Notes

To the outcome regarding EFL Teachers' Self-Efficacy along with Combined Efficiency on Kids' Engagement.
Ovarian cancer (OC) is a severe malignancy featuring a poor prognosis due to rapid metastasis and chemotherapy resistance. In this study, we extensively investigated the upstream and downstream mechanisms of miR-548e in regulating OC progression and cisplatin resistance. Our results indicated that ZFAS1 was highly expressed and promoted OC cell proliferation, migration, invasion, and cisplatin resistance by directly suppressing miR-548e expression. ZFAS1 co-localized with miR-548e in the cytosols of OC cells. miR-548e repressed CXCR4 expression, and elevated CXCR4 expression promoted OC cell proliferation, migration, invasion, and cisplatin resistance. Cisplatin resistance induced by ZFAS1 and CXCR4 overexpression in OC cells was mediated by their suppression on let-7a and elevation of BCL-XL/S expression. ZFAS1 knockdown and miR-548e and let-7a overexpression impaired cisplatin resistance and suppressed lung metastatic nodule formation in nude mice. In conclusion, ZFAS1 binds with miR-548e to enhance CXCR4 expression to promote OC cell proliferation and metastasis, which also enhances cisplatin resistance by suppressing let-7a and elevating BCL-XL/S protein expression. Nanoplastics (NPs) and microplastics (MPs) are a heterogeneous class of pollutants with diverse sizes in aquatic environments. To evaluate the hazardous effects of N/MPs with different sizes, the accumulation, oxidative stress, cytochrome P450 (CYP) enzymes, neurotoxicity, and metabolomics changes were investigated in the red tilapia exposed to three sizes of polystyrene (PS) N/MPs (0.3, 5, and 70 - 90 μm). Gedatolisib After 14-d exposures, the largest particles (70 - 90 μm) showed the highest accumulation levels in most cases. Exposures to PS-MPs (5 and 70 - 90 μm) caused a more severe oxidative stress in red tilapia than PS-NPs. The activity of CYP3A-related enzyme was obviously inhibited by PS-NPs, whereas the CYP enzymes in the liver may not be sensitive to MP exposures. In the brain, only 5 μm PS-MPs significantly inhibited the acetylcholinesterase activity. After exposures, the treatments with 0.3, 5, and 70 - 90 μm N/MPs resulted in 31, 40, and 23 significantly differentially expressed metabolites, respectively, in which the pathway of tyrosine metabolism was significantly affected by all the three PS-N/MP exposures. Overall, the PS particles within the μm size posed more severe stress to red tilapia. Our results suggest that the toxicity of N/MPs may not show a simply monotonic negative correlation with their sizes. In spent lithium iron phosphate batteries, lithium has a considerable recovery value but its content is quite low, thus a low-cost and efficient recycling process has become a challenging research topic. In this paper, two methods about using the non-oxidizing inorganic iron salt - Fe2(SO4)3 to recover lithium from LiFePO4 are proposed. The method-1 is theoretical-molar Fe2(SO4)3 (Fe2(SO4)3 LiFePO4 =12) dosage is added and more than 97% of lithium can be leached in just 30 min even under a pretty high solid-liquid ratio of 500 g/L. Spectrophotometry provides the evidence of Fe2+/Fe3+ substitution in the leaching process. In the method-2, the generated Fe2+ originating from LiFePO4 is fully utilized with the addition of H2O2, and the dosage of Fe2(SO4)3 is decreased by two thirds (Fe2(SO4)3 LiFePO4 =16). Several sulphates (CuSO4, NiSO4, MgSO4) are employed to explore the leaching mechanism. All the results reveal that the reaction of Fe3+ substituting Fe2+ has a powerful driving force. In addition, these two leaching processes simultaneously present superior selectivity for the impurities. The Fe2(SO4)3 in two methods does not cause pollution and is easily regenerated by adding H2SO4. The proposed rapid, efficient and selective leaching thought would be a competitive candidate for recycling spent LiFePO4 batteries. Photocatalytic degradation of pollutants in high salinity wastewater usually shows extremely low activities and produces highly toxic by-products, often related to the presence of excess chloride ion (Cl-). Herein, we report for the first time that involvement of Cl- (quenching active species and generating chlorinated by-products) could be effectively blocked during photocatalytic processes. Based on a comprehensive investigation of its mechanism, we found that Cl- could quench superoxide radicals (O2-) through a cyclic indirect quenching model with holes (h+) and hydroxyl radicals (OH) quenching as "initiators". Thus, scavenging h+ and OH could successfully block the chain reactions between Cl- and O2-, and photocatalytic degradation of methyl orange (a refractory dye, with O2- as dominant attacking species) could be enhanced by nearly 50 times, even when Cl- content was up to 10 wt%. More importantly, both HPLC-MS analyses and DFT calculation validated that, by blocking its quenching effect, Cl- could be successfully excluded from the pollutant degradation processes, thus preventing the generation of toxic chlorinated by-products. This work provides new insights into control of chlorinated by-products and proposes feasible strategies to extend photocatalytic technology in high salinity wastewater. Nitro-polycyclic aromatic hydrocarbons (NPAHs) are of increasing global concern due to their ubiquitous occurrence and long-range transport in the environment. However, their potential metabolism-disrupting effects, especially nuclear receptor-related lipid disorders, are still poorly understood. Targeting estrogen receptor α (ERα), this study for the first time evaluated the lipid metabolic effects of NPAHs using in vitro and in vivo models. The results indicated that four of the five NPAHs tested exhibited significant ERα agonistic activities, and induced increased secretion of 17β-estradiol (E2) in HepG2 cells. Furthermore, lipidomic analysis showed that exposure to the candidate NPAH (3-nitrofluoranthene, 3-NFA) led to elevated hepatic levels of triacylglycerols (TAGs) and cholesteryl esters (CEs). Importantly, the lipid overload induced by 3-NFA was verified in the livers of zebrafish larvae using Oil Red O staining. Additionally, significant increases in E2 production and the expression levels of associated genes (17βHSD and C/EBP-α) further supported the involvement of the ERα signaling pathway in the lipid metabolic perturbation induced by 3-NFA. These results provide novel insight into the lipid metabolism-disrupting effects induced by NPAHs and may offer a better understanding of the environmental risks of NPAHs. Oxynitrides with narrow band gap are promising materials as visible-light sensitive photocatalysts, because introduction of nitrogen ions can negatively shift the position of valence band maximum of the corresponding oxides to negative side. (Zn1+xGe)(N2Ox) with wurtzite structure is one of the oxynitride materials. (Zn1+xGe)(N2Ox) with nanotube morphology was synthesized by nitridation of Zn2GeO4 nanorods at 800 °C for 6 h. During the nitridation process, the nanorod with smooth surface was transformed into nanotube with rough surface in spite of no template for formation of tube structure. The nanotube formation can be caused by ordered morphological transformation from Zn2GeO4 nanorod during the nitridation. (Zn1+xGe)(N2Ox) nanotube exhibited a large specific surface area due to its nanotube morphology and the ability to be responsive to visible light because of the narrow band gap of 2.76 eV. Compared to (Zn1+xGe)(N2Ox) synthesized by conventional solid state reaction, the optimized (Zn1+xGe)(N2Ox) nanotube possessed enhanced photocatalytic NOx decomposition activity under both ultraviolet and visible light irradiation. In this study, a novel Al°-CNTs-Cu2O composite, capable of activating O2 to generate H2O2 and further to reactive oxygen species (ROSs) at a wide pH range, was synthetized, characterized and applied for the degradation of sulfamerazine. In the activation of O2 by Al°-CNTs-Cu2O composite, H2O2 was generated from the reaction of O2 with Al°-CNTs, which could be catalytically decomposed into O2- and OH by Cu2O, the formed Cu(II) could be rapidly reduced to Cu2O by Al°-CNTs in composite, which made Al°-CNTs-Cu2O composite reusable and decreased the leaching of copper ions into solution. The removal efficiency of SMR and TOC was 73.91 % and 56.80 %, respectively at initial pH = 5.8, T = 20 °C, O2 flow rate = 100 mL/min, Al°-CNTs-Cu2O dosage = 2 g/L, SMR = 50 mg/L, and reaction time = 60 min. The removal efficiency of SMR kept almost unchanged and the concentration of copper ions in solution was below 0.5 mg/L. The Al°-CNTs-Cu2O/O2 process could be used as a novel catalyst for the degradation of refractory organic contaminants in water and wastewater by Fenton-like process at a wide pH range through the in situ generation of H2O2. Coal fly ash (CFA) is a valuable industrial solid waste, but conventional methods used for its disposal can lead to serious and long-lasting environmental issues. The study of technologies for CFA recycling has been of major concern, while the harm caused by CFA is only partially understood, limiting its reuse. In this review, the basic physico-chemical properties of CFA are introduced, followed by a systematic summary and discussion of the leachability of CFA via different leaching methods and the chemical speciation of some typical metal elements in CFA, which is related to its harmful effects. The specific harm that CFA causes to humans, wild animals, and plants and the study status of magnetic property of CFA are presented. Because of the pervasive concerns of many people, the utilisation of CFA in the USA and Europe and an economic and environmental analysis of its disposal is provided and discussed. Finally, some possible directions for future research involving CFA are proposed. China has applied the ultra-low emission technology in coal-fired power plants to control traditional air pollutants and to reduce Hg emissions synergically. In this study, we applied field experiment, model calculation, and literature review to evaluate the Hg control effect of ultra-low emission technology and the potential cross-media effect comprehensively. The dominant ultra-low emission technology significantly improves the atmospheric Hg removal efficiency from 75% to 87%. Such improvement mainly comes from the effect of dust removal devices. Based on the calculated distribution characteristic of Hg content of wastes, we find out that the improvement of Hg control effect of air pollution control devices significantly increase the Hg content of fly ash, which rises from 0.16 mg/kg to 0.33 mg/kg. However, the Hg content of gypsum decreases from 0.75 mg/kg to 0.51 mg/kg. Whether or not to carry out ultra-low emission retrofits, Hg contents of wastes from coal-fired power plants are overall lower than the limit of 25 mg/kg which is intended to be set as the limit for Hg-containing wastes. However, the embodied more than two hundreds of tons Hg in these wastes still require policies to guide the disposal of these wastes. V.Nanoscale zerovalent iron (nZVI) and sulfidated nanoscale zerovalent iron (S-nZVI) have been increasingly studied for heavy metal removal in the subsurface. However, a comprehensive comparison of the effectiveness of the technologies and the stability of derived metal-adsorbed composites is lacking. In this study, we evaluated the colloidal stability and transport of nZVI, S-nZVI and S-nZVI modified with nanosized silica (FeSSi). Furthermore, we monitored the metal immobilization performance of the three nanoparticles (NPs) under anoxic conditions in synthetic groundwater for 30 days. The NP-metal composites were thereafter discharged into a river water and metal remobilization was monitored for 20 days. Sulfidation improved the colloidal stability of nZVI in both simple media and in natural waters, although a lower initial agglomeration rate constant (ka) was observed in unmodified nZVI at acidic pH. The transport of nZVI in saturated soil column was enhanced with sulfidation due to decreased electrostatic attraction between the NPs and sand.
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