Preconcentration and separation of ultra-trace beryllium using quinalizarine-modified magnetic microparticles

被引:19
作者
Ashtari, Parviz [1 ,2 ]
Wang, Kemin [2 ]
Yang, Xiaohai [2 ]
Ahmadi, Seyed Javad [1 ]
机构
[1] Nucl Sci & Technol Res Inst, NFCS, Tehran, Iran
[2] Hunan Univ, Coll Chem & Chem Engn, Ctr Biomed Engn, State Key Lab Chemo Biosensing & Chemomet, Changsha 410082, Hunan, Peoples R China
关键词
Beryllium; Extraction; Magnetic microparticles; Quinalizarine; Separation; FLUORESCENCE METHOD; SOLVENT-EXTRACTION; WATER SAMPLES; PARTICLES; COPRECIPITATION; LANTHANIDES; ACTINIDES; RECOVERY; AIR;
D O I
10.1016/j.aca.2009.05.004
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Magnetically-assisted chemical separation/preconcentration method for the analysis of beryllium from aqueous solutions was developed. According to this method several extractants were coated on certain magnetic microparticles to assist the extraction of beryllium from the aqueous solutions. The influence of different parameters (type and amount of extractant, pH, equilibrium time and ionic strength) was investigated. Also, the interfering effect of various cationic and anionic species on the percent recovery of beryllium was studied. The applied spectro photo metric method showed good linearity and precision at a given wavelength (605.0 nm). Among the extractants used, quinalizarine resulted in almost a full recovery of beryllium at pH 7.4, which was the optimum extraction pH. The equilibrium time of the extraction was 10.0 min. The quantitative re-extraction was carried out by 0.5 M nitric acid. Also, the stability of the extractant-coated magnetic microparticles was 4 cycles (extraction and re-extraction) and the used magnetic microparticles showed good selectivity for beryllium against other cations and anions. Finally, the developed method was applicable for the preconcentration and separation of beryllium from spring water, tap water and certified reference waters. The obtained detection limit was 30 ng L-1. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 127
页数:5
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