首页> 美国卫生研究院文献>ACS Omega >Ambient Pressure Hybrid Silica Monoliths with Hexamethyldisilazane:From Vitreous Hydrophilic Xerogels to Superhydrophobic Aerogels
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Ambient Pressure Hybrid Silica Monoliths with Hexamethyldisilazane:From Vitreous Hydrophilic Xerogels to Superhydrophobic Aerogels

机译:六甲基二硅氮烷的常压混合二氧化硅整体料:从玻璃亲水性干凝胶到超疏水性气凝胶

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摘要

Hybrid silica-based monoliths were synthesized at ambient pressure, using minimum amounts of the silylating agent hexamethyldisilazane (HMDZ). Depending on the synthesis approach, the materials ranged from dense and vitreous xerogels to transparent and superhydrophobic aerogels. Emphasis was given to understanding the role of the silylating agent, its content and incorporation process on the final morphology, and properties of the xerogels/aerogels. It is proven that as a coprecursor, increasing HMDZ content contributes to increase the lipophilic/hydrophilic balance, induce high surface areas, and decrease densities, but there is a maximum usable content for producing monoliths. Conversely, as a postsynthesis modifier, there is an optimum HMDZ content that maximizes hydrophobicity (water contact angle of ∼144°) and induces high surface area (∼700 m2·g–1), keeping the density low (∼300 kg·m–3). It is proven that the aging period in the hydrophobizing solution is a crucial parameter. The most superhydrophobic xerogels were obtained using HMDZ as a postsynthesis modifier, achieving values of water contact angles as high as ∼173°, at the cost of densityincrease to ∼600 kg·m–3 and decreaseof the surface area to ∼300 m2·g–1. The best compromise between low density, high surface area, andsuperhydrophobicity is obtained using HMDZ both as a coprecursor andas a postsynthesis modifier, in a low HMDZ/tetraethoxysilane totalmolar ratio (<0.2), with an aging period of 16–24 h. Theuse of subcritical drying, along with the minimization of the expensiveorganic modifier quantities, allows envisaging a safe and low-costlarge-scale production of a variety of materials, including superhydrophobicaerogels with potential distinctive applications.
机译:使用最小量的甲硅烷基化剂六甲基二硅氮烷(HMDZ)在环境压力下合成杂化的基于二氧化硅的整体材料。取决于合成方法,材料的范围从致密和玻璃状干凝胶到透明和超疏水性干凝胶。重点在于理解甲硅烷基化剂的作用,其含量和掺入过程对最终形态的影响以及干凝胶/气凝胶的性能。事实证明,作为共前体,增加HMDZ含量有助于增加亲脂性/亲水性平衡,诱导高表面积并降低密度,但在生产整料中存在最大可用含量。相反,作为后合成改性剂,存在最佳的HMDZ含量,可最大程度地提高疏水性(水接触角约为144°)并诱导高表面积(约700 m 2 ·g –1 < / sup>),保持低密度(〜300 kg·m –3 )。事实证明,疏水化溶液中的老化时间是至关重要的参数。使用HMDZ作为后合成改性剂可获得最多的超疏水性干凝胶,以密度为代价达到高达173°的水接触角值增加到〜600 kg·m –3 并降低表面积的约300m 2 ·g -1 。低密度,高表面积和高密度之间的最佳折衷使用HMDZ作为共前体和在低HMDZ /四乙氧基硅烷总量中作为后合成改性剂摩尔比(<0.2),时效时间为16-24小时。的使用亚临界干燥,并尽量减少昂贵的物料有机改性剂的数量,可以设想一种安全且低成本的方法大规模生产包括超疏水在内的各种材料具有潜在独特应用的气凝胶。

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