Bertoldi Crislaine, Pucetaite Milda, Hansson Maria C, Troein Carl, van Praagh Martijn
Centre for Environmental and Climate Science (CEC), Lund University, Lund, Sweden.
Department of Biology, Lund University, Lund, Sweden.
J Hazard Mater. 2025 Sep 15;496:139448. doi: 10.1016/j.jhazmat.2025.139448. Epub 2025 Aug 4.
Microplastics (MPs) in biosolids used as soil amendments are of growing concern. The purpose of this study was to improve the characterization of MPs in complex biosolid matrices by optimizing sample preparation for morphological and chemical analyses with different spectroscopic techniques. We compared extraction procedures involving Fenton oxidation (F), Fenton plus sodium dodecyl sulfate (SDS), and Fenton plus cellulase (FE). We performed partial particle sample counting along with a helical shape, corresponding to 56 % of sample area, and total particle counting. Chemical characterization was performed using sub-micron optical-photothermal infrared (O-PTIR) spectroscopy, and the results were compared with those obtained via commonly employed Raman and Fourier transform infrared absorption microspectroscopy technique (µ-FTIR). Our FE protocol yielded a slightly higher total sample mass removal (97 %±0.3 %) compared to other pre-treatment methods. No significant difference was observed in the total MPs count between the two approaches, indicating a homogeneous distribution across the filter and supporting reliable quantification using only half the filter in the helical method. O-PTIR's high spatial resolution (down to 0.5 µm) and absence of spectral artefacts compared to Raman and µ-FTIR enabled accurate identification of fine fibers (2 µm wide) and small particles (∼5 µm). Single-frequency O-PTIR imaging revealed well-defined particles clearly separated from their surroundings, highlighting the technique's potential for particle identification. The findings highlight the need to combine effective sample pre-treatment with high-resolution chemical analysis to improve understanding of plastic fate in the environment and supporting future policy development or regulatory updates on plastic content in biosolids.
用作土壤改良剂的生物固体中的微塑料(MPs)日益受到关注。本研究的目的是通过优化用于不同光谱技术的形态和化学分析的样品制备,改进复杂生物固体基质中微塑料的表征。我们比较了涉及芬顿氧化(F)、芬顿加十二烷基硫酸钠(SDS)和芬顿加纤维素酶(FE)的提取程序。我们进行了部分颗粒样品计数以及对应于样品面积56%的螺旋形状计数和总颗粒计数。使用亚微米光热红外(O-PTIR)光谱进行化学表征,并将结果与通过常用的拉曼光谱和傅里叶变换红外吸收显微光谱技术(µ-FTIR)获得的结果进行比较。与其他预处理方法相比,我们的FE方案产生的总样品质量去除率略高(97%±0.3%)。两种方法之间在微塑料总数上没有观察到显著差异,这表明在过滤器上分布均匀,支持在螺旋法中仅使用过滤器的一半进行可靠定量。与拉曼光谱和µ-FTIR相比,O-PTIR的高空间分辨率(低至0.5 µm)和无光谱伪像能够准确识别细纤维(2 µm宽)和小颗粒(约5 µm)。单频O-PTIR成像显示出与周围环境清晰分离的明确颗粒,突出了该技术在颗粒识别方面的潜力。研究结果强调需要将有效的样品预处理与高分辨率化学分析相结合,以更好地了解塑料在环境中的归宿,并为未来关于生物固体中塑料含量的政策制定或监管更新提供支持。