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The release of phosphorus (P) from anaerobic sediments becomes the dominant source of P loading with effective control of external P pollution. As a crucial component responsible for binding P, vivianite (Fe(PO)·8HO) in sediment inevitably impacts the P level and transformation. The release of P from vivianite mediated by sulphide was investigated using simulated overlying water-sediment and chemical reaction systems. The percentage of redox-stable P in the sediments increased with vivianite input in the overlying water-sediment system. Increasing P concentrations in both the overlying water and interstitial water occurred before day 10, accompanied by a decreasing percentage of redox-sensitive P in the sediments driven by sulphide. The continuous release of P from vivianite clarifies the influence of sulphide on promoting vivianite dissolution in a chemical reaction system with vivianite and sulphide solution. Additionally, Mössbauer spectrum and nanoscale secondary ion mass spectrometry (NanoSIMS) images based on the chemical reaction with Fe isotope labelling demonstrated the presence of initial vivianite, newly produced vivianite, and FeS.
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http://dx.doi.org/10.1016/j.jes.2024.08.005 | DOI Listing |
Environ Res
September 2025
Guangdong Education Department Key Laboratory of Resources Comprehensive Utilization and Cleaner Production, School of Environmental Science and Engineering, Guangdong University of Technology, Guangzhou, 510006, China.
Catalytic pyrolysis, an efficient thermochemical process, offers a promising pathway to valorize thermoset photovoltaic backsheets (TPV) into high-value chemicals. This study investigates the ex situ catalytic pyrolysis of TPV using two acidic catalysts, ZSM-5 and FeNi-ZSM-5, under varied operational conditions, with a focus on product distribution and process efficiency. The catalytic intervention significantly enhanced pyrolysis performance.
View Article and Find Full Text PDFNitric Oxide
September 2025
Department of Physics, Wake Forest University, Winston-Salem, NC 27109, USA; Translational Science Center, Wake Forest University, Winston-Salem, NC 27109, USA. Electronic address:
We recently demonstrated a rapid reaction between labile ferric heme and nitric oxide (NO) in the presence of reduced glutathione (GSH) or other small thiols in a process called thiol-catalyzed reductive nitrosylation, yielding a novel signaling molecule, labile nitrosyl ferrous heme (NO-ferroheme), which we and others have shown can regulate vasodilation and platelet homeostasis. Red blood cells (RBCs) contain high concentrations of GSH, and NO can be generated in the RBC via nitrite reduction and/or RBC endothelial nitric oxide synthase (eNOS) so that NO-ferroheme could, in principle, be formed in the RBC. NO-ferroheme may also form in other cells and compartments, including in plasma, where another small and reactive thiol species, hydrogen sulfide (HS/HS), is also present and may catalyze NO-ferroheme formation akin to GSH.
View Article and Find Full Text PDFBioresour Technol
September 2025
Department of Earth Resources and Environmental Engineering, Hanyang University, Seoul 04763, Republic of Korea. Electronic address:
The rapid increase of electronic waste, particularly battery waste, presents significant environmental challenges such as pollutant emissions and resource depletion, emphasizing the need for effective valorization and reuse strategies. This study introduces a novel approach for repurposing end-of-life lithium iron phosphate (LFP) batteries as catalysts in the pyrolysis of walnut shells (WS). Characterization analyses revealed that LFP provides both Lewis and Brønsted acid sites, which alter the thermal decomposition pathway of WS.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Department of Chemical Engineering, Institute of Chemical Technology, Matunga (E), Mumbai, 400019, India. Electronic address:
Integrating multi-enzyme systems within metal-organic frameworks (MOFs) has garnered significant attention in biocatalysis due to their tunable structural properties and ability to enhance enzyme performance in cascade reactions. The unique features of MOFs, such as well-defined pore apertures, tailorable compositions, and high loading capacity, facilitate the design of robust multi-enzyme bio-composites with enhanced recyclability and specificity. This review explores systematic approaches for the compartmentalization and positional co-immobilization of multiple enzymes within MOFs, focusing on two key strategies: (i) layer-by-layer assembly and (ii) pore-engineered compartmentalization.
View Article and Find Full Text PDFWater Res
September 2025
State Key Laboratory of Soil Pollution Control and Safety, Department of Environmental Science, Zhejiang University, Hangzhou 310058, China; Future Environment Laboratory, Innovation Center of Yangtze River Delta, Zhejiang University, Jiaxing 314100, China. Electronic address:
Accelerating the rate-limiting surface Fe(III)/Fe(II) redox cycling is pivotal for efficient iron-mediated Fenton-like decontamination, yet conventional reductants (e.g., toxic hydroxylamine, thiosulfate) suffer from secondary toxicity, self-quenching, and heavy metal leaching.
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