手机版

扫一扫,手机访问

关于我们 加入收藏

麦克默瑞提克(上海)仪器有限公司

15 年金牌会员

已认证

拨打电话
获取底价
提交后,商家将派代表为您专人服务
立即发送
点击提交代表您同意 《用户服务协议》
当前位置:
美国麦克仪器 >公司动态 >

每周分享

每周分享
美国麦克仪器  2014-10-12  |  阅读:1879

手机扫码查看
    今天给大家分享的是2014年5月份 《Applied Catalysis A: General》上发表的一篇名为:Mechanistic insights into the effects of support on the reaction pathway for aqueous-phase hydrogenation of carboxylic acid over the supported Ru catalysts
 
文章摘要如下:
Several supported Ru catalysts, Ru/TiO2, Ru/ZrO2, Ru/SiO2, Ru/γ-Al2O3 and Ru/SiO2-Al2O3, were prepared and investigated for propanoic acid aqueous-phase hydrogenation. H2-TPR, NH3-TPD, pyridine-FTIR and propanoic acid-DRIFTS techniques were performed to explore the metal–support interaction, acid sites and key adsorption species. The effect of support on the reaction pathway of CO hydrogenation and decarbonylation of acyl species was discussed. Compared with Ru/ZrO2 and Ru/SiO2 catalysts, high selectivity of CO hydrogenation was obtained over the catalysts with more Lewis acid sites, such as Ru/γ-Al2O3 and Ru/SiO2-Al2O3 catalysts. The DRIFTS results suggest that the formation of adsorption species (acyl, carboxylate and carboxylic acid) is strongly depended on the nature of support. The metal–acid bifunctional sites are indispensable for the CO hydrogenation of acyl. However, the decarbonylation of acyl on the metal sites requires the relatively weak metal–support interaction and few of Lewis acid sites.
 
该文章中材料表征采用的是美国麦克仪器AutoChem 2920
 
详情可参考下面链接:
http://scholar.google.com.hk/scholar?start=20&q=Autochem+2920&hl=zh-CN&as_sdt=0,5&as_ylo=2014
留言咨询
(我们会第一时间联系您)
关闭
留言类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
(请留下您的联系方式,以便工作人员及时与您联系!)