首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Nearly monodisperse silica microparticles form in silicone (Pre)elastomer mixtures
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Nearly monodisperse silica microparticles form in silicone (Pre)elastomer mixtures

机译:有机硅(弹性体)弹性体混合物中形成几乎单分散的二氧化硅微粒

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The formation of silica from a tetraalkoxysilane in a sol-gel process usually requires a highly polar, typically aqueous, medium that aids in the hydrolysis of the silane and leads to electrostatic stabilization of the growing silica particles. Formation of such silica particles in a hydrophobic medium is much more challenging. We report the formation of silica microspheres within silicone oils (hydroxy-terminated poly(dimethylsiloxane), HO-PDMS) during elastomer cure using atmospheric humidity in a one-pot and one-step synthesis. Using tetraethyl orthosilicate (TEOS) as both cross-linker and silica precursor, and aminopropyl-terminated dimethylsiloxane oligomer (AT-PDMS) as a catalytic surfactant, silica particles of low polydispersity formed near or at the air interface of the elastomer: the presence of a hydrophilic polymer, poly(ethylene glycol) (PEG), had an indirect effect on the particle formation, as it assisted with water transmission into the system, which resulted in particle formation over a wider range of parameters and facilitated silicone elastomer cure further away from the air interface. Depending on the relative humidity during cure, the sizes of particles presenting at the air interface varied from ~6-7 μm under ambient conditions (20-30%RH) to ~7-9 μm at high relative humidity (90% RH). The origin of the controlled particle synthesis is ascribed to the relative solubility of the catalyst and the efficiency of water permeation through the silicone matrix. AT-PDMS preferentially migrates to the air interface, as shown by ninhydrin staining, where it both catalyzes alkoxysilane hydrolysis and condensation, and stabilizes the growing silica particles prior to aggregation. Since reactions in the presence of this catalyst are slow, TEOS can migrate from within the pre-elastomer body to the interface faster than water can penetrate the silicone, such that the main locus of hydrolysis/condensation leading both to silica formation and elastomer cross-linking is at the air interface.
机译:在溶胶-凝胶法中由四烷氧基硅烷形成二氧化硅通常需要高极性的,通常是水性的介质,该介质有助于硅烷的水解并导致生长的二氧化硅颗粒的静电稳定。在疏水性介质中形成这种二氧化硅颗粒更具挑战性。我们报告了在使用一站式和一步合成的大气湿度在弹性体固化过程中,在硅油(羟基封端的聚二甲基硅氧烷,HO-PDMS)中形成了硅微球。使用原硅酸四乙酯(TEOS)作为交联剂和二氧化硅前体,并用氨基丙基封端的二甲基硅氧烷低聚物(AT-PDMS)作为催化表面活性剂,在弹性体的空气界面附近或在空气界面处形成低多分散性的二氧化硅颗粒:亲水性聚合物聚乙二醇(PEG)对颗粒形成有间接影响,因为它有助于将水传输到系统中,从而导致在更宽范围的参数范围内形成颗粒,并促进了有机硅弹性体进一步固化从空中接口。取决于固化过程中的相对湿度,空气界面处存在的颗粒尺寸在环境条件(20-30%RH)下为〜6-7μm,在高相对湿度(90%RH)下为〜7-9μm。受控颗粒合成的起源归因于催化剂的相对溶解度和水通过有机硅基质的渗透效率。如茚三酮染色所示,AT-PDMS优先迁移至空气界面,在该处它既催化烷氧基硅烷水解和缩合,又使聚集的二氧化硅颗粒稳定下来。由于在这种催化剂的存在下反应很慢,因此TEOS可以比弹性体中的弹性体更快地从弹性体内部迁移到界面,从而导致水解/缩合的主要场所(导致二氧化硅形成和弹性体交叉)。链接位于空中接口。

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