US20060019842A1 - Aluminum complex grease - Google Patents
Aluminum complex grease Download PDFInfo
- Publication number
- US20060019842A1 US20060019842A1 US11/214,649 US21464905A US2006019842A1 US 20060019842 A1 US20060019842 A1 US 20060019842A1 US 21464905 A US21464905 A US 21464905A US 2006019842 A1 US2006019842 A1 US 2006019842A1
- Authority
- US
- United States
- Prior art keywords
- aluminum
- compound
- complex grease
- aluminum complex
- aluminium
- 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.)
- Abandoned
Links
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 53
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 239000004519 grease Substances 0.000 title claims abstract description 24
- 239000002562 thickening agent Substances 0.000 claims abstract description 33
- -1 aluminium carboxylate compound Chemical class 0.000 claims abstract description 29
- 239000007788 liquid Substances 0.000 claims abstract description 20
- 150000001399 aluminium compounds Chemical class 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000002480 mineral oil Substances 0.000 claims description 11
- 235000010446 mineral oil Nutrition 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 5
- 239000003921 oil Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000007942 carboxylates Chemical group 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- 230000001965 increasing effect Effects 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims 1
- 239000004411 aluminium Substances 0.000 abstract description 31
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 15
- 229940042472 mineral oil Drugs 0.000 description 10
- 239000000654 additive Substances 0.000 description 8
- 150000001735 carboxylic acids Chemical class 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 229940077746 antacid containing aluminium compound Drugs 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- NVXKDTVBVPMPAL-UHFFFAOYSA-N 1,2,2-trimethylquinoline Chemical compound C1=CC=C2C=CC(C)(C)N(C)C2=C1 NVXKDTVBVPMPAL-UHFFFAOYSA-N 0.000 description 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- UUNBFTCKFYBASS-UHFFFAOYSA-N C(CCCCCCC)C=1C(=C(C=CC1)NC1=CC=CC=C1)CCCCCCCC Chemical compound C(CCCCCCC)C=1C(=C(C=CC1)NC1=CC=CC=C1)CCCCCCCC UUNBFTCKFYBASS-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-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
- 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 1
- PEFNMPZKHOCMSW-UHFFFAOYSA-H [Al+3].[Al+3].[O-]O[O-].[O-]O[O-].[O-]O[O-] Chemical class [Al+3].[Al+3].[O-]O[O-].[O-]O[O-].[O-]O[O-] PEFNMPZKHOCMSW-UHFFFAOYSA-H 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000007866 anti-wear additive Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- YSIQDTZQRDDQNF-UHFFFAOYSA-L barium(2+);2,3-di(nonyl)naphthalene-1-sulfonate Chemical compound [Ba+2].C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1.C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1 YSIQDTZQRDDQNF-UHFFFAOYSA-L 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KDQZPXCKTHKGQM-UHFFFAOYSA-L bis(dipentylcarbamothioylsulfanyl)lead Chemical compound [Pb+2].CCCCCN(C([S-])=S)CCCCC.CCCCCN(C([S-])=S)CCCCC KDQZPXCKTHKGQM-UHFFFAOYSA-L 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- GBHRVZIGDIUCJB-UHFFFAOYSA-N hydrogenphosphite Chemical compound OP([O-])[O-] GBHRVZIGDIUCJB-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- PKPWVTWTIKKOMC-UHFFFAOYSA-M oxoalumanyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[Al]=O PKPWVTWTIKKOMC-UHFFFAOYSA-M 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- OGHBATFHNDZKSO-UHFFFAOYSA-N propan-2-olate Chemical compound CC(C)[O-] OGHBATFHNDZKSO-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000003039 volatile agent 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
- C10M123/00—Lubricating compositions characterised by the thickener being a mixture of two or more compounds covered by more than one of the main groups C10M113/00 - C10M121/00, each of these compounds being essential
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/069—Aluminium compounds without C-aluminium linkages
-
- 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
- C10M115/00—Lubricating compositions characterised by the thickener being a non-macromolecular organic compound other than a carboxylic acid or salt thereof
- C10M115/04—Lubricating compositions characterised by the thickener being a non-macromolecular organic compound other than a carboxylic acid or salt thereof containing oxygen
-
- 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
- C10M117/00—Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof
- C10M117/02—Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof having only one carboxyl group bound to an acyclic carbon atom, cycloaliphatic carbon atom or hydrogen
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
-
- 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
- C10M2207/006—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions used as thickening agents
-
- 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
- C10M2207/0206—Hydroxy compounds used as thickening agents
-
- 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
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/027—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
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/0413—Ethers; Acetals; Ortho-esters; Ortho-carbonates used as thickening agent
-
- 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
- C10M2207/09—Metal enolates, i.e. keto-enol metal complexes
- C10M2207/095—Metal enolates, i.e. keto-enol metal complexes used as thickening agent
-
- 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
- C10M2207/1225—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 used as thickening agent
-
- 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
- C10M2207/125—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
-
- 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
- C10M2207/125—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
- C10M2207/126—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 monocarboxylic
- C10M2207/1265—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 monocarboxylic used as thickening agent
-
- 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
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more 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
- C10M2207/16—Naphthenic acids
- C10M2207/166—Naphthenic acids used as thickening agents
-
- 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
- C10M2207/18—Tall oil acids
- C10M2207/186—Tall oil acids used as thickening agents
-
- 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
- C10M2207/20—Rosin acids
- C10M2207/206—Rosin acids used as thickening agents
-
- 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
- C10M2207/24—Epoxidised acids; Ester derivatives thereof
- C10M2207/246—Epoxidised acids; Ester derivatives thereof used as thickening agents
-
- 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
- C10N2010/06—Groups 3 or 13
Definitions
- This invention relates to a thickener component based on an aluminium carboxylate compound and to an aluminium complex grease made therefrom with addition of a base liquid.
- Aluminium complex greases have been known. They essentially comprise a mineral-oil base liquid and a thickener system containing one or more aluminium carboxylate compounds.
- the aluminium carboxylate compound is obtained by reacting a fatty acid and/or an aromatic carboxylic acid with an aluminium alcoholate derivative.
- the industrially used aluminium alcoholates comprise aluminium isopropoxylate and tri-oxy-aluminium-triisopropoxide. In theory, the reaction proceeds as shown hereinbelow:
- Aluminium complex greases are distinguished by a high dropping point, good conveyance and water resistance, and low separation of oil.
- the term ‘more effective’ shall mean that the grease exhibits better lubricating properties than conventional aluminium complex greases.
- the thickener component employed for making said aluminium complex greases be storable and marketable as such, thus enabling the grease manufacturer to produce the thickener-containing grease himself.
- hydrolysable aluminium compounds refers to aluminium compounds that are capable of forming aluminium-oxygen bonds by the action of protondonating compounds, such as water or organic acids.
- hydrolysable aluminium compounds are aluminium alcoholate- or aluminium-oxo-alcoholate compounds with the alcoholate group preferably being a C 2 - to C 4 -alcohol, particularly isopropanolate.
- the carboxylic acids can be branched or unbranched aliphatic monocarboxylic acids of the type R 1 —COOH, wherein R 1 represents a C 10 - to C 40 -radical, preferably a C 14 - to C 24 -radical, or a C 16 - to C 24 -radical.
- Carboxylic acid derivatives as used herein are defined as compounds which are capable of forming in combination with said aluminium compounds the aluminium-carboxylate bonds that would likewise be obtained when using the corresponding acids. Examples thereof include the anhydrides, acid chlorides, or amides of the aforesaid carboxylic acids.
- Ester compounds as used herein particularly refer to compounds which may be formed by reaction of the alcohols/alcoholates present in the reaction mixture with the carboxylic acids/carboxylate residues.
- the thickener component is prepared by reaction, preferably about equimolar reaction, i.e. about 1 mole of monocarboxylic acid per mole of aluminium atoms in the compound, of a hydrolysable aluminium compound with one or more of the abovementioned carboxylic acid(s) or carboxylic acid derivative(s) at a temperature not exceeding 145° C., most preferably 135° C., with a temperature profile most preferably increasing gradually by at least 20° C. during a period of at least 90 minutes being ensured. It is preferred that the hydrolysable aluminium compound be placed in the vessel first.
- reaction be carried out in a base liquid and the volatile compound released during the reaction, e.g. alcohol, be withdrawn from the equilibrium.
- volatile compound released during the reaction e.g. alcohol
- thickener as used herein is defined as a compound or mixture of compounds prepared from the thickener component, which thickener can be produced by reacting the thickener component with aromatic or cyclic monocarboxylic acids of the type R 2 —COOH, wherein R 2 represents a C 6 - to C 16 -radical, or with the derivatives thereof.
- aromatic or cyclic monocarboxylic acids of the type R 2 —COOH, wherein R 2 represents a C 6 - to C 16 -radical, or with the derivatives thereof.
- Said (aromatic or cyclic) carboxylic acid derivatives are defined as described hereinabove.
- aromatic monocarboxylic acid is defined as a carboxylic acid which has at least one benzene ring or condensed benzene ring and, in addition, may comprise aliphatic hydrocarbon radicals as well.
- compounds such as C 6 H 5 —CH 2 —CH 2 —. COOH or CH 3 —CH 2 —C 6 H 4 —COOH are explicitly included herein.
- the thickener as a constituent of the aluminium complex grease is produced by compounding the thickener component, optionally taken up in additional base liquid, with the aromatic or cyclic monocarboxylic acid.
- the production process of the invention ‘yields a raw material (thickener component) with a low ester content for making the real thickener that keeps its low ester content even upon storage.
- the aluminium complex greases of the invention also comprise a base liquid which is a hydrocarbon compound and/or a synthetic oil added to the overall composition in quantities of from 30 to 98 weight percent, preferably 60 to 95 weight percent.
- the hydrocarbon compound can be a paraffin-base or naphthenic mineral oil, a polyalphaolefin, or a white oil.
- Further synthetic oils which are suitable as base liquid include fatty acid esters based on mono- or multifunctional fatty acids having a chain length of from 8 to 24 carbon atoms and mono- or polyhydric alcohols. Additional constituents of the aluminium complex greases of the invention may be typical additives. Table 1 presents examples of suitable additives.
- the thickener components of the invention are useful as raw materials for producing thickeners included in aluminium complex greases exhibiting improved lubricating properties. They are preferably employed in high-temperature applications for which high dropping points are especially desirable, in central lubricators, and/or for lubricating machinery used for example for producing or processing foodstuffs.
- the thickener components as well contain 20 to 80 weight percent, most preferably 30 to 70 weight percent of the base liquid described hereinabove.
- Example 4 presents a high ester concentration, whereas the ester concentration in Example 5 (comparative example) is too high.
- the measurements were made on a thickener component having an aluminium content of 4.1 weight percent.
- the solvent in the aluminium-containing thickener component is identical with the base oil.
- the starting material is aluminium isopropanolate.
- the aliphatic monocarboxylic acid employed herein is a technical-grade stearic acid mixture.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Lubricants (AREA)
Abstract
This invention relates to a thickener component based on an aluminium carboxylate compound and to an aluminium complex grease made therefrom with addition of a base liquid.
Description
- This application is a divisional of U.S. patent application Ser. No. 10/221,336 filed on Feb. 03, 2003, for Thickener Component and Aluminum Complex Grease, the disclosure of which is incorporated herein by reference.
- 1. Field of the Invention
- This invention relates to a thickener component based on an aluminium carboxylate compound and to an aluminium complex grease made therefrom with addition of a base liquid.
- 2. Description of the Prior Art
- Aluminium complex greases have been known. They essentially comprise a mineral-oil base liquid and a thickener system containing one or more aluminium carboxylate compounds. The aluminium carboxylate compound is obtained by reacting a fatty acid and/or an aromatic carboxylic acid with an aluminium alcoholate derivative. The industrially used aluminium alcoholates comprise aluminium isopropoxylate and tri-oxy-aluminium-triisopropoxide. In theory, the reaction proceeds as shown hereinbelow:
- When using aluminium isopropoxylate, partial hydrolysis is performed with water before, during, or after reaction of the acids with aluminium alcoholate to produce the usually required free -OH group on the aluminium. Aluminium complex greases are distinguished by a high dropping point, good conveyance and water resistance, and low separation of oil.
- It is an object of this invention to provide more effective aluminium complex greases, in particular more suitable thickener components for manufacturing thickeners for aluminium complex greases. The term ‘more effective’ shall mean that the grease exhibits better lubricating properties than conventional aluminium complex greases. Furthermore, it is desired that the thickener component employed for making said aluminium complex greases be storable and marketable as such, thus enabling the grease manufacturer to produce the thickener-containing grease himself.
- According to this invention, the problem has been resolved by providing a thickener component comprising
-
- (A) from 99.99 to 94 weight percent, preferably 99.9 to 97 weight percent of an aluminium compound which can be prepared by reacting a hydrolysable aluminium compound with one or more aliphatic monocarboxylic acid(s) or aliphatic derivatives thereof, optionally in the presence of water and/or a C1- to C40-alcohol, thereby forming one or more aluminium compound(s) having at least one aluminium carboxylate bond per aluminium atom and, in addition, one or more aluminium-, hydroxy-, aluminium alcoholate-, and/or aluminium-oxygen-aluminium bond(s) and
- (B) from 0.01 to 6 weight percent, preferably 0.1 to 3 weight percent of an ester compound having from 6 to 60 carbon atoms,
each referring to the total of components (A) and (B).
- The term ‘hydrolysable aluminium compounds’ as used herein refers to aluminium compounds that are capable of forming aluminium-oxygen bonds by the action of protondonating compounds, such as water or organic acids. Preferably, such hydrolysable aluminium compounds are aluminium alcoholate- or aluminium-oxo-alcoholate compounds with the alcoholate group preferably being a C2- to C4-alcohol, particularly isopropanolate. The carboxylic acids can be branched or unbranched aliphatic monocarboxylic acids of the type R1—COOH, wherein R1 represents a C10- to C40-radical, preferably a C14- to C24-radical, or a C16- to C24-radical.
- Carboxylic acid derivatives as used herein are defined as compounds which are capable of forming in combination with said aluminium compounds the aluminium-carboxylate bonds that would likewise be obtained when using the corresponding acids. Examples thereof include the anhydrides, acid chlorides, or amides of the aforesaid carboxylic acids.
- Ester compounds as used herein particularly refer to compounds which may be formed by reaction of the alcohols/alcoholates present in the reaction mixture with the carboxylic acids/carboxylate residues.
- The thickener component is prepared by reaction, preferably about equimolar reaction, i.e. about 1 mole of monocarboxylic acid per mole of aluminium atoms in the compound, of a hydrolysable aluminium compound with one or more of the abovementioned carboxylic acid(s) or carboxylic acid derivative(s) at a temperature not exceeding 145° C., most preferably 135° C., with a temperature profile most preferably increasing gradually by at least 20° C. during a period of at least 90 minutes being ensured. It is preferred that the hydrolysable aluminium compound be placed in the vessel first.
- Moreover, it is preferred that the reaction be carried out in a base liquid and the volatile compound released during the reaction, e.g. alcohol, be withdrawn from the equilibrium.
- The term ‘thickener’ as used herein is defined as a compound or mixture of compounds prepared from the thickener component, which thickener can be produced by reacting the thickener component with aromatic or cyclic monocarboxylic acids of the type R2—COOH, wherein R2 represents a C6- to C16-radical, or with the derivatives thereof. Said (aromatic or cyclic) carboxylic acid derivatives are defined as described hereinabove.
- The resultant aluminium compound preferably has more than 40 mole % of aliphatic monocarboxylic acid radicals, referring to the amount of carboxylate groups (100 mole %=all the carboxylate groups). The remainder is comprised of aromatic or cyclic monocarboxylic acid radicals. As used herein, the term ‘aromatic monocarboxylic acid’ is defined as a carboxylic acid which has at least one benzene ring or condensed benzene ring and, in addition, may comprise aliphatic hydrocarbon radicals as well. Hence, compounds such as C6H5—CH2—CH2—. COOH or CH3—CH2—C6H4—COOH are explicitly included herein.
- The thickener as a constituent of the aluminium complex grease is produced by compounding the thickener component, optionally taken up in additional base liquid, with the aromatic or cyclic monocarboxylic acid.
- The production process of the invention ‘yields a raw material (thickener component) with a low ester content for making the real thickener that keeps its low ester content even upon storage.
- Besides the thickeners of the invention the aluminium complex greases of the invention also comprise a base liquid which is a hydrocarbon compound and/or a synthetic oil added to the overall composition in quantities of from 30 to 98 weight percent, preferably 60 to 95 weight percent.
- The hydrocarbon compound can be a paraffin-base or naphthenic mineral oil, a polyalphaolefin, or a white oil. Further synthetic oils which are suitable as base liquid include fatty acid esters based on mono- or multifunctional fatty acids having a chain length of from 8 to 24 carbon atoms and mono- or polyhydric alcohols. Additional constituents of the aluminium complex greases of the invention may be typical additives. Table 1 presents examples of suitable additives.
- The thickener components of the invention are useful as raw materials for producing thickeners included in aluminium complex greases exhibiting improved lubricating properties. They are preferably employed in high-temperature applications for which high dropping points are especially desirable, in central lubricators, and/or for lubricating machinery used for example for producing or processing foodstuffs.
- The prior art thickeners based on aluminium carboxylate compounds or the aluminium complex greases made therefrom have significantly higher ester concentrations. Surprisingly, compositions with lower ester concentrations, preferably less than 6 % in the thickener component, and improved lubricating properties have now become accessible by the process.
- It is preferred that the thickener components as well contain 20 to 80 weight percent, most preferably 30 to 70 weight percent of the base liquid described hereinabove.
- Examples of Tests
- Table 2 shows the rheometric values (Physica UDS 200, oscillating measurement, deformation=0.2%, frequency=0.1 Hz, temperature 20° C., plate/plate distance=1 mm) of aluminium complex greases of the invention. Example 4 presents a high ester concentration, whereas the ester concentration in Example 5 (comparative example) is too high. The measurements were made on a thickener component having an aluminium content of 4.1 weight percent. The solvent in the aluminium-containing thickener component is identical with the base oil. The starting material is aluminium isopropanolate. The aliphatic monocarboxylic acid employed herein is a technical-grade stearic acid mixture.
- Exemplary Synthesis
- Into a 5-litre agitated vessel equipped with a nitrogen supply line, a 30-cm column (metalized, packed with Raschig rings), and a reflux condenser there are placed 1.466 moles (299.5 g) of DOROX® D 10 (aluminium triisopropylate, liquid) and 500.0 g of Sera® 100 mineral oil (approx. 50 wt. % paraffin-base oil). The educts are heated to 97° C. (bottom temperature) while stirring. The stearic acid is heated to 75-80° C. to keep the product liquid upon feeding. 1.466 moles (393.5 g) of the liquid stearic acid (acid number=209 mg of KOH/g) and the mixture of water (1.372 moles=24.7 g) and 2-propanol (123.6 g) are charged steadily and simultaneously through separate submerged pipes during a period of 2.5 hours. The released 2-propanol is removed overhead (head temperature max. 85° C.). The bottom temperature is gradually increased to 127° C. during this period. Once the bottom temperature reaches 127° C., the pressure is reduced to 200 hPa during 20 minutes and the remainder of the low-boiling 2-propanol is drawn off. During the reaction a distillate comprised of 3.623 moles (217.7 g) of 2-propanol is removed from the reaction and the mixture (123.6 g). The product, oxo-aluminium-stearate, is obtained after purification and filtration. The total residence time of the product at 127° C. is 30 minutes (until end of vacuum phase). Filtration is performed at approx. 120° C. using a 60-μm sieve.
- The material parameters of the thickener component have been compiled in Table 3.
TABLE 1 Concentration Range, wt. % Extreme-pressure 2-10 dibenzyldisulfide with additives chlorinated paraffins; sulphurized fatty oils or terpenes Additives for enhancing 0.1-5 diisopropyl- or dilauryl film resistance hydrogen phosphite Rust-inhibiting additives 0.5-5 sodium petroleum sulfo- nates or barium dinonyl naphthalene sulfonate Copper deactivators 0.05-1 2-mercaptobenzthiazol Viscosity index improvers 0.1-1 polymethacrylates Desludgers 0.001 silicone oils Additives for producing 0.5-2 polymers ropiness Antiwear additives 0.1-2 tricresylic phosphate, zinc dialkyl dithio- phosphate Additives for producing 0.1-2 oil- or other vegetable water resistance fatty acids Deodorants 0.05-0.5 perfumes Anticorrosion additives 0.5-3 nonylphenoxy vinegar, ethylenediamine sulfonate, lead dinonylnaphthyl sul- fonate, barium sulfo- nates, lead- and zinc naphthenates Oxidation inhibitors diphenylamine, phenyl- α-naphthylamine, di- octyldiphenylamine, phenothiazine, poly- meric trimethyldi- hydroquinoline, 2,6- di-tert-butyl-4- methylphenol, lead diamyldithiocarbamate, dilaurylthiodipro- pionate-1/citric acid, ascorbic acid -
TABLE 2 Base Liquid Ester Concen- Base Liquid Thickener Base Liquid Concentra- tration in Concentration Component Benzoic Acid Viscosity tion in Thickener in Thickener Concentration Concentration Modulus of Modulus of at 40° C. Grease Component Component in Grease in Grease Elasticity Viscosity No. Base Liquid mm2/s wt. % wt. % wt. % wt. % wt. % Pa Pa 1 Paraffin- 100 91.3 1.4 60 7.3 1.4 860 330 based mineral oil 2 Paraffin- 100 87.1 1.4 60 10.9 2.0 5,720 1,030 based mineral oil 3 Paraffin- 100 82.8 1.4 60 14.5 2.7 35,100 5,400 based mineral oil 4 Paraffin- 100 87.1 3.9 60 10.9 2.0 1,100 270 based mineral oil 5 Paraffin- 100 87.1 8.7 60 10.9 2.0 800 170 based mineral oil 6 Naphthene- 100 87.1 1.2 50 10.9 2.0 5,820 1,000 based mineral oil 7 Naphthene- 40 87.1 1.2 50 10.9 2.0 2,680 450 based mineral oil 8 Polyalpha- 30 91.3 2.4 60 7.3 1.4 290 60 olefin 9 Polyalpha- 30 87.1 2.4 60 10.9 2.0 2,100 290 olefin 10 Polyalpha- 30 82.8 2.4 60 14.5 2.7 13,300 1,100 olefin -
TABLE 3 Method Al content 4.1% M 635 Turbidity 20 FNU DIN 38404 T2 Viscosity(25° C.) 1,500 mPa · s DIN 53015 Viscosity (100° C.) 100 mPa · s Rotation (200s−1) Pour point 16° C. DIN ISO 3016 2-Propanol concentration 3.5% Density (20° C.) 0.94 g/cm3 DIN 51757 Density (40° C.) 0.93 g/cm3 DIN 51757 Density (50° C.) 0.93 g/cm3 DIN 51757 Flash point 190° C. DIN 51758 Colour number 10 DIN 6162
Claims (12)
1-8. (canceled)
9. An aluminum complex grease comprising
a compound or compound mixture obtainable by reacting an ester thickener component with at least one aromatic and/or cyclic monocarboxylic acid, of the type R1—COOH, wherein R1 is a C6 to C16 organic moiety, and/or their derivatives and
a base liquid selected from the group consisting of hydrocarbon compounds, synthetic oils and mixtures thereof, said base liquid being present in the grease in an amount of from 30 to 98 weight percent
wherein the thickener component comprises
(A) from 99.99 to 94 weight percent of an aluminum compound obtainable by an approximately equimolar reaction of a hydrolysable aluminum compound with at least one aliphatic monocarboxylic acid or derivatives thereof, in the presence of water and a C1- to C40-alcohol to form one or more aluminum compound(s) having on average one aluminum carboxylate bond per aluminum atom and, in addition, one or more aluminum-hydroxy, aluminum-alcoholate, or aluminum-oxygen-aluminum bond(s) and
(B) from 0.01 to 6 weight percent of an ester compound having from 6 to 60 carbon atoms,
the weight percentage referring to the total of components (A) and (B).
10. An aluminum complex grease of claim 9 , characterized in that the hydrolysable aluminum compound is an aluminum-alcoholate or aluminum-oxo-alcoholate compound.
11. An aluminum complex grease according to claim 9 , characterized in that the base liquid has a viscosity of from 20 to 200 mm2/s at 40° C. measured in accordance with DIN 51562.
12. An aluminum complex grease according to claim 9 , characterized in that the base liquid is a mineral oil with a boiling point of greater than 250° C.
13. An aluminum complex grease according to claim 9 , wherein the base liquid is present in an amount of from 60 to 95 weight percent.
14. An aluminum complex grease according to claim 9 , characterized in that said aliphatic monocarboxylic acid is selected from the group consisting of branched or unbranched aliphatic monocarboxylic acids of the type R2—COOH, wherein R2 is a C10- to C40-radical, or a derivative thereof.
15. An aluminum complex grease according to claim 14 , wherein said R2 is a C14- to C24-radical.
16. An aluminum complex grease according to claim 9 , characterized in that a temperature of 145° C. is not exceeded during the preparation of the aluminum thickener compound by reacting said hydrolysable aluminum compound with said carboxylic acid or said carboxylic acid derivative.
17. An aluminum complex grease of claim 16 , wherein the temperature does not exceeded 135° C.
18. An aluminum complex grease according to any one of claims 16 and 17, characterized in that an increasing temperature profile presenting a temperature difference of at least 20° C. is maintained at a time interval of at least 90 min during the reaction.
19. An aluminum complex grease according to claim 9 , wherein the aluminium compound/compound mixture of the aluminum complex grease obtained has more than 40 mol % of aliphatic monocarboxylic acid radicals, referring to the amount of carboxylate groups, the reminder being aromatic and/or cyclic monocarboxylic acid radicals.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/214,649 US20060019842A1 (en) | 2000-03-10 | 2005-08-30 | Aluminum complex grease |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10011333A DE10011333A1 (en) | 2000-03-10 | 2000-03-10 | Thickener component used for a lubricating grease contains an aluminum compound and an ester compound |
DE10011333.8 | 2000-03-10 | ||
US10/221,336 US20040097381A1 (en) | 2000-03-10 | 2001-03-06 | Thickener component and lubricating grease containing an aluminium complex |
PCT/DE2001/000829 WO2001066675A2 (en) | 2000-03-10 | 2001-03-06 | Thickener component and lubricating grease containing an aluminium complex |
US11/214,649 US20060019842A1 (en) | 2000-03-10 | 2005-08-30 | Aluminum complex grease |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/221,336 Division US20040097381A1 (en) | 2000-03-10 | 2001-03-06 | Thickener component and lubricating grease containing an aluminium complex |
PCT/DE2001/000829 Division WO2001066675A2 (en) | 2000-03-10 | 2001-03-06 | Thickener component and lubricating grease containing an aluminium complex |
Publications (1)
Publication Number | Publication Date |
---|---|
US20060019842A1 true US20060019842A1 (en) | 2006-01-26 |
Family
ID=7634001
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/221,336 Abandoned US20040097381A1 (en) | 2000-03-10 | 2001-03-06 | Thickener component and lubricating grease containing an aluminium complex |
US11/214,649 Abandoned US20060019842A1 (en) | 2000-03-10 | 2005-08-30 | Aluminum complex grease |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/221,336 Abandoned US20040097381A1 (en) | 2000-03-10 | 2001-03-06 | Thickener component and lubricating grease containing an aluminium complex |
Country Status (4)
Country | Link |
---|---|
US (2) | US20040097381A1 (en) |
EP (1) | EP1268718B1 (en) |
DE (2) | DE10011333A1 (en) |
WO (1) | WO2001066675A2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7288506B2 (en) * | 2002-11-27 | 2007-10-30 | Baker Hughes Incorporated | Aluminum carboxylate drag reducers for hydrocarbon emulsions |
CN100540640C (en) * | 2006-01-25 | 2009-09-16 | 李政兆 | A kind of diesel car lubricant composition |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2768138A (en) * | 1952-10-18 | 1956-10-23 | California Research Corp | Complex basic aluminum soap greases |
US3345291A (en) * | 1963-12-17 | 1967-10-03 | Chevron Res | Production of complex basic aluminum soap greases |
US3591505A (en) * | 1968-06-18 | 1971-07-06 | Sun Oil Co | Aluminum complex soap greases |
US3620975A (en) * | 1968-07-03 | 1971-11-16 | Sun Oil Co | Mixed complex aluminum soap-clay grease composition |
US3791972A (en) * | 1972-01-13 | 1974-02-12 | Southwest Petro Chem Inc | Lubricating grease |
US5075473A (en) * | 1989-05-03 | 1991-12-24 | Komaromi Koolajipari V. | Process for the preparation of aluminum oxide carboxylate polymers containing at most two percent by weight of ester |
US5358664A (en) * | 1992-10-15 | 1994-10-25 | Caschem, Inc. | Gelled oil compositions |
US5387351A (en) * | 1993-05-18 | 1995-02-07 | Kumar; Anoop | Lubricating grease composition and process for preparing same |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0029589B1 (en) * | 1979-11-23 | 1984-07-04 | Chattem, Inc. | Process for making grease compositions |
GB2269169A (en) * | 1992-07-24 | 1994-02-02 | Rhone Poulenc Chemicals | Aluminium complexes useful for cross-linking coating compositions |
-
2000
- 2000-03-10 DE DE10011333A patent/DE10011333A1/en not_active Withdrawn
-
2001
- 2001-03-06 EP EP01929230A patent/EP1268718B1/en not_active Expired - Lifetime
- 2001-03-06 US US10/221,336 patent/US20040097381A1/en not_active Abandoned
- 2001-03-06 DE DE50106204T patent/DE50106204D1/en not_active Expired - Lifetime
- 2001-03-06 WO PCT/DE2001/000829 patent/WO2001066675A2/en active IP Right Grant
-
2005
- 2005-08-30 US US11/214,649 patent/US20060019842A1/en not_active Abandoned
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2768138A (en) * | 1952-10-18 | 1956-10-23 | California Research Corp | Complex basic aluminum soap greases |
US3345291A (en) * | 1963-12-17 | 1967-10-03 | Chevron Res | Production of complex basic aluminum soap greases |
US3591505A (en) * | 1968-06-18 | 1971-07-06 | Sun Oil Co | Aluminum complex soap greases |
US3620975A (en) * | 1968-07-03 | 1971-11-16 | Sun Oil Co | Mixed complex aluminum soap-clay grease composition |
US3791972A (en) * | 1972-01-13 | 1974-02-12 | Southwest Petro Chem Inc | Lubricating grease |
US5075473A (en) * | 1989-05-03 | 1991-12-24 | Komaromi Koolajipari V. | Process for the preparation of aluminum oxide carboxylate polymers containing at most two percent by weight of ester |
US5358664A (en) * | 1992-10-15 | 1994-10-25 | Caschem, Inc. | Gelled oil compositions |
US5387351A (en) * | 1993-05-18 | 1995-02-07 | Kumar; Anoop | Lubricating grease composition and process for preparing same |
Also Published As
Publication number | Publication date |
---|---|
EP1268718A2 (en) | 2003-01-02 |
EP1268718B1 (en) | 2005-05-11 |
DE10011333A1 (en) | 2001-09-20 |
WO2001066675A2 (en) | 2001-09-13 |
DE50106204D1 (en) | 2005-06-16 |
WO2001066675A3 (en) | 2002-06-27 |
US20040097381A1 (en) | 2004-05-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2843781C (en) | Synthetic ester-based lubricant compositions that exhibit improved oxidation stability and service life | |
EP0667389B1 (en) | Metal free hydraulic fluid with amine salt | |
JPH07103390B2 (en) | Lubricant additive | |
AU2018241897B2 (en) | Novel ester compounds, method for the production thereof and use thereof | |
US20210061750A1 (en) | Novel Ester Compounds, Method for the Production Thereof and Use Thereof | |
EP0193870A2 (en) | Cold rolling mill lubricant and method of manufacturing steel sheets | |
JP2002530476A (en) | Soluble complex alcohol ester compound and composition | |
CN102234555B (en) | Synthetic ester lubricant base oil and preparation method thereof | |
US20030104956A1 (en) | Synthetic lubricant base stock formed from high content branched chain acid mixtures | |
EP0518567B1 (en) | Synthetic lubricant base stock formed from high content branched chain acid mixtures | |
JPH0284494A (en) | Manufacture of concentrated additive used in lubricating oil | |
US20080317964A1 (en) | High Temperature Lubricant Compositions and Methods of Making the Same | |
JPH08183974A (en) | Oligoester and lubricating base oil comprising or containingsame | |
US20060019842A1 (en) | Aluminum complex grease | |
EP1051465B1 (en) | Biodegradable oleic estolide ester base stocks and lubricants | |
CN111320542A (en) | Antioxidant containing double hindered phenol structure and preparation method thereof | |
FR3092112A1 (en) | LUBRICATING BASE OIL SYNTHETIZED FROM POLYOL ESTERS AND FATTY ACIDS BIOSOURCES | |
EP0141643B1 (en) | Lubricating oil with corrosion inhibitor | |
US3822284A (en) | 1-and 3-substituted (3,5-di-t-butyl-4-hydroxybenzyl)carbazole | |
US3260672A (en) | Synthetic ester lubricating oil containing certain haloalkyl carboxylic acid esters | |
EP0039998A1 (en) | Lubricating oil composition containing sediment-reducing additive | |
US4260501A (en) | Lubricant compositions containing antioxidant mixtures comprising substituted thiazoles and substituted thiadiazole compounds | |
EP0004957A2 (en) | Compositions and use of chlorinated derivatives of butyric acid as additives for lubricants | |
JPH1081890A (en) | Heat-resistant lubricating oil composition | |
EP0639634A1 (en) | Colloidal products containing calcium and/or magnesium as well as sulfur and nitrogen, their preparation and their use, especially as additives for lubricants |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: SASOL GERMANY GMBH, GERMANY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:FINMANS, PETER;DIBLITZ, CHRISTINA;ALLMULLER, FRANK;AND OTHERS;REEL/FRAME:016942/0338;SIGNING DATES FROM 20021218 TO 20031218 |
|
AS | Assignment |
Owner name: SASOL SOLVENTS GERMANY GMBH, GERMANY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SASOL GERMANY GMBH;REEL/FRAME:021140/0424 Effective date: 20061129 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |