US2353170A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2353170A US2353170A US345614A US34561440A US2353170A US 2353170 A US2353170 A US 2353170A US 345614 A US345614 A US 345614A US 34561440 A US34561440 A US 34561440A US 2353170 A US2353170 A US 2353170A
- Authority
- US
- United States
- Prior art keywords
- sulfur
- thio
- compound
- halogen
- thionic
- 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
- 239000000314 lubricant Substances 0.000 title description 21
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 31
- -1 aliphatic organic compounds Chemical class 0.000 description 28
- 229910052736 halogen Inorganic materials 0.000 description 25
- 150000002367 halogens Chemical group 0.000 description 25
- 239000000203 mixture Substances 0.000 description 24
- 229910052717 sulfur Chemical group 0.000 description 24
- 239000011593 sulfur Chemical group 0.000 description 24
- 239000000463 material Substances 0.000 description 22
- 230000001050 lubricating effect Effects 0.000 description 17
- 239000010687 lubricating oil Substances 0.000 description 15
- 239000003795 chemical substances by application Substances 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 13
- 239000002480 mineral oil Substances 0.000 description 13
- 235000010446 mineral oil Nutrition 0.000 description 13
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 12
- 229910052802 copper Inorganic materials 0.000 description 12
- 239000010949 copper Substances 0.000 description 12
- 150000003464 sulfur compounds Chemical class 0.000 description 11
- 239000005864 Sulphur Substances 0.000 description 8
- 239000003921 oil Substances 0.000 description 7
- 235000019198 oils Nutrition 0.000 description 7
- 150000007824 aliphatic compounds Chemical class 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 150000002894 organic compounds Chemical class 0.000 description 5
- 150000002898 organic sulfur compounds Chemical class 0.000 description 5
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- OYHQOLUKZRVURQ-HZJYTTRNSA-M 9-cis,12-cis-Octadecadienoate Chemical class CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O OYHQOLUKZRVURQ-HZJYTTRNSA-M 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- UIJGNTRUPZPVNG-UHFFFAOYSA-N benzenecarbothioic s-acid Chemical compound SC(=O)C1=CC=CC=C1 UIJGNTRUPZPVNG-UHFFFAOYSA-N 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 229940049918 linoleate Drugs 0.000 description 3
- 125000001741 organic sulfur group Chemical group 0.000 description 3
- 150000003457 sulfones Chemical class 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- 239000001149 (9Z,12Z)-octadeca-9,12-dienoate Substances 0.000 description 2
- WTTJVINHCBCLGX-UHFFFAOYSA-N (9trans,12cis)-methyl linoleate Natural products CCCCCC=CCC=CCCCCCCCC(=O)OC WTTJVINHCBCLGX-UHFFFAOYSA-N 0.000 description 2
- LNJCGNRKWOHFFV-UHFFFAOYSA-N 3-(2-hydroxyethylsulfanyl)propanenitrile Chemical compound OCCSCCC#N LNJCGNRKWOHFFV-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- PKIXXJPMNDDDOS-UHFFFAOYSA-N Methyl linoleate Natural products CCCCC=CCCC=CCCCCCCCC(=O)OC PKIXXJPMNDDDOS-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- ABNDFSOIUFLJAH-UHFFFAOYSA-N benzyl thiocyanate Chemical compound N#CSCC1=CC=CC=C1 ABNDFSOIUFLJAH-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- ZCZLQYAECBEUBH-UHFFFAOYSA-L calcium;octadec-9-enoate Chemical compound [Ca+2].CCCCCCCCC=CCCCCCCCC([O-])=O.CCCCCCCCC=CCCCCCCCC([O-])=O ZCZLQYAECBEUBH-UHFFFAOYSA-L 0.000 description 2
- SKOLWUPSYHWYAM-UHFFFAOYSA-N carbonodithioic O,S-acid Chemical compound SC(S)=O SKOLWUPSYHWYAM-UHFFFAOYSA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 2
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 2
- 125000005456 glyceride group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 2
- 229940073769 methyl oleate Drugs 0.000 description 2
- HNKJADCVZUBCPG-UHFFFAOYSA-N methyl-phenyl-thioether Natural products CSC1=CC=CC=C1 HNKJADCVZUBCPG-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- GVIJJXMXTUZIOD-UHFFFAOYSA-N thianthrene Chemical compound C1=CC=C2SC3=CC=CC=C3SC2=C1 GVIJJXMXTUZIOD-UHFFFAOYSA-N 0.000 description 2
- 239000012991 xanthate Substances 0.000 description 2
- UWDABAWWHRTVNK-UHFFFAOYSA-N (benzyldisulfanyl)methylbenzene;(phenyldisulfanyl)benzene Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1.C=1C=CC=CC=1CSSCC1=CC=CC=C1 UWDABAWWHRTVNK-UHFFFAOYSA-N 0.000 description 1
- QMTFKWDCWOTPGJ-KVVVOXFISA-N (z)-octadec-9-enoic acid;tin Chemical compound [Sn].CCCCCCCC\C=C/CCCCCCCC(O)=O QMTFKWDCWOTPGJ-KVVVOXFISA-N 0.000 description 1
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 1
- SOQQSPURSLWWMI-UHFFFAOYSA-N 1,3-thiazole-4-carbothioamide Chemical compound NC(=S)C1=CSC=N1 SOQQSPURSLWWMI-UHFFFAOYSA-N 0.000 description 1
- KPNYBOIKZZNEKC-UHFFFAOYSA-N 1-(2,3-dimethylphenyl)sulfanyl-2,3-dimethylbenzene Chemical compound CC1=CC=CC(SC=2C(=C(C)C=CC=2)C)=C1C KPNYBOIKZZNEKC-UHFFFAOYSA-N 0.000 description 1
- MQQKTNDBASEZSD-UHFFFAOYSA-N 1-(octadecyldisulfanyl)octadecane Chemical compound CCCCCCCCCCCCCCCCCCSSCCCCCCCCCCCCCCCCCC MQQKTNDBASEZSD-UHFFFAOYSA-N 0.000 description 1
- LUYAMNYBNTVQJG-UHFFFAOYSA-N 1-chloro-2-(2-chloroethylsulfonyl)ethane Chemical compound ClCCS(=O)(=O)CCCl LUYAMNYBNTVQJG-UHFFFAOYSA-N 0.000 description 1
- TZOVOULUMXXLOJ-UHFFFAOYSA-N 1-methyl-4-[(4-methylphenyl)disulfanyl]benzene Chemical compound C1=CC(C)=CC=C1SSC1=CC=C(C)C=C1 TZOVOULUMXXLOJ-UHFFFAOYSA-N 0.000 description 1
- UKIRWOGXRCXNQA-UHFFFAOYSA-N 12-chlorododecyl thiocyanate Chemical compound ClCCCCCCCCCCCCSC#N UKIRWOGXRCXNQA-UHFFFAOYSA-N 0.000 description 1
- XQVYLDFSPBXACS-UHFFFAOYSA-N 2,4,6-Trimethyl-1,3,5-trithiane Chemical compound CC1SC(C)SC(C)S1 XQVYLDFSPBXACS-UHFFFAOYSA-N 0.000 description 1
- RFCQDOVPMUSZMN-UHFFFAOYSA-N 2-Naphthalenethiol Chemical compound C1=CC=CC2=CC(S)=CC=C21 RFCQDOVPMUSZMN-UHFFFAOYSA-N 0.000 description 1
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 description 1
- MOTOSAGBNXXRRE-UHFFFAOYSA-N 2-phenylsulfanylacetic acid Chemical compound OC(=O)CSC1=CC=CC=C1 MOTOSAGBNXXRRE-UHFFFAOYSA-N 0.000 description 1
- 244000126822 Albuca minor Species 0.000 description 1
- KYLIZBIRMBGUOP-UHFFFAOYSA-N Anetholtrithion Chemical group C1=CC(OC)=CC=C1C1=CC(=S)SS1 KYLIZBIRMBGUOP-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LUFPJJNWMYZRQE-UHFFFAOYSA-N Dibenzyl sulphide Natural products C=1C=CC=CC=1CSCC1=CC=CC=C1 LUFPJJNWMYZRQE-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- 241000639544 Dipara Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- HSRJKNPTNIJEKV-UHFFFAOYSA-N Guaifenesin Chemical compound COC1=CC=CC=C1OCC(O)CO HSRJKNPTNIJEKV-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 241001647090 Ponca Species 0.000 description 1
- KZTYYGOKRVBIMI-UHFFFAOYSA-N S-phenyl benzenesulfonothioate Natural products C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- FVFJGQJXAWCHIE-UHFFFAOYSA-N [4-(bromomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CBr)C=C1 FVFJGQJXAWCHIE-UHFFFAOYSA-N 0.000 description 1
- XWTFVTOZYCMQLA-UHFFFAOYSA-N [S].[Br] Chemical class [S].[Br] XWTFVTOZYCMQLA-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N anhydrous quinoline Natural products N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- KYNFOMQIXZUKRK-UHFFFAOYSA-N bishydroxyethyldisulfide Natural products OCCSSCCO KYNFOMQIXZUKRK-UHFFFAOYSA-N 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
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- FTOSZADXYFNRQP-UHFFFAOYSA-L calcium;2,2-dichlorooctadecanoate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCC(Cl)(Cl)C([O-])=O.CCCCCCCCCCCCCCCCC(Cl)(Cl)C([O-])=O FTOSZADXYFNRQP-UHFFFAOYSA-L 0.000 description 1
- LSCGCDXAEHGNMD-UHFFFAOYSA-N calcium;phenyl octadecanoate Chemical compound [Ca].CCCCCCCCCCCCCCCCCC(=O)OC1=CC=CC=C1 LSCGCDXAEHGNMD-UHFFFAOYSA-N 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- HHTWOMMSBMNRKP-UHFFFAOYSA-N carvacrol Natural products CC(=C)C1=CC=C(C)C(O)=C1 HHTWOMMSBMNRKP-UHFFFAOYSA-N 0.000 description 1
- RECUKUPTGUEGMW-UHFFFAOYSA-N carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 description 1
- 235000007746 carvacrol Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229940070335 chlor-phen Drugs 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000011365 complex material Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- MYXNWWDJRWCURH-UHFFFAOYSA-N ethoxymethanethioic s-acid Chemical compound CCOC(S)=O MYXNWWDJRWCURH-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910000286 fullers earth Inorganic materials 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- WYXXLXHHWYNKJF-UHFFFAOYSA-N isocarvacrol Natural products CC(C)C1=CC=C(O)C(C)=C1 WYXXLXHHWYNKJF-UHFFFAOYSA-N 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 125000005029 naphthylthio group Chemical group C1(=CC=CC2=CC=CC=C12)S* 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- GLSRRBHRRXRHAR-UHFFFAOYSA-N octadecyl thiocyanate Chemical compound CCCCCCCCCCCCCCCCCCSC#N GLSRRBHRRXRHAR-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- QWENMOXLTHDKDL-UHFFFAOYSA-N pentoxymethanedithioic acid Chemical compound CCCCCOC(S)=S QWENMOXLTHDKDL-UHFFFAOYSA-N 0.000 description 1
- LCLOXRAKDJBSMN-UHFFFAOYSA-N pentyl hydrogen carbonate Chemical compound CCCCCOC(O)=O LCLOXRAKDJBSMN-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- RZFBEFUNINJXRQ-UHFFFAOYSA-M sodium ethyl xanthate Chemical compound [Na+].CCOC([S-])=S RZFBEFUNINJXRQ-UHFFFAOYSA-M 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- JTHUJOZLDHAGIH-UHFFFAOYSA-M sodium;thiobenzate Chemical compound [Na+].[O-]C(=S)C1=CC=CC=C1 JTHUJOZLDHAGIH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000005323 thioketone group Chemical group 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/043—Sulfur; Selenenium; Tellurium
-
- 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty 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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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Definitions
- This invention relates, as indicated, to lubricating oils and more particularly to such compositions as new compositions of matter.
- the lubricant employed be also noncorrosive and stable to the rather high operating temperatures.
- Another object is to provide such a lubricant which also has the desirable property of high oiliness.
- Still another object is to provide a lubricant having the foregoing advantages and which is stable and noncorrosive in use.
- this invention comprises a lubricating composition
- a lubricating composition comprising a major amount of a lubricating oil and minor amounts of both a halogen and sulfur bearing organic compound and a thionic material.
- the thionic material which may be either an organic sulfur compound or elemental sulfur and when thus employed may "have sulphur present in either relatively active or inactive form, depending upon the particular use to which the composition is to be placed.
- both the halogen and sulfur bearing addition agent and the thionic material will preferably have a vapor pressure less than atmospheric at C. and for certain uses, a
- this conditlon may be expressed by stating that the boiling point of the compound should, in general, be higher than 140 C., and, for certain uses, such as in internal combustion engines, higher than 170 C.
- halogens While all of the halogens are eflective when employed in accordance with the present invention chlorine is generally preferred since it is the least expensive and one of the most effective of the halogens. Bromine and fluorine may be employed but are relatively expensive and the latter is somewhat difllcult to handle. Iodine, while effective, is at present too expensive to be employed on a large scale. It should also be noted that two or more different halogens may be present in the same molecule. The brom-chlor and fluorinated chlorine or bromine sulfur compounds give particularly satisfactory results.
- thionic material to be employed in this invention may be either elemental sulfur or an organic sulfur compound.
- the organic sulfur compound may be carbooyclic, aliphatic or heterocyclic in nature. '-We have also found that those thionic materials made by the direct sulfurlzing of organic compounds by the use of sulfur or a sulfur compound are of value in our invention. Of particular value are those thionic materials made by sulfurizing chemically unsaturated olefinio organic compounds;
- Thlophenates such as calcium thiocresolate Sulfurized olefinic material derived by halogenating, dehalogenating, and suliurizing petroleum Suliurized calcium oleate Sulfurized calcium'linoleate Sulfurized tin oleate Sulfurized tin linoleate Sulfurizedpotassium oleate Sulfurized potassium linoleate
- the thionic material to be used will be selected from those which will turn a copper strip black in less than 30 minutes at 210 1''.
- An example of such active thionic material is obtained by employing a physical solution or colloidal suspension of elemental sulphur in the lubricating composition. For many uses,
- the thionic material will be selected from .those which will not turn a copper strip black in less than 30 minutes at a temperature of 210 F.
- the copper strip test as above indicated is conducted by mixing of the addition agent with 90% of the base oil and then maintaining a clean copper strip therein for a period of 30 minutes at a temperature of 210 F.
- Sulfur compounds for use in this invention may be made by controlling the composition and by varying the physical and chemical factors involved in manufacturing until a sulfur compound is formed that will not blacken a copper strip when blended with mineral oil and heated to 210 I", for 30 minutes.
- a chemically unsaturated glyceride may be suifurized with 5, 10, or percent of sulfur and mineral oil blends of each of these may turn a copper strip black in less than 30 minutes at 210 F.
- control of the time and temperature of sulfurizing will convert all three of these to compounds that will not blacken a copper strip under the conditions of the foregoing test. Obviously, less time and lower temperatures will satisfactorily condition the glycerlde containing.
- sulfur compounds for use in this invention may be manufactured according to the above general method and the manufacturing process stopped short of complete conditioning of the sulfur compound to the copper strip test.
- only small amounts of sulfur or. sulfur compounds present in the desired product have a tendency to blacken the copper strip in the test prescribed.
- we remove the small amount of objectionable material by contacting the entire mass with treating agents that make the product satisfactory.
- these treating agents are finely divided metal such as copper, iron. mercury, etc., either as such or mixed with inert carriers like clay, fullers earth, pumice, kieselguhr, and the like.
- Other treating methods are known and may be employed to accomplish the desired ends.
- the oil base employed may be any suitable lubricating oil such as mineral oil or animal and vegetable oils of lubricating viscosity, and including synthetic, hydrogenated and volatilized oils.
- addition agents in the form of a concentrate in a suitable oil, said oil containing a rather high percentage of the addition agents.
- Such concentrates may beemployed for future blending with a lubricating oil in the proportions desired for the particular conditions of use.
- the invention contemplates the employmentof iron about .5 percent to about 10 percent by weight of thealiphatic halogen and sulfur bearing compound, based on the amount of mineral oil, and an equal or less amount of the thionic material.
- iron about .5 percent to about 10 percent by weight of thealiphatic halogen and sulfur bearing compound, based on the amount of mineral oil, and an equal or less amount of the thionic material.
- as little as .02 percent of one or the other addition agent may be eifective for certain uses, while for other uses as much as 20% may be employed.
- lubricants of this invention are superior in one or more respects depending upon the particular thionic material and halogen and sulfur bearing compound added to the mineral oil. For example, the corrosion or metal wear; is less with the combination lubricant. than with a lubricant containing only one of the addition agents.
- the sludging and oxidation characteristics of the lubricant in use are usually improved to a marked degree.
- the loadcarrying capacity of the lubricants of this invention may be higher than a lubricant made with the same mineral oil and only a thionic material or a. halogenand sulfur compound as such are defined by the invention.
- the oiliness character of the lubricants of this invention reflects the combined oiliness effect of the two separate types of compounds, namely, thionic material and halogen and sulfur compounds. The unexpected joint effectof the halogen and sulfur compound and the thionic material makes these lubricants outstanding. From these unexpected results we are of the opinion that there is a specific but incompletely understood effect of the thionic material on the halogen and sulfur compound and of the latter on the former.
- lubricating compositions which have been described herein as illustrating one embodiment of the invention have been generally referred' to as "oils," i. e., liquids
- this invention is, however, also applicable to the solid and semisolid types of lubricants commonly referred to in the trade as greases, bodied oils, etc., which contain metallic or nonmetallic salts or soaps such as calcium oleate.
- metallic or nonmetallic salts or soaps such as calcium oleate.
- sodium stearate, aluminum naph- The addition agents must, of course, be soluble thenate, calcium phenyl stearate, calcium dichlorostearate, ammonium oleate, or cadmium, nickel, zinc, or tin salts or soaps of various organic acids.
- a lubricating composition comprising a major proportion of lubricating oil and a minor amount of a halogen and sulfur bearing aliphatic ⁇ compound and a. minor amount of a thionic material.
- a lubricating composition comprising a major proportion of lubricating oil and a minor amountof a halogen and sulfur bearing aliphatic compound and a minor amount ofelemental sulfur.
- a lubricating composition comprising a major proportion of lubricating oil and a minor amount of a halogen and sulfur bearing aliphaticcompound and a minor amount of an organic sulfur compound.
- a "lubricating composition comprising a major proportion of lubricating oil'anda minor amount of a halogen and sulfur bearing aliphatic compound and a separate-organic sulfur compound of the type which does not blacken a copper strip placed in the composition at a temperature of 210 F. for thirty minutes.
- composition'at a temperature of 210 F. for I thirty minutes.
- a lubricating composition comprising a majorproportion of lubricating oil and minor proportions of both an organic sulfur-bearing compound and a halogen" and sulfur bearing aliphatic ester, said addition agents having vapor pressures of less than atmospheric at 140 C.
- a lubricating composition comprising a major proportion of lubricating oil and minor proportions of both an organic sulfur-bearing compound and a halogen and sulfur bearing salt of an aliphatic acid, said addition agents having vapor pressures of less than atmospheric at 140 C.
- a lubricating composition comprising a major proportion of lubricating oil and a minor amount of an aliphatic organic compound containinghalogen, sulphur and oxygen in the molecule, and a minor amount of an organic sulphur compound.
- a lubricating composition comprising a major proportion of lubricating oil and from about .02% to 20% of a halogen and sulphur bearing aliphatic compound having a vapor pressure less than atmospheric at 140 C. and'from about .02% to20% of a separate organic sulphur compound of the type which will blacken a copper strip placed in the composition at a temperature of 210 F. for thirty minutes.
- a lubricating composition comprising a -major proportion of lubricating oil and minor proportions of both an organicgsulphur bearing compound and a chlor naphtha xanthate, said addition agents having vapor pressures of less BlliRT H. Lmco'm.
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Description
F'atented July 11, 1944 UNITED STATES PATENT OFFICE LUBRICANT Bert E. Lincoln and Waldo L. Steiner, Ponca City, Okla, aasignors, by mesne assignments, to The Lubri -Zol Development Corporation, Cleveland, Ohio, a corporation of Delaware is Claims.
This invention relates, as indicated, to lubricating oils and more particularly to such compositions as new compositions of matter.
This application is a continuation in-part of our copending application Serial 293,276, filed September 2, 1939.
The present design of mechanical devices including internal combustion engines calls for high pressures on rubbing surfaces and the tendency is toward a still greaterincrease in such pressures. While conventional hydrocarbon lubricants vary somewhat in film strength the best of them are unableto withstand the extreme pressures imposed by modern design and the still higher pressures designers of mechanical devices would like to employ to take advantage of the improvements which might be achieved with higher rubbing pressures.
For many uses, as in the crankcase of an internal combustion engine, it is necessary that the lubricant employed be also noncorrosive and stable to the rather high operating temperatures.
Other desirable propertiesv include high oiliness, low pour point and resistance to sludge formation.
It is therefore a principal object of our invention to provide an effective extreme pressure lubricating composition capable of withstanding the high pressures imposed'on rubbing surfaces by modern mechanical design.
Another object is to provide such a lubricant which also has the desirable property of high oiliness.
Still another object is to provide a lubricant having the foregoing advantages and which is stable and noncorrosive in use.
Other objects of this invention will appear as the description proceeds.
To the accomplishment of the foregoing and related ends this invention, then, consists of the means hereinafter fully described and particularly pointed out in the claims.
The following description sets forth in detail certain approved combinations of ingredients embodying our invention, such disclosed means constituting, however, but one of various forms in which the principle of the invention may be used.
Broadly stated, this invention comprises a lubricating composition comprising a major amount of a lubricating oil and minor amounts of both a halogen and sulfur bearing organic compound and a thionic material. The thionic material which may be either an organic sulfur compound or elemental sulfur and when thus employed may "have sulphur present in either relatively active or inactive form, depending upon the particular use to which the composition is to be placed.
More particularly, both the halogen and sulfur bearing addition agent and the thionic material will preferably have a vapor pressure less than atmospheric at C. and for certain uses, a
vapor pressure less than atmospheric at C. In the case of compounds which are stable at temperatures up to their boiling points, this conditlon may be expressed by stating that the boiling point of the compound should, in general, be higher than 140 C., and, for certain uses, such as in internal combustion engines, higher than 170 C.
While all of the halogens are eflective when employed in accordance with the present invention chlorine is generally preferred since it is the least expensive and one of the most effective of the halogens. Bromine and fluorine may be employed but are relatively expensive and the latter is somewhat difllcult to handle. Iodine, while effective, is at present too expensive to be employed on a large scale. It should also be noted that two or more different halogens may be present in the same molecule. The brom-chlor and fluorinated chlorine or bromine sulfur compounds give particularly satisfactory results.
The following list includes a number of typical halogen and sulfur bearing aliphatic organic compounds found generally suitable for use in accordance with this invention. Itwill be. un-
derstood, however, that such list is intended for purposes of illustration only and is not intended to limit the scope of the invention to those compounds herein enumerated.
HALOGEN AND SULFUR BEARING ORGANIC COMPOUNDS 1. ALIPHATIC 5. Sulfones and sulfoxides Beta-chloroethyl sulfone The thionic material to be employed in this invention may be either elemental sulfur or an organic sulfur compound. The organic sulfur compound may be carbooyclic, aliphatic or heterocyclic in nature. '-We have also found that those thionic materials made by the direct sulfurlzing of organic compounds by the use of sulfur or a sulfur compound are of value in our invention. Of particular value are those thionic materials made by sulfurizing chemically unsaturated olefinio organic compounds;
I. CAssooYcuo Com'omms Examples of materials within this classification are:
Diphenyl sulfide Dibenzyl sulfide Di naphthyl sulfide Di paratolyl sulfide Di xylyl sulfide Di phenyl disulfide Di benzyl disulfide Di naphtyl disulfide Di para tolyl disulfide I Dibenzyl trisulfide Di phenol disulfide Diphenyl sulfone Dibenzylsuli'one Di par'atoyl sulfone Di naphthyl sulfone Di xylyl sulfone Di phenyl'sulioxide Dibenzyl sulioxide Dipara tolyl sulfoxide Di xylyl sulfoxide Di naphthyl sulfoxide Diphenyl 'thio urea Dibenzyl thio urea Dibenzyl thio urea Ortho tolyl thio urea Phenyl thio cyanate Benzyl thio cyan'ate Naphthyl thio cyanate Methyl phenyl thio ether Ethyl benzyl thio ether Propylnaphthyl thio ether Thioanthraquinone Thio phenol Ortho thio oresol Thio carvacrol Thio anisol Thio naphthol I l Ortho nitro thio phenol Phenyl thio carbonic chloride Chlor phen'yl mercaptan Phenyl thio glycolic acid Thio ben zoic acid Sodium thio benzoate: 4
Calcium thio benzoate Tin thio benzoate Benzene sulfonic acid Naphthalene sulionic acid 'I'hio aldehydes R,CHS in which R is any carbocyclic'i'adical including phenyl, tolyl, naphthyLxylyl, etc. v
Thio ketones R.CS.'R' in which either R or R' is Heterocyclic Dibenzothiophene 7 Thianthrene (diphenylene disulfide) 'I'rithioacetaldehyde Trithioacetaldehyde trisulfone Tetrahydrofurfuryl sulfide Methylmercaptobenzothiazole S-sulfhydryl quinoline Mercaptodibenzomrane Methylmercaptochlorodioxane Ethylene sym.-dithiocarbonate Aliphatic compounds Butyl sulfide Amyl sulfide Hexyl sulfide Octadecyl sulfide Heptyl sulfide Butyl disulfide Amyl disulfide Hexyl disulfide Hextyl disulfide Octadecyl disulfide Amy] sulfone Butyl sulfone Hexyl sulfone Hentyl sllJfOne Octadecyl sulfone Ethyl thio cyanate I Butyl thio cyanate Hexyl thio cyanate Heptyl thio cy'anate Octadecyl thio cyanate Naphtha xanthate Ethyl thio carbonic acid Amy] thio carbonic acid Thio ethyl carbonic ethyl ester Methyl'ester of dithio carbonic acid lAJnyl ester of dithio carbonic acid Sodium ethyl xanthate Calcium amyl xanthate Tri thio carbonic amyl ester Dithiodiglycol Ethyl di thio-oxalate Octadecyl mercaptan Sodium amyl thisulfate 'I'hiocarbamylamine (reaction product of amyl' amine and CS2) Amyl sulfate Mercapto stearic acid Calcium mercaptostearate Methyl mercaptostearate Sulfurized materials Sulfurized methyl linoleate Sulfurized methyl oleate' Sulfurized methyl aryl substituted linoleate Sulfurized animal and vegetable oi Sulfurized lard oil Sulfurized corn oil Sulfurized cottonseed oil Sulfurized sperm oil Sulfurized oleic acid Sulfurized olefinic hydrocarbons from P troleum any carbooyclic radical including phenyl tolyl,
xylyl;-naphthyl, etc. Thlophenates such as calcium thiocresolate Sulfurized olefinic material derived by halogenating, dehalogenating, and suliurizing petroleum Suliurized calcium oleate Sulfurized calcium'linoleate Sulfurized tin oleate Sulfurized tin linoleate Sulfurizedpotassium oleate Sulfurized potassium linoleate Where extreme or violent extreme pressure characteristics are encountered, the thionic material to be used will be selected from those which will turn a copper strip black in less than 30 minutes at 210 1''. An example of such active thionic material is obtained by employing a physical solution or colloidal suspension of elemental sulphur in the lubricating composition. For many uses,
however, where stability and freedom from corrosion and the like are of greater importance than extreme pressure characteristics, thenthe thionic material will be selected from .those which will not turn a copper strip black in less than 30 minutes at a temperature of 210 F. The copper strip test as above indicated is conducted by mixing of the addition agent with 90% of the base oil and then maintaining a clean copper strip therein for a period of 30 minutes at a temperature of 210 F.
Sulfur compounds for use in this invention may be made by controlling the composition and by varying the physical and chemical factors involved in manufacturing until a sulfur compound is formed that will not blacken a copper strip when blended with mineral oil and heated to 210 I", for 30 minutes. For example, a chemically unsaturated glyceride may be suifurized with 5, 10, or percent of sulfur and mineral oil blends of each of these may turn a copper strip black in less than 30 minutes at 210 F. However, control of the time and temperature of sulfurizing will convert all three of these to compounds that will not blacken a copper strip under the conditions of the foregoing test. Obviously, less time and lower temperatures will satisfactorily condition the glycerlde containing. 5 per cent sulfur than will be required for the glyceride containing 15 percent sulfur. To accomplish this result we regularly test the batch during manufacture and impose the minimum severity of manufacturing conditions. For some lubricating problems. it is necessary to have a controlled amount of both active and inactive sulfur in the lubricant.
In some instances sulfur compounds for use in this invention may be manufactured according to the above general method and the manufacturing process stopped short of complete conditioning of the sulfur compound to the copper strip test. In these instances, only small amounts of sulfur or. sulfur compounds present in the desired product have a tendency to blacken the copper strip in the test prescribed. In these instances we remove the small amount of objectionable material by contacting the entire mass with treating agents that make the product satisfactory. Examples of these treating agents are finely divided metal such as copper, iron. mercury, etc., either as such or mixed with inert carriers like clay, fullers earth, pumice, kieselguhr, and the like. Other treating methods are known and may be employed to accomplish the desired ends. v
The oil base employed may be any suitable lubricating oil such as mineral oil or animal and vegetable oils of lubricating viscosity, and including synthetic, hydrogenated and volatilized oils.
It is also within the contemplation of this invention to provide the addition agents in the form of a concentrate in a suitable oil, said oil containing a rather high percentage of the addition agents. Such concentrates may beemployed for future blending with a lubricating oil in the proportions desired for the particular conditions of use.
- permanently homogeneous composition when incorporated inthe 011 base.
In general, the invention contemplates the employmentof iron about .5 percent to about 10 percent by weight of thealiphatic halogen and sulfur bearing compound, based on the amount of mineral oil, and an equal or less amount of the thionic material. However, as little as .02 percent of one or the other addition agent may be eifective for certain uses, while for other uses as much as 20% may be employed.
For each combination of a specific halogen and sulfur compound and a specific thionic material, it will be found that there is a certain optimum proportional relationship which may be found by comparative tests. This also holds true where the halogen and sulfur or sulfur bearing component is in the form of a complex material.
It has been found that the addition of the thionic material in which the sulfur is present in relatively inactive form and the addition of the halogen and sulfur bearing organic compound to the same mineral oil results in lubricants far superior to lubricants made with the same mineral oil and only one or the other of the two classes of compounds. The lubricants of this invention are superior in one or more respects depending upon the particular thionic material and halogen and sulfur bearing compound added to the mineral oil. For example, the corrosion or metal wear; is less with the combination lubricant. than with a lubricant containing only one of the addition agents. The sludging and oxidation characteristics of the lubricant in use are usually improved to a marked degree. The loadcarrying capacity of the lubricants of this invention may be higher than a lubricant made with the same mineral oil and only a thionic material or a. halogenand sulfur compound as such are defined by the invention. The load-carrying capacity of lubricants of this invention'will remain fairly constant throughout the entire period of use of the lubricant which is one of the greatest practical advantages of these lubricants. The oiliness character of the lubricants of this invention reflects the combined oiliness effect of the two separate types of compounds, namely, thionic material and halogen and sulfur compounds. The unexpected joint effectof the halogen and sulfur compound and the thionic material makes these lubricants outstanding. From these unexpected results we are of the opinion that there is a specific but incompletely understood effect of the thionic material on the halogen and sulfur compound and of the latter on the former.
The addition agents, should of course, be stable at the operating temperatures to which they will be subjected.
While the lubricating compositions which have been described herein as illustrating one embodiment of the invention have been generally referred' to as "oils," i. e., liquids, this invention is, however, also applicable to the solid and semisolid types of lubricants commonly referred to in the trade as greases, bodied oils, etc., which contain metallic or nonmetallic salts or soaps such as calcium oleate. sodium stearate, aluminum naph- The addition agents must, of course, be soluble thenate, calcium phenyl stearate, calcium dichlorostearate, ammonium oleate, or cadmium, nickel, zinc, or tin salts or soaps of various organic acids.
- The following examples of our invention are not given as a limitation but to show certain practical combinations:
I Per cent (1) SAE 10 mineral oil.... 9B
' Chlorolauryl mercaptam 1 Sulfurized methyl linoleate 1 (2) SAE 20 mineral oil 98 Chloro amyl disulfide 1 Sulfurized methyl oleate 1 (3) SAE mineral oil 97 Chloro lauryl thio cyanide 2 Dibenzyl disulfide 1 (4) SAE 50 mineral oil 98 Chloroamyi suliate 1 Butyl disulfide. 1
(5) SAE 60 mineral oil 98 Chloro naphtha sulfate 1 Benzyl thiocyanate 1 We, therefore, particularly point out and dis- I tinctly claim as our invention: I
I 1. A lubricating composition comprising a major proportion of lubricating oil and a minor amount of a halogen and sulfur bearing aliphatic {compound and a. minor amount of a thionic material.
2. A lubricating composition comprising a major proportion of lubricating oil and a minor amountof a halogen and sulfur bearing aliphatic compound and a minor amount ofelemental sulfur.
3. A lubricating composition comprising a major proportion of lubricating oil and a minor amount of a halogen and sulfur bearing aliphaticcompound and a minor amount of an organic sulfur compound.
4. A "lubricating composition comprising a major proportion of lubricating oil'anda minor amount of a halogen and sulfur bearing aliphatic compound and a separate-organic sulfur compound of the type which does not blacken a copper strip placed in the composition at a temperature of 210 F. for thirty minutes.
the composition'at a temperature of 210 F. for I thirty minutes.
.7. A lubricating composition comprising major proportion of lubricating oil and from 2,sss,170
about 5 percent to about 10 percent each of a halogen and sulfur bearing aliphatic compound having a'vapor pressure less than atmospheric at C. and a relatively inactive organic sulfur-bearing compound having a vapor pressure less than atmospheric at 140 C.
proportions of both an organic sulfur compound and a halogen and sulfur-jbearing aliphatic hydrocarbon, said addition agents hav-,
ing vapor pressures of less than atmospheric at 140 C. a
9. A lubricating composition comprising a majorproportion of lubricating oil and minor proportions of both an organic sulfur-bearing compound and a halogen" and sulfur bearing aliphatic ester, said addition agents having vapor pressures of less than atmospheric at 140 C.
10. A lubricating composition comprising a major proportion of lubricating oil and minor proportions of both an organic sulfur-bearing compound and a halogen and sulfur bearing salt of an aliphatic acid, said addition agents having vapor pressures of less than atmospheric at 140 C.
11. A lubricating composition comprising a major proportion of lubricating oil and a minor amount of an aliphatic organic compound containinghalogen, sulphur and oxygen in the molecule, and a minor amount of an organic sulphur compound.
12. A lubricating composition comprising a major proportion of lubricating oil and from about .02% to 20% of a halogen and sulphur bearing aliphatic compound having a vapor pressure less than atmospheric at 140 C. and'from about .02% to20% of a separate organic sulphur compound of the type which will blacken a copper strip placed in the composition at a temperature of 210 F. for thirty minutes.
13. A lubricating composition comprising a major proportion of lubricating oil and from about .02% to 20% of a halogen and sulphur bearing aliphatic hydrocarbon having a vapor pressure less than atmospheric at 140 C. and from about .02% to 20% of a separate organic sulphur compound.
14. A lubricating composition comprising a -major proportion of lubricating oil and minor proportions of both an organicgsulphur bearing compound and a chlor naphtha xanthate, said addition agents having vapor pressures of less BlliRT H. Lmco'm.
WALDO L. s'rzmna.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US345614A US2353170A (en) | 1940-07-15 | 1940-07-15 | Lubricant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US345614A US2353170A (en) | 1940-07-15 | 1940-07-15 | Lubricant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2353170A true US2353170A (en) | 1944-07-11 |
Family
ID=23355740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US345614A Expired - Lifetime US2353170A (en) | 1940-07-15 | 1940-07-15 | Lubricant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2353170A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2546941A (en) * | 1946-07-25 | 1951-03-27 | Shell Dev | Lubricating oil |
| US2610182A (en) * | 1949-06-22 | 1952-09-09 | Standard Oil Dev Co | Hydrocarbon thiophosphoric acid salts of thialdine and certain homologues |
| US2900341A (en) * | 1956-01-25 | 1959-08-18 | Texaco Inc | Extreme pressure lubricant additive |
| US2932615A (en) * | 1957-07-22 | 1960-04-12 | Texnco Inc | Extreme pressure lubricant |
-
1940
- 1940-07-15 US US345614A patent/US2353170A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2546941A (en) * | 1946-07-25 | 1951-03-27 | Shell Dev | Lubricating oil |
| US2610182A (en) * | 1949-06-22 | 1952-09-09 | Standard Oil Dev Co | Hydrocarbon thiophosphoric acid salts of thialdine and certain homologues |
| US2900341A (en) * | 1956-01-25 | 1959-08-18 | Texaco Inc | Extreme pressure lubricant additive |
| US2932615A (en) * | 1957-07-22 | 1960-04-12 | Texnco Inc | Extreme pressure lubricant |
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