He Qingrong, Wang Xuwei, Liu Yimeng, Kong Weimin, Ren Shanshan, Liang Yun, Tang Min, Zhou Shuyuan, Dong Yanchun
School of Light Industry and Engineering, South China University of Technology, Guangzhou 510640, China.
State Key Laboratory of NBC Protection for Civilian, Beijing 100083, China.
Materials (Basel). 2023 May 16;16(10):3755. doi: 10.3390/ma16103755.
Carbon monoxide (CO) is a colourless, odourless, and toxic gas. Long-term exposure to high concentrations of CO causes poisoning and even death; therefore, CO removal is particularly important. Current research has focused on the efficient and rapid removal of CO via low-temperature (ambient) catalytic oxidation. Gold nanoparticles are widely used catalysts for the high-efficiency removal of high concentrations of CO at ambient temperature. However, easy poisoning and inactivation due to the presence of SO and HS affect its activity and practical application. In this study, a bimetallic catalyst, Pd-Au/FeO/AlO, with a Au:Pd ratio of 2:1 (wt%) was formed by adding Pd nanoparticles to a highly active Au/FeO/AlO catalyst. Its analysis and characterisation proved that it has improved catalytic activity for CO oxidation and excellent stability. A total conversion of 2500 ppm of CO at -30 °C was achieved. Furthermore, at ambient temperature and a volume space velocity of 13,000 h, 20,000 ppm CO was fully converted and maintained for 132 min. Density functional theory (DFT) calculations and in situ FTIR analysis revealed that Pd-Au/FeO/AlO exhibited stronger resistance to SO and HS adsorption than the Au/FeO/AlO catalyst. This study provides a reference for the practical application of a CO catalyst with high performance and high environmental stability.
一氧化碳(CO)是一种无色、无味的有毒气体。长期暴露于高浓度的CO会导致中毒甚至死亡;因此,去除CO尤为重要。目前的研究主要集中在通过低温(环境温度)催化氧化高效快速地去除CO。金纳米颗粒是在环境温度下高效去除高浓度CO的广泛使用的催化剂。然而,由于SO和HS的存在导致的易中毒和失活影响了其活性和实际应用。在本研究中,通过向高活性的Au/FeO/AlO催化剂中添加钯纳米颗粒,形成了一种金钯比为2:1(重量%)的双金属催化剂Pd-Au/FeO/AlO。其分析和表征证明它对CO氧化具有更高的催化活性和优异的稳定性。在-30°C下实现了2500 ppm的CO的完全转化。此外,在环境温度和13,000 h的体积空速下,20,000 ppm的CO被完全转化并保持了132分钟。密度泛函理论(DFT)计算和原位FTIR分析表明,Pd-Au/FeO/AlO比Au/FeO/AlO催化剂对SO和HS吸附表现出更强的抗性。本研究为高性能和高环境稳定性的CO催化剂的实际应用提供了参考。