Development of High Thermal Stability Geopolymer Composites Enhanced by Nano Metakaolin

This paper deals with study of thermal stability of geopolymer composites enhanced by nano metakaolin materials (NMK) and exposed to high firing temperature up to 1000 °C. The main geopolymer made up of water cooled slag having various kaolin ratios.  The activators used are Na2SiO3 and NaOH in the ratio of 3:3. The thermo-physical, micro-structural and mechanical properties of the geopolymers before and after the exposure to elevated temperatures of 300, 500, 600 800 and 1000 °C have been investigated. The fire shrinkage of the geopolymer specimens increased by increasing temperature up to 1000 oC. Also, the fire shrinkage increased slowly up to 500 °C. The mechanical strength of geopolymer specimens increased with temperature up to 500 oC. The good thermo-physical and mechanical properties for these geopolymer composites increase the possibility of vast application of these eco-friendly materials in construction sectors

Prevalence of Toxigenic and Methicillin Resistant Staphylococci in Poultry Chain Production

oai:ojs.pkp.sfu.ca:article/1Staphylococci are a worldwide cause of human and animal infection and are considered to be of the most common causes of infections in birds. Enterotoxins produced by some staphylococcal species were recognized as a causative agent of staphylococcal food poisoning (SFP). Only enterotoxins produced by Staphylococcus aureus were as yet well characterized. Much less is known about enterotoxigenic potential of coagulase-negative species of genus Staphylococcus (CNS). It has been reported that enterotoxigenic CNS strains have been associated with human and animal infections and food poisoning. Samples collected from chicken production cycle (un hatched eggs, baby chicks, broilers, chicken meat and table eggs) in Luxor, Egypt were tested to investigate the presence of Staphylococcus species and detection of their enterotoxines genes with more special attention for detection of methicillin resistance gene (mec A). Samples were tested for S. aureus and CNS on the basis of cultural and biochemical properties and confirmed by PCR amplification of 16S rRNA and clfa gene. Results showed that the presence of Staphylococci were 50/150 (33.3%), 14% of the samples were S. aureus (21/150), while, 19.33% were CNS (29/150). mecA gene was detected in 66.7% and 51.7% among S. aureus and CNS respectively. Enterotoxins genes (seb, sec and see) were found in 5 (23.8%) of S. aureus with a percent of (9.5%) for seb and sec and (4.8%) for see, while sec and see were found in 6 (20.6%) of CNS.  With a percent (10.3%) for each. &nbsp

Fabrication of an efficient vanadium redox flow battery electrode using a free-standing carbon-loaded electrospun nanofibrous composite

Vanadium redox flow batteries (VRFBs) are considered as promising electrochemical energy storage systems due to their efficiency, flexibility and scalability to meet our needs in renewable energy applications. Unfortunately, the low electrochemical performance of the available carbon-based electrodes hinders their commercial viability. Herein, novel free-standing electrospun nanofibrous carbon-loaded composites with textile-like characteristics have been constructed and employed as efficient electrodes for VRFBs. In this work, polyacrylonitrile-based electrospun nanofibers loaded with different types of carbon black (CB) were electrospun providing a robust free-standing network. Incorporation of CBs (14% and 50% weight ratio) resulted in fibers with rough surface and increased mean diameter. It provided higher BET surface area of 83.8 m2 g−1 for as-spun and 356.7 m2 g−1 for carbonized fibers compared to the commercial carbon felt (0.6 m2 g−1). These loaded CB-fibers also had better thermal stability and showed higher electrochemical activity for VRFBs than a commercial felt electrode

Development of High Thermal Stability Geopolymer Composites Enhanced by Nano Metakaolin

This paper deals with study of thermal stability of geopolymer composites enhanced by nano metakaolin materials (NMK) and exposed to high firing temperature up to 1000 °C. The main geopolymer made up of water cooled slag having various kaolin ratios.  The activators used are Na2SiO3 and NaOH in the ratio of 3:3. The thermo-physical, micro-structural and mechanical properties of the geopolymers before and after the exposure to elevated temperatures of 300, 500, 600 800 and 1000 °C have been investigated. The fire shrinkage of the geopolymer specimens increased by increasing temperature up to 1000 oC. Also, the fire shrinkage increased slowly up to 500 °C. The mechanical strength of geopolymer specimens increased with temperature up to 500 oC. The good thermo-physical and mechanical properties for these geopolymer composites increase the possibility of vast application of these eco-friendly materials in construction sectors

Unintended cation crossover influences CO2 reduction selectivity in Cu-based zero-gap electrolysers

Membrane electrode assemblies enable CO2 electrolysis at industrially relevant rates, yet their operational stability is often limited by formation of solid precipitates in the cathode pores, triggered by cation crossover from the anolyte due to imperfect ion exclusion by anion exchange membranes. Here we show that anolyte concentration affects the degree of cation movement through the membranes, and this substantially influences the behaviors of copper catalysts in catholyte-free CO2 electrolysers. Systematic variation of the anolyte (KOH or KHCO3) ionic strength produced a distinct switch in selectivity between either predominantly CO or C2+ products (mainly C2H4) which closely correlated with the quantity of alkali metal cation (K+) crossover, suggesting cations play a key role in C-C coupling reaction pathways even in cells without discrete liquid catholytes. Operando X-ray absorption and quasi in situ X-ray photoelectron spectroscopy revealed that the Cu surface speciation showed a strong dependence on the anolyte concentration, wherein dilute anolytes resulted in a mixture of Cu+ and Cu0 surface species, while concentrated anolytes led to exclusively Cu0 under similar testing conditions. These results show that even in catholyte-free cells, cation effects (including unintentional ones) significantly influence reaction pathways, important to consider in future development of catalysts and devices

Comparative Spectroscopic Study Revealing Why the CO2 Electroreduction Selectivity Switches from CO to HCOO– at Cu–Sn- and Cu–In-Based Catalysts

To address the challenge of selectivity toward single products in Cu-catalyzed electrochemical CO2 reduction, one strategy is to incorporate a second metal with the goal of tuning catalytic activity via synergy effects. In particular, catalysts based on Cu modified with post-transition metals (Sn or In) are known to reduce CO2 selectively to either CO or HCOO– depending on their composition. However, it remains unclear exactly which factors induce this switch in reaction pathways and whether these two related bimetal combinations follow similar general structure–activity trends. To investigate these questions systematically, Cu–In and Cu–Sn bimetallic catalysts were synthesized across a range of composition ratios and studied in detail. Compositional and morphological control was achieved via a simple electrochemical synthesis approach. A combination of operando and quasi-in situ spectroscopic techniques, including X-ray photoelectron, X-ray absorption, and Raman spectroscopy, was used to observe the dynamic behaviors of the catalysts’ surface structure, composition, speciation, and local environment during CO2 electrolysis. The two systems exhibited similar selectivity dependency on their surface composition. Cu-rich catalysts produce mainly CO, while Cu-poor catalysts were found to mainly produce HCOO–. Despite these similarities, the speciation of Sn and In at the surface differed from each other and was found to be strongly dependent on the applied potential and the catalyst composition. For Cu-rich compositions optimized for CO production (Cu85In15 and Cu85Sn15), indium was present predominantly in the reduced metallic form (In0), whereas tin mainly existed as an oxidized species (Sn2/4+). Meanwhile, for the HCOO–-selective compositions (Cu25In75 and Cu40Sn60), the indium exclusively exhibited In0 regardless of the applied potential, while the tin was reduced to metallic (Sn0) only at the most negative applied potential, which corresponds to the best HCOO– selectivity. Furthermore, while Cu40Sn60 enhances HCOO– selectivity by inhibiting H2 evolution, Cu25In75 improves the HCOO– selectivity at the expense of CO production. Due to these differences, we contend that identical mechanisms cannot be used to explain the behavior of these two bimetallic systems (Cu–In and Cu–Sn). Operando surface-enhanced Raman spectroscopy measurements provide direct evidence of the local alkalization and its impact on the dynamic transformation of oxidized Cu surface species (Cu2O/CuO) into a mixture of Cu(OH)2 and basic Cu carbonates [Cux(OH)y(CO3)y] rather than metallic Cu under CO2 electrolysis. This study provides unique insights into the origin of the switch in selectivity between CO and HCOO– pathways at Cu bimetallic catalysts and the nature of surface-active sites and key intermediates for both pathways

Poly(ionic liquid) nanovesicles via polymerization induced self-assembly and their stabilization of Cu nanoparticles for tailored CO2 electroreduction

Herein, we report a straightforward, scalable synthetic route towards poly(ionic liquid) (PIL) homopolymer nanovesicles (NVs) with a tunable particle size of 50 to 120 nm and a shell thickness of 15 to 60 nm via one-step free radical polymerization induced self-assembly. By increasing monomer concentration for polymerization, their nanoscopic morphology can evolve from hollow NVs to dense spheres, and finally to directional worms, in which a multilamellar packing of PIL chains occurred in all samples. The transformation mechanism of NVs’ internal morphology is studied in detail by coarse-grained simulations, revealing a correlation between the PIL chain length and the shell thickness of NVs. To explore their potential applications, PIL NVs with varied shell thickness are in situ functionalized with ultra-small (1 ∼ 3 nm in size) copper nanoparticles (CuNPs) and employed as electrocatalysts for CO2 electroreduction. The composite electrocatalysts exhibit a 2.5-fold enhancement in selectivity towards C1 products (e.g., CH4), compared to the pristine CuNPs. This enhancement is attributed to the strong electronic interactions between the CuNPs and the surface functionalities of PIL NVs. This study casts new aspects on using nanostructured PILs as new electrocatalyst supports in CO2 conversion to C1 products

Facile Synthesis of Hierarchical CuS and CuCo2S4 Structures from an Ionic Liquid Precursor for Electrocatalysis Applications

Covellite phase CuS and carrollite phase CuCo2S4 nano and microstructures were synthesized from tetrachloridometallate based ionic liquid precursors using a novel, facile, and highly controllable hot injection synthesis strategy. The synthesis parameters including reaction time and temperature were first optimized to produce CuS with a well controlled and unique morphology, providing the best electrocatalytic activity toward the oxygen evolution reaction OER . In an extension to this approach, the electrocatalytic activity was further improved by incorporating Co into the CuS synthesis method to yield CuCo2S4 microflowers. Both routes provide high microflower yields of gt;80 wt . The CuCo2S4 microflowers exhibit a superior performance for the OER in alkaline medium compared to CuS. This is demonstrated by a lower onset potential amp; 8764;1.45 V vs RHE 10 mA cm2 , better durability, and higher turnover frequencies compared to bare CuS flowers or commercial Pt C and IrO2 electrodes. Likely, this effect is associated with the presence of Co3 sites on which a better adsorption of reactive species formed during the OER e.g., OH, O, OOH, etc. can be achieved, thus reducing the OER charge transfer resistance, as indicated by X ray photoelectron spectroscopy and electrochemical impedance spectroscopy measurement