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硅酸钠溶液微观结构的硅/碱比依赖性。

Silica/alkali ratio dependence of the microscopic structure of sodium silicate solutions.

机构信息

Department of Applied Physics, Chalmers University of Technology, Gothenburg, Sweden.

出版信息

J Colloid Interface Sci. 2013 May 1;397:9-17. doi: 10.1016/j.jcis.2013.01.048. Epub 2013 Feb 9.

DOI:10.1016/j.jcis.2013.01.048
PMID:23484773
Abstract

Alkaline sodium silicate solutions with SiO2:Na2O molar ratios in the range 4-10 are known to be colloidally unstable manifested in phase separation or gelation. The mechanistic understanding of this instability is generally poor. To improve this situation the microscopic structure of a series of solutions with ratios in the range 3.3-8.9 has been characterised using small-angle X-ray scattering, Dynamic light scattering, Fourier transformed infrared spectroscopy, and (29)Si Nuclear magnetic resonance spectroscopy to cover the relevant length scales related to silica clusters, aggregates, and particles present. In the starting solution, with ratio 3.3, there are silica present in three fractions. The main part is present as small silica clusters with a radius of 0.7 nm. There are also a significant portion of monomers/small oligomeric silica species as well as a minute amount of larger colloidal silica particles. At a higher SiO2:Na2O ratio, above approximately 4, smaller spherical colloidal particles are formed due to condensation reactions. However, as a result of a too high ionic strength the suspension is not stable and the particles aggregate to fractal structures with a size that depends on ratio and ageing time. At the highest SiO2:Na2O ratio, fractals are not formed because of the lower ionic strength and the smaller colloidal particles are stable in the solution. By carefully adding small amounts of NaCl to the high ratio solution it is possible to induce gelation of the solution confirming the hypothesis that the instability region is due to too high electrolyte concentration for the silica species present under those conditions.

摘要

硅酸钠碱性溶液中 SiO2:Na2O 的摩尔比在 4-10 之间时,胶体是不稳定的,表现为相分离或凝胶化。这种不稳定性的机理理解通常很差。为了改善这种情况,使用小角 X 射线散射、动态光散射、傅里叶变换红外光谱和(29)Si 核磁共振波谱对一系列摩尔比在 3.3-8.9 范围内的溶液的微观结构进行了表征,以覆盖与二氧化硅团簇、聚集体和颗粒相关的相关长度尺度。在起始溶液中,摩尔比为 3.3,存在三种形式的二氧化硅。主要部分以半径为 0.7nm 的小二氧化硅簇形式存在。还有相当一部分单体/小寡聚硅物种以及微量的较大胶体二氧化硅颗粒。在更高的 SiO2:Na2O 比下,超过约 4,由于缩合反应形成更小的球形胶体颗粒。然而,由于离子强度过高,悬浮液不稳定,颗粒聚集形成分形结构,其大小取决于比和老化时间。在最高的 SiO2:Na2O 比下,由于离子强度较低,不会形成分形,较小的胶体颗粒在溶液中稳定。通过小心地向高比溶液中添加少量 NaCl,可以诱导溶液凝胶化,证实了这样的假设,即不稳定性区域是由于存在于这些条件下的硅物种的电解质浓度过高所致。

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