US2961408A - Power transmission mineral oil base fluids - Google Patents
Power transmission mineral oil base fluids Download PDFInfo
- Publication number
- US2961408A US2961408A US665660A US66566057A US2961408A US 2961408 A US2961408 A US 2961408A US 665660 A US665660 A US 665660A US 66566057 A US66566057 A US 66566057A US 2961408 A US2961408 A US 2961408A
- Authority
- US
- United States
- Prior art keywords
- reaction
- oil
- power transmission
- pyrophosphate
- carbon atoms
- 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
- 239000012530 fluid Substances 0.000 title claims description 27
- 230000005540 biological transmission Effects 0.000 title claims description 18
- 239000002480 mineral oil Substances 0.000 title description 13
- 235000010446 mineral oil Nutrition 0.000 title description 9
- 238000006243 chemical reaction Methods 0.000 claims description 25
- 239000007795 chemical reaction product Substances 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 16
- 235000011180 diphosphates Nutrition 0.000 claims description 14
- 238000000354 decomposition reaction Methods 0.000 claims description 11
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 11
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 claims description 8
- 239000010688 mineral lubricating oil Substances 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 3
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 32
- -1 saturated aliphatic monocarboxylic acid Chemical class 0.000 description 20
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 15
- 239000003921 oil Substances 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- 150000001412 amines Chemical class 0.000 description 12
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 10
- 235000021355 Stearic acid Nutrition 0.000 description 10
- 229910052791 calcium Inorganic materials 0.000 description 10
- 239000011575 calcium Substances 0.000 description 10
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 10
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 10
- 239000008117 stearic acid Substances 0.000 description 10
- 239000003208 petroleum Substances 0.000 description 9
- UMHKOAYRTRADAT-UHFFFAOYSA-N [hydroxy(octoxy)phosphoryl] octyl hydrogen phosphate Chemical compound CCCCCCCCOP(O)(=O)OP(O)(=O)OCCCCCCCC UMHKOAYRTRADAT-UHFFFAOYSA-N 0.000 description 7
- XXUJMEYKYHETBZ-UHFFFAOYSA-N ethyl 4-nitrophenyl ethylphosphonate Chemical compound CCOP(=O)(CC)OC1=CC=C([N+]([O-])=O)C=C1 XXUJMEYKYHETBZ-UHFFFAOYSA-N 0.000 description 7
- XMHIUKTWLZUKEX-UHFFFAOYSA-N hexacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O XMHIUKTWLZUKEX-UHFFFAOYSA-N 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 230000003068 static effect Effects 0.000 description 7
- 229910019142 PO4 Inorganic materials 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 235000021317 phosphate Nutrition 0.000 description 6
- 229910052788 barium Inorganic materials 0.000 description 5
- 230000007246 mechanism Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 150000004671 saturated fatty acids Chemical class 0.000 description 4
- 150000003871 sulfonates Chemical class 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 150000004982 aromatic amines Chemical class 0.000 description 3
- 239000002199 base oil Substances 0.000 description 3
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229920005573 silicon-containing polymer Polymers 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 125000003118 aryl group Chemical class 0.000 description 2
- 244000145845 chattering Species 0.000 description 2
- 125000000753 cycloalkyl group Chemical class 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- AQNVYUAYYQMVCF-UHFFFAOYSA-N didodecyl phosphono phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OP(O)(O)=O)OCCCCCCCCCCCC AQNVYUAYYQMVCF-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- ORLWXEYHGUZEHI-UHFFFAOYSA-N dioctadecyl phosphono phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(=O)(OP(O)(O)=O)OCCCCCCCCCCCCCCCCCC ORLWXEYHGUZEHI-UHFFFAOYSA-N 0.000 description 2
- 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 2
- AFVQQNICYUTZTM-UHFFFAOYSA-N dodecyl phosphono hydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(=O)OP(O)(O)=O AFVQQNICYUTZTM-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 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 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 2
- JGEYZICLFHQBOP-UHFFFAOYSA-N (4,4-dimethylcyclohexyl)sulfanyl-dihydroxy-sulfanylidene-lambda5-phosphane Chemical class CC1(CCC(CC1)SP(O)(O)=S)C JGEYZICLFHQBOP-UHFFFAOYSA-N 0.000 description 1
- RAADJDWNEAXLBL-UHFFFAOYSA-N 1,2-di(nonyl)naphthalene Chemical compound C1=CC=CC2=C(CCCCCCCCC)C(CCCCCCCCC)=CC=C21 RAADJDWNEAXLBL-UHFFFAOYSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 description 1
- HIVBGIWIIXMWOH-UHFFFAOYSA-N 3,5-dipentylphenol Chemical compound CCCCCC1=CC(O)=CC(CCCCC)=C1 HIVBGIWIIXMWOH-UHFFFAOYSA-N 0.000 description 1
- NKFIBMOQAPEKNZ-UHFFFAOYSA-N 5-amino-1h-indole-2-carboxylic acid Chemical compound NC1=CC=C2NC(C(O)=O)=CC2=C1 NKFIBMOQAPEKNZ-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- YSIQDTZQRDDQNF-UHFFFAOYSA-L barium(2+);2,3-di(nonyl)naphthalene-1-sulfonate Chemical compound [Ba+2].C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1.C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1 YSIQDTZQRDDQNF-UHFFFAOYSA-L 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- MKFUUBCXQNCPIP-UHFFFAOYSA-L calcium;2,3-di(nonyl)naphthalene-1-sulfonate Chemical compound [Ca+2].C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1.C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1 MKFUUBCXQNCPIP-UHFFFAOYSA-L 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- UALKIQHLONQBLF-UHFFFAOYSA-N cyclohexyloxy-methoxy-methylsulfanyl-sulfanylidene-lambda5-phosphane zinc Chemical compound P(=S)(SC)(OC)OC1CCCCC1.[Zn] UALKIQHLONQBLF-UHFFFAOYSA-N 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- JWOPLIXEIJVTGP-UHFFFAOYSA-N dihexadecoxy-sulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCCCCCCCCCCCCCOP(S)(=S)OCCCCCCCCCCCCCCCC JWOPLIXEIJVTGP-UHFFFAOYSA-N 0.000 description 1
- XQZPQRQQSHJDGK-UHFFFAOYSA-N dihexadecyl phosphono phosphate Chemical compound CCCCCCCCCCCCCCCCOP(=O)(OP(O)(O)=O)OCCCCCCCCCCCCCCCC XQZPQRQQSHJDGK-UHFFFAOYSA-N 0.000 description 1
- WDNQRCVBPNOTNV-UHFFFAOYSA-N dinonylnaphthylsulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1 WDNQRCVBPNOTNV-UHFFFAOYSA-N 0.000 description 1
- HTDKEJXHILZNPP-UHFFFAOYSA-N dioctyl hydrogen phosphate Chemical compound CCCCCCCCOP(O)(=O)OCCCCCCCC HTDKEJXHILZNPP-UHFFFAOYSA-N 0.000 description 1
- LAWOZCWGWDVVSG-UHFFFAOYSA-N dioctylamine Chemical compound CCCCCCCCNCCCCCCCC LAWOZCWGWDVVSG-UHFFFAOYSA-N 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 239000002783 friction material Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001421 myristyl 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])[H] 0.000 description 1
- HKUFIYBZNQSHQS-UHFFFAOYSA-N n-octadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC HKUFIYBZNQSHQS-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical class CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 1
- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
- FFQLQBKXOPDGSG-UHFFFAOYSA-N octadecyl benzenesulfonate Chemical compound CCCCCCCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 FFQLQBKXOPDGSG-UHFFFAOYSA-N 0.000 description 1
- LORXJTBATHQUMV-UHFFFAOYSA-N octadecyl phosphono hydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCCCOP(O)(=O)OP(O)(O)=O LORXJTBATHQUMV-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- SPGGJQWPRFTSMC-UHFFFAOYSA-N phosphono ditetradecyl phosphate Chemical compound CCCCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCCCC)OP(=O)(O)O SPGGJQWPRFTSMC-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- FSLSJTZWDATVTK-UHFFFAOYSA-N tris(6-methylheptyl) phosphate Chemical compound CC(C)CCCCCOP(=O)(OCCCCCC(C)C)OCCCCCC(C)C FSLSJTZWDATVTK-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/18—Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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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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- C10M2215/00—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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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/26—Amines
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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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- 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
- C10M2223/043—Ammonium or amine salts thereof
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- 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
- C10M2223/045—Metal containing thio derivatives
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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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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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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- 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
- 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
- C10M2225/041—Hydrocarbon polymers
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- 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
- 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
- C10M2229/02—Unspecified siloxanes; Silicones
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- 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
- 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
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- 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
- 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
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
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- 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
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
Definitions
- This invention pertains to improved functional fluids having good lubricating properties. More particularly this invention relates to mineral oil compositions for use in an apparatus by means of which mechanical forces are transmitted or absorbed such as in automotive and truck transmissions, hydraulic brakes, clutches, and various other mechanical equipment.
- the prior art discloses various functional or power transmission fluids of the mineral oil or synthetic type (organic esters and polyethers) containing as the improving agents, various organic phosphates, fatty acids and their esters, halogenated compounds, polymers such as polyacrylates and the like.
- Compositions of this type are objectionable because of their inability to eliminate chattering and noises caused by frictional vibrations and/or stick-slip phenomenon of clutch plates and the like, particularly in equipment which is subjected to high speeds and temperatures.
- an excellent functional or power transmission fluid which satisfactorily meets the above requirements, which comprises a highly refined mineral oil base containing an additive combination, in critical amounts, of from about 0.05% to about 2%, preferably from about 0.1% to about 1% each of (1) a saturated aliphatic monocarboxylic acid having at least 18 carbon atoms in the molecule and (2) a product of neutralization between an alpihatic amine having at least 8 carbon atoms with a monoor dialiphatic acid pyrophosphate having at least 8 carbon atoms.
- the long-chain aliphatic monocarboxylic acids include the saturated fatty acids of the C to C range such as stearic, arachidic, behenic, cerotic, montanic acids and mixtures thereof. Preferred are of saturated fatty acids having 18 to 26 carbon atoms such as stearic acid, be-. henic acid and cerotic acid and their mixtures.
- the second essential additive is a product of neutraltent O.
- the aliphatic amines suitable for reaction with the aliphatic acid pyrophosphates are the primary and secondary saturated or unsaturated aliphatic amines having from'8 to 18 carbon atoms or mixtures of such amines.
- Typical of such amine reactants are octylamine, dodecylamine, tetradecylamine, hexadecylamine, octadecylamine, octadecenylamine, octadecadienylamine, dioctylamine, didoceylamine, dioctadecylamine, dioctadecadienylamine and amines derived from fatty oils or fats such as cottonseed oil, soybean oil, coconut oil; lard, tallow, and the like, such as soyamine, cocoamine, tallowamine and mixtures thereof. Amines of this type are marketed by Armour and C0.
- Armeen under the trade name Armeen and include Armeen 12 and 12 D (dodecylamine), Armeen 14 and 14 D (tetradecylamine) Armeen 16 and 16 D (hexadecylamine) Armeen 18 and 18 D (octadecylamine), Armeen TD (mixture of tetradecyl, hexadecyl and octadecylamines), Armeen S and SD (mixtures of hexadecyl, octadecyl, octadecenyl and octadecadienyl amines).
- Duomeens such as Duorneen C, Duomeen S and Duomeen T, which are C1248 alkyl trimethylene dimonoand dioctyl pyrophosphate, monoand didodecyl pyrophosphate, monoand ditetradecyl pyrophosphate, monoand di-hexadecyl pyrophosphate, monoand di-octadecyl pyrophosphate, of which preferred are monooctyl pyrophosphate dioctyl pyrophosphate, monododecyl pyrophosphate, didodecyl pyrophosphate, mono-octadecyl pyrophosphate, dioctadecyl pyrophosphate and mixtures thereof.
- Duorneen C Duorneen C
- Duomeen S and Duomeen T which are C1248 alkyl trimethylene dimonoand dioctyl pyrophosphate, monoand dido
- the reaction betwen the amine and the pyrophosphate is exothermic and should be controlled so as to prevent decomposition.
- the temperature of the reaction should be between 50 and 100 C. and preferably below C.
- the mol ratio of the reactants should be within the ratio of 1 to 5 moles of the amine per mol of pyrophosphate compound, and preferably the reactants and reaction should be carried out under such conditions that the end product contains no free acid but can contain some free amine.
- free functional fluids should be high, as in fluids used in parking-brakes or the like, where it is desired that the frictional level be high enough (at least 0125 so that the force generates a frictional torque level sufiicient to overcome the gravitational pull on a 30 incline.
- a class of additives which when added, in amounts of from about 0.1% to about 10%, preferably from about 0.5% to 5% by weight, to functional fluids of this invention, increase their static coelficient of friction to at least 0.125;; are oil-soluble alkali metal or alkaline earth metal organic sulfonates.
- Materials for making oil-soluble sulfonates include various petroleum fractions such as mineral lubricating oil fractions, alkyl-substituted aromatic compounds such as alkylated benzene or naphthalene and alkyl substituted polar-containing aromatic compounds such as alkylated phenol, naphthol, aniline, etc.
- Specific sulfonates which are particularly suitable for increasing the static coeificient of friction of functional fluids of this invention oil-soluble sodium, potassium, calcium and barium petroleum sulfonate, tetra-tertiarybutylnaphthalene sulfonate, dinonyl naphthalene sulfonate, diwaxnaphthalene sulfonate, diwaxbenzene sulfonate, stearylbenzene sulfonate, tertiary-octylphenol sulfonate, waxphenol sulfonate and mixtures thereof.
- Preferred are the oil-soluble sodium, calcium and/or barium petroleum sulfonate and dinonylnaphthalene sulfonate.
- compositions of this invention In addition to the two essential additives present in compositions of this invention, as well as the frictional additive (sulfonate), it is preferred to incorporate into such compositions a small amount (0.1-5%) of specific anti-oxidants from groups (a) an oil-soluble organic thiophosphate salt of the metals of group II of the periodic tablehaving an atomic number of from 12 to 56 or (b) a mixture in about equal proportions of an alkyl phenol and an arylamine.
- groups (a) an oil-soluble organic thiophosphate salt of the metals of group II of the periodic tablehaving an atomic number of from 12 to 56 or (b) a mixture in about equal proportions of an alkyl phenol and an arylamine.
- the anti-oxidant of group (a) include the group H metal salts of alkyl, aryl, alkaryl, or cycloalkyl monoand di-acid thio or dithio-phosphoric acids such as calcium, barium or zinc alkyl, cyclo alkyl or aryl mono and dithiophosphates.
- Preferred compounds are calcium, barium and zinc methylphenyl dithiophosphate, dimethyl cyclohexyl dithiophosphate, dihexyl dithiophosphate, lauryl benzyl dithiophosphate and mixtures thereof.
- Lubri-Zol 66, 304, 360 or 1060 Libri-Zol Corp.
- Aerolube 70 American Cyanamid Co.
- Stan-Add 71 Stan-Add 71
- a particularly preferred class of such compounds includes the Zn and Ba salts of dimethylcyclohexyl dithiophosphate, Ba salt of P S polybutene reaction products and/ or P s -terpene (pinene) reaction products.
- Such products are commercially available from Lubri-Zol Corporation, Standard Oil Company of Indiana and Monsanto Chemical Company, respectively, under the above indicated trade names.
- the anti-oxidant mixture of group (b) include alkyl phenols, e.g., di and tri alkylphenols, for instance 2,4-, 2,3-, 3,4-, 2,6- and 3,5-diamyl phenol, 2,4-dimethyl-6- tertbutyl phenol, 2,6-ditertbutyl-4-methyl phenol; and arylamines such as phenyl-a-naphthylamine, or phenyl-B- naphthylamine.
- alkyl phenols e.g., di and tri alkylphenols, for instance 2,4-, 2,3-, 3,4-, 2,6- and 3,5-diamyl phenol, 2,4-dimethyl-6- tertbutyl phenol, 2,6-ditertbutyl-4-methyl phenol
- arylamines such as phenyl-a-naphthylamine, or phenyl-B- naphthylamine
- compositions of this invention can be used in compositions of this invention such as anti-foaming agent e.g., silicone polymers (DC 200 fluids) ranging in viscosity in centistokes from 100 to 1000 at 25 C. or Silicone Type A fluid made by DowCorning Co. and described in US. Patents 2,563,588 and 2,662,055.
- anti-foaming agent e.g., silicone polymers (DC 200 fluids) ranging in viscosity in centistokes from 100 to 1000 at 25 C. or Silicone Type A fluid made by DowCorning Co. and described in US. Patents 2,563,588 and 2,662,055.
- the base oil is a hydrocarbon oil preferably of wide viscosity range and having a high viscosity index and a low pour point. These oils can range in viscosity from 40 l SUS at F. to SUS at 210 F., and include mineral spray oil, transformer oil as well as lubricating oils having SAE numbers of 10, 20, 30, etc. Oils of this type have the following properties:
- Another suitable base oil is a refined, highly refined transformer oil (A) having the following properties:
- composition A Stearic acid percent wt 0.2
- Example I additiv do 0.2 Calcium petroleum sulfonate do 5 Zinc dimethyl cyclohexyl dithiophosphate.... do 0.5 Dimethyl silicone polymer (1000 cs. at 25 C.) p.p.m- 5 Mineral oil (B) Balance Composition B Stearic acid percent Wt 0.2
- Compositions of this invention eliminate noise, frictional vibrations and stick-slip sliding in various equip ment such as liquid cooled hydraulic brake systems in which the friction members were made of steel and resilient, or semi-metallic, or full sintered metallic friction materials. Evaluation was done in actual automobile tests wherein the noise created after accelerating and suddenly stopping the vehicle was rated, 10 being excellent, no noise or stick-slip and zero (0) being poor, severe noise and stick-slip.
- compositions A, B, C, and D With compositions A, B, C, and D the ratings were between 8 and 10. Mineral oils (A) and (B), each containing 0.2% stearic acid, or 0.2% cerotic acid gave ratings of 4 and 5 respectively, whilethe same oils each containing 0.2% stearic acid and 5% Lubri-Zol66 gave ratings of 5.
- compositions of this invention possess with respect to eliminating noise and stick-slip in brake systems.
- mineral oils containing a fatty acid e.g., stearic or cerotic acids alone or in combination thiophosphates or mineral oils containing various acid phosphates alone or in combination with a metal thiophosphate gave poor results.
- the data shows that the static coeflicient friction of compositions of the present invention can be increased to a desired value by addition to such compositions certain oil-soluble sulfonates and that other metal salts e.g. naphthenates or salicylates or phosphate esters are not effective when used for this purpose in compositions of this invention.
- a noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from about 0.05% to about 2% each of an aliphatic monocarboxylic acid having from 18 to 26 carbon atoms in the molecule and a reaction product prepared by reacting from 1 to 5 moles of an aliphatic amine having from 8 to 18 carbon atoms with a mol of an aliphatic acid pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
- a noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubrieating oil and from about 0.05% to about 2% each of a saturated fatty acid having from 18 to 26 carbon atoms in the molecule and a reaction product prepared by reacting from 1 to 5 moles of a C aliphatic amine with a mol of an aliphatic acid pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
- a noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from 0.05 to about 2% each of a saturated fatty acid having from 18 to 26 carbon atoms in the molecule and a reaction product prepared by reacting from 1 to 5 moles of a C alkyl amine with a mol of an alkyl acid pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
- a noise-free power transmission fluid consisting essentially of a major amount of'a refined mineral lubricating oil and from about,0.05% to about 2% each of stearic acid and a reaction product of a C aliphatic amine with 21 mol of an alkyl pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially cornpleted, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs, '5.
- a noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from about 0.05% to about 2% each of stearic acid and a reaction product prepared by reacting from 1 to 5 moles of a C aliphatic amine with a mol of octyl pyrophosphate until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
- a noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from about 0.05 to 2% each of stearic acid and a reaction product prepared by reacting from Ito 5 moles of a C aliphatic amine with a mol of dioctyl pyrophosphate until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
- a noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from about 0.05 to 2% each of cerotic acid and a reaction product prepared by reacting from 1 to 5 moles of a C aliphatic amine with a mo] of an alkyl pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
- the power transmission fluid of claim 1 containing from about 0.1% to about 10% of an oil-soluble metal organic sulfonate the metal portion of the salt being selected from the group consisting of alkali and alkaline earth metals.
- the power transmission fluid of claim 4 containing from about 0.1% to 10% of oil-soluble calcium petroleum sulfonate and from about 0.1 to about 5% of oil-soluble zinc cycloalkyl dithiophosphate.
- the power transmission fluid of claim 5 containing from about 0.1% to 10% of oil-soluble sodium petroleum sulfonate.
- a noise-free power transmission fluid consisting essentially of about 0.2% stearic acid, about 0.2% of a reaction product prepared by reacting from 1 to 5 moles of C C aliphatic amine with a mol of dioctyl pyrophosphate until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs, and about 0.1-0.5% of a mixture of an alkyl phenol and an aryl amine and the balance being a refined transformer mineral oil.
- a noise-free power transmission fluid consisting essentially of about 0.2% stearic acid, about 0.2% of a reaction product prepared by reacting from 1 to 5 moles of C1648 aliphatic amine with a mol of dioctyl pyrophosphate until the reaction is substantially completed,
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Description
States Unite 13 Claims. (Cl. 25275) This invention pertains to improved functional fluids having good lubricating properties. More particularly this invention relates to mineral oil compositions for use in an apparatus by means of which mechanical forces are transmitted or absorbed such as in automotive and truck transmissions, hydraulic brakes, clutches, and various other mechanical equipment.
The smooth functioning of various power transmitting mechanisms particularly the more complicated automotive transmissions, fluid cooled brake mechanisms, oil lubricated wet clutches, planetary gears and hydraulic control mechanisms depends on adequate cooling and lubrication of the equipment. Rigorous requirements have been set up to quality fluids for this service which includes wide temperature stability at both high and low temperatures and a low pour point to insure proper pumpability and fluidity at low temperatures. The fluids must not have a detrimental effect on parts with which they come in contact such as metal surfaces e.g., copper and solid non-metallic surfaces such as organic resins and the like. They must possess desired frictional properties and, in some cases extreme pressure characteristics, to afford proper lubrication of gears, clutch plates and other parts of the mechanism in which they are used, such as automotive and truck equipment. Also, the fluids must not cause chattering, squawking, squealing or produce other noises caused by the frictional vibrations and/or stick-slip phenomenon of clutch plates or other parts of such mechanisms.
The prior art discloses various functional or power transmission fluids of the mineral oil or synthetic type (organic esters and polyethers) containing as the improving agents, various organic phosphates, fatty acids and their esters, halogenated compounds, polymers such as polyacrylates and the like. Compositions of this type are objectionable because of their inability to eliminate chattering and noises caused by frictional vibrations and/or stick-slip phenomenon of clutch plates and the like, particularly in equipment which is subjected to high speeds and temperatures.
-It has now been discovered that an excellent functional or power transmission fluid is provided, which satisfactorily meets the above requirements, which comprises a highly refined mineral oil base containing an additive combination, in critical amounts, of from about 0.05% to about 2%, preferably from about 0.1% to about 1% each of (1) a saturated aliphatic monocarboxylic acid having at least 18 carbon atoms in the molecule and (2) a product of neutralization between an alpihatic amine having at least 8 carbon atoms with a monoor dialiphatic acid pyrophosphate having at least 8 carbon atoms.
The long-chain aliphatic monocarboxylic acids include the saturated fatty acids of the C to C range such as stearic, arachidic, behenic, cerotic, montanic acids and mixtures thereof. Preferred are of saturated fatty acids having 18 to 26 carbon atoms such as stearic acid, be-. henic acid and cerotic acid and their mixtures.
The second essential additive is a product of neutraltent O."
2,961,408 Patented Nov. 22 1960 ization between an aliphatic amine having at least 8' carbon atoms and a monoor dialiphatic acid pyrophosphate the aliphatic group containing at least 8 carbon atoms. The aliphatic amines suitable for reaction with the aliphatic acid pyrophosphates are the primary and secondary saturated or unsaturated aliphatic amines having from'8 to 18 carbon atoms or mixtures of such amines. Typical of such amine reactants are octylamine, dodecylamine, tetradecylamine, hexadecylamine, octadecylamine, octadecenylamine, octadecadienylamine, dioctylamine, didoceylamine, dioctadecylamine, dioctadecadienylamine and amines derived from fatty oils or fats such as cottonseed oil, soybean oil, coconut oil; lard, tallow, and the like, such as soyamine, cocoamine, tallowamine and mixtures thereof. Amines of this type are marketed by Armour and C0. under the trade name Armeen and include Armeen 12 and 12 D (dodecylamine), Armeen 14 and 14 D (tetradecylamine) Armeen 16 and 16 D (hexadecylamine) Armeen 18 and 18 D (octadecylamine), Armeen TD (mixture of tetradecyl, hexadecyl and octadecylamines), Armeen S and SD (mixtures of hexadecyl, octadecyl, octadecenyl and octadecadienyl amines). Preferred are the unsatu rated amines such as octadecadienylamine or Armeen S and Armeen SD. Polyamines are also included as reactants with the pyrophosphates. Polyamines' which are preferred are the N-alkyl alklene diamines which are prepared by the method described in U.S. 2,736,658 and and are marked by Armour and Co. under the trade name Duomeens such as Duorneen C, Duomeen S and Duomeen T, which are C1248 alkyl trimethylene dimonoand dioctyl pyrophosphate, monoand didodecyl pyrophosphate, monoand ditetradecyl pyrophosphate, monoand di-hexadecyl pyrophosphate, monoand di-octadecyl pyrophosphate, of which preferred are monooctyl pyrophosphate dioctyl pyrophosphate, monododecyl pyrophosphate, didodecyl pyrophosphate, mono-octadecyl pyrophosphate, dioctadecyl pyrophosphate and mixtures thereof.
The reaction betwen the amine and the pyrophosphate is exothermic and should be controlled so as to prevent decomposition. Generally'the temperature of the reaction should be between 50 and 100 C. and preferably below C. The mol ratio of the reactants should be within the ratio of 1 to 5 moles of the amine per mol of pyrophosphate compound, and preferably the reactants and reaction should be carried out under such conditions that the end product contains no free acid but can contain some free amine.
The amine-acid pyrophosphate reaction products in the molar proportions indicated in Table I were made as follows:
TABLE I Molar ratio of Temper- Example Amine Acid pyrophosphate amine ature,
to pyro- 0. phosphate I Armeen SD Dioctylpyrophosphate 2/1 70 do do 5/1 70 do do 2.2/1 70 Octadecy Lauryl pyrophosphate 5/1 80 annne. Dodecy1- Dodecyl pyrophos- 5/1 80' amine. phate. VI DuomeenTL- Dioctylpyrophosphate 4/1 70 35% oetadecenylamine and 45% oetadecadienylamine I Duomeen T=Oi iutrimethy1ene diamine derived trom tailow.
free functional fluids should be high, as in fluids used in parking-brakes or the like, where it is desired that the frictional level be high enough (at least 0125 so that the force generates a frictional torque level sufiicient to overcome the gravitational pull on a 30 incline. A class of additives which when added, in amounts of from about 0.1% to about 10%, preferably from about 0.5% to 5% by weight, to functional fluids of this invention, increase their static coelficient of friction to at least 0.125;; are oil-soluble alkali metal or alkaline earth metal organic sulfonates. Materials for making oil-soluble sulfonates include various petroleum fractions such as mineral lubricating oil fractions, alkyl-substituted aromatic compounds such as alkylated benzene or naphthalene and alkyl substituted polar-containing aromatic compounds such as alkylated phenol, naphthol, aniline, etc. Specific sulfonates which are particularly suitable for increasing the static coeificient of friction of functional fluids of this invention oil-soluble sodium, potassium, calcium and barium petroleum sulfonate, tetra-tertiarybutylnaphthalene sulfonate, dinonyl naphthalene sulfonate, diwaxnaphthalene sulfonate, diwaxbenzene sulfonate, stearylbenzene sulfonate, tertiary-octylphenol sulfonate, waxphenol sulfonate and mixtures thereof. Preferred are the oil-soluble sodium, calcium and/or barium petroleum sulfonate and dinonylnaphthalene sulfonate.
In addition to the two essential additives present in compositions of this invention, as well as the frictional additive (sulfonate), it is preferred to incorporate into such compositions a small amount (0.1-5%) of specific anti-oxidants from groups (a) an oil-soluble organic thiophosphate salt of the metals of group II of the periodic tablehaving an atomic number of from 12 to 56 or (b) a mixture in about equal proportions of an alkyl phenol and an arylamine. The anti-oxidant of group (a) include the group H metal salts of alkyl, aryl, alkaryl, or cycloalkyl monoand di-acid thio or dithio-phosphoric acids such as calcium, barium or zinc alkyl, cyclo alkyl or aryl mono and dithiophosphates. Preferred compounds are calcium, barium and zinc methylphenyl dithiophosphate, dimethyl cyclohexyl dithiophosphate, dihexyl dithiophosphate, lauryl benzyl dithiophosphate and mixtures thereof. Compounds of this type are available commercially under the trade names of Lubri-Zol 66, 304, 360 or 1060 (Lubri-Zol Corp.); Aerolube 70 (American Cyanamid Co.) and Stan-Add 71 (Standard Oil Co. of Indiana). A particularly preferred class of such compounds includes the Zn and Ba salts of dimethylcyclohexyl dithiophosphate, Ba salt of P S polybutene reaction products and/ or P s -terpene (pinene) reaction products. Such products are commercially available from Lubri-Zol Corporation, Standard Oil Company of Indiana and Monsanto Chemical Company, respectively, under the above indicated trade names.
The anti-oxidant mixture of group (b) include alkyl phenols, e.g., di and tri alkylphenols, for instance 2,4-, 2,3-, 3,4-, 2,6- and 3,5-diamyl phenol, 2,4-dimethyl-6- tertbutyl phenol, 2,6-ditertbutyl-4-methyl phenol; and arylamines such as phenyl-a-naphthylamine, or phenyl-B- naphthylamine.
Also optional additives can be used in compositions of this invention such as anti-foaming agent e.g., silicone polymers (DC 200 fluids) ranging in viscosity in centistokes from 100 to 1000 at 25 C. or Silicone Type A fluid made by DowCorning Co. and described in US. Patents 2,563,588 and 2,662,055. These optional agents when used in compositions of this invention are employed in amounts of from 0.0001% to 10% and preferably between 0.l% and 5%.
The base oil is a hydrocarbon oil preferably of wide viscosity range and having a high viscosity index and a low pour point. These oils can range in viscosity from 40 l SUS at F. to SUS at 210 F., and include mineral spray oil, transformer oil as well as lubricating oils having SAE numbers of 10, 20, 30, etc. Oils of this type have the following properties:
SAE 10 mineral oil Viscosity, SUS, at 100 F Viscosity, SUS, at 210 F 45.2 Viscosity index 106, Flash, 9 F 395 Fire, F- 440 Pour point, F -35 Another suitable base oil is a refined, highly refined transformer oil (A) having the following properties:
Sp. gr., API 30.9 Color V 30 Viscosity, SUS, at 100 F 56.9 Flash, COC, F 290 Fire, COC, F 320 Pour point, F Below --70 Still another suitable base oil is a refined mineral oil (B) having the following properties:
Sp. Gr., API 31.2 Color, ASTM -1 Pour point ---30 Flash, F 270 Fire, F 295 Viscosity, SUS, at 100 F 48 Viscosity index 33 The following compositions are illustrative of the present invention.
Composition A Stearic acid percent wt 0.2
Example I additiv do 0.2 Calcium petroleum sulfonate do 5 Zinc dimethyl cyclohexyl dithiophosphate.... do 0.5 Dimethyl silicone polymer (1000 cs. at 25 C.) p.p.m- 5 Mineral oil (B) Balance Composition B Stearic acid percent Wt 0.2
Compositions of this invention eliminate noise, frictional vibrations and stick-slip sliding in various equip ment such as liquid cooled hydraulic brake systems in which the friction members were made of steel and resilient, or semi-metallic, or full sintered metallic friction materials. Evaluation was done in actual automobile tests wherein the noise created after accelerating and suddenly stopping the vehicle was rated, 10 being excellent, no noise or stick-slip and zero (0) being poor, severe noise and stick-slip.
With compositions A, B, C, and D the ratings were between 8 and 10. Mineral oils (A) and (B), each containing 0.2% stearic acid, or 0.2% cerotic acid gave ratings of 4 and 5 respectively, whilethe same oils each containing 0.2% stearic acid and 5% Lubri-Zol66 gave ratings of 5. Transformer oil (A) or mineral oils (B) each containing 0.5% of n-octyl acid phosphate, dioctyl phosphate and triisooctyl phosphate gave ratingsof 4, 1 and 1, respectively, while transformer oil (A) containing 0.4% lauryl acid phosphate gave a rating of 3 and transformer oil (A) containing 0.2% lauryl acid phosphate and 2.5% Lubri-Zol 1060 gave a rating of 1.
The static coetficient of friction of Compositions B, C and D was about 0.04 whereas the static coefficient of friction of Composition A containing 2.5% neutral calcium petroleum sulfonate increased the coefficient of friction to 0.130 The addition of 2.5% of neutral calcium dinonylnaphthalene sulfonate or barium dinonylnaphthalene sulfonate, or neutral calcium petroleum sulfonate to Composition C increased the static coefiicient of friction of the compositions from 0.0411. to 15211., 1.88 1 and 1.42,, respectively. These values are far above the required minimum of 0.125 1. On the other hand, the addition of 2.5% of calcium naphthenate, or calcium C1448 alkyl salicylate, or zinc dimethylcyclohexyl dithiophosphate or tricresyl phosphate to Composition C gave static coeflicient of friction values of 0.086 0.49 0052 1 and 0.091 respectively. These values are below the required minimum of 0.125
Thus the data shows the outstanding properties which compositions of this invention possess with respect to eliminating noise and stick-slip in brake systems. On the other hand, mineral oils containing a fatty acid, e.g., stearic or cerotic acids alone or in combination thiophosphates or mineral oils containing various acid phosphates alone or in combination with a metal thiophosphate gave poor results. Also the data shows that the static coeflicient friction of compositions of the present invention can be increased to a desired value by addition to such compositions certain oil-soluble sulfonates and that other metal salts e.g. naphthenates or salicylates or phosphate esters are not effective when used for this purpose in compositions of this invention.
We claim as our invention:
1. A noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from about 0.05% to about 2% each of an aliphatic monocarboxylic acid having from 18 to 26 carbon atoms in the molecule and a reaction product prepared by reacting from 1 to 5 moles of an aliphatic amine having from 8 to 18 carbon atoms with a mol of an aliphatic acid pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
2. A noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubrieating oil and from about 0.05% to about 2% each of a saturated fatty acid having from 18 to 26 carbon atoms in the molecule and a reaction product prepared by reacting from 1 to 5 moles of a C aliphatic amine with a mol of an aliphatic acid pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
3. A noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from 0.05 to about 2% each of a saturated fatty acid having from 18 to 26 carbon atoms in the molecule and a reaction product prepared by reacting from 1 to 5 moles of a C alkyl amine with a mol of an alkyl acid pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
4. A noise-free power transmission fluid consisting essentially of a major amount of'a refined mineral lubricating oil and from about,0.05% to about 2% each of stearic acid and a reaction product of a C aliphatic amine with 21 mol of an alkyl pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially cornpleted, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs, '5. A noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from about 0.05% to about 2% each of stearic acid and a reaction product prepared by reacting from 1 to 5 moles of a C aliphatic amine with a mol of octyl pyrophosphate until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
6. A noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from about 0.05 to 2% each of stearic acid and a reaction product prepared by reacting from Ito 5 moles of a C aliphatic amine with a mol of dioctyl pyrophosphate until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
7. A noise-free power transmission fluid consisting essentially of a major amount of a refined mineral lubricating oil and from about 0.05 to 2% each of cerotic acid and a reaction product prepared by reacting from 1 to 5 moles of a C aliphatic amine with a mo] of an alkyl pyrophosphate having from 8 to 18 carbon atoms until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs.
8. The power transmission fluid of claim 1 containing from about 0.1% to about 10% of an oil-soluble metal organic sulfonate the metal portion of the salt being selected from the group consisting of alkali and alkaline earth metals.
9. The power transmission fluid of claim 4 containing from about 0.1% to 10% of oil-soluble calcium petroleum sulfonate and from about 0.1 to about 5% of oil-soluble zinc cycloalkyl dithiophosphate.
10. The power transmission fluid of claim 5 containing from about 0.1% to 10% of oil-soluble sodium petroleum sulfonate.
11. A noise-free power transmission fluid consisting essentially of about 0.2% stearic acid, about 0.2% of a reaction product prepared by reacting from 1 to 5 moles of C C aliphatic amine with a mol of dioctyl pyrophosphate until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs, and about 0.1-0.5% of a mixture of an alkyl phenol and an aryl amine and the balance being a refined transformer mineral oil.
12. A noise-free power transmission fluid consisting essentially of about 0.2% stearic acid, about 0.2% of a reaction product prepared by reacting from 1 to 5 moles of C1648 aliphatic amine with a mol of dioctyl pyrophosphate until the reaction is substantially completed,
aliphatic amine with a mol of dioctyl pyrophosphate until the reaction is substantially completed, the reaction being carried out at a temperature below that at which substantial decomposition of the reaction product occurs, about 7 2.5-5% calcium petroleum sulfonate, about 0.5% zinc dimethylcyelohexyl di thiophosphate, and about 5 p.p.m. dimethyl silicone polymer and the balance being a refined transformer mineral oil.
References Cited in the file of this patent UNITED STATES PATENTS 2,005,619 Graves June 18, 1 935 8 Benniug May 11, 1937 Baker Aug. 24, 1948 Watson May 30, 1950 Rudel Apr. 29, 1952 Woodstock et a1. Dec. 29, 1953 Watson Aug. 17, 1954 Jones Nov. 9, 1954 Wasson et a1. Apr. 15, 1958 Chenicek Aug. 19, 1958
Claims (1)
1. A NOISE-FREE POWER TRANSMISSION FLUID CONSISTING ESSENTIALLY OF A MAJOR AMOUNT OF A REFINED MINERAL LUBRICATING OIL FROM ABOUT 0.05% TO ABOUT 2% OF EACH OF AN ALIPHATIC MONOCARBOXYLIC ACID HAVINNG FROM 18 TO 26 CARBON ATOMS IN THE MOLECULE AND A REACTION PRODUCT PREPARED BY REACING FROM 1 TO 5 MOLES OF AN ALIPHATIC AMINE HAVING FROM 8 TO 18 CARBON ATOMS WITH A MOL OF AN ALIPHATIC ACID PYROPHOSPHATE HAVING FROM 8 TO 18 CARBON ATOMS UNTIL THE REACTION IS SUBSTANTIALLY COMPLETED, THE REACTION BEING CARRIED OUT AT A TEMPERATURE BELOW THAT AT WHICH SUBSTANTIAL DECOMPOSITION OF THE REACTION PRODUCT OCCURS.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US665660A US2961408A (en) | 1957-06-14 | 1957-06-14 | Power transmission mineral oil base fluids |
| GB19001/58A GB827704A (en) | 1957-06-14 | 1958-06-13 | Power transmission fluid |
| DEN15224A DE1083010B (en) | 1957-06-14 | 1958-06-14 | Power transmission fluid |
| FR1208510D FR1208510A (en) | 1957-06-14 | 1958-06-14 | Force transmission fluid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US665660A US2961408A (en) | 1957-06-14 | 1957-06-14 | Power transmission mineral oil base fluids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2961408A true US2961408A (en) | 1960-11-22 |
Family
ID=24671030
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US665660A Expired - Lifetime US2961408A (en) | 1957-06-14 | 1957-06-14 | Power transmission mineral oil base fluids |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2961408A (en) |
| DE (1) | DE1083010B (en) |
| FR (1) | FR1208510A (en) |
| GB (1) | GB827704A (en) |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3087895A (en) * | 1959-05-14 | 1963-04-30 | Celanese Corp | Automatic transmission fluids containing a triaryl phosphate |
| US3125528A (en) * | 1964-03-17 | Method of lubricating automotive | ||
| US3169923A (en) * | 1962-03-22 | 1965-02-16 | Universal Oil Prod Co | Oil of lubricating viscosity |
| US3203895A (en) * | 1962-03-22 | 1965-08-31 | Universal Oil Prod Co | Lubricating oils containing amine salts of phosphates |
| US3203896A (en) * | 1962-03-28 | 1965-08-31 | Universal Oil Prod Co | Lubricating composition |
| US3250726A (en) * | 1962-03-29 | 1966-05-10 | On silica | |
| US3267033A (en) * | 1963-04-15 | 1966-08-16 | Lubrizol Corp | Lubricating composition having desirable frictional characteristics |
| US3275559A (en) * | 1963-01-14 | 1966-09-27 | Texaco Inc | Hydraulic fluid |
| US3360468A (en) * | 1965-06-28 | 1967-12-26 | Standard Oil Co | Water-in-oil emulsion useful as fireresistant hydraulic fluid |
| US3450636A (en) * | 1967-08-22 | 1969-06-17 | Sinclair Research Inc | Automatic transmission fluid of reduced susceptibility oxidative degradation |
| US3547820A (en) * | 1968-12-20 | 1970-12-15 | Gaf Corp | Lubricating oil compositions |
| US20080058235A1 (en) * | 2004-03-25 | 2008-03-06 | Katsuya Takigawa | Lubricative Composition for Industrial Machinery and Equipment |
| WO2018200664A1 (en) * | 2017-04-27 | 2018-11-01 | The Lubrizol Corporation | Method of lubricating a mechanical device with high pyrophosphate level lubricant |
| US11352582B2 (en) | 2015-11-06 | 2022-06-07 | The Lubrizol Corporation | Lubricant with high pyrophosphate level |
| US11384308B2 (en) | 2016-07-20 | 2022-07-12 | The Lubrizol Corporation | Alkyl phosphate amine salts for use in lubricants |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1218097B (en) * | 1961-04-01 | 1966-06-02 | Bayer Ag | Hydraulic oils |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2005619A (en) * | 1934-11-10 | 1935-06-18 | Du Pont | Esters of acids of phosphorus |
| US2080299A (en) * | 1935-04-12 | 1937-05-11 | Du Pont | Inhibiting corrosion of metals |
| US2447483A (en) * | 1944-04-15 | 1948-08-24 | Us Navy | Additives for silicone oils |
| US2509620A (en) * | 1947-05-13 | 1950-05-30 | Shell Dev | Nonflammable hydraulic fluid |
| US2595170A (en) * | 1949-11-14 | 1952-04-29 | Standard Oil Dev Co | Stabilized mineral oil |
| US2664400A (en) * | 1949-08-13 | 1953-12-29 | Victor Chemical Works | Reaction products of an octyl acid pyrophosphate and soyamine and lubricants containing the same |
| US2686760A (en) * | 1951-10-27 | 1954-08-17 | Shell Dev | Hydraulic fluids and lubricating compositions |
| US2694045A (en) * | 1951-12-14 | 1954-11-09 | Standard Oil Dev Co | Stabilizer for petroleum products |
| US2830956A (en) * | 1954-02-12 | 1958-04-15 | Exxon Research Engineering Co | Hydraulic power transmission fluids |
| US2848414A (en) * | 1955-11-23 | 1958-08-19 | Universal Oil Prod Co | Corrosion inhibitor |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2605226A (en) * | 1949-11-30 | 1952-07-29 | Tide Water Associated Oil Comp | Compounded lubricating oil |
| US2768953A (en) * | 1952-08-26 | 1956-10-30 | Exxon Research Engineering Co | Hydraulic transmission fluid |
| US2731418A (en) * | 1952-08-26 | 1956-01-17 | Exxon Research Engineering Co | Hydraulic transmission fluid |
| US2777819A (en) * | 1954-04-27 | 1957-01-15 | Shell Dev | Lubricating compositions |
-
1957
- 1957-06-14 US US665660A patent/US2961408A/en not_active Expired - Lifetime
-
1958
- 1958-06-13 GB GB19001/58A patent/GB827704A/en not_active Expired
- 1958-06-14 FR FR1208510D patent/FR1208510A/en not_active Expired
- 1958-06-14 DE DEN15224A patent/DE1083010B/en active Pending
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2005619A (en) * | 1934-11-10 | 1935-06-18 | Du Pont | Esters of acids of phosphorus |
| US2080299A (en) * | 1935-04-12 | 1937-05-11 | Du Pont | Inhibiting corrosion of metals |
| US2447483A (en) * | 1944-04-15 | 1948-08-24 | Us Navy | Additives for silicone oils |
| US2509620A (en) * | 1947-05-13 | 1950-05-30 | Shell Dev | Nonflammable hydraulic fluid |
| US2664400A (en) * | 1949-08-13 | 1953-12-29 | Victor Chemical Works | Reaction products of an octyl acid pyrophosphate and soyamine and lubricants containing the same |
| US2595170A (en) * | 1949-11-14 | 1952-04-29 | Standard Oil Dev Co | Stabilized mineral oil |
| US2686760A (en) * | 1951-10-27 | 1954-08-17 | Shell Dev | Hydraulic fluids and lubricating compositions |
| US2694045A (en) * | 1951-12-14 | 1954-11-09 | Standard Oil Dev Co | Stabilizer for petroleum products |
| US2830956A (en) * | 1954-02-12 | 1958-04-15 | Exxon Research Engineering Co | Hydraulic power transmission fluids |
| US2848414A (en) * | 1955-11-23 | 1958-08-19 | Universal Oil Prod Co | Corrosion inhibitor |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3125528A (en) * | 1964-03-17 | Method of lubricating automotive | ||
| US3087895A (en) * | 1959-05-14 | 1963-04-30 | Celanese Corp | Automatic transmission fluids containing a triaryl phosphate |
| US3169923A (en) * | 1962-03-22 | 1965-02-16 | Universal Oil Prod Co | Oil of lubricating viscosity |
| US3203895A (en) * | 1962-03-22 | 1965-08-31 | Universal Oil Prod Co | Lubricating oils containing amine salts of phosphates |
| US3203896A (en) * | 1962-03-28 | 1965-08-31 | Universal Oil Prod Co | Lubricating composition |
| US3250726A (en) * | 1962-03-29 | 1966-05-10 | On silica | |
| US3275559A (en) * | 1963-01-14 | 1966-09-27 | Texaco Inc | Hydraulic fluid |
| US3267033A (en) * | 1963-04-15 | 1966-08-16 | Lubrizol Corp | Lubricating composition having desirable frictional characteristics |
| US3360468A (en) * | 1965-06-28 | 1967-12-26 | Standard Oil Co | Water-in-oil emulsion useful as fireresistant hydraulic fluid |
| US3450636A (en) * | 1967-08-22 | 1969-06-17 | Sinclair Research Inc | Automatic transmission fluid of reduced susceptibility oxidative degradation |
| US3547820A (en) * | 1968-12-20 | 1970-12-15 | Gaf Corp | Lubricating oil compositions |
| US20080058235A1 (en) * | 2004-03-25 | 2008-03-06 | Katsuya Takigawa | Lubricative Composition for Industrial Machinery and Equipment |
| US11352582B2 (en) | 2015-11-06 | 2022-06-07 | The Lubrizol Corporation | Lubricant with high pyrophosphate level |
| US11384308B2 (en) | 2016-07-20 | 2022-07-12 | The Lubrizol Corporation | Alkyl phosphate amine salts for use in lubricants |
| WO2018200664A1 (en) * | 2017-04-27 | 2018-11-01 | The Lubrizol Corporation | Method of lubricating a mechanical device with high pyrophosphate level lubricant |
| US11180710B2 (en) | 2017-04-27 | 2021-11-23 | The Lubrizol Corporation | Method of lubricating a mechanical device with high pyrophosphate level lubricant |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1208510A (en) | 1960-02-24 |
| DE1083010B (en) | 1960-06-09 |
| GB827704A (en) | 1960-02-10 |
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