Preparation of TiO2/MCM-41 by plasma enhanced chemical vapor deposition method and its photocatalytic activity

Shenghung WANG , Kuohua WANG , Jihmirn JEHNG , Lichen LIU

Front. Environ. Sci. Eng. ›› 2012, Vol. 6 ›› Issue (3) : 304 -312.

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Front. Environ. Sci. Eng. ›› 2012, Vol. 6 ›› Issue (3) : 304 -312. DOI: 10.1007/s11783-010-0297-8
RESEARCH ARTICLE
RESEARCH ARTICLE

Preparation of TiO2/MCM-41 by plasma enhanced chemical vapor deposition method and its photocatalytic activity

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Abstract

Titanium dioxide is coated on the surface of MCM-41 wafer through the plasma enhanced chemical vapor deposition (PECVD) method using titanium isopropoxide (TTIP) as a precursor. Annealing temperature is a key factor affecting crystal phase of titanium dioxide. It will transform an amorphous structure to a polycrystalline structure by increasing temperature. The optimum anatase phase of TiO2 which can acquire the best methanol conversion under UV-light irradiation is obtained under an annealing temperature of 700°C for 2 h, substrate temperature of 500°C, 70 mL·min-1 of oxygen flow rate, and 100 W of plasma power. In addition, the films are composed of an anatase-rutile mixed phase, and the ratio of anatase to rutile varies with substrate temperature and oxygen flow rate. The particle sizes of titanium dioxide are between 30.3 nm and 59.9 nm by the calculation of Scherrer equation. Under the reaction conditions of 116.8 mg·L-1 methanol, 2.9 mg·L-1 moisture, and 75°C of reaction temperature, the best conversion of methanol with UV-light is 48.2% by using the anatase-rutile (91.3/8.7) mixed phase TiO2 in a batch reactor for 60 min. While under fluorescent light irradiation, the best photoactivity appears by using the anatase-rutile (55.4/44.6) mixed phase TiO2 with a conversion of 40.0%.

Keywords

photocatalyst / titanium dioxide / MCM-41 / plasma enhanced chemical vapor deposition (PECVD)

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Shenghung WANG, Kuohua WANG, Jihmirn JEHNG, Lichen LIU. Preparation of TiO2/MCM-41 by plasma enhanced chemical vapor deposition method and its photocatalytic activity. Front. Environ. Sci. Eng., 2012, 6(3): 304-312 DOI:10.1007/s11783-010-0297-8

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