JP2007520335A5 - - Google Patents

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JP2007520335A5
JP2007520335A5 JP2006547169A JP2006547169A JP2007520335A5 JP 2007520335 A5 JP2007520335 A5 JP 2007520335A5 JP 2006547169 A JP2006547169 A JP 2006547169A JP 2006547169 A JP2006547169 A JP 2006547169A JP 2007520335 A5 JP2007520335 A5 JP 2007520335A5
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catalyst
sulfur
noble metal
waxy hydrocarbon
base oil
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JP2006547169A
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JP4796508B2 (en
JP2007520335A (en
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Priority claimed from US10/747,152 external-priority patent/US20050139513A1/en
Priority claimed from US10/747,524 external-priority patent/US20050139514A1/en
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Priority claimed from PCT/US2004/042467 external-priority patent/WO2005065212A2/en
Publication of JP2007520335A publication Critical patent/JP2007520335A/en
Publication of JP2007520335A5 publication Critical patent/JP2007520335A5/ja
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Claims (26)

ワックス質炭化水素供給原料から潤滑基油を製造する方法であって、
a)形状選択的、中孔径、貴金属含有モレキュラーシーブ触媒を硫化して、硫化された触媒を提供するステップであって、硫化された触媒中のイオウ対貴金属のモル比は1を超えるステップと、
b)ワックス質炭化水素供給原料を水素化異性化条件で硫化された触媒と接触させることにより、ワックス質炭化水素供給原料を水素化異性化して、潤滑基油を製造するステップと、
を含む方法。
A method for producing a lubricating base oil from a waxy hydrocarbon feedstock comprising:
a) sulfiding a shape selective, medium pore size, noble metal-containing molecular sieve catalyst to provide a sulphided catalyst, wherein the molar ratio of sulfur to noble metal in the sulphided catalyst is greater than 1.
b) hydrolytically isolating the waxy hydrocarbon feedstock by contacting the waxy hydrocarbon feedstock with a catalyst sulfided under hydroisomerization conditions to produce a lubricating base oil;
Including methods.
前記硫化ステップが事前硫化ステップである、請求項1に記載の方法。   The method of claim 1, wherein the sulfiding step is a pre-sulfiding step. 前記硫化ステップが操業中の硫化ステップである、請求項1に記載の方法。   The method of claim 1, wherein the sulfidation step is an operating sulfidation step. 事前硫化ステップが、水素の存在下で、前記触媒をイオウ含有種と接触させることを含み、前記イオウ含有種が、硫化水素、二硫化炭素、及びメルカプタンからなる群から選択される、請求項2に記載の方法。The pre-sulfiding step comprises contacting the catalyst with a sulfur-containing species in the presence of hydrogen, wherein the sulfur-containing species is selected from the group consisting of hydrogen sulfide, carbon disulfide, and mercaptans. The method described in 1. ワックス質炭化水素供給原料が10ppm未満のイオウを含む、請求項4に記載の方法。5. The method of claim 4, wherein the waxy hydrocarbon feed contains less than 10 ppm sulfur. 水素化異性化ステップに先立って硫化された触媒中のイオウ対貴金属のモル比が少なくとも2:1であり、水素化異性化ステップ中に硫化された触媒中のイオウ対貴金属のモル比が少なくとも3:1である、請求項2、4又は5に記載の方法。The sulfur to noble metal molar ratio in the catalyst sulfided prior to the hydroisomerization step is at least 2: 1 and the sulfur to noble metal molar ratio in the catalyst sulfided during the hydroisomerization step is at least 3 The method according to claim 2, 4 or 5. 硫化された触媒中のイオウ対貴金属のモル比が少なくとも3:1である、請求項2、4、5又は6に記載の方法。The process according to claim 2, 4, 5, or 6, wherein the molar ratio of sulfur to noble metal in the sulfurized catalyst is at least 3: 1. 硫化された触媒中のイオウ対貴金属のモル比が少なくとも5:1である、請求項2、4、5、6又は7に記載の方法。The process according to claim 2, 4, 5, 6 or 7, wherein the molar ratio of sulfur to noble metal in the sulfurized catalyst is at least 5: 1. ワックス質炭化水素供給原料が、ガス油、潤滑油原料、合成油、フィッシャー−トロプシュ由来のワックス、オリゴマー化フィッシャー−トロプシュ由来のオレフィン、ワックス下油、粗ワックス、脱油ワックス、直鎖α−オレフィンワックス、微晶ワックス、及びこれらの混合物からなる群から選択される、前記請求項1から8までのいずれかに記載の方法。The waxy hydrocarbon feedstock is gas oil, lubricating oil feedstock, synthetic oil, Fischer-Tropsch derived wax, oligomerized Fischer-Tropsch derived olefin, wax lower oil, crude wax, deoiled wax, linear α-olefin 9. A method according to any preceding claim, wherein the method is selected from the group consisting of waxes, microcrystalline waxes, and mixtures thereof. ワックス質炭化水素供給原料がフィッシャー−トロプシュ由来のワックスである、請求項9に記載の方法。10. A process according to claim 9, wherein the waxy hydrocarbon feedstock is a Fischer-Tropsch derived wax. 前記モレキュラーシーブが、4.0〜7.1Åの範囲のチャネル径を有する、前記請求項1から10までのいずれかに記載の方法。The method according to any one of claims 1 to 10, wherein the molecular sieve has a channel diameter in the range of 4.0 to 7.1 mm. 前記モレキュラーシーブが非ゼオライト系である、請求項11に記載の方法。The method according to claim 11, wherein the molecular sieve is non-zeolitic. 前記触媒がSAPO触媒である、請求項12に記載の方法。The method of claim 12, wherein the catalyst is a SAPO catalyst. SAPO触媒が、SAPO−11、SAPO−31、及びSAPO−41からなる群から選択される、請求項13に記載の方法。14. The method of claim 13, wherein the SAPO catalyst is selected from the group consisting of SAPO-11, SAPO-31, and SAPO-41. 前記貴金属が、白金、パラジウム、及びこれらの混合物からなる群から選択される、前記請求項1から14までのいずれかに記載の方法。15. A method according to any preceding claim, wherein the noble metal is selected from the group consisting of platinum, palladium, and mixtures thereof. ワックス質炭化水素供給原料が、イオウ強化供給原料である、前記請求項1から15までのいずれかに記載の方法。   16. A method according to any preceding claim, wherein the waxy hydrocarbon feedstock is a sulfur enhanced feedstock. 水素化異性化条件が、150と1000ポンド/平方インチゲージの間の全圧を含む、前記請求項1から16までのいずれかに記載の方法。   17. A process according to any preceding claim, wherein the hydroisomerization conditions comprise a total pressure between 150 and 1000 pounds per square inch gauge. 水素化異性化条件が、150と500ポンド/平方インチゲージの間の全圧を含む、請求項17に記載の方法。   18. The method of claim 17, wherein the hydroisomerization conditions comprise a total pressure between 150 and 500 pounds per square inch gauge. 水素化異性化条件が、150と300ポンド/平方インチゲージの間の全圧を含む、請求項18に記載の方法。   19. The method of claim 18, wherein the hydroisomerization conditions comprise a total pressure between 150 and 300 pounds per square inch gauge. 水素化異性化条件が、500と1000ポンド/平方インチゲージの間の全圧を含む、請求項17に記載の方法。   The method of claim 17, wherein the hydroisomerization conditions comprise a total pressure between 500 and 1000 pounds per square inch gauge. 40と95重量パーセントの間の潤滑基油が、650と1400°Fの間の沸点を有する、前記請求項1から20までのいずれかに記載の方法。   21. A method according to any preceding claim, wherein between 40 and 95 weight percent of the lubricating base oil has a boiling point between 650 and 1400 ° F. 潤滑基油が140と190の間の粘度指数を有する、前記請求項1から21までのいずれかに記載の方法。   22. A method according to any preceding claim, wherein the lubricating base oil has a viscosity index between 140 and 190. 潤滑基油が−5と−60℃の間の流動点を有する、前記請求項1から22までのいずれかに記載の方法。   23. A method according to any preceding claim, wherein the lubricating base oil has a pour point between -5 and -60 <0> C. 潤滑基油が、3センチストークを超える100℃における粘度を有する、前記請求項1から23までのいずれかに記載の方法。   24. A method according to any preceding claim, wherein the lubricating base oil has a viscosity at 100 <0> C of greater than 3 centistokes. 潤滑基油の少なくとも一部を溶媒脱ワックスし、これにより粗ワックスを除去するステップをさらに含む、前記請求項1から24までのいずれかに記載の方法。   25. A method according to any preceding claim, further comprising the step of solvent dewaxing at least a portion of the lubricating base oil, thereby removing the crude wax. 前記粗ワックスを、ワックス質炭化水素供給原料と共に水素化異性化するステップをさらに含む、請求項25に記載の方法。   26. The method of claim 25, further comprising hydroisomerizing the crude wax with a waxy hydrocarbon feedstock.
JP2006547169A 2003-12-30 2004-12-16 Hydroisomerization using sulfurized catalyst Expired - Fee Related JP4796508B2 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US10/747,152 2003-12-30
US10/747,152 US20050139513A1 (en) 2003-12-30 2003-12-30 Hydroisomerization processes using pre-sulfided catalysts
US10/747,524 2003-12-30
US10/747,524 US20050139514A1 (en) 2003-12-30 2003-12-30 Hydroisomerization processes using sulfided catalysts
PCT/US2004/042467 WO2005065212A2 (en) 2003-12-30 2004-12-16 Hydroisomerization processes using sulfided catalysts

Publications (3)

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JP2007520335A JP2007520335A (en) 2007-07-26
JP2007520335A5 true JP2007520335A5 (en) 2008-01-31
JP4796508B2 JP4796508B2 (en) 2011-10-19

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JP (1) JP4796508B2 (en)
AU (1) AU2004311767B2 (en)
BR (1) BRPI0418260A (en)
GB (1) GB2409864B (en)
NL (1) NL1027901C2 (en)
WO (1) WO2005065212A2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7662271B2 (en) * 2005-12-21 2010-02-16 Chevron U.S.A. Inc. Lubricating oil with high oxidation stability
US7547666B2 (en) * 2005-12-21 2009-06-16 Chevron U.S.A. Inc. Ashless lubricating oil with high oxidation stability

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU8842482A (en) * 1981-09-30 1983-04-14 Mobil Oil Corp. Activating zeolite catalysts
DE3562987D1 (en) * 1984-10-30 1988-07-07 Eurecat Europ Retrait Catalys Method for presulfiding a catalyst for the treatment of hydrocarbons
ES2076360T3 (en) * 1989-02-17 1995-11-01 Chevron Usa Inc ISOMERIZATION OF LUBRICATING OILS, WAXES AND OIL WAXES USING A SILICOALUMINOPHOSPHATE MOLECULAR SCREEN CATALYST.
US5284985A (en) * 1992-10-05 1994-02-08 Mobil Oil Corp. Process for the selective hydrocracking of distillates to produce naphta range high octane isoparaffins
US5562817A (en) * 1994-12-20 1996-10-08 Exxon Research And Engineering Company Reforming using a Pt/Re catalyst
US5786293A (en) * 1996-06-17 1998-07-28 Shell Oil Company Process for presulfiding hydrocarbon processing catalysts
US6663768B1 (en) * 1998-03-06 2003-12-16 Chevron U.S.A. Inc. Preparing a HGH viscosity index, low branch index dewaxed
GB2388611B (en) * 2001-05-11 2004-05-26 Chevron Usa Inc Co-hydroprocessing of hydrocarbon synthesis products and crude oil fractions
EP1559769A1 (en) * 2003-12-19 2005-08-03 Shell Internationale Researchmaatschappij B.V. Process to prepare base oils having different viscosity index

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