US2951809A - Lubricating oil thickened with a metal soap of an alpha sulfo-fatty acid - Google Patents
Lubricating oil thickened with a metal soap of an alpha sulfo-fatty acid Download PDFInfo
- Publication number
- US2951809A US2951809A US491540A US49154055A US2951809A US 2951809 A US2951809 A US 2951809A US 491540 A US491540 A US 491540A US 49154055 A US49154055 A US 49154055A US 2951809 A US2951809 A US 2951809A
- Authority
- US
- United States
- Prior art keywords
- grease
- alpha
- soap
- fatty acid
- sulfo
- 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
Links
- 239000000344 soap Substances 0.000 title claims description 29
- 239000000194 fatty acid Substances 0.000 title claims description 8
- 239000010687 lubricating oil Substances 0.000 title claims description 4
- 229910052751 metal Inorganic materials 0.000 title description 8
- 239000002184 metal Substances 0.000 title description 8
- 239000004519 grease Substances 0.000 claims description 33
- 239000000203 mixture Substances 0.000 claims description 26
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229910006069 SO3H Inorganic materials 0.000 claims 1
- 150000001721 carbon Chemical class 0.000 claims 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 14
- 229910052791 calcium Inorganic materials 0.000 description 14
- 239000011575 calcium Substances 0.000 description 14
- 239000003921 oil Substances 0.000 description 14
- 239000002253 acid Substances 0.000 description 10
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 7
- 229910052744 lithium Inorganic materials 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000018044 dehydration Effects 0.000 description 4
- 238000006297 dehydration reaction Methods 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000007127 saponification reaction Methods 0.000 description 4
- -1 sulfo fatty acid Chemical class 0.000 description 4
- XQITUXIEASXIMZ-UHFFFAOYSA-N 2-sulfooctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(C(O)=O)S(O)(=O)=O XQITUXIEASXIMZ-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- RXPKHKBYUIHIGL-UHFFFAOYSA-L calcium;12-hydroxyoctadecanoate Chemical compound [Ca+2].CCCCCCC(O)CCCCCCCCCCC([O-])=O.CCCCCCC(O)CCCCCCCCCCC([O-])=O RXPKHKBYUIHIGL-UHFFFAOYSA-L 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 1
- ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1h-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 description 1
- CJAJEZSCULAKCB-UHFFFAOYSA-N 2-sulfohexadecanoic acid Chemical class CCCCCCCCCCCCCCC(C(O)=O)S(O)(=O)=O CJAJEZSCULAKCB-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 229940067597 azelate Drugs 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- PQVSTLUFSYVLTO-UHFFFAOYSA-N ethyl n-ethoxycarbonylcarbamate Chemical compound CCOC(=O)NC(=O)OCC PQVSTLUFSYVLTO-UHFFFAOYSA-N 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- GLXDVVHUTZTUQK-UHFFFAOYSA-M lithium hydroxide monohydrate Substances [Li+].O.[OH-] GLXDVVHUTZTUQK-UHFFFAOYSA-M 0.000 description 1
- 229940040692 lithium hydroxide monohydrate Drugs 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N n-hexadecanoic acid Natural products CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940098695 palmitic acid Drugs 0.000 description 1
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/028—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/102—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the ring
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/106—Thiadiazoles
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/02—Macromolecular compounds obtained by reactions of monomers involving only carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/09—Complexes with metals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
Definitions
- the fatty component in such premium greases is, generally, hydrogenated castor oil or 12-hydroxy stearic acid, and continued and increased uses of these greases have made the search for substitutes forthe fatty components and the lithium nec l in casive
- One of the characteristics which classifies a grease as a premium grease is a high dropping point; thus, a lithium l2-hydrox'y steara'te grease willhave a dropping point in the range-of above about 400 F. andanhydrous calcium l2-hydroxy s'tearate grease drops at about 300 F.
- the present invention is particularly related to grease compositions evidencing high dropping points.
- high dropping point grease compositions which are characterized by high dropping points.
- These high dropping point grease compositions in general comprise a lubricating oil thickened to grease consistency with a soap of an alpha sulfo fatty acid, preferably a saturated fatty acid, having. 12 to 22 carbon atoms per molecule.
- These sulfo-fatty acids include, to:"example,'alpha sulfmmyristic acid, alpha-snlfo stearic acid and alpha-sulfo-palmitic acids. Mixtures of the various acids Within the class can also be used.
- Particularly desirable greases result when the fatty component employed is alpha-sulfo-stearic acid, alpha-sulfo palm itic acid, or a mixture of the alpha-sulfo stearic and pah nitic acids.
- the fatty material can be saponified to produce the soaps employed in my invention.
- alkali metals and alkaline earth metals constitute the main groups of metals which can be used.
- Particular components include, for example, sodium, calcium, lithium, potassium, magnesium, strontium, barium and mixtures of the foregoing, with calcium, lithium and mixturesof sodium and calcium being especially desirable.
- Saponifying components are used in any of the usual forms, for
- hydroxides as hydroxides, oxides, carbonates and the like.
- the resulting soaps generally constitute about 5 to '25 Weight percent of the compositions and preferably about 10 to 20 percent.
- the mineral oil fraction can be obtained from Mid-Continent, paraffinic and naphthenic crudes. In general, it is preferred that a mineral lubricating oil fraction having a viscosity within the range of about 50 SUS at F. to 1500 SUS at 210 F. be employed.
- The'oil traction can be highly refined and solvent treated, if desired, by known means.
- the'synthetic lubricants which can be used are polymerized olefins, alkyl'ated aromatics, silicone polymers, polyalkylene glycols and their partial or complete ethers and esters. Also I can use synthetic lubricants such as diesters of dibasic acids, e.g. di(2-e thyl hexyl) adipate and di(isooctyl) azelate, and the like.
- Grease compositions of the present invention are prepared by thickeningthe oil fraction with soap of an alpha-'sulfo fatty acid of the class described.
- the soaps employed can be preformed, or they can be prepared in situ.
- soap formation can be effected. by any of the procedures known to the art. For example, both low and high temperature saponification procedures are eifective as are saponification in part of or all of the oil of the final composition.
- saponification of the fatty component with a divalent material introduces a measure of flexibility permitting difierent soaps tobe produced.
- soaps which can be produced include polymeric a monovalent metal or esterifying such remaining acid groups, particularly with a lower alkyl alcohol.
- Preferred calcium greases are produced by employing about 1.50 to 2.50 moles of calcium per mole of fatty component and adding the calcium incrementally, for example adding about half of the calcium slurried in starting oil, to a mixture of the acid and Water and then adding the remainder of calcium after reaction has been initiated.
- the soap resulting appears to have the structure indicated under III above.
- Premium grease compositions characteristically are substantially anhydrous, i.e., the finished greases have a Water content below about 0.10 weight percent and preferably below about 0.05 weight percent.
- Grease'compositions of the instant invention also are substantially anhydrous. Dehydration to result in this state can be accomplished in any manner but preferably by maintaining the temperature of the reaction mass, after completion of saponification, at a temperature above the boiling point of water for about 2 to 4 hours. While dehydration can be affected after finishing oil has been added, it is preferred to dehydrate prior to the addition of finishing oil in order that less material need be handled.
- Grease compositions of the present invention can be formulated with a plurality of soaps.
- the use of a soap of an alpha-sulfo fatty acid, as noted before, results in a grease composition characterized by a high dropping point.
- This advantageous property can be obtained in a grease composition without the necessity of employing the alpha-sulfo soap to the exclusion of other soaps.
- grease compositions can be made employing calcium 12-hydroxy stearate and calcium alpha-sulfo stearate with the result that a higher dropping point will be evidenced than would be evidenced by the grease containing only calcium 12-hydroxy stearate.
- Plural soap greases of this nature are additionally advantageous in that the stabilizing agents normally employed as in calcium containing greases need not be employed since calcium soaps of alpha-sulfo-saturated fatty acids unexpectedly exert a stabilizing efiect on compositions of which they form a part. Where soaps of alpha-sulfa saturated fatty acids are employed in conjunction with other soaps, the former generally constitutes about 5 to 75 weight percent of the total soap content.
- oxidation inhibitors Materials normally incorporated in greases to impart special characteristics can be added to my compositions. These include oxidation inhibitors, corrosion inhibitors, extreme pressure agents and anti-wear agents.
- the amount of additives added to the grease compositions usually ranges from about 0.01 Weight percent up to about 10 weight percent and, in general, can be employed in any amounts desired so long as the present invention is not deleteriously aifected.
- Anhydrous calcium grease was prepared as follows: 195 grams of alpha-sulfo stearic acid were treated with 22 grams of lime slurried in 400 grams of conventionally refined naphtenic type oil, having a viscosity of 200 SUS at F. and 195 grams of water. This mixture was stirred in a jacketed grease kettle at room temperature for 15 minutes. Steam was gradually introduced into the jacket until the kettle contents were heated to F. Then an additional 25 grams of lime slurried in 400 grams of the oil were added to the kettle and the temperature was slowly raised to 250 F. The temperature was held at about 250 F. for 2 /2 hours to insure essentiallycomplete dehydration and to form the desired soap grease structure.
- Age-Rite Resin D-oxidation inhibitor trimethyldihydroquinaline polymer marketed by B. F. Goodrich
- finishing oil was added amounting to about 700 grams of oil and the grease was stirred until it cooled to 200 F.
- a grease composition consisting essentially ofa lubri cating oil base thickened with a soap of a fatty acid'hav ing twelve to twenty-two carbon atoms per molecule and a SO H radical attached to the alpha carbon atom and a metal selected from the group consistingof metals and alkaline earth metals.
- the grease composition of claim 1 soap is a calcium soap
- The'grease composition of soap is a lithium 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
2,951,809 rnromunn WITH A METAL SOAP or AN ALPHA SULFO-FATTY ACID John Nelson, Lansing, lll., assignor to Sinclair Refining Company, New York, N.Y., acorporation of Maine w No Drawing; FiledMar. 1, 1955, Set. No. 491,540
3 Claims. 01.252 33) droppin point greases in particular, is the soap empi'dyeuas the thickener. Consequently, these in the art areednstanuy insea'rch of means for reducing the amount ap ifiequired in a grease of a given penetration, ing tor alternate fatty substances which may be in r supply or otherwise less expensive and attempting to ub'stitiite less expensive saponitying components for these presently used. These considerations are especially acute with the so-called premium greases such as those containing lithium l 2-hyd'roiiy stearate. The fatty component in such premium greases is, generally, hydrogenated castor oil or 12-hydroxy stearic acid, and continued and increased uses of these greases have made the search for substitutes forthe fatty components and the lithium nec l in casive One of the characteristics which classifies a grease as a premium grease is a high dropping point; thus, a lithium l2-hydrox'y steara'te grease willhave a dropping point in the range-of above about 400 F. andanhydrous calcium l2-hydroxy s'tearate grease drops at about 300 F.
while ordinary calcium stearate cup greases have low tlropping points on the order of 220 F. The present invention is particularly related to grease compositions evidencing high dropping points.
I have now discovered novel grease compositions which are characterized by high dropping points. These high dropping point grease compositions in general comprise a lubricating oil thickened to grease consistency with a soap of an alpha sulfo fatty acid, preferably a saturated fatty acid, having. 12 to 22 carbon atoms per molecule.
Grease compositions within the scope of the present invention'includ'e as the thickening component soaps of alpha-sulfo faty acids. These sulfo-fatty acids include, to:"example,'alpha sulfmmyristic acid, alpha-snlfo stearic acid and alpha-sulfo-palmitic acids. Mixtures of the various acids Within the class can also be used. Particularly desirable greases result when the fatty component employed is alpha-sulfo-stearic acid, alpha-sulfo palm itic acid, or a mixture of the alpha-sulfo stearic and pah nitic acids.
The fatty material can be saponified to produce the soaps employed in my invention. In general, alkali metals and alkaline earth metals constitute the main groups of metals which can be used. Particular componentsinclude, for example, sodium, calcium, lithium, potassium, magnesium, strontium, barium and mixtures of the foregoing, with calcium, lithium and mixturesof sodium and calcium being especially desirable. Saponifying components are used in any of the usual forms, for
example, as hydroxides, oxides, carbonates and the like.
The resulting soaps generally constitute about 5 to '25 Weight percent of the compositions and preferably about 10 to 20 percent.
Mineral oils or synthetic oils which normally are used in preparing grease compositions can be used in the present invention. The mineral oil fraction can be obtained from Mid-Continent, paraffinic and naphthenic crudes. In general, it is preferred that a mineral lubricating oil fraction having a viscosity within the range of about 50 SUS at F. to 1500 SUS at 210 F. be employed. The'oil traction can be highly refined and solvent treated, if desired, by known means. Among the'synthetic lubricants which can be used are polymerized olefins, alkyl'ated aromatics, silicone polymers, polyalkylene glycols and their partial or complete ethers and esters. Also I can use synthetic lubricants such as diesters of dibasic acids, e.g. di(2-e thyl hexyl) adipate and di(isooctyl) azelate, and the like.
Grease compositions of the present invention are prepared by thickeningthe oil fraction with soap of an alpha-'sulfo fatty acid of the class described. The soaps employed can be preformed, or they can be prepared in situ. When a mono-v alent saponifying component is employed, soap formation can be effected. by any of the procedures known to the art. For example, both low and high temperature saponification procedures are eifective as are saponification in part of or all of the oil of the final composition. On the other hand, saponification of the fatty component with a divalent material introduces a measure of flexibility permitting difierent soaps tobe produced. Thus considering the following formula H where R is an alkyl group for instance having 12 to 20 carbon atoms it can be observed that a divalent metal canetlect joinder of a plurality of molecules of the acid in a variety of ways. Examples include the following where M is a divalent metal:
The two functional groups of a single molecule also can be. joined as follows:
Other soaps which can be produced include polymeric a monovalent metal or esterifying such remaining acid groups, particularly with a lower alkyl alcohol.
The various embodiments may be obtained through use of conventional blocking procedures, since the two acid groups present are of such diverse strength. Preferred calcium greases are produced by employing about 1.50 to 2.50 moles of calcium per mole of fatty component and adding the calcium incrementally, for example adding about half of the calcium slurried in starting oil, to a mixture of the acid and Water and then adding the remainder of calcium after reaction has been initiated. The soap resulting appears to have the structure indicated under III above.
Premium grease compositions characteristically are substantially anhydrous, i.e., the finished greases have a Water content below about 0.10 weight percent and preferably below about 0.05 weight percent. Grease'compositions of the instant invention also are substantially anhydrous. Dehydration to result in this state can be accomplished in any manner but preferably by maintaining the temperature of the reaction mass, after completion of saponification, at a temperature above the boiling point of water for about 2 to 4 hours. While dehydration can be affected after finishing oil has been added, it is preferred to dehydrate prior to the addition of finishing oil in order that less material need be handled.
Grease compositions of the present invention can be formulated with a plurality of soaps. The use of a soap of an alpha-sulfo fatty acid, as noted before, results in a grease composition characterized by a high dropping point. This advantageous property can be obtained in a grease composition without the necessity of employing the alpha-sulfo soap to the exclusion of other soaps. For example, grease compositions can be made employing calcium 12-hydroxy stearate and calcium alpha-sulfo stearate with the result that a higher dropping point will be evidenced than would be evidenced by the grease containing only calcium 12-hydroxy stearate. Plural soap greases of this nature are additionally advantageous in that the stabilizing agents normally employed as in calcium containing greases need not be employed since calcium soaps of alpha-sulfo-saturated fatty acids unexpectedly exert a stabilizing efiect on compositions of which they form a part. Where soaps of alpha-sulfa saturated fatty acids are employed in conjunction with other soaps, the former generally constitutes about 5 to 75 weight percent of the total soap content.
Materials normally incorporated in greases to impart special characteristics can be added to my compositions. These include oxidation inhibitors, corrosion inhibitors, extreme pressure agents and anti-wear agents. The amount of additives added to the grease compositions usually ranges from about 0.01 Weight percent up to about 10 weight percent and, in general, can be employed in any amounts desired so long as the present invention is not deleteriously aifected.
The invention will be described further in conjunction with the following specific examples. It should be understood that the invention is not to be limited by the details disclosed in the examples.
EXAMPLE I An anhydrous calcium grease was prepared as follows: 195 grams of alpha-sulfo stearic acid were treated with 22 grams of lime slurried in 400 grams of conventionally refined naphtenic type oil, having a viscosity of 200 SUS at F. and 195 grams of water. This mixture was stirred in a jacketed grease kettle at room temperature for 15 minutes. Steam was gradually introduced into the jacket until the kettle contents were heated to F. Then an additional 25 grams of lime slurried in 400 grams of the oil were added to the kettle and the temperature was slowly raised to 250 F. The temperature was held at about 250 F. for 2 /2 hours to insure essentiallycomplete dehydration and to form the desired soap grease structure. One percent of Age-Rite Resin D-oxidation inhibitor (trimethyldihydroquinaline polymer marketed by B. F. Goodrich) was then'added, finishing oil was added amounting to about 700 grams of oil and the grease was stirred until it cooled to 200 F.
Tests on the grease are as follows:
. Table I Penetration data: A Unworked 306 Worked, 60 strokes 352 Dropping point, F. {374 EXAMPLE II i In the preparation of a lithium alpha-sulfo'stearate grease, 51 got lithium hydroxide mono-hydrate dissolved in 250 grams of boiling water were added to 198 grams of alpha-sulfo stearic acid dispersed in 600 grams of a conventionally refined napthenic oil, having a viscosity of 750 SUS at 100 F. at 200 F. The temperature was raised to 338 F. during dehydration. One percent-Iof Age-Rite Resin D oxidation inhibitor was added in con junction with finishing oil in the usual manner, while the grease cooled. to about 200 F. The grease was milled-at .005 clearance in a conventional colloid mill.
Tests on this grease indicated:
From the above examples it is readily apparent that greases of my invention are characterized by veryhigh dropping points.
What is claimed is: i y
l. A grease composition consisting essentially ofa lubri cating oil base thickened with a soap of a fatty acid'hav ing twelve to twenty-two carbon atoms per molecule and a SO H radical attached to the alpha carbon atom and a metal selected from the group consistingof metals and alkaline earth metals. i
2. The grease composition of claim 1 soap is a calcium soap;
3. The'grease composition of soap is a lithium soap.
which said claim f wa e 5 6 References Cited in the file of this patent OTHER REFERENCES UNITED STATES PATENTS Recueil des Travaux Chimiques Des Pay-Bas, v01. 18,
, pp. 211-214, 1899. SEE 2:; et a1 "32? 5 Chemical Technology and Analysis of Oils, Fats, and 2666744 Dixon 1954 Waxes, Lewkowitsch, fifth ed., v01. 1, Macmillan C0.,
N. Y., 1913, pp. 145 and 146.
FORE GN PATENTS Evidence for Alpha Sulfonation in the Reaction of 288 612 Great Britain p 21 1928 Pahnitic Acid With Sulfur Trioxide, J. K. Well at al., 607:204 Great Britain Aug. 28, 194:; JACS 2526 (1953)-
Claims (1)
1. A GREASE COMPOSITION CONSISTING ESSENTIALLY OF A LUBRICATING OIL BASE THICKENED WITH A SOAP OF A FATTY ACID HAVING TWELVE TO TWENTY-TWO CARBON ATOMS PER MOLECULE AND A-SO3H RADICAL ATTACHED TO THE ALPHA CARBON ATOM AND A METAL SELECTED FROM THE GROUP CONSISTING OF ALKALI METALS AND ALKALINE EARTH METALS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US491540A US2951809A (en) | 1955-03-01 | 1955-03-01 | Lubricating oil thickened with a metal soap of an alpha sulfo-fatty acid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US491540A US2951809A (en) | 1955-03-01 | 1955-03-01 | Lubricating oil thickened with a metal soap of an alpha sulfo-fatty acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2951809A true US2951809A (en) | 1960-09-06 |
Family
ID=23952657
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US491540A Expired - Lifetime US2951809A (en) | 1955-03-01 | 1955-03-01 | Lubricating oil thickened with a metal soap of an alpha sulfo-fatty acid |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2951809A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5587500A (en) * | 1993-09-17 | 1996-12-24 | The Chemithon Corporation | Sulfonation of fatty acid esters |
| US6696394B1 (en) * | 2002-11-14 | 2004-02-24 | Ecolab Inc. | Conveyor lubricants for use in the food and beverage industries |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB288612A (en) * | 1926-06-21 | 1928-09-21 | Ig Farbenindustrie Ag | Improvements in the manufacture and production of sulphonic acids derived from non-aromatic carboxylic acids |
| US1926442A (en) * | 1927-06-07 | 1933-09-12 | Ig Farbenindustrie Ag | Production of sulfonic acids of aliphatic and hydroaromatic carboxylic acids |
| US1939169A (en) * | 1929-05-08 | 1933-12-12 | Horwitz Alexander | Method of preparing an aluminum sulphostearate |
| GB607204A (en) * | 1943-09-28 | 1948-08-26 | Innovations Chimiques Soc D | Improved process of obtaining aliphatic sulphonic acids |
| US2666744A (en) * | 1952-03-05 | 1954-01-19 | California Research Corp | Sulfurized grease compositions |
-
1955
- 1955-03-01 US US491540A patent/US2951809A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB288612A (en) * | 1926-06-21 | 1928-09-21 | Ig Farbenindustrie Ag | Improvements in the manufacture and production of sulphonic acids derived from non-aromatic carboxylic acids |
| US1926442A (en) * | 1927-06-07 | 1933-09-12 | Ig Farbenindustrie Ag | Production of sulfonic acids of aliphatic and hydroaromatic carboxylic acids |
| US1939169A (en) * | 1929-05-08 | 1933-12-12 | Horwitz Alexander | Method of preparing an aluminum sulphostearate |
| GB607204A (en) * | 1943-09-28 | 1948-08-26 | Innovations Chimiques Soc D | Improved process of obtaining aliphatic sulphonic acids |
| US2666744A (en) * | 1952-03-05 | 1954-01-19 | California Research Corp | Sulfurized grease compositions |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5587500A (en) * | 1993-09-17 | 1996-12-24 | The Chemithon Corporation | Sulfonation of fatty acid esters |
| US6696394B1 (en) * | 2002-11-14 | 2004-02-24 | Ecolab Inc. | Conveyor lubricants for use in the food and beverage industries |
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