Abiotic reduction of iron (oxyhydr)oxides by aqueous Fe(II) is one of the key processes affecting the Fe cycle in soil. Lepidocrocite (Lep) occurs naturally in anaerobic, clayey, non-calcareous soils in cooler and temperate regions; however, little is known about the impacts of co-precipitated humic acid (HA) on Fe(II)-induced Lep transformation and its consequences for heavy metal immobilization. In this study, the Fe(II)-induced phase transformation of Lep-HA co-precipitates was analyzed as a function of the C/Fe ratio, and its implications for subsequent Cd(II) concentration dynamic in dissolved and solid form was further investigated. The results revealed that secondary Fe(II)-bearing magnetite commonly formed during the Fe(II)-induced transformation of Lep, which further changed the mobility and distribution of Cd(II). The co-precipitated HA resulted in a decrease in the Fe solid phase transformation as the C/Fe ratios increased. Magnetite was found to be a secondary mineral in the 0.3C/Fe ratio Lep-HA co-precipitate, while only Lep was observed at a C/Fe ratio of 1.2 using X-ray diffraction (XRD) and Mössbauer spectroscopy. Based on XRD, scanning electron microscopy (SEM), Mössbauer, X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FTIR) results, newly formed magnetite may immobilize Cd(II) through surface complexes, incorporation, or structural substitution. The presence of HA was beneficial for binding Cd(II) and affected the mineralogical transformation of Lep into magnetite, which further induced the distribution of Cd(II) into the newly formed secondary minerals. These results provide insights into the behavior of Cd(II) in response to reaction between humic matter and iron (oxyhydr)oxides in anaerobic environments.
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http://dx.doi.org/10.1016/j.scitotenv.2022.160624 | DOI Listing |
Environ Res
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Ministry of Ecology and Environment South China Institute of Environmental Sciences, Guangzhou 510655, China; Key Laboratory of Water Environmental Simulation and Pollution Control, Ministry of Ecology and Environment, Guangzhou 510655, China. Electronic address:
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Dpt. Chemistry, Lomonosov Moscow State University, Moscow 119991, Russia.
The enzyme-catalyzed synthesis of calcium phosphate is a promising method for producing calcium-based nanomaterials for biomedical applications. The purpose of this work was to determine the type of phosphate that forms when alkaline phosphatase catalyzes the reaction, and to identify the role of natural biopolymers in calcium phosphate formation. In this research, we analyzed calcium phosphates that were synthesized in the presence of alkaline phosphatase from either E.
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January 2025
School of Minerals Processing and Bioengineering, Central South University, Changsha 410083, PR China. Electronic address:
Bubble-microplastic (MP) interaction is a significant process that changes the routes of MP circulation in marine environment and thereby determines the risk of MPs, which could be strongly influenced by natural organic matter (NOM) in oceans. However, the quantitative interaction mechanisms between bubbles and MPs under the effect of NOM remain elusive. Herein, bubble-MP interactions in simulated seawater were quantified at nanoscale based on atomic force microscope coupled with the Stokes-Reynold-Young-Laplace model.
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Institute of Biotechnology and Nuclear Technology, Sichuan Academy of Agricultural Sciences, Chengdu, China.
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January 2025
College of Architecture & Civil Engineering, Beijing University of Technology, Beijing, People's Republic of China.
The release of algal organic matter (AOM) during seasonal algal blooms increases the complexity and heterogeneity of natural organic matter (NOM) in water sources, altering its hydrophilic-hydrophobic balance and posing significant challenges to conventional water treatment processes. This study aims to verify whether the (Granular activated carbon) GAC selected for the adsorption of NOM in sand filtration effluent can adapt to water quality fluctuations caused by AOM release, and identify the criteria influencing GAC adsorption performance. Results indicated that external surface area, mesopore volume, pore size and surface functional groups were key indicators of GAC adsorption performance.
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