School of Veterinary Medicine and Animal Science, São Paulo State University (UNESP), Botucatu, Brazil.
Institute of Biosciences, São Paulo State University (UNESP), Botucatu, Brazil.
Biol Trace Elem Res. 2018 Aug;184(2):517-522. doi: 10.1007/s12011-017-1212-y. Epub 2017 Dec 2.
This paper presents a slurry sampling method for total mercury determination by graphite furnace atomic absorption spectrometry (GFAAS) in tissue of fish from the Amazon. The tissue samples were lyophilized and macerated, and then the slurry samples were prepared by putting 20 mg of tissue, added to a solution containing Triton X-100, Suprapur HNO, and zirconium nitrate directly in sampling vials of a spectrometer. Mercury standard solutions were prepared under the same conditions as the slurry samples. The slurry samples and the mercury standard solutions were sonicated for 20 s. Twenty microliters of slurry samples were injected into the graphite tube, which contained an internal wall lined with tungsten carbide. Under these conditions, it was possible to thermally stabilize the mercury up to an atomization temperature of 1700 °C. The method was validated by mercury determination in reference materials DORM-4 and DOLT-4. The LOD and LOQ were 0.014 and 0.045 mg kg, respectively, and recovery percentages in relation to the concentration values were certified in the order of 98%.
本文提出了一种用于通过石墨炉原子吸收光谱法(GFAAS)测定亚马逊鱼类组织中总汞的浆体采样方法。将组织样品冻干并粉碎,然后将 20mg 组织加入含有 Triton X-100、Suprapur HNO 和硝酸氧锆的溶液中,直接放入光谱仪的采样小瓶中制备浆体样品。汞标准溶液在与浆体样品相同的条件下制备。将浆体样品和汞标准溶液超声处理 20 秒。将 20 微升浆体样品注入含有碳化钨内涂层的石墨管中。在这些条件下,可以将汞热稳定至 1700°C 的原子化温度。通过对参考材料 DORM-4 和 DOLT-4 中的汞进行测定来验证该方法。LOD 和 LOQ 分别为 0.014 和 0.045mgkg,与浓度值相关的回收率百分比在 98%的范围内得到了认证。