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Verified CAS / Academic Author2 Decoded Studies

Prof. Shucheng Li

School of Materials Science and Engineering, Zhengzhou University

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3814-2

Directional Micro-Grooved Fibers with Theoretical Infinite-Length Toward Liquid Self-Transport

Micro-structured surfaces have attracted increasing attention due to their great potential applications. However, it is still a challenge to continuously fabricate micro-structured surfaces based on thermoplastics by a facile, low-cost, and environmentally-friendly method. Herein, with the help of the extrusion molding method and an elaborately designed mold, micro-grooved fiber (MGF) based on high-density polyethylene (HDPE) is continuously prepared. Theoretically, infinitely long MGFs with feature sizes down to a few microns can be efficiently fabricated because of the continuous fabrication characteristic of the melt extrusion method. Interestingly, left- and right-handed micro-grooves with different helix angles can be produced by applying twisting at the die exit, and the macroscopically MGF springs can be further fabricated via a self-designed three-dimensional helical enwind device. By regulating wettability, MGF can achieve liquid self-transport on predefined paths. In addition, MGF fabric exhibits rapid evaporation behavior, whose evaporation rate is about 4 times higher than that of the Smooth fiber (SMF) fabric and 2 times higher than that of the most popular commercial quick-drying fabric (i.e., Cool-max fabric). This work proposes a facile and environmentally-friendly method for continuously preparing low-cost and flexible MGF, opening a new pathway to develop fiber-based microfluidic systems following the concept of "functionalized processing for thermoplastics".

Journal of Fuel Chemistry and Technology2026DOI: 10.1016/S1872-5813(26)60653-6

Study on the coke deposition characteristics of hierarchical ZSM-5 zeolites with synergistic regulation of pore structure and temperature in benzene catalysis

Carbon deposition caused by mass transfer limitations is a key challenge for traditional microporous ZSM-5 zeolites in coal tar catalytic cracking. To address this, benzene was used as a model compound. Parent ZSM-5 (NL-ZSM-5) was modified with tetraethylammonium hydroxide (TEAOH) to prepare hierarchical ZSM-5 zeolites with different mesopore sizes. Characterization (XRD, FT-IR, BET, TEM) confirmed successful mesopore introduction via selective desilication while retaining the MFI structure. At TEAOH concentration of 0.4 mol/L (ZSM-5-C), total pore volume increased from 0.24 to 0.43 cm3/g, and Brønsted acid amount increased from 0.28 to 0.67 mmol/g, with improved acid site accessibility. Catalytic experiments and carbon deposition analysis showed that hierarchical pore structure inhibits coking via a synergistic effect of diffusion enhancement and adsorption-site regulation. The coke amount of ZSM-5-C was 4.0%, only one-third of that of NL-ZSM-5 (11.9%). Molecular dynamics simulations confirmed that the diffusion coefficient of benzene in a 3.0 nm mesopore model is an order of magnitude higher than in a 2.0 nm model. Adsorption capacity decreases with increasing mesopore size, shortening residence time. Increasing temperature enhances diffusion but exponentially intensifies surface condensation reactions (Arrhenius effect), which dominates coke formation; hierarchical pores mitigate this negative effect. This research provides a theoretical basis for designing high-efficiency, coke-resistant catalysts for coal tar conversion.