期刊
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
卷 61, 期 11, 页码 3850-3859出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.1c03760
关键词
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资金
- National Key Research and Development Program of China [2017YFA0206803]
- National Nature Science Foundation of China [22078338]
- Major Program of National Science Foundation of China [21890760]
- Key Programs of the Chinese Academy of Sciences [KFZD-SW-413]
- K.C. Wong Education Foundation [GJTD-2018-04]
A series of tunable-acidity VPO catalysts modified by LDO were fabricated, and the relationship between the surface properties and catalytic performance was explored. The appropriate surface acidity significantly improved the performance, and a synergistic catalysis mechanism between Lewis and Bronsted acid sites was proposed to enhance the catalytic performance.
A series of tunable-acidity vanadium phosphorus oxide (VPO) catalysts modified by layered double oxide (LDO)werefirst fabricated by a mechanical milling approach. The optimum Zn2Mg1Al1O-VPO sample achieved 63.2% yield of maleicanhydride (MA), which is 8.9% higher than that of Blank-VPO. Various characterizations were used to explore the relationshipbetween the surface properties such as the crystal structure, surface P/V ratio, surface acidity, and catalytic performance. The NH3-TPD and pyridine IR analysis demonstrated that the appropriate surface acidity could significantly improve the performance of theVPO catalyst. A synergistic catalysis mechanism between the Lewis and Bronsted acid sites is tentatively proposed to enhance thecatalytic performance of VPO. The Lewis acid sites accelerate the C-H bond activation and cleavage, thereby increasing theconversion ofn-butane. Moreover, the Bronsted acid sites can stabilize the reaction intermediates and facilitate the desorption ofMA, consequently improving the selectivity of MA.
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