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机构地区:[1]山东大学实验中心 [2]山东大学化学院 [3]济南出口商品检验局
出 处:《山东大学学报(自然科学版)》1999年第2期202-207,共6页Journal of Shandong University(Natural Science Edition)
摘 要:GFAAS法测试生物样品中微量锗的主要干扰因素及其消除方法.采用了Pd(NO3)2和LiNO3复合基体改进剂加Ba(NO3)2辅助基体改进剂,锗的热稳定性及体系的抗干扰能力远高于采用单一基体改进剂.灰化温度达1600℃,未见锗产生挥发损失.试样中NaCl量达6.0g/L,Na2SO4量高达600mg/L也未干扰锗的测定.本法用于实际样品分析效果良好.用X射线衍射光谱法确证了Pd(NO3)2存在下锗在石墨管内加热至≥1200℃的灰化产物为锗钯金属化合物.Various matrix interferences on the determination of trace germanium in biological samples were studied dy GF-AAS.The thermostability and the interference-resisting property of germanium were increased remaredly when palladium and lithium nitrates were used as complexing matrix modifiers and barium nitrate as a supplementary matrix modifier.There were no losses of evaporated germanium when ashing temperature increased to 1 600 ℃,and there were no interferences to the determination of germanium even when the coexistent content of sodium chloride was up to 6.0 g/L,the content of sodium sulfate was up to 600 mg/L in the samples. The X-ray diffraction analysis affirmed that the ashing product was germanium-palladium intermetallic compounds when germanium and palladium nitrates were heated simultaniously up to 1 200 ℃ in the graphite furnace.
关 键 词:锗 GF-AAS光谱分析 热稳定性 抗干扰能力
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