首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Combined Electrospray-Scanning Mobility Particle Sizer (ES-SMPS) and Time-Resolved Synchrotron Radiation-Small-Angle X-ray Scattering (SR-SAXS) Investigation of Colloidal Silica Aggregation. Part II. Influence of Aggregation Initiator on Gel Stability
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Combined Electrospray-Scanning Mobility Particle Sizer (ES-SMPS) and Time-Resolved Synchrotron Radiation-Small-Angle X-ray Scattering (SR-SAXS) Investigation of Colloidal Silica Aggregation. Part II. Influence of Aggregation Initiator on Gel Stability

机译:结合电喷雾扫描迁移率粒度仪(ES-SMPS)和时间分辨同步辐射-小角X射线散射(SR-SAXS)研究胶体二氧化硅聚集。第二部分聚集引发剂对凝胶稳定性的影响

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The effect of ion specificity on the slow aggregation of silica nanoparticles with various initial morphology was investigated with an electrospray-scanning mobility particle sizer (ES-SMPS) and time-resolved synchrotron radiation-small-angle X-ray scattering (SR-SAXS). This combination provides a unique tool to monitor and resolve the early aggregate development in detail, Aggregation was induced by varying the K2CO3 or,KCl concentration to obtain a fixed gelation time of ~40 min, and the results were compared with those obtained in a previous paper (Johnsson et al. J. Phys. Chem. B 2011,1 15, 765-775) for NaCl. All dispersions produced gels that contained free primary particles well past the point of gelation (PoG). The initial aggregate formation and obtained gel morphologies were independent of the aggregation initiator. Nevertheless, ion-specific effects were observed for the rate of the stability increase of the 3-dimensional (3D) gel structure. The formation of a stable structure was fastest in the presence of the strongly hydrated counterions, and a clear anion effect was observed. The obtained gel stabilities were interpreted by relating the rate of formation of covalent siloxane bonds to the polarization of the water molecules surrounding structure-maker ions.
机译:使用电喷雾扫描迁移率粒度仪(ES-SMPS)和时间分辨同步辐射-小角度X射线散射(SR-SAXS)研究了离子特异性对具有各种初始形态的二氧化硅纳米粒子缓慢聚集的影响。这种组合提供了一个独特的工具来详细监测和解决早期聚集体的发展,通过改变K2CO3或KCl的浓度诱导聚集,以获得约40分钟的固定胶凝时间,并将结果与​​以前的结果进行了比较。 NaCl的论文(Johnsson et al.J.Phys.Chem.B 2011,1 15,15,765-775)。所有分散体产生的凝胶都含有游离的初级颗粒,远远超过了凝胶化点(PoG)。初始聚集体形成和获得的凝胶形态与聚集引发剂无关。但是,对于3维(3D)凝胶结构的稳定性增加的速率,观察到了离子特异性效应。在强烈水合的抗衡离子存在下,稳定结构的形成最快,并且观察到明显的阴离子作用。通过将共价硅氧烷键的形成速率与围绕结构制造者离子的水分子的极化相关联来解释获得的凝胶稳定性。

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