Yang Liu , Zhenyu Jin , Zhiwen Chen , Jiacong Chen , Hang Yang , Ming Zhao
{"title":"超高温水气转换的合理性与实用性——短流合成气改造的开创性探索","authors":"Yang Liu , Zhenyu Jin , Zhiwen Chen , Jiacong Chen , Hang Yang , Ming Zhao","doi":"10.1016/j.ccst.2025.100472","DOIUrl":null,"url":null,"abstract":"<div><div>Water-gas shift (WGS) reaction is an important process linking gasification syngas upgrading to downstream synthesis of pure H<sub>2</sub> or hydrogen-based fuels such as ammonia, methanol, and sustainable aviation fuel (SAF). The conventional WGS reaction is a long process that includes syngas cleaning and cooling, pressurization, and multistep medium- and low-temperature shift reactions. The latest progress in biomass gasification has led to breakthroughs in the production of low-tar and pressurized syngas, which could facilitate a short process flow for the WGS at high temperatures with minimized heat loss and maximized shift kinetics. However, WGS still faces thermodynamic limitations at high temperatures. Herein, a new ultrahigh-temperature WGS (UT-WGS) strategy is explored using a Cr-free hybrid catalyst that contains both catalytic and adsorptive sites. The results revealed that the optimum reaction temperature and H<sub>2</sub>O/CO ratio are 600 °C and 2, respectively, while the maximum CO conversion and H<sub>2</sub> content are 67.73 % and 75.42 %. Our research contributes to direct upgrading of gasification syngas and low-cost production of hydrogen-based fuels, which will appeal to a broad scientific and engineering audience.</div></div>","PeriodicalId":9387,"journal":{"name":"Carbon Capture Science & Technology","volume":"16 ","pages":"Article 100472"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rationality and practicability of performing water-gas shift at ultrahigh-temperatures: pioneering exploration for short-flow syngas upgrading\",\"authors\":\"Yang Liu , Zhenyu Jin , Zhiwen Chen , Jiacong Chen , Hang Yang , Ming Zhao\",\"doi\":\"10.1016/j.ccst.2025.100472\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Water-gas shift (WGS) reaction is an important process linking gasification syngas upgrading to downstream synthesis of pure H<sub>2</sub> or hydrogen-based fuels such as ammonia, methanol, and sustainable aviation fuel (SAF). The conventional WGS reaction is a long process that includes syngas cleaning and cooling, pressurization, and multistep medium- and low-temperature shift reactions. The latest progress in biomass gasification has led to breakthroughs in the production of low-tar and pressurized syngas, which could facilitate a short process flow for the WGS at high temperatures with minimized heat loss and maximized shift kinetics. However, WGS still faces thermodynamic limitations at high temperatures. Herein, a new ultrahigh-temperature WGS (UT-WGS) strategy is explored using a Cr-free hybrid catalyst that contains both catalytic and adsorptive sites. The results revealed that the optimum reaction temperature and H<sub>2</sub>O/CO ratio are 600 °C and 2, respectively, while the maximum CO conversion and H<sub>2</sub> content are 67.73 % and 75.42 %. Our research contributes to direct upgrading of gasification syngas and low-cost production of hydrogen-based fuels, which will appeal to a broad scientific and engineering audience.</div></div>\",\"PeriodicalId\":9387,\"journal\":{\"name\":\"Carbon Capture Science & Technology\",\"volume\":\"16 \",\"pages\":\"Article 100472\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-07-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbon Capture Science & Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772656825001113\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Capture Science & Technology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772656825001113","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Rationality and practicability of performing water-gas shift at ultrahigh-temperatures: pioneering exploration for short-flow syngas upgrading
Water-gas shift (WGS) reaction is an important process linking gasification syngas upgrading to downstream synthesis of pure H2 or hydrogen-based fuels such as ammonia, methanol, and sustainable aviation fuel (SAF). The conventional WGS reaction is a long process that includes syngas cleaning and cooling, pressurization, and multistep medium- and low-temperature shift reactions. The latest progress in biomass gasification has led to breakthroughs in the production of low-tar and pressurized syngas, which could facilitate a short process flow for the WGS at high temperatures with minimized heat loss and maximized shift kinetics. However, WGS still faces thermodynamic limitations at high temperatures. Herein, a new ultrahigh-temperature WGS (UT-WGS) strategy is explored using a Cr-free hybrid catalyst that contains both catalytic and adsorptive sites. The results revealed that the optimum reaction temperature and H2O/CO ratio are 600 °C and 2, respectively, while the maximum CO conversion and H2 content are 67.73 % and 75.42 %. Our research contributes to direct upgrading of gasification syngas and low-cost production of hydrogen-based fuels, which will appeal to a broad scientific and engineering audience.