An integrated multimethod approach for size-specific assessment of potentially toxic element adsorption onto micro- and nanoplastics: implications for environmental risk†

IF 5.1 3区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Nanoscale Pub Date : 2025-03-11 DOI:10.1039/D5NR00353A
Swaroop Chakraborty, Roland Drexel, Prathmesh Bhadane, Nathan Langford, Pankti Dhumal, Florian Meier and Iseult Lynch
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Abstract

Micro- and nanoscale plastics (MnPs), arising from the environmental degradation of plastic waste, pose significant environmental and health risks as carriers for potentially toxic element (PTE) metals. This study employs asymmetrical flow field-flow fractionation (AF4) coupled with multi-angle light scattering (MALS) and inductively coupled plasma mass spectrometry (ICP-MS) to provide a size-resolved assessment of chromium (Cr), arsenic (As), and selenium (Se) adsorption onto carboxylated polystyrene nanoparticles (COOH-PSNPs) of 100 nm, 500 nm, and 1000 nm. Cr exhibited the highest adsorption, with adsorption per particle surface area increasing from 9.45 × 10−15 μg nm−2 for 100 nm particles to 6.87 × 10−14 μg nm−2 for 1000 nm particles, driven by chemisorptive interactions with carboxyl groups. In contrast, As and Se exhibited slower adsorption rates and significantly weaker interactions, attributed to outer-sphere complexation and electrostatic repulsion. Smaller particles exhibited enhanced adsorption efficiency per unit mass due to their larger surface area-to-volume ratios and higher carboxyl group density (18.5 μEq g−1 for 100 nm compared to 7.9 μEq g−1 for 1000 nm particles). Se adsorption remained negligible across all sizes, near detection limits, highlighting its low affinity for carboxylated surfaces. Our study demonstrates the superior resolution of AF4-MALS-ICP-MS compared to that of bulk ICP-MS, which lacks the ability to discern particle-specific adsorption trends. Unlike bulk ICP-MS, which provides average adsorption values, AF4-MALS-ICP-MS reveals the size-dependent mechanisms influencing metal binding, offering critical insights into the role of MnPs as PTE vectors. The findings highlight the environmental implications of MnPs in facilitating PTE transport and highlights the need for size-specific mitigation strategies. This work sets a foundation for developing more precise risk assessment frameworks and advanced remediation approaches for MnP-contaminated environments.

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微塑料和纳米塑料吸附潜在有毒元素的综合多方法评估:对环境风险的影响
塑料废弃物环境降解产生的微米级和纳米级塑料(MnPs)作为潜在有毒元素(PTEs)金属的载体,对环境和健康构成了重大风险。本研究采用非对称流场-流分馏(AF4)结合多角度光散射(MALS)和电感耦合等离子体质谱法(ICP-MS),对 100 nm、500 nm 和 1000 nm 的羧基聚苯乙烯纳米颗粒(COOH-PSNPs)上的铬(Cr)、砷(As)和硒(Se)吸附进行了粒度分辨评估。在与羧基的化学吸附作用的驱动下,铬的吸附量最高,单位颗粒表面积的吸附量从 100 纳米颗粒的 9.45 × 10-¹⁵ µg/nm² 增加到 1000 纳米颗粒的 6.87 × 10-¹⁴ µg/nm²。相比之下,砷和硒的吸附速度较慢,相互作用明显较弱,这归因于外球复合和静电排斥作用。较小的颗粒由于表面积与体积比更大,羧基密度更高(100 nm 的颗粒为 18.5 μEq/g,而 1000 nm 的颗粒为 7.9 μEq/g),因此单位质量的吸附效率更高。在所有尺寸的颗粒中,硒的吸附量仍然微乎其微,接近检测极限,这表明硒对羧基化表面的亲和力较低。我们的研究表明,AF4-MALS-ICP-MS 的分辨率优于大体积 ICP-MS,后者缺乏辨别特定颗粒吸附趋势的能力。与提供平均吸附值的大容量 ICP-MS 不同,AF4-MALS-ICP-MS 揭示了影响金属结合的尺寸依赖机制,为了解 MnPs 作为 PTEs 载体的作用提供了重要见解。研究结果强调了 MnPs 在促进 PTEs 迁移过程中对环境的影响,并强调需要制定针对具体尺寸的减缓策略。这项工作为制定更精确的风险评估框架和针对 MnP 污染环境的先进修复方法奠定了基础。
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来源期刊
Nanoscale
Nanoscale CHEMISTRY, MULTIDISCIPLINARY-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
12.10
自引率
3.00%
发文量
1628
审稿时长
1.6 months
期刊介绍: Nanoscale is a high-impact international journal, publishing high-quality research across nanoscience and nanotechnology. Nanoscale publishes a full mix of research articles on experimental and theoretical work, including reviews, communications, and full papers.Highly interdisciplinary, this journal appeals to scientists, researchers and professionals interested in nanoscience and nanotechnology, quantum materials and quantum technology, including the areas of physics, chemistry, biology, medicine, materials, energy/environment, information technology, detection science, healthcare and drug discovery, and electronics.
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