Adsorbable organic halogen (AOX) is a bulk organic parameter conventionally used to indicate all adsorbable halogenated organic disinfection byproducts formed in disinfected water. Analytically, AOX is determined by three sequential steps: 1) concentration and separation of AOX from halides with activated carbon, 2) conversion of AOX into halides with pyrolysis, and 3) quantification of halides via microcoulometry or ion chromatography (IC). Because the approach is relatively costly and cannot effectively recover non-adsorbable compounds, we herein proposed a facile and green pretreatment tool to measure the nonionic portion of total organic halogen (NTOX) with a new three-step approach: 1) separation of NTOX and halides with electrodialysis (ED), 2) conversion of NTOX into halides with ultraviolet, and 3) analysis of halides with IC. To verify this proposal, this study presented the efficiency of ED in separating halides and NTOX under a variety of operational and environmental conditions. The results showed that ED removed ≥98.5% of fluoride, chloride, bromide, and iodide from all tested waters (up to 1000 mg-X/L) within 1.5 h. Meanwhile, ED recovered an average of 87.9% of fourteen small molecular weight model compounds with each at 100 μg/L. By using electrospray ionization-triple quadrupole mass spectrometry, the whole pictures of high molecular weight compounds in a chlorinated drinking water before and after ED pretreatment were compared, which revealed 79.7% and 83.6% recoveries of overall polar chlorinated and brominated compounds, respectively. In addition, the quantity and property of the dissolved organic matter were largely maintained by ED, and the retained organics may be used for later characterization. The study hence presents a novel use of ED as a pretreatment tool to enable subsequent NTOX measurement.

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http://dx.doi.org/10.1016/j.watres.2018.08.065DOI Listing

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