A Case Study of Swine Wastewater Treatment via Electrochemical Oxidation by Ti4O7 Anode.

With the rapid development of breeding industry, the efficient treatment of dramatically increasing swine wastewater is gradually becoming urgent. In particular, the development of application technologies suitable for the relatively small piggeries is critical due to the time cost and space requirements of conventional biological methods. In this study, Electrochemical oxidation (EO) was selected to systematically explore the treatment performance of three different swine wastewaters by Ti4O7 anode. It was observed that the colors changed from dark brown to light yellow after 60 min treatment at 50 mA/cm2, and the removal rates of turbidity and suspended solids ranged from 89.36% to 93.65% and 81.31% to 92.55%, respectively. The chemical oxygen demand (COD), ammonia nitrogen (NH3-N) and total phosphorus (TP) of all the three swine wastewaters were simultaneously removed to a very low concentration in 120 min, especially for sample III, 61 ± 9 mg/L of COD, 6.6 ± 0.4 mg/L of NH3-N and 5.7 ± 1.1 mg/L of TP, which met the Discharge Standard of Pollutants for Livestock and Poultry Breeding (GB 18596-2001). Moreover, 70.93%-85.37% mineralization rates were also achieved in 120 min, confirming that EO treatment by Ti4O7 could efficiently remove the organic matters in wastewater. Excitation-emission matrix (EEM) and UV-vis spectrum characterization results further proved that aromatic compounds and macromolecules in wastewater were rapidly removed, which played important roles in the mineralization processes. The findings here provided an efficient and environment-friendly technology for swine wastewater treatment.

An electrocoagulation and electrooxidation treatment train to remove and degrade per- and polyfluoroalkyl substances in aqueous solution.

This study examined the feasibility of a novel treatment train that combines electrocoagulation (EC) with electrooxidation (EO) treatment to remove and degrade per- and polyfluoroalkyl substances (PFASs) from water. Electrocoagulation with a zinc anode could effectively remove PFASs from water, and long-chain PFASs (C7-C10) tended to have a higher removal rate. Foam was generated when a relatively high current density (>1 mA cm-2) was applied to a relatively high PFAS concentration (each PFAS > 0.1 µM) during EC, which promoted the separation of PFASs from the bulk solution, especially for long-chain PFASs. Isotherm-like adsorption results indicated that competitive adsorption on floc occurred between PFASs when no foam was produced in a solution containing 10 different PFASs. Acid dissolution methods could recover and concentrate 10 PFASs in controlled volumes from both the floc and the foam, and it was also successfully applied in groundwater collected from a contaminated site. The concentrated PFASs in the acid solutions were efficiently destructed using EO treatment with a Ti4O7 anode at 10 mA cm-2, and no supplement of electrolyte was needed for the floc dissolved solution. This electrochemical-based process can economically separate, concentrate and destroy PFASs in groundwater and wastewater.