Gold supported on surface acidity modified Y-type and iron/Y-type zeolite for CO oxidation
A modified method for the preparation of gold in Y-type zeolite was developed in this research. Prior to the preparation of gold catalysts, the surface property of the zeolite (with or without iron) was adjusted in a 1N sodium nitrate solution at pH 6. After drying, the zeolite was added into a chlo...
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description | A modified method for the preparation of gold in Y-type zeolite was developed in this research. Prior to the preparation of gold catalysts, the surface property of the zeolite (with or without iron) was adjusted in a 1N sodium nitrate solution at pH 6. After drying, the zeolite was added into a chloroauric acid solution at pH 6 for gold loading. The resulted catalysts (i.e. Au/Y or Au/Fe/Y) possessed much better activity and stability for CO oxidation than those (i.e. Au/Y(NP) or Au/Fe/Y(NP)) without any surface pretreatment. Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) studies indicate that the gold particles in Au/Y are smaller and more uniformly distributed than those in Au/Y(NP). XPS and temperature-programmed reduction (TPR) results suggest the strong interaction between gold and iron in Y-type zeolite. Furthermore, it was found from this research that Au/Fe/Y had full initial activity for CO oxidation at 0°C and Au/Y required an induction period to reach a comparable activity to Au/Fe/Y. However, the stability of the activated Au/Y was much better than that of Au/Fe/Y. It can be concluded from XPS results that the formation of carbonate-like species, which covered the active sites for CO oxidation, was the main cause for the deactivation of Au/Fe/Y. On the other hand, TEM study suggests that the sintering of nano-gold particles was the main reason for the slight deactivation of Au/Y. |
doi_str_mv | 10.1016/S0926-3373(01)00276-4 |
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Prior to the preparation of gold catalysts, the surface property of the zeolite (with or without iron) was adjusted in a 1N sodium nitrate solution at pH 6. After drying, the zeolite was added into a chloroauric acid solution at pH 6 for gold loading. The resulted catalysts (i.e. Au/Y or Au/Fe/Y) possessed much better activity and stability for CO oxidation than those (i.e. Au/Y(NP) or Au/Fe/Y(NP)) without any surface pretreatment. Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) studies indicate that the gold particles in Au/Y are smaller and more uniformly distributed than those in Au/Y(NP). XPS and temperature-programmed reduction (TPR) results suggest the strong interaction between gold and iron in Y-type zeolite. Furthermore, it was found from this research that Au/Fe/Y had full initial activity for CO oxidation at 0°C and Au/Y required an induction period to reach a comparable activity to Au/Fe/Y. However, the stability of the activated Au/Y was much better than that of Au/Fe/Y. It can be concluded from XPS results that the formation of carbonate-like species, which covered the active sites for CO oxidation, was the main cause for the deactivation of Au/Fe/Y. On the other hand, TEM study suggests that the sintering of nano-gold particles was the main reason for the slight deactivation of Au/Y.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/S0926-3373(01)00276-4</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>CO oxidation ; Gold ; Iron ; Iron oxide ; Surface acidity ; Y-type zeolite</subject><ispartof>Applied catalysis. B, Environmental, 2002-02, Vol.36 (1), p.19-29</ispartof><rights>2002 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-c0e605e10683b7d5d5ce65af4c894f5d7796a162231fe1e5574958f8c49845353</citedby><cites>FETCH-LOGICAL-c474t-c0e605e10683b7d5d5ce65af4c894f5d7796a162231fe1e5574958f8c49845353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0926-3373(01)00276-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids></links><search><creatorcontrib>Lin, Jiunn-Nan</creatorcontrib><creatorcontrib>Chen, Jen-Ho</creatorcontrib><creatorcontrib>Hsiao, Chih-Yang</creatorcontrib><creatorcontrib>Kang, Yih-Ming</creatorcontrib><creatorcontrib>Wan, Ben-Zu</creatorcontrib><title>Gold supported on surface acidity modified Y-type and iron/Y-type zeolite for CO oxidation</title><title>Applied catalysis. B, Environmental</title><description>A modified method for the preparation of gold in Y-type zeolite was developed in this research. Prior to the preparation of gold catalysts, the surface property of the zeolite (with or without iron) was adjusted in a 1N sodium nitrate solution at pH 6. After drying, the zeolite was added into a chloroauric acid solution at pH 6 for gold loading. The resulted catalysts (i.e. Au/Y or Au/Fe/Y) possessed much better activity and stability for CO oxidation than those (i.e. Au/Y(NP) or Au/Fe/Y(NP)) without any surface pretreatment. Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) studies indicate that the gold particles in Au/Y are smaller and more uniformly distributed than those in Au/Y(NP). XPS and temperature-programmed reduction (TPR) results suggest the strong interaction between gold and iron in Y-type zeolite. Furthermore, it was found from this research that Au/Fe/Y had full initial activity for CO oxidation at 0°C and Au/Y required an induction period to reach a comparable activity to Au/Fe/Y. However, the stability of the activated Au/Y was much better than that of Au/Fe/Y. It can be concluded from XPS results that the formation of carbonate-like species, which covered the active sites for CO oxidation, was the main cause for the deactivation of Au/Fe/Y. On the other hand, TEM study suggests that the sintering of nano-gold particles was the main reason for the slight deactivation of Au/Y.</description><subject>CO oxidation</subject><subject>Gold</subject><subject>Iron</subject><subject>Iron oxide</subject><subject>Surface acidity</subject><subject>Y-type zeolite</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLAzEUhYMoWKs_QZiV6GJsMnlMshIpWoVCF-pCN2FMbiAynYxJKtZf7_SBW1eXc-93DtyD0DnB1wQTMXnCqhIlpTW9xOQK46oWJTtAIyJrWlIp6SEa_SHH6CSlDzxQtJIj9DYLrS3Squ9DzGCL0A0iusZA0RhvfV4Xy2C988Pttczrfth3tvAxdJO9_oHQ-gyFC7GYLorw7W2TfehO0ZFr2gRn-zlGL_d3z9OHcr6YPU5v56VhNculwSAwB4KFpO-15ZYbELxxzEjFHLd1rURDRFVR4oAA5zVTXDppmJKMU07H6GKX28fwuYKU9dInA23bdBBWSRMmMFZKDSDfgSaGlCI43Ue_bOJaE6w3Teptk3pTk8ZEb5vUbPDd7HwwfPHlIepkPHQGrI9gsrbB_5PwC_jzekc</recordid><startdate>20020208</startdate><enddate>20020208</enddate><creator>Lin, Jiunn-Nan</creator><creator>Chen, Jen-Ho</creator><creator>Hsiao, Chih-Yang</creator><creator>Kang, Yih-Ming</creator><creator>Wan, Ben-Zu</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>20020208</creationdate><title>Gold supported on surface acidity modified Y-type and iron/Y-type zeolite for CO oxidation</title><author>Lin, Jiunn-Nan ; Chen, Jen-Ho ; Hsiao, Chih-Yang ; Kang, Yih-Ming ; Wan, Ben-Zu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-c0e605e10683b7d5d5ce65af4c894f5d7796a162231fe1e5574958f8c49845353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>CO oxidation</topic><topic>Gold</topic><topic>Iron</topic><topic>Iron oxide</topic><topic>Surface acidity</topic><topic>Y-type zeolite</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Jiunn-Nan</creatorcontrib><creatorcontrib>Chen, Jen-Ho</creatorcontrib><creatorcontrib>Hsiao, Chih-Yang</creatorcontrib><creatorcontrib>Kang, Yih-Ming</creatorcontrib><creatorcontrib>Wan, Ben-Zu</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Applied catalysis. B, Environmental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Jiunn-Nan</au><au>Chen, Jen-Ho</au><au>Hsiao, Chih-Yang</au><au>Kang, Yih-Ming</au><au>Wan, Ben-Zu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gold supported on surface acidity modified Y-type and iron/Y-type zeolite for CO oxidation</atitle><jtitle>Applied catalysis. B, Environmental</jtitle><date>2002-02-08</date><risdate>2002</risdate><volume>36</volume><issue>1</issue><spage>19</spage><epage>29</epage><pages>19-29</pages><issn>0926-3373</issn><eissn>1873-3883</eissn><abstract>A modified method for the preparation of gold in Y-type zeolite was developed in this research. Prior to the preparation of gold catalysts, the surface property of the zeolite (with or without iron) was adjusted in a 1N sodium nitrate solution at pH 6. After drying, the zeolite was added into a chloroauric acid solution at pH 6 for gold loading. The resulted catalysts (i.e. Au/Y or Au/Fe/Y) possessed much better activity and stability for CO oxidation than those (i.e. Au/Y(NP) or Au/Fe/Y(NP)) without any surface pretreatment. Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) studies indicate that the gold particles in Au/Y are smaller and more uniformly distributed than those in Au/Y(NP). XPS and temperature-programmed reduction (TPR) results suggest the strong interaction between gold and iron in Y-type zeolite. Furthermore, it was found from this research that Au/Fe/Y had full initial activity for CO oxidation at 0°C and Au/Y required an induction period to reach a comparable activity to Au/Fe/Y. However, the stability of the activated Au/Y was much better than that of Au/Fe/Y. It can be concluded from XPS results that the formation of carbonate-like species, which covered the active sites for CO oxidation, was the main cause for the deactivation of Au/Fe/Y. On the other hand, TEM study suggests that the sintering of nano-gold particles was the main reason for the slight deactivation of Au/Y.</abstract><pub>Elsevier B.V</pub><doi>10.1016/S0926-3373(01)00276-4</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | CO oxidation Gold Iron Iron oxide Surface acidity Y-type zeolite |
title | Gold supported on surface acidity modified Y-type and iron/Y-type zeolite for CO oxidation |
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