Aqueous-phase reforming of Fischer-Tropsch alcohols over nickel-based catalysts to produce hydrogen: Product distribution and reaction pathways

[Display omitted] •The alcohols in Fischer-Tropsch derived wastewaters can converted into valuable products through catalytic aqueous-phase reforming (APR).•Hydrogen was one of the main products in the APR of C1-C3 alcohols over Ni-based catalysts that allowed alcohol conversions up to 60%.•Copper d...

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Veröffentlicht in:Applied catalysis. A, General General, 2018-10, Vol.567, p.112-121
Hauptverfasser: Coronado, Irene, Pitínová, Martina, Karinen, Reetta, Reinikainen, Matti, Puurunen, Riikka L., Lehtonen, Juha
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container_end_page 121
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container_start_page 112
container_title Applied catalysis. A, General
container_volume 567
creator Coronado, Irene
Pitínová, Martina
Karinen, Reetta
Reinikainen, Matti
Puurunen, Riikka L.
Lehtonen, Juha
description [Display omitted] •The alcohols in Fischer-Tropsch derived wastewaters can converted into valuable products through catalytic aqueous-phase reforming (APR).•Hydrogen was one of the main products in the APR of C1-C3 alcohols over Ni-based catalysts that allowed alcohol conversions up to 60%.•Copper doping improved the stability of a nickel-copper catalyst; however, it limited the hydrogen yield.•The alcohol chain-length, the location of the hydroxyl group in the alcohol and the catalysts have a strong effect on the on the reaction pathway. Catalytic aqueous-phase reforming (APR) can be applied to process the organic compounds in the water fractions derived from the Fischer-Tropsch (FT) synthesis. This work aimed at finding an active nickel-based catalyst to convert organic compounds typically found in FT-derived waters, such as alcohols, into hydrogen. In addition, this work aimed at proposing potential reaction pathways that explain the product distribution resulting from the APR of C1–C3 alcohols. Solutions with 5% mass fraction of either methanol, ethanol, propan-1-ol or propan-2-ol in water were processed in APR at 230 °C and 3.2 MPa over different nickel-based catalysts in a continuous packed-bed reactor. Methanol was successfully reformed into hydrogen and carbon monoxide with conversions up to 60%. The conversion of C2–C3 alcohols achieved values in the range of 12% to 55%. The results obtained in the APR of C2–C3 alcohols suggest that in addition to reforming to hydrogen and carbon monoxide, the alcohols underwent dehydrogenation and decarbonylation. The most stable catalyst, nickel-copper supported on ceria-zirconia, reached feedstock conversions between 20% and 60% and high hydrogen selectivity. Monometallic nickel supported on ceria-zirconia catalysts reached higher H2 yields; however, the yield of side products, such as alkanes, was also higher over the monometallic catalysts. Accordingly, ceria-zirconia nickel-based supported catalysts constitute suitable candidates to process the alcohols in the water fractions derived from the FT synthesis.
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Catalytic aqueous-phase reforming (APR) can be applied to process the organic compounds in the water fractions derived from the Fischer-Tropsch (FT) synthesis. This work aimed at finding an active nickel-based catalyst to convert organic compounds typically found in FT-derived waters, such as alcohols, into hydrogen. In addition, this work aimed at proposing potential reaction pathways that explain the product distribution resulting from the APR of C1–C3 alcohols. Solutions with 5% mass fraction of either methanol, ethanol, propan-1-ol or propan-2-ol in water were processed in APR at 230 °C and 3.2 MPa over different nickel-based catalysts in a continuous packed-bed reactor. Methanol was successfully reformed into hydrogen and carbon monoxide with conversions up to 60%. The conversion of C2–C3 alcohols achieved values in the range of 12% to 55%. The results obtained in the APR of C2–C3 alcohols suggest that in addition to reforming to hydrogen and carbon monoxide, the alcohols underwent dehydrogenation and decarbonylation. The most stable catalyst, nickel-copper supported on ceria-zirconia, reached feedstock conversions between 20% and 60% and high hydrogen selectivity. Monometallic nickel supported on ceria-zirconia catalysts reached higher H2 yields; however, the yield of side products, such as alkanes, was also higher over the monometallic catalysts. 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A, General</title><description>[Display omitted] •The alcohols in Fischer-Tropsch derived wastewaters can converted into valuable products through catalytic aqueous-phase reforming (APR).•Hydrogen was one of the main products in the APR of C1-C3 alcohols over Ni-based catalysts that allowed alcohol conversions up to 60%.•Copper doping improved the stability of a nickel-copper catalyst; however, it limited the hydrogen yield.•The alcohol chain-length, the location of the hydroxyl group in the alcohol and the catalysts have a strong effect on the on the reaction pathway. Catalytic aqueous-phase reforming (APR) can be applied to process the organic compounds in the water fractions derived from the Fischer-Tropsch (FT) synthesis. This work aimed at finding an active nickel-based catalyst to convert organic compounds typically found in FT-derived waters, such as alcohols, into hydrogen. In addition, this work aimed at proposing potential reaction pathways that explain the product distribution resulting from the APR of C1–C3 alcohols. Solutions with 5% mass fraction of either methanol, ethanol, propan-1-ol or propan-2-ol in water were processed in APR at 230 °C and 3.2 MPa over different nickel-based catalysts in a continuous packed-bed reactor. Methanol was successfully reformed into hydrogen and carbon monoxide with conversions up to 60%. The conversion of C2–C3 alcohols achieved values in the range of 12% to 55%. The results obtained in the APR of C2–C3 alcohols suggest that in addition to reforming to hydrogen and carbon monoxide, the alcohols underwent dehydrogenation and decarbonylation. The most stable catalyst, nickel-copper supported on ceria-zirconia, reached feedstock conversions between 20% and 60% and high hydrogen selectivity. Monometallic nickel supported on ceria-zirconia catalysts reached higher H2 yields; however, the yield of side products, such as alkanes, was also higher over the monometallic catalysts. Accordingly, ceria-zirconia nickel-based supported catalysts constitute suitable candidates to process the alcohols in the water fractions derived from the FT synthesis.</description><subject>Alcohol</subject><subject>Alcohols</subject><subject>Alkanes</subject><subject>Aqueous-phase reforming</subject><subject>Carbon monoxide</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Cerium oxides</subject><subject>Chemical synthesis</subject><subject>Copper converters</subject><subject>Dehydrogenation</subject><subject>Ethanol</subject><subject>Fischer-Tropsch water fraction</subject><subject>Hydrogen</subject><subject>Hydrogen storage</subject><subject>Methanol</subject><subject>Nickel</subject><subject>Nickel-based catalysts</subject><subject>Organic compounds</subject><subject>Reforming</subject><subject>Selectivity</subject><subject>Zirconium dioxide</subject><issn>0926-860X</issn><issn>1873-3875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kMtO5DAQRa0RSNPA_MEsLLFOxo_ESWaBhBAMSEiwAImd5dhl4p4QB9tp1F_BL-OmWbOqh-rWrToI_aakpISKP-tSzVolVTJC25J0JaH8B1rRtuEFb5v6AK1Ix0TRCvL0Ex3FuCaEsKqrV-j9_HUBv8RiHlQEHMD68OKmZ-wtvnJRDxCKh-DnnGE1aj_4MWK_gYAnp__DWPRZZvDOfdzGFHHyeA7eLBrwsDXBP8P0F99_dhI2Lqbg-iU5P2E1meyn9GcxqzS8qW08QYdWjRF-fcVj9Hh1-XBxXdze_bu5OL8tdEWbVDDb8r5uLIVKCKKqtle9tbo2VjPNuSBW9VQLaBhUDe9AVFXd1z23rQBTG-DH6HS_Nx-bCcQk134JU7aUjHLGWMcIy1PVfkoHH2OGI-fgXlTYSkrkDr1cyz16uUMvSScz-iw728sgf7BxEGTUDiYNxgXQSRrvvl_wATVTkzc</recordid><startdate>20181025</startdate><enddate>20181025</enddate><creator>Coronado, Irene</creator><creator>Pitínová, Martina</creator><creator>Karinen, Reetta</creator><creator>Reinikainen, Matti</creator><creator>Puurunen, Riikka L.</creator><creator>Lehtonen, Juha</creator><general>Elsevier B.V</general><general>Elsevier Science SA</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20181025</creationdate><title>Aqueous-phase reforming of Fischer-Tropsch alcohols over nickel-based catalysts to produce hydrogen: Product distribution and reaction pathways</title><author>Coronado, Irene ; Pitínová, Martina ; Karinen, Reetta ; Reinikainen, Matti ; Puurunen, Riikka L. ; Lehtonen, Juha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-2f83b57f1e4660a48babffc5dfc2c3360fab1c6e72e4739e6445b5b3f86ed5de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Alcohol</topic><topic>Alcohols</topic><topic>Alkanes</topic><topic>Aqueous-phase reforming</topic><topic>Carbon monoxide</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Cerium oxides</topic><topic>Chemical synthesis</topic><topic>Copper converters</topic><topic>Dehydrogenation</topic><topic>Ethanol</topic><topic>Fischer-Tropsch water fraction</topic><topic>Hydrogen</topic><topic>Hydrogen storage</topic><topic>Methanol</topic><topic>Nickel</topic><topic>Nickel-based catalysts</topic><topic>Organic compounds</topic><topic>Reforming</topic><topic>Selectivity</topic><topic>Zirconium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Coronado, Irene</creatorcontrib><creatorcontrib>Pitínová, Martina</creatorcontrib><creatorcontrib>Karinen, Reetta</creatorcontrib><creatorcontrib>Reinikainen, Matti</creatorcontrib><creatorcontrib>Puurunen, Riikka L.</creatorcontrib><creatorcontrib>Lehtonen, Juha</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied catalysis. A, General</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coronado, Irene</au><au>Pitínová, Martina</au><au>Karinen, Reetta</au><au>Reinikainen, Matti</au><au>Puurunen, Riikka L.</au><au>Lehtonen, Juha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aqueous-phase reforming of Fischer-Tropsch alcohols over nickel-based catalysts to produce hydrogen: Product distribution and reaction pathways</atitle><jtitle>Applied catalysis. A, General</jtitle><date>2018-10-25</date><risdate>2018</risdate><volume>567</volume><spage>112</spage><epage>121</epage><pages>112-121</pages><issn>0926-860X</issn><eissn>1873-3875</eissn><abstract>[Display omitted] •The alcohols in Fischer-Tropsch derived wastewaters can converted into valuable products through catalytic aqueous-phase reforming (APR).•Hydrogen was one of the main products in the APR of C1-C3 alcohols over Ni-based catalysts that allowed alcohol conversions up to 60%.•Copper doping improved the stability of a nickel-copper catalyst; however, it limited the hydrogen yield.•The alcohol chain-length, the location of the hydroxyl group in the alcohol and the catalysts have a strong effect on the on the reaction pathway. Catalytic aqueous-phase reforming (APR) can be applied to process the organic compounds in the water fractions derived from the Fischer-Tropsch (FT) synthesis. This work aimed at finding an active nickel-based catalyst to convert organic compounds typically found in FT-derived waters, such as alcohols, into hydrogen. In addition, this work aimed at proposing potential reaction pathways that explain the product distribution resulting from the APR of C1–C3 alcohols. Solutions with 5% mass fraction of either methanol, ethanol, propan-1-ol or propan-2-ol in water were processed in APR at 230 °C and 3.2 MPa over different nickel-based catalysts in a continuous packed-bed reactor. Methanol was successfully reformed into hydrogen and carbon monoxide with conversions up to 60%. The conversion of C2–C3 alcohols achieved values in the range of 12% to 55%. The results obtained in the APR of C2–C3 alcohols suggest that in addition to reforming to hydrogen and carbon monoxide, the alcohols underwent dehydrogenation and decarbonylation. The most stable catalyst, nickel-copper supported on ceria-zirconia, reached feedstock conversions between 20% and 60% and high hydrogen selectivity. Monometallic nickel supported on ceria-zirconia catalysts reached higher H2 yields; however, the yield of side products, such as alkanes, was also higher over the monometallic catalysts. Accordingly, ceria-zirconia nickel-based supported catalysts constitute suitable candidates to process the alcohols in the water fractions derived from the FT synthesis.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcata.2018.09.013</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Alcohol
Alcohols
Alkanes
Aqueous-phase reforming
Carbon monoxide
Catalysis
Catalysts
Cerium oxides
Chemical synthesis
Copper converters
Dehydrogenation
Ethanol
Fischer-Tropsch water fraction
Hydrogen
Hydrogen storage
Methanol
Nickel
Nickel-based catalysts
Organic compounds
Reforming
Selectivity
Zirconium dioxide
title Aqueous-phase reforming of Fischer-Tropsch alcohols over nickel-based catalysts to produce hydrogen: Product distribution and reaction pathways
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