Efficient microwave degradation of humic acids in water using persulfate and activated carbon

Environmental Chemistry Letters - Humic acids are complex mixtures of organic molecules of different sizes, molecular weights and functional groups such as phenols, carboxyls, quinones and amino...     

UV light induces Ag nanoparticle formation: roles of natural organic matter,iron, and oxygen

Nanoparticles occurring in the environment originate either from engineered, synthetically produced nanoparticles, or from naturally produced nanoparticles. The latter can be formed in natural media by light-induced reduction of metal ions in presence of natural organic matter, such as humic substances occurring widely in waters, soils and sediments. There is actually few knowledge on the effect of sunlight and of the nature of organic matter on nanoparticle formation. Therefore, we studied here the photoreduction of silver(I) ion to silver nanoparticles with and without ferrous ion under oxic and anoxic conditions, using humic and fulvic acids as proxies of natural organic matter. UV light-induced formation of silver nanoparticles was monitored up to 60 min by measuring surface plasmon resonance in air-saturated mixture and nitrogen-saturated mixture of silver(I) ion–organic matter. Results show that the surface plasmon resonance intensity was about 2.5 times higher in the nitrogen-purged solution mixture than the air-saturated solution. This finding suggests the oxygen-containing species had no major role in forming silver nanoparticles. Therefore, photo-driven formation of silver nanoparticles most likely involved photoactivation of silver(I) ion and natural organic matter complexes. We observed also that both iron(II) and iron(III) ions highly modified the surface plasmon resonance spectra of the particles with broader features. Results also reveal that in the presence of humic acid, the intensity of the surface plasmon resonance peak decreased by at least 50 %, while almost no change in the intensity was seen when fulvic acid was used. Overall, our findings demonstrate that the ligand–metal charge transfer process, affected by the nature of organic matter, i.e., humic acid versus fulvic acid, was influenced by redox iron species.     

A comparison of concentrations of polycyclic aromatic compounds detected in dust samples from various regions of the world

Settled house dust can be a source of human exposure to toxic polycyclic aromatic hydrocarbons (PAHs) through non-dietary ingestion and dermal contact. Information regarding the concentrations of various contaminants in house dust would be useful in estimating the risk associated with exposure to these compounds. This study reports on the surface loading, variability and distribution of PAHs in settled house dust collected from homes in three locations: Sumgayit, Azerbaijan; Shanxi Province, China; and southern Texas, United States. The highest PAH floor surface loadings were observed in China, followed by Azerbaijan and Texas. Median concentrations of high molecular weight (four ring and larger) PAHs ranged from a low of 0.11 microg/m(2) in Texas, to 2.9 microg/m(2) in Azerbaijan and 162 microg/m(2) in China. These trends in total surface loading and relative carcinogenicity indicate that the risk of health effects from exposure to PAHs in house dust is highest in the Chinese population and lowest in the Texas population. As anticipated, variability among dust samples from different houses within the same region was high, with coefficients of variation greater than 100%. Alkylated PAHs comprised 30-50% of the total mass of PAHs. Based on a comparison of the composition of specific components, PAHs in China and Azerbaijan were determined to be derived mainly from combustion sources rather than from unburned fossil fuels such as petroleum. These results, coupled with ongoing investigation of appropriate PAH exposure biomarkers in humans, will guide future efforts to identify ways to reduce exposures in the study areas.     

Bacterial community structure and microorganism inactivation following water treatment with ferrate(VI) or chlorine

Drinking water disinfection plays a critical role in protecting humans from waterborne pathogens. Ferrate(VI) (Fe^VIO₄ ^2?) has also been proposed as a disinfectant. This is the first study investigating the bacterial microbiomes of ferrate(VI)-treated water compared to chlorinated water. Tested water was collected after sand filtration and before disinfection from a drinking water treatment plant at Jiaxing, Zhejiang Province, China. A culture-independent method utilizing propidium monoazide was used with quantitative polymerase chain reaction and pyrosequencing of 16S rRNA genes to distinguish between the viable and nonviable bacterial populations. The operational taxonomic units and α-diversity indexes of the live bacterial phylotypes in the samples were determined. Viable bacteria remained in all samples following chlorination or ferrate treatment. However, the genera Vibrio, Salmonella, Shigella, Escherichia, Campylobacter, Yersinia, Plesiomonas, Legionella, and Helicobacter, which contain important human pathogens, were not present among the 25 dominant genera seen in these samples. The profiles of the bacteria remaining after treatment with either chlorine or ferrate differed. The ferrate-treated samples showed a reduced percent relative abundance of operational taxonomic units of the class Alphaproteobacteria within the total remaining viable bacteria. The genera Flavobacterium and Duganella were relatively resistant to treatment by either chlorine or ferrate(VI). At the highest doses of chlorine and ferrate(VI), the genus Sphingobium represented a greater percentage of live bacteria in the chlorinated sample than in the ferrate(VI)-treated sample. The results suggest that ferrate(VI) and chlorine could inactivate slightly different sets of bacteria and could have different mechanisms of bacterial inactivation.