NIPPON KAGAKU KAISHI
Online ISSN : 2185-0925
Print ISSN : 0369-4577
Photocatalytic Activities of Titanium(IV) Oxide Prepared from Titanium(IV) Sulfate
Sei-ichi NISHIMOTOBunsho OHTANIAkira SAKAMOTOTsutomu KAGIYA
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JOURNAL FREE ACCESS

1984 Volume 1984 Issue 2 Pages 246-252

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Abstract

A series of TiO2 powders was prepared by calcining titanium(N) hydroxide slurry, which was provided by hydrolysis of titanium(N) sulfate, in the temperature range (To) of 170 to 1000°C. The content of anatase (CA) in the TiO2 powder and the corresponding crystallite size (LA) increased with increasing To up to 700°C (Fig.1). The transition from anatase to rutile occurred at 740-830°C. The BET surface area (S) of the TiO2 powder was directly proportional to the content of amorphous TiO2 (CAM) (Fig.2). The residual sulfate ions in the TiO2 powder decreased linearly with increasing To, disappearing almost completely above 800°C (Fig.4). The amount of hydroxyl groups located on the TiO2 surface decreased monotonously with increasing To (Fig.6). The To dependence of the photocatalytic activity of Pt (5 wt%)loaded TiO2 (Fig.9), with reference to the above structural characteristics of the TiO2, suggested that the anatase, but not the rutile, has a sufficient photocatalytic activity to reduce 11+ and oxidize 2-propanol when loaded with a small amount of platinum black (Pt)(see also Fig.8).
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However, in another reaction system consisting of 2-propanol and silver salts, even the rutile TiO2 without Pt could effectively photocatalyze the reduction of Ag+ to Ag metal onto the TiO2 and oxidation of 2-propanol to acetone (Table 1).

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