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      <dc:title>Cold vapour generation electrothermal atomic absorption spectrometry and solid phase extraction based on a new nanosorbent for sensitive HG determination in environmental samples (sea water and river water)</dc:title>
      <dc:creator>Vereda-Alonso, Elisa Isabel</dc:creator>
      <dc:creator>Siles-Cordero, María Teresa</dc:creator>
      <dc:creator>López-Guerrero, María del Mar</dc:creator>
      <dc:creator>García-de-Torres, Amparo</dc:creator>
      <dc:creator>Cano-Pavón, José Manuel</dc:creator>
      <dc:subject>Mercurio</dc:subject>
      <dc:description>Reunión bianual del Grupo Regional Andaluz de la Sociedad Española de Química Analítica</dc:description>
      <dc:description>Mercury is not an essential element for plant or animal life and it is a potential&#xd;
environmental toxic because of its tendency to form covalent bonds with organic&#xd;
molecules and the high stability of the Hg-C bond. Reports estimate a total mercury&#xd;
concentration in natural waters ranging from 0.2 to 100 ng L-1. Due to this fact, highly&#xd;
sensitive methods are required for direct determination of such extremely low levels. In&#xd;
this work, a rapid and simple method was developed for separation and preconcentration&#xd;
of mercury by flow injection solid phase extraction coupled with on-line&#xd;
chemical vapour generation electrothermal atomic absorption spectrometry. The&#xd;
system is based on chelating retention of the analyte onto the mini column filled with a&#xd;
mesoporous silica functionalized with 1,5 bis (di-2-pyridyl) methylene&#xd;
thiocarbohydrazide. The main aim of this work was to develop a precise and accurate&#xd;
method for the determination of the Hg. Under the optima conditions and 120 s&#xd;
preconcentration time, the detection limit obtained was 0.009 μg L-1, with RSDs 3.7 %&#xd;
for 0.2 μg L-1, 4.8 % for 1 μg L-1 and enrichment factor 4, Furthermore, the method&#xd;
proposed has permitted the determination of Hg with a reduction in the analysis time,&#xd;
the sample throughput was about 18 h-1, low consumption of reagents and sample&#xd;
volume.&#xd;
The method was applied to the determination of Hg in sea water and river water. For&#xd;
the quality control of the analytical performance and the validation of the newly&#xd;
developed method, the analysis of two certified samples, TMDA 54.4 Fortified Lake,&#xd;
and LGC6187 River sediment was addressed. The results showed good agreement&#xd;
with the certified values.</dc:description>
      <dc:date>2016-07-07T11:35:53Z</dc:date>
      <dc:date>2016-07-07T11:35:53Z</dc:date>
      <dc:date>2016</dc:date>
      <dc:date>2016-07-07</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>http://hdl.handle.net/10630/11771</dc:identifier>
      <dc:identifier>http://orcid.org/0000-0001-9502-4424</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>XV Reunión GRASEQA</dc:relation>
      <dc:relation>Almería (España)</dc:relation>
      <dc:relation>30/06/2016</dc:relation>
      <dc:rights>open access</dc:rights>
      <dc:rights>by-nc-nd</dc:rights>
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