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GB669947A - Improvements in or relating to lubricating grease compositions - Google Patents

Improvements in or relating to lubricating grease compositions

Info

Publication number
GB669947A
GB669947A GB24741/49A GB2474149A GB669947A GB 669947 A GB669947 A GB 669947A GB 24741/49 A GB24741/49 A GB 24741/49A GB 2474149 A GB2474149 A GB 2474149A GB 669947 A GB669947 A GB 669947A
Authority
GB
United Kingdom
Prior art keywords
per cent
oil
acids
furfural
grease
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
GB24741/49A
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
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 US57565A external-priority patent/US2516136A/en
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB669947A publication Critical patent/GB669947A/en
Expired legal-status Critical Current

Links

Classifications

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    • 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
    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/104Aromatic fractions
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/106Naphthenic fractions
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
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    • C10M2211/044Acids; Salts or esters thereof
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    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
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    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2229/02Unspecified siloxanes; Silicones
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    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
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    • C10N2050/10Semi-solids; greasy
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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

Salts of heterocyclic carboxylic acids are prepared by the Cannizzaro reaction from the corresponding aldehydes and strong alkali. The so-formed salts may be incorporated in lubricating grease compositions (see Group III). If desired, the reaction may be carried out in the presence of a hydrocarbon oil diluent, which oil may be the same as that to serve as the liquid phase of the grease. Furfural is preferred, but aldehydes from thiophene and alkyl substituted homologues of furfural may also be used. In an example (IX) furfural is reacted in a grease kettle with caustic soda in about its own amount of mineral oil as the first stage of a grease manufacture. The Specification as open to inspection under Sect. 91, refers also to the use of benzaldehyde and other aromatic aldehydes, glyoxal and formaldehyde as suitable for simultaneous oxidation and reduction as in the Cannizzaro reaction. Chloro- and nitro-ring-substituted aromatic aldehydes may also be used, as well as thioaldehydes. This subject-matter does not appear in the Specification as accepted.ALSO:Lubricating oil is thickened to a grease with a metal soap of a fatty acid having from 12 to 22 carbon atoms in the molecule and from 2 to 20 per cent by weight, based on the total composition, of a metal salt of a heterocyclic carboxylic acid. The lubricating oil may be a mineral base lubricating oil of viscosity from 35 to 1,000 S.S.U. at 210 DEG F. (preferably 35-200 S.S.U. at 210 DEG F.). Vegetable oils, e.g. castor oil, and synthetic oils may also be used, for instance ester oils, such as di-2-ethylhexyl sebacate and glycollates, or the esters from oxo-alcohols and dibasic acids, or fluorinated hydrocarbons, polyglycols, and silicone oils. Suitable heterocyclic acids are furoic acid and its alkyl-substituted homologues and the thiophene carboxylic acids. The metal salt and metal soap may be compounds of the same metal. Sodium, lithium and calcium salts and soaps are preferred, but potassium, strontium, magnesium and barium compounds may be employed. If desired, the metal salt of the heterocyclic acid may be prepared from the corresponding aldehyde by the Cannizzaro reaction, e.g. sodium furoate from furfural. This reaction may be controlled by a diluent such as a hydrocarbon oil, which may be the same as that to serve as the liquid phase of the grease. Any undesirable reaction products such as water may be removed by evaporation, but the alcohol produced in the reaction may be allowed to remain in the grease, where it may be esterified with the fatty acids subsequently added, or left unchanged. The alcohol may also be polymerised. At the same time, or preferably subsequently, the soap may be formed by adding the C12-C20 acids to the Cannizzaro reaction mixture and p neutralising with a base. Instead of adding furfural to a hydrocarbon oil as such, the reaction may be carried out on the raffinate from the furfural extraction of mineral lubricating oil base stocks (which raffinate contains a minor proportion of furfural) the amount of furfural being adjusted if necessary to between 2 and 20 per cent. The raffinate from refining of drying oils (which contains non-drying oils) or the furfural-containing effluent from a solvent refining of fatty oils or fatty acids may also be employed. The relative proportions of the soap and salt may be between 1 and 4 mols of soap to between 1 and 4 mols of salt. It is preferred that these proportions should be more nearly equal, 1 to 2 mols of soap being used with 1 to 1.5 mols of salt. In general the amount of soap is from 3 to 30 per cent by weight. The soap may be made from hydrogenated fish oil acids, but unsaturated or hydroxy acids of similar molecular weight may be used. Detergent materials (e.g. sodium toluene-C12-alkylate sulphonates), oxidation inhibitors (phenyl-alpha-naphthylamine), corrosion inhibitors, extreme pressure agents, and/or tackiness agents may also be added. If the Cannizzaro reaction is not used, alcohols such as oleyl and cetyl alcohols may be added to react with an excess of the C12-C20 acids forming the soap to give ester plasticizers, the amount of ester being from 0.01 to 5 per cent of the total composition. In an example a grease is prepared using 15 per cent (by weight of the total composition) of hydrogenated fish oil acids, 6 per cent of furoic acid, 5 per cent of sodium hydroxide and 74 per cent low cold test lubricating oil of 50 S.S.U. viscosity at 210 DEG F. The acids together with about one-third of the mineral oil are charged into a grease kettle and heated. The caustic soda is added as a 30 per cent aqueous solution and the temperature raised to dry out the mixed soap and salt. The remainder of the oil is added slowly with stirring, the final temperature being 480 DEG F. A further example (IX) describes the application of the Cannizzaro reaction using 10 per cent (by weight of the total composition) of furfural, 5.4 per cent sodium hydroxide, 15.0 per cent hydrogenated fish oil acids and 68.6 per cent naphtheric lubricating oil of 55 S.S.U. viscosity at 210 DEG F. The furfural, about an equal amount of the oil and about 60 per cent of the alkali as a 33.3 per cent aqueous solution are reacted in a grease kettle. After about 2 hours the fatty acids and about one-third of the mineral oil are added, the kettle heated to 150-160 DEG F. and the remainder of the caustic soda added while the temperature is raised to 350 DEG F. The remainder of the oil is then added slowly and the temperature raised to 450 DEG F. to evaporate water and other volatile constituents. The heating is discontinued, phenyl-alpha-naphthylamine added and the grease cooled while being stirred. The Specification as open to inspection under Sect. 91, refers also to the use of benzaldehyde and other aromatic aldehydes, glyoxal and formaldehyde as suitable aldehydes for simultaneous oxidation and reduction as in the Cannizzaro reaction. Chloro- and nitro-ring-substituted aromatic aldehydes may also be used, as well as thioaldehydes. This subject-matter does not appear in the Specification as accepted.
GB24741/49A 1948-10-30 1949-09-27 Improvements in or relating to lubricating grease compositions Expired GB669947A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US57565A US2516136A (en) 1948-10-30 1948-10-30 Lubricating grease compositions
US86586A US2576031A (en) 1948-10-30 1949-04-09 Lubricating grease containing soaps of tall oil

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GB669947A true GB669947A (en) 1952-04-09

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GB24741/49A Expired GB669947A (en) 1948-10-30 1949-09-27 Improvements in or relating to lubricating grease compositions
GB7576/50A Expired GB684697A (en) 1948-10-30 1950-03-27 Lubricating grease containing soaps of tall oil

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GB7576/50A Expired GB684697A (en) 1948-10-30 1950-03-27 Lubricating grease containing soaps of tall oil

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US (1) US2576031A (en)
DE (1) DE845228C (en)
FR (1) FR998260A (en)
GB (2) GB669947A (en)
NL (3) NL73227C (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2790770A (en) * 1957-04-30 Grease composition
US2801974A (en) * 1952-12-22 1957-08-06 Exxon Research Engineering Co Grease process utilizing the alkali fusion products of cyclic alcohols
US2834732A (en) * 1954-11-29 1958-05-13 Standard Oil Co Extreme pressure lubricant
US2946748A (en) * 1956-05-08 1960-07-26 Swift & Co Liquid hydrocarbon gels and uses thereof
US3252906A (en) * 1963-06-07 1966-05-24 Standard Oil Co Grease
US11760952B2 (en) 2021-01-12 2023-09-19 Ingevity South Carolina, Llc Lubricant thickener systems from modified tall oil fatty acids, lubricating compositions, and associated methods

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2182137A (en) * 1937-02-01 1939-12-05 Shell Dev Soda soap grease
GB583303A (en) * 1944-10-17 1946-12-13 Bataafsche Petroleum Improvements in or relating to the manufacture of lithium base greases
US2514286A (en) * 1947-12-31 1950-07-04 Standard Oil Dev Co Lubricating grease and method of preparing same
US2516137A (en) * 1948-10-30 1950-07-25 Standard Oil Dev Co High-temperature lubricating greases
US2516136A (en) * 1948-10-30 1950-07-25 Standard Oil Dev Co Lubricating grease compositions

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NL75829C (en)
NL73227C (en)
FR998260A (en) 1952-01-16
US2576031A (en) 1951-11-20
DE845228C (en) 1952-07-31
GB684697A (en) 1952-12-24

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