Use of superoxide as an electron shuttle for iron acquisition by the marine cyanobacterium Lyngbya majuscula

Reduction of iron from the ferric state to the ferrous state is one strategy employed by microorganisms in nearneutral environments to increase its biological availability. In recent years, the existence of mobile reducing agents produced bymicroorganismsto promote iron reduction, known as electron shuttles, has been demonstrated. Production of electron shuttles has been shown for several organisms, employing a variety of mostly organic molecules as the electron carrier. Here we show that the coastal cyanobacterium Lyngbya majuscula produces iron-reducing superoxide radicals (02*-) and that this facilitates increased iron uptake. We suggest that superoxide is a useful electron shuttle because it reacts rapidly and almost indiscriminately with Fe(lll)-organic complexes and its precursor, dissolved oxygen, is ubiquitous in the photic zone. We further suggest that, for these reasons, the generation of superoxide by marine oxygenic photosynthetic microorganisms and its use in facilitating iron uptake may be a reasonably widespread process.     

Wet air oxidation of glucose with hydrogen peroxide and metal salts

Wet air oxidation (the patented Zimmermann process) destroys organic matter in sewage sludge by bringing a sludge-air mixture to elevated temperature (260 to 370 °C) and pressure (12.4 MPa) and holding it for a reaction time of 35 to 55 min. These conditions result in 70 to 80% COD removal with carbon dioxide, water, short chain aliphatic acids, and ash as products. Energy recovery provisions enable the process to be self-contained at sludge concentrations of 4.5 to 5% which are difficult to obtain. An additive to the process which would enable successful oxidation to proceed with less concentrated sludge, at lower pressures and shorter times would be useful. Hydrogen peroxide in combination with several metal salts was tested as an additive. Hydrogen peroxide plus dichromate was found to destroy 70% of the COD of a glucose solution (500 mg/1 COD) at 150 °C and 5.2 MPa in 15 min. The ratio of the equivalents of the substances glucose: hydrogen peroxide: dichromate stood as 13 : 6.5 : 1. The amount of COD destroyed exceeded the oxidative equivalents of peroxide and dichromate present; hence it was concluded that molecular oxygen was incorporated in the reaction.     

Diagonal horn integrated with micromachined waveguide forsubmillimetre applications

The feasibility of coupling silicon micromachines rectangular waveguide to a modified diagonal horn antenna using a model at 110 GHz is demonstrated. The antenna patterns obtained are similar to those obtained with a standard diagonal horn. A method of reducing the on-axis cross polarization response of diagonal horns is also presented     

Immunological characterisation of barley polypeptides in lager foam

Eight monoclonal antibodies (mAb) recognising barley polypeptides have been identified from a library developed to wheat prolamins. The specificity or the mAb has been determined using enzyme-linked immunosorbent assay (ELISA) and immunoblotting. Six were of broad specificity, recognising D, B, C and γ-hordeins to varying degrees by both techniques. IFRN 0610 preferentially recognised γ-hordeins by ELISA but was highly specific for this hordein group by immunoblotting. Another mAb, IFRN 0624, bound to a M_r ∽ 18000 polypeptide belonging to the CM protein (trypsin/α-amylase inhibitor) family by immunoblotting. This, or a related protein, was detected by 0624 in all hordein fractions using ELISA. These mAb, together with two others described previously and found to recognise the repeat motif of C hordein, were used in ELISA and immunoblot analysis of Octyl-Sepharose fractions of lager foam. Hordein polypeptides were found in all foam fractions, indicating that much foam protein originates from the malt. The CM-like protein was found present in a virtually unmodified form. In contrast, the repeat motif of C hordein was not detected, indicating that it had either been destroyed or masked by other beer constituents. The foam stabilising agent, propylene glycol alginate (PGA), increased the apparent hydrophobicity of hordein fragments suggesting that at least part of the activity of PGA is mediated by interactions with the hordein components of foam.     

E-waste: An assessment of global production and environmental impacts

E-waste comprises discarded electronic appliances, of which computers and mobile telephones are disproportionately abundant because of their short lifespan. The current global production of E-waste is estimated to be 20-25 million tonnes per year, with most E-waste being produced in Europe, the United States and Australasia. China, Eastern Europe and Latin America will become major E-waste producers in the next ten years. Miniaturisation and the development of more efficient cloud computing networks, where computing services are delivered over the internet from remote locations, may offset the increase in E-waste production from global economic growth and the development of pervasive new technologies. E-waste contains valuable metals (Cu, platinum group) as well as potential environmental contaminants, especially Pb, Sb, Hg, Cd, Ni, polybrominated diphenyl ethers (PBDEs), and polychlorinated biphenyls (PCBs). Burning E-waste may generate dioxins, furans, polycyclic aromatic hydrocarbons (PAHs), polyhalogenated aromatic hydrocarbons (PHAHs), and hydrogen chloride. The chemical composition of E-waste changes with the development of new technologies and pressure from environmental organisations on electronics companies to find alternatives to environmentally damaging materials. Most E-waste is disposed in landfills. Effective reprocessing technology, which recovers the valuable materials with minimal environmental impact, is expensive. Consequently, although illegal under the Basel Convention, rich countries export an unknown quantity of E-waste to poor countries, where recycling techniques include burning and dissolution in strong acids with few measures to protect human health and the environment. Such reprocessing initially results in extreme localised contamination followed by migration of the contaminants into receiving waters and food chains. E-waste workers suffer negative health effects through skin contact and inhalation, while the wider community are exposed to the contaminants through smoke, dust, drinking water and food. There is evidence that E-waste associated contaminants may be present in some agricultural or manufactured products for export.     

Liquidus Temperature of SrO-Al2O3-SiO2 Glass-Forming Compositions

Despite the important role of strontium aluminosilicate glasses in various technologies, there is no available phase diagram for this ternary system in the ACerS-NIST Phase Equilibria Diagrams Database. Establishing the liquidus surface (liquidus temperature T_liq and primary devitrification phase) is crucial for glass composition design, because the liquidus temperature is intimately connected with the glass-forming ability of the melt. In this work, we have determined the liquidus surface by X-ray diffraction phase analyses of isothermally reacted samples from powder mixtures of 24 compositions. In the composition range of interest for industrial glasses, T_liq tends to decrease with increasing strontium-to-alumina ratio. We find that cristobalite, mullite, and slawsonite are the dominant devitrification phases for the compositions with high SiO₂, SiO₂+Al₂O₃, and SrO contents, respectively. By comparison with the phase diagrams for CaO-Al₂O₃-SiO₂ and MgO-Al₂O₃-SiO₂ systems, we have found that for the highest [RO]/[Al₂O₃] ratios, T_liq exhibits a minimum value for R = Ca. Based on the phase diagram established here, the composition of glass materials, for example, for liquid crystal display substrates, belonging to the SrO-Al₂O₃-SiO₂ family may be designed with a more exact control of the glass-forming ability by avoiding the regions of high liquidus temperature.     

Potentials with small‐angle neutron scattering technique for understanding structure–property relation of 3D‐printed materials

Carbon fiber (CF)‐embedded acrylonitrile butadiene styrene polymer composites printed on the large‐scale printer at Oak Ridge National Laboratory were investigated by small‐angle neutron scattering to correlate the microstructure of the composites with their mechanical strength. The microstructure of the polymer domains and the alignment of CF were characterized across the interfaces between layers of the hot‐melt extruded material and were compared with CF‐free ABS. The small‐angle neutron scattering data show that the CF‐containing material displays strong anisotropic scatterings suggesting molecular alignment along the printing direction that is not present in the CF‐free ABS. Scattering data analysis across the interfacial layer revealed enhanced molecular alignment along the printing direction near the boundaries and inhomogeneous size distribution of polymer domains upon the addition of CF. We attribute the compromised strength across interfacial layers from CF‐containing material to this inhomogeneous size distribution which prevents effective lateral interaction between layers. POLYM. ENG. SCI., 59:E65–E70, 2019. © 2018 Society of Plastics Engineers     

Apportionment of primary and secondary organic aerosols in southern California during the 2005 study of organic aerosols in riverside (SOAR-1)

Ambient sampling was conducted in Riverside, California during the 2005 Study of Organic Aerosols in Riverside to characterize the composition and sources of organic aerosol using a variety of state-of-the-art instrumentation and source apportionmenttechniques. The secondary organic aerosol (SOA) mass is estimated by elemental carbon and carbon monoxide tracer methods, water soluble organic carbon content, chemical mass balance of organic molecular markers, and positive matrix factorization of high-resolution aerosol mass spectrometer data. Estimates obtained from each ofthese methods indicate that the organic fraction in ambient aerosol is overwhelmingly secondary in nature during a period of several weeks with moderate ozone concentrations and that SOA is the single largest component of PM1 aerosol in Riverside. Average SOA/OA contributions of 70-90% were observed during midday periods, whereas minimum SOA contributions of approximately 45% were observed during peak morning traffic periods. These results are contraryto previous estimates of SOAthroughout the Los Angeles Basin which reported that, other than during severe photochemical smog episodes, SOA was lower than primary OA. Possible reasons for these differences are discussed.     

B-HIVE: Beeswax hydrogen isotopes as validation of environment. Part I: Bulk honey and honeycomb stable isotope analysis

Stable isotope analysis is an established method for detecting honey adulteration. We extend its application to include honey and honeycomb region-of-origin assignment using hydrogen (δ²H) and oxygen (δ¹⁸O) isotopes. We observed that liquid honey δ²H and δ¹⁸O values had the potential to change because of water absorption and H atom exchange between sugars and water vapour. This suggested that liquid honey has limited use for geo-location, because specimens will record analysis location humidity. Paired liquid honey and honeycomb δ²H values were significantly correlated; therefore, we propose using wax δ²H values for region-of-origin assignment. We observed significant correlations between beeswax δ²H values and both mean annual precipitation and tap water δ²H values predicted for hive locations, suggesting that geographical variation in water δ²H values are recorded by beeswax δ²H values. This survey demonstrates the promise of stable isotopes for region-of-origin assignment, using honeycomb wax δ²H values, which complements carbon isotope analysis to detect adulteration.     

Performance of a CO2 sorbent for indoor air cleaning applications: Effects of environmental conditions,sorbent aging,and adsorption of co-occurring formaldehyde

Indoor air cleaning systems that incorporate CO₂ sorbent materials enable HVAC load shifting and efficiency improvements. This study developed a bench-scale experimental system to evaluate the performance of a sorbent under controlled operation conditions. A thermostatic holder containing 3.15 g sorbent was connected to a manifold that delivered CO₂-enriched air at a known temperature and relative humidity (RH). The air stream was also enriched with 0.8-2.1 ppm formaldehyde. The CO₂ concentration was monitored in real-time upstream and downstream of the sorbent, and integrated formaldehyde samples were collected at different times using DNPH-coated silica cartridges. Sorbent regeneration was carried out by circulating clean air in countercurrent. Almost 200 loading/regeneration cycles were performed in the span of 17 months, from which 104 were carried out at reference test conditions defined by loading with air at 25°C, 38% RH, and 1000 ppm CO₂, and regenerating with air at 80°C, 3% RH and 400 ppm CO₂. The working capacity decreased slightly from 43-44 mg CO₂ per g sorbent to 39-40 mg per g over the 17 months. The capacity increased with lower loading temperature (in the range 15-35°C) and higher regeneration temperature, between 40 and 80°C. The CO₂ capacity was not sensitive to the moisture content in the range 6-9 g/m³, and decreased slightly when dry air was used. Loading isothermal breakthrough curves were fitted to three simple adsorption models, verifying that pseudo-first-order kinetics appropriately describes the adsorption process. The model predicted that equilibrium capacities decreased with increasing temperature from 15 to 35°C, while adsorption rate constants slightly increased. The formaldehyde adsorption efficiency was 80%-99% in different cycles, corresponding to an average capacity of 86 ± 36 µg/g. Formaldehyde was not quantitatively released during regeneration, but its accumulation on the sorbent did not affect CO₂ adsorption.