Combined Steam and Carbon Dioxide Reforming of Methane on Ni/MgAl₂O₄: Effect of CeO₂ Promoter to Catalytic Performance

The catalytic performance during combined steam and carbon dioxide reforming of methane (SCR) was investigated on Ni/MgAl₂O₄ catalyst promoted with CeO₂. The SCR catalyst was prepared by co-impregnation method using nickel and cerium metal precursors on hydrotalcite-like MgAl₂O₄ support. In terms of...

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Veröffentlicht in:Catalysis letters 2011-02, Vol.141 (2), p.224-234
Hauptverfasser: Baek, Seung-Chan, Bae, Jong-Wook, Cheon, Joo Yeong, Jun, Ki-Won, Lee, Kwan-Young
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Cheon, Joo Yeong
Jun, Ki-Won
Lee, Kwan-Young
description The catalytic performance during combined steam and carbon dioxide reforming of methane (SCR) was investigated on Ni/MgAl₂O₄ catalyst promoted with CeO₂. The SCR catalyst was prepared by co-impregnation method using nickel and cerium metal precursors on hydrotalcite-like MgAl₂O₄ support. In terms of catalytic activity and stability, CeO₂-promoted Ni/MgAl₂O₄ catalyst is superior to Ni-CeO₂/Al₂O₃ or Ni/MgAl₂O₄ catalysts because of high resistance to coke formation and suppressed aggregation of nickel particles. The role of CeO₂ on Ni/MgAl₂O₄ catalyst was elucidated by carrying out the various characterization methods in the viewpoint of the aggregation of nickel particles and metal-support interactions. The observed superior catalytic performance on CeO₂-promoted Ni/MgAl₂O₄ catalyst at the weight ratio of MgO/Al₂O₃ of 3/7 seems to be closely related to high dispersion and low aggregation of active metals due to their strong interaction with the MgAl₂O₄ support and the adjacent contact of Ni and CeO₂ species. The CeO₂ promoter also plays an important role to suppress particle aggregation by forming an appropriate interaction of NiO-CeO₂ as well as Ni-MgAl₂O₄ with the concomitant enhancement of mobile oxygen content. Graphical Abstract The catalytic performance during combined steam and carbon dioxide reforming of methane was investigated on Ni/MgAl₂O₄ catalyst promoted with CeO₂. In terms of catalytic activity and stability, CeO₂-promoted Ni/MgAl₂O₄ catalyst (b) is superior to Ni/MgAl₂O₄ catalyst (a) because of high resistance to coke formation and suppressed aggregation of nickel particles at the following reaction conditions; T = 850 °C, P = 1.0 MPa, CH₄/CO₂/H₂O/N₂ molar ratio of 3/1.2/3/3 and SV = 200,000 mL(CH₄)/gcat/h. [graphic removed]
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The SCR catalyst was prepared by co-impregnation method using nickel and cerium metal precursors on hydrotalcite-like MgAl₂O₄ support. In terms of catalytic activity and stability, CeO₂-promoted Ni/MgAl₂O₄ catalyst is superior to Ni-CeO₂/Al₂O₃ or Ni/MgAl₂O₄ catalysts because of high resistance to coke formation and suppressed aggregation of nickel particles. The role of CeO₂ on Ni/MgAl₂O₄ catalyst was elucidated by carrying out the various characterization methods in the viewpoint of the aggregation of nickel particles and metal-support interactions. The observed superior catalytic performance on CeO₂-promoted Ni/MgAl₂O₄ catalyst at the weight ratio of MgO/Al₂O₃ of 3/7 seems to be closely related to high dispersion and low aggregation of active metals due to their strong interaction with the MgAl₂O₄ support and the adjacent contact of Ni and CeO₂ species. The CeO₂ promoter also plays an important role to suppress particle aggregation by forming an appropriate interaction of NiO-CeO₂ as well as Ni-MgAl₂O₄ with the concomitant enhancement of mobile oxygen content. Graphical Abstract The catalytic performance during combined steam and carbon dioxide reforming of methane was investigated on Ni/MgAl₂O₄ catalyst promoted with CeO₂. In terms of catalytic activity and stability, CeO₂-promoted Ni/MgAl₂O₄ catalyst (b) is superior to Ni/MgAl₂O₄ catalyst (a) because of high resistance to coke formation and suppressed aggregation of nickel particles at the following reaction conditions; T = 850 °C, P = 1.0 MPa, CH₄/CO₂/H₂O/N₂ molar ratio of 3/1.2/3/3 and SV = 200,000 mL(CH₄)/gcat/h. 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The SCR catalyst was prepared by co-impregnation method using nickel and cerium metal precursors on hydrotalcite-like MgAl₂O₄ support. In terms of catalytic activity and stability, CeO₂-promoted Ni/MgAl₂O₄ catalyst is superior to Ni-CeO₂/Al₂O₃ or Ni/MgAl₂O₄ catalysts because of high resistance to coke formation and suppressed aggregation of nickel particles. The role of CeO₂ on Ni/MgAl₂O₄ catalyst was elucidated by carrying out the various characterization methods in the viewpoint of the aggregation of nickel particles and metal-support interactions. The observed superior catalytic performance on CeO₂-promoted Ni/MgAl₂O₄ catalyst at the weight ratio of MgO/Al₂O₃ of 3/7 seems to be closely related to high dispersion and low aggregation of active metals due to their strong interaction with the MgAl₂O₄ support and the adjacent contact of Ni and CeO₂ species. The CeO₂ promoter also plays an important role to suppress particle aggregation by forming an appropriate interaction of NiO-CeO₂ as well as Ni-MgAl₂O₄ with the concomitant enhancement of mobile oxygen content. Graphical Abstract The catalytic performance during combined steam and carbon dioxide reforming of methane was investigated on Ni/MgAl₂O₄ catalyst promoted with CeO₂. In terms of catalytic activity and stability, CeO₂-promoted Ni/MgAl₂O₄ catalyst (b) is superior to Ni/MgAl₂O₄ catalyst (a) because of high resistance to coke formation and suppressed aggregation of nickel particles at the following reaction conditions; T = 850 °C, P = 1.0 MPa, CH₄/CO₂/H₂O/N₂ molar ratio of 3/1.2/3/3 and SV = 200,000 mL(CH₄)/gcat/h. [graphic removed]</description><subject>Agglomeration</subject><subject>Aluminum oxide</subject><subject>Carbon dioxide</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Ceria</subject><subject>Cerium oxides</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Coke</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>High resistance</subject><subject>Hydrotalcite</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Methane</subject><subject>Ni/MgAl₂O</subject><subject>Nickel</subject><subject>Organometallic Chemistry</subject><subject>Oxygen content</subject><subject>Physical Chemistry</subject><subject>Reforming</subject><subject>Selective catalytic reduction</subject><subject>Stability</subject><subject>Steam and carbon dioxide reforming of methane</subject><subject>Strong interactions (field theory)</subject><subject>Synthesis gas (syngas)</subject><subject>Theory of reactions, general kinetics. 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Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baek, Seung-Chan</creatorcontrib><creatorcontrib>Bae, Jong-Wook</creatorcontrib><creatorcontrib>Cheon, Joo Yeong</creatorcontrib><creatorcontrib>Jun, Ki-Won</creatorcontrib><creatorcontrib>Lee, Kwan-Young</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Catalysis letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baek, Seung-Chan</au><au>Bae, Jong-Wook</au><au>Cheon, Joo Yeong</au><au>Jun, Ki-Won</au><au>Lee, Kwan-Young</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined Steam and Carbon Dioxide Reforming of Methane on Ni/MgAl₂O₄: Effect of CeO₂ Promoter to Catalytic Performance</atitle><jtitle>Catalysis letters</jtitle><stitle>Catal Lett</stitle><date>2011-02-01</date><risdate>2011</risdate><volume>141</volume><issue>2</issue><spage>224</spage><epage>234</epage><pages>224-234</pages><issn>1011-372X</issn><eissn>1572-879X</eissn><abstract>The catalytic performance during combined steam and carbon dioxide reforming of methane (SCR) was investigated on Ni/MgAl₂O₄ catalyst promoted with CeO₂. The SCR catalyst was prepared by co-impregnation method using nickel and cerium metal precursors on hydrotalcite-like MgAl₂O₄ support. In terms of catalytic activity and stability, CeO₂-promoted Ni/MgAl₂O₄ catalyst is superior to Ni-CeO₂/Al₂O₃ or Ni/MgAl₂O₄ catalysts because of high resistance to coke formation and suppressed aggregation of nickel particles. The role of CeO₂ on Ni/MgAl₂O₄ catalyst was elucidated by carrying out the various characterization methods in the viewpoint of the aggregation of nickel particles and metal-support interactions. The observed superior catalytic performance on CeO₂-promoted Ni/MgAl₂O₄ catalyst at the weight ratio of MgO/Al₂O₃ of 3/7 seems to be closely related to high dispersion and low aggregation of active metals due to their strong interaction with the MgAl₂O₄ support and the adjacent contact of Ni and CeO₂ species. The CeO₂ promoter also plays an important role to suppress particle aggregation by forming an appropriate interaction of NiO-CeO₂ as well as Ni-MgAl₂O₄ with the concomitant enhancement of mobile oxygen content. Graphical Abstract The catalytic performance during combined steam and carbon dioxide reforming of methane was investigated on Ni/MgAl₂O₄ catalyst promoted with CeO₂. In terms of catalytic activity and stability, CeO₂-promoted Ni/MgAl₂O₄ catalyst (b) is superior to Ni/MgAl₂O₄ catalyst (a) because of high resistance to coke formation and suppressed aggregation of nickel particles at the following reaction conditions; T = 850 °C, P = 1.0 MPa, CH₄/CO₂/H₂O/N₂ molar ratio of 3/1.2/3/3 and SV = 200,000 mL(CH₄)/gcat/h. [graphic removed]</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><doi>10.1007/s10562-010-0483-0</doi><tpages>11</tpages></addata></record>
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subjects Agglomeration
Aluminum oxide
Carbon dioxide
Catalysis
Catalysts
Catalytic activity
Ceria
Cerium oxides
Chemistry
Chemistry and Materials Science
Coke
Exact sciences and technology
General and physical chemistry
High resistance
Hydrotalcite
Industrial Chemistry/Chemical Engineering
Methane
Ni/MgAl₂O
Nickel
Organometallic Chemistry
Oxygen content
Physical Chemistry
Reforming
Selective catalytic reduction
Stability
Steam and carbon dioxide reforming of methane
Strong interactions (field theory)
Synthesis gas (syngas)
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
title Combined Steam and Carbon Dioxide Reforming of Methane on Ni/MgAl₂O₄: Effect of CeO₂ Promoter to Catalytic Performance
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