TiO2 is a well-known mineral that occurs in three phases: rutile, anatase, and brookite [ 1 ], each having different structures. All the three phases have been studied for their high photocatalitic activity, high
Metal oxides, such as TiO2 , SnO 2 , ZnO, WO 3 , and Fe 2 O 3 , are well known for their remarkable ability to change the electrical resistivity in response to oxidizing and reducing gases. Gas sensing properties
, this method does not require any additional reagent such as ammonia or ozone.
Titanium dioxide or titania (TiO2 ) is usually preferred as an excellent material for photocatalytic applications because of its slower electron–hole recombination
effect of the oxidants in the UV/TiO2 system on the degradation rate of 4-chloro-2-methylphenol were found to follow the order IO 4 − > BrO 3 − > H 2 O 2 > O 2 > ClO 3 − [ 6 ]. Syoufian and Nakashima [ 8 ] indicated that the effectiveness of the
photocatalysts is more and more prevalent [ 1 , 2 ]. This particular field of catalysis initiated intensive scientific interest in the last few decades, particularly for TiO2 assisted photocatalysis, which has already proved to be a promising tool in water and
Titanium dioxide (TiO2 ) is a well-researched material in the environmental applications of photocatalysis because of its many desirable properties such as being inexpensive, readily available, biologically and
The inorganic semiconducting material TiO2 has attracted great attention because it can photocatalytically split water [ 1 ] and degrade organic pollutants [ 2 – 7 ]. Nevertheless, the wide band gap (3.2 eV) of
The effect of certain promoters on TiO2 crystal structure transformation was studied by mean thermal and X-ray analyses. It was found that the addition of rutile nuclei and potassium, phosphorus, zinc, magnesium, and aluminium compounds to hydrated titanium dioxide before calcination process influences on the initial temperature and anatase transformation.
The efficiency of color removal from aqueous Congo Red dye (CR) solution has been investigated in TiO2 suspensions irradiated with artificial UV light. Batch photocatalytic tests were carried out by varying the amount of TiO2 and the irradiation time using the same initial CR concentration. The experimental results indicated that the decolorization
rate follows pseudo first-order kinetics with respect to CR concentration. The doses of TiO2 were 0.25, 0.5 and 1.0 g L−1 and the wavelength of incident ultraviolet light was predominantly 254 nm. CR adsorption on the surface of TiO2 is also investigated and described.