US2088997A - Antiknock gasoline - Google Patents
Antiknock gasoline Download PDFInfo
- Publication number
- US2088997A US2088997A US74195A US7419536A US2088997A US 2088997 A US2088997 A US 2088997A US 74195 A US74195 A US 74195A US 7419536 A US7419536 A US 7419536A US 2088997 A US2088997 A US 2088997A
- Authority
- US
- United States
- Prior art keywords
- cobalt
- carbonyl
- salts
- gasoline
- hydrides
- 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
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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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/12—Inorganic compounds
- C10L1/1233—Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof
- C10L1/1241—Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof metal carbonyls
Definitions
- This invention relates to the use oi carbonyl hydride derivatives of cobalt and iron in caseline type fuels to improve their antilmoclb properties.
- nickel and other metals when dissolved in cgmoline have the ability of suppressina the latter's tendency to knock.
- the carbonyl hydrides are so unstable that they decompose within a short period i to the respective carbonyls and water. Though relatively unstable, such hydrides can be con verted into stable salts.
- a typical example of the production oi salts of the type herein described is as i'ollows: carbon monoxide, or gases containing carbon monoidde. are contacted under. normalor superatmospheric pressure and at normal or elevated temperatures with an aqueous alkaline suspension or a solution of cobalt cyanide.
- the carbon monoidde no reacts with the cobalt cyanide, forming the alkali salt of cobalt carbonyl hydride and in addition alkali carbonate as well as alhali salts oi complex compounds of. cobalt cyanide.
- the resulting mixture is slightly acidified and the liberated its cobalt carbonyl hydride canbe removed by dis- While these carbonyls are carbonyis are used.
- the freshly distilled hydride is introduced into an aqueous solution of mercuric chloride, forming a mercuric cobalt carbonyl of the iormum la l-lgOtJMCOM): which is then isolated.
- This compound is soluble in gasoline, forming stable solutions.
- 0.2% of cobalt in the form of the mercuric cobalt carbonyl dissolved in a standard gasoline raises the octane number 35 points L barium salts, as well as thallium and lead salts.
- Salts of the monovalent metal or metal equivalents such as the sodium, ammonium and silver saltswere found to be as unstable as the free 30 carbonyls themselves.
- db antiirnock motor fuel comprising gasoline type hydrocarbons and a small amount oi it the mercuric salt of cobalt carbonyl hydride.
- an antlhnock motor luel comprising gasoline type hydrocarbons and about .2% of cobalt
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
particles.
'umrso STATES PATENT OFFICE f 2,088,997 1 immoox Gnsonmn Y Nicolaas Max, Amsterdam, Netherlands, assignor to Shell Development @ompany, san Francisco, Calit... accrporation oi Delaware t i'llaims.
, This invention relates to the use oi carbonyl hydride derivatives of cobalt and iron in caseline type fuels to improve their antilmoclb properties.
a It is known that carbonyls oi iron, cobalt,
nickel and other metals when dissolved in cgmoline have the ability of suppressina the latter's tendency to knock.
quite emcient as antidetonants, their use has is been restricted because their solutions in liquid hydrocarbons have proven to be unstable, particularly when exposed to light. Ciasolines containing, for instance, cobalt carbonyl develop upon standing a flocculent precipitate of a coin bait compound, and when this gasoline is used in an internal combustion engine, a rapid wear and erosion of the cylinders and valves takes place, due to a formation of hard metallic I have found that the dimculty oi excessive wear can be overcome by using certain oilsoluble derivatives of carbonyl hydrides rather than the carbonyis themselves. "The term derivatives of carbonyl hydrides, as herein used,
an refers to metal salts'of the carbonyihydrides oi iron and cobalt, which hydrides appear to have the formulas HaFHCOM and JHC'MC'OM respectively. The carbonyl hydrides are so unstable that they decompose within a short period i to the respective carbonyls and water. Though relatively unstable, such hydrides can be con verted into stable salts.
A typical example of the production oi salts of the type herein described is as i'ollows: carbon monoxide, or gases containing carbon monoidde. are contacted under. normalor superatmospheric pressure and at normal or elevated temperatures with an aqueous alkaline suspension or a solution of cobalt cyanide. The carbon monoidde no reacts with the cobalt cyanide, forming the alkali salt of cobalt carbonyl hydride and in addition alkali carbonate as well as alhali salts oi complex compounds of. cobalt cyanide. The resulting mixture is slightly acidified and the liberated its cobalt carbonyl hydride canbe removed by dis- While these carbonyls are carbonyis are used. and no iouli application April it, 1936, Serial in theltetheriands April 2d, 1935 (or. are) tillation in a stream ofan inert gas, such as nitroren. instead of Jusing cobalt cyanide as a starting material, certain other cobalt salts such as cobalt thioglycolates, cobalt hexacyanides, cobalt mercaptides and the lilre, may be reacted M with carbon monoxide. to produce cobalt carbonyl hydride. The freshly distilled hydride is introduced into an aqueous solution of mercuric chloride, forming a mercuric cobalt carbonyl of the iormum la l-lgOtJMCOM): which is then isolated. This compound is soluble in gasoline, forming stable solutions. 0.2% of cobalt in the form of the mercuric cobalt carbonyl dissolved in a standard gasoline, raises the octane number 35 points L barium salts, as well as thallium and lead salts.
Salts of the monovalent metal or metal equivalents, such as the sodium, ammonium and silver saltswere found to be as unstable as the free 30 carbonyls themselves.
Engine tests in which fuels containing salts of the carbonyl hydrides have been used, have not revealed excessive wear of cylinders, piston rings and valves, as is frequently found when free at g of spark plugs has been evidenced.
' I claim as my invention: a
1. db antiirnock motor fuel comprising gasoline type hydrocarbons and a small amount oi it the mercuric salt of cobalt carbonyl hydride.
2. an antlhnock motor luel comprising gasoline type hydrocarbons and about .2% of cobalt
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL2088997X | 1935-04-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2088997A true US2088997A (en) | 1937-08-03 |
Family
ID=19873639
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US74195A Expired - Lifetime US2088997A (en) | 1935-04-24 | 1936-04-13 | Antiknock gasoline |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2088997A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2647149A (en) * | 1947-10-20 | 1953-07-28 | California Research Corp | Production of oxygen-containing carbon compounds |
| US2767048A (en) * | 1951-09-07 | 1956-10-16 | Exxon Research Engineering Co | Preparation of metallic hydrocarbonyls |
| US3100137A (en) * | 1958-03-13 | 1963-08-06 | Basf Ag | Production of manganese pentacarbonyl hydride |
| US3252753A (en) * | 1964-05-19 | 1966-05-24 | Ethyl Corp | Process for preparing manganese carbonyl hydride |
-
1936
- 1936-04-13 US US74195A patent/US2088997A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2647149A (en) * | 1947-10-20 | 1953-07-28 | California Research Corp | Production of oxygen-containing carbon compounds |
| US2767048A (en) * | 1951-09-07 | 1956-10-16 | Exxon Research Engineering Co | Preparation of metallic hydrocarbonyls |
| US3100137A (en) * | 1958-03-13 | 1963-08-06 | Basf Ag | Production of manganese pentacarbonyl hydride |
| US3252753A (en) * | 1964-05-19 | 1966-05-24 | Ethyl Corp | Process for preparing manganese carbonyl hydride |
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