...
首页> 外文期刊>Journal of analytical chemistry >Determination of uranium and thorium in natural waters by ICP-OES after on-line solid phase extraction and preconcentration in the presence of 2,3-dihydro-9,10-dihydroxy-1,4-antracenedion
【24h】

Determination of uranium and thorium in natural waters by ICP-OES after on-line solid phase extraction and preconcentration in the presence of 2,3-dihydro-9,10-dihydroxy-1,4-antracenedion

机译:在线固相萃取并在2,3-二氢-9,10-二羟基-1,4-邻苯二甲酰存在下进行预浓缩后,通过ICP-OES测定天然水中的铀和th

获取原文
获取原文并翻译 | 示例
           

摘要

An on-line solid phase extraction method, linked to inductively coupled plasma optical emission spectrometry (ICP-OES), has been examined using octadecyl-bonded silica cartridge for determination of low levels of uranium and thorium in aqueous samples. 2,3-dihydro-9,10-dihydroxy-1,4-anthracenedion forms a hydrophobic complex with cations and the resulted complex was retained on SPE. The retained complex was eluted using an acidic solution and introduced into ICP for determination. Various effective parameters and chemical variables such as sample pH, amount of ligand (as a complexing agent), sampling and eluting flow rates and concentration of the eluent were optimized. Under optimal conditions, calibration curves with dynamic linear ranges of 1-200 mu g/L (r (2) = 0.9999) and 1-500 mu g/L (r (2) = 0.9994) for U and Th were obtained, respectively. Detection limits based on three times of standard deviations of blank by 6 replicates were 0.69 mu g/L and 0.84 mu g/L for U and Th, respectively. Sample throughput was 10 samples/h. The interference effects of several metal ions on percentage of recovery of U and Th were also studied. The method was applied to the recovery and sequential determination of these actinide elements in different water samples.
机译:已使用十八烷基键合硅胶柱检查了在线固相萃取方法,该方法与电感耦合等离子体发射光谱法(ICP-OES)相连,用于测定水性样品中的低含量铀和th。 2,3-二氢-9,10-二羟基-1,4-蒽二酮与阳离子形成疏水复合物,并将所得复合物保留在SPE上。使用酸性溶液洗脱保留的复合物,并将其引入ICP中进行测定。优化了各种有效参数和化学变量,例如样品的pH值,配体(作为络合剂)的量,采样和洗脱流速以及洗脱液的浓度。在最佳条件下,分别获得了U和Th的线性线性范围分别为1-200μg / L(r(2)= 0.9999)和1-500μg / L(r(2)= 0.9994)的校准曲线。基于六次重复空白的标准偏差的三倍,U和Th的检出限分别为0.69μg / L和0.84μg / L。样品处理量为10个样品/小时。还研究了几种金属离子对铀和Th的回收率的影响。该方法用于不同水样中这些act系元素的回收和顺序测定。

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