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After impregnating the Ba species, admitted NO molecules were oxidized with enough O2 and stored very strongly as ionic nitrate (NO3-) onto the Ba species even after heating at 500 °C. This preliminary study is helpful for designing mesoporous deNOx catalysts combined with unique storage/adsorption property.Cobalt-mediated activation of peroxymonosulfate (PMS) has been extensively investigated for the degradation of emerging organic pollutants. In this study, PMS activation via cobalt-impregnated biochar towards atrazine (ATZ) degradation was systematically examined, and the underlying reaction mechanism was explicated. It was found that persistent free radicals (PFRs) contained in biochar play a pivotal role in PMS activation process. The PFRs enabled an efficient transfer electron to both cobalt atom and O2, facilitating the recycle of Co(III)/Co(II), and thereby leaded to an excellent catalytic performance. In contrast to oxic condition, the elimination of dissolved oxygen significantly retarded the ATZ degradation efficiency from 0.76 to 0.36 min-1. Radical scavenging experiments and electron paramagnetic resonance (EPR) analysis confirmed that the ATZ degradation was primarily due to SO4·- and, to a lesser extent, ·OH. In addition, dual descriptor (DD) method was carried out to reveal reactive sites on ATZ for radicals attacking and predicted derivatives. Meanwhile, the possible ATZ degradation pathways were accordingly proposed, and the ecotoxicity evaluation of the oxidation intermediates was also conducted by ECOSAR. Consequently, the cobalt-impregnated biochar could be an efficient and environmentally friendly catalyst to activate PMS for abatement and detoxication of ATZ.Gut microbiota is intimately involved in numerous aspects of human health. Arsenite expouse can perturb gut microbiota and is linked to increased susceptibility of individual to arsenite-related diseases. However, how microbiome factors influence arsenite-induced neurotoxicity remains largely unknown. In this study, after treating of healthy adult female mice with arsenite via drinking water for 6 months, our results clearly revealed that chronic arsenite exposure not only perturbed the composition of gut microbiota but also caused neurobehavioral dysfunctions, which manifested by learning and memory deficits and anxiety-like behavior. Given that the overactive autophagy directly leads to gut pathological changes, we further assessed whether inhibiton of autophagy by genetic mean could reverse arsenite-induced neurobehavioral dysfunctions. Our results illustrated for the first time that heterozygous disruption of beclin 1, which played a central role in autophagy, alleviated the perturbation of gut microbiome phenotypes induced by arsenite, and ultimately leading to the improvement of neurobehavioral deficits through gut-brain communication. These findings provide a new clue that regulation of autophagy is a potential approach for probing the functional impacts of arsenite on the gut microbiome, and it also may be severed as a way for protection strategies against arsenite neurotoxicity.In recent years, nutrient management has gained much attention for mitigating metal stress. But, role of nutrients like calcium (Ca) and sulfur (S) in mitigating Cr(VI) toxicity along with their mechanism of action are still limited. Therefore, the present study was performed to explore role of Ca and S in ameliorating Cr(VI) toxicity in 21 days old seedlings of Solanum lycopersicum L. and Solanum melongena L. Chromium (VI) reduced tolerance index and altered root traits due to greater Cr accumulation in the cell wall and cellular organelles due to down-regulation in thiols and phytochelatins that lead to alterations in photosynthesis. However, Ca or S stimulated vacuolar sequestration of Cr(VI) and reduced its uptake at the cell wall. This was coincided with up-regulation in glutathione-S-transferase activity, and amounts of thiols and phytochelatins. Cr(VI) caused oxidative stress together with up-regulation in superoxide dismutase and catalase, and proline metabolism while Ca and S reversed these effects. Chromium (VI) inhibited nitrate reductase activity while Ca and S reversed this response. NG-nitro-l-arginine methyl ester augmented Cr(VI) toxicity but sodium nitroprusside (SNP) mitigated Cr(VI) toxicity. Overall results show that Ca and S both are able in ameliorating Cr(VI) toxicity and require nitric oxide for this task.Despite the unique properties of single semiconductor nanomaterials and quantum dots, poor photocatalytic activity has characterized them and the fabrication of nanocomposites has become necessary to enhance their photocatalytic performance. Thus, AgInS2 quantum dots (AIS QDs, 4.0 ± 1.6 nm), have been successfully prepared and loaded onto ZnO nanopyramids (ZnO NPy). PT100 The effect of the nominal amount of AIS QDs decorating ZnO NPy on the morphology, optical properties, structure and surface chemistry of the nanocomposites was systematically studied. Photocatalytic tests revealed that the 1%AIS@ZnO NPy sample reported the highest photoactivity for phenol degradation in aqueous phase (92 % after one hour of irradiation, λ > 350 nm) that was 4 and 68 times the reported for bare ZnO NPy and AIS QDs, respectively. Accordingly, the maximum photocatalytic hydrogen evolution, under UV-vis light, for the same sample corresponded to 17 and 21 times the estimated for pristine ZnO NPy and AIS QDs, respectively. Hence, the AIS QDs - ZnO system has been applied in the photocatalytic field for the first time in this work and a synergetic effect was confirmed owing to a strong heterojunction formation between both semiconductors that allows an enhanced charge carrier separation, improving the photocatalytic activity.In the present study, catalytically inactive or low-active Ti4+ (d0) or Zn2+ (d10) ions were doped to α-Fe2O3 to tune the geometric and electronic engineering for Fe active center. X-ray absorption near edge structure (XANES) and Powder X-ray diffraction (XRD) analyses coupled with density functional theory (DFT) calculation show that the added of Ti4+ could occupy the interstitial octahedral or tetrahedral sites, resulting in surface Fe2+ species are oxidized to octahedrally coordinated Fe3+. As a result, more oxygen vacancies are generated, which improve the catalytic performance for toluene combustion. On the other hand, Fe2+ was substituted by Zn2+ ion could result in the partial destruction of hematite crystal structure, forming an additional phase of ZnFe2O4, and meanwhile part of Zn2+ ions replace the octahedrally coordinated Fe3+ sites, and therefore significantly decreasing the toluene catalytic performance. Moreover, our studies demonstrate that the combustions of toluene over Fe-based catalysts involve both the MvK and L-H mechanisms.