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Green chemical incorporation of silicon into polyoxoanions of molybdenum: characterization, thermal kinetics study and their photocatalytic water splitting activityElectronic supplementary information (ESI) available: One figure showing dependence of activation energy E with conversion α obtained by FWO and KAS methods for stages I and II and one table giving the expressions for reaction models have been made available as ESI available. See DOI: 10.1039/c4ra12331j
Cetylpyridinium silicomolybdate (CSM) nanorods were successfully synthesized by applying green chemistry principles using sodium molybdate and a structure directing cationic surfactant, cetyl pyridinium chloride (CPC) at room temperature. The composition and morphology of the nanorods were establish...
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creator | D'Cruz, Bessy Samuel, Jadu George, Leena |
description | Cetylpyridinium silicomolybdate (CSM) nanorods were successfully synthesized by applying green chemistry principles using sodium molybdate and a structure directing cationic surfactant, cetyl pyridinium chloride (CPC) at room temperature. The composition and morphology of the nanorods were established by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TG) and inductively coupled plasma atomic emission spectroscopic (ICP-AES) techniques. The thermal decomposition kinetics of CSM nanorods were investigated by a non-isothermal thermogravimetric analyzer at various heating rates. The thermal decomposition of CSM occurred in two stages. The activation energies of the first and second stages of thermal decomposition for all heating rates have been estimated using the iso-conventional methods of Flynn-Wall-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS) and the results are found to be in good agreement with each other. The invariant kinetic parameter (IKP) method and master plot method were also used to evaluate the kinetic parameters and mechanism for the thermal decomposition of CSM. The photocatalytic water oxidation mechanism using the CSM catalyst in the presence of platinum (Pt) co-catalyst enhances the H
2
evolution and was found to be 1.946 mmol g
−1
h
−1
.
Cetylpyridinium silicomolybdate nanorods were synthesized by following green chemical paths. The decomposition kinetics was studied by thermo gravimetric analysis. It acts as a good catalyst for photocatalytic water oxidation. |
doi_str_mv | 10.1039/c4ra12331j |
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2
evolution and was found to be 1.946 mmol g
−1
h
−1
.
Cetylpyridinium silicomolybdate nanorods were synthesized by following green chemical paths. The decomposition kinetics was studied by thermo gravimetric analysis. It acts as a good catalyst for photocatalytic water oxidation.</description><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c4ra12331j</identifier><language>eng</language><creationdate>2014-11</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>D'Cruz, Bessy</creatorcontrib><creatorcontrib>Samuel, Jadu</creatorcontrib><creatorcontrib>George, Leena</creatorcontrib><title>Green chemical incorporation of silicon into polyoxoanions of molybdenum: characterization, thermal kinetics study and their photocatalytic water splitting activityElectronic supplementary information (ESI) available: One figure showing dependence of activation energy E with conversion α obtained by FWO and KAS methods for stages I and II and one table giving the expressions for reaction models have been made available as ESI available. See DOI: 10.1039/c4ra12331j</title><description>Cetylpyridinium silicomolybdate (CSM) nanorods were successfully synthesized by applying green chemistry principles using sodium molybdate and a structure directing cationic surfactant, cetyl pyridinium chloride (CPC) at room temperature. The composition and morphology of the nanorods were established by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TG) and inductively coupled plasma atomic emission spectroscopic (ICP-AES) techniques. The thermal decomposition kinetics of CSM nanorods were investigated by a non-isothermal thermogravimetric analyzer at various heating rates. The thermal decomposition of CSM occurred in two stages. The activation energies of the first and second stages of thermal decomposition for all heating rates have been estimated using the iso-conventional methods of Flynn-Wall-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS) and the results are found to be in good agreement with each other. The invariant kinetic parameter (IKP) method and master plot method were also used to evaluate the kinetic parameters and mechanism for the thermal decomposition of CSM. The photocatalytic water oxidation mechanism using the CSM catalyst in the presence of platinum (Pt) co-catalyst enhances the H
2
evolution and was found to be 1.946 mmol g
−1
h
−1
.
Cetylpyridinium silicomolybdate nanorods were synthesized by following green chemical paths. The decomposition kinetics was studied by thermo gravimetric analysis. It acts as a good catalyst for photocatalytic water oxidation.</description><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFUcFuEzEQXZCQqEov3JGGG0i07GZLpOaGIC0RhxyCxDGatWd3p3hty3aSbv-KH-mN_2G8RcoBCXwZa97Mm_dmiuJlVV5UZX31Xl0GrGZ1Xd0-LU5m5eX8fFbOr54XZzHelvLmH6rZvDp58usmEFlQPQ2s0ABb5YJ3ARM7C66FyIaVfNkmB96Z0d05tALGjA6SaDTZ3bAQDgyoEgW-n7rfQeopDEL6gy0lVhFi2ukR0OoMcQDfu-QUJjSj4HBA6YboDafEtgNh4z2ncWlIpeCslMSd94YGsgnDKKJaJxMmrW-Wm9VbwD2ywcbQAtaWoOVuFwhi7w6ZUJMnK3IVZfET_WMzWQrdCEs4cOpB_O4pxAw8_ATXJBQDGpoRrr-vJ_lfP25goNQ7HUEkiDHsKMJqAlePwcn8lKVAJy5kungGuvOBYpz2lxsDZRUyaHCaTIQe9wRNPsmAmo52ACOIwWPiAjZE8Hm9WsDfN39RPGvRRDr7E0-LV9fLb5--nIeotj7wIMvbHsvr0-L1v_Ct1239P47frlLYmA</recordid><startdate>20141124</startdate><enddate>20141124</enddate><creator>D'Cruz, Bessy</creator><creator>Samuel, Jadu</creator><creator>George, Leena</creator><scope/></search><sort><creationdate>20141124</creationdate><title>Green chemical incorporation of silicon into polyoxoanions of molybdenum: characterization, thermal kinetics study and their photocatalytic water splitting activityElectronic supplementary information (ESI) available: One figure showing dependence of activation energy E with conversion α obtained by FWO and KAS methods for stages I and II and one table giving the expressions for reaction models have been made available as ESI available. See DOI: 10.1039/c4ra12331j</title><author>D'Cruz, Bessy ; Samuel, Jadu ; George, Leena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c4ra12331j3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>D'Cruz, Bessy</creatorcontrib><creatorcontrib>Samuel, Jadu</creatorcontrib><creatorcontrib>George, Leena</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>D'Cruz, Bessy</au><au>Samuel, Jadu</au><au>George, Leena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Green chemical incorporation of silicon into polyoxoanions of molybdenum: characterization, thermal kinetics study and their photocatalytic water splitting activityElectronic supplementary information (ESI) available: One figure showing dependence of activation energy E with conversion α obtained by FWO and KAS methods for stages I and II and one table giving the expressions for reaction models have been made available as ESI available. See DOI: 10.1039/c4ra12331j</atitle><date>2014-11-24</date><risdate>2014</risdate><volume>4</volume><issue>18</issue><spage>63328</spage><epage>63337</epage><pages>63328-63337</pages><eissn>2046-2069</eissn><abstract>Cetylpyridinium silicomolybdate (CSM) nanorods were successfully synthesized by applying green chemistry principles using sodium molybdate and a structure directing cationic surfactant, cetyl pyridinium chloride (CPC) at room temperature. The composition and morphology of the nanorods were established by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TG) and inductively coupled plasma atomic emission spectroscopic (ICP-AES) techniques. The thermal decomposition kinetics of CSM nanorods were investigated by a non-isothermal thermogravimetric analyzer at various heating rates. The thermal decomposition of CSM occurred in two stages. The activation energies of the first and second stages of thermal decomposition for all heating rates have been estimated using the iso-conventional methods of Flynn-Wall-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS) and the results are found to be in good agreement with each other. The invariant kinetic parameter (IKP) method and master plot method were also used to evaluate the kinetic parameters and mechanism for the thermal decomposition of CSM. The photocatalytic water oxidation mechanism using the CSM catalyst in the presence of platinum (Pt) co-catalyst enhances the H
2
evolution and was found to be 1.946 mmol g
−1
h
−1
.
Cetylpyridinium silicomolybdate nanorods were synthesized by following green chemical paths. The decomposition kinetics was studied by thermo gravimetric analysis. It acts as a good catalyst for photocatalytic water oxidation.</abstract><doi>10.1039/c4ra12331j</doi><tpages>1</tpages></addata></record> |
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title | Green chemical incorporation of silicon into polyoxoanions of molybdenum: characterization, thermal kinetics study and their photocatalytic water splitting activityElectronic supplementary information (ESI) available: One figure showing dependence of activation energy E with conversion α obtained by FWO and KAS methods for stages I and II and one table giving the expressions for reaction models have been made available as ESI available. See DOI: 10.1039/c4ra12331j |
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