2007
DOI: 10.1016/j.apcatb.2006.12.015
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Immobilization of TiO2 on perlite granules for photocatalytic degradation of phenol

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Cited by 266 publications
(110 citation statements)
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“…The strong adsorption of the pollutants over the activated carbon was the main reason pointed by the authors to explain the occurred phenomenon. Recently, porous non-metal minerals have been taken into account as supports of TiO 2 -based photocatalysts, such as perlite, zeolite and diatomite due to their low costs [11][12][13][14]. The use of porous minerals as support induces a synergistic effect by improving the photo-efficiency of the immobilized TiO 2 NPs.…”
Section: Introductionmentioning
confidence: 99%
“…The strong adsorption of the pollutants over the activated carbon was the main reason pointed by the authors to explain the occurred phenomenon. Recently, porous non-metal minerals have been taken into account as supports of TiO 2 -based photocatalysts, such as perlite, zeolite and diatomite due to their low costs [11][12][13][14]. The use of porous minerals as support induces a synergistic effect by improving the photo-efficiency of the immobilized TiO 2 NPs.…”
Section: Introductionmentioning
confidence: 99%
“…Typical procedure given in [6], with some changes, was applied in order to prepare TiO2/perlite composites. According to that, a determined amount of TiO2 (Degussa P-25), then, 5 mL of diluted nitric acid (at pH 3.3), was added into 50 mL of absolute ethanol in an ultrasonic bath.…”
Section: Methodsmentioning
confidence: 99%
“…TiO2 can be strongly attached to the perlite surface with Ti-O-Si bonds effectively, hence, stable photocatalysts could be developed. Expanded perlite, has been widely used as photocatalyst support in recently published works in order to photocatalytic degradation of different pollutant like ammonia [2,3], sulfamethoxazole [4], ethylbenzene [5], phenol [6,7], and furfural [8]. None of them investigated the effect of preparation conditions onto degradation efficiency by any experimental design approach.…”
Section: Introductionmentioning
confidence: 99%
“…The direct reaction of •OH with the phenol molecules also gives rise to phenoxy radical. This radical, as detailed by Hosseini et al (2007), is in resonance with radical structures in o-and p-positions [24] and becomes the starting point for the formation of different intermediates. More hydroxylated compounds such as catechol, hydroquinone, benzoquinone or hydroxyl hydroquinone are then produced from subsequent reactions of the intermediates with •OH [25].…”
Section: Uv/h2o2/o3 Processmentioning
confidence: 98%