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Abstract Organic phosphorus (Po) is an important constituent of P pool. Soil phoD community is primarily involved Po transformation. However, influences of agriculturally-driven land-use change on different Po fractions, phosphatase activities and phoD community are largely unknown. Here, an investigation was carried out containing three treatments: vegetable field (VF), cropland (CF) and uncultivated land (UL). Various Po fractions were measured by Hedley’s sequential extraction and 31P-NMR methods. The activities of alkaline phosphomonoesterase (ALP), acid phosphomonoesterase (ACP), phosphodiesterase activity (PD) and phytase were assayed; the abundance, and diversity of phoD community and its co-occurrence networks were analyzed. Compared with the UL treatment, soil total organic P (total-Po) in the VF and CF treatments significantly increased by 75.9% and 53.0%, respectively, mainly attributed to the increases in NaHCO3-Po, NaOH-Po and C.HCl-Po. 31P-NMR spectra showed that, when land was reclaimed from uncultivated land into agriculture fields (i.e., VF and CF), myo-inositol hexaphosphate (myo-IHP), α-glycerophosphate (α-glyc) and β-glycerophosphate (β-glyc) were increased by 9.5, 3.9 and 2.0 times, respectively. The activities of ACP, ALP and PD in the VF and CF treatments were higher than in the UL treatment. The α-diversity of phoD community was also significantly increased by land reclamation. Moreover, the linkage between soil Po and Po-cycling-related biological parameters (ACP, ALP and PD and phoD community) was more pronounced by NaHCO3-Po and NaOH-Po than the Po fractions measured by 31P-NMR method. Topological parameters (edges, node degree, and betweenness centrality) of phoD community’s network in the VF and CF networks were higher than in the UL network, implying that land reclamation favored to construct a more cooperative network of phoD community. Collectively, our findings demonstrated that when uncultivated land was converted to cropland, soil Po was notably increased, and phoD community’s co-occurrence network was also strengthened. The outcomes of this study emphasize that when land was reclaimed from nature (uncultivated land) into agriculture fields, the fertilization strategy of organic combined with chemical fertilizers application was beneficial for improving P fertility and assembling organic P-cycling related community.

Abstract Biochar and biochar-based materials have been studied extensively in multidisciplinary areas because of their outstanding physicochemical properties. In this review article, biochar and biochar-based materials in the removal of environmental pollutants, hydrogen generation and carbon dioxide capture were summarized and compared. The interaction mechanisms were discussed from the experimental results and characterization analysis. The high porous structures, active surface sites, (co)doping of single metals/nonmetals, and incorporation of metal oxides or other materials improved the high activity of biochar-based materials in their applications. However, there are still some challenges such as: (1) the fact that H2 generation with high selectivity or the produced syngas to meet the real application requirement in industrial is the main challenge in H2 production; (2) the fact that the selective capture of CO2 with high stability, high adsorption capacity and recyclability at low-cost should be considered and focused on; (3) the sorption-(photo)degradation of the organic chemicals; and (4) the fact that the sorption-reduction-extraction/solidification of metals/radionuclides are efficient methods for the elimination of environmental pollutants. In the end, the perspectives, challenges and possible techniques for biochar-based materials’ real application in future were described. Graphical Abstract

Abstract Herein, a biochar-based composite (Ti3C2Tx@biochar-PDA/PEI) was constructed by decorating Ti3C2Tx and polydopamine on coconut shell biochar via electrostatic self-assembly method. Different characterization techniques were applied to explore the structure, morphology and composition of the sorbents. It was found that the higher porosity and diverse functional groups were conducive for Ti3C2Tx@biochar-PDA/PEI to capture radionuclides, and the water environmental conditions made a great contribution to the adsorption process. The process of removing U(VI)/Cs(I) well complied with the Langmuir isotherm and Pseudo-second-order equations, which indicated that the single layer chemical adsorption occurred on the solid liquid interface. Meanwhile, this produced composite exhibited superior removal performance under complex co-existing ion environment, and the maximum adsorption amounts of U(VI) and Cs(I) reached up to 239.7 and 40.3 mg g−1. Impressively, this adsorbent still exhibited good adsorption performance after three cycles of regeneration. The spectral analysis and DFT calculation demonstrated that adsorption of U(VI) might be a chemical process, while the adsorption of Cs(I) should be ion exchange or electrostatic attraction. This study demonstrated the potential application of Ti3C2Tx@biochar-PDA/PEI as an effective remediation strategy for radioactive wastewater cleanup. Graphical Abstract

The East Zhejiang Canal is an artificial waterway located in the plains of East China. Because of its role in providing social services, it is frequently subjected to human activities affecting its health. To improve the water resource management and condition of this canal, assessment of its ecological health is necessary. We measured water quality variables and benthic diatom and macroinvertebrate assemblages to evaluate the ecological status of the canal. We found that the canal was eutrophic with an average chemical trophic level index of 64.3 and an average trophic diatom index of 68.1 (with Nitzschia palea, Melosira varians, and Navicula rostellata, Encyonema minutum abundant). Macroinvertebrate assemblages also showed that the canal was eutrophic based on the dominance of Limnodrilus sp. A low BMWP (Biological Monitoring Working Party) score further indicated the poor water quality of the canal. Correlation analysis indicated that phosphorus was the main driver of eutrophication in the canal. Consequently, more attention should be paid to reduce phosphorus loadings.

ABSTRACTGlycogen storage disease type Ia (GSD-Ia) is caused by a deficiency in the glucose-6-phosphatase (G6Pase, G6pc) enzyme, which catalyses the final step of gluconeogenesis and glycogenolysis. Accumulation of G6pc can lead to an increase in glycogen and development of fatty liver. Ductular reactions refer to the proliferation of cholangiocytes and hepatic progenitors, which worsen fatty liver progress. To date, however, ductular reactions in GSD-Ia remain poorly understood. Here, we studied the development and potential underlying mechanism of ductular reactions in GSD-Ia in mice. We first generated GSD-Ia mice using CRISPR/Cas9 to target the exon 3 region of the G6pc gene. The typical GSD-Ia phenotype in G6pc−/− mice was then analysed using biochemical and histological assays. Ductular reactions in G6pc−/− mice were tested based on the expression of cholangiocytic markers cytokeratin 19 (CK19) and epithelial cell adhesion molecule (EpCAM). Yes-associated protein 1 (Yap) signalling activity was measured using western blot (WB) analysis and quantitative real-time polymerase chain reaction (qRT-PCR). Verteporfin was administered to the G6pc−/− mice to inhibit Yap signalling. The CRISPR/Cas9 system efficiently generated G6pc−/− mice, which exhibited typical GSD-Ia characteristics, including retarded growth, hypoglycaemia, and fatty liver disease. In addition, CK19- and EpCAM-positive cells as well as Yap signalling activity were increased in the livers of G6pc−/− mice. However, verteporfin treatment ameliorated ductular reactions and decreased Yap signalling activity. This study not only improves our understanding of GSD-Ia pathophysiology, but also highlights the potential of novel therapeutic approaches for GSD-Ia such as drug targeting of ductular reactions.

Abstract Formation of chlorate (ClO3 −) and perchlorate (ClO4 −) as by-products in electrooxidation process has raised concern. In the present study, the formation of ClO3 − and ClO4 − in the presence of 1.0 mM Cl− on boron doped diamond (BDD) and Magneli phase titanium suboxide (Ti4O7) anodes were evaluated. The Cl− was transformed to ClO3 − (temporal maximum 276.2 μM) in the first 0.5 h on BDD anodes with a constant current density of 10 mA cm2, while approximately 1000 μM ClO4 − was formed after 4.0 h. The formation of ClO3 − on the Ti4O7 anode was slower, reaching a temporary maximum of approximately 350.6 μM in 4.0 h, and the formation of ClO4 − was also slower on the Ti4O7 anode, taking 8.0 h to reach 780.0 μM. Compared with the BDD anode, the rate of ClO3 − and ClO4 − formation on the Ti4O7 anode were always slower, regardless of the supporting electrolytes used in the experiments, including Na2SO4, NaNO3, Na2B4O7, and Na2HPO4. It is interesting that the formation of ClO4 − during electrooxidation was largely mitigated or even eliminated, when methanol, KI, and H2O2 were included in the reaction solutions. The mechanism of the inhibition on Cl− transformation by electrooxidation was explored.

Highlights 1. Adsorption-photocatalytic degradation of organic pollutants by biochar-based catalysts is summarized. 2. Adsorption-(photo)catalytic reduction-solidification of heavy metal ions is discussed. 3. Mechanism and active free radicals on the degradation/reduction of contaminants are compared and described. 4. The methods to improve the photocatalysis performance of biochar-based catalysts are introduced. 5. The challenges for the real application of biochar-based materials are provided.

In this study, a novel synergistic photocatalyst (Fe3O4/GO/g-C3N4 composites) were constructed by chemical precipitation of Fe3O4 nanoparticles on surface of GO/g-C3N4 suspension. The characterization results indicated that Fe3O4/GO/g-C3N4 composites exhibited high efficient separation of photogenerated electron–hole pair, narrow bandgap (∼2.38 eV) and wide absorption range. The incorporation of Fe3O4 significantly increased the photocatalytic performance of GO/g-C3N4 composites due to synergistic effect. More than 90% of U(VI) was photo-reduced by Fe3O4/GO/g-C3N4 composites within 2 h under visible light irradiation. The trapping experiments and XPS analysis indicated that the photogenerated electrons and superoxide (⋅O2) radicals are responsible for U(VI) removal. These findings indicated that magnetic g-C3N4 composites can be used as excellent candidates for the high efficient removal of U(VI) in actual environmental cleanup.

Metal-organic frameworks (MOFs) have garnered multidisciplinary attention due to their structural tailorability, controlled pore size, and physicochemical functions, and their inherent properties can be exploited by applying them as precursors and/or templates for fabricating derived hollow porous nanomaterials. The fascinating, functional properties and applications of MOF-derived hollow porous materials primarily lie in their chemical composition, hollow character, and unique porous structure. Herein, a comprehensive overview of the synthetic strategies and emerging applications of hollow porous materials derived from MOF-based templates and/or precursors is given. Based on the role of MOFs in the preparation of hollow porous materials, the synthetic strategies are described in detail, including (1) MOFs as removable templates, (2) MOF nanocrystals as both self-sacrificing templates and precursors, (3) MOF@secondary-component core-shell composites as precursors, and (4) hollow MOF nanocrystals and their composites as precursors. Subsequently, the applications of these hollow porous materials for chemical catalysis, electrocatalysis, energy storage and conversion, and environmental management are presented. Finally, a perspective on the research challenges and future opportunities and prospects for MOF-derived hollow materials is provided. Public summary: • MOFs have garnered multi-disciplinary attention due to their unique inherent properties • Various synthetic strategies of MOFs-derived hollow porous materials are summarized • Emerging applications of MOFs-derived hollow porous materials are reviewed

Acid stress is a challenging condition that yeast cells must overcome during fermentation. Enhancing the inherent tolerance of industrial Saccharomyces cerevisiae to organic acid stresses is crucial for increasing fermentation efficiency and reducing economic costs. In a previous study, we constructed a Saccharomyces cerevisiae strain SWY85S with improved tolerance to citric acid stress by modifying the second PEP4-allele. Malic acid is a dominant organic acid in grapefruit, which forms the acidic constituents of wine fermentation mash and finished products. We investigated the malic acid stress tolerance of the strain SWY85S in comparison with that of a strain with one PEP4-allele disrupted and the wild-type strain in this study. Our results revealed that the strain SWY85S demonstrated greater tolerance of malic acid stress, regardless of whether it was cultured with adequate nutrient supplies or under amino acid starvation. Moreover, the strain SWY85S performed remarkably in converting glucose to ethanol during fermentation under malic acid stress. This study provides insights into the role of a vacuolar PEP4-allele coding product in response to environmental stress and the physiological mechanism of yeast to withstand organic acid stress.

In this work, a CdS/BiVO4 step-scheme (S-scheme) heterojunction with self-photothermally enhanced photocatalytic effect was synthesized and applied for efficient U(VI) photoextraction. Characterizations such as transient absorption spectroscopy and Tafel test together confirmed the formation of S-scheme heterojunctions, which allows CdS/BiVO4 to avoid photocorrosion while retaining the strong reducing capacity of CdS and the oxidizing capacity of BiVO4. Experimental results such as radical quenching experiments and electron spin resonance show that U(VI) is rapidly oxidized by photoholes/•OH to insoluble UO2(OH)2 after being reduced to U(IV) by photoelectrons/•O2-, which precisely avoids the depletion of electron sacrificial agents. The rapid recombination of electron-hole pairs triggered by the S-scheme heterojunction is found to release large amounts of heat and accelerate the photocatalysis. This work offers a new enhanced strategy for photocatalytic uranium extraction and presents a direction for the design and development of new photocatalysts.

Phthalic acid esters (PAEs) pollution has become an increasing issue worldwide, but little is known about its effects on ammonia-oxidizers and nitrous oxide (N2O) in the soil environment. Here, a 50-day soil microcosm experiment was conducted using low and high doses bis (2-Ethylhexyl) phthalate (DEHP) to estimate the effect of DEHP exposure on soil N2O emissions and the nitrifying community in calcareous soil. The results showed that DEHP exposure at 10 and 100 mg kg-1 doses significantly reduced N2O by 67.5% and 73.6%, respectively, relative to the DEHP absent treatment. The microbial biomass carbon and nitrogen (MBC and MBN) were consistently and significantly decreased with DEHP exposure at 5, 22, and 50 days after incubation, especially with high-dose. The bipartite association networks showed that DEHP exposure changed the compositions of both ammonia-oxidizing archaea (AOA) and ammonia-oxidizing bacteria (AOB) communities. Moreover, the AOA and AOB amoA gene abundances were significantly decreased by DEHP addition to the soil (P

Summary: Covalent organic frameworks (COFs) are a new type of crystalline porous polymers known for chemical stability, excellent structural regularity, robust framework, and inherent porosity, making them promising materials for capturing various types of pollutants from aqueous solutions. This review thoroughly presents the recent progress and advances of COFs and COF-based materials as superior adsorbents for the efficient removal of toxic heavy metal ions, radionuclides, and organic pollutants. Information about the interaction mechanisms between various pollutants and COF-based materials are summarized from the macroscopic and microscopic standpoints, including batch experiments, theoretical calculations, and advanced spectroscopy analysis. The adsorption properties of various COF-based materials are assessed and compared with other widely used adsorbents. Several commonly used strategies to enhance COF-based materials’ adsorption performance and the relationship between structural property and sorption ability are also discussed. Finally, a summary and perspective on the opportunities and challenges of COFs and COF-based materials are proposed to provide some inspiring information on designing and fabricating COFs and COF-based materials for environmental pollution management.

Microplastics (MPs), a kind of novel contaminant, have potential to concentrate and transport heavy metals in the aquatic environment. This feature may affect the distribution and bioavailability of heavy metals. In order to determine the sorption behaviors of heavy metals onto the MPs, the sorption kinetics and mechanisms were investigated between the MPs (polyvinylchloride PVC, polyethylene PE, polystyrene PS) and Pb(II). The results suggested that the Pb(II) sorption onto the MPs were pH- and ionic strength-dependent. The sorption processes were best fitted by the pseudo-second-order model, and the rate-limiting steps were the intraparticle diffusion and final equilibrium process. The maximum sorption capacities of PVC, PE and PS were 483.1 μg/g, 416.7 μg/g and 128.5 μg/g under the condition of 0.01 M NaCl, pH 6.0, T = 298 K. The sorption rate constants were in the following order: PVC

Metal-enhanced photocatalysis has recently received increasing interest, mainly due to the ability of metal to directly or indirectly degrade pollutants. In this review, we briefly review the recent breakthroughs in metal-enhanced photocatalysis. We discussed the recent progress of surface plasmon resonance (SPR) effect and small size effect of metal nanoparticles on photocatalysis; in particular, we focus on elucidating the mechanism of energy transfer and hot electron injection/transfer effect of metal nanoparticles and clusters while as photocatalysts or as cophotocatalysts. Finally, we discuss the potential applications of metal-enhanced photocatalysis, and we also offer some perspectives for further investigations.

With the fast development of industry and nuclear energy, large amounts of different radionuclides are inevitably released into the environment. The efficient solidification or elimination of radionuclides is thereby crucial to environmental pollution and human health because of the radioactive hazardous of long-lived radionuclides. The properties of negatively or positively charged radionuclides are quite different, which informs the difficulty of simultaneous elimination of the radionuclides. Herein, we summarized recent works about the selective sorption or catalytic reduction of target radionuclides using different kinds of nanomaterials, such as carbon-based nanomaterials, metal–organic frameworks, and covalent organic frameworks, and their interaction mechanisms are discussed in detail on the basis of batch sorption results, spectroscopy analysis and computational calculations. The sorption-photocatalytic/electrocatalytic reduction of radionuclides from high valent to low valent is an efficient strategy for in situ solidification/immobilization of radionuclides. The special functional groups for the high complexation of target radionuclides and the controlled structures of nanomaterials can selectively bind radionuclides from complicated systems. The challenges and future perspective are finally described, summarized, and discussed.

The selective elimination of long-lived radioactive actinides from complicated solutions is crucial for pollution management of the environment. Knowledge about the species, structures and interaction mechanism of actinides at solid–water interfaces is helpful to understand and to evaluate physicochemical behavior in the natural environment. In this review, we summarize recent works about the sorption and interaction mechanism of actinides (using U, Np, Pu, Cm and Am as representative actinides) on natural clay minerals and man-made nanomaterials. The species and microstructures of actinides on solid particles were investigated by advanced spectroscopy techniques and computational theoretical calculations. The reduction and solidification of actinides on solid particles is the most effective way to immobilize actinides in the natural environment. The contents of this review may be helpful in evaluating the migration of actinides in near-field nuclear waste repositories and the mobilization properties of radionuclides in the environment.

The novel carbon based acid has been synthesized via one-step hydrothermal carbonization of furaldehyde and hydroxyethylsulfonic acid. A highly efficient procedure for the synthesis of fructone has been developed using the novel carbon based acid. The results showed that the catalyst possessed high activity for the reaction, giving a yield of over 95%. The advantages of high activity, stability, reusability and low cost for a simple synthesis procedure and wide applicability to various diols and β-keto esters make this novel carbon based acid one of the best choices for the reaction.