PL445249A1 - Bifunctional catalyst for the synthesis of dimethyl ether by a single-step method, method for obtaining a bifunctional catalyst and its use - Google Patents
Bifunctional catalyst for the synthesis of dimethyl ether by a single-step method, method for obtaining a bifunctional catalyst and its useInfo
- Publication number
- PL445249A1 PL445249A1 PL445249A PL44524923A PL445249A1 PL 445249 A1 PL445249 A1 PL 445249A1 PL 445249 A PL445249 A PL 445249A PL 44524923 A PL44524923 A PL 44524923A PL 445249 A1 PL445249 A1 PL 445249A1
- Authority
- PL
- Poland
- Prior art keywords
- oxide
- bifunctional catalyst
- synthesis
- obtaining
- dimethyl ether
- Prior art date
Links
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 title abstract 4
- 239000003054 catalyst Substances 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 4
- 230000001588 bifunctional effect Effects 0.000 title abstract 3
- 230000015572 biosynthetic process Effects 0.000 title abstract 2
- 238000003786 synthesis reaction Methods 0.000 title abstract 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 abstract 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 4
- 230000018044 dehydration Effects 0.000 abstract 3
- 238000006297 dehydration reaction Methods 0.000 abstract 3
- 229910052751 metal Inorganic materials 0.000 abstract 3
- 239000002184 metal Substances 0.000 abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 abstract 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052814 silicon oxide Inorganic materials 0.000 abstract 2
- 239000011787 zinc oxide Substances 0.000 abstract 2
- 239000005751 Copper oxide Substances 0.000 abstract 1
- 229910017278 MnxOy Inorganic materials 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 229910000431 copper oxide Inorganic materials 0.000 abstract 1
- 229910052593 corundum Inorganic materials 0.000 abstract 1
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 1
Classifications
-
- 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
-
- 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
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—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
- B01J23/80—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 zinc, cadmium or mercury
-
- 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
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—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
- 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
- B01J23/889—Manganese, technetium or rhenium
-
- 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
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
- B01J29/72—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65 containing iron group metals, noble metals or copper
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/15—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively
- C07C29/151—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases
- C07C29/153—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/09—Preparation of ethers by dehydration of compounds containing hydroxy groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
Pierwszym przedmiotem zgłoszenia jest bifunkcyjny katalizator zawierający komponent metaliczny i komponent dehydratacyjny do syntezy eteru dimetylowego metodą jednoetapową, charakteryzujący się tym, że stosunek wagowy komponentu metalicznego do komponentu dehydratacyjnego wynosi od 1:1 do 1:3 i komponent metaliczny zawiera tlenek miedzi (II), tlenek cynku, tlenek glinu oraz tlenek manganu, gdzie stosunek molowy tlenków CuO:ZnO:Al2O3:MnxOy wynosi 4-6:2-4:0,25-0,75:0,25-0,75 i komponent dehydratacyjny zawiera tlenek krzemu i tlenek glinu w stosunku 100:1 do 1:100 oraz tlenek miedzi w ilości od 1% - 50% molowych względem tlenku krzemu. Zgłoszenie obejmuje również sposób otrzymywania katalizatora oraz jego zastosowanie.The first subject of the application is a bifunctional catalyst containing a metal component and a dehydration component for the synthesis of dimethyl ether by a single-stage method, characterized in that the weight ratio of the metal component to the dehydration component is from 1:1 to 1:3 and the metal component contains copper (II) oxide, zinc oxide, aluminum oxide and manganese oxide, where the molar ratio of CuO:ZnO:Al2O3:MnxOy oxides is 4-6:2-4:0.25-0.75:0.25-0.75 and the dehydration component contains silicon oxide and aluminum oxide in a ratio of 100:1 to 1:100 and copper oxide in an amount of 1% - 50% by moles relative to silicon oxide. The application also covers a method of obtaining the catalyst and its use.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL445249A PL445249A1 (en) | 2023-06-16 | 2023-06-16 | Bifunctional catalyst for the synthesis of dimethyl ether by a single-step method, method for obtaining a bifunctional catalyst and its use |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL445249A PL445249A1 (en) | 2023-06-16 | 2023-06-16 | Bifunctional catalyst for the synthesis of dimethyl ether by a single-step method, method for obtaining a bifunctional catalyst and its use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL445249A1 true PL445249A1 (en) | 2024-12-23 |
Family
ID=94644277
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL445249A PL445249A1 (en) | 2023-06-16 | 2023-06-16 | Bifunctional catalyst for the synthesis of dimethyl ether by a single-step method, method for obtaining a bifunctional catalyst and its use |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL445249A1 (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105170179A (en) * | 2015-09-15 | 2015-12-23 | 沈阳化工大学 | Method for preparing dimethyl ether mesoporous catalyst by hydrogenating carbon dioxide |
| US20160318006A1 (en) * | 2013-12-16 | 2016-11-03 | Cool Planet Energy Systems, Inc. | Low Pressure Dimethyl Ether Synthesis Catalyst |
| US11452995B2 (en) * | 2017-12-20 | 2022-09-27 | Basf Se | Catalyst and process for preparing dimethyl ether |
-
2023
- 2023-06-16 PL PL445249A patent/PL445249A1/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20160318006A1 (en) * | 2013-12-16 | 2016-11-03 | Cool Planet Energy Systems, Inc. | Low Pressure Dimethyl Ether Synthesis Catalyst |
| CN105170179A (en) * | 2015-09-15 | 2015-12-23 | 沈阳化工大学 | Method for preparing dimethyl ether mesoporous catalyst by hydrogenating carbon dioxide |
| US11452995B2 (en) * | 2017-12-20 | 2022-09-27 | Basf Se | Catalyst and process for preparing dimethyl ether |
Non-Patent Citations (2)
| Title |
|---|
| ATEKA, A., SÁNCHEZ-CONTADOR, M., EREÑA, J., AGUAYO, A. T., & BILBAO, J., CATALYST CONFIGURATION FOR THE DIRECT SYNTHESIS OF DIMETHYL ETHER FROM CO AND CO2 HYDROGENATION ON CUO–ZNO–MNO/SAPO-18 CATALYSTS. REACTION KINETICS, MECHANISMS AND CATALYSIS, (2018), 124(1), 401–418. HTTPS://DOI.ORG/10.1007/S11144-018-1344-X * |
| PALGUNADI, J., YATI, I., & JUNG, K. D., CATALYTIC ACTIVITY OF CU–ZN–AL–MN ADMIXED WITH GAMMA-ALUMINA FOR THE SYNTHESIS OF DME FROM SYNGAS: MANGANESE EFFECT OR JUST METHOD OF PREPARATION?, REACTION KINETICS, MECHANISMS AND CATALYSIS, (2010),101(1), 117–128. DOI:10.1007/S11144-010-0205-Z * |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MY208681A (en) | Catalysts containing copper, zinc oxide, alumina and silica | |
| ATE272605T1 (en) | METHOD FOR PRODUCING AMINES | |
| JPS55158202A (en) | Water-dispersible metal powder composition | |
| NO924807L (en) | LUBRICATING COMPOSITIONS | |
| PL445249A1 (en) | Bifunctional catalyst for the synthesis of dimethyl ether by a single-step method, method for obtaining a bifunctional catalyst and its use | |
| RU93058626A (en) | PIRIDINSULPHONAMID, METHOD FOR ITS PREPARATION AND APPLICATION, INTERMEDIATE PRODUCT FOR ITS SYNTHESIS AND METHOD OF ITS PREPARATION | |
| Larrieu et al. | Theoretical study of nitrous acid electronic spectrum and photofragmentation | |
| RU2015113941A (en) | The method of producing alpha, omega-diiodoperfluoroalkanes | |
| RU2003112977A (en) | SYNTHETIC POROUS CRYSTALLINE MSM-71, ITS SYNTHESIS AND APPLICATION | |
| PL446061A1 (en) | Nanocomposite catalyst for carbon oxide conversion and method for obtaining it | |
| JPS5335124A (en) | Converter | |
| RU2003102481A (en) | METHOD FOR PREPARING THE CATALYST FOR THE CONVERSION OF CARBON OXIDE | |
| PL429375A1 (en) | Alloy catalyst precursor for the synthesis and decomposition of ammonia | |
| KR970012810A (en) | Manufacturing method of soft magnetic ferrite | |
| Fallis et al. | A route to the polyacetylenic C 18-acids containing 1-en-4-yne unsaturation | |
| MX2023005382A (en) | Aldehyde composition. | |
| MD20220006A2 (en) | Trinuclear zinc coordination compound with photoluminescent properties, based on 2,3-dihydroxybenzaldehyde semicarbazone and pivalate anions as coligands | |
| OKAMOTO | Surface States of Cu-ZnO Catalysts and Catalytic Activity for Methanol Synthesis | |
| PL444513A1 (en) | Method of obtaining cement composites doped with deep eutectic mixtures and metal oxides | |
| DEM0001684MA (en) | Feeding device for gas generators | |
| PL441075A1 (en) | Magnetorheological fluid based on metal oxides and method of its preparation | |
| UA132475U (en) | A METHOD OF IMPROVING PIGS 'REPRODUCTIVE ABILITY WITH THE USE OF NANOAKHACHELATES | |
| RU2013106113A (en) | METHOD FOR PRODUCING 1,8- {BIS [(PENT-2,4-DION-3-IL) METHYLSULFANIL]} - 3,6-DIOXOACTANE AND 4,4 '- {BIS [(PENT-2,4-DION-3 -Yl) methylsulfanyl]} - diphenyloxide | |
| Kim et al. | Hydration and Setting Properties of Alkali-free Accelerator for Shotcrete using Aluminum sulfate | |
| PL417163A1 (en) | Method for producing the iron catalyst precursor for synthesis of ammonia |