Gao Xingsu, Dai Jiayong, Zhao Hongyan, Zhu Jun, Luo Lan, Zhang Rui, Zhang Zhan, Li Lei
Department of Hygiene Analysis and Detection, School of Public Health, Nanjing Medical University 101 Longmian Avenue Nanjing 211166 Jiangsu P. R. China
Nanjing Entry-exit Inspection and Quarantine Bureau 110 Jiangjun Avenue Nanjing 211106 Jiangsu P. R. China.
RSC Adv. 2018 May 18;8(33):18364-18371. doi: 10.1039/c8ra01891j. eCollection 2018 May 17.
Mercury species have aroused wide concern in the past several decades due to their high toxicity. However, it is still difficult to detect ultra-trace mercury species due to their biochemical transformation in complex samples. To establish a simpler and more sensitive method for pre-concentration and determination of trace mercury species, molybdenum disulfide (MoS) nanosheets with sulfur-rich characteristics and enlarged interlayer spacing were prepared by a hydrothermal method coupled with a sonication-assisted liquid exfoliation method and acted as solid-phase extraction adsorbent. The nano-MoS had high adsorption capacity, fast adsorption rate and excellent selectivity towards mercury ions (Hg), methyl mercury (MeHg) and ethyl mercury (EtHg) in a wide pH range and complex matrices. And it could be easily regenerated by 4 mol L HCl and reused several times. After optimizing HPLC-UV-HG-AFS conditions, a great linearity (1.0-10.0 μg L, = 0.999 for Hg, MeHg and EtHg), lower detection limits (0.017, 0.037 and 0.021 ng mL for Hg, MeHg and EtHg, respectively), relative standard deviations (<5%) and addition recoveries of the samples within 82.75-113.38% were observed. In summary, trace inorganic and organic mercury species in environmental and biological samples could be selectively enriched by the prepared nano-MoS and efficiently seperated and detected by HPLC-UV-HG-AFS. The present study will help provide a better strategy for environmental monitoring and health assessment of mercury pollutants.
在过去几十年中,汞物种因其高毒性而引起了广泛关注。然而,由于其在复杂样品中的生化转化,超痕量汞物种的检测仍然困难。为了建立一种更简单、更灵敏的痕量汞物种预浓缩和测定方法,采用水热法结合超声辅助液体剥离法制备了具有富硫特性和扩大层间距的二硫化钼(MoS)纳米片,并将其用作固相萃取吸附剂。纳米MoS在较宽的pH范围和复杂基质中对汞离子(Hg)、甲基汞(MeHg)和乙基汞(EtHg)具有高吸附容量、快速吸附速率和优异的选择性。并且它可以很容易地用4 mol L盐酸再生并重复使用几次。优化高效液相色谱-紫外-氢化物发生-原子荧光光谱(HPLC-UV-HG-AFS)条件后,观察到Hg、MeHg和EtHg具有良好的线性关系(1.0-10.0 μg L,Hg、MeHg和EtHg的相关系数均为0.999)、较低的检测限(Hg、MeHg和EtHg分别为0.017、0.037和0.021 ng mL)、相对标准偏差(<5%)以及样品加标回收率在82.75-113.38%之间。综上所述,环境和生物样品中的痕量无机和有机汞物种可以通过制备的纳米MoS进行选择性富集,并通过HPLC-UV-HG-AFS进行有效分离和检测。本研究将有助于为汞污染物的环境监测和健康评估提供更好的策略。