This study interrogated multi-layer heterojunction anodes were interrogated for potential applications to water treatment. The multi-layer anodes with outer layers of SnO2/Bi2O3 and/or TiO2/Bi2O3 onto IrO2/Ta2O5 electrodes were prepared by thermal decomposition and characterized in terms of reactive chlorine species (RCS) generation in 50 mM NaCl solutions. The IrO2/Ta2O5 layer on Ti substrate (Anode 1) primarily served as an electron shuttle. The current efficiency (CE) and energy efficiency (EE) for RCS generation were significantly enhanced by the further coating of SnO2/Bi2O3 (Anode 2) and TiO2/Bi2O3 (Anode 3) layers onto the Anode 1, despite moderate losses in electrical conductivity and active surface area. The CE of the Anode 3 was found to show the highest RCS generation rate, whereas the multi-junction architecture (Anode 4, sequential coating of IrO2/Ta2O5, SnO2/Bi2O3, and TiO2/Bi2O3) showed marginal improvement. The microscopic observations indicated that the outer TiO2/Bi2O3 could form a crack-free layer by an incorporation of anatase TiO2 particles, potentially increasing the service life of the anode. The results of this study are expected to broaden the usage of dimensionally stable anodes in water treatment with an enhanced RCS generation and lifetime.

The sol-gel method was used to prepare binary metal oxide (IrO2-RuO2) pH sensor. The electrodes that mole percent compositions (mol%) of IrO2 and RuO2 were 70:30 and 30:70 were selected. The characterizations of Nernstian response over pH range, response rate, interference on alkaline metals and reproducibility were investigated. Also the electroanalytical properties of these electrodes were evaluated in comparison with a commercial glass pH electrode. The composition of IrO2:RuO2 70:30 mol% was chosen as better electrode formulation. The electrode was not susceptible to the action of interfering ions such as Li+, Na+ and K+.

In this work, we prepared a heterojunction anode with a surface layer of SnO2-Sb-Ni (SSN) on a Ti/IrO2 electrode by thermal decomposition to improve the electrochemical activity of the Ti/IrO2 electrode. The Ti/IrO2-SSN electrode showed significantly improved electrochemical activity compared with Ti/IrO2. For the 0.1 M NaCl and 0.1 M Na2SO4 electrolytes, the onset potential of the Ti/IrO2-SSN electrode shifted in the positive direction by 0.1 VSCE and 0.4 VSCE, respectively. In 2.0-2.5 V voltages, the concentration in Ti/IrO2-SSN was 2.59-214.6 mg/L Cl2, and Ti/IrO2 was 0.55-49.21 mg/L Cl2. Moreover, the generation of the reactive chlorine species and degradation of Eosin-Y increased by 3.79-7.60 times and 1.06-2.15 times compared with that of Ti/IrO2. Among these voltages, the generation of the reactive chlorine species and degradation of Eosin-Y were the most improved at 2.25 V. Accordingly, in the Ti/IrO2-SSN electrode, it can be assumed that the competitive reaction between chlorine ion oxidation and water oxidation is minimized at an applied voltage of 2.25V.

Soluble Cutting Fluids (SCFs) have been used in metal machining processes to improve the quality of metal processing equipment and products. Although SCFs are useful and essential material, wasted soluble cutting fluids are harmful in hydroecological systems because of the high concentration of COD and nitrogen material. If discharged to hydroecological systems without specific treatment, they may cause eutrophication in rivers and lakes. Therefore, the removal efficiency of the COD contained in the SCFs is investigated in this study using electrochemical treatment with an insoluble electrode. The electrode was made of titanium with iridium plating, made from a perforated metal sheet to agitate the sample in the reactor. Cathode and anode electrodes were inserted into acrylic reactor alternately and the reaction time was one hour. The experimental results were as follows: First, for 60 A/m2, 80 A/m2, and 100 A/m2 current densities, the COD removal efficiencies were 42.0%, 63.9%, and 78.4%, respectively.

As industry continues to develop, the contents of various recalcitrant substances that are not removed by conventional wastewater treatment have increased in modern society. The metal working fluids (MWFs) used in the metal working process contain chemical substances, such as mineral oils, anticorrosive agents, extreme-pressure additives, and stabilizers, as well as high concentrations of organics and ammonia-nitrogen. Accordingly, MWFs are required to develop advanced treatments to conserve hydro-ecological resources. This study investigated the removal efficiency of ammonia nitrogen from MWFs according to operating time, applied voltage, and NaCl concentration using a Ti/IrO2 electrode in a batch-type reactor. The experimental results showed that ammonia-nitrogen removal efficiencies without NaCl were 89% and 92% when voltage was adjusted to 15 and 20 V for 60 min and removal efficiency was 90% at 25 V for 40 min. Removal efficiencies of 10 mM NaCl were 4% and 2% greater than those of not adding NaCl at 15 V for 50 min and 20 V for 30 min.