TL;DR: In this article, the authors present two reuse strategies for reverse osmosis (RO) concentrate produced by an integrated membrane system (IMS) from a wastewater reclamation facility, including bipolar membrane electrodialysis (BMED) and electrochlorination (EC) for onsite chlorine generation.
TL;DR: A semi-quantitative analysis of various volatile species produced during the electrolysis of highly saline water (0.6 M NaCl) at BDD electrode has been conducted by differential electrochemical mass spectrometry (DEMS) using the dual thin layer flow through cell as mentioned in this paper.
TL;DR: An electrochlorination and electrochemical system for the onsite generation and treatment of municipal water supplies and other reservoirs of water, by using a custom mixed oxidant and mixed reductant generating system for enhanced destruction of water borne contaminants by creating custom oxidation-reduction-reactant chemistries with real time monitoring is described in this article.
Abstract: An electrochlorination and electrochemical system for the on-site generation and treatment of municipal water supplies and other reservoirs of water, by using a custom mixed oxidant and mixed reductant generating system for the enhanced destruction of water borne contaminants by creating custom oxidation-reduction-reactant chemistries with real time monitoring. A range of chemical precursors are provided that when acted upon in an electrochemical cell either create an enhanced oxidation, or reduction environment for the destruction or control of contaminants. Chemical agents that can be used to control standard water quality parameters such as total hardness, total alkalinity, pH, total dissolved solids, and the like are introduced via the chemical precursor injection subsystem infrequently or in real time based on sensor inputs and controller set points.
TL;DR: Electrochemical activation of sulfate to SO4- at BDD anodes enhanced the removal of an antibiotic sulfamethoxazole (SMX) in this study, and the peak intensities of chlorinated TPs were three orders of magnitude lower in Na2SO4 than in NaNO3 anolyte, suggesting that addition of sulfates may lower the formation ofchlorinated organics.
TL;DR: In this article, the authors investigated the mechanisms of electrochemical (EC) wastewater disinfection and found that the major killing function of EC disinfection is provided by short-lived and high-energy intermediate EC products, such as free radicals.
Abstract: Laboratory experiments were carried out to investigate the mechanisms of electrochemical (EC) wastewater disinfection. Artificial wastewater contaminated by \IEscherichia coli\N (\IE. coli\N) culture, and which contained different salts of NaCl, Na\d2SO\d4, and NaNO\d3, was used as the test medium. The experimental results do not favor the hypotheses that the EC bactericidal action was due to cell destruction by the electric field and the production of persulfate. In comparison to direct chlorination, the EC process displayed a much stronger disinfecting capability than that of electrochlorination assumed for EC disinfection. Observations with scanning electron microscopy on the \IE. coli\N bacteria of wastewater treated by different means of disinfection suggested that the cells were likely killed during the EC treatment by chemical products with oxidizing and germicidal powers similar to that of ozone and much stronger than that of chlorine. All of the findings support the theory that the major killing function of EC disinfection is provided by short-lived and high-energy intermediate EC products, such as free radicals.