Ran Wang , Xin Zhang , Yuanyuan Huang , Wei Shen , Liyuan Xu , Haoyi Tong , Pengbin Pan , Yuan-Gen Yao
{"title":"研究了钾改性对zno -活性炭催化剂分解甲酸甲酯的催化活性和稳定性的影响","authors":"Ran Wang , Xin Zhang , Yuanyuan Huang , Wei Shen , Liyuan Xu , Haoyi Tong , Pengbin Pan , Yuan-Gen Yao","doi":"10.1016/j.mcat.2025.114946","DOIUrl":null,"url":null,"abstract":"<div><div>Methyl formate (MF) decomposition is essential for producing valuable chemicals, but finding efficient and stable catalysts is challenging. This study explores the catalytic performance of ZnO/AC, K8-10-4/AC, and Zn5K8-10-4/AC in MF decomposition. The catalysts were synthesized by varying the potassium-to-carbon ratios and the calcination temperatures and durations, and characterized using nitrogen adsorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), CO<sub>2</sub>-TPD, and <em>in-situ</em> DRIFTS. Zn5K8-10-4/AC demonstrated significantly higher activity, with a conversion rate of 99.3%, compared to ZnO/AC (18.4%) and K8-10-4/AC (2.4%) at 210 °C. Potassium addition enhanced the basicity and surface properties, facilitating ester bond cleavage and HCOO species formation. Zn5K8-10-16/AC also exhibited excellent stability over 100 hours, in contrast to the rapid deactivation observed with K8-10-16/AC. This study highlights the synergistic effect of zinc and potassium for improving catalytic performance and stability, offering insights for designing more efficient catalysts for MF decomposition and similar reactions.</div></div>","PeriodicalId":393,"journal":{"name":"Molecular Catalysis","volume":"576 ","pages":"Article 114946"},"PeriodicalIF":4.9000,"publicationDate":"2025-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigating the role of potassium modification in the catalytic activity and stability of ZnO-activated carbon catalysts for methyl formate decomposition\",\"authors\":\"Ran Wang , Xin Zhang , Yuanyuan Huang , Wei Shen , Liyuan Xu , Haoyi Tong , Pengbin Pan , Yuan-Gen Yao\",\"doi\":\"10.1016/j.mcat.2025.114946\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Methyl formate (MF) decomposition is essential for producing valuable chemicals, but finding efficient and stable catalysts is challenging. This study explores the catalytic performance of ZnO/AC, K8-10-4/AC, and Zn5K8-10-4/AC in MF decomposition. The catalysts were synthesized by varying the potassium-to-carbon ratios and the calcination temperatures and durations, and characterized using nitrogen adsorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), CO<sub>2</sub>-TPD, and <em>in-situ</em> DRIFTS. Zn5K8-10-4/AC demonstrated significantly higher activity, with a conversion rate of 99.3%, compared to ZnO/AC (18.4%) and K8-10-4/AC (2.4%) at 210 °C. Potassium addition enhanced the basicity and surface properties, facilitating ester bond cleavage and HCOO species formation. Zn5K8-10-16/AC also exhibited excellent stability over 100 hours, in contrast to the rapid deactivation observed with K8-10-16/AC. This study highlights the synergistic effect of zinc and potassium for improving catalytic performance and stability, offering insights for designing more efficient catalysts for MF decomposition and similar reactions.</div></div>\",\"PeriodicalId\":393,\"journal\":{\"name\":\"Molecular Catalysis\",\"volume\":\"576 \",\"pages\":\"Article 114946\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-02-22\",\"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/S2468823125001324\",\"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/S2468823125001324","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Investigating the role of potassium modification in the catalytic activity and stability of ZnO-activated carbon catalysts for methyl formate decomposition
Methyl formate (MF) decomposition is essential for producing valuable chemicals, but finding efficient and stable catalysts is challenging. This study explores the catalytic performance of ZnO/AC, K8-10-4/AC, and Zn5K8-10-4/AC in MF decomposition. The catalysts were synthesized by varying the potassium-to-carbon ratios and the calcination temperatures and durations, and characterized using nitrogen adsorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), CO2-TPD, and in-situ DRIFTS. Zn5K8-10-4/AC demonstrated significantly higher activity, with a conversion rate of 99.3%, compared to ZnO/AC (18.4%) and K8-10-4/AC (2.4%) at 210 °C. Potassium addition enhanced the basicity and surface properties, facilitating ester bond cleavage and HCOO species formation. Zn5K8-10-16/AC also exhibited excellent stability over 100 hours, in contrast to the rapid deactivation observed with K8-10-16/AC. This study highlights the synergistic effect of zinc and potassium for improving catalytic performance and stability, offering insights for designing more efficient catalysts for MF decomposition and similar reactions.
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