Al-Harahsheh M, Kingman S, Somerfield C, Ababneh F
College of Mining and Environmental Engineering, Al-Hussein Bin Talal University, P.O. Box 20, Ma'an 71111, Jordan.
Anal Chim Acta. 2009 Apr 6;638(1):101-5. doi: 10.1016/j.aca.2009.02.030. Epub 2009 Feb 25.
A new two-stage microwave-assisted digestion procedure using concentrated HNO(3), HCl, HF and H(3)BO(3) has been developed for the chemical analysis of major and trace elements in sulphide ore samples prior to inductively coupled plasma atomic emission spectroscopy (ICP-AES) analysis. In the first stage 0.2 g of the certified reference material (CRM) sample was digested with a combination of acids (HNO(3), HCl, and HF) in a closed Teflon vessel and heated in the microwave to 200 degrees C for 30 min. After cooling, H(3)BO(3) was added and the vessel was reheated to 170 degrees C for 15 min. The precision of the method was checked by comparing the results against six certified reference materials. The analytical results obtained were in good agreement with the certified values, in most cases the recoveries were in the range 95-105%. Based on at least 17 replicates of sample preparation and analysis, the precision of the method was found to be < or = 5%.
一种新的两阶段微波辅助消解方法已被开发出来,该方法使用浓硝酸(HNO₃)、盐酸(HCl)、氢氟酸(HF)和硼酸(H₃BO₃),用于在电感耦合等离子体原子发射光谱法(ICP - AES)分析之前对硫化矿样品中的主要和微量元素进行化学分析。在第一阶段,将0.2克有证标准物质(CRM)样品与酸(HNO₃、HCl和HF)的混合物在密闭的聚四氟乙烯容器中消解,并在微波中加热至200℃ 30分钟。冷却后,加入H₃BO₃,然后将容器重新加热至170℃ 15分钟。通过将结果与六种有证标准物质进行比较来检查该方法的精密度。获得的分析结果与认证值吻合良好,在大多数情况下回收率在95 - 105%范围内。基于至少17次样品制备和分析的重复实验,发现该方法的精密度≤5%。