GB627865A - An improved mineral oil composition - Google Patents
An improved mineral oil compositionInfo
- Publication number
- GB627865A GB627865A GB3006346A GB3006346A GB627865A GB 627865 A GB627865 A GB 627865A GB 3006346 A GB3006346 A GB 3006346A GB 3006346 A GB3006346 A GB 3006346A GB 627865 A GB627865 A GB 627865A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- heat
- condensation product
- prepared
- paraffin wax
- 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
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/22—Alkylation reaction products with aromatic type compounds, e.g. Friedel-crafts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/101—Condensation polymers of aldehydes or ketones and phenols, e.g. Also polyoxyalkylene ether derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/042—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds between the nitrogen-containing monomer and an aldehyde or ketone
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/043—Mannich bases
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)
- Lubricants (AREA)
Abstract
Low-pour test mineral oil compositions comprise a major proportion of a waxy mineral oil, e.g. a lubricating oil, a pour-depressing amount of a high molecular weight condensation product of a long-chain aliphatic compound having at least 10 carbon atoms in the molecule with an aromatic hydrocarbon or a hydroxy or amino derivative thereof, and a pour stability promoting amount of a condensation product prepared (see Group IV (b)) by heat-thickening at about 400 DEG to 750 DEG F., a compound of the formula R-COX, where R is a member of the class consisting of alkyl and aryl alkyl radicals having at least 10 carbon atoms in an aliphatic chain, e.g. the stearyl radical, and X is a halogen, e.g. chlorine. The composition may contain about 0.1-2.0 per cent, e.g. 1.0 to 1.25 per cent of a high mol. wt. condensation product of a chlorinated paraffin wax with naphthalene and about 0.01 to 1.5 per cent, e.g. 0.5-0.75 per cent of stearyl chloride heat-thickened at 400 DEG to 750 DEG F. The aromatic compound used in making the alkyl-aromatic condensation product may be diphenyl, benzene, toluene, amyl-benzene, anthracene, phenol, naphthol, cresol, aniline or xylidine. The long chain aliphatic compound is preferably paraffin wax chlorinated to about 10-20 per cent chlorine content. Alternatively the chlorinated wax may be dehydrochlorinated to produce corresponding olefines and the latter may be condensed with the aromatic compound. Alternative long chain aliphatic compounds which may be used are stearic acid, stearyl chloride, octadecyl alcohol, or cetyl alcohol. The acyl halide used in the preparation of the other condensation product may be prepared from palmitic or behenic acid or mixtures of acids obtained by the oxidation of paraffin wax. The oil base stocks may be waxy paraffinic or mixed base mineral oils and may have been partially dewaxed. Their viscosity may lie within the normal range for lubricating oils or may be of much lower viscosity, e.g. hydraulic oils of viscosity as low as 40 s.u.s. at 100 DEG F. U.S.A. Specifications 1,815,022 and 2,251,550 are referred to.ALSO:Condensation products which may be used as additives in mineral lubricating &c. oils (see Group III) are prepared by heat-thickening at about 400-750 DEG F. compounds of the formula R-COX, where R is an alkyl or aralkyl radical having at least 10 carbon atoms in an aliphatic chain, and X is a halogen. In the example stearyl chloride is heated for 3 hours at 580 DEG C. until the evolution of hydrogen chloride has ceased and the heat-thickened product heated to 600 DEG F. at 10-20 mm. mercury pressure to remove volatile impurities. Alternatively, the acyl halide may be prepared from palmitic, behenic or paraffin wax oxidation acids, and after heat thickening, the product may be dissolved in a solvent and washed free from acid prior to heating under reduced pressure. U.S.A. Specification 2,251,550 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3006346A GB627865A (en) | 1946-10-08 | 1946-10-08 | An improved mineral oil composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3006346A GB627865A (en) | 1946-10-08 | 1946-10-08 | An improved mineral oil composition |
Publications (1)
Publication Number | Publication Date |
---|---|
GB627865A true GB627865A (en) | 1949-08-17 |
Family
ID=10301651
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3006346A Expired GB627865A (en) | 1946-10-08 | 1946-10-08 | An improved mineral oil composition |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB627865A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3020384A (en) * | 1959-04-20 | 1962-02-06 | Maxwell K Murphy | Dual radiant heater |
-
1946
- 1946-10-08 GB GB3006346A patent/GB627865A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3020384A (en) * | 1959-04-20 | 1962-02-06 | Maxwell K Murphy | Dual radiant heater |
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