材料科学
化学工程
纳米复合材料
聚合物
甲基丙烯酸甲酯
原子转移自由基聚合
高分子化学
纳米颗粒
甲基丙烯酸酯
乙二醇
复合材料
聚合
纳米技术
工程类
作者
Zongyu Wang,Hao Chen,Yangyang Wang,Jihua Chen,Mark A. Arnould,Bin Hu,Ilja Popovs,Shannon M. Mahurin,Sheng Dai
标识
DOI:10.1021/acsami.1c04342
摘要
Three different types of polymer ligands, poly(methyl methacrylate) (PMMA), poly(methyl methacrylate-random-poly(ethylene glycol)methyl ether methacrylate) (PMMA-r-PEGMEMA), and poly(ionic liquid)s (PIL), were grafted onto the surface of 15 nm solid and large hollow porous silica nanoparticles (average particle size ∼60 nm) by surface-initiated atom transfer radical polymerization (SI-ATRP) to demonstrate the enhanced carbon dioxide (CO2) permeability as well as mechanical properties. After characterizing the purified products, free-standing bulk films were fabricated by the solvent-casting method. The poly(ionic liquid) nanocomposite films exhibited a much higher carbon dioxide permeance than PMMA and PMMA-r-PEGMEMA systems with a similar silica content. Also, the hollow silica-mixed matrix membranes showed a significant enhancement in CO2 permeability compared to the 15 nm solid silica films because of the pore structure. Despite the transparency loss due to the scattering of larger particle sizes, the hollow silica particle brush films exhibited the same mechanical properties as the 15 nm solid silica-derived ones.
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