MOF‐derived/zeolite hybrid catalyst for the production of light olefins from CO 2
In this contribution we propose an alternative catalytic system based on MOF derivatives and small pore zeolites for the selective conversion of CO 2 into light olefins, using the lowest metal loadings and highest GHSV reported in literature. The catalyst synthesis involves deriving In−Zr oxides fro...
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Veröffentlicht in: | ChemCatChem 2020-11, Vol.12 (22), p.5750-5758 |
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creator | Martín, Nuria Portillo, Ander Ateka, Ainara Cirujano, Francisco G. Oar‐Arteta, Lide Aguayo, Andrés T. Dusselier, Michiel |
description | In this contribution we propose an alternative catalytic system based on MOF derivatives and small pore zeolites for the selective conversion of CO
2
into light olefins, using the lowest metal loadings and highest GHSV reported in literature. The catalyst synthesis involves deriving In−Zr oxides from MOFs containing these metals in their structure, i. e. (Zr)UiO‐67‐bipy‐In, via direct calcination in the presence of the zeolite, avoiding co‐precipitation, washing and mixing steps. This effectively creates a truly bifunctional In−Zr zeolite catalyst, opposed to physical mixtures of two catalysts using different precursors. The good dispersion and low loadings of the MOF‐derived In−Zr oxide supplemented with the strong acidity of chabazite‐type zeolites allows to couple the activation of CO
2
with C−C coupling, obtaining space time yields of 0.1 mol of CO
2
converted to light olefins per gram of In per hour at 375 °C, under the GHSV conditions employed. |
doi_str_mv | 10.1002/cctc.202001109 |
format | Article |
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2
into light olefins, using the lowest metal loadings and highest GHSV reported in literature. The catalyst synthesis involves deriving In−Zr oxides from MOFs containing these metals in their structure, i. e. (Zr)UiO‐67‐bipy‐In, via direct calcination in the presence of the zeolite, avoiding co‐precipitation, washing and mixing steps. This effectively creates a truly bifunctional In−Zr zeolite catalyst, opposed to physical mixtures of two catalysts using different precursors. The good dispersion and low loadings of the MOF‐derived In−Zr oxide supplemented with the strong acidity of chabazite‐type zeolites allows to couple the activation of CO
2
with C−C coupling, obtaining space time yields of 0.1 mol of CO
2
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2
into light olefins, using the lowest metal loadings and highest GHSV reported in literature. The catalyst synthesis involves deriving In−Zr oxides from MOFs containing these metals in their structure, i. e. (Zr)UiO‐67‐bipy‐In, via direct calcination in the presence of the zeolite, avoiding co‐precipitation, washing and mixing steps. This effectively creates a truly bifunctional In−Zr zeolite catalyst, opposed to physical mixtures of two catalysts using different precursors. The good dispersion and low loadings of the MOF‐derived In−Zr oxide supplemented with the strong acidity of chabazite‐type zeolites allows to couple the activation of CO
2
with C−C coupling, obtaining space time yields of 0.1 mol of CO
2
converted to light olefins per gram of In per hour at 375 °C, under the GHSV conditions employed.</description><issn>1867-3880</issn><issn>1867-3899</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNo90LFOwzAUhWELgUQprMx-gaTXceLaI6ooIBV1oHuUXF8To7SubINUJh6BZ-RJUAXqdP7pDB9jtwJKAVDNEDOWFVQAQoA5YxOh1byQ2pjzU2u4ZFcpvQEoI-fNhL08r5c_X9-Wov8gO_ukMPpMfDj00VuOXe7GQ8rchcjzQHwfg33H7MOOB8dH_zpkHkZyfpe4i2HLF2teXbML142Jbv53yjbL-83isVitH54Wd6sCdW0KCUIpVA2oHoiwqh1KqXSv0GmlsbZIjUIS2DfKaNs7Qb1TjTWdBNMYI6es_LvFGFKK5Np99NsuHloB7VGkPYq0JxH5C-JJVew</recordid><startdate>20201119</startdate><enddate>20201119</enddate><creator>Martín, Nuria</creator><creator>Portillo, Ander</creator><creator>Ateka, Ainara</creator><creator>Cirujano, Francisco G.</creator><creator>Oar‐Arteta, Lide</creator><creator>Aguayo, Andrés T.</creator><creator>Dusselier, Michiel</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-2483-6158</orcidid><orcidid>https://orcid.org/0000-0002-3074-2318</orcidid></search><sort><creationdate>20201119</creationdate><title>MOF‐derived/zeolite hybrid catalyst for the production of light olefins from CO 2</title><author>Martín, Nuria ; Portillo, Ander ; Ateka, Ainara ; Cirujano, Francisco G. ; Oar‐Arteta, Lide ; Aguayo, Andrés T. ; Dusselier, Michiel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c849-30166c6506b0eec24fc3368b6cf868c4dce56ce1cb5698dbf1ebf65d9a3095993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martín, Nuria</creatorcontrib><creatorcontrib>Portillo, Ander</creatorcontrib><creatorcontrib>Ateka, Ainara</creatorcontrib><creatorcontrib>Cirujano, Francisco G.</creatorcontrib><creatorcontrib>Oar‐Arteta, Lide</creatorcontrib><creatorcontrib>Aguayo, Andrés T.</creatorcontrib><creatorcontrib>Dusselier, Michiel</creatorcontrib><collection>CrossRef</collection><jtitle>ChemCatChem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martín, Nuria</au><au>Portillo, Ander</au><au>Ateka, Ainara</au><au>Cirujano, Francisco G.</au><au>Oar‐Arteta, Lide</au><au>Aguayo, Andrés T.</au><au>Dusselier, Michiel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MOF‐derived/zeolite hybrid catalyst for the production of light olefins from CO 2</atitle><jtitle>ChemCatChem</jtitle><date>2020-11-19</date><risdate>2020</risdate><volume>12</volume><issue>22</issue><spage>5750</spage><epage>5758</epage><pages>5750-5758</pages><issn>1867-3880</issn><eissn>1867-3899</eissn><abstract>In this contribution we propose an alternative catalytic system based on MOF derivatives and small pore zeolites for the selective conversion of CO
2
into light olefins, using the lowest metal loadings and highest GHSV reported in literature. The catalyst synthesis involves deriving In−Zr oxides from MOFs containing these metals in their structure, i. e. (Zr)UiO‐67‐bipy‐In, via direct calcination in the presence of the zeolite, avoiding co‐precipitation, washing and mixing steps. This effectively creates a truly bifunctional In−Zr zeolite catalyst, opposed to physical mixtures of two catalysts using different precursors. The good dispersion and low loadings of the MOF‐derived In−Zr oxide supplemented with the strong acidity of chabazite‐type zeolites allows to couple the activation of CO
2
with C−C coupling, obtaining space time yields of 0.1 mol of CO
2
converted to light olefins per gram of In per hour at 375 °C, under the GHSV conditions employed.</abstract><doi>10.1002/cctc.202001109</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-2483-6158</orcidid><orcidid>https://orcid.org/0000-0002-3074-2318</orcidid></addata></record> |
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title | MOF‐derived/zeolite hybrid catalyst for the production of light olefins from CO 2 |
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