Li Hui-Zhi, Zhai Dian-Tang, Xu Chong-Juan, Pei Mei-Shan
School of Chemistry and Chemical Engineering, Ji'nan University, Ji'nan 250022, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2007 Jun;27(6):1204-6.
The present paper describes the determination of trace Ni, Fe, Mo, Mn and B in Ti/TiC composite material using carbon powder, calcium carbonate, cupric oxide and beryllium oxide-as buffer by atomic emission spectrometry (ASE). Be 298.61 nm was selected as internal standard line. Sample separation and chemistry treatment were not requirel. The sample was directly loaded into ordinary electrode. The method is simple, rapid and accurate. The requirement of determination, and factors of influence were studied. A new method has developed for the determination of Ni, Fe, Mo, Mn and B. The analysis lines of Ni, Fe, Mo, Mn and B are 300.36, 248.33, 315.82, 260.57 and 249.68 nm respectively. The internal standard line of Be is 298.61 nm. The linear ranges of the determination of Ni, Fe, Mo, Mn and B are 0.003%-0.30%, 0.001%-0.20%, 0.003%-0.30%, 0.001%-0.20%, 0.001%-0.20% respectively. The detection limits of Ni, Fe, Mo, Mn and B are 0.003%; 0.001%, 0.003%, 0.001% and 0.001% respectively. The ranges of the recovery of Ni, Fe, Mo, Mn and B are 95.80%-104.8%, and the standard relative deviations (RSD) are less than 5.0% (n = 9). The method has been applied to the determination of Ni, Fe, Mo, Mn and B with satisfactory results.
本文描述了采用碳粉、碳酸钙、氧化铜和氧化铍作为缓冲剂,通过原子发射光谱法(ASE)测定Ti/TiC复合材料中痕量镍、铁、钼、锰和硼的方法。选择铍的298.61nm作为内标线。无需进行样品分离和化学处理。将样品直接装入普通电极。该方法简便、快速、准确。研究了测定要求及影响因素。开发了一种测定镍、铁、钼、锰和硼的新方法。镍、铁、钼、锰和硼的分析线分别为300.36、248.33、315.82、260.57和249.68nm。铍的内标线为298.61nm。镍、铁、钼、锰和硼的测定线性范围分别为0.003% - 0.30%、0.001% - 0.20%、0.003% - 0.30%、0.001% - 0.20%、0.001% - 0.20%。镍、铁、钼、锰和硼的检出限分别为0.003%、0.001%、0.003%、0.001%和0.001%。镍、铁、钼、锰和硼的回收率范围为95.80% - 104.8%,标准相对偏差(RSD)小于5.0%(n = 9)。该方法已应用于镍、铁、钼、锰和硼的测定,结果令人满意。