Keyi Wang, Yuanting Du, Yang Li, Xingkun Qi, Weijun Shan, Haibiao Yu, Ying Xiong
{"title":"F127 辅助合成用于在杂质气体存在时催化 N2O 分解的 Bi 促进 Co3O4 催化剂","authors":"Keyi Wang, Yuanting Du, Yang Li, Xingkun Qi, Weijun Shan, Haibiao Yu, Ying Xiong","doi":"10.1016/j.mcat.2024.114604","DOIUrl":null,"url":null,"abstract":"<div><div>In this paper, Bi promoted Co<sub>3</sub>O<sub>4</sub> catalysts used for catalyzing N<sub>2</sub>O decomposition were successfully prepared by improved sol-gel method with the assistance of F127. It was found that the doping of additive Bi not only did not change the unique “Yardang Landform” microstructure of the 3.0F-Co<sub>3</sub>O<sub>4</sub>, but also prompted Co<sub>3</sub>O<sub>4</sub> to expose more active crystal planes, such as (422), (533) and (620). Moreover, the doping of the additive Bi also enhanced the catalyst's specific surface area, and further weakened the surface Co-O bond. The optimum 3.0F-Bi<sub>0.015</sub>Co catalyst achieved >88 % N<sub>2</sub>O conversion (2000 ppmv N<sub>2</sub>O/Ar, <em>GHSV</em>=20,000 <em>h</em><sup>−1</sup>) at 300 °C, and its corresponding <strong><em>TOF</em></strong> value increased from 1.50 × 10<sup>−3</sup> <em>s</em><sup>−1</sup> for 3.0F-Co<sub>3</sub>O<sub>4</sub> to 3.63 × 10<sup>−3</sup> <em>s</em><sup>−1</sup>. Meanwhile, the <strong><em>E<sub>a</sub></em></strong> of 3.0F-Bi<sub>0.015</sub>Co was as low as 47.0 kJ mol<sup>−1</sup>. Most importantly, the catalyst has good resistance to O<sub>2</sub> and H<sub>2</sub>O. Under the harsh condition (both 5 vol.% O<sub>2</sub>, 100 ppmv NO and 2 vol.% H<sub>2</sub>O were coexisted in the reaction system), the N<sub>2</sub>O conversion over the 3.0F-Bi<sub>0.015</sub>Co catalyst can be stable above 90 % at 400 °C.</div></div>","PeriodicalId":393,"journal":{"name":"Molecular Catalysis","volume":"569 ","pages":"Article 114604"},"PeriodicalIF":3.9000,"publicationDate":"2024-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"F127 assisted synthesis of Bi promoted Co3O4 catalyst for catalyzing N2O decomposition in presence of impurity gases\",\"authors\":\"Keyi Wang, Yuanting Du, Yang Li, Xingkun Qi, Weijun Shan, Haibiao Yu, Ying Xiong\",\"doi\":\"10.1016/j.mcat.2024.114604\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this paper, Bi promoted Co<sub>3</sub>O<sub>4</sub> catalysts used for catalyzing N<sub>2</sub>O decomposition were successfully prepared by improved sol-gel method with the assistance of F127. It was found that the doping of additive Bi not only did not change the unique “Yardang Landform” microstructure of the 3.0F-Co<sub>3</sub>O<sub>4</sub>, but also prompted Co<sub>3</sub>O<sub>4</sub> to expose more active crystal planes, such as (422), (533) and (620). Moreover, the doping of the additive Bi also enhanced the catalyst's specific surface area, and further weakened the surface Co-O bond. The optimum 3.0F-Bi<sub>0.015</sub>Co catalyst achieved >88 % N<sub>2</sub>O conversion (2000 ppmv N<sub>2</sub>O/Ar, <em>GHSV</em>=20,000 <em>h</em><sup>−1</sup>) at 300 °C, and its corresponding <strong><em>TOF</em></strong> value increased from 1.50 × 10<sup>−3</sup> <em>s</em><sup>−1</sup> for 3.0F-Co<sub>3</sub>O<sub>4</sub> to 3.63 × 10<sup>−3</sup> <em>s</em><sup>−1</sup>. Meanwhile, the <strong><em>E<sub>a</sub></em></strong> of 3.0F-Bi<sub>0.015</sub>Co was as low as 47.0 kJ mol<sup>−1</sup>. Most importantly, the catalyst has good resistance to O<sub>2</sub> and H<sub>2</sub>O. Under the harsh condition (both 5 vol.% O<sub>2</sub>, 100 ppmv NO and 2 vol.% H<sub>2</sub>O were coexisted in the reaction system), the N<sub>2</sub>O conversion over the 3.0F-Bi<sub>0.015</sub>Co catalyst can be stable above 90 % at 400 °C.</div></div>\",\"PeriodicalId\":393,\"journal\":{\"name\":\"Molecular Catalysis\",\"volume\":\"569 \",\"pages\":\"Article 114604\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468823124007867\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468823124007867","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
F127 assisted synthesis of Bi promoted Co3O4 catalyst for catalyzing N2O decomposition in presence of impurity gases
In this paper, Bi promoted Co3O4 catalysts used for catalyzing N2O decomposition were successfully prepared by improved sol-gel method with the assistance of F127. It was found that the doping of additive Bi not only did not change the unique “Yardang Landform” microstructure of the 3.0F-Co3O4, but also prompted Co3O4 to expose more active crystal planes, such as (422), (533) and (620). Moreover, the doping of the additive Bi also enhanced the catalyst's specific surface area, and further weakened the surface Co-O bond. The optimum 3.0F-Bi0.015Co catalyst achieved >88 % N2O conversion (2000 ppmv N2O/Ar, GHSV=20,000 h−1) at 300 °C, and its corresponding TOF value increased from 1.50 × 10−3s−1 for 3.0F-Co3O4 to 3.63 × 10−3s−1. Meanwhile, the Ea of 3.0F-Bi0.015Co was as low as 47.0 kJ mol−1. Most importantly, the catalyst has good resistance to O2 and H2O. Under the harsh condition (both 5 vol.% O2, 100 ppmv NO and 2 vol.% H2O were coexisted in the reaction system), the N2O conversion over the 3.0F-Bi0.015Co catalyst can be stable above 90 % at 400 °C.
期刊介绍:
Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are:
Heterogeneous catalysis including immobilized molecular catalysts
Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis
Photo- and electrochemistry
Theoretical aspects of catalysis analyzed by computational methods