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    <doi_batch_id>_1591959923</doi_batch_id>
    <timestamp>1591959923</timestamp>
    <depositor>
      <depositor_name>Hamid Shirkhanloo</depositor_name>
      <email_address>sahar.zi67@gmail.com</email_address>
    </depositor>
    <registrant>Hamid Shirkhanloo</registrant>
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    <journal>
      <journal_metadata>
        <full_title>Analytical Methods in Environmental Chemistry Journal</full_title>
        <abbrev_title>AMECJournal</abbrev_title>
        <issn media_type="electronic">2645-5382</issn>
        <issn media_type="print">2645-5552</issn>
      </journal_metadata>
      <journal_issue>
        <publication_date media_type="online">
          <month>12</month>
          <day>01</day>
          <year>2018</year>
        </publication_date>
        <journal_volume>
          <volume>1</volume>
        </journal_volume>
        <issue>01</issue>
      </journal_issue>
      <journal_article xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1" publication_type="full_text" metadata_distribution_opts="any">
        <titles>
          <title>Solid phase extraction and determination of indium using multiwalled carbon nanotubes modified with magnetic nanoparticles</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first">
            <given_name>Ehsan</given_name>
            <surname>Zolfonoun</surname>
          </person_name>
        </contributors>
        <jats:abstract xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1">
          <jats:p>In this work MWCNTs-Fe3O4 nanocomposite was used as an adsorbent for extraction and preconcentration of indium from aqueous solutions. The magnetic MWCNTs with adsorbed analytes were easily separated from the aqueous solution by applying an external magnetic field. After elution of the adsorbed analytes, the concentration of indium was determined using inductively coupled plasma optical emission spectrometry determination. The effects of pH, sorbent amount, eluent type, chelating reagent concentration, sample volume and time on the recovery of the In(III) were investigated. Under the optimum conditions, the detection limit for In(III) was 0.28 μg L−1. The precision of the method, evaluated as the relative standard deviation obtained by analyzing a series of ten replicates, was 3.1 %. The method was successfully applied for the determination of In(III) in environmental water samples.</jats:p>
        </jats:abstract>
        <publication_date media_type="online">
          <month>12</month>
          <day>31</day>
          <year>2018</year>
        </publication_date>
        <pages>
          <first_page>5</first_page>
          <last_page>10</last_page>
        </pages>
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          <doi>10.24200/amecj.v1.i01.14</doi>
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