Duo-hua LIAO, Liang YANG, Geng-zhe SONG, Xue-dong MA, Shuang LI
{"title":"ZnO-ZrO2催化剂催化乙烷氧化脱氢制乙烯","authors":"Duo-hua LIAO, Liang YANG, Geng-zhe SONG, Xue-dong MA, Shuang LI","doi":"10.1016/S1872-5813(23)60360-3","DOIUrl":null,"url":null,"abstract":"<div><p>The ZnO-ZrO<sub>2</sub> catalyst was prepared by the deposition-precipitation method using ZrO<sub>2</sub> as the carrier obtained from calcining commercial zirconium hydroxide (Zr(OH)<sub>4</sub>). And the catalytic performance was evaluated at 873 K in CO<sub>2</sub>-assisted ethane oxidative dehydrogenation reaction (CO<sub>2</sub>-ODHE). The physical-chemical properties and morphology were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), Raman spectra, High-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectra (XPS), CO<sub>2</sub> temperature-programmed desorption (CO<sub>2</sub>-TPD). The results show that ZnO were doped into the surface lattice of ZrO<sub>2</sub> on the 5%ZnO-ZrO<sub>2</sub> catalyst, generating highly dispersed ZnO species and oxygen-deficient regions on catalyst surface. 5%ZnO-ZrO<sub>2</sub> catalyst could selectively breaking C–H bond instead of C–C bond, delivering excellent catalytic performance. 210 μmol/(g<sub>cat</sub>·min) of C<sub>2</sub>H<sub>4</sub> formation rate could compare favorably with the data reported on noble metal and transition metal carbides. Additionally, the possible mechanism is discussed.</p></div>","PeriodicalId":15956,"journal":{"name":"燃料化学学报","volume":"51 10","pages":"Pages 1421-1431"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CO2-assisted oxidative dehydrogenation of ethane to ethylene over the ZnO-ZrO2 catalyst\",\"authors\":\"Duo-hua LIAO, Liang YANG, Geng-zhe SONG, Xue-dong MA, Shuang LI\",\"doi\":\"10.1016/S1872-5813(23)60360-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The ZnO-ZrO<sub>2</sub> catalyst was prepared by the deposition-precipitation method using ZrO<sub>2</sub> as the carrier obtained from calcining commercial zirconium hydroxide (Zr(OH)<sub>4</sub>). And the catalytic performance was evaluated at 873 K in CO<sub>2</sub>-assisted ethane oxidative dehydrogenation reaction (CO<sub>2</sub>-ODHE). The physical-chemical properties and morphology were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), Raman spectra, High-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectra (XPS), CO<sub>2</sub> temperature-programmed desorption (CO<sub>2</sub>-TPD). The results show that ZnO were doped into the surface lattice of ZrO<sub>2</sub> on the 5%ZnO-ZrO<sub>2</sub> catalyst, generating highly dispersed ZnO species and oxygen-deficient regions on catalyst surface. 5%ZnO-ZrO<sub>2</sub> catalyst could selectively breaking C–H bond instead of C–C bond, delivering excellent catalytic performance. 210 μmol/(g<sub>cat</sub>·min) of C<sub>2</sub>H<sub>4</sub> formation rate could compare favorably with the data reported on noble metal and transition metal carbides. Additionally, the possible mechanism is discussed.</p></div>\",\"PeriodicalId\":15956,\"journal\":{\"name\":\"燃料化学学报\",\"volume\":\"51 10\",\"pages\":\"Pages 1421-1431\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"燃料化学学报\",\"FirstCategoryId\":\"1087\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1872581323603603\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Energy\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"燃料化学学报","FirstCategoryId":"1087","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872581323603603","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Energy","Score":null,"Total":0}
CO2-assisted oxidative dehydrogenation of ethane to ethylene over the ZnO-ZrO2 catalyst
The ZnO-ZrO2 catalyst was prepared by the deposition-precipitation method using ZrO2 as the carrier obtained from calcining commercial zirconium hydroxide (Zr(OH)4). And the catalytic performance was evaluated at 873 K in CO2-assisted ethane oxidative dehydrogenation reaction (CO2-ODHE). The physical-chemical properties and morphology were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), Raman spectra, High-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectra (XPS), CO2 temperature-programmed desorption (CO2-TPD). The results show that ZnO were doped into the surface lattice of ZrO2 on the 5%ZnO-ZrO2 catalyst, generating highly dispersed ZnO species and oxygen-deficient regions on catalyst surface. 5%ZnO-ZrO2 catalyst could selectively breaking C–H bond instead of C–C bond, delivering excellent catalytic performance. 210 μmol/(gcat·min) of C2H4 formation rate could compare favorably with the data reported on noble metal and transition metal carbides. Additionally, the possible mechanism is discussed.
期刊介绍:
Journal of Fuel Chemistry and Technology (Ranliao Huaxue Xuebao) is a Chinese Academy of Sciences(CAS) journal started in 1956, sponsored by the Chinese Chemical Society and the Institute of Coal Chemistry, Chinese Academy of Sciences(CAS). The journal is published bimonthly by Science Press in China and widely distributed in about 20 countries. Journal of Fuel Chemistry and Technology publishes reports of both basic and applied research in the chemistry and chemical engineering of many energy sources, including that involved in the nature, processing and utilization of coal, petroleum, oil shale, natural gas, biomass and synfuels, as well as related subjects of increasing interest such as C1 chemistry, pollutions control and new catalytic materials. Types of publications include original research articles, short communications, research notes and reviews. Both domestic and international contributors are welcome. Manuscripts written in Chinese or English will be accepted. Additional English titles, abstracts and key words should be included in Chinese manuscripts. All manuscripts are subject to critical review by the editorial committee, which is composed of about 10 foreign and 50 Chinese experts in fuel science. Journal of Fuel Chemistry and Technology has been a source of primary research work in fuel chemistry as a Chinese core scientific periodical.