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Particulate matter (PM) is emitted during thermal decomposition of waste. During this process, aromatic compounds chemisorb to the surface of metal-oxide-containing PM, forming a surface-stabilized environmentally persistent free radical (EPFR). We hypothesized that EPFR-containing PM redox cycle to produce ROS and that this redox cycle is maintained in biological environments. To test our hypothesis, we incubated model EPFRs with the fluorescent probe dihydrorhodamine (DHR). Marked increases in DHR fluorescence were observed. Using a more specific assay, hydroxyl radicals ((•)OH) were also detected, and their level was further increased by cotreatment with thiols or ascorbic acid (AA), known components of epithelial lining fluid. Next, we incubated our model EPFR in bronchoalveolar lavage fluid (BALF) or serum. Detection of EPFRs and (•)OH verified that PM generate ROS in biological fluids. Moreover, incubation of pulmonary epithelial cells with EPFR-containing PM increased (•)OH levels compared to those in PM lacking EPFRs. Finally, measurements of oxidant injury in neonatal rats exposed to EPFRs by inhalation suggested that EPFRs induce an oxidant injury within the lung lining fluid and that the lung responds by increasing antioxidant levels. In summary, our EPFR-containing PM redox cycle to produce ROS, and these ROS are maintained in biological fluids and environments. Moreover, these ROS may modulate toxic responses of PM in biological tissues such as the lung.
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http://dx.doi.org/10.1021/tx400227s | DOI Listing |
J Hazard Mater
September 2025
Shandong Key Laboratory of Water Pollution Control and Resource Reuse, Shandong Key Laboratory of Environmental Processes and Health, School of Environmental Science and Engineering, Shandong University, Qingdao 266237, China. Electronic address:
Advanced oxidation processes (AOPs) are among the most effective methods for industrial wastewater treatment, but their applications to remove trace organic contaminants (TrOCs) are hampered by a lack of "selectivity". Here, an AOP was established using Cr(III) to activate periodate (PI) (Cr(III)/PI system) realizing rapid TrOCs removal, in which 2 μM tetracycline hydrochloride was completely degraded within 8 min (with 29 μM Cr(III) and 30 μM PI, pH 8). Mechanism analysis revealed the positive effect of Cr(III) complexation on enhancing both the efficiency and selectivity of TrOCs removal.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemistry, Jadavpur University, Kolkata - 700032, India.
An interesting ruthenium(III) complex, -[Ru(HL)Cl(PPh)], has been synthesized using a redox-active tetradentate bis-azo diamine ligand (HL). This complex represents the first example of a structurally robust, air- and moisture-stable coordination compound featuring a redox non-innocent ligand that provides a unique N4 donor set comprising both strong π-acidic (azo) and σ-donating (amido) groups. The complex has been comprehensively characterized by elemental analysis, various spectroscopic techniques, and single-crystal X-ray diffraction (SCXRD) studies.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
School of Integrated Circuits, State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Huazhong University of Science and Technology, Wuhan, 430074, China.
Low-temperature rechargeable batteries face great challenges due to the sluggish reaction kinetics. Redox covalent organic frameworks (COFs) with porous structures provide a viable solution to accelerate the ionic diffusion and reaction kinetics at low temperatures. However, the applications of COFs in low-temperature batteries are still at their infancy stage.
View Article and Find Full Text PDFAdv Mater
September 2025
School of Materials Science and Engineering, Anhui University, Hefei, 230601, China.
Modulating the electronic structure of catalysts to maximize their power holds the key to address the challenges faced by zinc-iodine batteries (ZIBs), including the shuttle effect and slow redox kinetics at the iodine cathode. Herein, oxygen vacancies is innovatively introduced into CoO lattice to create high-spin-state Co active sites in nonstoichiometric CoO nanocrystals supported by carbon nanofibers (H-CoO/CNFs). This simple strategy intensifies crystal field splitting of Co 3d orbitals, optimizing the spin-orbital coupling between Co 3d orbitals and iodine species.
View Article and Find Full Text PDFAdv Sci (Weinh)
September 2025
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu, 225009, P. R. China.
Lithium-sulfur batteries (LSBs) hold great potential as next-generation energy storage systems due to their high theoretical energy density and relatively low cost. However, their practical application is hindered by issues such as the shuttle phenomenon caused by soluble lithium polysulfides (LiPSs), slow redox reaction rates, and unsatisfactory cycling stability. In this study, novel conjugated metal-organic frameworks, MM″(HHTP) (M, M″ = Ni, Co, Cu) is reported, as a functional coating on polypropylene (PP) separators.
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