Wang Haodi, Jiao Feng, Ding Yi, Liu Wenjuan, Xu Zhaochao, Pan Xiulian, Bao Xinhe
State Key Laboratory of Catalysis, 2011-Collaborative Innovation Center of Chemistry for Energy Materials, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Natl Sci Rev. 2022 Jul 26;9(9):nwac146. doi: 10.1093/nsr/nwac146. eCollection 2022 Sep.
The OXZEO (oxide-zeolite) bifunctional catalyst concept has enabled selective syngas conversion to a series of value-added chemicals and fuels such as light olefins, aromatics and gasoline. Herein we report for the first time a dynamic confinement of SAPO-17 cages on the selectivity control of syngas conversion observed during an induction period. Structured illumination microscopy, intelligent gravimetric analysis, UV-Raman, X-ray diffraction, thermogravimetry and gas chromatography-mass spectrometer analysis indicate that this is attributed to the evolution of carbonaceous species as the reaction proceeds, which gradually reduces the effective space inside the cage. Consequently, the diffusion of molecules is hindered and the hindering is much more prominent for larger molecules such as C. As a result, the selectivity of ethylene is enhanced whereas that of C is suppressed. Beyond the induction period, the product selectivity levels off. For instance, ethylene selectivity levels off at 44% and propylene selectivity at 31%, as well as CO conversion at 27%. The findings here bring a new fundamental understanding that will guide further development of selective catalysts for olefin synthesis based on the OXZEO concept.
OXZEO(氧化物-沸石)双功能催化剂概念已实现将合成气选择性转化为一系列增值化学品和燃料,如轻质烯烃、芳烃和汽油。在此,我们首次报道了在诱导期观察到的SAPO-17笼的动态限域对合成气转化选择性控制的影响。结构光照显微镜、智能重量分析、紫外拉曼光谱、X射线衍射、热重分析和气相色谱-质谱分析表明,这归因于反应进行过程中碳质物种的演变,其逐渐减小了笼内的有效空间。因此,分子扩散受到阻碍,对于较大分子如C而言,这种阻碍更为显著。结果,乙烯的选择性增强,而C的选择性受到抑制。在诱导期之后,产物选择性趋于稳定。例如,乙烯选择性稳定在44%,丙烯选择性稳定在31%,CO转化率稳定在27%。此处的研究结果带来了一种新的基础认识,将指导基于OXZEO概念的烯烃合成选择性催化剂的进一步开发。