US2820010A - Lubricating compositions - Google Patents
Lubricating compositions Download PDFInfo
- Publication number
- US2820010A US2820010A US527876A US52787655A US2820010A US 2820010 A US2820010 A US 2820010A US 527876 A US527876 A US 527876A US 52787655 A US52787655 A US 52787655A US 2820010 A US2820010 A US 2820010A
- Authority
- US
- United States
- Prior art keywords
- oil
- soluble
- silver
- compositions
- lubricating oil
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 34
- 230000001050 lubricating effect Effects 0.000 title description 5
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 19
- 239000004332 silver Substances 0.000 claims description 19
- 229910052709 silver Inorganic materials 0.000 claims description 19
- 239000011575 calcium Substances 0.000 claims description 18
- 239000003208 petroleum Substances 0.000 claims description 16
- 239000003921 oil Substances 0.000 claims description 13
- 239000007859 condensation product Substances 0.000 claims description 11
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 11
- 239000010688 mineral lubricating oil Substances 0.000 claims description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 7
- 239000010687 lubricating oil Substances 0.000 claims description 6
- 230000009972 noncorrosive effect Effects 0.000 claims description 6
- 159000000007 calcium salts Chemical class 0.000 claims description 4
- MCPSMQGVSYDFLC-UHFFFAOYSA-N formaldehyde;2-octylphenol Chemical compound O=C.CCCCCCCCC1=CC=CC=C1O MCPSMQGVSYDFLC-UHFFFAOYSA-N 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- -1 Babbitt surfaces Inorganic materials 0.000 description 12
- 239000000463 material Substances 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 239000000654 additive Substances 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- 229910052698 phosphorus Inorganic materials 0.000 description 7
- 150000003871 sulfonates Chemical class 0.000 description 7
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 150000005002 naphthylamines Chemical class 0.000 description 5
- 229920001568 phenolic resin Polymers 0.000 description 5
- 239000011574 phosphorus Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- VKCLPVFDVVKEKU-UHFFFAOYSA-N S=[P] Chemical compound S=[P] VKCLPVFDVVKEKU-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N N-phenyl aniline Natural products C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000000346 nonvolatile oil Substances 0.000 description 2
- 125000005561 phenanthryl group Chemical group 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- GRFGKFDKQNHGIP-UHFFFAOYSA-N 1,1-bis(2-methylphenyl)ethane-1,2-diamine Chemical compound CC1=CC=CC=C1C(N)(CN)C1=CC=CC=C1C GRFGKFDKQNHGIP-UHFFFAOYSA-N 0.000 description 1
- BOJZPUPAXYETRK-UHFFFAOYSA-N 1,1-diphenylethane-1,2-diamine Chemical compound C=1C=CC=CC=1C(N)(CN)C1=CC=CC=C1 BOJZPUPAXYETRK-UHFFFAOYSA-N 0.000 description 1
- YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 description 1
- JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 1
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- WZKXBGJNNCGHIC-UHFFFAOYSA-N Leucomalachite green Chemical compound C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)N(C)C)C1=CC=CC=C1 WZKXBGJNNCGHIC-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- YKBJQDXMLXQZTP-UHFFFAOYSA-N [Cl].[P].[S] Chemical compound [Cl].[P].[S] YKBJQDXMLXQZTP-UHFFFAOYSA-N 0.000 description 1
- PFRUBEOIWWEFOL-UHFFFAOYSA-N [N].[S] Chemical compound [N].[S] PFRUBEOIWWEFOL-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000001118 alkylidene group Chemical group 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 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
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005266 diarylamine group Chemical group 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral 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
- 239000010699 lard oil Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 230000003137 locomotive effect Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- HDINWBRYKNUCEC-UHFFFAOYSA-N methyl 2,2-dichlorooctadecanoate Chemical compound CCCCCCCCCCCCCCCCC(Cl)(Cl)C(=O)OC HDINWBRYKNUCEC-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- FGGAOQTXQHKQOW-UHFFFAOYSA-N n,n-diphenylnaphthalen-1-amine Chemical class C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=CC=C1 FGGAOQTXQHKQOW-UHFFFAOYSA-N 0.000 description 1
- GMEFLMYTWJUZQZ-UHFFFAOYSA-N n-benzyl-n-phenylnaphthalen-1-amine Chemical class C=1C=CC=CC=1CN(C=1C2=CC=CC=C2C=CC=1)C1=CC=CC=C1 GMEFLMYTWJUZQZ-UHFFFAOYSA-N 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
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- PFUPABFCHVRLLY-UHFFFAOYSA-N nonanophenone Chemical compound CCCCCCCCC(=O)C1=CC=CC=C1 PFUPABFCHVRLLY-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002895 organic esters Chemical class 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
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 210000000707 wrist Anatomy 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/027—Neutral salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/028—Overbased salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
-
- 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
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/402—Castor oils
-
- 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
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/101—Condensation polymers of aldehydes or ketones and phenols, e.g. Also polyoxyalkylene ether derivatives thereof
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl amines
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- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/067—Polyaryl amine alkanes
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/068—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings having amino groups bound to polycyclic aromatic ring systems, i.e. systems with three or more condensed rings
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/046—Overbased sulfonic acid salts
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/12—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
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- C10M2225/00—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2225/04—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of macromolecualr compounds not containing phosphorus in the monomers
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/041—Siloxanes with specific structure containing aliphatic substituents
Definitions
- This invention relates to new and improved lubricating compositions. More particularly, it relates to highly detergent mineral oil lubricating compositions which are non-corrosive and wear resistant to metals such as silver and alloys of silver, copper and lead containing metal and the like.
- one of the best additive combinations for imparting detergency to lubricants is the combination of a particular class of oil-soluble metal sulfonates and oil-soluble metal phenates.
- the supplemental use of conventional antioxidants, corrosion and wear inhibitors such as nitrogen-sulfur-containing compounds such as thiocarbamates or organic thiophosphates such as zinc or calcium dialkyl dithiophosphates and the like although effective in inhibiting oxidation, corrosion and/ or wear of conventional metal surfaces such as steel, steel alloys, Babbitt surfaces, cadmium and the like, have been found to be ineffective for oils which contact silver metal-wearing surfaces, such as are used in certain rail road diesel engines, for instance the silver wrist pin bushings, or in aircraft engines which have silver bearing surfaces.
- the sulfonates are oil-soluble neutral and/ or basic polyvalent metal petroleum sulfonates, of which petroleum sulfonates of the metals of group II of the periodic table having an atomic number of from 12 to 56, inclusive, are preferred, and especially of the alkaline earth metals.
- Suitable sulfonates include the neutral and/or basic calcium, barium and magnesium petroleum sulfonates of oilsoluble petroleum sulfonic acids.
- the acids can range in molecular weight from about 350 to 550 and preferably are in the range of from 400 to 500.
- basic petroleum sulfonates is meant that the amount of neutralizing agent, such as calcium carbonate and/ or calcium hydroxide, which is used to neutralize the petroleum sulfonic acid, is in excess of that which is normally required to neutralize the acid. The excess should be from to 100 and preferably between and 60 percent that normally required to neutralize the acid.
- neutralizing agent such as calcium carbonate and/ or calcium hydroxide
- the phenates used in compositions of this invention are oil-soluble neutral and/or basic polyvalent metal polyphenates.
- polyphenates is meant to include a plurality of phenolic radicals linked together through a carbon such as where a plurality of simple phenates are condensed at positions ortho and/ or para to the phenolic hydroxy group through alkylidene (methylene) radicals.
- the cationic portion of the phenate can be the same as that in the sulfonate and usually will be, but different cations may be used.
- the alkaline earth metal salts of the condensation product of an alkylphenol e. g.
- p-octylphenol with formaldehyde, acetaldehyde or benzaldehyde, e. g. calcium or barium salts of octylphenol-formal- 2,820,010 Patented Jan. 14-, 1958 dehyde condensation products ranging in molecular weight of from 500 to 1100, are particularly suitable and are preferred.
- the additives which render detergent lubricants of the described class useful in the lubrication of silver and silver alloys constitute a particular class of oil-soluble phosphorus-sulfur-halogen-containing materials.
- One group of such materials can be prepared by reacting phosphorus sulfide with halogenated fatty materials. Reaction products of this type can be readily prepared by reacting, at temperatures of above 270 F.
- halogenated fatty materials such as chlorinated sperm oil, chlorinated whale oil, chlorinated degras, or derivatives thereof such as the chlorinated free fatty acids or esters derived from said oils, with a phosphorus sulfide such as P 8 and P 8
- a phosphorus sulfide such as P 8 and P 8
- the amount of phosphorus sulfide used in making reaction products of this type should be at least about equivalent to the theoretical amount required to replace the oxygen in the halogenated material. Generally the amount of phosphorus sulfide will be in the range of from 15% to 35% by weight of the halogenated fatty material.
- reaction product of this type was prepared by reacting chlorinated sperm oil containing 30% by weight chlorine with 20% by weight phosphorus pentasu'lfide at a temperature of about 300 F. for about one hour. The sludge formed was removed and the final oil-soluble product recovered contained phosphorus, sulfur and chlorine.
- Compounds of this type are commercially available under the trade name Parapoid 16S and contain 7% sulfur, 1.3% chlorine and 4.75% phosphorus.
- Other examples include reaction products of P 8 or P 8 with chlorinated degras,
- chlorinated castor oil chlorinated glycerol monoleate
- chlorinated materials include chlorinated waxes, chlorinated rosins and the like and reacted with P 3 or P 8 as described.
- Suitable phosphorus-sulfur-halogen containing materials which can be used include additives described in U. S. Patents 2,307,183, 2,494,332 and 2,623,018. Suitable commercially available products are made by Monsanto Chemical Company and sold under the trade name of Santopoid 29, 32 and 33. Suitable materials available under these trade names have the following properties:
- Such arylarnines preferably have at least two aromatic rings.
- Preferred compounds are, forv example, the naphthylamines: primary, secondary or tertiary alkyl, aryl or aralkyl naphthylamines in which the alkyl, aryl or aralkyl radicals are attached directly to a nuclear carbon atom of the aromatic nucleus or preferably to the nitrogen atom, suchas phenylalpha, or beta-naphthylamine, tetralin naphthylamine, alpha alpha, alpha beta, or beta beta dinaphthylamines, various phenanthryl-, anthryl-naphthylamines, xenyl naphthylamines, benzyl phenyl naphthylamines, diphenyl naphthylamines, phenyl xenyl naphthththth
- aryl amines may be used, such as diamino diaryl alkanes, e. g., diamino diphenyl methane, tetrametbyl diamino diphenyl methane, tetra methyl diamino triphenyl methane, tetra ethyl diarnino triphenyl methane, diamino diphenyl ethane, diamino ditolyl ethane, etc., alkylated diaryl amines, e.
- diamino diaryl alkanes e. g., diamino diphenyl methane, tetrametbyl diamino diphenyl methane, tetra methyl diamino triphenyl methane, tetra ethyl diarnino triphenyl methane, diamino diphenyl ethane, diamino ditolyl e
- p-ethyl diphenylamine g., p-ethyl diphenylamine, m-ethyl diphenylamine, p-isopropyl diphenylamine, monoand poly-amyl, hexyl, heptyl, octyl, nonyl, decyl, hexadecyl, cyclohexyl, methyl cyclohexyl and other alkyl substituted diphenylamines, etc.
- the base for additives of this invention can be any natural or synthetic material having lubricating properties.
- the base may be a hydrocarbon oil obtained from a paraflinic, naphthenic, mid-continent or Coastal stock and/ or mixtures thereof.
- the viscosity of these oils may vary over a Wide range such as from 45 SUS at 100 F. to 100 SUS at 210 F.
- the hydrocarbon oils may be blended with fixed oils such as castor oil, lard oil and the like and/or with synthetic lubricants such as polymerized olefins, copolymers of alkylene glycols and alkylene oxides, organic esters, e.
- the synthetic lubricants may be used as the sole base lubricant or admixed with fixed oils and derivatives thereof.
- compositions of this invention may be represented by:
- compositions are illustrative of preferred compositions of this invention:
- compositions A through F of this invention were tested in a modified four-ball machine similar in principle to the Boerlage apparatus described in Engineering, vol. 136, July 13, 1933, using a rotating steel top ball and 3 silver discs, operated at 700 R. P. M. spindle speed, 50 pound load and 302 F. oil temperature.
- compositions 1 and 2 Compositions 1 and 2 were also tested for a period of hours in a Model 567-B diesel engine.
- the conditions of the silver bushings were rated on the basis of a number scale from 0 to 10, with 10 being excellent, indicating no scufiing or removal of silver from the bushing and below 6 signifying failure.
- compositions A through F rated between 8 and 10, while Composition 1 rated 4 and Composition 2 rated 3; Composition 3 (mineral oil+0.2% wt phenyl-a-naphthylamine-l-ZA% wt.
- oil-soluble Ca petroleum sulfonate +1.5% wt. oil-soluble Ca salt of octylphenol-formaldehyde condensation product
- Compositions A and B were also field tested in E. M. D. F-7 freight locomotives using model 567-B engines having silver bushings. After more than 100,000 miles of operation on these compositions, the engines were in excellent condition showing no sign of wear of the silver bushings, while Composition 1 proved unsatisfactory and silver bushing failure was noted in less than 10,000 miles of operation.
- lubricating oil compositions contemplated herein may contain other agents, such as pour-point depressants, oiliness agents, blooming agents, compounds for enhancing the viscosity index of the lubricating oil, peptizing agents, etc.
- a lubricating oil composition which is non-corrosive and wear resistant toward silver consisting essentially of a major proportion of mineral lubricating oil containing from 1.2% to 2.4% of oil-soluble calcium petroleum sulfonate, from 1.0% to 1.5% of oil-soluble calcium salt of octyl phenol-formaldehyde condensation product, and from 0.2% to 0.4% each of phenyl-ot-naphthylamine and 0.25% to 0.5% P 8 treated chlorinated sperm oil.
- a lubricating oil composition which is non-corrosive and wear resistant toward silver, consisting essentially of a major proportion of mineral lubricating oil containing 1.5% of oil-soluble calcium petroleum sulfonate, 1.2% of oil-soluble calcium salt of octyl phenolformaldehyde condensation product, 0.4% of phenyl-otnaphthylamine and 0.5% of P 8 treated chlorinated sperm oil.
- a lubricating oil composition which is non-corrosive and wear resistant toward silver, consisting essentially of a major proportion of mineral lubricating oil containing 1.2% of oil-soluble calcium petroleum sulfonate, 1.0% of oil-soluble calcium salt of octyl phenyl-formaldehyde condensation product, 0.2% of phenyl-u-naphthylamine and 0.5 of P 8 treated chlorinated sperm oil.
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Description
United States Patent LUBRICATING COMPOSITIONS Roland Frederick Bergstrom and Harvey M. Trowbridge,
Martinez, and Robert C. Jones, Berkeley, Calif., assignors to Shell Development Company, New York, N. Y., a corporation of Delaware No Drawing. Application August 11, 1955 Serial No. 527,876
3 Claims. (Cl. 25233.4)
This invention relates to new and improved lubricating compositions. More particularly, it relates to highly detergent mineral oil lubricating compositions which are non-corrosive and wear resistant to metals such as silver and alloys of silver, copper and lead containing metal and the like.
It has been observed that one of the best additive combinations for imparting detergency to lubricants is the combination of a particular class of oil-soluble metal sulfonates and oil-soluble metal phenates. The supplemental use of conventional antioxidants, corrosion and wear inhibitors such as nitrogen-sulfur-containing compounds such as thiocarbamates or organic thiophosphates such as zinc or calcium dialkyl dithiophosphates and the like, although effective in inhibiting oxidation, corrosion and/ or wear of conventional metal surfaces such as steel, steel alloys, Babbitt surfaces, cadmium and the like, have been found to be ineffective for oils which contact silver metal-wearing surfaces, such as are used in certain rail road diesel engines, for instance the silver wrist pin bushings, or in aircraft engines which have silver bearing surfaces.
It has now been discovered that these detergent lubricants containing this particular oil-soluble sulfonate-phenate additive combination can be rendered non-corrosive and wear resistant toward silver surfaces when supplemented with minor amounts of a particular class of phosphorus-sulfur-halogen-containing organic compounds.
The sulfonates are oil-soluble neutral and/ or basic polyvalent metal petroleum sulfonates, of which petroleum sulfonates of the metals of group II of the periodic table having an atomic number of from 12 to 56, inclusive, are preferred, and especially of the alkaline earth metals. Suitable sulfonates include the neutral and/or basic calcium, barium and magnesium petroleum sulfonates of oilsoluble petroleum sulfonic acids. The acids can range in molecular weight from about 350 to 550 and preferably are in the range of from 400 to 500. By basic petroleum sulfonates is meant that the amount of neutralizing agent, such as calcium carbonate and/ or calcium hydroxide, which is used to neutralize the petroleum sulfonic acid, is in excess of that which is normally required to neutralize the acid. The excess should be from to 100 and preferably between and 60 percent that normally required to neutralize the acid.
The phenates used in compositions of this invention are oil-soluble neutral and/or basic polyvalent metal polyphenates. By polyphenates is meant to include a plurality of phenolic radicals linked together through a carbon such as where a plurality of simple phenates are condensed at positions ortho and/ or para to the phenolic hydroxy group through alkylidene (methylene) radicals. The cationic portion of the phenate can be the same as that in the sulfonate and usually will be, but different cations may be used. The alkaline earth metal salts of the condensation product of an alkylphenol (e. g. p-octylphenol) with formaldehyde, acetaldehyde or benzaldehyde, e. g. calcium or barium salts of octylphenol-formal- 2,820,010 Patented Jan. 14-, 1958 dehyde condensation products ranging in molecular weight of from 500 to 1100, are particularly suitable and are preferred.
The additives which render detergent lubricants of the described class useful in the lubrication of silver and silver alloys constitute a particular class of oil-soluble phosphorus-sulfur-halogen-containing materials. One group of such materials can be prepared by reacting phosphorus sulfide with halogenated fatty materials. Reaction products of this type can be readily prepared by reacting, at temperatures of above 270 F. and preferably in the range of 285 to 325 F., halogenated fatty materials such as chlorinated sperm oil, chlorinated whale oil, chlorinated degras, or derivatives thereof such as the chlorinated free fatty acids or esters derived from said oils, with a phosphorus sulfide such as P 8 and P 8 The amount of phosphorus sulfide used in making reaction products of this type should be at least about equivalent to the theoretical amount required to replace the oxygen in the halogenated material. Generally the amount of phosphorus sulfide will be in the range of from 15% to 35% by weight of the halogenated fatty material. For example, a reaction product of this type was prepared by reacting chlorinated sperm oil containing 30% by weight chlorine with 20% by weight phosphorus pentasu'lfide at a temperature of about 300 F. for about one hour. The sludge formed was removed and the final oil-soluble product recovered contained phosphorus, sulfur and chlorine. Compounds of this type are commercially available under the trade name Parapoid 16S and contain 7% sulfur, 1.3% chlorine and 4.75% phosphorus. Other examples include reaction products of P 8 or P 8 with chlorinated degras,
chlorinated castor oil, chlorinated glycerol monoleate,
methyl dichlorostearate and mixtures thereof. Other chlorinated materials include chlorinated waxes, chlorinated rosins and the like and reacted with P 3 or P 8 as described.
Other suitable phosphorus-sulfur-halogen containing materials which can be used include additives described in U. S. Patents 2,307,183, 2,494,332 and 2,623,018. Suitable commercially available products are made by Monsanto Chemical Company and sold under the trade name of Santopoid 29, 32 and 33. Suitable materials available under these trade names have the following properties:
Santopoid Property Color, ASIM (diluted) 8 5% 5 Pour point, F 5 +5 +25 Flash point, F. (0. O. C.) 250 250 250 Snecific gravity at G0l60 F 1. 09 1.18 1.14 Visc sity S. U. S. at 100 F 268 2, 400 550 S. U. S. at 210 F. 48 59 Sulfur, percent wt- 8.5 8. 2 8. 5 Ohorine, percent wt 24. 0 26. 0 26. 0 Ph sphorus, percent 0.56 0.56 0. 55 Metals, percent wt None None None Still another phosphorus-sulfur-chlorine-containing material which is commercialy available as Anglamol 88, made by Lubrizol Corporation, and which contains 3% sulfur, 18% chlorine and 0.3% phosphorus. This product can be also used in compositions of the present invention.
The addition of minor amounts ofarylamines to thev above additive combination is essential. Such arylarnines preferably have at least two aromatic rings. Preferred compounds are, forv example, the naphthylamines: primary, secondary or tertiary alkyl, aryl or aralkyl naphthylamines in which the alkyl, aryl or aralkyl radicals are attached directly to a nuclear carbon atom of the aromatic nucleus or preferably to the nitrogen atom, suchas phenylalpha, or beta-naphthylamine, tetralin naphthylamine, alpha alpha, alpha beta, or beta beta dinaphthylamines, various phenanthryl-, anthryl-naphthylamines, xenyl naphthylamines, benzyl phenyl naphthylamines, diphenyl naphthylamines, phenyl xenyl naphthylamines, dixenyl naphthylamines; also various phenanthryl, anthryl or picyl phenyl amines, etc. The N-aryl substituted naphthylamines are in general more useful for the present purpose.
If desired, however, other aryl amines may be used, such as diamino diaryl alkanes, e. g., diamino diphenyl methane, tetrametbyl diamino diphenyl methane, tetra methyl diamino triphenyl methane, tetra ethyl diarnino triphenyl methane, diamino diphenyl ethane, diamino ditolyl ethane, etc., alkylated diaryl amines, e. g., p-ethyl diphenylamine, m-ethyl diphenylamine, p-isopropyl diphenylamine, monoand poly-amyl, hexyl, heptyl, octyl, nonyl, decyl, hexadecyl, cyclohexyl, methyl cyclohexyl and other alkyl substituted diphenylamines, etc.
The base for additives of this invention can be any natural or synthetic material having lubricating properties. Thus, the base may be a hydrocarbon oil obtained from a paraflinic, naphthenic, mid-continent or Coastal stock and/ or mixtures thereof. The viscosity of these oils may vary over a Wide range such as from 45 SUS at 100 F. to 100 SUS at 210 F. The hydrocarbon oils may be blended with fixed oils such as castor oil, lard oil and the like and/or with synthetic lubricants such as polymerized olefins, copolymers of alkylene glycols and alkylene oxides, organic esters, e. g., 2-ethyl hexyl sebacate, dioctyl phthalate, trioctyl phosphate; polymeric tetrahydrofuran, polyalkyl silicones, e. g., dimethyl silicone and the like. If desired, the synthetic lubricants may be used as the sole base lubricant or admixed with fixed oils and derivatives thereof.
The general formulations of compositions of this invention may be represented by:
Broad Limited range, range percent (percent wt Oil-s luble polyvalent metal polyphenates 005-15 0. 1-6 Oil-soluble polyvalent petroleum sultonates 0. 05-5 Arylanune .i 0. 01-5 0. 05-2 Base 011 (natural and/or synthetic) Balance Balance The following compositions are illustrative of preferred compositions of this invention:
Composition A Percent weight Oil-soluble Ca petroleum sulfonate (40% excess Santopoid 33 (8.5% S, 26% Cl, 0.55% P) 0.25 Mineral lubricating oil Balance Composition C Oil-soluble Ca petroleum sulfonate (40% excess base) 1.2 Oil-soluble Ca salt of octyl phenolformaldehyde condensation product (av. mol wt. 1000)--.." 1.0 .Phenyl-a-naphthylamine 0.2
4 Parapoid 16S 0.5 Mineral lubricating oil--- Balance Composition D Oil-soluble Ca petroleumv sulfonate (40% excess base) 1.2 Oil-soluble Ca salt. of octyl phenolformaldehyde condensation product (av. mol wt. 1000) 1.0. Phenyl-u-naphthylamine 0.2 Santopoid 33" 0.25 Mineral lubricating oil Balance Composition E Oil-soluble Ca petroleum sulfonate (40% excess base) 1.2 Oil-soluble Ca salt of octyl phenolformaldehyde condensation product (av. mol wt. 1000) 1.0 Phenylra-naphthylamine 0.4 Parapoid 165 0.5 Mineral lubricating oil Balance Composition F Oil-soluble Ca petroleum sulfonate (40% excess base) 2.4 Oil-soluble Ca salt of octyl phenolformaldehyde condensation product (av. mol wt. 1000) 1.5 Phenyl-a-naphthylamine 0.2 Anglamol 88 (3% S, 18% Cl, 0.3% phosphorus) 0.25 Mineral lubricating oil Balance The mineral lubricating oil used in Compositions A-F was a solvent refined distillate blend meeting the following specification:
Gravity, API min. 23 Color, ASTM 4-6 Pour point, F max. 0 Flash point, F min. 440 Viscosity, SUS, at 210 F 75-80 Viscosity index min. 55
the lubrication of silver surfaces has been demonstrated by the results of comparative tests.
Compositions A through F of this invention were tested in a modified four-ball machine similar in principle to the Boerlage apparatus described in Engineering, vol. 136, July 13, 1933, using a rotating steel top ball and 3 silver discs, operated at 700 R. P. M. spindle speed, 50 pound load and 302 F. oil temperature. The results showed a reduction in sending and wear of the silver surfaces in the range of from 60% to 90% over similar oil compositions except that the Parapoid 16S, Anglamol 88 and Santopoid 33 were replaced by various amounts ranging from 0.2% to 2% by weight of zinc dialkyl dithiophosphate, or zinc dibutyl-dithiocarbamate (Compositions 1 and 2, respectively) Compositions A through F were also tested for a period of hours in a Model 567-B diesel engine. The conditions of the silver bushings were rated on the basis of a number scale from 0 to 10, with 10 being excellent, indicating no scufiing or removal of silver from the bushing and below 6 signifying failure. Compositions A through F rated between 8 and 10, while Composition 1 rated 4 and Composition 2 rated 3; Composition 3 (mineral oil+0.2% wt phenyl-a-naphthylamine-l-ZA% wt.
oil-soluble Ca petroleum sulfonate+1.5% wt. oil-soluble Ca salt of octylphenol-formaldehyde condensation product) rated 6, indicating failure of the silver bushing.
Compositions A and B were also field tested in E. M. D. F-7 freight locomotives using model 567-B engines having silver bushings. After more than 100,000 miles of operation on these compositions, the engines were in excellent condition showing no sign of wear of the silver bushings, while Composition 1 proved unsatisfactory and silver bushing failure was noted in less than 10,000 miles of operation.
In addition to the additives already described lubricating oil compositions contemplated herein may contain other agents, such as pour-point depressants, oiliness agents, blooming agents, compounds for enhancing the viscosity index of the lubricating oil, peptizing agents, etc.
This application is a continuation-in-part of our copending patent application Serial No. 278,112, filed March 22, 1952, and now abandoned.
We claim as our invention:
1. A lubricating oil composition which is non-corrosive and wear resistant toward silver consisting essentially of a major proportion of mineral lubricating oil containing from 1.2% to 2.4% of oil-soluble calcium petroleum sulfonate, from 1.0% to 1.5% of oil-soluble calcium salt of octyl phenol-formaldehyde condensation product, and from 0.2% to 0.4% each of phenyl-ot-naphthylamine and 0.25% to 0.5% P 8 treated chlorinated sperm oil.
2. A lubricating oil composition which is non-corrosive and wear resistant toward silver, consisting essentially of a major proportion of mineral lubricating oil containing 1.5% of oil-soluble calcium petroleum sulfonate, 1.2% of oil-soluble calcium salt of octyl phenolformaldehyde condensation product, 0.4% of phenyl-otnaphthylamine and 0.5% of P 8 treated chlorinated sperm oil.
3. A lubricating oil composition which is non-corrosive and wear resistant toward silver, consisting essentially of a major proportion of mineral lubricating oil containing 1.2% of oil-soluble calcium petroleum sulfonate, 1.0% of oil-soluble calcium salt of octyl phenyl-formaldehyde condensation product, 0.2% of phenyl-u-naphthylamine and 0.5 of P 8 treated chlorinated sperm oil.
References Cited in the file of this patent UNITED STATES PATENTS 2,307,183 Zimmer et a1. Ian. 5, 1943 2,444,948 Musselman et al. July 13, 1948 2,580,274 Bergstrom et al. Dec. 25, 1951 2,629,693 Barton et a1. Feb. 24, 1953
Claims (1)
1. A LUBRICATING OIL COMPOSITION WHICH IS NON-CORROSIVE AND WATER RESISTANT TOWARD SILVER CONSISTING ESSENTIALLY OF A MAJOR PROPORTION OF MINERAL LUBRICATING OIL CONTAINING FROM 1.2% TO 2.4% OF OIL-SOLUBLE CALCIUM PETROLEUM SULFONATE, FROM 1.0% TO 1.5% OF OIL-SOLUBLE CALCIUM SALT OF OCTYL PHENOL-FORMALDEHYDE CONDENSATION PRODUCT, AND FROM 0.2% TO 0.4% EACH OF PHENYL-A-NAPHTHYLAMINE AND 0.25% TO 0.5% P2S5 TREATED CHLORINATED SPERM OIL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US527876A US2820010A (en) | 1955-08-11 | 1955-08-11 | Lubricating compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US527876A US2820010A (en) | 1955-08-11 | 1955-08-11 | Lubricating compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2820010A true US2820010A (en) | 1958-01-14 |
Family
ID=24103310
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US527876A Expired - Lifetime US2820010A (en) | 1955-08-11 | 1955-08-11 | Lubricating compositions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2820010A (en) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2307183A (en) * | 1939-05-09 | 1943-01-05 | Standard Oil Dev Co | Extreme pressure lubricant |
| US2444948A (en) * | 1945-05-17 | 1948-07-13 | Standard Oil Co | Lubricant |
| US2580274A (en) * | 1947-03-08 | 1951-12-25 | Shell Dev | Lubricant |
| US2629693A (en) * | 1947-07-01 | 1953-02-24 | Shell Dev | Lubricating composition |
-
1955
- 1955-08-11 US US527876A patent/US2820010A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2307183A (en) * | 1939-05-09 | 1943-01-05 | Standard Oil Dev Co | Extreme pressure lubricant |
| US2444948A (en) * | 1945-05-17 | 1948-07-13 | Standard Oil Co | Lubricant |
| US2580274A (en) * | 1947-03-08 | 1951-12-25 | Shell Dev | Lubricant |
| US2629693A (en) * | 1947-07-01 | 1953-02-24 | Shell Dev | Lubricating composition |
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