Maya Shopska, Krassimir Tenchev, Georgi Kadinov, Hristo Kolev, Martin Fabian, Katerina Aleksieva
{"title":"Heterogeneity of adsorption and reaction sites on the surface of (10%Co + 0.5%Pd)/TiO2 catalysts during CO hydrogenation","authors":"Maya Shopska, Krassimir Tenchev, Georgi Kadinov, Hristo Kolev, Martin Fabian, Katerina Aleksieva","doi":"10.1007/s11144-024-02644-8","DOIUrl":null,"url":null,"abstract":"<div><p>Adsorption and reaction site heterogeneity of titania-supported (10%Co + 0.5%Pd) catalysts in CO hydrogenation was studied by chemisorption, temperature-programmed desorption, and diffuse reflectance infrared Fourier transform spectroscopy techniques. Precursor material was treated in various media as reductive, inert, or oxidative. Cobalt metal sites and TiO<sub>2</sub> support heterogeneity were proved. Upon H<sub>2</sub> chemisorption, a pre-reduced sample exposed mostly homogeneous metal surface. Surface heterogeneity toward CO chemisorption depended on preliminary treatment. A catalyst prepared in inert medium revealed moderate activity dynamics of adsorption and reaction sites. Weak to medium strength sites toward hydrogen adsorption were relatively strong in terms of CO adsorption. Carbonate-(like) species occupied medium and strong sites on the support. Sites of weak strength for CO adsorption were active in hydrogenation but very strong in terms of CH<sub>x</sub> intermediates adsorption.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":750,"journal":{"name":"Reaction Kinetics, Mechanisms and Catalysis","volume":"137 4","pages":"2147 - 2171"},"PeriodicalIF":1.7000,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Kinetics, Mechanisms and Catalysis","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11144-024-02644-8","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Adsorption and reaction site heterogeneity of titania-supported (10%Co + 0.5%Pd) catalysts in CO hydrogenation was studied by chemisorption, temperature-programmed desorption, and diffuse reflectance infrared Fourier transform spectroscopy techniques. Precursor material was treated in various media as reductive, inert, or oxidative. Cobalt metal sites and TiO2 support heterogeneity were proved. Upon H2 chemisorption, a pre-reduced sample exposed mostly homogeneous metal surface. Surface heterogeneity toward CO chemisorption depended on preliminary treatment. A catalyst prepared in inert medium revealed moderate activity dynamics of adsorption and reaction sites. Weak to medium strength sites toward hydrogen adsorption were relatively strong in terms of CO adsorption. Carbonate-(like) species occupied medium and strong sites on the support. Sites of weak strength for CO adsorption were active in hydrogenation but very strong in terms of CHx intermediates adsorption.
期刊介绍:
Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields:
-kinetics of homogeneous reactions in gas, liquid and solid phase;
-Homogeneous catalysis;
-Heterogeneous catalysis;
-Adsorption in heterogeneous catalysis;
-Transport processes related to reaction kinetics and catalysis;
-Preparation and study of catalysts;
-Reactors and apparatus.
Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.