Flow control using bifrequency motion

We used a second-order approximation for the periodic lift coefficient of a circular cylinder under monofrequency and bifrequency cross-flow motions. Two lock-in modes exist under monofrequency fundamental (i.e., near the Strouhal number) motion. In the first mode, the work is done by the flow on the cylinder, whereas in the second mode the work is done by the cylinder on the flow. Under monofrequency superharmonic (i.e., near three times the Strouhal number) motion, the work is always done on the flow. We then replaced the monofrequency motions by a bifrequency one, consisting of a fundamental term combined with a small-magnitude superharmonic term. We examined the effect of the magnitude and phase of the superharmonic motion term on the two modes of lock-in which we obtained when only the fundamental motion term is applied, considering two different frequencies that belonged to the two lock-in modes. Under the bifrequency motion, the work can be done on the flow or on the cylinder. This can be controlled using the superharmonic motion term, even when its magnitude is 5% of magnitude of the fundamental motion term. Other flow variables, such as the magnification of the lift, can be remarkably altered through the added superharmonic motion term. The phase of the third superharmonic lift-coefficient component relative to the fundamental one is the most responsive variable to the phase of the superharmonic motion component relative to the fundamental one.     

Electron Ionization Mass Spectra of Organophosphorus Compounds Part I: The Mass Fragmentation Pathways of Cyclic α-Aminophosphonates Monoester Containing 1,2,4-Triazinone Moiety

Abstract

The electron impact induced fragmentation reactions of 3-(4-chlorophenyl)-3,4- dihydro-2-ethoxy-2-oxido-7-methyl-2H,6H-[1,2,4]triazino[4,3-e][1,4,5,2]thiadiazaphosphin in-6-one (1), 3,7-dimethyl-2-ethoxy-2-oxido-1,2,3,4-tetrahydro-6H-[1,2,4]triazino[4,3-b][1,2,4,5]triazaphosphinin-6-one (2), and 9-amino-3,7-dimethyl-4-ethoxy-4-oxido-2,3,4,9-tetrahydro-8H-[1,2,4]triazino[3,2-c][1,2,4,5]triazaphosphinin-8-one (3) are presented and compared. The 1,2,4-triazine rings have almost identical fragmentation routes. The 1,2,4-triazine rings are rather stable relative to the phosphorus rings. Therefore, fragmentation of the phosphorus rings is more favorable for the compounds than the stable 1,2,4-triazine rings.     

One-way and two-way couplings of CFD and structural models and application to the wake-body interaction

The current study focuses on the wake-body interaction of a circular cylinder, whose transverse free vibration is modeled by a mass-spring-damper system coupled to a computational fluid dynamics (CFD) model for the flow and wake. We first simulate the free vibration of the elastically-mounted cylinder and the wake, and analyze the transverse load it exerts on the cylinder and its phase with the vibration. We vary the damping by three orders of magnitude and examine the difference in the wake-body interaction for slightly-damped and highly-damped systems. We then use the spectral properties of the free vibration and use them to construct two different types of forced vibrations: one consists only of the fundamental component of the free vibration, and the other accounts for all spectral properties of it. We compare the wake load for each type to that corresponding to the free vibration. The forced vibrations correspond to a one-way coupling and the information is communicated from the CFD model to the structural model, whereas the free vibration corresponds to a two-way coupling of the models. By comparing the spectral properties of the wake load, including the phase relation of its components with the vibration, which we obtained for the free vibration and for the equivalent forced vibration, we identify the effects of the wake feedback. The findings show that a forced vibration does not reproduce exactly the wake load at small and intermediate levels of structural damping. As the damping increases, the vibration changes from being in-phase with the wake load to being 90° out-of-phase with it, corresponding to two different wake states, and the forced vibration gives wake load that is very close to the one occurring in the case of full wake-body interaction.     

Ultrasonic,FTIR and thermal investigations of SiO2–Na2O–CaO–P2O5 glasses doped with CeO2

The longitudinal and shear ultrasonic wave velocities for different compositions of SiO₂–Na₂O–CaO–P₂O₅ glasses were measured at room temperature (305 K) using a pulse-echo method at a frequency of 4 MHz. The elastic moduli, Poisson's ratio, microhardness, Debye temperature and other ultrasonic parameters were obtained from experimental data and analyzed using bond compression theory. By calculating the number of network bonds per unit volume, the average stretching constant, and the average ring size, information about the structure of the glass can be deduced. Structural changes after doping with CeO₂ were investigated by FTIR spectroscopy, and by measurements of the thermal expansion coefficient, glass transition and softening temperature to throw more light on the characterization of these glasses.     

Structural studies and mechanical properties of some borate glasses doped with different alkali and cobalt oxides

Mixed alkali borate glasses doped with CoO, have been prepared by the melt quenching technique. Elastic properties and FT-IR spectroscopic studies have been employed to study the role of CoO and the mixed alkali effect on the structure of the investigated glass system. Elastic properties and Debye temperature have been investigated using sound wave velocity measurements at 4 MHz at room temperature. The density, molar volume and glass transition temperatures were employed to investigate the structure of these glasses. Infrared spectra of these glasses revealed that the borate network is affected by the increase in the concentration of CoO content and the mixed alkali oxides. These results are interpreted in terms of the change in the topology of these glass structures. The elastic moduli are observed to increase with the increase of CoO content due to the increased average bond connectivity.     

Chemical composition and antioxidant activity of the coriander cake obtained by extrusion

This study was designed to examine the effect of operating conditions on essential oil composition and antioxidant activity of coriander cakes. Twenty-nine components were determined in essential oils, which were mostly alcohol monoterpenes. The highest essential oil yields (0.11%) were obtained by the nozzle diameter of 5 mm. The main components of cake essential oil linalool, γ-terpinene, geranyl acetate, linalyl acetate and camphor showed significant variations with different nozzle diameter.The total phenol contents and condensed flavonoid contents varied between different nozzle diameters; the highest values obtained of small diameters (5 and 6 mm). Significant differences were also found in total tannin contents among different nozzle diameters. The total phenol contents decreased significantly (p < 0.05) when increased the nozzle diameter to 9 mm and reached 9.11 mg GAE/g.The screening of antioxidant activity of the different coriander cakes using the di(phenyl)-(2,4,6-trinitrophenyl) iminoazanium radical (DPPH) assay showed an appreciable reduction of the stable radical DPPH, although small nozzle diameter was the most efficient method with an IC₅₀ reached of 55 μg/ml as compared with bigger diameter (IC₅₀ = 88 μg/ml).All the extracts had lower β-carotene bleaching activity than that of synthetic antioxidant BHA and BHT. Coriander cake extracts presented a very low reducing power ability (EC₅₀ ≈ 700 μg/ml) compared to ascorbic acid (EC₅₀ = 40 μg/ml).     

Piperidinium Hydrogen Sulfate (PHS) as an Efficient Ionic Liquid Catalyst for the Synthesis of Imidazole Derivative under Solvent‐Free Condition

Piperidinium hydrogen sulfate is used as a very important new catalyst for the synthesis of the biologically active compounds from a series of multi‐substituted imidazole components by the simple reaction of benzyl with different aromatic aldehydes, ammonium acetate, and phenethylamine or butylamine as amine derivatives. The key merits of this method are very shorter reaction times, excellent yield, and ease of stabilization. Furthermore, the produced products can be purified by a non‐chromatographic technique, and the catalyst is reusable. All of these new synthesized components have been characterized and checked from spectral data: IR, ¹H‐NMR, and ¹³C‐NMR spectra and elemental analyses.     

Optical study of Ce ion in gamma-irradiated binary barium-borate glasses

Absorption spectra measurements of cerium-doped binary system from barium-borate glasses have been measured. The effects of dopant concentration of CeO₂ and Al₂O₃ in the concentration range 0.54-2.9 and 4.8-9.2 mol%, respectively, and exposed to different irradiation doses have been measured in the range 1-7 eV and the result have been interpreted in terms of structural concepts. The radiation-induced broad band at 2.25-1.88 eV in the base glass is observed to be suppressed by the presence of cerium due to the transformation of Ce⁴⁺ to Ce³⁺. The released electrons are then used to annihilate positive holes responsible for this band. The resolution of the observed absorption spectra show two to seven induced bands depending on the glass composition. Absorption spectra of the irradiated binary glass system are found to be controlled by the cerium concentration. From the absorption edge studies, the values of optical band gap E_opt and Urbach energy ΔE have been evaluated. The oxidoreduction (redox) reaction Ce³⁺/Ce⁴⁺ is assumed to be related to the glass basicity and the possible complex-ion formation. The oxygen ion activity (O²⁻) is believed to be related to the basicity and to the possible oxygen ion formation in the glass melt, and the redox equilibrium is shifted toward the reduced state.