CA2613438C - Fluide sans zinc pour tracteur agricole - Google Patents
Fluide sans zinc pour tracteur agricole Download PDFInfo
- Publication number
- CA2613438C CA2613438C CA2613438A CA2613438A CA2613438C CA 2613438 C CA2613438 C CA 2613438C CA 2613438 A CA2613438 A CA 2613438A CA 2613438 A CA2613438 A CA 2613438A CA 2613438 C CA2613438 C CA 2613438C
- Authority
- CA
- Canada
- Prior art keywords
- percent
- oil
- fatty
- composition
- thiadiazole
- 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.)
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- 239000012530 fluid Substances 0.000 title description 29
- -1 amine salt Chemical class 0.000 claims abstract description 93
- 239000000203 mixture Substances 0.000 claims abstract description 86
- 239000002253 acid Substances 0.000 claims abstract description 55
- 150000002148 esters Chemical class 0.000 claims abstract description 37
- 239000011574 phosphorus Substances 0.000 claims abstract description 31
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 31
- 230000001050 lubricating effect Effects 0.000 claims abstract description 28
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 26
- 150000001639 boron compounds Chemical class 0.000 claims abstract description 24
- 229910052751 metal Inorganic materials 0.000 claims abstract description 24
- 239000002184 metal Substances 0.000 claims abstract description 24
- 239000003599 detergent Substances 0.000 claims abstract description 22
- 239000003607 modifier Substances 0.000 claims abstract description 22
- 239000003112 inhibitor Substances 0.000 claims abstract description 14
- 239000011701 zinc Substances 0.000 claims abstract description 14
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 11
- 150000001412 amines Chemical class 0.000 claims description 55
- 239000003921 oil Substances 0.000 claims description 51
- 239000002270 dispersing agent Substances 0.000 claims description 31
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 22
- 239000000194 fatty acid Substances 0.000 claims description 22
- 229930195729 fatty acid Natural products 0.000 claims description 22
- 150000003839 salts Chemical class 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 21
- 239000007795 chemical reaction product Substances 0.000 claims description 15
- 150000004665 fatty acids Chemical class 0.000 claims description 13
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical compound S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 claims description 10
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 9
- 239000004327 boric acid Substances 0.000 claims description 8
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 7
- 239000011575 calcium Substances 0.000 claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 7
- 150000002462 imidazolines Chemical class 0.000 claims description 7
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 6
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 5
- 230000000996 additive effect Effects 0.000 claims description 5
- 239000003963 antioxidant agent Substances 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 239000002518 antifoaming agent Substances 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 238000005260 corrosion Methods 0.000 abstract description 12
- 230000007797 corrosion Effects 0.000 abstract description 10
- 238000005461 lubrication Methods 0.000 abstract description 3
- ATWQTGLWGFGTRE-UHFFFAOYSA-N copper;thiadiazole Chemical compound [Cu].C1=CSN=N1 ATWQTGLWGFGTRE-UHFFFAOYSA-N 0.000 abstract description 2
- 235000019198 oils Nutrition 0.000 description 50
- 125000004432 carbon atom Chemical group C* 0.000 description 36
- 125000001183 hydrocarbyl group Chemical group 0.000 description 32
- 239000000463 material Substances 0.000 description 30
- 235000014786 phosphorus Nutrition 0.000 description 29
- 125000000217 alkyl group Chemical group 0.000 description 21
- 239000000306 component Substances 0.000 description 21
- 150000002924 oxiranes Chemical class 0.000 description 21
- 239000000314 lubricant Substances 0.000 description 20
- 150000007513 acids Chemical class 0.000 description 19
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 18
- 238000012360 testing method Methods 0.000 description 15
- 150000001336 alkenes Chemical class 0.000 description 14
- 229910052717 sulfur Inorganic materials 0.000 description 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 13
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- 229910052796 boron Inorganic materials 0.000 description 12
- 239000011593 sulfur Substances 0.000 description 12
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 11
- 150000001642 boronic acid derivatives Chemical class 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 9
- 150000001299 aldehydes Chemical class 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 9
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 9
- 229920000768 polyamine Polymers 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 235000010338 boric acid Nutrition 0.000 description 8
- 229960002645 boric acid Drugs 0.000 description 8
- XXUJMEYKYHETBZ-UHFFFAOYSA-N ethyl 4-nitrophenyl ethylphosphonate Chemical compound CCOP(=O)(CC)OC1=CC=C([N+]([O-])=O)C=C1 XXUJMEYKYHETBZ-UHFFFAOYSA-N 0.000 description 8
- 229920013639 polyalphaolefin Polymers 0.000 description 8
- 230000005540 biological transmission Effects 0.000 description 7
- 239000007859 condensation product Substances 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 239000010949 copper Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 6
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 150000001733 carboxylic acid esters Chemical class 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 150000003335 secondary amines Chemical class 0.000 description 5
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 4
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 235000006708 antioxidants Nutrition 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 4
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003333 secondary alcohols Chemical class 0.000 description 4
- 239000003784 tall oil Substances 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 150000007942 carboxylates Chemical class 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 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 3
- 150000005690 diesters Chemical class 0.000 description 3
- 150000002194 fatty esters Chemical class 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 3
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229920000193 polymethacrylate Polymers 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 150000003138 primary alcohols Chemical class 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229960002317 succinimide Drugs 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 3
- 150000003751 zinc Chemical class 0.000 description 3
- 150000003752 zinc compounds Chemical class 0.000 description 3
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- SKDGWNHUETZZCS-UHFFFAOYSA-N 2,3-ditert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(O)=C1C(C)(C)C SKDGWNHUETZZCS-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 238000006683 Mannich reaction Methods 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- UDSAIICHUKSCKT-UHFFFAOYSA-N bromophenol blue Chemical compound C1=C(Br)C(O)=C(Br)C=C1C1(C=2C=C(Br)C(O)=C(Br)C=2)C2=CC=CC=C2S(=O)(=O)O1 UDSAIICHUKSCKT-UHFFFAOYSA-N 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000012612 commercial material Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 229940043237 diethanolamine Drugs 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- 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 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
- LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000013020 final formulation Substances 0.000 description 2
- 150000002314 glycerols Chemical class 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 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 2
- 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 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000010688 mineral lubricating oil Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- 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 2
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 235000021313 oleic acid Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920002866 paraformaldehyde Polymers 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 150000003017 phosphorus Chemical class 0.000 description 2
- 239000005077 polysulfide Substances 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 150000008117 polysulfides Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000036647 reaction Effects 0.000 description 2
- 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 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
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- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
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- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
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- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- LGQXXHMEBUOXRP-UHFFFAOYSA-N tributyl borate Chemical compound CCCCOB(OCCCC)OCCCC LGQXXHMEBUOXRP-UHFFFAOYSA-N 0.000 description 1
- 150000003628 tricarboxylic acids Chemical group 0.000 description 1
- BOOITXALNJLNMB-UHFFFAOYSA-N tricyclohexyl borate Chemical compound C1CCCCC1OB(OC1CCCCC1)OC1CCCCC1 BOOITXALNJLNMB-UHFFFAOYSA-N 0.000 description 1
- AJSTXXYNEIHPMD-UHFFFAOYSA-N triethyl borate Chemical compound CCOB(OCC)OCC AJSTXXYNEIHPMD-UHFFFAOYSA-N 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- KDQYHGMMZKMQAA-UHFFFAOYSA-N trihexyl borate Chemical compound CCCCCCOB(OCCCCCC)OCCCCCC KDQYHGMMZKMQAA-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Chemical class 0.000 description 1
- DTBRTYHFHGNZFX-UHFFFAOYSA-N trioctyl borate Chemical compound CCCCCCCCOB(OCCCCCCCC)OCCCCCCCC DTBRTYHFHGNZFX-UHFFFAOYSA-N 0.000 description 1
- JLPJTCGUKOBWRJ-UHFFFAOYSA-N tripentyl borate Chemical compound CCCCCOB(OCCCCC)OCCCCC JLPJTCGUKOBWRJ-UHFFFAOYSA-N 0.000 description 1
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 description 1
- LTEHWCSSIHAVOQ-UHFFFAOYSA-N tripropyl borate Chemical compound CCCOB(OCCC)OCCC LTEHWCSSIHAVOQ-UHFFFAOYSA-N 0.000 description 1
- WAXLMVCEFHKADZ-UHFFFAOYSA-N tris-decyl borate Chemical compound CCCCCCCCCCOB(OCCCCCCCCCC)OCCCCCCCCCC WAXLMVCEFHKADZ-UHFFFAOYSA-N 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
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical class [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 description 1
- 239000004711 α-olefin Chemical group 0.000 description 1
Classifications
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- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/045—Mixtures of base-materials and additives the additives being a mixture of compounds of unknown or incompletely defined constitution and non-macromolecular compounds
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- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
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- C10M169/048—Mixtures of base-materials and additives the additives being a mixture of compounds of unknown or incompletely defined constitution, non-macromolecular and macromolecular compounds
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- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M2207/028—Overbased salts thereof
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- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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- C10M2223/043—Ammonium or amine salts thereof
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- C10M2223/047—Thioderivatives not containing metallic elements
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- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
-
- 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
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/046—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
-
- 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
- C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
- C10N2060/14—Chemical after-treatment of the constituents of the lubricating composition by boron or a compound containing boron
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
L'invention concerne une composition lubrifiante qui comprend : une huile de viscosité lubrifiante ; un sel d'amine d'un ester d'acide phosphoreux ; un inhibiteur de corrosion du cuivre de type thiadiazole ; un détergent métallique superbasique ; un composé bore ; et au moins un modificateur de frottement. Cette composition permet d'assurer une bonne lubrification pour un dispositif mécanique de type tracteur agricole, même si ladite composition est sensiblement exempte de dialkyldithiophosphate de zinc.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US69511505P | 2005-06-29 | 2005-06-29 | |
US60/695,115 | 2005-06-29 | ||
PCT/US2006/024988 WO2007005423A2 (fr) | 2005-06-29 | 2006-06-27 | Fluide sans zinc pour tracteur agricole |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2613438A1 CA2613438A1 (fr) | 2007-01-11 |
CA2613438C true CA2613438C (fr) | 2014-03-25 |
Family
ID=37508276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2613438A Active CA2613438C (fr) | 2005-06-29 | 2006-06-27 | Fluide sans zinc pour tracteur agricole |
Country Status (6)
Country | Link |
---|---|
US (1) | US20090215657A1 (fr) |
EP (1) | EP1910505B1 (fr) |
AU (1) | AU2006266095B2 (fr) |
BR (1) | BRPI0611715B1 (fr) |
CA (1) | CA2613438C (fr) |
WO (1) | WO2007005423A2 (fr) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080194442A1 (en) * | 2007-02-13 | 2008-08-14 | Watts Raymond F | Methods for lubricating a transmission |
CA2716473C (fr) * | 2008-03-19 | 2017-07-04 | The Lubrizol Corporation | Composition anti usure renfermant un compose hydroxycarboxylique |
CN105623778A (zh) * | 2008-07-23 | 2016-06-01 | 路博润公司 | 润滑拖拉机液压系统的方法 |
US9029304B2 (en) * | 2008-09-30 | 2015-05-12 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
CN102630249B (zh) * | 2009-09-14 | 2014-03-05 | 卢布里佐尔公司 | 具有良好的水耐受性的农用拖拉机润滑组合物 |
KR20120109594A (ko) * | 2009-12-29 | 2012-10-08 | 이데미쓰 고산 가부시키가이샤 | 윤활유 조성물 |
SG183389A1 (en) * | 2010-02-19 | 2012-09-27 | Infineum Int Ltd | Wet friction clutch-lubricant systems providing high dynamic coefficients of friction through the use of borated detergents |
US9156859B2 (en) * | 2010-09-30 | 2015-10-13 | The United States Of America, As Represented By The Secretary Of Agriculture | Boron containing vegetable oil based antiwear/antifriction additive and their preparation |
US20140100147A1 (en) * | 2011-05-27 | 2014-04-10 | Jx Nippon Oil & Energy Corporation | Lubricant additive and lubricant oil composition |
US9546341B2 (en) | 2014-04-17 | 2017-01-17 | Chemtura Corporation | Low ash lubricant and fuel additive comprising polyamine |
US11072758B2 (en) * | 2015-11-06 | 2021-07-27 | Lubrizol Corporation | Lubricant composition containing an antiwear agent |
JP2018053027A (ja) * | 2016-09-27 | 2018-04-05 | 出光興産株式会社 | 産業機械用潤滑油組成物、及び潤滑方法 |
US10647939B2 (en) | 2016-11-18 | 2020-05-12 | International Petroleum Products & Additives Company, Inc. | Thiadiazole components, compositions, and methods |
CA3069718A1 (fr) * | 2017-07-17 | 2019-01-24 | The Lubrizol Corporation | Composition de lubrifiant a faible teneur en zinc |
WO2024211259A1 (fr) * | 2023-04-06 | 2024-10-10 | Chevron Oronite Company Llc | Compositions de fluide hydraulique pour machines agricoles |
Family Cites Families (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2191125A (en) | 1937-10-20 | 1940-02-20 | Collins Douglas | Auxiliary steering mechanism |
US2760933A (en) | 1952-11-25 | 1956-08-28 | Standard Oil Co | Lubricants |
US2719126A (en) | 1952-12-30 | 1955-09-27 | Standard Oil Co | Corrosion inhibitors and compositions containing same |
US2719125A (en) | 1952-12-30 | 1955-09-27 | Standard Oil Co | Oleaginous compositions non-corrosive to silver |
US3087932A (en) | 1959-07-09 | 1963-04-30 | Standard Oil Co | Process for preparing 2, 5-bis(hydrocarbondithio)-1, 3, 4-thiadiazole |
US3087937A (en) | 1961-03-22 | 1963-04-30 | Tesi Giorgio | Bis (perfluoromethyl) phosphinic nitride |
US3907601A (en) | 1970-02-17 | 1975-09-23 | Union Carbide Corp | Vinyl battery separators |
US3853772A (en) | 1971-06-01 | 1974-12-10 | Chevron Res | Lubricant containing alkali metal borate dispersed with a mixture of dispersants |
US3819521A (en) | 1971-06-07 | 1974-06-25 | Chevron Res | Lubricant containing dispersed borate and a polyol |
US3877899A (en) | 1972-09-28 | 1975-04-15 | Richard P Bundy | Apparatus for separating particulate matter from a gas stream |
US3980569A (en) | 1974-03-15 | 1976-09-14 | The Lubrizol Corporation | Dispersants and process for their preparation |
US3997454A (en) | 1974-07-11 | 1976-12-14 | Chevron Research Company | Lubricant containing potassium borate |
US4089790A (en) | 1975-11-28 | 1978-05-16 | Chevron Research Company | Synergistic combinations of hydrated potassium borate, antiwear agents, and organic sulfide antioxidants |
US4454059A (en) | 1976-11-12 | 1984-06-12 | The Lubrizol Corporation | Nitrogenous dispersants, lubricants and concentrates containing said nitrogenous dispersants |
CA1188704A (fr) | 1981-05-26 | 1985-06-11 | Kirk E. Davis | Compositions a teneur de bore destinees a servir d'additifs pour lubrifiants |
US4584115A (en) | 1982-02-11 | 1986-04-22 | The Lubrizol Corporation | Method of preparing boron-containing compositions useful as lubricant additives |
US4618539A (en) * | 1984-12-06 | 1986-10-21 | The Lubrizol Corporation | Corrosion-inhibiting compositions, and oil compositions containing said corrosion-inhibiting compositions |
US4752416A (en) | 1986-12-11 | 1988-06-21 | The Lubrizol Corporation | Phosphite ester compositions, and lubricants and functional fluids containing same |
US4792410A (en) | 1986-12-22 | 1988-12-20 | The Lubrizol Corporation | Lubricant composition suitable for manual transmission fluids |
IN172215B (fr) | 1987-03-25 | 1993-05-08 | Lubrizol Corp | |
US5157088A (en) | 1987-11-19 | 1992-10-20 | Dishong Dennis M | Nitrogen-containing esters of carboxy-containing interpolymers |
US4957651A (en) | 1988-01-15 | 1990-09-18 | The Lubrizol Corporation | Mixtures of partial fatty acid esters of polyhydric alcohols and sulfurized compositions, and use as lubricant additives |
US4959168A (en) | 1988-01-15 | 1990-09-25 | The Lubrizol Corporation | Sulfurized compositions, and additive concentrates and lubricating oils containing same |
DE68912307T2 (de) | 1988-10-24 | 1994-05-05 | Exxon Chemical Patents Inc | Amid enthaltende reibungsmodifizierungsmittel zur verwendung bei leistungstransmissionsfluiden. |
JP2919611B2 (ja) | 1990-01-05 | 1999-07-12 | ザ ルブリゾル コーポレイション | 普遍的な駆動系流体 |
US5284591A (en) | 1991-05-15 | 1994-02-08 | The Lubrizol Corporation | Functional fluid with borated epoxides, carboxylic solubilizers, zinc salts, calcium complexes and sulfurized compositions |
AU662595B2 (en) | 1991-08-09 | 1995-09-07 | Lubrizol Corporation, The | Functional fluid with triglycerides, detergent-inhibitor additives and viscosity modifying additives |
US5597785A (en) * | 1991-10-02 | 1997-01-28 | R. T. Vanderbilt Company, Inc. | Succinimide derivatives of 2,5-dimercapto-1,3,4-thiadiazole |
US5358652A (en) * | 1992-10-26 | 1994-10-25 | Ethyl Petroleum Additives, Limited | Inhibiting hydrolytic degradation of hydrolyzable oleaginous fluids |
JPH07150183A (ja) * | 1993-08-20 | 1995-06-13 | Lubrizol Corp:The | 熱安定性が向上し、そしてスリップ性能が限定された潤滑組成物 |
US5843673A (en) * | 1994-10-25 | 1998-12-01 | Curators Of The University Of Missouri | Method of screening for endometriosis |
JPH08209171A (ja) * | 1994-11-15 | 1996-08-13 | Lubrizol Corp:The | チオカーバメートおよびリン含有エステルを含有する潤滑剤および流体 |
CA2162439A1 (fr) | 1994-11-15 | 1996-05-16 | Betsy J. Butke | Lubrifiants et fluides renfermant des thiocarbamates et des phosphonates |
AU710294B2 (en) | 1995-09-12 | 1999-09-16 | Lubrizol Corporation, The | Lubrication fluids for reduced air entrainment and improved gear protection |
US5635459A (en) | 1995-10-27 | 1997-06-03 | The Lubrizol Corporation | Borated overbased sulfonates for improved gear performance in functional fluids |
ZA97222B (en) | 1996-01-16 | 1998-02-18 | Lubrizol Corp | Lubricating compositions. |
DE19653887C1 (de) * | 1996-12-21 | 1997-10-30 | Deutsche Forsch Luft Raumfahrt | Prüfvorrichtung zum Beaufschlagen einer Probe mit einem hochenergetischen Gasstrahl |
US6001783A (en) * | 1997-03-24 | 1999-12-14 | The Lubrizol Corporation | Mixed polysulfides and lubricants and functional fluids containing the same |
US6451745B1 (en) * | 1999-05-19 | 2002-09-17 | The Lubrizol Corporation | High boron formulations for fluids continuously variable transmissions |
CA2374501A1 (fr) * | 1999-05-24 | 2000-11-30 | The Lubrizol Corporation | Huiles minerales pour engrenages et liquides a transmissions |
US6617287B2 (en) * | 2001-10-22 | 2003-09-09 | The Lubrizol Corporation | Manual transmission lubricants with improved synchromesh performance |
KR101022920B1 (ko) * | 2002-07-12 | 2011-03-16 | 더루우브리졸코오포레이션 | 변속기용 윤활유에 항진동 성능 향상과 높은 정지 마찰을제공하기 위한 마찰 개질제 |
US7285516B2 (en) | 2002-11-25 | 2007-10-23 | The Lubrizol Corporation | Additive formulation for lubricating oils |
US7056871B2 (en) * | 2003-04-25 | 2006-06-06 | Chevron Oronite Company Llc | Lubricating oil composition which decreases copper corrosion and method of making same |
US20050014656A1 (en) | 2003-07-16 | 2005-01-20 | The Lubrizol Corporation | Transmission lubricating compositions with improved performance, containing acid/polyamine condensation product |
US7439213B2 (en) | 2004-10-19 | 2008-10-21 | The Lubrizol Corporation | Secondary and tertiary amines as friction modifiers for automatic transmission fluids |
-
2006
- 2006-06-27 US US11/917,540 patent/US20090215657A1/en not_active Abandoned
- 2006-06-27 BR BRPI0611715A patent/BRPI0611715B1/pt active IP Right Grant
- 2006-06-27 EP EP06785653.4A patent/EP1910505B1/fr not_active Revoked
- 2006-06-27 AU AU2006266095A patent/AU2006266095B2/en not_active Ceased
- 2006-06-27 WO PCT/US2006/024988 patent/WO2007005423A2/fr active Application Filing
- 2006-06-27 CA CA2613438A patent/CA2613438C/fr active Active
Also Published As
Publication number | Publication date |
---|---|
WO2007005423A2 (fr) | 2007-01-11 |
BRPI0611715A2 (pt) | 2010-09-28 |
EP1910505B1 (fr) | 2013-08-07 |
EP1910505A2 (fr) | 2008-04-16 |
WO2007005423A3 (fr) | 2007-03-01 |
CA2613438A1 (fr) | 2007-01-11 |
US20090215657A1 (en) | 2009-08-27 |
AU2006266095A1 (en) | 2007-01-11 |
BRPI0611715B1 (pt) | 2016-03-15 |
AU2006266095B2 (en) | 2010-08-05 |
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Legal Events
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EEER | Examination request |