Promising PtIr, catalysts for hydrocarbon transformation: Comparison of different preparation methods

PtIr/Al 2O 3 catalysts were prepared adding Ir by successive impregnation (SI) or by organometallic grafting (OG). The OG catalyst (with PtIr active sites) was most active in methylcyclopentane ring opening. Ir–Pt/Al 2O 3 catalysts were prepared by adding Ir to Pt catalysts using two methods: succes...

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Veröffentlicht in:Chinese journal of catalysis 2010-06, Vol.272 (2), p.315-319
Hauptverfasser: Poupin, Christophe, Pirault-Roy, Laurence, Fontaine, Camille La, Tóth, Lajos, Chamam, Mounir, Wootsch, Attila, Paál, Zoltán
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container_end_page 319
container_issue 2
container_start_page 315
container_title Chinese journal of catalysis
container_volume 272
creator Poupin, Christophe
Pirault-Roy, Laurence
Fontaine, Camille La
Tóth, Lajos
Chamam, Mounir
Wootsch, Attila
Paál, Zoltán
description PtIr/Al 2O 3 catalysts were prepared adding Ir by successive impregnation (SI) or by organometallic grafting (OG). The OG catalyst (with PtIr active sites) was most active in methylcyclopentane ring opening. Ir–Pt/Al 2O 3 catalysts were prepared by adding Ir to Pt catalysts using two methods: successive impregnation (SI) or organometallic grafting (OG). These resulted in different structures: with the first method (SI) Pt and Ir sites were separated, whereas bimetallic Pt–Ir sites are created by the second method (OG), as demonstrated also by electron microscopy. We tested the bimetallic catalysts obtained by these two preparation methods using hydrocarbon transformation, particularly the reaction of ring opening of methylcyclopentane (MCP). The OG catalyst shows a very promising behavior in ring opening reaction of MCP, showing high activity and producing ring opening products (ROP) with high selectivities even at high conversion values.
doi_str_mv 10.1016/j.jcat.2010.04.013
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The OG catalyst (with PtIr active sites) was most active in methylcyclopentane ring opening. Ir–Pt/Al 2O 3 catalysts were prepared by adding Ir to Pt catalysts using two methods: successive impregnation (SI) or organometallic grafting (OG). These resulted in different structures: with the first method (SI) Pt and Ir sites were separated, whereas bimetallic Pt–Ir sites are created by the second method (OG), as demonstrated also by electron microscopy. We tested the bimetallic catalysts obtained by these two preparation methods using hydrocarbon transformation, particularly the reaction of ring opening of methylcyclopentane (MCP). 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The OG catalyst (with PtIr active sites) was most active in methylcyclopentane ring opening. Ir–Pt/Al 2O 3 catalysts were prepared by adding Ir to Pt catalysts using two methods: successive impregnation (SI) or organometallic grafting (OG). These resulted in different structures: with the first method (SI) Pt and Ir sites were separated, whereas bimetallic Pt–Ir sites are created by the second method (OG), as demonstrated also by electron microscopy. We tested the bimetallic catalysts obtained by these two preparation methods using hydrocarbon transformation, particularly the reaction of ring opening of methylcyclopentane (MCP). The OG catalyst shows a very promising behavior in ring opening reaction of MCP, showing high activity and producing ring opening products (ROP) with high selectivities even at high conversion values.</description><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemical Sciences</subject><subject>Chemistry</subject><subject>Electron microscopes</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Hydrocarbons</subject><subject>Inorganic chemistry</subject><subject>Material chemistry</subject><subject>Methylcyclopentane ring opening</subject><subject>Organometallic grafting</subject><subject>PtIr</subject><subject>PtIrGe</subject><subject>PtIrSn</subject><subject>Successive impregnation</subject><subject>Theory of reactions, general kinetics. Catalysis. 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Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poupin, Christophe</creatorcontrib><creatorcontrib>Pirault-Roy, Laurence</creatorcontrib><creatorcontrib>Fontaine, Camille La</creatorcontrib><creatorcontrib>Tóth, Lajos</creatorcontrib><creatorcontrib>Chamam, Mounir</creatorcontrib><creatorcontrib>Wootsch, Attila</creatorcontrib><creatorcontrib>Paál, Zoltán</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Chinese journal of catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poupin, Christophe</au><au>Pirault-Roy, Laurence</au><au>Fontaine, Camille La</au><au>Tóth, Lajos</au><au>Chamam, Mounir</au><au>Wootsch, Attila</au><au>Paál, Zoltán</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Promising PtIr, catalysts for hydrocarbon transformation: Comparison of different preparation methods</atitle><jtitle>Chinese journal of catalysis</jtitle><date>2010-06-15</date><risdate>2010</risdate><volume>272</volume><issue>2</issue><spage>315</spage><epage>319</epage><pages>315-319</pages><issn>0021-9517</issn><issn>1872-2067</issn><eissn>1090-2694</eissn><coden>JCTLA5</coden><abstract>PtIr/Al 2O 3 catalysts were prepared adding Ir by successive impregnation (SI) or by organometallic grafting (OG). The OG catalyst (with PtIr active sites) was most active in methylcyclopentane ring opening. Ir–Pt/Al 2O 3 catalysts were prepared by adding Ir to Pt catalysts using two methods: successive impregnation (SI) or organometallic grafting (OG). These resulted in different structures: with the first method (SI) Pt and Ir sites were separated, whereas bimetallic Pt–Ir sites are created by the second method (OG), as demonstrated also by electron microscopy. We tested the bimetallic catalysts obtained by these two preparation methods using hydrocarbon transformation, particularly the reaction of ring opening of methylcyclopentane (MCP). 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subjects Catalysis
Catalysts
Chemical Sciences
Chemistry
Electron microscopes
Exact sciences and technology
General and physical chemistry
Hydrocarbons
Inorganic chemistry
Material chemistry
Methylcyclopentane ring opening
Organometallic grafting
PtIr
PtIrGe
PtIrSn
Successive impregnation
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
title Promising PtIr, catalysts for hydrocarbon transformation: Comparison of different preparation methods
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