Abstract:The effect of water adsorption and heat treatment at various temperatures between 200 and 1100°C on the dielectric dispersions of silica gel was measured in the frequency range from 50 to 3×106 Hz and 9.81 GHz and in the temperature range from −196°C to 180°C. Two anomalous dispersions (Dispersion I and II) and one anomaly (Anomaly III) were found. The mechanisms of those anomalies were discussed in relation to some physical properties and silica crystal structures. Dispersion I, having activation energy ΔE eq… Show more
“…65 Such an interpretation is furthermore consistent with an earlier study on high temperature treated silica gel, where a fast process with similar activation energy was attributed to the rotation of surface bonded hydroxyl groups. 66 A similar result was also obtained for water in montmorillonite (hydrated clays) 67 and more recently in hydrated ordinary Portland cement where a decrease in the elastic intensity occurs at about 190 K and attributed to the activation of OH − motions. 68 In addition, studies on dried amorphous polysaccharides (cellulose and dextran) with two and three hydroxyl groups per ring, respectively, have shown on a weak relaxation similar to the here obtained process 1, however, with a somewhat higher activation energy of 0.33 eV.…”
Section: Possible Molecular Origin Of the Fastest Relaxation In C-s-hsupporting
Articles you may be interested inCause of the fragile-to-strong transition observed in water confined in C-S-H gel In this study, the rotational dynamics of hydration water confined in calcium-silicate-hydrate (C-S-H) gel with a water content of 22 wt.% was studied by broadband dielectric spectroscopy in broad temperature (110-300 K) and frequency (10 −1 -10 8 Hz) ranges. The C-S-H gel was used as a 3D confining system for investigating the possible existence of a fragile-to-strong transition for water around 220 K. Such transition was observed at 220 K in a previous study
“…65 Such an interpretation is furthermore consistent with an earlier study on high temperature treated silica gel, where a fast process with similar activation energy was attributed to the rotation of surface bonded hydroxyl groups. 66 A similar result was also obtained for water in montmorillonite (hydrated clays) 67 and more recently in hydrated ordinary Portland cement where a decrease in the elastic intensity occurs at about 190 K and attributed to the activation of OH − motions. 68 In addition, studies on dried amorphous polysaccharides (cellulose and dextran) with two and three hydroxyl groups per ring, respectively, have shown on a weak relaxation similar to the here obtained process 1, however, with a somewhat higher activation energy of 0.33 eV.…”
Section: Possible Molecular Origin Of the Fastest Relaxation In C-s-hsupporting
Articles you may be interested inCause of the fragile-to-strong transition observed in water confined in C-S-H gel In this study, the rotational dynamics of hydration water confined in calcium-silicate-hydrate (C-S-H) gel with a water content of 22 wt.% was studied by broadband dielectric spectroscopy in broad temperature (110-300 K) and frequency (10 −1 -10 8 Hz) ranges. The C-S-H gel was used as a 3D confining system for investigating the possible existence of a fragile-to-strong transition for water around 220 K. Such transition was observed at 220 K in a previous study
“…Dielectric studies of adsorbed water on inorganic surfaces and in porous systems [27][28][29][30][31][32][33][34][35] are also of relevance in this context. In all these cases, molecular and interfacial effects overlap.…”
The dielectric properties of composite samples prepared by polymerizing ethylene on the surface of filler are compared to those of mechanical mixtures consisting of CaCO3 and ultra high molecular weight polyethylene. After presenting the normalized master curves of AC dispersion and loss measured at different relative humidities, the field strength dependence of the 50 Hz AC and DC responses were studied. With one exception, the effect is small. Thermally stimulated polarization (TSP) and depolarization (TSD) curves are presented; the peak appearing on the TSP curves of the samples stored under ambient conditions is interpreted as a result of water desorption. The high temperature DC conductivity and the depolarization current density are higher in the composites and mechanical mixtures than in the matrix. The dielectric properties of the wet filler particles were calculated from the measured composite and matrix data using various mixture formulae. The results can be understood and interpreted if the dielectric properties of adsorbed water are described by the cluster theory of dielectric relaxation.
“…Results were similar to that of mesoporous silicas SBA-15, which uses costly P123 as framework, respectively. Because mesoporous materials have a significant effect on the removal of heavy metal in aqueous solution, − the adsorbents used in this study were place in a complex solution environment. According to the experimental data, the removal ability of heavy metals in aqueous solution is not only related to electrostatic attraction, surface precipitation, and chemical interaction between the metal ions and the surface functional groups, but also related to its surface free energy − and its pore system.…”
Section: Introductionmentioning
confidence: 99%
“…16 This type of urea− formaldehyde framework mesoporous silica has a complex pore structure. To maintain the surface area 17 and a high surface activity, 18 urea−formaldehyde polymer/SiO 2 composite microspheres were heated gradually after attaching SiO 2 colloid onto the framework under strict temperature and pH conditions. Superpure high activity silica was obtained.…”
A mesoporous silica prototype (MSP) was produced by attaching SiO 2 colloid to urea formaldehyde resin. Treatment of the MSP using different grafting methods yielded three different amino-functionalized mesoporous silica samples. The materials were characterized by scanning electron microscopy, energy-dispersive spectroscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, 13 C nuclear magnetic resonance, zeta potential measurements, and isothermal N 2 sorption/desorption. For a 1:2000 solid-to-liquid ratio, all adsorbents could almost completely remove uranyl from sulfate and carbonate solutions of 3.6 mg L −1 U(VI) at pH 3.5 to 5.5 and pH 6.5 to 9.5, respectively. The adsorption equilibrium time was less than 30 min. The adsorption equilibrium curve showed that the maximum sorption capacity was 117 mg L −1 at pH 4.0. Through the experimental adsorption, it was found that the most effective sample could reduce the U(VI) concentration from 3.6 mg L −1 to 0.79 μg L −1 with 99.98% removed. In desorption experiments, 0.1 mol L −1 nitric acid could desorb U(VI) almost completely from the adsorbent. However, this kind of adsorbent is unsuitable for use in high acid or alkaline environments.
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