Abstract
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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This work was in part supported by a Grant-in-Aid for Challenging Exploratory Research [grant number 25550064] from the Japan Society for the Promotion of Science for H. I.
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Fukushi, K., Fujita, Y., Nonogaki, J. et al. Capillary zone electrophoresis determination of fluoride in seawater using transient isotachophoresis. Anal Bioanal Chem 410, 1825–1831 (2018). https://doi.org/10.1007/s00216-017-0838-0
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DOI: https://doi.org/10.1007/s00216-017-0838-0