US3377281A - Lubricating composition - Google Patents
Lubricating composition Download PDFInfo
- Publication number
- US3377281A US3377281A US435707A US43570765A US3377281A US 3377281 A US3377281 A US 3377281A US 435707 A US435707 A US 435707A US 43570765 A US43570765 A US 43570765A US 3377281 A US3377281 A US 3377281A
- Authority
- US
- United States
- Prior art keywords
- calcium
- weight
- sulfonate
- oil
- base number
- 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
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- 239000000203 mixture Substances 0.000 title claims description 24
- 230000001050 lubricating effect Effects 0.000 title claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 54
- 239000011575 calcium Substances 0.000 claims description 54
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 49
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 37
- -1 METHACRYLATE ESTER Chemical class 0.000 claims description 19
- 239000002480 mineral oil Substances 0.000 claims description 10
- 235000010446 mineral oil Nutrition 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- 239000010687 lubricating oil Substances 0.000 claims description 8
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 3
- 229960002317 succinimide Drugs 0.000 claims description 2
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 description 15
- 239000000654 additive Substances 0.000 description 13
- 239000003921 oil Substances 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 238000012360 testing method Methods 0.000 description 11
- 239000012141 concentrate Substances 0.000 description 8
- 241000158728 Meliaceae Species 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 150000003460 sulfonic acids Chemical class 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000002199 base oil Substances 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000010688 mineral lubricating oil Substances 0.000 description 4
- 239000010802 sludge Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 230000006315 carbonylation Effects 0.000 description 3
- 238000005810 carbonylation reaction Methods 0.000 description 3
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 230000003472 neutralizing effect Effects 0.000 description 3
- 125000000962 organic group Chemical group 0.000 description 3
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 229940043430 calcium compound Drugs 0.000 description 2
- 150000001674 calcium compounds Chemical class 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- HVSYRUKKSFWIKV-UHFFFAOYSA-K dioxido-sulfanylidene-sulfido-lambda5-phosphane nickel(3+) Chemical class [Ni+3].[O-]P([O-])([S-])=S HVSYRUKKSFWIKV-UHFFFAOYSA-K 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920005573 silicon-containing polymer Polymers 0.000 description 2
- 229940014800 succinic anhydride Drugs 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WGFYKSNMQJBURX-UHFFFAOYSA-N 1-methyl-1-pentyl-2-propylhydrazine Chemical compound CCCCCN(C)NCCC WGFYKSNMQJBURX-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- DILRJUIACXKSQE-UHFFFAOYSA-N n',n'-dimethylethane-1,2-diamine Chemical compound CN(C)CCN DILRJUIACXKSQE-UHFFFAOYSA-N 0.000 description 1
- VSEKEMQDOIJVFY-UHFFFAOYSA-N n',n'-dimethylmethanediamine Chemical compound CN(C)CN VSEKEMQDOIJVFY-UHFFFAOYSA-N 0.000 description 1
- GZUCMODGDIGMBI-UHFFFAOYSA-N n',n'-dipropylpropane-1,3-diamine Chemical compound CCCN(CCC)CCCN GZUCMODGDIGMBI-UHFFFAOYSA-N 0.000 description 1
- UVSDKMISWYGPIQ-UHFFFAOYSA-N n'-butyl-n-propylethane-1,2-diamine Chemical compound CCCCNCCNCCC UVSDKMISWYGPIQ-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
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- 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
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
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- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
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- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular 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
- C10M2209/084—Acrylate; Methacrylate
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- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/086—Imides
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- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/26—Amines
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- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/28—Amides; Imides
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- 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
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
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- 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
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- 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
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- 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
- C10M2219/046—Overbasedsulfonic acid salts
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/02—Unspecified siloxanes; Silicones
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/041—Siloxanes with specific structure containing aliphatic substituents
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/043—Siloxanes with specific structure containing carbon-to-carbon double bonds
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/044—Siloxanes with specific structure containing silicon-to-hydrogen bonds
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/14—Group 7
-
- 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
- C10N2010/16—Groups 8, 9, or 10
Definitions
- the present invention relates to mineral lubricating oils having improved detergent-dispersant properties and more particularly to mineral lubricating oils containing small amounts of each of a combination of two different types of basic alkaline earth metal sulfonates and an ashless polymeric detergent.
- additives include detergentdispersants, corrosion inhibitors, antioxidants, pour depressors, etc. each of which is generally employed to impart a particular characteristics to the oil.
- detergentdispersants include detergentdispersants, corrosion inhibitors, antioxidants, pour depressors, etc. each of which is generally employed to impart a particular characteristics to the oil.
- these lubricating oil compositions have not been entirely satisfactory for commercial use since apparently an additive agent which imparts a beneficial effect of one type may impart a detrimental efiect with respect to one or more of other desired characteristics.
- many additive combinations fail to meet the low temperature dispersancy characteristics required by the Ordnance MIL- L-2104B specification.
- Other additive combinations although meeting the low temperature detergency qualification fail to come up to the required standards in the other properties required by this specification.
- the two calcium aromatic sulfonates of the invention are obtained from aromatic oil-soluble sulfonic acids, preferably having an average molecular weight of about 350 to 600 such as the sulfonic acids produced in the treatment of petroleum hydrocarbons usually boiling primarily in the range from 600 to 1000 F. with a sulfonating agent such as sulfuric acid.
- aromatic oil-soluble sulfonic acids preferably having an average molecular weight of about 350 to 600
- the petroleum sulfonic acids produced by the acid treatment are composed to a large extent of aromatic hydrocarbons having either one or two aromatic rings per molecule, possibly with one or more long-chain alkyl groups containing from about 8 to 24 or more carbon atoms attached to the ring nucleus.
- aromatic sulfonic acids are the synthetic alkaryl sulfonic acids prepared by the reaction of paraffin chains of 8 to 24 carbons or more with aromatic nuclei followed by sulfonation with fuming sulfuric acid.
- the preferred sulfonic acids are the mahogany sulfonic acids.
- the basic calcium sulfonate of the invention can be prepared by neutralizing the aromatic sulfonic acid with an excess of a calcium compound over the stoichiometric amount required for neutralization.
- the basic calcium sulfonate contains about 1 to 5 percent by weight calcium, has a measureable titratable alkalinity and a base number of generally about 10 to 60, preferably 20 to-SO.
- base number is meant the quantity of acid expressed in terms of the equivalent number of milligrams of potassium hydroxide required to neutralize one gram of sample, titrating electrometrically according to ASTM-D 664.
- base number is meant the quantity of acid expressed in terms of the equivalent number of milligrams of potassium hydroxide required to neutralize one gram of sample, titrating electrometrically according to ASTM-D 664.
- at least about 2 equivalents of the calcium neutralizing compound are reacted; however as little as about 1.1 equivalents may be employed, if desired.
- a suitable basic calcium sulfonate can be prepared by sulfonating a sweet West Texas gas-oil of 150 SUS at F., viscosity and an average molecular weight of 450 with three 50 pounds per barrel oleum dumps.
- the oil solution is decanted from the insoluble sludge and the clear oil solution of sulfonic acids is neutralized by adding a slurry of about 2 equivalents of calcium oxide in twice its weight of water.
- the water is topped oif and the product filtered clear to obtain a basic calcium sulfonate concentrate in gas-oil containing about 1 to 5% calcium and having a base number of 10 to 50.
- the overbased calcium aromatic sulfonates of the present invention like the basic calcium sulfonates described above, also contain an excess of calcium above that required for neutralization to prepare the normal salt but are further distinguished in that the overbased calcium sulfonates have a base number of about 200 to 500, preferably about 250 to 400, and contain about 8 to 30 weight percent calcium.
- the overbased salts can be obtained by employing neutralization methods of the art known to provide a calcium aromatic sulfonate having a base number in the described range.
- One method comprises employing as a starting material a basic calcium aromatic sulfonate, as described above, and subjecting the basic calcium sulfonate to treatment with carbon dioxide followed by reaction with calcium methylate. More than one of such successive carbonylation and calcium methylate reactions may be necessary to provide a calcium sulfonate having the defined base number.
- the basic calcium sulfonate may be dissolved in a suitable mineral oil and reacted with an excess of carbon dioxide, usually at a temperature of about to 250 C., for a time sufiicient to effect reaction of one mole of carbon dioxide per mole of basic calcium sulfonate.
- the reaction mixture is cooled to from about 25 C. to 60 C. and a solution of calcium methylate, usually in methanol, is added in an amount sufiicient to provide at least about 1 equivalent of calcium per mole of basic calcium sulfonate.
- the reaction mixture is then reheated at a temperature of about 150 to 250 C.
- an overbased calcium sulfonate of greater calcium content and base number can be prepared by subjecting the product thus prepared to further carbonylation and calcium methylate treatments.
- oil-soluble alkenyl succinimides of the invention can be represented by the following formula:
- R is an alkenyl radical of about 30 to 200 carbon atoms; R is a divalent alkylene radical of 2 to 4 or more carbon atoms; R and R hydrogen or lower alkyl radicals of say 1 to 4 carbon atoms; and n is an integer having a value of 1 to 6, preferably 2 to 4.
- R is preferably a polymer of an a-monoolefin of 2 to 5 carbon atoms, wherein the polymer has a molecular weight from 400 to 3000, more particularly from about 900 to about 1200.
- the alkenyl sucoinimide component of the invention can be prepared by first reacting the polyolefin with maleic anhydride to form an alkenyl succinic anhydride and then reacting the resulting anhydride with a suitable polyamide.
- suitable polyamides include dialkylaminoalkylamines and polyalkylenepolyamines.
- dialkylaminoalkylamines are dimethylaminomethylamine, dimethylaminoethylamine, dimethyl aminopropylamine, dimethylaminobutylam'ine, diethylaminopropylamine, diethylaminoamylarnine, dipropylaminopropylamine, methylpropylaminoamylamine, propylbutylaminoethylamine, etc.
- Non-limiting examples of polya'lkylene polyamines are diethylenetriamine, triethylenetetraamine, tetraethylenepentamine, hexapropyleneheptamine, tetrabutylenepentamine, etc.
- each of the additives of the invention is added to the mineral-oils in small effective amounts which may vary depending upon the particular mineral oil employed.
- the basic calcium sulfonate and the overbased calcium sulfonate are added in amounts that provide the final composition with a minimum total base number of at least about 2, preferably up to about 7.
- the ratio of basic sulfonate to overbased sulfonate is such that about 5 to 25%, preferably 5 to of the totalbase number is provided by the basic sulfonate component while about 75 to 95%, preferably 85 to 95% of the total base number is provided by the overbased sulfonate.
- the amounts employed usually fall in the range of about 0.2% to 3% by weight of the basic sulfonate and about 0.1 to 1% by weight of the overbased sulfonate-The weight percent in each case is on a dry soap basis.
- the N-substituted alkenyl succinirnide component is usually added in an amount of about 0.25% to 2.5%, preferably 0.1 to 1.5%, by weight on a dry basis.
- the mineral oil base stock used in the present invention is of lubricating viscosity, e.g. 35 to 225 SUS at 210 F. and may be solvent extracted, solvent refined, acid treated, hydrogenated, a combination thereof, or an oil obtained in accordance with conventional methods of treating lubricating oils.
- the base oil may be derived from parafiinic, naphthenic, asphaltic or mixed base crudes, shale oils, or, if desired, a blend of solvent-treated MidContinent neutrals and Mid-Continent bright stocks may be employed.
- a particularly suitable base oil is a blend of solvent-treated Mid-Continent neutral and bright stock having a viscosity indexof about 95.
- additive agents such as pour depressors, antioxidants, antifoam additives and the like can be employed to improve the oil in one or more respects.
- nickel and zinc dithiophosphate diesters which are obtaned from a wide variety of diester dithiophosphoric acids conventionally prepared by reacting a sulfide of phosphorous, such as phosphorous pentasulfide, with an alcohol, phenol or mercaptan.
- the organic groups in the acid esters may be aryl, alkyl, aralkyl or cycloalkyl groups which contain from about 4 to 20 carbon atoms, preferably about 6 to 14 carbon atoms, and the organic groups may be further substituted if desired.
- a suitable zinc dithiophosphate which may be employed is the zinc salt obtained from a mixed dithiophosphate prepared by reacting a technical mixture of C secondary and C primary alcohols, mainly the former, with phosphorous pentasulfide.
- Nickel dithiophosphates which can be employed may be prepared from a di-Z-ethylhexyl dithiophosphate obtained by reacting a technical mixture of 2-ethylhexanol with phosphorous pentasulfide.
- the zinc and nickel dithiophosphates are used in the lubricating compositions in a minor amount sufficient to inhibit oxidation and bearing corrosion and in most instances the amount employed provides about 0.02 to 0.2 percent by weight of phosphorous to the oil in which it is incorporated.
- Preferred additives for improving pour point and viscosity index in lubricating oils are the methacrylate type additive agents. These additives are the oil-compatible methacrylate ester polymers which have the formula:
- R is an alkyl group of 4 to 20 carbon atoms and x is the number of molecules condensed together to form a high molecular weight polymer of 5,000 to 20,000 molecular weight.
- These materials include a series of commercially available polymers known as the Acryloids some of which are described in U.S. Patent No.
- Anti-foam agents are particularly desirable in the lubricating composition for inhibiting foam and gas entrainment and for this purpose silicone oxide condensation polymer products such as polymers of dimethyl silicone, methyl phenyl silicone, ethyl butyl silicone, etc. can be employed. These materials and their method of preparation are well known to the art and are described in U.S. Patent No. 2,662,055.
- Thesilicone oxide anti-foam agents are conveniently handled as a 10 percent concentrate in a hydrocarbon solvent such as kerosene, and in the specific examples shown below a concentrate was prepared by dissolving 10 grams of dimethyl silicone polymer in a sufiicient amount of kerosene to make up a total volume of cc.
- the silicone polymer concentrate is preferably employed in the hydrocarbon base oil in a proportion of about .00001 to 0.05 percent by weight.
- lubricating oil compositions of the invention are further illustrated by the following example.
- Base oil Vol. percent Solvent refined Mid-Continent neutral oil, 200 SUS 1 gPfegarled from 4 moles of phenol with one mole of P285 at A 45% concentrate in mineral oil solution which analyzes 3% calcium; Base 1N0. 28.0.
- Acryloid 150 a 40% concentrate in mineral oil of methacrylate polymer in which the ester groups are derived from a mixture of alcohols in the C5 to C14 range.
- the total Base No. of the oil composition was 2.85, about 8% of which was provided by the basic calcium mahogany sulfonate and about 92% of which was provided by the over-based calcium mahogany sulfonate.
- a lubricating oil composition consisting essentially of a major amount of a mineral oil of lubricating viscosity, about 0.2% to 3% by weight of a basic calcium aromatic sulfonate having a base number of about 10 to and a calcium content of about 1 to 5%, about 0.1 to 1% by weight of an overbased calcium aromatic sulfonate having a base number of about 200 to 500 and a calcium content of about 8 to 30%, and about 0.25 to 2.5% by weight of an alkenyl succinimide having the formula:
- R is an alkenyl radical of about 30 to 200 carbon atoms
- R is a divalent alkylene radical of about 2 to 4 carbon atoms
- R and R are selected from the group consisting of hydrogen and a lower alkyl radical and n is an integer having a value of 1 to 6, with the proviso that when n is 1, R" and R are lower alkyl and when n is greater than 1, R" and R" are hydrogen, said composition having a total base number of about 2 to 7 with said basic calcium aromatic sulfonate providing about 5 to 25% of said total base number and said overbased calcium aromatic sulfonate providing about to 95% of said total base number.
- composition of claim 1 which contains a small amount of zinc dithiophosphate diester in which the organic groups contain from about 4 to 20 carbon atoms, said amount being sufficient to provide a phosphorous level of from about 0.02 to 0.2% by weight and about .001 to 1 percent by weight of a methacrylate ester polymer in which the ester radical contains 4 to 20 carbon atoms.
- composition of claim 2 wherein the basic calcium aromatic sulfonate is a basic calcium mahogany sulfonate having a base number of 20 to 50 and the overba-sed calcium aromatic sulfonate is an overbased calcium mahogany sulfonate having a base number of 250 to 400.
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Description
United States Patent 3,377,281 LUBRICATING COMPOSITION Howard D. Gower, Munster, Ind., assignor to Sinclair Research, Inc., New York, N.Y., a corporation of Delaware No Drawing. Filed Feb. 26, 1965, Ser. No. 435,707 4 Claims. (Cl. 25232.7)
The present invention relates to mineral lubricating oils having improved detergent-dispersant properties and more particularly to mineral lubricating oils containing small amounts of each of a combination of two different types of basic alkaline earth metal sulfonates and an ashless polymeric detergent.
With the advent of higher compression internal combustion engines and increased horsepower it has become common practice to incorporate into lubricating oils a variety of additives to insure successful operation of the oil under severe conditions. These additives include detergentdispersants, corrosion inhibitors, antioxidants, pour depressors, etc. each of which is generally employed to impart a particular characteristics to the oil. Unfortunately, however, while many of the proposed additive agents improve mineral lubricating oils, quite frequently these lubricating oil compositions have not been entirely satisfactory for commercial use since apparently an additive agent which imparts a beneficial effect of one type may impart a detrimental efiect with respect to one or more of other desired characteristics. For example, many additive combinations fail to meet the low temperature dispersancy characteristics required by the Ordnance MIL- L-2104B specification. Other additive combinations although meeting the low temperature detergency qualification fail to come up to the required standards in the other properties required by this specification.
It has now been found that the addition to mineral lubricating oils of small amounts of each of an oil-soluble basic calcium aromatic sulfonate, an oil-soluble, overbased calcium aromatic sulfonate and certain oil-soluble alkenyl succinimides provides a composition which not only possessess highly desirable detergent-dispersant properties but also on addition thereto of an antioxidant and a pour depressor, readily passes the Ordance MIL-L- 2104B specification.
The two calcium aromatic sulfonates of the invention are obtained from aromatic oil-soluble sulfonic acids, preferably having an average molecular weight of about 350 to 600 such as the sulfonic acids produced in the treatment of petroleum hydrocarbons usually boiling primarily in the range from 600 to 1000 F. with a sulfonating agent such as sulfuric acid. The petroleum sulfonic acids produced by the acid treatment are composed to a large extent of aromatic hydrocarbons having either one or two aromatic rings per molecule, possibly with one or more long-chain alkyl groups containing from about 8 to 24 or more carbon atoms attached to the ring nucleus. However, other useful aromatic sulfonic acids are the synthetic alkaryl sulfonic acids prepared by the reaction of paraffin chains of 8 to 24 carbons or more with aromatic nuclei followed by sulfonation with fuming sulfuric acid. The preferred sulfonic acids are the mahogany sulfonic acids.
The basic calcium sulfonate of the invention can be prepared by neutralizing the aromatic sulfonic acid with an excess of a calcium compound over the stoichiometric amount required for neutralization. The basic calcium sulfonate contains about 1 to 5 percent by weight calcium, has a measureable titratable alkalinity and a base number of generally about 10 to 60, preferably 20 to-SO. By base number is meant the quantity of acid expressed in terms of the equivalent number of milligrams of potassium hydroxide required to neutralize one gram of sample, titrating electrometrically according to ASTM-D 664. Generally at least about 2 equivalents of the calcium neutralizing compound are reacted; however as little as about 1.1 equivalents may be employed, if desired. Usually little is gained by using more than about 4 equivalents of the calcium compound. When desired, the high base strength of the basic calcium sulfonate can be decreased by further reacting with CO without decreasing the neutralizing power for strong acids. More specifically, a suitable basic calcium sulfonate can be prepared by sulfonating a sweet West Texas gas-oil of 150 SUS at F., viscosity and an average molecular weight of 450 with three 50 pounds per barrel oleum dumps. The oil solution is decanted from the insoluble sludge and the clear oil solution of sulfonic acids is neutralized by adding a slurry of about 2 equivalents of calcium oxide in twice its weight of water. The water is topped oif and the product filtered clear to obtain a basic calcium sulfonate concentrate in gas-oil containing about 1 to 5% calcium and having a base number of 10 to 50.
The overbased calcium aromatic sulfonates of the present invention, like the basic calcium sulfonates described above, also contain an excess of calcium above that required for neutralization to prepare the normal salt but are further distinguished in that the overbased calcium sulfonates have a base number of about 200 to 500, preferably about 250 to 400, and contain about 8 to 30 weight percent calcium. The overbased salts can be obtained by employing neutralization methods of the art known to provide a calcium aromatic sulfonate having a base number in the described range.
One method comprises employing as a starting material a basic calcium aromatic sulfonate, as described above, and subjecting the basic calcium sulfonate to treatment with carbon dioxide followed by reaction with calcium methylate. More than one of such successive carbonylation and calcium methylate reactions may be necessary to provide a calcium sulfonate having the defined base number.
According to this method the basic calcium sulfonate may be dissolved in a suitable mineral oil and reacted with an excess of carbon dioxide, usually at a temperature of about to 250 C., for a time sufiicient to effect reaction of one mole of carbon dioxide per mole of basic calcium sulfonate. When the carbonylation has been completed, the reaction mixture is cooled to from about 25 C. to 60 C. and a solution of calcium methylate, usually in methanol, is added in an amount sufiicient to provide at least about 1 equivalent of calcium per mole of basic calcium sulfonate. The reaction mixture is then reheated at a temperature of about 150 to 250 C. After complete removal of uncombined methanol, the reaction mixture is filtered to provide the overbased calcium sulfonate in oil solution. An overbased calcium sulfonate of greater calcium content and base number can be prepared by subjecting the product thus prepared to further carbonylation and calcium methylate treatments.
Another method of preparing the overbased calcium sulfonates is described in U.S. Patent No. 3,150,088 to M. W. Hunt, Gerald L. Nield and Richard M. Tillman issued Sept. 22, 1964.
The oil-soluble alkenyl succinimides of the invention can be represented by the following formula:
C Hswherein R is an alkenyl radical of about 30 to 200 carbon atoms; R is a divalent alkylene radical of 2 to 4 or more carbon atoms; R and R hydrogen or lower alkyl radicals of say 1 to 4 carbon atoms; and n is an integer having a value of 1 to 6, preferably 2 to 4. When n is 1, -R" and R are lower alkyl and when n is greater than one, R" and R are hydrogen. R is preferably a polymer of an a-monoolefin of 2 to 5 carbon atoms, wherein the polymer has a molecular weight from 400 to 3000, more particularly from about 900 to about 1200.
The alkenyl sucoinimide component of the invention can be prepared by first reacting the polyolefin with maleic anhydride to form an alkenyl succinic anhydride and then reacting the resulting anhydride with a suitable polyamide. These polyamides include dialkylaminoalkylamines and polyalkylenepolyamines.
Examples of suitable dialkylaminoalkylamines are dimethylaminomethylamine, dimethylaminoethylamine, dimethyl aminopropylamine, dimethylaminobutylam'ine, diethylaminopropylamine, diethylaminoamylarnine, dipropylaminopropylamine, methylpropylaminoamylamine, propylbutylaminoethylamine, etc. Non-limiting examples of polya'lkylene polyamines are diethylenetriamine, triethylenetetraamine, tetraethylenepentamine, hexapropyleneheptamine, tetrabutylenepentamine, etc.
The reaction of the polyolefin with maleic anhydride and the reaction of the resulting alkenyl succinirnide in turn with the polyamine are reactions well known in the art having been described in many publications as, for instance, U.S. Patent 3,018,291, and British Patent No. 922,831. These patents along with U.S. Patent Nos. 3,018,250; 3,024,195 and 3,131,150 described N-substituted alkenyl succinimides of the type considered suitable for use in the composition of this invention.
-Each of the additives of the invention is added to the mineral-oils in small effective amounts which may vary depending upon the particular mineral oil employed. The basic calcium sulfonate and the overbased calcium sulfonate are added in amounts that provide the final composition with a minimum total base number of at least about 2, preferably up to about 7.
The ratio of basic sulfonate to overbased sulfonate is such that about 5 to 25%, preferably 5 to of the totalbase number is provided by the basic sulfonate component while about 75 to 95%, preferably 85 to 95% of the total base number is provided by the overbased sulfonate. Ordinarily the amounts employed usually fall in the range of about 0.2% to 3% by weight of the basic sulfonate and about 0.1 to 1% by weight of the overbased sulfonate-The weight percent in each case is on a dry soap basis. The N-substituted alkenyl succinirnide component is usually added in an amount of about 0.25% to 2.5%, preferably 0.1 to 1.5%, by weight on a dry basis.
The mineral oil base stock used in the present invention is of lubricating viscosity, e.g. 35 to 225 SUS at 210 F. and may be solvent extracted, solvent refined, acid treated, hydrogenated, a combination thereof, or an oil obtained in accordance with conventional methods of treating lubricating oils. The base oil may be derived from parafiinic, naphthenic, asphaltic or mixed base crudes, shale oils, or, if desired, a blend of solvent-treated MidContinent neutrals and Mid-Continent bright stocks may be employed. A particularly suitable base oil is a blend of solvent-treated Mid-Continent neutral and bright stock having a viscosity indexof about 95.
In addition to the three additives discussed above, other additive agents such as pour depressors, antioxidants, antifoam additives and the like can be employed to improve the oil in one or more respects. For example, to improve the antioxidant properties of the composition of the invention, nickel and zinc dithiophosphate diesters which are obtaned from a wide variety of diester dithiophosphoric acids conventionally prepared by reacting a sulfide of phosphorous, such as phosphorous pentasulfide, with an alcohol, phenol or mercaptan. The organic groups in the acid esters may be aryl, alkyl, aralkyl or cycloalkyl groups which contain from about 4 to 20 carbon atoms, preferably about 6 to 14 carbon atoms, and the organic groups may be further substituted if desired. A suitable zinc dithiophosphate which may be employed is the zinc salt obtained from a mixed dithiophosphate prepared by reacting a technical mixture of C secondary and C primary alcohols, mainly the former, with phosphorous pentasulfide. Nickel dithiophosphates which can be employed may be prepared from a di-Z-ethylhexyl dithiophosphate obtained by reacting a technical mixture of 2-ethylhexanol with phosphorous pentasulfide. The zinc and nickel dithiophosphates are used in the lubricating compositions in a minor amount sufficient to inhibit oxidation and bearing corrosion and in most instances the amount employed provides about 0.02 to 0.2 percent by weight of phosphorous to the oil in which it is incorporated.
Preferred additives for improving pour point and viscosity index in lubricating oils are the methacrylate type additive agents. These additives are the oil-compatible methacrylate ester polymers which have the formula:
in which R is an alkyl group of 4 to 20 carbon atoms and x is the number of molecules condensed together to form a high molecular weight polymer of 5,000 to 20,000 molecular weight. These materials include a series of commercially available polymers known as the Acryloids some of which are described in U.S. Patent No.
Anti-foam agents are particularly desirable in the lubricating composition for inhibiting foam and gas entrainment and for this purpose silicone oxide condensation polymer products such as polymers of dimethyl silicone, methyl phenyl silicone, ethyl butyl silicone, etc. can be employed. These materials and their method of preparation are well known to the art and are described in U.S. Patent No. 2,662,055. Thesilicone oxide anti-foam agents are conveniently handled as a 10 percent concentrate in a hydrocarbon solvent such as kerosene, and in the specific examples shown below a concentrate was prepared by dissolving 10 grams of dimethyl silicone polymer in a sufiicient amount of kerosene to make up a total volume of cc. The silicone polymer concentrate is preferably employed in the hydrocarbon base oil in a proportion of about .00001 to 0.05 percent by weight.
The lubricating oil compositions of the invention are further illustrated by the following example.
EXAMPLE A lubricating oil was prepared having the following composition:
Base oil: Vol. percent Solvent refined Mid-Continent neutral oil, 200 SUS 1 gPfegarled from 4 moles of phenol with one mole of P285 at A 45% concentrate in mineral oil solution which analyzes 3% calcium; Base 1N0. 28.0.
As an approximately 20% concentrate in mineral oil solution analyzing approximately 11.5% by weight calcium and having a Base No. 275.
An approximately 48% concentrate in mineral oil of the reaction product prepared by reacting polyisobutylene having a. molecular weight of approximately 1000 with maleic anhy- (lride and then reacting the resulting polybuteuyl succinic anhydride with teraethylenepentamine.
Acryloid 150; a 40% concentrate in mineral oil of methacrylate polymer in which the ester groups are derived from a mixture of alcohols in the C5 to C14 range.
The total Base No. of the oil composition was 2.85, about 8% of which was provided by the basic calcium mahogany sulfonate and about 92% of which was provided by the over-based calcium mahogany sulfonate.
In accordance with the requirements of Ordnance MIL-L-2104B the oil composition was subjected to the following tests:
(A) Caterpillar 1H test-In this test the grooves are rated for deposits-a minimum of 30% top groove filling being allowable. The test is run for 480 hours.
(B) Low temperature sludge dispersancy test.This test is run for 180 hours.
(C) Oldsmobile Sequence II rust test.
(D) CLR L-38 oxidation test.
Caterpillar 1H test Pass-0.1% top groove filling. Low temperature sludge test Passtotal sludge 47.1. Oldsmobile Sequence II rust test Pass9.6 average rust. L-38 test PassCu-Pb bearing weight loss 31 mgs.
It is claimed:
1. A lubricating oil composition consisting essentially of a major amount of a mineral oil of lubricating viscosity, about 0.2% to 3% by weight of a basic calcium aromatic sulfonate having a base number of about 10 to and a calcium content of about 1 to 5%, about 0.1 to 1% by weight of an overbased calcium aromatic sulfonate having a base number of about 200 to 500 and a calcium content of about 8 to 30%, and about 0.25 to 2.5% by weight of an alkenyl succinimide having the formula:
wherein R is an alkenyl radical of about 30 to 200 carbon atoms, R is a divalent alkylene radical of about 2 to 4 carbon atoms, R and R are selected from the group consisting of hydrogen and a lower alkyl radical and n is an integer having a value of 1 to 6, with the proviso that when n is 1, R" and R are lower alkyl and when n is greater than 1, R" and R" are hydrogen, said composition having a total base number of about 2 to 7 with said basic calcium aromatic sulfonate providing about 5 to 25% of said total base number and said overbased calcium aromatic sulfonate providing about to 95% of said total base number.
2. The composition of claim 1 which contains a small amount of zinc dithiophosphate diester in which the organic groups contain from about 4 to 20 carbon atoms, said amount being sufficient to provide a phosphorous level of from about 0.02 to 0.2% by weight and about .001 to 1 percent by weight of a methacrylate ester polymer in which the ester radical contains 4 to 20 carbon atoms.
3. The composition of claim 2 wherein the basic calcium aromatic sulfonate is a basic calcium mahogany sulfonate having a base number of 20 to 50 and the overba-sed calcium aromatic sulfonate is an overbased calcium mahogany sulfonate having a base number of 250 to 400.
4. The composition of claim 3 wherein the basic calcium mahogany sulfonate provides about 5 to 15% of the total base number and the overbased calcium mahogany sulfonate provides about to of the total base number.
References Cited UNITED STATES PATENTS 3,150,088 9/1964 Hunt et a1. 252-33 X 3,172,892 3/1965 LeSuer et al.
FOREIGN PATENTS 677,917 8/1952 Great Britain.
DANIEL E. WYMAN, Primary Examiner.
C. F. DEES, Assistant Examiner.
Claims (2)
1. A LUBRICATING OIL COMPOSITON CONSITING ESSENTIALLY OF A MAJOR AMOUNT OF A MINERAL OIL OF LUBRICATING VISCOSITY, ABOUT 0.2% TO 3% BY WEIGHT OF A BASIC CALCIUM AROMATIC SULFONATE HAVING A BASE NUMBER OF ABOUT 10 TO 60 AND A CALCIUM CONTENT OF ABOUT 1 TO 5%, ABOUT 0.1 TO 1% BY WEIGHT OF A OVERBASED CALCIUM AROMATIC SULFONATE HAVING A BASE NUMBER OF AOBUT 200 TO 500 AND A CALCIUM CONTENT OF ABOUT 8 TO 30%, AND ABOUT 0.25 TO 2.5% BY WEIGHT OF AN ALKENYL SUCCINIMIDE HAVING THE FORMULA:
2. THE COMPOSITION OF CLAIM 1 WHICH CONTAINS A SMALL AMOUNT OF ZINC DITHIOPHOSPHATE DIESTER IN WHICH THE ORGANIC GROUPS CONTAIN FROM ABOUT 4 TO 20 CARBON ATOMS, SAID AMOUNT BEING SUFFICIENT TO PROVIDE A PHOSPHORUS LEVEL OF FROM ABOUT 0.02 TO 0.2% BY WEIGHT AND ABOUT .001 TO 1 PERCENT BY WEIGHT OF A METHACRYLATE ESTER POLYMER IN WHICH THE ESTER RADICAL CONTAINS 4 TO 20 CARBON ATOMS.
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US435707A US3377281A (en) | 1965-02-26 | 1965-02-26 | Lubricating composition |
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US435707A US3377281A (en) | 1965-02-26 | 1965-02-26 | Lubricating composition |
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US3377281A true US3377281A (en) | 1968-04-09 |
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ID=23729505
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US435707A Expired - Lifetime US3377281A (en) | 1965-02-26 | 1965-02-26 | Lubricating composition |
Country Status (1)
Country | Link |
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US (1) | US3377281A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3539511A (en) * | 1967-11-24 | 1970-11-10 | Standard Oil Co | Preparation of alkaline earth sulfonates |
US3627681A (en) * | 1970-01-23 | 1971-12-14 | Shell Oil Co | Lubricant compositions |
US3852204A (en) * | 1966-02-01 | 1974-12-03 | Cosden Oil & Chem Co | Lubricant compositions |
USB329476I5 (en) * | 1973-02-05 | 1975-01-28 | ||
US3898168A (en) * | 1972-07-21 | 1975-08-05 | Standard Oil Co | Prevention of magnesium carbonate precipitation by water from crankcase oil containing high base magnesium sulfonate |
US3899432A (en) * | 1974-06-03 | 1975-08-12 | Chevron Res | All-purpose lubricating oil composition with anti-chatter characteristics for wet disc brakes |
US3909425A (en) * | 1974-07-01 | 1975-09-30 | Texaco Inc | Lubricating oil composition |
US4113633A (en) * | 1976-12-15 | 1978-09-12 | Gibbons Paul J | Penetrating oil composition |
US4169799A (en) * | 1976-12-27 | 1979-10-02 | Texaco Inc. | Lubricating oil composition |
US4171270A (en) * | 1976-12-27 | 1979-10-16 | Texaco Inc. | Sulfurized overbased calcium alkylphenolate lubricant composition |
US4171269A (en) * | 1976-12-27 | 1979-10-16 | Texaco Inc. | Sulfurized lubricant composition |
WO1996031120A1 (en) * | 1995-04-05 | 1996-10-10 | Australian Petroleum Pty. Limited | Oil for agricultural use |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB677917A (en) * | 1948-12-06 | 1952-08-27 | Bataafsche Petroleum | Lubricating oil compositions |
US3150088A (en) * | 1962-03-23 | 1964-09-22 | Continental Oil Co | Highly basic calcium-containing additive agent |
US3172892A (en) * | 1959-03-30 | 1965-03-09 | Reaction product of high molecular weight succinic acids and succinic anhydrides with an ethylene poly- amine |
-
1965
- 1965-02-26 US US435707A patent/US3377281A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB677917A (en) * | 1948-12-06 | 1952-08-27 | Bataafsche Petroleum | Lubricating oil compositions |
US3172892A (en) * | 1959-03-30 | 1965-03-09 | Reaction product of high molecular weight succinic acids and succinic anhydrides with an ethylene poly- amine | |
US3150088A (en) * | 1962-03-23 | 1964-09-22 | Continental Oil Co | Highly basic calcium-containing additive agent |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3852204A (en) * | 1966-02-01 | 1974-12-03 | Cosden Oil & Chem Co | Lubricant compositions |
US3539511A (en) * | 1967-11-24 | 1970-11-10 | Standard Oil Co | Preparation of alkaline earth sulfonates |
US3627681A (en) * | 1970-01-23 | 1971-12-14 | Shell Oil Co | Lubricant compositions |
US3898168A (en) * | 1972-07-21 | 1975-08-05 | Standard Oil Co | Prevention of magnesium carbonate precipitation by water from crankcase oil containing high base magnesium sulfonate |
US3920562A (en) * | 1973-02-05 | 1975-11-18 | Chevron Res | Demulsified extended life functional fluid |
USB329476I5 (en) * | 1973-02-05 | 1975-01-28 | ||
US3899432A (en) * | 1974-06-03 | 1975-08-12 | Chevron Res | All-purpose lubricating oil composition with anti-chatter characteristics for wet disc brakes |
US3909425A (en) * | 1974-07-01 | 1975-09-30 | Texaco Inc | Lubricating oil composition |
US4113633A (en) * | 1976-12-15 | 1978-09-12 | Gibbons Paul J | Penetrating oil composition |
US4169799A (en) * | 1976-12-27 | 1979-10-02 | Texaco Inc. | Lubricating oil composition |
US4171270A (en) * | 1976-12-27 | 1979-10-16 | Texaco Inc. | Sulfurized overbased calcium alkylphenolate lubricant composition |
US4171269A (en) * | 1976-12-27 | 1979-10-16 | Texaco Inc. | Sulfurized lubricant composition |
WO1996031120A1 (en) * | 1995-04-05 | 1996-10-10 | Australian Petroleum Pty. Limited | Oil for agricultural use |
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