US2441720A - Lubricant - Google Patents

Lubricant Download PDF

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US2441720A
US2441720A US602667A US60266745A US2441720A US 2441720 A US2441720 A US 2441720A US 602667 A US602667 A US 602667A US 60266745 A US60266745 A US 60266745A US 2441720 A US2441720 A US 2441720A
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Prior art keywords
grease
per cent
greases
water
oil
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US602667A
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Theodore G Roehner
George W Murray
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ExxonMobil Oil Corp
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Socony Vacuum Oil Co Inc
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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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    • 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
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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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
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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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • C10M2201/042Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/10Compounds containing silicon
    • C10M2201/102Silicates
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    • 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
    • C10M2205/20Natural rubber; Natural resins
    • 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
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    • 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/404Fatty vegetable or animal oils obtained from genetically modified species
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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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
    • C10M2209/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical
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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
    • C10M2209/06Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
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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
    • C10M2209/06Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
    • C10M2209/062Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/109Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/12Polysaccharides, e.g. cellulose, biopolymers
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    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/044Polyamides
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/045Polyureas; Polyurethanes
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/02Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
    • C10M2219/024Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
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    • C10N2010/00Metal present as such or in compounds
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
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    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/08Groups 4 or 14
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
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    • 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 has to do with lubricants and more particularly has to do with lubricants characterized by a high order of effectiveness under severe operating conditions.
  • the greases contemplated herein contain as a characterizing or reinforcing agent, a small amount of a water-dispersible, or oil-insoluble and water soluble, thermoplastic material, representative of which are cellulose derivatives such as methyl-, hydroxyethyl-, and sodium carboxymethyl-cellulose; polymerized glycols typified by polyethylenet glycols and esters thereof; esters of polyhydric alcohols and polyvalent inorganic acids; polyvinyl alcohols; natural gums such as gum arabic; proteins; etc.
  • a characterizing or reinforcing agent a small amount of a water-dispersible, or oil-insoluble and water soluble, thermoplastic material, representative of which are cellulose derivatives such as methyl-, hydroxyethyl-, and sodium carboxymethyl-cellulose; polymerized glycols typified by polyethylenet glycols and esters thereof; esters of polyhydric alcohols and polyvalent inorganic acids; polyvinyl alcohols; natural gums such as gum
  • water-dispersibie cellulose ethers and, of this class, water-soluble methyl-cellulose containing from 1 to 1.2 methoxy groups per glucose unit is particularly preferred. All of these materials are well known in the art and it is believed to be unnecessary to discuss them further.
  • the greases containing one or more of the aforesaid characterizing agents are of the soda.
  • These greases have a high soap content of the order of 36-50 per cent on the basis of the final product. They are generally prepared by heating a fat or a fatty acid, or a mixture thereof, with a mineral oil and thereafter heating the resultant mixture with caustic soda at elevated temperatures, to obtain a substantially anhydrous soda soap grease.
  • the final product generally contains: 31-44 per cent fat or fatty acid; 4.8-6.8 per cent caustic soda (dry basis); 50-64 per cent mineral oil.
  • the mixture may be cooked, for example, at temperatures of 250-400 F. Available steam cooked greases do not maintain their shape at elevated temperatures and fire cooked greases are typified by bleeding under such conditions.
  • the mineral oil constituent of the greases contemplated herein may vary considerably in character and includes residual or distilled oils. Preference is accorded, however, to oils having a viscosity (8. U. V.) of -250 seconds at 210 F.
  • the fats and fatty acids which may be used are those generally found in soap type greases. Representative of such materials are vegetable, animal and fish fatty oils, and hydrogenated fatty materials thereof. While sodium hydroxide is preferred in view of cost considerations, other metal hydroxides may be used in our greases, preferably where the soap constituent of the grease is prepared by direct saponification in aqueous phase.
  • a fat or fatty acid, or mixture thereof is added to mineral oil in order to provide a blend thereof; if necessary the materials may be heated in order to thoroughly distribute the fatty material in the mineral oil.
  • a characterizing material such as oil-insoluble, water-soluble, methyl cellulose, is dissolved or dispersed in water, and the resulting water solution is dispersed or emulsified with the blend of fatty material and mineral oil. The resulting dispersion or emulsion is thereafter saponified with a metal hydroxide solution, such as caustic soda.
  • the. saponified mixture may also be steam cooked at temperatures of the order of 250-330 F., or fire cooked at temperatures in the range of 300-450 F.
  • the grease is then withdrawn from the vessel in which it was prepared and run into a suitable mold. The grease is allowed to cool whereupon it solidifies. The solid grease may then be cut into cakes of the desired size.
  • the characterizing agent is incorporated in the grease in an extremely fine dispersed state and the grease is provided with a high order of effectiveness.
  • the greases this invention are illustrated by k the following typical example.
  • spatula to determine whether there was any deformation or "slumping" of the cube.
  • the sample should show only a slight spreading at the base of the cube and no tree oil at the base of the cube, after the third test period oi 350 F.
  • the results (average of 4 tests) of these tests solidified.
  • the final product, hereinafter re- 35 are tabulated in Table I below.
  • the characterizing materials of this invention may be used in various amounts in our greases. In general, from about per cent to about per cent will provide satisfactory greases, with preferred amounts being of the order of per cent to 3 per cent. Accordingly, the various constituents (on a dry basis) of our greases may vary within the following limits:
  • the greases .of this invention may also contain other characterizing agents and fillers.
  • they may contain grease antioxidants such as amines, phenols, sulfides, etc.; fillers such as asbestos, graphite,
  • mica, talc, etc. mica, talc, etc.; and lubricity improving agents.
  • a lubricating grease composition prepared from about 30 to about 50 per cent of a fatty material. about 4.5 to about 7.5 per cent of an UNITED STATES PATENTS Number Name Date 1,882,816 Hagedom Oct. 18,1932 1,963,901 Hickman June 19, 1934 2,070,781 Brunstrum et al. Feb. 16, 1937 2,079,783 Wiezevich May 11, 1937 2,104,408 Wiezevich Jan. 4, 1938 2,109,644 Brunstrum Feb. 15, 1938 2,303,558 Kaufman et al Dec. 1, 1942 2,346,124 Dew Apr. 4, 1944 2,352,811 Swenson July 4, 1944 FOREIGN PATENTS Number Country Date 45.863 Sweden Oct. 4, 1919 alkaline material selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides, about 0.5 to about 10 per cent of a water-dispersible cellulose ether and the balance, mineral oil.
  • a lubricating grease composition prepared from about 30 to about 50 per cent of a fatty material, about 4.5 to about 7.5 per cent of an alkaline material selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides, about 0.5 to about 10 per cent of water-dispersible methyl cellulose and the balance, mineral oil.
  • a lubricating grease composition prepared from about 30 to about 50 per cent of a fatty material, about 4.5 to about 7.5 per cent of an alkali metal hydroxide, about 0.5 to about 10 per cent of a water-dispersible cellulose ether and the balance, mineral oil.
  • a lubricating grease composition prepared from about 30 to about 50 per cent of a fatty material, about 4.5 to about 7.5 per cent of an alkaline earth metal hydroxide, about 0.5 to about 10 per cent of a water-dispersible cellulose ether and the balance, mineral oil.
  • a soda soap lubricating grease characterized by resistance to deformation and bleeding comprising a sodium soap content of from about 36 to about 50 per cent and from about 0.5 to about 10 per cent of a water-dispersible cellulose ether.
  • a soda soap lubricating grease characterized by resistance to deformation and bleeding comprising a sodium soap content of from about 36 to about 50 per cent and from about 0.5 to about 3 per cent of water-dispersible methyl cellulose.

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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)

Description

Patented May 18, 1948 LUBRICANT Theodore G. Roehner, Mount Vernon, and George W. Murray, Pleasantviile, N. Y., assign orsto Socony-Vacuum Oil Company, Incorporated, a corporation of New York No Drawing. Applioationlune so, 1945,
' Serial N0. 602,687
9 Claims. (01. 252-38) This invention has to do with lubricants and more particularly has to do with lubricants characterized by a high order of effectiveness under severe operating conditions.
It is well known that lubricants generally lose some or all of their effectiveness when subjected to high temperature and pressure conditions, and
this is particularly true of greases exposed to such conditions. In lubricating machine parts with a grease, it is essential to provide a grease which will substantially retain its character under the foregoing conditions; failure to do so results in high consumption of the lubricant and frequent servicing. In general, available greases suffer from a marked tendency to change in character when used over a wide range of temperature. For example, the consistency of a conventional grease is prone to change over a wide range of temperature. Certain soda base greases, for example, have a pronounced and undesirable property of changing from a short to a long fibre structure, with temperature change. Some conventional greases are also characterized by excessive softening when exposed to elevated temperatures, thereby being extruded too rapidly from the area being lubricated to provide efficient lubrication. In addition, some greases tend to lose their oil content when used at elevated temperatures and pressures; this condition is generally referred to in the art as bleeding.
We have now discovered a grease which is characterized by a high order of effectiveness 'under severe operating conditions and which is substantially free from the shortcomings discussed hereinabove. -The greases contemplated herein contain as a characterizing or reinforcing agent, a small amount of a water-dispersible, or oil-insoluble and water soluble, thermoplastic material, representative of which are cellulose derivatives such as methyl-, hydroxyethyl-, and sodium carboxymethyl-cellulose; polymerized glycols typified by polyethylenet glycols and esters thereof; esters of polyhydric alcohols and polyvalent inorganic acids; polyvinyl alcohols; natural gums such as gum arabic; proteins; etc. Preferred of such materials, however, are the water-dispersibie cellulose ethers and, of this class, water-soluble methyl-cellulose containing from 1 to 1.2 methoxy groups per glucose unit is particularly preferred. All of these materials are well known in the art and it is believed to be unnecessary to discuss them further.
The greases containing one or more of the aforesaid characterizing agents are of the soda.
base type. These greases have a high soap content of the order of 36-50 per cent on the basis of the final product. They are generally prepared by heating a fat or a fatty acid, or a mixture thereof, with a mineral oil and thereafter heating the resultant mixture with caustic soda at elevated temperatures, to obtain a substantially anhydrous soda soap grease. The final product generally contains: 31-44 per cent fat or fatty acid; 4.8-6.8 per cent caustic soda (dry basis); 50-64 per cent mineral oil. In obtaining the grease, the mixture may be cooked, for example, at temperatures of 250-400 F. Available steam cooked greases do not maintain their shape at elevated temperatures and fire cooked greases are typified by bleeding under such conditions.
. The mineral oil constituent of the greases contemplated herein may vary considerably in character and includes residual or distilled oils. Preference is accorded, however, to oils having a viscosity (8. U. V.) of -250 seconds at 210 F. Similarly the fats and fatty acids which may be used are those generally found in soap type greases. Representative of such materials are vegetable, animal and fish fatty oils, and hydrogenated fatty materials thereof. While sodium hydroxide is preferred in view of cost considerations, other metal hydroxides may be used in our greases, preferably where the soap constituent of the grease is prepared by direct saponification in aqueous phase. Accordingly, such other metal hydroxides as those of lithium, potassium, magnesium, calcium, barium, etc., are contemplated here, with the alkali metal hydroxides preferred. It will be understood, there fore, that the term soap type grease used herein, and in the appended claims, is used generically and includes such greases wherein metal constituents such as those mentioned above are present in place of sodium.
We have further discovered that the characterizing or reinforcing agents described hereinabove are most advantageously incorporated in soap type greases prior to or during the saponification stage, as illustrated by the following procedure. A fat or fatty acid, or mixture thereof, is added to mineral oil in order to provide a blend thereof; if necessary the materials may be heated in order to thoroughly distribute the fatty material in the mineral oil. A characterizing material, such as oil-insoluble, water-soluble, methyl cellulose, is dissolved or dispersed in water, and the resulting water solution is dispersed or emulsified with the blend of fatty material and mineral oil. The resulting dispersion or emulsion is thereafter saponified with a metal hydroxide solution, such as caustic soda. Following the latter treatment, water-of solution and of reactionis evaporated by heating and stirring the saponifled mixture at a temperature above about 220 F., preferably at 260 F. In this evaporation operation, the. saponified mixture may also be steam cooked at temperatures of the order of 250-330 F., or fire cooked at temperatures in the range of 300-450 F. The grease is then withdrawn from the vessel in which it was prepared and run into a suitable mold. The grease is allowed to cool whereupon it solidifies. The solid grease may then be cut into cakes of the desired size. By following this preferred procedure, the characterizing agent is incorporated in the grease in an extremely fine dispersed state and the grease is provided with a high order of effectiveness.
The greases this invention are illustrated by k the following typical example.
' EXAMPLE One part (by weight) of an oil-insoluble, water-soluble, methyl cellulose having about one methoxy group per glucose unit, was dissolved, with stirring in parts of cold water. Sixteen parts of mineral oil (S. U. V.=165 seconds at 210 F. and ll parts of a fatty material were then added, with stirring, to the methyl cellulose solution and heated. The fatty material is a mixture of hydrogenated fatty acids (9 parts) obtained by hydrogenation of fish oil fatty acids, and hydrogenated fat (2 parts) obtained by hydrogenating fish oil fat. The methyl cellulose-oil-iat solution was heated at about 160 F. and agitated vigorously whereupon an emulsion was obtained. Caustic soda solution per cent aqueous solution, 3 parts) was added to the emulsion at 160 F. addition being completed in ten minutes. The mixture thus obtained was heated, and agitated, for three hours at 280 F. to complete the saponification, and was substantially dehydrated (water content, 0.1 per cent) thereafter by heating or fire cooking to a. temperature of 330 F. The grease was then allowed to cool, whereupon it 4 art. The latter greases (II and III) are identifled by the following:
11 III (Fire (Steam Cooked) Cooked) Hydrogenated Fatty Acidsmfl 3i. 8 31.3 Hydrogenated Fat 7. 7 7. 6 6. 0 5. 8 l 64. 5 65. 3 none none) One inch cubes were out from one inch thickgrease slabs which were representative cross sections of the grease blocks under test. The cubes were placed on an open tray and the tray was placed on a shelf in a constant temperature electric oven. The cubes were heated at 250 F. for one hour, at 300 F. for one hour and finally at 350 F. without being removed from the oven. After each of the aforesaid heating periods, the top side of each cube was slightly pressed down with the flat side of a. spatula to determine whether there was any deformation or "slumping" of the cube. In order to pass the test, the sample should show only a slight spreading at the base of the cube and no tree oil at the base of the cube, after the third test period oi 350 F. The results (average of 4 tests) of these tests solidified. The final product, hereinafter re- 35 are tabulated in Table I below.
Table 2 Dimensions of Test Cubes Per Cent Per Cent Grease Increase Decrease Oil at in Base in Base Beiore Heating After Heating Area Height sec 1.031" I! 1.031"... 1.100": 1.004".. I Height 1.031"... 09mm. 14 6 H ass 1.000" x 1.063"... 1 its": 1.140".. 24 12 {Consideri o iw i'dii tw ne? Height 1.000" 0.813" 59 rerred to as grease I, is identified by the follow- The outstanding character of the aforesaid grease is shown by established deformation and bleeding" tests shown hereinafter which were run on samples of the said grease, and comparable and typical soda soap greases known in the It will be apparent from the foregoing results that grease I, which contains methyl cellulose, is greatly superior to grease II in its resistance to bleeding as shown by the oil extruded from the latter grease. and also in its substantially smaller degree of deformation. Grease I is also far superior to grease III in regard to deformation.
High temperature penetration tests were also carried out with grease test cubes, three inches on a side, after heating the same in an oven of the aforesaid type for three hours at 300 F. At the end of the heating period, A. S. T. M. penetration values (using a 300 gram load) were obtained at 300 F. Concurrently, measurements of each cube were taken to determine the degree of deformation. Test results are shown in Table II.
Table II 1* 5 Wm A. s. 'r. M. Dimensions oi Test Cubes Pffitlggofl as: Cent 5e1- Cent Grease m m Remarks 1086 ml! 2 Before Heating Mei-Heating 3 g (dma) I I Heart-.1 are"; a a m III. 363 fig f fl ,25%}"52: M 83 Blumpedmoreon one side.
Here again, test results effectively demonstrate the outstanding character of greases of the type contemplated herein.
It will be apparent from the foregoing that the greases contemplated herein have considerable application. For example, they are outstanding greases for lubricating locomotive driving journals where high temperatures and pressures are encountered. They also find application as antifriction bearing greases, for example, ball bearing and roller greases. Other applications will be apparent to those skilled in the'art.
The characterizing materials of this invention may be used in various amounts in our greases. In general, from about per cent to about per cent will provide satisfactory greases, with preferred amounts being of the order of per cent to 3 per cent. Accordingly, the various constituents (on a dry basis) of our greases may vary within the following limits:
Per cent Fatty material 30-50 Alkali 4 -7 Mineral oil 40-60 Characterizing material /2-10 It is to be understood that the greases .of this invention may also contain other characterizing agents and fillers. For example, they may contain grease antioxidants such as amines, phenols, sulfides, etc.; fillers such as asbestos, graphite,
mica, talc, etc.; and lubricity improving agents.
following ingredients in the indicated proportions:
, Per cent Fatty material 30-50 Alkali 4 -7 Mineral oil 40-60 Water-dispersible, cellulose ether -10 2-11 lubricating grease composition characterized by resistance to deformation and bleeding, comprising the reaction products of the following ingredients in the indicated proportions:
Per cent Hydrogenated fatty acids 30.3 Hydrogenated fat 7.3 Sodium hydroxide 5.!
Mineral oil 53.9 Water-dlspersible methyl cellulose 2.8
3. A lubricating grease composition prepared from about 30 to about 50 per cent of a fatty material. about 4.5 to about 7.5 per cent of an UNITED STATES PATENTS Number Name Date 1,882,816 Hagedom Oct. 18,1932 1,963,901 Hickman June 19, 1934 2,070,781 Brunstrum et al. Feb. 16, 1937 2,079,783 Wiezevich May 11, 1937 2,104,408 Wiezevich Jan. 4, 1938 2,109,644 Brunstrum Feb. 15, 1938 2,303,558 Kaufman et al Dec. 1, 1942 2,346,124 Dew Apr. 4, 1944 2,352,811 Swenson July 4, 1944 FOREIGN PATENTS Number Country Date 45.863 Sweden Oct. 4, 1919 alkaline material selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides, about 0.5 to about 10 per cent of a water-dispersible cellulose ether and the balance, mineral oil.
4. A lubricating grease compositionprepared from about 30 to about 50 per cent of a fatty material, about 4.5 to about 7.5 per cent of an alkaline material selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides, about 0.5 to about 10 per cent of water-dispersible methyl cellulose and the balance, mineral oil.
5. A lubricating grease composition prepared from about 30 to about 50 per cent of a fatty material, about 4.5 to about 7.5 per cent of an alkali metal hydroxide, about 0.5 to about 10 per cent of a water-dispersible cellulose ether and the balance, mineral oil.
6. A lubricating grease composition prepared from about 30 to about 50 per cent of a fatty material, about 4.5 to about 7.5 per cent of an alkaline earth metal hydroxide, about 0.5 to about 10 per cent of a water-dispersible cellulose ether and the balance, mineral oil.
7. A soda soap lubricating grease characterized by resistance to deformation and bleeding," comprising a sodium soap content of from about 36 to about 50 per cent and from about 0.5 to about 10 per cent of a water-dispersible cellulose ether.
8. A soda soap lubricating grease characterized by resistance to deformation and "bleeding," comprising a sodium soap content of from about 36 to about 50 per cent and'from about 0.5 to
about 10 per cent of water-dlspersible methyl cellulose.
9. A soda soap lubricating grease characterized by resistance to deformation and bleeding," comprising a sodium soap content of from about 36 to about 50 per cent and from about 0.5 to about 3 per cent of water-dispersible methyl cellulose.
THEODORE G. ROEHNER. GEORGE W. MURRAY.
REFERENCES CITED The following references are of record in the file of this patent:
US602667A 1945-06-30 1945-06-30 Lubricant Expired - Lifetime US2441720A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
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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
US2576033A (en) * 1949-12-17 1951-11-20 Standard Oil Dev Co Preparing high-temperature lubricating greases
US2694683A (en) * 1952-12-24 1954-11-16 Standard Oil Dev Co Lubricating grease containing pectic acid salt
US2754268A (en) * 1953-07-15 1956-07-10 Exxon Research Engineering Co Lubricating grease containing a metal salt of algin
US2801976A (en) * 1952-12-11 1957-08-06 Exxon Research Engineering Co Lubricating greases containing alkali fusion products of polysaccharides
WO2013066810A1 (en) * 2011-10-31 2013-05-10 Shell Oil Company Fuel and engine oil composition and its use
US9347313B2 (en) 2011-06-13 2016-05-24 Shell Oil Company Hydraulic fracture monitoring using active seismic sources with receivers in the treatment well

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US1882816A (en) * 1928-11-29 1932-10-18 Ig Farbenindustrie Ag Process of enhancing the viscosity of technical oils
US1963901A (en) * 1931-04-17 1934-06-19 Eastman Kodak Co Lubricant containing a cellulose derivative
US2070781A (en) * 1935-02-13 1937-02-16 Standard Oil Co Grease
US2079783A (en) * 1933-08-16 1937-05-11 Standard Oil Dev Co Lubricant
US2104408A (en) * 1933-09-20 1938-01-04 Standard Oil Dev Co Lubricant
US2108644A (en) * 1934-03-22 1938-02-15 Standard Oil Co Grease
US2303558A (en) * 1940-08-10 1942-12-01 Texas Co Premium cup grease of improved heat and texture stability
US2346124A (en) * 1939-12-08 1944-04-04 Du Pont Bullet lubrication
US2352811A (en) * 1941-06-27 1944-07-04 Standard Oil Co Lubricant

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Publication number Priority date Publication date Assignee Title
SE45863C1 (en) *
US1882816A (en) * 1928-11-29 1932-10-18 Ig Farbenindustrie Ag Process of enhancing the viscosity of technical oils
US1963901A (en) * 1931-04-17 1934-06-19 Eastman Kodak Co Lubricant containing a cellulose derivative
US2079783A (en) * 1933-08-16 1937-05-11 Standard Oil Dev Co Lubricant
US2104408A (en) * 1933-09-20 1938-01-04 Standard Oil Dev Co Lubricant
US2108644A (en) * 1934-03-22 1938-02-15 Standard Oil Co Grease
US2070781A (en) * 1935-02-13 1937-02-16 Standard Oil Co Grease
US2346124A (en) * 1939-12-08 1944-04-04 Du Pont Bullet lubrication
US2303558A (en) * 1940-08-10 1942-12-01 Texas Co Premium cup grease of improved heat and texture stability
US2352811A (en) * 1941-06-27 1944-07-04 Standard Oil Co Lubricant

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US2576033A (en) * 1949-12-17 1951-11-20 Standard Oil Dev Co Preparing high-temperature lubricating greases
US2801976A (en) * 1952-12-11 1957-08-06 Exxon Research Engineering Co Lubricating greases containing alkali fusion products of polysaccharides
US2694683A (en) * 1952-12-24 1954-11-16 Standard Oil Dev Co Lubricating grease containing pectic acid salt
US2754268A (en) * 1953-07-15 1956-07-10 Exxon Research Engineering Co Lubricating grease containing a metal salt of algin
US9347313B2 (en) 2011-06-13 2016-05-24 Shell Oil Company Hydraulic fracture monitoring using active seismic sources with receivers in the treatment well
WO2013066810A1 (en) * 2011-10-31 2013-05-10 Shell Oil Company Fuel and engine oil composition and its use

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