IL106285A - Grease compositions - Google Patents
Grease compositionsInfo
- Publication number
- IL106285A IL106285A IL10628593A IL10628593A IL106285A IL 106285 A IL106285 A IL 106285A IL 10628593 A IL10628593 A IL 10628593A IL 10628593 A IL10628593 A IL 10628593A IL 106285 A IL106285 A IL 106285A
- Authority
- IL
- Israel
- Prior art keywords
- sulfur
- grease
- grease composition
- phosphorus
- composition
- Prior art date
Links
- 239000004519 grease Substances 0.000 title claims abstract description 124
- 239000000203 mixture Substances 0.000 title claims abstract description 119
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 74
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 73
- 239000011593 sulfur Substances 0.000 claims abstract description 73
- 229910052751 metal Inorganic materials 0.000 claims abstract description 59
- 239000002184 metal Substances 0.000 claims abstract description 59
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 55
- 239000011574 phosphorus Substances 0.000 claims abstract description 55
- 239000000344 soap Substances 0.000 claims abstract description 53
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 52
- 150000001875 compounds Chemical class 0.000 claims abstract description 47
- 238000000034 method Methods 0.000 claims abstract description 29
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910052796 boron Inorganic materials 0.000 claims abstract description 15
- -1 C24 mono-carboxylic acid Chemical class 0.000 claims description 64
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 58
- 125000004432 carbon atom Chemical group C* 0.000 claims description 51
- 239000002585 base Substances 0.000 claims description 40
- 229910052739 hydrogen Inorganic materials 0.000 claims description 29
- 150000001412 amines Chemical class 0.000 claims description 28
- 239000001257 hydrogen Substances 0.000 claims description 28
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 27
- 229910052760 oxygen Inorganic materials 0.000 claims description 27
- 239000001301 oxygen Substances 0.000 claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 20
- 239000000194 fatty acid Substances 0.000 claims description 20
- 229930195729 fatty acid Natural products 0.000 claims description 20
- 150000004665 fatty acids Chemical class 0.000 claims description 19
- 239000000047 product Substances 0.000 claims description 17
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 125000002947 alkylene group Chemical group 0.000 claims description 15
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 12
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 12
- 230000002378 acidificating effect Effects 0.000 claims description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 7
- 125000001118 alkylidene group Chemical group 0.000 claims description 7
- 150000003973 alkyl amines Chemical class 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 5
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 229910052744 lithium Inorganic materials 0.000 claims description 4
- 230000003472 neutralizing effect Effects 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 claims 2
- 229940114069 12-hydroxystearate Drugs 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 150000002118 epoxides Chemical group 0.000 claims 1
- 150000003464 sulfur compounds Chemical class 0.000 abstract description 2
- 239000002253 acid Substances 0.000 description 37
- 150000007513 acids Chemical class 0.000 description 22
- 239000003921 oil Substances 0.000 description 22
- 235000019198 oils Nutrition 0.000 description 21
- 239000002562 thickening agent Substances 0.000 description 16
- 239000004215 Carbon black (E152) Substances 0.000 description 15
- 239000000654 additive Substances 0.000 description 15
- 229930195733 hydrocarbon Natural products 0.000 description 15
- 150000002430 hydrocarbons Chemical class 0.000 description 15
- 230000001050 lubricating effect Effects 0.000 description 14
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 150000002148 esters Chemical class 0.000 description 10
- 239000003925 fat Substances 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 9
- 239000000314 lubricant Substances 0.000 description 9
- 230000000996 additive effect Effects 0.000 description 8
- 150000002924 oxiranes Chemical class 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 150000003141 primary amines Chemical class 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
- 239000002199 base oil Substances 0.000 description 7
- XXUJMEYKYHETBZ-UHFFFAOYSA-N ethyl 4-nitrophenyl ethylphosphonate Chemical compound CCOP(=O)(CC)OC1=CC=C([N+]([O-])=O)C=C1 XXUJMEYKYHETBZ-UHFFFAOYSA-N 0.000 description 7
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 6
- QCJQWJKKTGJDCM-UHFFFAOYSA-N [P].[S] Chemical compound [P].[S] QCJQWJKKTGJDCM-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- FPLIHVCWSXLMPX-UHFFFAOYSA-M lithium 12-hydroxystearate Chemical compound [Li+].CCCCCCC(O)CCCCCCCCCCC([O-])=O FPLIHVCWSXLMPX-UHFFFAOYSA-M 0.000 description 6
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- 125000005842 heteroatom Chemical group 0.000 description 5
- 150000002440 hydroxy compounds Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 150000003335 secondary amines Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- AAIUWVOMXTVLRG-UHFFFAOYSA-N 8,8-dimethylnonan-1-amine Chemical compound CC(C)(C)CCCCCCCN AAIUWVOMXTVLRG-UHFFFAOYSA-N 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- UDSAIICHUKSCKT-UHFFFAOYSA-N bromophenol blue Chemical compound C1=C(Br)C(O)=C(Br)C=C1C1(C=2C=C(Br)C(O)=C(Br)C=2)C2=CC=CC=C2S(=O)(=O)O1 UDSAIICHUKSCKT-UHFFFAOYSA-N 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 125000000853 cresyl group Chemical group C1(=CC=C(C=C1)C)* 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000003879 lubricant additive Substances 0.000 description 3
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 230000008719 thickening Effects 0.000 description 3
- 150000005691 triesters Chemical class 0.000 description 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- 125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 235000015278 beef Nutrition 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000005265 dialkylamine group Chemical group 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 125000005456 glyceride group Chemical group 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- 239000010689 synthetic lubricating oil Substances 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- GOLAKLHPPDDLST-HZJYTTRNSA-N (9z,12z)-octadeca-9,12-dien-1-amine Chemical compound CCCCC\C=C/C\C=C/CCCCCCCCN GOLAKLHPPDDLST-HZJYTTRNSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- ZBUAAIKWLHWSPO-UHFFFAOYSA-N (Z)-20-aminoicos-11-en-1-ol Chemical compound OCCCCCCCCCCC=C/CCCCCCCCN ZBUAAIKWLHWSPO-UHFFFAOYSA-N 0.000 description 1
- YHLRMABUJXBLCK-LBCXAKKBSA-N (z)-methyl-oxido-[[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethylimino]azanium Chemical compound C\[N+]([O-])=N\CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O YHLRMABUJXBLCK-LBCXAKKBSA-N 0.000 description 1
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1 -dodecene Natural products CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- YDBHSDRXUCPTQQ-UHFFFAOYSA-N 1-methylcyclohexan-1-amine Chemical compound CC1(N)CCCCC1 YDBHSDRXUCPTQQ-UHFFFAOYSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical class C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- XDJWZONZDVNKDU-UHFFFAOYSA-N 1314-24-5 Chemical compound O=POP=O XDJWZONZDVNKDU-UHFFFAOYSA-N 0.000 description 1
- MCIKGVLBLIZYRY-UHFFFAOYSA-N 2-(hexylamino)ethanol Chemical compound CCCCCCNCCO MCIKGVLBLIZYRY-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
- BITAPBDLHJQAID-KTKRTIGZSA-N 2-[2-hydroxyethyl-[(z)-octadec-9-enyl]amino]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCN(CCO)CCO BITAPBDLHJQAID-KTKRTIGZSA-N 0.000 description 1
- GIACMWUKBLHAAG-UHFFFAOYSA-N 2-[hexyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCCCN(CCO)CCO GIACMWUKBLHAAG-UHFFFAOYSA-N 0.000 description 1
- NJWSNNWLBMSXQR-UHFFFAOYSA-N 2-hexyloxirane Chemical compound CCCCCCC1CO1 NJWSNNWLBMSXQR-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- KDTZBYPBMTXCSO-UHFFFAOYSA-N 2-phenoxyphenol Chemical class OC1=CC=CC=C1OC1=CC=CC=C1 KDTZBYPBMTXCSO-UHFFFAOYSA-N 0.000 description 1
- TWXCJZHSMRBNGO-UHFFFAOYSA-N 3-decoxypropan-1-amine Chemical compound CCCCCCCCCCOCCCN TWXCJZHSMRBNGO-UHFFFAOYSA-N 0.000 description 1
- JPNCZSADMGXVPA-UHFFFAOYSA-N 3-tridecoxypropan-1-amine Chemical compound CCCCCCCCCCCCCOCCCN JPNCZSADMGXVPA-UHFFFAOYSA-N 0.000 description 1
- APXVJJBVNYZEDD-UHFFFAOYSA-N 4-(3-chlorophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid Chemical compound CC(C)(C)OC(=O)NC(CC(O)=O)CC1=CC=CC(Cl)=C1 APXVJJBVNYZEDD-UHFFFAOYSA-N 0.000 description 1
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 241000766026 Coregonus nasus Species 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 101500021084 Locusta migratoria 5 kDa peptide Proteins 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C10M169/06—Mixtures of thickeners and additives
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- C10M137/10—Thio derivatives
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- 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
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- C10M2207/16—Naphthenic acids
- C10M2207/166—Naphthenic acids used as thickening agents
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- C10M2207/206—Rosin acids used as thickening agents
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- C10M2207/24—Epoxidised acids; Ester derivatives thereof
- C10M2207/246—Epoxidised acids; Ester derivatives thereof used as thickening agents
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- C10M2223/045—Metal containing thio derivatives
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- C10M2223/047—Thioderivatives not containing metallic elements
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
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- C10N2010/02—Groups 1 or 11
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C10N2010/00—Metal present as such or in compounds
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Edible Oils And Fats (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/911,833 US5256321A (en) | 1992-07-10 | 1992-07-10 | Grease compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL106285A0 IL106285A0 (en) | 1993-11-15 |
| IL106285A true IL106285A (en) | 1996-06-18 |
Family
ID=25430930
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL10628593A IL106285A (en) | 1992-07-10 | 1993-07-08 | Grease compositions |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US5256321A (de) |
| EP (1) | EP0580331B1 (de) |
| JP (1) | JPH06184584A (de) |
| CN (1) | CN1082100A (de) |
| AT (1) | ATE158015T1 (de) |
| AU (1) | AU658517B2 (de) |
| BR (1) | BR9302459A (de) |
| CA (1) | CA2100216A1 (de) |
| DE (1) | DE69313751T2 (de) |
| ES (1) | ES2109439T3 (de) |
| IL (1) | IL106285A (de) |
| MX (1) | MX201211B (de) |
| SG (1) | SG47440A1 (de) |
| TW (1) | TW276268B (de) |
| ZA (1) | ZA934958B (de) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5362409A (en) * | 1992-07-10 | 1994-11-08 | The Lubrizol Corporation | Grease compositions |
| JP3370829B2 (ja) * | 1995-04-21 | 2003-01-27 | 株式会社日立製作所 | 潤滑グリース組成物 |
| AU708775B2 (en) * | 1995-09-19 | 1999-08-12 | Lubrizol Corporation, The | Additive compositions for lubricants and functional fluids |
| US5693598A (en) * | 1995-09-19 | 1997-12-02 | The Lubrizol Corporation | Low-viscosity lubricating oil and functional fluid compositions |
| US5674820A (en) * | 1995-09-19 | 1997-10-07 | The Lubrizol Corporation | Additive compositions for lubricants and functional fluids |
| AU719520B2 (en) * | 1995-09-19 | 2000-05-11 | Lubrizol Corporation, The | Additive compositions for lubricants and functional fluids |
| US5858934A (en) * | 1996-05-08 | 1999-01-12 | The Lubrizol Corporation | Enhanced biodegradable vegetable oil grease |
| CN1042949C (zh) * | 1996-06-05 | 1999-04-14 | 中国石化兰州炼油化工总厂 | 润滑油组合物 |
| US5834407A (en) * | 1996-08-21 | 1998-11-10 | The Lubrizol Corporation | Lubricants and functional fluids containing heterocyclic compounds |
| US6001783A (en) * | 1997-03-24 | 1999-12-14 | The Lubrizol Corporation | Mixed polysulfides and lubricants and functional fluids containing the same |
| US6100226A (en) * | 1998-05-20 | 2000-08-08 | The Lubrizol Corporation | Simple metal grease compositions |
| US6063742A (en) * | 1999-03-01 | 2000-05-16 | The Lubrizol Corporation | Grease compositions |
| US7018958B2 (en) * | 2002-10-22 | 2006-03-28 | Infineum International Limited | Lubricating oil compositions |
| US20070238625A1 (en) * | 2006-04-06 | 2007-10-11 | Kaperick Joseph P | Grease Composition And Additive For Improving Bearing Life |
| EP2054363B1 (de) | 2006-07-27 | 2013-04-17 | F. Hoffmann-La Roche AG | Asymmetrische hydrierung von 1,1,1-trifluoraceton |
| MX2010001742A (es) | 2007-08-13 | 2010-03-10 | Hoffmann La Roche | Nuevos derivados de piperazina-amida. |
| CN102245570A (zh) | 2008-12-16 | 2011-11-16 | 弗·哈夫曼-拉罗切有限公司 | 制备吡咯烷-3-甲酸类的方法 |
| US20110040091A1 (en) | 2009-08-13 | 2011-02-17 | Stephan Bachmann | Process for the preparation of (r)-2-phenyl propionic acid derivatives |
| US20110054174A1 (en) | 2009-08-28 | 2011-03-03 | Stephan Bachmann | Process for the preparation of a glucokinase activator compound |
| JP5818075B2 (ja) * | 2011-07-22 | 2015-11-18 | 協同油脂株式会社 | 潤滑グリース組成物 |
| US9944879B2 (en) * | 2014-10-08 | 2018-04-17 | Afton Chemical Corporation | Phosphorous-containing compounds and uses thereof |
| KR101819132B1 (ko) | 2015-02-09 | 2018-01-16 | 가부시키가이샤 모레스코 | 윤활제 조성물과 그 이용 및 지방족 에테르 화합물 |
| CN113680535B (zh) * | 2021-08-24 | 2023-03-21 | 中南大学 | 一种烷基醚基二硫代磷酸盐捕收剂及其制备方法与应用 |
| WO2025122708A1 (en) | 2023-12-07 | 2025-06-12 | Chevron Phillips Chemical Company Lp | Pao-based-compositions for lubricant applications |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2802856A (en) * | 1953-09-08 | 1957-08-13 | Lubrizol Corp | Methods of preparing tri-esters of thiophosphoric acids |
| US3341633A (en) * | 1955-01-27 | 1967-09-12 | Lubrizol Corp | Reaction of o, o-dihydrocarbyl phosphorodithioic acids with epoxides |
| US2923682A (en) * | 1957-09-17 | 1960-02-02 | Exxon Research Engineering Co | Lubricating compositions containing mixed salts |
| US3033787A (en) * | 1959-08-11 | 1962-05-08 | Exxon Research Engineering Co | Mixed salt lubricant compositions having improved base oils |
| US3174931A (en) * | 1961-12-05 | 1965-03-23 | Sinclair Research Inc | Grease compositions |
| US3197405A (en) * | 1962-07-09 | 1965-07-27 | Lubrizol Corp | Phosphorus-and nitrogen-containing compositions and process for preparing the same |
| US3318807A (en) * | 1963-05-13 | 1967-05-09 | Texaco Inc | Lubricating greases containing finely divided inorganic metal salts and method of preparation therefor |
| US3389085A (en) * | 1964-03-31 | 1968-06-18 | Exxon Research Engineering Co | Lubricants containing mixed metal salts of mono- and polybasic acids |
| GB1345522A (de) * | 1970-05-21 | 1974-01-30 | ||
| JPS6014795B2 (ja) * | 1979-08-16 | 1985-04-16 | 日本精工株式会社 | リチウムコンプレツクスグリ−ス及びその製造法 |
| SU981350A1 (ru) * | 1981-05-26 | 1982-12-15 | Московский Ордена Октябрьской Революции И Ордена Трудового Красного Знамени Институт Нефтехимической И Газовой Промышленности Им.М.Губкина | Пластична смазка |
| US4961868A (en) * | 1983-01-10 | 1990-10-09 | Mobil Oil Corporation | Grease composition |
| US4582617A (en) * | 1983-08-03 | 1986-04-15 | Mobil Oil Corporation | Grease composition containing borated epoxide and hydroxy-containing soap grease thickener |
| US4600517A (en) * | 1984-08-22 | 1986-07-15 | Mobil Oil Corporation | Grease composition containing boronated alcohols, and hydroxy-containing thickeners |
| US4743386A (en) * | 1983-01-10 | 1988-05-10 | Mobil Oil Corporation | Grease compositions containing phenolic- or thio-amine borates and hydroxy-containing soap thickeners |
| US5084194A (en) * | 1984-03-07 | 1992-01-28 | Mobil Oil Corporation | Grease composition |
| US4780227A (en) * | 1984-08-22 | 1988-10-25 | Mobil Oil Corporation | Grease composition containing borated alkoxylated alcohols |
| US4536308A (en) * | 1984-10-01 | 1985-08-20 | Texaco Inc. | Lithium soap grease additive |
| US5068045A (en) * | 1985-08-27 | 1991-11-26 | Mobil Oil Corporation | Grease composition containing alkoxylated amide borates |
| US4828734A (en) * | 1985-08-27 | 1989-05-09 | Mobil Oil Corporation | Grease compositions containing borated oxazoline compounds and hydroxy-containing soap thickeners |
| US4781850A (en) * | 1985-08-27 | 1988-11-01 | Mobil Oil Corporation | Grease compositions containing borated catechol compounds and hydroxy-containing soap thickeners |
| US4655948A (en) * | 1985-08-27 | 1987-04-07 | Mobil Oil Corporation | Grease compositions containing borated catechol compounds and hydroxy-containing soap thickeners |
| US4752416A (en) * | 1986-12-11 | 1988-06-21 | The Lubrizol Corporation | Phosphite ester compositions, and lubricants and functional fluids containing same |
| US4828732A (en) * | 1987-05-20 | 1989-05-09 | Mobil Oil Corporation | Grease compositions comprising borated diols and hydroxy-containing thickeners |
| US4842752A (en) * | 1988-03-22 | 1989-06-27 | Conoco Inc. | Stable extreme pressure grease |
| US4897210A (en) * | 1988-07-12 | 1990-01-30 | Pennzoil Products Company | Lithium complex grease thickener and high dropping point thickened grease |
-
1992
- 1992-07-10 US US07/911,833 patent/US5256321A/en not_active Expired - Lifetime
-
1993
- 1993-07-03 TW TW82105310A patent/TW276268B/zh active
- 1993-07-06 AU AU41754/93A patent/AU658517B2/en not_active Ceased
- 1993-07-08 IL IL10628593A patent/IL106285A/en not_active IP Right Cessation
- 1993-07-08 MX MX9304125A patent/MX201211B/es not_active IP Right Cessation
- 1993-07-08 BR BR9302459A patent/BR9302459A/pt not_active IP Right Cessation
- 1993-07-09 CN CN93108162A patent/CN1082100A/zh active Pending
- 1993-07-09 ZA ZA934958A patent/ZA934958B/xx unknown
- 1993-07-09 CA CA002100216A patent/CA2100216A1/en not_active Abandoned
- 1993-07-09 AT AT93305393T patent/ATE158015T1/de not_active IP Right Cessation
- 1993-07-09 DE DE69313751T patent/DE69313751T2/de not_active Expired - Fee Related
- 1993-07-09 SG SG1996001412A patent/SG47440A1/en unknown
- 1993-07-09 ES ES93305393T patent/ES2109439T3/es not_active Expired - Lifetime
- 1993-07-09 EP EP93305393A patent/EP0580331B1/de not_active Expired - Lifetime
- 1993-07-12 JP JP5171926A patent/JPH06184584A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06184584A (ja) | 1994-07-05 |
| EP0580331A1 (de) | 1994-01-26 |
| MX201211B (es) | 2001-04-05 |
| SG47440A1 (en) | 1998-04-17 |
| TW276268B (en) | 1996-05-21 |
| BR9302459A (pt) | 1994-03-01 |
| IL106285A0 (en) | 1993-11-15 |
| EP0580331B1 (de) | 1997-09-10 |
| US5256321A (en) | 1993-10-26 |
| AU4175493A (en) | 1994-01-13 |
| CA2100216A1 (en) | 1994-01-11 |
| ATE158015T1 (de) | 1997-09-15 |
| ZA934958B (en) | 1994-02-01 |
| ES2109439T3 (es) | 1998-01-16 |
| AU658517B2 (en) | 1995-04-13 |
| DE69313751D1 (de) | 1997-10-16 |
| MX9304125A (es) | 1994-01-31 |
| CN1082100A (zh) | 1994-02-16 |
| DE69313751T2 (de) | 1998-02-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| RH | Patent void |