{"title":"将二氧化碳和甲醇直接转化为碳酸二甲酯的高效氧化铈-氧化锰技术","authors":"Yue Yu, Xiaolu Chen, Ping He, Zhiwen Xu, Xiao Wu, Hong Chen, Songlin Yang, Jia Yu, Shuang Gao","doi":"10.1007/s11144-024-02722-x","DOIUrl":null,"url":null,"abstract":"<p>A number of Ce<sub>1-x</sub>Mn<sub>x</sub> catalysts with different Mn contents were prepared by resol-assisted cationic coordinative co-assembly approach and used for the synthesis of dimethyl carbonate (DMC) from CO<sub>2</sub> and methanol. Multiple characterizations of XRD, FT-IR, TEM, BET, CO<sub>2</sub>-TPD, NH<sub>3</sub>-TPD, H<sub>2</sub>-TPR, XPS analyses were applied to investigate the surface properties of the Ce<sub>1-x</sub>Mn<sub>x</sub> catalysts. It turned out that adjusting the proper concentration of Mn ions not only increased the pore volumes, but also improved the content of medium acidic and medium basic sites. When a small amount of Mn was added, the presence of Mn<sup>2+</sup> on the catalyst surface enhanced, facilitating the conversion of Ce<sup>4+</sup> to Ce<sup>3+</sup>, and leading to higher oxygen vacancy concentration. Consequently, the adsorption and activation of CO<sub>2</sub> and methanol were promoted, and the catalytic efficiency of the reaction was improved. It was found that Ce<sub>0.95</sub>Mn<sub>0.05</sub> catalyst exhibited the best catalytic activity, achieving a high DMC yield of 6.44 mmol/g (120 °C, 6.5 MPa, 4 h).</p><h3 data-test=\"abstract-sub-heading\">Graphical Abstract</h3>\n","PeriodicalId":750,"journal":{"name":"Reaction Kinetics, Mechanisms and Catalysis","volume":"46 1","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficient ceria-manganese oxide for the direct conversion of CO2 and methanol to dimethyl carbonate\",\"authors\":\"Yue Yu, Xiaolu Chen, Ping He, Zhiwen Xu, Xiao Wu, Hong Chen, Songlin Yang, Jia Yu, Shuang Gao\",\"doi\":\"10.1007/s11144-024-02722-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A number of Ce<sub>1-x</sub>Mn<sub>x</sub> catalysts with different Mn contents were prepared by resol-assisted cationic coordinative co-assembly approach and used for the synthesis of dimethyl carbonate (DMC) from CO<sub>2</sub> and methanol. Multiple characterizations of XRD, FT-IR, TEM, BET, CO<sub>2</sub>-TPD, NH<sub>3</sub>-TPD, H<sub>2</sub>-TPR, XPS analyses were applied to investigate the surface properties of the Ce<sub>1-x</sub>Mn<sub>x</sub> catalysts. It turned out that adjusting the proper concentration of Mn ions not only increased the pore volumes, but also improved the content of medium acidic and medium basic sites. When a small amount of Mn was added, the presence of Mn<sup>2+</sup> on the catalyst surface enhanced, facilitating the conversion of Ce<sup>4+</sup> to Ce<sup>3+</sup>, and leading to higher oxygen vacancy concentration. Consequently, the adsorption and activation of CO<sub>2</sub> and methanol were promoted, and the catalytic efficiency of the reaction was improved. It was found that Ce<sub>0.95</sub>Mn<sub>0.05</sub> catalyst exhibited the best catalytic activity, achieving a high DMC yield of 6.44 mmol/g (120 °C, 6.5 MPa, 4 h).</p><h3 data-test=\\\"abstract-sub-heading\\\">Graphical Abstract</h3>\\n\",\"PeriodicalId\":750,\"journal\":{\"name\":\"Reaction Kinetics, Mechanisms and Catalysis\",\"volume\":\"46 1\",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-08-29\",\"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://doi.org/10.1007/s11144-024-02722-x\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Kinetics, Mechanisms and Catalysis","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s11144-024-02722-x","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Efficient ceria-manganese oxide for the direct conversion of CO2 and methanol to dimethyl carbonate
A number of Ce1-xMnx catalysts with different Mn contents were prepared by resol-assisted cationic coordinative co-assembly approach and used for the synthesis of dimethyl carbonate (DMC) from CO2 and methanol. Multiple characterizations of XRD, FT-IR, TEM, BET, CO2-TPD, NH3-TPD, H2-TPR, XPS analyses were applied to investigate the surface properties of the Ce1-xMnx catalysts. It turned out that adjusting the proper concentration of Mn ions not only increased the pore volumes, but also improved the content of medium acidic and medium basic sites. When a small amount of Mn was added, the presence of Mn2+ on the catalyst surface enhanced, facilitating the conversion of Ce4+ to Ce3+, and leading to higher oxygen vacancy concentration. Consequently, the adsorption and activation of CO2 and methanol were promoted, and the catalytic efficiency of the reaction was improved. It was found that Ce0.95Mn0.05 catalyst exhibited the best catalytic activity, achieving a high DMC yield of 6.44 mmol/g (120 °C, 6.5 MPa, 4 h).
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.