Frandsenlawrence1520

From DigitalMaine Transcription Project
Revision as of 23:35, 21 November 2024 by Frandsenlawrence1520 (talk | contribs) (Created page with "Moreover, the re-used of the optimum photocatalyst was evaluated. Finally, a mechanism for the photocatalytic decomposition of the antibiotic was suggested. Exposure to fine p...")
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to: navigation, search

Moreover, the re-used of the optimum photocatalyst was evaluated. Finally, a mechanism for the photocatalytic decomposition of the antibiotic was suggested. Exposure to fine particulate matter (PM2.5) have been associated with adverse respiratory outcomes, but long-term effect of personal exposure on lung function remains largely unknown. We conducted a panel study of 158 adult residents with 394 measurements of personal PM2.5 concentration and lung function within six years to investigate the long-term association. Linear mixed models were used to identify the associations between lung function changes in relation to different levels of persistent personal PM2.5 exposure in three or six years. We further attempted to validate resident areas (city) and smoking status as potential predictors of the long-term PM2.5 exposure levels (persistently high/ persistently low) by generating ROC curves. Compared with subjects who had persistently low exposure level, those with persistently high levels of personal PM2.5 exposure had an additional 3.63 % decline in FEV1/FVC in three years (-3.63 [-7.25, -0.02]), while 7.15 % decline in six years (-7.15 [-14.27, -0.03]). BMI can modify the association. The AUCs were 0.68 (95 %CI 0.54, 0.82), 0.75 (0.64, 0.86), and 0.82 (0.71, 0.93) for models including smoking status, resident areas, and smoking status combining resident areas respectively. These findings provide new evidence for the long-term effect of personal PM2.5 exposure on lung function decline. Selleck Pentylenetetrazol In this study, a method of disposing food waste is introduced via catalytic pyrolysis under CO2 condition. The catalyst and CO2 hindered the generation of condensable compounds, leading to enhancing non-condensable gas generation. However, they did not affect the amount of solid residues left after the thermal reaction. The amount of condensable cyclic compounds was reduced when the catalyst and/or CO2 were used. The enhancement of non-condensable gas production and reduction of cyclic compounds formation were maximized when the Pt catalyst and CO2 were simultaneously applied to the pyrolysis of food waste. For instance, approximately 67.3 % less cyclic compounds, including benzene derivatives, were generated at 700 °C in the presence of the catalyst under a CO2 atmosphere compared to non-catalytic conditions without CO2. The results suggest that a CO2-assisted catalytic pyrolysis is as environmentally benign disposal method for food waste. Piezoelectricity, as a kind of physical phenomenon, is a coupling between a material's mechanical and electrical behavior. Herein, the local accumulated charges on the surface of piezoelectric material were used to break OO bond of peroxymonosulfate (PMS) to induce its activation for the benzothiazole (BTH) removal. Taking BaTiO3 as a model piezocatalyst, up to 97 % of BTH was degraded within 30 min in BaTiO3/PMS/force system, which was respective 40 %, 79 %, 83 % higher than that in BaTiO3/force piezocatalysis, force/PMS oxidation, and BaTiO3/PMS adsorption. A significant synergistic effect was observed since the reaction rate constant of BaTiO3/PMS/force was 3 times higher than the sum of those later three processes. The possible activated mechanism was proposed based on reactive species analysis, DFT calculation and LCMS determination. The stability of the piezocatalyst and the treatment performance for real wastewater were studied to investigate the potential in practical applicability. All the results demonstrated that the BaTiO3 piezoelectricity can efficiently activate PMS to enhance BTH removal, which is a promising strategy for PMS activation, as well as a valuable insight for the piezoelectrical application in wastewater remediation. Silver nanoparticles (AgNPs) are compounds used in numerous consumer products because of their desirable optical, conductive and antibacterial properties. However, several in vivo and in vitro studies have raised concerns about their potential developmental toxicity. Here, we employed a human embryonic stem cell model to evaluate the potential ectodermal toxicity of AgNPs, at human relevant concentrations. Among the four major ectodermal lineages tested, only cranial placode specification was significantly affected by AgNPs and AgNO3, morphology-wise and in the expression of specific markers, such as SIX3 and PAX6. Mechanistically, we found that the effects of AgNPs on the cranial placode differentiation were probably due to Ag ion leakage and mediated by the FGF signaling. Thus, AgNPs may have the ability to alter the early stages of embryonic development. Nitrated nonylphenols (2-nitro-nonylphenols, NNPs) are metabolites of the endocrine-disrupter nonylphenols (NPs). While they have been detected in the environment, their fate in activated sludge has yet to be determined. In this study, we used synthesized NNP isomers and a 14C-tracer technique to study the degradation and transformation of four NNP isomers (NNP111, NNP112, NNP38, and NNP65) in nitrifying activated sludge (NAS) and heterotrophic bacteria-enhanced activated sludge (HAS). Our results showed that the degradation of NNPs in both NAS and HAS was isomer-specific. The half-lives of the NNPs decreased in the order NNP111 > NNP112 > NNP38 > NNP65. After 36 days of incubation, 9.48 % and 4.01 % of the 14C-NNP111 was mineralized in NAS and HAS, respectively. In addition to mineralization, five metabolites of NNPs containing hydroxyl, carbonyl, and carboxyl substituents on the alkyl chains were formed in NAS but not in HAS. The transformation of NNPs differed in NAS and HAS, mainly due to the differences in their microbial communities and the activities thereof in NAS and HAS. This is the first study of the isomer-specific fate of NNP isomers in activated sludge. Future studies should assess the toxicity, stability and potential risks of NNP metabolites in the environment. The influence of digestate dissolved organic matter (DOM) on chemical behavior of soil heavy metals (HMs) in an abandoned copper mining areas was explored by fluorescence quenching titration and heavy metal extracting experiment. Five fluorescent components were obtained from digestate DOM by PARAFAC model combined with the EEM data. The stability constant (log KM) values were in the range of 4.95-5.53, 5.05-5.29, 5.21-6.00, and 4.12-4.75 for DOM-Cr(III), DOM-Cu(II), DOM-Fe(III) and DOM-Pb(II) complexes, respectively. Alcohols, ethers and esters in digestate DOM were preferentially combined with Fe(III), Cu(II) and Zn(II). However, phenolic hydroxyl groups were more likely to combine with Cr(III) and Pb(II). The speciation distribution of HMs indicated that mining resulted in a higher concentration of Cu(II) in the grassland soil (GS) than those in the agricultural soil (AS) and forest land soil (FS). Fe-Mn oxides and organic forms of Pb(II) increased dramatically due to mining. Digestate DOM extraction can increase the content of Cr(III), Fe(III) and Pb(II), and decrease the content of Cu(II) and Zn(II) in the AS, GS, and FS.