Porous Silsesquioxane-Imine Frameworks as Highly Efficient Adsorbents for Cooperative Iodine Capture

被引:88
作者
Janeta, Mateusz [1 ]
Bury, Wojciech [1 ]
Szafert, Slawomir [1 ]
机构
[1] Univ Wroclaw, Fac Chem, 14 F Joliot Curie, PL-50383 Wroclaw, Poland
关键词
microporous polymer; iodine capture; gas storage; porosity; aerogel; imine; silsesquioxane; COVALENT ORGANIC FRAMEWORKS; CONJUGATED MICROPOROUS POLYMERS; CARBON-DIOXIDE CAPTURE; VOLATILE IODINE; NANOBUILDING BLOCKS; CO2; ADSORPTION; SURFACE-AREA; GAS-STORAGE; HYBRID; NETWORKS;
D O I
10.1021/acsami.8b03023
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The efficient capture and storage of radioactive iodine (I-129 or I-131), which can be formed during nuclear energy generation or nuclear waste storage, is of paramount importance. Herein, we present highly efficient aerogels for reversible iodine capture, namely, porous silsesquioxane- imine frameworks (PSIFs), constructed by condensation of octa(3-aminopropypsilsesquioxane cage compound and selected multitopic aldehydes. The resulting PSIFs are permanently porous (Brunauer-Emmet-Teller surface areas up to 574 m(2)/g), thermally stable, and present a combination of micro-, meso-, and macropores in their structures. The presence of a large number of imine functional groups in combination with silsesquioxane cores results in extremely high I-2 affinity with uptake capacities up to 485 wt %, which is the highest reported to date. Porous properties can be controlled by the strut length and rigidity of linkers. In addition, PSIF-1a could be recycled at least four times while maintaining 94% I-2 uptake capacity. Kinetic studies of I-2 desorption show two strong binding sites with apparent activation energies of 77.0 and 89.0 kJ/mol. These energies are considerably higher than the enthalpy of sublimation of bulk I-2.
引用
收藏
页码:19964 / 19973
页数:10
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