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作 者:刘文龙[1] 刘臣辉[1] 陆小龙[1] 姚哲源 宋波
机构地区:[1]扬州大学农学院理化测试中心
出 处:《分析试验室》1997年第3期90-93,共4页Chinese Journal of Analysis Laboratory
基 金:江苏省自然科学基金
摘 要:本文应用氢化物发生ICP-AES法研究了药用植物样品中痕量锗的测定方法,系统地研究了ICP-AES仪器参数及氢化物发生条件对锗谱线信背比的影响,考察了13种共存元素的干扰,并比较了植物样品的3种前处理方法。选定H3PO4-HNO3-H2O2消化,在3mol/LH3PO4介质中,以15g/LNaBH4还原,测定药用植物样品中的锗,相对标准偏差≤2.9%,回收率为94%~103%。方法检出限达0.13μg/L。A method for the determination of Ge inmedicinal plants was studied by hydride generation ICP AES in this paper. The influences of ICP AES operating parameters and hydride generation conditions on signal/background(S/B) ratio of Ge 209.426nm spectral line were investigated.The interferences of 13 co elements were studied.Three wet digestion procedures for plant samples were compared.When we digested medicinal plant samples using H 3PO 4 HNO 3 H 2O 2 procedure and determined Ge by the hydride generation ICP AES using 15g/L NaBH 4 as reducing agent in the medium of 3mol/L H 3PO 4,the RSD was less than 2.9% and the recovery of Ge was 94% ̄103%.The detection limit of this method reached 0.13μg/L.
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