2018
DOI: 10.1016/j.cattod.2017.02.045
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Preparation and catalytic properties of cobalt salts of Keggin type heteropolyacids supported on mesoporous silica

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Cited by 15 publications
(12 citation statements)
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“…[36] The Mo 3d spectrum is deconvoluted into 2 doublets at 232.6 eV and 233.45 eV, which are contributing to Mo 6 + in MoO 3 existed in the keggin anion and more electropositive surrounded Mo 6 + , respectively. [37] The broad peak between 515 and 521 eV assigned to V 2p3/2 of all samples is deconvoluted to V 5 + and V 4 + species at 517.8 � 0.1 and 516 � 0.1 eV, respectively. V 5 + is the dominate unit of Keggin structure with existence of less V 4 + due to the redox equilibrium at the surface of catalyst.…”
Section: Resultsmentioning
confidence: 93%
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“…[36] The Mo 3d spectrum is deconvoluted into 2 doublets at 232.6 eV and 233.45 eV, which are contributing to Mo 6 + in MoO 3 existed in the keggin anion and more electropositive surrounded Mo 6 + , respectively. [37] The broad peak between 515 and 521 eV assigned to V 2p3/2 of all samples is deconvoluted to V 5 + and V 4 + species at 517.8 � 0.1 and 516 � 0.1 eV, respectively. V 5 + is the dominate unit of Keggin structure with existence of less V 4 + due to the redox equilibrium at the surface of catalyst.…”
Section: Resultsmentioning
confidence: 93%
“…The peaks at 135 eV and 134 eV are corresponding to P 2p1/2 and P 2p3/2, indicating that P(V) is existed in the HPAs [36] . The Mo 3d spectrum is deconvoluted into 2 doublets at 232.6 eV and 233.45 eV, which are contributing to Mo 6+ in MoO 3 existed in the keggin anion and more electropositive surrounded Mo 6+ , respectively [37] . The broad peak between 515 and 521 eV assigned to V 2p3/2 of all samples is deconvoluted to V 5+ and V 4+ species at 517.8±0.1 and 516±0.1 eV, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…The high conversion rate of 1-butanol and the selectivity of butenes indicated that Zn-Mn-Co/γ-Al 2 O 3 exhibited excellent activity at low temperature. Zinc, manganese, and cobalt oxides exhibited high activity in alcohol dehydration, as already proven [15][16][17]29]. The modification of metal ions improved the acidity of the catalyst, and the Lewis acid sites played an important role in the catalytic dehydration of alcohols [30].…”
Section: Catalytic Activity Of γ-Al2o3 and Zn-mn-co/γ-al2o3mentioning
confidence: 52%
“…WHSV mainly affected the retention time of 1-butanol in the catalyst micro-reactor system, and high WHSV was not conducive to the adsorption of butanol by a catalyst, which resulted in a decline of the conversion rate of 1-butanol. Zinc, manganese, and cobalt oxides exhibited excellent catalytic activity in the dehydration reaction of alcohol [15][16][17] and they are also used as active components to be loaded onto a catalyst carrier [16,19]. In this study, zinc, manganese, and cobalt were loaded onto γ-Al 2 O 3 , and the modified catalyst showed superior catalytic activity, which was attributed to the catalytic ability of the active components and the increase of the catalyst's acidity.…”
Section: Optimization Of Temperature and Whsv For Butanol Dehydrationmentioning
confidence: 88%
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