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Vortex-assisted liquid–liquid microextraction and indirect spectrophotometric determination of chromium(vi)

机译:涡流辅助液-液微萃取和间接分光光度法测定铬(vi)

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A novel, simple, sensitive and selective method for the indirect spectrophotometric determination of chromium( VI ) was developed on the basis of vortex-assisted liquid–liquid microextraction (VALLME) of an ion association pair formed between the triiodide anion (I _(3) ~(?) ) and cationic dye Astrazone Brilliant Red 4G (ABR). The indirect spectrophotometric determination of chromium( VI ) was based on the redox-reaction of Cr( VI ) with iodide and formed I _(3) ~(?) . The triiodide anion was determined spectrophotometrically at 530 nm following VALLME of an ion association pair with ABR. The calibration plot was linear in the range 0.050–4.2 μg L ~(?1) ( R ~(2) = 0.998), and limit of detection (LOD) was 0.015 μg L ~(?1) for Cr( VI ). The suggested procedure was successfully applied for the determination Cr( VI ) in water samples (RSD 3.3–5.7%, recovery 97.7–102.8% when determining ultratrace levels Cr( VI ) at 0.55–5.77 μg L ~(?1) ), the accuracy of the method was assessed through a comparison with reference methods and certified reference materials.
机译:基于三碘化物阴离子之间形成的离子缔合对的涡旋液-液微萃取(VALLME),开发了一种间接分光光度法测定铬(VI)的新颖,简单,灵敏,选择性的方法。 )和阳离子染料Astrazone亮红色4G(ABR)。铬(VI)的间接分光光度法是基于铬(VI)与碘的氧化还原反应而形成的I_(3)〜(?)。在离子缔合对与ABR进行VALLME之后,在530 nm处用分光光度法测定了三碘化物阴离子。校准曲线在0.050–4.2μgL〜(?1)范围内呈线性(R〜(2)= 0.998),Cr(VI)的检出限(LOD)为0.015μgL〜(?1)。所建议的方法已成功用于水样品中的Cr(VI)测定(RSD为3.3-5.7%,当测定0.55-5.77μgL〜(?1)时的痕量Cr(VI)时,回收率为97.7-102.8%)。通过与参考方法和经认证的参考材料进行比较来评估方法的准确性。

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