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The Core-Shell Approach to Formation of Ordered Nanoporous Silicas by MPEG-b-PLA Block Copolymers

机译:MPEG-b-PLA嵌段共聚物形成有序纳米多孔二氧化硅的核-壳方法

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摘要

Selected MPEG-b-PLA block copolymer templates have been synthesized by ring-opening polymerization,with systematic variation of the chain lengths of the hydrophilic and hydrophobic blocks.The size and shape of the micelles that spontaneously form in solution are controlled by the characteristics of the block copolymer template.Tunable pore sizes ranging from 2 to 8 nm were achieved in the templated synthesis of ordered nanoporous silica by increasing the hydrophobic chain lengths.The highest surface area observed by BET analysis was 660 m~2/g.The formation mechanism of these nanoporous structures,obtained by controlling the micelle size,has been confirmed using both liquid and solid state ~13C and ~29Si NMR techniques.This work verifies the formation mechanism of nanoporous structures in which the pore size and wall thickness are closely dependent on the size of the hydrophobic cores and hydrophilic shells of the block copolymer templates.
机译:选定的MPEG-b-PLA嵌段共聚物模板是通过开环聚合反应合成的,亲水性和疏水性嵌段的链长有系统性的变化。溶液中自发形成的胶束的大小和形状受分子结构的控制。通过增加疏水链长度在模板化有序纳米多孔二氧化硅的模板化合成中可调节的孔径为2至8 nm,BET分析观察到的最大表面积为660 m〜2 / g。通过使用液态和固态〜13C和〜29Si NMR技术证实了通过控制胶束尺寸获得的这些纳米多孔结构。这项工作验证了孔径和壁厚密切相关的纳米多孔结构的形成机理。嵌段共聚物模板的疏水核和亲水壳的大小。

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