SCI和EI收录∣中国化工学会会刊

中国化学工程学报 ›› 2025, Vol. 85 ›› Issue (9): 128-139.DOI: 10.1016/j.cjche.2025.03.019

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The sulfur and water resistance improvement of Pt/TiO2 catalyst for CO oxidation reaction by anatase and rutile TiO2 crystal interfaces

Zhenxing Feng1, Bin Song1, Zongcheng Zhan2, Lei Xu1, Hanlei Sun1, Shuo Yao1, Hongzhi Wang1, Licheng Liu1   

  1. 1. Key Laboratory of Marine Chemistry Theory and Technology (Ministry of Education), College of Chemistry & Chemical Engineering, Ocean University of China, Qingdao 266100, China;
    2. Qingdao Huashijie Environment Technology Co., Ltd., Qingdao 266510, China
  • 收稿日期:2025-01-14 修回日期:2025-03-18 接受日期:2025-03-21 出版日期:2025-09-28 发布日期:2025-04-26
  • 通讯作者: Licheng Liu,E-mail:liulicheng@ouc.edu.cn
  • 基金资助:
    This work was financially supported by the National Key Research & Development Program of China (2024YFC3908400), the National Natural Science Foundation of China (U21B2099) and Fundamental Research Funds for the Central Universities, Ocean University of China (202364004).

The sulfur and water resistance improvement of Pt/TiO2 catalyst for CO oxidation reaction by anatase and rutile TiO2 crystal interfaces

Zhenxing Feng1, Bin Song1, Zongcheng Zhan2, Lei Xu1, Hanlei Sun1, Shuo Yao1, Hongzhi Wang1, Licheng Liu1   

  1. 1. Key Laboratory of Marine Chemistry Theory and Technology (Ministry of Education), College of Chemistry & Chemical Engineering, Ocean University of China, Qingdao 266100, China;
    2. Qingdao Huashijie Environment Technology Co., Ltd., Qingdao 266510, China
  • Received:2025-01-14 Revised:2025-03-18 Accepted:2025-03-21 Online:2025-09-28 Published:2025-04-26
  • Contact: Licheng Liu,E-mail:liulicheng@ouc.edu.cn
  • Supported by:
    This work was financially supported by the National Key Research & Development Program of China (2024YFC3908400), the National Natural Science Foundation of China (U21B2099) and Fundamental Research Funds for the Central Universities, Ocean University of China (202364004).

摘要: Catalytic oxidation is an effective strategy for eliminating CO pollutant. Pt/TiO2 catalyst are one of the most active catalysts as used, but facing the issue of sulfur and water deactivation. In this study, TiO2 was synthesized using a sol-gel method, while Pt/TiO2 was prepared by impregnation method. By varying the calcination temperature of the TiO2 support, Pt/TiO2 catalysts with different proportions of anatase and rutile phases were synthesized. At the calcination temperature of 500 ℃, the catalysts exhibited approximately equal proportions of anatase and rutile, resulting in exceptional catalytic activity for CO oxidation, as well as improved resistance to sulfur and water in the flue gas. Consequently, the Pt/TiO2-500 catalyst achieved a CO conversion of 93% at 160 ℃. Even under conditions of 8% (vol) H2O and 0.016% (vol) SO2 (GHSV = 300000 ml·h-1·g-1), the CO conversion remained above 95% at 220 ℃ for 46 h. The catalysts were characterized and analyzed using various techniques. The results indicated that anatase-phase TiO2 exhibited weak CO adsorption capacity but strong SO2 adsorption capacity, whereas rutile-phase TiO2 demonstrated strong CO adsorption capacity and weak SO2 adsorption capacity. The presence of the anatase phase mitigated the CO self-poisoning phenomenon of the catalyst, while the biphase interface reduced the adsorption and oxidation of SO2 on the catalyst’s surface, significantly inhibiting the deposition of TiOSO4. Consequently, the Pt/TiO2-500 catalyst displayed the highest CO catalytic activity along with superior resistance to sulfur and water.

关键词: CO oxidation, Pt/TiO2 catalysts, TiO2 support, Crystal phase, Sulfur tolerance

Abstract: Catalytic oxidation is an effective strategy for eliminating CO pollutant. Pt/TiO2 catalyst are one of the most active catalysts as used, but facing the issue of sulfur and water deactivation. In this study, TiO2 was synthesized using a sol-gel method, while Pt/TiO2 was prepared by impregnation method. By varying the calcination temperature of the TiO2 support, Pt/TiO2 catalysts with different proportions of anatase and rutile phases were synthesized. At the calcination temperature of 500 ℃, the catalysts exhibited approximately equal proportions of anatase and rutile, resulting in exceptional catalytic activity for CO oxidation, as well as improved resistance to sulfur and water in the flue gas. Consequently, the Pt/TiO2-500 catalyst achieved a CO conversion of 93% at 160 ℃. Even under conditions of 8% (vol) H2O and 0.016% (vol) SO2 (GHSV = 300000 ml·h-1·g-1), the CO conversion remained above 95% at 220 ℃ for 46 h. The catalysts were characterized and analyzed using various techniques. The results indicated that anatase-phase TiO2 exhibited weak CO adsorption capacity but strong SO2 adsorption capacity, whereas rutile-phase TiO2 demonstrated strong CO adsorption capacity and weak SO2 adsorption capacity. The presence of the anatase phase mitigated the CO self-poisoning phenomenon of the catalyst, while the biphase interface reduced the adsorption and oxidation of SO2 on the catalyst’s surface, significantly inhibiting the deposition of TiOSO4. Consequently, the Pt/TiO2-500 catalyst displayed the highest CO catalytic activity along with superior resistance to sulfur and water.

Key words: CO oxidation, Pt/TiO2 catalysts, TiO2 support, Crystal phase, Sulfur tolerance