5-(4-氟苯基)-喹啉-8-醇分光光度法测定水中Zn2+离子

Maryam Al-Jabri, Salma M.Z. Al-Kindy, Fakhr Eldin O. Suliman, Beena Varghese, Saleh N. Al-Busafi, Haider J. Al-Lawati
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引用次数: 7

摘要

建立了一种基于Zn2+离子与5-(4-氟苯基)-喹啉-8-醇络合物形成的荧光光谱法,用于快速测定痕量锌离子。该方法灵敏度高,选择性好。形成的配合物在535 nm处发出强辐射,激发波长为394 nm。通过考察pH、金属与配体的摩尔比和缓冲液类型对络合反应的影响,优化了络合反应的形成。研究表明,当溶液pH为8.0,缓冲液为0.2 M碳酸盐,金属与配体的化学计量比为1:2时,络合效果最好。在最佳条件下,其检出限为3 ppb。方法经适当验证,相对标准偏差小于2% (n = 5),可用于自来水、矿泉水、鲜奶和奶油样品中微量Zn2+离子的测定。
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Spectrofluorimetric determination of Zn2+ ions in aqueous medium using 5-(4-flourophenyl)-quinolin-8-ol

A spectrofluorimetric method based on complex formation between Zn2+ ions and 5-(4-flourophenyl)-quinolin-8-ol has been developed for the rapid determination of trace levels of zinc ions. The method is sensitive and selective. The complex formed emit strongly at 535 nm with excitation wavelength at 394 nm. Complexation formation was optimized by studying the effect of pH, molar ratio of the metal to the ligand and the type of buffers. The study indicated that maximum complexation resulted when the pH of the mixture was maintained at 8.0 with 0.2 M carbonate buffer and metal to ligand was at a stoichiometric ratio of 1:2. Under the optimum conditions, the detection limit was 3 ppb. Appropriate validation of the method, yielded acceptable relative standard deviations of less than 2% (n = 5). The method was applied to the trace determination of Zn2+ ions in tap water, mineral water, fresh milk and cream samples successfully.

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