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首页> 外文期刊>Fullerenes, nanotubes, and carbon nanostructures >Liquid-liquid extraction, separation, preconcentration, and ICP-AES determination of lanthanum and cerium with N-phenyl-(1,2-methanofullerene C-60)61-formohydroxamic acid
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Liquid-liquid extraction, separation, preconcentration, and ICP-AES determination of lanthanum and cerium with N-phenyl-(1,2-methanofullerene C-60)61-formohydroxamic acid

机译:N-苯基-(1,2-甲基富勒烯C-60)61-甲氧肟酸的液-液萃取,分离,预浓缩和ICP-AES测定镧和铈

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摘要

A novel method for liquid-liquid extraction, separation, preconcentration, and simultaneous trace determination of cerium(IV) and lanthanum(III) with N-phenyl-(1,2-methanofulterene C-60)61-formohydroxamic acid (PMFFA) is reported. Lanthanum and cerium are extracted at pH 8.5 and 9.5, respectively in chloroform and recovered from monazite sands in the presence of thorium, uranium, and large number of cations and anions in high purity (99.98%). The extraction mechanism is investigated. The influence of PMFFA, pH, diverse ions, and temperature on the distribution constants of lanthanum and cerium was examined. The overall stability constants (log beta(2)K(e)) and extraction constants (K-ex) for lanthanum(III) are 22.50 and 5.0 x 10(-9), respectively and for cerium(IV) are 21.51 and 3.9 x 10-9, respectively. Lanthanum(III) gives a colourless complex with PMFFA which is extracted into chloroform having molar absorptivity 5.5 x 10(4) L mol(-1) cm(-1) at 395 nm, and Beer's law 0.12-2.52 mug mL(-1), while cerium(IV) forms a red coloured complex, lambda(max) 460 nm, molar absorptivity 1.5 x 10(4) L mol(-1) cm(-1), and Beer's law 0.46-9.26 mug mL(-1). For trace determination the extracts were directly inserted into the plasma for inductively coupled plasma atomic emission spectrometry ICP-AES measurements of lanthanum and cerium which increases the sensitivity 60 folds and obey Beer's law in the range, 2.1-37.5 ng mL(-1) for lanthanum and 9.2-186.4 ng mL(-1) for cerium. The method is applied for the determination of lanthanum and cerium in real and standard samples, sea water, and environmental samples.
机译:N-苯基-(1,2-甲亚富富烯烯C-60)61-甲氧基异羟肟酸(PMFFA)液-液萃取,分离,预浓缩和同时痕量测定铈(IV)和镧(III)的新方法是报告。镧和铈分别在氯仿中以pH 8.5和9.5萃取,并在and,铀以及大量高纯度(99.98%)阳离子和阴离子存在下从独居石砂中回收。研究了提取机理。研究了PMFFA,pH,各种离子和温度对镧和铈的分布常数的影响。镧(III)的总体稳定性常数(log beta(2)K(e))和提取常数(K-ex)分别为22.50和5.0 x 10(-9),铈(IV)的总体稳定性常数为21.51和3.9 x 10-9。镧(III)与PMFFA形成无色络合物,将其萃取到氯仿中,在395 nm处的摩尔吸收率为5.5 x 10(4)L mol(-1)cm(-1),比尔定律为0.12-2.52毫升(-1) ),铈(IV)形成红色络合物,λ(最大)460 nm,摩尔吸收率1.5 x 10(4)L mol(-1)cm(-1),比尔定律0.46-9.26杯mL(- 1)。为了进行痕量测定,将提取物直接插入血浆中以进行电感耦合等离子体原子发射光谱法ICP-AES测定镧和铈,这将灵敏度提高了60倍,并遵守比尔定律,其范围为2.1-37.5 ng mL(-1)。镧和铈的9.2-186.4 ng mL(-1)。该方法用于测定真实和标准样品,海水和环境样品中的镧和铈。

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