Over the past several years, synthesized mesoporous nanosilica (SiO2) powders have been developed by many different methods. The methods include precipitation and microemulsion, the St?ber method, chemistry, and technology. In this study, mesoporous silica powders are synthesized by the sol-gel method. The sol-gel method obtains a high purity silica powder; however, the process yields a low percentage. Past syntheses of SiO2 powder precursors are expensive, but this study needs to find a replacement precursor for low cost alternatives. A high surface area was used to form an anion surfactant sodium dodecyl sulfate, which regulates the molar concentration. The particles size variability was changed by the precursor molar ratio of the sodium silicate solution with hydrochloric acid. 1. Introduction The silica powders are considered competent materials because of their unique characteristics, such as low density, low thermal conductivity, high surface area, high thermal shock resistance, and high specific strength [1, 2]. They also have the potential to be used in a wide range of applications, including catalysts, thermal and electrical insulators, adsorbents, filters, light-weight structural materials, optoelectronic devices, humidity sensors, chemical polishing, and other fine precision equipments [3–6]. According to recent academic and technical reports, various chemical methods have been developed to control the particle shapes, size, and distribution of fine silica particles. In the conventional method, ammonia-catalyzed reactions of tetraethylorthosilicate with water in low-molecular-weight alcohols are synthesized by St?ber method. However, this method has to use a high cost alkoxide or organometallic compound. In this work, we demonstrate a sol-gel method that controls the sphere size, cubic shapes, and mesoporous silica using the low cost sodium silicate solution with surfactant sodium dodecyl sulfate (SDS). The pore size and surface area of the silica varied with pH and aging time. The characteristics of the silica varied with the change in surface area, pore volume, and particle shapes. 2. Experimental 2.1. Synthesis The flow chart in Figure 1 shows the experimental steps involved in the rapid processing of cubic silica powders. In a study on the typical synthesis, the water glass solution was prepared in a beaker and the 1?M?HCl solution dripped for 30 minutes. The mixture was stirred for 10 hours with a magnetic bar at 400?rpm using a churner [7]. The water glass solution was diluted with the desired weight percentage of silica in the starting
References
[1]
S. Smitha, P. Shajesh, P. Mukundan, T. D. R. Nair, and K. G. K. Warrier, “Synthesis of biocompatible hydrophobic silica-gelatin nano-hybrid by sol-gel process,” Colloids and Surfaces B, vol. 55, no. 1, pp. 38–43, 2007.
[2]
N. N. Ghosh and P. Pramanik, “Synthesis of nano-sized ceramic powders using precipitated silica in aqueous sol-gel method,” Nanostructured Materials, vol. 8, no. 8, pp. 1041–1045, 1997.
[3]
P. W. J. G. Wijnen, T. P. M. Beelen, K. P. J. Rummens, H. C. P. L. Saeijs, and R. A. van Santen, “Silica gel from water glass: a SAXS study of the formation and ageing of fractal aggregates,” Journal of Applied Crystallography, vol. 24, no. 5, pp. 759–764, 1991.
[4]
A. Fouzri, R. Dorbez-Sridi, and M. Oumezzine, “Water confined in silica gel and in vycor glass at low and room temperature, x-ray diffraction study,” Journal of Chemical Physics, vol. 116, no. 2, pp. 791–797, 2002.
[5]
M. Helmich and F. Rauch, “On the mechanism of diffusion of water in silica glass,” Glastechnische Berichte, vol. 66, no. 8, pp. 195–200, 1993.
[6]
T. Matsuzawa, K. Mase, and S. Inoue, “Synthesis and application of a silica nanocomposite filler using water glass and a resole-type phenol resin,” Journal of Applied Polymer Science, vol. 112, no. 6, pp. 3748–3753, 2009.
[7]
A. Agarwal, M. Tomozawa, and W. A. Lanford, “Effect of stress on water diffusion in silica glass at various temperatures,” Journal of Non-Crystalline Solids, vol. 167, no. 1-2, pp. 139–148, 1994.
[8]
K. Aramaki, “Synergistic inhibition of zinc corrosion in 0.5 M NaCl by combination of cerium(III) chloride and sodium silicate,” Corrosion Science, vol. 44, no. 4, pp. 871–886, 2002.
[9]
J. Yatabe, T. Yamada, T. Mogi, S. Yamada, T. Ikawa, and T. Kageyama, “Preparation of porous amorphous silica from water glass as raw materials,” Nippon Kagaku Kaishi, vol. 3, 304 pages, 1993.
[10]
J. Chandradass, S. Kang, and D.-S. Bae, “Synthesis of silica aerogel blanket by ambient drying method using water glass based precursor and glass wool modified by alumina sol,” Journal of Non-Crystalline Solids, vol. 354, no. 34, pp. 4115–4119, 2008.
[11]
Y. Arai, H. Segawa, and K. Yoshida, “Synthesis of nano silica particles for polishing prepared by sol-gel method,” Journal of Sol-Gel Science and Technology, vol. 32, no. 1–3, pp. 79–83, 2004.
[12]
A. Borisov, Y. Lahaye, and H. Palme, “The effect of sodium on the solubilities of metals in silicate melts,” American Mineralogist, vol. 91, no. 5-6, pp. 762–771, 2006.
[13]
K. M. Davis and M. Tomozawa, “Water diffusion into silica glass: structural changes in silica glass and their effect on water solubility and diffusivity,” Journal of Non-Crystalline Solids, vol. 185, no. 3, pp. 203–220, 1995.
[14]
M. Tomozawa, D.-L. Kim, and V. Lou, “Preparation of high purity, low water content fused silica glass,” Journal of Non-Crystalline Solids, vol. 296, no. 1-2, pp. 102–106, 2001.
[15]
K. Kamiya, A. Oka, H. Nasu, and T. Hashimoto, “Comparative study of structure of silica gels from different sources,” Journal of Sol-Gel Science and Technology, vol. 19, no. 1–3, pp. 495–499, 2000.
[16]
F. W. Chang, M. T. Tsay, M. S. Kuo, and C. M. Yang, “Characterization of nickel catalysts on RHA-Al2O3 composite oxides prepared by ion exchange,” Applied Catalysis A, vol. 226, no. 1-2, pp. 213–224, 2002.
[17]
B. Andri?i?, T. Kova?i?, and I. Klari?, “Kinetic analysis of the thermooxidative degradation of poly(vinyl-chloride) in poly(vinyl chloride)/methyl methacrylate-butadiene-styrene blends—2. Nonisothermal degradation,” Polymer Degradation and Stability, vol. 79, no. 2, pp. 265–270, 2003.