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The meta-analysis in regards to the piling up regarding volatile organic compounds customer base through Sedum alfredii and Sedum plumbizincicola within infected garden soil.
Risk assessment indicated that the MP-associated pharmaceuticals posed low risks to organisms, and warm-blooded organisms suffered relatively higher risks than cold-blooded ones. This study reveals important information to understand the ecological risks of co-existed MPs and pollutants in the environment. The emergence of more and more persistent organic molecules as contaminants in water simulates research towards the development of more advanced technologies, among which photocatalysis is a feasible choice. However, it is still challenging to design a photocatalyst that fulfills all the requirements for industrial application, i.e., active under visible-light irradiation, shape with handy convenience, highly uniform distribution of active sites, substrate with excellent electronic properties, etc. In this study, we report an attempt to solve these issues at once by designing a film-like photocatalyst with uniform distribution of nitrogen-doped ZnO nanoparticles along nitrogen-doped carbon ultrafine nanofibers with three-dimensional interconnected structure. Under visible-light irradiation, the product exhibited remarkable reactivity for the degradation of two model pollutants tetracycline hydrochloride and 2,4-dichlorophenol within 100 min. The cyclic experiments demonstrated only a slight loss (ca. 5 %) of reactivity after five consecutive photocatalytic reactions. We also investigated the detailed relationship between the structural features and the superior properties of this product, as well as the degradation mechanisms. The convenient shape of the product with excellent performances for the treatment of real polluted water increases its suitability for larger scale application. Our work provides a rational design of photocatalysts for environmental remediation. A considerable amount of volatile organic compounds (VOCs) is emitted, and a vast amount of citric acid residue (CAR) waste is simultaneously produced during citric acid production. Thus, a suitable method realizing the clean production of citric acid must be developed. This study investigated the adsorption of the multicomponent VOCs in a homemade CAR waste-based activated carbon (CAR-AC). A fixed-bed experimental setup was used to explore the adsorption and desorption of single- and multi-component VOCs. Surface adsorption and diffusion molecular models with different defects were built to study the underlying adsorption and diffusion mechanisms of multicomponent VOCs on CAR-AC. The adsorption amount of ethyl acetate in CAR-AC from multicomponent VOCs was 3.04 and 5.91 times higher than those of acetone and acetaldehyde, respectively, and the interaction energy between ethyl acetate and C surfaces was low at -13.41 kcal/mol. During desorption, the most weakly adsorbed acetaldehyde desorbed from the surface of CAR-AC first, followed by acetone and ethyl acetate. The regeneration efficiencies of acetaldehyde, acetone, and ethyl acetate reached 88.77, 85.55, and 91.46 %, respectively, after four adsorption/desorption cycles. We aimed to provide a new strategy to realize the recycle use of CAR and the clean production of citric acid. Flotation is an effective and clean separation technology to realize the recovery of metal in waste printed circuit boards (WPCBs). The flotation kinetic of metal and non-metal components was concerned in this study. In addition, the loading of bubbles, the collision and shedding of particles and bubbles were used to assist in proving the particle dynamics results. By analyzing the force on the particles, the load of bubbles on particles was analyzed, and the appropriate volume ratio of bubbles to particles was 1.5-8.0, depending on the particle density. Moreover, Clift model and Schiller-Naumann model has high fitting accuracy for the final bubble velocity. In addition, metal particles have greater settling velocity, which results in shorter collision time with bubbles. In the process of bubble-particle rising, the shedding probability gradually decreases, and the shedding probability of metal particles is much higher than that of non-metal particles. The results of flotation kinetics show that the removal of impurity particles represented by silicon mainly occurs in the initial stage of flotation process. The loss of copper increases with flotation time and collector dosage. This study reveals the flotation kinetics of particles from the perspectives of bubble loading, bubble-particle collision and shedding. Covalent organic frameworks (COFs) have attracted tremendous attention due to their excellent performance in wastewater remediation, but their practical application still suffers from various challenges. The development of highly-efficient magnetic COFs along with fast adsorption kinetic and high adsorption capacity is very promising. To achieve the purpose, thiol-functionalized magnetic covalent organic frameworks (M-COF-SH) with abundant accessible chelating sites were designed and synthesized by utilizing disulfide derivative as building blocks and subsequently cutting off the disulfide linkage. After the cutting process, the crystallinity, porosity, superparamagnetism of pristine M-COF are well maintained, and the resultant M-COF-SH turned out to be an effective and selective platform for Hg2+ capture from water. Impressively, the resulting composite exhibited a maximum adsorption capacity of Hg2+ as high as 383 mg g-1. In addition, it also displays a rapid kinetic, where the adsorption equilibrium can be achieved within 10 min. More importantly, there is no significant loss of its adsorption performance even after recycling 5 times. This work not only offers a reliable platform for wastewater remediation but also provides a conceptual guide to prepare functionalized M-COF composites which cannot be obtained through conventional approaches. A new strategy was applied by periodic stacking of active sites of Cu and reduced graphene oxide (rGO) in the form of Cu-rGO LDH nanohybrid material. The experimental results revealed that newly prepared Cu-rGO LDH nanohybrid material was extremely reactive in PMS activation as evident from the degradation rate of 0.115 min-1, much higher than Mn-rGO LDH (0.071 min-1), Zn-rGO LDH (0.023 min-1) or other benchmarked material used during the degradation of bisphenol A (BPA). This excellent activity of Cu-rGO LDH nanohybrid was attributed to the better PMS utilization efficiency as compared to the other catalysts. Additionally, the characterization techniques disclosed that the layer by layer arrangement of active sites in the Cu-rGO LDH catalyst promotes interfacial electron mobility owing to the synergistic association between Cu in LDH and interlayered rGO. Based on the in-situ electron paramagnetic resonance spectroscopy (EPR) and chemical scavengers, singlet oxygen (1O2) was unveiled as dominant reactive species for pollutant removal, resulting from the recombination of superoxides (O2-) or reduction of active Cu centers. We believe that this novel Cu-rGO LDH/PMS system will open up a new avenue to design efficient metal-carbon nanohybrid catalysts for the degradation of emerging aquatic pollutants in a real application. This work demonstrates a facile route to assemble MIL-53(Fe) by solvothermal method. Sulfate radical-based advanced oxidation processes (SR-AOPs) coupling with photocatalysis based on MIL-53(Fe) were investigated under visible light. The catalytic effect of MIL-53(Fe) for the degradation of tetracycline hydrochloride (TC-HCl) was systematically studied, as well as the reusability of the catalyst and the effect of operating parameters. The results indicated that 99.7 % of TC (300 mg/L) could be degraded within 80 min in the SR-AOPs coupling with photocatalysis processes, as compared to 71.4 % for the SR-AOPs and only 17.1 % for the photocatalysis. The trapping experiments and electron spin-resonance spectroscopy (ESR) showed the photogenerated electrons of MIL-53(Fe) under visible light irritation were trapped by persulfate to generated sulfate radicals which effectively suppressed the recombination of photogenerated carriers. And also, the SO4- could be formed by the conversion between Fe (Ⅲ) and Fe (Ⅱ) in MIL-53(Fe). Moreover, OH and O2- generated by the reaction increased significantly due to the increase of SO4- which generated more OH and reduced photogenerated carrier recombination respectively. Thus, the degradation efficiency of TC-HCl was improved. Furthermore, the degradation pathway for TC-HCl was proposed using the theoretical calculations and liquid chromatography coupled with mass spectrometry. External organic sources could make up for the lack of carbon in the treatment of chlorophenol; but the impact on external carbon concentration on the degradation of 2,4,6-trichlorophenol (2,4,6-TCP) has rarely been studied. In this study, the effect of carbon addition on the degradation of 2,4,6-TCP was investigated using the lab-scale sequencing batch reactor (SBR). The results indicated that excessive carbon amounts inhibited 2,4,6-TCP degradation in the long-term operation and a typical cycle, while a suitable dosage could increase the removal of 2,4,6-TCP. The application of external carbon rapidly decreased the dissolved oxygen level of the system, resulting in inhibited chlorophenol removal. The concentration of removed 2,4,6-TCP could be increased from 35.49-152.89 mg L-1 by adjusting the carbon dosage. At the phylum level, Proteobacteria and Acidobacteria phylum bacteria, related to 2,4,6-TCP removal, were dominant when no carbon source was added, while excessive carbon levels resulted in the overgrowth of Saccharibacteria (50.19 %), responsible for carbon metabolism. In co-metabolism systems, chlorophenol-contaminated wastewater can effectively be treated by adjusting the external carbon source. Here we present photoelectrochemical (PEC) bacterial inactivation properties of large-scale fabricable Ti/MoS2/MoOx photoanode with a strong solar light absorbance capacity. Specifically, by thermal oxidation of the as-prepared MoS2/Ti film at 250 °C for 15 min in aerobic condition, the visible light performance of photocurrent generation and Escherichia coli (E. coli) inactivation are markedly enhanced. Complete inactivation of 106 CFU/mL E. coli in NaCl electrolyte is achieved with 0.5 V bias in 2 h under visible light irradiation, and H2O2 and O2- have been found as key reactive oxidative species to destroy E. coli. The bacteria inactivation performance of present photoanode is comparable with reported visible light photoanodes such as Cu2O or N-doped TiO2. The markedly improved PEC performance and inhibited photocorrosion could be attributed to the formation of heterojunction of MoS2/MoOx on the surface due to thermal oxidation. Furthermore, the PEC E. coli inactivation performance and stability of the large dimensional electrode are evaluated in a scale-up reactor. As an example of self-sustainable PEC water treatment system powered by only solar panels, wastewater containing inorganic, organic, macromolecule and microbial pollutants is attempted to be treated employing the developed electrodes under illumination of LED lamps. selleck products Rational design of highly active and selective photocatalyst for NO removal is significant for the commercial application of photocatalytic technology because the secondary byproduct caused by insufficient and non-selective pollutant oxidation process is a major challenge. In this work, Pd nanoparticles decorated C3N4 (PdCN) is designed by density functional theory (DFT) at first. The PdCN exhibits superiority to CN in terms of both kinetics and thermodynamics performances, as reflected in the lower activation barrier of rate-determining step and higher selectivity for the final product (nitrate) instead of toxic intermediate (NO2). The as-designed highly selective and efficient photocatalyst is then fabricated by a facile method with an extremely low content of Pd particles supported on C3N4. Compared to bare CN, the synthesized PdCN exhibits highly enhanced purification of NO in air and strong inhibition of toxic NO2 by-product as supported by in-situ DRIFTS investigation, which is consistent with the theoretical prediction.
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