<?xml version="1.0" encoding="UTF-8"?><marc:collection xmlns:marc="http://www.loc.gov/MARC21/slim">
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    <marc:controlfield tag="003">CaOODSP</marc:controlfield>
    <marc:controlfield tag="005">20241203113649</marc:controlfield>
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    <marc:controlfield tag="008">190531s1990    onca   #ob   f000 0 eng d</marc:controlfield>
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      <marc:subfield code="a">eng</marc:subfield>
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      <marc:subfield code="a">Baxter, R. M., </marc:subfield>
      <marc:subfield code="e">author.</marc:subfield>
    </marc:datafield>
    <marc:datafield tag="245" ind1="1" ind2="0">
      <marc:subfield code="a">Reductive dechlorination of certain chlorinated organic compounds by reduced hematin compared with their behaviour in the environment / </marc:subfield>
      <marc:subfield code="c">R.M. Baxter.</marc:subfield>
    </marc:datafield>
    <marc:datafield tag="264" ind1=" " ind2="1">
      <marc:subfield code="a">Burlington, Ontario : </marc:subfield>
      <marc:subfield code="b">Environment Canada, National Water Research Institute = Environnement Canada, Institut national de recherche sur les eaux, </marc:subfield>
      <marc:subfield code="c">[1990]</marc:subfield>
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      <marc:subfield code="a">computer</marc:subfield>
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      <marc:subfield code="a">online resource</marc:subfield>
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      <marc:subfield code="a">NWRI contribution ; </marc:subfield>
      <marc:subfield code="v">90-27</marc:subfield>
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      <marc:subfield code="a">Title from cover.</marc:subfield>
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      <marc:subfield code="a">Digitized edition from print [produced by Environment and Climate Change Canada].</marc:subfield>
    </marc:datafield>
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      <marc:subfield code="a">Includes bibliographical references.</marc:subfield>
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      <marc:subfield code="a">"A number of chlorinated organic compounds of environmental concern were tested for their ability to react with reduced hematin. Within any class of substances the reactivity correlated fairly well with environmental persistence. DDT and DDD reacted but DDE did not. The least persistent BHC isomer, lindane, was the most reactive. Aldrin and heptachlor, which are less persistent than their epoxides, proved more reactive. Chlordene was detected as a dechlorination product of heptachlor. Mirex proved to be an exception, being fairly reactive in spite of its great persistence. Two dechlorination products were detected, representing the loss of one and two chlorine atoms, respectively. Hexachlorobutadiene reacted slowly, and octachlorostyrene reacted very slowly, yielding heptachlorostyrene. Purely aromatic compounds did not react"--Abstract.</marc:subfield>
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      <marc:subfield code="a">Includes abstract and management perspective in English and French.</marc:subfield>
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      <marc:subfield code="2">gccst</marc:subfield>
      <marc:subfield code="a">Pollutants</marc:subfield>
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      <marc:subfield code="a">Heme</marc:subfield>
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      <marc:subfield code="a">Organic compounds</marc:subfield>
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      <marc:subfield code="a">Canada. </marc:subfield>
      <marc:subfield code="b">Environment Canada.</marc:subfield>
    </marc:datafield>
    <marc:datafield tag="710" ind1="2" ind2=" ">
      <marc:subfield code="a">National Water Research Institute (Canada)</marc:subfield>
    </marc:datafield>
    <marc:datafield tag="830" ind1="#" ind2="0">
      <marc:subfield code="a">NWRI contribution ;</marc:subfield>
      <marc:subfield code="v">90-27.</marc:subfield>
      <marc:subfield code="w">(CaOODSP)9.844121</marc:subfield>
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    <marc:datafield tag="856" ind1="4" ind2="0">
      <marc:subfield code="q">PDF</marc:subfield>
      <marc:subfield code="s">1.40 MB</marc:subfield>
      <marc:subfield code="u">https://publications.gc.ca/collections/collection_2019/eccc/en13-5/En13-5-90-27-eng.pdf</marc:subfield>
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