首页> 外文期刊>Analytica chimica acta >Simultaneous preconcentration of vanadium(V/IV) species with palmitoyl quinolin-8-ol bonded to amberlite XAD 2 and their separate spectrophotometric determination with 4-(2-pyridylazo)-resorcinol using CDTA as masking agent
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Simultaneous preconcentration of vanadium(V/IV) species with palmitoyl quinolin-8-ol bonded to amberlite XAD 2 and their separate spectrophotometric determination with 4-(2-pyridylazo)-resorcinol using CDTA as masking agent

机译:钒(V / IV)物种同时预浓缩与Amberlite XAD 2键合的棕榈酰基喹啉8-醇对钒(V / IV)物种的分离,并使用CDTA作为掩蔽剂用4-(2-吡啶基偶氮)-间苯二酚分光光度法测定

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摘要

This paper reports the simultaneous preconcentration and separation of trace amounts of V species in synthetic solutions and seawater with palmitoyl quinolin-8-ol bonded amberlite XAD 2 copolymer resin column prior to simultaneous speciation analysis.Both V(IV) and V(V) species could be sorbed and preconcentrated by the resin.Both vanadium species were quantitatively eluted together from the resin column using HC1 as stripping agent and used for speciation studies.For the speciation analysis of eluted V species,the selected route involved spectrophotometric determination of total vanadium with 4-(2-pyridylazo)-resorcinol (PAR) and vanadate estimation by masking vanadyl with 1,2 cyclohexanediaminetetraacetic acid (CDTA).The preconcentrated V species were assayed spectrophotometrically with PAR at 542 nm,and the results were compared with those of FAAS.The detection limits of V(V) with spectrophotometry and FAAS were 1.6 and 0.9mug l~(-1),respectively.The optimal experimental parameters such as pH,sample flow rate,desorption flow rate,redox behaviour of V(IV) and V(V) in resin and volume of eluent and sample were investigated.The values obtained for the preconcentration factor by the two methods were nearly consistent,and were in the range 150-fold.Analysis of certified reference material (IAEA-405) by the proposed method showed good agreement with the certified value.The established procedure was employed for preconcentrating the vanadium species from artificial and real seawater.
机译:本文报道了在同时形态分析之前,棕榈酰喹啉8-ol键合的Amberlite XAD 2共聚物树脂柱同时富集和分离合成溶液和海水中的痕量V物种.V(IV)和V(V)物种用HC1作为汽提剂将两种钒物种从树脂柱中定量洗脱出来并用于形态学研究。为洗脱的V物种进行形态分析,选择的途径包括分光光度法测定总钒4-(2-吡啶基偶氮)-间苯二酚(PAR)并通过用1,2环己二胺四乙酸(CDTA)掩蔽钒来估算钒酸盐。使用PAR在542 nm处分光光度法测定预浓缩的V物种,并将结果与​​FAAS进行比较分光光度法和FAAS对V(V)的检出限分别为1.6和0.9mug l〜(-1)。最佳实验参数考察了pH值,样品流速,解吸流速,树脂中V(IV)和V(V)的氧化还原行为以及洗脱液和样品的体积。两种方法测得的预富集系数值基本一致,范围在150倍以内。所提出的方法对认证标准物质(IAEA-405)的分析与认证值具有良好的一致性。采用既定程序从人工和真实海水中预浓缩了钒。

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