化工进展 ›› 2024, Vol. 43 ›› Issue (4): 1851-1862.DOI: 10.16085/j.issn.1000-6613.2023-0525

• 工业催化 • 上一篇    

蛭石基FeCeO x 催化剂及CO选择性催化还原NO

高飞1(), 刘志松1, 潘珂珂1, 刘敏敏1, 代斌1(), 但建明1(), 于锋1,2()   

  1. 1.石河子大学化学化工学院化工绿色过程兵团重点实验室,新疆 石河子 832003
    2.石河子大学兵团工业技术 研究院碳中和与环境催化技术研究室,新疆 石河子 832003
  • 收稿日期:2023-04-06 修回日期:2023-06-11 出版日期:2024-04-15 发布日期:2024-05-13
  • 通讯作者: 代斌,但建明,于锋
  • 作者简介:高飞(1998—),男,硕士研究生,研究方向为氮氧化物脱除。E-mail:1138896836@qq.com
  • 基金资助:
    兵团区域创新计划(2021BB005);兵团科技创新团队计划(2020CB006);兵团重大科技计划(2018AA002)

Vermiculite-supported FeCe bimetallic catalyst for selective catalytic reduction of NO with CO

GAO Fei1(), LIU Zhisong1, PAN Keke1, LIU Minmin1, DAI Bin1(), DAN Jianming1(), YU Feng1,2()   

  1. 1.Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan, School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003, Xinjiang, China
    2.Carbon Neutralization and Environmental Catalytic Technology Laboratory, Bingtuan Industrial Technology Research Institute, Shihezi University, Shihezi 832003, Xinjiang, China
  • Received:2023-04-06 Revised:2023-06-11 Online:2024-04-15 Published:2024-05-13
  • Contact: DAI Bin, DAN Jianming, YU Feng

摘要:

以CO为还原剂去除NO的选择性催化还原(CO-SCR)技术受到了广泛关注。本文以天然矿物蛭石为载体,采用共沉淀辅助浸渍法(CP-IM)制备了蛭石负载的铁铈双金属氧化物(FeCe/VMT)用于CO-SCR脱硝反应。表征结果显示,相比传统的浸渍法(IM),共沉淀辅助浸渍制备的FeCe/VMT催化剂具有更大的比表面积(106.9m2/g)和更多氧空位,可以提供更多的活性位点。共沉淀过程形成更多Fe3+,并促进了FeCe间的协同作用,有利于提高CO-SCR的催化活性和稳定性。性能测试表明,在300℃和50000h-1的空速下,NO转化率可达100%,48h后NO转化率几乎无衰减。当温度降至250℃时,NO的转化率依然可以达到97%。同时,利用原位红外光谱和密度泛函理论计算技术,揭示了相应的催化反应机理,为制备大比表面积的负载型催化剂提供了一种方法。

关键词: 催化剂, 一氧化碳, 选择催化还原, 纳米材料, 多相反应

Abstract:

NO removal by CO selective catalytic reduction (CO-SCR) has gained great attentions. In this paper, vermiculite-supported Fe-Ce bimetallic oxides (FeCe/VMT) for CO-SCR were prepared by coprecipitation-assisted impregnation (CP-IM) with the natural mineral vermiculite as the carrier. The characterization results showed that compared with the traditional impregnation method (IM), FeCe/VMT (CP-IM) prepared by coprecipitation-assisted impregnation had larger specific surface area (106.9m2/g) and more oxygen vacancies due to more active sites available. The enhanced synergistic effect between FeCe was beneficial to the increase of both catalytic activity and stability in CO-SCR reaction. Performance tests showed that NO conversion reached 100% at 300℃ with 50000h-1 gas hourly space velocity (GHSV), and the performance of the catalyst didn't decrease within 48h. When the temperature dropped to 250℃, the conversion of NO could still reach 97%. At the same time, insitu infrared spectroscopy and density functional theory were used to reveal the corresponding catalytic mechanism. This research provided a promising method for preparing supported catalysts with large specific surface area.

Key words: catalyst, carbon monoxide, selective catalytic reduction (SCR), nanomaterials, multiphase reaction

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