Principle and application of ball SAW devices

A thin beam of waves usually diverges due to diffraction, which is a limitation of any device using such waves. However, a surface acoustic wave (SAW) on a sphere with an appropriate aperture does not diverge but is collimated, realizing ultra‐multiple roundtrips along an equator of the sphere. This effect is caused by the balance between diffraction and focusing on a spherical surface, and it enables realization of high‐performance ball SAW sensors. © 2009 Wiley Periodicals, Inc. Electr Eng Jpn, 168(1): 41–51, 2009; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20817     

Characterisation of a uranium ore using multiple X-ray diffraction based methods

Uranium bearing ores are often a complex mixture of minerals and compounds, a number of which are not of economic importance and are commonly referred to as gangue materials. In order to improve the efficiency of the dissolution stage of the overall uranium extraction process, a greater understanding of the minerals and compounds present in the ore is required. A greater knowledge of the gangue materials present is important as they can influence various aspects of the dissolution process such as providing potential adsorption sites for aqueous uranium species and through influencing the equilibrium of reactions involving aqueous uranium species. In this study the mineralogy of a uranium ore was investigated using a range of X-ray diffraction (XRD) based methods including in situ high temperature XRD and XRD using a synchrotron beam line. The results obtained from standard XRD (Cu Kα), high temperature XRD and synchrotron XRD (16.534 keV) were compared and a number of minerals were identified. The improved spatial resolution and intensity of the synchrotron data allowed for superior phase identification of a variety of minerals where standard X-ray techniques gave inconclusive results.     

Newly-modeled graphene-based ternary nanocomposite for the magnetophotocatalytic reduction of CO2 with electrochemical performance

The development of CO₂ into hydrocarbon fuels has emerged as a green method that could help mitigate global warning. The novel structured photocatalyst is a promising material for use in a photocatalytic and magneto-electrochemical method that fosters the reduction of CO₂ by suppressing the recombination of electron−hole pairs and effectively transferring the electrons to the surface for the chemical reaction of CO₂ reduction. In our study, we have developed a novel-structured AgCuZnS₂–graphene–TiO₂ to analyze its catalytic activity toward the selective evolution of CO₂. The selectivity of each nanocomposite substantially enhanced the activity of the AgCuZnS₂–graphene–TiO₂ ternary nanocomposite due to the successful interaction, and the selectivity of the final product was improved to a value 3 times higher than that of the pure AgCuZnS₂ and 2 times higher than those of AgCuZnS₂–graphene and AgCuZnS₂–TiO₂ under ultra-violet (UV)-light (λ = 254 nm) irradiation in the photocatalytic process. The electrochemical CO₂ reduction test was also conducted to analyze the efficacy of the AgCuZnS₂–graphene–TiO₂ when used as a working electrode in laboratory electrochemical cells. The electrochemical process was conducted under different experimental conditions, such as various scan rates (mV·s^–1), under UV-light and with a 0.07 T magnetic-core. The evolution of CO₂ substantially improved under UV-light (λ = 254 nm) and with 0.07 T magnetic-core treatment; these improvements were attributed to the facts that the UV-light activated the electron-transfer pathway and the magnetic core controlled the pathway of electron-transmission/prevention to protect it from chaotic electron movement. Among all tested nanocomposites, AgCuZnS₂–graphene–TiO₂ absorbed the CO₂ most strongly and showed the best ability to transfer the electron to reduce the CO₂ to methanol. We believe that our newly-modeled ternary nanocomposite opens up new opportunities for the evolution of CO₂ to methanol through an electrochemical and photocatalytic process.     

Economical treatment of reverse osmosis reject of textile industry effluent by electrodialysis–evaporation integrated process

Membrane separation methods such as electrodialysis (ED) can reduce the volume load on evaporators by facilitating further concentration of rejects from reverse osmosis (RO) plants. ED studies were carried out on a bench-scale system using five membrane cell pairs to obtain a textile effluent concentrate containing approximately 6 times the quantity of salts present in the RO reject. The limiting current densities were determined to be in the range 2.15–3.35 amp/m² for feed flow rates varying from 18 to 108 L/h. Apart from feed rate, the influence of volume of concentrate and current on membrane performance was evaluated to optimize current utilization. An estimation of energy requirement of an integrated process constituting ED and evaporation for concentration of inorganics present in textile effluent from 4.35% to 24% was made and found to be approximately one eighth of the operating cost incurred by evaporation alone. Detailed design of a commercial ED system revealed that a membrane area of 13.1 m² was required to treat a feed rate of 1500 L/h. The payback period to recover capital investment was found to be 110 days.     

A convenient crosslinking method for sulfonated poly(ether ether ketone) membranes via friedel–crafts reaction using 1,6‐dibromohexane and aluminum trichloride

In this study, sulfonated poly(ether ether ketone) (SPEEK) was very efficiently crosslinked via a Friedel–Craft reaction using 1,6‐dibromohexane and AlCl₃. The resulting crosslinked SPEEK (c‐SPEEK) membranes exhibited improved dimensional stability, thermal and chemical stability, and mechanical strength with slight reduction in the elongation. The methanol permeability was reduced by approximately two orders of magnitude by the crosslinking reaction. The proton conductivities of c‐SPEEK membranes were greater than Nafion‐212 in the temperature range of 30–90°C. Overall, this new crosslinking method can be conveniently and efficiently applicable to most aromatic hydrocarbon polymer membranes. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40695.     

Polystyrene-poly(2-ethylhexylmethacrylate) block copolymers: Synthesis,bulk phase behavior,and thin film structure

Anionic polymerization was employed to synthesize well-defined diblock copolymers of polystyrene and poly(2-ethylhexylmethacrylate), PS-PEHMA. Diblock morphologies in bulk and in substrate-supported thin films were characterized by small-angle X-ray scattering (SAXS) and atomic force microscopy (AFM), respectively. PS-PEHMA diblocks exhibited thermotropic order-disorder transitions; one diblock showed a thermoreversible transition between lamellae and a higher-temperature morphology assigned as perforated lamellae. Unlike PS-poly(alkylmethacrylate) diblocks where the alkyl group is n-butyl or n-pentyl, PS-PEHMA diblocks showed a typical decreasing Flory interaction parameter with increasing temperature. Thin films of PS-cylinder-forming PS-PEHMA diblocks showed a strong preference for the cylinders to lie in the plane of the film; films of incommensurate thickness readily formed terraces. Films of commensurate thickness were easily aligned over macroscopic areas through the application of mechanical shear.     

Friction and wear behavior of graphite fiber-reinforced composites

Friction and wear behavior of continuous graphite fiber composites was studied for different fiber orientations against the sliding direction. The effect of fiber orientation on friction and wear of the composite and on deformation of the counterface was investigated experimentally. A pin on disk type testing machine was built and employed to generate friction and wear data. A graphite fiber composite plate was produced by the bleeder ply molding in an autoclave and machined into rectangular pin specimens with specific fiber orientations, i.e., normal, transverse, and longitudinal directions. Three different wear conditions were employed for two different periods of time, 24 and 48 hours. The wear track of the worn specimens and the metal counterface was examined and a scanning electron microscope (SEM) to observe the damaged fibers on the sliding surface of the specimen and wear film generation on the counterface. A wear mechanism of the continuous graphite fiber composite during sliding wear is proposed based on the experimental results.     

Brief Review of Precipitated Iron-Based Catalysts for Low-Temperature Fischer–Tropsch Synthesis

Topics in Catalysis - Fischer–Tropsch synthesis (FTS) is a promising way to produce clean liquid fuels and high value-added chemicals from low-value carbon-containing resources such as coal,...     

Developement of neutral polymeric bonding agents for propellants with polar composites filled with organic nitramine crystals

Versatile neutral polymeric bonding agents (NBPA's) have been developed for energetic propellants in which polar HMX particles are dispersed in a polar binder matrix containing highly polar plasticizers (TMETN, NG, etc.). Using a semi-empirical approach through adjustment of solubility parameters and molecular weight, neutral acrylonitrile interpolymers were synthesized which mix uniformly with the submix and still have a high affinity for the HMX particles when they are added. Addition of about 0.2 % w/w of NPBA to HMX-filled PEG binders increases the strength by a factor of as high as five compared to samples with no NPBA, and also eliminates the sudden decrease in modulus (knee) which occurs at relatively low elongation. The degree of filler reinforcement achieved by our NPBA's in energetic propellants is far superior to that achieved by adding nitrocellulose or any other previously proposed bonding agents, and similar to the effect of precoating the HMX particles with polyurea shells.     

Comparison of the Antimicrobial and Sanitizer Resistance of Salmonella Isolates from Chicken Slaughter Processes in Korea

Salmonella is a foodborne pathogen worldwide. Outbreaks of Salmonella are commonly associated with consumption of contaminated foods such as poultry products. Therefore, the objective of this study was to determine the occurrence, biofilm formation, antibiotic resistance, and sanitizer resistance of Salmonella enterica isolated from chicken carcasses. A total of 318 samples were collected from 15 chicken slaughterhouses in 8 provinces of Korea. They were then examined for Salmonella contamination. S. enterica isolates were tested for their susceptibilities to 15 antimicrobials by broth microdilution method. Their biofilm formation ability and resistance to sanitizers were also evaluated. Eighty‐two isolates of S. enterica were obtained from the 318 samples. There were 14 serotypes and 2 untypable isolates. Fifty‐seven (69.5%) isolates were resistant to at least one antibiotic while 30 (36.6%) isolates were resistant to 5 or more antibiotics. Two S. Senftenberg and 3 S. Montevideo isolates exhibited considerable biofilm formation ability (A₆₀₀>0.2) following incubation in Luria‐Bertani (LB) broth for 48 h. Biofilm cell survival and recovery growth assay after sanitization showed that most isolates were highly susceptible to 2.5% lactic acid and 0.1% cetylpyridinium chloride. Therefore, lactic acid and cetylpyridinium chloride might be alternatively or additionally used in addition to chlorine‐based sanitizers that are frequently used to reduce Salmonella contamination of chicken carcasses. Our results provide basic information on the distribution of Salmonella serotypes in chicken slaughterhouses. This study also highlights the necessity to improve farming practices and use antimicrobial agents cautiously. This study also suggests that sanitization during the slaughtering process might be necessary to reduce Salmonella contamination of chicken carcasses.