Preconcentration and spectrophotometric determination of low concentrations of malachite green and leuco-malachite green in water samples by high performance solid phase extraction using maghemite nanoparticles

被引:160
作者
Afkhami, Abbas [1 ]
Moosavi, Razieh [1 ]
Madrakian, Tayyebeh [1 ]
机构
[1] Bu Ali Sina Univ, Fac Chem, Hamadan, Iran
关键词
Malachite green; Leuco-malachite green; Spectrophotometric determination; Maghemite nanoparticles; Preconcentration; IRON-OXIDE NANOPARTICLES; LEUCOMALACHITE GREEN; LIQUID-CHROMATOGRAPHY; AQUEOUS-SOLUTIONS; WASTE-WATER; CRYSTAL VIOLET; ADSORPTION; FISH; REMOVAL; RESIDUES;
D O I
10.1016/j.talanta.2010.05.054
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
A novel and sensitive extraction procedure using maghemite nanoparticles (gamma-Fe2O3) modified with sodium dodecyl sulfate (SDS), as an efficient solid phase, was developed for removal. preconcentration and spectrophotometric determination of trace amounts of malachite green (MG) and leuco-malachite green (LMG). Combination of nanoparticle adsorption and easily magnetic separation was used to extraction and desorption of MG and LMG. The adsorption capacity was evaluated using both the Langmuir and Freundlich adsorption isotherm models. Maghemite nanoparticles were prepared by co-precipitation method and their surfaces were modified by SDS. The size and properties of the produced maghemite nanoparticles was determined by X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM) and BET analysis. MG and LMG became adsorbed at pH 3.0. LMG was oxidized to MG by adsorption on maghemite nanoparticles. The adsorbed MG was then desorbed and determined spectrophotometrically. The calibration graph was linear in the range 0.50-250.00 ng mL(-1) of MG and LMG with a correlation coefficient of 0.9991. The detection limit of the method for determination of MG was 0.28 ng mL(-1) and the relative standard deviation (R.S.D.) for 10.00 and 50.00 ng mL(-1) of malachite green was 1.60% (n = 3) and 0.86% (n = 5). respectively. A preconcentration factor of 50 was achieved in this method. The Langmuir adsorption capacity (q(max)) was found to be 227.3 mg g(-1) of the adsorbent. The method was applied to the determination of MG in fish farming water samples. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:785 / 789
页数:5
相关论文
共 52 条
[1]
Adsorptive removal of Congo red, a carcinogenic textile dye, from aqueous solutions by maghemite nanoparticles [J].
Afkhami, Abbas ;
Moosavi, Razieh .
JOURNAL OF HAZARDOUS MATERIALS, 2010, 174 (1-3) :398-403
[3]
Quantitative and confirmatory analyses of malachite green and leucomalachite green residues in fish and shrimp [J].
Andersen, WC ;
Turnipseed, SB ;
Roybal, JE .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (13) :4517-4523
[4]
[Anonymous], 2002, Off. J. Eur. Comm, VL221, P8
[5]
[Anonymous], 1996, Off. J. Eur. Commun, VL125, P10
[6]
Advantages of PARAFAC calibration in the determination of malachite green and its metabolite in fish by liquid chromatography-tandem mass spectrometry [J].
Arroyo, David ;
Ortiz, M. Cruz ;
Arabia, Luis A. S. ;
Palacios, Francisco .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1187 (1-2) :1-10
[7]
Determination and identification, according to European Union Decision 2002/657/EC, of malachite green and its metabolite in fish by liquid chromatography-tandem mass spectrometry using an optimized extraction procedure and three-way calibration [J].
Arroyo, David ;
Cruz Ortiz, M. ;
Sarabia, Luis A. ;
Palacios, Francisco .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (29) :5472-5482
[8]
Determination of residues of malachite green in aquatic animals [J].
Bergwerff, AA ;
Scherpenisse, P .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2003, 788 (02) :351-359
[9]
Sorption of malachite green by eucalyptus bark as a non-conventional low-cost biosorbent [J].
Boutemedjet, Sihem ;
Hamdaoui, Oualid .
DESALINATION AND WATER TREATMENT, 2009, 8 (1-3) :201-210
[10]
Protein separations using colloidal magnetic nanoparticles [J].
Bucak, S ;
Jones, DA ;
Laibinis, PE ;
Hatton, TA .
BIOTECHNOLOGY PROGRESS, 2003, 19 (02) :477-484