1 Ocak 2013 Dergi makalesi Açık Erişim

Uslu, Musa; Uluturk, Hakan; Yartasi, Ahmet; Doker, Serhat

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{
  "@context": "https://schema.org/", 
  "@id": 12533, 
  "@type": "ScholarlyArticle", 
  "creator": [
    {
      "@type": "Person", 
      "affiliation": "Cankiri Karatekin Univ, Fac Sci, Dept Chem, Cankiri, Turkey", 
      "name": "Uslu, Musa"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Cankiri Karatekin Univ, Fac Sci, Dept Chem, Cankiri, Turkey", 
      "name": "Uluturk, Hakan"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Cankiri Karatekin Univ, Fac Engn, Dept Chem Engn, Cankiri, Turkey", 
      "name": "Yartasi, Ahmet"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Cankiri Karatekin Univ, Fac Sci, Dept Chem, Cankiri, Turkey", 
      "name": "Doker, Serhat"
    }
  ], 
  "datePublished": "2013-01-01", 
  "description": "A simple, fast, and low-cost analytical procedure was developed for trace-level determination of inorganic vanadium species by dispersive liquid-liquid microextraction in combination with spectrophotometry. Vanadium in pentavalent form, V(V), was quantitatively extracted into organic phase as 4-(2-pyridylazo)-recorcinol (PAR) complex in the presence of N-cetyl-N,N,N-trimethyl ammonium bromide (CTAB) as counter-ion. Vanadium (IV) was masked with 1,2-diaminocyclohexanetetraacetic acid to allow speciation analysis. Total vanadium was determined after oxidation of V(IV) to V(V). The main factors affecting preconcentration and spectrophotometric detection of vanadium species such as pH, concentration of PAR and CTAB, the type and volume of the extraction, and disperser solvents were optimized. The limit of detection and enhancement factor obtained under optimum conditions were found to be 0.06g L-1 and 98, respectively. Relative standard deviations for V(IV) and V(V) at 3.0g L-1 were less than 2.4%. The presented procedure was applied to environmental water samples for selective determination of vanadium species. Moreover, the method was applied to determination of vanadium in edible salt samples, due to its applicability in high-NaCl-containing solutions. The validity of proposed method was proven by spike recovery experiments and also independent analysis by inductively coupled plasma mass spectrometry.", 
  "headline": "A sensitive method for selective determination of vanadium species by dispersive liquid- liquid microextraction ( DLLME) with spectrophotometric detection", 
  "identifier": 12533, 
  "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", 
  "license": "http://www.opendefinition.org/licenses/cc-by", 
  "name": "A sensitive method for selective determination of vanadium species by dispersive liquid- liquid microextraction ( DLLME) with spectrophotometric detection", 
  "url": "https://aperta.ulakbim.gov.tr/record/12533"
}