TWI243708B - Hydrothermally synthesized Mo-V-M-X oxide catalysts for the selective oxidation of hydrocarbons - Google Patents
Hydrothermally synthesized Mo-V-M-X oxide catalysts for the selective oxidation of hydrocarbons Download PDFInfo
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- TWI243708B TWI243708B TW091112636A TW91112636A TWI243708B TW I243708 B TWI243708 B TW I243708B TW 091112636 A TW091112636 A TW 091112636A TW 91112636 A TW91112636 A TW 91112636A TW I243708 B TWI243708 B TW I243708B
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- 239000003054 catalyst Substances 0.000 title claims abstract description 159
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 51
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 6
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- DHRLEVQXOMLTIM-UHFFFAOYSA-N phosphoric acid;trioxomolybdenum Chemical compound O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.OP(O)(O)=O DHRLEVQXOMLTIM-UHFFFAOYSA-N 0.000 description 1
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- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
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- 229960004889 salicylic acid Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
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- JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 description 1
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 229940071536 silver acetate Drugs 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- 229940096017 silver fluoride Drugs 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
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- FJOLTQXXWSRAIX-UHFFFAOYSA-K silver phosphate Chemical compound [Ag+].[Ag+].[Ag+].[O-]P([O-])([O-])=O FJOLTQXXWSRAIX-UHFFFAOYSA-K 0.000 description 1
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- LMEWRZSPCQHBOB-UHFFFAOYSA-M silver;2-hydroxypropanoate Chemical compound [Ag+].CC(O)C([O-])=O LMEWRZSPCQHBOB-UHFFFAOYSA-M 0.000 description 1
- CLDWGXZGFUNWKB-UHFFFAOYSA-M silver;benzoate Chemical compound [Ag+].[O-]C(=O)C1=CC=CC=C1 CLDWGXZGFUNWKB-UHFFFAOYSA-M 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
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- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
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- 239000011593 sulfur Substances 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- LAJZODKXOMJMPK-UHFFFAOYSA-N tellurium dioxide Chemical compound O=[Te]=O LAJZODKXOMJMPK-UHFFFAOYSA-N 0.000 description 1
- SWLJJEFSPJCUBD-UHFFFAOYSA-N tellurium tetrachloride Chemical compound Cl[Te](Cl)(Cl)Cl SWLJJEFSPJCUBD-UHFFFAOYSA-N 0.000 description 1
- ZUUZGQPEQORUEV-UHFFFAOYSA-N tetrahydrate;hydrochloride Chemical compound O.O.O.O.Cl ZUUZGQPEQORUEV-UHFFFAOYSA-N 0.000 description 1
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 description 1
- 229910003452 thorium oxide Inorganic materials 0.000 description 1
- OMDXFCRSKHYDTM-UHFFFAOYSA-J thorium(4+);tetrabromide Chemical compound Br[Th](Br)(Br)Br OMDXFCRSKHYDTM-UHFFFAOYSA-J 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- KBXXFKPVKJZGJG-UHFFFAOYSA-K tribromoiridium;hydrate Chemical compound O.Br[Ir](Br)Br KBXXFKPVKJZGJG-UHFFFAOYSA-K 0.000 description 1
- DANYXEHCMQHDNX-UHFFFAOYSA-K trichloroiridium Chemical compound Cl[Ir](Cl)Cl DANYXEHCMQHDNX-UHFFFAOYSA-K 0.000 description 1
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- 238000009777 vacuum freeze-drying Methods 0.000 description 1
- MSRILKIQRXUYCT-UHFFFAOYSA-M valproate semisodium Chemical compound [Na+].CCCC(C(O)=O)CCC.CCCC(C([O-])=O)CCC MSRILKIQRXUYCT-UHFFFAOYSA-M 0.000 description 1
- 229960000604 valproic acid Drugs 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- UUUGYDOQQLOJQA-UHFFFAOYSA-L vanadyl sulfate Chemical compound [V+2]=O.[O-]S([O-])(=O)=O UUUGYDOQQLOJQA-UHFFFAOYSA-L 0.000 description 1
- 229940041260 vanadyl sulfate Drugs 0.000 description 1
- 229910000352 vanadyl sulfate Inorganic materials 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 150000003746 yttrium Chemical class 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- KVSXXOUZYJZCPY-UHFFFAOYSA-L zinc;4-cyclohexylbutanoate Chemical compound [Zn+2].[O-]C(=O)CCCC1CCCCC1.[O-]C(=O)CCCC1CCCCC1 KVSXXOUZYJZCPY-UHFFFAOYSA-L 0.000 description 1
- MQWLIFWNJWLDCI-UHFFFAOYSA-L zinc;carbonate;hydrate Chemical compound O.[Zn+2].[O-]C([O-])=O MQWLIFWNJWLDCI-UHFFFAOYSA-L 0.000 description 1
Classifications
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- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
- C07C51/252—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
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- 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
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- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
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- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
- B01J27/057—Selenium or tellurium; Compounds thereof
- B01J27/0576—Tellurium; Compounds thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/24—Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/24—Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons
- C07C253/26—Preparation of carboxylic acid nitriles by ammoxidation of hydrocarbons or substituted hydrocarbons containing carbon-to-carbon multiple bonds, e.g. unsaturated aldehydes
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
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- 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
- B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
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- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/08—Heat treatment
- B01J37/10—Heat treatment in the presence of water, e.g. steam
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
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| US29921301P | 2001-06-18 | 2001-06-18 |
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| TW583023B (en) * | 2000-12-22 | 2004-04-11 | Nippon Kayaku Kk | Alkane oxidizing catalyst, method for producing the same and method for producing unsaturated oxygen-containing compound |
| US6919472B2 (en) * | 2001-12-21 | 2005-07-19 | Saudi Basic Industries Corporation | Catalyst compositions for the selective conversion of alkanes to unsaturated carboxylic acids, methods of making and methods of using thereof |
| DE10247784A1 (de) * | 2002-10-14 | 2004-04-22 | Bayer Ag | Ein Katalysator für die Oxidation von Kohlenwasserstoffen zu Epoxiden |
| JP4155034B2 (ja) * | 2003-01-21 | 2008-09-24 | 東亞合成株式会社 | 金属酸化物触媒の製造方法 |
| US8383158B2 (en) * | 2003-04-15 | 2013-02-26 | Abbott Cardiovascular Systems Inc. | Methods and compositions to treat myocardial conditions |
| US20050054869A1 (en) * | 2003-06-06 | 2005-03-10 | Lugmair Claus G. | Mixed metal oxide catalysts for propane and isobutane oxidation and ammoxidation, and methods of preparing same |
| US7642214B2 (en) * | 2003-06-10 | 2010-01-05 | Nippon Kayaku Kabushiki Kaisha | Catalyst for oxidation of alkane, process for preparing thereof and process for producing unsaturated oxygen-containing compound |
| DE102004009985A1 (de) | 2004-03-01 | 2005-09-22 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Magnetische Manipulation von biologischen Proben |
| BRPI0500615B1 (pt) * | 2004-03-10 | 2015-07-14 | Rohm And Haas Company | Catalisador modificado, e, sistema de catalisador modificado |
| US7009075B2 (en) * | 2004-06-30 | 2006-03-07 | Saudi Basic Industries Corporation | Process for the selective conversion of alkanes to unsaturated carboxylic acids |
| US20060122055A1 (en) * | 2004-12-06 | 2006-06-08 | Gaffney Anne M | (Amm)oxidation catalyst and catalytic (amm)oxidation process for conversion of lower alkanes |
| EP1693107A1 (en) | 2005-02-11 | 2006-08-23 | Rohm And Haas Company | Method for preparing mixed-metal oxide catalysts and the catalysts produced thereby |
| US20060183626A1 (en) * | 2005-02-11 | 2006-08-17 | Cavalcanti Fernando Antonio Pe | Process for preparing catalysts and catalysts produced therefrom |
| DE102006018886A1 (de) * | 2006-04-18 | 2007-10-31 | Leibnitz-Institut für Katalyse e.V. an der Universität Rostock | Vanadiumhaltige Mischoxide des Cs(WNb)5O14 - Strukturtyps |
| US7875571B2 (en) * | 2006-09-07 | 2011-01-25 | Rohm And Haas Company | Activated mixed metal oxide oxidation catalysts |
| KR100962082B1 (ko) * | 2008-07-31 | 2010-06-09 | 희성촉매 주식회사 | 수소를 이용한 질소산화물의 환원제거용 촉매 및 이를이용한 질소산화물의 환원제거 방법 |
| WO2010087262A1 (ja) * | 2009-01-30 | 2010-08-05 | 旭化成ケミカルズ株式会社 | シリカ担持触媒の製造方法、及び不飽和カルボン酸又は不飽和ニトリルの製造方法 |
| KR102764897B1 (ko) | 2015-11-16 | 2025-02-07 | 에이치헬리, 엘엘씨 | 에너지 저장 용도, 촉매 용도, 광전지 용도 및 센서 용도를 위한 합성된 표면-관능화된, 산성화 금속 산화물 재료 |
| WO2018093945A1 (en) | 2016-11-15 | 2018-05-24 | Hheli, Llc. | A surface-functionalized, acidified metal oxide material in an acidified electrolyte system or an acidified electrode system |
| CN117727928A (zh) | 2017-04-10 | 2024-03-19 | 氢氦锂有限公司 | 具有新型组分的电池 |
| JP7309619B2 (ja) | 2017-05-17 | 2023-07-18 | ヒーリー，エルエルシー | 酸性化カソードおよびリチウムアノードを有する電池 |
| CA3062617C (en) | 2017-05-17 | 2023-09-19 | HHeLI, LLC | A high capacity battery cell with low active material loading |
| US10978731B2 (en) | 2017-06-21 | 2021-04-13 | HHeLI, LLC | Ultra high capacity performance battery cell |
| WO2019060773A1 (en) | 2017-09-22 | 2019-03-28 | HHeLI, LLC | CONSTRUCTION OF VERY HIGH CAPACITY PERFORMANCE BATTERY ELEMENTS |
| JP7410934B2 (ja) | 2018-09-10 | 2024-01-10 | ヒーリー、エルエルシー | 超大容量高性能電池セルの使用方法 |
| SG11202111125TA (en) | 2019-05-02 | 2021-11-29 | Dow Global Technologies Llc | Process for aldehyde byproduct reduction in acrylic acid production using highly active and selective catalysts |
| US12278342B2 (en) | 2019-06-12 | 2025-04-15 | HHeLI, LLC | Alkaline and acidified metal oxide blended active materials |
| US12401018B2 (en) | 2019-06-12 | 2025-08-26 | HHeLI, LLC | Blended active materials for battery cells |
| US12128386B2 (en) * | 2019-07-18 | 2024-10-29 | Nova Chemicals (International) S.A. | ODH catalyst formulations |
| CN111569924B (zh) * | 2020-04-22 | 2023-08-22 | 中南民族大学 | 氨氧化法制备2,6-二氯苯腈的专用催化剂及其制备方法和用途 |
| CN119776892B (zh) * | 2024-12-31 | 2025-11-21 | 广东工业大学 | 一种碳包覆二氧化铱电解水制氢催化剂及其制备方法和应用 |
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|---|---|---|---|---|
| KR920021498A (ko) * | 1991-05-09 | 1992-12-18 | 에또 다께또시 | 니트릴의 제조 방법 |
| EP0529853B1 (en) * | 1991-08-08 | 1996-02-28 | Mitsubishi Chemical Corporation | Catalyst and process for producing nitriles |
| DE69402567T2 (de) * | 1993-01-28 | 1997-11-27 | Mitsubishi Chem Corp | Methode zur Herstellung einer ungesättigten Carbonsäure |
| JP3500663B2 (ja) | 1993-08-18 | 2004-02-23 | 三菱化学株式会社 | アクリル酸の製造方法 |
| JP2000143244A (ja) | 1998-07-24 | 2000-05-23 | Mitsubishi Chemicals Corp | 複合金属酸化物の製造方法 |
| CN1166452C (zh) * | 1998-08-28 | 2004-09-15 | 旭化成株式会社 | 从丙烷或异丁烷生产丙烯腈或甲基丙烯腈中所使用的氧化催化剂的制备方法 |
| US6043185A (en) * | 1999-04-02 | 2000-03-28 | The Standard Oil Company | Gallium promoted molybdenum vanadium-antimony-oxide based catalyst for selective paraffin ammoxidation |
-
2002
- 2002-06-07 EP EP02253989A patent/EP1270068B1/en not_active Expired - Lifetime
- 2002-06-07 DE DE60210709T patent/DE60210709T2/de not_active Expired - Lifetime
- 2002-06-10 US US10/165,892 patent/US6746983B2/en not_active Expired - Fee Related
- 2002-06-11 TW TW091112636A patent/TWI243708B/zh active
- 2002-06-13 MX MXPA02005875A patent/MXPA02005875A/es unknown
- 2002-06-17 BR BR0202283-4A patent/BR0202283A/pt active Search and Examination
- 2002-06-18 KR KR1020020034031A patent/KR100905958B1/ko not_active Expired - Fee Related
- 2002-06-18 JP JP2002176924A patent/JP2003088758A/ja not_active Ceased
- 2002-06-18 CN CNB02122658XA patent/CN1275694C/zh not_active Expired - Fee Related
-
2004
- 2004-03-23 US US10/806,582 patent/US7074956B2/en not_active Expired - Fee Related
-
2006
- 2006-01-04 US US11/324,909 patent/US20060106244A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| DE60210709T2 (de) | 2007-01-11 |
| US20030004379A1 (en) | 2003-01-02 |
| EP1270068B1 (en) | 2006-04-19 |
| KR100905958B1 (ko) | 2009-07-06 |
| CN1275694C (zh) | 2006-09-20 |
| US20040181084A1 (en) | 2004-09-16 |
| BR0202283A (pt) | 2003-04-22 |
| EP1270068A1 (en) | 2003-01-02 |
| KR20020096982A (ko) | 2002-12-31 |
| US6746983B2 (en) | 2004-06-08 |
| US7074956B2 (en) | 2006-07-11 |
| DE60210709D1 (de) | 2006-05-24 |
| US20060106244A1 (en) | 2006-05-18 |
| CN1395997A (zh) | 2003-02-12 |
| JP2003088758A (ja) | 2003-03-25 |
| MXPA02005875A (es) | 2005-09-08 |
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