Nanostructured ZnO-TiO2 thin film oxide as anode material in electrooxidation of organic pollutants. Application to the removal of dye Amido black 10B from water.

Electrochemical oxidative degradation of diazo dye Amido black 10B (AB10B) as model pollutant in water has been studied using nanostructured ZnO-TiO2 thin films deposited on graphite felt (GrF) substrate as anode. The influence of various operating parameters, namely the current intensity, the nature and concentration of catalyst, the nature of electrode materials (anode/cathode), and the adsorption of dye and ambient light were investigated. It was found that the oxidative degradation of AB10B followed pseudo first-order kinetics. The optimal operating conditions for the degradation of 0.12 mM (74 mg L-1) dye concentration and mineralization of its aqueous solution were determined as GrF-ZnO-TiO2 thin film anode, 100 mA current intensity, and 0.1 mM Fe2+ (catalyst) concentration. Under these operating conditions, discoloration of AB10B solution was reached at 60 min while 6 h treatment needed for a mineralization degree of 91 %. Therefore, this study confirmed that the electrochemical process is effective for the degradation of AB10B in water using nanostructured ZnO-TiO2 thin film anodes.

Simultaneous removal of Cr(VI) and Amido black 10B (AB10B) from aqueous solutions using quaternized chitosan coated bentonite.

In this study, simultaneous removal of Cr(VI) and Amido Black 10B (AB10B) using quaternized chitosan coated bentonite was investigated by a batch method. The factors affecting adsorption process such as pH, adsorbent dosage, contact time and initial concentration and the interaction of two components in binary solutions have been studied. The results showed that the antagonism effect existed between Cr(VI) and AB10B in binary systems. The equilibrium time for Cr(VI) adsorption was less than the one for AB10B adsorption. The maximum adsorption capacities of the modified bentonite, according to the Langmuir isotherm model were 847.5mg/g for AB10B and 66.6mg/g for Cr(VI) at 298K. The experimental results demonstrated that both Cr(VI) and AB10B were well described by the pseudo-second-order model. Thermodynamic study depicted that the adsorption of Cr(VI) and AB10B onto the modified bentonite was both spontaneous. The adsorption for Cr(VI) was exothermic while the one for AB10B was endoth- ermic in nature.

Adsorption of an anionic azo dye by cross-linked chitosan/bentonite composite.

In this study, cross-linked chitosan (CCS)/bentonite (BT) composite was prepared by the intercalation of chitosan in bentonite and the cross-linking reaction between chitosan and glutaraldehyde. CCS/BT composite was characterized by using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD) and thermal gravimetric analyses (TGA). Their adsorption characteristics were assessed by using an azo dye (Amido Black 10B) as a model adsorbate. The adsorption of Amido Black 10B onto the CCS/BT composite was found to be optimal at pH 2. The adsorption isotherm was well described by the Langmuir model and the maximum adsorption capacity was 323.6 mg/g at 293K and pH 2. Amido Black 10B adsorption kinetics followed a pseudo-second-order kinetic model. The calculated thermodynamic parameters showed that the adsorption of Amido Black 10B by CCS/BT composite was spontaneous and endothermic in nature.

Ag2S-ZnO--an efficient photocatalyst for the mineralization of Acid Black 1 with UV light.

The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 °C for 12 h. The catalyst was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) images, energy dispersive spectra (EDS), diffuse reflectance spectra (DRS) photoluminescence spectra (PL) and BET surface area measurements. The photocatalytic activity of Ag(2)S-ZnO was investigated for the degradation of Acid Black (AB 1) in aqueous solution using UV light. Ag(2)S-ZnO is found to be more efficient than commercial ZnO, prepared ZnO and TiO(2)-P25 at pH 9 for the mineralization of Acid Black 1. The effects of operational parameters such as the amount of photocatalyst, dye concentration, initial pH on photo mineralization have been analyzed. Mechanism of degradation by Ag(2)S-ZnO is proposed. The mineralization of Acid Black 1 has also been confirmed by COD measurements. The catalyst is found to be reusable.

Ethylenediamine modified starch as biosorbent for acid dyes.

This work investigated the sorption performance of the ethylenediamine modified starch (CAS) for the removal of acid dyes from aqueous solutions. The influence of pH on adsorption of acid orange 10 (AO10), acid green 25 (AG25) and amido black 10B (AB10B) was evaluated. The sorption kinetics, equilibrium uptake and desorption of the loaded dyes in sodium sulfate solution were studied. It was found that the interaction mechanism was based on electrostatic attraction and hydrogen bonding. The adsorption of AG25 and AB10B followed pseudo-second-order model, whereas AO10 followed both pseudo-first-order and pseudo-second-order models. The best isotherm was Langmuir equation and the capacities followed the sequence AB10B>AG25>AO10. The different behaviors of individual dyes adsorption on CAS were largely dependent on the number of hydrophilic functional groups, which had strong tendency to form hydrogen bonds with the biosorbent. Dye release in sodium sulfate solutions was determined by the salt concentration and nature of dyes.