Abstract
This work reported a comparative study on the electrochemical incineration of nitrilotriacetic acid (NTA) in the presence of different supporting electrolytes (Na2SO4 and NaCl). Galvanostatic electrolyses were conducted in an undivided electrochemical cell containing boron-doped diamond (BDD) anode and platinum cathode. Initial solution pH, flow rate, applied current density, and supporting electrolyte concentration were selected as variables, besides the mineralization efficiency of NTA that was selected as response. Central composite rotatable design and response surface methodology were employed here to examine the statistical significance of the selected variables, as well as to determine the optimal conditions of the degradation process. Under the same operating conditions, two regression models were thus constructed to illustrate the differing impact of supporting electrolytes in BDD anode cells. The kinetics for NTA degradation followed different reaction orders for the two scenarios (in the absence and presence of NaCl), indicating the complex interaction between hydroxyl radicals and active chlorine. Despite this, the experimental results demonstrated that effective mineralization of NTA might also be achieved in the presence of chlorides (of lower concentrations). Besides, in the case of chlorides, the average mass transfer coefficient of the system was found to be strongly dependent on the initial solution pH. Lastly, a plausible reaction sequence concerning the electrolytic oxidation of NTA in chloride media was also proposed.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.