The fate of Zn and other sorbed heavy metals during microbial reduction of iron oxides is different when comparing synthetic Fe-(hydr)oxides and natural sediments undergoing a similar degree of iron reduction. Batch experiments with the iron-reducing organism Shewanella putrefaciens were conducted to examine the effects of an aqueous complexant (nitrilotriacetic acid or NTA), two solid-phase complexants (kaolinite and montmorillonite), an electron carrier (anthraquinone disulfonic acid or AQDS), and a humic acid on the speciation of Zn during microbial reduction of synthetic goethite. Compared to systems containing only goethite and Zn, microbial Fe(III) reduction in the presence of clay resulted in up to a 50% reduction in Zn immobilization (insoluble in a 2 h 0.5 M HCl extraction) without affecting Fe(II) production. NTA (3 mM) increased Fe(II) production 2-fold and resulted in recovery of nearly 75% of Zn in the aqueous fraction. AQDS (50 microM) resulted in a 12.5% decrease in Fe(II) production and a 44% reduction in Zn immobilization. Humic acid additions resulted in up to a 25% decrease in Fe(II) production and 51% decrease in Zn immobilization. The results suggest that all the components examined here as either complexing agents or electron shuttles reduce the degree of Zn immobilization by limiting the availability of Zn for incorporation into newly formed biogenic minerals. These results have implications for the remediation of heavy metals in a variety of natural sediments.
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http://dx.doi.org/10.1021/es0525197 | DOI Listing |
Inorg Chem
January 2025
Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, Tehran P.O. Box 14117-13116, Islamic Republic of Iran.
Several studies were focused on the application of MIL-100(Fe) (FeO(OH)(HO)(BTC), HBTC is 1,3,5-benzene tricarboxylic acid) in the photo-Fenton reaction, but it still suffers from low efficiency. In this work, MIL-100(Fe) was synthesized at ambient conditions and low pHs using Fe(II) precursors in homogeneous aqueous media to develop a sample with high activity in the photo-Fenton reaction, even better than Fe-porphyrin metal-organic frameworks. The as-synthesized sample is highly crystalline with 30.
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 PDFJ Pharm Sci
January 2025
Department of Pharmaceutical Chemistry, University of Kansas, 2093 Constant Avenue, Lawrence, KS 66047, USA. Electronic address:
Iron-catalyzed oxidation reactions are common degradation pathways in pharmaceutical formulations. Buffers can influence oxidation reactions promoted by iron (Fe) and hydrogen peroxide (H₂O₂). However, mechanistically, the specific role of buffers in such reactions is not well understood.
View Article and Find Full Text PDFChemMedChem
January 2025
National Taiwan University, Chemistry, No.1, Sec.4, Roosevelt Road, Deptartment of Chemistry, Rm A521, 106319, Taipei, TAIWAN.
Cofactors are non-protein entities necessary for proteins to operate. They provide "functional groups" beyond those of the 20 canonical amino acids and enable proteins to carry out more diverse functions. Such a viewpoint is rarely mentioned, if at all, when it comes to natural products and is the theme of this Concept.
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.
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