US2250545A - Lubricating composition - Google Patents

Lubricating composition Download PDF

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Publication number
US2250545A
US2250545A US235778A US23577838A US2250545A US 2250545 A US2250545 A US 2250545A US 235778 A US235778 A US 235778A US 23577838 A US23577838 A US 23577838A US 2250545 A US2250545 A US 2250545A
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US
United States
Prior art keywords
xanthogen
oil
oils
lubricating
sulfur
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
US235778A
Inventor
Louis A Mikeska
Lieber Eugene
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
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Filing date
Publication date
Priority to NL51053D priority Critical patent/NL51053C/xx
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Priority to US235778A priority patent/US2250545A/en
Priority to GB13059/39A priority patent/GB522189A/en
Priority to FR855166D priority patent/FR855166A/en
Priority to DEST59124D priority patent/DE710095C/en
Application granted granted Critical
Publication of US2250545A publication Critical patent/US2250545A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/12Thio-acids; Thiocyanates; Derivatives thereof
    • C10M135/14Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
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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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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/14Synthetic waxes, e.g. polythene waxes
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    • 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
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    • C10M2205/17Fisher Tropsch reaction products
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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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    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
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    • 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
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
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    • 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
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    • C10M2207/28Esters
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    • C10M2207/40Fatty vegetable or animal oils
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    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/404Fatty vegetable or animal oils obtained from genetically modified species
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    • 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
    • C10M2209/082Macromolecular 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 monocarboxylic
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    • 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
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    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/042Alcohols; Ethers; Aldehydes; Ketones
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    • C10M2211/044Acids; Salts or esters thereof
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    • C10M2211/06Perfluorinated compounds
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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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    • C10M2219/06Thio-acids; Thiocyanates; Derivatives thereof
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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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    • C10N2040/244Metal working of specific metals
    • C10N2040/246Iron or steel
    • 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
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/247Stainless steel
    • 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

Definitions

  • This invention deals with lubricating composl-1 tions. More specifically, it relates to the use in such compositions of small amounts of soluble organic xanthogen tetrasulfldes which are believed to possess a structure corresponding to the following formula:
  • Rand R represent alkyl, cyclic, or-cycloalkyl organic groups.
  • Potassium hydroxide is dissolved in absolute a1coho1'(fair excess over that required for reaction) and the required amount of carbon disulflde is added with cooling and mechanical agitation. Potassium xanthate precipitates out. The amount of xanthate is further increased by the addition of ether. excess alcohol being saturated with xanthate could be used again, avoiding the use of ether as a precipitant.) The solid product is recovered by filtration and dried.
  • the potassium xanthate is suspended in benzene (other inert solvents such as light naphtha could be used), stirred and a benzene solution of sulfur monochloride added with cooling. After the sulfur chloride has been added, the reaction mixture is refluxed for 2 hours to complete the condensation, and then poured into water. The benzene layer is removed and dried. After stripping off the benzene, the xanthogen tetrasulflde remains as a residue.
  • benzene other inert solvents such as light naphtha could be used
  • 'I'hese compounds are also compatible with soap, fatty oils and other ingredients normally employed in soluble oils, cutting oils, greases, motor oils, compounded, and industrial lubricants, without causing precipitation. or settling out of sulfur or sulfur compounds.
  • the xanthogen tetrasulfides e. g. ethyl xanthogen tetrasulflde
  • 3% of this material will carry the full load (580 lbs.) on the S. A. E. machine at 1000 R. P. M., and in addition, it meets the requirements of the Packard Stability Test.
  • This test involves the heating of the blend in an oven at 200 F. for 64 hrs. and running the thus-treated oil on the S. A. E. machine at 1000 R. P. M. and 83.6 lbs/sec. loading rate, the rubbing ratio being 14.6:1.
  • the blend must carry a full load of 550 lbs. scale pull.
  • Blends containing these xanthogen tetrasulxanthate salt prior to condensation Since these products pick up some of the mercaptan odor which is dimcult to remove, they are not as desirable as the corresponding alcohol derivatives.
  • compositions which are the subject of this invention are in the field of cutting oils.
  • a high E. P. eflect is desired without any detrimental odor or discoloration oi! the base stock, so as to give clean work pieces without need for further handling or processing.
  • Soluble cut ting oils are prepared by the addition of emulsihere such as sodium naphthenate, mahogany 1 in which the tetrasuliide is an alkyl xanthogen tetrasulilde.
  • a cutting oil comprising a mineral lubricating oil and about 2 to% oia soluble xanthogen tetrasulfide having the probable structure:
  • R and R are alkyl, cyclic or cyclo-alkyl groups, and the oxygen atoms may be replaced by sulfur.
  • the lubricating oil base stocks are generally crude or refined mineral oils of about 70 viscosity at 100 F. (Saybolt) to about 5000 viscosity at 100 F.
  • compositions may be employed i conjunction with linear polymer V.
  • linear polymer V. I. improvers, pour inhibitors, dyes, resins, voltolized'iats and/ or mineral oils or waxes, ester and other oiliness agents, phenolic or amino oxidation inhibitors, soaps, such as calcium stearate, lead oleate, lead naphthenate, aluminum naphthenate, and the like, dyes, halogenated compounds, such aschlorinated esters, chlorinated parailin waxes, etc., wetting agents, insecticides, germicides, fungicides, and the like.
  • composition of matter comprising any oil selected from the group consisting oi mineral oils and fatty oils, and a small amount of organic xanthogen tetrasulfide.
  • a lubricating composition comprising a lubricating oil base stock and at least about .01% of a soluble xanthogen sulfide having the general formula:
  • n-x-ti-(s)l-ii-x a where R and R are like or unlike alkyl, cyclic hydrocarbon, or mixed cyclo-alkyl radicals,'and X is either oxygen or sulfur.

Description

Patented July 29, 194i LUBRIYCATING COMPOSITION Louis A. Mikeska, Westiield, and Eugene liieber,
Linden, N. J., assignors to Standard Oil Development Company, a corporation of Delaware No Drawing. Application October 19,1938,
sci-a1 No. 235,771;
3 Claims. (Cl. 252-46) This invention deals with lubricating composl-1 tions. More specifically, it relates to the use in such compositions of small amounts of soluble organic xanthogen tetrasulfldes which are believed to possess a structure corresponding to the following formula:
where Rand R. represent alkyl, cyclic, or-cycloalkyl organic groups.
These compounds are condensation products which may be obtained in high yields according to the following reactions:
. Z3 ROH+CS:+KOH R-0-C +1110 Potassium xanthate Xsnthogen tetrasulflde An example in the preparation of such a material (ethyl xanthogen tetrasulfide) is as follows:
Potassium hydroxide is dissolved in absolute a1coho1'(fair excess over that required for reaction) and the required amount of carbon disulflde is added with cooling and mechanical agitation. Potassium xanthate precipitates out. The amount of xanthate is further increased by the addition of ether. excess alcohol being saturated with xanthate could be used again, avoiding the use of ether as a precipitant.) The solid product is recovered by filtration and dried.
The potassium xanthate is suspended in benzene (other inert solvents such as light naphtha could be used), stirred and a benzene solution of sulfur monochloride added with cooling. After the sulfur chloride has been added, the reaction mixture is refluxed for 2 hours to complete the condensation, and then poured into water. The benzene layer is removed and dried. After stripping off the benzene, the xanthogen tetrasulflde remains as a residue.
The overall yield averages around 86.7%.
These xanthogen tetrasulfldes possess such un- (In large production, the
and corrosion inhibiting properties. They likewise .exhibit exceptionally potentextreme pressure lubricating properties. Although they are sulfur compounds (ethyl xanthogen tetrasulfide contains about 63% S), they are light colored, oil soluble compounds, possessing a faint pleasant odor, and thus impart no objectionable characteristics to the mineral or other oil base stockin which they are blended.
'I'hese compounds are also compatible with soap, fatty oils and other ingredients normally employed in soluble oils, cutting oils, greases, motor oils, compounded, and industrial lubricants, without causing precipitation. or settling out of sulfur or sulfur compounds.
In the extreme pressure lubricating art the common practice is to add to the lubricating 'oil a sulfurized mineral or fatty 'oil. These com- .pounds are generally dark colored, odorous materials, poor in combined sulfur. Alkyl sulfides and polysulfides have been proposed for this purpose but their pungent and sickening odor markedly limits their uses in this direction. Xanthogen disulfldes, prepared by the oxidation of xanthic salts show relatively poor load carryirig properties, a 5% blend failing on the S. A. E
machine at 200 lbs. load. Although ethyl xanusual characteristics as to impart to lubricating and other oils, new and unexpected properties. For example, they possess excellent antioxidant thogen'trisulfide shows fair load carrying properties, it tends to settle out free sulfur on standing, and is therefore excluded from use to some extent because of its instability. An improved composition can be obtained by chilling the trisulflde or its solutions and filtering to remove the separated material.
However, the xanthogen tetrasulfides (e. g. ethyl xanthogen tetrasulflde) such as'those embodied in the present invention, give excellent results as extreme pressure blending agents. When used alone in mineral lubricating oil, 3% of this material will carry the full load (580 lbs.) on the S. A. E. machine at 1000 R. P. M., and in addition, it meets the requirements of the Packard Stability Test. This test involves the heating of the blend in an oven at 200 F. for 64 hrs. and running the thus-treated oil on the S. A. E. machine at 1000 R. P. M. and 83.6 lbs/sec. loading rate, the rubbing ratio being 14.6:1. The blend must carry a full load of 550 lbs. scale pull.
Blends containing these xanthogen tetrasulxanthate salt prior to condensation. Since these products pick up some of the mercaptan odor which is dimcult to remove, they are not as desirable as the corresponding alcohol derivatives.
One exceptionally wide use for the compositions which are the subject of this invention, is in the field of cutting oils. Here a high E. P. eflect is desired without any detrimental odor or discoloration oi! the base stock, so as to give clean work pieces without need for further handling or processing. For this purpose, it is desired to employ about 2 to 10% of the tetrasulfide condensation products previously described. Soluble cut ting oils are prepared by the addition of emulsihere such as sodium naphthenate, mahogany 1 in which the tetrasuliide is an alkyl xanthogen tetrasulilde.
3. A lubricating composition according to claim 1 in which the tetrasulflde is ethyl xanthyl tetrasulilde.
4. A lubricating composition according to claim i in which the mineral oil is an oil oi. high viscosity index. j
5. A cutting oil comprising a mineral lubricating oil and about 2 to% oia soluble xanthogen tetrasulfide having the probable structure:
where R and R are alkyl, cyclic or cyclo-alkyl groups, and the oxygen atoms may be replaced by sulfur.
soaps, rosin soaps, glycerol, alcohol and similar ingredients. 1 The lubricating oil base stocks are generally crude or refined mineral oils of about 70 viscosity at 100 F. (Saybolt) to about 5000 viscosity at 100 F.
In many cases, where antioxidant and anticorrosion effects are more desired, about 0.01 to 2% of the xanthate tetrasulildes is sumcient. For the preparation or E. P. greases and gear oils, higher viscosity base stocks may be employed, and there is often an advantage to employ stocks of high viscosity index, e. g. above 50. v
The present compositions may be employed i conjunction with linear polymer V. I. improvers, pour inhibitors, dyes, resins, voltolized'iats and/ or mineral oils or waxes, ester and other oiliness agents, phenolic or amino oxidation inhibitors, soaps, such as calcium stearate, lead oleate, lead naphthenate, aluminum naphthenate, and the like, dyes, halogenated compounds, such aschlorinated esters, chlorinated parailin waxes, etc., wetting agents, insecticides, germicides, fungicides, and the like.
The invention is not limited to any theory or structure or action, but islimited only by the 6. A composition of matter comprising any oil selected from the group consisting oi mineral oils and fatty oils, and a small amount of organic xanthogen tetrasulfide.
7. A lubricating composition comprising a lubricating oil base stock and at least about .01% of a soluble xanthogen sulfide having the general formula:
n-x-ti-(s)l-ii-x a where R and R are like or unlike alkyl, cyclic hydrocarbon, or mixed cyclo-alkyl radicals,'and X is either oxygen or sulfur.
8. The method of preparing improved lubrieating compositions which comprises reacting a compound having the general formula R--XH where R is an alkyl, cyclic hydrocarbon,-or mixed cyclo-alkyl radical and X is either oxygen or sulfur, with carbon disuliide and with a metal hydroxide to form a xanthate having the general formula:
I where M represents the nietal, then reacting 2 claims in which it is the intention to cover the s DISCLAIMER- mols or such xanthate in whichthe R constitu- -2,250,545ritual A. Mantra, Westfield, and' Eugene Lieber, Linden, N. .1. Lunaros'rma Courosrrrou. 'Patent dated July' 29, 1941. Disclaimer. filed 4 April 14, 1942, by the assignee, StandardOtl Development Company. Hereby enters this disclaimer to claims 1, 2, 3, 6, and 7.
[Oficial Gazette June 2, 1942.]
US235778A 1938-10-19 1938-10-19 Lubricating composition Expired - Lifetime US2250545A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
NL51053D NL51053C (en) 1938-10-19
US235778A US2250545A (en) 1938-10-19 1938-10-19 Lubricating composition
GB13059/39A GB522189A (en) 1938-10-19 1939-05-02 Improved lubricating compositions
FR855166D FR855166A (en) 1938-10-19 1939-05-23 Lubricant
DEST59124D DE710095C (en) 1938-10-19 1939-09-27 Mineral lubricating oils

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2431010A (en) * 1941-07-19 1947-11-18 Standard Oil Dev Co Soluble cutting oil
US2498863A (en) * 1945-08-30 1950-02-28 Socony Vacuum Oil Co Inc Lubricating oil composition
US2574457A (en) * 1947-08-05 1951-11-13 Phillips Petroleum Co Manufacture of alkyl sulfenyl trithiocarbonates
US2615804A (en) * 1947-05-08 1952-10-28 Goodrich Co B F Herbicidal composition
US2615802A (en) * 1948-10-23 1952-10-28 Monsanto Chemicals Herbicidal composition and method
US2743210A (en) * 1952-12-24 1956-04-24 Stauffer Chemical Co Xanthogen and dtthiocarbonyl tetrasulfides as pesticides
US2743209A (en) * 1952-12-24 1956-04-24 Robert H Jones Xanthyl and trithiocarbonyl, sulfides, sulfoxides, and sulfones as pesticides
US2813890A (en) * 1954-10-15 1957-11-19 Exxon Research Engineering Co Manufacture of alkyl xanthogen sulfides
US2925386A (en) * 1952-08-25 1960-02-16 Huels Chemische Werke Ag Mineral oil base lubricant
US3864374A (en) * 1973-11-19 1975-02-04 Canadian Ind Manufacture of alkali metal xanthates

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2431010A (en) * 1941-07-19 1947-11-18 Standard Oil Dev Co Soluble cutting oil
US2498863A (en) * 1945-08-30 1950-02-28 Socony Vacuum Oil Co Inc Lubricating oil composition
US2615804A (en) * 1947-05-08 1952-10-28 Goodrich Co B F Herbicidal composition
US2574457A (en) * 1947-08-05 1951-11-13 Phillips Petroleum Co Manufacture of alkyl sulfenyl trithiocarbonates
US2615802A (en) * 1948-10-23 1952-10-28 Monsanto Chemicals Herbicidal composition and method
US2925386A (en) * 1952-08-25 1960-02-16 Huels Chemische Werke Ag Mineral oil base lubricant
US2743210A (en) * 1952-12-24 1956-04-24 Stauffer Chemical Co Xanthogen and dtthiocarbonyl tetrasulfides as pesticides
US2743209A (en) * 1952-12-24 1956-04-24 Robert H Jones Xanthyl and trithiocarbonyl, sulfides, sulfoxides, and sulfones as pesticides
US2813890A (en) * 1954-10-15 1957-11-19 Exxon Research Engineering Co Manufacture of alkyl xanthogen sulfides
US3864374A (en) * 1973-11-19 1975-02-04 Canadian Ind Manufacture of alkali metal xanthates

Also Published As

Publication number Publication date
NL51053C (en)
DE710095C (en) 1941-09-03
FR855166A (en) 1940-05-04
GB522189A (en) 1940-06-11

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