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Ethanol steam reforming: understanding changes in the activity and stability of Rh/M x O y catalysts as function of the support
We reported herein a systematic investigation on how the nature of the support affected the catalytic performances of Rh nanoparticles. The prepared catalysts were denoted as Rh/MxOy, where M corresponded to Ce, Ti, Si, Zn, and Al, and Rh was Rh3+ reduction to Rh nanoparticles on the surface of oxid...
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Published in: | Journal of materials science 2019-09, Vol.54 (17), p.11400-11416 |
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container_title | Journal of materials science |
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creator | Rodrigues, Thenner S Silva, Felipe A e Candido, Eduardo G Anderson G M da Silva Rafael dos S Geonmonond Camargo, Pedro H C Linardi, Marcelo Fonseca, Fabio C |
description | We reported herein a systematic investigation on how the nature of the support affected the catalytic performances of Rh nanoparticles. The prepared catalysts were denoted as Rh/MxOy, where M corresponded to Ce, Ti, Si, Zn, and Al, and Rh was Rh3+ reduction to Rh nanoparticles on the surface of oxides. This strategy was performed in a single step using urea as a mediator and in the absence of any other stabilizer or capping agent. The Rh nanoparticles displayed relatively similar sizes, shapes, and uniform distribution over the supports, differing only in terms of the nature of the support. This strongly affected the metal–support interaction between Rh nanoparticles and the respective oxides, leading to significant differences in their catalytic performances toward the ethanol steam reforming. Here, not only the catalytic activity (in terms of ethanol conversion) was affected, but both the selectivity and stability were also influenced by the nature of the oxide support. Interestingly, the reaction paths as well as the deactivation profile were completely changed as function of the employed support. Such differences were associated with differences in the oxygen storage, oxygen mobility, and acidity/basicity of the supports. We believe that our results can contribute to the development and understanding of Rh-supported catalysts for the applications toward gas-phase transformations such as the ethanol steam reforming reaction. |
doi_str_mv | 10.1007/s10853-019-03660-z |
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The prepared catalysts were denoted as Rh/MxOy, where M corresponded to Ce, Ti, Si, Zn, and Al, and Rh was Rh3+ reduction to Rh nanoparticles on the surface of oxides. This strategy was performed in a single step using urea as a mediator and in the absence of any other stabilizer or capping agent. The Rh nanoparticles displayed relatively similar sizes, shapes, and uniform distribution over the supports, differing only in terms of the nature of the support. This strongly affected the metal–support interaction between Rh nanoparticles and the respective oxides, leading to significant differences in their catalytic performances toward the ethanol steam reforming. Here, not only the catalytic activity (in terms of ethanol conversion) was affected, but both the selectivity and stability were also influenced by the nature of the oxide support. Interestingly, the reaction paths as well as the deactivation profile were completely changed as function of the employed support. Such differences were associated with differences in the oxygen storage, oxygen mobility, and acidity/basicity of the supports. We believe that our results can contribute to the development and understanding of Rh-supported catalysts for the applications toward gas-phase transformations such as the ethanol steam reforming reaction.</description><identifier>ISSN: 0022-2461</identifier><identifier>EISSN: 1573-4803</identifier><identifier>DOI: 10.1007/s10853-019-03660-z</identifier><language>eng</language><publisher>New York: Springer Nature B.V</publisher><subject>Aluminum ; Basicity ; Catalysts ; Catalytic activity ; Catalytic converters ; Deactivation ; Ethanol ; Materials science ; Nanoparticles ; Phase transitions ; Reforming ; Rhodium ; Selectivity ; Silicon ; Stability ; Titanium ; Zinc</subject><ispartof>Journal of materials science, 2019-09, Vol.54 (17), p.11400-11416</ispartof><rights>Journal of Materials Science is a copyright of Springer, (2019). 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The prepared catalysts were denoted as Rh/MxOy, where M corresponded to Ce, Ti, Si, Zn, and Al, and Rh was Rh3+ reduction to Rh nanoparticles on the surface of oxides. This strategy was performed in a single step using urea as a mediator and in the absence of any other stabilizer or capping agent. The Rh nanoparticles displayed relatively similar sizes, shapes, and uniform distribution over the supports, differing only in terms of the nature of the support. This strongly affected the metal–support interaction between Rh nanoparticles and the respective oxides, leading to significant differences in their catalytic performances toward the ethanol steam reforming. Here, not only the catalytic activity (in terms of ethanol conversion) was affected, but both the selectivity and stability were also influenced by the nature of the oxide support. Interestingly, the reaction paths as well as the deactivation profile were completely changed as function of the employed support. Such differences were associated with differences in the oxygen storage, oxygen mobility, and acidity/basicity of the supports. We believe that our results can contribute to the development and understanding of Rh-supported catalysts for the applications toward gas-phase transformations such as the ethanol steam reforming reaction.</description><subject>Aluminum</subject><subject>Basicity</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Catalytic converters</subject><subject>Deactivation</subject><subject>Ethanol</subject><subject>Materials science</subject><subject>Nanoparticles</subject><subject>Phase transitions</subject><subject>Reforming</subject><subject>Rhodium</subject><subject>Selectivity</subject><subject>Silicon</subject><subject>Stability</subject><subject>Titanium</subject><subject>Zinc</subject><issn>0022-2461</issn><issn>1573-4803</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqNjMFKxDAURYMoWB1_wNUD13FekqadcSsjbkQQ90Omk047dJKal4h146-bgh_g6nK4517GbgXeC8R6SQJXWnEUa46qqpB_n7FC6FrxcoXqnBWIUnJZVuKSXREdEVHXUhTsZxM74_wAFK05QbCtD6feHR4gub0NFI3bZ4QmWwdL0DuInQXTxP6zjxPkOk_Nrh9m8i28dcsX-IJXmKAx0QwTRQJD0CaXN97NzvxAaRx9iAt20ZqB7M1fXrO7p8374zMfg_9IluL26FNwudpKqXW5lrKs1f-sX_zmVwk</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Rodrigues, Thenner S</creator><creator>Silva, Felipe A e</creator><creator>Candido, Eduardo G</creator><creator>Anderson G M da Silva</creator><creator>Rafael dos S Geonmonond</creator><creator>Camargo, Pedro H C</creator><creator>Linardi, Marcelo</creator><creator>Fonseca, Fabio C</creator><general>Springer Nature B.V</general><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>L6V</scope><scope>M7S</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope></search><sort><creationdate>20190901</creationdate><title>Ethanol steam reforming: understanding changes in the activity and stability of Rh/M x O y catalysts as function of the support</title><author>Rodrigues, Thenner S ; 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The prepared catalysts were denoted as Rh/MxOy, where M corresponded to Ce, Ti, Si, Zn, and Al, and Rh was Rh3+ reduction to Rh nanoparticles on the surface of oxides. This strategy was performed in a single step using urea as a mediator and in the absence of any other stabilizer or capping agent. The Rh nanoparticles displayed relatively similar sizes, shapes, and uniform distribution over the supports, differing only in terms of the nature of the support. This strongly affected the metal–support interaction between Rh nanoparticles and the respective oxides, leading to significant differences in their catalytic performances toward the ethanol steam reforming. Here, not only the catalytic activity (in terms of ethanol conversion) was affected, but both the selectivity and stability were also influenced by the nature of the oxide support. Interestingly, the reaction paths as well as the deactivation profile were completely changed as function of the employed support. Such differences were associated with differences in the oxygen storage, oxygen mobility, and acidity/basicity of the supports. We believe that our results can contribute to the development and understanding of Rh-supported catalysts for the applications toward gas-phase transformations such as the ethanol steam reforming reaction.</abstract><cop>New York</cop><pub>Springer Nature B.V</pub><doi>10.1007/s10853-019-03660-z</doi></addata></record> |
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subjects | Aluminum Basicity Catalysts Catalytic activity Catalytic converters Deactivation Ethanol Materials science Nanoparticles Phase transitions Reforming Rhodium Selectivity Silicon Stability Titanium Zinc |
title | Ethanol steam reforming: understanding changes in the activity and stability of Rh/M x O y catalysts as function of the support |
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