{"title":"Ga/H-ZSM-5 中 Ga2O22+ 上丙烷的 C-H 键活化及其机理影响","authors":"Zhaoqi Zhao, Yunzhu Zhong, Xiaoxia Chang, Bingjun Xu","doi":"10.1016/S1872-2067(24)60065-3","DOIUrl":null,"url":null,"abstract":"<div><p>Propane dehydrogenation (PDH) on Ga/H-ZSM-5 catalysts is a promising reaction for propylene production, while the detail mechanism remains debatable. Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> stabilized by framework Al pairs have been identified as the most active species in Ga/H-ZSM-5 for PDH in our recent work. Here we demonstrate a strong correlation between the PDH activity and a fraction of Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species corresponding to the infrared GaH band of higher wavenumber (GaHHW) in reduced Ga/H-ZSM-5, instead of the overall Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species, by employing five H-ZSM-5 supports sourced differently with comparable Si/Al ratio. This disparity in Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species stems from their differing capacity in completing the catalytic cycle. Spectroscopic results suggest that PDH proceeds <em>via</em> a two-step mechanism: (1) C–H bond activation of propane on H-Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species (rate determining step); (2) β-hydride elimination of adsorbed propyl group, which only occurs on active Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species corresponding to GaHHW.</p></div>","PeriodicalId":9832,"journal":{"name":"Chinese Journal of Catalysis","volume":"64 ","pages":"Pages 32-43"},"PeriodicalIF":15.7000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"C–H bond activation of propane on Ga2O22+ in Ga/H-ZSM-5 and its mechanistic implications\",\"authors\":\"Zhaoqi Zhao, Yunzhu Zhong, Xiaoxia Chang, Bingjun Xu\",\"doi\":\"10.1016/S1872-2067(24)60065-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Propane dehydrogenation (PDH) on Ga/H-ZSM-5 catalysts is a promising reaction for propylene production, while the detail mechanism remains debatable. Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> stabilized by framework Al pairs have been identified as the most active species in Ga/H-ZSM-5 for PDH in our recent work. Here we demonstrate a strong correlation between the PDH activity and a fraction of Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species corresponding to the infrared GaH band of higher wavenumber (GaHHW) in reduced Ga/H-ZSM-5, instead of the overall Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species, by employing five H-ZSM-5 supports sourced differently with comparable Si/Al ratio. This disparity in Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species stems from their differing capacity in completing the catalytic cycle. Spectroscopic results suggest that PDH proceeds <em>via</em> a two-step mechanism: (1) C–H bond activation of propane on H-Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species (rate determining step); (2) β-hydride elimination of adsorbed propyl group, which only occurs on active Ga<sub>2</sub>O<sub>2</sub><sup>2+</sup> species corresponding to GaHHW.</p></div>\",\"PeriodicalId\":9832,\"journal\":{\"name\":\"Chinese Journal of Catalysis\",\"volume\":\"64 \",\"pages\":\"Pages 32-43\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1872206724600653\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872206724600653","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
C–H bond activation of propane on Ga2O22+ in Ga/H-ZSM-5 and its mechanistic implications
Propane dehydrogenation (PDH) on Ga/H-ZSM-5 catalysts is a promising reaction for propylene production, while the detail mechanism remains debatable. Ga2O22+ stabilized by framework Al pairs have been identified as the most active species in Ga/H-ZSM-5 for PDH in our recent work. Here we demonstrate a strong correlation between the PDH activity and a fraction of Ga2O22+ species corresponding to the infrared GaH band of higher wavenumber (GaHHW) in reduced Ga/H-ZSM-5, instead of the overall Ga2O22+ species, by employing five H-ZSM-5 supports sourced differently with comparable Si/Al ratio. This disparity in Ga2O22+ species stems from their differing capacity in completing the catalytic cycle. Spectroscopic results suggest that PDH proceeds via a two-step mechanism: (1) C–H bond activation of propane on H-Ga2O22+ species (rate determining step); (2) β-hydride elimination of adsorbed propyl group, which only occurs on active Ga2O22+ species corresponding to GaHHW.
期刊介绍:
The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.