4.6 Article

Temperature dependent microstructure of MTES modified hydrophobic silica aerogels

期刊

MATERIALS LETTERS
卷 65, 期 4, 页码 606-609

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.matlet.2010.11.026

关键词

Silica aerogels; Hydrophobic; MTES; Thermal stability; Single step sol-gel process

资金

  1. NASF [10976013]

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Hydrophobic silica aerogels were prepared using a single step sol-gel process followed by ethanol supercritical drying. Using tetraethoxysilane (TEOS) as a precursor and ammonium hydroxide as a catalyst the aerogel surface was chemically modified with methyltriethoxysilane (MTES). A MTES/TEOS molar ratio of 0.5 (M5) was used. The microstructure of the surface modified aerogels was evaluated as a function of heat treatment temperature over a range of 200-500 degrees C. The thermal stability was analyzed by simultaneous thermogravimetry and differential scanning calorimetry (TG-DSC) and the microstructure was evaluated by physisorption analysis (BET) and scanning electron microscopy (SEM). The chemical composition and hydrophobicity/hydrophilicity of the aerogels were investigated by Fourier Transform-Infrared (FT-IR) spectroscopy. The M5 aerogels, which were initially hydrophobic, exhibited partial hydrophilicity at treatments above 244.5 degrees C and complete hydrophilicity above 429.9 degrees C. The surface area of the aerogels ranged from 776.65-850.20 m(2)/g. Pore size increased after heat treatment, ranging from 16.25 to 18.52 nm vs. an initial pore size of 14.71 nm. The maximum pore size of 18.52 nm was found at the lowest heat treatment temperature (similar to 200 degrees C). Heat treatment had a mixed effect on the pore volume, as pore volumes decreased at lower treatments (similar to 200-400 degrees C) and increased at higher heat treatments (similar to 450-500 degrees C) relative to the untreated aerogels. With initial heat treatment the Si-CH(3) group began to oxidize to Si-OH. Aerogels heated above 429.9 degrees C exhibited hydroxyl polymerization leading to aerogels with large particles and a dense microstructure. (C) 2010 Elsevier B.V. All rights reserved.

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