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A novel digestion method based on a choline chloride-oxalic acid deep eutectic solvent for determining Cu, Fe, and Zn in fish samples

机译:基于氯化胆碱-草酸深共熔溶剂的新型消解方法测定鱼样品中的铜,铁和锌

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A novel and efficient digestion method based on choline chloride-oxalic acid (ChCl-Ox) deep eutectic solvent (DES) was developed for flame atomic absorption spectrometry (FAAS) determination of Cu, Zn, and Fe in biological fish samples. Key parameters that influence analyte recovery were investigated and optimized, using the fish protein certified reference material (CRM, DORM-3) throughout the procedure. In this method, 100 mg of the sample was dissolved in ChCl-Ox (1:2, molar ratio) at 100 °C for 45 min. Then, 5.0 mL HNO3 (1.0 M) was added. After centrifugation, the supernatant solution was filtered, diluted to a known volume, and analyzed by FAAS. Under optimized conditions, an excellent agreement between the obtained results and the certified values was observed, using Student's t-test (P=0.05); the extraction recovery of the all elements was greater than 95.3%. The proposed method was successfully applied to the determination of analytes in different tissues (muscle, liver, and gills) having a broad concentration range in a marine fish sample. The reproducibility of the method was validated by analyzing all samples by our method in a different laboratory, using inductively coupled plasma optical emission spectrometry (ICP-OES). For comparison, a conventional acid digestion (CAD) method was also used for the determination of analytes in all studied samples. The simplicity of the proposed experimental procedure, high extraction efficiency, short analysis time, lack of concentrated acids and oxidizing agents, and the use of safe and inexpensive components demonstrate the high potential of ChCl-Ox (1:2) for routine trace metal analysis in biological samples.
机译:建立了一种基于氯化胆碱-草酸(ChCl-Ox)深共熔溶剂(DES)的新型高效消解方法,用于火焰原子吸收光谱法(FAAS)测定生物鱼类样品中的铜,锌和铁。在整个过程中,使用鱼蛋白认证的参考材料(CRM,DORM-3)对影响分析物回收的关键参数进行了研究和优化。在此方法中,将100 mg的样品在100°C下溶解于ChCl-Ox(1:2,摩尔比)中45分钟。然后,加入5.0mL HNO 3(1.0M)。离心后,将上清液过滤,稀释至已知体积,并通过FAAS分析。在最佳条件下,使用Student's t检验观察到所得结果与认证值之间的极佳一致性(P = 0.05);所有元素的提取回收率均大于95.3%。所提出的方法已成功地用于测定海水鱼样品中浓度范围较广的不同组织(肌肉,肝脏和腮)中的分析物。该方法的重现性通过使用电感耦合等离子体发射光谱法(ICP-OES)在不同实验室中通过我们的方法分析所有样品而得到验证。为了进行比较,还使用常规的酸消解(CAD)方法确定所有研究样品中的分析物。拟议的实验程序简单,提取效率高,分析时间短,缺乏浓酸和氧化剂以及使用安全廉价的组分证明了ChCl-Ox(1:2)在常规痕量金属分析中的巨大潜力在生物样品中。

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