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作 者:倪文山[1,2] 张萍[1,2] 姚明星[1,2] 李贤珍[1,2]
机构地区:[1]中国地质科学院郑州矿产综合利用研究所,河南郑州450006 [2]国家非金属矿资源综合利用工程技术研究中心,河南郑州450006
出 处:《冶金分析》2010年第8期50-53,共4页Metallurgical Analysis
摘 要:通过微波加热,氢氟酸溶解矿石样品,再以酒石酸溶液处理,使铌、钽完全进入溶液。以铌316.340{106}nm光谱线和钽268.517{125}nm光谱线为分析线,在选定的仪器参数下用电感耦合等离子体原子发射光谱法(ICP-AES)测定了溶液中的铌和钽。铌、钽原子发射光谱强度与ρ(Nb2O5)和ρ(Ta2O5)在0~6μg/mL范围内呈良好的线性关系,铌、钽的校准曲线相关系数r均为0.999 9,方法检出限分别为0.018μg/mL、0.051μg/mL。用于实际样品分析,加标回收率为97%~102%,铌和钽的相对标准偏差(n=6)分别为0.23%~0.86%和1.5%~2.3%;用于标准样品分析,测定值与认定值相符。The ore sample was digested with hydrofluoric acid by microwave heating,and then treated with tartaric acid solution to make niobium and tantalum in ore sample completely dissolve in solution.The niobium and tantalum in the prepared solution were determined by inductively coupled plasma atomic emission spectrometry(ICP-AES) under the selected instrumental parameters using Nb 316.340{106} nm and Ta 268.517{125} nm as analytical lines.The emission spectral intensity of niobium and tantalum showed good linear relationship with ρ(Nb2O5)and ρ(Ta2O5)in the range of 0-6 μg/mL.The correlation coefficients of calibration curve for niobium and tantalum were both 0.999 9.The detection limits for niobium and tantalum were 0.018 μg/mL and 0.051 μg/mL,respectively.The proposed method was applied to the determination of actual sample,giving the recovery rate of 97 %-102 % and the relative standard deviations(RSD,n=6) of 0.23 %-0.86 % for niobium and 1.5 %-2.3 % for tantalum.This method was applied to the analysis of standard sample,and the results were consistent with the certified values.
关 键 词:微波消解 酒石酸 铌 钽 电感耦合等离子体原子发射光谱法
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