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用于碳氢化合物(C2 - C3)储存、二氧化碳捕集与分离的动态缠结多孔框架

Dynamic Entangled Porous Framework for Hydrocarbon (C2-C3) Storage, CO2 Capture, and Separation.

作者信息

Sikdar Nivedita, Bonakala Satyanarayana, Haldar Ritesh, Balasubramanian Sundaram, Maji Tapas Kumar

机构信息

Chemistry and Physics of Materials Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore-, 560064, India.

New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, India.

出版信息

Chemistry. 2016 Apr 18;22(17):6059-70. doi: 10.1002/chem.201505217. Epub 2016 Mar 11.

Abstract

Storage and separation of small (C1-C3) hydrocarbons are of great significance as these are alternative energy resources and also can be used as raw materials for many industrially important materials. Selective capture of greenhouse gas, CO2 from CH4 is important to improve the quality of natural gas. Among the available porous materials, MOFs with permanent porosity are the most suitable to serve these purposes. Herein, a two-fold entangled dynamic framework {[Zn2 (bdc)2 (bpNDI)]⋅4DMF}n with pore surface carved with polar functional groups and aromatic π clouds is exploited for selective capture of CO2 , C2, and C3 hydrocarbons at ambient condition. The framework shows stepwise CO2 and C2 H2 uptake at 195 K but type I profiles are observed at 298 K. The IAST selectivity of CO2 over CH4 is the highest (598 at 298 K) among the MOFs without open metal sites reported till date. It also shows high selectivity for C2 H2 , C2 H4 , C2 H6 , and C3 H8 over CH4 at 298 K. DFT calculations reveal that aromatic π surface and the polar imide (RNC=O) functional groups are the primary adsorption sites for adsorption. Furthermore, breakthrough column experiments showed CO2 /CH4 C2 H6 /CH4 and CO2 /N2 separation capability at ambient condition.

摘要

储存和分离小分子(C1 - C3)碳氢化合物具有重要意义,因为这些是替代能源,也可用作许多重要工业材料的原料。从CH4中选择性捕获温室气体CO2对于提高天然气质量很重要。在现有的多孔材料中,具有永久孔隙率的金属有机框架(MOF)最适合用于这些目的。在此,利用一种具有极性官能团和芳香π云刻蚀孔表面的双折缠结动态框架{[Zn2 (bdc)2 (bpNDI)]⋅4DMF}n在环境条件下选择性捕获CO2、C2和C3碳氢化合物。该框架在195 K时显示出逐步的CO2和C2H2吸附,但在298 K时观察到I型吸附等温线。在迄今为止报道的无开放金属位点的MOF中,CO2对CH4的理想吸附溶液理论(IAST)选择性最高(298 K时为598)。它在298 K时对C2H2、C2H4、C2H6和C3H8也显示出对CH4的高选择性。密度泛函理论(DFT)计算表明,芳香π表面和极性酰亚胺(RNC=O)官能团是吸附的主要吸附位点。此外,突破柱实验表明在环境条件下具有CO2/CH4、C2H6/CH4和CO2/N2的分离能力。

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