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Rehydroxylation of dehydrated silica surfaces by water vapor adsorption
Affiliation:1. Laboratoire de Chimie, Catalyse, Polymères et Procédés, UMR 5265 CNRS/ESCPELyon/UCBL, ESCPE Lyon, F-308-43, Boulevard du 11 Novembre 1918, F-69616 Villeurbanne Cedex, France;2. Université Lille Nord de France, CNRS UMR8181, Unité de Catalyse et de Chimie du Solide, UCCS USTL, F-59655 Villeneuve d''Ascq, France;3. Kjemisk Institutt, Universitetet i Bergen, Allégaten 41, N-5007 Bergen, Norway;1. Phys. Dept. Fac. of Appl. Med. Sci., Turabah 21995, Taif University, Saudi Arabia;2. Nano and thin film lab. Phys. Dept., Fac. of Sci., South Valley Univ., Qena 83523, Egypt;3. Phys. Dept, Phys. Dept., Fac. of Sci., Damietta Univ., New Damietta 34517, Egypt;4. Physics Department, Damietta Cancer Institute, Damietta, Egypt
Abstract:The rehydroxylation reaction of siloxane bridges was studied for silica gel particles dehydrated by preheating. Adsorption isotherms of water vapor at 298 K were measured for the samples which were preheated at different temperatures. The amounts of total adsorption and irreversible adsorption were examined against the preheating temperature and vapor pressure. The number of the hydroxyl groups produced by the rehydroxylation of siloxane was measured by thermogravimetrican alysis to determine the adsorption isotherms for chemisorption of water. For the surface preheated at 673 K, the siloxane bridges were fully rehydroxylated for about 3 h at a relative pressure of 0.3. The surface preheatedat 873 K was gradually rehydroxylated with increasing pressure and the rehydroxylation was not complete even for 90 h at a relative pressure lower than 0.7. In the high-pressure region, the rehydroxylation was promoted by condensed water. The number of surface hydroxyls after rehydroxylation became greater than that on the original surface. The possibility of the generation of the geminal hydroxyls was suggested from the degree of rehydroxylation on the surface.
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