Department of Chemistry, Payame Noor University, 19395-4697 Tehran, Iran.
Spectrochim Acta A Mol Biomol Spectrosc. 2011 Aug;79(3):603-7. doi: 10.1016/j.saa.2011.03.042. Epub 2011 Apr 9.
This paper describes the development of a new design of hollow fiber solid/liquid phase microextraction (HF-SLPME) for determination of brilliant green (BG) residues in water fish ponds. This method consists of an aqueous donor phase and carbon nanotube reinforced organic solvent (acceptor phase) operated in direct immersion sampling mode. The multi-walled carbon nanotube dispersed in the organic solvent is held in the pores and lumen of a porous polypropylene hollow fiber. It is in contact directly with the aqueous donor phase. In this method the solid/liquid extractor phase is supported using a polypropylene hollow fiber membrane. Both ends of the hollow fiber segment are sealed with magnetic stoppers. This device is placed inside the donor solution and plays the rule of a pseudo-stir bar. It is disposable, so single use of the fiber reduces the risk of carry-over problems. Brilliant green (BG) after extraction from the aqueous samples with mentioned HF-SLPME device was determined by ultraviolet-visible spectroscopy with diode array detection (UV-vis/DAD). The absorption wavelength was set to 625 nm (λ(max)). The effect of different variables on the extraction was evaluated and optimized to enhance the sensitivity and extraction efficiency of the proposed method. The calibration curve was linear in the range of 1.00-10,000 μg L(-1) of BG in the initial solution with R(2)=0.979. Detection limit, based on three times the standard deviation of the blank, was 0.55 μg L(-1). All experiments were carried out at room temperature (25±0.5°C).
本文介绍了一种新型中空纤维固/液萃取(HF-SLPME)的设计,用于测定水产养殖池塘水中的亮绿残留。该方法由水相和碳纳米管增强有机溶剂(有机相)组成,采用直接浸入式采样模式。多壁碳纳米管分散在有机溶剂中,保留在多孔聚丙烯中空纤维的孔隙和内腔中。它与水相直接接触。在该方法中,固/液萃取相采用聚丙烯中空纤维膜支撑。中空纤维段的两端用磁性塞密封。该装置置于供体溶液内,起到类似搅拌棒的作用。由于它是一次性使用的,因此单次使用纤维可降低交叉污染的风险。采用上述 HF-SLPME 装置从水样中萃取亮绿(BG)后,用紫外可见分光光度法结合二极管阵列检测(UV-vis/DAD)进行测定。吸收波长设定为 625nm(λ(max))。评估了不同变量对萃取的影响,并对其进行了优化,以提高所提出方法的灵敏度和萃取效率。在初始溶液中 BG 的浓度为 1.00-10,000μg/L 时,校准曲线呈线性,R(2)=0.979。基于空白三倍标准偏差的检测限为 0.55μg/L。所有实验均在室温(25±0.5°C)下进行。