Chen Hui, Chen Qi, Hu Xiaomin, Ding Chenyu, Huang Lihong, Wang Ning
State Key Laboratory of Geohazard Prevention and Geoenvironment Protection, Chengdu University of Technology, Chengdu 610059, China.
College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu 610059, China.
Materials (Basel). 2024 May 22;17(11):2490. doi: 10.3390/ma17112490.
The x%Ni/SmO-MnO (x = 0, 10, 15, 20) catalysts derived from SmMnO mullite were prepared by solution combustion and impregnation method; auto-thermal reforming (ATR) of acetic acid (HAc) for hydrogen production was used to explore the metal-support effect induced by Ni loadings on the catalytic reforming activity and product distribution. The 15%Ni/SmO-MnO catalyst exhibited optimal catalytic performance, which can be due to the appropriate Ni loading inducing a strong metal-support interaction to form a stable Ni/SmO-MnO active center, while side reactions, such as methanation and ketonization, were well suppressed. According to characterizations, SmO-MnO mixed oxides derived from SmMnO mullite were formed with oxygen vacancies; nevertheless, loading of Ni metal further promoted the formation of oxygen vacancies, thus enhancing adsorption and activation of oxygen-containing intermediate species and resulting in higher reactivity with HAc conversion near 100% and hydrogen yield at 2.62 mol-H/mol-HAc.
通过溶液燃烧法和浸渍法制备了源自SmMnO莫来石的x%Ni/SmO-MnO(x = 0、10、15、20)催化剂;采用乙酸(HAc)自热重整制氢来探究镍负载量引起的金属-载体效应对催化重整活性和产物分布的影响。15%Ni/SmO-MnO催化剂表现出最佳的催化性能,这可能是由于适量的镍负载量诱导了强烈的金属-载体相互作用,形成了稳定的Ni/SmO-MnO活性中心,同时甲烷化和酮化等副反应得到了很好的抑制。根据表征结果,源自SmMnO莫来石的SmO-MnO混合氧化物形成了氧空位;然而,镍金属的负载进一步促进了氧空位的形成,从而增强了含氧化合物中间物种的吸附和活化,导致乙酸转化率接近100%且氢气产率为2.62 mol-H/mol-HAc时具有更高的反应活性。