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Controlled synthesis of conjugated polycarbazole polymers via structure tuning for gas storage and separation applications

机译:通过结构调整可控制地合成共轭聚咔唑聚合物,用于气体存储和分离应用

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摘要

A series of conjugated microporous polymers (CMPs) based on 1,3,6,8-tetrabromocarbazole (N4CMP-1–5) is synthesized via Suzuki cross-coupling or Sonogashira polycondensation. The porosity properties and surface area of these polymer networks can be finely tuned by using a linker with different geometries or strut length. These polymers show the Brunauer-Emmett-Tellerthe (BET) surface areas ranging from 592 to 1426?m2?g?1. The dominant pore sizes of the polymers on the basis of the different linker are located between 0.36 and 0.61?nm. Gas uptake increases with BET surface area and micropore volume, N4CMP-3 polymer can capture CO2 with a capacity of 3.62?mmol?g?1 (1.05?bar and 273?K) among the obtained polymers. All of the polymers show high isosteric heats of CO2 adsorption (25.5–35.1?kJ?mol?1), and from single component adsorption isotherms, IAST-derived ideal CO2/N2 (28.7–53.8), CO2/CH4 (4.6–5.2) and CH4/N2 (5.7–10.5) selectivity. Furthermore, N4CMPs exhibit the high CO2 adsorption capacity of 542–800?mg?g?1 at 318?K and 50?bar pressure. These data indicate that these materials are a promising potential for clean energy application and environmental field.
机译:通过Suzuki交叉偶联或Sonogashira缩聚合成一系列基于1,3,6,8-四溴咔唑(N4CMP-1-5)的共轭微孔聚合物(CMP)。这些聚合物网络的孔隙率特性和表面积可以通过使用具有不同几何形状或支杆长度的连接剂来进行微调。这些聚合物的Brunauer-Emmett-Tellerthe(BET)表面积为592至1426?m2?g?1。基于不同的连接基,聚合物的主要孔尺寸在0.36和0.61?nm之间。气体吸收随BET表面积和微孔体积的增加而增加,N4CMP-3聚合物可以在所获得的聚合物中以3.62?mmol?g?1(1.05?bar和273?K)的容量捕获CO2。所有聚合物均表现出较高的等高吸附CO2(25.5–35.1?kJ?mol?1),并且从单组分吸附等温线得出的是IAST衍生的理想CO2 / N2(28.7–53.8),CO2 / CH4(4.6–5.2) )和CH4 / N2(5.7-10.5)的选择性。此外,N4CMP在318?K和50?bar的压力下具有542-​​800?mg?g?1的高CO2吸附能力。这些数据表明,这些材料在清洁能源应用和环境领域具有广阔的发展前景。

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