US2836560A - Water- and corrosion-resistant lubricating greases gelled with inorganic colloids - Google Patents
Water- and corrosion-resistant lubricating greases gelled with inorganic colloids Download PDFInfo
- Publication number
- US2836560A US2836560A US568431A US56843156A US2836560A US 2836560 A US2836560 A US 2836560A US 568431 A US568431 A US 568431A US 56843156 A US56843156 A US 56843156A US 2836560 A US2836560 A US 2836560A
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- US
- United States
- Prior art keywords
- grease
- water
- corrosion
- lubricating
- inorganic
- 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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- 230000001050 lubricating effect Effects 0.000 title description 30
- 238000005260 corrosion Methods 0.000 title description 13
- 230000007797 corrosion Effects 0.000 title description 10
- 239000000084 colloidal system Substances 0.000 title description 4
- 239000004519 grease Substances 0.000 claims description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- 239000003349 gelling agent Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 13
- 239000010687 lubricating oil Substances 0.000 claims description 11
- 150000007824 aliphatic compounds Chemical class 0.000 claims description 7
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 150000004679 hydroxides Chemical class 0.000 claims description 4
- 229910052809 inorganic oxide Inorganic materials 0.000 claims description 4
- 150000004760 silicates Chemical class 0.000 claims description 4
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 4
- 229910052806 inorganic carbonate Inorganic materials 0.000 claims description 3
- 229910001853 inorganic hydroxide Inorganic materials 0.000 claims description 3
- 229910052909 inorganic silicate Inorganic materials 0.000 claims description 3
- 229910052920 inorganic sulfate Inorganic materials 0.000 claims description 3
- 229910052945 inorganic sulfide Inorganic materials 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 150000003568 thioethers Chemical class 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 239000010688 mineral lubricating oil Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- -1 hydroxy fatty acid Chemical class 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 150000001335 aliphatic alkanes Chemical class 0.000 description 4
- 239000008119 colloidal silica Substances 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 150000004763 sulfides Chemical class 0.000 description 3
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- RWNKSTSCBHKHTB-UHFFFAOYSA-N Hexachloro-1,3-butadiene Chemical compound ClC(Cl)=C(Cl)C(Cl)=C(Cl)Cl RWNKSTSCBHKHTB-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000017 hydrogel Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000005049 silicon tetrachloride Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 235000011044 succinic acid Nutrition 0.000 description 2
- 150000003444 succinic acids Chemical class 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 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
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical class OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical class O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 1
- 229910000271 hectorite Inorganic materials 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
- 239000004535 oil miscible liquid Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003330 sebacic acids Chemical class 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000012808 vapor phase 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
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/043—Sulfur; Selenenium; Tellurium
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/063—Peroxides
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/065—Sulfides; Selenides; Tellurides
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- C10M2201/08—Inorganic acids or salts thereof
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- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/081—Inorganic acids or salts thereof containing halogen
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- C10M2201/082—Inorganic acids or salts thereof containing nitrogen
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/102—Silicates
- C10M2201/103—Clays; Mica; Zeolites
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- C10M2201/105—Silica
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
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- C10M2205/20—Natural rubber; Natural resins
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
- C10M2207/128—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
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- C10M2207/28—Esters
- C10M2207/287—Partial esters
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- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
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- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/042—Alcohols; Ethers; Aldehydes; Ketones
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/044—Acids; Salts or esters thereof
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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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated compounds
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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
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl amines
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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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
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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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
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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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/024—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
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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
- C10M2229/02—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
- C10M2229/041—Siloxanes with specific structure containing aliphatic substituents
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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
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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
- C10N2010/08—Groups 4 or 14
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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
- 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
- This invention relates to improved grease compositions. More particularly, it is concerned with greases gelled with inorganic colloids and improved with respect to water resistance and corrosion protection by the presence of certain haloepoxides.
- Lubricating greases contain a lubricating oil base and a gelling agent.
- the gelling agent is usually a soap of a fatty acid or a hydroxy fatty acid. Soaps are subject to phase changes as the temperature increases, so that soap-gelled lubricating greases soften at elevated temperature and finally become liquid.
- Inorganic colloids have already been used as gelling agents in lubricating greases.
- Lubricating greases containing such gelling agents are able to retain their consistency over a far Wider temperature range.
- Lubricating greases containing an inorganic gelling agent generaly have, however, a poor resistance to disintegration by the action of water.
- surface-active agents such as long chain amines, amides, ammonium salts and salts of higher fatty acids, have already been incorporated therein.
- aliphatic compounds containing a halogen atom and an epoxy-oxygen atom are effective to improve the water resistance of lubricating greases containing an inorganic gelling agent.
- the said aliphatic compounds have the additional advantage of improving the corrosion properties of lubricating greases at the same time; this is particularly the case when the greases are applied to highly sensitive steel surfaces.
- epoxy-oxygen atom means an oxygen atom which is present in a radical of the following formula:
- the present invention provides a lubricating grease comprising a hydrocarbon lubricating oil base, thickened to a lubricating grease consistency by means of a normally hydrophilic inorganic gelling agent, and a minor proportion of an aliphatic compound containing a halogen atom and an epoxy-oxygen atom.
- the preferred class comprises those compounds containing 3-10 carbon atoms per molecule, of which the chloroepoxyalkanes have the most satisfactory effect.
- the proportion used depends, among other things, on the desired improvement of water resistance and the amount of hydrophilic inorganic gelling agent present in the grease. Generally the proportion of the aliphatic compound lies between 0.01 and 3% by weight, based on the whole lubricating grease. In many cases a proportion of from 0.05 to 0.5% by weight (0.25%25% by weight of the gelling agent), and particularly of approximately 0.1% by weight, imparts satisfactory properties to the lubricating greases.
- the preferred anti-corrosion agents for this purpose are the aliphatic polycarboxylic acids containing one or more alkyl or alkenyl groups with at least 3 carbon atoms, and the corresponding thio acids, as well as the amides, anhydrides and esters of these acids.
- suitable acids are the malonic, succinic, glutaric, adipic, pimelic, sebacic, azelaic, tartaric, citric, maleic and citraconic acids which are substituted by alkyl or alkenyl groups of the type mentioned above, particularly those containing 10 to 18 carbon atoms.
- Suitable amides and esters are the mono-amides of alkyl-substituted succinic acids, the mono-oleyl esters of alkenyl-substituted succinic acids and the mono-octyl esters of alkyl-substituted sebacic acids. Dimerized unsaturated fatty acids also are suitable corrosion inhibitors for use in these compositions.
- anti-corrosion additives When additional anti-corrosion additives are used these are employed in minor proportions, suitably in proportions of from 0.01 to 3% by weight, and particularly from 0.05 to 1% by weight, based on the whole lubricating grease.
- a mineral lubricating oil is generally used as the hydrocarbon lubricating oil base.
- the mineral lubricating oils used may be of any origin and their properties may vary within wide limits.
- the viscosity generally lies within a range of 1 to 50 E. at 50 C. and the viscosity index between 0 and 80, but oils with a viscosity and a viscosity index outside these limits may also be used.
- hydrocarbon oils are preferred as the grease base, other non-ester oleaginous fluids such as silicones and halocarbons (e. g. dimethyl silicone or hexachlorobutadiene) may be utilized.
- Suitable gelling agents are the known normally hydrophilic inorganic gelling agents. Colloidal inorganic oxides, hydroxides, sulfides, sulfates, silicates and carbonates, such a silica, alumina, magnesia, calcium oxide, copper sulfide, calcium sulfate and mixtures thereof, particularly mixtures of silica withmagnesia, as well as Synthetic zeolites, and natural clays, such as hectorite and bentonite, may be used.
- the gelling agent is used in a proportion sufficient to thicken the lubricating oil base to the desired lubricating grease consistency. The proportion of the gelling agent generally lies between 2 and 20% by weight based on the whole lubricating grease.
- anti-oxidants especially phenolic anti-oxidants, suchas alkyl phenols, e. g. 2,6-di-tert.- butyl-4'-methyl"phenol, and amines,. such as phenylanaphthylamine, extremepressurc agents such as sulfur, lead naphthenate and sulfurized and/or chlorinated fats or fatty oils and tackiness agents such as rubber and 'poly-isobutylene, f 1
- phenolic anti-oxidants suchas alkyl phenols, e. g. 2,6-di-tert.- butyl-4'-methyl"phenol
- amines such as phenylanaphthylamine
- extremepressurc agents such as sulfur, lead naphthenate and sulfurized and/or chlorinated fats or fatty oils
- tackiness agents such as rubber and 'poly-isobutylene, f 1
- the lubricating grease's' may. be prepared by any one of theknown methods.
- a volatile silicon compound such as silicon tetrachloride
- silicon tetrachloride may be burnt in 7 meters long and 15 millimeters wide.
- the glass strip'is grease should extend above the water so that the degree of change of the grease may be better assessed.
- the strip is allowed to stand in the water for 48 hours at 20? C.
- additives desired in the lubricating grease can be incorporated in thejlubricating grease mixture at any stageof these processes, provided'of course, that such a stage is not chosen that the additives are Washed away or destroyed during the further course of the process.
- the following example illustrates the benefits of this invention; 0 I I 1 Three lubricating greases were prepared-having the The mineral oil was a lubricating oil with a viscosity of 19 Engler at C. obtained by distillation and extraction of a Venezuelan crude .oil.
- the silicawas a colloidal silica obtained by'burning'in air hydrogen saturated with silicon tetrachloride. 1
- the'oil was gradually poured'o n to thesilica, while constantly stirring.
- the penetration was determined according to the A. S. .T. M. Method D217-48 (so-called .worked penetrationi), I j
- the lubricating greases were applied in a thin layer on steel plates. A quantity of 2 grams of the grease to be tested was placed on the plates and then uniformly distributed over the whole plate by rubbing in at moderate pressure with a pad (twisted rag) which had, been previously soaked in the same grease. The plates were then placed in a glass cupboard for four weeks at 40 C., in an atmosphere with a relative humidity of in such a way as to be protected from water condensing on the glass wallsand running or trickling down. After this period the corrosion of the plates is assessed.
- a grease composition consisting essentially iof a hydrocarbon lubricating oil, a grease-forming proportion of an inorganic hydrophilic colloidal gelling agent of the group consisting of inorganic oxides, hydroxides, sulfides,
- a grease composition consisting essentially, of a mineral lubricating oil, a grease-forming proportion of an inorganic hydrophilic colloidal amorphous silica; gelling agent, and from about 0.01% to about 3% by weight of a monohaloepoxyalkane having '3 10 carbon atoms per molecule, the amount of'said alkane being 'suflicient 'to improve the water resistant characteristic of the grease.
- a grease composition consisting essentially of a mineral lubricating oil, a grease forming proportion of an inorganic hydrophilic colloidal clay gelling agent and I from about 0.05% to about 1% by weight of a monochloroepoxyalkane having 3-10 carbonatoms per molecule, the amountof said alkane being sufiicientto improve the water resistant characteristic of the grease.
- a grcasecomposition consisting essentially of a
- a grease composition consisting essentially of a mineral lubricating oil, a grease-forming proportion of an inorganic hydrophilic colloidal silica gelling agent and from about 0.05% to about 1% by Weight of a monochloroepoxyalkane having 310 carbon atoms per molecule, the amount of said alkane being suflicient to improve the Water resistant characteristic of the grease.
- a grease composition consisting essentially of a mineral lubricating oil, a grease-forming proportion of an inorganic hydrophih'c colloidal silica gel and from about 0.05% to about 1% by weight of epichlorohydrin.
- a grease composition consisting essentially of a major proportion of a mineral lubricating oil and a grease- 6 forming proportion of an inorganic hydrophilic colloidal gelling agent of the group consisting of inorganic oxides, hydroxides, sulfides, sulfates, silicates and carbonates, rendered water-resistant by the addition of 0.01-3% by weight of a haloepoxyalkane having 3-10 carbon atoms per molecule.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
WATER- AND CORROSION-RESISTANT LUBRI- CATING GREASES GELLED WITH INORGANIC COLLOIDS Ronald Sowerby Teale, Beaconsfield, England, and Hans Seeles, Hamburg, and Helmut Richard Karl Ferdinand Rolf Konau, Hambisrg-Ghlsdorf, Germany, assignors to Shell Development Company, New York, N. Y., a corporation of Delaware No Drawing. Application February 29, 1956 Serial No. 568,431
Claims priority, application Great Britain May 2,1955
7 Claims. (Cl. 25228) This invention relates to improved grease compositions. More particularly, it is concerned with greases gelled with inorganic colloids and improved with respect to water resistance and corrosion protection by the presence of certain haloepoxides.
Lubricating greases contain a lubricating oil base and a gelling agent. The gelling agent is usually a soap of a fatty acid or a hydroxy fatty acid. Soaps are subject to phase changes as the temperature increases, so that soap-gelled lubricating greases soften at elevated temperature and finally become liquid.
Inorganic colloids have already been used as gelling agents in lubricating greases. Lubricating greases containing such gelling agents are able to retain their consistency over a far Wider temperature range.
Lubricating greases containing an inorganic gelling agent generaly have, however, a poor resistance to disintegration by the action of water. In order to improve such lubricating greases in this respect surface-active agents, such as long chain amines, amides, ammonium salts and salts of higher fatty acids, have already been incorporated therein.
It has now been found that aliphatic compounds containing a halogen atom and an epoxy-oxygen atom (e. g. haloepoxyalkanes), are effective to improve the water resistance of lubricating greases containing an inorganic gelling agent. The said aliphatic compounds have the additional advantage of improving the corrosion properties of lubricating greases at the same time; this is particularly the case when the greases are applied to highly sensitive steel surfaces.
The expression epoxy-oxygen atom means an oxygen atom which is present in a radical of the following formula:
Accordingly, the present invention provides a lubricating grease comprising a hydrocarbon lubricating oil base, thickened to a lubricating grease consistency by means of a normally hydrophilic inorganic gelling agent, and a minor proportion of an aliphatic compound containing a halogen atom and an epoxy-oxygen atom. The preferred class comprises those compounds containing 3-10 carbon atoms per molecule, of which the chloroepoxyalkanes have the most satisfactory effect.
Patented May 27, 1958 ice Examples of suitable halo-epoxy aliphatic compounds are:
1,2-epoxy-3-chloropropane (epichlorohydrin) 2,3-epoxy-4-chlorobutane l,2-epoxy-3-isopropy1-3-iodopropane 1,2-epoxy-4-chlorobutane 1,2-epoxy-5-chloropentane 1,2-epoxy-3-methyl-3-chloropropan 1,Z-epoxy-S,3-dimethyl-3-chloropropane 1,2-epoxy-2-methyl-3-bromopropane 2,3-epoxy-4-methyl-l-chlorohexane 1,2-epoxy-4-methyl-5-bromopentane These compounds are added to the lubricating greases in minor proportions. The proportion used depends, among other things, on the desired improvement of water resistance and the amount of hydrophilic inorganic gelling agent present in the grease. Generally the proportion of the aliphatic compound lies between 0.01 and 3% by weight, based on the whole lubricating grease. In many cases a proportion of from 0.05 to 0.5% by weight (0.25%25% by weight of the gelling agent), and particularly of approximately 0.1% by weight, imparts satisfactory properties to the lubricating greases.
Although the said compounds improve the corrosion properties of the lubricating greases, a further improvement of these properties is generally obtained by adding a further anti-corrosion agent. The preferred anti-corrosion agents for this purpose are the aliphatic polycarboxylic acids containing one or more alkyl or alkenyl groups with at least 3 carbon atoms, and the corresponding thio acids, as well as the amides, anhydrides and esters of these acids. Examples of suitable acids are the malonic, succinic, glutaric, adipic, pimelic, sebacic, azelaic, tartaric, citric, maleic and citraconic acids which are substituted by alkyl or alkenyl groups of the type mentioned above, particularly those containing 10 to 18 carbon atoms. Examples of suitable amides and esters are the mono-amides of alkyl-substituted succinic acids, the mono-oleyl esters of alkenyl-substituted succinic acids and the mono-octyl esters of alkyl-substituted sebacic acids. Dimerized unsaturated fatty acids also are suitable corrosion inhibitors for use in these compositions.
When additional anti-corrosion additives are used these are employed in minor proportions, suitably in proportions of from 0.01 to 3% by weight, and particularly from 0.05 to 1% by weight, based on the whole lubricating grease.
A mineral lubricating oil is generally used as the hydrocarbon lubricating oil base. The mineral lubricating oils used may be of any origin and their properties may vary within wide limits. The viscosity generally lies within a range of 1 to 50 E. at 50 C. and the viscosity index between 0 and 80, but oils with a viscosity and a viscosity index outside these limits may also be used. While hydrocarbon oils are preferred as the grease base, other non-ester oleaginous fluids such as silicones and halocarbons (e. g. dimethyl silicone or hexachlorobutadiene) may be utilized.
Suitable gelling agents are the known normally hydrophilic inorganic gelling agents. Colloidal inorganic oxides, hydroxides, sulfides, sulfates, silicates and carbonates, such a silica, alumina, magnesia, calcium oxide, copper sulfide, calcium sulfate and mixtures thereof, particularly mixtures of silica withmagnesia, as well as Synthetic zeolites, and natural clays, such as hectorite and bentonite, may be used. The gelling agent is used in a proportion sufficient to thicken the lubricating oil base to the desired lubricating grease consistency. The proportion of the gelling agent generally lies between 2 and 20% by weight based on the whole lubricating grease.
If desired, minor proportions, e. g. 0.01 to 5% by weight, based on the whole lubricating grease, of other additives may be incorporated in the lubricating greases in orderto improve specific properties. As such may be mentioned, for example, anti-oxidants, especially phenolic anti-oxidants, suchas alkyl phenols, e. g. 2,6-di-tert.- butyl-4'-methyl"phenol, and amines,. such as phenylanaphthylamine, extremepressurc agents such as sulfur, lead naphthenate and sulfurized and/or chlorinated fats or fatty oils and tackiness agents such as rubber and 'poly-isobutylene, f 1
The lubricating grease's'may. be prepared by any one of theknown methods. For "instance, a volatile silicon compound, such as silicon tetrachloride, may be burnt in 7 meters long and 15 millimeters wide. The glass strip'is grease should extend above the water so that the degree of change of the grease may be better assessed. The strip is allowed to stand in the water for 48 hours at 20? C.
After this period it is determined how far the water has 7 become turbid and the grease has emulsified or decomthe vapor phase,[thus' forming a' colloidal silica which a may be dispersed in the lubricating oil base in any'desired way, e. g. by milling. It is also possible to start from a hydrogel and expel' the'water therefrom by means of a low-boiling organic liquid, such as methyl orethyl alcohol oracetone, after which'th e gel is heated to above the critical temperature of the liquid and the latter is evaporated. The resultant so-called aeorgel'is then dispersed in the lubricating oil base. the water present in a hydrogel by a waterand oilmiscible liquid, and then again expel the liquid by means of the lubricating oil base. In most cases, more than one organic'liquid is used.- The water'is first expelled,
' for example, bymeansof alcohol or acetone, this liquid It is also possible to expel,
being expelled by means of the lubricating oil base. The
additives desired in the lubricating grease can be incorporated in thejlubricating grease mixture at any stageof these processes, provided'of course, that such a stage is not chosen that the additives are Washed away or destroyed during the further course of the process. The following example illustrates the benefits of this invention; 0 I I 1 Three lubricating greases were prepared-having the The mineral oil was a lubricating oil with a viscosity of 19 Engler at C. obtained by distillation and extraction of a Venezuelan crude .oil.
The silicawas a colloidal silica obtained by'burning'in air hydrogen saturated with silicon tetrachloride. 1
In order to prepare the lubricating greases, the'oil was gradually poured'o n to thesilica, while constantly stirring.
ln preparingthe lubricating greases: B and. C, the epichlorohydrinand the anti corrosion agent were previously dissolved in the oil. The mLxture thus obtained was twice passed through a roll mill. Q 7 T I The penetration, water resistance and corrosion properties of the lubricating greases were determined.
The penetration was determined according to the A. S. .T. M. Method D217-48 (so-called .worked penetrationi), I j
The water resistance of the lubricating greases was tested in the so-ca'lled glass strip test? In this test a layerof grease lOO millimeters long, 10 millimeters wide and 1 millimeter thick is laid on a glass strip 160"milliposed.
In order to test the corrosion properties. the lubricating greases were applied in a thin layer on steel plates. A quantity of 2 grams of the grease to be tested was placed on the plates and then uniformly distributed over the whole plate by rubbing in at moderate pressure with a pad (twisted rag) which had, been previously soaked in the same grease. The plates were then placed in a glass cupboard for four weeks at 40 C., in an atmosphere with a relative humidity of in such a way as to be protected from water condensing on the glass wallsand running or trickling down. After this period the corrosion of the plates is assessed.
table:
' Resistance Lubricating grease Penetration to Water Corrosion of the plates 205 poor B weak to medium weak. 207 good very weak. 210 good traces.
a The grease decomposed completely.
tendency to emulsify; the water was still clear.
The unexpected improvementin Water resistanceoflthe compositions, caused by the additionof such. small quantities' of low 'molecular'weight materialste. g. epichloro llydrin) indicates the possibility that reaction may have occurred between the additive and the gel surface, or that the gel may have catalyzed the polymerization. of the additive to form poly(alkylene oxide) coatings having hydrophobic haloalkyl (chloromethyl) substituents. The remaining possibility'comprises simple. adsorption 10f the additive on the gel surfaces. We claim as our invention: 7 r
1. A grease composition consisting essentially iof a hydrocarbon lubricating oil, a grease-forming proportion of an inorganic hydrophilic colloidal gelling agent of the group consisting of inorganic oxides, hydroxides, sulfides,
sulfates, silicates and carbonates, and from about 0.01% to about.3% by weight of an aliphaticcompound having 7 3-10 carbon atoms per molecule and containinga halogen atom and an epoxy-oxygen atom, the amount of said compound being suflicient to improve the water resistant characteristicflof the grease. 1 i
2. A grease composition consisting essentially, of a mineral lubricating oil, a grease-forming proportion of an inorganic hydrophilic colloidal amorphous silica; gelling agent, and from about 0.01% to about 3% by weight of a monohaloepoxyalkane having '3 10 carbon atoms per molecule, the amount of'said alkane being 'suflicient 'to improve the water resistant characteristic of the grease.
3. A grease composition consisting essentially of a mineral lubricating oil, a grease forming proportion of an inorganic hydrophilic colloidal clay gelling agent and I from about 0.05% to about 1% by weight of a monochloroepoxyalkane having 3-10 carbonatoms per molecule, the amountof said alkane being sufiicientto improve the water resistant characteristic of the grease.
4. A grcasecomposition consisting essentially of a;
the amount of said alkane being sutficient to improve the water resistant characteristic of the grease.
The results of the tests are summarized in the following 5. A grease composition consisting essentially of a mineral lubricating oil, a grease-forming proportion of an inorganic hydrophilic colloidal silica gelling agent and from about 0.05% to about 1% by Weight of a monochloroepoxyalkane having 310 carbon atoms per molecule, the amount of said alkane being suflicient to improve the Water resistant characteristic of the grease.
6. A grease composition consisting essentially of a mineral lubricating oil, a grease-forming proportion of an inorganic hydrophih'c colloidal silica gel and from about 0.05% to about 1% by weight of epichlorohydrin.
7. A grease composition consisting essentially of a major proportion of a mineral lubricating oil and a grease- 6 forming proportion of an inorganic hydrophilic colloidal gelling agent of the group consisting of inorganic oxides, hydroxides, sulfides, sulfates, silicates and carbonates, rendered water-resistant by the addition of 0.01-3% by weight of a haloepoxyalkane having 3-10 carbon atoms per molecule.
Weike et a1. Mar. 20, 1956 Peterson et a1. May 29, 1956
Claims (1)
1. A GREASE COMPOSITION CONSISTING ESSENTIALLY OF A HYDROCARBON LUBRICATING OIL, A GREASE-FORMING PROPORTION OF AN INORGANIC HYDROPHILIC COLLODIAL GELLING AGENT OF THE GROUP CONSISTING OF INORGANIC OXIDES, HYDROXIDES, SULFIDES, SULFATES, SILICATES AND CARBONATES, AND FROM ABOUT 0.01% TO ABOUT 3% BY WEIGHT OF AN ALIPHATIC COMPOUND HAVING 3-10 CARBON ATOMS PER MOLECULE AND CONTAINING A HALOGEN ATOM AND EPOXY-OXYGEN ATOM, THE AMOUNT OF SAID COMPOUND BEING SUFFICIENT TO IMPROVE THE WATER RESISTANT CHARACTERISTIC OF THE GREASE.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2836560X | 1955-05-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2836560A true US2836560A (en) | 1958-05-27 |
Family
ID=10916234
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US568431A Expired - Lifetime US2836560A (en) | 1955-05-02 | 1956-02-29 | Water- and corrosion-resistant lubricating greases gelled with inorganic colloids |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2836560A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3180827A (en) * | 1961-04-19 | 1965-04-27 | Pure Oil Co | Thickened compositions containing a hydrate of an alum |
| US3222279A (en) * | 1963-06-25 | 1965-12-07 | Shell Oil Co | Lubricant compositions |
| US3639237A (en) * | 1969-05-14 | 1972-02-01 | Exxon Research Engineering Co | Extreme pressure greases |
| US4122022A (en) * | 1976-08-03 | 1978-10-24 | Shell Internationale Research Maatschap Iij B.V. | Method for preparing clay-based grease compositions |
| US20040102330A1 (en) * | 2001-02-13 | 2004-05-27 | Jian Zhou | Viscoelastic compositions |
| US8785355B2 (en) | 2001-02-13 | 2014-07-22 | Schlumberger Technology Corporation | Viscoelastic compositions |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2739121A (en) * | 1951-12-14 | 1956-03-20 | Degussa | Thickened hydrophobic lubricating compositions |
| US2748081A (en) * | 1952-06-02 | 1956-05-29 | Shell Dev | Water-resistant non-soap grease containing alkaline agents |
-
1956
- 1956-02-29 US US568431A patent/US2836560A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2739121A (en) * | 1951-12-14 | 1956-03-20 | Degussa | Thickened hydrophobic lubricating compositions |
| US2748081A (en) * | 1952-06-02 | 1956-05-29 | Shell Dev | Water-resistant non-soap grease containing alkaline agents |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3180827A (en) * | 1961-04-19 | 1965-04-27 | Pure Oil Co | Thickened compositions containing a hydrate of an alum |
| US3222279A (en) * | 1963-06-25 | 1965-12-07 | Shell Oil Co | Lubricant compositions |
| US3639237A (en) * | 1969-05-14 | 1972-02-01 | Exxon Research Engineering Co | Extreme pressure greases |
| US4122022A (en) * | 1976-08-03 | 1978-10-24 | Shell Internationale Research Maatschap Iij B.V. | Method for preparing clay-based grease compositions |
| USRE31307E (en) * | 1976-08-03 | 1983-07-12 | Shell Internationale Research Maatschap, IIJ B.V. | Method for preparing clay-based grease compositions |
| US20040102330A1 (en) * | 2001-02-13 | 2004-05-27 | Jian Zhou | Viscoelastic compositions |
| US7704926B2 (en) * | 2001-02-13 | 2010-04-27 | Schlumberger Technology Corporation | Viscoelastic compositions |
| US8785355B2 (en) | 2001-02-13 | 2014-07-22 | Schlumberger Technology Corporation | Viscoelastic compositions |
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