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首页> 外文期刊>Bulletin of the Korean Chemical Society >Study on Solid Phase Extraction and Spectrophotometric Determination of Nickel in Waters and Biological Samples
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Study on Solid Phase Extraction and Spectrophotometric Determination of Nickel in Waters and Biological Samples

机译:水和生物样品中固相萃取和分光光度法测定镍的研究

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A sensitive, selective and rapid method for the determination of nickel based on the rapid reaction of nickel(II) with QADMAA and the solid phase extraction of the Ni(II)-QADMAA chelate with C18 membrane disks has been developed. In the presence of pH 6.0 buffer solution and sodium dodecyl sulfonate (SDS) medium, QADMAA reacts with nickel to form a violet complex of a molar ratio of 1 : 2 (nickel to QADMAA). This chelate was enriched by solid phase extraction with C18 membrane disks. An enrichment factor of 50 was obtained by elution of the chelates form the disks with the minimal amount of isopentyl alcohol. The molar absorptivity of the chelate was 1.32 】 105 L mol-1 cm-1 at 590 nm in the measured solution. Beer`s law was obeyed in the range of 0.01-0.6 レg/mL. This method was applied to the determination of nickel in water and biological samples with good results.
机译:基于镍(II)与QADMAA的快速反应和C 18 膜盘固相萃取Ni(II)-QADMAA螯合物的灵敏,选择性,快速的测定镍的方法已经被开发出来。在pH 6.0缓冲溶液和十二烷基磺酸钠(SDS)介质存在下,QADMAA与镍反应形成摩尔比为1:2的紫色络合物(镍与QADMAA)。通过C 18 膜片的固相萃取富集了这种螯合物。通过用最小量的异戊醇从圆盘上洗脱螯合物获得富集因子为50。在被测溶液中,螯合物的摩尔吸光度在590 nm处为1.32】10 5 L mol -1 cm -1 。遵守比尔定律,范围为0.01-0.6微克/毫升。该方法用于水和生物样品中镍的测定,结果良好。

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