US2365377A - Method of stabilizing carbonyl containing motor fuels - Google Patents
Method of stabilizing carbonyl containing motor fuels Download PDFInfo
- Publication number
- US2365377A US2365377A US415065A US41506541A US2365377A US 2365377 A US2365377 A US 2365377A US 415065 A US415065 A US 415065A US 41506541 A US41506541 A US 41506541A US 2365377 A US2365377 A US 2365377A
- Authority
- US
- United States
- Prior art keywords
- motor fuel
- iron
- lecithin
- gasoline
- mercaptide
- 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
- 239000000446 fuel Substances 0.000 title description 47
- 238000000034 method Methods 0.000 title description 11
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 title description 9
- 230000000087 stabilizing effect Effects 0.000 title description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 36
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 21
- 239000000787 lecithin Substances 0.000 description 21
- 229940067606 lecithin Drugs 0.000 description 21
- 235000010445 lecithin Nutrition 0.000 description 21
- 229910052742 iron Inorganic materials 0.000 description 17
- 239000002184 metal Substances 0.000 description 14
- 229910052751 metal Inorganic materials 0.000 description 14
- 150000001728 carbonyl compounds Chemical class 0.000 description 12
- DBLMXLQJTBGLMP-UHFFFAOYSA-N iron tetracarbonyl hydride Chemical group [Fe].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-] DBLMXLQJTBGLMP-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 9
- 239000002244 precipitate Substances 0.000 description 8
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 229910017052 cobalt Inorganic materials 0.000 description 4
- 239000010941 cobalt Substances 0.000 description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 235000009508 confectionery Nutrition 0.000 description 3
- CFWRDBDJAOHXSH-SECBINFHSA-N 2-azaniumylethyl [(2r)-2,3-diacetyloxypropyl] phosphate Chemical compound CC(=O)OC[C@@H](OC(C)=O)COP(O)(=O)OCCN CFWRDBDJAOHXSH-SECBINFHSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229940087654 iron carbonyl Drugs 0.000 description 2
- 150000002506 iron compounds Chemical class 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- RKAGSDNHCHISPT-UHFFFAOYSA-N 4-amino-2-(2-methylpropyl)phenol Chemical compound C(C(C)C)C1=C(C=CC(=C1)N)O RKAGSDNHCHISPT-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical class [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/103—Liquid carbonaceous fuels containing additives stabilisation of anti-knock agents
Definitions
- This invention relates to a method of stabilizing against loss in octane value, motor fuel to which has been added metal carbonyl compounds, and to the stabilized motor fuel.
- hydrocarbon motor fuels which contain metal carbonyl compounds can be stabilized against deterioration and decomposition by incorporating in the motor fuel phosphatides such as lecithin and cephalin.
- the phosphatide may be added to the motor fuel either be fore, together with or after th addition of themetal carbonyl compound, but I prefer to have the phosphatide present in the motor fuel at the time the carbonyl is added, particularly in those cases where the motor fuel contains mercaptans and a polymeric carbonyl such as iron tetracarbonyl. capable of reacting with the mercaptans to form iron tricarbonyl mercaptide, is added.
- 1 B may be any alkyl or aryl radical.
- lecithin-that is, amounts comparable to amounts of inhibitors which are commonly added to motor fuelhave substantially no effect in inhibiting deterioration of the carbonyl compounds.
- lecithin or other phosphatide should be added in amounts approximately .50 to 10 grams per gallon of motor fuel and preferably in amounts approximately corresponding to the amount of iron contained in the carbonyl compound added to the motor fuel, in order to get sufficient stability for commercial purposes. Larger amounts of lecithin will give increased stability and smaller amounts will give decreased stability.
- a motor fuel comprising a major portion of hydrocarbons boiling within the gasoline boilin range, a minor but sufilcient amount of a metal carbonyl compound to rmse the anti-knock ratwhich the metal carbonyl compound is an iron compound.
- a motor fuel comprising a major portion of hydrocarbons boiling within the gasoline boiling range, a minor but suflicient amount of metal tricarbonyl mercaptide to raise the anti-knock rating of the motor fuel and a phosphatide in an amount at least approximately equal in weight to the metal present as tricarbonyl mercaptide.
- a motor fuel comprising a major portion of hydrocarbons boiling within the gasoline boiling range, a minor portion of iron tricarbonyl mercaptide but sufficient to raise the anti-knock rat ing of the motor fuel and lecithin in an amount approximately corresponding to the amount of iron in the mercaptide.
- the method of preparing a motor fuel of improved octane rating which comprises adding an iron carbonyl compound to said fuel in the presence of a phosphatide in amount at least approximately equal to the amount of iron present as carbonyl compound.
- the method of preparing a motor fuel which is sweet to the doctor test and which possesses a high octane number, from a sour motor fuel of low octane number which comprises adding to said motor fuel sufficient polymeric metal carbonyl to react with the mercaptans in said fuel in the presence of sufiicient phosphatide to prevent precipitation of metal compounds and agitating the mixture at a temperature sufllcient to cause reaction between said carbonyl and said mercaptans.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Liquid Carbonaceous Fuels (AREA)
Description
loss of octane value of the motor fuel.
Patented cc. 19, 1944 METHOD OF STABILIZING CARBONYL CONTAINING MOTOR FUELS Richmond T. Bell, Deerfield, 111., assignor to The Pure Oil Company, Chicago, 111., a corporation of Ohio No Drawing. Application October 15, 1941, Serial No. 415,065
18 Claims.
This invention relates to a method of stabilizing against loss in octane value, motor fuel to which has been added metal carbonyl compounds, and to the stabilized motor fuel.
It is known that various metal carbonyls such as iron, cobalt and nickel pentacarbonyl, iron tetracarbonyl, iron and cobalt tricarbonyl mercaptide and various metal nitrosyl carbonyls im- )IOVB the antiknock characteristics of hydrocarbon motor fuels. However, the various metal carbonyl compounds are unstable, decomposing in the presence of air and/r light with the formation of heavy precipitates and resultant Although I have discovered that metal tricarbonyl mercaptides' are more stable than the metal carbonyls, even the meroaptides decompose upon storage when exposed to daylight and air for a sufiicient period of time.
I have discovered that hydrocarbon motor fuels which contain metal carbonyl compounds can be stabilized against deterioration and decomposition by incorporating in the motor fuel phosphatides such as lecithin and cephalin.
In accordance with my invention the phosphatide may be added to the motor fuel either be fore, together with or after th addition of themetal carbonyl compound, but I prefer to have the phosphatide present in the motor fuel at the time the carbonyl is added, particularly in those cases where the motor fuel contains mercaptans and a polymeric carbonyl such as iron tetracarbonyl. capable of reacting with the mercaptans to form iron tricarbonyl mercaptide, is added.
In my co-pending application Serial No. 385,869 I have disclosed and claimed a method for increasing antiknock of motor fuels and for sweetening mercaptan-containing motor fuels by adding thereto iron or cobalt tetracarbonyl. At temperatures of approximately 160200 F. the tetra... carbonyl readily reacts with the mercaptans to form the tricarbonyl mercaptide. Although the resulting motor fuel has greatly improved antiknock, the process is attendant with certain disadvantages. Upon reaction of the mercaptans in the motor fuel with the tetracarbonyl, a light precipitate forms which is composed chiefly of iron oxide with small amounts of other iron compounds. This precipitate must be separated from the motor fuel before using. Moreover, the
motor fuel upon storage in the daylight exposed to air slowly deteriorates. A series of samples were prepared in some of which iron tricarbonyl phenyl mercaptide was added to sweet straight run petroleum naphtha having an octane number of and in some of which iron tetracarbonyl was added to sour gasoline having an octane of 61.9 and. prepared by blending gasoline from high pressure thermal cracking of petroleum oil and straight run gasoline, and the mixture heated to -180 for a period of thirty minutes to one hour. These samples were permitted to stand in glass bottles exposed to daylight at room temperature with an air space in the top of the bottle.
1 B may be any alkyl or aryl radical.
A sample of the same sour gasoline was sweetened with iron tetracarbonyl inthe same manner as previously described except that 2.3 grams of lecithin per gallon of gasoline was dissolved therein before introduction of the iron tetracarbonyl. The reaction. appeared to proceed in the same manner as it did without the lecithin. The dark green color of the iron tetracarbonyl in solution changed to dark red, but the resulting motor fuel was clear and free of any precipitate. It was observed that the color of the motor fuel was a somewhat darker red than that obtained without the presence of lecithin. The resulting gasoline had an octane number of 68 as compared with 68.2 obtained when the gasoline was sweetened without the presence of lecithin. The same amount of iron tetracarbonyl was required to sweetent the gasoline with and without the presence of lecithin. This amount was found to be 7 grams or the equivalent of 2.3 grams of iron per gallon of gasoline. Thus, by sweetening in the presence of the phosphatide,'loss of iron and the necess'ity of filtering the gasoline are avoided.
In order to demonstrate the relative stability of motor fuel made with and without the presence of lecithin, a number of samples were prepared and the samples were observed daily over a period of 26 days. The following results were obtained:
ing of the motor fuel and a phosphatide in an amount at leastapproximately equal in weight Table IL Time of cloud and precipitate formation, days Sample Identification precipitate Solution Precipitate during reaction Clear Cloudy Slight Appreciable Large for after alter after after Gasoline sweetened by addition of 7 1;. Fe; (00) end filtered. Appreciable. $4 l 1% 3 No lecithin present. Sample l+16ii lecithin/1,000 bbls l -d0 34 l l 2 4 salnzfilcblilfi lecithin/1,000 bbls+16# isobutyl p-amlnophenol/ do. e.. $6 1 2 3 6 Q Gasoline sweetened by addition 017 g. Fei(C0)4 with 2138 leci- None 26 thin/1,000 bbis. present during reaction. Sample 4+1 isobutyl p-aminophenol/LOOO bbls d0 l1 10 ll Gasoline sweetened by addition of 7 g. Fe (C0)4. 213 #lecrthm/ Appreclable. 26
1,000 bbls. added after reaction but before filtration.
It will be seen from Table II that the addition of lecithin in the amount of 16 pounds per 1000 barrels of gasoline had no appreciable effect on the stability of the motor fuel, but that upon addition of larger quantities of lecithin the stability was markedly improved as shown by the fact that it remained clear for a period of 26 days. The addition of a well known gum inhibitor-namely, isobutyl p-a'minophe'noL-in quantities commonly added to gasoline was harmful in that it detracted from the stability of the motor fuel, as shown by a comparison of samples 4 and 5. It will also be noted from the results tabulated in Table II that by having the lecithin present in the gasoline during the reaction between the iron tetracarbonyl and the mercaptans, precipitation was avoided during reaction, whereas where the lecithin was not added until after the reaction, an appreciable precipitate formed. The stability of the resulting motor fuel in both cases was the same.
Stability tests were also made on iron pentacarbonyl and it was found that the effect of lecithin in stabilizing motor fuel containing this material was similar to its effect in connection with iron tricarbonyl mercaptide, but the stability of the fuel was not as great as in the case of the mercaptide compound.
As previously shown, small amounts of lecithin-that is, amounts comparable to amounts of inhibitors which are commonly added to motor fuelhave substantially no effect in inhibiting deterioration of the carbonyl compounds. I have found that lecithin or other phosphatide should be added in amounts approximately .50 to 10 grams per gallon of motor fuel and preferably in amounts approximately corresponding to the amount of iron contained in the carbonyl compound added to the motor fuel, in order to get sufficient stability for commercial purposes. Larger amounts of lecithin will give increased stability and smaller amounts will give decreased stability.
I claim:
1. A motor fuel comprising a major portion of hydrocarbons boiling within the gasoline boilin range, a minor but sufilcient amount of a metal carbonyl compound to rmse the anti-knock ratwhich the metal carbonyl compound is an iron compound.
5. A motor fuel comprising a major portion of hydrocarbons boiling within the gasoline boiling range, a minor but suflicient amount of metal tricarbonyl mercaptide to raise the anti-knock rating of the motor fuel and a phosphatide in an amount at least approximately equal in weight to the metal present as tricarbonyl mercaptide.
6. A motor fuel in accordance with claim 5 in which the metal tricarbonyl mercaptide is cobalt tricarbonyl mercaptide.
7. A motor fuel in accordance with claim 5 in which the phosphatide is lecithin.
8. A motor fuel in accordance with claim 5 in which the phosphatide is cep-halin.
9. A motor fuel comprising a major portion of hydrocarbons boiling within the gasoline boiling range, a minor portion of iron tricarbonyl mercaptide but sufficient to raise the anti-knock rat ing of the motor fuel and lecithin in an amount approximately corresponding to the amount of iron in the mercaptide.
'10. A motor fuel in accordance with claim 9 in which the quantity of iron present in the form of iron tricarbonyl mercaptide is between .25 and 10 grams per gallon of motor fuel and the quantity of lecithin ranges from 0.50 to 10 rams per gallon.
11. A motor fuel in accordance with claim 1 in which the metal carbonyl compound is iron pentacarbonyl.
12. The method of preparing a motor fuel of improved octane rating which comprises adding an iron carbonyl compound to said fuel in the presence of a phosphatide in amount at least approximately equal to the amount of iron present as carbonyl compound.
13. The method in accordance with claim 12 in which the iron carbonyl compound is iron tricarbonyl mercaptide.
14. The method of preparing a motor fuel which is sweet to the doctor test and which possesses a high octane number, from a sour motor fuel of low octane number which comprises adding to said motor fuel sufficient polymeric metal carbonyl to react with the mercaptans in said fuel in the presence of sufiicient phosphatide to prevent precipitation of metal compounds and agitating the mixture at a temperature sufllcient to cause reaction between said carbonyl and said mercaptans.
15. The method in accordance with claim 14 in which the phosphatide is present in amounts of at least 0.50 gram per gallon.
16. The method in accordance with claim 14 in which the carbonyl is iron tetracarbonyl and the phosphatide is lecithin.
1'7. The method of preparing a motor fuel which is sweet to the doctor test and which possesses a high octane number comprising adding to sour hydrocarbon motor fuel iron tetracarbonyl RICHMOND T. BELL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US415065A US2365377A (en) | 1941-10-15 | 1941-10-15 | Method of stabilizing carbonyl containing motor fuels |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US415065A US2365377A (en) | 1941-10-15 | 1941-10-15 | Method of stabilizing carbonyl containing motor fuels |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2365377A true US2365377A (en) | 1944-12-19 |
Family
ID=23644230
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US415065A Expired - Lifetime US2365377A (en) | 1941-10-15 | 1941-10-15 | Method of stabilizing carbonyl containing motor fuels |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2365377A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3034875A (en) * | 1956-08-06 | 1962-05-15 | Union Oil Co | Automotive fuel |
| DE2320856A1 (en) * | 1972-04-25 | 1973-11-08 | Oestergren | STABILIZED METAL CARBONYL SOLUTIONS IN ORGANIC SOLVENTS, IN PARTICULAR HYDROCARBONS AND METHODS FOR THE PREPARATION OF THE SAME |
-
1941
- 1941-10-15 US US415065A patent/US2365377A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3034875A (en) * | 1956-08-06 | 1962-05-15 | Union Oil Co | Automotive fuel |
| DE2320856A1 (en) * | 1972-04-25 | 1973-11-08 | Oestergren | STABILIZED METAL CARBONYL SOLUTIONS IN ORGANIC SOLVENTS, IN PARTICULAR HYDROCARBONS AND METHODS FOR THE PREPARATION OF THE SAME |
| US3880612A (en) * | 1972-04-25 | 1975-04-29 | Jarl Olle Borje Ostergren | Stabilization of metal carbonyls |
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