氯膦酸钠水溶液和尿液的络合测定。

V Virtanen, J Pursiainen, L H Lajunen
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引用次数: 2

摘要

介绍了用Th-EDTA-XO或th - dta -XO (XO =二甲酚橙)配合物测定氯膦酸盐的三种不同方法。根据UV-VIS和13C NMR测量,在微酸性溶液中,混合配体Th-EDTA-XO或Th-DCTA-XO配合物中的XO被氯钠阴离子定量取代。该配体替代反应可用于氯膦酸钠的痕量测定。研究的方法包括目视络合滴定法、分光光度滴定法和常规分光光度测定法。通过目视络合滴定法,可以直接测定人尿中的氯膦酸盐,准确度和精密度在0.5-2.5 mg l-1范围内。通过用水1:10稀释更浓的尿液样本,可以以可接受的准确度和精度测定高达80 mg l-1的样本。该方法的工作范围在16 mg l-1的水溶液中呈线性,rsd值在0.7 ~ 3.8%之间变化。研究了人尿中主要物质对测定的干扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Complexometric determination of clodronate in aqueous solutions and urine.

Three different procedures for the determination of clodronate by means of Th-EDTA-XO or Th-DCTA-XO (XO = xylenol orange) complexes are presented. According to the UV-VIS and 13C NMR measurements, XO is quantitatively replaced by the clodronate anion in the mixed ligand Th-EDTA-XO or Th-DCTA-XO complexes in slightly acidic solutions. This ligand replacement reaction can be applied to the determination of traces of clodronate. Procedures studied involve visual complexometric titration, spectrophotometric titration and conventional spectrophotometric determination. By visual complexometric titration it is possible to determine clodronate directly in human urine with acceptable accuracy and precision in the range 0.5-2.5 mg l-1. By diluting more concentrated urine samples 1:10 with water, samples of up to 80 mg l-1 can be determined with acceptable accuracy and precision. The working range of the method is linear up to 16 mg l-1 in aqueous solutions with the RSD-value varying between 0.7 and 3.8%. Interference caused by the major substances of human urine on the determination were studied.

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