Institute of Environmental Research at Greater Bay Area, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, People's Republic of China.
School of Environmental Science and Engineering, Shandong University, Jinan 250100, People's Republic of China.
Anal Chem. 2020 Apr 7;92(7):4765-4770. doi: 10.1021/acs.analchem.0c00262. Epub 2020 Feb 28.
Toxicity and transport of metal-based nanoparticles (M-NPs) in environmental waters strongly depend on their speciation. A detailed understanding of the composition and speciation of M-NPs is necessary in order to move this field forward. Unfortunately, there is a shortage of analytical methods for metal-sulfide nanoparticles (MS-NPs) in the environment. In this work, a cloud point extraction (CPE) method combined with liquid chromatography hyphenated to inductively coupled plasma mass spectrometry (LC-ICPMS) is developed for sensitive determination of AgS- and ZnS-NPs. Under the condition of 0.15% (w/v) of Triton X-114 (TX-114), pH 5, 20 mM NaNO, incubation temperature of 45 °C, and time of 15 min, MS-NPs and non-MS-NPs were extracted into the surfactant-rich phase. With the sequent addition of 10 mM bis(p-sulfonatophenyl)phenylphosphane dehydrate dipotassium (BSPP) aqueous solution (100 μL) into the CPE-obtained extract, the non-MS-NPs were selectively dissociated into their ionic counterparts while maintaining the original size and shape of AgS- and ZnS-NPs. Interestingly, the micelle-mediated behavior suddenly disappeared with the addition of BSPP. Thus, the extract can be injected to LC-ICPMS for speciation analysis of trace AgS- and ZnS-NPs. This method exhibited excellent reproducibility (relative standard deviations < 4.9%), high sensitivity with the respective detection limits of 8 ng/L for AgS-NPs and 15 ng/L for ZnS-NPs, enabling recoveries of 81.3-96.6% for AgS-NPs and 83.9-93.5% for ZnS-NPs when they were spiked into three environmental water samples. Due to its potential applicability to low concentrations of AgS- and ZnS-NPs, this method is particularly convenient for monitoring the transformations of AgNPs and ZnO-NPs in the environment.
金属基纳米粒子(M-NPs)在环境水中的毒性和迁移强烈依赖于其形态。为了推动该领域的发展,需要详细了解 M-NPs 的组成和形态。不幸的是,环境中金属硫化物纳米粒子(MS-NPs)的分析方法还很缺乏。在这项工作中,开发了一种浊点萃取(CPE)方法,结合液相色谱与电感耦合等离子体质谱(LC-ICPMS),用于灵敏测定 AgS-和 ZnS-NPs。在 0.15%(w/v)Triton X-114(TX-114)、pH5、20mMNaNO3、45°C 孵育温度和 15min 时间的条件下,MS-NPs 和非 MS-NPs 被萃取到表面活性剂富相。随后,向 CPE 获得的提取物中加入 10mM 双(对磺酸盐苯基)二苯基膦二钾盐(BSPP)水溶液(100μL),非 MS-NPs 被选择性地解离成其离子对应物,同时保持 AgS-和 ZnS-NPs 的原始大小和形状。有趣的是,随着 BSPP 的加入,胶束介导的行为突然消失。因此,提取物可以注入 LC-ICPMS 进行痕量 AgS-和 ZnS-NPs 的形态分析。该方法表现出良好的重现性(相对标准偏差<4.9%)和高灵敏度,AgS-NPs 的检测限为 8ng/L,ZnS-NPs 的检测限为 15ng/L,当 AgS-NPs 和 ZnS-NPs 分别被加入到三种环境水样中时,回收率为 81.3-96.6%和 83.9-93.5%。由于其对低浓度 AgS-和 ZnS-NPs 的潜在适用性,该方法特别方便用于监测 AgNPs 和 ZnO-NPs 在环境中的转化。