Degradation of ranitidine and changes in N-nitrosodimethylamine formation potential by advanced oxidation processes: Role of oxidant speciation and water matrix. (15th September 2021)

• Record Type: Journal Article
• Authors: Seid, Mingizem Gashaw; Lee, Changha; Cho, Kangwoo; Hong, Seok Won
• Is Part Of: Water research. Volume 203(2021)
• Publication Date: 2021-09-15
• Subjects: N-nitrosodimethylamine formation potential -- Reactive radical species -- (Photo/electro)chemical oxidation -- Ranitidine chloramination -- Reverse osmosis; Water -- Pollution -- Research -- Periodicals; 363.7394
• DOI: 10.1016/j.watres.2021.117495
• Languages: English
• ISSNs: 0043-1354

Abstract

Highlights: l Roles of OH, Cl, SO4 −, and Fe(IV) were interrogated to reduce NDMA-FP. l Activated PDS showed a higher % RSE as compared to H2 O2 treatment. l Increasing pretreatment pH overall alleviated the reduction in NDMA-FP. l OH alone was ineffective and UV/H2 O2 even increased NDMA-FP of ranitidine. l e-Fenton and e-PDS were cost-effective method for RO brine treatment. Abstract: This study investigated the effects of thirteen (photo/electro) chemical oxidation processes on the formation potential (FP) of N -nitrosodimethylamine (NDMA) during the chloramination of ranitidine in reverse osmosis (RO) permeate and brine. The NDMA-FP varied significantly depending on the pretreatment process, initial pH, and water matrix types. At higher initial pH values (> 7.0), most pretreatments did not reduce the NDMA-FP, presumably because few radical species and more chloramine-reactive byproducts were generated. At pH < 7.0, however, electrochemical oxidation assisted by chloride and Fe 2+ /H2 O2, catalytic wet peroxide oxidation and peroxydisulfate-induced pretreatments removed up to 85% of NDMA-FP in the RO brine. Ultraviolet (UV) irradiation or prechlorination alone did not reduce the NDMA-FP effectively, but combined UV/chlorine treatment effectively reduced the NDMA-FP. In contrast, after UV irradiation (2.1 mW cm −2 for 0.5 h) in the presence of H2 O2 and chloramine, NDMA formation increased substantially (up to 26%) during the post-chloramination of the RO permeate. Mass spectrometric analysis and structural elucidation of the oxidation byproducts indicated that compared with the reactive nitrogen species generated by UV/NH2 Cl, sulfate radicals and (photo/electro)chemically generated reactive chlorine species were more promising for minimizing NDMA-FP. Unlike, the hemolytic OH driven by UV/H2 O2, the OH from Fe(IV)-assisted pretreatments showed a significant synergistic effect on NDMA-FP reduction. Overall, the results suggest the need for a careful assessment of the type of radical species to be used for treating an RO water system containing amine-functionalized compounds. Graphical abstract: Image, graphical abstract