The occurrence of in situ degradation of chlorinated ethenes was investigated using an integrated approach in a complex groundwater system consisting of several geological units. The assessment of hydrogeochemistry and chlorinated ethenes distribution using principal component analysis (PCA) in combination with carbon stable isotope analysis revealed that chlorinated ethenes were subjected to substantial biodegradation. Shifts in isotopic values up to 20.4 per thousand, 13.9 per thousand, 20.1 per thousand and 31.4 per thousand were observed between geological units for tetrachloroethene (PCE), trichloroethene (TCE), cis-dichloroethene (cDCE) and vinyl chloride (VC), respectively. The use of specific biomarkers (16S rRNA gene) indicated the presence of Dehalococcoides sp. DNA in 20 of the 33 evaluated samples. In parallel, the analysis of changes in the bacterial community composition in the aquifers using canonical correspondence analysis (CCA) indicated the predominant influence of the chlorinated ethene concentrations (56.3% of the variance, P=0.005). The integrated approach may open new prospects for the assessment of spatial and temporal functioning of bioattenuation in contaminated groundwater systems.
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http://dx.doi.org/10.1016/j.watres.2007.08.035 | DOI Listing |
J Hazard Mater
January 2025
School of Earth and Environmental Sciences, Seoul National University, Seoul 08826, South Korea. Electronic address:
Chlorinated ethenes are prevalent contaminants in industrial wastewater that detrimentally affect human health. As elevated tetrachloroethene (PCE) concentrations (18.0-18.
View Article and Find Full Text PDFACS Catal
January 2025
School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Partial oxidation of ethylene over silver catalysts produces more than 30 million metric tons of ethylene oxide (EO) annually. However, the form of active silver surfaces, reactive oxygen species, and dominant pathways of this chemical reaction remains controversial despite decades of research. Here, we use Raman spectroscopy and transient kinetic measurements to demonstrate that higher coverages of peroxide species, present only upon Ag oxide surfaces that form , correlate with greater selectivities to EO.
View Article and Find Full Text PDFChempluschem
January 2025
L V Pisarzhevskii Institute of Physical Chemistry NAS of Ukraine: Institut fiziceskoj himii imeni L V Pisarzevskogo Nacional'na akademia nauk Ukraini, Department of free radicals, UKRAINE.
This study unveils a novel property of polyaniline by establishing its catalytic activity in heterogeneous hydrogenation with molecular hydrogen. Polyaniline was activated by heat-treating at different temperatures in a hydrogen atmosphere. The sample treated at 300 °C exhibited the highest catalytic activity for ethylene hydrogenation in the gas phase at atmospheric pressure and for p-nitrotoluene or α-methylstyrene hydrogenation in the liquid phase.
View Article and Find Full Text PDFChemosphere
January 2025
Department of Civil and Environmental Engineering, University of Massachusetts Lowell, Massachusetts, United States. Electronic address:
There is significant interest in monitoring abiotic decomposition of chlorinated solvents at contaminated sites due to large uncertainties regarding the rates of abiotic attenuation of trichloroethylene (TCE) and perchloroethylene (PCE) under field conditions. In this study, an innovative passive sampling tool was developed to quantify acetylene, a characteristic product of abiotic reduction of TCE or PCE, in groundwater. The sampling mechanism is based on the highly specific and facile click reaction between acetylene and an azide compound to form a biologically and chemically stable triazole product.
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January 2025
University of Chinese Academy of Sciences, Beijing, 100049, China; Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China. Electronic address:
The degradation of rubber seal (RS), particularly ethylene-propylene-diene (EPDM), in the drinking water networks has been confirmed, yet the role of RS as a disinfection by-product (DBP) precursor remains unknown. This study provides explicit proof of the formation of halogenated disinfection by-products (X-DBPs) from RS in chlorinated drinking water within water supply systems. Over time, exposure to chlorinated water ages RS, releasing high levels of organic compounds, which act as DBP precursors.
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