首页> 外文期刊>Analytical methods >A cloud point extraction procedure for gallium, indium and thallium determination in liquid crystal display and sediment samples
【24h】

A cloud point extraction procedure for gallium, indium and thallium determination in liquid crystal display and sediment samples

机译:浊点萃取法测定液晶显示器和沉积物样品中的镓,铟和al

获取原文
获取原文并翻译 | 示例
           

摘要

A simple, sensitive and rapid cloud point extraction (CPE) methodology has been developed for the selective separation and preconcentration of gallium, indium and thallium, after complexation with gallic acid in the presence of Triton X-114 as a non-ionic surfactant. The quantitative extraction of gallium, indium and thallium was performed at pH 2.5, with 0.04 mmol L-1 gallic acid, and 0.05% (w/v) Triton X-114 at 40 degrees C. The dilution of the surfactant-rich phase with acidified methanol was performed after phase separation, and the metal ions were determined using flame atomic absorption spectrometry. Under the optimized experimental conditions, the calibration curve is linear over the concentration range of 6-150 ng mL(-1) for gallium, 2-150 ng mL(-1) for indium, and 2-100 ng mL(-1) for thallium. The limits of detection, based on three times the standard deviation of a blank signal by seven replicate measurements were 3.50, 1.25 and 0.92 ng mL(-1). The relative standard deviations of this method were 1.55, 1.40 and 1.82% for gallium, indium and thallium, respectively (C = 50 ng mL(-1), n = 7). The results showed that the developed method was not susceptible to interference effects, providing good recoveries. The developed method was successfully applied to gallium, indium and thallium determination in sediments and mobile phone liquid crystal display samples with satisfactory results.
机译:在Triton X-114作为非离子型表面活性剂存在下,与没食子酸络合后,已开发出一种简单,灵敏,快速的浊点萃取(CPE)方法,用于选择性分离和预浓缩镓,铟和al。在pH值为2.5的条件下,用0.04 mmol L-1没食子酸和0.05%(w / v)Triton X-114在40°C下进行镓,铟和al的定量萃取。相分离后进行酸化的甲醇,并使用火焰原子吸收光谱法测定金属离子。在优化的实验条件下,校准曲线在镓的浓度范围为6-150 ng mL(-1),铟的浓度范围为2-150 ng mL(-1)和2-100 ng mL(-1)范围内是线性的th基于七次重复测量的空白信号标准偏差的三倍,检测限为3.50、1.25和0.92 ng mL(-1)。镓,铟和th的这种方法的相对标准偏差分别为1.55%,1.40和1.82%(C = 50 ng mL(-1),n = 7)。结果表明,所开发的方法不易受到干扰的影响,具有良好的回收率。该方法成功应用于沉积物和手机液晶显示样品中镓,铟和al的测定,结果令人满意。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号