Chen Qizhi, Yang Yong, Luo Hang, Liu Zuohua, Tong Zhangfa, Tao Changyuan, Du Jun
School of Chemistry and Chemical Engineering, Guangxi University Nanning 530004 China.
Guangxi Huiyuan Manganese Industry Co., Ltd. China.
RSC Adv. 2020 Nov 4;10(66):40047-40054. doi: 10.1039/d0ra06639g. eCollection 2020 Nov 2.
Ce modified MnO /SAPO-34 was prepared and investigated for low-temperature selective catalytic reduction of NO with ammonia (NH-SCR). The 0.3Ce-Mn/SAPO-34 catalyst had nearly 95% NO conversion at 200-350 °C at a space velocity of 10 000 h. Microporous SAPO-34 as the support provided the catalyst with increased hydrothermal stability. XPS and H-TPR results proved that the Mn and O content increased after incorporation of Ce, this promoted the conversion of NO at low temperature a 'fast SCR' route. NH-TPD measurements combined oxidation experiments of NO, NH indicated the reduction of both the surface acidity and the amount of acid sites, which effectively decreased the NH oxditaion to NO or NO at elevated temperature and promoted the catalytic selectivity for nitrogen. A redox cycle between manganese oxide and Ce was assumed for the active oxygen transfer and facilitated the catalyst durability.
制备了铈改性的MnO₂/SAPO-34,并对其用于氨(NH₃-SCR)低温选择性催化还原NO进行了研究。0.3Ce-Mn/SAPO-34催化剂在200-350℃、空速为10000 h⁻¹时,NO转化率接近95%。作为载体的微孔SAPO-34提高了催化剂的水热稳定性。XPS和H-TPR结果表明,掺入铈后,Mn和O含量增加,这促进了低温下NO的转化,形成了“快速SCR”途径。NH₃-TPD测量结合NO、NH₃的氧化实验表明,表面酸度和酸位数量均降低,这有效地减少了高温下NH₃氧化为NO或NO₂的情况,并提高了对氮气的催化选择性。假定氧化锰和铈之间存在氧化还原循环以实现活性氧转移,并提高了催化剂的耐久性。