Some Generalised Characteristics of the Electro-dynamics of the Plasma Focus in Its Axial Phase: Illustrated by an Application to Independantly Determine the Drive Current Fraction and the Mass Swept-Up Fraction

We describe the axial phase of the Mather plasma focus by two coupled equations of motion and circuit. We non-dimensionalised these equations resulting in two coupled equations which are characterised by only three scaling parameters α, β and δ which are ratios of electrical to transit times, inductances and impedances respectively. The normalised current waveform, trajectory and speed profile are unique for each combination of α, β, δ which are the ratios of characteristic times (electrical discharge vs. axial transit), inductances (tube inductance vs. static inductance) and impedances (stray resistance vs. electrical surge impedance). This leads to important information and insight into various aspects of the axial phase. In the present work we show that in a time-matched plasma focus shot we deduce the value of axial phase current fraction f_c simply by measuring the calibrated voltage waveform and the uncalibrated current waveform. The scaling parameters β and δ are fixed; and by form-fitting the measured current waveform to the normalised current waveform using the value of α of the shot is determined uniquely; from which the peak current and the ratio of peak to average speed [the speed form factor (SFF)] are obtained. The average transit speed is measured by time-of-flight using the voltage upturn as indicator of end of axial phase. Then the SFF yields the peak speed. The measured voltage (back EMF), peak current and peak axial speed (all at the end of axial phase) allows the unambiguous measurement of f_c. The value of the mass swept-up fraction f_m is deduced from α which is the ratio of the characteristic discharge and the characteristic transit times, both deduced during the non-dimensionalisation of the equations. Analysis of a time-matched shot in the INTI PF at 15 kV, 3 Torr D₂ gave f_c = 0.68 and f_m = 0.05.     

A comprehensive survey of AI-enabled phishing attacks detection techniques

In recent times, a phishing attack has become one of the most prominent attacks faced by internet users, governments, and service-providing organizations. In a phishing attack, the attacker(s) collects the client’s sensitive data (i.e., user account login details, credit/debit card numbers, etc.) by using spoofed emails or fake websites. Phishing websites are common entry points of online social engineering attacks, including numerous frauds on the websites. In such types of attacks, the attacker(s) create website pages by copying the behavior of legitimate websites and sends URL(s) to the targeted victims through spam messages, texts, or social networking. To provide a thorough understanding of phishing attack(s), this paper provides a literature review of Artificial Intelligence (AI) techniques: Machine Learning, Deep Learning, Hybrid Learning, and Scenario-based techniques for phishing attack detection. This paper also presents the comparison of different studies detecting the phishing attack for each AI technique and examines the qualities and shortcomings of these methodologies. Furthermore, this paper provides a comprehensive set of current challenges of phishing attacks and future research direction in this domain.

     

The sinuous antenna-A dual polarized feed for reflector-based searching systems

The sinuous antennas have a numerous applications in military and civil systems such as direction finding systems and reflector feeds due to their superior broadband characteristics and simultaneous polarization capability. In this paper, design, construction and measurements of planar sinuous antennas are investigated for 1–5 GHz frequency range. Feeding sections of this antenna are realized by using microstrip tapered baluns. We have determined the microstrip tapered balun dimensions using Ansoft HFSS-simulation program. The performances of the manufactured antenna are measured using HP vector network analyzer. Polarization patterns and return loss characteristics of the designed antenna that have been measured in anechoic chamber, are presented.     

Hydrogen Generation from CO2 Reforming of Biomass-Derived Methanol on Ni/SiO2 Catalyst

Topics in Catalysis - CO2 reforming of methanol for producing hydrogen was experimentally carried out in a fixed-bed reactor on 10%Ni/SiO2. The 10%Ni/SiO2 was completely reduced during H2...     

Preparation of Silane-Grafted and Moisture Cross-Linked Low Density Polyethylene: Part I: Factors Affecting Performance of Grafting and Cross-Linking

In the present work, the silane grafting and water cross-linking of low density polyethylene (LDPE) were investigated. The grafting reaction was carried out in an internal mixer and polyethylene cross-linking was done in hot water. The effect of silane, peroxide, catalyst, carbon black, cross-linking time, and cross-linking temperature on the grafting and cross-linking processes are reported. Vinyl trimethoxy silane (VTMO) and di-cumyl peroxide (DCP) were selected as grafting agent and initiator respectively. Silane grafting on polyethylene was determined using Fourier transform infrared (FTIR) spectroscopy and torque monitoring of the mixer. Absorption peak due to –Si–OCH₃ groups in FTIR and torque increasing due to silane grafting in the mixer illustrated that silane-grafting reactions occurred. The FTIR data demonstrated that the extent of silane grafting was increased as the concentration of silane and peroxide was increased. Thermogravimetry analysis (TGA) determined that the thermal stability of LDPE increased by increasing the amount of silane grafting. Gel fraction increased with silane and peroxide concentration. As the percent of of catalyst increase the time scale for specified gel content shifted to shorter times. Incorporation of carbon black into LDPE decreased the extent of silane grafting and gel fraction. Water temperature increasing in cross-linking stage reduced the time to maximum degree of cross-linking.     

Rheological characterization of polypropylene/poly(ethylene-<Emphasis Type="Italic">co</Emphasis>-propylene) in-reactor blends synthesized under different polymerization conditions

In-reactor blends of polypropylene/poly(ethylene-co-propylene) with complex microstructure, synthesized through different polymerization procedures; two-step (one homopolymerization and one copolymerization under high ethylene concentration) and three-step (with an additional copolymerization step under low ethylene concentration), were characterized by rheological measurements. The effects of a change in the polymerization process on the types and amounts of block copolymers in the blends were evaluated using small amplitude oscillation rheometry in the linear viscoelastic region. The Palierne model in its complete form was employed to model the rheological behavior of the blends. For this analysis the reactor products were separated into xylene cold insoluble (XCI) and xylene cold soluble fractions. Besides, another two copolymer fractions at 80 and 100 °C, which are crystallizable copolymer fractions and contain block copolymers rich in polyethylene and polypropylene, respectively, were separated from XCI fraction by xylene using temperature gradient elution fractionation method. Considering all copolymer fractions as dispersed and the remained fraction (mostly polypropylene) as matrix phase, it was shown that the rheological properties of the blends could not be predicted by Palierne model. It was found that only by considering part of block copolymer fractions having long polypropylene sequences along with polypropylene homopolymer as one phase, the rheological properties of the blends could be predicted by Palierne model. By rheological modeling, it was confirmed that the amounts of copolymers with long polypropylene sequences which are miscible with the matrix are higher in the case of three-step blends and also the elasticity of three-step polymerized blends is higher than two-step polymerized blends.     

Comparing thermal and mechanochemical decomposition of ammonium paratungstate (APT)

In this research, the possibility of mechanochemical decomposition of ammonium paratungstate (APT) has been studied, and compared with thermal decomposition method. For this purpose, APT powders were milled using a planetary ball mill up to 36 h and under air atmosphere. For thermal decomposition, APT powders were heated for 30 minutes at 300 and 450 °C in air atmosphere. X-ray diffraction (XRD), differential scanning calorimeter (DSC), and thermo gravimetric analyzer (TGA) were used to study the decomposition progress, and products. The XRD results showed that APT completely decomposed to WO₃ by thermal decomposition, while the final product of mechanochemical decomposition was WO₃ (H₂O)_0.5. According to DSC and TGA results, during thermal decomposition, ammonia and water released in four steps, and leaved WO₃. By mechanochemical decomposition crystal water and ammonia liberated from APT structure, but structural water of APT remained. In both methods, an X-ray amorphous phase was the intermediate product of APT decomposition.     

Morphological,mechanical, and rheological studies of PVC/ABS blends in the presence of maleic anhydride

A novel method of enhancing compatibility in PVC/ABS blends is the use of ABS‐grafted‐(maleic anhydride) (ABS‐g‐MAH) as a compatibilizer. In this study, maleic anhydride was grafted onto ABS (initiated by peroxide) in an internal mixer. Grafting degree was determined by a back‐titration method, and certain amounts of the resultant ABS‐g‐MAH were added to PVC/ABS blends during their melt blending in the mixer. The weight ratio of PVC to ABS was kept at 70:30. Evaluation of compatibilization was accomplished via tensile and notched Izod impact tests, scanning electron microscopy (SEM), and rheological studies. According to the SEM micrographs, better dispersion of the rubber phase and its finer size in properly compatibilized blends were indications of better compatibility. Besides, in the presence of a proper amount [5 parts per hundred parts of PVC (php)] of ABS‐g‐MAH, PVC/ABS blends showed significantly higher impact strengths than uncompatibilized blends. This result, in turn, would be an indication of better compatibility. In the presence of 5 php of compatibilizer, the higher complex viscosity and storage modulus, as well as a lower loss modulus and loss factor in the range of frequency studied, indicated stronger interfacial adhesion as a result of interaction between maleic anhydride and the PVC‐SAN matrix. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers     

Supplementing with L-Tryptophan Increases Medium Protein and Alters Expression of Genes and Proteins Involved in Milk Protein Synthesis and Energy Metabolism in Bovine Mammary Cells

The objective of this study was to investigate the effects of supplementing with L-tryptophan (L-Trp) on milk protein synthesis using an immortalized bovine mammary epithelial (MAC-T) cell line. Cells were treated with 0, 0.3, 0.6, 0.9, 1.2, and 1.5 mM of supplemental L-Trp, and the most efficient time for protein synthesis was determined by measuring cell, medium, and total protein at 0, 24, 48, 72, and 96 h. Time and dose tests showed that the 48 h incubation time and a 0.9 mM dose of L-Trp were the optimal values. The mechanism of milk protein synthesis was elucidated through proteomic analysis to identify the metabolic pathway involved. When L-Trp was supplemented, extracellular protein (medium protein) reached its peak at 48 h, whereas intracellular cell protein reached its peak at 96 h with all L-Trp doses. β-casein mRNA gene expression and genes related to milk protein synthesis, such as mammalian target of rapamycin (mTOR) and ribosomal protein 6 (RPS6) genes, were also stimulated (p < 0.05). Overall, there were 51 upregulated and 59 downregulated proteins, many of which are involved in protein synthesis. The results of protein pathway analysis showed that L-Trp stimulated glycolysis, the pentose phosphate pathway, and ATP synthesis, which are pathways involved in energy metabolism. Together, these results demonstrate that L-Trp supplementation, particularly at 0.9 mM, is an effective stimulus in β-casein synthesis by stimulating genes, proteins, and pathways related to protein and energy metabolism.