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   <dc:title>Simple and fast methods based on solid-phase extraction coupled to liquid chromatography with UV detection for the monitoring of caffeine in natural and waste waters as marker of anthropogenic impact</dc:title>
   <dc:creator>Moret Solà, Sònia</dc:creator>
   <dc:creator>Hidalgo Muñoz, Manuela</dc:creator>
   <dc:creator>Sánchez Navarro, Juan Manuel</dc:creator>
   <dc:subject>Cafeïna</dc:subject>
   <dc:subject>Caffeine</dc:subject>
   <dc:subject>Aigua -- Contaminació</dc:subject>
   <dc:subject>Water pollution</dc:subject>
   <dc:subject>Cromatografia de líquids</dc:subject>
   <dc:subject>Liquid chromatography</dc:subject>
   <dc:subject>Aigües residuals -- Anàlisi</dc:subject>
   <dc:subject>Sewage -- Analysis</dc:subject>
   <dc:subject>Síntesi en fase sólida</dc:subject>
   <dc:subject>Solid-phase synthesis</dc:subject>
   <dc:description>Two concentration methods for fast and routine determination of caffeine (using HPLC-UV detection) in surface, and wastewater are evaluated. Both methods are based on solid-phase extraction (SPE) concentration with octadecyl silica sorbents. A common “offline” SPE procedure shows that quantitative recovery of caffeine is obtained with 2 mL of an elution mixture solvent methanol-water containing at least 60% methanol. The method detection limit is 0.1 μg L−1 when percolating 1 L samples through the cartridge. The development of an “online” SPE method based on a mini-SPE column, containing 100 mg of the same sorbent, directly connected to the HPLC system allows the method detection limit to be decreased to 10 ng L−1 with a sample volume of 100 mL. The “offline” SPE method is applied to the analysis of caffeine in wastewater samples, whereas the “on-line” method is used for analysis in natural waters from streams receiving significant water intakes from local wastewater treatment plants</dc:description>
   <dc:date>2012</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/10256/8411</dc:identifier>
   <dc:identifier>http://hdl.handle.net/10256/8411</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.5402/2012/487138</dc:relation>
   <dc:relation>info:eu-repo/semantics/altIdentifier/issn/2090-8636</dc:relation>
   <dc:rights>Attribution 3.0 Spain</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Hindawi Publishing Corporation</dc:publisher>
   <dc:source>ISRN Chromatography, 2012, vol. 2012, núm. ID 487138</dc:source>
   <dc:source>Articles publicats (D-Q)</dc:source>
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