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Carbon-based materials have been applied as cost-effective electrocatalysts to reduce carbon dioxide (CO2) into valuable chemicals. Here, an environment-friendly method is proposed to obtain nitrogen-doped porous carbons (NPCs) from digested sludge, which is an abundant waste product from sewage treatment plants. The materials were used as a metal-free electrocatalyst for electrochemical reduction of CO2 to formate. The synthesized material (NPC-600) had a mesoporous and microporous structure with a specific surface area of 246.21 m2 g-1 and pore volume of 0.494 cm3 g-1. Active sites based on nitrogen atoms accounted for 2.98 atom% of the content and included pyrrolic-, pyridinic-, and graphitic-N, which is useful for CO2 adsorption and electron transfer in electrochemical reduction. The Faradaic efficiency for formate production from CO2 in the presence of NPC-600 was 68% at the potential of -1.5 V vs. SCE. Tafel analysis indicated that the pathway of CO2 conversion involved the reduction of CO2 to CO2*- intermediate, which was then converted to HCOO*- and finally formate.A relevant but yet unconsidered subset of particles that may alter the fate of extracellular antibiotic resistance genes (eARGs) are nano-scale particles (NPs), which are ubiquitous in natural environments and have unique properties. GDC-1971 mouse In this study, sorption isotherms were developed describing the association of linear DNA fragments isolated from widespread eARGs (blaI and nptII) with either micon-sized kaolinite or silica nanoparticles (SNPs), to determine if sorption capacity was enhanced at the nanoscale. For each isotherm, eARG fragments were added at five starting concentrations (5-40 μg/mL) to mixed batch systems with 0.25 g of particles and nuclease-free water. Sorption was quantified by the removal of DNA from solution, as detected by a Qubit fluorimeter. Isotherms were developed for eARGs of various fragment lengths (508, 680 and 861 bp), guanine-cytosine (GC) contents (34%, 47% and 54%) and both double and single stranded eARGs, to assess the impact of DNA properties on particle association. Sorption isotherms were also developed in systems with added humic acid and/or CaCl2, to assess the impact of these environmental parameters on sorption. FTIR analysis was performed to analyze the conformation of sorbed eARGs. Desorption of eARGs was studied by quantifying the removal of eDNA from washed and vortexed post-sorption particles. Statistically significant irreversible sorption of eARGs to environmentally relevant NPs (humic acid functionalized silica nanoparticles) was demonstrated for the first time. Nano-emergent properties did not increase sorption capacity of eARGs, but led to a unique compressed conformation of sorbed eARGs. The addition of humic acid, increased CaCl2 concentration and small DNA fragment size favored sorption. NPs showed a slight preference for the sorption of single-stranded DNA over double-stranded DNA. These findings suggest that NP association with eARGs may be a significant and unique environmental phenomenon that could influence the spread of antibiotic resistance.With observational analysis and WRF-Chem simulation on a heavy air pollution event in January 2019 over the Twain-Hu Basin (THB) in Central China, this study characterized the regional transport of PM2.5 emitted from the North China Plain (NCP) to the THB region in Central China and quantitatively assessed the influence of the regional PM2.5 transport and precipitation washout on PM2.5 change in the wintertime heavy air pollution over the THB. It was found that the THB's heavy air pollution event was exacerbated by the strong northeasterly winds driving a quasi 2-day time lag of regional PM2.5 transport from the NCP to the THB. The multi-scale atmospheric circulations of cold air invasion influenced by East Asian winter monsoon and the terrain block of THB altered the structures of regional PM2.5 transport in deteriorating air quality to the THB. It was assessed for the THB region that the enhancing contribution of regional PM2.5 transport to the high air pollution level reached up to 70.5% in the heavy air pollution, and the precipitation washout could contribute the 55.3% PM2.5 removal to dissipating the PM2.5 pollution over the THB with frequent precipitation and wet environment, distinguishing from the dominance of wind-cleaning air pollution in the other regions in China.The utilization of biomass pyrolysis volatile-derived water-dissolved organic matter (WOM, often called wood vinegar) determines sustainable recycling of biomass. Further, pyrolysis temperature significantly controls the cracking of biomass components, resulting in various molecular compositions and biological responses of WOM. Although it has been widely used in the agriculture, the relationship between molecular compositions and biological responses affected by heating temperature is still unclear. Here, it was observed that the WOM concentration increased with increasing temperatures and the pyrolysis of 1 g biomass can generate ~ WOM with 36.24 mg C. Moreover, with increasing pyrolysis temperatures, the generated WOM consisted of more phenols but fewer alcohols, furans, acids, and ketones, and demonstrated characteristics of higher aromaticity and lower m/z molecular weight. Due to the enhanced polarity, high temperatures promoted the solubility of WOM. Germination tests show that low pyrolysis temperatures-derived WOM ( 400 °C) with small-molecular-weight and high oxygen-containing (high O/Cwa) inhibited growth. These results suggest that WOM can be separately collected at different pyrolysis temperatures to achieve sustainable recycling of pyrolysis volatile.To eliminate the spread of a novel coronavirus breaking out in the end of 2019 (COVID-19), the Chinese government has implemented a nationwide lockdown policy after the Chinese lunar New Year of 2020, resulting in a sharp reduction in air pollutant emissions. To investigate the impact of the lockdown on aerosol chemistry, the number fraction, size distribution and formation process of oxalic acid (C2) containing particles and its precursors were studied using a single particle aerosol mass spectrometer (SPAMS) at the urban site of Liaocheng in the North China Plain (NCP). Our results showed that five air pollutants (i.e., PM2.5, PM10, SO2, NO2, and CO) decreased by 30.0-59.8% during the lockdown compared to those before the lockdown, while O3 increased by 63.9% during the lockdown mainly due to the inefficient titration effect of O3 via NO reduction. The increased O3 concentration can boost the atmospheric oxidizing capacity and further enhance the formation of secondary organic aerosols, thereby significantly enhancing the C2 particles and its precursors as observed during the lockdown.

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