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Water-Dispersible Silica-Polyelectrolyte Nanocomposites Prepared via Acid-Triggered Polycondensation of Silicic Acid and Directed by Polycations

机译:通过酸引发的硅酸的缩聚反应并由聚阳离子指导制备的水分散性二氧化硅-聚合物纳米复合材料

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摘要

The present work describes the acid-triggered condensation of silicic acid, Si(OH)(4), as directed by selected polycations in aqueous solution in the pH range of 6.5-8.0 at room temperature, without the use of additional solvents or surfactants. This process results in the formation of silica-polyelectrolyte (S-PE) nanocomposites in the form of precipitate or water-dispersible particles. The mean hydrodynamic diameter (d(h)) of size distributions of the prepared water-dispersible S-PE composites is presented as a function of the solution pH at which the composite formation was achieved. Poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) and block copolymers of DMAEMA and oligo(ethylene glycol) methyl ether methacrylate (OEGMA) were used as weak polyelectrolytes in S-PE composite formation. The activity of the strong polyelectrolytes poly(methacryloxyethyl trimethylammonium iodide) (PMOTAI) and PMOTAI-b-POEGMA in S-PE formation is also examined. The effect of polyelectrolyte strength and the OEGMA block on the formation of the S-PE composites is assessed with respect to the S-PE composites prepared using the PDMAEMA homopolymer. In the presence of the PDMAEMA(60) homopolymer (M-w = 9400 g/mol), the size of the dispersible S-PE composites increases with solution pH in the range pH 6.6-8.1, from d(h) = 30 nm to d(h) = 800 nm. S-PDMAEMA(60) prepared at pH 7.8 contained 66% silica by mass (TGA). The increase in dispersible S-PE particle size is diminished when directed by PDMAEMA(300) (M-w = 47,000 g/mol), reaching a maximum of d(h) = 75 nm. S-PE composites formed using PDMAEMA-b-POEGMA remain in the range d(h) = 20-30 nm across this same pH regime. Precipitated S-PE composites were obtained as spheres of up to 200 nm in diameter (SEM) and up to 65% mass content of silica (TGA). The conditions of pH for the preparation of dispersible and precipitate S-PE nanocomposites, as directed by the five selected polyelectrolytes PDMAEMA(60), PDMAEMA(300), PMOTAI(60), PDMAEMA(60)-b-POEGMA(38) and PMOTAI(60)-b-POEGMA(38) is summarized.
机译:目前的工作描述了在室温下,在不使用其他溶剂或表面活性剂的情况下,通过选择的聚阳离子在pH为6.5-8.0的水溶液中进行酸引发的硅酸Si(OH)(4)的缩合反应。该过程导致形成沉淀或水分散性颗粒形式的二氧化硅-聚电解质(S-PE)纳米复合材料。所制备的水分散性S-PE复合材料的尺寸分布的平均流体动力学直径(d(h))是实现复合材料形成的溶液pH的函数。聚(2-(二甲基氨基)乙基甲基丙烯酸酯)(PDMAEMA)和DMAEMA与低聚(乙二醇)甲基醚甲基丙烯酸甲酯(OEGMA)的嵌段共聚物在S-PE复合材料的形成中用作弱聚电解质。还检查了强聚电解质聚(甲基丙烯酰氧基乙基三甲基碘化铵)(PMOTAI)和PMOTAI-b-POEGMA在S-PE形成中的活性。对于使用PDMAEMA均聚物制备的S-PE复合物,评估了聚电解质强度和OEMGA嵌段对S-PE复合物形成的影响。在PDMAEMA(60)均聚物(Mw = 9400 g / mol)的存在下,溶液pH在6.6-8.1的范围内,从d(h)= 30 nm到d,可分散S-PE复合材料的尺寸会增加(h)= 800nm。在pH 7.8下制备的S-PDMAEMA(60)包含66质量%的二氧化硅(TGA)。当由PDMAEMA(300)指导(M-w = 47,000 g / mol)时,可分散S-PE粒径的增加减小,最大d(h)= 75 nm。在相同的pH范围内,使用PDMAEMA-b-POEGMA形成的S-PE复合材料的d(h)= 20-30 nm。获得沉淀的S-PE复合材料,其直径最大为200 nm(SEM),二氧化硅的质量含量最高为65%(TGA)。按照五个选定的聚电解质PDMAEMA(60),PDMAEMA(300),PMOTAI(60),PDMAEMA(60)-b-POEGMA(38)和pH的指导,制备可分散和沉淀S-PE纳米复合材料的pH条件。总结了PMOTAI(60)-b-POEGMA(38)。

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