GB719776A - Diesel fuel - Google Patents
Diesel fuelInfo
- Publication number
- GB719776A GB719776A GB30525/50A GB3052550A GB719776A GB 719776 A GB719776 A GB 719776A GB 30525/50 A GB30525/50 A GB 30525/50A GB 3052550 A GB3052550 A GB 3052550A GB 719776 A GB719776 A GB 719776A
- Authority
- GB
- United Kingdom
- Prior art keywords
- lead
- sulphonate
- benzene
- per cent
- petroleum
- 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
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/08—Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
-
- 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
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
-
- 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
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Lead sulphonates and naphthenates are employed as ingredients in fuel oil compositions (see Group III). Specification 674,765, [Group III], is referred to. Lead mahogany sulphonate.-Crude calcium mahogany sulphonate (50 per cent oil) is dissolved in a petroleum distillate (boiling range 185-290 DEG F.) and the solution is repeatedly washed with aqueous lead nitrate in the presence of ethyl alcohol with steam agitation. A small amount of litharge is added to neutralize any acidity and the petroleum distillate is distilled off, leaving a concentrate of lead mahogany sulphonate. Lead alkyl benzene sulphonate.-Benzene is alkylated with polypropylene (a C12-C15 olefin cut) and the alkylated benzene is sulphonated with concentrated sulphuric acid and then neutralized with sodium hydroxide. The sodium sulphonate is reacted with lead nitrate to obtain the lead sulphonate. Basic lead alkyl benzene sulphonate.-The alkyl benzene sulphonic acid prepared as above is reacted with a 100 per cent stoichiometric excess of litharge to obtain the basic lead salt. Lead naphthenate.-Petroleum gas oil is washed with aqueous caustic soda and the aqueous sodium naphthenate solution is treated with strong sulphuric acid to release the naphthenic acid. This is distilled and then treated with litharge. Lead naphthenate is extracted from the reaction mixture with Stoddard solvent.ALSO:A composition which, in spite of its sulphur content, causes little engine wear when employed as a fuel for diesel engines comprises a petroleum distillate boiling in the range of about 350-750 DEG F. and having an A.P.I. gravity above 20 DEG and a sulphur content above about 0.5 per cent. by weight, together with a minor proportion of an oil-soluble lead naphthenate, lead sulphonate and/or lead salt of a fatty acid, sufficient to give the composition a lead content of about 0.005-0.07 per cent. by weight. The sulphonic acids from which suitable lead sulphonates are prepared are preferably those having a molecular weight above about 400, for example sulphonic acids obtained by sulphonating white oils, petroleum lubricating oil fractions, higher boiling fractions of SO2 extracts of petroleum gas oils, and high boiling synthetic alkylated aromatic hydrocarbons, such as those formed by alkylating benzene with propylene polymers, butylene polymers or mixed propylene-butylene polymers. Lead salts of fatty acids mentioned are the oleate, palmitate, and stearate, and the soaps prepared from unrefined fats. In the examples, the normal or basic lead salt of naphthenic acids of molecular weight above about 225, or of sulphonic acids prepared by alkylating benzene with polypropylene (C12-C15 cut) and sulphonating the product, is added to the petroleum distillate. Specification 674,765 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US135507A US2691572A (en) | 1949-12-28 | 1949-12-28 | High sulfur diesel fuel containing organic lead salts |
Publications (1)
Publication Number | Publication Date |
---|---|
GB719776A true GB719776A (en) | 1954-12-08 |
Family
ID=22468414
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB30525/50A Expired GB719776A (en) | 1949-12-28 | 1950-12-14 | Diesel fuel |
Country Status (2)
Country | Link |
---|---|
US (1) | US2691572A (en) |
GB (1) | GB719776A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1034918B (en) * | 1956-05-03 | 1958-07-24 | Exxon Standard Sa | Fuel for internal combustion engines working with carburettors and spark ignition |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2789892A (en) * | 1952-10-22 | 1957-04-23 | California Research Corp | Diesel fuel composition |
DE1077358B (en) * | 1957-08-22 | 1960-03-10 | Exxon Research Engineering Co | Heating oil |
BE581117A (en) * | 1958-09-26 | |||
DE1545266B1 (en) * | 1966-04-27 | 1969-10-16 | Dasic Chemicals Ltd | Compensation for heavy heating oils with a high sulfur content |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB599222A (en) * | 1945-09-21 | 1948-03-08 | Anglo Iranian Oil Co Ltd | Improvements relating to motor fuels |
US2045788A (en) * | 1933-07-11 | 1936-06-30 | Standard Oil Dev Co | Fuel for high pressure liquid fuel injection engines |
US2230642A (en) * | 1938-08-13 | 1941-02-04 | Standard Oil Dev Co | Fuel oil |
GB561328A (en) * | 1941-07-05 | 1944-05-15 | Standard Oil Dev Co | Improvements relating to fuel oils |
US2575003A (en) * | 1948-07-03 | 1951-11-13 | Shell Dev | Fuel oil composition |
-
1949
- 1949-12-28 US US135507A patent/US2691572A/en not_active Expired - Lifetime
-
1950
- 1950-12-14 GB GB30525/50A patent/GB719776A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1034918B (en) * | 1956-05-03 | 1958-07-24 | Exxon Standard Sa | Fuel for internal combustion engines working with carburettors and spark ignition |
Also Published As
Publication number | Publication date |
---|---|
US2691572A (en) | 1954-10-12 |
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