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Square wave voltammetry for analytical determination of paraquat at carbon paste electrode modified with fluoroapatite

机译:方波伏安法测定氟磷灰石修饰的碳糊电极上的百草枯

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摘要

This paper describes the construction of a carbon paste electrode (CPE) impregnated with fluoroapatite (FAP). The new electrode (FAP-CPE) was revealed an interesting determination of paraquat. The latter was accumulated on the surface of the modified electrode by adsorbing onto fluoroapatite and reduced in 0.1 mol L~(-1) K_2SO_4 electrolyte at -0.70 and -1.0 V for peaks 1 and 2, respectively. Experimental conditions were optimized by varying the accumulation time, FAP loading and measuring solution pH. Under the optimized working conditions, calibration graphs were linear in the concentration ranging from 5 × 10~(-8) to 7 × 10~(-5)molL~(-1) with detection limits (DL,3σ) of 3.5 × 10~(-9)and 7.4 × 10~(-9)mol L~(-1) respectively, for peaks 1 and 2. Fluoroapatite was characterized by X-ray diffraction XRD analysis; Fourier-transform infrared spectros-copy FT-IR and inductively coupled plasma-atomic emission spectrometry (ICP-AES) analysis.
机译:本文介绍了用氟磷灰石(FAP)浸渍的碳糊电极(CPE)的构造。新的电极(FAP-CPE)被发现是百草枯的有趣测定方法。后者通过吸附到氟磷灰石上而积累在修饰电极的表面上,并分别在-0.70和-1.0 V的0.1 mol L〜(-1)K_2SO_4电解质中还原,用于峰1和2。通过改变累积时间,FAP上样量和溶液pH值来优化实验条件。在优化的工作条件下,校准曲线在5×10〜(-8)至7×10〜(-5)molL〜(-1)浓度范围内呈线性,检出限(DL,3σ)为3.5×10峰1和2分别为〜(-9)和7.4×10〜(-9)mol L〜(-1)。用X射线衍射XRD分析表征氟磷灰石。傅立叶变换红外光谱FT-IR和电感耦合等离子体原子发射光谱法(ICP-AES)分析。

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