Solar degradation of Direct Blue 71 using surface modied iron doped ZnO hybrid nanomaterials A. Maleki and B. Shahmoradi ABSTRACT This paper reports photodegradation of Direct Blue 71 under irradiation by sunlight. We synthesized Fe:ZnO nanomaterials under mild hydrothermal conditions ( P ¼ autogenous, T ¼ 100 W C, t ¼ 18 h). The precursors were Fe 2 O 3 as dopant, n-butylamine as surface modier, NaOH as mineralizer and reagent grade ZnO. The systematic experiments on the photodegradation of Direct Blue 71 were carried out by changing different effective parameters. The variables in this study were type of nanomaterials synthesized (4 types), nanomaterial dosage (0.41.0 g/L), contact time (30120 min), pH (311), and dye concentration (20100 ppm). The photodegradation efciency was determined using a UV-Vis spectrophotometer. Determination of total organic carbon (TOC) amount was used to nd out mineralization efciency. Our experimental results revealed that the nanomaterials synthesized had higher efciency compared with the reagent grade ZnO. The best efciency was achieved at the following conditions: 1.0 g/L nanomaterials loading, 120 min contact time, pH 5, and photodegradation efciency from more than 75 up to 99% depending upon the dye concentration. A. Maleki B. Shahmoradi (corresponding author) Environmental Health Research Center, Faculty of Health, Kurdistan University of Medical Science, Sanadaj, Kurdistan, Iran E-mail: bshahmorady@gmail.com; bshahmoradi@ymail.com Key words | Direct Blue 71, Fe:ZnO nanomaterials, mild hydrothermal, solar degradation, surface modier INTRODUCTION More than 30,000 commercial dyes based on ca 8,000 different chemical structures are used in textile, food, pharmaceutical, paper, and ink industries, and they are dis- charged in wastewater (Molinari et al. ). The efuents are usually treated by physico-chemical, oxidative or, most commonly, active sludge biochemical processes. The main drawback of the above-mentioned processes is that they gen- erally produce secondary pollution due to the introduction of chemicals and/or the possible accumulation of other bioresistant species in the environment. As azo dyes are intentionally designed to resist degradation, traditional methods such as occulation, carbon adsorption, reverse osmosis, and the activated sludge process have low mineral- ization efciency for this class of xenobiotics. In recent years, advanced oxidation processes (AOPs) have emerged as contemporary oxidative techniques for degradation of detrimental organic compounds both in industrial pretreatment and in full-scale treatment (Pare et al. ; Rezaee et al. ). In this regard, nanomaterials such as TiO 2 and ZnO have been known as suitable photo- catalysts. Compared with other II-IV semiconductors, ZnO is a versatile and unique material with a direct band gap (E g ¼ 3.37 eV) and large exciton binding energy of 60 meV (Gyu-Ghul et al. ; Qiuxiang et al. ). Most ZnO nanomaterials have been fabricated through the traditional high temperature solid-state method, which is energy con- suming and in which the particle properties are difcult to control. These nanomaterials could be synthesized at low cost using simple solution-based methods, such as chemical precipitation (Daneshvar et al. ), sol-gel (Xu et al. ), or solvothermal/hydrothermal reactions (Byrappa et al. ). The hydrothermal technique is a promising and known alternative synthetic method because of low process temperature and pressure, and the particle size is easily con- trolled. Moreover, the hydrothermal technique has several advantages over other processes such as use of simple equip- ment, catalyst-free growth, costeffectiveness large area uniform production, eco-friendliness, high product purity, high crystallinity, and no need for post-treatment (Adschiri & Byrappa ). However, ZnO nanomaterials are active in the UV range only due to their wide band gap energy. Moreover, they are 1923 © IWA Publishing 2012 Water Science & Technology | 65.11 | 2012 doi: 10.2166/wst.2012.091