Krawczyk-Coda Magdalena, Stanisz Ewa
Faculty of Chemical Technology, Poznan University of Technology, Berdychowo 4, 60-965, Poznań, Poland.
Anal Bioanal Chem. 2017 Nov;409(27):6439-6449. doi: 10.1007/s00216-017-0589-y. Epub 2017 Aug 29.
This work presents ultrasound-assisted dispersive micro solid phase extraction (USA DMSPE) for preconcentration of fluorine (F) in water and herb samples. TiO nanoparticles (NPs) were used as an adsorbent. The determination with slurry sampling was performed via molecular absorption of calcium monofluoride (CaF) at 606.440 nm using a high-resolution continuum source electrothermal absorption spectrometry (HR-CS ET MAS). Several factors influencing the efficiency of the preconcentration technique, such as the amount of TiO, pH of sample solution, ultrasonication and centrifugation time and TiO slurry solution preparation before injection to HR-CS ET MAS, were investigated in detail. The conditions of detection step (wavelength, calcium amount, pyrolysis and molecule-forming temperatures) were also studied. After extraction, adsorbent with the analyte was mixed with 200 μL of HO to prepare a slurry solution. The concentration limit of detection was 0.13 ng mL. The achieved preconcentration factor was 7. The relative standard deviations (RSDs, %) for F in real samples were 3-15%. The accuracy of this method was evaluated by analyses of certified reference materials after spiking: INCT-MPH-2 (Mixed Polish Herbs), INCT-SBF-4 (Soya Bean Flour), ERM-CAO11b (Hard Drinking Water) and TMDA-54.5 (Lake Ontario Water). The measured F contents in reference materials were in satisfactory agreement with the added amounts, and the recoveries were found to be 97-109%. Under the developed extraction conditions, the proposed method has been successfully applied for the determination of F in real water samples (lake, sea, tap water) and herbs.
本研究提出了一种用于预富集水和草药样品中氟(F)的超声辅助分散微固相萃取(USA DMSPE)方法。使用二氧化钛纳米颗粒(NPs)作为吸附剂。采用高分辨率连续光源电热吸收光谱法(HR-CS ET MAS),通过在606.440 nm处对一氟化钙(CaF)进行分子吸收,以悬浮液进样方式进行测定。详细研究了影响预富集技术效率的几个因素,如二氧化钛的用量、样品溶液的pH值、超声处理和离心时间以及将二氧化钛悬浮液注入HR-CS ET MAS之前的制备方法。还研究了检测步骤的条件(波长、钙含量、热解温度和分子形成温度)。萃取后,将吸附有分析物的吸附剂与200 μL水混合以制备悬浮液。检测限为0.13 ng/mL。实现的预富集因子为7。实际样品中氟的相对标准偏差(RSDs,%)为3-15%。通过对加标后的有证标准物质(INCT-MPH-2(波兰混合草药)、INCT-SBF-4(大豆粉)、ERM-CAO11b(硬饮用水)和TMDA-54.5(安大略湖水))进行分析,评估了该方法的准确性。标准物质中氟的测定含量与添加量吻合良好,回收率为97-109%。在优化后的萃取条件下,该方法已成功应用于实际水样(湖水、海水、自来水)和草药中氟的测定。