Hendriks Lyndsey, Egger Matthias, Mitrano Denise M
Institute of Analytical Chemistry, University of Vienna Währingerstraße 38 1090 Vienna Austria
The Ocean Cleanup Coolsingel 6 3011 AD Rotterdam The Netherlands.
J Anal At Spectrom. 2025 Sep 8. doi: 10.1039/d5ja00223k.
Plastic pollution in marine environments poses ecological risks, in part because plastic debris can release hazardous substances, such as metal-based additives. While microplastics have received considerable attention as vectors of contaminants, less is known about larger macroplastics and their role in the spatial and temporal redistribution of substances. In this study, pristine, store-bought plastic items and macroplastics recovered from the North Pacific Subtropical Gyre (NPSG) were analysed using Fourier-Transform Infrared Spectroscopy (FTIR) to identify polymer types, and bulk acid digestion followed by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) for total metal quantification. These techniques were complemented by high resolution elemental mapping by Laser Ablation Inductively Coupled Plasma Time-of-Flight Mass Spectrometry (LA-ICP-TOFMS). Detailed elemental maps revealed native metal distribution in pristine plastics, and evidence of both sorption and intrinsic metal depletion in weathered plastics. In particular, weathered plastics showed surface depletion of intrinsic metals, and enrichment of seawater-derived elements (, Na, Mg, I). Linear regressions were used to quantify spatial distribution trends across cross sections, providing statistical support for directional gradients. Since pristine and weathered plastics were opportunistically collected, variability in product type, polymer chemistry, and weathering time limited direct comparisons. Instead, this study demonstrates the utility of LA-ICP-TOFMS for mapping elemental distribution in plastics, offering a novel analytical approach for investigating spatial metal distribution in plastics and laying the groundwork for future studies on weathering processes in marine environments.
海洋环境中的塑料污染带来了生态风险,部分原因是塑料碎片会释放有害物质,如金属基添加剂。虽然微塑料作为污染物载体已受到广泛关注,但对于较大的宏观塑料及其在物质时空再分配中的作用,人们了解较少。在本研究中,使用傅里叶变换红外光谱(FTIR)分析了从北太平洋亚热带环流(NPSG)回收的原始的、从商店购买的塑料物品和宏观塑料,以确定聚合物类型,并采用酸消解后电感耦合等离子体质谱(ICP-MS)进行总金属定量分析。这些技术通过激光烧蚀电感耦合等离子体飞行时间质谱(LA-ICP-TOFMS)进行的高分辨率元素映射得到补充。详细的元素图谱揭示了原始塑料中的天然金属分布,以及风化塑料中吸附和固有金属消耗的证据。特别是,风化塑料显示出固有金属的表面消耗以及海水来源元素(如氯、钠、镁、碘)的富集。使用线性回归来量化横截面的空间分布趋势,为方向梯度提供统计支持。由于原始塑料和风化塑料是机会性收集的,产品类型、聚合物化学和风化时间的变异性限制了直接比较。相反,本研究证明了LA-ICP-TOFMS在绘制塑料中元素分布方面的实用性,为研究塑料中金属的空间分布提供了一种新颖的分析方法,并为未来海洋环境中风化过程的研究奠定了基础。