JP5746671B2 - 駆動伝達装置用潤滑油組成物 - Google Patents
駆動伝達装置用潤滑油組成物 Download PDFInfo
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- JP5746671B2 JP5746671B2 JP2012209924A JP2012209924A JP5746671B2 JP 5746671 B2 JP5746671 B2 JP 5746671B2 JP 2012209924 A JP2012209924 A JP 2012209924A JP 2012209924 A JP2012209924 A JP 2012209924A JP 5746671 B2 JP5746671 B2 JP 5746671B2
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- oil
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- lubricating
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- 239000010687 lubricating oil Substances 0.000 title claims description 148
- 239000000203 mixture Substances 0.000 title claims description 137
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- 229920006395 saturated elastomer Polymers 0.000 claims description 109
- 150000001875 compounds Chemical class 0.000 claims description 50
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 33
- 125000004122 cyclic group Chemical group 0.000 claims description 33
- 229910052698 phosphorus Inorganic materials 0.000 claims description 33
- 239000011574 phosphorus Substances 0.000 claims description 33
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- 125000003118 aryl group Chemical group 0.000 claims description 22
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 21
- 239000011630 iodine Substances 0.000 claims description 21
- 229910052740 iodine Inorganic materials 0.000 claims description 21
- 125000002619 bicyclic group Chemical group 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- -1 monocyclic aromatic compounds Chemical class 0.000 description 112
- 239000001993 wax Substances 0.000 description 94
- 239000003921 oil Substances 0.000 description 93
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- 229910052751 metal Inorganic materials 0.000 description 63
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- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 19
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 239000002585 base Substances 0.000 description 10
- 230000002265 prevention Effects 0.000 description 10
- 230000003197 catalytic effect Effects 0.000 description 9
- 239000003599 detergent Substances 0.000 description 9
- 230000006870 function Effects 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- 230000001590 oxidative effect Effects 0.000 description 9
- 229920000768 polyamine Polymers 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
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- TYQTYRXEMJXFJG-UHFFFAOYSA-N phosphorothious acid Chemical compound OP(O)S TYQTYRXEMJXFJG-UHFFFAOYSA-N 0.000 description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 8
- 238000000926 separation method Methods 0.000 description 8
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- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 7
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- 239000010779 crude oil Substances 0.000 description 7
- 125000000753 cycloalkyl group Chemical group 0.000 description 7
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- 239000000395 magnesium oxide Substances 0.000 description 7
- 229910052750 molybdenum Inorganic materials 0.000 description 7
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- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 229910017464 nitrogen compound Inorganic materials 0.000 description 7
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- 238000000746 purification Methods 0.000 description 7
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- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 150000001342 alkaline earth metals Chemical class 0.000 description 6
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- 229920001577 copolymer Polymers 0.000 description 6
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 6
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- 238000005292 vacuum distillation Methods 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 5
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 5
- 125000002877 alkyl aryl group Chemical group 0.000 description 5
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- 239000002518 antifoaming agent Substances 0.000 description 5
- 125000003710 aryl alkyl group Chemical group 0.000 description 5
- 239000004927 clay Substances 0.000 description 5
- 238000005984 hydrogenation reaction Methods 0.000 description 5
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- 230000000737 periodic effect Effects 0.000 description 5
- OTYNBGDFCPCPOU-UHFFFAOYSA-N phosphane sulfane Chemical compound S.P[H] OTYNBGDFCPCPOU-UHFFFAOYSA-N 0.000 description 5
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- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 4
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- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 125000002460 pentacosyl 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])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
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004346 phenylpentyl group Chemical group C1(=CC=CC=C1)CCCCC* 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- 150000008301 phosphite esters Chemical class 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000004929 pyrrolidonyl group Chemical group N1(C(CCC1)=O)* 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 125000004151 quinonyl group Chemical group 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 239000008165 rice bran oil Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000000371 solid-state nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000002336 sorption--desorption measurement Methods 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- PPEZWDDRWXDXOQ-UHFFFAOYSA-N tributoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound CCCCOP(=S)(OCCCC)OCCCC PPEZWDDRWXDXOQ-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- XTTGYFREQJCEML-UHFFFAOYSA-N tributyl phosphite Chemical compound CCCCOP(OCCCC)OCCCC XTTGYFREQJCEML-UHFFFAOYSA-N 0.000 description 1
- 125000002469 tricosyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005040 tridecenyl group Chemical group C(=CCCCCCCCCCCC)* 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- YVFHKLYMBACKFA-UHFFFAOYSA-N trioctoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound CCCCCCCCOP(=S)(OCCCCCCCC)OCCCCCCCC YVFHKLYMBACKFA-UHFFFAOYSA-N 0.000 description 1
- QOQNJVLFFRMJTQ-UHFFFAOYSA-N trioctyl phosphite Chemical compound CCCCCCCCOP(OCCCCCCCC)OCCCCCCCC QOQNJVLFFRMJTQ-UHFFFAOYSA-N 0.000 description 1
- IKXFIBBKEARMLL-UHFFFAOYSA-N triphenoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 IKXFIBBKEARMLL-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 125000005065 undecenyl group Chemical group C(=CCCCCCCCCC)* 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Lubricants (AREA)
Description
M A /M B ≦3 (1)
(式中、M A は1環飽和分の質量を示し、M B は2環以上の飽和分を示す。)
また、飽和分を90質量%以上含有し、且つ該飽和分に占める環状飽和分の割合が40質量%以下であり、粘度指数が110以上であり、ヨウ素価が2.5以下である潤滑油基油と、ポリ(メタ)アクリレート系粘度指数向上剤と、リン含有化合物とを含有することを特徴とする駆動伝達装置用潤滑油組成物を提供する。
(1)パラフィン基系原油及び/又は混合基系原油の常圧蒸留による留出油
(2)パラフィン基系原油及び/又は混合基系原油の常圧蒸留残渣油の減圧蒸留による留出油(WVGO)
(3)潤滑油脱ろう工程により得られるワックス(スラックワックス等)及び/又はガストゥリキッド(GTL)プロセス等により得られる合成ワックス(フィッシャートロプシュワックス、GTLワックス等)
(4)基油(1)〜(3)から選ばれる1種又は2種以上の混合油及び/又は当該混合油のマイルドハイドロクラッキング処理油
(5)基油(1)〜(4)から選ばれる2種以上の混合油
(6)基油(1)、(2)、(3)、(4)又は(5)の脱れき油(DAO)
(7)基油(6)のマイルドハイドロクラッキング処理油(MHC)
(8)基油(1)〜(7)から選ばれる2種以上の混合油。
(9)上記基油(1)〜(8)から選ばれる基油又は当該基油から回収された潤滑油留分を水素化分解し、その生成物又はその生成物から蒸留等により回収される潤滑油留分について溶剤脱ろうや接触脱ろうなどの脱ろう処理を行い、または当該脱ろう処理をした後に蒸留することによって得られる水素化分解鉱油
(10)上記基油(1)〜(8)から選ばれる基油又は当該基油から回収された潤滑油留分を水素化異性化し、その生成物又はその生成物から蒸留等により回収される潤滑油留分について溶剤脱ろうや接触脱ろうなどの脱ろう処理を行い、または、当該脱ろう処理をしたあとに蒸留することによって得られる水素化異性化鉱油。
NH3脱着温度依存性評価においてNH3の全脱着量に対する300〜800℃でのNH3の脱着量の分率が80%以下である担体に、周期律表第VIa族金属のうち少なくとも1種類と、第VIII族金属のうち少なくとも1種類とが担持された水素化分解触媒を準備する第1工程と、
水素化分解触媒の存在下、スラックワックスを50容量%以上含む原料油を、水素分圧0.1〜14MPa、平均反応温度230〜430℃、LHSV0.3〜3.0hr−1、水素油比50〜14000scf/bで水素化分解する第2工程と、
第2工程で得られた分解生成油を蒸留分離して潤滑油留分を得る第3工程と、
第3工程で得られた潤滑油留分を脱ろう処理する第4工程と
を備える。
上記製造方法Aにおいては、スラックワックスを50容量%以上含有する原料油が用いられる。なお、本発明でいう「スラックワックスを50容量%以上含有する原料油」とは、スラックワックスのみからなる原料油と、スラックワックスと他の原料油との混合油であってスラックワックスを50容量%以上含有する原料油との双方が包含される。
上記製造方法Aでは、NH3脱着温度依存性評価においてNH3の全脱着量に対する300〜800℃でのNH3の脱着量の分率が80%以下である担体に、周期律表第VIa族金属のうち少なくとも1種類と、第VIII族金属のうち少なくとも1種類とが担持された水素化分解触媒が用いられる。
上記製造方法Aにおいては、上記の水素化分解触媒の存在下、スラックワックスを50容量%以上含む原料油を、水素分圧が0.1〜14MPa、好ましくは1〜14MPa、より好ましくは2〜7MPa;平均反応温度が230〜430℃、好ましくは330〜400℃、より好ましくは350〜390℃;LHSVが0.3〜3.0hr−1、好ましくは0.5〜2.0hr−1;水素油比が50〜14000scf/b、好ましくは100〜5000scf/bで水素化分解する。
(分解率(容量%))=100−(生成物中の沸点が360℃以上の留分の割合(容量%))
のように定義すると、分解率は3〜90容量%であることが好ましい。分解率が3容量%未満では、原料油中に含まれる流動点の高い高分子量n−パラフィンの分解異性化によるイソパラフィンの生成や、粘度指数の劣る芳香族分や多環ナフテン分の水素化分解が不十分となり、また、分解率が90容量%を超えると潤滑油留分の収率が低くなり、それぞれ好ましくない。
次いで、上記の水素化分解工程により得られる分解生成油から潤滑油留分を蒸留分離する。この際、軽質分として燃料油留分も得られる場合がある。
上記の蒸留分離工程において、分解生成油から分留した潤滑油留分は流動点が高いので、所望の流動点を有する潤滑油基油を得るために脱ろうする。脱ろう処理は溶剤脱ろう法又は接触脱ろう法などの通常の方法で行うことができる。このうち、溶剤脱ろう法は一般にMEK、トルエンの混合溶剤が用いられるが、ベンゼン、アセトン、MIBK等の溶剤を用いてもよい。脱ろう油の流動点を−10℃以下にするために溶剤/油比1〜6倍、ろ過温度−5〜−45℃、好ましくは−10〜−40℃の条件で行うことが好ましい。なお、ここで除去されるろう分は、スラックワックスとして、水素化分解工程に再び供することができる。
触媒の存在下、パラフィン系炭化水素を含有する原料油を水素化分解及び/又は水素化異性化する第5工程と、
第5工程で得られる生成物又はその生成物から蒸留等により回収される潤滑油留分を脱ろう処理する第6工程と、
を備える。
上記製造方法Bにおいては、パラフィン系炭化水素を含有する原料油が用いられる。なお、本発明でいう「パラフィン系炭化水素」とは、パラフィン分子の含有率が70質量%以上の炭化水素をいう。パラフィン系炭化水素の炭素数は特に制限されないが、通常、10〜100程度のものが用いられる。また、パラフィン系炭化水素の製法は特に制限されず、石油系及び合成系の各種パラフィン系炭化水素を用いることができるが、特に好ましいパラフィン系炭化水素としては、ガストゥリキッド(GTL)プロセス等により得られる合成ワックス(フィッシャートロプシュワックス(FTワックス)、GTLワックス等)が挙げられ、中でもFTワックスが好ましい。また、合成ワックスは、炭素数が好ましくは15〜80、より好ましくは20〜50のノルマルパラフィンを主成分として含むワックスが好適である。
製造方法Bで用いられる触媒は特に制限されないが、アルミノシリケートを含有する担体に、活性金属成分として周期律表第VI属b金属及び第VIII属金属から選ばれる1種以上が担持された触媒が好ましく用いられる。
上記製造方法Bにおいては、上記触媒の存在下、パラフィン系炭化水素を含有する原料油を水素化分解/水素化異性化する。かかる水素化分解/水素化異性化工程は、固定床反応装置を用いて行うことができる。水素化分解/水素化異性化の条件としては、例えば温度は250〜400℃、水素圧は0.5〜10MPa、原料油の液空間速度(LHSV)は0.5〜10h−1がそれぞれ好ましい。
次いで、上記の水素化分解/水素化異性化工程により得られる分解生成油から潤滑油留分を蒸留分離する。なお、製造方法Bにおける蒸留分離工程は製造方法Aにおける蒸留分離工程と同様であるため、ここでは重複する説明を省略する。
次いで、上記の蒸留分離工程において分解生成油から分留した潤滑油留分を脱ろうする。かかる脱ろう工程は、溶剤脱ろう又は接触脱ろう等の従来公知の脱ろうプロセスを用いて行うことができる。ここで、分解/異性化生成油中に存在する沸点370℃以下の物質が脱ろうに先立ち高沸点物質から分離されていない場合、分解/異性化生成油の用途に応じて、全水素化異性化物を脱ろうしてもよく、あるいは沸点370℃以上の留分を脱ろうしてもよい。
(ガスクロマトグラフィ条件)
カラム:液相無極性カラム(長さ25mm、内径0.3mmφ、液相膜厚さ0.1μm)
昇温条件:50℃〜400℃(昇温速度:10℃/min)
キャリアガス:ヘリウム(線速度:40cm/min)
スプリット比:90/1
試料注入量:0.5μL(二硫化炭素で20倍に希釈した試料の注入量)
1.435≦n20−0.002×kv100≦1.453 (2)
[式中、n20は潤滑油基油の20℃における屈折率を示し、kv100は潤滑油基油の100℃における動粘度(mm2/s)を示す。]
(I)100℃における動粘度が1.5mm2/s以上3.5mm2/s未満、より好ましくは2.0〜3.0mm2/sの潤滑油基油
(II)100℃における動粘度が3.0mm2/s以上4.5mm2/s未満、より好ましくは3.5〜4.1mm2/sの潤滑油基油
(III)100℃における動粘度が4.5〜20mm2/s、より好ましくは4.8〜11mm2/s、特に好ましくは5.5〜8.0mm2/sの潤滑油基油。
(IV)40℃における動粘度が6.0mm2/s以上12mm2/s未満、より好ましくは8.0〜12mm2/sの潤滑油基油
(V)40℃における動粘度が12mm2/s以上28mm2/s未満、より好ましくは13〜19mm2/sの潤滑油基油
(VI)40℃における動粘度が28〜50mm2/s、より好ましくは29〜45mm2/s、特に好ましくは30〜40mm2/sの潤滑油基油。
ρ=0.0025×kv100+0.820 (3)
[式中、kv100は潤滑油基油の100℃における動粘度(mm2/s)を示す。]
A=4.1×kv100+97 (4)
[式中、kv100は潤滑油基油の100℃における動粘度(mm2/s)を示す。]
(A−1)一般式(5)中のR1がメチル基又は炭素数12〜15の直鎖アルキル基であるモノマーを主成分とする重合体
(A−2)一般式(5)中のR1がメチル基又は炭素数12〜15、16、18の直鎖アルキル基であるモノマーを主成分とする重合体
(A−3)一般式(5)中のR1がメチル基又は炭素数12〜15、16、18の直鎖アルキル基であるモノマーと、一般式(5)中のR1が炭素数20〜30の直鎖又は分枝アルキル基であるモノマーとの重合体。
R5―Sx―R6 (8)
R7―Sy―R8 (9)
(D−1)炭素数40〜400のアルキル基又はアルケニル基を分子中に少なくとも1個有するコハク酸イミド、あるいはその誘導体
(D−2)炭素数40〜400のアルキル基又はアルケニル基を分子中に少なくとも1個有するベンジルアミン、あるいはその誘導体
(D−3)炭素数40〜400のアルキル基又はアルケニル基を分子中に少なくとも1個有するポリアミン、あるいはその誘導体。
R26−NH−(CH2CH2NH)n−H (18)
(基油1〜3)
溶剤精製基油を精製する工程において減圧蒸留で分離した留分を、フルフラールで溶剤抽出した後で水素化処理し、次いで、メチルエチルケトン−トルエン混合溶剤で溶剤脱ろうした。かかる溶剤脱ろうの際に除去されたワックス分(以下、「WAX1」という)を、潤滑油基油の原料として用いた。WAX1の性状を表1に示す。
実施例1〜3においては、上記基油1、2、並びに下記の基油4及び添加剤A1、A2、B1、C1を用いて、表4に示す組成を有する潤滑油組成物を調製した。また、比較例1〜3においては、上記表3に示す基油5、6、並びに下記の基油4及び添加剤A1、A2、B1、C1を用いて、表5に示す組成を有する潤滑油組成物を調製した。基油5、6の各種性状及び評価試験結果を表3に示す。得られた潤滑油組成物の40℃及び100℃における動粘度、粘度指数及びリン含有量を表4、5に示す。
(基油)
基油4:パラフィン系溶剤精製基油(飽和分:60.1質量%、芳香族分:35.7質量%、樹脂分:4.2質量%、硫黄分:0.51質量%、100℃における動粘度:32mm2/s、粘度指数:95)
基油5:パラフィン系水素化分解基油
基油6:パラフィン系水素化分解基油
基油7:パラフィン系水素化分解基油
(粘度指数向上剤)
A1:非分散型ポリメタクリレート(一般式(5)におけるR1がメチル基、炭素数12〜15の直鎖アルキル基であるモノマーを主成分とするモノマー混合物の共重合体、重量平均分子量:25,000)
A2:分散型ポリメタクリレート(一般式(5)におけるR1がメチル基、炭素数12、14、16、18の直鎖アルキル基であるモノマーを主成分とし、一般式(6)又は(7)で表される含窒素モノマーを含むモノマー混合物の共重合体、重量平均分子量:40,000)
(リン含有化合物)
B1:亜リン酸と亜リン酸エステルとの混合物
(パッケージ添加剤)
C1:パッケージ添加剤(潤滑油組成物への添加量:12.5質量%、潤滑油組成物中、無灰分散剤:4.0質量%、アルカリ土類金属スルホネート:0.01質量%(アルカリ土類金属元素換算値)、腐食防止剤:0.1質量%、酸化防止剤:0.2質量%、摩擦調整剤:3.5質量%、ゴム膨潤剤:1.0質量%、消泡剤:0.003質量%、希釈剤:残部)。
ASTM D 2983に準拠し、各潤滑油組成物の−40℃におけるBF粘度を測定した。得られた結果を表4、5に示す。本試験においては、BF粘度の値が小さいものほど低温流動性に優れていることを意味する。
JASO M347−95に準拠し、下記条件で超音波せん断試験を行い、試験後の各潤滑油組成物の100℃における動粘度を測定した。得られた結果を表4、5に示す。本試験においては、超音波せん断を受けた後の粘度低下が小さく、100℃における動粘度が高い値を示すものほどせん断安定性に優れていることを意味する。
(試験条件)
試験油量:30ml
超音波周波数:10kHz
試験油温度:40℃
試験時間:1時間。
JPI−5S−32−90に準拠し、下記条件で四球試験を行い、試験後の摩耗痕径を測定した。得られた結果を表4、5に示す。本試験においては、摩耗痕径が小さいものほど耐摩耗性に優れていることを意味する。
(試験条件)
回転数:1800rpm
荷重:392N
試験油量:75℃
試験時間:1時間。
先ず、各潤滑油組成物の酸価を測定した。次に、JIS K 2514に準拠し、ISOTにて165℃、144時間の条件で各潤滑油組成物を強制劣化させてその酸価を測定し、試験前後の酸価の測定値から酸価の増加量を求めた。得られた結果を表4、5に示す。本試験においては、酸価の増加量が小さいものほど熱・酸化安定性に優れていることを意味する。
実施例4、5においては、上記基油2、3及び添加剤A1、並びに下記添加剤A3、B2、C2を用いて表6に示す組成を有する潤滑油組成物を調製した。また、比較例4、5においては、前記表3に示した基油6及び添加剤A1、並びに前記表3に示した基油7及び添加剤A3、B2、C2を用いて表6に示す組成を有する潤滑油組成物を調製した。得られた潤滑油組成物の40℃及び100℃における動粘度、粘度指数及びリン含有量を表6に示す。
(粘度指数向上剤)
A3:非分散型ポリメタクリレート(一般式(5)におけるR1がメチル基、炭素数12、14、16、18の直鎖アルキル基であるモノマーを主成分とするモノマー混合物の共重合体、重量平均分子量:60,000)
(リン含有化合物)
B2:ジアルキルジチオリン酸亜鉛(Pri−ZDTPとSec−ZDTPとの混合物)(パッケージ添加剤)
C2:パッケージ添加剤(潤滑剤組成物への添加量:6.0質量%、潤滑油組成物中、アルカリ土類金属スルホネート:0.25質量%(アルカリ土類金属元素換算値)、腐食防止剤:0.1質量%、酸化防止剤:0.5質量%、摩擦調整剤:1.0質量%、ゴム膨潤剤:0.5質量%、消泡剤:0.001質量%、希釈剤:残部)。
Claims (3)
- 飽和分を90質量%以上含有し、且つ該飽和分に占める環状飽和分の割合が1.5〜20質量%であり、該飽和分に占める2環以上の飽和分の割合が2.6質量%以上であり、前記環状飽和分に含まれる1環飽和分と2環以上の飽和分との質量比が下記式(1)で表される条件を満たし、粘度指数が110以上であり、ヨウ素価が2.5以下であり、100℃における動粘度が3.0mm2/s以上4.5mm2/s未満であり、流動点が−17.5℃以下である潤滑油基油と、
ポリ(メタ)アクリレート系粘度指数向上剤と、
リン含有化合物と
を含有することを特徴とする駆動伝達装置用潤滑油組成物。
M A /M B ≦3 (1)
(式中、M A は1環飽和分の質量を示し、M B は2環以上の飽和分を示す。) - 前記潤滑油基油において、前記飽和分に占める2環以上の飽和分の割合が3質量%以上であることを特徴とする、請求項1に記載の駆動伝達装置用潤滑油組成物。
- 前記潤滑油基油が芳香族分を0.1〜5質量%含有することを特徴とする、請求項1又は2に記載の駆動伝達装置用潤滑油組成物。
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