Adsorption of pyridine onto the metal organic framework MIL-101

被引:36
作者
Kim, Mi Jin [1 ,2 ]
Park, Se Min [1 ,2 ]
Song, Sun-Jung [3 ]
Won, Jiyeon [4 ]
Lee, Jin Yong [4 ]
Yoon, Minyoung [5 ,6 ]
Kim, Kimoon [5 ,6 ]
Seo, Gon [1 ,2 ]
机构
[1] Chonnam Natl Univ, Sch Appl Chem Engn, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Res Inst Catalysis, Kwangju 500757, South Korea
[3] Chonnam Natl Univ, Ctr Funct Nano Fine Chem, Kwangju 500757, South Korea
[4] Sungkyunkwan Univ, Dept Chem, Suwon 440746, South Korea
[5] Pohang Univ Sci & Technol, Natl Creat Res Initiat Ctr Smart Supramol, Pohang 790784, South Korea
[6] Pohang Univ Sci & Technol, Dept Chem, Pohang 790784, South Korea
基金
新加坡国家研究基金会;
关键词
MOF MIL-101; Pyridine; Adsorption; Theoretical calculation; SPECTRA; SURFACE;
D O I
10.1016/j.jcis.2011.05.067
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The adsorption of pyridine onto the metal organic framework MIL-101 was investigated by experimental and theoretical methods. The amount of pyridine adsorbed on MIL-101 was extraordinarily large at 20 degrees C, corresponding to about 950 mg/g of dried MIL-101 and approximately half of the voids being filled. Most of the pyridine that had filled the voids was rapidly removed by evacuation at room temperature, but some of the pyridine was so strongly adsorbed that it was retained even under evacuation at 150 degrees C. Although IR spectra of the adsorbed pyridine indicated the adsorption of pyridine as pyridinium ions and coordinated pyridine at low temperatures, increasing the adsorption temperature induced partial cleavage of the pyridine rings. The high stabilization energy of pyridine on the coordinative unsaturated sites (CUS) of MIL-101, obtained by theoretical calculation, -103 kJ/mol, supported the strong adsorption of pyridine on the CUS. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:612 / 617
页数:6
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