Photoluminescence emission of nanoporous anodic aluminum oxide films prepared in phosphoric acid

The photoluminescence emission of nanoporous anodic aluminum oxide films formed in phosphoric acid is studied in order to explore their defect-based subband electronic structure. Different excitation wavelengths are used to identify most of the details of the subband states. The films are produced under different anodizing conditions to optimize their emission in the visible range. Scanning electron microscopy investigations confirm pore formation in the produced layers. Gaussian analysis of the emission data indicates that subband states change with anodizing parameters, and various point defects can be formed both in the bulk and on the surface of these nanoporous layers during anodizing.     

A Novel Algebraic Technique for the Construction of Strong Substitution Box

Magnetic induction applications mostly rely on resonance for inducing maximum magnetic fields to system loads and hence for each resonant frequency dedicated circuits are required. Unfortunately, the frequency responses of such inductive systems manifest several peaks (frequency splitting) when their coupling coefficients are equal to or larger than critical coupling. Such frequency responses with several peaks are detrimental when the objective is to transfer maximum energy. Frequency splitting between inductive coils have been seen to date as detrimental to wireless power transfer and inductive communication systems. In this paper it is demonstrated that frequency splitting is a welcome phenomenon with advantage in the design of inductive filter banks and multi-frequency inductive systems. The centre frequencies of the filter banks result from split bands of inductive systems. This phenomenon is applied in conjunction with an innovative recursive algorithm to design inductive filter banks. The filters straddle both sides of the resonant frequency position and can be resolved individually.     

The Plastome Sequences of Triticum sphaerococcum (ABD) and Triticum turgidum subsp. durum (AB) Exhibit Evolutionary Changes,Structural Characterization,Comparative Analysis,Phylogenomics and Time Divergence

The mechanism and course of Triticum plastome evolution is currently unknown; thus, it remains unclear how Triticum plastomes evolved during recent polyploidization. Here, we report the complete plastomes of two polyploid wheat species, Triticum sphaerococcum (AABBDD) and Triticum turgidum subsp. durum (AABB), and compare them with 19 available and complete Triticum plastomes to create the first map of genomic structural variation. Both T. sphaerococcum and T. turgidum subsp. durum plastomes were found to have a quadripartite structure, with plastome lengths of 134,531 bp and 134,015 bp, respectively. Furthermore, diploid (AA), tetraploid (AB, AG) and hexaploid (ABD, AGA^m) Triticum species plastomes displayed a conserved gene content and commonly harbored an identical set of annotated unique genes. Overall, there was a positive correlation between the number of repeats and plastome size. In all plastomes, the number of tandem repeats was higher than the number of palindromic and forward repeats. We constructed a Triticum phylogeny based on the complete plastomes and 42 shared genes from 71 plastomes. We estimated the divergence of Hordeum vulgare from wheat around 11.04–11.9 million years ago (mya) using a well-resolved plastome tree. Similarly, Sitopsis species diverged 2.8–2.9 mya before Triticum urartu (AA) and Triticum monococcum (AA). Aegilops speltoides was shown to be the maternal donor of polyploid wheat genomes and diverged ~0.2–0.9 mya. The phylogeny and divergence time estimates presented here can act as a reference framework for future studies of Triticum evolution.     

Investigation of miscibility and phase structure of a novel blend of poly(lactic acid) (PLA)/acrylic rubber (ACM) and its nanocomposite with nanosilica

In this work, a novel polymer blend containing poly(lactic acid) (PLA) as a biocompatible and biodegradable thermoplastic and acrylic rubber (ACM) is prepared and the miscibility and phase structure of the blend and its nanocomposite (PLA/ACM/nanosilica) are investigated through theoretical and experimental methods. To predict the phase diagram of the blend, a compressible regular solution model was employed, in which an upper critical solution temperature was observed. The model predicted that PLA/ACM blends are immiscible over the whole composition range at temperatures below 260 °C. Performing scanning force microscopy on the blend showed phase separated structures for the blends containing different amounts of the PLA and ACM. This was in accordance with the results of dynamic mechanical analysis, which revealed two distinct glass transition temperatures for the studied blends. The effect of nanometer sized silica particle on morphology and rheological properties of these blends was also investigated. Scanning force microscopy results showed much reduction of droplet size in the blends containing 2 wt % nanosilica. This was attributed to the suppression effect of nanosilica on the droplets coalescences. Rheological measurements confirmed the interaction of both components with the silica nanofiller. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45499.     

Prevalence of virulent Yersinia enterocolitica in bulk raw milk and retail cheese in northern-west of Iran

To determine the prevalence of virulent Yersinia enterocolitica, 554 samples consisting of 354 bulk raw milks and 200 traditional cheeses were collected from different parts of Eastern-Azerbaijan province, during a 23-month period from 2008 to 2010. The occurrence of virulent strains of Y. enterocolitica in samples enriched in peptone sorbitol bile broth (PSBB) was evaluated via the detection of attachment invasion locus (ail) gene by PCR. The viability of virulent Y. enterocolitica in the PCR-positive samples was tested using conventional culture method and the isolates were confirmed by the second-phase ail-PCR. According to the results, 8.66% of total samples including 7.62% of bulk raw milks and 10.5% of raw milk cheeses were found ail-positive by PCR method; subsequently Y. enterocolitica was isolated by the culture method and confirmed by the second phase ail-PCR in 2.88% of total samples including 2.26% of raw milks and 4% of cheese samples. It was concluded that, a sample enrichment followed by ail-PCR was more sensitive and robust to detect and distinguish the virulent strains of Y. enterocolitica compared to the conventional culture method.     

Zr‐Doped Indium Oxide (IZRO) Transparent Electrodes for Perovskite‐Based Tandem Solar Cells

Parasitic absorption in transparent electrodes is one of the main roadblocks to enabling power conversion efficiencies (PCEs) for perovskite‐based tandem solar cells beyond 30%. To reduce such losses and maximize light coupling, the broadband transparency of such electrodes should be improved, especially at the front of the device. Here, the excellent properties of Zr‐doped indium oxide (IZRO) transparent electrodes for such applications, with improved near‐infrared (NIR) response, compared to conventional tin‐doped indium oxide (ITO) electrodes, are shown. Optimized IZRO films feature a very high electron mobility (up to ≈77 cm² V^?1 s^?1), enabling highly infrared transparent films with a very low sheet resistance (≈18 Ω □^?1 for annealed 100 nm films). For devices, this translates in a parasitic absorption of only ≈5% for IZRO within the solar spectrum (250–2500 nm range), to be compared with ≈10% for commercial ITO. Fundamentally, it is found that the high conductivity of annealed IZRO films is directly linked to promoted crystallinity of the indium oxide (In₂O₃) films due to Zr‐doping. Overall, on a four‐terminal perovskite/silicon tandem device level, an absolute 3.5 mA cm^?2 short‐circuit current improvement in silicon bottom cells is obtained by replacing commercial ITO electrodes with IZRO, resulting in improving the PCE from 23.3% to 26.2%.     

The influence of depth of cut on the machinability of an alloyed austempered ductile iron

The volume fraction of high carbon austenite present in the microstructure of austempered ductile iron (ADI) is one of the important factors that influence the mechanical and physical properties of the alloy. Formation of martensite by TRIP (transformation induced plasticity) mechanism during the machining operation in which a large amount of stress is applied to the microstructure results in a decrease in machinability of austempered ductile iron which has affected the expansion of ADI in industry. In this article, the effect of depth of cut as a machining variable is assessed in an alloyed austempered ductile iron containing Cu, Ni and Mo. The measurements of mechanical properties including impact energy, tensile strength, hardness and microhardness along the cross-section of samples are reported for samples austenitized at 870 °C followed by austempering at 375, 340 and 300 °C. Results indicate that contrary to the behavior of many alloys, in austempered ductile iron, reducing the depth of cut will not improve the machinability. In the case of studied composition, cutting with depths of 0.5 and 0.1 mm had the best and worst results, respectively.     

Cathodic electrodeposition of Y(OH)3 and Y2O3 nanostructures from chloride bath. Part II: Effect of the bath temperature on the crystal structure,composition and morphology

Ultra-fine nanoparticles, mono-dispersed nanospheres and nanorods of Y(OH)₃ and Y₂O₃ were successfully prepared via electrodeposition from chloride bath at different temperatures of 10, 25, 40 and 80 °C followed by heat-treatments at 600 °C in dry air atmosphere. Thermal behavior of the hydroxide samples was investigated by differential scanning calorimetry (DSC) and thermogravimetric (TG) analysis. The structural and morphological characteristics of the products were determined by X-ray diffraction (XRD), FT-IR, scanning and transmission electron microscopy (SEM and TEM). Effects of bath temperature on the mechanism of base electrogeneration and deposit formation on the cathode surface were proposed and discussed. The results showed that the crystal structure, composition and morphology of the products are mainly affected by the temperature of electrodeposition bath.