Sensitive Voltammetric Determination of Titanium(IV) in Catalytic Adsorptive Mandelic Acid-Chlorate(V) System on Renewable Silver Amalgam Film Electrode

被引:6
作者
Piech, Robert [1 ]
机构
[1] AGH Univ Sci & Technol, Fac Mat Sci & Ceram, PL-30059 Krakow, Poland
关键词
Catalytic adsorptive stripping voltammetry; Renewable mercury film electrode; Ti-mandelic acid-chlorate(V) system; Titanium(IV) trace analysis; PERFORMANCE LIQUID-CHROMATOGRAPHY; CURRENT STRIPPING POTENTIOMETRY; VIOLET RS COMPLEXES; TRACE TITANIUM; PLASMA; WATER; PRECONCENTRATION; ACCUMULATION; SPECTROMETRY; IRON(III);
D O I
10.1002/elan.201200350
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The renewable mercury film electrode, applied for the determination of titanium(IV) ultratraces using differential pulse catalytic adsorptive cathodic stripping voltammetry (DP CAdSV) in the presence of mandelic acid as a ligand and chlorate(V) as an oxidant is represented. The calibration graph obtained for Ti(IV) is linear from 0.05nM (2.39ngL1) to 95nM (4.55 mu gL1) for a preconcentration time of 30s, with correlation coefficient of 0.9995. For the renewable mercury electrode (Hg(Ag)FE) with a surface area of 8.6mm2 the detection limit for a preconcentration time of 180s is as low as 0.006nM (0.29ngL1). The repeatability of the method at a concentration level of the analyte as low as 23.9ngL1, expressed as RSD is 1.8% (n=5). The proposed method was successfully applied and validated by studying the certified reference material NWTM-26.3 and simultaneously recovery of Ti(IV) from spiked samples.
引用
收藏
页码:716 / 722
页数:7
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