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作 者:任红英 杨小红 REN Hong-Ying, YANG Xiao-Hong(Food Quality and Safety Supervision Inspection Center of Yongzhou City, Yongzhou 425000, Chin)
机构地区:[1]永州市食品质量安全监督检验中心,永州425000
出 处:《食品安全质量检测学报》2018年第5期1163-1168,共6页Journal of Food Safety and Quality
摘 要:目的建立γ-氯丙基三乙氧基硅烷改性纳米Si-HAP分离富集-火焰原子吸收法测定痕量锰、钴、镍的新方法。方法研究γ-氯丙基三乙氧基硅烷改性纳米Si-HAP在不同p H、吸附温度和时间、洗脱条件及共存离子对锰、钴、镍分离富集的影响。结果在最佳吸附条件下,该方法检出限分别为锰0.21μg/L,钴0.18μg/L,镍0.24μg/L,相对标准偏差分别为锰0.90%(1μg/mL),钴0.78%(2μg/mL),镍0.18%(5μg/mL)(n=11),样品加标回收率在95.0%~108.0%之间。结论该方法适用于水样中痕量锰、钴、镍的测定。Objective To establish a new method for the determination of trace manganese (Mn), cobalt (Co) and nickel (Ni) by flame atomic absorption spectrometry after separation/preconcentration with nanometer silicon hydroxyapatite (Si-HAP) modified with 3-chloropropyl trimethoxy silane. Methods The effects of different pH, adsorption temperature and time, elution conditions and co-existing ions on the separation and enrichment of Mn, Co and Ni by Si-HAP modified with 3-chloropropyl trimethoxy silane were studied. Results Under the optimum conditions, the limits of detection were 0.21 μg/L, 0.18 μg/L and 0.24 μg/L for Mn, Co and Ni, respectively. The relative standard deviations for the elements were 0.90 %, 0.78 % and 0.18 % for Mn (1 μg/mL), Co (2 μg/mL) and Ni (5 μg/mL) (n=11), and the recoveries were in the range of 95.0%~108.0%. Conclusion This method is suitable for the determination of trace Mn, Co and Ni in water samples.
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