US2620303A - Mercaptothiazines as sulfur-corrosion inhibiting agents - Google Patents
Mercaptothiazines as sulfur-corrosion inhibiting agents Download PDFInfo
- Publication number
- US2620303A US2620303A US103936A US10393649A US2620303A US 2620303 A US2620303 A US 2620303A US 103936 A US103936 A US 103936A US 10393649 A US10393649 A US 10393649A US 2620303 A US2620303 A US 2620303A
- Authority
- US
- United States
- Prior art keywords
- silver
- sulfur
- oils
- oil
- agents
- 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
- 238000005260 corrosion Methods 0.000 title description 21
- 230000002401 inhibitory effect Effects 0.000 title description 4
- RLHFVQZGAHOKPT-UHFFFAOYSA-N 2h-thiazine-3-thiol Chemical class SC1=CC=CSN1 RLHFVQZGAHOKPT-UHFFFAOYSA-N 0.000 title 1
- 229910052709 silver Inorganic materials 0.000 claims description 60
- 239000004332 silver Substances 0.000 claims description 60
- 229910052717 sulfur Inorganic materials 0.000 claims description 43
- 239000011593 sulfur Substances 0.000 claims description 43
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 42
- 239000010687 lubricating oil Substances 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 11
- YZZWZWGTNAEJIN-UHFFFAOYSA-N 2-sulfanylthiazine Chemical compound SN1SC=CC=C1 YZZWZWGTNAEJIN-UHFFFAOYSA-N 0.000 claims description 9
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 60
- 239000003921 oil Substances 0.000 description 37
- 239000003223 protective agent Substances 0.000 description 24
- 230000007797 corrosion Effects 0.000 description 20
- 229910052751 metal Inorganic materials 0.000 description 19
- 239000002184 metal Substances 0.000 description 19
- 150000001875 compounds Chemical class 0.000 description 18
- 239000003795 chemical substances by application Substances 0.000 description 17
- -1 organo thiophosphates Chemical class 0.000 description 16
- 239000000314 lubricant Substances 0.000 description 12
- 230000003647 oxidation Effects 0.000 description 12
- 238000007254 oxidation reaction Methods 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 11
- 239000000654 additive Substances 0.000 description 10
- 150000002739 metals Chemical class 0.000 description 10
- 150000003464 sulfur compounds Chemical class 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 239000011575 calcium Substances 0.000 description 7
- 229910052791 calcium Inorganic materials 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- 150000001336 alkenes Chemical class 0.000 description 6
- 239000002199 base oil Substances 0.000 description 6
- 230000001050 lubricating effect Effects 0.000 description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- DLBJODXBDQMKRQ-UHFFFAOYSA-N 4,6,6-trimethyl-3h-1,3-thiazine-2-thione Chemical compound CC1=CC(C)(C)SC(=S)N1 DLBJODXBDQMKRQ-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 4
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 3
- BLDKZNOCHFGWQD-UHFFFAOYSA-L P(=S)(SCCCCCCCCCCCCCCCC)(OC1=CC=CC=C1)[O-].[Zn+2].C(CCCCCCCCCCCCCCC)SP(=S)(OC1=CC=CC=C1)[O-] Chemical compound P(=S)(SCCCCCCCCCCCCCCCC)(OC1=CC=CC=C1)[O-].[Zn+2].C(CCCCCCCCCCCCCCC)SP(=S)(OC1=CC=CC=C1)[O-] BLDKZNOCHFGWQD-UHFFFAOYSA-L 0.000 description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical class CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000003751 zinc Chemical class 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-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
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical compound [Cu].[Pb] WIKSRXFQIZQFEH-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
- 230000002411 adverse Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper 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
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 239000005077 polysulfide Substances 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 150000008117 polysulfides Polymers 0.000 description 2
- 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
- 150000004763 sulfides Chemical class 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
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- 229910000897 Babbitt (metal) Inorganic materials 0.000 description 1
- 229910000906 Bronze Inorganic materials 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
- FGOQDABVCOAPHM-UHFFFAOYSA-N CC=1NSC=CC1 Chemical compound CC=1NSC=CC1 FGOQDABVCOAPHM-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 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
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- DHHCPMGCLXWUQS-UHFFFAOYSA-H P(=S)([S-])([O-])[O-].[Ba+2].P(=S)([S-])([O-])[O-].[Ba+2].[Ba+2] Chemical compound P(=S)([S-])([O-])[O-].[Ba+2].P(=S)([S-])([O-])[O-].[Ba+2].[Ba+2] DHHCPMGCLXWUQS-UHFFFAOYSA-H 0.000 description 1
- NXEUTNOJLUEESD-UHFFFAOYSA-L P(OCCCCCCCCCCCCCCCC)([O-])=S.[Ca+2].C(CCCCCCCCCCCCCCC)OP([O-])=S Chemical compound P(OCCCCCCCCCCCCCCCC)([O-])=S.[Ca+2].C(CCCCCCCCCCCCCCC)OP([O-])=S NXEUTNOJLUEESD-UHFFFAOYSA-L 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 208000036366 Sensation of pressure Diseases 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 230000000397 acetylating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001266 acyl halides Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000002547 anomalous effect Effects 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 239000010974 bronze Substances 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
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NSAODVHAXBZWGW-UHFFFAOYSA-N cadmium silver Chemical compound [Ag].[Cd] NSAODVHAXBZWGW-UHFFFAOYSA-N 0.000 description 1
- DHJGVCITGOCTCA-UHFFFAOYSA-L calcium;hexadecyl phosphate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCOP([O-])([O-])=O DHJGVCITGOCTCA-UHFFFAOYSA-L 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000002079 cooperative effect Effects 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 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
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000003599 detergent Substances 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
- HHECSPXBQJHZAF-UHFFFAOYSA-N dihexyl hexanedioate Chemical compound CCCCCCOC(=O)CCCCC(=O)OCCCCCC HHECSPXBQJHZAF-UHFFFAOYSA-N 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
- 150000002019 disulfides Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000012208 gear oil Substances 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
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000005461 lubrication Methods 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
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 150000002825 nitriles Chemical class 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
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 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
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 150000003461 sulfonyl halides Chemical class 0.000 description 1
- 150000003463 sulfur Chemical class 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical class [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- YVFHKLYMBACKFA-UHFFFAOYSA-N trioctoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound CCCCCCCCOP(=S)(OCCCCCCCC)OCCCCCCCC YVFHKLYMBACKFA-UHFFFAOYSA-N 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
-
- 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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/022—Ethene
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—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
-
- 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
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- C10M2223/042—Metal salts thereof
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- C10M2223/065—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur
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- C10M2223/12—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
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- C10M2225/00—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2225/04—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of macromolecualr compounds not containing phosphorus in the monomers
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
Definitions
- the present invention relates to lubricating oils compounded with active sulfur-containing compounds such as metal salts of thiophosphate's, which compounded oils are severely corrosive to silver and like metals, and to the prevention of such sulfur attack on silver by incorporatin'gin said severely corrosive compounded oils certain protective agents such as 2-mercapto-4,6,6-trimethyl thiazine.
- active sulfur-containing compounds such as metal salts of thiophosphate's
- oils compounded with such active sulfur-containing compounds are severely corrosive to silver and like metals.
- the deleterious action involves a direct attack of the metals by sulfur, resulting in a rapid darkening of the metal surfaces and formation of sulfides and the subsequent sloughing off of the sulfides during engine operation.
- This sulfur attack may be designated as sulfur corrosion, as distinguished from corrosion caused by the action of acids and peroxides which are found as products of oxidation of lubricating oils, particularly highly refined lubricating oils.
- This latter type of corrosion -which may be called oxidation corrosion or acid corrosion, adversely affects such hard metal alloys as cadmium-silver, copper-lead, etc., but does not seriously affect silver or bronze.
- Such oxidation corrosion is usually minimized by the presence of oxidation inhibitors, which reduce the formation of the corrosive acids and peroxides.
- the present invention concerns the combination of a lubricant compounded with active sulfur compounds, which compounded lubricant is severely corrosive to silver and a silver protective agent which greatly minimizes the attack on silver by sulfur of the compounded lubricant but without adversely affecting the desired functioning of the sulfur compound.
- the action of the silver protective agents 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 pres sure agents which are believed to act by reaction with the metal surface.
- the silver protective agents of this invention are 2-thiothiazines.
- the simplest member of this class of compounds is z-mercaptothiazine.
- Also included are the derivatives of 2-mercaptothiazine, wherein the mercapto-hydrogen may be replaced by a hydrolyzable group and wherein there may be substituents on the ring carbon atoms.
- the hydrolyzable group is one which may reradicals (e. g., cyclohexylamide radical), and
- organic carboxyl and thionyl radicals e. g., benzoic and diethyl dithiocarbonyl radicals.
- the hydrogen atoms of the ring may be substituted by short-chain saturated and unsaturated aliphatic radicals (e. g., methyl, ethyl, propyl, butyl, octyl, ethenyl, propenyl, butenyl, octenyl, etc.)
- short-chain saturated and unsaturated aliphatic radicals e. g., methyl, ethyl, propyl, butyl, octyl, ethenyl, propenyl, butenyl, octenyl, etc.
- short-chain aliphatic radicals is meant aliphatic radicals containing not more than 8 carbon atoms.
- Z-thiothiazines are: 2-mercapto- 4,6,6-trimethylthiazine; the zinc salt of 2-mercapto 4,6,6 trimethylthiazine; 2 mercapto- 1,3 dihydrothiazine; 4,6,6 trimethylthiazine z-cyclohexyl sulfenamide; 2'-mercapto-2,4,1-trimethylthiazine; 2-mercapto-4-methylthiazine; 2- mercapto 4 ethylthiazine; 2 mercapto 4,6- dimethyl-thiazine; and 2-mercapto-4-isobutenyl- 6,6-dimethylthiazine.
- 2 thiothiaz'ine examples include the reaction products obtained by reacting Z-thiothiazine with the following: carboxylic acids, alpha-beta unsaturated ketones, esters, olefins, nitriles, sulfonyl halides, organometallic compounds, anhydrides, ethylene oxides and acyl halides.
- the 2-thiothiazines embraced in this invention vary in effectiveness as silver protective agents. Because of the greater effectiveness obtained, it is preferred to use 2-mercapto4,6,6- trimethylthiazine.
- the 2-thiothiazines embraced in this invention vary in effectiveness as silver protective agents. Some of the compounds, for example, are effective when used in amounts as low as 0.001% (by weight of total composition). Certain of the compounds have only limited solubility in the lubricating oiland are effective at that solubility. All of the compounds having sufficient solubility are effective when they are used in amount as great as 5.0%. However, it is preferred that the compounds of this invention be used in amounts sufficient substantially to reduce the corrosion of silver. For example, it is preferred to use amounts of from 0.05 to 1.5%. The major portion of the lubricating composition of this invention is the base oil.
- Suitable base oils include a wide variety of lubricating oils such as naphthenic base, paraffin base, and mixed base mineral oils, other hydrocarbon lubricants, e. g., lubricating oil derived from coal products, and synthetic oils, e. g., alkylene polymers (such as polymers of propylene, butylene, etc., and mixtures thereof), alkylenroxide-type polymers, dicarboxylic acid esters and liquid esters of acids of phosphorus.
- synthetic oils of the alkylene-oxide type polymer 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, and esters of alkylene-oxide type polymers, e. g., acetylated propylene oxide polymers prepared by acetylating propylene oxide polymers containing hydroxyl groups.
- 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 di-butyl adipate, di-hexyl adipate, di-2- ethyl-hexyl sebacate, dim-hexyl fumarate polymer, 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., di-ethyl 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 al., U. S. patentapplication No. 86,856)
- the improved lubricant of the present invention is used wherever elemental sulfur or sulfur compounds having active sulfur present attackmetals and are severly corrosive" to metals which are being lubricated.
- Severely corrosive is defined as that corrosion which causes a weight los greate than 30 milligrams in the silver strip test noted hereinbelow.
- a silver metal strip having the dimensions of 2 inches by inch by inch 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 milliliter beaker in such a manner that the strip was completely immersed when 300 grams 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 anide wash was noted and recorded as the weight,
- the agents of this invention are especially effective as protective agents for silver.
- the protective agents of this invention are also effective in protecting other sulfur sensitive metals from sulfur attack.
- Such other sulfursensitive metals include copper, aluminum and alloys of copper and aluminum. 1
- 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 pentasulfide, organic trisulfides, tetrasulfides and pentasulfides (e. g., parafiin 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 with lubricating oils containing the polyvalent metal salts of organo-substituted thioacids of phosphorus (e. g., zinc cetyl phenyl dithiophosphate), they may be used in lubricating oils also containing such compounds as phenates (e. g., calcium cetyl phosphate), phenols (e. g., 2,6-di-tertiary-butyl-4-methyl phenol), phosphonates (e. g., calcium white oil phosphonate), thiophosphonates (e. g., calcium cetyl thiophosphonate), etc.
- phenates e. g., calcium cetyl phosphate
- phenols e. g., 2,6-di-tertiary-butyl-4-methyl phenol
- phosphonates e. g., calcium white oil phosphonate
- thiophosphonates
- the silver protective agents of this invention may be added to lubricating compositions containing other agents than sulfur-active agents, that'is, other agents which are advantageously present as oiliness agents, blooming agents, viscosity index improvers, pour point depressants, peptizing agents, etc.
- the protective agents of this invention were incorporated in a mineral petroleum lubricating oil containing various sulfurcorrosive additives.
- Table I below presents'data of various compounds tested by the silver strip test.
- the various silver protective agents were added to a California solvent refined S.
- Table II below presents silver strip test data of various compounds incorporated in a California solvent refined S.
- A. E. 30 parafiinlc base oil containing a calcium petroleum sulfonate. a sulfurized calcium cetyl phenate and zinc cetyl phenyl dithiophosphate.
- Table IV presents data showing the eifectiveness of the compounds of this invention as protective agents in a California solvent refined S.
- A. E. 30 paraflinic base 011 containing calcium petroleum sulfonate, sulfurized diparafiin sulfide, a barium dithiophosphate, and trioctyl thiophosphate, which composite oil without the protective agent is extremely corrosive to silver.
- Table IV I Amount of frotgcttlived lilver$ trip gen se est, t eight Fromm Agent in Lubricating Loss in Oil (Percent Milligrams by Wgt.)
- the silver wrist-pin bushing is weighed before it is placed into position for a test run. In order to prevent scoring of the silver wrist-pin bushing while it is being inserted into the connecting rod, the silver wrist-pin itself is cooled with solid CO2 and the connecting rod eye is heated.v After the silver wrist-pin bushinghas been inserted, the temperature is allowed to reachv equilibrium.
- the engine is run for 8 hours in order to break in the new wrist-pin bushing.
- the oil is then drained from the engine, fresh oil is added and the engine is run for an additional three-hour test period to make the. final engine adjustments, after which the oil is again drained and the test 011 added.
- the engine is then run for the full 200 hours at the conditions noted hereinabove.
- the compounded oils to which the protective agents oi! this invention were added contained calcium cetyl phenyl dithiophosphate and zinc" cetyl phenyl dithiophosphate as the sulfur corrosive agents. Following the 200-hour test, the silver wrist-pin bushing was weighed to determine-the-loss of silver due to sulfur corrosion.
- test oil compounded as noted hereinabove was tested in an engine according to the LA-Test Method. described in pages 394-418 of the CRC Handbook compiled by the Coordinating Research Council, Inc. in 1946 and printed by the-J- J; Littleand; Ives Company. New York. This.te'st'is'-usedito determine the oxidation corrosiveness of the oils.
- the L-4 procedure test engine is a stock 1942 Chevrolet engine, having a bore of 3.5 inches, a stroke of 3.75 inches and a compression ratio of 6.5 to 1.
- the rod bearings are babbitt, but with provisions for inserting cooper-lead bearings in place of the babbitt. For each test run, two
- the engine is flushed twice with uncompounded hydrocarbon lubricating oil (using. 4' quarts of the oil each time) by running the engine at a speed of 1500 R. P..M.- for 15 minutes
- the copper leadbearing inserts are-washed free of oil, then weighed" to determine the weight lost.
- a sulfur-containing, lubricating oil composition severely corrosive to silver and. a small amount sufiicient substantially to reduce the sulfur attack on silver of. a zinc salt of a 2-mercapto-v thiazine containing no more than 3 aliphatic. radicals, said aliphatic radicals having 'no more than 8 carbon atoms.
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Description
Patented Dec. 2, 1952 UNITED STATES PATENT 2,620,303 9 F F! C E 2,620,303 MERCAPTOTHIAZINES AS SULFUR- C-ORROSION INHIBITING AGENTS Delaware No Drawing. Application July 9, 1949, Serial No. 103,936
The present invention relates to lubricating oils compounded with active sulfur-containing compounds such as metal salts of thiophosphate's, which compounded oils are severely corrosive to silver and like metals, and to the prevention of such sulfur attack on silver by incorporatin'gin said severely corrosive compounded oils certain protective agents such as 2-mercapto-4,6,6-trimethyl thiazine.
Of the various lubricating oil compounding agents, many of the most effective are compounds containing 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. Unfortunately, oils compounded with such active sulfur-containing compounds are severely corrosive to silver and like metals. The deleterious action involves a direct attack of the metals by sulfur, resulting in a rapid darkening of the metal surfaces and formation of sulfides and the subsequent sloughing off of the sulfides during engine operation. Thus, there is a considerable loss of bearing metal and a pitting of'bearing surfaces. This sulfur attack may be designated as sulfur corrosion, as distinguished from corrosion caused by the action of acids and peroxides which are found as products of oxidation of lubricating oils, particularly highly refined lubricating oils. This latter type of corrosion,-which may be called oxidation corrosion or acid corrosion, adversely affects such hard metal alloys as cadmium-silver, copper-lead, etc., but does not seriously affect silver or bronze. Such oxidation corrosion is usually minimized by the presence of oxidation inhibitors, which reduce the formation of the corrosive acids and peroxides.
It is apparent that 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.
Therefore, it isan object of this invention to provide a non-silver-corrosive lubricant containing active sulfur compounds.
In the attainment of this object, the present invention concerns the combination of a lubricant compounded with active sulfur compounds, which compounded lubricant is severely corrosive to silver and a silver protective agent which greatly minimizes the attack on silver by sulfur of the compounded lubricant but without adversely affecting the desired functioning of the sulfur compound.
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 difficult to prevent sulfur attack of the silver surfaces. Because the silver surfaces (e. g., the silver wrist-pin bush- 7 Claims. (Cl. 252-4237) ings) are susceptible to attack by the sulfur of the sulfur-containing lubricating oil additive, there has been a tendency to eliminate highly effective sulfur-containing additives from the diesel lubrieating 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 wrist-pin bushings without sulfur attack of 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.
It is of extreme advantage to be able to use a lubricant composition which is effective not only in inhibiting oxidation corrosion but is also effective in preventing sulfur attack on metals. In railroad oils, for example, it has been a handicap to use lubricants which inhibit corrosion resulting from oxidation products but permitting unhampered attack on metals by compounds having active sulfur present. I While the outstanding advantages of the cooperative action of the 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 use in hypoid gears, cutting oils, soluble oils, greases, etc.
The action of the silver protective agents 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 pres sure agents which are believed to act by reaction with the metal surface.
The silver protective agents of this invention are 2-thiothiazines. The simplest member of this class of compounds is z-mercaptothiazine. Also included are the derivatives of 2-mercaptothiazine, wherein the mercapto-hydrogen may be replaced by a hydrolyzable group and wherein there may be substituents on the ring carbon atoms.
The hydrolyzable group is one which may reradicals (e. g., cyclohexylamide radical), and
organic carboxyl and thionyl radicals (e. g., benzoic and diethyl dithiocarbonyl radicals).
In z-thiothiazine, the hydrogen atoms of the ring may be substituted by short-chain saturated and unsaturated aliphatic radicals (e. g., methyl, ethyl, propyl, butyl, octyl, ethenyl, propenyl, butenyl, octenyl, etc.)
It is preferred that there should be not more than 4 substituents on the ring and that each substituent contain not more than 4 carbon atoms. Furthermore, it is preferred that the substituents on the ring have a total of not more than 16 carbon atoms.
By short-chain aliphatic radicals is meant aliphatic radicals containing not more than 8 carbon atoms.
Examples of Z-thiothiazines are: 2-mercapto- 4,6,6-trimethylthiazine; the zinc salt of 2-mercapto 4,6,6 trimethylthiazine; 2 mercapto- 1,3 dihydrothiazine; 4,6,6 trimethylthiazine z-cyclohexyl sulfenamide; 2'-mercapto-2,4,1-trimethylthiazine; 2-mercapto-4-methylthiazine; 2- mercapto 4 ethylthiazine; 2 mercapto 4,6- dimethyl-thiazine; and 2-mercapto-4-isobutenyl- 6,6-dimethylthiazine. Further examples of 2 thiothiaz'ine include the reaction products obtained by reacting Z-thiothiazine with the following: carboxylic acids, alpha-beta unsaturated ketones, esters, olefins, nitriles, sulfonyl halides, organometallic compounds, anhydrides, ethylene oxides and acyl halides.
The 2-thiothiazines embraced in this invention vary in effectiveness as silver protective agents. Because of the greater effectiveness obtained, it is preferred to use 2-mercapto4,6,6- trimethylthiazine.
The 2-thiothiazines embraced in this invention vary in effectiveness as silver protective agents. Some of the compounds, for example, are effective when used in amounts as low as 0.001% (by weight of total composition). Certain of the compounds have only limited solubility in the lubricating oiland are effective at that solubility. All of the compounds having sufficient solubility are effective when they are used in amount as great as 5.0%. However, it is preferred that the compounds of this invention be used in amounts sufficient substantially to reduce the corrosion of silver. For example, it is preferred to use amounts of from 0.05 to 1.5%. The major portion of the lubricating composition of this invention is the base oil.
Suitable base oils include a wide variety of lubricating oils such as naphthenic base, paraffin base, and mixed base mineral oils, other hydrocarbon lubricants, e. g., lubricating oil derived from coal products, and synthetic oils, e. g., alkylene polymers (such as polymers of propylene, butylene, etc., and mixtures thereof), alkylenroxide-type polymers, dicarboxylic acid esters and liquid esters of acids of phosphorus. Synthetic oils of the alkylene-oxide type polymer 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, and esters of alkylene-oxide type polymers, e. g., acetylated propylene oxide polymers prepared by acetylating propylene oxide polymers containing hydroxyl groups.
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 di-butyl adipate, di-hexyl adipate, di-2- ethyl-hexyl sebacate, dim-hexyl fumarate polymer, 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., di-ethyl 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 al., U. S. patentapplication No. 86,856)
The improved lubricant of the present invention is used wherever elemental sulfur or sulfur compounds having active sulfur present attackmetals and are severly 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 sulfu compounds may now be used without fear of corrosion by incorporating therein the present protective agents. Severely corrosive is defined as that corrosion which causes a weight los greate than 30 milligrams 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. Thi silver strip corrosion test was performed as follows:
A silver metal strip having the dimensions of 2 inches by inch by inch 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 milliliter beaker in such a manner that the strip was completely immersed when 300 grams 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 anide wash was noted and recorded as the weight,
loss due to corrosion by the sulfur compound.
The agents of this invention are especially effective as protective agents for silver. However, the protective agents of this invention are also effective in protecting other sulfur sensitive metals from sulfur attack. Such other sulfursensitive metals include copper, aluminum and alloys of copper and aluminum. 1
' 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 pentasulfide, organic trisulfides, tetrasulfides and pentasulfides (e. g., parafiin wax polysulfide), polyvalent metal salts of organo-substituted acids of phosphorus (e. g., zinc hexyldithiophosphate), sulfurized olefins (e. g., sulfurized terpene), xanthic acid derivatives (e. g.. dibutyl xanthogen disulfide), etc.
Some of the above indicated additives are more vigorous in their attack on silver than others, and consequently such attack is more difficult to minimize. However, the silver protective agents are advantageously used even with the more act'ive sulfur additives.
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.
Although the silver protective agents are especially desirable and preferably used in combination with lubricating oils containing the polyvalent metal salts of organo-substituted thioacids of phosphorus (e. g., zinc cetyl phenyl dithiophosphate), they may be used in lubricating oils also containing such compounds as phenates (e. g., calcium cetyl phosphate), phenols (e. g., 2,6-di-tertiary-butyl-4-methyl phenol), phosphonates (e. g., calcium white oil phosphonate), thiophosphonates (e. g., calcium cetyl thiophosphonate), etc. The silver protective agents of this invention may be added to lubricating compositions containing other agents than sulfur-active agents, that'is, other agents which are advantageously present as oiliness agents, blooming agents, viscosity index improvers, pour point depressants, peptizing agents, etc.
For the purposes of the tests described hereinabove and below, the protective agents of this invention were incorporated in a mineral petroleum lubricating oil containing various sulfurcorrosive additives.
, Table I below presents'data of various compounds tested by the silver strip test. The various silver protective agents were added to a California solvent refined S. A. E. 30 paramnic base oil containing sulfurized calcium cetyl phenate; sulfurized diparafiin sulfide; calcium petroleum sulfonate, and zinc cetyl phenyl dithiophosphate.
Table II below presents silver strip test data of various compounds incorporated in a California solvent refined S. A. E. 30 parafiinlc base oil containing a calcium petroleum sulfonate. a sulfurized calcium cetyl phenate and zinc cetyl phenyl dithiophosphate.
Further silver strip tests were made by incorporating the protective agents of this invention in a California solvent refined S. A. E. 30 paraflinic base oil to which had been added calcium petroleum sulfonate, sulfurized diparaffin sulfide and a commercial oxidation inhibitor containing sulfurized olefins. The results of these tests are presented below in Table III.
Table III Amount of frotgcivel Tilei$trilp v gen se es ei t Protecme Agent in Lubricating Loss in Oil (Percent Milligrams by Wgt.)
1. None 93.0 2. 2-Meroapto 4,6,6-Trimethyl 'lhiazine 0.3 20. 1
Table IV presents data showing the eifectiveness of the compounds of this invention as protective agents in a California solvent refined S. A. E. 30 paraflinic base 011 containing calcium petroleum sulfonate, sulfurized diparafiin sulfide, a barium dithiophosphate, and trioctyl thiophosphate, which composite oil without the protective agent is extremely corrosive to silver.
Table IV I Amount of frotgcttlived lilver$ trip gen se est, t eight Fromm Agent in Lubricating Loss in Oil (Percent Milligrams by Wgt.)
1. None 852.1 2. 2 Mercapt0 4,6,6Trin1ethyl Thiazine 0.3 116. 9
In order to show further the effectiveness of the compounds of this invention as protective agents against sulfur corrosion," compounded oils were tested in a General Motors 4-71 engine. This engine has silver-plated wrist-pin bushings, a bore of 4.25 inches, 2. stroke of 5.0 inches, a compression ratio of 16 to 1, and is operated at a speed of 2,000 R. P. M., an oil sump temperature of 230 F., and a jacket temperature of 180 F.
The silver wrist-pin bushing is weighed before it is placed into position for a test run. In order to prevent scoring of the silver wrist-pin bushing while it is being inserted into the connecting rod, the silver wrist-pin itself is cooled with solid CO2 and the connecting rod eye is heated.v After the silver wrist-pin bushinghas been inserted, the temperature is allowed to reachv equilibrium.
After the silver wrist-pin bushing has been inserted for the test, the engine is run for 8 hours in order to break in the new wrist-pin bushing. The oil is then drained from the engine, fresh oil is added and the engine is run for an additional three-hour test period to make the. final engine adjustments, after which the oil is again drained and the test 011 added. The engine is then run for the full 200 hours at the conditions noted hereinabove.
The compounded oils to which the protective agents oi! this invention were added contained calcium cetyl phenyl dithiophosphate and zinc" cetyl phenyl dithiophosphate as the sulfur corrosive agents. Following the 200-hour test, the silver wrist-pin bushing was weighed to determine-the-loss of silver due to sulfur corrosion.
The results of the General Motors engine tests are presented below in Table. V.
Table V Amount of Protectivc Agent Added.
Appearance of Silver gg %g:
Protective Agent -Added. Wrist-Pin Bushing Y (Milligrams) The results presented in Table V show that the agents of this invention are remarkable in protecting the metals from attack by sulfur.
In order to show that the compounds oithis invention are not present in the lubricants for the-purpose of reducing the oxidation corrosion characteristics of the compounded oil, the test oil compounded as noted hereinabove was tested in an engine according to the LA-Test Method. described in pages 394-418 of the CRC Handbook compiled by the Coordinating Research Council, Inc. in 1946 and printed by the-J- J; Littleand; Ives Company. New York. This.te'st'is'-usedito determine the oxidation corrosiveness of the oils.
The L-4 procedure test engine is a stock 1942 Chevrolet engine, having a bore of 3.5 inches, a stroke of 3.75 inches and a compression ratio of 6.5 to 1. The rod bearings are babbitt, but with provisions for inserting cooper-lead bearings in place of the babbitt. For each test run, two
of the babbitt bearings were replaced with i weighed copper-lead inserts. In preparation for the test, the engine is flushed twice with uncompounded hydrocarbon lubricating oil (using. 4' quarts of the oil each time) by running the engine at a speed of 1500 R. P..M.- for 15 minutes At the end of the 20-hour test run, the copper leadbearing inserts are-washed free of oil, then weighed" to determine the weight lost. The
Table VI Base Oil Protective Agent Added ggggi gg Lead- Bearing b Insert (Milli- I y grams) v A 2-Mercapto4, 6, (i- Tri- 0.3 32
methyl Thiazine.
We claim: I
1. A sulfur-containing lubricating oil 'composi-j tion severely corrosive to silver, and a small. amount, sufiicient substantially to reduce the sulfur attack on silver of a 2-thiothiazinev selected from the group consisting of a Z-mercapt'othiazine and a zinc salt of a 2 mercaptothiazine, wherein said 2-mercaptothiazine contains. no more than 3 aliphatic radicals, said aliphatic radicals having no more than 8 carbon atoms.
2. Asuliur-containing lubricating oil'fcomp'os'i tion severely corrosive. to silver and a small amount, sufiicient substantially. to reduce the sulfur attack on silver of a'Z-mercaptothiazine.con taming. no more. than. 3 aliphatic radicals, said. aliphatic radicals having no. more than 8 carbon atoms.
3. The lubricatin oil composition of claim 2 whereinthe 2-mercaptothiazine. contains no more. than 3 methyl radicals.
4. A sulfur-containing, lubricating oil composition severely corrosive to silver and. a small amount sufiicient substantially to reduce the sulfur attack on silver of. a zinc salt of a 2-mercapto-v thiazine containing no more than 3 aliphatic. radicals, said aliphatic radicals having 'no more than 8 carbon atoms.
5. The lubricating oil composition of' claim 4 wherein said 2-mercaptothiazine contains no more than 3 methyl radicals.
6. The lubricating oil composition of claim 4- wherein said 2-mercaptothiazine is 2-inercapto- 4,6,6-trimethylthiazine.
7. A- sulfur-containing lubricating oilseverely.v corrosive to. silver, and a small amount. suflicient substantially to reduce the sulfur attack on silver, of 'a Z-mercapto-4,6,6-trimethyl thiazine.
WARREN LOWE. JAMES O. CLAYTON.
REFERENCES CITED The following references are of record in thefile of this patent:
UNITED STATES PATENTS Number Name Date 2,154,096 Loane Apr. 11, 1939 2,160,293 Shoemaker May 30, 1939 2,190,648 Cantrell Feb. 20, 1940 2,201,258 Busse May 21, 19.40. 2,293,237 Bartlett Aug. 18, 1942 2,318,629 Prutton May 11, 1943' 2,414,257 Evans et al Jan. 14, 1947 2,440,095 Janes Apr. 20, 1948-
Claims (1)
1. A SULFUR-CONTAINING LUBRICATING OIL COMPOSITION SEVERELY CORROSIVE TO SILVER, AND A SMALL AMOUNT, SUFFICENT SUBSTANTIALLY TO REDUCE THE SULFUR ATTACK ON SILVER OF A 2-THIOTHIAZINE SELECTED FROM THE GROUP CONSISTING OF A 2-MERCAPTOTHIAZINE AND A ZINC SALT OF A 2-MERCAPTOTHIAZINE, WHEREIN SAID 2-MERCAPTOTHIAZINE CONTAINS NO MORE THAN 3 ALIPHATIC RADICALS, SAID ALIPHATIC RADICALS HAVING NO MORE THAN 8 CARBON ATOMS,
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US103936A US2620303A (en) | 1949-07-09 | 1949-07-09 | Mercaptothiazines as sulfur-corrosion inhibiting agents |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US103936A US2620303A (en) | 1949-07-09 | 1949-07-09 | Mercaptothiazines as sulfur-corrosion inhibiting agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2620303A true US2620303A (en) | 1952-12-02 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US103936A Expired - Lifetime US2620303A (en) | 1949-07-09 | 1949-07-09 | Mercaptothiazines as sulfur-corrosion inhibiting agents |
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| US (1) | US2620303A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4210545A (en) * | 1979-03-30 | 1980-07-01 | Standard Oil Company (Indiana) | Oxidation resistant lubricant composition |
| EP0416909A1 (en) * | 1989-09-07 | 1991-03-13 | Exxon Research And Engineering Company | Lubricating oil composition |
| US10786080B1 (en) * | 2019-12-06 | 2020-09-29 | Dooli Products, LLC | Anti-tipping mechanisms integrated into furniture |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2154096A (en) * | 1936-11-16 | 1939-04-11 | Standard Oil Co | Lubricating oil |
| US2160293A (en) * | 1936-12-05 | 1939-05-30 | Standard Oil Co | Lubricant |
| US2190648A (en) * | 1936-06-09 | 1940-02-20 | Gulf Oil Corp | Lubrication of alloy bearings |
| US2201258A (en) * | 1936-08-11 | 1940-05-21 | Goodrich Co B F | Extreme pressure lubricant |
| US2293237A (en) * | 1939-12-29 | 1942-08-18 | Standard Oil Dev Co | Hydrocarbon product |
| US2318629A (en) * | 1938-03-04 | 1943-05-11 | Lubri Zol Corp | Lubricating composition |
| US2414257A (en) * | 1942-07-29 | 1947-01-14 | Wakefield & Co Ltd C C | Lubricating oil |
| US2440095A (en) * | 1944-10-05 | 1948-04-20 | Goodrich Co B F | 2-mercapto thiazines and method of preparing same |
-
1949
- 1949-07-09 US US103936A patent/US2620303A/en not_active Expired - Lifetime
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2190648A (en) * | 1936-06-09 | 1940-02-20 | Gulf Oil Corp | Lubrication of alloy bearings |
| US2201258A (en) * | 1936-08-11 | 1940-05-21 | Goodrich Co B F | Extreme pressure lubricant |
| US2154096A (en) * | 1936-11-16 | 1939-04-11 | Standard Oil Co | Lubricating oil |
| US2160293A (en) * | 1936-12-05 | 1939-05-30 | Standard Oil Co | Lubricant |
| US2318629A (en) * | 1938-03-04 | 1943-05-11 | Lubri Zol Corp | Lubricating composition |
| US2293237A (en) * | 1939-12-29 | 1942-08-18 | Standard Oil Dev Co | Hydrocarbon product |
| US2414257A (en) * | 1942-07-29 | 1947-01-14 | Wakefield & Co Ltd C C | Lubricating oil |
| US2440095A (en) * | 1944-10-05 | 1948-04-20 | Goodrich Co B F | 2-mercapto thiazines and method of preparing same |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4210545A (en) * | 1979-03-30 | 1980-07-01 | Standard Oil Company (Indiana) | Oxidation resistant lubricant composition |
| EP0416909A1 (en) * | 1989-09-07 | 1991-03-13 | Exxon Research And Engineering Company | Lubricating oil composition |
| US10786080B1 (en) * | 2019-12-06 | 2020-09-29 | Dooli Products, LLC | Anti-tipping mechanisms integrated into furniture |
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