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Anaerobic pond was found to perform well also by removing 97.8% of COD in POME but require long retention time and larger land. Hence, this study aims to provide intensive review of the performance of the anaerobic biofilm reactor in treating POME and the recent advancements in this technology. The limitations and future perspectives in utilization of anaerobic biofilm reactor during its operation in treating POME are discussed.Despite growing interest in developing extensive fuel treatment programs to prevent catastrophic wildfires in the Mediterranean region, there is little information on the projected effectiveness of fuel treatments in terms of avoided exposure and risk. In Portugal, a fuel management plan aiming to prevent loss of lives, reduce large fires (>500 ha), and reduce annual burned area is under implementation, with particular emphasis on the nation-wide fuel break network (FBN). In this study, we evaluated the effectiveness of the planned FBN in terms of meeting fire management objectives, costs, and benefits. We first estimated the overall effectiveness of the FBN at intersecting modeled large fires (>500 ha) and at reducing exposure to protected areas and residential buildings using wildfire simulation modeling. Then, the fuel break burn-over percentage, i.e. the percentage of fires that are not contained at the FBN, was modeled as a function of pre-defined flame length thresholds for individual FBN segments. For the planned FBN, the results suggested a potential reduction of up to 13% in the annual burned area due to large fires (ca. 13,000 ha), of up to 8% in the annual number of residential buildings exposed (ca. 100 residential buildings), and up to 14% in the annual burned area in protected areas (ca. 2400 ha). The expected burn-over percentage was highly variable among the segments in response to estimated fire intensity, and an average decrease of 40% of the total benefits was estimated. The most important fuel breaks typically showed a higher percentage of fire burn-over, and hence reduction in effectiveness. We also showed that the current implementation of FBN follows a random sequence, suboptimal for all objectives. Our results suggest that additional landscape-scale fuel reduction strategies are required to meet short-term national wildfire management targets.Lithium-sulfur battery(LSB)'s commercial manufacturing has been mainly retarded by the "shuttle effect" and low electrical conductivity of polysulfides (LiPSs). Designing a cathode with hollow and hierarchically porous structures was expected to solve the above problems. Herein, a kind of TiN particles with the hierarchical hollow double-shelled structures was synthesized and applied to cathodes of LSB. The Fig-like hollow TiO2 particles (FHTiO2s) were firstly synthesized by the hard-template method. Subsequently, the Fig-like hierarchical hollow double-shelled TiN particles (FHTiNs) were synthesized by the template-free sequential transformation and separation approach (STSA). It was verified that the heating temperature and time were key parameters. Special Fig-like double-shell hollow structures could greatly increase the loading of S, and the excellent initial capacity of FHTiNs cathodes was up to 1159 mAh/g. On the one hand, the Fig-like framework in internal cavity and double-shell structures could promote the ultrahigh specific surface area, and the adsorption to LiPSs was improved by increasing active sites; On the other hand, the shuttle effect of LiPSs was weakened by the fig-like framework and double-shell structures, which slowed down the massive dissolution of sulfur in the electrolyte. As a result, the pleasant rate performance of FHTiNs cathodes was up to 400 mAh/g at 5C. This novel structures and synthesis method provided a new strategy for the designing of LSB cathodes.Aqueous zinc ion batteries have attracted extensive concern as a promising candidate for large-scale energy storage because of their high theoretical specific capacity, low cost and inherent safety. However, the lacking of applicable cathode materials with outstanding electrochemical performance have severely hindered the further development of aqueous zinc ion batteries. Herein, we report a hierarchical accordion-like manganese oxide@carbon (MnO@C) hybrid with strong interaction heterointerface and comprehensively inquire into its electrochemical performance as cathode materials for aqueous zinc ion batteries. The unique hierarchical accordion-like layered structure coupling with strong interaction heterointerface between small MnO and carbon matrix efficaciously improve the ion/electron transfer process and enhance structure stability of the MnO@C hybrid. Benefitting from these unique advantages, the MnO@C hybrid bestows excellent specific capacity of 456 mAh g-1 at 50 mA g-1. Impressively, the MnO@C hybrid presents distinguished long-term cycling stability with fairly low decay rates of only 0.0079 % per cycle even over 2000 cycles at 2000 mA g-1. Moreover, comprehensive characterizations are executed to elucidate the mechanism involved. Therefore, this work affords a new idea for developing outstanding performance manganese-based cathode materials for aqueous zinc ion batteries.Silicon (Si) is attracted much attention due to its outstanding theoretical capacity (4200 mAh/g) as the anode of lithium-ion batteries (LIBs). However, the large volume change and low electron/ion conductivity during the charge and discharge process limit the electrochemical performance of Si-based anodes. Here we demonstrate a foldable acrylic yarn-based composite carbon nanofiber embedded by Si@SiOx particles (Si@SiOx-CACNFs) as the anode material. Since the amorphous SiOx and carbon (C) coating on the outside of the Si particles can provide a double buffer for volume expansion while reducing the contact between the Si core and the electrolyte to form a thin and stable solid electrolyte interface (SEI) film. Simultaneous in-situ electrochemical impedance spectroscopy (in-situ EIS) and galvanostatic intermittent titration technique (GITT) tests show that SiOx and C have higher ion/electron transport rates, and in addition, using acrylic fiber yarn and Zn(Ac)2 as raw materials reduces the manufacturing cost and enhanced mechanical properties. Therefore, the half-cell can achieve a high initial Coulombic efficiency (ICE) of 82.3% and a reversible capacity of 1358.2 mAh/g after 180 cycles. It can return to its original shape and remain intact after four consecutive folds, and the soft-pack full battery can also light up LED lights under different bending conditions.

Layered double hydroxide (LDH) loaded with orthophosphate (PO

) are suggested as slow-release P fertilizers. However, PO

-LDHs have a low maximal P content, related to high charge HPO



/PO



anions occupying the anion exchange capacity (AEC) of LDHs. We postulate that the P content of LDHs can be enhanced by exchanging them with polymeric-P (i.e. trimetaphosphate, P

O

), which has a lower molar charge/P ratio than its monomer.

Adsorption capacities were compared between PO

and P

O

for as-synthesized and calcined MgAl LDHs with Mg/Al ratio of 2, 3, or 4; the P-LDHs were characterized (XRD, FTIR). Dialysis and soil incubation experiments were performed with PO



LDHs, P

O



LDHs, and corresponding soluble fertilizers to compare their P release and P solubility (CaCl

extract).

The P adsorption capacities were 1.25-1.60 fold larger for P

O

compared to PO

, yet the high theoretical P contents with P

O

were not achieved (incomplete loading, P

O

depolymerization). P

O

-Mg

Al released polymeric-P whereas P

O

-Mg

Al released depolymerized PO

, and P release from P

O

-LDHs was slower than that of PO

-LDHs. With soil incubation, soluble P from P

O

-LDH was initially lower but later converged to that of PO

-LDH as result of continued hydrolysis, yet did not exceed that of the soluble P

O

and PO

fertilizers.

The P adsorption capacities were 1.25-1.60 fold larger for P3O9 compared to PO4, yet the high theoretical P contents with P3O9 were not achieved (incomplete loading, P3O9 depolymerization). P3O9-Mg3Al released polymeric-P whereas P3O9-Mg2Al released depolymerized PO4, and P release from P3O9-LDHs was slower than that of PO4-LDHs. With soil incubation, soluble P from P3O9-LDH was initially lower but later converged to that of PO4-LDH as result of continued hydrolysis, yet did not exceed that of the soluble P3O9 and PO4 fertilizers.Obtaining of non-noble metal catalyst with bifunctional effect for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in water splitting is highly desired to get high purity hydrogen. Here in, we design and fabricate Cu/Ni bimetallic phosphides with Graphdiyne (GDY) to form hybrid nanomaterial CuNiPx-GDY on Ni foam for the first time. The synergistical effect between GDY and transition metal phosphides, and the atomic scale heterojunctions between Cu3P and Ni2P, effectively accelerate the catalytical process both in HER and OER, resulting in extraordinarily small overpotentials of 178 mV and 110 mV at 10 mA cm-2 for OER and HER in CuNiPx-GDY(11) in 1 M KOH, respectively. Density functional theory results show that, compared with pure CuNiPx, the introduced GDY can considerably improve the activity of OER and generate different active sites for OER and HER in CuNiPx-GDY(11). Thus CuNiPx-GDY(11) exhibits good catalytical performance and stability as catalyst for overall water splitting. selleck chemicals This study provides a new sight into the structure and catalytic properties of GDY and transition metal phosphides hybrid nanomaterial, and also offers a new way to obtain advanced materials with remarkable catalytic properties.It is imperative to design and manufacture electrocatalysts towards oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) for popularization of rechargeable Zn-air batteries. Herein, FeNi alloy confined in N-doped carbon nanosheets (FeNi@NCSs) was harvested via a facile complexation-pyrolysis strategy from the mixture of guanine and metal chlorides. After strictly exploring the pyrolysis temperature and metal types, the resulted FeNi@NCSs showed greatly improved performances on both the ORR (onset potential of 0.93 V and half-wave potential of 0.84 V) and OER (overpotential of 318 mV at 10 mA cm-2 and 379 mV at 100 mA cm-2). Further, the FeNi@NCSs based Zn-air battery exhibited a higher open circuit voltage (1.496 V), a larger power density (128.8 mW cm-2), and prominent durability (360 cycles, 120 h). This study provides an appealing approach to utilize biomass for synthesis of low-cost and high-efficiency electrocatalysts in energy associated systems.Lead-free inorganic Cs2AgBiBr6 double perovskites have emerged as promising materials in perovskite solar cells (PSCs) to tackle the inferior stability and toxicity issues of organic-inorganic hybrid PSCs. However, the power conversion efficiencies (PCEs) of Cs2AgBiBr6 solar cells are remarkably restricted by the intrinsic and extrinsic defects of Cs2AgBiBr6 films. More specifically, the fast crystallization process in the formation of Cs2AgBiBr6 films strongly prevents the homogeneous growth of perovskite crystals, leading to inferior Cs2AgBiBr6 film quality. This work introduces a facile strategy to retard the crystallization of Cs2AgBiBr6 perovskites by introducing Lewis base additives into the precursor solution. The incorporation of a strongly coordinated thiourea additive with a sulfur donor leads to the generation of a Lewis acid base adduct, which retards the crystallization process for Cs2AgBiBr6 crystals, improves the quality of the Cs2AgBiBr6 film, decreases the defect density and inhibits charge carrier recombination.