Comparative determination of Ba, Cu, Fe, Pb and Zn in tea leaves by slurry sampling electrothermal atomic absorption and liquid sampling inductively coupled plasma atomic emission spectrometry

被引:60
作者
Mierzwa, J [1 ]
Sun, YC [1 ]
Chung, YT [1 ]
Yang, MH [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Nucl Sci, Hsinchu 30043, Taiwan
关键词
electrothermal atomic absorption spectrometry; inductively coupled plasma-atomic emission spectrometry; slurry sampling; microwave-assisted wet digestion; tea leaves; heavy metals determination;
D O I
10.1016/S0039-9140(98)00214-8
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The comparative determination of barium, copper, iron, lead and zinc in tea leaf samples by two atomic spectrometric techniques is reported. At first, slurry sampling electrothermal atomization atomic absorption spectrometry (ETAAS) was applied. The results of Ba and Pb determination were calculated using the method of standard additions, and results of Cu, Fe and Zn from the calibration graphs based on aqueous standards. These results were compared with the results obtained after microwave-assisted wet (nitric + hydrochloric + hydrofluoric acids) digestion in closed vessels followed by inductively coupled plasma-atomic emission spectrometric (ICP-AES) determination with the: calibration by means of aqueous standards. The exception was lead determined after a wet digestion procedure by ETAAS. The accuracy of the studied methods was checked by the use of the certified reference material Tea GBW-07605. The recoveries of the analytes varied in the range from 91 to 99% for slurry sampling ETAAS, and from 92.5 to 102% for liquid sampling ICP-AES. The advantages of slurry sampling ETAAS method are simplicity of sample preparation and very good sensitivity. Slurry sampling ETAAS method is relatively fast but if several elements must be: determined in one sample, the time of the whole microwave-assisted digestion procedure and ICP-AES determination will be shorter. However, worse detection limits of ICP-AES must also be taken into the consideration in a case of some analytes. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1263 / 1270
页数:8
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