Tunable schiff-based networks with different bonding sites for enhanced photocatalytic activity under visible-light irradiation: The effects of steric hindrance.

Organic polymers hold great potential in photocatalysis considering their low cost, structural tailorability, and well-controlled degree of conjugation for efficient electron transfer. Among the polymers, Schiff base networks (SNWs) with high nitrogen content have been noticed. Herein, a series of SNWs is synthesized based on the melamine units and dialdehydes with different bonding sites. The chemical and structural variation caused by steric hindrance as well as the related photoelectric properties of the SNW samples are investigated, along with the application exploration on photocatalytic degradation and energy production. The results demonstrate that only SNW-o based on o-phthalaldehyde responds to visible light, which extends to over 550 nm. SNW-o shows the highest tetracycline degradation rate of 0.02516 min-1, under 60-min visible light irradiation. Moreover, the H2O2 production of SNW-o is 2.14 times higher than that of g-C3N4. The enhanced photocatalytic activity could be ascribed to the enlarged visible light adsorption and intramolecular electron transfer. This study indicates the possibility to regulate the optical and electrical properties of organic photocatalysts on a molecular level, providing an effective strategy for rational supramolecular engineering to the applications of organic materials in photocatalysis.

Water-compatible halloysite-imprinted polymer by Pickering emulsion polymerization for the selective recognition of herbicides.

A water-compatible molecularly imprinted polymer was prepared by Pickering emulsion polymerization using halloysite nanotubes as stabilized solid particles. During polymerization, we used 4-vinylpyridine as monomer, divinylbenzene as cross-linking agent, toluene as porogen, 2,2-azobisisobutyronitrile as initiator, 2,4-dichlorophenoxyacetic acid as template to form the oil phase, and Triton X-100 aqueous solution to form the water phase. The halloysite nanotubes molecularly imprinted polymer was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. Kinetic and equilibrium bindings were also employed to evaluate the adsorption properties of the imprinted polymer. The imprinted polymer showed better selectivity, more rapid kinetic binding (60 min) for 2,4-dichlorophenoxyacetic acid in pure water compared with rebinding in toluene. The imprinted polymer was used as a sorbent to enrich and separate 2,4-dichlorophenoxyacetic acid from water, and was detected by high-performance liquid chromatography with UV detection.

Microplastics in landfill and leachate: Occurrence, environmental behavior and removal strategies.

Plastic wastes buried in landfill are gradually broken and decomposed into microplastics under physical, chemical and biological effects, bringing environmental risks to the exploitation of waste resources. Landfill leachate as a potential source of environmental microplastics has not good attention. Microplastics in leachate carry toxic and harmful pollutants and antibiotic resistance genes, and these vectors pose greater risks to human and environmental health without systematic treatment. Recently, the main technologies of landfill leachate treatment process include order batch activated sludge process, membrane biological reaction process, flocculation process, combined filtration process, and constructed wetland process. However, there is still little knowledge about microplastic removal of the existing leachate treatment facilities, and some technologies to alleviate the sources of such microplastics should be timely developed. This paper systematically summarizes the occurrence of plastics, microplastics and nanoplastics in leachate and their interactive pollution with other toxic pollutants. Meanwhile, the prospects of their environmental behaviors in landfill and leachate are put forward. The microplastic removal by existing leachate treatment equipment and the limitations and challenges to upgrading process of development and implementation are also discussed. The paper can provide a scientific basis for studying the fate of microplastics in landfill and leachate.

Advanced oxidation processes for the elimination of microplastics from aqueous systems: Assessment of efficiency, perspectives and limitations.

Microplastics act as a vector of heavy metals, organic pollutants, pathogens and resistance genes in the environment further aggravate the pollution of plastics. The conventional wastewater/water treatment processes can physically capture and remove most of microplastics, but the success rates varies. How to quickly remove a large amount of microplastics from aqueous system is a key research topic at present. Recently, advanced oxidation processes (AOPs) as a green elimination strategy has attracted attention because of its effective elimination, strong destruction and safety. The molecular chain of microplastics can be gradually degraded into small molecular organics until H2O and CO2 by strong oxidizing free radical produced by AOPs. Unfortunately, problematically, the elimination of microplastics in aqueous system by AOPs is recently carried out on a laboratory scale. The application and implementation of this strategy are restricted by long reaction time, low liquid phase degradation efficiency and the formation of nanoplastics. Generally, the technology is still in its infancy, and most studies are carried out under laboratory conditions. The degradation of microplastics in aqueous system also needs appropriate conditions, but it is not always feasible under field conditions in AOPs. Although AOPs can be used as a green degradation technology to eliminate microplastics in aqueous systems in theory, it still needs to be furtherly explored in practical application. Consequently, before AOPs as a green elimination strategy is successfully applied to the effective remove microplastics, more in-depth research is still required, such as the setting from single condition to complex environment, the transfer from laboratory scale to field scale, and systematic toxicity evaluation of corresponding products.

Recent advances in impacts of microplastics on nitrogen cycling in the environment: A review.

Nitrogen cycling plays a decisive role in biogeochemistry, and largely depends on microbial driven nitrogen transformation. The environmental problems caused by microplastics are becoming more serious, and the analysis and control of its pollution in the environment have become a research hotspot in the field. The nitrogen transformation and nitrogen cycling in the environment are mainly driven by microorganisms in the environment, and the existence of microplastics can affect the microbial population, abundance and type, thus affecting the transformation of nitrogen. The effect of microplastics on microorganisms involved in nitrogen transformation is briefly described. This paper mainly reviews the research progress on the impacts of microplastics on nitrogen transformation and nitrogen cycling in water, soil, sediment and sewage sludge. Microplastic type, size and concentration can cause obvious difference in the impacts of microplastics on nitrogen transformation. Then, response and mechanism of microplastics to microorganism mediated nitrogen transformation and nitrogen cycling are introduced. Processes of nitrogen transformation are affected by interfering with microorganism diversity and structure, enzyme activities and related coding genes and oxygen flux. Additionally, additives released from microplastics can also affect the microbial activity. However, mechanisms of microplastics on environmental nitrogen transformation and nitrogen cycling are not fully understood due to the lack of relevant research. There are effective strategies to evaluate complex environmental systems, prolong action time, strengthen multi factor and multi-level research, and assist molecular biology and stable isotope technology. This review article can provide valuable insights into the impact of microplastics on microorganisms mediated nitrogen transformation processes and evaluate the impact on ecological and environmental health.

Lignocellulosic biomass derived N-doped and CoO-loaded carbocatalyst used as highly efficient peroxymonosulfate activator for ciprofloxacin degradation.

Burning lignocellulosic biomass wastes in an outdoor atmosphere has placed heavy burden on ecological environment and increased risk on human health. Converting solid agricultural wastes into functional materials is a research hotspot. In this study, N-doped and CoO-loaded carbocatalyst (CoO-N/BC) was successfully synthesized from the cotton stalk biomass via a simple synthesis process of impregnation and carbonization. Compared with cotton stalk biomass derived pristine biochar, the CoO-N/BC possessed a higher specific surface area (466.631 m2 g-1vs 286.684 m2 g-1) as well as a better catalytic performance in the activation of peroxymonosulfate (PMS) for CIP degradation. The superior catalytic efficiency was ascribed to the directional flow of electrons on the well-organized carbon network of CoO-N/BC, which accelerated electron migration and improved electron conduction ability. Based on the results of radical quenching experiment and electron paramagnetic resonance (EPR), both radical and non-radical process conjointly led to the stepwise decomposition of CIP, and singlet oxygen (1O2) mediated non-radical pathway was discovered to play a dominant role. Besides, the carbon-bridge mediated non-radical pathway was proved to accelerate this degradation process through the experiments of prolong the time of adding CIP at different time intervals. Nitrogen doped sites and CoO active sites as well as defects formed in sp2-hybridized carbon network were supposed to be the active sites for PMS. Furthermore, EIS and LSV were employed to confirm the electron transfer mediated non-radical process of reaction system. This work provides a modified strategy for the disposition of lignocellulosic biomass wastes and illuminates the underlying mechanism of heterogeneous catalysis by CoO-N/BC.

Benzyl butyl phthalate activates prophage, threatening the stable operation of waste activated sludge anaerobic digestion.

The stable operation of the anaerobic digestion of waste activated sludge (WAS) is threatened by numerous emerging contaminants. Meanwhile, the extensive microplastic pollution increased the environmental exposure risk of plasticizer benzyl butyl phthalate (BBP), the BBP content has reached a substantial level in WAS. However, the effect of BBP on WAS anaerobic digestion is still unknown. Here we show that high-level BBP brings on anaerobic digestion upset. The presence of 10.0 mg/L BBP (in sludge with 17,640 ± 510 mg/L TSS) led to deferred cell lysis, which was confirmed by the results of continuous parallel factor analysis of dissolved organic matter and the liberation of lactate dehydrogenase. Further, the deferred cell rupture was confirmed associate with prophage activation during WAS anaerobic digestion. Besides solubilization, the hydrolysis, acetogenesis and methanogenesis were also affected by the addition of BBP. The long-term effects of BBP revealed that the dominant microbial structure in anaerobic digester was stable, but the abundance of many functional microorganisms was changed, including short chain fatty acid producers and consumers. This work highlights one of the susceptibility mechanisms for WAS anaerobic digestion processes and provides new perspectives for the comprehensive assessment of emerging contaminant's environmental risks.

Efficient conversion of myricetin from Ampelopsis grossedentata extracts and its purification by MIP-SPE.

In this study, we developed an efficient conversion process of dihydromyricetin to myricetin from Ampelopsis grossedentata extracts. The content of myricetin increased from 2.38% to 85.57%, demonstrating the successful dehydrogenation of dihydromyricetin. Molecularly imprinted polymers (MIPs) were prepared by surface imprinting method using silica microspheres as the support matrices and myricetin as template. The MIPs were applied for the selective adsorption of myricetin. The chemical structure of the MIPs was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. Static, dynamic and selective adsorption experiments showed that the MIPs exhibited good adsorption ability, rather fast template rebinding kinetics, and appreciate selectivity over structurally related compounds. Accordingly, the MIPs were applied as the selective sorbent in SPE to purify myricetin obtained through dehydrogenation, followed by HPLC-UV analysis. The recoveries of myricetin and dihydromyricetin were 92.7% and 55.6%, respectively. This study demonstrates the feasibility of using the developed MIP-SPE method to purify and enrich myricetin in the natural products.