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作 者:翟好英[1] 张学艳[1] 阮尚全[1] 谭学蓉[1]
机构地区:[1]内江师范学院化学与生命科学系,四川内江641112
出 处:《冶金分析》2009年第12期17-20,共4页Metallurgical Analysis
基 金:四川省教育厅科研项目资助(No.2006B101)
摘 要:在pH4.39的Walpole缓冲溶液中,Ag^+分别与曙红B(EB)和曙红Y(EY)反应形成络合物微粒,使溶液的共振散射(RS)强度显著增强,其最大散射峰均位于282nm处。在优化的实验条件下,在0.0108~1.30μg/mL范围内,Ag^+浓度分别与EB和EY体系的共振散射强度(ΔI282nm)之间呈较好的线性关系,检出限分别为74.2ng/L(EB)和86.5ng/L(EY)。该方法应用于废胶片中痕量银的测定,相对标准偏差为1.3%~3.4%,回收率在96.7%~104.3%之间。In Walpole buffer solution at pH 4.39, Ag^+ reacted with Eosin B and Eosin Y, respectively, forming two kinds of ion-association complexes. The resonance scattering intensity of the solution was obviously strengthened, and their maximum resonance scattering peaks were all at 282 nm. Under the optimum experimental conditions, there was a good linear relationship between the resonance scattering intensity (ΔI282.m) of the EB or EY system and the Ag^+ concentration in the range of 0. 010 8- 1.30 μg/mL. The detection limits were 74. 2 ng/L (EB) and 86.5 ng/L (EY). This method has been applied to determine trace silver in waste film with the RSD of 1.3%- 3.4% and the recovery of 96. 7%-104. 3%.
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