首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Supported liquid membrane coupled on-line to potentiometric stripping analysis at a mercury-coated reticulated vitreous carbon electrode for trace metal determinations in urine
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Supported liquid membrane coupled on-line to potentiometric stripping analysis at a mercury-coated reticulated vitreous carbon electrode for trace metal determinations in urine

机译:支撑的液膜在线耦合到电位计上的汞涂覆的玻璃化玻璃碳碳电极上的溶出分析,用于尿液中痕量金属的测定

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摘要

A method for trace metal determinations in complex matrices is presented, The method combines supported liquid membrane (SLM) sample clean-up and enrichment with potentiometric stripping analysis (PSA) in a flow system using reticulated vitreous carbon (RVC) as the electrode material, The membrane contained 40% mim di-2-ethylhexylphosphoric acid dissolved in kerosene, Lead was used as a model substance in high-purity water and urine samples. The samples were enriched after a simple pH adjustment, The SLM enrichment time was 10 min when the last 5 min electrodeposition on the RVC electrode at -1.0 V (versus Ag/AgCl) was performed simultaneously, The influence of various experimental parameters such as deposition time, deposition potential and flow rate on the lead signal was investigated, With a 10 min SLM enrichment including a 5 min deposition time, the detection limit for lead was 0.3 mu g l(-1), The relative standard deviation for lead concentrations in the range 4-20 mu g l(-1) was 0.05%, The overall SLM-PSA system was found to be stable for at least 100 urine analyses, The method was validated by running a reference urine sample, The result obtained (five replicates) was 9.7 mu g l(-1) (standard deviation 1.8 mu g l(-1)) which is within the recommended range of 9.2-10.8 mu g l(-1). [References: 19]
机译:提出了一种在复杂的基质中测定痕量金属的方法,该方法在以网状玻璃碳(RVC)为电极材料的流动系统中,将支持液膜(SLM)样品的净化和富集与电位剥离分析(PSA)相结合,该膜含有溶解在煤油中的40%mim二-2-乙基己基磷酸。铅被用作高纯水和尿液样品中的模型物质。通过简单的pH调节富集样品,同时在-1.0 V(相对于Ag / AgCl)下在RVC电极上进行最后5分钟的电沉积时,SLM富集时间为10分钟,沉积等各种实验参数的影响研究了铅信号上的时间,沉积电位和流速,采用10分钟SLM富集(包括5分钟沉积时间),铅的检出限为0.3 mu gl(-1),铅中铅的相对标准偏差范围4-20 mu gl(-1)为0.05%,发现整个SLM-PSA系统对于至少100次尿液分析是稳定的,通过运行参考尿液样品对该方法进行了验证,获得的结果(重复5次)为9.7 mu gl(-1)(标准偏差为1.8 mu gl(-1)),该值在9.2-10.8 mu gl(-1)的建议范围内。 [参考:19]

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