CA2444285A1 - Method for preparing hydrogenation purification catalyst - Google Patents
Method for preparing hydrogenation purification catalyst Download PDFInfo
- Publication number
- CA2444285A1 CA2444285A1 CA002444285A CA2444285A CA2444285A1 CA 2444285 A1 CA2444285 A1 CA 2444285A1 CA 002444285 A CA002444285 A CA 002444285A CA 2444285 A CA2444285 A CA 2444285A CA 2444285 A1 CA2444285 A1 CA 2444285A1
- Authority
- CA
- Canada
- Prior art keywords
- pseudo
- boehmite
- less
- producing
- hydrorefining catalyst
- 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.)
- Granted
Links
- 239000003054 catalyst Substances 0.000 title claims abstract 18
- 238000000034 method Methods 0.000 title claims abstract 5
- 238000005984 hydrogenation reaction Methods 0.000 title 1
- 238000000746 purification Methods 0.000 title 1
- 239000011148 porous material Substances 0.000 claims abstract 38
- VXAUWWUXCIMFIM-UHFFFAOYSA-M aluminum;oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Al+3] VXAUWWUXCIMFIM-UHFFFAOYSA-M 0.000 claims abstract 26
- 238000004519 manufacturing process Methods 0.000 claims abstract 15
- 239000000843 powder Substances 0.000 claims abstract 15
- 229910052751 metal Inorganic materials 0.000 claims abstract 10
- 239000002184 metal Substances 0.000 claims abstract 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract 5
- 238000001354 calcination Methods 0.000 claims abstract 4
- 229910052809 inorganic oxide Inorganic materials 0.000 claims abstract 4
- 229910052782 aluminium Inorganic materials 0.000 claims 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 4
- 230000007704 transition Effects 0.000 claims 3
- 230000002378 acidificating effect Effects 0.000 claims 2
- 238000006386 neutralization reaction Methods 0.000 claims 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims 2
- 230000002902 bimodal effect Effects 0.000 abstract 2
Classifications
-
- B01J35/60—
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
- B01J21/04—Alumina
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G45/00—Compounds of manganese
- C01G45/04—Carbonyls
-
- 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
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
- C10G45/04—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
-
- 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
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
- C10G45/04—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
- C10G45/12—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing crystalline alumino-silicates, e.g. molecular sieves
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/24—Chromium, molybdenum or tungsten
- B01J23/28—Molybdenum
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J27/188—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
- B01J27/19—Molybdenum
-
- B01J35/69—
Abstract
A method for producing a hydrorefining catalyst is used to produce the hydrorefining catalyst which contains an inorganic oxide carrier and a hydrogenation-active metal and which has such a bimodal pore characteristic that pores having pore diameters of not more than 50 nm have a pore volume of not less than 0.4 cm3/g, pores having pore diameters of not less than 50 nm have a pore volume of not less than 0.2 cm3/g, and pores having pore diameters of not less than 1000 nm have a pore volume of not more than 0.1 cm3/g. The method comprises the steps of mixing and forming a pseudo-boehmite powder having a dispersibility index of 0.13 to 0.28, and calcinating the formed pseudo-boehmite under a condition in which the pseudo-boehmite is converted into .gamma.-alumina. The hydrorefining catalyst, which has the bimodal pore characteristic, can be produced easily at low cost.
Claims (14)
1. A method for producing a hydrorefining catalyst containing an inorganic oxide carrier and a hydrogenation-active metal in which pores having pore diameters of not more than 50 nm have a pore volume of not less than 0.4 cm3/g, pores having pore diameters of not less than 50 nm have a pore volume of not less than 0.2 cm3/g, and pores having pore diameters of not less than 1000 nm have a pore volume of not more than 0.1 cm3/g, the method comprising the steps of:
mixing and forming a pseudo-boehmite powder having a dispersibility index of 0.13 to 0.28; and calcinating the formed pseudo-boehmite under a condition in which the pseudo-boehmite is converted into .gamma.-alumina.
mixing and forming a pseudo-boehmite powder having a dispersibility index of 0.13 to 0.28; and calcinating the formed pseudo-boehmite under a condition in which the pseudo-boehmite is converted into .gamma.-alumina.
2. The method for producing the hydrorefining catalyst according to claim 1, further comprising the step of allowing the calcinated pseudo-boehmite to contain the hydrogenation-active metal.
3. The method for producing the hydrorefining catalyst according to claim 1, wherein the pseudo-boehmite powder is allowed to contain the hydrogenation-active metal in the step of mixing and forming the pseudo-boehmite powder.
4. The method for producing the hydrorefining catalyst according to any one of claims 1 to 3, wherein a crystallite diameter in a (020) direction of the pseudo-boehmite powder is 2.0 to 3.0 nm, and a crystallite diameter in a (120) direction is 3.2 to 4.8 nm.
5. The method for producing the hydrorefining catalyst according to claim 4, wherein the pseudo-boehmite powder is produced by performing, under a predetermined condition, a neutralization reaction of an acidic aluminum solution and an alkaline aluminum solution.
6. The method for producing the hydrorefining catalyst according to any one of claims 1 to 3, wherein a phase transition temperature of the pseudo-boehmite powder to °-alumina is 1220 to 1240 °C.
7. The method for producing the hydrorefining catalyst according to claim 6, wherein the pseudo-boehmite powder is produced by performing, under a predetermined condition, a neutralization reaction of an acidic aluminum solution and an alkaline aluminum solution.
8. A method for producing a hydrorefining catalyst containing an inorganic oxide carrier and a hydrogenation-active metal in which pores having pore diameters of not more than 50 nm have a pore volume of not less than 0.4 cm3/g, pores having pore diameters of not less than 50 nm have a pore volume of not less than 0.2 cm3/g, and pores having pore diameters of not less than 1000 nm have a pore volume of not more than 0.1 cm3/g, the method comprising the steps of:
mixing and forming a pseudo-boehmite powder in which a crystallite diameter in a (020) direction is 2.0 to 3.0 nm, and a crystallite diameter in a (120) direction is 3.2 to 4.8 nm; and calcinating the formed pseudo-boehmite under a condition in which the pseudo-boehmite is converted into .gamma.-alumina.
mixing and forming a pseudo-boehmite powder in which a crystallite diameter in a (020) direction is 2.0 to 3.0 nm, and a crystallite diameter in a (120) direction is 3.2 to 4.8 nm; and calcinating the formed pseudo-boehmite under a condition in which the pseudo-boehmite is converted into .gamma.-alumina.
9. The method for producing the hydrorefining catalyst according to claim 8, further comprising the step of allowing the calcinated pseudo-boehmite to contain the hydrogenation-active metal.
10. The method for producing the hydrorefining catalyst according to claim 8, wherein the pseudo-boehmite powder is allowed to contain the hydrogenation-active metal in the step of mixing and forming the pseudo-boehmite powder.
11. The method for producing the hydrorefining catalyst according to any one of claims 8 to 10, wherein a phase transition temperature of the pseudo-boehmite powder to .alpha.-alumina is 1220 to 1240 °C.
12. A method for producing a hydrorefining catalyst containing an inorganic oxide carrier and a hydrogenation-active metal in which pores having pore diameters of not more than 50 nm have a pore volume of not less than 0.4 cm3/g, pores having pore diameters of not less than 50 nm have a pore volume of not less than 0.2 cm3/g, and pores having pore diameters of not less than 1000 nm have a pore volume of not more than 0.1 cm3/g, the method comprising the steps of:
mixing and forming a pseudo-boehmite powder which has a phase transition temperature to .alpha.-alumina of 1220 to 1240 °C; and calcinating the formed pseudo-boehmite under a condition in which the pseudo-boehmite is converted into .gamma.-alumina.
mixing and forming a pseudo-boehmite powder which has a phase transition temperature to .alpha.-alumina of 1220 to 1240 °C; and calcinating the formed pseudo-boehmite under a condition in which the pseudo-boehmite is converted into .gamma.-alumina.
13. The method for producing the hydrorefining catalyst according to claim 12, further comprising the step of allowing the calcinated pseudo-boehmite to contain the hydrogenation-active metal.
14. The method for producing the hydrorefining catalyst according to claim 12, wherein the pseudo-boehmite powder is allowed to contain the hydrogenation-active metal in the step of mixing and forming the pseudo-boehmite powder.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2727661A CA2727661C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
CA2727654A CA2727654C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002-28868 | 2002-02-06 | ||
JP2002028868 | 2002-02-06 | ||
PCT/JP2003/001182 WO2003066215A1 (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2727654A Division CA2727654C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
CA2727661A Division CA2727661C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2444285A1 true CA2444285A1 (en) | 2003-08-14 |
CA2444285C CA2444285C (en) | 2011-03-29 |
Family
ID=27677871
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2727661A Expired - Lifetime CA2727661C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
CA2727654A Expired - Lifetime CA2727654C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
CA2444285A Expired - Lifetime CA2444285C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2727661A Expired - Lifetime CA2727661C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
CA2727654A Expired - Lifetime CA2727654C (en) | 2002-02-06 | 2003-02-05 | Method for preparing hydrogenation purification catalyst |
Country Status (7)
Country | Link |
---|---|
US (1) | US6919294B2 (en) |
EP (1) | EP1473082B1 (en) |
JP (2) | JP4537713B2 (en) |
KR (1) | KR100895632B1 (en) |
AU (1) | AU2003207232A1 (en) |
CA (3) | CA2727661C (en) |
WO (1) | WO2003066215A1 (en) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7265075B2 (en) * | 2001-07-10 | 2007-09-04 | Japan Energy Corporation | Hydro-refining catalyst, carrier for use therein and method for production thereof |
CN1942242B (en) * | 2004-03-12 | 2011-07-27 | 圣戈本陶瓷及塑料股份有限公司 | Spray dried alumina for catalyst carrier |
US7560412B2 (en) * | 2004-08-14 | 2009-07-14 | Sud-Chemie Inc. | Fluid/slurry bed cobalt-alumina catalyst made by compounding and spray drying |
AP2358A (en) | 2005-05-09 | 2012-01-30 | Achillion Pharmaceuticals Inc | Thiazole compounds and methods of use. |
US9307925B2 (en) | 2005-06-16 | 2016-04-12 | Aaken Laboratories | Methods and systems for generating electrical property maps of biological structures |
JP4916157B2 (en) * | 2005-10-28 | 2012-04-11 | 日揮触媒化成株式会社 | Alumina support for hydrodemetallation catalyst, production method thereof, and hydrodemetallation catalyst using the same |
US7820587B2 (en) * | 2005-11-28 | 2010-10-26 | Uchicago Argonne, Llc | Porous anodic aluminum oxide membranes for nanofabrication |
CN100577288C (en) * | 2006-09-29 | 2010-01-06 | 中国石油化工股份有限公司 | Hydroactivity protector and its production method |
JP2010528019A (en) | 2007-05-22 | 2010-08-19 | アキリオン ファーマシューティカルズ,インコーポレーテッド | Heteroaryl substituted thiazole |
ES2433220T5 (en) * | 2008-09-10 | 2024-02-12 | Haldor Topsoe As | Hydroconversion process and catalyst |
JP5745960B2 (en) * | 2011-07-11 | 2015-07-08 | 出光興産株式会社 | Method for determination of metals and metal-containing catalysts in heavy oil |
RU2624024C2 (en) | 2011-09-01 | 2017-06-30 | Адванст Рифайнинг Текнолоджиз Ллк | Catalyst carrier and catalysts, obtained on its basis |
CN102989517B (en) * | 2011-09-09 | 2015-07-29 | 中国石油天然气股份有限公司 | Alumina support of bimodal pore size distribution and preparation method thereof |
FR2984180A1 (en) * | 2011-12-20 | 2013-06-21 | IFP Energies Nouvelles | PROCESS FOR PRODUCING SPHEROIDAL ALUMINA PARTICLES |
JP6236647B2 (en) * | 2014-02-26 | 2017-11-29 | 国立研究開発法人産業技術総合研究所 | Alumina particles |
FR3022157B1 (en) | 2014-06-13 | 2017-09-01 | Ifp Energies Now | BIMODAL CATALYST WITH COMALATED ACTIVE PHASE, PROCESS FOR PREPARING THE SAME, AND USE THEREOF IN HYDROTREATMENT OF RESIDUES |
FR3022158B1 (en) | 2014-06-13 | 2018-02-23 | IFP Energies Nouvelles | MESOPOROUS CATALYST OF RESIDUAL HYDROCONVERSION AND METHOD OF PREPARATION |
FR3022159B1 (en) | 2014-06-13 | 2018-04-27 | IFP Energies Nouvelles | MESOPOROUS AND MACROPOROUS CATALYST OF RESIDUAL HYDROCONVERSION AND METHOD OF PREPARATION |
FR3022156B1 (en) | 2014-06-13 | 2018-02-23 | Ifp Energies Now | CATALYST AND MACROPOROUS CATALYST WITH COMALATED ACTIVE PHASE, PROCESS FOR THE PREPARATION THEREOF AND USE THEREOF IN HYDROTREATMENT OF RESIDUES |
EP4049972A1 (en) | 2021-02-26 | 2022-08-31 | Nabaltec AG | Method for the preparation of pseudoboehmite |
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-
2003
- 2003-02-05 EP EP03703186.1A patent/EP1473082B1/en not_active Expired - Lifetime
- 2003-02-05 CA CA2727661A patent/CA2727661C/en not_active Expired - Lifetime
- 2003-02-05 WO PCT/JP2003/001182 patent/WO2003066215A1/en active Application Filing
- 2003-02-05 JP JP2003565633A patent/JP4537713B2/en not_active Expired - Lifetime
- 2003-02-05 KR KR1020037012992A patent/KR100895632B1/en active IP Right Grant
- 2003-02-05 AU AU2003207232A patent/AU2003207232A1/en not_active Abandoned
- 2003-02-05 US US10/474,712 patent/US6919294B2/en not_active Expired - Lifetime
- 2003-02-05 CA CA2727654A patent/CA2727654C/en not_active Expired - Lifetime
- 2003-02-05 CA CA2444285A patent/CA2444285C/en not_active Expired - Lifetime
-
2008
- 2008-10-10 JP JP2008264203A patent/JP5227134B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP5227134B2 (en) | 2013-07-03 |
US20040126315A1 (en) | 2004-07-01 |
US6919294B2 (en) | 2005-07-19 |
EP1473082B1 (en) | 2013-10-09 |
WO2003066215A1 (en) | 2003-08-14 |
CA2727654C (en) | 2014-08-05 |
AU2003207232A1 (en) | 2003-09-02 |
EP1473082A4 (en) | 2007-12-05 |
KR100895632B1 (en) | 2009-05-07 |
JP4537713B2 (en) | 2010-09-08 |
KR20040084634A (en) | 2004-10-06 |
CA2727654A1 (en) | 2003-08-14 |
EP1473082A1 (en) | 2004-11-03 |
JPWO2003066215A1 (en) | 2005-05-26 |
JP2009072777A (en) | 2009-04-09 |
CA2727661A1 (en) | 2003-08-14 |
CA2727661C (en) | 2013-09-10 |
CA2444285C (en) | 2011-03-29 |
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