Araujo Rennan G O, Oleszczuk Nédio, Rampazzo Roger T, Costa Pedro A, Silva Márcia M, Vale Maria Goreti R, Welz Bernhard, Ferreira Sérgio L C
Universidade Federal da Bahia, Instituto de Química, Grupo de Pesquisa em Química Analítica, Campus Ondina, 40170-290 Salvador, BA, Brazil.
Talanta. 2008 Oct 19;77(1):400-6. doi: 10.1016/j.talanta.2008.06.047. Epub 2008 Jul 9.
Two analytical methods for the determination of cadmium in wheat flour by electrothermal atomic absorption spectrometry without prior sample digestion have been compared: direct solid sampling analysis (SS) and slurry sampling (SlS). Besides the conventional modifier mixture of palladium and magnesium nitrates (10 microg Pd+3 microg Mg), 0.05% (v/v) Triton X-100 has been added to improve the penetration of the modifier solution into the solid sample, and 0.1% H(2)O(2) in order to promote an in situ digestion for SS. For SlS, 30 microg Pd, 12 microg Mg and 0.05% (v/v) Triton X-100 have been used as the modifier mixture. Under these conditions, and using a pyrolysis temperature of 800 degrees C, essentially no background absorption was observed with an atomization temperature of 1600 degrees C. About 2 mg of sample have been typically used for SS, although as much as 3-5 mg could have been introduced. In the case of SlS multiple injections had to be used to achieve the sensitivity required for this determination. Calibration against aqueous standards was feasible for both methods. The characteristic mass obtained with SS was 0.6 pg, and that with SlS was 1.0 pg. The limits of detection were 0.4 and 0.7 ng g(-1), the limits of quantification were 1.3 and 2.3 ng g(-1) and the relative standard deviation (n=5) was 6-16% and 9-23% for SS and SlS, respectively. The accuracy was confirmed by the analysis of certified reference materials. The two methods were applied for the determination of cadmium in six wheat flour samples acquired in supermarkets of different Brazilian cities. The cadmium content varied between 8.9+/-0.5 and 13+/-2 ng g(-1) (n=5). Direct SS gave results similar to those obtained with SlS using multi-injections; the values of both techniques showed no statistically significant difference at the 95% confidence level. Direct SS was finally adopted as the method of choice, due to its greater simplicity, the faster speed of analysis and the better figures of merit.
直接固体进样分析(SS)和悬浮液进样(SlS)。除了常规的钯和硝酸镁混合改性剂(10μg钯 + 3μg镁)外,还添加了0.05%(v/v)的 Triton X - 100以提高改性剂溶液渗入固体样品的能力,并添加了0.1%的H₂O₂以促进SS的原位消解。对于SlS,使用30μg钯、12μg镁和0.05%(v/v)的Triton X - 100作为改性剂混合物。在这些条件下,使用800℃的热解温度,在1600℃的原子化温度下基本未观察到背景吸收。对于SS,通常使用约2mg样品,尽管最多可引入3 - 5mg。在SlS的情况下,必须使用多次进样才能达到该测定所需的灵敏度。两种方法均可行以水标准溶液进行校准。SS获得的特征质量为0.6pg,SlS为1.0pg。检测限分别为0.4和0.7ng g⁻¹,定量限分别为1.3和2.3ng g⁻¹,SS和SlS的相对标准偏差(n = 5)分别为6 - 16%和9 - 23%。通过分析有证标准物质确认了准确性。这两种方法用于测定在巴西不同城市超市采集的六个小麦粉样品中的镉。镉含量在8.9±0.5和13±2ng g⁻¹之间(n = 5)。直接SS得到的结果与多次进样的SlS相似;两种技术的值在95%置信水平下无统计学显著差异。由于直接SS更简单、分析速度更快且性能指标更好,最终被选为首选方法。