DE748244C - Prevention of the oxidation of lubricants - Google Patents
Prevention of the oxidation of lubricantsInfo
- Publication number
- DE748244C DE748244C DEST59307D DEST059307D DE748244C DE 748244 C DE748244 C DE 748244C DE ST59307 D DEST59307 D DE ST59307D DE ST059307 D DEST059307 D DE ST059307D DE 748244 C DE748244 C DE 748244C
- Authority
- DE
- Germany
- Prior art keywords
- oil
- oils
- alcohol
- salt
- phenol
- 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
Links
- 239000000314 lubricant Substances 0.000 title claims description 7
- 230000003647 oxidation Effects 0.000 title claims description 5
- 238000007254 oxidation reaction Methods 0.000 title claims description 5
- 230000002265 prevention Effects 0.000 title 1
- LJKQIQSBHFNMDV-UHFFFAOYSA-N 7-thiabicyclo[4.1.0]hepta-2,4-dien-6-ol Chemical class C1=CC=CC2(O)C1S2 LJKQIQSBHFNMDV-UHFFFAOYSA-N 0.000 claims description 8
- 150000002736 metal compounds Chemical class 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000003921 oil Substances 0.000 description 33
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 24
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- 235000019441 ethanol Nutrition 0.000 description 11
- -1 nitro, nitroso, amino Chemical group 0.000 description 11
- 150000003839 salts Chemical class 0.000 description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- 159000000007 calcium salts Chemical class 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 239000010687 lubricating oil Substances 0.000 description 5
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 229910052788 barium Inorganic materials 0.000 description 4
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 239000010685 fatty oil Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 150000003568 thioethers Chemical class 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 3
- 230000001476 alcoholic effect Effects 0.000 description 3
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 239000003502 gasoline Substances 0.000 description 3
- 239000010688 mineral lubricating oil Substances 0.000 description 3
- 150000002815 nickel Chemical group 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 229910052711 selenium Inorganic materials 0.000 description 3
- 239000011669 selenium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- MHRFIEZKKQESCC-UHFFFAOYSA-N 5,6-bis(2-methylpropyl)-7-thiabicyclo[4.1.0]hepta-2,4-dien-1-ol Chemical compound C(C(C)C)C=1C2(C(C=CC1)(O)S2)CC(C)C MHRFIEZKKQESCC-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000013495 cobalt Nutrition 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920001021 polysulfide Polymers 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 150000003498 tellurium compounds Chemical class 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical class [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- MUBKMWFYVHYZAI-UHFFFAOYSA-N [Al].[Cu].[Zn] Chemical compound [Al].[Cu].[Zn] MUBKMWFYVHYZAI-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 1
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- 239000010727 cylinder oil Substances 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- XDKQUSKHRIUJEO-UHFFFAOYSA-N magnesium;ethanolate Chemical compound [Mg+2].CC[O-].CC[O-] XDKQUSKHRIUJEO-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Chemical class 0.000 description 1
- 239000011572 manganese Chemical class 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- 239000004058 oil shale Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- 239000011701 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011787 zinc oxide 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio 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
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/20—Thiols; Sulfides; Polysulfides
- C10M135/28—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to a carbon atom of a six-membered aromatic ring
- C10M135/30—Thiols; Sulfides; Polysulfides containing sulfur atoms bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/041—Carbon; Graphite; Carbon black
-
- 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
- C10M2201/041—Carbon; Graphite; Carbon black
- C10M2201/042—Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
-
- 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
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
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Description
Es wurde gefunden, daß man die Oxydation von Schmiermitteln verhindern oder zum mindesten wesentlich herabsetzen kann, wenn man ihnen geringe Mengen von Metallverbindungen von Phenolsulfiden oder den entsprechenden Selen- oder Tellurverbindungen zusetzt. Diese Maßnahme eignet sich insbesondere zur Verbesserung der Oxydationsbeständigkeit von Schmierölen, vorzugsweise mineralischen Schmierölen.It has been found that one can prevent or at least prevent the oxidation of lubricants can be significantly reduced if you give them small amounts of metal compounds of phenol sulfides or the corresponding selenium or tellurium compounds. This measure is particularly suitable for improving the resistance to oxidation of lubricating oils, preferably mineral lubricating oils.
Die zugesetzten Metallsalze der Phenolsulfide entsprechen der allgemeinen FormelThe added metal salts of the phenol sulfides correspond to the general formula
MOMO
Ar —Zv—R'.
R x Ar —Z v —R '.
R x
Hierin bedeutet Ar eine beliebige cyclische Gruppe, die einen oder mehrere Benzolringe, im letzten Falle z. B. in Form eines kondensierten Ringsystems, enthalten kann. M stellt ein Metall dar, z.B. Lithium, Natrium, Kalium, Magnesium, Barium, Calcium, Aluminium, Kupfer, Zink, Kadmium, Zinn, Blei, Chrom, Mangan, Eisen, Kobalt oder Nickel. Falls M ein mehrwertiges Metall ist, kann es mit seinen anderen Valenzen an andere anorganische oder organische Gruppen gebunden sein, beispielsweise an Halogen, Schwefel, Sauerstoff oder an Alkyl- oder Arvlgruppen, alkoholische Reste, phenolische Verbindungen, Mercaptane oder organische oder anorganische Säuren. R' kann eine Aryl·, Alkyl-, Aralkyl- oder alkylierte Arylgruppe sein, die auch andere Substituenten, wie Halogen, insbesondere Chlor, oder die Nitro-, Nitroso-, Amino-,Herein Ar means any cyclic group that contains one or more benzene rings, in the latter case z. B. in the form of a condensed ring system may contain. M represents a metal, e.g. lithium, sodium, potassium, magnesium, barium, calcium, aluminum, Copper, zinc, cadmium, tin, lead, chromium, manganese, iron, cobalt or nickel. If M is a polyvalent metal, it can with its other valences to other inorganic ones or organic groups, for example to halogen, sulfur, oxygen or to alkyl or aromatic groups, alcoholic residues, phenolic compounds, mercaptans or organic or inorganic Acids. R 'can be an aryl, alkyl, aralkyl or alkylated aryl group, which also has other substituents, such as halogen, in particular Chlorine, or the nitro, nitroso, amino,
Oxy-, Carboxy-, Alkoxy-, Aroxy- oder Mercaptogruppe enthalten kann. R bedeutet ebenfalls eine organische Gruppe, die der gleichen Klasse wie R'angehören kann, vorzugsweise aber eine Alkylgruppe mit etwa 4 bts S Kohlenstoffatomen. Z bedeutet Schwefel, Selen oder Tellur, χ ist eine ganze Zahl von 1 bis 5. vorzugsweise 1 oder 2. May contain oxy, carboxy, alkoxy, aroxy or mercapto groups. R likewise denotes an organic group which can belong to the same class as R ′, but preferably an alkyl group with about 4 to 5 carbon atoms. Z denotes sulfur, selenium or tellurium, χ is an integer from 1 to 5, preferably 1 or 2.
Besonders wirksam sind Metallsalze von •10 Alkylphenolsulfiden oder -polysulfide!! und deren Polymepen, die z. B. den folgenden Formeln entsprechen können:Metal salts of • 10 alkylphenol sulfides or polysulfides are particularly effective !! and their Polymepen z. B. can correspond to the following formulas:
i. Alkylphenolthioätheri. Alkyl phenol thioether
OH OHOH OH
R,R,
OHOH
oder S/ or S /
S/S /
OH OHOH OH
R S \ , RR S \, R
Zweckmäßig werden symmetrische Verbindungen dieser Art benutzt, doch können auch einer oder mehrere der Benzolkerne andere Substituenten enthalten, wie z. B. in der folgenden Formel dargestellt ist:Symmetrical connections of this type are expediently used, but can one or more of the benzene nuclei also contain other substituents, such as. B. in the is shown in the following formula:
OHOH
NO.,NO.,
y S' ~-s "NO2 y S ' ~ -s "NO 2
(Dinitrophenylalkylphenolsulfid)(Dinitrophenylalkylphenol sulfide)
In allen diesen Formeln bedeutet R vorzugsweise eine Alkylgruppe mit 4 bis 6 Kohlen-Stoffatomen. In den genannten Verbindungen kann der Wasserstoff in einer oder mehreren Hydroxylgruppen durch, ein Metall ersetzt werden. Bei Anwendung mehrwertiger Metalle können diese mit zwei Hydroxylgruppen des gleichen Moleküls verbunden sein oder auch zwei'gleiche oder verschiedene Moleküle, von denen mindestens eines ein Phenolsulfid ist, miteinander verbinden. F-Ur die Metallverbindungen ergeben sich also beispielsweise folgende Formeln:In all of these formulas, R preferably denotes an alkyl group having 4 to 6 carbon atoms. In the compounds mentioned, the hydrogen in one or more hydroxyl groups can be replaced by a metal. If polyvalent metals are used, these can be linked to two hydroxyl groups of the same molecule or else two identical or different molecules, of which at least one is a phenol sulfide, can be linked to one another. F - For example, the following formulas result for the metal compounds:
0 —Na 0 —Ca —0 0 —Ni-OR"0 —Na 0 —Ca —0 0 —Ni-OR "
R, A R. A, A ,R R / ,R, A R. A, A, RR / ,
V--Sx-R' V-' ■V - S x -R 'V-' ■
Hierbei bedeutet OR" vorzugsweise die gleiche Gruppe, die mit der anderen Valenz des Nickelatoms verbunden ist. Die Herstellung / ■ Here, OR "preferably means the same group that is connected to the other valence of the nickel atom. The production / ■
Sx- R' S x - R '
solcher Metallverbindungen soll an Hand der folgenden Beispiele näher beschrieben werden.such metal compounds will be described in more detail with reference to the following examples will.
Beispiel ιExample ι
ι Mol tert. Amylphenolthioäther (der nach dem Verfahren der französischen Patentschrift 824 600 hergestellt werden kann) wird in etwa der i^fachen Raummenge absoluten Äthylalkohols gelöst und dann zu einer Lösung von Natriumäthylat, die aus 2 Mol metallischem Natrium und einem Überschuß absoluten Äthylalkohols hergestellt ist, zugegeben. Es bildet sich das Natriumsalz des tert. Amylphenolthioäthers, das von dem überschüssigen Äthylalkohol gelöst wird. Es kann durch Verdampfen des Alkohols gewonnen werden, oder man, kann auch die alkoholische Lösung unmittelbar einem Schmieröl zugeben und dann, wenn das Schmieröl einen hohen Flammpunkt haben soll, den Alkohol durch Verdampfen entfernen.ι mol tert. Amylphenol thioether (the after the process of French patent 824 600 can be produced) about i ^ times the absolute amount of space Ethyl alcohol and then dissolved into a solution of sodium ethylate, which consists of 2 moles of metallic Sodium and an excess of absolute ethyl alcohol is prepared, added. The sodium salt of is formed tert. Amylphenol thioether, which is dissolved from the excess ethyl alcohol. It can can be obtained by evaporating the alcohol, or one can also use the alcoholic Add the solution immediately to a lubricating oil and then when the lubricating oil has a high Should have a flash point, remove the alcohol by evaporation.
Salze anderer Metalle können aus dem Natriumsalz durch doppelte Umsetzung im Sinne des folgenden Beispiels hergestellt werden.Salts of other metals can be derived from the sodium salt by double conversion of the following example.
Ein geringer Überschuß über die berechnete Menge eines wasserfreien Halogenide des gewünschten Metalls (zweckmäßig verwendet man das Chlorid oder Bromid), beispielsweise Calciumchlorid, wird in absolutem Äthylalkohol gelöst und unter Rühren der nach Beispiel 1 erhaltenen alkoholischen Lösung des Natriumsalzes zugegeben. Es bildet sich einerseits das Calciumsalz des tert. ΑΠ13Ί-phenolthioäthers, andererseits Natriumchlorid, das in dem absoluten Alkohol unlöslich ist und daher ausgefällt wird. Das Natriumchlorid wird abfiltriert und der Alkohol aus dem Filtrat durch Verdampfen entfernt, wobei man gegen Schluß zweckmäßig im Vakuum arbeitet. Falls durch die Anwesenheit geringer Mengen Wasser nicht alles Natriumchlorid entfernt sein sollte, kann man das Produkt in beliebiger Weise davon befreien, beispielsweise indem man das getrocknete Produkt in Abwesenheit von Wasser in Benzin löst, wobei das Natriumchlorid ungelöst bleibt und durch Filtrieren entfernt wird.A slight excess over the calculated amount of an anhydrous halide of the desired Metal (it is advisable to use the chloride or bromide), for example calcium chloride, is in absolute ethyl alcohol dissolved and with stirring the alcoholic solution of the obtained according to Example 1 Sodium salt added. On the one hand, the calcium salt of tert is formed. ΑΠ13Ί-phenol thioether, on the other hand sodium chloride, which is insoluble in the absolute alcohol and is therefore precipitated. The sodium chloride is filtered off and the alcohol is removed from the filtrate by evaporation, wherein it is advisable to work in a vacuum towards the end. If not all of the sodium chloride is present due to the presence of small amounts of water should be removed, the product can be freed from it in any way, for example by removing the dried Product dissolves in gasoline in the absence of water, the sodium chloride being undissolved remains and is removed by filtration.
In analoger Weise kann man auch die Salze des Bariums, Aluminiums, Zinks, Mangans oder Kobalts herstellen. In den meisten Fällen sind die Chloride dieser Metalle gut geeignet, jedoch empfiehlt es sich im Falle des Bariums, mit dem Bromid zu arbeiten, da dieses in absolutem Alkohol leichter löslich ist*The salts of barium, aluminum, zinc and manganese can also be used in an analogous manner or make cobalts. In most cases the chlorides of these metals are well suited to however, in the case of barium, it is advisable to work with the bromide, as this is more soluble in absolute alcohol *
Unter Umständen wird zusammen mit dem Natriumchlorid auch eine gewisse Menge des Metallsalzes des Phenolthioäthers ausgefällt. Es kann dann aus dem getrockneten Niederschlag durch Extraktion mit Benzin (54° Be) gewönnen werden.A certain amount of the sodium chloride may also be used together with the sodium chloride Metal salt of phenol thioether precipitated. It can then come from the dried precipitate by extraction with gasoline (54 ° Be).
fio An Stelle von absolutem Äthylalkohol kann man auch absoluten Methylalkohol als Lösungsmittel verwenden. Dies empfiehlt sich . bei der Herstellung der Nickelsalze, da Nickelchlorid in Äthylalkohol nur wenig löslich ist.fio Instead of absolute ethyl alcohol, you can also use absolute methyl alcohol as a solvent use. This is recommended. in the manufacture of nickel salts, as nickel chloride is only sparingly soluble in ethyl alcohol.
Salze von solchen Metallen, die genügend basische Oxyde bilden, können auch durch unmittelbare Umsetzung des Phenolthioäthers und des Metalloxyds in der folgenden Weise gewonnen werden: Eine Mischung aus 107 "Teilen tert. Amylphenolthioäther, 214Teilen Xylol, 10,8 Teilen Wasser und 16,8 Teilen Calciumhydroxyd wird unter einem Rückflußkühler zum Sieden erhitzt, der mit einer Vorrichtung zur Abscheidung von Wasser aus dem Rückflußkondensat versehen ist. Man erhitzt, bis alles anfangs vorhandene und während der Reaktion gebildete Wasser (16,5 Teile) entfernt ist. Man erhält eine Lösung des Galciumsalzes des Thioäthers in Xylol, aus der das überschüssige Calciumhydroxyd durch Filtrieren entfernt werden kann.Salts of such metals, which form sufficient basic oxides, can also be obtained by direct Reaction of the phenol thioether and the metal oxide in the following manner obtained: A mixture of 107 "parts of tert. amylphenol thioether, 214 parts Xylene, 10.8 parts of water and 16.8 parts Calcium hydroxide is heated to boiling under a reflux condenser, which is equipped with a Device for separating water from the reflux condensate is provided. One heats until all water initially present and formed during the reaction (16.5 Parts) is removed. A solution of the calcium salt of thioether in xylene is obtained, from which the excess calcium hydroxide can be removed by filtration.
In ähnlicher Weise kann man mit den Oxyden oder Hydroxyden des Bariums, Natriums oder Kaliums arbeiten.One can work in a similar way with the oxides or hydroxides of barium and sodium or potassium work.
Man stellt eine Suspension von Magnesiumäthylat durch Verrühren von metallischem Magnesium mit einem Überschuß von absolutem Äthylalkohol in Gegenwart von Quecksilberchlorid und Jod als Katalysatoren her und gibt dann eine Lösung von tert. Amylphenolthioäther in absolutem Äthylalkohol zu. Die Masse wird 24 Stunden unter einem Rückflußkühler zum Sieden erhitzt und dann heiß filtriert. Beim Eindampfen des Filtrats bis zur Trockne erhält man als Rückstand das Magnesiumsalz.A suspension of magnesium ethylate is made by stirring metallic Magnesium with an excess of absolute ethyl alcohol in the presence of mercury chloride and iodine as catalysts and then gives a solution of tert. Amyl phenol thioether in absolute ethyl alcohol too. The mass is heated to boiling under a reflux condenser for 24 hours and then filtered hot. When the filtrate is evaporated to dryness, the residue is obtained Magnesium salt.
1 Zu einer Lösung von 1 Teil wasserfreiem Natriumhydroxyd in 3 Teilen 98 °/oigem Isopropylalkohol gibt man die theoretische Menge tert. Amylphenolthioäther und erhitzt die Mischung zum Sieden, bis 2 Teile Alkohol abdestilliert sind. Hierbei geht gleichzeitig das Wasser über, da das Destillat 9i%igen Isopropylalkohol darstellt, und man erhält einen praktisch wasserfreien Destillationsrückstand, der unmittelbar in der in Beispiel 2 beschriebenen Weise mit Metallhalogeniden umgesetzt werden kann. 1 To a solution of 1 part of anhydrous sodium hydroxide ° / isopropyl alcohol is added the theoretical amount of tert in 3 parts 98th Amylphenol thioether and heat the mixture to the boil until 2 parts of alcohol have distilled off. At the same time, the water passes over, since the distillate is 91% strength isopropyl alcohol, and a practically anhydrous distillation residue is obtained, which can be reacted directly with metal halides in the manner described in Example 2.
Zu einer Mischung von 25 Teilen tert. Amylphenolthioäther, der zur Salzbildung benötigten Menge Natriumhydroxyd und 100 Teilen 95°/„igem Alkohol gibt man 100 Teile Benzol und erhitzt die Masse zum Sieden. Das gebildete Wasser wird als konstant siedendesTo a mixture of 25 parts tert. Amylphenol thioether, which is needed for salt formation 100 parts of benzene are added to the amount of sodium hydroxide and 100 parts of 95% alcohol and heats the mass to a boil. The water formed is called constant boiling
Gemisch von Benzol, Wasser und Alkohol abdestilliert. Dann gibt man wasserfreies Calciumchlorid zu und verfährt weiter, wie in Beispiel 2 beschrieben.Mixture of benzene, water and alcohol distilled off. Then you give anhydrous calcium chloride and proceed as described in Example 2.
An Stelle von wasserfreiem Calciumchlorid kann man auch eine Lösung von Calciumchlorid in 95"%igem Äthylalkohol verwenden, wobei das ini Alkohol enthaltene Wasser durch azeotrope Destillation entfernt wird. ίο In entsprechender Weise kann man auch die Metallsalze von Alkylphenolpolysuljden sowie von kettenförmigen Alkylphenolthioäthern oder -polysulfiden herstellen. Ebenso verfährt man bei der Gewinnung der Metallsalze der entsprechenden Selen- oder Tellurverbindungen. Instead of anhydrous calcium chloride you can also use a solution of calcium chloride Use in 95 "% ethyl alcohol, with the water contained in alcohol through azeotropic distillation is removed. ίο In a corresponding way one can also the metal salts of alkylphenol polysulides and of chain-like alkylphenol thioethers or polysulphides. The same applies to the extraction of the metal salts the corresponding selenium or tellurium compounds.
Gewünschtenfalls kann man die rohen Produkte noch einer weiteren Reinigung unterwerfen, beispielsweise durch fraktionierte Kristallisation oder Extraktion oder Fällung mit selektiven Lösungsmitteln. Auch durch Behandlung mit Adsorptionsmittel]!, wie Bleicherde, können Verunreinigungen entfernt werden.If desired, the raw products can be subjected to further purification, for example by fractional crystallization or extraction or precipitation with selective solvents. Also through Treatment with adsorbent] !, such as fuller's earth, can remove impurities will.
Zur Verbesserung der Schmiermittel können die Metallverbindungen in beliebiger Konzentration, soweit sie überhaupt löslich sind, angewandt werden. Vorzugsweise verwendet man Mengen von 0,05 oder 0,1 bis 0,25%· Bei Anwendung verhältnismäßig· großer Mengen von etwa 5% oder mehr wird auch die Schmierfähigkeit der Öle erhöht.To improve the lubricant, the metal compounds can be used in any concentration, insofar as they are at all soluble, can be used. Amounts of 0.05 or 0.1 to 0.25% are preferably used When using relatively large amounts of about 5% or more, the Increased lubricity of the oils.
Wie bereits erwähnt, eignen sich die Metallverbindungen besonders gut zur Verbesserung von Kohlenwasserstoffschmierölen, die beliebiger Art sein können. Die Öle können ungereinigt oder einer Raffination, beispielsweise durch Destillation, Voltolisierung oder • Behandlung mit chemischen oder Adsorptionsmitteln, unterworfen sein, Paraffin enthalten oder nicht. Beispielsweise eignen sich Steinkohlenteere,- Ölschieferdestillate, Rückstandsöle, Fraktionen von Spaltrückständen oder durch Kondensation oder Polymerisation gewonnene Öle. Insbesondere kommen in Frage hochraffinierte Öle, wie sie z. B. durch Extraktion mit Lösungsmitteln, wie Phenol. Dichlordiäthyläther. Furfurol, Propan, Xitrobenzol, Crotonaldehyd oder Gemischen von ■50 Propan und Kresol, oder durch Behandlung mit Bleicherde oder Säuren oder Aluminiumchlorid gewonnen werden, ferner auch durch Hydrierung gewonnene oder -synthetisch hergestellte Öle. Die Zusätze können sowohl bei verhältnismäßig leichten Ölen, wie Spindeloder Textilölen, als auch bei beliebigen anderen Ölen, wie Schneideölen, Turbinenölen, Transformatorenöle!!, Motorensehmierölen, H ei Pi dampf zylinderölen und Schmierfetten 6u angewandt werden. Sie kommen besonders in Frage bei Kurbehvellensehmierölen und anderen Schmiermitteln, die bei erhöhter Temperatur oberhalb etwa 150 bis 200c angewandt werden.As already mentioned, the metal compounds are particularly suitable for improving hydrocarbon lubricating oils, which can be of any type. The oils may be unpurified or subjected to refining, for example by distillation, voltolization or treatment with chemical or adsorbents, and may or may not contain paraffin. For example, coal tars, oil shale distillates, residual oils, fractions of fission residues or oils obtained by condensation or polymerization are suitable. In particular, highly refined oils come into question, as they are, for. B. by extraction with solvents such as phenol. Dichlorodiethyl ether. Furfural, propane, xitrobenzene, crotonaldehyde or mixtures of propane and cresol, or by treatment with fuller's earth or acids or aluminum chloride, and also oils obtained or synthetically produced by hydrogenation. The additives can be used both with relatively light oils, such as spindle or textile oils, and with any other oils such as cutting oils, turbine oils, transformer oils, engine sealing oils, steam cylinder oils and lubricating greases 6u. They are particularly suitable for Kurbehvellensehmierölen and other lubricants that are used at elevated temperatures above about 150 to 200 c .
Die Schmiermittel können auch noch andere Zusatzstoffe enthalten, wie z. B. Farbstoffe, Seifen, Stockpunktserniedriger. Schlamniverteilungsmittel, Oxydationsverhinderer, Verdickungsmittel, Mittel zur Erhöhung des Viscositätsindex, ferner Harze, Kautschuk, fette öle, durch Erhitzen verdickte fette Öle. geschwefelte fette Öle, Mittel zur Erhöhung der Druekbtständigkeit, metallorganische Verbindungen,. Rückstandsöle, Voltolisierungsprodukte von . fetten oder mineralischen Ölen oder Paraffin, ferner kolloidale feste Störte, wie Graphit oder Zinkoxyd.The lubricants can also contain other additives, such as. B. dyes, Soaps, pour point depressants. Sludge distributing agents, antioxidants, thickening agents, Means for increasing the viscosity index, also resins, rubber, fatty oils, fatty oils thickened by heating. sulphurized fatty oils, agents to increase pressure, organometallic compounds. Residual oils, voltolization products from. fatty or mineral oils or paraffin, also colloidal solid disturbances, like graphite or zinc oxide.
Die Anwendung der Metallverbindungen auf Schmiermittel soll in den folgenden Beispielen erläutert werden.The application of the metal compounds to lubricants is illustrated in the following examples explained.
Man setzt einem naphthenisehen Mineralschmieröl mit einer Viscosität von 1,7293E bei 99° 1% de-s in Beispiel 2 beschriebenen Caleiumsalzes zu. Beim Dieselöl-Oxydationstest ergeben sich folgende Vergleichswerte:It is a naphthenisehen mineral lubricating oil having a viscosity of 1.729 3 E 1% at 99 ° d e - s described in Example 2 to Caleiumsalzes. The following comparative values result from the diesel oil oxidation test:
Behandiungsz^it 48 Std. 72 Std. ui'< Std.Treatment time 48 hours 72 hours ui '< hours
Öl ohne Zusatz 1 2 4Oil without additives 1 2 4
Öl + ι % CalciumsalzOil + ι% calcium salt
nach Beispiel 2 ... 1 1 1according to example 2 ... 1 1 1
Bei diesem Test wird das Öl bei 149' die angegebene Zeitlang oxydiert, worauf eine io-g-Probe durch Filtrierpapier nitriert und die auf dem Papier verbleibende Rückstandsmenge abgeschätzt wird. Dabei bedeutet die Bewertungszahl 1 die kleinste und die Zahl 10 die größte Menge Niederschlag.In this test, the oil is at 149 'the oxidized for the specified time, whereupon an io-g sample nitrated through filter paper and the amount of residue remaining on the paper is estimated. The means Rating number 1 is the smallest and number 10 is the largest amount of precipitation.
Bei spielSFor example S.
Man mischt eine Probe des in Beispiel 7 beschriebenen Öles mit 0,5 °/0 des in Beispiel 2 beschriebenen Caleiumsalzes bzw. mit 0,5°/0 des entsprechenden Aluminiumsalzes und vergleicht die so gewonnenen Mischungen mit dem ursprünglichen Öl im verlx?sserten Sligh-Test (dieser wird nach den Angaben in Proc. A. S. T. M. 24, 964, TI (1924). aber während 24 Stunden, durchgeführt), wobei 11t sich folgende Werte ergeben:Mixing a sample of the oil described in Example 7 with 0.5 ° / 0 of the Caleiumsalzes described in Example 2 or 0.5 ° / 0 of the corresponding aluminum salt, and compares the thus obtained mixtures with the original oil in verlx? Sserten Sligh -Test (this is carried out according to the information in Proc. ASTM 24, 964, TI (1924), but for 24 hours), whereby the following values result:
Schlummi ücksuind in Milligr.-iinmSchlummi ücksuind in milligrams
Öl ohne Zusatz OiOil with no added Oi
öl 4- 0.5% Calciumsalzoil 4- 0.5% calcium salt
nach Beispiel 2 32.7according to example 2 32.7
Öl J- 0,5 % AluminiumsalzOil J- 0.5% aluminum salt
nach Heispiel 2 21.9according to example 2 21.9
Beispiel 9 lao Example 9 lao
Man setzt einem raffinierten paniflhiisehen Mineralschmieröl mit einer Viscosität vonOne sets a refined paniflhiisehen Mineral lubricating oil with a viscosity of
2,31° E bei 990 in einer Menge von 0,25% verschiedene nach Beispiel 2 erhältliche Salze zu und vergleicht die so erhaltenen Mischungen mit dem Öl ohne Zusatz, indem man die Öle unter vergleichbaren Bedingungen in einem C. F. R.- (Cooperative Fuel Research-) Motor verwendet. Jede Probe dauert 14 Stunden und wird bei einer Mantel temperatur von 1900 durchgeführt. Nach jedem Versuch wird die Maschine auseinandergenommen und der Zustand der Kolben, Ventile und Zylinder bewertet, wobei die Bewertungsziffer um so höher ist, je schlechter die einzelnen Maschinenteile aussehen. Setzt man die Bewertung bei dem Öl ohne Zusatz gleich 100, so ergeben sich für die Öle mit -den Zusätzen niedrigere Zahlen, und die Verhältniszahl ergibt sich dann als2.31 ° E at 99 0 in an amount of 0.25% different salts obtainable according to Example 2 and compares the mixtures obtained in this way with the oil without addition by comparing the oils under comparable conditions in a CFR (Cooperative Fuel Research -) Motor used. Each sample lasts 14 hours and is carried out at a jacket temperature of 190 0. After each test, the machine is dismantled and the condition of the pistons, valves and cylinders is assessed, the rating number being higher the worse the individual machine parts look. If the rating for the oil without additives is set equal to 100, lower numbers result for the oils with -the additives, and the ratio then results as
Bewertung bei der Mischung
Bewertung bei dem Öl ohne ZusatzEvaluation of the mix
Evaluation of the oil without additives
XiooXioo
Öl ohne Zusatz ..' Oil without additives .. '
Öl + Aluminiumsalz nach Beispiel:
Öl + Bariumsalz
Öl + Calciumsalz
Öl + Nickelsalz
Öl + KobaltsalzOil + aluminum salt according to the example:
Oil + barium salt
Oil + calcium salt
Oil + nickel salt
Oil + cobalt salt
Verhältniszahl Ratio
100
24
10100
24
10
17
12 17th
12th
Gegenüber der bekannten Verwendung der Phenolsulfide mit freien Hydroxylgruppen besitzen die vorstehend beschriebenen Metallsalze der Phenolsulfide den Vorteil, daß sie wesentlich wirksamer sind. So ergibt sich z. B. bei einem Schmieröl ohne Zusatz in einem Otto-Motor eine zulässige Laufzeit des Motors von 22 Stunden, bei Zusatz von 0,2% Diisobutylphenolsulfideine solche von 24 Stunden und bei Zusatz des Aluminium- bzw. Bleir bzw. Kupfersalzes desDiisobutylphenolsulfids, ebenfalls in Mengen von 0,2%) Z'U dem gleichen Öl eine Laufzeit von 28,5 bzw. 33 bzw. 35,5 Stunden. Auch im. Aussehen des Motors ergeben sich Vorteile, da die Verunreinigung der Kolbenringnuten und der Unterseite des Kolbens wie auch die aus dem Öl ausgeschiedene Kohlenstoffmenge im Falle der Metallverbindungen der Phenolsulfide wesentlich geringer ist, als wenn man die Phenolsulfide mit freien Hydroxylgruppen verwendet.Compared to the known use of phenol sulfides with free hydroxyl groups, the metal salts of phenol sulfides described above have the advantage that they are significantly more effective. So z. B. with a lubricating oil without additive in a gasoline engine a permissible running time of the engine of 22 hours, with the addition of 0.2% diisobutylphenol sulfide one such of 24 hours and with the addition of the aluminum or lead or copper salt of diisobutylphenol sulfide, likewise in quantities of 0.2%) Z 'U the same oil a running time of 28.5 or 33 or 35.5 hours. Also in. The appearance of the engine results in advantages, since the contamination of the piston ring grooves and the underside of the piston as well as the amount of carbon precipitated from the oil is significantly less in the case of the metal compounds of the phenol sulfides than when the phenol sulfides with free hydroxyl groups are used.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US246073A US2362289A (en) | 1938-12-16 | 1938-12-16 | Lubricating compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
DE748244C true DE748244C (en) | 1944-10-31 |
Family
ID=22929227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEST59307D Expired DE748244C (en) | 1938-12-16 | 1939-12-15 | Prevention of the oxidation of lubricants |
Country Status (4)
Country | Link |
---|---|
US (2) | US2362289A (en) |
DE (1) | DE748244C (en) |
FR (1) | FR862357A (en) |
GB (2) | GB547972A (en) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2493987A (en) * | 1939-12-27 | 1950-01-10 | Standard Oil Dev Co | Aluminum salts of alkylated phenol sulfides |
US2362293A (en) * | 1939-12-27 | 1944-11-07 | Standard Oil Dev Co | Lubricant |
US2514186A (en) * | 1945-10-22 | 1950-07-04 | Firestone Tire & Rubber Co | Antimony phenol sulfides |
US2542831A (en) * | 1945-10-23 | 1951-02-20 | Socony Vacuum Oil Co Inc | Mineral oil composition and improving agent therefor |
US2459063A (en) * | 1946-05-09 | 1949-01-11 | American Cyanamid Co | Divalent metal salts of halogen substituted phenylol sulfides |
US2459754A (en) * | 1946-05-23 | 1949-01-18 | Firestone Tire & Rubber Co | Purification of phenol sulfides and preparation of metallic salts thereof |
US2472518A (en) * | 1947-07-08 | 1949-06-07 | Gulf Oil Corp | Addition agents for mineral oil lubricants |
US2610982A (en) * | 1950-02-11 | 1952-09-16 | Texas Co | Manufacture of magnesium salts of high molecular weight alkylated hydroxy aromatic copounds and their use in lubricating oils |
US2721845A (en) * | 1951-04-18 | 1955-10-25 | Texas Co | Metal soap grease containing alkaline earth metal alkyl phenol sulfide |
US2690998A (en) * | 1951-04-18 | 1954-10-05 | Texas Co | Metal soap grease containing alkaline earth metal phenolate |
US2673881A (en) * | 1951-10-31 | 1954-03-30 | Standard Oil Developoment Comp | Lubricant additives and production thereof |
US2849398A (en) * | 1953-08-19 | 1958-08-26 | Exxon Research Engineering Co | Mineral-base lubricating oils and methods for using same |
US3072707A (en) * | 1956-06-12 | 1963-01-08 | Goodyear Tire & Rubber | Aryl disulfides |
US2975132A (en) * | 1956-06-18 | 1961-03-14 | California Research Corp | Emulsifiable lubricant compositions |
US2992909A (en) * | 1958-12-31 | 1961-07-18 | Exxon Research Engineering Co | Additives to improve the electrical properties of combustible organic liquids |
US2971941A (en) * | 1959-05-15 | 1961-02-14 | Ferro Corp | Nickel bis-(p-octylphenol) monosulphide stabilized polyethylene |
US3035908A (en) * | 1959-08-10 | 1962-05-22 | Gulf Research Development Co | Stable gasoline motor fuels |
US3248361A (en) * | 1959-08-10 | 1966-04-26 | Gulf Research Development Co | Hydrocarbon lubricating oil composition |
US3238263A (en) * | 1962-12-31 | 1966-03-01 | Exxon Research Engineering Co | Calcium salts of bridged phenols |
GB1019924A (en) * | 1963-08-26 | 1966-02-09 | Ici Ltd | Stabilisation of chlorinated hydrocarbons |
US3699172A (en) * | 1969-11-28 | 1972-10-17 | Crown Zellerbach Corp | Hydroxymethyl, methylthio phenols |
US3741896A (en) * | 1970-12-11 | 1973-06-26 | Chevron Res | Basic alkylene amine and sulfur bridged alkylphenoxides for use in lubricating oils |
US4151100A (en) * | 1977-11-21 | 1979-04-24 | Mobil Oil Corporation | Novel cobalt thiobis(alkylphenolates) and antioxidant compositions thereof |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB365534A (en) * | 1929-10-19 | 1932-01-15 | Chem Fab Vormals Sandoz | Non dyeing sulphurized derivatives of phenols |
GB370458A (en) * | 1931-01-08 | 1932-04-08 | Ig Farbenindustrie Ag | Improvements in or relating to the manufacture of sulphurized phenols |
FR40616E (en) * | 1931-07-27 | 1932-07-27 | Prod Chim Fab De | Process for the preparation of new sulfur derivatives of phenol |
US2125961A (en) * | 1937-08-16 | 1938-08-09 | Standard Oil Co | Color stable viscous hydrocarbon oil |
US2230542A (en) * | 1937-11-27 | 1941-02-04 | Standard Oil Dev Co | Process for preparing improved oxidation inhibitors and products thereof |
NL51441C (en) * | 1937-12-04 | |||
US2229528A (en) * | 1938-03-23 | 1941-01-21 | Standard Oil Co | Stabilized hydrocarbon oil |
US2310449A (en) * | 1939-08-12 | 1943-02-09 | Jasco Inc | Age resisting rubbery material and method of making |
US2366874A (en) * | 1940-04-10 | 1945-01-09 | Socony Vacuum Oil Co Inc | Composition of matter |
US2331448A (en) * | 1940-10-05 | 1943-10-12 | Standard Oil Dev Co | Chemical process |
-
1938
- 1938-12-16 US US246073A patent/US2362289A/en not_active Expired - Lifetime
-
1939
- 1939-11-17 GB GB30306/39A patent/GB547972A/en not_active Expired
- 1939-12-15 DE DEST59307D patent/DE748244C/en not_active Expired
- 1939-12-15 FR FR862357D patent/FR862357A/en not_active Expired
-
1943
- 1943-04-08 GB GB5622/43A patent/GB603216A/en not_active Expired
-
1944
- 1944-10-18 US US559254A patent/US2461335A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US2362289A (en) | 1944-11-07 |
GB547972A (en) | 1942-09-21 |
US2461335A (en) | 1949-02-08 |
GB603216A (en) | 1948-06-11 |
FR862357A (en) | 1941-03-12 |
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