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    <doi_batch_id>_1603473520</doi_batch_id>
    <timestamp>1603473520</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>09</month>
          <day>30</day>
          <year>2020</year>
        </publication_date>
        <journal_volume>
          <volume>3</volume>
        </journal_volume>
        <issue>03</issue>
        <doi_data>
          <doi>10.24200/amecj.v3.i03</doi>
          <resource>http://journal.amecj.com/index.php/AMECJ-01/issue/view/15</resource>
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          <title>Dispersive liquid–liquid microextraction technique combined with UV–Vis spectrophotometry for determination of zirconium in aqueous samples</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>Dispersive liquid–liquid microextraction coupled with UV–Vis spectrophotometry was applied for the determination of zirconium in aqueous samples. In this method a small amount of chloroform as the extraction solvent was dissolved in pure ethanol as the disperser solvent, then the binary solution was rapidly injected by a syringe into the water sample solution containing Zr(IV), xylenol orange and cetyltrimethylammonium bromide. The formed ion-associate was extracted into the fine chloroform droplets. The detection limit for Zr(IV) was 0.010 µg mL−1. The precision of the method, evaluated as the relative standard deviation obtained by analyzing of 10 replicates, was 2.7 %. The practical applicability of the developed method was examined using natural waters and ceramic samples.</jats:p>
        </jats:abstract>
        <publication_date media_type="online">
          <month>09</month>
          <day>27</day>
          <year>2020</year>
        </publication_date>
        <pages>
          <first_page>18</first_page>
          <last_page>24</last_page>
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          <doi>10.24200/amecj.v3.i03.107</doi>
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