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深共晶溶剂液相微萃取-非水相氢化物发生原子荧光光谱法测定无机砷

Determination of Inorganic Arsenic Using Non-Aqueous Hydride Generation–Atomic Fluorescence Spectrometry Coupled with Deep Eutectic Solvent-Based Liquid Phase Microextraction

  • 摘要: 分析水体等环境介质和生物样品中砷的含量及其赋存状态,对于地质灾害预警、生态安全评估等具有重要意义。传统氢化物发生原子荧光光谱法存在过渡金属离子干扰、还原剂溶液不稳定等问题,而对于砷价态的分析,通常离不开离子色谱柱和相关联用仪器,限制了其广泛应用和发展。本文利用吡咯烷二硫代氨基甲酸铵(APDC)选择性络合As(Ⅲ),并借助超声辅助将APDC-As(Ⅲ)络合物萃取至制备的疏水性深共晶溶剂中,在样品富集的同时,消除了潜在的过渡金属离子干扰,进一步通过固体硼氢化钾粉末直接还原萃取的As(Ⅲ),建立了一种超声辅助液液微萃取(UA-DLLME)-氢化物发生原子荧光光谱法测定砷的高灵敏新方法。首先以百里香酚、薄荷醇和氯化胆碱为氢键受体(HBAs),正辛酸、癸酸和月桂酸为氢键供体(HBDs),制备并筛选了疏水性和稳定性良好的共晶溶剂用于无机砷的萃取,进一步优化了影响微萃取和氢化物发生过程的各项参数。在选定的实验条件下,该方法对砷的检出限低至0.02ng/mL,增强因子为72。以1% L-抗坏血酸和硫脲还原样品中的As(Ⅴ)后,采用该法测定无机砷总量,结合差减法计算得到As(Ⅴ)含量,从而实现无机砷的价态分析。采用砷含量标准参考物质验证了方法的准确性,测定值与参考值吻合,同时对乌木泉水(四川)、瓶装水、自来水和白醋等实际样品中的无机砷进行测定,加标回收率为96.0%~104%。该法在环境水样和生物样品的无机砷测定中具有潜在应用前景。

     

    Abstract: The analysis of arsenic content and its speciation in environmental media such as water and biological samples is of great significance to the early warning of geological disaster and ecological safety assessment. Traditional hydride generation atomic fluorescence spectrometry (HG-AFS) suffers from severe interference from transition metal ions and instability of the reductant solution. For the analysis of arsenic valence states, ion chromatography columns and coupled instruments are usually required, which limits its wide application and development. Here, ammonium pyrrolidine dithiocarbamate (APDC) was used to selectively extract As(Ⅲ), and the formed APDC-As(Ⅲ) complex was extracted into the prepared hydrophobic deep eutectic solvent with the assistance of ultrasound. Enrichment of the analyte was achieved while potential interference from transition metal ions was eliminated. Furthermore, solid potassium borohydride powder was directly used to reduce the extracted As(Ⅲ), establishing a new and highly sensitive method for arsenic determination. Firstly, using thymol, menthol and choline chloride as hydrogen bond acceptors (HBAs), and n-octanoic acid, decanoic acid and lauric acid as hydrogen bond donors (HBDs), deep eutectic solvents with good hydrophobicity and stability were prepared and screened for the extraction of inorganic arsenic. The parameters affecting the microextraction and hydride generation process were further optimized. Under the selected experimental conditions, the detection limit of this method for arsenic was as low as 0.02ng/mL, with an enhancement factor of 72. After reducing As(Ⅴ) in the sample with 1% L-ascorbic acid and thiourea, the total inorganic arsenic was determined, and the content of As(Ⅴ) was calculated by the difference, thereby achieving the speciation analysis of inorganic arsenic. The accuracy of the method was verified by certified reference materials, and the measured values were in good agreement with the certified values. Meanwhile, the inorganic arsenic in actual samples such as Wumu spring water (Sichuan), bottled water, tap water and white vinegar was determined, with recoveries of 96.0%–104.0%. This method has potential application prospects in the determination of inorganic arsenic in environmental water samples and biological samples.

     

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