Li Hui-zhi, Yang Chun-xia, Zhai Dian-tang
Department of Applied Chemistry, Ji'nan University, Ji'nan 250022, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2005 Feb;25(2):283-5.
This paper describes the determination of trace Zr and Hf in the sample using carbon powder and titanium oxide as the buffer by Atomic Emission Spectrometry (AES). Titanium was selected for the internal standard line. Sample separation and chemical treatment were not required. The sample was directly loaded into an ordinary electrode. The method is simple, rapid and accurate. The conditions for the determination, and the factors of influence have been studied. A new method has been developed for the determination of zirconium and hafnium. The analytical lines of Zr and Hf were 327.3 and 286.6 nm respectively. The internal standard line of Ti was 308.8 nm. The linear range of the determination of Zr and Hf was 0-0.50% and 0-0.25% respectively. The detection limit of Zr and Hf was 0.0010% and 0.010% respectively. The range of the recovery of zirconium and hafnium was 96.67%-105.0%. The results for these elements in standard sample are in agreement with certified values with a precision of 3.61% RSD for Zr (n = 9), and 4.82% RSD for Hf (n = 9). The method has been applied to the determination of Zr and Hf with satisfactory results.
本文描述了采用碳粉和氧化钛作为缓冲剂,通过原子发射光谱法(AES)测定样品中的痕量锆和铪。选择钛作为内标线。无需进行样品分离和化学处理。将样品直接装入普通电极。该方法简单、快速且准确。研究了测定条件及影响因素。开发了一种测定锆和铪的新方法。锆和铪的分析线分别为327.3和286.6 nm。钛的内标线为308.8 nm。锆和铪测定的线性范围分别为0 - 0.50%和0 - 0.25%。锆和铪的检出限分别为0.0010%和0.010%。锆和铪的回收率范围为96.67% - 105.0%。标准样品中这些元素的测定结果与认定值相符,锆的相对标准偏差(RSD,n = 9)为3.61%,铪的相对标准偏差(RSD,n = 9)为4.82%。该方法已应用于锆和铪的测定,结果令人满意。