{"title":"湿生物质模型化合物在氧化铝支撑金属催化剂上的水相转化制氢过程","authors":"Rohini S. Zambare, Prakash D. Vaidya","doi":"10.1002/kin.21704","DOIUrl":null,"url":null,"abstract":"<p>Catalytic aqueous-phase reforming (APR) of wet biomass such as microalgae and activated sludge is a potential technique for the production of H<sub>2</sub>-rich gaseous products. In the present work, model compounds such as ethylene glycol, xylose and alanine were selected as representatives of the polyols, carbohydrates and proteins in wet biomass. APR trials were performed in a stirred batch reactor using commercial Pt/Al<sub>2</sub>O<sub>3</sub> and Ru/Al<sub>2</sub>O<sub>3</sub> catalysts. The reforming reactions were investigated at different conditions: temperature (T), 498 to 518 K, feed concentration, 1 to 5 wt. %, catalyst loading (ω), 2 to 6 kg/m<sup>3</sup>, and reaction time (t), 1 to 6 h. The commercial Pt/Al<sub>2</sub>O<sub>3</sub> catalyst exhibited higher reforming activity. The influence of reaction parameters on turnover frequency (TOF<sub>H₂</sub>), hydrogen yield (Y-H<sub>2</sub>) and carbon-to-gas conversion (C to G conversion) was studied. The values of TOF<sub>H₂</sub> for Pt/Al<sub>2</sub>O<sub>3</sub> were measured at T = 518 K, ω = 2 kg/m<sup>3</sup> and t = 3 h using 1 wt% feed and these values were 19.2, 4 and 6 1/min for ethylene glycol, xylose and alanine. The values of TOF<sub>H₂</sub> over Ru/Al<sub>2</sub>O<sub>3</sub> under identical conditions were: ethylene glycol–12.4, xylose–1.4 and alanine–5.4 1/min. The activation energies for H<sub>2</sub> production from ethylene glycol, xylose and alanine over Pt/Al<sub>2</sub>O<sub>3</sub> and Ru/Al<sub>2</sub>O<sub>3</sub> catalysts were determined. APR of the mixture of model compounds was also studied over laboratory-made Pt/Al<sub>2</sub>O<sub>3</sub> and Ru/Al<sub>2</sub>O<sub>3</sub> catalysts at the optimum reaction conditions. Thus, this work has provided crucial insights into the production of H<sub>2</sub> from model compounds of wet biomass using Al<sub>2</sub>O<sub>3</sub>-supported catalysts.</p>","PeriodicalId":13894,"journal":{"name":"International Journal of Chemical Kinetics","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2023-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Aqueous-phase reforming of model compounds of wet biomass to hydrogen on alumina-supported metal catalysts\",\"authors\":\"Rohini S. Zambare, Prakash D. Vaidya\",\"doi\":\"10.1002/kin.21704\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Catalytic aqueous-phase reforming (APR) of wet biomass such as microalgae and activated sludge is a potential technique for the production of H<sub>2</sub>-rich gaseous products. In the present work, model compounds such as ethylene glycol, xylose and alanine were selected as representatives of the polyols, carbohydrates and proteins in wet biomass. APR trials were performed in a stirred batch reactor using commercial Pt/Al<sub>2</sub>O<sub>3</sub> and Ru/Al<sub>2</sub>O<sub>3</sub> catalysts. The reforming reactions were investigated at different conditions: temperature (T), 498 to 518 K, feed concentration, 1 to 5 wt. %, catalyst loading (ω), 2 to 6 kg/m<sup>3</sup>, and reaction time (t), 1 to 6 h. The commercial Pt/Al<sub>2</sub>O<sub>3</sub> catalyst exhibited higher reforming activity. The influence of reaction parameters on turnover frequency (TOF<sub>H₂</sub>), hydrogen yield (Y-H<sub>2</sub>) and carbon-to-gas conversion (C to G conversion) was studied. The values of TOF<sub>H₂</sub> for Pt/Al<sub>2</sub>O<sub>3</sub> were measured at T = 518 K, ω = 2 kg/m<sup>3</sup> and t = 3 h using 1 wt% feed and these values were 19.2, 4 and 6 1/min for ethylene glycol, xylose and alanine. The values of TOF<sub>H₂</sub> over Ru/Al<sub>2</sub>O<sub>3</sub> under identical conditions were: ethylene glycol–12.4, xylose–1.4 and alanine–5.4 1/min. The activation energies for H<sub>2</sub> production from ethylene glycol, xylose and alanine over Pt/Al<sub>2</sub>O<sub>3</sub> and Ru/Al<sub>2</sub>O<sub>3</sub> catalysts were determined. APR of the mixture of model compounds was also studied over laboratory-made Pt/Al<sub>2</sub>O<sub>3</sub> and Ru/Al<sub>2</sub>O<sub>3</sub> catalysts at the optimum reaction conditions. Thus, this work has provided crucial insights into the production of H<sub>2</sub> from model compounds of wet biomass using Al<sub>2</sub>O<sub>3</sub>-supported catalysts.</p>\",\"PeriodicalId\":13894,\"journal\":{\"name\":\"International Journal of Chemical Kinetics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2023-12-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Chemical Kinetics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/kin.21704\",\"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":"International Journal of Chemical Kinetics","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/kin.21704","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Aqueous-phase reforming of model compounds of wet biomass to hydrogen on alumina-supported metal catalysts
Catalytic aqueous-phase reforming (APR) of wet biomass such as microalgae and activated sludge is a potential technique for the production of H2-rich gaseous products. In the present work, model compounds such as ethylene glycol, xylose and alanine were selected as representatives of the polyols, carbohydrates and proteins in wet biomass. APR trials were performed in a stirred batch reactor using commercial Pt/Al2O3 and Ru/Al2O3 catalysts. The reforming reactions were investigated at different conditions: temperature (T), 498 to 518 K, feed concentration, 1 to 5 wt. %, catalyst loading (ω), 2 to 6 kg/m3, and reaction time (t), 1 to 6 h. The commercial Pt/Al2O3 catalyst exhibited higher reforming activity. The influence of reaction parameters on turnover frequency (TOFH₂), hydrogen yield (Y-H2) and carbon-to-gas conversion (C to G conversion) was studied. The values of TOFH₂ for Pt/Al2O3 were measured at T = 518 K, ω = 2 kg/m3 and t = 3 h using 1 wt% feed and these values were 19.2, 4 and 6 1/min for ethylene glycol, xylose and alanine. The values of TOFH₂ over Ru/Al2O3 under identical conditions were: ethylene glycol–12.4, xylose–1.4 and alanine–5.4 1/min. The activation energies for H2 production from ethylene glycol, xylose and alanine over Pt/Al2O3 and Ru/Al2O3 catalysts were determined. APR of the mixture of model compounds was also studied over laboratory-made Pt/Al2O3 and Ru/Al2O3 catalysts at the optimum reaction conditions. Thus, this work has provided crucial insights into the production of H2 from model compounds of wet biomass using Al2O3-supported catalysts.
期刊介绍:
As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.