US2430050A - Gas odorizing - Google Patents
Gas odorizing Download PDFInfo
- Publication number
- US2430050A US2430050A US574447A US57444745A US2430050A US 2430050 A US2430050 A US 2430050A US 574447 A US574447 A US 574447A US 57444745 A US57444745 A US 57444745A US 2430050 A US2430050 A US 2430050A
- Authority
- US
- United States
- Prior art keywords
- gas
- mercaptan
- odorant
- oxygen
- odor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000007789 gas Substances 0.000 description 38
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 31
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 22
- 239000003205 fragrance Substances 0.000 description 22
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 18
- -1 alkyl mercaptans Chemical class 0.000 description 16
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 16
- 229910052760 oxygen Inorganic materials 0.000 description 16
- 239000001301 oxygen Substances 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000003112 inhibitor Substances 0.000 description 9
- 239000003345 natural gas Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- 150000002989 phenols Chemical class 0.000 description 8
- 238000009835 boiling Methods 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 6
- 238000005562 fading Methods 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- ZRKMQKLGEQPLNS-UHFFFAOYSA-N 1-Pentanethiol Chemical compound CCCCCS ZRKMQKLGEQPLNS-UHFFFAOYSA-N 0.000 description 5
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 230000008016 vaporization Effects 0.000 description 4
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 150000001555 benzenes Chemical class 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 230000009965 odorless effect Effects 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- KAEAMHPPLLJBKF-UHFFFAOYSA-N iron(3+) sulfide Chemical compound [S-2].[S-2].[S-2].[Fe+3].[Fe+3] KAEAMHPPLLJBKF-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- 206010003497 Asphyxia Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241001307210 Pene Species 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical class CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J1/00—Production of fuel gases by carburetting air or other gases without pyrolysis
Definitions
- This invention relates to improvements in the distribution of combustible or fuel gas, such as natural gas, manufactured gas, or their mixtures.
- my invention relates to improvements in the odorization of odor deficient gases of the foregoing class by the addition of malodorants generally added to raise the odor intensity of the gas to aid in the detection of leaks, and wherein the malodorants employed are composed essentially of alkyl mercaptans.
- efilcacy of the introduced alkyl mercaptan odorant may be maintained in substantially uniform degree over several hundred miles of distribution mains without necessity for unequal or too high odorization at the point of introduction 'or distribution points adjacent thereto, or requirement for re-introduction at successive points in th system, all with an attendant economy in materials, and labor, more satisfactory and uniform results, and the attendant enhanced factor of safety.
- the antioxidants, or rather polymerization inhibitors which I employ by vaporization in admixture with the mercaptan odorants, or by direct vaporization into the gas mains are the mono or polyhydrie derivatives of benzene or its homologs, and particularly the mono and polyhydric phenols, having a boiling point not greater than about 210 C., atmospheric pressure, such as cresol, ortho. tertiary butyl phenol, 2-4 (ll-tertiary butyl phenol and the like.
- Typical systems wherein the practice of my invention is adapted may be illustrated by the average city distribution system utilizing either a mixture of natural gas and manufactured gas or straight natural gas, or by the high pressure transmission of natural gas derived from distillate producing wells that operate under a partial vacuum. In the latter instance although the gas is substantially dry, any leakage on the suction side of the first compressor station results in air leaking into the gas with the oxygen content sometimes rising to as much as 2%.
- the oxygen reacts with the iron sulfide formed as above, to form sulfur and iron oxide, the regenerated iron oxide being then again free to react with the mercaptan.
- the iron oxide acts as a catalyst for the reaction of the mercaptan with oxygen to form free sulfur, water and alkyl sulfides.
- the system containing both moisture and oxygen in addition to the iron oxide it appears that bOth reactionstake place, that is, direct reaction of the mercaptan with the iron oxide and reaction of the mercaptan with oxygen under the influence of the iron oxide.
- the following reactions appear to be typical and further illustrative of the conversion of the malodorous mercaptans to relatively odorless compounds. They further illustrate that the destructive action results from reaction with the polymers, rather than the mercaptan monomers, that is, it is first necessary for two molecules of mercaptan to come together in order to split off two molecules of hydrogen and one of sulfur to produce the reaction products? That such is the mechanics of the reaction has been demonstrated In a system containing rust, oxygen and substantially dry gas, such as the natural gas high pressure transmission system previously described, the reaction is essentially the latter (4).
- oxidative destruction of these odorants can be prevented by inhibiting the polymerization of the mercaptans vaporized into the gas line by incorporation with the mercaptan approximately A; of 1% by weight thereof of a suitable polymerization inhibitor.
- These inhibitors are of the class generally useful as vapor phase gum formation inhibitors in gas distribution systems and, as previously described comprise the mono and poly hydric derivatives of benzene and its homologs, particularly the. mono and polyby for example the polymerization of amyl mercaptan in the liquid phase to a relatively nonvolatile liquid.
- this polymerized material was distilled at atmospheric pressure, regular amyl mercaptan was recovered.
- the normally liquid material is vaporized into the gas line in a similar manner, but from the resulting reactions in the gas distribution system it is apparent that it polymerizes therein. 1
- the ferric oxide appearsto react with mercaptan under the uence of. the ferric oxide as a catalyst as follows;
- hydric phenols such as cresol, the alkylated phenols, etc, which boil preferably below 210 C.
- the inhibitor normal use may be made of small proportions of the conventional alkyl mercaptan odorants such as ethyl, propyl, butyl and amyl mercaptans or mixtures thereof.
- cresol and its homologs as an inhibitor will cause the odor produced by the mercaptan to be detected in two days in a city gas distribution of the class previously described, where previously odorant in the form of puremercaptan had been added to the gas for over a year without penetration to the ends of the system.
- a mercaptan based malodorant with a suitable inhibitor added to it will enable the odor of the mercaptan to be detected at the extreme end of a 400 mile long high pressure gas distribution main containing only pound of mercaptan odorant per million cubic feet of gas. Without the use of the inhibitor, even as much as thirty pounds of pure mercaptan failed to give a sufficiently strong odor at the end of the line, even though the gas immediately downstream from the point of odorant introduction was too highly odorized.
- inhibitors may be vaporized into the gas stream near the introduction point of the mercaptan odorant, or added to the odorant and jointly vaporized therewith into the gas stream.
- a suitable composition has been found to be a petroleum distillate fraction containing in admixture both ethyl, propyl and butyl mercaptans together with ortho, meta and para cresols.
- a method for preventing odor fading due to oxidation of mercaptan bearing odorant in a combustible gas'free from gum forming constituents which comprises incorporating and vaporizing with. said odorant a small proportion of acompound selected from the class consisting of mono and poly hydric derivatives of benzene and its homologs boiling below about 210 C.
- a method for preventing odor fading due to oxidation of alkyl mercaptan odorant containedin a combustible gas stream free from gum forming constituents which comprises vaporizing into the gas stream, adjacent the point of introduction of the mercaptan odorant, a compound selected from the class consisting of the mono and poly hydric phenols boiling below about 210 C.
- a method for preventing odor fading of alkyl mercaptan odorant contained in a combustible natural gas stream by oxidation due to the presence of iron oxide and moisture whichcomprises incorporating therewith in .vaporous form a small proportion of a compound selected from the class consisting of the mono and polyhydric phenols boiling below about 210 C.
- a method for preventing odor fading of alkyl mercaptan odorant contained 'in a combustible natural gas stream by oxidation due to the presence of iron oxide and oxygen which comprises incorporating therewith in vaporous and poly hydric phenols to inhibit polymerization of said odorant, said compound being normally liquid and having a boiling point below about 210 C.
- a method of odorizing an odor deficient combustible gas stream free from gum forming constituents and for preventing odor fading form a small proportion of a compound selected from the class consisting of the mono and poly hydric phenols boiling below about 210 C.
- a method for preventing odor fading of alkyl mercaptan odorant contained in a combustible natural gas stream by oxidation due to the presence of iron oxide, oxygen and moisture which comprises incorporating therewith in vaporous form a smallproportion of a compound thereof due to oxidizing agents present in the gas distribution conduits which comprises introducing into the gas stream in vaporized form alkyl mercaptan odorant and a small proportion of a compound selected from the class consisting of the mono and poly hydric phenols boiling below about 210 C.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Description
Patented Nov. 4, 1941 UNITED STATES 'PATENT OFFICE GAS ODOBIZING Charles E. Gill, Chicago, Ill.
" No Drawing. Application January 24, 1945,
Serial N0. 574,447
. 7 Claims. 1
This invention relates to improvements in the distribution of combustible or fuel gas, such as natural gas, manufactured gas, or their mixtures.
More particularly my invention relates to improvements in the odorization of odor deficient gases of the foregoing class by the addition of malodorants generally added to raise the odor intensity of the gas to aid in the detection of leaks, and wherein the malodorants employed are composed essentially of alkyl mercaptans.
It has, however, been found that when pure alkyl mercaptans are employed that their characteristlc odor tends to fade and disappear due to progressive oxidation of the mercaptan content of the odorant when the gas is transported for bustlble gas as both the public and distribution personnel have learned to depend upon the odor of the gas for detection and consequently explosions or asphyxiation can occur in a gas system that has been conscientiously endeavoring to provide every safety factor against them.
It is therefore the object of my invention to provide a method for the successful and dependable employment or alkyl mercaptan odorants for the odorizing of combustible gas in distribu- 'tion systemsv therefor in a manner whereby the efficiency of the odorant will be maintained from the point of introduction to the extreme ends of the distribution system, and the mercaptans permitted to flow unhindered throughout the system with the gas and odorize the gas until it is burned or otherwise utilized. Also, by proceeding in accordance with the method of my invention, the
efilcacy of the introduced alkyl mercaptan odorant may be maintained in substantially uniform degree over several hundred miles of distribution mains without necessity for unequal or too high odorization at the point of introduction 'or distribution points adjacent thereto, or requirement for re-introduction at successive points in th system, all with an attendant economy in materials, and labor, more satisfactory and uniform results, and the attendant enhanced factor of safety.
In general I accomplish the objects of my invention by preventing the oxidation of the mercaptans in the gas distribution system, or rather by inhibiting the polymerization of the mercaptans, since it appears that their polymers, rather than their monomers are subject to oxidation under the conditions prevailing, as will be later more fully described. The antioxidants, or rather polymerization inhibitors which I employ by vaporization in admixture with the mercaptan odorants, or by direct vaporization into the gas mains are the mono or polyhydrie derivatives of benzene or its homologs, and particularly the mono and polyhydric phenols, having a boiling point not greater than about 210 C., atmospheric pressure, such as cresol, ortho. tertiary butyl phenol, 2-4 (ll-tertiary butyl phenol and the like.
Typical systems wherein the practice of my invention is adapted may be illustrated by the average city distribution system utilizing either a mixture of natural gas and manufactured gas or straight natural gas, or by the high pressure transmission of natural gas derived from distillate producing wells that operate under a partial vacuum. In the latter instance although the gas is substantially dry, any leakage on the suction side of the first compressor station results in air leaking into the gas with the oxygen content sometimes rising to as much as 2%.
Experience has proven that when pure or substantially pure alkyl mercaptans are utilized; under such circumstances, the odor cannot pene, trate or be relied upon to completely enetrate to the extreme ends of the distribution system, and in a system containing rust and moisture but substantially free of oxygen, this situation prevails until the iron oxide in the system has been saturated with mercaptan, but which may require several years for the condition of equilibrium to be reached with attendant intervening hazard. Thus in a gas distribution line containing iron oxide (Fe-20s) moisture and vaporized alkyl mercaptan, the iron oxide, in the presence of the moisture, reacts with the mercaptan to .form water, iron sulfide and relatively odorless alkyl sulfides. If no oxygen is admitted, the system after a long time will become "saturated and the odor will progress to the end 0f-the line. However, pockets or odorless areas remain in the distribution system for as much as seven or eight 55 years after odorization has begun, because of the slow flow of gas in these particular areas and thereby constitute potential hazards.
In the event that the system contains in addition an appreciable amount of oxygen, the oxygen reacts with the iron sulfide formed as above, to form sulfur and iron oxide, the regenerated iron oxide being then again free to react with the mercaptan. In the event that the system contains iron oxide but where the gas is a substantially dry, but oxygen containing natural gas, the iron oxide acts as a catalyst for the reaction of the mercaptan with oxygen to form free sulfur, water and alkyl sulfides. In the system containing both moisture and oxygen in addition to the iron oxide, it appears that bOth reactionstake place, that is, direct reaction of the mercaptan with the iron oxide and reaction of the mercaptan with oxygen under the influence of the iron oxide.
The following reactions appear to be typical and further illustrative of the conversion of the malodorous mercaptans to relatively odorless compounds. They further illustrate that the destructive action results from reaction with the polymers, rather than the mercaptan monomers, that is, it is first necessary for two molecules of mercaptan to come together in order to split off two molecules of hydrogen and one of sulfur to produce the reaction products? That such is the mechanics of the reaction has been demonstrated In a system containing rust, oxygen and substantially dry gas, such as the natural gas high pressure transmission system previously described, the reaction is essentially the latter (4).
In accordance with my present invention I have found that oxidative destruction of these odorants can be prevented by inhibiting the polymerization of the mercaptans vaporized into the gas line by incorporation with the mercaptan approximately A; of 1% by weight thereof of a suitable polymerization inhibitor. These inhibitors are of the class generally useful as vapor phase gum formation inhibitors in gas distribution systems and, as previously described comprise the mono and poly hydric derivatives of benzene and its homologs, particularly the. mono and polyby for example the polymerization of amyl mercaptan in the liquid phase to a relatively nonvolatile liquid. When this polymerized material was distilled at atmospheric pressure, regular amyl mercaptan was recovered. In employment of the mercaptans as odorants, the normally liquid material is vaporized into the gas line in a similar manner, but from the resulting reactions in the gas distribution system it is apparent that it polymerizes therein. 1
Thus in a system containing alkyl mercaptan, rust and moisture, the following reactions appear to occur.
2 R.SH R--SR (mercaptan polymer) t (2) H Moisture when all of the ferric oxide has been reacted with, further action stops and if no oxygen is admitted to react with the ferric sulfide then the line is said to be saturated and the'odor will not be adversely affected in the saturated part of the distribution system.
Should the system, however, contain oxygen, the oxygen reacts with the ferric sulfide to regenerate ferric oxide as follows:
2Fe2 S3+3Oz 6S+2Fe2O3 whereupon the cycle repeats itself, the ferric oxide reacting with mercaptan polymer as in (2) aboveg,
In addition tothe foregoing when the system fcontains both oxygen and moisture, the ferric oxide appearsto react with mercaptan under the uence of. the ferric oxide as a catalyst as follows;
4 H I F620:
hydric phenols, such as cresol, the alkylated phenols, etc, which boil preferably below 210 C. By the employment of the inhibitor, normal use may be made of small proportions of the conventional alkyl mercaptan odorants such as ethyl, propyl, butyl and amyl mercaptans or mixtures thereof.
Thus I have found that the use of cresol and its homologs as an inhibitor will cause the odor produced by the mercaptan to be detected in two days in a city gas distribution of the class previously described, where previously odorant in the form of puremercaptan had been added to the gas for over a year without penetration to the ends of the system.
I have also found that a mercaptan based malodorant with a suitable inhibitor added to it will enable the odor of the mercaptan to be detected at the extreme end of a 400 mile long high pressure gas distribution main containing only pound of mercaptan odorant per million cubic feet of gas. Without the use of the inhibitor, even as much as thirty pounds of pure mercaptan failed to give a sufficiently strong odor at the end of the line, even though the gas immediately downstream from the point of odorant introduction was too highly odorized.
These inhibitors may be vaporized into the gas stream near the introduction point of the mercaptan odorant, or added to the odorant and jointly vaporized therewith into the gas stream. A suitable composition has been found to be a petroleum distillate fraction containing in admixture both ethyl, propyl and butyl mercaptans together with ortho, meta and para cresols.
I claim as my invention:
1. A method for preventing odor fading due to oxidation of mercaptan bearing odorant in a combustible gas'free from gum forming constituents which comprises incorporating and vaporizing with. said odorant a small proportion of acompound selected from the class consisting of mono and poly hydric derivatives of benzene and its homologs boiling below about 210 C.
A method for preventing odor fading due to oxidation of alkyl mercaptan odorant containedin a combustible gas stream free from gum forming constituents which comprises vaporizing into the gas stream, adjacent the point of introduction of the mercaptan odorant, a compound selected from the class consisting of the mono and poly hydric phenols boiling below about 210 C.
3. A method for preventing odor fading of alkyl mercaptan odorant contained in a combustible natural gas stream by oxidation due to the presence of iron oxide and moisture whichcomprises incorporating therewith in .vaporous form a small proportion of a compound selected from the class consisting of the mono and polyhydric phenols boiling below about 210 C.
4. A method for preventing odor fading of alkyl mercaptan odorant contained 'in a combustible natural gas stream by oxidation due to the presence of iron oxide and oxygen which comprises incorporating therewith in vaporous and poly hydric phenols to inhibit polymerization of said odorant, said compound being normally liquid and having a boiling point below about 210 C.
7. A method of odorizing an odor deficient combustible gas stream free from gum forming constituents and for preventing odor fading form a small proportion of a compound selected from the class consisting of the mono and poly hydric phenols boiling below about 210 C.
5. A method for preventing odor fading of alkyl mercaptan odorant contained in a combustible natural gas stream by oxidation due to the presence of iron oxide, oxygen and moisture which comprises incorporating therewith in vaporous form a smallproportion of a compound thereof due to oxidizing agents present in the gas distribution conduits which comprises introducing into the gas stream in vaporized form alkyl mercaptan odorant and a small proportion of a compound selected from the class consisting of the mono and poly hydric phenols boiling below about 210 C.
CHARLES E. GILL.
REFERENCES CITED 7 The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,986,333 Fulweiler Jan. 1, 1935 OTHER REFERENCES American Gas Journal. July 1938, page 15.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US574447A US2430050A (en) | 1945-01-24 | 1945-01-24 | Gas odorizing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US574447A US2430050A (en) | 1945-01-24 | 1945-01-24 | Gas odorizing |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2430050A true US2430050A (en) | 1947-11-04 |
Family
ID=24296172
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US574447A Expired - Lifetime US2430050A (en) | 1945-01-24 | 1945-01-24 | Gas odorizing |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2430050A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2807592A (en) * | 1952-12-27 | 1957-09-24 | California Research Corp | Oxidation inhibitor for gas odorants |
| US2823104A (en) * | 1955-03-07 | 1958-02-11 | California Research Corp | Warning agent and process for the odorization of a hydrocarbon fuel gas therewith |
| US20060009372A1 (en) * | 2002-08-27 | 2006-01-12 | Symrise Gmbh & Co. Kg | Low-sulphur odorants for liquid gas |
| US9587191B2 (en) | 2013-10-01 | 2017-03-07 | Aygaz Anonim Sirketi | Sulphur-free gas odorant |
| US11279895B2 (en) * | 2017-04-25 | 2022-03-22 | Arkema France | Process for cryogenic fluid odorisation |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1986333A (en) * | 1935-01-01 | Prevention of gum formation in gas |
-
1945
- 1945-01-24 US US574447A patent/US2430050A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1986333A (en) * | 1935-01-01 | Prevention of gum formation in gas |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2807592A (en) * | 1952-12-27 | 1957-09-24 | California Research Corp | Oxidation inhibitor for gas odorants |
| US2823104A (en) * | 1955-03-07 | 1958-02-11 | California Research Corp | Warning agent and process for the odorization of a hydrocarbon fuel gas therewith |
| US20060009372A1 (en) * | 2002-08-27 | 2006-01-12 | Symrise Gmbh & Co. Kg | Low-sulphur odorants for liquid gas |
| US9587191B2 (en) | 2013-10-01 | 2017-03-07 | Aygaz Anonim Sirketi | Sulphur-free gas odorant |
| US11279895B2 (en) * | 2017-04-25 | 2022-03-22 | Arkema France | Process for cryogenic fluid odorisation |
| US11814596B2 (en) | 2017-04-25 | 2023-11-14 | Arkema France | Process for cryogenic fluid odorisation |
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