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As a short-chain PFAS, GenX has gained increasing attention in recent years as a hazardous and emerging contaminant in water bodies. However, there is only limited research outcome up to date to address GenX remediation from water. In this research, we investigated amidoxime surface-functionalized PAN nanofibrous material from electrospinning as adsorbent to remove GenX from water. The nanofibrous adsorbent from 10 min treatment of electrospun PAN nanofibrous material in hydroxylamine (ASFPAN10) realized 35% GenX removal from a 100 mg/L aqueous solution at pH = 4 and 0.24 g/L loading after a simple one-time filtration with a GenX removal capacity of ~0.6 mmol/g. The mechanism study indicated that the GenX adsorption on PAN nanofibrous adsorbent could be mainly ascribed to hydrophobic interaction and dipole-dipole interaction between CN and C-F while the GenX adsorption on ASFPAN10 nanofibrous adsorbent could be mainly attributed to coulomb force between positive-charged CN+(OH)-H from ASFPAN10 and negative-charged COO- from GenX. Compared to that of PAN, the more hydrophilic surface of ASFPAN10 facilitated water access to the nanofibrous adsorbent surface and also contributed to the higher GenX removal efficiency. For the first time, this research pointed out a direction to use common economic materials for effective remediation of short-chain PFAS from water bodies especially at relatively high PFAS centration.Coal fly ash (CFA) is fine particles generated from coal combustion, and large amount of CFA causes environmental pollution. Traditionally, CFA is added into construction materials, which has realized effective reduction. As the exploration of CFA properties goes deeper, finer utilization has been studied to maximize the recycling of CFA. Summarized from plenty of investigations, structure reconstruction has become the most crucial part for re-production as well as pre-treatments. Various zeolites and other complex materials have been synthesized by structure reconstruction. In this work, the state of the art of structure reconstruction were technically collated in the order of pre-treatments, mechanisms, specific techniques, and novel optimizing strategies. It has been found the crystalline types are closely related to the reaction conditions, that certain types of products could be obtained via accurate condition controls, especially the ratio of Si to Al. The current as-synthesized products were listed as well as their crystalline structure characteristics. Recently, combined materials and techniques have been innovatively investigated. However, the challenge remains as low purity, not only impurities in CFA but also different types of zeolites formed in one process.Structure, reactivity and physico-chemical properties of polyhalogenated compounds determine their up-take, transport, bio-accumulation, transformation and toxicity and their environmental fate. In technical mixtures of chlorinated paraffins (CPs), these properties are distributed due to the presence of thousands of homologues. We hypothesized that roles of CP dehalogenation reactions, catalyzed by the haloalkane dehalogenase LinB, depend on structural properties of the substrates, e.g. chlorination degree and carbon-chain length. Tradipitant purchase We exposed mixtures of chlorinated undecanes, dodecanes and tridecanes in-vitro to LinB from Sphingobium Indicum bacteria. These single-chain CP-materials also contain small amounts of chlorinated olefins (COs), which can be distinct by mathematical deconvolution of respective mass-spectra. With this procedure, we obtained homologue-specific transformation kinetics of substrates differing in saturation degree, chlorination degree and carbon chain-length. For all homologues, two-stage first-order kinetic models were established, which described the faster conversion of reactive material and the slower transformation of more persistent material. Half-lifes of 0.5-3.2 h and 56-162 h were determined for more reactive and more persistent CP-material. Proportions of persistent material increased steadily from 18 to 67% for lower (Cl6) to higher (Cl11) chlorinated paraffins and olefins. Conversion efficiencies decreased with increasing chlorination degree from 97 to 70%. Carbon-chain length had only minor effects on transformation rates. Hence, the conversion was faster and more efficient for lower-chlorinated material, and slower for higher-chlorinated and longer-chained CPs and COs. Current legislation has banned short-chain chlorinated paraffins (SCCPs) and forced a transition to longer-chain CPs. This may be counterproductive with regard to enzymatic transformation with LinB.The potential application of silage fermentation on abandoned fresh tea leaves (AFTL) was investigated. Dynamic profiles of fermentation-related components, characteristic components and the bacterial community of AFTL during ensiling were analysed. The results showed that after ensiling for 60 days, the concentrations of lactic, acetic and propionic acid increased, whereas a high pH value (4.80) and NH3-N content (106 g/kg TN) were detected. Characteristic components, including caffeine, polyphenols, theanine and catechins, were well preserved. The microbial community changed significantly, and Lactobacillus (63.6%) became the dominant phylum. Spearman rank correlation revealed a positive correlation between lactic acid concentration and the abundance of Lactobacillus (63.6%) and Klebsiella (25.0%), whereas the abundance of Klebsiella was negatively correlated with catechin concentration. In conclusion, ensiling could be an effective utilization for AFTL and provides a new idea for utilizing idle resources on tea plantations.Compared with the Z-scheme and type-II heterojunctions, p-n type heterojunctions are more favorable for the migration of photo-induced carriers owing to the advantage of built-in electric fields. In addition, it is still of great significance to understand the carrier migration properties of the p-n heterojunction. Therefore, the development of new p-n heterojunctions and the development of high-efficiency catalysts with effective modulation of light responsiveness and rapid transfer of charge to achieve photocatalytic inactivation have attracted much attention. In this study, we synthesized a Ag2S/g-C3N4 heterojunction via the in situ deposition of Ag2S onto the g-C3N4 substrate. The prepared Ag2S/g-C3N4 composite facilitated photo-generated charge carrier transfer and exhibited outstanding photocatalytic inactivation of bacteria compared to that of a single catalyst under visible light irradiation. In addition, the ACN-2 composites fully deactivated 7 log10 CFU/mL E. coli and 7 log10 CFU/mL S. aureus cells in 90 min under visible light.

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