A Clathrate‐Like Methane Trap for Capture of Mine Ventilation Air Methane

F Feifei Zhang Y Yating Wang M Mengyue Lu (College of Chemistry and Chemical Engineering Taiyuan University of Technology Taiyuan P. R. China) X Xiaomin Li (Department of Chemistry, Shanghai Stomatological Hospital & School of Stomatology, State Key Laboratory of Molecular Engineering of Polymers, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials) X Xiaowei Bai X Xiaoqing Wang (Hefei National Research Center for Physical Sciences at the Microscale and Synergetic Innovation Center of Quantum Information & Quantum Physics, New Cornerstone Science Laboratory) J Jinping Li J Jiangfeng Yang

Abstract

ABSTRACT Adsorption‐based processes offer an efficient approach for the treatment of ventilation air methane (VAM). However, existing separation mechanisms typically distinguish CH 4 and N 2 based on their insignificant differences in polarizability and size, and remain largely ineffective for VAM with extremely low CH 4 concentrations. Here, we reported a clathrate‐like methane trap featuring dense arrays of electronegative O/N atoms as in methane hydrate, which exhibited electrostatic potential and shape complementarity toward CH 4 , realizing precise CH 4 recognition. The clathrate‐like methane trap exhibited a high isosteric heat of adsorption ( Q st ) of 36.0 kJ mol −1 for CH 4 , a benchmark Q st difference between CH 4 and N 2 (19.6 kJ mol −1 ), and the highest reported equilibrium‐kinetic combined selectivity (19.0). Breakthrough experiments confirmed that this trap efficiently captured CH 4 from a CH 4 /N 2 (1/99) mixture, providing a record‐high breakthrough selectivity (3.8). Its practical potential was validated by conducting a two‐bed, six‐step, variable‐pressure swing adsorption process, and 25% purity CH 4 could be obtained from a CH 4 /N 2 (1/99) mixture. In situ infrared spectroscopy and computational modelling studies revealed that the rational arrangement of dense N/O binding sites imparted a synergy between optimal pore shape and surface electrostatic potential that boosted CH 4 affinity.

Article Details

Volume / Issue Vol. 65, Issue 22
Published May 25, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

F

Feifei Zhang

Y

Yating Wang

M

Mengyue Lu

College of Chemistry and Chemical Engineering Taiyuan University of Technology Taiyuan P. R. China

X

Xiaomin Li

Department of Chemistry, Shanghai Stomatological Hospital & School of Stomatology, State Key Laboratory of Molecular Engineering of Polymers, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials

X

Xiaowei Bai

X

Xiaoqing Wang

Hefei National Research Center for Physical Sciences at the Microscale and Synergetic Innovation Center of Quantum Information & Quantum Physics, New Cornerstone Science Laboratory

J

Jinping Li

J

Jiangfeng Yang