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Synthesis of Nitrogen-Rich Polymers by Click Polymerization Reaction and Gas Sorption Property

机译:通过点击聚合反应和气体吸附性能合成富氮聚合物

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摘要

Microporous organic polymers (MOPs) are promising materials for gas sorption because of their intrinsic and permanent porosity, designable framework, and low density. The introduction of nitrogen-rich building block in MOPs will greatly enhance the gas sorption capacity. Here, we report the synthesis of MOPs from the 2,4,6-tris(4-ethynylphenyl)-1,3,5-triazine unit and aromatic azides linkers by click polymerization reaction. Fourier transform infrared (FTIR) and solid-state 13C CP-MAS (Cross Polarization-Magic Angle Spinning) NMR confirm the formation of the polymers. CMOP-1 and CMOP-2 exhibit microporous networks with a BET (Brunauer–Emmett–Teller) surface area of 431 m2·g−1 and 406 m2·g−1 and a narrow pore size distribution under 1.2 nm. Gas sorption isotherms including CO2 and H2 were measured. CMOP-1 stores a superior CO2 level of 1.85 mmol·g−1 at 273 K/1.0 bar, and an H2 uptake of up to 2.94 mmol·g−1 at 77 K/1.0 bar, while CMOP-2, with its smaller surface area, shows a lower CO2 adsorption capacity of 1.64 mmol·g−1 and an H2 uptake of 2.48 mmol·g−1. In addition, I2 vapor adsorption was tested at 353 K. CMOP-1 shows a higher gravimetric load of 160 wt%. Despite the moderate surface area, the CMOPs display excellent sorption ability for CO2 and I2 due to the nitrogen-rich content in the polymers.
机译:微孔有机聚合物(MOP)由于其固有的和永久的孔隙率,可设计的框架和低密度而成为具有前景的气体吸附材料。在拖把中引入富氮构件将大大提高气体的吸附能力。在这里,我们报道了通过点击聚合反应由2,4,6-三(4-乙炔基苯基)-1,3,5-三嗪单元和芳族叠氮化物连接基合成MOP。傅里叶变换红外光谱(FTIR)和固态 13 C CP-MAS(交叉极化-魔角旋转)NMR证实了聚合物的形成。 CMOP-1和CMOP-2的微孔网络的BET(Brunauer–Emmett–Teller)表面积为431 m 2 ·g -1 和406 m 2 ·g -1 且孔径小于1.2 nm。测量了包括CO 2和H 2的气体吸附等温线。 CMOP-1在273 K / 1.0 bar时具有出色的CO2水平1.85 mmol·g -1 ,在H2吸收高达2.94 mmol·g -1 77 K / 1.0 bar,而CMOP-2具有较小的表面积,显示出较低的CO2吸附容量1.64 mmol·g -1 和H2吸收2.48 mmol·g - 1 。另外,在353 K下测试了I2蒸气吸附。CMOP-1显示出160 wt%的较高重量负载。尽管表面积适中,但由于聚合物中富含氮,因此CMOP对CO2和I2表现出出色的吸附能力。

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