烷烃
微型多孔材料
选择性
吸附
限制
石油化工
吸附
分子
合理设计
化学
选择性吸附
金属有机骨架
化学工程
材料科学
有机化学
纳米技术
碳氢化合物
催化作用
机械工程
工程类
作者
Li Wang,Zhaozhuang Liu,Yating Wang,Jiaqi Liu,Jinping Li,Jiangfeng Yang
标识
DOI:10.1002/advs.202516118
摘要
Abstract Efficient separation of light hydrocarbons—including the removal of CH 4 from N 2 and the purification of olefins such as C 2 H 4 and C 3 H 6 from their corresponding alkanes (C 2 H 6 and C 3 H 8 )—is critical in natural gas upgrading, steam cracking, and downstream petrochemical production. Traditional adsorbents are tailored to specific mixtures, limiting their broader applicability. The development of multifunctional adsorbents that can efficiently operate across multiple gas separation systems represents a promising strategy to simplify material design and broaden industrial relevance. Herein, methyl‐functional groups are innovatively introduced into porous coordination polymers (PCPs), synthesizing PCP‐BDC‐M and PCP‐BDC‐DM with precisely tailored microporous structures. Notably, the dimethyl‐functionalized PCP‐BDC‐DM demonstrates superior multifunctional selectivity toward CH 4 /N 2 , C 2 H 6 /C 2 H 4 , and C 3 H 8 /C 3 H 6 gas mixtures. Adsorption isotherms and Ideal Adsorbed Solution Theory (IAST) calculations reveal significantly higher alkane selectivity in PCP‐BDC‐DM compared to PCP‐BDC‐M and existing alkane‐selective adsorbents. Grand Canonical Monte Carlo (GCMC) simulations provide molecular‐level insight, confirming that methyl groups effectively enhance interactions between alkane molecules and the framework. Dynamic breakthrough experiments further validate PCP‐BDC‐DM's excellent practical separation capability and structural stability. This study offers valuable insights into designing advanced adsorbents for alkane‐selective gas separation.
科研通智能强力驱动
Strongly Powered by AbleSci AI