Boosting the Performance of Pt-Based Honeycomb Monolithic Catalysts for CO Preferential Oxidation in Hydrogen-Rich Streams via the Channel Rotation

被引:0
作者
Sun, Zongzhuang [1 ]
Zhang, Xiaoqian [1 ]
Cao, Jianlin [1 ]
Wang, Qing [1 ]
Yuan, Juncong [1 ]
Li, Weiguo [2 ]
Lu, Yiwu [3 ]
Fu, Xiaoli [4 ]
Sui, Jiancai [2 ]
Zhou, Xin [5 ]
Tuo, Yongxiao [1 ]
Feng, Xiang [1 ]
Yang, Chaohe [1 ]
Chen, De [6 ]
机构
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Qingdao 266580, Shandong, Peoples R China
[2] Natl Engn Res Ctr Coal Gasificat & Coal Based Adv, Jinan 250000, Peoples R China
[3] Yankuang Lunan Chem Co Ltd, Zaozhuang 277500, Peoples R China
[4] ShanDong Energy Grp Co Ltd, Jinan 250000, Peoples R China
[5] Ocean Univ China, Dept Chem & Chem Engn, Qingdao 266100, Shandong, Peoples R China
[6] Norwegian Univ Sci & Technol, Dept Chem Engn, N-7491 Trondheim, Norway
基金
中国国家自然科学基金;
关键词
CARBON-MONOXIDE; HEAT-TRANSFER; MECHANICAL STABILITY; REACTOR;
D O I
10.1021/acs.iecr.4c01926
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
CO preferential oxidation (CO-PROX) in H2-rich streams has garnered considerable attention because of the emerging hydrogen economy, including advanced fuel cell technology. Particularly, mass transfer and diffusion at low CO concentrations (1 vol %) are critical factors influencing CO-PROX performance of structured catalyst. In this study, Pt/Fe3O4 catalysts were uniformly coated on honeycomb ceramics, and the stacked arrangement of rotating channels with varying angles (0 degrees, 15 degrees, 30 degrees, and 45 degrees) was proposed to enhance CO diffusion in channels. By employing computational fluid dynamics (CFD), the velocity, CO mole fraction, and pressure were systematically analyzed, and the underlying angle-performance relationship was then elucidated. Through this cost-effective rotation strategy, flow perturbations were induced as gas transitions between monoliths, which prompted a shift from laminar to turbulent flow and altered velocity and reactant distribution. At a rotation angle of 45 degrees, the CO conversion was boosted by 5-13%. This work underscores the pivotal role of our innovative catalyst design in revolutionizing the CO-PROX reactions to pave the way for enhanced efficiency and practical implementation in various industrial applications.
引用
收藏
页码:15073 / 15082
页数:10
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