GB622311A - Improvements in or relating to lubricating compositions - Google Patents

Improvements in or relating to lubricating compositions

Info

Publication number
GB622311A
GB622311A GB2801/47A GB280147A GB622311A GB 622311 A GB622311 A GB 622311A GB 2801/47 A GB2801/47 A GB 2801/47A GB 280147 A GB280147 A GB 280147A GB 622311 A GB622311 A GB 622311A
Authority
GB
United Kingdom
Prior art keywords
alkenes
carbon
carbon atoms
molecule
product
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
Application number
GB2801/47A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
KENNETH DARLING GRICE
Shell Refining and Marketing Co Ltd
Original Assignee
KENNETH DARLING GRICE
Shell Refining and Marketing Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by KENNETH DARLING GRICE, Shell Refining and Marketing Co Ltd filed Critical KENNETH DARLING GRICE
Priority to GB2801/47A priority Critical patent/GB622311A/en
Publication of GB622311A publication Critical patent/GB622311A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
    • C10M2211/022Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

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

An extreme pressure or high film strength lubricant comprises a mineral lubricating oil or a lubricating grease and a small proportion, e.g. about 1 per cent of an additive comprising a product obtainable by the addition reaction of a carbon tetrahalide or a trihalomethane and an alkene-1 containing 8 or more carbon atoms in the molecule or a mixture of such alkenes. The carbon tetrahalide may be carbon tetrachloride and the trihalomethane may be chloroform. The product may be partially dehydrohalogenated, e.g. by heating to about 100 DEG C., prior to being added to the oil in order to obtain a more stable product. The addition products before partial dehydrohalogenation are believed to be compounds or mixtures of compounds having the general formula <FORM:0622311/III/1> wherein Y represents a halogen atom, X represents a hydrogen or halogen atom and R represents an aliphatic hydrocarbon radical of at least six carbon atoms. The alkenes-1 used as starting material may be isolated from the mixture of alkenes-1, other alkenes, alkanes and other aliphatic hydrocarbons obtained by the cracking of paraffin wax or the crude complex of cracked hydrocarbons may be used. The addition products may be prepared in the presence of peroxide condensing agents such as benzoyl peroxide or acetyl peroxide. Examples are given of the preparation of the addition products from cracked wax alkenes-1 containing 12 or 14 carbon atoms in the molecule and carbon tetrachloride, chloroform, carbon tetrabromide and bromotrichloromethane respectively [see Group IV (b)].ALSO:Halogen-containing organic compounds, suitable for use as additives in lubricants (see Group III), are obtained by the addition reaction of a carbon tetrahalide or a trihalomethane and an alkene-1 containing 8 or more carbon atoms in the molecule, in the presence of peroxide condensing agents such as benzoyl peroxide or acetyl peroxide. The products are believed to be compounds or mixtures of compounds having the general formula <FORM:0622311/IV (b)/1> wherein Y represents a halogen atom, X represents a hydrogen or halogen atom and R represents an aliphatic hydrocarbon radical of at least six carbon atoms. In some cases the addition product tends to lose hydrogen halide on being subjected to an elevated temperature, but may be stabilized by a partial dehydrohalogenation, for example by heating to about 100 DEG C. In an example, 30 parts by weight of commercial benzoyl peroxide are dehydrated in a Dean and Stark apparatus by refluxing with 770 parts of carbon tetrachloride. 168 parts by weight of a mixture of alkenes-1 containing on an average 12 carbon atoms in the molecule and obtained by the cracking of paraffin wax are added and the mixture refluxed for 17 hours. The excess of carbon tetrachloride is then distilled off, the residue dissolved in 200 parts by volume of acetone and extracted successively with a concentrated aqueous solution of potassium iodide, an aqueous solution of sodium thiosulphate and water. The residual acetone was distilled off, leaving the product in the form of a mobile reddish oil miscible with mineral lubricating oils at room temperature and containing 44 per cent by weight of chlorine. On heating the product to constant weight at 100 DEG C. under 12 m.m. mercury pressure, the chlorine content fell to 23.0 per cent. Additional examples are given of the preparation by similar methods of addiion products from cracked paraffin wax alkenes-1 containing 12 or 14 carbon atoms in the molecule and chloroform, carbon tetrabromide and bromotrichloromethane respectively.
GB2801/47A 1947-01-29 1947-01-29 Improvements in or relating to lubricating compositions Expired GB622311A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2801/47A GB622311A (en) 1947-01-29 1947-01-29 Improvements in or relating to lubricating compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2801/47A GB622311A (en) 1947-01-29 1947-01-29 Improvements in or relating to lubricating compositions

Publications (1)

Publication Number Publication Date
GB622311A true GB622311A (en) 1949-04-29

Family

ID=9746172

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2801/47A Expired GB622311A (en) 1947-01-29 1947-01-29 Improvements in or relating to lubricating compositions

Country Status (1)

Country Link
GB (1) GB622311A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0201015A2 (en) * 1985-05-04 1986-11-12 BASF Aktiengesellschaft Use of 1,1,1-trichloromethyl compounds as lubricant additives, and lubricants containing these additives

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0201015A2 (en) * 1985-05-04 1986-11-12 BASF Aktiengesellschaft Use of 1,1,1-trichloromethyl compounds as lubricant additives, and lubricants containing these additives
EP0201015A3 (en) * 1985-05-04 1987-10-28 BASF Aktiengesellschaft Use of 1,1,1-trichloromethyl compounds as lubricant additives, and lubricants containing these additives

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