Hybridation des méthodes de recherche taboue et du recuit simulé pour l’optimisation d’une antenne en réseau adaptative

The increasing pollution of the electromagnetic environment has prompted the study of array pattern nulling techniques. These techniques are very important in radar, sonar and communication systems for minimising degradation in signal-to-noise ratio performance due to undesired interferences. Adaptive array antennas backed by strong signal processing algorithms are able to automatically change the beam pattern in accordance with the changing signal environment. It not only directs maximum radiation in the direction of the desired mobile user but also introduces nulls for interfering directions while tracking the desired mobile user at the same time. The adaptation is achieved by multiplying the incoming signals with complex weights and then summing them together to obtain the desired radiation pattern. Adaptive array optimization is an NP-hardproblem. In this paper, a technique based on the coupling between tabu search and simulated annealing methods is presented to solve this problem. Several illustrative examples of patterns with imposed single and multiple null directions are given to show the versatility of the present method.     

Patterned assembly of genetically modified viral nanotemplates via nucleic acid hybridization

The patterning of nanoparticles represents a significant obstacle in the assembly of nanoscale materials and devices. In this report, cysteine residues were genetically engineered onto the virion surface of tobacco mosaic virus (TMV), providing attachment sites for fluorescent markers. To pattern these viruses, labeled virions were partially disassembled to expose 5' end RNA sequences and hybridized to virus-specific probe DNA linked to electrodeposited chitosan. Electron microscopy and RNAase treatments confirmed the patterned assembly of the virus templates onto the chitosan surface. These findings demonstrate that TMV nanotemplates can be dimensionally assembled via nucleic acid hybridization.     

Analysis of grapefruit sulphur volatiles using SPME and pulsed flame photometric detection

Sulphur volatiles are major factors in the perceived aroma of grapefruit juice, GFJ. The objective of this study was to develop a procedure to concentrate, separate, identify and quantify the major volatile sulphur compounds, VSC’s, in grapefruit juices. SPME parameters such as headspace atmosphere, fibre coating, extraction time and temperature were evaluated. High resolution capillary GC using ZB-5, DB-Wax and PLOT columns coupled with pulsed flame photometric detection, PFPD, were employed for separation and detection. Thirteen sulphur volatiles were identified including; hydrogen sulphide, sulphur dioxide, methanethiol, dimethyl sulphide, carbon disulphide, dimethyl disulphide, 2-methyl thiophene, 3-methyl thiophene, methional, dimethyl trisulphide, 3-mercaptohexylacetate, 2,8-epithio-cis-p-menthane and 1-p-menthene-8-thiol. Five additional VSC’s were tentatively identified. Canned reconstituted GFJ had more total sulphur volatiles and a greater number than fresh GFJ. Hydrogen sulphide comprised over 80% of total sulphur volatiles in fresh GFJ but only 5% in canned GFJ.     

Wear Behavior of Composites Based on ZA-27 Alloy Reinforced by Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Particles Under Dry Sliding Condition

In present study, the effect of Al₂O₃ particle reinforcement on the sliding behavior of ZA-27 alloy composites was investigated. The composites with 3, 5, and 10 wt% of Al₂O₃ particles were produced by the compocasting procedure. Tribological properties of unreinforced alloy and composite were studied, using block-on-disk tribometer under unlubricated sliding conditions at different specific loads and sliding speeds. The worn surfaces of samples were examined by the scanning electron microscopy (SEM). The test results revealed that those composite specimens exhibited significantly lower wear rate than the ZA-27 matrix alloy specimens in all combinations of applied loads and sliding speeds. The difference in the wear resistance of composite with respect to the matrix alloy, increased with the increase of the applied load/sliding speed and Al₂O₃ particle content. The highest degree of improvement of the ZA-27 alloy tribological behavior corresponded with change of the Al₂O₃ particles content from 3 to 5 wt%. At low sliding speed, moderate lower wear rate of the composites over that of the matrix alloy was noticed. This has been attributed to micro cracking tendency of the composites. Significantly reduced wear rate, experienced by the composite over that of the matrix alloy at the higher sliding speeds and loads, could be explained due to enhanced compatibility of matrix alloy with dispersoid phase and greater thermal stability of the composite in view of the presence of the dispersoid. Level of wear rate of tested ZA-27/Al₂O₃ samples pointed to the process of mild wear, which was primarily controlled by the formation and destruction of mechanical mixed layers (MMLs).     

Correction of pressure drop in a heavily loaded hybrid bearing when starting by using a constant flow lubrication system- Application to a rotary cement mill

We analyzed a lubricated journal plain bearing supporting heavy loaded rotary mill. During start-up operating, after the shaft is lifted by high external pressure lubricant, the speed of the shaft grows from 0 to the operating hydrodynamic speed when, suddenly after the first thirty seconds of shaft rotation, the pressure drops in one recess causing excessive damage to the pad bearing interface. The aim was to understand and provide some answers to the pressure drop in order to give an appropriate correction. Misalignment between the shaft and bearing surfaces was considered and analyzed in first part of the study. According to the obtained results the proposed correction is to use a suitable constant flow lubrication system which avoids the pressure to drop in recesses. A real application was made on a partial pad bearing supporting a heavy rotary cement mill localized at the cement plant of Chlef in Algeria.

     

Aerobic Training in Young Men Increases the Transfer of Cholesterol to High Density Lipoprotein In Vitro: Impact of High Density Lipoprotein Size

Exercise training not only improves the plasma lipid profile but also reduces risk of developing coronary heart disease. We investigate whether plasma lipids and high density lipoprotein (HDL) metabolism are affected by aerobic training and whether the high-density lipoprotein cholesterol (HDL-C) levels at baseline influence exercise-induced changes in HDL. Seventy-one male sedentary volunteers were evaluated and allocated in two subgroups, according to the HLD-C levels (< or >40 mg/dL). Participants underwent an 18-week aerobic training period. Blood was sampled before and after training for biochemical analysis. Plasma lipids, apolipoproteins, HDL diameter, and VO₂ peak were determined. Lipid transfers to HDL were determined in vitro by incubating plasma samples with a donor lipid artificial nanoemulsion. After the 18-week period of aerobic training, the VO₂ peak increased, while the mean body mass index (BMI) decreased. HDL-C concentration was higher after the training period, but low-density lipoprotein cholesterol (LDL-C) and non-HDL-C did not change. The transfer of esterified cholesterol and phospholipids was greater after exercise training, but the triacylglycerol and unesterified cholesterol transfers were unchanged. The HDL particle diameter increased after aerobic training in all participants. When the participants were separated in low-HDL and normal-HDL groups, the postaerobic exercise increment in HDL-C was higher in the low-HDL group, while the transfer of esterified cholesterol was lower. In conclusion, aerobic exercise training increases the lipid transfers to HDL, as measured by an in vitro method, which possibly contributes to the classical elevation of the HDL-C associated with training.     

Nanocomposites of ultrahigh molar mass polyethylene and modified carbon nanotubes

In this work, the use of a laboratory twin-screw extruder was evaluated to process ultrahigh molar mass polyethylene and composites with carbon nanotubes (CNTs). Commercial polymer samples with lubricant (1%) and different percentages (0.01%, 0.05%, and 0.1%) of pure, oxidized, and chemically surface treated multi-walled carbon nanotubes (MWCNTs) were evaluated. The results showed that polymer melting and crystallization temperatures were not affected by CNTs, although an increase in the degree of crystallinity in all nanocomposites was observed along with a decrease in crystal size. Therefore, CNTs behaved as nucleating agents. All ultrahigh molar mass polyethylene (UHMWPE)/CNT samples showed increased initial degradation temperature, although this was not very great when introducing acetylated and stearic acid modified CNTs. Both oxidized CNTs and stearic acid CNTs did not markedly improve the composites' mechanical properties. Therefore, the nanocomposites containing pure CNTs and most of those with acetylated CNTs resulted in higher reinforcement for UHMWPE. The addition of the lubricant allowed the polymer matrix to be processed in the extruder, whereas the increase in CNT content in UHMWPE improved the stiffness of the material. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47459     

Synthesis and Characterization of Hetero-metallic Oxides-Reduced Graphene Oxide Nanocomposites for Photocatalytic Applications

A new AgO.CuO.WO₃/rGO nanocomposite was designed for the investigation of the degradation ability of the hybrid material under visible light irradiation. The AgO, CuO, WO₃ NPs, and AgO.CuO.WO₃ hetero-metallic oxides were fabricated via the chemical co-precipitation method. The crystallite sizes and phase analyses were investigated by recording X-ray diffraction patterns. The crystallite sizes of three metal oxides in the AgO.CuO.WO₃ hetero metal oxide were 16.7, 15.9, and 16.9 nm, respectively. The FESEM images at various magnifications were probed to study the morphology of synthesized materials. The micrographs of hetero-metallic oxides AgO.CuO.WO₃ exposed that three metal oxides merged like small particles and gives a large bulbous appearance. EDX analyses confirmed the formation of required materials with high purity. FTIR data was in agreement with the literature which facilitated to ensure the purity of synthesized samples. The optical bandgap energy was calculated via the Tauc plot indicating that the blend of three metal oxides generated a new energy level in the electronic structure is suitable for photocatalysis in the presence of visible light. The bandgap energy of hetero metallic oxides was 1.25 eV which is less than individual metal oxides signifying the tuning of the bandgap. The incorporation of rGO in AgO.CuO.WO₃ hetero-metallic oxides gives a new photocatalyst for optimum photodegradation of methylene blue in minimum time. The percentage degradation via AgO.CuO.WO₃ was 87.20% in 70 min while the percentage degradation via AgO.CuO.WO₃/rGO recorded by photocatalytic experiment was 95% in 40 min. The photocatalysis data revealed that AgO.CuO.WO₃ hetero-metallic oxides-rGO nanocomposite ensured a strong potential to uptake organic dyes from water by promoting redox reactions during photocatalysis in the minimum time limit.     

Synthesis and Characterization of Sulfanilamide-Based Nonionic Surfactants and Evaluation of Their Nano-Vesicular Drug Loading Application

Nonionic surfactants are highly stable and cost-effective and receiving acceptance for applications in many diverse fields including drug delivery, due to their distinctive properties. Here, we report on the synthesis and characterization of sulfanilamide-based nonionic surfactants for nanoscale vesicular drug loading applications. Nonionic surfactants were synthesized through alkylation of sulfanilamide with alkyl halides that possessed diverse degrees of lipophilicity. They were explored for their nanovesicular drug loading with Cefixime as a hydrophobic model drug. Drug-loaded nanovesicles were characterized for surface morphologies, size, size distribution, surface charge, and drug loading efficiency using atomic force microscopy (AFM), dynamic light scattering (DLS), and UV–visible spectrophotometry. All of the synthesized nonionic surfactants revealed their CMC values in 0.055–0.035 mM range depending upon the lipophilic chain length of surfactants. They caused a decreased hemoglobin release and low toxicity against cell culture. They self-assembled and loaded an increased amount of drug in the form of nanorange spherical shape niosomal vesicles. Results of the current study verify these synthesized nonionic surfactants are hemocompatible, nontoxic, and capable of self-assembling into nanorange niosomal vesicles. These niosomal vesicles can be suggested as safe and highly efficient nanocarriers for hydrophobic drug loading and delivery.