SPECTROPHOTOMETRIC DETERMINATION OF COPPER (II) AFTER DISPERSIVE LIQUID-LIQUID EXTRACTION OF ITS COMPLEX WITH 6,7-DIHYDROXY-4-METHYL-2-PHENYLBENZOPYRYLIUM CHLORIDE

D. Snigur
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Abstract

The specificity of the dispersive liquid-liquid semi-microextraction of Copper (II) complex with 6,7-dihydroxy-4-methyl-2-phenylbenzopyryl chloride has been studied. It is noted that the transition to semi-microextraction technology can significantly reduce the toxic organic solvents consumption, and the use of dispersion solvent can intensify the complex extraction of Сopper (II) complex with 6,7-dihydroxy-4-methyl-2-phenylbenzopyryl chloride. Optimal conditions for spectrophotometric determination of Сopper (II) after dispersive liquid-liquid semi-microextraction of its complex with 6,7-dihydroxy-4-methyl-2-phenylbenzopyrylium chloride were found to be: 1.5 mL of chloroform, 1.5 mL of methanol, pH 4.5, λmax = 535 nm, l = 1 cm. The main analytical characteristics of the developed dispersive liquid-liquid semi-microextraction-spectrophotometric method are calculated: the calibration graph is linear in the wide range of concentrations of 17-480 μg/L, and the limit of detection and limit of determination are 5 and 17 μg/L, respectively. The molar ratios Copper (II) : interferer, in which there is no effect on the quantitative determination of Copper(II) by the proposed dispersive liquid-liquid semi-microextraction-spectrophotometric method have been established. The proposed method for Copper (II) spectrophotometric quantification after preconcentration via dispersive liquid-liquid semi-microextraction as a complex with 6,7-dihydroxy-4-methyl-2-phenylbenzopyrilium chloride was tested in the analysis of model solutions and water samples. The accuracy of the developed dispersive liquid-liquid semi-microextraction-spectrophotometric method was checked by the "spiked-found" method and the relative standard deviation does not exceed 3.9%. The proposed technique is simple, sensitive and environmentally friendly.
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6,7-二羟基-4-甲基-2-苯基苯并吡氯铵分散液-液萃取络合物分光光度法测定铜(ii)
研究了6,7-二羟基-4-甲基-2-苯基苯并吡氯分散液-液半微萃取铜(II)配合物的特异性。注意到过渡到半微萃取技术可以显著减少有毒有机溶剂的消耗,并且使用分散溶剂可以强化与6,7-二羟基-4-甲基-2-苯基苯并吡氯配合物Сopper (II)的配合物萃取。采用6,7-二羟基-4-甲基-2-苯基苯并氯吡啶对其配合物进行分散液-液半微萃取,测定Сopper (II)的最佳工艺条件为:氯仿1.5 mL,甲醇1.5 mL, pH 4.5, λmax = 535 nm, l = 1 cm。计算了所建立的分散液-液半微萃取-分光光度法的主要分析特性:在17 ~ 480 μg/L的浓度范围内,标定图呈线性关系,检出限为5,测定限为17 μg/L。建立了铜(II)与干扰物的摩尔比,该摩尔比对分散液-液半微萃取-分光光度法测定铜(II)的含量无影响。以6,7-二羟基-4-甲基-2-苯基苯并氯化吡啶为络合物,采用分散液-液半微萃取法对铜(II)进行预富集,并对模型溶液和水样进行了分析。建立的分散液-液半微萃取-分光光度法的准确度经“尖峰发现”法检验,相对标准偏差不超过3.9%。该技术简单、灵敏、环保。
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