Pore surface engineering in porous, chemically stable covalent organic frameworks for water adsorption

被引:169
作者
Biswal, Bishnu P. [1 ,2 ]
Kandambeth, Sharath [1 ,2 ]
Chandra, Suman [1 ,2 ]
Shinde, Digambar Balaji [2 ]
Bera, Saibal [1 ,2 ]
Karak, Suvendu [1 ,2 ]
Garai, Bikash [1 ,2 ]
Kharul, Ulhas K. [3 ]
Banerjee, Rahul [1 ,2 ]
机构
[1] Acad Sci & Innovat Res AcSIR, New Delhi, India
[2] CSIR, Natl Chem Lab, Phys Mat Chem Div, Pune 411008, Maharashtra, India
[3] CSIR, Natl Chem Lab, Polymer Sci & Engn Div, Pune 411008, Maharashtra, India
关键词
HYDROGEN-BONDS; STABILITY; DEHUMIDIFICATION; CRYSTALLINE; ADSORBENTS;
D O I
10.1039/c5ta07998e
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
Herein, we have explored the possibility of a class of covalent organic frameworks (COFs) as water adsorbing materials. We have selected, synthesized 12 chemically stable functionalized Schiff base COFs and thoroughly studied their water uptake behaviour. Further, a deep understanding was developed with these COFs towards the effects of condensation pressure of water and hydrophilic/hydrophobic groups present in the COF pores on water absorption capacity and ultimately, their recyclability. Among all reported COFs, TpPa-1 shows the highest water uptake of 30 wt% (368 cm(3) g(-1); 17 mmol g(-1)) at P/P-0 = 0.3, which is also comparable with the recently reported carbon materials and few well known MOFs. This study also reveals that the overall water uptake of COFs can be tuned systematically based on chemical functionality and pore size in a wider window of relative pressures.
引用
收藏
页码:23664 / 23669
页数:6
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