US2908645A - Blended lithium calcium base grease - Google Patents
Blended lithium calcium base grease Download PDFInfo
- Publication number
- US2908645A US2908645A US504659A US50465955A US2908645A US 2908645 A US2908645 A US 2908645A US 504659 A US504659 A US 504659A US 50465955 A US50465955 A US 50465955A US 2908645 A US2908645 A US 2908645A
- Authority
- US
- United States
- Prior art keywords
- grease
- acids
- lithium
- molecular weight
- component
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004519 grease Substances 0.000 title claims description 68
- USOPFYZPGZGBEB-UHFFFAOYSA-N calcium lithium Chemical compound [Li].[Ca] USOPFYZPGZGBEB-UHFFFAOYSA-N 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims description 38
- 239000000344 soap Substances 0.000 claims description 34
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 33
- 229910052744 lithium Inorganic materials 0.000 claims description 33
- 239000002253 acid Substances 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 26
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 12
- 239000000194 fatty acid Substances 0.000 claims description 12
- 229930195729 fatty acid Natural products 0.000 claims description 12
- 150000004665 fatty acids Chemical class 0.000 claims description 12
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 10
- 229910052791 calcium Inorganic materials 0.000 claims description 10
- 239000011575 calcium Substances 0.000 claims description 10
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 description 23
- 239000002184 metal Substances 0.000 description 23
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical class CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 21
- 150000007513 acids Chemical class 0.000 description 21
- 150000001735 carboxylic acids Chemical class 0.000 description 21
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- 230000001050 lubricating effect Effects 0.000 description 11
- 239000002562 thickening agent Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 9
- 239000002585 base Substances 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 229960000583 acetic acid Drugs 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 7
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 6
- 239000000920 calcium hydroxide Substances 0.000 description 6
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 6
- 235000011116 calcium hydroxide Nutrition 0.000 description 6
- 239000010688 mineral lubricating oil Substances 0.000 description 6
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 6
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 5
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 150000004715 keto acids Chemical class 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000004359 castor oil Substances 0.000 description 4
- 235000019438 castor oil Nutrition 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- FZRNJOXQNWVMIH-UHFFFAOYSA-N lithium;hydrate Chemical compound [Li].O FZRNJOXQNWVMIH-UHFFFAOYSA-N 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 150000001734 carboxylic acid salts Chemical class 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 125000002524 organometallic group Chemical group 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 2
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- -1 aliphatic monocarboxylic acids Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229940116226 behenic acid Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 235000021323 fish oil Nutrition 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- FPLIHVCWSXLMPX-UHFFFAOYSA-M lithium 12-hydroxystearate Chemical compound [Li+].CCCCCCC(O)CCCCCCCCCCC([O-])=O FPLIHVCWSXLMPX-UHFFFAOYSA-M 0.000 description 2
- 150000002642 lithium compounds Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- RVWOWEQKPMPWMQ-UHFFFAOYSA-N methyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OC RVWOWEQKPMPWMQ-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 229960002446 octanoic acid Drugs 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 229910052712 strontium Inorganic materials 0.000 description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 2
- 239000010689 synthetic lubricating oil Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-Hydroxyoctadecanoic acid Natural products CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 125000002015 acyclic group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229940067597 azelate Drugs 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
- 239000001639 calcium acetate Substances 0.000 description 1
- 235000011092 calcium acetate Nutrition 0.000 description 1
- 229960005147 calcium acetate Drugs 0.000 description 1
- NDWWLJQHOLSEHX-UHFFFAOYSA-L calcium;octanoate Chemical compound [Ca+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O NDWWLJQHOLSEHX-UHFFFAOYSA-L 0.000 description 1
- JHVJHCOGRSPCSN-UHFFFAOYSA-L calcium;octanoate;acetate Chemical compound [Ca+2].CC([O-])=O.CCCCCCCC([O-])=O JHVJHCOGRSPCSN-UHFFFAOYSA-L 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000003240 coconut oil Chemical class 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid group Chemical group C(CCCCCC)(=O)O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid group Chemical group C(CCCCC)(=O)O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N pentanoic acid group Chemical group C(CCCC)(=O)O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003760 tallow Chemical class 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- QERYCTSHXKAMIS-UHFFFAOYSA-N thiophene-2-carboxylic acid Chemical compound OC(=O)C1=CC=CS1 QERYCTSHXKAMIS-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
-
- 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
- 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
-
- 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
- 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
- C10M2207/122—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
-
- 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
- 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
-
- 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
- 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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Definitions
- This invention relates to improved lubricating grease compositions having outstanding lubricating life and water resistance characteristics. More particularly, the invention "pertains to blends of separate grease components to form' greases having excellent water emulsion stability and long lubrication service.
- the invention in brief compass, relates to lubricating grease compositions comprising a blend of two component greases, one component being a lubricating oil thickened to grease consistency with an organo-metallic soap-salt or mixed salt complex, having a high combined but active metal content, and the other component being a lithium soap thickened grease.
- These two-component greases areimade separately and then blended togetherby thorough mixing or by the use of a suitable homogenizer or grease mill.
- organo-metallic complexes having high metal content as grease thickeners has recently been suggested.
- these complex thickeners have been prepared from the metal salts of low molecular weight carboxylic acids in combination with metal soaps ofhigh molecular weight carboxylic acids, metal salts of intermediate molecular weight carboxylic acids, or metal salts of medium molecular weight carboxylioacids 'and metal soaps of high molecular weight ca'rboxylicacids.
- the metal constituents of the complex thickeners have usually been selected from the 'divalent metals, especially the alkaline earth metals. Calcium is particularly preferred.
- Greases containing these complex thickeners have been found to have outstanding extreme pressure properties and long lubricating lives, but they tend to form fluid emulsions when water is churned into them. f
- lithium soaps in grease-making is well known in theart.
- Such lithium soap type thickeners have been prepared from the conventional soap-forming high molecular weight carboxylic acids, including their hydroxy derivatives and esters thereof.
- Lithium-containing grease thickeners have also been prepared from mixtures of lithium and calcium soaps of high; molecular Weight fatty acids. Greases thickened with these lithiumcontaining soaps, such asthe lithium soap of hydroxy stearic acid, haveexcellent water resistance but notably poor lubricating lives.
- carbon atoms per molecule between the high and medium molecular weight carboxylic acid is at least 7, preferably about 7 to 15.
- the high molecular Weight carboxylic acids useful for preparing the complex thickeners described above are those saturated and unsaturated, grease-making fatty acids thatare commonly known to the art. In general, these fatty acids have from about 12 to 30 carbon atoms, preferably about 16 to 22 carbon atoms per molecule, and
- fatty acids include such fatty acids as myristic acid, palmitic acid,
- stearic acid the various hydroxy s'tearic acids, oleic acid, arachidic acid, behenic acid and the like.
- -Mixtures in any proportions of these high molecular weight fatty acids are also operable.
- Naturally occurring high molecular weight acids such as fish oil acids, tallow acids, castor oil acids, coconut oil acids may also be utilized either in their natural state or after partial or complete saturation by hydrogenation.
- Preferred acids are mixtures derived from natural sources such as hydrogenated fish oil acids,
- the intermediate molecular Weightacids are those aliphatic monocarboxylic acids containing from about7 to 10 carbon atoms, preferably about 8 to 9 carbon atoms, per molecule. Either saturated or unsaturated fatty acids may be utilized, though the saturated fatty acids are preferred.
- branched chain acids are useful in the prepara- .tion ofsofter greases, Single or mixed intermediate weight acids having an average saponification valueof 3 from about 310 to 44 0, especially about 320 to 420', are preferred.
- Suitable acids include:
- OX0 acids are those formed by the well known Oxo process of synthesis with carbon monoxide, hydrogen and olefins, the latter being 0; and C polymers of propylene with or without some butylene, for making C and C Oxo acids.
- the medium molecular weight carboxylic acids include straight and branched chain saturated aliphatic carboxylic acids, hydroxy aliphatic monoand poly-carboxylic acids, aromatic monoand poly-carboxylic acids and anhydrides thereof, and heterocyclic acids containing from about 3 to 10, preferably 6 to 9, carbon atoms per molecule.
- Suitable carboxylic acids are as follows:
- Pentanoic valeric Glyceric Hexanoic (caproic) Lactic Heptanoic (enanthic) Citric Octanoic (caprylic) Benzoic Nonanoic (pelargonic) Hydroxy benzoic Decanoic (capric) Toluic Isobutyric o-Phthalic C OX0 acids Phthalic anhydride C Oxo acids Terephthalic C Oxo acids Furoic C Oxo acids Thiophene carboxylic Mixed as well as single medium molecular Weight carboxylic acids may be employed in the preparation of these complex thickeners.
- the low molecular weight carboxylic acids contemplated in this invention include saturated and unsaturated carboxylic acids having from about 1 to 3 carbon atoms, such as formic, acetic, propionic, acyclic and similar acids including their hydroxy derivatives, e.g. lactic acid. Monocarboxylic acids are particularly useful, and acetic acid is especially preferred.
- the low molecular weight carboxylic acid employed should have a saponification value of above about 600, preferably about 750 to 1300.
- Mixed low molecular weight carboxylic acids, wherein the acids contain from about 1 to 3 carbon atoms, having saponification values above about 600 may also be employed.
- the acetic acid can be either glacial acetic acid or an aqueous solution of acetic acid. When the latter is employed, the concentration of acid in solution may vary from about 60 to 99.9 wt. percent, and is preferably about 80 wt. percent.
- the metal component of the complexes described above is used in a form which can combine chemically with carboxylic acids to form salts or soaps. Ordinarily the metal hydroxide is used.
- the alkaline earth metal hydroxides or carbonates such as those of calcium, barium and strontium are particularly useful for the purposes of this invention. Calcium hydroxide is especially preferred.
- the alkaline earth metals differ in this respect from the alkali metals, i.e. sodium, potassium and lithium.
- Complexes having a high alkali metal content and which consist of the combinations of acids, mol ratios, etc. of the alkaline earth metal complexes of this invention yield greases with poor structural stability. 7 It is preferred, therefore, to use metals having a valency of two. Metals such as magnesium and zinc are also useful for the purposes of this invention.
- the soap-salt complex thickening agents may be utilized in combination with a Wide variety of mineral as well as synthetic lubricating oils.
- Mineral base lubricating oils ranging in viscosity from about 30 to 1000 SUS at 100 F. are preferably employed as the liquid phase of the grease composition within the range of about 50 to wt. percent based on the total weight of the final grease composition.
- These naturally occurring mineral lubricating oils may be derived from any petroleum crude source, whether paraffinic or naphthenic in type, and may be refined by any of the well known refining techniques of the petroleum industry.
- Suitable synthetic lubricating oils include the hydrocarbon, hydrocarbon polymer, ester, complex ester, formal, mercaptal, polyalkylene oxide, silicone and similar types. Synthetic oils such as di-Z-ethylhexyl sebacate, di-C Oxo azelate and other branched chain simple esters of dicarboxylic acids can be used, as well as complex esters prepared from glycols, dicarboxylic acids, and alcohols or monocarboxylic acids.
- the high metal content soap-salt complex or salt complexes may be prepared by coneutralization of a mixture of the acids employed with suitable bases, particularly the hydroxides and/or carbonates of the metals desired.
- This coneutralization step may be carried out in situ in the liquid menstruum to which the complex is to be applied in actual use.
- the mixed acids may be coneutralized in a portion or all of the lubricating oil forming the dispersant of a grease to be thickened by the soap-salt or salt complexes.
- the coneutralized material is heated to high temperatures of about 400 to 550 F. or higher prior to use in order to dehydrate the product and to promote the formation of the complex.
- this heating step is carried out in a liquid dispersant, the latter should have a boiling point above the heating temperature or the heating should be carried out under pressure.
- the high meta'l soap-salt or salt complexes may also be prepared by separately preforming at least a portion of the high molecular weight carboxylic acid soap, when employed, and/or the low and intermediate molecular weight carboxylic acid salts. This method is particularly useful when different metals are employed as bases.
- Soap-salt or salt complex proportions of about 530- wt. percent, preferably about 10-20 wt. percent, based on the total grease composition may be employed in preparing the greases constituting component 1 of this invention.
- Component 2 is a lithium base grease, i.e. a lubricating oil thickened to grease consistency with lithium soaps of high molecular weight carboxylic acids. Mixtures of lithium and strontium or lithium and calcium soaps may also be employed to prepare these greases.
- the grease-forming fats or high molecular weight fatty acids listed above are also suitable for preparing the component 2 grease.
- the grease can be made ximm J genesis
- the conventional methods of grease manufacture such as cooking in a fire heated kettle followed by drawing into thin pans or deep. cakes for cooling may be em ployed in preparing the lithium soap thickened greases. They may also be prepared in steam heated kettles followed by cooling with stirring while running cold water through the kettle jacket or by a continuous method of manufacture.
- US. Patent 2,397,956 discloses the preparation of greases containing a lithium soap of 12-hydroxy stearic or the lithium soap of hydrogenated castor oil as a thickener.
- the lithium soaps are present in amounts up to 50%, preferably 8 to 40%, of the total weight of the grease.
- these greases are preferably prepared at temperatures of between about 400 to 425 F.
- any suitable lithium compound may be used such as lithium hydroxide, lithium carbonate, lithium oxide and the like.
- the lithium compound used is lithium monohydrate which contains from 53 to 55% .of lithium hydroxide.
- operable proportions include from about 20 to 80% of component 1 and from about 20 to 80% of component 2.
- Preferred proportions are from about 40 to 80% of component 1 and from about 20 to 60% of component 2.
- the temperatures of blending are within the range of about 100 to 300 F., preferably about 180 to 225 F.
- the maximum temperature range may be just below the phase change in the lithium grease, i.e. when the grease changes in structure from a rubbery fibrous product to a smooth homogeneous product.
- the two grease components are blended together by thorough mixing or by being passed through a Gaulin homogenizer or Morehouse mill at a temperature suflicient to give an outlet temperature below the phase change of the lithium soap thickened grease component.
- Grease B I A grease was prepared from the following ingredients:
- the fatty acid and about one half of the mineral oil were added to steam kettle, and the calcium hydroxide was stirred in at a temperature of about 155 F. Heating and stirring were continued, and the lithium hydroxide added as a 10% aqueous solution at a temperature of 198 F.
- the grease batch was then heated to a temperature of about 290 F. to eifect dehydration. During this period the viscosity of the mass was cut down by the addition of small amounts of oil. Thereafter the heat was shut oif, and the balance of the mineral oil added while stirring over a period of about 1 to 2 hours.
- the grease was finished by being passed through a Morehouse rnillat an inlet temperature of about 90 F. and an outlet temperature of about 118 F.
- Greases C, D, E and F These greases were prepared by blending Greases A and B, separately prepared as described above, in accordance with formulations listed in the table below at a temperature of 125 F.
- Grease G A grease was prepared from the following ingredients:
- the mixture 'of acetic acid and caprylic acid was charged to the kettle, and the temperature raised with stirring to about 480 F. At this temperature, heating was discontinued and the mixture cooled to about 250 F. with stirring. Phenyl alpha naphthylamine was. then added, and cooling continued to a temperature of about 200 F. The resulting grease composition was milled through a Gaulin homogenizer and filtered.
- Grease H A grease was prepared from the following ingredients:
- the methyl 12-hydroxy stearate and the mineral oil were charged to a fire heated kettle and warmed while mixing to F.
- a 20% aqueous boiling water solution of the lithium monohydrate was then added and the grease heated to 400 F.
- the fluid grease was cooled while stirring to 350 F. where the grease was just starting to solidify.
- the phenyl alpha naphthylamine was then added, and the grease drawn into pans for cooling.
- Greases I, J, K, L and M These greases were prepared by blending Greases G and H, separately prepared as described above, in accordance with the formulations listed in the table below at a temperature of 180 F.
- this invention relates to new and improved lubricating grease compositions comprising blends of l) soap-salt complex or mixed salt complex thickened greases having a high combined metal content and (2) lithium soap thickened greases.
- the blended grease compositions prepared in accordance with the invention have lubricating lives superior to the individual lithium soap thickened greases and a water resistance superior to the individual complex thickened greases.
- Blends containing from about 20' The invention is not necessarily limited to the specific conditions and materials of the foregoing example. These conditions and materials may be varied within the limits indicated in the general portions of the specification. Moreover, the conventional grease additives such as oxidation inhibitors, pour point depressors, corrosion inhibitors and the like can be effectively incorporated in the grease blends of this invention.
- a blended grease composition comprising a blend of two component greases, one component being a grease thickened with a calcium mixed salt complex of lowand intermediate molecular weight mono-carboxylic acids, wherein the mol ratio of low to intermediate weight acid is about 2:1 to 40:1, the other component being a lithium base grease thickened with the lithium soap of a highmolecular weight fatty acid, said blend consisting essentially of from 40 to 80% by Weight of the first component and 20 to by weight of the second component.
- blended grease composition of claim 1 wherein said blend consists essentially of from about 40 to 60% by weight of the first component and from about 40 to 60% by weight of'the second component.
- the blended grease composition of claim 1, wherein said calcium mixed salt complex is a mixed salt complex of a low molecular weight carboxylicacid having from 1 to 3 carbon atoms per molecule and an intermediate molecular weight carboxylic acid having from 7 to 10 carbon atoms per molecule.
- the blended grease composition of claim 1 wherein the first component is a grease thickened with the mixed salt complex of calcium acetate and calcium caprylate, and the second component is a lithium base grease thickened with lithium 12-hydroxystearate said blend consisting essentially of from about 40 to 60% by weight of the first component and 40 to 60% by weight of the second component.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL104990D NL104990C (cs) | 1955-04-28 | ||
BE546805D BE546805A (cs) | 1955-04-28 | ||
US504659A US2908645A (en) | 1955-04-28 | 1955-04-28 | Blended lithium calcium base grease |
GB9885/56A GB793484A (en) | 1955-04-28 | 1956-03-29 | Improved grease compositions |
FR1152678D FR1152678A (fr) | 1955-04-28 | 1956-04-18 | Graisses composées lubrifiantes |
DEE12287A DE1064667B (de) | 1955-04-28 | 1956-04-24 | Schmierfett und Verfahren zu seiner Herstellung |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US504659A US2908645A (en) | 1955-04-28 | 1955-04-28 | Blended lithium calcium base grease |
Publications (1)
Publication Number | Publication Date |
---|---|
US2908645A true US2908645A (en) | 1959-10-13 |
Family
ID=24007212
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US504659A Expired - Lifetime US2908645A (en) | 1955-04-28 | 1955-04-28 | Blended lithium calcium base grease |
Country Status (6)
Country | Link |
---|---|
US (1) | US2908645A (cs) |
BE (1) | BE546805A (cs) |
DE (1) | DE1064667B (cs) |
FR (1) | FR1152678A (cs) |
GB (1) | GB793484A (cs) |
NL (1) | NL104990C (cs) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3223633A (en) * | 1963-07-01 | 1965-12-14 | Exxon Research Engineering Co | Lubricant |
US3298953A (en) * | 1964-04-01 | 1967-01-17 | Exxon Research Engineering Co | Lubricants containing mixed metal salts of fatty acid and aromatic polybasic acid |
US3389085A (en) * | 1964-03-31 | 1968-06-18 | Exxon Research Engineering Co | Lubricants containing mixed metal salts of mono- and polybasic acids |
US5015403A (en) * | 1990-03-23 | 1991-05-14 | Shell Oil Company | Preparation of lithium-calcium grease compositions |
WO2015021052A1 (en) * | 2013-08-05 | 2015-02-12 | Sr Lubricant Solutions, Llc | Lubricant with spherical copper and bismuth powders |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL258842A (cs) * | 1959-12-11 | |||
DE2027403C2 (de) * | 1970-06-04 | 1983-12-15 | Exxon Research and Engineering Co., 07036 Linden, N.J. | Dauerschmierfett |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2397956A (en) * | 1943-01-15 | 1946-04-09 | Internat Lubricant Corp | Production of lubricants |
US2417428A (en) * | 1946-09-19 | 1947-03-18 | Union Oil Co | Lubricating composition |
US2641577A (en) * | 1951-06-22 | 1953-06-09 | Standard Oil Dev Co | Lithium-calcium lubricating grease composition |
US2844536A (en) * | 1954-04-30 | 1958-07-22 | Exxon Research Engineering Co | High temperature complex grease manufacturing processes |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2712527A (en) * | 1952-08-26 | 1955-07-05 | Exxon Research Engineering Co | Improved lubricating greases containing dihydroxy stearic acid soap |
-
0
- BE BE546805D patent/BE546805A/xx unknown
- NL NL104990D patent/NL104990C/xx active
-
1955
- 1955-04-28 US US504659A patent/US2908645A/en not_active Expired - Lifetime
-
1956
- 1956-03-29 GB GB9885/56A patent/GB793484A/en not_active Expired
- 1956-04-18 FR FR1152678D patent/FR1152678A/fr not_active Expired
- 1956-04-24 DE DEE12287A patent/DE1064667B/de active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2397956A (en) * | 1943-01-15 | 1946-04-09 | Internat Lubricant Corp | Production of lubricants |
US2417428A (en) * | 1946-09-19 | 1947-03-18 | Union Oil Co | Lubricating composition |
US2641577A (en) * | 1951-06-22 | 1953-06-09 | Standard Oil Dev Co | Lithium-calcium lubricating grease composition |
US2844536A (en) * | 1954-04-30 | 1958-07-22 | Exxon Research Engineering Co | High temperature complex grease manufacturing processes |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3223633A (en) * | 1963-07-01 | 1965-12-14 | Exxon Research Engineering Co | Lubricant |
US3389085A (en) * | 1964-03-31 | 1968-06-18 | Exxon Research Engineering Co | Lubricants containing mixed metal salts of mono- and polybasic acids |
US3298953A (en) * | 1964-04-01 | 1967-01-17 | Exxon Research Engineering Co | Lubricants containing mixed metal salts of fatty acid and aromatic polybasic acid |
US5015403A (en) * | 1990-03-23 | 1991-05-14 | Shell Oil Company | Preparation of lithium-calcium grease compositions |
WO2015021052A1 (en) * | 2013-08-05 | 2015-02-12 | Sr Lubricant Solutions, Llc | Lubricant with spherical copper and bismuth powders |
Also Published As
Publication number | Publication date |
---|---|
GB793484A (en) | 1958-04-16 |
FR1152678A (fr) | 1958-02-21 |
BE546805A (cs) | |
NL104990C (cs) | |
DE1064667B (de) | 1959-09-03 |
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