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Verified CAS / Academic Author2 Decoded Studies

Prof. TAN Minghui

National Engineering Center for Large-Scale Coal Gasification and Coal-Based New Materials, Shandong Energy Group

Co-Affiliations:State Key Laboratory of Clean and Efficient Coal Utilization, College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, China

Research Publications & English Decoded Briefs

Showing 2 publications
Journal of Fuel Chemistry and Technology2026DOI: 10.1016/S1872-5813(25)60624-4

Recent Advances in Catalysts for the Highly Selective Conversion of Syngas into Para-Xylene

Para-xylene (PX) is a critical chemical feedstock for producing polyesters, plastics, and fibers, with China's 2024 consumption reaching 40 million tons (63% of global total) and an import dependency of 17%. Conventional naphtha-based routes face feedstock security and cost volatility, prompting interest in syngas conversion. This review systematically examines recent catalyst developments for direct syngas-to-PX-rich aromatics, focusing on three systems: Fischer-Tropsch synthesis (FTS) catalyst/zeolite coupling, methanol synthesis catalyst/zeolite synergy, and dual-engine/zeolite catalysis. Critical parameters such as active component electronic structure, promoter effects, and zeolite pore topology are analyzed to reveal governing principles of activity, selectivity, and stability. Reaction mechanisms via olefin, methanol, and dual-intermediate pathways are explored. Current bottlenecks include coordinated optimization of activity and stability, and unclear regulation of PX selectivity. Future research directions are proposed to address these challenges.

Journal of Fuel Chemistry and Technology2026DOI: 10.1016/S1872-5813(26)60663-9

Calcination Atmosphere-Engineered Cu/SiO2 Catalysts for Efficient Hydrogenation of Dimethyl Succinate to 1,4-Butanediol

The catalytic hydrogenation of biomass-derived dimethyl succinate (DMS) to 1,4-butanediol (BDO) is a pivotal route for producing high-value C4 chemicals in green chemistry. Cu/SiO2 catalysts are known for high selectivity in hydrogenating ester groups, with performance correlated to copper species microstructure. Although calcination critically defines this active structure, systematic influence of calcination atmosphere remains underexplored. Here, Cu/SiO2 catalysts were prepared via urea-assisted hydrothermal method and calcined under different atmospheres to elucidate effects on physicochemical properties and hydrogenation performance. Comprehensive characterization (N2 physisorption, FT-IR, H2-TPR, XRD, TEM, N2O pulse chemisorption, XPS, NH3-TPD) revealed that calcination atmosphere profoundly alters metal-support interaction, regulating dispersion and chemical state of copper species. Specifically, air calcination promoted stronger metal-support interaction, enhancing copper dispersion and increasing proportion of key active Cu+ species. Consequently, air-calcined catalyst achieved 92.37% DMS conversion and 64.15% BDO yield under optimized conditions (210 °C, 5.0 MPa, WHSV 0.6 h−1, H2/DMS molar ratio 100). This work underscores calcination atmosphere engineering as potent strategy for optimizing metal-support interactions in heterogeneous catalysts for efficient hydrogenation.