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Ultrasound-assisted cloud point extraction of manganese, zinc and tin from digested food samples for their determination by FAAS

机译:超声辅助消化点样中锰,锌和锡的浊点萃取,用FAAS测定

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The current study is focused on the determination of the trace levels of manganese, zinc and tin in wet acid digested foods by flame atomic absorption spectrometry (FAAS) after preconcentration with ultrasound assisted-cloud point extraction (UA-CPE). The preconcentration procedure is making use of 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one (Quercetin) as the chelating agent, the cationic surfactant cetyltrimethylammonium bromide (CTAB) as the counter ion, the non-ionic surfactant polyoxyethylenesorbitan monolaurate (Tween 20) as the extracting agent, and acidic methanol as the diluting agent. The significant analytical parameters were optimized, and the selected values were a pH of 4.0, a chelating agent concentration of 8.5 mu mol L-1, cationic and nonionic surfactant concentrations of 30 mu mol L-1 and 0.5% w/v, a sample volume of 10 mL, an equilibrium temperature of 60 degrees C, an incubation time of 15 min and a diluting agent amount of 1.25 mL. Under optimum conditions, the detection limits for manganese, zinc and tin were 0.34, 0.15 and 0.7 mu g L-1 with sensitivity enhancement factors of 116, 175 and 153, respectively. The precision was evaluated as relative standard deviations (RSDs%) for solution containing 15 mu g L-1 of Mn(II), 40 mu g L-1 of Zn(II), and 20 mu g L-1 of Sn(II), and was found to be 2.3, 2.0 and 2.5% (n: 5), respectively. The accuracy of the method was evaluated by analysis of standard reference materials (SRMs) and through recovery rates from spiked aqueous samples. The obtained results were statistically in good agreement with the certified values at the 95% confidence limit, in which the recoveries for target analytes varied in the range of 95.6-104.2%. The method was successfully applied to the analysis of manganese, zinc and tin contents of various food samples, which are generally of plant origin, including black and green tea after dry ashing and wet digestion steps.
机译:当前的研究重点是在超声辅助浊点萃取(UA-CPE)预浓缩后,通过火焰原子吸收光谱法(FAAS)测定湿酸消化食品中的痕量锰,锌和锡。预浓缩步骤是使用2-(3,4-二羟基苯基)-3,5,7-三羟基-4H-铬-4-酮(槲皮素)作为螯合剂,阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)作为螯合剂。在抗衡离子中,非离子表面活性剂聚氧乙烯脱水山梨糖醇单月桂酸酯(吐温20)作为萃取剂,酸性甲醇作为稀释剂。优化了重要的分析参数,选择的值为pH 4.0,螯合剂浓度为8.5μmolL-1,阳离子和非离子表面活性剂浓度为30μmolL-1和0.5%w / v(样品)体积为10毫升,平衡温度为60摄氏度,孵育时间为15分钟,稀释剂的量为1.25毫升。在最佳条件下,锰,锌和锡的检出限分别为0.34、0.15和0.7微克L-1,灵敏度增强因子分别为116、175和153。对于包含15μg L-1的Mn(II),40μgL-1的Zn(II)和20μgL-1的Sn(II)的溶液,以相对标准偏差(RSDs%)评估精度。 ),分别为2.3%,2.0%和2.5%(n:5)。通过分析标准参考物质(SRM)以及通过加标含水样品的回收率来评估该方法的准确性。在95%的置信度下,所获得的结果与标准值在统计学上高度吻合,其中目标分析物的回收率在95.6-104.2%的范围内变化。该方法成功地用于分析各种食品样品中的锰,锌和锡含量,这些食品通常是植物来源的,包括干灰化和湿消化步骤后的红茶和绿茶。

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