Tirumalesh K
Isotope Applications Division, Bhabha Atomic Research Centre, Mumbai 400085, India.
Talanta. 2008 Feb 15;74(5):1428-34. doi: 10.1016/j.talanta.2007.09.021. Epub 2007 Sep 29.
This study describes a new ion chromatography method using a low-capacity anion exchange column with amperometric and absorbance detection for rapid and simultaneous determination of Br(-) and NO(3)(-) in contaminated waters where one of these ions is present in excess compared to other. The use of two detectors overcomes the problem of baseline separation for Br(-) and NO(3)(-) for accurate quantification, which was commonly encountered when using a low-capacity anion exchange column and suppressed conductivity detection mode. The method achieved accurate quantification of these two ions without requirement of baseline separation. The accuracy of 2.8% for NO(3)(-) was determined using a quality control sample obtained from UN GEMS/Water PE Study No. 6. The detection limits for Br(-) and NO(3)(-) were 20 and 6 microg l(-1) (25 microl sample), respectively. Linearity of these two ions was over three orders of magnitude with a correlation coefficient >0.998. The influence of potential interfering ions was also studied followed by the determination of Br(-) and NO(3)(-) in seawater, unsaturated zone water, soil extract and groundwater.
本研究描述了一种新的离子色谱方法,该方法使用低容量阴离子交换柱,并结合安培检测和吸光度检测,用于快速同时测定受污染水体中的Br(-)和NO(3)(-),其中这两种离子中的一种相对于另一种过量存在。使用两个检测器克服了使用低容量阴离子交换柱和抑制电导检测模式时常见的Br(-)和NO(3)(-)基线分离问题,从而实现准确的定量分析。该方法无需基线分离即可对这两种离子进行准确定量。使用从联合国全球环境监测系统/水项目第6号研究中获得的质量控制样品,测定出NO(3)(-)的准确度为2.8%。Br(-)和NO(3)(-)的检测限分别为20和6 μg l(-1)(25 μl样品)。这两种离子的线性范围超过三个数量级,相关系数>0.998。还研究了潜在干扰离子的影响,随后测定了海水中、非饱和带水、土壤提取物和地下水中的Br(-)和NO(3)(-)。