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Effects of Tin on Product Distribution and Catalyst Stability in Hydrodechlorination of CCl4 over Pt-Sn/γ-Al2O3
The Pt−Sn/γ-Al2O3 catalyst with a moderate amount of tin showed an enhanced catalytic stability and selectivity to CHCl3 in hydrodechlorination of CCl4 compared to monometallic platinum catalyst. The tin added in consecutive order to 1.0wt%Pt/γ-Al2O3 acted as a diluting component of platinum ensembl...
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Published in: | Industrial & engineering chemistry research 2007-03, Vol.46 (6), p.1721-1730 |
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container_title | Industrial & engineering chemistry research |
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creator | Bae, Jong Wook Jang, Eun Joo Lee, Byoung In Lee, Jae Sung Lee, Kyung Hee |
description | The Pt−Sn/γ-Al2O3 catalyst with a moderate amount of tin showed an enhanced catalytic stability and selectivity to CHCl3 in hydrodechlorination of CCl4 compared to monometallic platinum catalyst. The tin added in consecutive order to 1.0wt%Pt/γ-Al2O3 acted as a diluting component of platinum ensemble sites and resulted in reducing the formation of C2 compounds and carbon deposition. Furthermore, tin addition modifies the electronic state of supported platinum particles by the electron transfer from tin to platinum, results in the reduction of the binding energy of intermediate species, and suppresses the complete hydrodechlorination activity of surface intermediates. Thus on Pt−Sn/γ-Al2O3 catalysts, adsorbed CCl4 is readily desorbed as CHCl3 instead of residing too long on the surface until it is completely dechlorinated to form CH4. |
doi_str_mv | 10.1021/ie061334l |
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The tin added in consecutive order to 1.0wt%Pt/γ-Al2O3 acted as a diluting component of platinum ensemble sites and resulted in reducing the formation of C2 compounds and carbon deposition. Furthermore, tin addition modifies the electronic state of supported platinum particles by the electron transfer from tin to platinum, results in the reduction of the binding energy of intermediate species, and suppresses the complete hydrodechlorination activity of surface intermediates. 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Thus on Pt−Sn/γ-Al2O3 catalysts, adsorbed CCl4 is readily desorbed as CHCl3 instead of residing too long on the surface until it is completely dechlorinated to form CH4.</description><subject>Applied sciences</subject><subject>Catalysis</subject><subject>Catalytic reactions</subject><subject>Chemical engineering</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Reactors</subject><subject>Theory of reactions, general kinetics. Catalysis. 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Eng. Chem. Res</addtitle><date>2007-03-14</date><risdate>2007</risdate><volume>46</volume><issue>6</issue><spage>1721</spage><epage>1730</epage><pages>1721-1730</pages><issn>0888-5885</issn><eissn>1520-5045</eissn><coden>IECRED</coden><abstract>The Pt−Sn/γ-Al2O3 catalyst with a moderate amount of tin showed an enhanced catalytic stability and selectivity to CHCl3 in hydrodechlorination of CCl4 compared to monometallic platinum catalyst. The tin added in consecutive order to 1.0wt%Pt/γ-Al2O3 acted as a diluting component of platinum ensemble sites and resulted in reducing the formation of C2 compounds and carbon deposition. Furthermore, tin addition modifies the electronic state of supported platinum particles by the electron transfer from tin to platinum, results in the reduction of the binding energy of intermediate species, and suppresses the complete hydrodechlorination activity of surface intermediates. 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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Applied sciences Catalysis Catalytic reactions Chemical engineering Chemistry Exact sciences and technology General and physical chemistry Reactors Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Effects of Tin on Product Distribution and Catalyst Stability in Hydrodechlorination of CCl4 over Pt-Sn/γ-Al2O3 |
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