In phosphate-rich environments, vivianite (Fe(II)(3)(PO(4))(2), 8H(2)O) is an important sink for dissolved Fe(II) and is considered as a very stable mineral due to its low solubility at neutral pH. In the present study, we report the mineralogical transformation of vivianite in cultures of the nitrate-reducing iron-oxidizing bacterial strain BoFeN1 in the presence of dissolved Fe(II). Vivianite was first transformed into a greenish phase consisting mostly of an amorphous mixed valence Fe-phosphate. This precipitate became progressively orange and the final product of iron oxidation consisted of an amorphous Fe(III)-phosphate. The sub-micrometer analysis by scanning transmission X-ray microscopy of the iron redox state in samples collected at different stages of the culture indicated that iron was progressively oxidized at the contact of the bacteria and at a distance from the cells in extracellular minerals. Iron oxidation in the extracellular minerals was delayed by a few days compared with cell-associated Fe-minerals. This led to strong differences of Fe redox in between these two types of minerals and finally to local heterogeneities of redox within the sample. In the absence of dissolved Fe(II), vivianite was not significantly transformed by BoFeN1. Whereas Fe(II) oxidation at the cell contact is most probably directly catalyzed by the bacteria, vivianite transformation at a distance from the cells might result from oxidation by nitrite. In addition, processes leading to the export of Fe(III) from bacterial oxidation sites to extracellular minerals are discussed including some involving colloids observed by cryo-transmission electron microscopy in the culture medium.
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http://dx.doi.org/10.1111/j.1472-4669.2009.00203.x | DOI Listing |
Ecotoxicol Environ Saf
January 2025
Hubei Key Laboratory of Yangtze Catchment Environmental Aquatic Science, School of Environmental Studies, China University of Geosciences, Wuhan 430074, PR China. Electronic address:
Microorganisms that utilize organic matter to reduce Fe oxides/hydroxides constitute the primary geochemical processes controlling the formation of high-arsenic (As) groundwater. Biogenic secondary iron minerals play a significant role in As migration. However, the influence of quinone electron shuttles and competitive anionic phosphate on this process has not been thoroughly studied.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Fenton-like reactions between organic peroxides and transition-metal ions in the atmospheric aqueous phase have profound impacts on the chemistry, composition, and health effects of aerosols. However, the kinetics, mechanisms, and key influencing factors of such reactions remain poorly understood. In this study, we synthesized a series of monoterpene-derived α-acyloxyalkyl hydroperoxides (AAHPs), an important class of organic peroxides formed from Criegee intermediates during the ozonolysis of alkenes, and investigated their Fenton-like reactions with iron ions in the aqueous phase.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
Zachry Department of Civil & Environmental Engineering, Texas A&M University, College Station, Texas 77843, United States.
This study quantifies the contribution of the HO-dependent pathway to hydroxyl radical (OH) production from the photolysis of dissolved organic matter (DOM). OH formation rates were cross-validated using benzoate and terephthalate as probe compounds for diverse DOM sources (reference isolates and whole waters). Catalase addition revealed that the HO-dependent pathway accounts for 10-20% of the total OH production in DOM isolate materials, but no significant correlation was observed between ambient iron (Fe) concentrations and HO-dependent OH formation.
View Article and Find Full Text PDFJ Colloid Interface Sci
April 2025
Department of Environmental Science and Engineering, College of Environment and Resources, Xiangtan University, Xiangtan 411105, China.
Ferrous oxalate (FeCO)-based composite has been recognized as an eminent catalyst for Cr(III)-ethylenediamine tetraacetic acid (Cr(III)-EDTA) decomplexation. However, their practical application has been limited by low cycling capacity and an ambiguous mechanism. In this research, a composite catalyst consisting of biotite loaded with nano FeCO (CFS90) was prepared directly from iron-containing silicate tailing.
View Article and Find Full Text PDFSci Total Environ
December 2024
State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing 210023, China.
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