 [22] Filed May 17, 1967 [45] Patented Feb.9, 1971 [73] Assignee American Machine 8: Foundry Company a corporation of New Jersey [54] PROCESS OF MANUFACTURING RECONSTITUTED TOBACCO OF LIGHT COLOR 1 Claim, No Drawings [52] US. Cl 131/143, 131/17 [51] Int. Cl A241) 03/14, A24b 15/08 [50] Field ofSearch 131/15,17, l40144(1nd. all) [56] References Cited UNITED STATES PATENTS 267,764 11/1882 Wood 131/17UX 720,830 2/1903 Marsden 13 l/17UX 3,255,760 6/1966 13l/2X 802,487 10/1905 131/143 3,351,066 11/1967 Colgate 131/140 3,390,685 7/1968 Von Bethmann et al. 131/143 3,145,717 8/1964 Osborne et al. l31/143X Primary Examiner-Melvin D. Rein Attorneys-George W. Price and Murray Schaffer ABSTRACT: A process of treating tobacco in the manufacture of reconstituted tobacco is disclosed wherein the color of the finished reconstituted product is lightened by the removal of basic polyphenols present in the starting batch. The process involves washing the tobacco with water to form an aqueous extract thereof, separating the extract and treating it with absorbent agents such as activated alumina or polyamids to remove the basic polyphenols and finally reincorporating the extract minus the removed polyphenols into the fibrous tobacco mass.
raocsss or MANUFACTURTNG RECONSTITUTED TOBACCO or [.IGHT COLOR The present invention relates to a method for the preparation of reconstituted tobacco sheet and more particularly to an improved process for preparing light colored reconstitutet. tobacco sheet, despite the use of heat as a processing aid at any step of the process.
The commercial method for the manufacture of reconstituted tobacco sheet requires the application of heat at some stage in the processing e.g. either in the preparative stages and/or in the drying. it is known that the color of the finished tobacco product darkens because of the heating; the level of darkening being a function of temperature and heating time. As a rule, it is desirable to produce a light colored tobacco sheet and various steps are taken to achieve this goal, for example, the addition of dyes or coloring chemicals, the addition a of color masking agents (whiteners") such as titanium dioxcially if excessive amounts are needed to produce the desired results. Excessive use of dyes can produce leaching" problems while excessive use of whiteners" can result in sheets which are greyish in appearance or lack proper physical structure. In the case of controlled temperature and heating time, undesirable limits are put upon the manufacturing procedures. The invention herein revealed makes it possible to produce a light colored, reconstituted tobacco sheet without the resort to dyes for color preservation and without any undue limitations on the temperature and heating time used in the process. This is achieved by selectively removing from the tobacco the agents responsible for the darkening of the tobacco on heating.
In the preparation of additive reconstituted tobacco, tobacco, such as stems, field scrap, cuttings, whole leaf and the like, -is preferably uniformly comminuted and formed into tobacco sheet suitable for later machine processing. On the other hand, in the preparation of all-tobacco reconstituted sheet or i in reconstituted sheets wherein a more efficient utilization of the natural gums of the tobacco is desired, the tobacco is usually ground to colloid-forming size particles by a wet process or refining. However, the large amount of energy and time required for the preparation of these colloid-forming size' tobacco particles has limited its use for the preparation of reconstituted sheets.
To reduce the energy expended and time involved to comminute the tobacco particles in the wet process, it is desirable to cook the tobacco prior to refining. This cooking operation reduces the refining time and simultaneously improves the physical properties of the finished product. However, the cooking causes darkening of. the tobacco and hence darkens the sheets made from this cooked tobacco material, thereby making, such sheets unacceptable in a number of manufac-' tured tobacco products.
Many attempts have been made heretofore to produce reconstituted tobacco sheets using heat at some stage in the processing without the adverse darkening of the tobacco,
using various techniques and methods, but, in general, such at- The present invention provides a solutionto this longstand problem, and results in a great reduction in energy and time required to obtain good quality reconstituted tobacco sheets of acceptable color. A further object of the present invention is to provide a method for producing a light colored reconstituted tobacco sheet despite the use of heat as a processing aid.
A still further object of the present invention is to remove Still another object of the present invention is to provide a.
method for accomplishing all of the above, which can be used in processing large quantities of tobacco resulting in a reconstituted sheet of tobacco having an acceptable color and to do so in an economical and easily controlable method.
Other objects and advantages of the present invention will be apparent from the further reading of the specification and of the appended claims.
Tobacco as defined for this invention includes any type of tobacco suitable for the manufacture: of reconstituted tobacco sheet, such as stern, veins, scrap and waste tobacco, cuttings and the like, as well as whole leaf or portions thereof.
In general, the method of the present invention discloses a method of removing from the tobacco washings the agents responsible for the darkening of the tobacco when it is exposed to heat. The treated washings are then returned to the tobacco being processed, and the product prepared in a conventional manner to provide a reconstituted tobacco sheet of good physical properties without detriment to the sheet color. lthas long been commonly believed that the agents responsible for the darkening of the tobacco on cooking were the carbohydrates and the amino acids, which react during the heating to form dark colored compounds, the process being called the Mai1lard" reaction. We have discovered that neither'the carbohydrates nor the :amino acids darken the tobacco significantly on heating, but that polyphenols contained in the tobacco, especially the basic-polyphenols, do cause a significant darkening of the tobacco upon exposure to heating. This phenomenon is also pH dependent.
A series of tests were run to isolate and determine the agents which caused tobacco darkening upon heating. The following procedure illustrates how the polyphenols were identified as the agents which cause tobacco darkening during heating. A sample of Bright stern dust weighing 10 g. was mixed with ml. of distilled water. The slurry was filtered on a Buchner funnel using Whatrnan No. l filter paper. The filter cake and filtrate were retained. The filter cake was subsequently mixed with 90 ml. of a predleterrnined liquid and the slurry transferred to a vessel, such as a mason jar, which was sealed and placed in a pressure cooker, where it washeated at 250 F. at 15 psi. for 2 hours. Upon cooling, three sheets having a thickness of about 0.25-0.30 mm. were cast from the slurry on 20 cm. x 20 cm. glass plates. The sheets were dried in an ovenat ll0-l15 C. for about 15-20 minutes and the color of each sheet was read in a Gardner automatic color difference meter, Model AC-2 A, Series 200. Readings were made by placing the plate over the Gardner aperture with the tobacco side facing the aperture. A number of readings were 'taken at different points on each plate so as to obtain an overall average.
The test results in table lwere obtained with various add i tives in the predetermined liquid and serve to illustrate that polyphenols are the agents causing the darkening of the tobacco on exposure to heat. Water-washed Bright stern dust was used in all cases, unless otherwise indicated. The weight of the washed tobacco in each sample was 7 g. dry weight and this was suspended in 90 ml. of liquid prior to heating.
3 4 TABLE 1.COLOR F SHEETS PREPARED FROM BRiGglITggglgi DUST HEATED IN SOLVENIS CONTAINING VARIOUS pH before pH after Materials heating heating Rd a+ b+ Washed tobacco plus water (positive control) 24 9 3. 1 21.5 Unwashed tobacco plus water 16. 3 Washed tobacco plus washings (negative control) 16. 4 Washed tobacco plus sucrose (2 gm.) plus water 25. 4 Washed tobacco plus glucose (2 gm.) plus water.. 25. 2 Washed tobacco plus fructose (2 gm.) plus water 24. 7 Washed tobacco plus sucrose, fructose, glucose (2 gm. each) plus water 26. 8 Washed tobacco plus tryptone (1 gm.) (casein digest) plus water 22. 3 2. 7 Washed tobacco plus tryptone plus sucrose (1 gm. each) plus water. 22. 9 2. 5 Washed tobacco plus tryptone plus glucose (1 gm. each) plus water 22. 2 3. 3 Washed tobacco plus tryptone plus fructose (1 gm. each) plus water 22. 0 2. 5 Washed tobacco plus tryptone plus glucose, fructose, sucrose (1 gm. each) plus water. 21. 9 3. 8 Washed tobacco plus water plus acidic polyphenols 22. 6 3. 5 Basic polyphenols plus washed tobacco plus water 12. 4 5. 8 Acidified basic polyphenols plus washed tobacco plus wate 17. 2 4. 7 Washed tobacco plus Pb acetate sol. (10%) water 23. 4
NorE.Rd=Brightness factor; black=0; white=l00; a+, b+=Coordinates on a chromaticity diagram; P Acetate=lead acetate.
The polyphenol fractions shown in table I were obtained as follows: 90 ml. of a tobacco-water extract, prepared as described above, was mixed with ml. ofa 10 percent lead acetate solution, and the formed precipitate was removed by centrifugation. This precipitate comprised the acidic polyphenol fraction.
Adding more lead acetate solution to the supernatant caused no more precipitation. An alkaline reagent, such as ammonium hydroxide (NH4OH) was added to the supernatant until the pH was about 8.59. The formed precipitate, which was collected by centrifugation, constituted the basic polyphenol fraction.
As seen from the experimental results shown in table I, the basic polyphenols make a sheet darker than even the negative control (Rd readings 12.4 and 16.4, respectively). Furthermore, it is seen that while acidifying the basic polyphenols improves the color, it is still far below the positive control (Rd readings of 17.2 and 24.9, respectively). These results show that the sugars and amino acids do not affect the sheet color and similarly neither does the lead acetate solution used to precipitate the polyphenols.
Processes for the neutralization or removal of the polyphenol from tobacco with the addition of chemical substances are fully disclosed and described in our copending application, Ser. No. 639,066 filed even date herewith. The present disclosure confines itself to the removal of polyphenols without chemical substances.
in order to extract the basic polyphenols from the tobacco without adding any chemical additive to the reconstituted tobacco sheet, the tobacco water washings can be treated with adsorbent material, which adds nothing to the extract, but selectively removes the darkening agent or agents by adsorption. For example, tobacco water washings are passed through a column containing a selected adsorbent material, such as activated alumina. The adsorbent removes the darkening material, but leaves the other valuable tobacco constituents unchanged in the extract. The treated extract is then recombined with the original washed tobacco and the combination is processed into reconstituted tobacco sheet, which retains its commercially acceptable light color with no additives.
In accordance with the present invention, untreated tobacco, such as broken leaves, cuttings, stemmings, various fragments or waste, field scrap, is subjected to a water extraction operation so as to separate the water-soluble constituents.
The water-soluble constituents of the tobacco or extract are separated from the insoluble portion by any convenient process, such as draining, pressing, or centrifuging. The aqueous extract contains various water-soluble materials, including polyphenols. This aqueous extract can then be passed through a column containing an adsorbent material, such as activated alumina. Continuous operation in a column can be effected by placing the adsorbent material and passing the aqueous extract continuously through a column. The adsorbent material removes the color-forming bodies, but leaves the other valuable tobacco constituents unchanged in the column effluent. The effluent is then recombined with the original washed tobacco and the combination is processed in a conventional form and a light colored reconstituted tobacco sheet is produced. The extracted coloring materials can be eluted from the adsorbent so that it can be reused as desired.
The following examples are set forth to demonstrate the method of this invention.
A glass column (25 cm. x 3 cm.) was filled with a slurry of 100 gm. of activated alumina (8l4 mesh) in water. The water was allowed to drain and the column was washed repeatedly with about 500l000 ml. fresh water. A water extract of tobacco dust obtained by the method described previously was passed over the column at a flow rate such that effluent was collected at 0.5 ml. per minute. The column was then washed with water until the washings were colorless. The combined water washings and collected effluent were then concentrated to 100 ml. under vacuum in a flash evaporator using a temperature range of 36-38 C. The solids content in the concentrate, as well as in the original water tobacco extract were determincd and the recovery of material from the column calculated from these values. The test results are presented in table 2.
TABLE 2.SOLIDS IN TOBACCO-WATER EXTRACTS AND IN COLUMN EFFLUENT FROM ALUMINA COLUMNS Solids Solids in Solids put recovered in 0 1120 on concentrated Tobacco extract, column efliuents Percent Sample stems percent (gm.) (gm.) recovery 1 Bright-.. 4.50 9.00 6.73 74.5 2 d 4. 57 9. 14 6. 72 74. 5 3 .-do. 4. 52 9. 04 6. 52 72. 5 5 5 4 4. 55 9. 10 3. 17 6. 34 3. 15 6. 30 5. 63 89. 2 3. 15 6. 30 5. 64 89. 3 3. 14 6.28 5. 67 90. 5
The figures in table 2 show that the solids recovery is 73- 75 percent for Bright stem extracts and 89-91 percent for Penn. stem extracts.
The material not removed from the column by water washing was eluted off by passing 2 normal formic acid through the column. Fractions were collected at a rate of 0.5 ml. per minute. The eluted samples were very dark in color. The 2 normal formic acid removed all the adsorbed material leaving the activated alumina free of color. The alumina was washed with water until free of acid, dried in the oven l30-l40 C.) overnight and used again.
The formic acid was removed from the eluate (i.e., the
basic-polyphenols) by evaporation under vacuum in a flash evaporator. The remaining dark brown material was made up to a ml. volume with water and tested for carbohydrates by a thin layer chromatographv method. such as rlpcorihri in the Journal of Chromatography l8, l70-l74 (1965 Samples of the effluent concentrate from the column previously referred to as well as the original tobacco-water extract were also examined for carbohydrates. The results showed that practically all of the carbohydrates found in the original tobacco-water extract were recovered in the concentrated effluent while only significant amounts were found in the formic acid eluate.
It should be noted that the material. which could not be removed from the column by water could be eluted off by other suitable solvents, such as 50 percent ethanol containing 2 normal HCl or by 2 normal HCl solution. Advantageously, formic acid is preferred, since it is easily removed by evaporation under vacuum. This makes it possible to recover the solids from the formic acid eluate and their subsequent utilization in the color experiments. In an operation where these solids are of no consequence, their removal from the alumina would be carried out more economically with a 2 normal HCI solution.
The effluent concentrates were made up to volume and recombined with the washed tobacco. The slurries were treated in a manner as described above. The obtained sheets were examined in a Gardner colorimeter, and the results are presented in table 3.
these materials are fine meshed and pack easily in the columns, so as to reduce flow through the columns. A pressure source would be necessary to obtain satisfactory flow through columns using these adsorbent materials. It is understood that the preferred adsorbents need not be used in a column. They can also be employed effectively in slurry-type removal polyphenols.
By the practice of the present invention, there is produced a reconstituted tobacco sheet using heat, which contains all the desirable portions of the original tobacco, and which is lighter in color than sheets made of untreated tobacco.
Various changes and modifications may be made in practicing this invention without departing from the spirit and scope thereof, and therefore, the invention is not to be limited, except as defined in the appended claims.
We claim:
TABLE fir-GARDNER READINGS 0N SHEETS PREPARED WITH VARIOUS EFFLUENTS AND ELUATES FROM ALUMINA COLUMNS pH of Tobacco Fraction tob. slurry Rd a+ b+ Brlght Efliuent con- 5.8 21.5 3 7 17.5
centrate. Do -do 5.6 24.6 Do do 4.7 24.6 5.4 34.4 Do 3. 2 17. 4 4. 1 22. 7 Bright (positive c 1) 5. 3 24. 8 3. 9 35. 0 Bright (negative control) 4. 8 16. 8 4. 8 22. 3 Penn 6.3 19.6 so 24.6
3. 8 17. 1 6. 1 23.3 7.0 19.3 5.2 24.6 6. 2 17.4 5. 3 22. 8 Efliuent con- 5.1 15.8
centrate. Bulgarian (postive control) 6.7 15.3 Bulgarian (negative control) 5.2 11. 3
Note.--Posltive control consists of washed tobacco (7 gm. Negative control consists of washed tobacco plus the obtained washing The figures in table 3 show that the effluent concentrate from the adsorbent column is similar in its color properties to the positive control, while the formic acid eluate, after removing the formic acid and adjusting to volume with water, is similar to the negative control. This is particularly apparent in the Rd values.
Adsorbents, other than activated alumina, were examined. Regenerated alumina worked as well as unused alumina.
Polyamide and silica gelalso gave satisfactory results.
Other adsorbent materials could be used, such as magnesol, silicic acid or adsorption alumina, and the like. However,
ry weight) plus new water.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63903267A | 1967-05-17 | 1967-05-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3561451A true US3561451A (en) | 1971-02-09 |
Family
ID=24562448
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US639032A Expired - Lifetime US3561451A (en) | 1967-05-17 | 1967-05-17 | Process of manufacturing reconstituted tobacco of light color |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US3561451A (en) |
| DE (1) | DE1767523A1 (en) |
| GB (1) | GB1162510A (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5005593A (en) * | 1988-01-27 | 1991-04-09 | R. J. Reynolds Tobacco Company | Process for providing tobacco extracts |
| US5025812A (en) * | 1989-08-10 | 1991-06-25 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5065775A (en) * | 1990-02-23 | 1991-11-19 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5131414A (en) * | 1990-02-23 | 1992-07-21 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5234008A (en) * | 1990-02-23 | 1993-08-10 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5243999A (en) * | 1991-09-03 | 1993-09-14 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5377698A (en) * | 1993-04-30 | 1995-01-03 | Brown & Williamson Tobacco Corporation | Reconstituted tobacco product |
| US5601097A (en) * | 1991-12-31 | 1997-02-11 | Imasco Limited | Tobacco treatment |
| US6058940A (en) * | 1997-04-21 | 2000-05-09 | Lane; Kerry Scott | Method and system for assay and removal of harmful toxins during processing of tobacco products |
| WO2001028367A1 (en) * | 1997-04-21 | 2001-04-26 | Kerry Scott Lane | Method and system for assay and removal of harmful toxins during processing of tobacco products |
| US6298859B1 (en) * | 1998-07-08 | 2001-10-09 | Novozymes A/S | Use of a phenol oxidizing enzyme in the treatment of tobacco |
| US6679270B2 (en) | 2000-10-05 | 2004-01-20 | Nicolas Baskevitch | Reduction of nitrosamines in tobacco and tobacco products |
| US20050005947A1 (en) * | 2003-07-11 | 2005-01-13 | Schweitzer-Mauduit International, Inc. | Smoking articles having reduced carbon monoxide delivery |
| US20050056294A1 (en) * | 2002-11-19 | 2005-03-17 | Wanna Joseph T. | Modified reconstituted tobacco sheet |
| US20050263161A1 (en) * | 2004-05-27 | 2005-12-01 | Brown & Williamson Tobacco Corporation | Tobacco filler of low nitrogen content |
| US20050279374A1 (en) * | 2004-04-14 | 2005-12-22 | Philip Morris Usa Inc. | Reduction of phenolic compound precursors in tobacco |
| US20060162733A1 (en) * | 2004-12-01 | 2006-07-27 | Philip Morris Usa Inc. | Process of reducing generation of benzo[a]pyrene during smoking |
| US20060174904A1 (en) * | 2005-02-07 | 2006-08-10 | Schweitzer-Mauduit International, Inc. | Smoking articles having reduced analyte levels and process for making same |
| US20070295348A1 (en) * | 2006-06-01 | 2007-12-27 | Schweitzer-Mauduit International, Inc. | Free air burning smoking articles with reduced ignition proclivity characteristics |
| US20080006286A1 (en) * | 2002-11-19 | 2008-01-10 | John-Paul Mua | Reconstituted Tobacco Sheet and Smoking Article Therefrom |
| US20080178894A1 (en) * | 2007-01-26 | 2008-07-31 | Philip Morris Usa Inc. | Methods and apparatus for the selective removal of constituents from aqueous tobacco extracts |
| WO2012170761A1 (en) | 2011-06-10 | 2012-12-13 | Schweitzer-Mauduit International, Inc. | Tobacco material containing non-isometric calcium carbonate microparticles |
| WO2013170028A1 (en) | 2012-05-09 | 2013-11-14 | Lanig Le Bec | Tobacco product that produces lower carbon monoxide to tar ratio |
| WO2014134254A1 (en) | 2013-02-28 | 2014-09-04 | Schweitzer-Mauduit International, Inc. | Composition for making a tea beverage or herbal and vegetable broths |
| WO2014141201A2 (en) | 2013-03-15 | 2014-09-18 | Fall Safall | Method of reducing tobacco-specific nitrosamines |
| WO2014140346A1 (en) | 2013-03-15 | 2014-09-18 | Philip Morris Products S.A | Methods for reducing one or more tobacco specific nitrosamines in tobacco material |
| WO2014207704A2 (en) | 2013-06-26 | 2014-12-31 | Pan Jiayi | Filter media |
| US9149068B2 (en) | 2012-10-11 | 2015-10-06 | Schweitzer-Mauduit International, Inc. | Wrapper having reduced ignition proclivity characteristics |
| US20150296872A1 (en) * | 2012-11-26 | 2015-10-22 | British American Tobacco (Investments) Limited | Treatment of tobacco material |
| US10178872B2 (en) | 2010-10-29 | 2019-01-15 | Schweitzer-Manduit International, Inc. | Method for producing articles of plant origin impregnated with a liquid plant substance |
| EP3561179A1 (en) | 2014-03-28 | 2019-10-30 | SWM Luxembourg s.a.r.l. | Reconstituted plant material and its use for packaging, wrapping and food appliances |
| US10729662B2 (en) | 2013-08-20 | 2020-08-04 | Schweitzer-Mauduit International, Inc. | Product comprising a plant for medicinal, cosmetic, coloring or dermatologic use |
| US10751282B2 (en) | 2013-08-02 | 2020-08-25 | Schweitzer-Mauduit International, Inc. | Edible product comprising reconstituted plant material |
| US11035079B2 (en) | 2016-04-05 | 2021-06-15 | Schweitzer-Mauduit International, Inc. | Vegetable paper comprising fibres of a plant |
| US11484497B2 (en) | 2013-02-28 | 2022-11-01 | Schweitzer-Mauduit International, Inc. | Composition for making a tea beverage or herbal and vegetable broths |
| US11737472B2 (en) | 2015-03-02 | 2023-08-29 | Mativ Holdings, Inc. | Low bulk density composition for making a tea beverage having reduced dust or fines |
| US12201142B2 (en) | 2020-09-11 | 2025-01-21 | SWM Holdings US, LLC | Filter for smoking or vaping article comprising a nonwoven substrate |
| US12543775B2 (en) | 2013-03-15 | 2026-02-10 | Philip Morris Products S.A. | Methods for reducing one or more tobacco specific nitrosamines in tobacco material |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US267764A (en) * | 1882-11-21 | Manufacture of tobacco | ||
| US720830A (en) * | 1902-04-17 | 1903-02-17 | Mark W Marsden | Tobacco wrapper and process of making same. |
| US802487A (en) * | 1903-12-28 | 1905-10-24 | Karl Wimmer | Treatment of tobacco for the removal of nicotin. |
| US3145717A (en) * | 1959-10-22 | 1964-08-25 | C H Dexter & Sons Inc | Methods of making tobacco web material |
| US3255760A (en) * | 1962-08-03 | 1966-06-14 | Kimberly Clark Co | Tobacco product which produces less tars |
| US3351066A (en) * | 1965-07-20 | 1967-11-07 | Harry R Colgate | Chemical composition alteration of tobacco |
| US3390685A (en) * | 1965-03-11 | 1968-07-02 | Eresta Warenhandelsgmbh | Process for extracting substances from plant particles |
-
1967
- 1967-05-17 US US639032A patent/US3561451A/en not_active Expired - Lifetime
-
1968
- 1968-04-30 GB GB20442/68A patent/GB1162510A/en not_active Expired
- 1968-05-17 DE DE19681767523 patent/DE1767523A1/en active Pending
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US267764A (en) * | 1882-11-21 | Manufacture of tobacco | ||
| US720830A (en) * | 1902-04-17 | 1903-02-17 | Mark W Marsden | Tobacco wrapper and process of making same. |
| US802487A (en) * | 1903-12-28 | 1905-10-24 | Karl Wimmer | Treatment of tobacco for the removal of nicotin. |
| US3145717A (en) * | 1959-10-22 | 1964-08-25 | C H Dexter & Sons Inc | Methods of making tobacco web material |
| US3255760A (en) * | 1962-08-03 | 1966-06-14 | Kimberly Clark Co | Tobacco product which produces less tars |
| US3390685A (en) * | 1965-03-11 | 1968-07-02 | Eresta Warenhandelsgmbh | Process for extracting substances from plant particles |
| US3351066A (en) * | 1965-07-20 | 1967-11-07 | Harry R Colgate | Chemical composition alteration of tobacco |
Cited By (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5005593A (en) * | 1988-01-27 | 1991-04-09 | R. J. Reynolds Tobacco Company | Process for providing tobacco extracts |
| US5025812A (en) * | 1989-08-10 | 1991-06-25 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5065775A (en) * | 1990-02-23 | 1991-11-19 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5131414A (en) * | 1990-02-23 | 1992-07-21 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5234008A (en) * | 1990-02-23 | 1993-08-10 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5243999A (en) * | 1991-09-03 | 1993-09-14 | R. J. Reynolds Tobacco Company | Tobacco processing |
| US5601097A (en) * | 1991-12-31 | 1997-02-11 | Imasco Limited | Tobacco treatment |
| US5377698A (en) * | 1993-04-30 | 1995-01-03 | Brown & Williamson Tobacco Corporation | Reconstituted tobacco product |
| US6058940A (en) * | 1997-04-21 | 2000-05-09 | Lane; Kerry Scott | Method and system for assay and removal of harmful toxins during processing of tobacco products |
| WO2001028367A1 (en) * | 1997-04-21 | 2001-04-26 | Kerry Scott Lane | Method and system for assay and removal of harmful toxins during processing of tobacco products |
| US6298859B1 (en) * | 1998-07-08 | 2001-10-09 | Novozymes A/S | Use of a phenol oxidizing enzyme in the treatment of tobacco |
| AU775920B2 (en) * | 1999-10-18 | 2004-08-19 | Kerry Scott Lane | Method and system for assay and removal of harmful toxins during processing of tobacco products |
| AP1894A (en) * | 1999-10-18 | 2008-09-29 | Kerry Scott Lane | Method and system for assay and removal of harmful toxins during processing of tobacco products. |
| US6679270B2 (en) | 2000-10-05 | 2004-01-20 | Nicolas Baskevitch | Reduction of nitrosamines in tobacco and tobacco products |
| US8136533B2 (en) | 2002-11-19 | 2012-03-20 | R.J. Reynolds Tobacco Company | Reconstituted tobacco sheet and smoking article therefrom |
| US20050056294A1 (en) * | 2002-11-19 | 2005-03-17 | Wanna Joseph T. | Modified reconstituted tobacco sheet |
| US20080006286A1 (en) * | 2002-11-19 | 2008-01-10 | John-Paul Mua | Reconstituted Tobacco Sheet and Smoking Article Therefrom |
| US8443812B2 (en) | 2003-07-11 | 2013-05-21 | Schweitzer-Mauduit International, Inc. | Smoking articles having reduced carbon monoxide delivery |
| US8353301B2 (en) | 2003-07-11 | 2013-01-15 | Schweitzer-Mauduit International, Inc. | Smoking articles having reduced carbon monoxide delivery |
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| US20090283104A1 (en) * | 2003-07-11 | 2009-11-19 | Hampl Jr Vladimir | Smoking Articles Having Reduced Carbon Monoxide Delivery |
| US20050279374A1 (en) * | 2004-04-14 | 2005-12-22 | Philip Morris Usa Inc. | Reduction of phenolic compound precursors in tobacco |
| US7581543B2 (en) | 2004-04-14 | 2009-09-01 | Philip Morris Usa Inc. | Reduction of phenolic compound precursors in tobacco |
| US20050263161A1 (en) * | 2004-05-27 | 2005-12-01 | Brown & Williamson Tobacco Corporation | Tobacco filler of low nitrogen content |
| US20060162733A1 (en) * | 2004-12-01 | 2006-07-27 | Philip Morris Usa Inc. | Process of reducing generation of benzo[a]pyrene during smoking |
| US8151806B2 (en) | 2005-02-07 | 2012-04-10 | Schweitzer-Mauduit International, Inc. | Smoking articles having reduced analyte levels and process for making same |
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| US20110000497A1 (en) * | 2005-02-07 | 2011-01-06 | Schweitzer-Mauduit International, Inc. | Smoking Articles Having Reduced Analyte Levels and Process For Making Same |
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| US9049886B2 (en) | 2007-01-26 | 2015-06-09 | Philip Morris Usa Inc. | Methods and apparatus for the selective removal of constituents from aqueous tobacco extracts |
| US10178872B2 (en) | 2010-10-29 | 2019-01-15 | Schweitzer-Manduit International, Inc. | Method for producing articles of plant origin impregnated with a liquid plant substance |
| WO2012170761A1 (en) | 2011-06-10 | 2012-12-13 | Schweitzer-Mauduit International, Inc. | Tobacco material containing non-isometric calcium carbonate microparticles |
| US10098378B2 (en) | 2011-06-10 | 2018-10-16 | Stephane Rouillard | Tobacco material containing non-isometric calcium carbonate microparticles |
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Also Published As
| Publication number | Publication date |
|---|---|
| GB1162510A (en) | 1969-08-27 |
| DE1767523A1 (en) | 1971-10-21 |
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