GB987440A - High molecular weight esters - Google Patents

High molecular weight esters

Info

Publication number
GB987440A
GB987440A GB45366/61A GB4536661A GB987440A GB 987440 A GB987440 A GB 987440A GB 45366/61 A GB45366/61 A GB 45366/61A GB 4536661 A GB4536661 A GB 4536661A GB 987440 A GB987440 A GB 987440A
Authority
GB
United Kingdom
Prior art keywords
acid
diol
esters
ethyl
diol mixture
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
GB45366/61A
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.)
Evonik Operations GmbH
Original Assignee
Technochemie GmbH
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
Priority claimed from DET19458A external-priority patent/DE1186042B/en
Priority claimed from DET19846A external-priority patent/DE1186456B/en
Application filed by Technochemie GmbH filed Critical Technochemie GmbH
Publication of GB987440A publication Critical patent/GB987440A/en
Expired legal-status Critical Current

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
    • C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
    • C07C69/28—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with dihydroxylic compounds
    • 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
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28—Esters
    • C10M2207/283—Esters of polyhydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/08—Resistance to extreme temperature
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/12—Gas-turbines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/12—Gas-turbines
    • C10N2040/13—Aircraft turbines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2070/00—Specific manufacturing methods for lubricant compositions
    • C10N2070/02—Concentrating of additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

A high molecular weight ester having at least 21 carbon atoms in its molecule is derived from a monocarboxylic acid and an aliphatic saturated polyhydric alcohol, the hydroxy groups of which are linked to an uninterrupted hydro-carbon chain, which alcohol has at least 12 carbon atoms in its molecule. In examples of preparation of the esters (1) nonadecane diol and 2-ethyl-hexanoic acid are melted together and treated with dry hydrogen chloride at 200 DEG C.; (2) a diol mixture is prepared by reacting oleic acid with carbon monoxide and hydrogen in the presence of a cobalt catalyst; the product is dissolved in methanol, mixed with urea and cooled, when solid impurities form and are removed; the purified diol is esterified with 2-ethyl-hexanoic acid, lauric acid, or 9,10-dimethyl-stearic acid; (3) the diol mixture obtained as in (2) is dissolved in methanol and cooled to deposit solid impurities before forming the ester; other suitable low boiling organic solvents are specified; (4) the diol mixture is heated with formic acid in the presence of hydrogen chloride to produce formic acid esters which are reacted with urea in methanol solution; the solid addition products are decomposed with dilute acid and the purified ester saponified and the diol mixture esterified with 2-ethyl-hexanoic acid; acetic acid may be used instead of formic acid. The esters are useful as lubricants stable at high and low temperatures and also as plasticizers and rubber additives.
GB45366/61A 1960-12-23 1961-12-18 High molecular weight esters Expired GB987440A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DET0019848 1960-12-23
DET19458A DE1186042B (en) 1960-12-23 1960-12-23 Process for the production of an ester serving as a high-performance lubricating oil
DET19847A DE977102C (en) 1960-12-23 1961-03-23 Process for the production of ester mixtures used as high-performance lubricants
DET19846A DE1186456B (en) 1961-03-23 1961-03-23 Process for the preparation of ester mixtures serving as lubricants

Publications (1)

Publication Number Publication Date
GB987440A true GB987440A (en) 1965-03-31

Family

ID=27437607

Family Applications (1)

Application Number Title Priority Date Filing Date
GB45366/61A Expired GB987440A (en) 1960-12-23 1961-12-18 High molecular weight esters

Country Status (3)

Country Link
BE (1) BE610685A (en)
GB (1) GB987440A (en)
NL (1) NL120567C (en)

Also Published As

Publication number Publication date
NL120567C (en)
BE610685A (en) 1964-12-09

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