Enhanced TiO2 photocatalytic degradation of bisphenol E by β-cyclodextrin in suspended solutions

Enhancement of beta-cyclodextrin (beta-CD) on TiO2 Photocatalytic degradation of bisphenol E (BPE, bis(4-hydroxyphenyl)ethane) was investigated under a 250 W metal halide lamp ( lambda >= 365 nm) in this work. In the system of photocatalytic degradation of BPE, the photodegradation rate of BPE in aqueous solutions containing beta-CD and TiO2 was obviously faster than that in aqueous solutions containing only Tio(2). After 40 min of irradiation, beta-CD could increase the photodegradation efficiency by about 26% for 10 mg l(-1) BPE in the UV-vis/TiO2 system and the photodegradation of 2.5-20.0 mg l(-1) BPE in aqueous solutions was found to follow pseudo-first-order law and the adsorption constant and the reaction rate constant of BPE in the system containing beta-CD and TiO2 are obviously higher than those in the system containing only TiO2, the influence factors on photode.-radation of BPE were studied and described in details, such as beta-CD concentration, pH, BPE initial concentration and gas medium. The formation of CO2 as a result of mineralization of BPE was observed during the photodegradation process. After 120 min of irradiation, the mineralization efficiency of BPE reached 61% in the presence of beta-CD, whereas mineralization efficiency was only 23% in the absence of beta-CD. The enhancement of photodegradation of BPE could be dependent on the enhancement of adsorption of BPE on TiO2 surface and moderate inclusion-depth of BPE in the beta-CD cavity. (c) 2005 Elsevier B.V. All rights reserved.