Distinct electrochemical and metabolic responses of anode respiring bacteria to sulfamethoxazole in microbial fuel cells coupled with constructed wetlands.

The influence of sulfamethoxazole (SMX) on the electrochemical activity, bacterial community, and metabolic state of anode respiring microbes was investigated in constructed-wetland-coupled microbial fuel cells (CW-MFCs). Results suggested that SMX shortened the acclimatisation period and enhanced the maximal power density of the CW-MFC at 0.1 mg/L. Cyclic voltammetry (CV) results indicated that SMX may trigger an electrocatalytic process related to an extra redox-active compound. Exposure to SMX significantly altered the bacterial communities, leading to decreased abundances of Desulfurivibrio and Pseudomonas, while increasing the contents of Rhodobacter and Anaerovorax. Furthermore, metabolites related to amino acids and nucleotide metabolism were suppressed at 10 mg/L SMX, while the related metabolites increased at 0.1 mg/L SMX. The upregulated pathway of biofilm formation indicated that the bacteria tended to form biofilms under the influence of SMX. This study provides valuable insights into the complex interactions between SMX and electrochemically active bacteria.

Functional Electrospun Nanofibrous Hybrid Materials for Colorimetric Sensors: A Review.

Electrospun nanofibrous hybrid materials have several advantageous characteristics, including easy preparation, high porosity, and a large specific surface area. Meanwhile, they can be more suitable for colorimetric detection in environmental and food areas than organic materials due to the advantages of inorganic nanomaterials, i.e., stability, low toxicity, and durability. In addition to being able to immobilize nanomaterials to avoid particle aggregation, electrospinning hybrid materials also have the advantages of high specific surface area and high porosity, which is beneficial for constructing colorimetric sensors. This review mainly summarizes the fabrication methods of electrospun nanofibrous hybrid materials and the application of electrospun nanofibrous hybrid material based colorimetric sensors. First, the preparation strategies of electrospun nanofibrous hybrid materials were discussed. Then, the applications of the obtained electrospun nanofibrous hybrid materials in the colorimetric sensors for environmental molecules in the gas and liquid phase were further investigated. Finally, this review looks forward to the development prospects and challenges of electrospun hybrid materials in practical applications of colorimetric sensors in order to support the application of colorimetric sensors in practical detection.

Coordination-Polymer-Derived Cu-CoO/C Nanocomposite Used in Fenton-like Reaction to Achieve Efficient Degradation of Organic Compounds.

In this paper, carbon-matrix-supported copper (Cu) and cobaltous oxide (CoO) nanoparticles were obtained by using coordination polymers (CPs) as a precursor. The aqueous solutions of copper methacrylate (CuMA) and cobalt methacrylate (CoMA) were preferentially prepared, which were then mixed with anhydrous ethanol to fabricate dual metal ion coordination polymers (CuMA/CoMA). After calcination under an argon atmosphere, the Cu-CoO/C nanocomposite was obtained. Scanning electron microscope (SEM) and transmission electron microscope (TEM) showed that the material has banded morphology, and the dual functional nanoparticles were highly dispersed in the carbon matrix. The prepared material was used in a heterogeneous Fenton-like reaction, with the aim of replacing traditional ferric catalysts to solve pH constraints and the mass production of ferric slime. The obtained nanocomposite showed excellent catalytic performance on the degradation of methylene blue (MB) at near-neutral conditions; the discoloration efficiency is about 98.5% within 50 min in the presence of 0.15 mmol/mL H2O2 and 0.5 mg/mL catalyst. And good reusability was verified via eight cycles. The plausible pathway for MB discoloration and the possible catalytic mechanism was also proposed.

Enhanced power generation, organics removal and water desalination in a microbial desalination cell (MDC) with flow electrodes.

This study introduced a flow electrode microbial desalination cell (FE-MDC), which used activated carbon (AC) particles and carbon nanotubes (CNTs) as the electrode to promote electron harvesting. The recovered electricity energy (0.371 KWh/m3) and columbic efficiency (66.7 %) of the FE-MDC were over 2 times higher than those of the conventional MDC without the flow electrode. Consequently, the salt and COD removal efficiencies were enhanced to 77.8 % and 91.2 %, respectively. Electrochemical analysis implied that the charge transfer resistance of the system was reduced by the flow electrode. Electron accumulation and charging-discharging experiments proved that the flow electrode could accumulate electrons and transfer the electrons to the fixed anode. Bacterial community analysis indicated that the bacterial activity was improved by the flow electrode. The content of the exoelectrogen Pseudomonas increased from 5.0 % to 14.7 %, and Hydrogenophaga improved from 1.4 % to 5.9 %. Finally, a continuous operation mode of the FE-MDC was established, and the flow electrode slurry was returned to the anodic chamber for recirculated utilization. The voltage output, COD removal, and salt removal during the operation mode reached 610 mV, 78.8 %, and 76.1 %, respectively. This study proved that the flow electrode is a promising way to promote the practical application of MDC technology.

Analysis on ecological status and spatial-temporal variation of Tamarix chinensis forest based on spectral characteristics and remote sensing vegetation indices.

The reserve of Tamarix forest, located in Changyi, China, is the only national marine special reserve taking Tamarix as the main object of protection. Compared with conventional monitoring technology, remote sensing technology can more comprehensively reflect the ecological environment status and spatial-temporal variation of monitoring objects. Based on spectral characteristics and remote sensing vegetation indices, the ecological status and spatial-temporal variation of Tamarix chinensis forest in the reserve deserve further exploration. Therefore, spectral characteristic, typical vegetation indices, comprehensive health index, VFC, and REP were analyzed based on Sentinel-2A images. Spatial-temporal variation analysis during 2014 to 2018 was analyzed based on GF-1 images. The research result indicated that ecological quality of protection zone showed an overall growth trend with the help of artificial ecological restoration, and it is possible to continuously implement ecological recovery towards the protection zone.

Bioelectrochemical process for simultaneous removal of copper, ammonium and organic matter using an algae-assisted triple-chamber microbial fuel cell.

Considering the adverse effect of heavy metals (such as Cu2+) on biological wastewater treatment processes, an algae-assisted triple-chamber microbial fuel cell (MFC) was established to remove Cu2+, COD and nitrogen sequentially, and also generate electricity. About 86.2% of the Cu2+ was removed in the first cathodic chamber, and the remaining Cu2+ was largely eliminated by algal uptake, contributing to an overall Cu2+ removal rate of 99.9% across the whole system. The nitrogen removal rate reached 79% in the system. The majority of the ammonium was assimilated by algae, and nitrogen oxides formed during the light period were denitrified at the cathode in the dark period. The variation in electrode potentials indicated that the cathode and anode potentials not only depended on the respective substrate concentrations, but also affected each other. The influence of algae on the microbial communities was greater than that of Cu2+ or the system structure. Devosia, Thauera, Pseudomonas, Acinetobacter and Flavobacterium may influence nitrogen removal, while Delftia, Thauera and Pseudomonas may play an important role in power generation. The present study has developed a practical method for removing pollutants from the wastewater containing heavy metals.

Construction of magnetic NiO/C nanosheets derived from coordination polymers for extraordinary adsorption of dyes.

Herein, a facial stratagem for the large-scale synthesis of NiO/C nanosheets used as magnetic adsorbents is proposed by using nanoscale coordination polymers (nanoCPs) as precursors. The NiO nanoparticles (NPs) scattered on the NiO/C nanosheets have an untrasmall size (~3 nm) as well as uniform dispersion, since the Ni2+ ions are preassembled into the nanoCPs precursors by coordination bonds and transformed to NiO NPs in situ under the restriction of carbon layers. Thanks to the small size and spatially uniform distribution of NiO NPs, fully exposed carbon matrix containing part of graphene structures, and the high specific surface area of the special nanosheet structure, the magnetic NiO/C nanosheets have an a great breakthrough in the adsorption performance toward Congo Red (CR) among many reported NiO-based materials. The maximum adsorption capacity for CR is up to 2000 mg/g, and the adsorption kinetics and thermodynamics are also systematically studied. Moreover, the NiO/C nanosheets can be separated from water and reused simply by an external magnetic field. The NiO/C nanosheets with low cost and extraordinary adsorption ability have great potential in water pollution treatment area.

A general autocatalytic route toward silica nanospheres with ultrasmall sized and well-dispersed metal oxide nanoparticles.

A facile and efficient approach for the synthesis of metal ions@silica nanospheres is proposed by using an intramolecular autocatalytic route. By the rational selection of reactants, metal ions@silica nanospheres can be obtained via successive spontaneous reactions under near neutral conditions. After thermal treatment, spherical silica equipped with ultrasmall and highly dispersed metal oxides nanoparticles was obtained.

Directed self-assembly of dual metal ions with ligands: towards the synthesis of noble metal/metal oxide composites with controlled facets.

The large-scale synthesis of noble metal/metal oxide spheres with controlled facets was for the first time enabled by making use of a bottom-up self-assembly strategy.

The development of novel Au/CaO nanoribbons from bifunctional building block for biodiesel production.

Herein, a novel and facile high-yield strategy is reported to efficiently fabricate 1D self-supported Au/CaO nanocatalysts using dual metal co-ordination polymers as templates. Significantly, a uniform distribution of dual metal nanoparticles can be ensured due to the fact that both Ca2+ and Au3+ ions are initially introduced into the co-ordination polymer via chemical bonding with bifunctional organic linkers and then, the Au and CaO nanoparticles are formed simultaneously in one pot via calcination. Furthermore, the as-prepared Au/CaO nanoribbons exhibit excellent catalytic performance in the transesterification reaction, which can be attributed to the small size and high distribution of CaO nanoparticles as well as the special 1D structure with high surface area. Moreover, leaching and deactivation, which are the main problems of CaO-based catalysts, are remarkably reduced due to the presence of hydrophobic Au nanoparticles on the surface of the CaO nanoribbons. Consequently, the Au/CaO nanoribbons can be used as recyclable catalysts with high activity for biodiesel production.

Autocatalytic synthesis of multifunctional precursors for fabricating silica microspheres with well-dispersed Ag and Co3O4 nanoparticles.

Herein, an autocatalytic route to fabricate dual metal ion-equipped organic/inorganic hybrid silica, an ideal precursor for multifunctional silica-based composites integrated with well-dispersed Ag and Co3O4 nanoparticles was demonstrated. Significantly, by rational selection of reactants, such dual metal ion-equipped organic/inorganic hybrid silica can be synthesized through successive spontaneous reactions under near neutral conditions without an additional catalyst. Both the Ag+ and Co2+ ions are introduced into silica by chemical bonds, which favor the formation of small-sized and well-dispersed Ag and Co3O4 nanoparticles without aggregation in the entire silica matrix. After calcination, multifunctional silica composites equipped with well-dispersed Ag and Co3O4 nanoparticles were obtained. The as-obtained silica composites, as indicated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), have a spherical morphology and smooth surface. TEM tests also reveal the well dispersed fashion of Ag and Co3O4 nanoparticles. In addition, the obtained Ag-Co3O4@SiO2 composites exhibit good catalytic performance in the reduction of methylene blue (MB) with NaBH4 as a reducing agent, and can be readily recycled by an external magnetic field due to their superparamagnetic properties.

A simple way to prepare Au@polypyrrole/Fe3O4 hollow capsules with high stability and their application in catalytic reduction of methylene blue dye.

Metal nanoparticles are promising catalysts for dye degradation in treating wastewater despite the challenges of recycling and stability. In this study, we have introduced a simple way to prepare Au@polypyrrole (PPy)/Fe3O4 catalysts with Au nanoparticles embedded in a PPy/Fe3O4 capsule shell. The PPy/Fe3O4 capsule shell used as a support was constructed in one-step, which not only dramatically simplified the preparation process, but also easily controlled the magnetic properties of the catalysts through adjusting the dosage of FeCl2·4H2O. The component Au nanoparticles could catalyze the reduction of methylene blue dye with NaBH4 as a reducing agent and the reaction rate constant was calculated through the pseudo-first-order reaction equation. The Fe3O4 nanoparticles permitted quick recycling of the catalysts with a magnet due to their room-temperature superparamagnetic properties; therefore, the catalysts exhibited good reusability. In addition to catalytic activity and reusability, stability is also an important property for catalysts. Because both Au and Fe3O4 nanoparticles were wrapped in the PPy shell, compared with precursor polystyrene/Au composites and bare Fe3O4 nanoparticles, the stability of Au@PPy/Fe3O4 hollow capsules was greatly enhanced. Since the current method is simple and flexible to create recyclable catalysts with high stability, it would promote the practicability of metal nanoparticle catalysts in industrial polluted water treatment.