2019
DOI: 10.1016/j.jcat.2019.06.041
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The oxidation of chlorinated organic compounds over W-modified Pt/CeO2 catalysts

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Cited by 80 publications
(25 citation statements)
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“…Meanwhile, the inorganic chlorine species deposited on the spent MoPt-110Mn (2.57%) was less than that of Pt-110Mn (7.99%), because the abundant surface hydroxyl groups as Brønsted sites promoted the removal of adsorbed Cl species in form of HCl, and the surface molybdate species such as monomolybdate and polymolybdate as polyoxometalate anion suppressed the adsorption of Cl species. By the way, the latter was practicable for vanadate-, tungstate-, sulfate-, or phosphate-modified other oxides catalysts. , …”
Section: Resultsmentioning
confidence: 99%
“…Meanwhile, the inorganic chlorine species deposited on the spent MoPt-110Mn (2.57%) was less than that of Pt-110Mn (7.99%), because the abundant surface hydroxyl groups as Brønsted sites promoted the removal of adsorbed Cl species in form of HCl, and the surface molybdate species such as monomolybdate and polymolybdate as polyoxometalate anion suppressed the adsorption of Cl species. By the way, the latter was practicable for vanadate-, tungstate-, sulfate-, or phosphate-modified other oxides catalysts. , …”
Section: Resultsmentioning
confidence: 99%
“…The use of a catalyst reduces the activation energy and makes it possible to oxidize VOCs at a lower temperature. The catalytic oxidation of benzene (B), chlorobenzene (CB), and 1,2dichlorobenzene (1,2-DCB) over W-modified Pt/CeO 2 catalysts has been studied [143]. A decrease in the strength of Cl adsorption on Ce and Pt sites can be promoted by the addition of W. The interaction of W with Pt species led to the formation of Pt-O-W structures, which promoted the reducibility and availability of surface oxygen.…”
Section: Oxidation Of Volatile Organic Compounds (Vocs)mentioning
confidence: 99%
“…One of the main challenges is to select suitable, economical and highly efficient catalysts from large number of potential alternatives. Solid catalytic materials commonly investigated are supported precious metal catalysts [10][11][12][13][14][15][16], solid acid catalysts [16][17][18][19][20][21][22] and transition metal/rare earth oxide catalysts [23][24][25][26][27][28][29][30][31][32][33][34][35][36].…”
Section: Introductionmentioning
confidence: 99%
“…Particularly, WO 3-x with abundant oxygen vacancies, noticeable resistance to thermal shock and hydrochloric acid corrosion can be used as the active or additive component of catalyst [37][38][39][40][41]. It has both acidity and oxidizability, showing certain catalytic activity for Cl-VOCs degradation [35,37,38]. Acidity can improve the adsorption and activation of chlorinated organic molecules on the catalyst surface, and oxidizability is helpful for the deep oxidation of intermediates to form CO 2 and H 2 O [17][18][19][20][21].…”
Section: Introductionmentioning
confidence: 99%