TY - JOUR
T1 - Facile synthesis and thermal properties of waterglass-based silica xerogel nanocomposites containing reduced graphene oxide
AU - Oikawa, Kazuma
AU - Toyota, Kei
AU - Sakatani, Shigeaki
AU - Hayashi, Yamato
AU - Takizawa, Hirotsugu
N1 - Publisher Copyright:
© 2018 Elsevier Ltd and Techna Group S.r.l.
PY - 2019/3
Y1 - 2019/3
N2 - In this study, new rGO-silica xerogel nanocomposites (SX-rGO) and its glass fiber reinforced composites (GFR-SX-rGO) were prepared, and its microstructure and thermal properties were evaluated. The raw material was a mixed dispersion prepared by adding 0.01–2.5 wt% of reduced graphene oxide (rGO) to waterglass (6% SiO2). A hydrogel was prepared via sol-gel reaction of this raw material, which was then immersed in hydrochloric acid, hydrophobized in a siloxane/2-propanol reaction system, and then dried at ambient pressure to obtain a hydrophobic carbon-silica xerogel composite. The obtained samples were characterized by N2 physisorption (at 77 K), solid 29Si Magic angle spinning nuclear magnetic resonance spectroscopy, Fourier-transform infrared spectroscopy, Raman spectroscopy, differential scanning calorimetry, thermogravimetric analysis, hydrophobicity, and thermal conductivity. It was found that as the amount of rGO was increased, the specific surface area of the nanocomposite decreased by ~25% from 535 to 403 cm2/g, and the average pore size and pore volume were almost halved. The thermal decomposition temperature of the SX-rGO was increased markedly by the addition of rGO. Moreover, the GFR-SX-rGO-0.5 showed low density (0.208 g/cm3), high contact angle (146°) and low thermal conductivity (0.0199 W/mK).
AB - In this study, new rGO-silica xerogel nanocomposites (SX-rGO) and its glass fiber reinforced composites (GFR-SX-rGO) were prepared, and its microstructure and thermal properties were evaluated. The raw material was a mixed dispersion prepared by adding 0.01–2.5 wt% of reduced graphene oxide (rGO) to waterglass (6% SiO2). A hydrogel was prepared via sol-gel reaction of this raw material, which was then immersed in hydrochloric acid, hydrophobized in a siloxane/2-propanol reaction system, and then dried at ambient pressure to obtain a hydrophobic carbon-silica xerogel composite. The obtained samples were characterized by N2 physisorption (at 77 K), solid 29Si Magic angle spinning nuclear magnetic resonance spectroscopy, Fourier-transform infrared spectroscopy, Raman spectroscopy, differential scanning calorimetry, thermogravimetric analysis, hydrophobicity, and thermal conductivity. It was found that as the amount of rGO was increased, the specific surface area of the nanocomposite decreased by ~25% from 535 to 403 cm2/g, and the average pore size and pore volume were almost halved. The thermal decomposition temperature of the SX-rGO was increased markedly by the addition of rGO. Moreover, the GFR-SX-rGO-0.5 showed low density (0.208 g/cm3), high contact angle (146°) and low thermal conductivity (0.0199 W/mK).
KW - Carbons
KW - D.SiO
KW - Silica xerogel
KW - Thermal properties
KW - Waterglass
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U2 - 10.1016/j.ceramint.2018.11.089
DO - 10.1016/j.ceramint.2018.11.089
M3 - Article
AN - SCOPUS:85057234120
SN - 0272-8842
VL - 45
SP - 4201
EP - 4207
JO - Ceramics International
JF - Ceramics International
IS - 4
ER -