JP2020514048A5 - - Google Patents
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- Publication number
- JP2020514048A5 JP2020514048A5 JP2019553157A JP2019553157A JP2020514048A5 JP 2020514048 A5 JP2020514048 A5 JP 2020514048A5 JP 2019553157 A JP2019553157 A JP 2019553157A JP 2019553157 A JP2019553157 A JP 2019553157A JP 2020514048 A5 JP2020514048 A5 JP 2020514048A5
- Authority
- JP
- Japan
- Prior art keywords
- supported catalyst
- alkali metal
- aqueous solution
- weight
- cesium
- 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
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- 238000000034 method Methods 0.000 claims description 114
- 239000003054 catalyst Substances 0.000 claims description 74
- 229910021536 Zeolite Inorganic materials 0.000 claims description 56
- 239000010457 zeolite Substances 0.000 claims description 56
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 51
- 229910052783 alkali metal Inorganic materials 0.000 claims description 41
- 150000001340 alkali metals Chemical class 0.000 claims description 37
- 239000007864 aqueous solution Substances 0.000 claims description 32
- 239000002585 base Substances 0.000 claims description 30
- 238000005406 washing Methods 0.000 claims description 21
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 16
- 229910052792 caesium Inorganic materials 0.000 claims description 13
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 10
- 229910052700 potassium Inorganic materials 0.000 claims description 10
- 239000011591 potassium Substances 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 9
- 239000011148 porous material Substances 0.000 claims description 9
- 229910052723 transition metal Inorganic materials 0.000 claims description 8
- 150000003624 transition metals Chemical class 0.000 claims description 8
- 238000004140 cleaning Methods 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 229910052701 rubidium Inorganic materials 0.000 claims description 7
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 claims description 7
- 238000001354 calcination Methods 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 238000002407 reforming Methods 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 5
- -1 alkali metal salt Chemical class 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 239000008367 deionised water Substances 0.000 claims description 3
- 229910021641 deionized water Inorganic materials 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000001103 potassium chloride Substances 0.000 claims description 2
- 235000011164 potassium chloride Nutrition 0.000 claims description 2
- 238000004438 BET method Methods 0.000 claims 3
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 2
- AIYUHDOJVYHVIT-UHFFFAOYSA-M caesium chloride Chemical compound [Cl-].[Cs+] AIYUHDOJVYHVIT-UHFFFAOYSA-M 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- NOWPEMKUZKNSGG-UHFFFAOYSA-N azane;platinum(2+) Chemical compound N.N.N.N.[Pt+2] NOWPEMKUZKNSGG-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- 238000005899 aromatization reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 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 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- CLSUSRZJUQMOHH-UHFFFAOYSA-L platinum dichloride Chemical compound Cl[Pt]Cl CLSUSRZJUQMOHH-UHFFFAOYSA-L 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- VEHXKUNAGOJDJB-UHFFFAOYSA-N (4-formyl-2-methoxyphenyl) 4-methoxybenzoate Chemical compound C1=CC(OC)=CC=C1C(=O)OC1=CC=C(C=O)C=C1OC VEHXKUNAGOJDJB-UHFFFAOYSA-N 0.000 description 1
- KLFRPGNCEJNEKU-FDGPNNRMSA-L (z)-4-oxopent-2-en-2-olate;platinum(2+) Chemical compound [Pt+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O KLFRPGNCEJNEKU-FDGPNNRMSA-L 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910003480 inorganic solid Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- NWAHZABTSDUXMJ-UHFFFAOYSA-N platinum(2+);dinitrate Chemical compound [Pt+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O NWAHZABTSDUXMJ-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15/384,366 | 2016-12-20 | ||
| US15/384,366 US10226761B2 (en) | 2016-12-20 | 2016-12-20 | Aromatization catalyst preparation with alkali metal present during a washing step |
| PCT/US2017/066254 WO2018118604A1 (en) | 2016-12-20 | 2017-12-14 | Aromatization catalyst preparation with alkali metal present during a washing step |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020514048A JP2020514048A (ja) | 2020-05-21 |
| JP2020514048A5 true JP2020514048A5 (enExample) | 2021-01-28 |
| JP7101190B2 JP7101190B2 (ja) | 2022-07-14 |
Family
ID=60991534
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019553157A Active JP7101190B2 (ja) | 2016-12-20 | 2017-12-14 | 洗浄工程におけるアルカリ金属存在下での芳香族化触媒の製造 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US10226761B2 (enExample) |
| EP (2) | EP3718631A1 (enExample) |
| JP (1) | JP7101190B2 (enExample) |
| KR (2) | KR20190091463A (enExample) |
| RU (1) | RU2725671C1 (enExample) |
| SA (2) | SA519402130B1 (enExample) |
| WO (1) | WO2018118604A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11260376B2 (en) | 2016-12-21 | 2022-03-01 | Chevron Phillips Chemical Company Lp | Methods of preparing an aromatization catalyst |
| US10487025B2 (en) * | 2016-12-21 | 2019-11-26 | Chevron Phillips Chemical Company Lp | Methods of preparing an aromatization catalyst |
| CN110152719A (zh) * | 2019-04-22 | 2019-08-23 | 中海油天津化工研究设计院有限公司 | 一种以海绵铂为铂源制备Pt/KL链烷烃芳构化催化剂的方法 |
| EP4182077A1 (en) * | 2020-07-17 | 2023-05-24 | Chevron Phillips Chemical Company Lp | Aromatization catalyst activity and selectivity improvement with alcohol addition during catalyst preparation |
| US11529617B2 (en) | 2020-08-12 | 2022-12-20 | Chevron Phillips Chemical Company, Lp | Catalyst supports and catalyst systems and methods |
| FR3143385A1 (fr) | 2022-12-19 | 2024-06-21 | IFP Energies Nouvelles | Catalyseur d’aromatisation a haute teneur en zeolithe kl |
| US12473498B2 (en) | 2023-04-10 | 2025-11-18 | Chevron Phillips Chemical Company Lp | In-reactor activation of a high chloride aromatization catalyst |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2323664A1 (fr) * | 1975-09-10 | 1977-04-08 | Erap | Procede de deshydrocyclisation d'hydrocarbures aliphatiques |
| US4448891A (en) * | 1982-09-28 | 1984-05-15 | Exxon Research & Engineering Co. | Zeolite L catalyst for reforming |
| US4456527A (en) | 1982-10-20 | 1984-06-26 | Chevron Research Company | Hydrocarbon conversion process |
| DE3590575T1 (de) | 1984-11-08 | 1986-11-20 | Chevron Research Co., San Francisco, Calif. | Verjüngung eines entaktivierten Katalysators |
| US4681865A (en) | 1985-05-07 | 1987-07-21 | Research Association For Utilization Of Light Oil | Catalyst for the production of aromatic hydrocarbons |
| JPS6257653A (ja) * | 1985-05-07 | 1987-03-13 | Res Assoc Util Of Light Oil | 芳香族製造用触媒およびこれを用いる芳香族炭化水素の製造方法 |
| US4678764A (en) | 1985-11-21 | 1987-07-07 | Mobil Oil Corporation | Reactivation of noble metal-zeolite catalysts |
| US5196631A (en) | 1986-10-04 | 1993-03-23 | Research Association For Utilization Of Light Oil | Catalyst for production of aromatic hydrocarbons and process for production of aromatic hydrocarbons using same |
| US4855269A (en) | 1986-12-19 | 1989-08-08 | Chevron Research Company | Process for regenerating a monofunctional large-pore zeolite catalyst having high selectivity for paraffin dehydrocyclization |
| US4987109A (en) | 1988-10-19 | 1991-01-22 | Exxon Chemical Patents Inc. | Zeolites for reforming catalysts |
| JP2606991B2 (ja) | 1991-10-03 | 1997-05-07 | 出光興産株式会社 | 失活触媒の再生方法 |
| US5401386A (en) | 1992-07-24 | 1995-03-28 | Chevron Research And Technology Company | Reforming process for producing high-purity benzene |
| WO1994009878A1 (en) | 1992-10-28 | 1994-05-11 | Chevron Chemical Company | High purity benzene production using extractive distillation |
| US5389235A (en) | 1992-12-02 | 1995-02-14 | Uop | Catalytic reaction zone for sulfur contaminant sensitive catalyst |
| JP3409352B2 (ja) * | 1993-03-01 | 2003-05-26 | 東ソー株式会社 | 芳香族化合物の製造方法 |
| US5705726A (en) * | 1994-11-18 | 1998-01-06 | Mobil Oil Corporation | Xylene isomerization on separate reactors |
| RU2223818C2 (ru) * | 1997-06-12 | 2004-02-20 | Идемицу Козан Ко., Лтд. | Галогенсодержащий катализатор и способ его получения |
| WO1998056502A1 (fr) | 1997-06-12 | 1998-12-17 | Idemitsu Kosan Co., Ltd. | Catalyseur contenant un halogene et procede de fabrication |
| US6812180B2 (en) | 1997-12-10 | 2004-11-02 | Idemitsu Kosan Co., Ltd. | Method for preparing catalyst |
| US6190539B1 (en) | 1998-01-08 | 2001-02-20 | Chevron Chemical Company Llc | Reforming using a bound halided zeolite catalyst |
| US6207042B1 (en) | 1998-01-08 | 2001-03-27 | Chevron Chemical Company Llc | Reforming using a bound halided zeolite catalyst |
| US6406614B1 (en) | 1999-12-22 | 2002-06-18 | Phillips Petroleum Company | Method for zeolite platinization |
| US7153801B2 (en) | 2003-06-18 | 2006-12-26 | Chevron Phillips Chemical Company Lp | Aromatization catalyst and methods of making and using same |
| US7932425B2 (en) | 2006-07-28 | 2011-04-26 | Chevron Phillips Chemical Company Lp | Method of enhancing an aromatization catalyst |
| US8993468B2 (en) * | 2007-05-24 | 2015-03-31 | Saudi Basic Industries Corporation | Catalyst for conversion of hydrocarbons, process of making and process of using thereof—Ge zeolites |
| US9221723B2 (en) | 2007-05-24 | 2015-12-29 | Saudi Basic Industries Corporation | Catalyst for conversion of hydrocarbons, process of making and process of using thereof—incorporation-1 |
| US8263518B2 (en) | 2007-12-13 | 2012-09-11 | Chevron Phillips Chemical Company Lp | Catalyst having an improved crush strength and methods of making and using same |
| US8664145B2 (en) | 2008-12-23 | 2014-03-04 | Chevron Phillips Chemical Company Lp | Methods of preparing an aromatization catalyst |
| US8835341B2 (en) | 2011-09-07 | 2014-09-16 | Chevron Phillips Chemical Company Lp | Processed support and methods of making and using same |
| RU2549836C1 (ru) * | 2014-02-18 | 2015-04-27 | Открытое акционерное общество "Нефтяная компания "Роснефть" | Способ получения катализатора циклизации нормальных алканов |
| EP3509747A1 (en) * | 2016-09-08 | 2019-07-17 | Chevron Phillips Chemical Company LP | Acid aromatization catalyst with improved activity and stability |
| US10118167B2 (en) | 2016-12-20 | 2018-11-06 | Chevron Phillips Chemical Company Lp | Methods for regenerating sulfur-contaminated aromatization catalysts |
-
2016
- 2016-12-20 US US15/384,366 patent/US10226761B2/en active Active
-
2017
- 2017-12-14 RU RU2019118883A patent/RU2725671C1/ru active
- 2017-12-14 KR KR1020197017577A patent/KR20190091463A/ko not_active Ceased
- 2017-12-14 JP JP2019553157A patent/JP7101190B2/ja active Active
- 2017-12-14 EP EP20176073.3A patent/EP3718631A1/en not_active Withdrawn
- 2017-12-14 EP EP17829781.8A patent/EP3554698A1/en not_active Ceased
- 2017-12-14 WO PCT/US2017/066254 patent/WO2018118604A1/en not_active Ceased
- 2017-12-14 KR KR1020227041899A patent/KR102622547B1/ko active Active
-
2019
- 2019-01-18 US US16/251,196 patent/US11141718B2/en active Active
- 2019-06-18 SA SA519402130A patent/SA519402130B1/ar unknown
- 2019-06-18 SA SA522433232A patent/SA522433232B1/ar unknown
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