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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 μg nm for 100 nm particles to 6.87 × 10 μg nm 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 for 100 nm compared to 7.9 μEq g 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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http://dx.doi.org/10.1039/d5nr00353a | DOI Listing |
ACS Nano
September 2025
Eastern Institute for Advanced Study, Eastern Institute of Technology, Ningbo, Zhejiang 315200, P. R. China.
Ni-Fe (oxy)hydroxides are among the most active oxygen evolution reaction (OER) catalysts in alkaline media. However, achieving precise control over local asymmetric Fe-O-Ni active sites in Ni-Fe oxyhydroxides for key oxygenated intermediates' adsorption steric configuration regulation of the OER is still challenging. Herein, we report a two-step dealloying strategy to fabricate asymmetric Fe-O-Ni pair sites in the shell of NiOOH@FeOOH/NiOOH heterostructures from NiFe Prussian blue analogue (PBA) nanocubes, involving anion exchange and structure reconstruction.
View Article and Find Full Text PDFJ Phys Chem A
September 2025
Department of Basic Science, School of Arts and Sciences, The University of Tokyo, Komaba, Meguro, Tokyo 153-8902, Japan.
Desorption processes of HO molecules from AlO(HO) ( = 3, 5, 7) and AlO(HO)H ( = 4, 6, 8) clusters were investigated using gas-phase thermal desorption spectrometry to evaluate the HO storage capacity and mechanisms of aluminum oxide clusters. The clusters stored approximately 10 HO molecules at ∼300 K, depending on the size (), and released them upon heating. Even after heating to ∼1000 K, 2-4 HO molecules remained bound.
View Article and Find Full Text PDFNano Lett
September 2025
School of Materials and Chemistry, University of Shanghai for Science & Technology, Shanghai 200093, China.
Developing low-temperature gas sensors for parts per billion-level acetone detection in breath analysis remains challenging for non-invasive diabetes monitoring. We implement dual-defect engineering via one-pot synthesis of Al-doped WO nanorod arrays, establishing a W-O-Al catalytic mechanism. Al doping induces lattice strain to boost oxygen vacancy density by 31.
View Article and Find Full Text PDFMikrochim Acta
September 2025
Department of Public Health Laboratory Sciences, College of Public Health, Hengyang Medical School, University of South China, 28 Changsheng West Road, Hengyang, 421001, Hunan, China.
We systematically evaluated the DNA adsorption and desorption efficiencies of several nanoparticles. Among them, titanium dioxide (TiO₂) nanoparticles (NPs), aluminum oxide (Al₂O₃) NPs, and zinc oxide (ZnO) NPs exhibited strong DNA-binding capacities under mild conditions. However, phosphate-mediated DNA displacement efficiencies varied considerably, with only TiO₂ NPs showing consistently superior performance.
View Article and Find Full Text PDFMikrochim Acta
September 2025
Key Laboratory of Water Security and Water Environment Protection in Plateau Intersection (NWNU), Ministry of Education, Northwest Normal University, Lanzhou, 730070, China.
An electrochemical sensor based on MXene/PANI/SnO nanomaterials was developed for the detection of 4-aminophenol (4-AP). In situ oxidative growth of PANI on the MXene surface effectively hindered the stacking of the lamellae and increased the specific surface area of the composites. Further complexation of tin dioxide with swelling properties of the structure provided adsorption and catalytic sites for 4-AP.
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