Search

Burkholderia gladioli (B. gladioli) may cause food poisoning through the production of the toxin bongkrekic acid (BA), and could induce lung infections in patients with cystic fibrosis (CF). Edible mushrooms are a route of B. gladioli transmission; however, little effort has been focused on the prevalence of B. gladioli in edible mushrooms. In this study, 25 of the 325 edible mushroom samples were positive for B. gladioli , which showed moderate or strong biofilm formation capacity with a wide range of motility. Seventeen strains were capable of producing BA, while the isolates without toxin production lacked BA synthesis pathway genes bonK or bonR2. Antibiotic susceptibility testing indicated that all isolates were multidrug resistant. A considerable proportion of isolates were resistant to polymyxin B (100 %), chloramphenicol (84.62 %), aztreonam (84.62 %), ceftriaxone (84.62 %), and ticarcillin (61.54 %). None of the strains grew under environmental conditions such as pH below 4.0 or NaCl concentrations above 3.0 g/100 mL. Furthermore, 10 novel sequence typings (STs) were detected among the 25 isolates by multilocus sequence typing. This study provides valuable information for the control and prevention of B. gladioli contamination in common edible mushrooms for the first time. • Dried black fungus was contaminated with B. gladioli at a rate of 25.61 %. • Strong or moderate biofilm-forming ability was observed in B. gladioli isolates. • B. gladioli not producing BA were found to lack the bonK or bonR2 genes. • Ten STs were detected from edible mushrooms for the first time. [ABSTRACT FROM AUTHOR]

[Display omitted] The creation of high-performance thermal insulation and flame-retardant materials is of great importance for minimizing energy consumption and reducing fire risk for modern buildings. Herein, we report the creation of a new composite aerogel, which was prepared by incorporation of 9,10-Dihydro-9-oxa-10-phosphaphenanthrene 10-Oxide-3-Aminopropyl triethoxysilane (DOPO-KH550) modified hollow glass microspheres (HGM) into polyvinyl alcohol (PVA) using citric acid as a cross-linker, as a kind of thermal insulation and flame retardant materials (abbreviated as PVA-DKHGM). The as-synthesized PVA-DKHGM composite exhibits superior thermal conductivity of 0.0187 W m−1 K−1, owing to the hollow structure of the hollow glass microspheres and rich porosity. Besides, it reaches V-0 level at the UL-94 test and the peak heat release rate (pHRR) was measured to be 114.93 (kW/m2) which is lower than most composites now. These results are attributed to the synergy effect of the hollow glass microsphere and DOPO-KH550 which offers the composites aerogel excellent flame retardancy. Owing to its advantages such as lightweight, highly porous, thermally stable, simple to prepare, high mechanical strength, and can be further scaled up, our PVA-DKHGM aerogel may hold great potential for practical applications in construction of energy-saving modern buildings. [ABSTRACT FROM AUTHOR]

Novel Fe N C electrocatalysts derived from conjugated microporous polymers based on pre-functionalization of monomers was developed, which exhibits great potential for cathodic oxygen reduction reaction in fuel cell and provides a feasible strategy of developing multi-atoms doping catalysts for heterogeneous catalysis. [Display omitted] Porous iron–nitrogen-doped carbons (Fe N C) offer a great platform for construction of cathodic oxygen reduction reaction (ORR) catalysts in fuel cells. However, challenges still remain regarding with the collapse of carbon-skeleton during pyrolysis, uneven distribution of active sites and aggregation of metal atoms. In this work, we synthesized Fe, N co-doped conjugated microporous polymer (FeN-CMP) through a facile bottom-up strategy using 1,3,5-triethynylbenzene and iron-chelated 3,8-dibromo-1,10-phenanthroline as monomers, ensuring the uniform coordination of N with Fe element in network. Then, the resulting FeN-CMP was treated by pyrolysis without structural collapse to obtain porous Fe N C electrocatalyst for ORR. The most active catalyst was fabricated under 900 °C, which exhibits remarkable ORR activity in alkaline medium with half-wave potential of 0.796 V (18 mV and 105 mV positive deviation from the commercial Pt/C catalyst and post-doping catalyst), high selectivity with nearly 4e- transfer process and excellent methanol tolerance. Our study first developed porous Fe N C electrocatalysts derived from Fe, N -anchoring CMPs based on pre-functionalization of monomers, which exhibits great potential as an alternative to commercial Pt/C catalyst for ORR, and provides a feasible strategy of developing multi-atoms doping catalysts for energy storage and conversion as well as heterogeneous catalysis. [ABSTRACT FROM AUTHOR]

[Display omitted] The development and preparation of multifunctional photothermal conversion materials has far-reaching significance for the utilization of solar energy resources in response to the energy crisis. Herein, we propose a Janus membrane for interfacial solar evaporation and phase change energy storage. The membranes were fabricated via combining the PVA film with multi-shelled hollow spheres (MHS). The membranes have asymmetric wettability, that is, one side is hydrophilic and the other side is hydrophobic. The as-resulted membranes obtain outstanding light absorption without further processing. According to these two advantages, the membranes were applied to solar evaporation. The evaporation rate of the membrane is 1.41 kg*m−2h−1 and the evaporation efficiency is 92.4 % under 1sun irradiation. Moreover, the membrane prepared by impregnating 1-Hexadecanamine (HDA) into MHS possesses excellent tensile strength (2.21 MPa) and photothermal conversion ability. The light-to-thermal conversion efficiency can reach 81.9 % under 1sun irradiation. Therefore, the membranes have broad application prospects in the field of photothermal conversion. [ABSTRACT FROM AUTHOR]

[Display omitted] Water environmental pollution especially caused by bacteria, viruses and other microorganisms always would accelerate the spread of infectious diseases and has been one of the issues highly concerned by the World Health Organization for a long time. The development of novel antibacterial materials with high activity for water cleanness was of great importance for public health and ecological sustainable development. In this work, we developed two really free-standing conjugated microprous polymers (CMPs) film with large size and processibility by a simple and convenient solid surface-assisted polymerization between bromo- and aryl-acetylene monomers. With the solid interfacial orientation from silica nanofibers, the resulting CMPs film exhibited nanotube-liked morphology with BET surface area of 379.5 m2 g−1 and 480.1 m2 g−1. The introduction of antibacterial isocyanurate and acetanilide group into polymer skeleton brings the resulting CMPs film intrinsically antimicrobial capability and durability. The growth of E. coli can be completely inhibited by the resulting CMPs film even after several cycles. Our work was suggested to provide a new route for rational design of CMPs film or membrane with antibacterial activity for water treatment and sterilization. [ABSTRACT FROM AUTHOR]

• Catalytic partial oxidation (CPOX) processing experimentally investigated to use Methane in SOFC. • Reynolds number effects on electrochemical performance of the SOFCs. • Carbon deposition prevented by utilizing oxygen with methane in favorable operating conditions. • Investigation of the carbon deposition through the NiO-YSZ anode by EDAX and SEM. The development of high-performance non-precious metal electrocatalysts is of great importance for construction of next generation fuel cells. Herein, we report for the first time the creation of new metal-free porous carbon framework catalysts derived from N -rich hypercrosslinked polymers (HCPs) using pyrrole as building blocks for oxygen reduction reaction (ORR) (denoted as PCF-HCPs). The PCF-HCPs obtained at the pyrolysis temperature of 900 °C (PCF-HCP-900), displayed outstanding catalytic activity towards the ORR compared with other PCF-HCPs pyrolysis temperature. Due to PCF-HCP-900 with large specific surface, excellent porosity and, importantly, exposed active sites caused by N doping with high density, the catalysts exhibited outstanding ORR activity in alkaline medium, i.e., the PCF-HCP-900 yielded a half-wave potential of 0.84 V, which was 10 mV higher than that of the state of-the-art Pt/C catalyst (0.83 V), and onset potential of 0.95 V (vs. RHE), a high diffusion limiting current density of 4.8 mA cm−2, better methanol tolerance and long-term stability (2 mV negative shift after 3000 potential cycles) than commercial Pt/C. Furthermore, PCF-HCP-900 shows a favorable 4-electron transfer process (n ≈ 3.96) and lower H 2 O 2 yield. Based on these merits, the PCF-HCP-900 may open a new possibility for design of ORR metal-free catalyst of fuel-cell technologies. [ABSTRACT FROM AUTHOR]

[Display omitted] The inevitable intermittency of solar illumination during the interfacial evaporation process can cause a reduction in the evaporation performance of solar evaporators. Here, we report the fabrication of a new solar-driven interfacial evaporator using MXene nanosheets as the photothermal layer, modifying them with conjugated microporous polymer hollow microspheres, and then compounding them with the phase change material, in this case, cetyl alcohol, to form a composite evaporator (CE) that can perform all-weather solar interfacial evaporation. By combining interfacial evaporation photothermal conversion with energy storage, the evaporator achieves an evaporation rate of 1.57 kg⋅m−2⋅h−1 at a light intensity of 1 kW⋅m−2 and 2.79 kg⋅m−2⋅h−1 at a light intensity of 2 kW⋅m−2. In addition, the evaporator attains an excellent solar evaporation efficiency of over 91% in both cases and even in salt water. In addition, interestingly, our CE exhibits excellent continuous evaporation ability, e.g., the mass of evaporated water was increased by 0.36 kg⋅m−2 at a light intensity of 2 kW⋅m−2 compared to the cavity evaporator without the phase change material (PCM) when solar light was turned off. These results could be attributed to the fact that the energy released by the incorporated phase change material allows the evaporator to maintain stable evaporation under conditions of insufficient or intermittent solar irradiation, potentially providing a new opportunity for addressing the intermittent problem of evaporation at the solar interface due to unstable light intensity, thus showing great potential for practical continuous desalination. [ABSTRACT FROM AUTHOR]