CA2673613A1 - Inhibiteur de la corrosion de multiples metaux - Google Patents
Inhibiteur de la corrosion de multiples metaux Download PDFInfo
- Publication number
- CA2673613A1 CA2673613A1 CA002673613A CA2673613A CA2673613A1 CA 2673613 A1 CA2673613 A1 CA 2673613A1 CA 002673613 A CA002673613 A CA 002673613A CA 2673613 A CA2673613 A CA 2673613A CA 2673613 A1 CA2673613 A1 CA 2673613A1
- Authority
- CA
- Canada
- Prior art keywords
- group
- formula
- borate
- triazole
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000005260 corrosion Methods 0.000 title claims abstract description 18
- 230000007797 corrosion Effects 0.000 title claims abstract description 18
- 229910052751 metal Inorganic materials 0.000 title description 9
- 239000002184 metal Substances 0.000 title description 9
- 239000003112 inhibitor Substances 0.000 title description 2
- -1 borate ester Chemical class 0.000 claims abstract description 58
- 150000003852 triazoles Chemical class 0.000 claims abstract description 47
- 239000000314 lubricant Substances 0.000 claims abstract description 44
- 239000000203 mixture Substances 0.000 claims abstract description 34
- 239000006078 metal deactivator Substances 0.000 claims abstract description 26
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 15
- 239000010949 copper Substances 0.000 claims abstract description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052802 copper Inorganic materials 0.000 claims abstract description 13
- 239000011133 lead Substances 0.000 claims abstract description 12
- 239000011701 zinc Substances 0.000 claims abstract description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 10
- 239000010452 phosphate Substances 0.000 claims abstract description 8
- 229910052742 iron Inorganic materials 0.000 claims abstract description 5
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- 239000012964 benzotriazole Substances 0.000 claims description 14
- 235000021317 phosphate Nutrition 0.000 claims description 14
- 125000003118 aryl group Chemical group 0.000 claims description 11
- 125000002015 acyclic group Chemical group 0.000 claims description 8
- 125000002723 alicyclic group Chemical group 0.000 claims description 8
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 150000002431 hydrogen Chemical group 0.000 claims description 6
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 3
- AVBBHCMDRGQBNW-UHFFFAOYSA-N 2-ethyl-n-(2-ethylhexyl)-n-(1,2,4-triazol-1-ylmethyl)hexan-1-amine Chemical compound CCCCC(CC)CN(CC(CC)CCCC)CN1C=NC=N1 AVBBHCMDRGQBNW-UHFFFAOYSA-N 0.000 claims description 3
- JEKIXEKZNDOZOH-UHFFFAOYSA-N 4-[6-(1-cyclohexyloxybutyl)-6-methylcyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound C1=CC=CC(C=2N=NNC=2)C1(C)C(CCC)OC1CCCCC1 JEKIXEKZNDOZOH-UHFFFAOYSA-N 0.000 claims description 3
- VPBPQUMKWCDSCO-UHFFFAOYSA-N 4-[6-(1-cyclohexyloxyheptyl)-6-methylcyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound C1=CC=CC(C=2N=NNC=2)C1(C)C(CCCCCC)OC1CCCCC1 VPBPQUMKWCDSCO-UHFFFAOYSA-N 0.000 claims description 3
- PMMXOGKGAOMJNY-UHFFFAOYSA-N 4-[6-(2-methoxypropan-2-yl)-6-methylcyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound COC(C)(C)C1(C)C=CC=CC1C1=CNN=N1 PMMXOGKGAOMJNY-UHFFFAOYSA-N 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 3
- JZSFJRODQAKRNT-UHFFFAOYSA-N 6-methyl-n-(6-methylheptyl)-n-(1,2,4-triazol-1-ylmethyl)heptan-1-amine Chemical compound CC(C)CCCCCN(CCCCCC(C)C)CN1C=NC=N1 JZSFJRODQAKRNT-UHFFFAOYSA-N 0.000 claims description 2
- LJOUMIFRRRQONS-KTKRTIGZSA-N [(z)-octadec-9-enoxy]boronic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCOB(O)O LJOUMIFRRRQONS-KTKRTIGZSA-N 0.000 claims description 2
- BOOITXALNJLNMB-UHFFFAOYSA-N tricyclohexyl borate Chemical compound C1CCCCC1OB(OC1CCCCC1)OC1CCCCC1 BOOITXALNJLNMB-UHFFFAOYSA-N 0.000 claims description 2
- AJSTXXYNEIHPMD-UHFFFAOYSA-N triethyl borate Chemical group CCOB(OCC)OCC AJSTXXYNEIHPMD-UHFFFAOYSA-N 0.000 claims description 2
- KDQYHGMMZKMQAA-UHFFFAOYSA-N trihexyl borate Chemical compound CCCCCCOB(OCCCCCC)OCCCCCC KDQYHGMMZKMQAA-UHFFFAOYSA-N 0.000 claims description 2
- DTBRTYHFHGNZFX-UHFFFAOYSA-N trioctyl borate Chemical compound CCCCCCCCOB(OCCCCCCCC)OCCCCCCCC DTBRTYHFHGNZFX-UHFFFAOYSA-N 0.000 claims description 2
- JLPJTCGUKOBWRJ-UHFFFAOYSA-N tripentyl borate Chemical compound CCCCCOB(OCCCCC)OCCCCC JLPJTCGUKOBWRJ-UHFFFAOYSA-N 0.000 claims description 2
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 claims description 2
- LTEHWCSSIHAVOQ-UHFFFAOYSA-N tripropyl borate Chemical compound CCCOB(OCCC)OCCC LTEHWCSSIHAVOQ-UHFFFAOYSA-N 0.000 claims description 2
- WAXLMVCEFHKADZ-UHFFFAOYSA-N tris-decyl borate Chemical compound CCCCCCCCCCOB(OCCCCCCCCCC)OCCCCCCCCCC WAXLMVCEFHKADZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims 1
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 239000010705 motor oil Substances 0.000 abstract description 12
- 238000009472 formulation Methods 0.000 abstract description 6
- 239000002270 dispersing agent Substances 0.000 description 14
- 229910052698 phosphorus Inorganic materials 0.000 description 14
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 10
- 239000002956 ash Substances 0.000 description 10
- 239000011574 phosphorus Substances 0.000 description 10
- 235000014786 phosphorus Nutrition 0.000 description 10
- 239000003599 detergent Substances 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 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 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000008186 active pharmaceutical agent Substances 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000005864 Sulphur Substances 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000012530 fluid Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 229920001515 polyalkylene glycol Polymers 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- GONFBOIJNUKKST-UHFFFAOYSA-N 5-ethylsulfanyl-2h-tetrazole Chemical compound CCSC=1N=NNN=1 GONFBOIJNUKKST-UHFFFAOYSA-N 0.000 description 2
- 229910000881 Cu alloy Inorganic materials 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000007866 anti-wear additive Substances 0.000 description 2
- SCJNCDSAIRBRIA-DOFZRALJSA-N arachidonyl-2'-chloroethylamide Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NCCCl SCJNCDSAIRBRIA-DOFZRALJSA-N 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000005078 molybdenum compound Substances 0.000 description 2
- 150000002752 molybdenum compounds Chemical class 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003873 salicylate salts Chemical class 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- DTEVPEVVQOSRSM-UHFFFAOYSA-N (diphenyl-lambda4-sulfanylidene)-dihydroxy-[2-(2-methylpropyl)phenoxy]-lambda5-phosphane Chemical compound CC(C)CC1=CC=CC=C1OP(O)(O)=S(C=1C=CC=CC=1)C1=CC=CC=C1 DTEVPEVVQOSRSM-UHFFFAOYSA-N 0.000 description 1
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical class S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 description 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- DZNCHORQQWFQFG-UHFFFAOYSA-N 3-hydroxy-1,3$l^{5}-thiaphosphetane 3-oxide Chemical compound OP1(=O)CSC1 DZNCHORQQWFQFG-UHFFFAOYSA-N 0.000 description 1
- APZCUVKBZIJIPW-UHFFFAOYSA-N 4-[6-(1-butoxy-2-methylpropyl)-6-methylcyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CCCCOC(C(C)C)C1(C)C=CC=CC1C1=NNN=C1 APZCUVKBZIJIPW-UHFFFAOYSA-N 0.000 description 1
- BSMKQSXZGWAHLC-UHFFFAOYSA-N 4-[6-(1-cyclohexyloxypropyl)-6-methylcyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound C1=CC=CC(C=2N=NNC=2)C1(C)C(CC)OC1CCCCC1 BSMKQSXZGWAHLC-UHFFFAOYSA-N 0.000 description 1
- VKMZCQWIOWSRAF-UHFFFAOYSA-N 4-[6-(1-dodecoxybutyl)-6-methylcyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CCCCCCCCCCCCOC(CCC)C1(C)C=CC=CC1C1=NNN=C1 VKMZCQWIOWSRAF-UHFFFAOYSA-N 0.000 description 1
- JLRQKAQMQJOZHC-UHFFFAOYSA-N 4-[6-[1-(2-ethoxyethoxy)butyl]-6-methylcyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CCOCCOC(CCC)C1(C)C=CC=CC1C1=NNN=C1 JLRQKAQMQJOZHC-UHFFFAOYSA-N 0.000 description 1
- SAZOPPSYUBEVTC-UHFFFAOYSA-N 4-[6-[1-(2-methoxyethoxy)butyl]-6-methylcyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound COCCOC(CCC)C1(C)C=CC=CC1C1=NNN=C1 SAZOPPSYUBEVTC-UHFFFAOYSA-N 0.000 description 1
- JPPVALDHUKQXCY-UHFFFAOYSA-N 4-[6-methyl-6-(1-octoxybutyl)cyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CCCCCCCCOC(CCC)C1(C)C=CC=CC1C1=NNN=C1 JPPVALDHUKQXCY-UHFFFAOYSA-N 0.000 description 1
- DHDDLCZFOKQQKI-UHFFFAOYSA-N 4-[6-methyl-6-(1-propan-2-yloxybutyl)cyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CCCC(OC(C)C)C1(C)C=CC=CC1C1=NNN=C1 DHDDLCZFOKQQKI-UHFFFAOYSA-N 0.000 description 1
- SWHSMKLIBBLERP-UHFFFAOYSA-N 4-[6-methyl-6-(1-propan-2-yloxyethyl)cyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CC(C)OC(C)C1(C)C=CC=CC1C1=NNN=C1 SWHSMKLIBBLERP-UHFFFAOYSA-N 0.000 description 1
- GSCVVUUTIXGLMJ-UHFFFAOYSA-N 4-[6-methyl-6-(1-propan-2-yloxypropyl)cyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CC(C)OC(CC)C1(C)C=CC=CC1C1=NNN=C1 GSCVVUUTIXGLMJ-UHFFFAOYSA-N 0.000 description 1
- YKBXYLXDWPLJQE-UHFFFAOYSA-N 4-[6-methyl-6-[1-(2-methylpropoxy)butyl]cyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CC(C)COC(CCC)C1(C)C=CC=CC1C1=NNN=C1 YKBXYLXDWPLJQE-UHFFFAOYSA-N 0.000 description 1
- RWIQIWCIJOIQDK-UHFFFAOYSA-N 4-[6-methyl-6-[1-[(2-methylpropan-2-yl)oxy]butyl]cyclohexa-2,4-dien-1-yl]-2h-triazole Chemical compound CCCC(OC(C)(C)C)C1(C)C=CC=CC1C1=NNN=C1 RWIQIWCIJOIQDK-UHFFFAOYSA-N 0.000 description 1
- JXPFXQIZXHIDRS-UHFFFAOYSA-N 5,9-diethyl-7-(1,2,4-triazol-1-yl)tridecan-7-amine Chemical compound CCCCC(CC)CC(N)(CC(CC)CCCC)N1C=NC=N1 JXPFXQIZXHIDRS-UHFFFAOYSA-N 0.000 description 1
- ODIRCEMRICGASB-UHFFFAOYSA-N 5,9-diethyl-7-(4-methylbenzotriazol-1-yl)tridecan-7-amine Chemical group C1=CC=C2N(C(N)(CC(CC)CCCC)CC(CC)CCCC)N=NC2=C1C ODIRCEMRICGASB-UHFFFAOYSA-N 0.000 description 1
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 1
- YQNBWBRMWDRTHX-UHFFFAOYSA-N C=1C=CC=CC=1S(C=1C=CC=CC=1)(=P(O)(O)O)C1=CC=CC=C1.C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 Chemical compound C=1C=CC=CC=1S(C=1C=CC=CC=1)(=P(O)(O)O)C1=CC=CC=C1.C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 YQNBWBRMWDRTHX-UHFFFAOYSA-N 0.000 description 1
- MWFYBHJZZZJQOG-UHFFFAOYSA-O CCCCC(CC)CN(CC(CC)CCCC)C[S+]1C(S)=NC2=CC=CC=C12 Chemical compound CCCCC(CC)CN(CC(CC)CCCC)C[S+]1C(S)=NC2=CC=CC=C12 MWFYBHJZZZJQOG-UHFFFAOYSA-O 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical class OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910003873 O—P—O Inorganic materials 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- MAOGTIAUZWTWSQ-UHFFFAOYSA-N [(2,3-diphenylphenyl)-nonyl-lambda4-sulfanylidene]-trihydroxy-lambda5-phosphane Chemical compound CCCCCCCCCS(=P(O)(O)O)C1=CC=CC(=C1C2=CC=CC=C2)C3=CC=CC=C3 MAOGTIAUZWTWSQ-UHFFFAOYSA-N 0.000 description 1
- VPIGOGDSZWTTAG-UHFFFAOYSA-N [5-[2,3-bis(2-ethylhexyl)-6-methylphenyl]-2H-triazol-4-yl]methanamine Chemical compound C(C)C(CC1=C(C(=C(C=C1)C)C=1N=NNC=1CN)CC(CCCC)CC)CCCC VPIGOGDSZWTTAG-UHFFFAOYSA-N 0.000 description 1
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical group [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical group C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 239000001996 bearing alloy Substances 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 101150047356 dec-1 gene Proteins 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical group C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 description 1
- JHNNEDALALNBGM-UHFFFAOYSA-N ethyl 2-di(propan-2-yloxy)phosphinothioylsulfanylpropanoate Chemical compound CCOC(=O)C(C)SP(=S)(OC(C)C)OC(C)C JHNNEDALALNBGM-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- WKPVNNKDJXZZEQ-UHFFFAOYSA-N ethyl octan-4-ylcarbamothioylsulfanylformate Chemical compound CCCCC(CCC)NC(=S)SC(=O)OCC WKPVNNKDJXZZEQ-UHFFFAOYSA-N 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- VDTIMXCBOXBHER-UHFFFAOYSA-N hydroxy-bis(sulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound OP(S)(S)=S VDTIMXCBOXBHER-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 239000003879 lubricant additive Substances 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
- NTIGMHLFJNXNBT-UHFFFAOYSA-N manganese tin Chemical compound [Mn].[Sn] NTIGMHLFJNXNBT-UHFFFAOYSA-N 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical class CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003136 n-heptyl 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])* 0.000 description 1
- 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 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- PDEDQSAFHNADLV-UHFFFAOYSA-M potassium;disodium;dinitrate;nitrite Chemical compound [Na+].[Na+].[K+].[O-]N=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PDEDQSAFHNADLV-UHFFFAOYSA-M 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- LGQXXHMEBUOXRP-UHFFFAOYSA-N tributyl borate Chemical compound CCCCOB(OCCCC)OCCCC LGQXXHMEBUOXRP-UHFFFAOYSA-N 0.000 description 1
- SMVBWTKCDCPTQG-UHFFFAOYSA-N tris[2-(7-methyloctyl)phenoxy]-sulfanylidene-$l^{5}-phosphane Chemical compound CC(C)CCCCCCC1=CC=CC=C1OP(=S)(OC=1C(=CC=CC=1)CCCCCCC(C)C)OC1=CC=CC=C1CCCCCCC(C)C SMVBWTKCDCPTQG-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon 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
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/12—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic compound containing atoms of elements not provided for in groups C10M141/02 - C10M141/10
-
- 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
- C10M139/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing atoms of elements not provided for in groups C10M127/00 - C10M137/00
-
- 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
- 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
-
- 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
- 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
- C10M2209/1033—Polyethers, i.e. containing di- or higher polyoxyalkylene groups 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/223—Five-membered rings containing nitrogen and carbon 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
- C10M2215/28—Amides; Imides
-
- 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
- C10M2223/043—Ammonium or amine 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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
-
- 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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
- C10M2227/062—Cyclic esters
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
-
- 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
- C10N2040/25—Internal-combustion engines
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US89994607P | 2007-02-07 | 2007-02-07 | |
| US60/899,946 | 2007-02-07 | ||
| PCT/EP2008/050932 WO2008095805A2 (fr) | 2007-02-07 | 2008-01-28 | Inhibiteur de la corrosion de multiples métaux |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2673613A1 true CA2673613A1 (fr) | 2008-08-14 |
Family
ID=39462073
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002673613A Abandoned CA2673613A1 (fr) | 2007-02-07 | 2008-01-28 | Inhibiteur de la corrosion de multiples metaux |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US20080200357A1 (fr) |
| EP (1) | EP2118245A2 (fr) |
| JP (1) | JP2010518205A (fr) |
| KR (1) | KR20090109086A (fr) |
| CN (1) | CN101600784A (fr) |
| CA (1) | CA2673613A1 (fr) |
| WO (1) | WO2008095805A2 (fr) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2954346B1 (fr) | 2009-12-18 | 2013-02-08 | Total Raffinage Marketing | Composition additive pour huile moteur |
| WO2013062890A1 (fr) | 2011-10-27 | 2013-05-02 | The Lubrizol Corporation | Lubrifiants présentant une compatibilité avec des produits d'étanchéité améliorée |
| MX360197B (es) * | 2013-10-29 | 2018-10-11 | Mexicano Inst Petrol | Composicion inhibidora de corrosion para oleoductos, proceso de obtencion y de sintesis. |
| GB201502002D0 (en) * | 2015-02-06 | 2015-03-25 | Castrol Ltd | Uses and compositions |
| AU2016307780B2 (en) | 2015-08-14 | 2019-02-21 | Vanderbilt Chemicals, Llc | Additive for lubricant compositions comprising an organomolybdenum compound, and a derivatized triazole |
| CA2993995A1 (fr) * | 2015-08-14 | 2017-02-23 | Vanderbilt Chemicals, Llc | Nouveaux derives de diphenylamine alkylee de triazole et compositions lubrifiantes les contenant |
| JP6741239B2 (ja) * | 2016-03-28 | 2020-08-19 | 出光興産株式会社 | 潤滑油組成物 |
| CA3031232A1 (fr) | 2016-07-20 | 2018-01-25 | The Lubrizol Corporation | Sels d'amine d'alkyl-phosphate destines a etre utilises dans des lubrifiants |
| CN109715765B (zh) * | 2016-07-20 | 2022-09-30 | 路博润公司 | 用于润滑剂中的烷基磷酸酯胺盐 |
| CN109679717B (zh) * | 2017-10-18 | 2022-06-24 | 中国石油化工股份有限公司 | 压缩机润滑油组合物及其制备方法 |
| US10704009B2 (en) * | 2018-01-19 | 2020-07-07 | Chevron Oronite Company Llc | Ultra low ash lubricating oil compositions |
| US10640723B2 (en) * | 2018-03-16 | 2020-05-05 | Afton Chemical Corporation | Lubricants containing amine salt of acid phosphate and hydrocarbyl borate |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4595523A (en) * | 1983-07-01 | 1986-06-17 | Petrolite Corporation | Corrosion inhibition in engine fuel systems |
| GB8408617D0 (en) * | 1984-04-04 | 1984-05-16 | Ciba Geigy Ag | Metal deactivators |
| US4791206A (en) * | 1985-05-16 | 1988-12-13 | Ciba-Geigy Corporation | Triazole-organodithiophosphate reaction product additives for functional fluids |
| GB8730220D0 (en) * | 1987-12-29 | 1988-02-03 | Exxon Chemical Patents Inc | Detergents |
| GB8824402D0 (en) * | 1988-10-18 | 1988-11-23 | Ciba Geigy Ag | Lubricant compositions |
| US5171463A (en) * | 1989-07-14 | 1992-12-15 | Ciba-Geigy Corporation | N-substituted triazole compounds |
| US5580482A (en) * | 1995-01-13 | 1996-12-03 | Ciba-Geigy Corporation | Stabilized lubricant compositions |
| US6774091B2 (en) * | 1997-08-27 | 2004-08-10 | Ashland Inc. | Lubricant and additive formulation |
| US6010986A (en) * | 1998-07-31 | 2000-01-04 | The Lubrizol Corporation | Alcohol borate esters to improve bearing corrosion in engine oils |
| US6008165A (en) * | 1998-07-31 | 1999-12-28 | The Lubrizol Corporation | Alcohol borate esters and borated dispersants to improve bearing corrosion in engine oils |
| EP1054052B1 (fr) * | 1999-05-19 | 2006-06-28 | Ciba SC Holding AG | Des compositions lubrifiantes hydroraffinées et hydrodéparaffinées stabilisées |
| US20040038835A1 (en) * | 2002-08-06 | 2004-02-26 | Chasan David E. | Engine oils that are non-aggressive towards lead |
| MY136312A (en) * | 2003-05-21 | 2008-09-30 | Ciba Holding Inc | Borate ester lubricant additives |
| US20080020952A1 (en) * | 2004-10-19 | 2008-01-24 | Kazuhiro Yagishita | Lubricant Composition |
-
2008
- 2008-01-28 CN CNA2008800014488A patent/CN101600784A/zh active Pending
- 2008-01-28 KR KR1020097013098A patent/KR20090109086A/ko not_active Application Discontinuation
- 2008-01-28 JP JP2009548648A patent/JP2010518205A/ja active Pending
- 2008-01-28 WO PCT/EP2008/050932 patent/WO2008095805A2/fr active Application Filing
- 2008-01-28 EP EP08708255A patent/EP2118245A2/fr not_active Withdrawn
- 2008-01-28 CA CA002673613A patent/CA2673613A1/fr not_active Abandoned
- 2008-02-04 US US12/012,590 patent/US20080200357A1/en not_active Abandoned
-
2010
- 2010-03-15 US US12/723,879 patent/US20100173808A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008095805A2 (fr) | 2008-08-14 |
| US20080200357A1 (en) | 2008-08-21 |
| US20100173808A1 (en) | 2010-07-08 |
| CN101600784A (zh) | 2009-12-09 |
| JP2010518205A (ja) | 2010-05-27 |
| WO2008095805A3 (fr) | 2008-10-23 |
| KR20090109086A (ko) | 2009-10-19 |
| EP2118245A2 (fr) | 2009-11-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2673613A1 (fr) | Inhibiteur de la corrosion de multiples metaux | |
| US7531487B2 (en) | Lubricating oil compositions with improved performance | |
| AU2003253351B2 (en) | Engine oils comprising lead corrosion-inhibitors | |
| WO2006029966A1 (fr) | Additifs d'alkylaminoacetamide pour lubrifiants | |
| US7291581B2 (en) | Borate ester lubricant additives | |
| JP3523235B2 (ja) | 潤滑剤用イミダゾールチオン添加剤 | |
| US7897552B2 (en) | Additives and lubricant formulations for improved antioxidant properties | |
| EP3212746A1 (fr) | Amides alcoxylés, esters et agents anti-usure dans des compositions lubrifiantes | |
| JP2018090714A (ja) | 潤滑油組成物及びその製造方法 | |
| JP4111918B2 (ja) | 潤滑剤向け１，３，４−オキサジアゾール添加剤 | |
| EP4202023B1 (fr) | Compositions lubrifiantes capables de donner une flotte mixte | |
| EP0588561A1 (fr) | Compositions d'huile moteur à faible teneur en phosphore et compositions d'additifs | |
| JP4141951B2 (ja) | 摩擦調整剤としての有機モリブデン配位化合物 | |
| JP4128523B2 (ja) | 潤滑剤のためのチアジアゾリジン添加剤 | |
| CN118291198A (zh) | 减少异常燃烧事件的方法 | |
| JP4241949B2 (ja) | 磨耗抑制効果を有するフルオロカーボンエラストマーとの相容性を改良する薬剤 | |
| CN118251483A (zh) | 在旨在用于机动化系统的润滑剂中作为添加剂用于改善与弹性体的相容性的碳二亚胺 | |
| EP0918083A1 (fr) | Utilisation de dérivés du dithioéthylène en tant qu'agents améliorant la compatibilité avec les élastomers fluorocarbonés |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |
Effective date: 20130128 |