KR970704859A - Vi 선택성 촉매를 사용하여 윤활유를 제조하는 방법 - Google Patents
Vi 선택성 촉매를 사용하여 윤활유를 제조하는 방법 Download PDFInfo
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- KR970704859A KR970704859A KR1019970700639A KR19970700639A KR970704859A KR 970704859 A KR970704859 A KR 970704859A KR 1019970700639 A KR1019970700639 A KR 1019970700639A KR 19970700639 A KR19970700639 A KR 19970700639A KR 970704859 A KR970704859 A KR 970704859A
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
- C10G47/02—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions characterised by the catalyst used
- C10G47/10—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions characterised by the catalyst used with catalysts deposited on a carrier
- C10G47/12—Inorganic carriers
- C10G47/16—Crystalline alumino-silicate carriers
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
- C10G47/02—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions characterised by the catalyst used
- C10G47/10—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions characterised by the catalyst used with catalysts deposited on a carrier
- C10G47/12—Inorganic carriers
- C10G47/16—Crystalline alumino-silicate carriers
- C10G47/18—Crystalline alumino-silicate carriers the catalyst containing platinum group metals or compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1074—Vacuum distillates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/202—Heteroatoms content, i.e. S, N, O, P
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/30—Physical properties of feedstocks or products
- C10G2300/301—Boiling range
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/40—Characteristics of the process deviating from typical ways of processing
- C10G2300/4018—Spatial velocity, e.g. LHSV, WHSV
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/10—Lubricating oil
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Catalysts (AREA)
- Lubricants (AREA)
Abstract
높은 점도 지수 선택성 및 낮은 오염률을 가진 촉매로 양질의 윤활유를 제조하는 방법을 제공한다. 촉매는 소량의 제올라이트를 함유하며 큰 기공이 상당량있는 것으로 특징되는 기공 크기 분포를 갖는다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (23)
- 수소화분해 조건하에서 제올라이트, 수소화 성분 및 무기 산화물 매트릭스 물질을 포함하고, 기공부피가 약 0.25 내지 약 0.60cm3/g이고 평균기공직경이 약 40Å 내지 약 1OOÅ이며 기공부피의 약 5%이상은 기공직경이 200Å이상인 촉매를 함탄화수소 공급원료와 접촉시키는 것을 특징으로 하는 윤활유 기제 공급원료의 제조방법.
- 제 1 항에 있어서, 평균기공직경이 약 40 내지 80Å인 제조방법.
- 제 1 항에 있어서,기공부피의 약 10%이상은 기공직경이 200Å이상인 제조방법.
- 제 1 항에 있어서, 기공부피의 약 15%이상은 기공직경이 200Å이상인 제조방법.
- 제 4 항에 있어서, 기공부피의 약 1%이상은 기공직경이 1OOOÅ이상인 제조방법.
- 제 1 항에 있어서, 제올라이트가 제올라이트 Y, 탈알루미나화된 제올라이트 Y 및 초안정(ultrastable) 제올라이트 Y인 제조방법.
- 제 1 항에 있어서, 촉매가 제올라이트를 약 1 내지 약 20 중량% 포함하는 제조방법.
- 제 1 항에 있어서, 촉매가 제올라이트를 약 1 내지 약 10중량% 포함하는 제조방법.
- 제 1 항에 있어서, 제올라이트는 Si02/A1203의 몰비가 약 5 내지 약 100인 제조방법.
- 제 1 항에 있어서, 제올라이트는 Si02/A1203의 몰비가 약 5 내지 약 60인 제조방법.
- 제 1 항에 있어서, 촉매가 수소화 성분을 약 0.01 내지 약 45중량% 함유하는 제조방법.
- 제 11 항에 있어서, 수소화성분이 금속 삼산화물로서 텅스텐, 몰리브덴, 및 이의 결합물로부터 선택된 하나이상의 VIB족 금속의 약 5 내지 약 30중량%를 함유하는 제조방법.
- 제 12 항에 있어서, 수소화성분이 금속 일산화물로서 니켈, 코발트 및 이의 결합물로부터 선택된 하나이상의 VⅢ족 염기 금속의 약 1 내지 약 15중량%를 함유하는 제조방법.
- 제 1 항에 있어서, 촉매가 무기 산화물 매트릭스 물질을 약 30 내지 90중량%를 함유하는 제조방법.
- 제 1 항에 있어서, 무기산화물 매트릭스 물질이 알루미나, 실리카 알루미나 및 이의 결합물로부터 선택되는 제조방법.
- 제 1 항에 있어서, 함탄화수소 공급원료가 정상 비점범위가 약 350 내지 590℃인 진공가스오일인 제조방법.
- 제 1 항에 있어서, 함탄화수소 공급원료가 정상 비점 범위가 약 480 내지 650℃인 탈아스팔트화된 잔유인 제조방법.
- 제 1 항에 있어서, 수소화분해 조건이 400℉(204℃) 내지 950℉(510℃)의 온도, 500 내지 3500psig(3550 내지 24200 KPa abs)압력, O.1 내지 20.0의 액체 시간당 공간속도, 및 함탄화수소 공급원료 1 밸럴당 200 내지 20,000 SCF 수소(43-4300 std H2/kg 원료)의 총 수소공급을 포함하는 제조방법.
- 제 1 항에 있어서, 약 10 내지 약 80 중량% 전화가 제공되는 제조방법.
- 제 1 항에 있어서, 윤활유 기제 공급원료중 650℉(343℃)이상 분획이 탈납, 수소화마무리, 또는 이를 결합하여 수행되는 제조방법.
- 제 20 항에 있어서, 탈납이 촉매 탈납 또는 용매탈납 조건에서 수행되는 제조방법.
- 수소화분해 조건하에서 a) 파우자사이트 구조를 갖는 제올라이트가 약 1 내지 10 중량%이고; b) 금속일산화물로서 니켈, 코발트 및 이의 결합물로부터 선택된 하나 이상의 VⅢ족 금속이 약 1 내지 15 중량% 이고 금속 삼산화물로서 텅스텐, 몰리브덴 및 이의 결합물로 선택된 하나이상의 ⅥB 족 금속이 약 5 내지 30중량%이고; c) 무형의 실리카-알루미나 매트릭스 물질이 약 45 내지 75중량%이고; d) 100중량%를 만들기 위하여 충분한 알루미나 지지체 물질을 포함하며, 기공부피가 약 0.25 내지 약 0.45cm3/g이고 평균기공직경이 약 40Å 내지 약 1OOÅ이며 기공부피의 약 5%이상은 기공직경이 200Å이상안 촉매를 정상비점 범위가 약 350 내지 590℃의 진공 가스오일인 함탄화수소 공급원료와 접촉시키는 것을 특징으로 하는 윤활유 기제 공급원료의 제조방법.
- a) 수소화전화 조건하에서 함탄화수소 공급원료를 수소화전화 촉매와 접촉시켜 lOOppm이하의 질소함량을 갖는 수소화처리된 생성물을 제조하고; b) 수소화분해 조건하에서 수소화처리된 생성물을 파우자사이트 구조, 수소화성분, 및 실리카-알루미나 매트릭스 물질를 포함하고, 기공부피가 약 0.25 내지 약 0.60cm3/g이고 평균기공직경이 약 40Å 내지 약 1OOÅ이며 기공부피의 약 5%이상은 기공직경이 200Å이상인 촉매와 접촉시키는 것을 특징으르 하는 윤활유 기제 공급원료의 제조방법.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/284,933 | 1994-08-01 | ||
US08/284,933 US5543035A (en) | 1994-08-01 | 1994-08-01 | Process for producing a high quality lubricating oil using a VI selective catalyst |
PCT/US1995/008018 WO1996004354A1 (en) | 1994-08-01 | 1995-06-20 | Lubricating oil production with vi-selective catalyst |
Publications (1)
Publication Number | Publication Date |
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KR970704859A true KR970704859A (ko) | 1997-09-06 |
Family
ID=23092091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019970700639A KR970704859A (ko) | 1994-08-01 | 1995-06-20 | Vi 선택성 촉매를 사용하여 윤활유를 제조하는 방법 |
Country Status (17)
Country | Link |
---|---|
US (1) | US5543035A (ko) |
EP (1) | EP0775184B2 (ko) |
JP (1) | JPH10503542A (ko) |
KR (1) | KR970704859A (ko) |
CN (1) | CN1046544C (ko) |
AT (1) | ATE281504T1 (ko) |
AU (1) | AU692574B2 (ko) |
BR (1) | BR9508454A (ko) |
CA (1) | CA2194975A1 (ko) |
CZ (1) | CZ4397A3 (ko) |
DE (1) | DE69533716T3 (ko) |
FI (1) | FI970395A (ko) |
HU (1) | HU218039B (ko) |
PL (1) | PL179172B1 (ko) |
RU (1) | RU2140966C1 (ko) |
SK (1) | SK10697A3 (ko) |
WO (1) | WO1996004354A1 (ko) |
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CN102485332B (zh) * | 2010-12-03 | 2013-10-16 | 中国石油天然气股份有限公司 | 一种含分子筛的馏分油加氢脱酸催化剂及其制备和应用 |
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US4699707A (en) * | 1985-09-25 | 1987-10-13 | Union Oil Company Of California | Process for producing lubrication oil of high viscosity index from shale oils |
US4695365A (en) * | 1986-07-31 | 1987-09-22 | Union Oil Company Of California | Hydrocarbon refining process |
US4976848A (en) * | 1988-10-04 | 1990-12-11 | Chevron Research Company | Hydrodemetalation and hydrodesulfurization using a catalyst of specified macroporosity |
US5089463A (en) * | 1988-10-04 | 1992-02-18 | Chevron Research And Technology Company | Hydrodemetalation and hydrodesulfurization catalyst of specified macroporosity |
US5171422A (en) * | 1991-01-11 | 1992-12-15 | Mobil Oil Corporation | Process for producing a high quality lube base stock in increased yield |
US5177047A (en) * | 1991-10-02 | 1993-01-05 | Chevron Research And Technology Company | High activity resid catalyst |
US5215955A (en) * | 1991-10-02 | 1993-06-01 | Chevron Research And Technology Company | Resid catalyst with high metals capacity |
US5393408A (en) * | 1992-04-30 | 1995-02-28 | Chevron Research And Technology Company | Process for the stabilization of lubricating oil base stocks |
US5308472A (en) * | 1992-06-11 | 1994-05-03 | Texaco Inc. | Mild hydrocracking process using catalysts containing dealuminated y-zeolites |
US5342507A (en) * | 1992-06-11 | 1994-08-30 | Texaco Inc. | Mild hydrocracking process employing catalysts containing dealuminated y-zeolites |
CN1046308C (zh) * | 1992-06-19 | 1999-11-10 | 中国石油化工总公司石油化工科学研究院 | 馏分油的深度选择裂化方法 |
US5397456A (en) * | 1993-02-19 | 1995-03-14 | Texaco Inc. | Hydroconversion process employing catalyst with specified pore size distribution |
US5393409A (en) * | 1993-03-08 | 1995-02-28 | Uop | Hydrocracking process using a controlled porosity catalyst |
-
1994
- 1994-08-01 US US08/284,933 patent/US5543035A/en not_active Expired - Lifetime
-
1995
- 1995-06-20 AT AT95924684T patent/ATE281504T1/de not_active IP Right Cessation
- 1995-06-20 EP EP95924684A patent/EP0775184B2/en not_active Expired - Lifetime
- 1995-06-20 AU AU29096/95A patent/AU692574B2/en not_active Expired
- 1995-06-20 PL PL95318267A patent/PL179172B1/pl unknown
- 1995-06-20 JP JP8506488A patent/JPH10503542A/ja not_active Ceased
- 1995-06-20 CN CN95194378A patent/CN1046544C/zh not_active Expired - Fee Related
- 1995-06-20 WO PCT/US1995/008018 patent/WO1996004354A1/en not_active Application Discontinuation
- 1995-06-20 KR KR1019970700639A patent/KR970704859A/ko not_active Application Discontinuation
- 1995-06-20 BR BR9508454A patent/BR9508454A/pt not_active IP Right Cessation
- 1995-06-20 RU RU97103141A patent/RU2140966C1/ru active
- 1995-06-20 DE DE69533716T patent/DE69533716T3/de not_active Expired - Lifetime
- 1995-06-20 SK SK106-97A patent/SK10697A3/sk unknown
- 1995-06-20 CZ CZ9743A patent/CZ4397A3/cs unknown
- 1995-06-20 HU HU9700299A patent/HU218039B/hu not_active IP Right Cessation
- 1995-06-20 CA CA002194975A patent/CA2194975A1/en not_active Abandoned
-
1997
- 1997-01-30 FI FI970395A patent/FI970395A/fi unknown
Also Published As
Publication number | Publication date |
---|---|
CA2194975A1 (en) | 1996-02-15 |
JPH10503542A (ja) | 1998-03-31 |
FI970395A0 (fi) | 1997-01-30 |
US5543035A (en) | 1996-08-06 |
SK10697A3 (en) | 1997-06-04 |
EP0775184B2 (en) | 2012-05-02 |
EP0775184A4 (en) | 1998-11-04 |
AU2909695A (en) | 1996-03-04 |
CN1154130A (zh) | 1997-07-09 |
PL318267A1 (en) | 1997-05-26 |
CZ4397A3 (en) | 1997-06-11 |
CN1046544C (zh) | 1999-11-17 |
FI970395A (fi) | 1997-01-30 |
RU2140966C1 (ru) | 1999-11-10 |
WO1996004354A1 (en) | 1996-02-15 |
EP0775184B1 (en) | 2004-11-03 |
HUT77419A (hu) | 1998-04-28 |
AU692574B2 (en) | 1998-06-11 |
EP0775184A1 (en) | 1997-05-28 |
DE69533716D1 (de) | 2004-12-09 |
DE69533716T3 (de) | 2012-09-20 |
HU218039B (hu) | 2000-05-28 |
ATE281504T1 (de) | 2004-11-15 |
BR9508454A (pt) | 1998-07-14 |
DE69533716T2 (de) | 2006-02-02 |
PL179172B1 (pl) | 2000-07-31 |
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