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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Single granular activated carbon microextraction and graphite furnace atomic absorption spectrometry determination for trace amount of gold in aqueous and geological samples
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Single granular activated carbon microextraction and graphite furnace atomic absorption spectrometry determination for trace amount of gold in aqueous and geological samples

机译:一次颗粒活性炭微萃取-石墨炉原子吸收光谱法测定水样和地质样品中的痕量金

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摘要

A new and simple method was developed for preconcentration trace amount of gold in aqueous and mineral samples. The method was based on the sorption of gold on granular activated carbon (AC) in acidic medium (hydrochloric acid) and subsequently direct determination by graphite furnace atomic absorption spectrometry (GFAAS). A small particle of adsorbent was delivered to small volume of sample. After extraction, AC removed and analyzed directly by GFAAS. Several factors influencing the extraction efficiency, such as the hydrochloric acid concentration, sample volume and extraction time were studied as well as effect of potential interfering ions. The preconcentration factor 50 was obtained. The limit of detection (LOD) of gold in water and soil samples was 0.007μgL-1 and 0.9ngg-1, respectively. The proposed method was applied successfully to the determination of trace amount of gold in environmental and geological samples. In order to validate the developed method, two certified reference materials: Platinum Ore (SARM-7B) and Copper Ore Mill Heads (No. 330) were analyzed and the determined values obtained were in good agreement with the certified values and recovery was obtained in the range of 80-118%. The relative standard deviations (RSD) for the spiking levels of 0.5μgL-1 in the real samples was 4%, (n=15).
机译:开发了一种新的简单方法来预富集水和矿物样品中的痕量金。该方法基于在酸性介质(盐酸)中金在颗粒状活性炭(AC)上的吸附,然后直接通过石墨炉原子吸收光谱法(GFAAS)测定。一小部分吸附剂被输送到少量样品中。提取后,去除AC,直接用GFAAS分析。研究了影响萃取效率的几个因素,例如盐酸浓度,样品量和萃取时间以及潜在干扰离子的影响。获得预浓缩因子50。水和土壤样品中金的检出限(LOD)分别为0.007μgL-1和0.9ngg-1。该方法成功地用于环境和地质样品中痕量金的测定。为了验证所开发的方法,分析了两种认证的参考材料:铂矿(SARM-7B)和铜矿磨头(No. 330),获得的测定值与认证值高度一致,并在范围为80-118%。实际样品中0.5μgL-1的加标水平的相对标准偏差(RSD)为4%(n = 15)。

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