Polymer-derived amorphous silica-based inorganic-organic hybrids having alkoxy groups

Alkoxy group-functionalized amorphous silica-based inorganic-organic hybrid materials were designed through polymer precursor route, in order to develop a novel route for the fabrication of microporous amorphous silica-based materials. Commercial perhydropolysilazane (PHPS) was chemically modified w...

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Veröffentlicht in:Journal of the Ceramic Society of Japan 2015-01, Vol.123 (1441), p.732-732
Hauptverfasser: Nazri MOHD SOKRI, Mohd, ONISHI, Takahiro, MOULINE, Zineb, DAIKO, Yusuke, HONDA, Sawao, IWAMOTO, Yuji
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Sprache:eng
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Zusammenfassung:Alkoxy group-functionalized amorphous silica-based inorganic-organic hybrid materials were designed through polymer precursor route, in order to develop a novel route for the fabrication of microporous amorphous silica-based materials. Commercial perhydropolysilazane (PHPS) was chemically modified with alcohols (R-OH, R = n-C5H11OH, n-C10H21OH) at a PHPS (Si basis) to ROH molar ratio of 4/1, and subsequently oxidized to afford alkoxy group-functionalized amorphous silica by exposure to aqueous ammonia vapours at room temperature. Then, the oxidized materials were heat-treated at 600°C in air. Nitrogen sorption analysis revealed that micropore volume of the amorphous silica increased upon alkoxy group-functionalization prior to the heat treatment. As a result, higher micropore volume of 0.204 cm3/g was achieved, with a specific surface area of 387 m2/g for the PHPS-derived amorphous silica chemically modified with n-C10H21OH at the Si/n-C10H21OH molar ratio of 2/1. The micropores evaluated by the SF method were in the size range of 0.43 to 1.6 nm, and the resulting micropore size distribution plot exhibited a peak at 0.43 nm. The in-situ formation of the microporosity was further studied by the simultaneous thermogravimetry-mass spectrometry analysis. The relationship between the number of carbon atoms in the alkoxy group, the evolution of gaseous species during the heat treatment and the resulting microporosity is discussed.
ISSN:1882-0743
1348-6535