| Nano-TiO2 has received much attention due to its strong redox ability, chemical stability,non-toxicity, and cheapness. However, the nano-TiO2 powder is easy to lose in liquid-phasephotocatalytic reaction and difficult to be collected after the reaction, which disturbs therecycle of photocatalyst and hampers the practical applications of nano-TiO2 powder.Immobilization of nano-TiO2 overcomes the difficulties in separation and recycles ofphotocatalyst, enhances the concentration of substrates near the TiO2, as well as restrainsaggregation and deactivation of the catalyst particles. In this work, the research on nano-TiO2supported on zeolites or porous silica and their hydrophobical modification was reviewed.Therefore, the significance of theory and practice about the study on photocatalyticdegradation of MO over TiO2/HZSM-5, as well as adsorption and photocatalytic properties ofTiO2/MCM-41, which includes cationic template within the framework of MCM-41-drymaterials, has been shown in this paper.TiO2/HZSM-5 photocatalysts were prepared by impregnation, sol-gel, and solid statedispersion methods, using ammonium titanyl oxalate, tetrabutyl titanate, and P-25 as titaniumsource, respectively. The photocatalytic reactivity of the prepared samples for the degradationof methyl orange (MO) under UV light irradiation were investigated. The catalyst prepared bysimple, easy to control and organic-solvent-free impregnation method showed a higherphotocatalytic activity than that prepared by sol-gel and solid state dispersion methods. Inaddition, effect of Si/Al ratios and TiOB2 Bloadings on catalyst, which prepared by impregnation,for photocatalytic activity of degradation of MO were investigated. It was found that, at 15wt% and Si/Al=500, TiO2/HZSM-5 showed a higher photocatalytic activity. The structure ofthe catalysts were characterized by XRD,UV-vis DRS and BET technologies. It was foundthat TiO2/HZSM-5 prepared by impregnation had a higher surface area and the nano-TiO2particles well dispersed on the surface of zeolite leading to a higher photocatalytic activity.The effect of surfactant template in MCM-41 on the removal of o-CP and o-CNB wasinvestigated. The comparison of adsorption of o-CP and o-CNB on uncalcined MCM-41noted as MCM-41-dry) and calcined MCM-41 (noted as MCM-41-cal) was investigated.MCM-41-dry exhibited significant adsorption capacity for o-CP and o-CNB as compared to MCM-41-cal, which may be because of the hydrophobicity created by surfactant template inMCM-41-dry. In addition, batch adsorption studies were carried out to study the effect ofvarious parameters like adsorbent dose, pH, initial concentration and the presence ofco-existing ions. It was found that adsorption of o-CP and o-CNB depends upon the solutionpH as well as co-existing ions present in the aqueous solution. . From the sorption studies itwas observed that the uptake of o-CP was higher than that of o-CNB. The equilibriumadsorption data for o-CP and o-CNB was analyzed by using Freundlich adsorption isothermmodel.The photocatalytic activity of TiO2 supported on MCM-41-dry and MCM-41-cal wasinvestigated using the photooxidation of o-CP as test reactions. The photocatalytic activity ofTiO2 supported on MCM-41-dry was observed to be higher than that of TiO2 supported onMCM-41-cal. Moreover, it was found that the photocatalytic activity of TiO2/MCM-41-dryincreased with the increase in pH value of reactant solution and decrease in initialconcentration of o-CP. |