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Liquid–liquid extraction and separation of lead(II) by using N-n-octylcyclohexylamine as an extractant: analysis of real samples

机译:以N-正辛基环己胺为萃取剂液-液萃取分离铅(II):实际样品分析

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A method for the determination of micro amounts of lead(II) is described. N-n-Octylcyclohexylamine (N-n-OCA) was employed as an ion-pair forming a neutral [N-n-OCAH+PbCl3a?’] complex in hydrochloric acid medium. The quantitative extraction of lead(II) was observed with N-n-OCA (0.03 to 0.055 M) in a dichloromethane (DCM) and xylene mixture (1:4), from hydrochloric acid medium (3.0 to 5.0 M). The extracted ion-pair complex was back stripped with 0.5 M nitric acid and determined spectrophotometrically with PAR. The quantitative extraction of lead(II) was found in the DCM:xylene ratio of 1:4 as a mixed solvent system. The various parameters studied, such as concentration of acid, N-n-OCA concentration, equilibrium time, solvent study, back stripping agents and loading capacity were optimized for the quantitative extraction of lead(II). The stoichiometry of the extracted ion-pair complex was determined on the basis of the slope analysis method, and it was found to be 1:3:1 (metal:chloride:extractant). The proposed method was successfully applied to the analysis of diverse ions, binary mixtures of associated metal ions, ternary mixtures, alloys, ayurvedic samples and water samples, by using N-n-OCA and lead(II) was determined using PAR and the results of analysis were confirmed by ICP-OES.
机译:描述了一种测定微量铅(II)的方法。使用N-正辛基环己胺(N-n-OCA)作为离子对,在盐酸介质中形成中性[N-n-OCAH + PbCl3a′’]络合物。在二氯甲烷(DCM)和二甲苯混合物(1:4)中,用N-n-OCA(0.03至0.055 M)从盐酸介质(3.0至5.0 M)中定量提取了铅(II)。用0.5 M硝酸反萃取萃取的离子对络合物,并用PAR分光光度法测定。发现以混合溶剂体系DCM:二甲苯的比例为1:4定量萃取铅(II)。研究中优化了各种参数,如酸的浓度,N-n-OCA的浓度,平衡时间,溶剂研究,反萃取剂和负载量,以定量萃取铅(II)。通过斜率分析法求出所提取的离子对络合物的化学计量,结果为1:3:1(金属:氯化物:萃取剂)。采用Nn-OCA方法成功地将所提出的方法用于各种离子,相关金属离子的二元混合物,三元混合物,合金,阿育吠陀样品和水样品的分析,并用PAR测定了铅(II)并分析了结果由ICP-OES确认。

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