US2451895A - Synthetic grease - Google Patents

Synthetic grease Download PDF

Info

Publication number
US2451895A
US2451895A US675332A US67533246A US2451895A US 2451895 A US2451895 A US 2451895A US 675332 A US675332 A US 675332A US 67533246 A US67533246 A US 67533246A US 2451895 A US2451895 A US 2451895A
Authority
US
United States
Prior art keywords
grease
acid
soap
radicals
greases
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 - Lifetime
Application number
US675332A
Inventor
White Ellis Ross
Harman Denham
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.)
Shell Development Co
Original Assignee
Shell 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
Application filed by Shell Development Co filed Critical Shell Development Co
Priority to US675332A priority Critical patent/US2451895A/en
Priority to GB14330/47A priority patent/GB642410A/en
Application granted granted Critical
Publication of US2451895A publication Critical patent/US2451895A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • C10M7/00Solid or semi-solid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single solid or semi-solid substances
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16Paraffin waxes; Petrolatum, e.g. slack wax
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/18Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/122Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/128Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/16Naphthenic acids
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/18Tall oil acids
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/20Rosin acids
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/084Acrylate; Methacrylate
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • 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
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • 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
    • C10M2215/064Di- and triaryl amines
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • 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
    • C10M2215/064Di- and triaryl amines
    • C10M2215/065Phenyl-Naphthyl amines
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • 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
    • C10M2215/066Arylene diamines
    • 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/084Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof
    • 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
    • C10N2010/00Metal present as such or in 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/06Groups 3 or 13
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/08Resistance to extreme temperature
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/12Gas-turbines
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/12Gas-turbines
    • C10N2040/13Aircraft turbines
    • 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
    • C10N2050/08Solids
    • 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
    • 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
    • C10N2060/00Chemical after-treatment of the constituents of the lubricating composition
    • C10N2060/04Oxidation, e.g. ozonisation

Definitions

  • Airplanes are controlled in flight by special mechanisms such as rudders, elevators, and ailerons which are adapted to the main portions of the airplane such as fuselage and wings by specially designed hinges. These hinges have metal to metal contact bearing surfaces which oifer a very difilcult lubrication problem. Airplanes are operated under the most severe changes in climatic conditions and since the failure of even one part of the mechanism might well result in a catastrophe, it is imperative that all parts should be free and well lubricated at all times.
  • High temperature greases such. as sodium greases are known to the art. However, they are quite water-soluble and readily disintegrate under humid conditions. Water-insoluble greases such as calcium soap greases, are also known, but these compositions will not withstand high temperatures. Aluminum soap greases are also water insoluble, but have a relatively low transition point where they become fluid and run out of the bearing. Barium soap greases are only slowly affected by the presence of water and eifectlvely withstand elevated temperatures, but have the disadvantages of losing their grease structure on standing at lower temperatures and of be- 2 coming quite stiff and heavy at elevated temperatures.
  • the common mineral oil and vegetable oil bases have shortcomings which limit their complete utility as grease bases. .
  • the viscosity indices of such bases are unsatisfactory where extreme conditions, both high and low temperatures and pressures, are to be met.
  • Various synthetic bases, suchv as chlorinated dlphenyl, have been investigated, but have not proved satisfactory for general use, especially because of their generally low thermal decomposition tem perature characteristics.
  • the soap comprises predominantly a lithium soap, although minor amounts of fatty acid salts of other metals, partlculariy sodium, potassium, calcium, barium,
  • the fatty acids which may be used in forming the lithium soaps useful in the invention comprise the lower fatty acid series as well as the higher v acid radicals, as well those of 2,3-diethylvaleric acid, 3'-propylcaproic acid, 4-isobutylheptolc acid,
  • the mono-oleiinic acids and the naphthenic acids are the preferred classes within this group.
  • the naphthenic acid derivatives are conveniently prepared from the naphthenic acids found in certain petroleum fractions. These acids, which are usually a mixture of various naphthenic acid homoiogues or alkylatedjderivatives thereof, are referred to hereinafteivas' petroleum naphthenic acids or simply as naphthenic acid.
  • the thin-- I other derivatives containing petroleum naphlard, various seed oils, wool fat, naphthenic acids such as may be derived from petroleum oils; rosin,
  • acids having twelve or more carbon atoms preferred for use in preparing lithium soaps, but those acids are most preferred which are saturated or contain no more than about one unsaturated linkage in the molecule. including saturated fatty acids, mono-oleflnic fatty acids and mono-acetylenic fatty acids, all having twelve or more carbon atoms.
  • the grease base for the greases which comprise this invention are thioether derivatives having the general structural formula 0 o m-d-o-as-san-o-ii-m in which R1 to Rs are hydrocarbon radicals.
  • R1 and R4 are non-aromatic, but instead are aliphatic or alicyclic.
  • the most useful grease bases of this class are those in which R1 and R4 are saturated aliphatic radicals, and of this group those having from 4 to 11 carbon atoms are preferred.
  • R1 and R4 form ester groups such as the valeric acid radicals, including normal valeric, isovaleric, tertiary valeric or trimethyl acetic, (which is the preferred acid radical) and (1-1 valeric (or methylethylacetic) acid radicals.
  • valeric acid radicals including normal valeric, isovaleric, tertiary valeric or trimethyl acetic, (which is the preferred acid radical) and (1-1 valeric (or methylethylacetic) acid radicals.
  • the saturated 5-carbon atom radicals together with the COO- group to which they are attached, comprise the caprolc- (or hexoic) acid radicals, including butyl-acetic, iso-caproic (or secondary butylacetic), pseudocaproic (or tertiary-butylacetic), secondary-caproic (or diethylacetic), secondary active-caproic (or methylpropylacetic) or tertiary-caproic (dimethylethyl acetic) acid radicals.
  • the groups R2 and Rs in the above general formula are either similar or dissimilar hydrocarbon radicals.
  • aliphatic radicals which may be saturated or may contain one or more unsaturateg linkagesoi' oletlnic or acetylenlccharacter and furthermore may contain elements such as sulfur, nitrogen, phosphorus, selenium and tellurlum.
  • each of these radicals is a saturated hydrocarbon radical, and still more preferably is a saturated straight chain hydrocarbon radical forming a primary linkage with the sulfur atom, giving the following general configuration:
  • R1 and R4 are hydrocarbon radicals and R4 and R3 are saturated aliphatic radicals.
  • R1 and R4 are hydrocarbon radicals and R4 and R3 are saturated aliphatic radicals.
  • those having similar ester groups and similar aliphatic radicals form the most suitable-grease bases and have the general formula:
  • drogen sulfide were subjected in a bomb to the radiation from a, 250 watt mercury arc lamp.
  • the pressure in the system rose steadily from 180 to 220 lbs/sq. in. after which it fell slowly to 170 lbs./sqin. at the end of the radiation period.
  • the temperature of the reactor increased from 16 C. to 0 in part due to the exothermic character fatty acid were absent. present, care must be taken that too much acid of the reaction, but mainly from the heat emitted by the mercury arc lamp.
  • reaction product was then distilled to remove unreacted allyl alco hol and the gamma-mercaptopropyl alcohol formed during reaction, leaving the desired product, namely, bis-(gamma hydroxypropyi) suifide. which boils above 134 C.
  • Greases having the compositions of the present invention may housed in unmodified form, or may be compounded with several other materials as stated hereinbefore to give greases having preferred properties for specific purposes.
  • the subject greases may be modified by the inclusion of a free fatty acid, either similar to an acid radical of the esterifying group, or to the acid radical of the soap, or it may be of a dissimilar nature.
  • the function of the free fatty acid appears to be that ofa peptizing agent, giving the soap 9. better texture, and allowing the use of a smaller amount of soap than if the free When a free acid is is not used, as the grease then becomes unduly soft for general use. Consequently, the composi-. tion should preferably contain from about 3% to about 30% (preferably 6% to lithium soap; from about 0.01 to about 1.0% (preferably 0.05% to 0.5%) free fatty acid; the remainder of the grease comprising the thio-ether derivative as specified hereinbefore. 4K
  • the free fatty acid may be any within the fatty acid series, but preferably is a saturated fatty acid, such as lauric, myristic, palmitic, stearic, arachic, behenic, hydroxystearic, etc.
  • the free fatty acid may be excess fatty acid added at the 50 time of saponification in the sulfide base.
  • the acid may be added to the thio-ether derivative prior to grease formation, or the grease may be modified therewith at any time prior to use.
  • the grease base is a thio-ether compound, it may show a tendency to oxidize under severe operating conditions, thus allowing the formation of decomposition products which may in time prove detrimental to optimum engine operation. Consequently an oxidation inhibitor, efgaa phenolic compound or a substituted aromatic amine,
  • composition may be added to the composition to improve its paraphenylenediamlne, alphaor beta-naphthyiamine, phenyl-alphaor beta-naphthylamine, al-
  • the compositions should comprise from about 4% to about 40% lithium soap (4% to 10% is preferred) and from about 0.01% to about 2.0% oxidation inhibitor (0.054% is preferred) the balance comprising the thio-ether derivative base defined hereinbefore.
  • the compositions ordinarily obtained have a rubbery texture which has only limited utility as greases.
  • the resulting grease is substantially toughened, becomes substantially waterproof and is resistant to syneresis or solution at low and high temperatures, respectively.
  • This toughened com.. position broadens the utility of the novel greases, since they thereby become useful for heavy duty purposes or where a water-proof grease is required.
  • the acrylic acid ester polymers have structural units of the general structure wherein R1, R2 and R3 are either hydrogen or alkyl groups, and COORA is an ester radical.
  • R1 is either hydrogen or a lower alkyl group, such as methyl, ethyl, isopropyl, butyl, isobutyl, amyl, etc.
  • R1 and R3 are preferably hydrogens.
  • R4 is an alkylgroup having 3 or more carbon atoms, and preferably has4 to 8 carbon atoms.
  • Optimum results are obtained when the polymeric ester is a polymer of isobutyl methacrylate.
  • the lithium soaps are prepared by direct saponification of either fatty acids or of fats, which generally are glycerides of the fatty acids.
  • the saponification is normally carried out by heating the fat or fatty acid with L120, its hydrates, or LiOH.
  • the lithium soaps thus formed, for exsq ample, at temperatures of about C. usually .contain a small amount of free fatty acid and water of neutralization. This latter may be relnoved by distillation, preferably at about C. or at lower temperatures if reduced pressures are employed. In some greases its presence is not ob- 70 jectionable.
  • a second method of forming the lithium soap comprises mixing the fatty acid material with the thio-ether derivatives which comprise the grease base, and subsequently adding a normal lithium 7s oxide, preferably in small amounts and at mod the lithium soap.
  • the composition may be purified as notedhbove.
  • the best, method of preparing the subject greases which involves no after-treatments orother steps such as dehydration, solvent removal, extraction of diluents or removal of excess reactants comprises the addition of a preformed lithiumsoap to a preformed dicarboxyalkyl thioether, usually at elevated temperatures to facilitate solution.
  • the thio-ether derivatives comprising the bases of the greases of this invention include those hav-. ing the general formula:
  • the esterifying acid and dihydroxy thlo-ether are uct may be purified by distillation, extraction. or usually heated together, preferably in the presence of an esterification catalyst and an inert solvent such as benzene, toluene, xylene, etc.
  • the reaction may be carried out with continuous or intermittent distillation of water formed during the esterification. or may be conducted in the presence of a dehydration catalyst, such as zinc chloride.
  • a dehydration catalyst such as zinc chloride.
  • the product may be purified by distillation, extraction, or other means for the removal of water. solvent, catalysts, dehydration agents, and unreacted esterifying acid and/or dihydroxy thio-ether.
  • solvent, catalysts, dehydration agents, and unreacted esterifying acid and/or dihydroxy thio-ether are listed in the section of this specification entitled The grease base.” A typical esteriflcation also is described in the latter section.
  • ingredients which may be added include various corrosion inhibitors, extreme pressure additives, anti-wear agents, stabilizers. viscosity index improvers, and the like, provided they do not interfere with the operation and utility of the grease.
  • the lithium map may be present in the subject greases to the extent of from about 4% to about 40% of the composition.
  • the soap concentration will befrom about 4% to about 10%.
  • Example I A grease having a composition according to the present invention was prepared as follows:
  • Bis-(gamma- 2 -ethylhexoyloxypropyl) sulfide was prepared as described hereinbefore. Substantially neutral lithium stearate was added to the sulfur compound while it was heated at about 185 C. The soap disperses at this temperature, after which it is rapidly cooled. The grease so formed was then homogenized'to remove any lumps that might be present therein. Amounts of the ingredients were such that the grease contained 10% of lithium stearate and per cent of the sulfide derivative. The grease was of buttery consistency at room temperature, and showed substantially no indications of syneresis. The buff-colored composition maintained suitable grease structure as high as C.
  • Example III Using the mixed naphthenlc acids derived from petroleum as the esterifying agent bis-(gammanaphthenoxypropyl) sulfide was prepared.
  • the naphthenic ester was mixed with lithium stearate at 185 C. "to form a 90:10 mixture of ester and soap. Upon rapid cooling followed by homogenizing the composition exhibited excellent grease properties, being light brown in color, showing no tendency to synerize, and maintaining its proper grease structure as high as l90 C.
  • a lubricating grease composition comprising as the major lubricating constituents thereof bis-(gamma-2-ethylhexoyloxypropyl) sulfide and R1-(")0-R2SR3-0- ()R4 wherein R1 and R4 are hydrocarbon radicals, R: and R: are aliphatic radicals, a lithium soap, from 4% to 40% of said major constituents being said soap and an oxidation inhibitor.
  • a water-resistant lubricating grease composition comprising as the major lubricating constituents thereof a thio-ether derivative havin the general formula wherein R1 and R4 are hydrocarbon radicals, R:
  • R1 and Rs are aliphatic radicals, a lithium soap and a minor amount of a polymer having recuring structural units of the general formula wherein R1 and Rs are radicals selected from the group consisting of hydrogen and alkyl radicals, and COORa is an ester radical.
  • a lubricating grease composition comprising as the major lubricating constituents thereof is present in said composition in amounts from.
  • a lubricating grease composition comprising as the major lubricating constituent thereof a thio-ether derivative having the general formula wherein R1 and R1 are hydrocarbon radicals and R2 and R: are aliphatic radicals, and a lithium soap from 4% to 40% of said major constituents being said soap.
  • a lubricating grease composition according to claim 5, wher in the lithium soap is derived from a mono-olefinic fatty acid.
  • a lubricating composition comprising 4- 40% of a lithium soap and, as the major lubricating componet, a thio-ether derivative having the general formula wherein m is an integer from 2 to 4, n is an integer from 1 to 4, the groups (CH-.0111 are identical saturated straight chain radicals and the groups (CH2); are identical saturated straight chain radicals.
  • a lubricatin rease composition comprising thio-ether derivative having the general formula wherein R1 and R4 are hydrocarbon radicals and W R: and Rs are saturated aliphatic radicals, and a lithium soap from 4%. to 40% of said major constituents being said soap.
  • a lubricating grease composition comprising as the major lubricating constituents thereof a thioether derivative having the general for mula wherein R1 and R4 are saturated aliphatic radicals having from 4 to 11 carbon atoms and R2 and R3 are aliphatic radicals, and a lithium soap from 4% to 40% of said major constituents beingsaid soap.
  • a lubricating grease composition comprising as the major lubricatin constituents thereof a thio-ether derivative shaving the. general formula o o RigORr-SR
  • a lubricating grease composition comprising as the major lubricating constituents thereof a thio-ether derivative having the general formula o R1-'d-o-a1-s-R1-o i-al wherein R1 through R1 are aliphatic radicals, and
  • a lithium soap from 4% to 40% of said major constituents being said soap.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Description

Patented Oct. 19, 1948 SYNTHETIC GREASE Ellis Ross Whit e, Berkeley, and Denlsam Harman, Albany, Calli'., assignors to Shell Development Company, San Francisco, Calif., a corporatlon of Delaware No Drawing. Application June 8, 1948, Serial No. 675,332
16 Claim]. (01. ZEH ZJ) 1 This invention relates to lubricants and to processes of preparing them, and refers more particularly to stable grease compositions comprising certain thioether derivatives and a lithilun soap. I
It is known in the art to prepare various lubricating grease compositions adapted for particular uses. The uses to which the various grease compositions are employed present a wide variety of conditions, and generally a grease prepared with a given set of conditions in mind is not suitable 'for use in a different environment. Conversely, all sets of conditions met in the great variety of lubricating systems encountered todayv cannot be satisfied by mineral oil base greases, for example.
To illustrate further: not only are high temperature conditions frequently met, but low temperature lubrication is becoming increasingly important. Airplanes are controlled in flight by special mechanisms such as rudders, elevators, and ailerons which are adapted to the main portions of the airplane such as fuselage and wings by specially designed hinges. These hinges have metal to metal contact bearing surfaces which oifer a very difilcult lubrication problem. Airplanes are operated under the most severe changes in climatic conditions and since the failure of even one part of the mechanism might well result in a catastrophe, it is imperative that all parts should be free and well lubricated at all times. It is not uncommon for a plane during a single trip to be subjected to extremely high ground temperatures, as well as subzero temperatures in the upper atmosphere, in addition to conditions of high humidity such as rain, snow or ice. Any lubricant used upon the control mechanisms oi the plane must therefore be capable of withstanding these conditions without disintegration.
High temperature greases such. as sodium greases are known to the art. However, they are quite water-soluble and readily disintegrate under humid conditions. Water-insoluble greases such as calcium soap greases, are also known, but these compositions will not withstand high temperatures. Aluminum soap greases are also water insoluble, but have a relatively low transition point where they become fluid and run out of the bearing. Barium soap greases are only slowly affected by the presence of water and eifectlvely withstand elevated temperatures, but have the disadvantages of losing their grease structure on standing at lower temperatures and of be- 2 coming quite stiff and heavy at elevated temperatures.
The common mineral oil and vegetable oil bases have shortcomings which limit their complete utility as grease bases. .The viscosity indices of such bases, for example, are unsatisfactory where extreme conditions, both high and low temperatures and pressures, are to be met. Various synthetic bases, suchv as chlorinated dlphenyl, have been investigated, but have not proved satisfactory for general use, especially because of their generally low thermal decomposition tem perature characteristics.
It is an object of this invention to produce a grease composition which will provide adequate lubrication at both high and low temperatures and will not decompose in the presence of excessive moisture or at relatively high temperatures. Another object of this invention is to provide grease compositions which are not unduly subject to thermal cracking such as is encountered with mineral and vegetable oil greases. A further object is to provide greases of uniform consistency and texture, and which vary from extreme hardness to extreme softness, in accordance with the nature and proportions of the ingredients. I
Now, in accordance with this invention, it has been found that superior greases are obtained :by the use of compositions predominating in an ester of a dihydroxy thioether, such as those having the general formula in which R1 and R4 are hydrocarbon radicals, and R2 and Rs are aliphatic radicals, and, in addition thereto, from about 4% to about 40% of a lithium soap. Lubricating greases having the above composition possess important features which render them highly desirable, such as substantial non-inflammability, thermal stability, etc. Also, in accordance with this invention, it has been found that such greases, although comparatively stable in regard to oxidation, are further improved in stability by the incorporation-therein of an inhibitor. Still in accordance with this invention thesegreases may be toughened by the addition thereto of a minor amount of polymers of an esteriiled methacrylic acid.
The several constituents of the grease will now be discussed.
The soap The particular type of soap employed comprises predominantly a lithium soap, although minor amounts of fatty acid salts of other metals, partlculariy sodium, potassium, calcium, barium,
zinc, aluminum, etc., may also be present. The fatty acids which may be used in forming the lithium soaps useful in the invention comprise the lower fatty acid series as well as the higher v acid radicals, as well those of 2,3-diethylvaleric acid, 3'-propylcaproic acid, 4-isobutylheptolc acid,
-etc. The higher molecular weight radicals, both saturated and unsaturated, likewise form suitable-ester groups in combination with the two -COO groups in thethioether molecule. The mono-oleiinic acids and the naphthenic acids are the preferred classes within this group. The naphthenic acid derivatives are conveniently prepared from the naphthenic acids found in certain petroleum fractions. These acids, which are usually a mixture of various naphthenic acid homoiogues or alkylatedjderivatives thereof, are referred to hereinafteivas' petroleum naphthenic acids or simply as naphthenic acid. The thin-- I other derivatives containing petroleum naphlard, various seed oils, wool fat, naphthenic acids such as may be derived from petroleum oils; rosin,
tall oil, oxidized paraflin, fish oils, olive oil, palm oil, etc.
Not only are the acids having twelve or more carbon atoms preferred for use in preparing lithium soaps, but those acids are most preferred which are saturated or contain no more than about one unsaturated linkage in the molecule. including saturated fatty acids, mono-oleflnic fatty acids and mono-acetylenic fatty acids, all having twelve or more carbon atoms.
The grease base The bases for the greases which comprise this invention are thioether derivatives having the general structural formula 0 o m-d-o-as-san-o-ii-m in which R1 to Rs are hydrocarbon radicals. Preferably, R1 and R4 are non-aromatic, but instead are aliphatic or alicyclic. The most useful grease bases of this class are those in which R1 and R4 are saturated aliphatic radicals, and of this group those having from 4 to 11 carbon atoms are preferred.
Together with the COO group to which they areattached, R1 and R4 form ester groups such as the valeric acid radicals, including normal valeric, isovaleric, tertiary valeric or trimethyl acetic, (which is the preferred acid radical) and (1-1 valeric (or methylethylacetic) acid radicals. The saturated 5-carbon atom radicals, together with the COO- group to which they are attached, comprise the caprolc- (or hexoic) acid radicals, including butyl-acetic, iso-caproic (or secondary butylacetic), pseudocaproic (or tertiary-butylacetic), secondary-caproic (or diethylacetic), secondary active-caproic (or methylpropylacetic) or tertiary-caproic (dimethylethyl acetic) acid radicals. The B-carbon saturated aliphatic radicals, together with the adjacent --COO- group.-form radicals of the'heptoic acid series, including enanthic. isoenanthic, methyldiethylacetic, ethylpropylacetic, methylbutylacetic, etc. acid radicals. The 'l-carbon atom saturated aliphatic radicals and the adjacent COO group form the octoic acid radicals Ce-u-OOO- including p'clargonic, capric. undecylic and iauric thenic acid radicals make especially suitable grease bases for lithium soaps.
The groups R2 and Rs in the above general formula are either similar or dissimilar hydrocarbon radicals. especially aliphatic radicals which may be saturated or may contain one or more unsaturateg linkagesoi' oletlnic or acetylenlccharacter and furthermore may contain elements such as sulfur, nitrogen, phosphorus, selenium and tellurlum. Preferably, however, each of these radicals is a saturated hydrocarbon radical, and still more preferably is a saturated straight chain hydrocarbon radical forming a primary linkage with the sulfur atom, giving the following general configuration:
T wherein R1 and R4 are hydrocarbon radicals and R4 and R3 are saturated aliphatic radicals. Of this group of trio-ether derivatives, those having similar ester groups and similar aliphatic radicals form the most suitable-grease bases and have the general formula:
When the grease bases have the above configuration, those giving the most satisfactory results have Ris which are saturated hydrocarbon groups having 4 to 11 carbon atoms, and Ra's which are saturated straight chain hydrocarbons having 1 to 8 carbon atoms, and preferably from 2 to 5 carbon atoms to give the formula in which n is an integer of from 3 to 10 and m is an integer of from 2 tall. The outstanding grease bases having this latter preferred general formula are those in which m is an integer of from 2 to 4.
Compounds having this latter general formula are readily prepared by the reaction of hydrogen sulfide with an oleflnic alcohol, such as allyl alcohol to give the bis-(gamma hydroxypropyl) sulflde. This in turn is esterifled with an acid, such as trimethylacetic acid or il-ethylhexoic acid. to give di-esters of thio-ether derivatives. A typical preparation is as follows:
Five hundred cc. allyl alcohol and 124 g. hy-
drogen sulfide were subjected in a bomb to the radiation from a, 250 watt mercury arc lamp. During the first hour the pressure in the system rose steadily from 180 to 220 lbs/sq. in. after which it fell slowly to 170 lbs./sqin. at the end of the radiation period. In this time the temperature of the reactor increased from 16 C. to 0 in part due to the exothermic character fatty acid were absent. present, care must be taken that too much acid of the reaction, but mainly from the heat emitted by the mercury arc lamp. The reaction product was then distilled to remove unreacted allyl alco hol and the gamma-mercaptopropyl alcohol formed during reaction, leaving the desired product, namely, bis-(gamma hydroxypropyi) suifide. which boils above 134 C.
In place of ultraviolet light, other free-radical promoting catalysts (preferably in the absence of metallic salts) may be used.
A mixture consisting of 150 grams of bis- (gamma-hydroxypropyl) sulfide, 432 grams of 2-. ethylhexoic acid, 8 grams of para-toluene sulfonic acid and 400 cc. of toluene was heated to boiling under a separating still head. This heating was continued until no further water was distilled ofi. All of the toluene was then evaporated, and the remaining product was distilled to yield 0.866 (348 g.) moles of bis-(gamma-Q-ethylhexoxypropyl) sulfide.
Other ingredients Greases having the compositions of the present invention may housed in unmodified form, or may be compounded with several other materials as stated hereinbefore to give greases having preferred properties for specific purposes.
The subject greases may be modified by the inclusion of a free fatty acid, either similar to an acid radical of the esterifying group, or to the acid radical of the soap, or it may be of a dissimilar nature. The function of the free fatty acid appears to be that ofa peptizing agent, giving the soap 9. better texture, and allowing the use of a smaller amount of soap than if the free When a free acid is is not used, as the grease then becomes unduly soft for general use. Consequently, the composi-. tion should preferably contain from about 3% to about 30% (preferably 6% to lithium soap; from about 0.01 to about 1.0% (preferably 0.05% to 0.5%) free fatty acid; the remainder of the grease comprising the thio-ether derivative as specified hereinbefore. 4K
The free fatty acid may be any within the fatty acid series, but preferably is a saturated fatty acid, such as lauric, myristic, palmitic, stearic, arachic, behenic, hydroxystearic, etc. The free fatty acid may be excess fatty acid added at the 50 time of saponification in the sulfide base. Alternatively, the acid may be added to the thio-ether derivative prior to grease formation, or the grease may be modified therewith at any time prior to use.
Since the grease base is a thio-ether compound, it may show a tendency to oxidize under severe operating conditions, thus allowing the formation of decomposition products which may in time prove detrimental to optimum engine operation. Consequently an oxidation inhibitor, efgaa phenolic compound or a substituted aromatic amine,
may be added to the composition to improve its paraphenylenediamlne, alphaor beta-naphthyiamine, phenyl-alphaor beta-naphthylamine, al-
Dh .alpha-, beta,beta-., or alpha,beta-dinaphthyl-- amine, etc.
When the greases of the present invention contain these substituted phenols or amines, the compositions should comprise from about 4% to about 40% lithium soap (4% to 10% is preferred) and from about 0.01% to about 2.0% oxidation inhibitor (0.054% is preferred) the balance comprising the thio-ether derivative base defined hereinbefore.
When thio-ether derivatives of the above-described structure are gelled with a polymer of one or a mixture of esters of acrylic acid or of. an alkylated derivative thereof, the compositions ordinarily obtained have a rubbery texture which has only limited utility as greases. However, when a minor amount of such an ester is incorporated in the compositions of the present invention, the resulting grease is substantially toughened, becomes substantially waterproof and is resistant to syneresis or solution at low and high temperatures, respectively. This toughened com.. position broadens the utility of the novel greases, since they thereby become useful for heavy duty purposes or where a water-proof grease is required. The acrylic acid ester polymers have structural units of the general structure wherein R1, R2 and R3 are either hydrogen or alkyl groups, and COORA is an ester radical. Preferably R1 is either hydrogen or a lower alkyl group, such as methyl, ethyl, isopropyl, butyl, isobutyl, amyl, etc., while R1 and R3 are preferably hydrogens. The most satisfactory degree of water-proofing is obtained when R4 is an alkylgroup having 3 or more carbon atoms, and preferably has4 to 8 carbon atoms. Optimum results are obtained when the polymeric ester is a polymer of isobutyl methacrylate.
When the homologues and analogues of polymerized acrylic acid esters are used as waterproofing and toughening agents for the greases of this invention, optimum over-all results are obtained when the composition comprises the following ingredients:
Poiymcrized acrylic ester (Ll-10% (preferred 0.5%-4%) Litliiumsoap 4-40% (preferred 4%-10%) Thio-ether derivative Balance (preferred 86%-95%) Preparation of .the grease and grease components The lithium soaps are prepared by direct saponification of either fatty acids or of fats, which generally are glycerides of the fatty acids. The saponification is normally carried out by heating the fat or fatty acid with L120, its hydrates, or LiOH. The lithium soaps thus formed, for exsq ample, at temperatures of about C. usually .contain a small amount of free fatty acid and water of neutralization. This latter may be relnoved by distillation, preferably at about C. or at lower temperatures if reduced pressures are employed. In some greases its presence is not ob- 70 jectionable.
A second method of forming the lithium soap comprises mixing the fatty acid material with the thio-ether derivatives which comprise the grease base, and subsequently adding a normal lithium 7s oxide, preferably in small amounts and at mod the lithium soap.
a subsequent to or during esteriflcation of the dihydroxyalkyl thio-ether and the preparation of --An alternative process which has been discovered comprises mixing the dihydroxyalkyl thioether and fatty acid material adding a normal lithium oxide at such temperatures and under such conditions that reaction will occur substantially only between the lithium oxide and the fatty acid. and subsequently adjusting conditions,
so that esterification of the dihydroxyalkyl thioether takes place, either with remaining free fatty acid or with a subsequently added fatty acid. If necessary, the composition may be purified as notedhbove.
The simultaneous formation of the esterifled dihydroxyalkyl thio-ether and of the lithium soap is also contemplated. I
The best, method of preparing the subject greases which involves no after-treatments orother steps such as dehydration, solvent removal, extraction of diluents or removal of excess reactants comprises the addition of a preformed lithiumsoap to a preformed dicarboxyalkyl thioether, usually at elevated temperatures to facilitate solution.
The thio-ether derivatives comprising the bases of the greases of this invention include those hav-. ing the general formula:
These are usually prepared by the esteriflcation of a dihydroxy thio-ether having the general formula:
The esterifying acid and dihydroxy thlo-ether are uct may be purified by distillation, extraction. or usually heated together, preferably in the presence of an esterification catalyst and an inert solvent such as benzene, toluene, xylene, etc. The reaction may be carried out with continuous or intermittent distillation of water formed during the esterification. or may be conducted in the presence of a dehydration catalyst, such as zinc chloride. Subsequent to esteriflcation. the product may be purified by distillation, extraction, or other means for the removal of water. solvent, catalysts, dehydration agents, and unreacted esterifying acid and/or dihydroxy thio-ether. The acids and dihydroxy thio-ethers, from which these esters are prepared, are listed in the section of this specification entitled The grease base." A typical esteriflcation also is described in the latter section.
Other ingredients which may be added include various corrosion inhibitors, extreme pressure additives, anti-wear agents, stabilizers. viscosity index improvers, and the like, provided they do not interfere with the operation and utility of the grease.
8 As pointed out hereinbefore, the lithium map may be present in the subject greases to the extent of from about 4% to about 40% of the composition. Preferably. however, the soap concentration will befrom about 4% to about 10%.
, or cold, are encountered.
The following examples illustrate the products of the present invention: I
Example I I A grease having a composition according to the present invention was prepared as follows:
Bis-(gamma- 2 -ethylhexoyloxypropyl) sulfide was prepared as described hereinbefore. Substantially neutral lithium stearate was added to the sulfur compound while it was heated at about 185 C. The soap disperses at this temperature, after which it is rapidly cooled. The grease so formed was then homogenized'to remove any lumps that might be present therein. Amounts of the ingredients were such that the grease contained 10% of lithium stearate and per cent of the sulfide derivative. The grease was of buttery consistency at room temperature, and showed substantially no indications of syneresis. The buff-colored composition maintained suitable grease structure as high as C.
Example II ture which showed no tendency to synerize, was
the color of cream, and had a satisfactory texture as high as about 194 C.
Example III Using the mixed naphthenlc acids derived from petroleum as the esterifying agent bis-(gammanaphthenoxypropyl) sulfide was prepared. The esteriflcation of bis-(gamma-hydroxypropyl) sulfide with this agent, was carried out by the process substantially as described hereinbefore for the preparation of bis-(gamma-Z-ethylhexoyloxypropyl) sulfide. The naphthenic ester was mixed with lithium stearate at 185 C. "to form a 90:10 mixture of ester and soap. Upon rapid cooling followed by homogenizing the composition exhibited excellent grease properties, being light brown in color, showing no tendency to synerize, and maintaining its proper grease structure as high as l90 C.
We claim as our invention:
1. A lubricating grease composition comprising as the major lubricating constituents thereof bis-(gamma-2-ethylhexoyloxypropyl) sulfide and R1-(")0-R2SR3-0- ()R4 wherein R1 and R4 are hydrocarbon radicals, R: and R: are aliphatic radicals, a lithium soap, from 4% to 40% of said major constituents being said soap and an oxidation inhibitor.
3. A water-resistant lubricating grease composition comprising as the major lubricating constituents thereof a thio-ether derivative havin the general formula wherein R1 and R4 are hydrocarbon radicals, R:
and R3 are aliphatic radicals, a lithium soap and a minor amount of a polymer having recuring structural units of the general formula wherein R1 and Rs are radicals selected from the group consisting of hydrogen and alkyl radicals, and COORa is an ester radical.
4. A water-resistant lubricating grease composition according to claim 14, wherein the polymer 1o ing as the major lubricating constituents thereof a thio-ether derivative having the general formula in which R1 and R4 are hydrocarbon radicals and R: and Rs are saturated aliphatic radicals, and a lithium soap from 4% to 40% of said major con- .10
stituents being said soap. 1
13. A lubricating grease composition comprising as the major lubricating constituents thereof is present in said composition in amounts from.
about 0.1 to about 10%. I
5. A lubricating grease composition comprising as the major lubricating constituent thereof a thio-ether derivative having the general formula wherein R1 and R1 are hydrocarbon radicals and R2 and R: are aliphatic radicals, and a lithium soap from 4% to 40% of said major constituents being said soap.
' 6. A lubricating grease composition according to claim 5, wherein the lithium soap comprises lithium napthenate.
7. A lubricating grease composition according to claim 5, wher in the lithium soap is derived from a mono-olefinic fatty acid.
8. A lubricating grease composition according to claim 5, wherein the lithium soap is derived from a saturated fatty acid having at least 12 car. bon atoms.
9. A lubricating grease composition according to claim 5, wherein the lithium soap contains at least 12 carbon atoms.
10. A lubricatin grease composition according to claim 5, wherein the lithium soap comprises from about 4 to about 40% of said composition.
11. A lubricating composition comprising 4- 40% of a lithium soap and, as the major lubricating componet, a thio-ether derivative having the general formula wherein m is an integer from 2 to 4, n is an integer from 1 to 4, the groups (CH-.0111 are identical saturated straight chain radicals and the groups (CH2); are identical saturated straight chain radicals.
12. A lubricatin rease composition comprisa thio-ether derivative having the general formula wherein R1 and R4 are hydrocarbon radicals and W R: and Rs are saturated aliphatic radicals, and a lithium soap from 4%. to 40% of said major constituents being said soap.
14. A lubricating grease composition comprising as the major lubricating constituents thereof a thioether derivative having the general for mula wherein R1 and R4 are saturated aliphatic radicals having from 4 to 11 carbon atoms and R2 and R3 are aliphatic radicals, anda lithium soap from 4% to 40% of said major constituents beingsaid soap.
15. A lubricating grease composition comprising as the major lubricatin constituents thereof a thio-ether derivative shaving the. general formula o o RigORr-SR|0 1h wherein R1 through R1 are saturated aliphatic radicals, and a lithium soap from 4% to 40% of said major constituents being said soap.
16. A lubricating grease composition comprising as the major lubricating constituents thereof a thio-ether derivative having the general formula o R1-'d-o-a1-s-R1-o i-al wherein R1 through R1 are aliphatic radicals, and
a lithium soap from 4% to 40% of said major constituents being said soap.
. ELLIS ROSS WHITE.
' DENHAM HARMAN.
REFERENCES CITED The following references are of record in the fileof this patent:
UNITED 's'm'ras m'mn'rs Lien July 2, 1m
US675332A 1946-06-08 1946-06-08 Synthetic grease Expired - Lifetime US2451895A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US675332A US2451895A (en) 1946-06-08 1946-06-08 Synthetic grease
GB14330/47A GB642410A (en) 1946-06-08 1947-05-29 Lubricating grease composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US675332A US2451895A (en) 1946-06-08 1946-06-08 Synthetic grease

Publications (1)

Publication Number Publication Date
US2451895A true US2451895A (en) 1948-10-19

Family

ID=24710008

Family Applications (1)

Application Number Title Priority Date Filing Date
US675332A Expired - Lifetime US2451895A (en) 1946-06-08 1946-06-08 Synthetic grease

Country Status (2)

Country Link
US (1) US2451895A (en)
GB (1) GB642410A (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2577706A (en) * 1948-11-26 1951-12-04 California Research Corp High melting-high water-resistant grease
US2585862A (en) * 1949-11-01 1952-02-12 Standard Oil Dev Co Synthetic lubricants
US2588273A (en) * 1950-08-02 1952-03-04 Standard Oil Dev Co Lubricating compositions
US2603604A (en) * 1948-11-01 1952-07-15 Shell Dev Lubricating composition
US2612472A (en) * 1949-05-28 1952-09-30 Standard Oil Dev Co Lubricating grease compositions
US2644793A (en) * 1950-08-30 1953-07-07 Standard Oil Dev Co Rust inhibiting composition
US2666033A (en) * 1951-04-11 1954-01-12 Texas Co Lithium soap grease containing methacrylate ester polymer for bearing noise suppression
US2683119A (en) * 1949-11-16 1954-07-06 Standard Oil Dev Co Compounded lubricant
US2807638A (en) * 1953-05-01 1957-09-24 Shell Dev Polyhydric alcohol ester of a tertiary alkyl-substituted cyclohexanecarboxylic acid
US3236805A (en) * 1960-08-01 1966-02-22 Montedison Spa Polypropylene stabilized with thioesters of long-chain alkyl compounds and process for preparing same
WO2004111163A1 (en) * 2003-06-10 2004-12-23 The Lubrizol Corporation Functionalized polymer composition for grease
US20080027181A1 (en) * 2006-07-28 2008-01-31 Loper John T Alkyl acrylate copolymer dispersants and uses thereof

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1422869A (en) * 1921-07-02 1922-07-18 Hoechst Ag Esters of dioxydiethylsulphide and process of making same
US2164393A (en) * 1935-04-15 1939-07-04 Wakefield & Co Ltd C C Lubricating oil
US2274674A (en) * 1940-04-05 1942-03-03 Clarence E Earle Lubricant containing a lithium compound
US2274673A (en) * 1940-04-05 1942-03-03 Clarence E Earle Lubricating composition
US2351384A (en) * 1942-11-18 1944-06-13 Shell Dev Lithium soap grease
US2351280A (en) * 1942-07-16 1944-06-13 Cities Service Oil Co Lubricant
US2356586A (en) * 1940-03-01 1944-08-22 Hentrich Winfrid Thio-diglycol ester plasticized polyvinyl chloride
US2362767A (en) * 1942-06-03 1944-11-14 Cities Service Oil Co Lubricants
US2366042A (en) * 1942-10-22 1944-12-26 Clties Service Oil Company Lubricants
US2383146A (en) * 1942-07-10 1945-08-21 Cities Service Oil Co Lubricants
US2403104A (en) * 1942-10-17 1946-07-02 Union Oil Co Lithium greases

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1422869A (en) * 1921-07-02 1922-07-18 Hoechst Ag Esters of dioxydiethylsulphide and process of making same
US2164393A (en) * 1935-04-15 1939-07-04 Wakefield & Co Ltd C C Lubricating oil
US2356586A (en) * 1940-03-01 1944-08-22 Hentrich Winfrid Thio-diglycol ester plasticized polyvinyl chloride
US2274674A (en) * 1940-04-05 1942-03-03 Clarence E Earle Lubricant containing a lithium compound
US2274673A (en) * 1940-04-05 1942-03-03 Clarence E Earle Lubricating composition
US2362767A (en) * 1942-06-03 1944-11-14 Cities Service Oil Co Lubricants
US2383146A (en) * 1942-07-10 1945-08-21 Cities Service Oil Co Lubricants
US2351280A (en) * 1942-07-16 1944-06-13 Cities Service Oil Co Lubricant
US2403104A (en) * 1942-10-17 1946-07-02 Union Oil Co Lithium greases
US2366042A (en) * 1942-10-22 1944-12-26 Clties Service Oil Company Lubricants
US2351384A (en) * 1942-11-18 1944-06-13 Shell Dev Lithium soap grease

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2603604A (en) * 1948-11-01 1952-07-15 Shell Dev Lubricating composition
US2577706A (en) * 1948-11-26 1951-12-04 California Research Corp High melting-high water-resistant grease
US2612472A (en) * 1949-05-28 1952-09-30 Standard Oil Dev Co Lubricating grease compositions
US2585862A (en) * 1949-11-01 1952-02-12 Standard Oil Dev Co Synthetic lubricants
US2683119A (en) * 1949-11-16 1954-07-06 Standard Oil Dev Co Compounded lubricant
US2588273A (en) * 1950-08-02 1952-03-04 Standard Oil Dev Co Lubricating compositions
US2644793A (en) * 1950-08-30 1953-07-07 Standard Oil Dev Co Rust inhibiting composition
US2666033A (en) * 1951-04-11 1954-01-12 Texas Co Lithium soap grease containing methacrylate ester polymer for bearing noise suppression
US2807638A (en) * 1953-05-01 1957-09-24 Shell Dev Polyhydric alcohol ester of a tertiary alkyl-substituted cyclohexanecarboxylic acid
US3236805A (en) * 1960-08-01 1966-02-22 Montedison Spa Polypropylene stabilized with thioesters of long-chain alkyl compounds and process for preparing same
WO2004111163A1 (en) * 2003-06-10 2004-12-23 The Lubrizol Corporation Functionalized polymer composition for grease
US20080027181A1 (en) * 2006-07-28 2008-01-31 Loper John T Alkyl acrylate copolymer dispersants and uses thereof
US8980804B2 (en) 2006-07-28 2015-03-17 Afton Chemical Corporation Alkyl acrylate copolymer dispersants and uses thereof

Also Published As

Publication number Publication date
GB642410A (en) 1950-09-06

Similar Documents

Publication Publication Date Title
US2182137A (en) Soda soap grease
US4536308A (en) Lithium soap grease additive
US2471115A (en) Lubricating oil
US2451895A (en) Synthetic grease
US2335017A (en) Lubricating composition
US3755176A (en) Sulfur-containing carboxylic acids as corrosion inhibitors
US2361804A (en) Lubricating composition
GB607013A (en) Corrosion inhibiting compositions
US2440530A (en) Stabilized organic compositions
US2820014A (en) Ester lubricants
US3174931A (en) Grease compositions
US2382700A (en) Compounded lubricating oil
US2614077A (en) Grease composition
US2625510A (en) Lubricating grease composition
US2250545A (en) Lubricating composition
US2652362A (en) Grease composition
US2489249A (en) Lubricant
US2281401A (en) Lubricating oil composition
US2398415A (en) Mineral oil composition and the like
US2355009A (en) Lubricant
US2676149A (en) Stabilized grease composition containing a sterol and a selenium compound
US2589973A (en) Lubricating grease composition
US2576031A (en) Lubricating grease containing soaps of tall oil
US2450321A (en) Rust-inhibiting greases
US2631132A (en) Lubricating oil additive