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    <doi_batch_id>_1609491427</doi_batch_id>
    <timestamp>1609491427</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>30</day>
          <year>2020</year>
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        <journal_volume>
          <volume>3</volume>
        </journal_volume>
        <issue>04</issue>
        <doi_data>
          <doi>10.24200/amecj.v3.i04</doi>
          <resource>http://journal.amecj.com/index.php/AMECJ-01/issue/view/16</resource>
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        <titles>
          <title>Dispersive solid phase extraction using graphitic carbon nitride microparticles for the determination of trace amounts of lead in water 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>In this work, ultrasound-assisted dispersive micro-solid phase extraction (USA-D-µSPE) technique using graphitized carbon nitride (g-C3N4) is proposed for the preconcentration of low level of lead in aqueous samples. In this method, microparticles of graphitized carbon nitride sorbent were dispersed in the samples using ultrasonic bath and Pb(II) ions were directly adsorbed on the surface of g-C3N4 particles. After adsorption and desorption of lead ions from g-C3N4 particles, the Pb concentration was determined by the inductively coupled plasma- optical emission spectroscopy (ICP-OES). The main advantages of this method are high speed, simplicity and cheapness. The effects of pH, sorbent amount, eluent type and time on the recovery of the analyte were investigated. Under the optimized conditions and preconcentration of 10 mL of sample, the detection limit of 1.24 μg L-1 was obtained. The results were validated by standard reference materials (NIST, SRM) and spiking of real samples by USA-D-µSPE procedure. </jats:p>
        </jats:abstract>
        <publication_date media_type="online">
          <month>12</month>
          <day>30</day>
          <year>2020</year>
        </publication_date>
        <pages>
          <first_page>52</first_page>
          <last_page>59</last_page>
        </pages>
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          <ai:license_ref>http://creativecommons.org/licenses/by/4.0</ai:license_ref>
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          <doi>10.24200/amecj.v3.i04.118</doi>
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