US3701730A - Extreme pressure properties of synthetic lubricants - Google Patents
Extreme pressure properties of synthetic lubricants Download PDFInfo
- Publication number
- US3701730A US3701730A US101098A US3701730DA US3701730A US 3701730 A US3701730 A US 3701730A US 101098 A US101098 A US 101098A US 3701730D A US3701730D A US 3701730DA US 3701730 A US3701730 A US 3701730A
- Authority
- US
- United States
- Prior art keywords
- lubricant
- parts
- weight
- ester
- extreme pressure
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000314 lubricant Substances 0.000 title abstract description 62
- -1 DIBROMINATED NEOPENTYL GLYCOL ESTER Chemical class 0.000 abstract description 38
- 239000002253 acid Substances 0.000 abstract description 31
- 229910019142 PO4 Inorganic materials 0.000 abstract description 15
- 239000010452 phosphate Substances 0.000 abstract description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 description 32
- 239000000203 mixture Substances 0.000 description 21
- 238000012360 testing method Methods 0.000 description 21
- LZJUZSYHFSVIGJ-UHFFFAOYSA-N ditridecyl hexanedioate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCCC LZJUZSYHFSVIGJ-UHFFFAOYSA-N 0.000 description 19
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 16
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 16
- NRTKYSGFUISGRQ-UHFFFAOYSA-N (3-heptanoyloxy-2,2-dimethylpropyl) heptanoate Chemical class CCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCC NRTKYSGFUISGRQ-UHFFFAOYSA-N 0.000 description 14
- 150000007513 acids Chemical class 0.000 description 11
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 10
- 239000002199 base oil Substances 0.000 description 9
- 150000001298 alcohols Chemical class 0.000 description 7
- 229940067597 azelate Drugs 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- MMXKVMNBHPAILY-UHFFFAOYSA-N ethyl laurate Chemical compound CCCCCCCCCCCC(=O)OCC MMXKVMNBHPAILY-UHFFFAOYSA-N 0.000 description 6
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical class OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 6
- 239000013638 trimer Substances 0.000 description 6
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 5
- ZWYAVGUHWPLBGT-UHFFFAOYSA-N bis(6-methylheptyl) decanedioate Chemical compound CC(C)CCCCCOC(=O)CCCCCCCCC(=O)OCCCCCC(C)C ZWYAVGUHWPLBGT-UHFFFAOYSA-N 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 239000000539 dimer Substances 0.000 description 4
- XIRNKXNNONJFQO-UHFFFAOYSA-N ethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical class [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 4
- 150000003014 phosphoric acid esters Chemical class 0.000 description 4
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 3
- LIAWCKFOFPPVGF-UHFFFAOYSA-N 2-ethyladamantane Chemical compound C1C(C2)CC3CC1C(CC)C2C3 LIAWCKFOFPPVGF-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- ZDWGXBPVPXVXMQ-UHFFFAOYSA-N bis(2-ethylhexyl) nonanedioate Chemical compound CCCCC(CC)COC(=O)CCCCCCCC(=O)OCC(CC)CCCC ZDWGXBPVPXVXMQ-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- OQCGQYSHNVXOJM-UHFFFAOYSA-N dicyclohexyl decanedioate Chemical compound C1CCCCC1OC(=O)CCCCCCCCC(=O)OC1CCCCC1 OQCGQYSHNVXOJM-UHFFFAOYSA-N 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 3
- 125000002948 undecyl 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])[H] 0.000 description 3
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- ALKCLFLTXBBMMP-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl hexanoate Chemical compound CCCCCC(=O)OC(C)(C=C)CCC=C(C)C ALKCLFLTXBBMMP-UHFFFAOYSA-N 0.000 description 2
- IHXYISPZQCLSIX-UHFFFAOYSA-N 6-o-(6-methylheptyl) 1-o-(8-methylnonyl) hexanedioate Chemical compound CC(C)CCCCCCCOC(=O)CCCCC(=O)OCCCCCC(C)C IHXYISPZQCLSIX-UHFFFAOYSA-N 0.000 description 2
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 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 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229940067592 ethyl palmitate Drugs 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 2
- WZZRCFLIGSUOOC-UHFFFAOYSA-N (2,2-dimethyl-3-octadecanoyloxypropyl) octadecanoate Chemical class CCCCCCCCCCCCCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCCCCCCCCCCCCC WZZRCFLIGSUOOC-UHFFFAOYSA-N 0.000 description 1
- XLEBGGMRMNRYRT-UHFFFAOYSA-N (3-butanoyloxy-2,2-dimethylpropyl) butanoate Chemical group CCCC(=O)OCC(C)(C)COC(=O)CCC XLEBGGMRMNRYRT-UHFFFAOYSA-N 0.000 description 1
- CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical compound OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-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
- SMTKGALBDOEZCA-UHFFFAOYSA-N 2-tetradecylpropanedioic acid Chemical compound CCCCCCCCCCCCCCC(C(O)=O)C(O)=O SMTKGALBDOEZCA-UHFFFAOYSA-N 0.000 description 1
- GPIWNUZDVBGDSM-UHFFFAOYSA-N C(CCCC)(=O)O.C(CCCC)(=O)O.C(CCCC)(=O)O.C(CCC)(=O)O Chemical compound C(CCCC)(=O)O.C(CCCC)(=O)O.C(CCCC)(=O)O.C(CCC)(=O)O GPIWNUZDVBGDSM-UHFFFAOYSA-N 0.000 description 1
- GFFMVPXGXPYMNT-UHFFFAOYSA-N CCC.CCCCCCC(O)=O.CCCCCCC(O)=O.CCCCCCC(O)=O Chemical compound CCC.CCCCCCC(O)=O.CCCCCCC(O)=O.CCCCCCC(O)=O GFFMVPXGXPYMNT-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- QAPVYZRWKDXNDK-UHFFFAOYSA-N P,P-Dioctyldiphenylamine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=C(CCCCCCCC)C=C1 QAPVYZRWKDXNDK-UHFFFAOYSA-N 0.000 description 1
- JPDHZHZDXCSZAT-UHFFFAOYSA-N [3-octanoyloxy-2-[[3-octanoyloxy-2,2-bis(octanoyloxymethyl)propoxy]methyl]-2-(octanoyloxymethyl)propyl] octanoate Chemical compound CCCCCCCC(=O)OCC(COC(=O)CCCCCCC)(COC(=O)CCCCCCC)COCC(COC(=O)CCCCCCC)(COC(=O)CCCCCCC)COC(=O)CCCCCCC JPDHZHZDXCSZAT-UHFFFAOYSA-N 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- LIYYARRTUJKZOT-UHFFFAOYSA-N butanoic acid hexanoic acid Chemical compound CCCC(O)=O.CCCCCC(O)=O.CCCCCC(O)=O.CCCCCC(O)=O LIYYARRTUJKZOT-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 1
- MZHWPEFVDZZOKM-UHFFFAOYSA-N dipentan-3-yl nonanedioate Chemical compound CCC(CC)OC(=O)CCCCCCCC(=O)OC(CC)CC MZHWPEFVDZZOKM-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000012208 gear oil Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid group Chemical group C(CCCCC)(=O)O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- YAFOVCNAQTZDQB-UHFFFAOYSA-N octyl diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)(OCCCCCCCC)OC1=CC=CC=C1 YAFOVCNAQTZDQB-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- PJHKBYALYHRYSK-UHFFFAOYSA-N triheptanoin Chemical compound CCCCCCC(=O)OCC(OC(=O)CCCCCC)COC(=O)CCCCCC PJHKBYALYHRYSK-UHFFFAOYSA-N 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
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/22—Acids obtained from polymerised unsaturated 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
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic 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
- C10M2207/282—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
- C10M2207/283—Esters of polyhydroxy compounds
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/044—Acids; Salts or esters 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated compounds
-
- 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
- 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
-
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/084—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms 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
- 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
- C10M2223/041—Triaryl phosphates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/08—Resistance to extreme temperature
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
- C10N2040/13—Aircraft turbines
Definitions
- This invention is the improvement of extreme pressure properties of synthetic lubricants.
- Timken Test involves apparatus known as the Timken Extreme Pressure Tester. In the test the tester is operated with a steel test cup rotating against a steel test block. The rotating speed is 405.88+2.54 rt/min. which is equivalent to a spindle speed of 800: r.p.m. Fluid samples are preheated to 100:5 F. before starting the test.
- lubricants for which we have developed improvements in extreme pressure properties are used typically in jet engines, automobile engines, gear oils, and the like.
- Suitable synthetic lubricant base stocks for the practice of the invention are esters of alcohols having 1 to 20, especially 4 to 12 carbons and aliphatic carboxylic acids having from 3 to 20, especially 4 to 12 carbons.
- the ester base may comprise a simple ester (reaction product of a monohydroxyalcohol and a monocarboxylic acid), a polyester (reaction product of an alcohol and an acid, one of which has more than one functional group), or a complex ester (reaction product of a polyfunctional acid with more than one alcohol, or of a polyfunctional alcohol with more than one acid).
- excellent synthetic lubricants may be formulated from mixtures of esters, such as major proportions of complex esters and minor amounts of diesters.
- Monohydric alcohols suitable for making ester base stocks include methyl, butyl, isooctyl, dodecyl and octadecyl alcohols.
- Oxo alcohols prepared by the reaction of ole-fine with carbon monoxide and hydrogen are suitable.
- Neo alcohols, i.e., alcohols having no hydrogens on the beta carbon atom are preferred. Examples of such alcohols are 2,2,4trimethyl-pentanol-1 and 2,2-dimethyl propanol.
- Polyalcohols used for the production of base oil esters preferably contain 1 to 12 carbons.
- dialcohols are 2-ethyl-1,3-hexanediol 2-propyl-3,3-heptanediol, 2-butyl-l,2-butanediol, 2,4-dimesityl-1,3-butanediol, and polypropylene glycols having molecular weights of from about to 300.
- Alcohols having 3,4,5 or more hydroxyl groups per molecule are also suitable. Examples of these polyols are pentaerythritol, dipentaerythritol, and trimethylolpropane. Mixtures of alcohols may also be used.
- Suitable carboxylic acids for making the ester base oils include monoand dibasic aliphatic carboxylic acids.
- appropriate acids are butyric, valeric, sebacic, azelaic, suberic, succinic, caproic, adipic, ethyl suberic, diethyl adipic, oxalic, malonic, glutaric, pentadecanedicarboxylic, diglycolic, thiodiglycolic, acetic, propionic, caprylic, lauric, palmitic, pimelic and mixtures thereof.
- Preferred acids are sebacic, azelaic, glutaric, adipic, and their mixtures.
- ester base oils examples include ethyl palmitate, ethyl laurate, butyl stearate, di-2-ethylhexyl sebacate, di- 2-ethylhexyl azelate, ethyl glycol dilaureate, di-2-ethylhexyl phthalate, diisooctyl sebacate, bis-(tridecyl) adipate, di-(1,3-methylbutyl) adipate, di-(l-ethylpropyl) azelate, diisopropyloxylate, dicyclohexyl sebacate, glycerol tri-nheptoate, di(undecyl) azelate, and tetraethylene glycol di- (2-ethylene caproate), and mixtures thereof.
- An especially preferred mixture of esters consists of about 50-80% wt. bis(2,2,4-trimethylpentyl) azelate
- esters for use as base stocks in the present invention are esters. of monocarboxylic acids having 3 to 12 carbons and polyalcohols such as pentaerythritol, dipentaerythritol and trimethylolpropane.
- esters examples include pentaerythrityl tetrabutyrate, pentaerythrityl tetravalerate, pentaerythrityl tetracaproate, pentaerythrityl dibutwratedicaproate, pentaerythrityl butyrate-caproate divalerate, pentaerythrityl butyrate trivalerate pentaerythrityl butyrate tricaproate, pentaerythrityl tributyrate-caproate, mixed C saturated fatty acid esters of pentaerythritol, dipentaerythrityl hexavalerate, dipentaerythrityl hexacaproate, dipentaerythrityl hexaheptoate, dipentaerythrityl hexacaprylate, dipentaerythrityl tributyratetricaproate, dipentaerythrityl trivalerate
- Esters which enable the above stated base stocks to exhibit improved extreme pressure properties by this invention include esters prepared from straight chain monobasic alkanoic acids having 2-36-(preferably 4-18) carbon atoms and a dibrominated neopentyl glycol having the following formula:
- R is hydrogenor an alkyl radical containing from 1-6 carbon atoms
- n is an integer from -8
- R and R" are alkyl radicals containing 1-3 carbon atoms.
- an object of this invention to provide a lubricant which exhibits improved extreme pressure properties. It is a further object to increase the extreme pressure properties of synthetic lubricantshaving an ester base. It is still a further object to improve the extreme pressure properties of synthetic lubricants which find use in jet engines, gears and in automobiles and the like. It is a further object of this invention to improve the extreme pressure properties of multipurpose oils and lubricants.
- dimers and trimers are defined as defined in The Condensed Chemical vDictionary, 5th ed., Reinhold Publicating Corporation, New York (1956). It is stated therein that a dimer is a molecule formed by union of two identical simpler molecules and a trimer is a molecule formed by union of three identical simpler molecules.
- a typical lubricant base stock bis(tridecyl) adipate (C H OOC(CH COOC H exhibits a Timken OK load of 6 pounds.
- a lubricant is prepared comprising 10 parts by weight of the same lubricant base stock (bis(tridecyl) adipate) and 1 part by weight of" a dibrominated neopentyl glycol ester, said ester having the formula 0 0mm 0 cnlonooom-b-omol a-(cnl -cni H Br A wherein n is an integer in the range of 0-20, and subjected to, the Timken Test, a Timken OK load of 24 pounds is obtained.
- dibrominated neopentyl glycol diheptanoate in a ratio of 10 parts to 100 parts lubricant base stock by weight,we have found that 5-30:100 parts by. weight also imparts improved extreme pressure properties.
- a lubricant comprising the same lubricant base stock bis(tridecyl) adipate, dibrominated neopentyl glycol dipheptanoate of the type listed supra, and a free polycarboxylic in a parts by weight ratio of about 100:5 to 30:0.005 to 0.2, preferably about 100 parts by weight base stock: 10 parts by weight halogenated ester:0.03 parts by weight polycarboxylic acid will exhibit a Timken OK load of pounds.
- a trimer, C acid described supra i.e. 3 molecules of an acid, having 18 carbon atoms have united to form the molecule having 54 carbon atoms
- the other polycarboxylic acids listed supra are also quite operable.
- R is an .aryl group having 6-12 carbon atoms, an alkyl group having 1 to 10 carbon atoms, an aralkyl'group having 7-22 carbon atoms or an alkaryl group having 7-22 carbon atoms, imparts improved extreme pressure properties to the lubricant base stock when admixed with the lubricant in a parts by weight ratio of lubricant base stockzphosphate ester of 100:0.5-5.
- a particularly effective phosphate ester is tricresyl phos- 4 phate.
- phosphate esters include cresyl diphenyl phosphate ester, tn'phenyl phosphate ester, trioctyl phosphate ester, and diphenyl octyl phosphate ester.
- a thus prepared lubricant will thereby provide a Ti-mken OK load value of about 9 pounds, or about 50% better than a lubricant without the phosphate ester.
- Timken OK load value can be increased as much as We prefer to use 100 parts by weight lubricant base stock: 10 parts by weight halogenated ester.
- parts by weight ratios in the range of 100:0.5 to 5:5 to 30 also produces excellent results.
- a typical lubricant base stock e.g., bis(tridecyl) adipate
- dibrominated neopentyl glycol diheptanoate e.g., bis(tridecyl) adipate
- a polycarboxylic acid preferably in a parts by weight ratio of 100 parts lubricant base stock: 10 parts dibrominated neopentyl glycol diheptanoate:3 parts phosphate ester:0.03 part polycarboxylic acid.
- bis(tridecyl) adipate is used as lubricant base stock to prepare a lubricant with improved extreme pressure properties.
- Said ester is preferably admixed with the following additives in parts by weight as follows:
- lubricant base stock e.g., bis(tridecyl) adipate
- phosphate ester e.g., tricresyl phosphate
- dibrominated neopentyl glycol diheptanoate 0.03 polycarboxylic acid having 2-54 carbon atoms 0.5 antioxidants, corrosion inhibitors, antifoamants, viscosity index improvers, demulsifiers, emulsifiers, and the like.
- Timken OK load value of about 50 pounds is obtained.
- the additives which may be used include antioxidants, e.g. p,p'-dioctyldiphenylamine; corrosion inhibitors, e.g. high molecular Weight dicarboxylic acids; antifoamants; and the like. (See Encyclopedia of Chemical Technology, 2nd ed., John Wiley & Sons (1965), vol. 6, pp. 317-346 and vol. 2, pp. 588-603.)
- the additives comprise 0-10 parts by weight of the total composition.
- composition is the preferred embodiment of our invention, any of the aforementioned dibrominated neopentyl glycol diheptanoate, phosphate esters, and/or polycarboxylic acids can be used.
- EXAMPLE 1 A commonly used base stock lubricant, bis(tridecyl) adipate was subjected to the heretofore described Timken Test as follows. The lubricant was placed in the test cup and block of the Timken apparatus and when the sump was about half-filled with the fluid the motor was started.
- the machine After a break in period of about 30 seconds, the machine was allowed to run for another 10 minutes at a load of 3 pounds. When it was found that the lubricant could withstand said weight (3 lbs.), the load was gradually increased with fresh lubricant until it was found the OK load value of 6 pounds.
- isooctylisodecyl adipate (Example 2) di-2-ethylhexyl adipate (Examples 3) diisooctyl sebacate (Example 4) C C pentaerythritol ester/w. (Example 5) diisodecyl adipate (Example 6) C -C trimethylolpropane ester (Example 7) di-2-ethylhexyl azelate (Example 8).
- EXAMPLE 9 A composition consisting essentially of 100 parts by weight bis(tridecyl) adipate, 10 parts dibrominated neopentylglycol diheptanoate, and 0.01 part sebacic acid was thoroughly mixed and subjected to the Timken Test as described in Example 1. A Timken OK load value of pounds was obtained.
- Example 10 was repeated except that adipic acid (Example 11) and azelaic acid (Example 12) were substituted for the sebacic acid. Timken OK load values of 15 pounds were obtained in each instance.
- EXAMPLE 13 A composition consisting essentially of 100 parts by weight bis(tridecyl) adipate was admixed thoroughly with 10 parts by weight dibrominated neopentylglycol diheptanoate and 3 parts by weight tricresyl phosphate and subjected to the Timken Test as described in Example 1. A Timken OK load value of 15 pounds was obtained.
- cresyldiphenyl phosphate (Example 14) triphenyl phosphate (Example 15), and trinonylphenyl phosphate (Example 16) were used instead of the tricresyl phosphate.
- EXAMPLE 17 100 parts by weight bis(tridecyl) adipate, 3 parts by weight tricresyl phosphate and 0.01 part by weight sebacic acid were thoroughly mixed and subjected to the Timken Test in Example 1. A Timken OK load value of 9 pounds was obtained.
- Example 17 was repeated except that adipic .acid (Example 18) and azelaic acid (Example 19) were substituted for the sebacic acid; the results, in each instance, were substantially identical with those obtained in Example l7.
- EXAMPLE 20 A homogeneous composition containing 100 parts by weight bis(tridecyl) adipate, 3 parts by weight tricresyl phosphate, 10 parts by weight dibrominated neopentylglycol diheptanoate and 0.01 part by weight sebacic acid
- EXAMPLE 21 This example illustrates the improved extreme pressure properties that can be attained by this invention.
- EXAMPLE 22 A composition consisting essentially of 100 parts by 'weight bis(tridecyl) adipate, 10 parts dibrominated neopentylglycol diheptanoate, and 0.028 part of a trimer C acid were thoroughly mixed and subjected to the Timken Test as described in Example 1. A Timken OK load value of 15 pounds was obtained.
- EXAMPLE 23 A composition consisting essentially of 100 parts by weight bis(tridecyl) adipate, 3 parts by weight tricresyl phosphate, and 0.028 part by weight of the trimer C acid were thoroughly mixed and subjected to the Timken Test as described in Example 1. A Timken OK load value of 6 pounds was obtained.
- Example 24 The composition of Example 23 was again prepared and admixed with 10 parts by weight dibrominated neopentylglycol diheptanoate and subjected to the Timken Test as described in Example 1. A Timken OK load value of 50 pounds was obtained.
- Example 25 The composition of Example 23 was again prepared and admixed with 5 parts by weight dibrominated neopentylglycol diheptanoate and subjected to the Timken Test as described in Example 1. A Timken OK load value of 18 pounds was obtained.
- Example 1 was repeated except that the dibrominated neopentyl glycol diheptanoate was replaced with dibrominated neopentyl glycol dibutyrate (Example 26) and dibrominated neopentyl glycol distearate (Example 27). Similar results were obtained.
- an extreme pressure lubricant comprising a major amount of an ester base oil selected from the group consisting of bis(tridecyl) adipate, ethyl palmiate, ethyl laurate, butyl stearate, di-2-ethylhexy1 sebacate, di-2- ethylhexyl azelate, ethyl glycol dilaureate, di-Z-ethylhexyl phthalate, diisooctyl sebacate, di(l,3-methyl'butyl) adipate, di-(l-ethylpropyl) azelate, diisopropyl oxylate, dicyclohexyl sebacate, glycerol tri-n-heptoate, di(undecyl) azelate, and tetraethylene glycol di-(Z-ethylene) caproate,
- an ester base oil selected from the group consisting of bis
- n is an integer in the range of -20, the weight ratio of ester baseoil-:to dibrominated neopentyl glycol ester being 100:10-30.
- an extreme pressure lubricant comprising a major amount of an ester base oil selected from the group consisting of bis(tridecyl) adipate, ethyl palmitate, ethyl laurate, butyl stearate, di-Z-ethylhexyl sebacate, di-Z-ethylhexyl azelate, ethyl glycol dilaureate, di-2-ethylhexyl phthalate, diisooctyl sebacate, di-(1,3-methylbutyl) adipate,;di-(1-ethylpropyl) azelate, diisopropyl oxylate, dicyclohexyl sebacate, glycerol tri-n-heptanoate, di(undecyl) azelate, and tetraethylene glycol di-(2-ethylene) caproate,
- an ester base oil selected from the group consisting of bis
- n is an integer in the range of 0-20
- a phosphate ester selected from the group consisting of tricresyl phosphate, cresyldiphenyl phosphate, triphenyl phosphate, trioctyl phosphate, diphenyloctylphosphate, and trinonylphenyl phosphate
- an aliphatic polycarboxylic acid having 2-54 carbon atoms, the weight ratio of ester base oil to dibrominated neopentyl glycol ester to phosphate ester to aliphatic polycarboxylic acid being :5-30:0.55:0.0020.28.
- the extreme pressure lubricant of claim 4 in which the aliphatic polycarboxylic acid is sebacic acid, adipic acid, azeolaic acid, a dimer C acid, or a trimer C acid.
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- Chemical & Material Sciences (AREA)
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Abstract
Description
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US10109870A | 1970-12-23 | 1970-12-23 |
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US3701730A true US3701730A (en) | 1972-10-31 |
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ID=22283032
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US101098A Expired - Lifetime US3701730A (en) | 1970-12-23 | 1970-12-23 | Extreme pressure properties of synthetic lubricants |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4178260A (en) * | 1974-10-31 | 1979-12-11 | Exxon Research & Engineering Co. | Ester based metal working lubricants |
US4187188A (en) * | 1978-11-13 | 1980-02-05 | The Dow Chemical Company | Electrical device containing a halogenated alkanoate dielectric fluid |
US4362634A (en) * | 1980-03-19 | 1982-12-07 | Stauffer Chemical Company | Metal working lubricant and lubricant emulsion |
US4440657A (en) * | 1982-09-01 | 1984-04-03 | Exxon Research And Engineering Co. | Synthetic ester lubricating oil composition containing particular t-butylphenyl substituted phosphates and stabilized hydrolytically with particular long chain alkyl amines |
US4514190A (en) * | 1982-10-25 | 1985-04-30 | Standard Oil Company (Indiana) | Synthetic fuel composition |
US4790957A (en) * | 1986-10-18 | 1988-12-13 | Basf Aktiengesellschaft | Polycarboxylic acid esters and lubricants containing these esters |
US5049448A (en) * | 1988-07-22 | 1991-09-17 | Fuji Photo Film Co., Ltd. | Magnetic recording medium containing an ester lubricant branched from the number 2 carbon position of the acid residue |
DE102006054511A1 (en) * | 2006-11-20 | 2008-05-21 | Lothar Bendel | Multi-component ester-based lubricant for internal combustion engines |
US20100216678A1 (en) * | 2009-02-24 | 2010-08-26 | Abhimanyu Onkar Patil | Lubricant compositions containing glycerol tri-esters |
-
1970
- 1970-12-23 US US101098A patent/US3701730A/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4178260A (en) * | 1974-10-31 | 1979-12-11 | Exxon Research & Engineering Co. | Ester based metal working lubricants |
US4187188A (en) * | 1978-11-13 | 1980-02-05 | The Dow Chemical Company | Electrical device containing a halogenated alkanoate dielectric fluid |
US4362634A (en) * | 1980-03-19 | 1982-12-07 | Stauffer Chemical Company | Metal working lubricant and lubricant emulsion |
US4440657A (en) * | 1982-09-01 | 1984-04-03 | Exxon Research And Engineering Co. | Synthetic ester lubricating oil composition containing particular t-butylphenyl substituted phosphates and stabilized hydrolytically with particular long chain alkyl amines |
US4514190A (en) * | 1982-10-25 | 1985-04-30 | Standard Oil Company (Indiana) | Synthetic fuel composition |
US4790957A (en) * | 1986-10-18 | 1988-12-13 | Basf Aktiengesellschaft | Polycarboxylic acid esters and lubricants containing these esters |
US5049448A (en) * | 1988-07-22 | 1991-09-17 | Fuji Photo Film Co., Ltd. | Magnetic recording medium containing an ester lubricant branched from the number 2 carbon position of the acid residue |
DE102006054511A1 (en) * | 2006-11-20 | 2008-05-21 | Lothar Bendel | Multi-component ester-based lubricant for internal combustion engines |
DE102006054511B4 (en) * | 2006-11-20 | 2009-06-10 | Lothar Bendel | Motor oil composition and its use |
US20100216678A1 (en) * | 2009-02-24 | 2010-08-26 | Abhimanyu Onkar Patil | Lubricant compositions containing glycerol tri-esters |
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