journal article·2019-10-28

Enhancing the Catalytic Activity and Selectivity of PdAu/SiO2 Bimetallic Catalysts for Dodecahydro-N-ethylcarbazole Dehydrogenation by Controlling the Particle Size and Dispersion

Zhao Jiang, Shuyi Guo, Tao Fang

ACS Applied Energy Materials· Volume 2· Issue 10
Publisher page

Abstract

The design and development of catalysts for dodecahydro-N-ethylcarbazole (12H-NECZ) dehydrogenation restrict the achievement of the cyclic hydrogenation/dehydrogenation process. In this work, the M/SiO2 (M = Pt, Pd, Ru, Rh, Au) and bimetallic PdAu/SiO2 catalysts are prepared, and their catalytic performances are measured. By XRD, XPS, HRTEM, and CO pulse chemisorption, we find that the alloy structure is not generated and the average particle size increases with the improvement of the Au amount in the bimetallic catalysts. Besides, the catalytic performance can be enhanced dramatically with introducing a small amount Au. Pd3Au1/SiO2 exhibits the best catalytic performance with the complete conversion, 94.9 selectivity to NECZ, and 5.7 wt % hydrogen release amount. The TOF values are up to 240.7 min–1, 2.26 times higher than that of Pd/SiO2. The qualitative and quantitative analyses indicate that 4H-NECZ dehydrogenation is the rate-limiting step. It can be proposed that controlling the particle size and dispersion of the PdAu/SiO2 bimetallic catalysts will bring a significant enhancement of catalytic performance.
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Research context

OpenAlex topics: Catalytic Processes in Materials Science · Carbon dioxide utilization in catalysis · Ammonia Synthesis and Nitrogen Reduction

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical Engineering, Shaanxi Key Laboratory of Energy Chemical Process Intensification, Xi’an Jiaotong University, Xi’an 710049, China

Funding

Ministry of Education of the People's Republic of China · National Natural Science Foundation of China · Natural Science Basic Research Plan in Shaanxi Province of China

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