首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Application of derivative and derivative ratio spectrophotometry to simultaneous trace determination of rhodamine B and rhodamine 6G after dispersive liquid-liquid microextraction
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Application of derivative and derivative ratio spectrophotometry to simultaneous trace determination of rhodamine B and rhodamine 6G after dispersive liquid-liquid microextraction

机译:导数和导数比分光光度法在分散液液微萃取后同时测定若丹明B和若丹明6G中的应用

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摘要

Two novel methods, first derivative spectrophotometric method (~1D) and first derivative ratio spectrophotometric method (~1DR), have been developed for the simultaneous trace determination of rhodamine B (RhB) and rhodamine 6G (Rh6G) in food samples after dispersive liquid-liquid microextraction (DLLME). The combination of derivative spectrophotometric techniques and DLLME procedure endows the presented methods with enhanced sensitivity and selectivity. Under optimum conditions, the linear calibration curves ranged from 5 to 450 ng mL~(-1), with the correlation coefficients (r) of 0.9997 for RhB and 0.9977 for Rh6G by ~1D method, and 0.9987 for RhB and 0.9958 for Rh6G by ~1DR method, respectively. The calculated limits of detection (LODs) based on the variability of the blank solutions (S/N = 3 criterion) for 11 measurements were in the range of 0.48-1.93 ng mL~(-1). The recoveries ranged from 88.1% to 111.6% (with RSD less than 4.4%) and 91.5-110.5% (with RSD less than 4.7%) for ~1D and ~1DR method, respectively. The influence of interfering substances such as foreign ions and food colorants which might be present in the food samples on the signals of RhB and Rh6G was examined. The developed methods have been successfully applied to the determination of RhB and Rh6G in black tea, red wine and chilli powder samples with the characteristics of simplicity, cost-effectiveness, environmental friendliness, and could be valuable for routine analysis.
机译:已经开发了两种新颖的方法,即一阶导数分光光度法(〜1D)和一阶导数比分光光度法(〜1DR),用于同时测定分散液中食品中的若丹明B(RhB)和若丹明6G(Rh6G)的痕量。液体微萃取(DLLME)。衍生的分光光度法技术与DLLME程序相结合,使所提出的方法具有更高的灵敏度和选择性。在最佳条件下,线性校准曲线的范围为5至450 ng mL〜(-1),〜1D方法的RhB相关系数(r)为0.9997,Rh6G为0.9977,RhB的相关系数(r)为0.9987,Rh6G为0.9958 〜1DR方法。根据空白溶液的变异性(S / N = 3标准)计算的11次测量的检测极限(LOD)在0.48-1.93 ng mL〜(-1)范围内。 〜1D和〜1DR方法的回收率分别为88.1%至111.6%(RSD小于4.4%)和91.5-110.5%(RSD小于4.7%)。检查了食物样品中可能存在的干扰物质(例如外来离子和食物色素)对RhB和Rh6G信号的影响。所开发的方法已经成功应用于红茶,红酒和辣椒粉样品中RhB和Rh6G的测定,具有操作简便,成本效益高,环境友好的特点,对常规分析具有重要的参考价值。

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