US2719827A - Lubricating oil compositions containing sulfur corrosive to silver - Google Patents
Lubricating oil compositions containing sulfur corrosive to silver Download PDFInfo
- Publication number
- US2719827A US2719827A US260112A US26011251A US2719827A US 2719827 A US2719827 A US 2719827A US 260112 A US260112 A US 260112A US 26011251 A US26011251 A US 26011251A US 2719827 A US2719827 A US 2719827A
- Authority
- US
- United States
- Prior art keywords
- silver
- sulfur
- thiadiazolyl
- oils
- lubricating oil
- 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.)
- Expired - Lifetime
Links
- 239000010687 lubricating oil Substances 0.000 title claims description 30
- 239000000203 mixture Substances 0.000 title claims description 18
- 229910052709 silver Inorganic materials 0.000 title description 56
- 239000004332 silver Substances 0.000 title description 56
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 title description 45
- 229910052717 sulfur Inorganic materials 0.000 title description 45
- 239000011593 sulfur Substances 0.000 title description 45
- 239000012990 dithiocarbamate Substances 0.000 claims description 16
- 239000000314 lubricant Substances 0.000 claims description 16
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 claims description 14
- SZRLKIKBPASKQH-UHFFFAOYSA-M dibutyldithiocarbamate Chemical compound CCCCN(C([S-])=S)CCCC SZRLKIKBPASKQH-UHFFFAOYSA-M 0.000 claims description 7
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 57
- 239000003921 oil Substances 0.000 description 30
- -1 thiadiazolyl dithiocarbamates Chemical class 0.000 description 30
- 230000007797 corrosion Effects 0.000 description 26
- 238000005260 corrosion Methods 0.000 description 26
- 239000003795 chemical substances by application Substances 0.000 description 17
- 231100001010 corrosive Toxicity 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 17
- 239000002184 metal Substances 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 15
- 239000000654 additive Substances 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 9
- 125000002947 alkylene group Chemical group 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- 239000003223 protective agent Substances 0.000 description 8
- 150000003464 sulfur compounds Chemical class 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 230000001050 lubricating effect Effects 0.000 description 7
- 125000001113 thiadiazolyl group Chemical group 0.000 description 7
- 229940054266 2-mercaptobenzothiazole Drugs 0.000 description 6
- 239000002199 base oil Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- OCVLSHAVSIYKLI-UHFFFAOYSA-N 3h-1,3-thiazole-2-thione Chemical compound SC1=NC=CS1 OCVLSHAVSIYKLI-UHFFFAOYSA-N 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 5
- 229940116901 diethyldithiocarbamate Drugs 0.000 description 5
- 230000002401 inhibitory effect Effects 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- LMBWSYZSUOEYSN-UHFFFAOYSA-N diethyldithiocarbamic acid Chemical compound CCN(CC)C(S)=S LMBWSYZSUOEYSN-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 150000004659 dithiocarbamates Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical class CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 3
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229940065287 selenium compound Drugs 0.000 description 3
- 150000003343 selenium compounds Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 150000004763 sulfides Chemical class 0.000 description 3
- 150000003871 sulfonates Chemical class 0.000 description 3
- 210000000707 wrist Anatomy 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-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
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical group C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 2
- NSAODVHAXBZWGW-UHFFFAOYSA-N cadmium silver Chemical compound [Ag].[Cd] NSAODVHAXBZWGW-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 229910001092 metal group alloy Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 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
- 239000003208 petroleum Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229920001296 polysiloxane Polymers 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
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- CFHLPYGPURTAMI-UHFFFAOYSA-N 4,5-diethyl-3h-1,3-thiazole-2-thione Chemical compound CCC=1N=C(S)SC=1CC CFHLPYGPURTAMI-UHFFFAOYSA-N 0.000 description 1
- KKHBRTFQIYIHEI-UHFFFAOYSA-N 4,5-dimethyl-3h-1,3-thiazole-2-thione Chemical compound CC=1N=C(S)SC=1C KKHBRTFQIYIHEI-UHFFFAOYSA-N 0.000 description 1
- FORKADXOPFAOHL-UHFFFAOYSA-N 4-ethyl-3h-1,3-thiazole-2-thione Chemical compound CCC1=CSC(S)=N1 FORKADXOPFAOHL-UHFFFAOYSA-N 0.000 description 1
- 125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 description 1
- JACGKHGTBZGVMW-UHFFFAOYSA-N 4-methyl-3h-1,3-benzothiazole-2-thione Chemical compound CC1=CC=CC2=C1N=C(S)S2 JACGKHGTBZGVMW-UHFFFAOYSA-N 0.000 description 1
- GUISIVZZEFLXQH-UHFFFAOYSA-N 4-phenyl-3h-1,3-benzothiazole-2-thione Chemical compound C1=CC=C2SC(=S)NC2=C1C1=CC=CC=C1 GUISIVZZEFLXQH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-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
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000925 Cd alloy Inorganic materials 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XTJFFFGAUHQWII-UHFFFAOYSA-N Dibutyl adipate Chemical compound CCCCOC(=O)CCCCC(=O)OCCCC XTJFFFGAUHQWII-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- NXEUTNOJLUEESD-UHFFFAOYSA-L P(OCCCCCCCCCCCCCCCC)([O-])=S.[Ca+2].C(CCCCCCCCCCCCCCC)OP([O-])=S Chemical class P(OCCCCCCCCCCCCCCCC)([O-])=S.[Ca+2].C(CCCCCCCCCCCCCCC)OP([O-])=S NXEUTNOJLUEESD-UHFFFAOYSA-L 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- PFUQSACCWFVIBW-UHFFFAOYSA-N [C].C1=CC=CC=C1 Chemical group [C].C1=CC=CC=C1 PFUQSACCWFVIBW-UHFFFAOYSA-N 0.000 description 1
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical compound [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 1
- 230000000397 acetylating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000002547 anomalous effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- DHJGVCITGOCTCA-UHFFFAOYSA-L calcium;hexadecyl phosphate Chemical class [Ca+2].CCCCCCCCCCCCCCCCOP([O-])([O-])=O DHJGVCITGOCTCA-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- DZQISOJKASMITI-UHFFFAOYSA-N decyl-dioxido-oxo-$l^{5}-phosphane;hydron Chemical compound CCCCCCCCCCP(O)(O)=O DZQISOJKASMITI-UHFFFAOYSA-N 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229940100539 dibutyl adipate Drugs 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 150000003959 diselenides Chemical class 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- KSNOVNHUMFSIDF-UHFFFAOYSA-N dodecylbenzene tetradecylbenzene Chemical compound C(CCCCCCCCCCCCC)C1=CC=CC=C1.C(CCCCCCCCCCC)C1=CC=CC=C1 KSNOVNHUMFSIDF-UHFFFAOYSA-N 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000012208 gear oil Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- OJXOOFXUHZAXLO-UHFFFAOYSA-M magnesium;1-bromo-3-methanidylbenzene;bromide Chemical compound [Mg+2].[Br-].[CH2-]C1=CC=CC(Br)=C1 OJXOOFXUHZAXLO-UHFFFAOYSA-M 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QCAZHHXMIVSLMW-UHFFFAOYSA-N o-butyl (butoxycarbothioyldisulfanyl)methanethioate Chemical compound CCCCOC(=S)SSC(=S)OCCCC QCAZHHXMIVSLMW-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000021317 phosphate Nutrition 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
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
- 229920003216 poly(methylphenylsiloxane) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Chemical class 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 150000003378 silver Chemical class 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
- 239000000126 substance Substances 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003463 sulfur Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- ZUEKXCXHTXJYAR-UHFFFAOYSA-N tetrapropan-2-yl silicate Chemical compound CC(C)O[Si](OC(C)C)(OC(C)C)OC(C)C ZUEKXCXHTXJYAR-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- PQRRMYYPKMKSNF-UHFFFAOYSA-N tris(4-methylpentan-2-yl) tris(4-methylpentan-2-yloxy)silyl silicate Chemical compound CC(C)CC(C)O[Si](OC(C)CC(C)C)(OC(C)CC(C)C)O[Si](OC(C)CC(C)C)(OC(C)CC(C)C)OC(C)CC(C)C PQRRMYYPKMKSNF-UHFFFAOYSA-N 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- XMFRQHDPDGAVEW-UHFFFAOYSA-L zinc;hexylsulfanyl-dioxido-sulfanylidene-$l^{5}-phosphane Chemical compound [Zn+2].CCCCCCSP([O-])([O-])=S XMFRQHDPDGAVEW-UHFFFAOYSA-L 0.000 description 1
Classifications
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- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/32—Heterocyclic sulfur, selenium or tellurium compounds
- C10M135/36—Heterocyclic sulfur, selenium or tellurium compounds the ring containing sulfur and carbon with nitrogen or oxygen
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- C10M2201/02—Water
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- C10M2205/024—Propene
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- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/044—Siloxanes with specific structure containing silicon-to-hydrogen bonds
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/045—Siloxanes with specific structure containing silicon-to-hydroxyl bonds
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/046—Siloxanes with specific structure containing silicon-oxygen-carbon bonds
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/047—Siloxanes with specific structure containing alkylene oxide groups
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- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/048—Siloxanes with specific structure containing carboxyl groups
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- 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
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
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- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
Definitions
- the present invention relates to lubricating oil compositions containing sulfur which is corrosive to silver and like metals, which corrosion is inhibited by the presence of 2-thio-thiazoles (e. g., 2-mercaptothiazole) and thiadiazolyl dithiocarbamates (e. g. 1,3,4-thiadiazolyl-2,5- bis(dialkyl dithiocarbamate)
- 2-thio-thiazoles e. g., 2-mercaptothiazole
- thiadiazolyl dithiocarbamates e. g. 1,3,4-thiadiazolyl-2,5- bis(dialkyl dithiocarbamate
- Some of the most effective agents which are added to lubricating oils for various purposes contain sulfur.
- sulfur For example, aliphatic polysulfides, metal salts of organo thiophosphates, etc., are highly effective oxidation inhibitors; and sulfurized olefins, xanthate esters and the like are excellent extreme pressure agents.
- the sulfur contained in these agents is severely corrosive to silver and like metals. This sulfur is not corrosive to such hard-metal alloys as cadmium-silver alloy, which cadmium alloy normally contains less than 1% of silver.
- sulfur readily attacks the pure silver metal wearing surfaces with which this invention is concerned. This attack results in a rapid darkening of the metal surface and the formation of sulfides which subsequently slough oif during engine operation. Thus, there is a considerable loss of metal wearing surface and a pitting of the surfaces.
- oxidation corrosion The corrosion and attack on metals by acidic bodies has been termed oxidation corrosion or acid corrosion, which corrosion is caused by action of acids and peroxides which are formed in lubricating oils as products of oxidation.
- sulfur corrosion The corrosion caused by sulfur is herein designated as sulfur corrosion.
- this object may be attained by the present invention which is concerned with lubricating oil compositions containing active sulfur, which lubricating oil compositions are severely corrosive to silver, and such agents which will inhibit the corrosivity of the sulfur to silver, minimizing the attack on the silver by the sulfur in the lubricant but without adversely affecting the desired functioning of the sulfur compounds per se.
- the combination of Z-thiothiazoles and thiadiazolyl dialkyl dithiocarbamates in lubricating oil compositions inhibits sulfur corrosion of silver.
- the lubricants of this invention comprise a major portion of oils of lubricating viscosity, and minor amounts each of 2-thio-thiazoles and thiadiazolyl dialkyl dithiocarbamates.
- the simplest member of the 2-thio-thiazole group is Z-mercapto-thiazole.
- Derivatives of Z-mercapto-thiazole, wherein there may be substituents in the ring carbon atoms, are also included herein.
- the hydrogen atoms of the thiazole ring may be substituted by short-chained saturated and unsaturated radicals (e. g., methyl, ethyl, propyl, butyl, ethenyl, propenyl, butenyl, etc.). It is preferred that the substitutents contain a total of not more than 20 carbon atoms.
- the two adjacent carbon atoms of the Z-thio-thiazoles may form parts of a benzene ring, such. as in Z-mercapto benzothiazole.
- the 2 mercapto-benzothiazole may be substituted on one or more benzene carbon atoms by short-chained saturated and unsaturated aliphatic radicals (e. g., methyl, ethyl, propyl, butyl, octyl, ethenyl, propenyl, octenyl, etc.). It is preferred that there be not more than four substituent groups on the ring and that these substituents contain a total of not more than 16 carbon atoms.
- Z-thio-thiazoles are: 2-mercapto-benzothiazole; N-cyclohexyl-Z-benzothiazyl sulfonamide, 2- mercapto-S-methyl thiazole; 2-mercapto-4-thiazole; 2- mercapto 4,5 dimethyl thiazole; 2-mercapto-4-ethyl thiazole; 2-mercapto-4,5-diethyl thiazole; phenyl mercapto-benzothiazole; and methyl mercapto-benzothiazole.
- the thiadiazolyl dithiocarbamates are represented by the following formulas:
- the Rs represent straight-chained or branched chained, saturated or unsaturated substantially hydrocarbon (hydrocarbonaceous) radicals selected from the group of alkyl, aralkyl and alkaryl radicals.
- the alkyl groups present as such or attached to a ring structure each contain from 1 to 20 or more carbon atoms, preferably 2 to 8 carbon atoms.
- the R groups may or may not be identical.
- R groups examples include: ethyl, propyl, propenyl, butyl, butenyl, octyl, octenyl, octadecyl, benzyl, phenyl butyl, phenyl octyl, ethyl phenyl, butyl phenyl, octyl phenyl, etc.
- hydrocarbon (hydrocarbonaceous) radical is meant those radicals which are composed mainly of hydrogen and carbon, and include such radicals which include, in addition, minor amounts of the substituents such as chlorine, bromine, oxygen, nitrogen, etc.
- thiadiazolyl dithiocarbamates of this invention include:
- the 2-thio-thiazoles and thiadiazolyl dithiocarbamates of this invention are effective in inhibiting silver corrosion when each is present in amounts as low as about 0.01% (by weight of total composition). Certain of these compounds have only limited solubility in the lubricating oil and are effective at that solubility. When the 2-thio-thiazoles and thiadiazolyl derivatives have sufficient solubility, they are effective when each one is used in amounts as great as 10%. However, it is preferred that the compounds of this invention be used in amounts sufiicient substantially to reduce the corrosion of silver.
- the 2-thiothiazole derivatives and the thiadiazolyl compounds each in amounts of from about 0.05% to 0.50%, so that the total is from about 0.10% to about 1.0%.
- the major proportion of the lubricating oil composition of this invention is the base oil.
- the 2-thio-thiazoles and the thiadiazolyl derivatives be used in equal amounts to obtain the greatest benefit therefrom.
- the ratio of 2-thio-thiazoles and thiadiazolyl derivatives can have values varying from 0.33 to 3.
- Suitable base oils include a wide variety of lubricating oils such as naphthenic base, paraffin base, and mixed mineral oils, other hydrocarbon lubricants, e. g., lubricating oils derived from coal products, and synthetic oils, e. g., alkylene polymers (such as polymers of propylene, butylenes, etc., and mixtures thereof), alkylene oxide type polymers, dicarboxylic acid esters, liquid esters of acids of phosphorus, alkyl benzene polymers, polymers of silicon, etc.
- synthetic oils of the alkylene oxide type polymers which may be used include those exemplified by the alkylene oxide polymers (e.
- propylene oxide polymers and derivatives, including alkylene oxide polymers prepared by polymerizing alkylene oxides, e. g., propylene oxide, in the presence of water or alcohols, e. g., ethyl alcohol; esters of alkylene oxide type polymers, e. g., acetylated propylene oxide polymers prepared by acetylating propylene oxide polymers containing hydroxyl groups; polyethers prepared from the alkylene glycols (e. g., ethylene glycol), etc.
- the polymeric products prepared from the various alkylene oxides and alkylene glycols may be polyoxyalkylene diols or polyalkylene glycol derivatives; that is, the terminal hydroxy group can remain as such, or one or both of the terminal hydroxy groups can be removed during the polymerization reaction by etherification or esterification.
- Synthetic oils of the dicarboxylic acid ester type include those which are prepared by esterifying such dicarboxylic acids as adipic acid, azelaic acid, suberic acid, sebacic acid, alkenyl succinic acid, fumaric acid, maleic acid, etc., with alcohols such as butyl alcohol, hexyl alcohol, 2-ethyl-hexyl alcohol, dodecyl alcohol, etc.
- Examples of dicarboxylic acid ester synthetic oils include dibutyl adipate, dihexyl adipate, di-2-ethylhexyl sebacate, di-n-hexyl fumaric polymer, etc.
- Synthetic oils of the alkyl benzene type include those which are prepared by alkylating benzene (e. g., dodecyl benzene tetradecyl benzene, etc.)
- Synthetic oils of the type of liquid esters of acids of phosphorus include the esters of phosphoric acid, e. g., tricresyl phosphate; the esters of phosphonic acid, e. g., diethyl ester of decane phosphonic acid (or other such esters as obtained by reacting alkyl phosphonyl chlorides with hydroxyl-containing compounds such as phenols and aliphatic alcohols) and with olefin oxides such as propylene oxide, as described in Jensen et 211., U. S. Patent Application 202,396.
- Synthetic oils of the type of polymers of silicon include the liquid esters of silicon and the polysiloxanes.
- the liquid esters of silicon and the polysiloxanes include those exemplified by tetraethyl silicate, tetraisopropyl silicate, tetra(methyl-2-butyl) silicate, tetra(4-methyl- 2-pentyl) silicate, tetra(l-methoxy-Z-propyl) silicate, hexa(4-methyl-2-pentoxy) disiloxane, poly (methyl siloxane), poly(methylphenyl siloxane), etc.
- the above base oils may be used individually as such or in various combinations (wherever miscible or whenever made so by the use of metal solvents).
- the improved lubricant of the present invention is used wherever elemental sulfur or sulfur compounds containing active sulfur attack metal and are severely corrosive to metals which are being lubricated.
- lubricants which normally are severely corrosive to metal parts due to attack by sulfur or active sulfur compounds may now be used without fear of corrosion by incorporating therein the combination of 2-thiothiazole compounds and thiadiazolyl compounds. Severely corrosive is defined as that corrosion which causes a weight loss greater than about 30 mg. in the silver strip test noted hereinbelow.
- a silver metal strip having the dimensions of 2%" x X was first cleaned with a Wire brush until the strip was highly polished. The strip was weighed and the weight recorded. This highly polished silver strip was then placed in a 600 ml. beaker in such a manner that the strip was completely immersed when 300 gm. of the oil being tested was poured into the beaker. The oil was stirred at a temperature of 300 F. for 20 hours, at which time the silver strip was removed and cleaned,
- 1,3,4-thiadiazolyl 2,5 bis(dialkyl dithiocarbamates) used in obtaining the dataset forth hereinbelow are manufactured by Sharples Chemicals, Inc., Philadelphia, Pa.
- Table I below presents data obtained in the silver strip test" and shows the remarkable effect of the combination of 2-thio-thiazole and thiadiazolyl dithiocarbamates as silver protective agents in reducing the attack on silver by a California solvent refined S.
- A. E. 30 paraflinic base oil containing a zinc alkyl phenyl dithiophosphate, 2- mercaptobenzothiazole and 1,3,4-thiadiazolyl 2,5-bis- (diethyldithiocarbarnate).
- the alkyl radical in the zinc alkyl phenyl dithiophosphate contained an average of 14 carbon atoms and was derived from a mixture of propene and butene polymers.
- Table II presents data obtained in the silver strip test of a solvent refined S.A.E. 30 parafiin base oil to which was added zinc alkyl phenyl dithiophosphate, 2- mercapto-benzothiazole and 1,3,4-thia-diazolyl 2,5-bis (dibutyl dithiocarbamate).
- the strips were rated as follows: a silver strip which was not discolored was given a rating of zero (0), while a strip which showed pronounced corrosion was given a rating of 5, with proportionate ratings for intermediate discoloration.
- the base oil was a mixture of equal parts by volume of isooctyl hexaoxypropylene acetate and tetra (Z-ethyl hexyl) ortho silicate. Incorporated in the oil was a sulfurcontaining extreme pressure additive commercially marketed by Lubri-Zol Corporation as Anglamol 82.
- sulfurized lubricating oils As illustrative of various sulfur containing extreme pressure agents, detergents, oxidation inhibitors, etc. which cause oils containing them to be severely corrosive to silver, the following may be mentioned: sulfurized lubricating oils, xanthate esters, chlorinated xanthate esters, dialkyl disulfides, sulfurized fatty oils, metal salts of reaction products of olefins and phosphorus penta sulfide, organic trisulfides, tetra sulfides and penta sulfides (e. g., paraifin wax polysulfide), polyvalent metal salts of organo-substituted acids of phosphorus (e.
- the silver protective agents of this invention are also efiective in reducing attack on silver by the sulfur in lubricating oils derived from some of the crude oils characterized by their high sulfur content.
- the silver protective agents are especially desirable and preferably used in combination in lubricating oils containing the polyvalent metal salts of organo-substituted thioacids of phosphorus (e. g., zinc alkylphenyl dithiophosphate); however, they can be used in lubricating oils containing such compounds as phenates (e. g.,
- the silver protective agents of this invention may be added to lubricating oil compositions containing other agents than sulfur active agents, that is, other agents which are advantageously present as oxidation inhibitors (e. g., phenyl alpha naphthylamine), anti-wear agents (e. g., tricresyl phosphate), rust inhibitors (e. g., metal sulfonates), oiliness agents, blooming agents, viscosity index improvers, pour point depressants, peptizing agents, thickening agents for greases, etc.
- oxidation inhibitors e. g., phenyl alpha naphthylamine
- anti-wear agents e. g., tricresyl phosphate
- rust inhibitors e. g., metal sulfonates
- oiliness agents e. g., blooming agents, viscosity index improvers, pour point depressants, peptizing agents, thickening agents for greases
- the combination of compounds of this invention is also effective in reducing corrosion of silver due to selenium compounds. That is, lubricants which contain active selenium compounds as additives, for example, dialkyl monoselem'des, dialkyl diselenides, dialkyl polyselenides, selenomercaptans, methyl alkyl selenides, etc. show attack on silver by selenium. However, the protective agents of this invention inhibit the attack on silver by lubricants containing selenium compounds.
- a lubricant comprising a major proportion of a silver-corrosive sulfur-containing lubricating oil composition, from 0.05% to 0.5% by weight of Z-mercaptobenzothiazole, and from 0.05% to 0.5 by weight of a thiadiazolyl dithiocarbamate selected from the group consisting of 1,3,4-thiadiazolyl-2,5-bis(diethyl dithio carbamate) and l,3,4-thiadiazolyl-2,5-bis(dibutyl dithiocarbamate).
- a lubricant comprising a major proportion of an oil of lubricating viscosity having incorporated therein sulfur-containing additives which are corrosive to silver, and which additives inhibit corrosion caused by oxidation, and from 0.05% to 0.5 by weight of Z-mercapto-benzothiazole, and from 0.05% to 0.5 by weight of a thiadiazolyl dithiocarbamate selected from the group consisting of 1,3,4-thiadiazolyl-2,5-bis(diethyl dithiocarbamate) and 1,3,4-thiadiazolyl-2,5-bis(dibutyl dithiocarbamate).
- a lubricant consisting essentially of a major proportion of an oil of lubricating viscosity having therein sulfur derived from the oil itself, which sulfur is corrosive to silver wearing surfaces, wherein the silver is prescut as substantially pure silver, and 0.05 to 0.5 by weight of 2-mercapto-benzothiazole, and from 0.05 to 0.5 by weight of a thiadiazolyl dithiocarbamate selected from the group consisting of 1,3,4-thiadiazolyl-2,S-bis- (diethyl dithiocarbamate) and 1,3,4-thiadiazolyl-2,5-bis- (dibutyl dithiocarbamate).
- a lubricant consisting essentially of a major proportion of an oil of lubricating viscosity having incorporated therein sulfur-containing compounds having sulfur corrosive to pure silver wearing surfaces, from 0.05% to 0.5% by weight of Z-mercapto-benzothiazole, and from 0.05% to 0.5% by weight of 1,3,4-thiadiazolyl-2,5-bis- (diethyl dithiocarbamate) 5.
- a lubricant consisting essentially of a major proportion of an oil of lubricating viscosity having incorporated therein sulfur-containing compounds having sulfur corrosive to pure silver wearing surfaces, from 0.05 to 0.5% by weight of 2-mercapto-benzothiazole, and from 0.05% to 0.5% by weight of 1,3,4-thiadiazolyl-2,S-bis- (dibutyl dithiocarbamate).
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Description
United States Patent LUBRICATING OIL COMPOSITIONS CONTAINING SULFUR CORROSIV E TO SILVER Warren Lowe, Berkeley, Calif., assignor to California Research Corporation, San Francisco, Calif., a corporation of Delaware No Drawing. Application December 5, 1951, Serial No. 260,112
5 Claims. (Cl. 25247) The present invention relates to lubricating oil compositions containing sulfur which is corrosive to silver and like metals, which corrosion is inhibited by the presence of 2-thio-thiazoles (e. g., 2-mercaptothiazole) and thiadiazolyl dithiocarbamates (e. g. 1,3,4-thiadiazolyl-2,5- bis(dialkyl dithiocarbamate) For the most part, internal combustion engines are operated at high speeds and at eleavted temperatures. At high speeds and elevated temperatures, the lubricating oil oxidizes to form acidic products. Furthermore, the engine fuel deposits acidic bodies which find their way into the lubricating oil chamber. These acidic products rapidly deteriorate the lubricating value of the oil. The acidic products thus formed in lubricating oil compositions are severely corrosive to hard metal alloys such as cadmium-silver, copper-lead, etc. This acid corrosion, which may also be called oxidation corrosion, is normally inhibited by the presence of additives which are incorporated in lubricating oil compositions to inhibit the deterioration of the lubricating oil.
Some of the most effective agents which are added to lubricating oils for various purposes contain sulfur. For example, aliphatic polysulfides, metal salts of organo thiophosphates, etc., are highly effective oxidation inhibitors; and sulfurized olefins, xanthate esters and the like are excellent extreme pressure agents. The sulfur contained in these agents is severely corrosive to silver and like metals. This sulfur is not corrosive to such hard-metal alloys as cadmium-silver alloy, which cadmium alloy normally contains less than 1% of silver. However, sulfur readily attacks the pure silver metal wearing surfaces with which this invention is concerned. This attack results in a rapid darkening of the metal surface and the formation of sulfides which subsequently slough oif during engine operation. Thus, there is a considerable loss of metal wearing surface and a pitting of the surfaces.
The corrosion and attack on metals by acidic bodies has been termed oxidation corrosion or acid corrosion, which corrosion is caused by action of acids and peroxides which are formed in lubricating oils as products of oxidation. The corrosion caused by sulfur is herein designated as sulfur corrosion.
In spite of the long desire to lubricate silver bearings with lubricants compounded with active sulfur compounds, it has been impractical to do so in view of the aforementioned severe corrosivity to silver.
Heretofore, in the lubrication of engines having silver metal wearing surfaces, for example, in certain-railroad Diesel engines which use silver wrist pin bushings, it has been diflicult to prevent sulfur attack of the'silver surfaces. Because the silver surfaces (e. g., the silver wrist pin bushings) are susceptible to attack by the sulfur of the sulfur-containing lubricating oil additives, there has been a tendency to eliminate highly effective sulfur-containing additives from the Diesel lubricating oils, thereby losing the remarkable benefits of these additives. As noted hereinabove, certain highly effective lubricating oil anti-oxidants contain sulfur, which is corrosive to silver. These effective anti-oxidants have not been used in Diesel engines containing silver wn'st pin bushings without sulfur attack on the silver. Alternative practices have been to eliminate the sulfur-containing additives from the oil, allowing the oil to deteriorate more rapidly through oxidation; or the sulfur-containing additives have been included in the oil formulation, with the resulting sulfur corrosion of the silver wrist pin bushings. Silver is also used in wearing surfaces in aircraft engines, but because of the presence of the silver, the highly effective sulfur-containing aviation oil additives are not used. Now, however, by using the compounds of this invention, lubricating oils compounded with sulfur-containing additives can be used in Diesel oils, aviation oils, and any other oils where sulfur corrosion of metals is a problem.
Numerous agents have been proposed for inhibiting the sulfur attack on silver; however, the combination of agents set forth in this invention has enhanced activities for reducing the corrosivity to silver by sulfur in lubricating oil compositions. The combination of compounds set forth hereinbelow produces a remarkable synergistic effect in inhibiting sulfur corrosion of silver.
It is, therefore, an object of this invention to provide a non-silver corrosive lubricant containing active sulfur compounds.
It has been ascertained that this object may be attained by the present invention which is concerned with lubricating oil compositions containing active sulfur, which lubricating oil compositions are severely corrosive to silver, and such agents which will inhibit the corrosivity of the sulfur to silver, minimizing the attack on the silver by the sulfur in the lubricant but without adversely affecting the desired functioning of the sulfur compounds per se.
According to the present invention, the combination of Z-thiothiazoles and thiadiazolyl dialkyl dithiocarbamates in lubricating oil compositions inhibits sulfur corrosion of silver. The lubricants of this invention comprise a major portion of oils of lubricating viscosity, and minor amounts each of 2-thio-thiazoles and thiadiazolyl dialkyl dithiocarbamates.
The simplest member of the 2-thio-thiazole group is Z-mercapto-thiazole. Derivatives of Z-mercapto-thiazole, wherein there may be substituents in the ring carbon atoms, are also included herein.
In Z-thio-thiazole, the hydrogen atoms of the thiazole ring may be substituted by short-chained saturated and unsaturated radicals (e. g., methyl, ethyl, propyl, butyl, ethenyl, propenyl, butenyl, etc.). It is preferred that the substitutents contain a total of not more than 20 carbon atoms.
The two adjacent carbon atoms of the Z-thio-thiazoles may form parts of a benzene ring, such. as in Z-mercapto benzothiazole. The 2 mercapto-benzothiazole may be substituted on one or more benzene carbon atoms by short-chained saturated and unsaturated aliphatic radicals (e. g., methyl, ethyl, propyl, butyl, octyl, ethenyl, propenyl, octenyl, etc.). It is preferred that there be not more than four substituent groups on the ring and that these substituents contain a total of not more than 16 carbon atoms.
Examples of Z-thio-thiazoles are: 2-mercapto-benzothiazole; N-cyclohexyl-Z-benzothiazyl sulfonamide, 2- mercapto-S-methyl thiazole; 2-mercapto-4-thiazole; 2- mercapto 4,5 dimethyl thiazole; 2-mercapto-4-ethyl thiazole; 2-mercapto-4,5-diethyl thiazole; phenyl mercapto-benzothiazole; and methyl mercapto-benzothiazole. The thiadiazolyl dithiocarbamates are represented by the following formulas:
wherein the Rs represent straight-chained or branched chained, saturated or unsaturated substantially hydrocarbon (hydrocarbonaceous) radicals selected from the group of alkyl, aralkyl and alkaryl radicals. The alkyl groups present as such or attached to a ring structure each contain from 1 to 20 or more carbon atoms, preferably 2 to 8 carbon atoms. The R groups may or may not be identical.
Examples of the R groups include: ethyl, propyl, propenyl, butyl, butenyl, octyl, octenyl, octadecyl, benzyl, phenyl butyl, phenyl octyl, ethyl phenyl, butyl phenyl, octyl phenyl, etc.
It is preferred to use thiadiazolyl dithiocarbamates wherein the Rs of the above formula represent alkyl radicals.
By essentially hydrocarbon (hydrocarbonaceous) radical is meant those radicals which are composed mainly of hydrogen and carbon, and include such radicals which include, in addition, minor amounts of the substituents such as chlorine, bromine, oxygen, nitrogen, etc.
Examples of thiadiazolyl dithiocarbamates of this invention include:
1,3,4-thiadiazolyl-2,5-bis (diethyl dithiocarbarnate) 1,3,4-thiadiazolyl-2,5-bis(dibutyl dithiocarbamate); 1,3,4-thiadiazolyl-2,S-bis (doctyl dithiocarbamate) 1,3,4-thiadiazolyl-2,5-bis(dioctadecyl dithiocarbamate); 1,2,4-thiadiazolyl-2-thiol-5-diethyl dithiocarbamate; l,3,4-thiadiazolyl-2-thiol-5-dibutyl dithioearbamate; 1,3,4-thiadiazolyl-2-thiol-5-dioctyl dithiocarbamate, etc.
The 2-thio-thiazoles and thiadiazolyl dithiocarbamates of this invention are effective in inhibiting silver corrosion when each is present in amounts as low as about 0.01% (by weight of total composition). Certain of these compounds have only limited solubility in the lubricating oil and are effective at that solubility. When the 2-thio-thiazoles and thiadiazolyl derivatives have sufficient solubility, they are effective when each one is used in amounts as great as 10%. However, it is preferred that the compounds of this invention be used in amounts sufiicient substantially to reduce the corrosion of silver. For example, it is preferred to use the 2-thiothiazole derivatives and the thiadiazolyl compounds each in amounts of from about 0.05% to 0.50%, so that the total is from about 0.10% to about 1.0%. The major proportion of the lubricating oil composition of this invention is the base oil.
It is preferred that the 2-thio-thiazoles and the thiadiazolyl derivatives be used in equal amounts to obtain the greatest benefit therefrom. However, the ratio of 2-thio-thiazoles and thiadiazolyl derivatives can have values varying from 0.33 to 3.
Suitable base oils include a wide variety of lubricating oils such as naphthenic base, paraffin base, and mixed mineral oils, other hydrocarbon lubricants, e. g., lubricating oils derived from coal products, and synthetic oils, e. g., alkylene polymers (such as polymers of propylene, butylenes, etc., and mixtures thereof), alkylene oxide type polymers, dicarboxylic acid esters, liquid esters of acids of phosphorus, alkyl benzene polymers, polymers of silicon, etc. Synthetic oils of the alkylene oxide type polymers which may be used include those exemplified by the alkylene oxide polymers (e. g., propylene oxide polymers) and derivatives, including alkylene oxide polymers prepared by polymerizing alkylene oxides, e. g., propylene oxide, in the presence of water or alcohols, e. g., ethyl alcohol; esters of alkylene oxide type polymers, e. g., acetylated propylene oxide polymers prepared by acetylating propylene oxide polymers containing hydroxyl groups; polyethers prepared from the alkylene glycols (e. g., ethylene glycol), etc. The polymeric products prepared from the various alkylene oxides and alkylene glycols may be polyoxyalkylene diols or polyalkylene glycol derivatives; that is, the terminal hydroxy group can remain as such, or one or both of the terminal hydroxy groups can be removed during the polymerization reaction by etherification or esterification.
Synthetic oils of the dicarboxylic acid ester type include those which are prepared by esterifying such dicarboxylic acids as adipic acid, azelaic acid, suberic acid, sebacic acid, alkenyl succinic acid, fumaric acid, maleic acid, etc., with alcohols such as butyl alcohol, hexyl alcohol, 2-ethyl-hexyl alcohol, dodecyl alcohol, etc. Examples of dicarboxylic acid ester synthetic oils include dibutyl adipate, dihexyl adipate, di-2-ethylhexyl sebacate, di-n-hexyl fumaric polymer, etc.
Synthetic oils of the alkyl benzene type include those which are prepared by alkylating benzene (e. g., dodecyl benzene tetradecyl benzene, etc.)
Synthetic oils of the type of liquid esters of acids of phosphorus include the esters of phosphoric acid, e. g., tricresyl phosphate; the esters of phosphonic acid, e. g., diethyl ester of decane phosphonic acid (or other such esters as obtained by reacting alkyl phosphonyl chlorides with hydroxyl-containing compounds such as phenols and aliphatic alcohols) and with olefin oxides such as propylene oxide, as described in Jensen et 211., U. S. Patent Application 202,396.
Synthetic oils of the type of polymers of silicon include the liquid esters of silicon and the polysiloxanes. The liquid esters of silicon and the polysiloxanes include those exemplified by tetraethyl silicate, tetraisopropyl silicate, tetra(methyl-2-butyl) silicate, tetra(4-methyl- 2-pentyl) silicate, tetra(l-methoxy-Z-propyl) silicate, hexa(4-methyl-2-pentoxy) disiloxane, poly (methyl siloxane), poly(methylphenyl siloxane), etc.
The above base oils may be used individually as such or in various combinations (wherever miscible or whenever made so by the use of metal solvents).
The improved lubricant of the present invention is used wherever elemental sulfur or sulfur compounds containing active sulfur attack metal and are severely corrosive to metals which are being lubricated. Thus, as a result of the present invention, lubricants which normally are severely corrosive to metal parts due to attack by sulfur or active sulfur compounds may now be used without fear of corrosion by incorporating therein the combination of 2-thiothiazole compounds and thiadiazolyl compounds. Severely corrosive is defined as that corrosion which causes a weight loss greater than about 30 mg. in the silver strip test noted hereinbelow.
In order to evaluate the agents of this invention for inhibiting corrosion due to active sulfur, a silver strip corrosion test was made on numerous agents of this invention. This silver strip corrosion test was performed as follows:
A silver metal strip having the dimensions of 2%" x X was first cleaned with a Wire brush until the strip was highly polished. The strip was weighed and the weight recorded. This highly polished silver strip was then placed in a 600 ml. beaker in such a manner that the strip was completely immersed when 300 gm. of the oil being tested was poured into the beaker. The oil was stirred at a temperature of 300 F. for 20 hours, at which time the silver strip was removed and cleaned,
first with chloroform then with petroleum ether. The appearance of the strip was noted. Those strips which had been severely attacked were quite black. The tested silver strips were washed in aqueous solution of potassium cyanide for about 5 minutes toremove the sulfide film adhering to'the strip. After the strip had been washed with potassium cyanide and dried, it was weighed. The difference in weight of the original strip and the strip after the potassium cyanide wash was noted and recorded as the weight loss due to corrosion by the sulfur compound.
The 1,3,4-thiadiazolyl 2,5 bis(dialkyl dithiocarbamates) used in obtaining the dataset forth hereinbelow are manufactured by Sharples Chemicals, Inc., Philadelphia, Pa.
Table I below presents data obtained in the silver strip test" and shows the remarkable effect of the combination of 2-thio-thiazole and thiadiazolyl dithiocarbamates as silver protective agents in reducing the attack on silver by a California solvent refined S. A. E. 30 paraflinic base oil containing a zinc alkyl phenyl dithiophosphate, 2- mercaptobenzothiazole and 1,3,4-thiadiazolyl 2,5-bis- (diethyldithiocarbarnate). The alkyl radical in the zinc alkyl phenyl dithiophosphate contained an average of 14 carbon atoms and was derived from a mixture of propene and butene polymers.
Table II presents data obtained in the silver strip test of a solvent refined S.A.E. 30 parafiin base oil to which was added zinc alkyl phenyl dithiophosphate, 2- mercapto-benzothiazole and 1,3,4-thia-diazolyl 2,5-bis (dibutyl dithiocarbamate).
TABLE II Amount of Amount gt 1,3i4-1tl21i5a(11)ia- Z-mercap o y is benzothiazole (dibutyl'dithiogg l aifi in lubricating carbamate) in Loss'in S oil (Percent lubricating oil g by Weight) (Percent by Weigh t) The eifectiveness of the combination of agents of this invention for inhibiting sulfur corrosion to silver is further shown by the data of Table III. These data were obtained according to a modified ASTM D130-SOT sulfur corrosion test. The silver strips were immersed in the test oils at 300 F. for a period of 3 hours, at which time the strips were removed, solvent-washed free of oil, and inspected visually. The strips were rated as follows: a silver strip which was not discolored was given a rating of zero (0), while a strip which showed pronounced corrosion was given a rating of 5, with proportionate ratings for intermediate discoloration. In these tests, the base oil was a mixture of equal parts by volume of isooctyl hexaoxypropylene acetate and tetra (Z-ethyl hexyl) ortho silicate. Incorporated in the oil was a sulfurcontaining extreme pressure additive commercially marketed by Lubri-Zol Corporation as Anglamol 82.
TABLE HI Amount of Amount of 2-mereapto igi gg g' Visual riffititttlt g g g isfit? car ama e by Weight) in on The action of the silver protective agents of this invention cannot be explained on any simple basis, since their apparent effect appears anomalous. On the one hand, the protective agents prevent destructive attack of the sensitive metal by active sulfur compounds, but on the other hand they do not interfere with the functioning of extreme pressure agents which are believed to act by reaction with the metal surfaces.
As illustrative of various sulfur containing extreme pressure agents, detergents, oxidation inhibitors, etc. which cause oils containing them to be severely corrosive to silver, the following may be mentioned: sulfurized lubricating oils, xanthate esters, chlorinated xanthate esters, dialkyl disulfides, sulfurized fatty oils, metal salts of reaction products of olefins and phosphorus penta sulfide, organic trisulfides, tetra sulfides and penta sulfides (e. g., paraifin wax polysulfide), polyvalent metal salts of organo-substituted acids of phosphorus (e. g., zinc hexyl dithiophosphate), sulfurized olefins (e. g., sulfurized terpenes), xanthic acid derivatives (e. g., dibutyl xanthogen disulfide), etc. The silver protective agents of this invention are also efiective in reducing attack on silver by the sulfur in lubricating oils derived from some of the crude oils characterized by their high sulfur content.
The silver protective agents are especially desirable and preferably used in combination in lubricating oils containing the polyvalent metal salts of organo-substituted thioacids of phosphorus (e. g., zinc alkylphenyl dithiophosphate); however, they can be used in lubricating oils containing such compounds as phenates (e. g.,
calcium cetyl phenates), sulfonates (e. g., calcium petroleum sulfonates) phosphates (e. g., calcium cetyl phosphates) phenols (e. g. 2,6-di-tertiary-butyl-4-methyl phenol), phosphonates (e. g., calcium white oil phosphonate), thiophosphonates (e. g., calcium cetyl thiophosphonates) While the outstanding advantages of these silver protective agents in otherwise severely corrosive lubricants containing sulfur compounds is particularly apparent in heavy duty motor oils, the inventive combination finds application in turbine oils, gear oils, such as for the use in hypoid gears, cutting oils, soluble oils, greases, etc. Thus, the silver protective agents of this invention may be added to lubricating oil compositions containing other agents than sulfur active agents, that is, other agents which are advantageously present as oxidation inhibitors (e. g., phenyl alpha naphthylamine), anti-wear agents (e. g., tricresyl phosphate), rust inhibitors (e. g., metal sulfonates), oiliness agents, blooming agents, viscosity index improvers, pour point depressants, peptizing agents, thickening agents for greases, etc.
The combination of compounds of this invention is also effective in reducing corrosion of silver due to selenium compounds. That is, lubricants which contain active selenium compounds as additives, for example, dialkyl monoselem'des, dialkyl diselenides, dialkyl polyselenides, selenomercaptans, methyl alkyl selenides, etc. show attack on silver by selenium. However, the protective agents of this invention inhibit the attack on silver by lubricants containing selenium compounds.
I claim:
1. A lubricant comprising a major proportion of a silver-corrosive sulfur-containing lubricating oil composition, from 0.05% to 0.5% by weight of Z-mercaptobenzothiazole, and from 0.05% to 0.5 by weight of a thiadiazolyl dithiocarbamate selected from the group consisting of 1,3,4-thiadiazolyl-2,5-bis(diethyl dithio carbamate) and l,3,4-thiadiazolyl-2,5-bis(dibutyl dithiocarbamate).
2. A lubricant comprising a major proportion of an oil of lubricating viscosity having incorporated therein sulfur-containing additives which are corrosive to silver, and which additives inhibit corrosion caused by oxidation, and from 0.05% to 0.5 by weight of Z-mercapto-benzothiazole, and from 0.05% to 0.5 by weight of a thiadiazolyl dithiocarbamate selected from the group consisting of 1,3,4-thiadiazolyl-2,5-bis(diethyl dithiocarbamate) and 1,3,4-thiadiazolyl-2,5-bis(dibutyl dithiocarbamate).
3. A lubricant consisting essentially of a major proportion of an oil of lubricating viscosity having therein sulfur derived from the oil itself, which sulfur is corrosive to silver wearing surfaces, wherein the silver is prescut as substantially pure silver, and 0.05 to 0.5 by weight of 2-mercapto-benzothiazole, and from 0.05 to 0.5 by weight of a thiadiazolyl dithiocarbamate selected from the group consisting of 1,3,4-thiadiazolyl-2,S-bis- (diethyl dithiocarbamate) and 1,3,4-thiadiazolyl-2,5-bis- (dibutyl dithiocarbamate).
4. A lubricant consisting essentially of a major proportion of an oil of lubricating viscosity having incorporated therein sulfur-containing compounds having sulfur corrosive to pure silver wearing surfaces, from 0.05% to 0.5% by weight of Z-mercapto-benzothiazole, and from 0.05% to 0.5% by weight of 1,3,4-thiadiazolyl-2,5-bis- (diethyl dithiocarbamate) 5. A lubricant consisting essentially of a major proportion of an oil of lubricating viscosity having incorporated therein sulfur-containing compounds having sulfur corrosive to pure silver wearing surfaces, from 0.05 to 0.5% by weight of 2-mercapto-benzothiazole, and from 0.05% to 0.5% by weight of 1,3,4-thiadiazolyl-2,S-bis- (dibutyl dithiocarbamate).
References Cited in the file of this patent UNITED STATES PATENTS
Claims (1)
1. A LUBRICANT COMPRISING A MAJOR PROPORTION OF A SILVER-CORROSIVE SULFUR-CONTAINING LUBRICATING OIL COMPOSITION, FROM 0.05% TO 0.5% BY WEIGHT OF 2-MERCAPTOBENZOTHIAZOLE, AND FROM 0.05% TO 0.5% BY WEIGHT OF A THIADIAZOLYL DITHIOCARBAMATE SELECTED FROM THE GROUP CONSISTING OF 1,3,4-THIADIAZOLYL-2,5-BIS(DIBUTYL DITHIOCABMATE) AND 1,3,4-THIADIAZOLYL-2,5-BIS(DIBUTYL DITHIOCARBAMATE).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US260112A US2719827A (en) | 1951-12-05 | 1951-12-05 | Lubricating oil compositions containing sulfur corrosive to silver |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US260112A US2719827A (en) | 1951-12-05 | 1951-12-05 | Lubricating oil compositions containing sulfur corrosive to silver |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2719827A true US2719827A (en) | 1955-10-04 |
Family
ID=22987815
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US260112A Expired - Lifetime US2719827A (en) | 1951-12-05 | 1951-12-05 | Lubricating oil compositions containing sulfur corrosive to silver |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2719827A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1097068B (en) * | 1957-08-16 | 1961-01-12 | Iashellia Res Ltd | Lubricants and heat transfer agents based on mineral or synthetic oils |
| US3105818A (en) * | 1959-06-02 | 1963-10-01 | Shell Oil Co | Lubricating compositions |
| US3533943A (en) * | 1966-11-10 | 1970-10-13 | Mobil Oil Corp | Lubricant compositions |
| US3853638A (en) * | 1973-06-25 | 1974-12-10 | Shell Oil Co | Quenching oil composition |
| WO1986004601A1 (en) | 1985-01-31 | 1986-08-14 | The Lubrizol Corporation | Sulfur-containing compositions, and additive concentrates and lubricating oils containing same |
| US4764298A (en) * | 1986-02-25 | 1988-08-16 | Union Oil Company Of California | Lubrication anti-wear additive |
| US4880668A (en) * | 1986-03-27 | 1989-11-14 | Ppg Industries, Inc. | Mirror protective composition comprising 2-mercaptothiazoline |
| US5008153A (en) * | 1988-12-08 | 1991-04-16 | Ppg Industries, Inc. | Corrosion inhibitive pretreatment for "copper-free" mirrors |
| US5180510A (en) * | 1988-03-31 | 1993-01-19 | Ethyl Petroleum Additives, Inc. | Antioxidant additive and lubricating oil containing same |
| US5686397A (en) * | 1997-02-03 | 1997-11-11 | Uniroyal Chemical Company, Inc. | Dithiocarbamate derivatives and lubricants containing same |
| EP0869165A3 (en) * | 1997-03-24 | 1998-12-16 | The Lubrizol Corporation | Mixed polysulfides and lubricants and functional fluids containing the same |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2154096A (en) * | 1936-11-16 | 1939-04-11 | Standard Oil Co | Lubricating oil |
| US2690999A (en) * | 1950-10-31 | 1954-10-05 | California Research Corp | Silver protective agents for sulfurcontaining lubricants |
-
1951
- 1951-12-05 US US260112A patent/US2719827A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2154096A (en) * | 1936-11-16 | 1939-04-11 | Standard Oil Co | Lubricating oil |
| US2690999A (en) * | 1950-10-31 | 1954-10-05 | California Research Corp | Silver protective agents for sulfurcontaining lubricants |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1097068B (en) * | 1957-08-16 | 1961-01-12 | Iashellia Res Ltd | Lubricants and heat transfer agents based on mineral or synthetic oils |
| US3105818A (en) * | 1959-06-02 | 1963-10-01 | Shell Oil Co | Lubricating compositions |
| US3533943A (en) * | 1966-11-10 | 1970-10-13 | Mobil Oil Corp | Lubricant compositions |
| US3853638A (en) * | 1973-06-25 | 1974-12-10 | Shell Oil Co | Quenching oil composition |
| WO1986004601A1 (en) | 1985-01-31 | 1986-08-14 | The Lubrizol Corporation | Sulfur-containing compositions, and additive concentrates and lubricating oils containing same |
| US4764298A (en) * | 1986-02-25 | 1988-08-16 | Union Oil Company Of California | Lubrication anti-wear additive |
| US4880668A (en) * | 1986-03-27 | 1989-11-14 | Ppg Industries, Inc. | Mirror protective composition comprising 2-mercaptothiazoline |
| US5180510A (en) * | 1988-03-31 | 1993-01-19 | Ethyl Petroleum Additives, Inc. | Antioxidant additive and lubricating oil containing same |
| US5008153A (en) * | 1988-12-08 | 1991-04-16 | Ppg Industries, Inc. | Corrosion inhibitive pretreatment for "copper-free" mirrors |
| US5686397A (en) * | 1997-02-03 | 1997-11-11 | Uniroyal Chemical Company, Inc. | Dithiocarbamate derivatives and lubricants containing same |
| EP0869165A3 (en) * | 1997-03-24 | 1998-12-16 | The Lubrizol Corporation | Mixed polysulfides and lubricants and functional fluids containing the same |
| US6001783A (en) * | 1997-03-24 | 1999-12-14 | The Lubrizol Corporation | Mixed polysulfides and lubricants and functional fluids containing the same |
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