Addition of phytochemical-rich plant extracts mitigate the antimicrobial activity of essential oil/wine mixtures against Escherichia coli O157:H7 but not against Salmonella enterica

Marinades for preparing raw meats for cooking are frequently made of wine and herbs. We simulated several formulations of potential antimicrobial marinades with these components and other food compatible/food derived extracts. Red wine formulations containing essential oils from oregano or thyme, or their primary active components carvacrol and thymol, respectively, and a mixture of plant extract powders from phytochemical-rich apple skin, green tea, and olive, were evaluated for inhibitory activity against the foodborne pathogens Escherichia coli O157:H7 and Salmonella enterica. Red wine alone exhibited low activity, as did the plant extract suspended in the wine. Surprisingly, the high activity of oregano or thyme essential oils in red wine was reduced in E. coli, but not in Salmonella, by addition of the plant extract. This study shows that essential oils in red wine can be an effective antimicrobial in food, however the possibility exists that phytochemicals, added to the treatment solution or natively present in the food itself, could adversely impact the antimicrobial activity and should be addressed with future studies.     

The utilization of carbon nitride to reinforce the mechanical and thermal properties of UV-curable waterborne polyurethane acrylate coatings

The waterborne polyurethane-acrylate (WPUA and Wsi-PUA) oligomers were prepared by anionic self-emulsifying method, using isophorone diisocyanate (IPDI), polyethylene glycol (PEG), dimethylol propionic acid (DMPA), vinyl hydroxyl silicone oil (VHSO) and hydroxyethyl methyl acrylate (HEMA) as raw materials. Then, a series of UV-curable waterborne Wsi-PUA–C₃N₄ composites containing different content of g-C₃N₄ were obtained with oligomer and photoinitiator Darocur 1173. FTIR, XRD, TEM, SEM, and TGA were employed to investigate the structure, morphology and thermal property of the Wsi-PUA–C₃N₄ composite films. The effect of g-C₃N₄ content on the performance was also investigated. The mechanical performance, water resistance and gel content of UV-PUA films were measured. It was found that with g-C₃N₄ particle was introduced into Wsi-PUA oligomer, the hardness, tensile strength, gel content, water resistance and thermal stability of composite films were significantly augmented. Moreover, when the content of g-C₃N₄ was 1.0 wt.%, the UV-curable film had the best mechanical property. The obtained composite is promising for a number of applications, e.g., for protecting the surfaces of metal and wood.     

Effects of thermodynamically coupled reaction diffusion in microalgae growth and lipid accumulation: Model development and stability analysis

This study investigates and presents the effects of thermodynamically coupled nonisothermal reaction-diffusion processes on microalgae growth, substrate consumption and neutral lipid production in a pond or wastewater treatment plant. The non-stirred chemostat hypothesis and linear nonequilibrium thermodynamics theory are applied to formulate the model equations that account the bulk phase compositions and temperature, resistances to the heat and mass transfers, and cross effects due to the thermodynamic coupling of heat and mass flow in the presence of chemical reaction. Nondimensional forms of the model equations are numerically solved. Bulk phase concentrations and temperatures, external resistances to heat and substrate transfers, and thermodynamic coupling may generate substantial number of new parameters that control the evolution and stability in microalgal growth and lipid production that are important for biofuels. Instabilities due to perturbations in nutrient concentrations may lead to spatial structures where the wavenumber plays important role in reaction diffusion systems.     

Selective hydrogenation of (E)-2-hexenal to (E)-2-hexen-1-ol over Co-based bimetallic catalysts

Hydrogenation of (E)-2-hexenal was carried out in a liquid phase using Co-based bimetallic catalysts (M–Co/Al₂O₃, M=Pd, Pt, Ru, Rh, Sn, Fe, or Cu). Pd–Co/Al₂O₃ showed the highest activity among the catalysts tested and catalyzed the hydrogenation of CC bond predominantly to produce hexanal and 1-hexanol. Pt–Co/Al₂O₃ was more active than monometallic Co/Al₂O₃ for the hydrogenation of CO bond. The excellent result, 92% selectivity to (E)-2-hexen-1-ol formation at 90% conversion, was obtained by the hydrogenation over Pt–Co/Al₂O₃ bimetallic catalyst. No improved activities were observed for the other bimetallic catalysts.     

Chemical conversion of wood by treatment in a semi-batch reactor with subcritical water

Sugi (Cryptomeria japonica D. Don) wood meal was extracted with subcritical water in a semi-batch reactor. About 70–90% by weight of the sugi wood meal was converted into water-soluble compounds. The main components of the water-soluble compounds were monosaccharides and oligosaccharides, as a result of hydrolysis of cellulose and hemicellulose. White precipitates appeared in the solution after settling for 48 h. X-ray diffractometry clearly showed that precipitates had crystallized into cellulose II. High yield of total saccharides (including the precipitates) was obtained at 310–320 °C, 25 MPa and 65 g min⁻¹ water flow rate from a wood meal charge of 2.0 g, while the decomposition reaction was completed within about 20 min. Moreover, the yield increased to more than 60% when the wood meal was pretreated for improved wettability. It is shown that saccharides can be produced from sugi wood powder quickly and effectively by treatment in subcritical water.     

Manganese oxide embedded graphene nanohybrid for pH-universal electrochemical overall water splitting

Efficient non-noble metal bifunctional electrocatalysts for overall water splitting in pH universal is highly desired in application. Herein, MnO₂/graphene composition are applied as efficient electrocatalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in pH-universal electrolytes with the help of plasma dc arc method. The couple of MnO₂ and graphene highly benefits to the H₂O, H⁺ and OH⁻ absorption respectively. The defects and stable Mn³⁺ contribute to the transfer of electron and charge. The low overpotentials and small Tafel slopes reveal attractive activities of HER and OER. The good electrocatalytic performances are attributed to the synergistic effect and abundant heterogeneous interfaces in MnO₂/graphene. These can offer rich electroactive sites and accelerate electron transfer. Thus, it may provide facile route for developing nonprecious electrocatalysts of water splitting.     

Deep-blue thermally activated delayed fluorescence emitter with a very high fluorescence rate

Conventional thermally activated delayed fluorescence (TADF) molecules achieve small energy differences between the lowest singlet and triplet excited states (ΔE_ST) by enhancing the intramolecular charge transfer, which inevitably leads to a wide emission spectrum and low fluorescence rate. Here, we prepared a deep blue TADF molecule via a small ΔE_ST pyridine-phenol fluoroboron complex as the acceptor. The small ΔE_ST is maintained when carbazole donors are attached to the 4-position of the phenyl rings in the fluoroboron complex. Benefiting from the strong electron coupling between the donor (D) and acceptor (A) moieties, the compound Cz-4-BF exhibits a high fluorescence rate of 4.8 × 10⁸ s⁻¹ and a small D-A dihedral angle change in the excited state. Consequently, a photoluminescence (PL) quantum yield of nearly 100% and a PL spectrum with full-width at half-maximum (FWHM) < 60 nm were obtained in solution and low-concentration doped films. A TADF-sensitized fluorescence (TSF) device containing Cz-4-BF achieves an external quantum efficiency of 21%, which is higher than the devices employing classical fluorescent emitters and multiple resonance-type TADF emitters. The Cz-4-BF-based TSF device shows significantly improved color coordinates of (0.14, 0.10) versus a control device without Cz-4-BF.     

Seasonal fluctuations of organochlorine and triazines pesticides in the aquatic system of Ioannina basin (Greece)

For the period September 1984 to November 1985 water samples from the aquatic system of Ioannina basin were analyzed every second month for organochlorine and triazines pesticides. The detected compounds were found to follow a seasonal pattern, with an increment during summer followed by a decrease during winter and an increase again during late spring. This pattern was apparent for Ioannina lake as well as for the Kalamas river connected to it through the Lapsista's canal and tunnel. The results are discussed in terms of the amounts of the detected pesticides used for farming in the vicinity of the Ioannina basin and the seasonal rainfall.