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    Formation of halogenated disinfection by-products during microfiltration and reverse osmosis treatment: implications for water recycling

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    Access Status
    Open access
    Authors
    Linge, Kathryn
    Blythe, J.
    Busetti, Francesco
    Blair, P.
    Rodriguez, C.
    Heitz, Anna
    Date
    2013
    Type
    Journal Article
    
    Metadata
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    Citation
    Linge, Kathryn L. and Blythe, Justin W. and Busetti, Francesco and Blair, Palenque and Rodriguez, Clemencia and Heitz, Anna. 2013. Formation of halogenated disinfection by-products during microfiltration and reverse osmosis treatment: implications for water recycling. Separation and Purification Technology 104: pp. 221-228.
    Source Title
    Separation and Purification Technology
    DOI
    10.1016/j.seppur.2012.11.031
    ISSN
    13835866
    Remarks

    NOTICE: this is the author’s version of a work that was accepted for publication in Separation and Purification Technology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Separation and Purification Technology, 104 (2013) 221- 228 http://dx.doi.org/10.1016/j.seppur.2012.11.031

    URI
    http://hdl.handle.net/20.500.11937/29338
    Collection
    • Curtin Research Publications
    Abstract

    A suite of 34 disinfection by-products (DBPs), including eight halomethanes, nine haloacetic acids, six haloacetonitriles, six haloaldehydes, four haloketones and the halonitromethane chloropicrin, were monitored in two microfiltration (MF) and reverse osmosis (RO) treatment plants as part of a larger study of chemical removal by MF/RO treatment for water recycling purposes. Both DBP detection frequency and concentration increased during treatment, and this was attributed to a chloramination step used to minimize RO membrane fouling. The degree of DBP formation was particularly related to plant residence time, with DBPs falling into two distinct groups; the first group in which DBP concentration increased with increasing residence time (e.g. chloroform and bromochloroacetaldehyde) and a second group in which increased residence time did not affect the concentration (e.g. dichloroacetic acid and 1,1-dichloropropanone). These results indicate that MF/RO plant design and wastewater quality are both important factors in minimizing DBP formation within MF/RO treatment. RO rejection was influenced by several chemical-specific properties, including pKa, log Kow and DBP class. Rejection of haloacetic acids, present as charged molecules, was consistently better than 90% and did not alter with log Kow. For all other DBPs, present as neutral molecules, rejection was much more variable, and decreased with decreasing log Kow, although the effect of MW and log Kow on rejection could not be separated. The DBP formation described in this study lead to variable estimations of DBP removal by RO and thus it is recommended that DBPs are used as indicators of RO removal efficiency with caution, and only after DBP formation within RO treatment has been studied.

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