Novel mesoporous composites based on natural rubber and hexagonal mesoporous silica: Synthesis and characterization |
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Authors: | Sakdinun Nuntang Sirilux Poompradub Suchada Butnark Toshiyuki Yokoi Takashi Tatsumi Chawalit Ngamcharussrivichai |
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Affiliation: | 1. Fuels Research Center, Department of Chemical Technology, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand;2. PTT Research and Technology Institute, PTT Public Company Limited, Wangnoi, Ayutthaya 13170, Thailand;3. Division of Catalytic Chemistry, Chemical Resources Laboratory, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8503, Japan;4. Center of Excellence on Petrochemical and Materials Technology (PETROMAT), Chulalongkorn University, Patumwan, Bangkok 10330, Thailand |
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Abstract: | ![]() The present study is the first report on the synthesis and characterization of mesoporous composites based on natural rubber (NR) and hexagonal mesoporous silica (HMS). A series of NR/HMS composites were prepared in tetrahydrofuran via an in situ sol–gel process using tetraethylorthosilicate as the silica precursor. The physicochemical properties of the composites were characterized by various techniques. The effects of the gel composition on the structural and textural properties of the NR/HMS composites were investigated. The Fourier-transform infrared spectroscopy (FTIR) and 29Si magic angle spinning nuclear magnetic resonance (29Si MAS NMR) results revealed that the surface silanol groups of NR/HMS composites were covered with NR molecules. The powder X-ray diffraction (XRD) and transmission electron microscopy (TEM) data indicated an expansion of the hexagonal unit cell and channel wall thickness due to the incorporation of NR molecules into the mesoporous structure. NR/HMS composites also possessed nanosized particles (∼79.4 nm) as confirmed by scanning electron microscopy (SEM) and particle size distribution analysis. From N2 adsorption–desorption measurement, the NR/HMS composites possessed a high BET surface area, large pore volume and narrow pore size distribution. Further, they were enhanced hydrophobicity confirmed by H2O adsorption–desorption measurement. In addition, the mechanistic pathway of the NR/HMS composite formation was proposed. |
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Keywords: | Composite materials Sol&ndash gel growth Surface properties Nanostructures |
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