GB961407A - Improved leaded motor fuel - Google Patents
Improved leaded motor fuelInfo
- Publication number
- GB961407A GB961407A GB16165/61A GB1616561A GB961407A GB 961407 A GB961407 A GB 961407A GB 16165/61 A GB16165/61 A GB 16165/61A GB 1616561 A GB1616561 A GB 1616561A GB 961407 A GB961407 A GB 961407A
- Authority
- GB
- United Kingdom
- Prior art keywords
- lead
- methyl
- alkyl
- tetra
- compounds
- 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
Links
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
- C10L1/14—Organic compounds
-
- 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
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1608—Well defined compounds, e.g. hexane, benzene
-
- 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
- C10L1/14—Organic compounds
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/305—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)
- C10L1/306—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond) organo Pb compounds
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
A gasoline composition contains from 3 to 65% by weight of methyl benzenes having from 1 to 4 methyl groups, and from 0.5 to 6.0 gms., preferably 1.05 to 3.17 gms., of lead per U.S. gallon in the form of tetra-alkyl lead in which at least 25% of the alkyl groups are methyl groups. The tetra-alkyl lead compound may be tetramethyl lead either alone or in admixture with one or more of tetraethyl, methyl triethyl, dimethyldiethyl, and trimethyl ethyl leads, while the list of optional additives also includes tetrapropyl lead and tetraphenyl lead. The tetra-alkyl lead compounds may be present as a physical mixture, or as the "chemical" mixture produced when a mixture of tetramethyl and tetraethyl lead is subject to the action of a catalyst such as an aluminium halide, e.g. AlCl3, an alkyl aluminium halide, e.g. ethyl aluminium sesquihalide, or an alkyl lead halide, e.g. triethyl lead chloride, whereby a random redistribution of the methyl and ethyl radicals takes place producing all possible combinations. Numerous specific mixtures of tetra-alkyl lead compounds are given. Of the monoto tetramethyl substituted benzenes those with higher degrees of substitution are preferred, although all possible compounds are specified. The base fuels may be straight run, catalytically or thermally cracked, alkylates or isomerized materials, and may contain benzene and other aromatics, many of which are specified in the examples. Other octane improving additives may be present, including methyl cyclopentadienyl manganese tricarbonyl, cyclopentadienyl nickel nitrosyl, manganese pentacarbonyl, iron carbonyl and dicyclopentadienyl iron. Additional antiknock improvers referred to are carboxylic acid esters, e.g. tert.-butyl acetate, and amine salts of organic acids, e.g. isobutylamine isobutyrate, ethyl amine a -a -dimethyl propionate, and n-propyl amine propionate. Organohalide scavengers may also be used, those referred to being aliphatic and/or aromatic halohydrocarbons, haloalkyl ethers, and halohydrogen and halonitro compounds, specific mention being made of ethylene dibromide, ethylene dichloride, dibromotoluene, and 1,2,4-trichlorobenzene. Other additives mentioned are antioxidants, e.g. N,N1 - di - sec - butyl - p - phenylene diamine, p-N-butylamino phenol, 4-methyl-2,6-di - tert. - butyl phenol, and 2,6 - di - tert.-butyl phenol, metal deactivators, e.g. N,N1-disalicylidene - 1,2 - diaminopropane, dyes, phosphorus additives, e.g. tri-(b -chloropropyl) thionophosphate, dimethyltolylphosphate, dimethylxylylphosphate, phenyldimethylphosphate, tricresylphosphate, phenyldicresylphosphate, cresyldiphenylphosphate, and trimethylphosphate, anti-icing agents, e.g. alcohols and salts of dehydroabietylamine, corrosion inhibitors, and detergents.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3151960A | 1960-05-25 | 1960-05-25 | |
US9161061A | 1961-02-27 | 1961-02-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB961407A true GB961407A (en) | 1964-06-24 |
Family
ID=26707344
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16165/61A Expired GB961407A (en) | 1960-05-25 | 1961-05-04 | Improved leaded motor fuel |
Country Status (2)
Country | Link |
---|---|
DE (2) | DE1420936A1 (en) |
GB (1) | GB961407A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2126246A (en) * | 1982-09-02 | 1984-03-21 | British Petroleum Co Plc | Preparation of motor spirit |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4126789A1 (en) * | 1990-12-19 | 1992-07-02 | Alcor Chem | FUEL ADDITIVE AND METHOD FOR PRODUCING THE SAME |
-
1961
- 1961-05-04 GB GB16165/61A patent/GB961407A/en not_active Expired
- 1961-05-12 DE DE19611420936 patent/DE1420936A1/en active Pending
- 1961-05-12 DE DE19611545490 patent/DE1545490A1/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2126246A (en) * | 1982-09-02 | 1984-03-21 | British Petroleum Co Plc | Preparation of motor spirit |
Also Published As
Publication number | Publication date |
---|---|
DE1420936A1 (en) | 1968-10-03 |
DE1545490A1 (en) | 1969-02-20 |
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