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Capillary zone electrophoresis determination of fluoride in seawater using transient isotachophoresis.
Fukushi, Keiichi; Fujita, Yuki; Nonogaki, Junpei; Tsujimoto, Jun-Ichi; Hattori, Takanari; Inui, Hideyuki; Beskoski, Vladimir P; Hotta, Hiroki; Hayashi, Mitsuru; Nakano, Takeshi.
Afiliação
  • Fukushi K; Kobe University Biosignal Research Center, 1-1, Rokkodai-cho, Nada-ku, Kobe, Hyogo, 657-8501, Japan. ppkp13580@leto.eonet.ne.jp.
  • Fujita Y; Kobe University Faculty of Maritime Sciences, 5-1-1 Fukaeminami-machi, Higashinada-ku, Kobe, Hyogo, 658-0022, Japan.
  • Nonogaki J; Kobe University Faculty of Maritime Sciences, 5-1-1 Fukaeminami-machi, Higashinada-ku, Kobe, Hyogo, 658-0022, Japan.
  • Tsujimoto JI; Kiso Chemical Enterprises Ltd., 1 Maya-futo, Nada-ku, Kobe, Hyogo, 657-0854, Japan.
  • Hattori T; Kobe University Graduate School of Maritime Sciences, 5-1-1 Fukae-minamimachi, Higashinada-ku, Kobe, Hyogo, 658-0022, Japan.
  • Inui H; Kobe University Biosignal Research Center, 1-1, Rokkodai-cho, Nada-ku, Kobe, Hyogo, 657-8501, Japan. hinui@kobe-u.ac.jp.
  • Beskoski VP; University of Belgrade Faculty of Chemistry, Studentski trg 12-16, Belgrade, 11000, Serbia.
  • Hotta H; Kobe University Graduate School of Maritime Sciences, 5-1-1 Fukae-minamimachi, Higashinada-ku, Kobe, Hyogo, 658-0022, Japan.
  • Hayashi M; Kobe University Graduate School of Maritime Sciences, 5-1-1 Fukae-minamimachi, Higashinada-ku, Kobe, Hyogo, 658-0022, Japan.
  • Nakano T; Osaka University Research Center for Environmental Preservation, 2-4 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Anal Bioanal Chem ; 410(6): 1825-1831, 2018 Feb.
Article em En | MEDLINE | ID: mdl-29313081
We developed capillary zone electrophoresis (CZE) with indirect UV detection for the determination of fluoride (F-) in seawater using transient isotachophoresis (tITP) as an on-line concentration procedure. A method of correcting sample salinity effects was also proposed so that F- concentrations were obtained using a calibration graph. The proposed method is simple: it requires no sample pretreatment aside from dilution. The following optimum conditions were established: background electrolyte (BGE), 5 mM 2,6-pyridinedicarboxylic acid (PDC) adjusted to pH 3.5 containing 0.03% m/v hydroxypropyl methylcellulose (HPMC); detection wavelength, 200 nm; vacuum (50 kPa) injection period of sample, 5 s (254 nL); and applied voltage, 23 kV with the sample inlet side as the cathode. The limit of detection (LOD, S/N = 3) and limit of quantification (LOQ, S/N = 10) for F- reached 0.024 and 0.070 mg/L, respectively. The respective values of the relative standard deviation (RSD) of the peak area, peak height, and migration time for F- were 2.5, 3.4, and 0.30%. The proposed method was applied for the determination of F- in seawater samples collected from coastal waters of western Japan during August 26-28, 2014. Both results obtained using standard addition method and a calibration graph agreed with those obtained using a conventional spectrophotometric method.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Anal Bioanal Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Anal Bioanal Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão