EP2307532B1 - Use as an antiwear hydraulic fluid composition - Google Patents
Use as an antiwear hydraulic fluid composition Download PDFInfo
- Publication number
- EP2307532B1 EP2307532B1 EP09803603.1A EP09803603A EP2307532B1 EP 2307532 B1 EP2307532 B1 EP 2307532B1 EP 09803603 A EP09803603 A EP 09803603A EP 2307532 B1 EP2307532 B1 EP 2307532B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- use according
- composition
- alkyl
- detergent additive
- hydraulic fluid
- 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.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims description 94
- 239000012530 fluid Substances 0.000 title claims description 83
- 239000003599 detergent Substances 0.000 claims description 85
- 239000000654 additive Substances 0.000 claims description 44
- 230000000996 additive effect Effects 0.000 claims description 38
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- 239000003921 oil Substances 0.000 claims description 26
- 239000003112 inhibitor Substances 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 150000005165 hydroxybenzoic acids Chemical class 0.000 claims description 15
- 239000002270 dispersing agent Substances 0.000 claims description 13
- 239000002199 base oil Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 150000007942 carboxylates Chemical class 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 8
- 230000005764 inhibitory process Effects 0.000 claims description 8
- 159000000007 calcium salts Chemical class 0.000 claims description 7
- 239000003995 emulsifying agent Substances 0.000 claims description 6
- 230000001050 lubricating effect Effects 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 5
- 238000007254 oxidation reaction Methods 0.000 claims description 5
- 239000006260 foam Substances 0.000 claims description 4
- 239000003607 modifier Substances 0.000 claims description 4
- 238000010998 test method Methods 0.000 claims description 4
- 230000000994 depressogenic effect Effects 0.000 claims description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 37
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 32
- -1 alkaline earth metal salt Chemical class 0.000 description 26
- 238000009472 formulation Methods 0.000 description 20
- 229910052751 metal Inorganic materials 0.000 description 20
- 239000002184 metal Substances 0.000 description 20
- 150000003839 salts Chemical class 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 15
- 229910052791 calcium Inorganic materials 0.000 description 14
- 239000011575 calcium Substances 0.000 description 14
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 13
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 11
- 239000002585 base Substances 0.000 description 11
- 229910052725 zinc Inorganic materials 0.000 description 11
- 239000011701 zinc Substances 0.000 description 11
- 239000007788 liquid Substances 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 5
- 235000006708 antioxidants Nutrition 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 5
- 239000002480 mineral oil Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 150000001340 alkali metals Chemical class 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229960001860 salicylate Drugs 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 4
- 239000004711 α-olefin Substances 0.000 description 4
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000004945 emulsification Methods 0.000 description 3
- 230000001804 emulsifying effect Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 150000003871 sulfonates Chemical class 0.000 description 3
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 description 2
- SZAQZZKNQILGPU-UHFFFAOYSA-N 2-[1-(2-hydroxy-3,5-dimethylphenyl)-2-methylpropyl]-4,6-dimethylphenol Chemical compound C=1C(C)=CC(C)=C(O)C=1C(C(C)C)C1=CC(C)=CC(C)=C1O SZAQZZKNQILGPU-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- ZMRQTIAUOLVKOX-UHFFFAOYSA-L calcium;diphenoxide Chemical compound [Ca+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 ZMRQTIAUOLVKOX-UHFFFAOYSA-L 0.000 description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-M carbamodithioate Chemical compound NC([S-])=S DKVNPHBNOWQYFE-UHFFFAOYSA-M 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000012990 dithiocarbamate Substances 0.000 description 2
- 150000002194 fatty esters Chemical class 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920013639 polyalphaolefin Polymers 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- HXKVLXJEOAAJSH-UHFFFAOYSA-L zinc;naphthalene-1-sulfonate Chemical compound [Zn+2].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1.C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HXKVLXJEOAAJSH-UHFFFAOYSA-L 0.000 description 2
- WJECKFZULSWXPN-UHFFFAOYSA-N 1,2-didodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1CCCCCCCCCCCC WJECKFZULSWXPN-UHFFFAOYSA-N 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- GSOYMOAPJZYXTB-UHFFFAOYSA-N 2,6-ditert-butyl-4-(3,5-ditert-butyl-4-hydroxyphenyl)phenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(C=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 GSOYMOAPJZYXTB-UHFFFAOYSA-N 0.000 description 1
- QHPKIUDQDCWRKO-UHFFFAOYSA-N 2,6-ditert-butyl-4-[2-(3,5-ditert-butyl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 QHPKIUDQDCWRKO-UHFFFAOYSA-N 0.000 description 1
- AKNMPWVTPUHKCG-UHFFFAOYSA-N 2-cyclohexyl-6-[(3-cyclohexyl-2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound OC=1C(C2CCCCC2)=CC(C)=CC=1CC(C=1O)=CC(C)=CC=1C1CCCCC1 AKNMPWVTPUHKCG-UHFFFAOYSA-N 0.000 description 1
- YFHKLSPMRRWLKI-UHFFFAOYSA-N 2-tert-butyl-4-(3-tert-butyl-4-hydroxy-5-methylphenyl)sulfanyl-6-methylphenol Chemical compound CC(C)(C)C1=C(O)C(C)=CC(SC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 YFHKLSPMRRWLKI-UHFFFAOYSA-N 0.000 description 1
- BGWNOSDEHSHFFI-UHFFFAOYSA-N 2-tert-butyl-4-[(3-tert-butyl-4-hydroxy-5-methylphenyl)methylsulfanylmethyl]-6-methylphenol Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CSCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 BGWNOSDEHSHFFI-UHFFFAOYSA-N 0.000 description 1
- PFANXOISJYKQRP-UHFFFAOYSA-N 2-tert-butyl-4-[1-(5-tert-butyl-4-hydroxy-2-methylphenyl)butyl]-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(CCC)C1=CC(C(C)(C)C)=C(O)C=C1C PFANXOISJYKQRP-UHFFFAOYSA-N 0.000 description 1
- MQWCQFCZUNBTCM-UHFFFAOYSA-N 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylphenyl)sulfanyl-4-methylphenol Chemical compound CC(C)(C)C1=CC(C)=CC(SC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O MQWCQFCZUNBTCM-UHFFFAOYSA-N 0.000 description 1
- BKZXZGWHTRCFPX-UHFFFAOYSA-N 2-tert-butyl-6-methylphenol Chemical compound CC1=CC=CC(C(C)(C)C)=C1O BKZXZGWHTRCFPX-UHFFFAOYSA-N 0.000 description 1
- MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 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
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- HBEMHMNHYDTVRE-UHFFFAOYSA-N ClC(CCCCCCCCCCCCCCCCC(=O)OC)(Cl)Cl Chemical compound ClC(CCCCCCCCCCCCCCCCC(=O)OC)(Cl)Cl HBEMHMNHYDTVRE-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-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
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical group [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- MQHWFIOJQSCFNM-UHFFFAOYSA-L Magnesium salicylate Chemical compound [Mg+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O MQHWFIOJQSCFNM-UHFFFAOYSA-L 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- AOZDHFFNBZAHJF-UHFFFAOYSA-N [3-hexanoyloxy-2,2-bis(hexanoyloxymethyl)propyl] hexanoate Chemical compound CCCCCC(=O)OCC(COC(=O)CCCCC)(COC(=O)CCCCC)COC(=O)CCCCC AOZDHFFNBZAHJF-UHFFFAOYSA-N 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- AVVIDTZRJBSXML-UHFFFAOYSA-L calcium;2-carboxyphenolate;dihydrate Chemical compound O.O.[Ca+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O AVVIDTZRJBSXML-UHFFFAOYSA-L 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 125000002704 decyl group Chemical group [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])C([H])([H])C([H])([H])* 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- LMODBLQHQHXPEI-UHFFFAOYSA-N dibutylcarbamothioylsulfanylmethyl n,n-dibutylcarbamodithioate Chemical compound CCCCN(CCCC)C(=S)SCSC(=S)N(CCCC)CCCC LMODBLQHQHXPEI-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- GHKVUVOPHDYRJC-UHFFFAOYSA-N didodecyl hexanedioate Chemical compound CCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCC GHKVUVOPHDYRJC-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 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 1
- 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 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 229910052744 lithium 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
- 229940072082 magnesium salicylate Drugs 0.000 description 1
- 125000002960 margaryl 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])([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 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002751 molybdenum Chemical class 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 125000001421 myristyl 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])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000001400 nonyl 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])([H])[H] 0.000 description 1
- 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 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 125000000913 palmityl 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])([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 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000002958 pentadecyl 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])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 125000004079 stearyl 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])([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])C([H])([H])[H] 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 150000003443 succinic acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000000954 titration curve Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 125000002889 tridecyl 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])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002948 undecyl 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])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- MBBWTVUFIXOUBE-UHFFFAOYSA-L zinc;dicarbamodithioate Chemical compound [Zn+2].NC([S-])=S.NC([S-])=S MBBWTVUFIXOUBE-UHFFFAOYSA-L 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
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/22—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing phenol radicals
-
- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/18—Ammonia
-
- 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
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
-
- 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
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl 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
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/028—Overbased 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
- C10M2207/26—Overbased carboxylic acid salts
- C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
-
- 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
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic 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
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic 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
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/289—Partial esters containing free 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
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/101—Condensation polymers of aldehydes or ketones and phenols, e.g. Also polyoxyalkylene ether derivatives 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/089—Overbased salts
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
-
- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/02—Viscosity; Viscosity index
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/24—Emulsion properties
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/40—Low content or no content compositions
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/52—Base number [TBN]
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
-
- 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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Definitions
- the present invention relates to detergents utilized in antiwear hydraulic fluid compositions.
- the present invention relates to the use of a composition as an antiwear hydraulic fluid which can be useful for certain mobile equipment applications (e.g., hydraulic fluids for construction equipment).
- Hydraulic fluids need to protect equipment from rust. To achieve this they are formulated with rust inhibitors. Typical rust inhibitors are metal sulfonates or succinic acid derivatives. Hydraulic fluids are also typically designed to separate readily from water (demulsify). Often, metallic rust inhibitors act to improve the demulsifying characteristics of the fluids.
- Japanese Patent Publication No. JP5311187A describes a composition containing (A) a base fluid of a sulfur content of up to 100 ppm, (B) 0.2-1 wt. % of zinc dithiophosphate, (C) 0.2-1 wt. % of an alkaline earth metal salt of salicylic acid and (D) 0.001-0.5 wt. % of a water-separating agent.
- WO0063325 describes a hydraulic fluid comprising lubricant base fluid, 0.001-5 wt.% of magnesium salicylate and 0.01-8 wt.% of zinc dithiophosphate.
- the hydraulic fluid composition also comprises a rust inhibitor.
- This publication also discloses the combination of a calcium salicylate, zinc dithiophosphate, and a rust inhibitor.
- compositions incorporating a metal salt of an alkyl salicylate, zinc dithiophosphate, and a rust inhibitor typically include demulsifiers to facilitate the separation of water from the fluid.
- demulsifiers to facilitate the separation of water from the fluid.
- fluids with enhanced detergent and dispersant characteristics e.g., so called HLPD and HVLPD fluids as defined by the German DIN 51 502 standard
- hydraulic fluids for certain mobile equipment applications e.g., hydraulic fluids for Caterpillar equipment, building machinery, excavators, hydraulic hoists, lifting platforms, presses, and the like
- Engine fluids which are typically formulated with large amounts of dispersants, are a way to provide these emulsifying characteristics. Hydraulic fluids with certain sulfonate detergents can also have these characteristics.
- US 2006/111252 discloses an emulsifier blend which includes at least one alkali metal sulfonate and at least one alkali metal alkyl salicylate.
- the emulsifier blend can be combined with a lubricant oil to provide a water-miscible lubricating oil concentrate capable of forming a stable aqueous emulsion when added to an aqueous medium.
- One aspect of this invention is the use of a composition comprising a major amount of a base fluid of lubricating viscosity and a minor amount of at least one oil soluble detergent additive; as an antiwear hydraulic fluid.
- This detergent additive comprises a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid.
- the composition has a Carboxylate Index of greater than 0.084.
- the antiwear hydraulic fluid composition is able to able to achieve an emulsion of 0 ml of fluid, 0 ml of water and 80 ml of emulsion (abbreviated 0-0-80) for 30 minutes or more, preferably 40 minutes or more in the ASTM D 1401 water separability test method.
- the hydraulic fluid composition is able to achieve a "pass" result in the ASTM D 665 rust inhibition test method.
- salts as described above exhibit excellent emulsifying and rust inhibition characteristics. This combined performance is unexpected when compared to other detergents.
- One advantage of the present invention is the reduction or removal of conventional rust inhibitors, such as metallic naphthalene sulfonic acid salts, (e.g., NA-SUL® from King Industries).
- Antiwear hydraulic fluids are used in hydraulic systems to prevent wear in mechanical equipment in hydraulic systems, for example, to prevent wear on moving metal on metal surfaces, such as steel on steel surfaces. Antiwear hydraulic fluids are useful, for example, in preventing wear in a variety of pumps, including but not limited to, vane pumps, piston pumps, and gear pumps, commonly used in hydraulic systems. Antiwear hydraulic fluids also provide protection for other parts of the hydraulic system such as motors, actuators, and pistons. Antiwear hydraulic fluids typically contain antiwear additves or extreme pressure agents, such as zinc dialkyl dithiophosphate.
- the antiwear hydraulic fluid of the present invention exhibits several performance features in addition to antiwear protection, in particular emulsification and rust protection.
- the antiwear hydraulic fluid of the present invention exhibits good oxidation stability, good filterability, good thermal stability, low internal friction, and good hydrolytic stability.
- the base oil of lubricating viscosity employed in the present invention may be mineral oil or synthetic oils.
- a base oil having a viscosity of at least 10 cSt (mm 2 /s) at 40 C. and a pour point below 20 C., preferably at or below 0 C. is desirable.
- the base oils may be derived from synthetic or natural sources.
- Mineral oils for use as the base oil in this invention include, for example, paraffinic, naphthenic and other fluids that are ordinarily used in lubricating oil compositions.
- Synthetic oils include, for example, both hydrocarbon synthetic oils and synthetic esters and mixtures thereof having the desired viscosity.
- Hydrocarbon synthetic oils may include, for example, liquid polymers having the proper viscosity prepared from the polymerization of ethylene or higher alpha olefins (polyalphaolefin or PAO), or from hydrocarbon synthesis procedures using carbon monoxide and hydrogen gases such as in a Fisher-Tropsch process.
- polyalphaolefin or PAO polyalphaolefin
- PAO polyalphaolefin
- the hydrogenated liquid oligomers of C 6 to C 12 alpha olefins such as 1-decene trimer.
- alkyl benzenes of proper viscosity such as didodecyl benzene, can be used.
- Useful synthetic esters include the esters of monocarboxylic acids and polycarboxylic acids, as well as mono-hydroxy alkanols and polyols.
- Typical examples are didodecyl adipate, pentaerythritol tetracaproate, di-2-ethylhexyl adipate, dilaurylsebacate, and the like.
- Complex esters prepared from mixtures of mono and dicarboxylic acids and mono and dihydroxy alkanols can also be used.
- Blends of mineral oils with synthetic oils are also useful. For example, blends of 10 wt % to 25 wt % hydrogenated 1-decene trimer with 75 wt % to 90 wt % 150 SUS (100F.) mineral oil make excellent lubricating oil bases.
- the base oil of the present invention is present in a "major amount.”
- a “major amount” of a base oil of lubricating viscosity refers to a concentration of the oil within the hydraulic fluid composition of at least about 40 wt %.
- "a major amount” of a base oil of lubricating viscosity refers to a concentration of the oil within the hydraulic fluid composition of at least about 50 wt %, at least about 60 wt %, at least about 70 wt %, at least about 80 wt %, or at least about 90 wt %.
- composition employed in the present invention comprises at least one suitable detergent additive that is oil soluble.
- the detergent additive comprises a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid.
- the Total Base Number (“TBN”) of the detergent additive is typically less than 200 mg KOH/g, and preferably less than 160 mg KOH/g.
- Total Base Number or “TBN” refers to the equivalent number of milligrams of KOH needed to neutralize 1 gram of a product. Therefore, a high TBN reflects strongly overbased products and, as a result, a higher base reserve for neutralizing acids.
- the TBN of a product can be determined by ASTM Standard No. D 2896 or equivalent procedure.
- An overbased detergent can be any detergent in which the TBN of the additive has been increased by a process such as the addition of a base source (such as lime) and an acidic overbasing compound (such as carbon dioxide).
- At least 75% (such as at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%) of the alkyl groups contained within the detergent (such as the alkyl groups of a carboxylate-containing detergent, or of an alkyl-substituted hydroxybenzoic acid) to be C 14 or greater, such as C 14 -C 40 , C 14 -C 35 , C 14 -C 30 , or C 14 -C 25 ,.
- At least 75% (such as at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%) of the alkyl groups contained within the detergent, with the remainder (such as 25% or less, about 20% or less, 15% or less, 10% or less, 5% or less, or even 1 % or less) of the alkyl groups contained within the detergent to be C 8 or greater (such as C 8 -C 14 , C 10 -C 14 , or even C 12 -C 14 ).
- the detergent comprises a calcium salt of an alkyl-substituted hydroxybenzoic acid that is derived from an alkyl-substituted hydroxybenzoic acid in which the alkyl groups are the residue of normal alpha-olefins containing at least 90% C 20 or greater normal alpha-olefins.
- the detergent comprises a calcium salt (e.g., an overbased salt) of an alkyl-substituted hydroxybenzoic acid.
- the detergent is in a mixture with an overbased salt (such as an overbased alkaline earth metal salt) of an alkyl-substituted phenol.
- the detergent is in a mixture with an overbased salt of an alkyl-substituted phenol, in combination or mixture with a non-overbased salt of one or more of: an alkyl-substituted hydroxybenzoic acid and an alkyl-substituted phenol.
- the composition comprises one or more detergents comprising an overbased calcium salt of an alkyl-substituted hydroxybenzoic acid and no other overbased salts (other than the salt of the detergent).
- the detergent additive in this regard, can comprise any suitable concentration of anion (e.g., organic anion) associated with the carboxylate salt (or salt of the alkyl-substituted hydroxybenzoic acid).
- Suitable detergents which may be used in combination with the non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid include alkyl or alkenyl aromatic sulfonates, borated sulfonates, sulfurized or unsulfurized metal salts of multi hydroxy alkyl or alkenyl aromatic compounds, alkyl or alkenyl hydroxy aromatic sulfonates, sulfurized or unsulfurized alkyl or alkenyl naphthenates, metal salts of alkanoic acids, metal salts of an alkyl or alkenyl multiacid, and chemical and physical mixtures thereof.
- suitable detergent additives include metal sulfonates, salicylates, phosphonates, thiophosphonates and combinations thereof.
- the metal can be any metal suitable for making sulfonate, salicylate or phosphonate detergents.
- suitable metals include alkali metals, alkaline metals and transition metals. In some embodiments, the metal is Ca, Mg, Ba, Sr, K, Na, Li or the like.
- the detergent additive employed in the present invention is generally soluble in oil as characterized by the following test: A mixture of a 600N oil and the additive at a content of 10% by weight with respect to the total weight of the mixture is centrifuged at a temperature of 60 C and for 30 minutes, the centrifugation being carried out under the conditions stipulated by the standard ASTM D2273 (it should be noted that centrifugation is carried out without dilution, i.e. without adding solvent); immediately after centrifugation, the volume of the deposit which forms is determined; if the deposit is less than 0.05% v/v (volume of the deposit with respect to the volume of the mixture), the product is considered as soluble in oil.
- the aforementioned oil soluble detergent additive in the antiwear hydraulic fluid composition of the present invention has a TBN typically less than 200 mg KOH/g, and preferably less than 160 mg KOH/g.
- the concentration of the oil soluble detergent additive itself will generally range from an amount of between about 0.05 wt % to about 0.3 wt%, and preferably about 0.07 wt% to about 0.25 wt %, based on the total weight of the hydraulic fluid composition.
- the detergent additive of the present invention is present in a "minor amount.”
- a “minor amount” of detergent additive refers to a concentration of the detergent additive within the hydraulic fluid composition of less than about 60 wt %.
- a “minor amount” of detergent additive refers to a concentration of the detergent additive within the hydraulic fluid composition of less than about 50 wt%, of less than about 30 wt %, of less than about 10 wt %, of less than about 1 wt %, or of less than about 0.5 wt %.
- detergents help control varnish, ring zone deposits, and rust by keeping insoluble particles in colloidal suspension.
- Metal-containing (or ash-forming detergents) function both as detergents to control deposits, and as acid neutralizers or rust inhibitors, thereby reducing wear and corrosion and extending equipment life.
- Detergents generally comprise a polar head with a long hydrophobic tail; with the polar head comprising a metal salt of an acidic organic compound.
- the salts may contain a substantially stoichiometric amount of the metal in which case they are usually described as normal or neutral salts.
- the detergent additives in the antiwear hydraulic fluid composition of the present invention can be characterized by the amount of potassium hydroxide equivalent to the amount of alkyl-substituted hydroxybenzoate (also referred to herein as a salt of an alkyl substituted hydroxybenzoic acid), or a sulfurized derivative thereof, present in the detergent expressed as mg KOH/g detergent and referred to as the Carboxylate Index (CI).
- CI Carboxylate Index
- the alkyl-substituted hydroxybenzoate detergent additive is dissolved in an organic solvent and washed three times with equal volumes of a dilute, strong acid solution.
- the aqueous layers are collected.
- the combined aqueous layers are washed with an organic solvent.
- the aqueous layer is removed and the organic layers are combined and subsequently washed with distilled water.
- the aqueous layer is decanted.
- the acidified extract is treated with pyridine and titrated with dilute, standardized base.
- Cl of antiwear hydraulic fluid composition Cl of alkyl - substituted hydroxybenzoate detergent x wt . % alkyl - substituted hydroxybenzoate detergent in fluid
- the CI of the antiwear hydraulic fluid composition is greater than 0.084, preferably greater than 0.10, and more preferably greater than 0.12.
- the CI of the antiwear hydraulic fluid composition is greater than 0.034, and more preferably greater than 0.04.
- the oil soluble detergent additive of the present invention can be employed as a concentrate which will typically contain a sufficient amount of an organic liquid diluent and the oil soluble detergent additive employed in the present invention.
- the concentrates contain sufficient organic liquid diluent to make them easy to handle during shipping and storage.
- the concentrate will contain from about 10 wt % to 90 wt %; preferably, from about 20 wt % to 70 wt %; and more preferably, from about 20 wt % to 35 wt %, of a compatible organic liquid diluent.
- Suitable organic liquid diluents which can be used include, for example, paraffinic base oils such as solvent refined 100N, e.g., Cit-Con 100N, and hydrotreated 100N, e.g., Chevron 100N, and the like.
- the organic liquid diluent preferably has a viscosity of from about 1 to 20 cSt at 100C. From about 10 wt % to 90 wt %; preferably, from about 30 wt % to 80 wt % of the concentrate is the oil soluble additive employed in the present invention.
- additive components are examples of some of the components that can be favorably employed in the present invention. These examples of additives are provided to illustrate the present invention, but they are not intended to limit it:
- a base-line formulation was prepared and used for assessing the performance of the detergent in Example 1 in the ASTM D 1401 water separability test.
- the base-line formulation contained 0.31 wt. % of a zinc dialkyldithiophosphate, 0.15 wt. % of a hindered phenol antioxidant, 0.044 wt. % of a succinate ester dispersant, 0.044 wt. % of a fatty ester friction modifier, 0.013 wt. % of an arylpolyol demulsifier and 0.008 wt. % of a foam inhibitor in a base fluid containing Shell HVI basestocks. All finished fluids in these Examples are ISO VG 46 with 8 wt. % of a polyalkyl methacrylate viscosity index improver.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.225 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 20 or greater and 0.06 wt. % of the succinate ester dispersant.
- the overbased calcium alkyl-substituted hydroxybenzoate detergent was prepared according to the method described in Example 1 of US Patent Application 2007/0027043 and has a calcium content of 5.35 wt. %, a TBN of 150 and a CI of 56.
- An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Example 1 except that 0.01 wt. % of a linear alcohol ethoxylate emulsifier and 0.16 wt% zinc dialkyl dithiophosphate was added.
- An antiwear hydraulic fluid composition was prepared consisting of the base-line formulation above with the addition of 0.041 wt. % of an overbased, sulfurized alkyl-substituted hydroxybenzoate-containing detergent, 0.024 wt. % of an overbased calcium phenate, 0.027 wt. % of a naphthalene sulfonic acid zinc salt rust inhibitor and 0.008 wt. % of a phenolic resin demulsifier.
- the overbased, sulfurized carboxylate-containing detergent was prepared according to the method described in Example 16 of US Patent Number 5808145 and has a calcium content of 9.3 wt. %, a sulfur content of 2.4 wt. %, a TBN of 260 and a CI of 28.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.075 wt. % of the 56 CI overbased calcium alkyl-substituted hydroxybenzoate as described in Example 1.
- An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Comparative Example 2 except that 0.06 wt. % of the succinate ester dispersant was added.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.15 wt. % of the 56 CI overbased calcium alkylhydroxybenzoate as described in Example 1.
- An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Comparative Example 4 except that 0.06 wt. % of the succinate ester dispersant was added.
- the water separability of antiwear hydraulic fluids is characterized in the ASTM D 1401 test method.
- a 40 mL volume of the sample material was emulsified with a 40 mL volume of distilled water by stirring the combined liquids in a graduated cylinder at 54°C for 5 minutes.
- the separation of the emulsion into organic and aqueous layers was characterized by monitoring the relative volumes of the respective fluid, water and emulsion layers after cessation of stirring. Results are set forth below in Table 1 as the respective mL fluid-mL water-mL emulsion observed at minutes after cessation of stirring.
- a base-line formulation was prepared and used for assessing the performance of various detergents in the ASTM D 665 rust prevention test.
- the base-line formulation contained 0.31 wt. % of a zinc dialkyldithiophosphate, 0.15 wt. % of a hindered phenol antioxidant, 0.044 wt. % of a succinate ester dispersant, 0.044 wt. % of a fatty ester friction modifier, 0.013 wt. % of an arylpolyol demulsifier, 0.008 wt. % of a phenolic resin demulsifier, 0.2 wt. % of a pour point depressant and 0.008 wt. % of a foam inhibitor in a base oil containing ExxonMobil AP/E CORE ® basestocks. All finished fluids in these Examples are ISO VG 68.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.075 wt. % of the 56 CI overbased calcium alkyl-substituted hydroxybenzoate detergent as described in Example 1.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.041 wt. % of the 28 CI overbased, sulfurized, alkyl-substituted hydroxybenzoate-containing detergent as described in Comparative Example 1, 0.024 wt. % of an overbased calcium phenate and 0.027 wt. % of a naphthalene sulfonic acid zinc salt rust inhibitor.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.067 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 14 -C 18 .
- the detergent has a TBN of 168 and a CI of 51.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.049 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 20 -C 28 .
- the detergent has a TBN of 230 and a CI of 46.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.035 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 20 -C 28 .
- the detergent has a TBN of 325 and a CI of 36.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.032 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C 20 or greater.
- the overbased calcium alkyl-substituted hydroxybenzoate detergent is prepared according to the method described in Example 1 of US Patent Application 2007/0027043 and has a calcium content of 12.5 wt. %, a TBN of 350 and a CI of 37.
- Rust inhibition of antiwear hydraulic fluids was determined using ASTM D 665.
- ASTM D 665 is directed at a test for determining the ability of fluid to aid in preventing the rusting of ferrous parts should water become mixed with the fluid.
- Procedure B of ASTM D 665 was employed. In this test, a mixture of 300 mL of the test fluid is stirred with 30 mL of synthetic sea water at a temperature of 60°C with a cylindrical steel specimen completely immersed therein for 24 hours. The rust test results are reported as either a "pass” or a "fail.” The results are presented in Table 2. Table 2 not according to the invention Ex. 3 Comp. Ex. 6 Comp. Ex. 7 Comp. Ex. 8 Comp. Ex.
- Example 3 demonstrated unexpected rust inhibiting performance when compared to other carboxylate/salicylate detergents (Comparative Examples 2-5) and also demonstrated unexpected rust inhibiting performance when compared to a formulation containing a rust inhibitor (Comparative Example 6).
- the formulation of Example 3 advantageously does not require the addition of a rust inhibitor in order to pass this test.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
- The present invention relates to detergents utilized in antiwear hydraulic fluid compositions. In particular, the present invention relates to the use of a composition as an antiwear hydraulic fluid which can be useful for certain mobile equipment applications (e.g., hydraulic fluids for construction equipment).
- Hydraulic fluids need to protect equipment from rust. To achieve this they are formulated with rust inhibitors. Typical rust inhibitors are metal sulfonates or succinic acid derivatives. Hydraulic fluids are also typically designed to separate readily from water (demulsify). Often, metallic rust inhibitors act to improve the demulsifying characteristics of the fluids.
- Japanese Patent Publication No.
JP5311187A - International Application No.
WO0063325 - The above publications describe compositions incorporating a metal salt of an alkyl salicylate, zinc dithiophosphate, and a rust inhibitor. Typically such compositions also include demulsifiers to facilitate the separation of water from the fluid. However, there is a need in some cases to have hydraulic fluids which emulsify, rather than demulsify, water. These include fluids with enhanced detergent and dispersant characteristics (e.g., so called HLPD and HVLPD fluids as defined by the German DIN 51 502 standard) and hydraulic fluids for certain mobile equipment applications (e.g., hydraulic fluids for Caterpillar equipment, building machinery, excavators, hydraulic hoists, lifting platforms, presses, and the like), wherein water separated from the fluid may not be adequately removed from the equipment leading to poor lubrication. Engine fluids, which are typically formulated with large amounts of dispersants, are a way to provide these emulsifying characteristics. Hydraulic fluids with certain sulfonate detergents can also have these characteristics.
-
US 2006/111252 discloses an emulsifier blend which includes at least one alkali metal sulfonate and at least one alkali metal alkyl salicylate. The emulsifier blend can be combined with a lubricant oil to provide a water-miscible lubricating oil concentrate capable of forming a stable aqueous emulsion when added to an aqueous medium. - One aspect of this invention is the use of a composition comprising a major amount of a base fluid of lubricating viscosity and a minor amount of at least one oil soluble detergent additive; as an antiwear hydraulic fluid. This detergent additive comprises a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid. The composition has a Carboxylate Index of greater than 0.084.
- Optionally, at least 90% of the alkyl groups of said alkyl-substituted hydroxybenzoic acid are C14 or greater. Furthermore, optionally, the antiwear hydraulic fluid composition is able to able to achieve an emulsion of 0 ml of fluid, 0 ml of water and 80 ml of emulsion (abbreviated 0-0-80) for 30 minutes or more, preferably 40 minutes or more in the ASTM D 1401 water separability test method. Furthermore, optionally, the hydraulic fluid composition is able to achieve a "pass" result in the ASTM D 665 rust inhibition test method.
- Surprisingly, we have found that salts as described above exhibit excellent emulsifying and rust inhibition characteristics. This combined performance is unexpected when compared to other detergents. One advantage of the present invention is the reduction or removal of conventional rust inhibitors, such as metallic naphthalene sulfonic acid salts, (e.g., NA-SUL® from King Industries).
- Antiwear hydraulic fluids are used in hydraulic systems to prevent wear in mechanical equipment in hydraulic systems, for example, to prevent wear on moving metal on metal surfaces, such as steel on steel surfaces. Antiwear hydraulic fluids are useful, for example, in preventing wear in a variety of pumps, including but not limited to, vane pumps, piston pumps, and gear pumps, commonly used in hydraulic systems. Antiwear hydraulic fluids also provide protection for other parts of the hydraulic system such as motors, actuators, and pistons. Antiwear hydraulic fluids typically contain antiwear additves or extreme pressure agents, such as zinc dialkyl dithiophosphate.
- The antiwear hydraulic fluid of the present invention exhibits several performance features in addition to antiwear protection, in particular emulsification and rust protection. In addition, the antiwear hydraulic fluid of the present invention exhibits good oxidation stability, good filterability, good thermal stability, low internal friction, and good hydrolytic stability.
- The base oil of lubricating viscosity employed in the present invention may be mineral oil or synthetic oils. A base oil having a viscosity of at least 10 cSt (mm2/s) at 40 C. and a pour point below 20 C., preferably at or below 0 C. is desirable. The base oils may be derived from synthetic or natural sources. Mineral oils for use as the base oil in this invention include, for example, paraffinic, naphthenic and other fluids that are ordinarily used in lubricating oil compositions. Synthetic oils include, for example, both hydrocarbon synthetic oils and synthetic esters and mixtures thereof having the desired viscosity. Hydrocarbon synthetic oils may include, for example, liquid polymers having the proper viscosity prepared from the polymerization of ethylene or higher alpha olefins (polyalphaolefin or PAO), or from hydrocarbon synthesis procedures using carbon monoxide and hydrogen gases such as in a Fisher-Tropsch process. Especially useful are the hydrogenated liquid oligomers of C6 to C12 alpha olefins such as 1-decene trimer. Likewise, alkyl benzenes of proper viscosity, such as didodecyl benzene, can be used. Useful synthetic esters include the esters of monocarboxylic acids and polycarboxylic acids, as well as mono-hydroxy alkanols and polyols. Typical examples are didodecyl adipate, pentaerythritol tetracaproate, di-2-ethylhexyl adipate, dilaurylsebacate, and the like. Complex esters prepared from mixtures of mono and dicarboxylic acids and mono and dihydroxy alkanols can also be used. Blends of mineral oils with synthetic oils are also useful. For example, blends of 10 wt % to 25 wt % hydrogenated 1-decene trimer with 75 wt % to 90 wt % 150 SUS (100F.) mineral oil make excellent lubricating oil bases.
- The base oil of the present invention is present in a "major amount." A "major amount" of a base oil of lubricating viscosity refers to a concentration of the oil within the hydraulic fluid composition of at least about 40 wt %. In some embodiments, "a major amount" of a base oil of lubricating viscosity refers to a concentration of the oil within the hydraulic fluid composition of at least about 50 wt %, at least about 60 wt %, at least about 70 wt %, at least about 80 wt %, or at least about 90 wt %.
- As discussed previously, composition employed in the present invention comprises at least one suitable detergent additive that is oil soluble.
- The detergent additive comprises a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid.
- The Total Base Number ("TBN") of the detergent additive is typically less than 200 mg KOH/g, and preferably less than 160 mg KOH/g. The term "Total Base Number" or "TBN" refers to the equivalent number of milligrams of KOH needed to neutralize 1 gram of a product. Therefore, a high TBN reflects strongly overbased products and, as a result, a higher base reserve for neutralizing acids. The TBN of a product can be determined by ASTM Standard No. D 2896 or equivalent procedure. An overbased detergent can be any detergent in which the TBN of the additive has been increased by a process such as the addition of a base source (such as lime) and an acidic overbasing compound (such as carbon dioxide).
- It is preferred that for at least 75% (such as at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%) of the alkyl groups contained within the detergent (such as the alkyl groups of a carboxylate-containing detergent, or of an alkyl-substituted hydroxybenzoic acid) to be C14 or greater, such as C14-C40, C14-C35, C14-C30, or C14-C25,. In some embodiments, at least 75% (such as at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%) of the alkyl groups contained within the detergent, with the remainder (such as 25% or less, about 20% or less, 15% or less, 10% or less, 5% or less, or even 1 % or less) of the alkyl groups contained within the detergent to be C8 or greater (such as C8-C14, C10-C14, or even C12-C14). In one preferred embodiment, the detergent comprises a calcium salt of an alkyl-substituted hydroxybenzoic acid that is derived from an alkyl-substituted hydroxybenzoic acid in which the alkyl groups are the residue of normal alpha-olefins containing at least 90% C20 or greater normal alpha-olefins.
- The detergent comprises a calcium salt (e.g., an overbased salt) of an alkyl-substituted hydroxybenzoic acid. In an embodiment, the detergent is in a mixture with an overbased salt (such as an overbased alkaline earth metal salt) of an alkyl-substituted phenol. In another embodiment, the detergent is in a mixture with an overbased salt of an alkyl-substituted phenol, in combination or mixture with a non-overbased salt of one or more of: an alkyl-substituted hydroxybenzoic acid and an alkyl-substituted phenol. In another embodiment, the composition comprises one or more detergents comprising an overbased calcium salt of an alkyl-substituted hydroxybenzoic acid and no other overbased salts (other than the salt of the detergent). The detergent additive, in this regard, can comprise any suitable concentration of anion (e.g., organic anion) associated with the carboxylate salt (or salt of the alkyl-substituted hydroxybenzoic acid).
- Some non-limiting examples of other suitable detergents which may be used in combination with the non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid include alkyl or alkenyl aromatic sulfonates, borated sulfonates, sulfurized or unsulfurized metal salts of multi hydroxy alkyl or alkenyl aromatic compounds, alkyl or alkenyl hydroxy aromatic sulfonates, sulfurized or unsulfurized alkyl or alkenyl naphthenates, metal salts of alkanoic acids, metal salts of an alkyl or alkenyl multiacid, and chemical and physical mixtures thereof. Other non-limiting examples of suitable detergent additives include metal sulfonates, salicylates, phosphonates, thiophosphonates and combinations thereof. The metal can be any metal suitable for making sulfonate, salicylate or phosphonate detergents. Non-limiting examples of suitable metals include alkali metals, alkaline metals and transition metals. In some embodiments, the metal is Ca, Mg, Ba, Sr, K, Na, Li or the like.
- The detergent additive employed in the present invention is generally soluble in oil as characterized by the following test: A mixture of a 600N oil and the additive at a content of 10% by weight with respect to the total weight of the mixture is centrifuged at a temperature of 60 C and for 30 minutes, the centrifugation being carried out under the conditions stipulated by the standard ASTM D2273 (it should be noted that centrifugation is carried out without dilution, i.e. without adding solvent); immediately after centrifugation, the volume of the deposit which forms is determined; if the deposit is less than 0.05% v/v (volume of the deposit with respect to the volume of the mixture), the product is considered as soluble in oil.
- The aforementioned oil soluble detergent additive in the antiwear hydraulic fluid composition of the present invention has a TBN typically less than 200 mg KOH/g, and preferably less than 160 mg KOH/g. In the antiwear hydraulic fluid composition of the present invention, the concentration of the oil soluble detergent additive itself will generally range from an amount of between about 0.05 wt % to about 0.3 wt%, and preferably about 0.07 wt% to about 0.25 wt %, based on the total weight of the hydraulic fluid composition. Alternatively speaking, the detergent additive of the present invention is present in a "minor amount." A "minor amount" of detergent additive refers to a concentration of the detergent additive within the hydraulic fluid composition of less than about 60 wt %. In some embodiments, a "minor amount" of detergent additive refers to a concentration of the detergent additive within the hydraulic fluid composition of less than about 50 wt%, of less than about 30 wt %, of less than about 10 wt %, of less than about 1 wt %, or of less than about 0.5 wt %.
- Generally speaking, detergents help control varnish, ring zone deposits, and rust by keeping insoluble particles in colloidal suspension. Metal-containing (or ash-forming detergents) function both as detergents to control deposits, and as acid neutralizers or rust inhibitors, thereby reducing wear and corrosion and extending equipment life. Detergents generally comprise a polar head with a long hydrophobic tail; with the polar head comprising a metal salt of an acidic organic compound. The salts may contain a substantially stoichiometric amount of the metal in which case they are usually described as normal or neutral salts.
- The detergent additives in the antiwear hydraulic fluid composition of the present invention can be characterized by the amount of potassium hydroxide equivalent to the amount of alkyl-substituted hydroxybenzoate (also referred to herein as a salt of an alkyl substituted hydroxybenzoic acid), or a sulfurized derivative thereof, present in the detergent expressed as mg KOH/g detergent and referred to as the Carboxylate Index (CI). Thus, a detergent additive with 56 mg KOH equivalent hydroxyphenyl carboxylate per gram of detergent would have a CI of 56 and would be referred to as 56 CI alkyl-substituted hydroxybenzoate.
- The alkyl-substituted hydroxybenzoate detergent additive is dissolved in an organic solvent and washed three times with equal volumes of a dilute, strong acid solution. The aqueous layers are collected. The combined aqueous layers are washed with an organic solvent. The aqueous layer is removed and the organic layers are combined and subsequently washed with distilled water. The aqueous layer is decanted. The acidified extract is treated with pyridine and titrated with dilute, standardized base.
- The Carboxylate Index (CI) of the detergent additive can then be calculated from the following formula:
wherein
V1 is the volume required to reach the first end point in the titration curve;
C is the concentration of the dilute, standardized base;
MWKOH is the molecular weight of KOH; and
W is the weight of the alkyl-substituted hydroxybenzoate detergent additive. - Once the CI of the detergent additive has been calculated, the CI of the antiwear hydraulic fluid composition can be readily determined from the amount of the alkyl-substituted hydroxybenzoate detergent additive present in the composition. This is expressed by the following formula:
In one embodiment of the invention, the CI of the antiwear hydraulic fluid composition is greater than 0.084, preferably greater than 0.10, and more preferably greater than 0.12. In another embodiment of the invention, the CI of the antiwear hydraulic fluid composition is greater than 0.034, and more preferably greater than 0.04. - The oil soluble detergent additive of the present invention can be employed as a concentrate which will typically contain a sufficient amount of an organic liquid diluent and the oil soluble detergent additive employed in the present invention. The concentrates contain sufficient organic liquid diluent to make them easy to handle during shipping and storage. Typically, the concentrate will contain from about 10 wt % to 90 wt %; preferably, from about 20 wt % to 70 wt %; and more preferably, from about 20 wt % to 35 wt %, of a compatible organic liquid diluent. Suitable organic liquid diluents which can be used include, for example, paraffinic base oils such as solvent refined 100N, e.g., Cit-Con 100N, and hydrotreated 100N, e.g., Chevron 100N, and the like. The organic liquid diluent preferably has a viscosity of from about 1 to 20 cSt at 100C. From about 10 wt % to 90 wt %; preferably, from about 30 wt % to 80 wt % of the concentrate is the oil soluble additive employed in the present invention.
- The following additive components are examples of some of the components that can be favorably employed in the present invention. These examples of additives are provided to illustrate the present invention, but they are not intended to limit it:
- 1. Dispersants: Alkenyl succinimides, alkenyl succinate esters, alkenyl succinimides modified with other organic compounds, alkenyl succinimides modified by posttreatment with ethylene carbonate or boric acid, pentaerythritols, phenate-salicylates and their post-treated analogs, alkali metal or mixed alkali metal, alkaline earth metal borates, dispersions of hydrated alkali metal borates, dispersions of alkaline-earth metal borates, polyamide ashless dispersants and the like or mixtures of such dispersants.
- 2. Anti-oxidants: Anti-oxidants reduce the tendency of mineral oils to deteriorate in service which deterioration is evidenced by the products of oxidation such as sludge and varnish-like deposits on the metal surfaces and by an increase in viscosity. Examples of anti-oxidants useful in the present invention include, but are not limited to, phenol type (phenolic) oxidation inhibitors, such as 4,4'-methylene-bis(2,6-di-tert-butylphenol), 4,4'-bis(2,6-di-tert-butylphenol), 4,4'-bis(2-methyl-6-tert-butylphenol), 2,2'-methylene-bis(4-methyl-6-tert-butyl-phenol), 4,4'-butylidene-bis(3-methyl-6-tert-butylphenol), 4,4'-isopropylidene-bis(2,6-di-tert-butylphenol), 2,2'-methylene-bis(4-me- thyl-6-nonylphenol), 2,2'-isobutylidene-bis(4,6-dimethylphenol), 2,2'-methylene-bis(4-methyl-6-cyclohexylphenol), 2,6-di-tert-butyl-4-methylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butylphenol, 2,4-dimethyl-6-tert-butyl-phenol, 2,6-di-tert-l-dimethylamino-p-cresol, 2,6-di-tert-4-(N,N'-dimethylamino- methylphenol), 4,4'-thiobis(2-methyl-6-tert-butylphenol), 2,2'-thiobis(4-methyl-6-tert-butylphenol), bis(3-methyl-4-hydroxy-5-tert--butylbenzyl)-sulfide, and bis(3,5-di-tert-butyl-4-hydroxybenzyl). Other types of oxidation inhibitors include alkylated diphenylamines (e.g., Irganox L-57 from Ciba-Geigy), metal dithiocarbamate (e.g., zinc dithiocarbamate), and methylenebis(dibutyldithiocarbamate).
- 3. Antiwear agents: As their name implies, these agents reduce wear of moving metallic parts. Examples of such agents include, but are not limited to, phosphates, phosphites, carbamates, esters, sulfur containing compounds, and molybdenum complexes.
- 4. Emulsifiers: Linear alcohol ethoxylates, including TERGITOL® 15-S-3 available from the Dow Chemical Company.
- 5. Demulsifiers: addition product of alkylphenol and ethylene oxide, polyoxyethylene alkyl ether, and polyoxyethylene sorbitan ester.
- 6. Extreme pressure agents (EP agents): zinc dialkyldithiophosphate (primary alkyl, secondary alkyl, and aryl type), sulfurized oils, diphenyl sulfide, methyl trichlorostearate, chlorinated naphthalene, fluoroalkylpolysiloxane, and lead naphthenate. A preferred EP agent is zinc dialkyl dithiophosphate (ZnDTP) as one of the co-additive components for the antiwear hydraulic fluid composition of the present invention, and is shown by the general formula:
- 7. Friction modifiers: fatty alcohol, fatty acid, fatty ester amine, borated ester, and other esters.
- 8. Multifunctional additives: sulfurized oxymolybdenum dithiocarbamate, sulfurized oxymolybdenum organo phosphorodithioate, oxymolybdenum monoglyceride, oxymolybdenum diethylate amide, amine-molybdenum complex compound, and sulfur-containing molybdenum complex compound.
- 9. Viscosity index improvers: polymethacrylate type polymers, ethylene-propylene copolymers, styrene-isoprene copolymers, hydrogenated styrene-isoprene copolymers, polyisobutylene, and dispersant type viscosity index improvers.
- 10. Pour point depressants: polymethacrylate type polymers.
- 11. Foam inhibitors: alkyl methacrylate polymers and dimethyl silicone polymers
- A base-line formulation was prepared and used for assessing the performance of the detergent in Example 1 in the ASTM D 1401 water separability test. The base-line formulation contained 0.31 wt. % of a zinc dialkyldithiophosphate, 0.15 wt. % of a hindered phenol antioxidant, 0.044 wt. % of a succinate ester dispersant, 0.044 wt. % of a fatty ester friction modifier, 0.013 wt. % of an arylpolyol demulsifier and 0.008 wt. % of a foam inhibitor in a base fluid containing Shell HVI basestocks. All finished fluids in these Examples are ISO VG 46 with 8 wt. % of a polyalkyl methacrylate viscosity index improver.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.225 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C20 or greater and 0.06 wt. % of the succinate ester dispersant. The overbased calcium alkyl-substituted hydroxybenzoate detergent was prepared according to the method described in Example 1 of
US Patent Application 2007/0027043 and has a calcium content of 5.35 wt. %, a TBN of 150 and a CI of 56. - An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Example 1 except that 0.01 wt. % of a linear alcohol ethoxylate emulsifier and 0.16 wt% zinc dialkyl dithiophosphate was added.
- An antiwear hydraulic fluid composition was prepared consisting of the base-line formulation above with the addition of 0.041 wt. % of an overbased, sulfurized alkyl-substituted hydroxybenzoate-containing detergent, 0.024 wt. % of an overbased calcium phenate, 0.027 wt. % of a naphthalene sulfonic acid zinc salt rust inhibitor and 0.008 wt. % of a phenolic resin demulsifier. The overbased, sulfurized carboxylate-containing detergent was prepared according to the method described in Example 16 of
US Patent Number 5808145 and has a calcium content of 9.3 wt. %, a sulfur content of 2.4 wt. %, a TBN of 260 and a CI of 28. - An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.075 wt. % of the 56 CI overbased calcium alkyl-substituted hydroxybenzoate as described in Example 1.
- An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Comparative Example 2 except that 0.06 wt. % of the succinate ester dispersant was added.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.15 wt. % of the 56 CI overbased calcium alkylhydroxybenzoate as described in Example 1.
- An antiwear hydraulic fluid composition was prepared in accordance with the formulation of Comparative Example 4 except that 0.06 wt. % of the succinate ester dispersant was added.
- The water separability of antiwear hydraulic fluids is characterized in the ASTM D 1401 test method. In this method, a 40 mL volume of the sample material was emulsified with a 40 mL volume of distilled water by stirring the combined liquids in a graduated cylinder at 54°C for 5 minutes. The separation of the emulsion into organic and aqueous layers was characterized by monitoring the relative volumes of the respective fluid, water and emulsion layers after cessation of stirring. Results are set forth below in Table 1 as the respective mL fluid-mL water-mL emulsion observed at minutes after cessation of stirring.
Table 1 Comp. Ex. 1 Comp. Ex. 2 Comp. Ex. 3 Comp. Ex. 4 Comp. Ex. 5 Ex. 1 Ex.2 56 Cl Ca alkyl-substituted hydroxybenzoate detergent (wt.%) - 0.075 0.075 0.15 0.15 0.225 0.225 28 Cl Ca alkyl-substituted hydroxybenzoate detergent (wt.%) 0.041 - - - - - - CI of antiwear hydraulic fluid composition1 0.01 0.042 0.042 0.084 0.084 0.126 0.126 Dispersant 0.044 0.044 0.1 0.044 0.1 0.1 0.1 Zinc dialkyl dithiophosphate 0.31 0.31 0.31 0.31 0.31 0.31 0.47 Rust inhibitor 0.027 - - - - - - Demulsifier 0.008 - - - - - - Emulsifier - - - - - - 0.01 ASTM D 665B (mL fluid-mL water-mL emulsion at minutes after stirring) 40-40-0 44-36-0 40-32-8 42-38-0 0-10-70 0-0-80 0-0-80 9 min 30 min 40 min 25 min 40 min 40 min 40 min 40-40-0 46-34-0 40-38-2 43-37-0 0-16-64 0-0-80 0-0-80 9 min 35 min 40 min 27 min 40 min 40 min 40 min 1CI of antiwear hydraulic fluid composition = (CI of alkyl-substituted hydroxybenzoate detergent) x (wt. % alkyl-substituted hydroxybenzoate detergent in fluid) - A base-line formulation was prepared and used for assessing the performance of various detergents in the ASTM D 665 rust prevention test. The base-line formulation contained 0.31 wt. % of a zinc dialkyldithiophosphate, 0.15 wt. % of a hindered phenol antioxidant, 0.044 wt. % of a succinate ester dispersant, 0.044 wt. % of a fatty ester friction modifier, 0.013 wt. % of an arylpolyol demulsifier, 0.008 wt. % of a phenolic resin demulsifier, 0.2 wt. % of a pour point depressant and 0.008 wt. % of a foam inhibitor in a base oil containing ExxonMobil AP/E CORE® basestocks. All finished fluids in these Examples are ISO VG 68.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.075 wt. % of the 56 CI overbased calcium alkyl-substituted hydroxybenzoate detergent as described in Example 1.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.041 wt. % of the 28 CI overbased, sulfurized, alkyl-substituted hydroxybenzoate-containing detergent as described in Comparative Example 1, 0.024 wt. % of an overbased calcium phenate and 0.027 wt. % of a naphthalene sulfonic acid zinc salt rust inhibitor.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.067 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C14-C18. The detergent has a TBN of 168 and a CI of 51.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.049 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C20-C28. The detergent has a TBN of 230 and a CI of 46.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.035 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C20-C28. The detergent has a TBN of 325 and a CI of 36.
- An antiwear hydraulic fluid composition was prepared consisting of the baseline formulation above with the addition of 0.032 wt. % of an overbased calcium alkyl-substituted hydroxybenzoate detergent wherein at least 90% of the alkyl groups are C20 or greater. The overbased calcium alkyl-substituted hydroxybenzoate detergent is prepared according to the method described in Example 1 of
US Patent Application 2007/0027043 and has a calcium content of 12.5 wt. %, a TBN of 350 and a CI of 37. - Rust inhibition of antiwear hydraulic fluids was determined using ASTM D 665. ASTM D 665 is directed at a test for determining the ability of fluid to aid in preventing the rusting of ferrous parts should water become mixed with the fluid. For the determining the rust prevention properties in the instant invention, Procedure B of ASTM D 665 was employed. In this test, a mixture of 300 mL of the test fluid is stirred with 30 mL of synthetic sea water at a temperature of 60°C with a cylindrical steel specimen completely immersed therein for 24 hours. The rust test results are reported as either a "pass" or a "fail." The results are presented in Table 2.
Table 2 not according to the invention Ex. 3 Comp. Ex. 6 Comp. Ex. 7 Comp. Ex. 8 Comp. Ex. 9 Comp. Ex. 10 56 Cl alkyl-substituted hydroxybenzoate detergent (wt.%) 0.075 - - - - - 28 Cl alkyl-substituted hydroxybenzoate (wt.%) - 0.041 - - - - 51 Cl alkyl-substituted hydroxybenzoate (wt.%) - - 0.067 - - - 46 Cl alkyl-substituted hydroxybenzoate (wt.%) - - - 0.049 - - 36 Cl alkyl-substituted hydroxybenzoate (wt.%) - - - - 0.035 - 37 Cl alkyl-substituted hydroxybenzoate (wt.%) - - - - - 0.032 Cl of antiwear hydraulic fluid composition1 0.042 0.011 0.034 0.023 0.013 0.012 Rust Inhibitor (wt. %) - 0.027 - - - - Rust Inhibition Result (ASTM D 665B) Pass Pass Fail Fail Fail Fail 1CI of antiwear hydraulic fluid composition = [CI of alkyl-substituted hydroxybenzoate detergent] x [wt.% alkyl-substituted hydroxybenzoate detergent in fluid] - The alkyl-substituted hydroxybenzoate from Example 3 demonstrated unexpected rust inhibiting performance when compared to other carboxylate/salicylate detergents (Comparative Examples 2-5) and also demonstrated unexpected rust inhibiting performance when compared to a formulation containing a rust inhibitor (Comparative Example 6). The formulation of Example 3 advantageously does not require the addition of a rust inhibitor in order to pass this test.
- As discussed previously, it is advantageous in certain hydraulic fluid applications, such as hydraulic fluids for certain mobile equipment applications and HLPD and HLVPD fluids, to emulsify water, rather than to demulsify water. Since the alkyl-substituted hydroxybenzoate from Example 1 also demonstrated good rust inhibition without the need for a metal sulfonate rust inhibitor and since metal sulfonate rust inhibitors are known to demulsify water, the alkyl-substituted hydroxybenzoate used in Example 1 provides additional performance advantages for such emulsifying hydraulic fluids.
Claims (13)
- The use of a composition comprising:(a) a major amount of a base oil of lubricating viscosity; and(b) a minor amount of at least one oil soluble detergent additive comprising a non-sulfurized calcium salt of an alkyl-substituted hydroxybenzoic acid;and further wherein said composition has a Carboxylate Index (as defined herein) of greater than 0.084;
as an antiwear hydraulic fluid. - The use according to claim 1, wherein said alkyl-substituted hydroxybenzoic acid comprises a linear or branched alkyl group or a mixture of linear and branched alkyl groups.
- The use according to claim 1 wherein at least 90% of the alkyl groups of said alkyl-substituted hydroxybenzoic acid are C14 or greater.
- The use according to claim 1 wherein said composition is able to achieve an emulsion of 0-0-80 at 40 minutes in the ASTM D 1401 water separability test method.
- The use according to claim 1, wherein said composition comprises no added rust inhibitors.
- The use according to claim 1, wherein said oil soluble detergent additive comprises a TBN of less than 200 mg KOH/g.
- The use according to claim 1, wherein said oil soluble detergent additive comprises a TBN of less than 160 mg KOH/g.
- The use according to claim 1, wherein said oil soluble detergent additive comprises greater than 0.1 weight percent of the total weight of said composition.
- The use according to claim 1, wherein said oil soluble detergent additive comprises greater than 0.2 weight percent of the total weight of said composition.
- The use according to claim 1, wherein the composition further comprises at least one of these co-additives: (a) an ashless dispersant; (b) an oxidation inhibitor; (d) a demulsifier; (e) an extreme pressure agent; (f) a friction modifier; (g) a multifunctional additive; (h) a viscosity index improver; (i) a pour point depressant; (j) a foam inhibitor; and (k) an emulsifier.
- The use according to claim 1 wherein said composition is able to achieve a pass result in the ASTM D 665 rust inhibition method.
- The use according to claim 1, wherein said oil soluble detergent additive comprises greater than 0.05 weight percent of the total weight of said composition.
- The use according to claim 1, wherein said oil soluble detergent additive comprises greater than 0.07 weight percent of the total weight of said composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP13180664.8A EP2669355A1 (en) | 2008-07-31 | 2009-07-30 | Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/184,094 US20100029525A1 (en) | 2008-07-31 | 2008-07-31 | Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties |
PCT/US2009/052286 WO2010014833A2 (en) | 2008-07-31 | 2009-07-30 | Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties |
Publications (3)
Publication Number | Publication Date |
---|---|
EP2307532A2 EP2307532A2 (en) | 2011-04-13 |
EP2307532A4 EP2307532A4 (en) | 2012-02-15 |
EP2307532B1 true EP2307532B1 (en) | 2013-08-21 |
Family
ID=41608974
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP13180664.8A Withdrawn EP2669355A1 (en) | 2008-07-31 | 2009-07-30 | Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties |
EP09803603.1A Active EP2307532B1 (en) | 2008-07-31 | 2009-07-30 | Use as an antiwear hydraulic fluid composition |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP13180664.8A Withdrawn EP2669355A1 (en) | 2008-07-31 | 2009-07-30 | Antiwear hydraulic fluid composition with useful emulsifying and rust prevention properties |
Country Status (7)
Country | Link |
---|---|
US (1) | US20100029525A1 (en) |
EP (2) | EP2669355A1 (en) |
JP (2) | JP5945414B2 (en) |
CN (1) | CN102105571B (en) |
CA (1) | CA2730058A1 (en) |
SG (2) | SG10201700780WA (en) |
WO (1) | WO2010014833A2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101261880B1 (en) | 2012-11-29 | 2013-05-08 | (주)이바이오텍 | A high-funcitional engine oil additives of multipurpose internal combustion engine and method of manufacturing |
CA3068667C (en) * | 2017-06-30 | 2024-04-16 | Chevron Oronite Company Llc | Lubricating oil compositions containing detergent compounds |
JP7304294B2 (en) * | 2017-06-30 | 2023-07-06 | シェブロン・オロナイト・カンパニー・エルエルシー | Lubricating oil magnesium detergent and method of making and using same |
CN109370736B (en) * | 2018-11-29 | 2021-02-09 | 郑州正赢石化有限公司 | Alkali-resistant ashless hydraulic oil |
CN110484332B (en) * | 2019-09-16 | 2021-08-31 | 辽宁百特润滑科技有限责任公司 | Hydraulic oil composite additive, preparation method thereof and hydraulic oil |
CN114075473B (en) * | 2020-08-18 | 2022-12-13 | 中国石油化工股份有限公司 | Emulsified hydraulic oil composition |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05311187A (en) * | 1992-05-01 | 1993-11-22 | Idemitsu Kosan Co Ltd | Heat-resistant hydraulic oil composition |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5691283A (en) * | 1994-03-01 | 1997-11-25 | Ethyl Petroleum Additives Limited | Use of transmission and gear oil lubricants having enhanced friction properties |
FR2717491B1 (en) | 1994-03-17 | 1996-06-07 | Chevron Chem Sa | Detergent-dispersant additives for lubricating oils of the alkylsalicylates-alkylphenates, alkaline-earth, sulphurized and over-alkalized type. |
JPH07258675A (en) * | 1994-03-28 | 1995-10-09 | Cosmo Sogo Kenkyusho:Kk | Hydraulic pressure oil composition for buffer |
FR2731427B1 (en) * | 1995-03-08 | 1997-05-30 | Chevron Chem Sa | ISOMERIZED LINEAR ALKYLARYL-SULFONATES USEFUL AS ADDITIVES FOR LUBRICATING OILS AND CORRESPONDING ALKYLARYL HYDOCARBONS |
DE69812873T2 (en) * | 1998-01-30 | 2004-01-22 | Chevron Chemical S.A. | Lubricating oil additives free of sulfur and alkali metals |
DE19813999C1 (en) | 1998-03-28 | 1999-11-25 | Seepex Seeberger Gmbh & Co | Eccentric screw pump |
JPH11302679A (en) * | 1998-04-24 | 1999-11-02 | Japan Energy Corp | Lubricating oil composition |
FR2783824B1 (en) * | 1998-09-25 | 2001-01-05 | Chevron Chem Sa | LOW-BASED ALKYLARYL SULFONATES AND LUBRICATING OIL CONTAINING THEM |
JP3927724B2 (en) * | 1999-04-01 | 2007-06-13 | 東燃ゼネラル石油株式会社 | Lubricating oil composition for internal combustion engines |
CA2370468C (en) | 1999-04-14 | 2008-01-15 | Shell Internationale Research Maatschappij B.V. | Hydraulic fluid |
US6569818B2 (en) * | 2000-06-02 | 2003-05-27 | Chevron Oronite Company, Llc | Lubricating oil composition |
EP1233052A1 (en) * | 2001-02-16 | 2002-08-21 | Infineum International Limited | Overbased detergent additives |
US7163911B2 (en) * | 2003-05-22 | 2007-01-16 | Chevron Oronite Company Llc | Carboxylated detergent-dispersant additive for lubricating oils |
US8618029B2 (en) * | 2003-12-22 | 2013-12-31 | Chevron Oronite S.A. | Overbased detergents for lubricating oil applications |
US8188020B2 (en) * | 2003-12-22 | 2012-05-29 | Chevron Oronite S.A. | Lubricating oil composition containing an alkali metal detergent |
US7585822B2 (en) * | 2004-11-23 | 2009-09-08 | Crompton Corporation | Emulsifier blends for lubricating oils |
US7662271B2 (en) * | 2005-12-21 | 2010-02-16 | Chevron U.S.A. Inc. | Lubricating oil with high oxidation stability |
US8030258B2 (en) * | 2005-07-29 | 2011-10-04 | Chevron Oronite Company Llc | Overbased alkaline earth metal alkylhydroxybenzoates having low crude sediment |
-
2008
- 2008-07-31 US US12/184,094 patent/US20100029525A1/en not_active Abandoned
-
2009
- 2009-07-30 SG SG10201700780WA patent/SG10201700780WA/en unknown
- 2009-07-30 SG SG2013058292A patent/SG193167A1/en unknown
- 2009-07-30 CA CA2730058A patent/CA2730058A1/en not_active Abandoned
- 2009-07-30 EP EP13180664.8A patent/EP2669355A1/en not_active Withdrawn
- 2009-07-30 CN CN200980129060.0A patent/CN102105571B/en active Active
- 2009-07-30 EP EP09803603.1A patent/EP2307532B1/en active Active
- 2009-07-30 WO PCT/US2009/052286 patent/WO2010014833A2/en active Application Filing
- 2009-07-30 JP JP2011521334A patent/JP5945414B2/en active Active
-
2014
- 2014-12-15 JP JP2014252608A patent/JP2015091982A/en not_active Ceased
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05311187A (en) * | 1992-05-01 | 1993-11-22 | Idemitsu Kosan Co Ltd | Heat-resistant hydraulic oil composition |
Also Published As
Publication number | Publication date |
---|---|
CN102105571B (en) | 2014-01-29 |
JP2015091982A (en) | 2015-05-14 |
US20100029525A1 (en) | 2010-02-04 |
WO2010014833A2 (en) | 2010-02-04 |
EP2307532A4 (en) | 2012-02-15 |
JP2011529994A (en) | 2011-12-15 |
JP5945414B2 (en) | 2016-07-05 |
EP2307532A2 (en) | 2011-04-13 |
SG193167A1 (en) | 2013-09-30 |
CA2730058A1 (en) | 2010-02-04 |
EP2669355A1 (en) | 2013-12-04 |
CN102105571A (en) | 2011-06-22 |
SG10201700780WA (en) | 2017-03-30 |
WO2010014833A3 (en) | 2010-05-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2308953B1 (en) | System oil formulation for marine two-stroke engines containing alkyl salicylates | |
CA2467640C (en) | Unsulfurized, carboxylate-containing additive for lubrication oils | |
EP1059301B1 (en) | Alkaline earth alkylaryl sulfonates, their application as an additive for lubricating oil, and methods of preparation | |
US20110028365A1 (en) | Anti-wear additive composition and lubricating oil composition containing the same | |
EP2307532B1 (en) | Use as an antiwear hydraulic fluid composition | |
EP1548089A1 (en) | Lubricating oil composition containing an alkali metal salicylate detergent | |
KR102260148B1 (en) | Tractor hydraulic fluid compositions | |
US20120165235A1 (en) | Glycerol-containing functional fluid | |
EP2776542B1 (en) | Glycerol-containing functional fluid | |
CA2852488A1 (en) | Diesel engine oils | |
JP2014533313A (en) | Glycerol-containing functional liquid | |
CA2756951C (en) | Lubricating oil compositions comprising polycyclic imides |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20110221 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA RS |
|
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20120117 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C10N 30/04 20060101ALI20120111BHEP Ipc: C10N 30/12 20060101ALI20120111BHEP Ipc: C10M 129/04 20060101AFI20120111BHEP Ipc: C10M 159/22 20060101ALI20120111BHEP Ipc: C10M 135/02 20060101ALI20120111BHEP Ipc: C10M 125/10 20060101ALI20120111BHEP |
|
17Q | First examination report despatched |
Effective date: 20120926 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R079 Ref document number: 602009018264 Country of ref document: DE Free format text: PREVIOUS MAIN CLASS: C10M0129040000 Ipc: C10N0030040000 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C10N 30/04 20060101AFI20130206BHEP Ipc: C10N 30/12 20060101ALI20130206BHEP Ipc: C10M 159/22 20060101ALI20130206BHEP |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
INTG | Intention to grant announced |
Effective date: 20130416 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: REF Ref document number: 628117 Country of ref document: AT Kind code of ref document: T Effective date: 20130915 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602009018264 Country of ref document: DE Effective date: 20131017 |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: T3 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 628117 Country of ref document: AT Kind code of ref document: T Effective date: 20130821 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20131121 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130717 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20131221 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20131223 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20131122 Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: BE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20140522 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602009018264 Country of ref document: DE Effective date: 20140522 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20140730 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: MM4A |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140731 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140731 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140730 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SM Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 8 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO Effective date: 20090730 Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 9 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 10 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20130821 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20200715 Year of fee payment: 12 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 602009018264 Country of ref document: DE Representative=s name: HL KEMPNER PATENTANWAELTE, SOLICITORS (ENGLAND, DE Ref country code: DE Ref legal event code: R082 Ref document number: 602009018264 Country of ref document: DE Representative=s name: HL KEMPNER PATENTANWALT, RECHTSANWALT, SOLICIT, DE |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MM Effective date: 20210801 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20210801 |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20230530 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20240606 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20240611 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20240604 Year of fee payment: 16 |