期刊文献+

Cu/SiO_(2)复合材料体系的构建及其高效催化醇类脱氢性能研究

Rational design of Cu/SiO_(2) system for improving activity in dehydrogenation of alcohols
下载PDF
导出
摘要 铜基催化剂对环己醇的非氧化脱氢具有较高的选择性,但转化率仍然不足,且铜基催化剂的稳定性因铜烧结而需要提高。通过湿化学法制备了Cu/SiO_(2)纳米颗粒,并对催化剂进行了XRD、SEM、TEM、FT-IR、BET、XPS和UV-Vis表征。结果表明,在280℃和WHSV为11.62 h^(-1)的条件下,该催化剂对环己醇脱氢制环己酮的选择性接近100%,摩尔转化率为81%。此外,该催化剂对苯甲醇脱氢制苯甲醛也有良好的性能,在260℃、WHSV为12.48 h^(-1)时,苯甲醇的摩尔转化率为75%,苯甲醛的收率为61%;该条件下,催化剂的活性在48 h内保持稳定。 Copper-based catalysts exhibit high selectivity for non-oxidative dehydrogenation of cyclohexanol,but deliver an insufficient conversion.Furthermore,the stability of copper-based catalysts needs to be improved due to copper sintering.Cu/SiO_(2) nanoparticles are prepared through wet chemical method,and characterized by means of XRD,SEM,TEM,FT-IR,BET,XPS and UV-Vis.It is shown that the selectivity of cyclohexanol dehydrogenation to cyclohexanone over the catalyst approaches 100%at 280℃and a WHSV of 11.62 h^(-1),and the molar conversion of cyclohexanol reaches 81%.In addition,the catalyst also has good performance for dehydrogenation of benzyl alcohol to benzaldehyde.At 260℃and a WHSV of 12.48 h^(-1),the molar conversion of benzyl alcohol reaches 75%,and the yield of benzaldehyde reaches 61%.Under these conditions,the activity of the catalyst remains stable within 48 h.
作者 李正萍 史明豪 李楠 马江权 LI Zheng-ping;SHI Ming-hao;LI Nan;MA Jiang-quan(Jiangsu Key Laboratory of Green Catalytic Materials and Technology,School of Petrochemical Engineering,Changzhou University,Changzhou 213164,China;Advanced Catalysis and Green Manufacturing Collaborative Innovation Center,Changzhou University,Changzhou 213164,China)
出处 《现代化工》 CAS CSCD 北大核心 2023年第8期191-197,共7页 Modern Chemical Industry
基金 常州市应用基础研究计划项目(CJ20220152) 常州大学、先进催化与绿色制造协同创新中心、江苏省常州市生物质精炼与优质利用国家地方联合工程研究中心及产业支撑项目(CE20195022) 浙江省国家重点研发计划(2019C01083) 江苏省教育厅科研基金(21KJB430035)。
关键词 环己醇脱氢 苯甲醇脱氢 铜催化剂 固定床反应器 cyclohexanol dehydrogenation benzyl alcohol dehydrogenation copper-based catalyst fixed bed reactor
  • 相关文献

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部