Ultrahigh iodine adsorption in porous organic frameworks

被引:244
作者
Pei, Cuiying [1 ]
Ben, Teng [2 ]
Xu, Shixian [1 ]
Qiu, Shilun [1 ]
机构
[1] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130023, Peoples R China
[2] Jilin Univ, Dept Chem, Changchun 130023, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTRICAL-CONDUCTIVITY; COORDINATION NETWORK; HYDROGEN ADSORPTION; AROMATIC FRAMEWORK; VAPOR-PRESSURE; SURFACE-AREA; I-2; SORPTION; POLYIODIDE; CRYSTALLINE; CONFINEMENT;
D O I
10.1039/c4ta00049h
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
We present two porous organic frameworks (POFs), PAF-1 and JUC-Z2, with ultrahigh iodine capture capacity. The iodine vapor uptake of PAF-1 and JUC-Z2 were 1.86 g g(-1) and 1.44 g g(-1) respectively at 298 K per 40 Pa, which is extremely high for such low pressure sorption conditions. In addition, PAF-1 and JUC-Z2 could adsorb iodine over water with the selectivity of 5.1 and 6.5 respectively. The isosteric enthalpy at zero surface coverage, calculated by a virial equation with the iodine vapor sorption isotherms at 298 K and 313 K of JUC-Z2, reached -51.1 kJ mol(-1), which was much higher than the coverage of PAF-1 (-14.9 kJ mol(-1)). Raman measurement confirmed the polyiodide to be I-5(-) in POFs. Furthermore, solvents with different polarities, such as n-hexane, chloroform, and methanol, were chosen to conduct iodine binding measurements on PAF-1 and JUC-Z2. The formation constant Kf for POFs in n-hexane, chloroform and methanol drastically decreased with the increase in polarity, thus illustrating the important role of solvents in iodine binding.
引用
收藏
页码:7179 / 7187
页数:9
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