Development of effervescence-assisted liquid phase microextraction based on fatty acid for determination of silver and cobalt ions using micro-sampling flame atomic absorption spectrometry

被引:57
作者
Moghadam, Ahmad Ghoochani [1 ]
Rajabi, Maryam [1 ]
Hemmati, Maryam [1 ]
Asghari, Alireza [1 ]
机构
[1] Semnan Univ, Dept Chem, Semnan 2333383193, Iran
关键词
Ag+ and Co2+ ions; Liquid-phase microextraction based on effervescence phenomenon; Micro-sampling flame atomic absorption spectrometry; Central composite design; Real samples; CLOUD POINT EXTRACTION; OPTICAL-EMISSION SPECTROMETRY; RESPONSE-SURFACE METHODOLOGY; WATER SAMPLES; ENVIRONMENTAL-SAMPLES; BIOLOGICAL MATRICES; SWITCHABLE SOLVENT; TRACE AMOUNTS; HUMAN URINE; PRECONCENTRATION;
D O I
10.1016/j.molliq.2017.07.038
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, coupling of effervescence-assisted dispersive liquid-liquid microextraction based on a medium chain fatty acid(EA-DLLME-FA) with accurate micro-sampling flame atomic absorption spectrometric (MSFAAS) analysis was developed for the first time as a swift, facile, and effective analytical procedure for the satisfactory analysis of Ag+ and Co2+ ions from different real samples. During the microextraction process, 1-phenyl-1,2-propanedione-2-oximethiosemicarbazone (PPDOT) was used as a proper chelating agent to form hydrophobic complex compounds, causing easy and effective penetration of metal ions into the organic extraction phase. On the other hand, by providing proper pH values via addition of an efficacious effervescent agent, the extraction medium could acquire a dual hydrophilicity/hydrophobicity nature, leading to a simple and efficient proceeding of the foresaid microextraction, followed by a quick and no labor intensive collection of the organic solvent (upper phase) in a special home-made extraction cell. Also simple, rapid, accurate, efficient, and inexpensive analyses via the MS-FAAS technique distinguished the determination of the foresaid metal ions. Under other optimum conditions enriched via the central composite design, the studied ions could be accurately determined in the wide linear dynamic ranges of 5.0-150 ng mL(-1) and 8.0-200 ng mL(-1) for the Ag+ and Co2+ ions, respectively, with the determination coefficients (R(2)s) higher than 0.98. The low limits of detection and the good percentage relative standard deviations were found to be in the span of 2.0-3.0 ng mL(-1) and 3.4-4.2%, respectively. The percentage extraction recoveries and the enrichment factors were found to be reasonably quantitative. These valuable results indicated the high quality of the developed procedure for the influential quantification of the aforementioned metal ions from cow milk, vitamin B12, orange juice, and tap water. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1176 / 1183
页数:8
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