Multivariate optimization of differential pulse polarographic-catalytic hydrogen wave technique for the determination of nickel(II) in real samples

被引:9
作者
Kanchi, S. [1 ]
Sabela, M. I. [1 ]
Singh, P. [1 ]
Bisetty, K. [1 ]
机构
[1] Durban Univ Technol, Dept Chem, POB 1334, ZA-4000 Durban, South Africa
基金
新加坡国家研究基金会;
关键词
Differential pulse polarographic catalytic hydrogen wave (DPP-CHW); Nickel(II); Box-Behnken design; Ammonium piperidine dithiocarbamates (APDC) and Ammonium morpholine dithiocarbamate (AMDC); Cyclic voltammetry; Density Functional Theory (DFT); CATHODIC STRIPPING VOLTAMMETRY; ATOMIC-ABSORPTION-SPECTROMETRY; SOLID-PHASE EXTRACTION; CLOUD POINT EXTRACTION; SPECTROPHOTOMETRIC DETERMINATION; SIMULTANEOUS PRECONCENTRATION; NATURAL-WATERS; TRACE NICKEL; COBALT; COPPER(II);
D O I
10.1016/j.arabjc.2013.07.061
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multivariate optimized experimental conditions were established for the determination of nickel(II) in 92 grape samples after complexation with ammonium piperidine dithiocarbamate (APDC) and ammonium morpholine dithiocarbamate (AMDC). Differential pulse polarographic (DPP) studies of the wave characteristics indicated that it is of the catalytic hydrogen wave (CHW) type sensitive to pH, concentration and scan rates. A single, sharp peak obtained at -1.22 V allowed for the trace determination of nickel(II) in the range of 3.2 x 10(-6) to 1.17 x 10(-3) M with a linear calibration and a detection limit of 1.8 x 10(-6) and 2.7 x 10(-6) M for APDC and AMDC respectively. Mechanistic aspects between APDC/AMDC and nickel(II) were confirmed with cyclic voltammetry and supported by theoretical calculations. The DFT calculations of piperidine adduct reveal a smaller HOMO-LUMO energy gap than morpholine adduct, suggesting that piperidine adduct has a greater tendency to act as an electron donor. (c) 2013 Production and hosting by Elsevier B.V.
引用
收藏
页码:S2260 / S2272
页数:13
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