Structure-performance correlations in the hybrid oxide-supported copper-zinc SAPO-34 catalysts for direct synthesis of dimethyl ether from CO.sub.2
Growing CO.sub.2 emissions lead to global warming, which is currently one of the most challenging environmental phenomena. Direct catalytic hydrogenation to dimethyl ether over hybrid catalysts enables CO.sub.2 utilization, hydrogen and energy storage and produces sustainable fuels and an important...
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Veröffentlicht in: | Journal of materials science 2022-02, Vol.57 (5), p.3268 |
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creator | Navarro-Jaén, Sara Virginie, Mirella Thuriot-Roukos, Joëlle Wojcieszak, Robert Khodakov, Andrei Y |
description | Growing CO.sub.2 emissions lead to global warming, which is currently one of the most challenging environmental phenomena. Direct catalytic hydrogenation to dimethyl ether over hybrid catalysts enables CO.sub.2 utilization, hydrogen and energy storage and produces sustainable fuels and an important platform molecule. In this paper, we evaluated structure-performance correlations in the bifunctional hybrid copper-zinc SAPO-34 catalysts for direct synthesis of dimethyl ether via CO.sub.2 prepared using zirconia, alumina and ceria used as oxide carriers. Higher copper dispersion and higher CO.sub.2 conversion rate were uncovered over the alumina and zirconia supported catalysts followed by ceria supported counterpart. The CO.sub.2 hydrogenation seems to be principally favoured by higher copper dispersion and to a lesser extent depends on the concentration of Bronsted acid sites in the studied catalysts. Because of lower reverse water gas-shift activity, the alumina supported catalyst exhibited a higher dimethyl ether yield compared to the zirconia and ceria supported counterparts. |
doi_str_mv | 10.1007/s10853-022-06890-w |
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Direct catalytic hydrogenation to dimethyl ether over hybrid catalysts enables CO.sub.2 utilization, hydrogen and energy storage and produces sustainable fuels and an important platform molecule. In this paper, we evaluated structure-performance correlations in the bifunctional hybrid copper-zinc SAPO-34 catalysts for direct synthesis of dimethyl ether via CO.sub.2 prepared using zirconia, alumina and ceria used as oxide carriers. Higher copper dispersion and higher CO.sub.2 conversion rate were uncovered over the alumina and zirconia supported catalysts followed by ceria supported counterpart. The CO.sub.2 hydrogenation seems to be principally favoured by higher copper dispersion and to a lesser extent depends on the concentration of Bronsted acid sites in the studied catalysts. 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Direct catalytic hydrogenation to dimethyl ether over hybrid catalysts enables CO.sub.2 utilization, hydrogen and energy storage and produces sustainable fuels and an important platform molecule. In this paper, we evaluated structure-performance correlations in the bifunctional hybrid copper-zinc SAPO-34 catalysts for direct synthesis of dimethyl ether via CO.sub.2 prepared using zirconia, alumina and ceria used as oxide carriers. Higher copper dispersion and higher CO.sub.2 conversion rate were uncovered over the alumina and zirconia supported catalysts followed by ceria supported counterpart. The CO.sub.2 hydrogenation seems to be principally favoured by higher copper dispersion and to a lesser extent depends on the concentration of Bronsted acid sites in the studied catalysts. Because of lower reverse water gas-shift activity, the alumina supported catalyst exhibited a higher dimethyl ether yield compared to the zirconia and ceria supported counterparts.</description><subject>Aluminum oxide</subject><subject>Catalysts</subject><subject>Cerium</subject><subject>Copper</subject><subject>Evaluation</subject><subject>Global temperature changes</subject><subject>Hydrogen</subject><subject>Hydrogenation</subject><subject>Methyl ether</subject><subject>Zirconium oxide</subject><issn>0022-2461</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpVj0tLAzEUhbNQsD7-gKtsXWRMMo90lqX4KBQqtvuSSW7ayMxkSDLY8W_4h43oQrlwL-dwzgcXoVtGM0apuA-MzsucUM4JreY1Je9naEa_JS8qdoEuQ3ijlJaCsxn63EY_qjh6IAN443wnewVYOe-hldG6PmDb43gEfJwabzV2J6uBhHEYnI-gU3RITfJhe4W3i5cNyQusZJTtFGLAiYi19aAiDlOfMMEG7EzyOojHqcVpg8fGuw4vN1kYm4xfo3Mj2wA3v_cK7R4fdstnst48rZaLNTmInBGuKl4aoRtDpeLCcM0KY3iTPqU8b8pCVlybqiorIZRQnNU1UFrkGoBB3Yj8CmU_2INsYW9746KXKo2GzirXg7HJX1Q145TVc5YKd_8KKRPhFA9yDGG_2r7-zX4BbXR6Fw</recordid><startdate>20220201</startdate><enddate>20220201</enddate><creator>Navarro-Jaén, Sara</creator><creator>Virginie, Mirella</creator><creator>Thuriot-Roukos, Joëlle</creator><creator>Wojcieszak, Robert</creator><creator>Khodakov, Andrei Y</creator><general>Springer</general><scope>ISR</scope></search><sort><creationdate>20220201</creationdate><title>Structure-performance correlations in the hybrid oxide-supported copper-zinc SAPO-34 catalysts for direct synthesis of dimethyl ether from CO.sub.2</title><author>Navarro-Jaén, Sara ; Virginie, Mirella ; Thuriot-Roukos, Joëlle ; Wojcieszak, Robert ; Khodakov, Andrei Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g731-2c625f7dbf0ac27f2d14ff2b002023b54a62df665677c7c2199e0043dee1e9b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Aluminum oxide</topic><topic>Catalysts</topic><topic>Cerium</topic><topic>Copper</topic><topic>Evaluation</topic><topic>Global temperature changes</topic><topic>Hydrogen</topic><topic>Hydrogenation</topic><topic>Methyl ether</topic><topic>Zirconium oxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Navarro-Jaén, Sara</creatorcontrib><creatorcontrib>Virginie, Mirella</creatorcontrib><creatorcontrib>Thuriot-Roukos, Joëlle</creatorcontrib><creatorcontrib>Wojcieszak, Robert</creatorcontrib><creatorcontrib>Khodakov, Andrei Y</creatorcontrib><collection>Gale In Context: Science</collection><jtitle>Journal of materials science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Navarro-Jaén, Sara</au><au>Virginie, Mirella</au><au>Thuriot-Roukos, Joëlle</au><au>Wojcieszak, Robert</au><au>Khodakov, Andrei Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure-performance correlations in the hybrid oxide-supported copper-zinc SAPO-34 catalysts for direct synthesis of dimethyl ether from CO.sub.2</atitle><jtitle>Journal of materials science</jtitle><date>2022-02-01</date><risdate>2022</risdate><volume>57</volume><issue>5</issue><spage>3268</spage><pages>3268-</pages><issn>0022-2461</issn><abstract>Growing CO.sub.2 emissions lead to global warming, which is currently one of the most challenging environmental phenomena. Direct catalytic hydrogenation to dimethyl ether over hybrid catalysts enables CO.sub.2 utilization, hydrogen and energy storage and produces sustainable fuels and an important platform molecule. In this paper, we evaluated structure-performance correlations in the bifunctional hybrid copper-zinc SAPO-34 catalysts for direct synthesis of dimethyl ether via CO.sub.2 prepared using zirconia, alumina and ceria used as oxide carriers. Higher copper dispersion and higher CO.sub.2 conversion rate were uncovered over the alumina and zirconia supported catalysts followed by ceria supported counterpart. The CO.sub.2 hydrogenation seems to be principally favoured by higher copper dispersion and to a lesser extent depends on the concentration of Bronsted acid sites in the studied catalysts. Because of lower reverse water gas-shift activity, the alumina supported catalyst exhibited a higher dimethyl ether yield compared to the zirconia and ceria supported counterparts.</abstract><pub>Springer</pub><doi>10.1007/s10853-022-06890-w</doi><tpages>12</tpages></addata></record> |
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subjects | Aluminum oxide Catalysts Cerium Copper Evaluation Global temperature changes Hydrogen Hydrogenation Methyl ether Zirconium oxide |
title | Structure-performance correlations in the hybrid oxide-supported copper-zinc SAPO-34 catalysts for direct synthesis of dimethyl ether from CO.sub.2 |
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