Rosenbergmcdermott5369

Iron-impregnated biochar-activated urea-hydrogen peroxide (FB-activated UHP) is a potential in-situ technology for simultaneously reducing soil sulfonamide antibiotic contaminants and improving soil fertility. To better understand the degradation of sulfonamide antibiotics by FB-activated UHP, a two-dimensional quantitative structure-activity relationship (2D-QSAR) model based on quantum chemical parameters and a three-dimensional QSAR (3D-QSAR) model based on molecular force field were developed to investigate the factors influencing the removal efficiencies (Re%). The optimal 2D-QSAR model was Re%= 0.858-8.930 E-5 EB3LYP-0.175 f(+)x with the evaluation indices of R2= 0.732, q2= 0.571, and Qext2= 0.673. The given 2D-QSAR model indicated that the molecular size (EB3LYP) and Fukui index with respect to nucleophilic attack (f(+)) were intrinsic factors influencing Re%. Three degradation pathways were subsequently proposed based on the f(+) distribution. Compared to the 2D-QSAR model, the developed 3D-QSAR model exhibited a better predictive ability, with the evaluation indices of R2= 0.989, q2= 0.696, and SEE= 0.001. The analysis of field contribution rates suggested that electrostatic field (48.2%), hydrophobic field (25.3%), and hydrogen-bond acceptor field (12.7%) were the main factors influencing Re%. These findings generated critical information for evaluating the degradation mechanisms/rules and provided theoretical bases for initially estimating the Re% of sulfonamide antibiotics undergoing FB-activated UHP process.Sulfur-fertilizer is commonly applied in croplands and in immobilizing Hg in contaminated soil. However, there is still great uncertainty and controversy concerning Hg transportability and transformation when supplying sulfur in paddies with complex conditions. Herein, we explored the effect of adding sulfate in paddy soil at different rice growth stages on soil Hg release and MeHg accumulation in rice and uncovered the correlation between sulfur induced MeHg production and the dynamically changed soil Eh, dissolved Fe, and dissolved organic carbon (DOC). In specific, sulfate addition at early stages (flooding period) triggered the decrease of Eh and increase of DOC and dissolved Fe, which in turn promoted Hg release and favored MeHg generation (increased by 235.19-555.07% vs control). Interestingly, adding sulfate at late stages (drainage condition), as compared with that at early stages, alleviated Hg release and MeHg production accompanied by the increase of Eh and decrease of dissolved Fe and DOC. The microcosmic experiment further confirmed the reduction of sulfate to sulfide promoted the change of Eh, thereby stimulating HgS dissolution in soil extract. selleckchem The results give clues on the rational application of sulfur-fertilizer and through the water-sulfur fertilizer management considering the correspondingly changed soil conditions to diminish Hg bioavailability and MeHg production in paddies and paddy-like environments.The prevalence of antibiotic resistance, as well as microplastics (MPs) as vectors for antibiotic resistant bacteria (ARB) and antibiotic resistance genes (ARGs) has attracting growing attention. However, the fate of ARB/ARGs on MPs treated by chlorination and Fenton oxidation were poorly understood. Herein, the removal and regrowth of ARGs/ARB on MPs and in MPs-surrounding landfill leachate (an important reservoir of MPs and ARGs) after chlorination and Fenton oxidation were comparatively analyzed. Target ARGs on MPs were reduced obviously less than that in leachate, with the largest percentages reduction of 34.0-46.3% vs. 54.3-77.6% after chlorination and 92.1-97.3% vs. > 99.9% after Fenton oxidation, and similar removal patterns were observed for ARB. Moreover, a considerable regrowth of ARGs/ARB in leachate were found after 48 h of storage at the end of chlorination (5, 10, 20 and 50 mg/L), and a greater regrowth of ARGs and ARB occurred on MPs with up to 17 and 139 fold, respectively. In contrast, Fenton oxidation achieved a reduced regrowth of target ARGs/ARB. These findings indicated that the removal of ARGs/ARB on MPs were more difficult than that in leachate, and ARGs/ARB in leachate and especially on MPs exhibited a considerable potential for rapid regrowth after chlorination.Understanding the future distribution of antibiotic resistance in natural soil ecosystems is important to forecast their impacts on ecosystem and human health under projected climate change scenarios. Therefore, it is critical and timely to decipher the links between climate warming and antibiotic resistance, two of Earth's most imminent problems. Here, we explored the role of five-year simulated climate warming (+ 4 °C) on the diversity and proportions of soil antibiotic resistance genes (ARGs) across three seasons in both plantation and natural forest ecosystems. We found that the positive effects of warming on the number and proportions of ARGs were dependent on the sampling seasons (summer, autumn and winter), and seasonality was a key factor driving the patterns of ARG compositions in forest soils. Fifteen ARGs, conferring resistance to common antibiotics including aminoglycoside, beta-lactam, macrolide-lincosamide-streptogramin B, multidrug, sulfonamide, and tetracycline, were significantly enriched in the warming treatment. We showed that changes in soil properties and community compositions of bacteria, fungi and protists can explain the changes in soil ARGs under climate warming. Taken together, these findings advance our understanding of environmental ARGs under the context of future climate change and suggest that elevated temperature may promote the abundance of specific soil ARGs, with important implications for ecosystem and human health.Hexafluoropropylene oxide trimer acid (HFPO-TA) is reported to have hepatotoxicity, lipotoxicity, and cytotoxicity. In this study, the toxicological effects of HFPO-TA on mitochondrial function and biogenesis were studied. Mice were exposed to drinking water which contained either 2, 20, or 200 μg/L HFPO-TA. Results showed exposure to HFPO-TA induced disadvantageous physiological changes in mice, including increases in liver weight, altered cell morphology, and inflammatory responses. Specifically, exposure to 200 μg/L HFPO-TA increased mitochondria number, relative mitochondrial DNA (mtDNA) content, and mRNA levels of mitochondrial genes encoded by mtDNA. Significant increases in TFAM mRNA and protein levels were also observed. Liver metabolome analysis also showed exposure to 200 μg/L HFPO-TA further enhanced increases in metabolites and altered metabolic pathways that correlated with mitochondrial function, especially the production of ATP. HFPO-TA exposure increased protein expression of mitochondrial complex I-V, and the activities of key enzymes involved in TCA cycle (α-ketoglutarate dehydrogenase, citrate synthase, and succinate dehydrogenase). Furthermore, exposure to 200 μg/L HFPO-TA significantly up-regulating mRNA and protein levels of Opa1, Mfn1, Mfn2, Fis1, and Mff, but did not change Drp1. These findings suggest HFPO-TA could have detrimental effects on health of animals, particularly it was associated with disrupted mitochondrial energy metabolism.Developing efficient modulation strategies to boost the degradation efficiencies of non-noble metal catalysts for toxic phenolic compounds involving peroxymonosulfate (PMS)-based oxidation processes is essential but remains an arduous challenge. This study reports the one-pot construction of in-situ surface vulcanized CoFe2O4 @carbon (Sx-CF@C) to boost the PMS activation for 4-nitrophenol (4-NP) destruction. The direct pyrolysis of an aerogel precursor consisted of cobalt nitrate, ferric nitrate, melamine, and thiourea enables the as-formed Sx-CF@C with hierarchical structure, rich oxygen vacancies, and electron/mass transfer, thereby considerably promoting PMS activation performance of Sx-CF@C toward 4-NP degradation. Specifically, the optimal S0.2-CF@C can achieve a removal efficiency of 99% for 4-NP destruction (20 mg/L) through PMS activation. Meanwhile, the catalyst also has generality to degrade a variety of antibiotic and dye organic pollutants. The radical quenching and electron paramagnetic resonance tests reveal the radical and non-radical activation mechanism in the S0.2-CF@C/PMS system. The degradation pathway for 4-NP destruction over the S0.2-CF@C/PMS system is proposed. This study provides an efficient approach to modulate the PMS activation performance of ferrite spinel materials toward the degradation of acute phenolic compounds.Electrochemical reduction of NO to NH3 (NORR) is an attractive approach to mildly realize NO removal and valuable NH3 production. The electrolyte, as function as the NO absorbent, is crucial to apply electrochemical technology in practical de-NO engineering. In this paper, the ferrous chelate acted as the electrolyte for effective NO absorption in NORR based on the Brown-ring reaction. The rGO and Au/rGO catalysts served as cathodes to realize ferrous regeneration for continuous NO reduction. The results revealed that ferric chelate could be fully reduced at lower onset potential on rGO electrode. The Au/rGO catalyst exhibited excellent average yield and selectivity for NH3 at - 0.1 V and pH = 6.32, (14.6 μmol* h-1 * cm-2 and 65.2%, respectively). The Faradaic Efficiency of NH3 could reach 98.3% at pH = 1.0. This work provides a valuable reference for effective NO adsorption and sustainable NO-to-NH3 conversion.The trade-off of Fenton-like catalysts in activity and stability remains a challenge in practical remediation applications. In this work, we successfully synthesized an efficient and stable catalyst comprised of single nickel (Ni) atoms dispersed on N-doped porous carbon (named Ni-SAs@CN) through a simple micropore confinement strategy. The catalyst exhibited outstanding catalytic performance with 25.8 min-1 turnover frequency for peroxymonosulfate (PMS) activation toward degradation of various organic pollutants (e.g., antibiotics, dyes, and plasticizers) in a wide pH range (4.5-10.8). Electron paramagnetic resonance and in situ Raman analyses demonstrated that both radical (including SO4•- and •OH) and Ni-PMS* dominated nonradical (via electron transfer) pathways played pivotal role in the decomposition of organics. The X-ray adsorption fine structure analysis and computational pieces of evidence demonstrate that the atomically dispersed NiN4 coordination is the intrinsic catalytic site for PMS activation. Meanwhile, pyrrolic N acts as a functional site to anchor target contaminants to the surface region for oxidation. In this process which is benefited from the dual active sites, the target contaminants were degraded via combined radical and nonradical pathways, which significantly boost the overall oxidation and mineralization kinetics.Despite the extensive uses of ZnO nanoparticles as promising antimicrobial agents to tackle the severe microbial infections, the systematic antibacterial studies on ZnO nanoparticles with manipulable nanoscale morphologies at the genetic expression level remain ill-defined. In this study, via a controllable thermal decomposition, ZnO nanoparticles of different morphologies were facilely prepared. Additionally, the surface PEGylation of ZnO was conducted to obtain the nanoparticles of low biotoxicity. While all the prepared ZnO nanoparticles exhibited the significantly chemical activities, the pronounced antibacterial effect of obtained ZnO nanoparticles was also identified, in which the ultra-small ones (~5 nm) showed the best performance. Moreover, the antibacterial activities of ZnO nanoparticles were studied by bacterial nucleic acid leakage, alkaline phosphatase, biofilm and reactive oxygen species (ROS) assays. Furthermore, the transcriptome analysis of ZnO nanoparticles with different morphologies against Escherichia coli (E.