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

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 synthesi...

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Detalles Bibliográficos
Autores principales: Song, Jing-Ru, Duan, Wen-Gui, Li, Dian-Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100294/
https://www.ncbi.nlm.nih.gov/pubmed/30012967
http://dx.doi.org/10.3390/molecules23071732
Descripción
Sumario: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 (13)C 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 m(2)·g(−1) and 406 m(2)·g(−1) and a narrow pore size distribution under 1.2 nm. Gas sorption isotherms including CO(2) and H(2) were measured. CMOP-1 stores a superior CO(2) level of 1.85 mmol·g(−1) at 273 K/1.0 bar, and an H(2) 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 CO(2) adsorption capacity of 1.64 mmol·g(−1) and an H(2) uptake of 2.48 mmol·g(−1). In addition, I(2) 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 CO(2) and I(2) due to the nitrogen-rich content in the polymers.