沸石
焦炭
催化作用
加氢脱氧
大孔隙
微型多孔材料
整体
介孔材料
化学工程
材料科学
碳化
愈创木酚
化学
有机化学
吸附
复合材料
选择性
冶金
工程类
作者
Fengli Gan,Xia Jiang,Ziheng Jin,Mingwu Tan,Xindi Xie,Q.J. Peng,Guangmei Cao,Shenggui Ma
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-08-22
卷期号:14 (17): 13324-13333
被引量:3
标识
DOI:10.1021/acscatal.4c02914
摘要
Mass transport in conventional microporous zeolite catalysts can be enhanced by introducing secondary mesopores during hydrodeoxygenation (HDO). However, the impact of the macropore architecture with intrinsic mass transfer advantages over mesopores on HDO performance remains elusive. In this study, a macroporous zeolite monolith catalyst without a template and binder was synthesized using a crystal space-confined growth method. This catalyst exhibited a 1.3 times higher macropore volume (0.566 m3/g) than a conventional zeolite catalyst, while the microporous structure was similar. Moreover, the high degree macropore connectivity was directly visualized and quantified with an advanced nanocomputed tomography technique. The macroporous catalyst achieved a higher guaiacol conversion rate of 93% and better coke resistance (3.2 wt % coke) than the conventional zeolite catalyst, which showed a 90% guaiacol conversion rate and 5.6 wt % coke. This improvement was primarily due to faster diffusion rates and an increased number of acid sites in the macropores.
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