Microporous organic polymers based on tetraethynyl building blocks with N-functionalized pore surfaces: synthesis, porosity and carbon dioxide sorption

RSC Advances ◽  
2016 ◽  
Vol 6 (115) ◽  
pp. 113826-113833 ◽  
Author(s):  
Hongjiang Zhang ◽  
Chong Zhang ◽  
Xunchang Wang ◽  
Zexiong Qiu ◽  
Xinmiao Liang ◽  
...  

We have synthesized nitrogen-rich polymers by copolymerization of tetraethynyl monomers with tris(4-iodophenyl)amine or 4,4′-diiodoazobenzene. Azobenzene-based polymers exhibited excellent CO2 adsorption selectivity against N2.

2011 ◽  
Vol 21 (34) ◽  
pp. 12958 ◽  
Author(s):  
K. Venkata Rao ◽  
Sudip Mohapatra ◽  
Chidambar Kulkarni ◽  
Tapas Kumar Maji ◽  
Subi J. George

RSC Advances ◽  
2014 ◽  
Vol 4 (71) ◽  
pp. 37767-37772 ◽  
Author(s):  
He Li ◽  
Zhongping Li ◽  
Yuwei Zhang ◽  
Xiaolong Luo ◽  
Hong Xia ◽  
...  

Three metallosalen-based microporous organic polymers were designed and synthesized. New materials display excellent porosity and good capacities for store and separation of carbon dioxide at 273 K and 1 bar.


2021 ◽  
Author(s):  
Timur Ashirov ◽  
Maymounah Alrayyani ◽  
Kyung Seob Song ◽  
Ognjen Miljanic ◽  
Ali Coskun

Porous organic polymers (POPs) incorporating macrocyclic units have been investigated in recent years in an effort to transfer macrocycles’ intrinsic host-guest properties onto the porous networks to achieve complex separations. In this regard, highly interesting building blocks are presented by the family of cyclotetrabenzoin macrocycles with rigid, well-defined, electron-deficient cavities. This macrocycle shows high affinity towards linear guest molecules such as carbon dioxide, thus offering an ideal building block for the synthesis of CO2-philic POPs. Herein, we report the synthesis of a porous organic polymer through the condensation reaction between cyclotetrabenzil with 1,2,4,5-tetraaminobenzene under ionothermal conditions using the eutectic zinc chloride/sodium chloride/potassium chloride salt mixture at 250 oC. Notably, following the condensation reaction, the macrocycle favors 3D growth rather than 2D one while retaining the cavity. The resulting polymer, named 3D-mPOP, showed a highly microporous structure with the BET surface area of 1142 m2 g−1 and a high carbon dioxide affinity with a binding enthalpy of 39 kJ mol−1. Moreover, 3D-mPOP showed very high selectivity for carbon dioxide in carbon dioxide/methane and carbon dioxide /nitrogen mixtures.


RSC Advances ◽  
2015 ◽  
Vol 5 (79) ◽  
pp. 64163-64169 ◽  
Author(s):  
Qing-Yu Ma ◽  
Bing-Xue Yang ◽  
Jian-Quan Li

Porous organic polymers show high and tunable porosity, and moderate CO2 uptake and CO2 selectivity over other gases simultaneously using tetrahedral silicon-centered monomers and a stereocontorted spirobifluorene-based precursor as building units.


RSC Advances ◽  
2015 ◽  
Vol 5 (121) ◽  
pp. 100322-100329 ◽  
Author(s):  
Yang Zhao ◽  
Xiaoyan Wang ◽  
Chong Zhang ◽  
Fangyuan Xie ◽  
Rui Kong ◽  
...  

Isoindigo-based microporous organic polymers show a high CO2 uptake ability of 3.30 mmol g−1 (1.13 bar/273 K) with a CO2/N2 sorption selectivity of 58.8 : 1.


2017 ◽  
Vol 13 ◽  
pp. 2131-2137 ◽  
Author(s):  
Tao Wang ◽  
Yan-Chao Zhao ◽  
Li-Min Zhang ◽  
Yi Cui ◽  
Chang-Shan Zhang ◽  
...  

We successfully employed bisphenol A and several different formyl-containing monomers as useful building blocks to construct a series of hydroxy-group-containing porous organic polymers in a sealed tube at high temperature. Fourier transform infrared and solid-state 13C CP/MAS NMR spectroscopy are utilized to characterize the possible structure of the obtained polymers. The highest Brunauer–Emmet–Teller specific surface area of the phenolic-resin porous organic polymers (PPOPs) is estimated to be 920 m2 g–1. The PPOPs exhibit a highest carbon dioxide uptake (up to 15.0 wt % (273 K) and 8.8 wt % (298 K) at 1.0 bar), and possess moderate hydrogen storage capacities ranging from 1.28 to 1.04 wt % (77 K) at 1.0 bar. Moreover, the highest uptake of methane for the PPOPs is measured as 4.3 wt % (273 K) at 1.0 bar.


2019 ◽  
Vol 38 (2) ◽  
pp. 187-194 ◽  
Author(s):  
Meng-Qi Du ◽  
Yu-Zheng Peng ◽  
Yuan-Chi Ma ◽  
Li Yang ◽  
Yuan-Lin Zhou ◽  
...  

2011 ◽  
Vol 4 (10) ◽  
pp. 4239 ◽  
Author(s):  
Robert Dawson ◽  
Ev Stöckel ◽  
James R. Holst ◽  
Dave J. Adams ◽  
Andrew I. Cooper

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