Department of Chemistry, Aarhus University, Langelandsgade 140, 8000, Aarhus, Denmark.
Department of Chemistry, Aarhus University, Langelandsgade 140, 8000, Aarhus, Denmark.
J Chromatogr A. 2024 Feb 22;1717:464622. doi: 10.1016/j.chroma.2023.464622. Epub 2024 Jan 5.
Microplastic is ubiquitous in the environment. Recently it was discovered that microplastic (MP, 1 μm-5 mm) contamination is present in the atmosphere where it can be transported over long distances and introduced to remote pristine environments. Sources, concentration levels, and transportation pathways of MP are still associated with large uncertainties. The abundance of atmospheric MP increases with decreasing particle size, suggesting that nanoplastics (NP, <1μm) could be of considerable atmospheric relevance. Only few analytical methods are available for detection of nanosized plastic particles. Thermoanalytical techniques are independent of particle size and are thus a powerful tool for MP and NP analysis. Here we develop a method for analysis of polystyrene on the nanogram scale using pyrolysis gas chromatography coupled to mass spectrometry. Pyrolysis was performed using a slow temperature ramp, and analytes were cryofocused prior to injection. The mass spectrometer was operated in selected ion monitoring (SIM) mode. A lower limit of detection of 1±1 ng and a lower limit of quantification of 2±2 ng were obtained (for the trimer peak). The method was validated with urban matrices of low (7 μg per sample) and high (53 μg per sample) aerosol mass loadings. The method performs well for low loadings, whereas high loadings seem to cause a matrix effect reducing the signal of polystyrene. This effect can be minimized by introducing a thermal desorption step prior to pyrolysis. The study provides a novel analysis method for qualitative and semi-quantitative analysis of PS on the nanogram scale in an aerosol matrix. Application of the method can be used to obtain concentration levels of polystyrene in atmospheric MP and NP. This is important in order to improve the understanding of the sources and sinks of MP and NP in the environment and thereby identify routes of exposure and uptake of this emerging contaminant.
微塑料在环境中无处不在。最近发现,微塑料(MP,1μm-5mm)污染存在于大气中,可以远距离传输,并引入到偏远的原始环境中。MP 的来源、浓度水平和传输途径仍存在很大的不确定性。大气中 MP 的丰度随着粒径的减小而增加,这表明纳米塑料(NP,<1μm)可能具有相当大的大气相关性。目前只有少数分析方法可用于检测纳米级塑料颗粒。热分析技术不依赖于颗粒尺寸,因此是分析 MP 和 NP 的有力工具。在这里,我们开发了一种使用热解气相色谱-质谱联用仪分析聚苯乙烯的方法,可对纳克级的聚苯乙烯进行分析。采用缓慢的升温速率进行热解,在进样前对分析物进行低温聚焦。质谱仪以选择离子监测(SIM)模式运行。获得了 1±1ng 的检测下限和 2±2ng 的定量下限(三聚物峰)。该方法用低(每个样品 7μg)和高(每个样品 53μg)气溶胶质量负荷的城市基质进行了验证。该方法对低负荷表现良好,而高负荷似乎会由于基质效应而降低聚苯乙烯的信号。通过在热解前引入热解吸步骤,可以最小化这种影响。该研究提供了一种在气溶胶基质中定性和半定量分析 PS 的纳米级分析方法。该方法的应用可以用来获得大气中 MP 和 NP 中聚苯乙烯的浓度水平。这对于提高对 MP 和 NP 环境来源和汇的理解以及确定这种新兴污染物的暴露和吸收途径非常重要。