Spatially developing secondary instabilities in compressible swept airfoil boundary layers

Two-dimensional eigenvalue analysis is used on a massive scale to study the spatial instabilities of compressible shear flows with two inhomogeneous directions. The main focus of the study is crossflow dominated swept-wing boundary layers although the methodology can also be applied to study other types of flows, such as the attachment-line flow. Certain unique aspects of formulating a spatial, two-dimensional eigenvalue problem for the secondary instability of finite amplitude crossflow vortices are discussed, namely, fixing the spatial growth direction unambiguously through a non-orthogonal formulation of the linearized disturbance equations. A primary test case used for parameter study corresponds to Numerical results are presented for the low-speed, NLF-0415(b) airfoil configuration as tested in the ASU Unsteady Wind Tunnel, wherein a spanwise periodic array of roughness elements was placed near the leading edge in order to excite stationary crossflow modes with a specified fundamental wavelength. The two classes of flow conditions selected for this analysis include those for which the roughness array spacing corresponds to either the naturally dominant crossflow wavelength, or a subcritical wavelength that serves to reduce the growth of the naturally excited dominant crossflow modes. Numerical predictions are compared with the measured database, both as indirect validation for the spatial instability analysis and to provide a basis for comparison with a higher Reynolds number, supersonic swept-wing configuration. Application of the eigenvalue analysis to the supersonic configuration reveals that a broad spectrum of stationary crossflow modes can sustain sufficiently strong secondary instabilities as to potentially cause transition over this configuration. In particular, the control mode itself, if initiated with too large an amplitude, may lead to an earlier transition.     

Hypersonic viscous flow over large roughness elements

Viscous flow over discrete or distributed surface roughness has great implications for hypersonic flight due to aerothermodynamic considerations related to laminar?Cturbulent transition. Current prediction capability is greatly hampered by the limited knowledge base for such flows. To help fill that gap, numerical computations are used to investigate the intricate flow physics involved. An unstructured mesh, compressible Navier?CStokes code based on the space?Ctime conservation element, solution element (CESE) method is used to perform time-accurate Navier?CStokes calculations for two roughness shapes investigated in wind tunnel experiments at NASA Langley Research Center. It was found through 2D parametric study that at subcritical Reynolds numbers, spontaneous absolute instability accompanying by sustained vortex shedding downstream of the roughness is likely to take place at subsonic free-stream conditions. On the other hand, convective instability may be the dominant mechanism for supersonic boundary layers. Three-dimensional calculations for both a rectangular and a cylindrical roughness element at post-shock Mach numbers of 4.1 and 6.5 also confirm that no self-sustained vortex generation from the top face of the roughness is observed, despite the presence of flow unsteadiness for the smaller post-shock Mach number case.     

Studies on etching behaviour of {101} faces of natural mesolite crystals

Etching behaviour of {101} habit faces of natural mesolite crystals is reported. Rectangular, truncated and elliptical etch pits are illustrated, and mechanism of their formation is assessed. Factors influencing kinetics of etching are discussed. From Arrhenius plots activation energy and pre-exponential factor are computed and reported.     

Thermoanalytical Study of Cu-Mg-Zn Ferrites

Homogeneous solid solution oxalates of Fe²⁺, Cu²⁺, Mg²⁺ and Zn²⁺ metals were prepared by co-precipitation from respective metal acetate solutions with oxalic acid solution. The thermogravimetric (TG) analysis of co-precipitated oxalate complexes with general formula Mg_xCu_(0.50-x)Zn_0.50Fe₂(C₂O₄)₃·nH₂O (x=0.00, 0.05, 0.10, 0.15, 0.20, 0.25, 0.30, 0.35, 0.40, 0.45, 0.50) were carried out by manual method in static air atmosphere. The total mass loss % and stepwise mass loss % values are in good agreement with theoretically calculated mass loss % values. The thermal decomposition of oxalate complexes occur at relatively lower temperatures (561 to 698 K). The lowering of decomposition temperatures may be attributed to earlier initiation of Fe²⁺ oxalate in oxalate complexes. At temperatures between 598–698 K the thermal decomposition of Cu-Mg-Zn-Fe solid solution oxalate complexes leads to formation of ferrites of spinel structure. After tampering at 873 and 1273 K, homogeneous ferrites arise, which is revealed from XRD studies. This revised version was published online in July 2006 with corrections to the Cover Date.     

Novel approach in the synthesis of imidazo [1, 2-a] pyridine from phenyl acrylic acids

This paper describes highly efficient concise method for the synthesis of imidazo[1,2-a] pyridine. It is a first report employing, amino pyridines, copper nitrate, and phenyl acrylic acids in the synthesis of imidazo[1,2-a] pyridine. The silent features of the devised protocol include the high yield, milder reaction conditions, and shorter reaction time.     

Determination of Dutasteride by LC: Validation and Application of the Method

A simple, rapid, and stability-indicating reversed-phase high-performance liquid chromatographic (LC) method for analysis for dutasteride has been successfully developed. Chromatography was performed on a 150 mm × 4.6 mm C₁₈ column with acetonitrile–water 60:40 (v/v) as isocratic mobile phase at 1.0 mL min^?1. Ultraviolet detection of dutasteride was at 210 nm. Its retention time was approximately 10 min and its peak was symmetrical. Response was a linear function of concentration over the range 0.2–1 μg mL^?1 (R ² = 0.997) and the limits of detection and quantitation were was 0.05 and 0.10 μg mL^?1, respectively. The method was validated for linearity, precision, repeatability, sensitivity, and selectivity. Selectivity was validated by subjecting dutasteride stock solution to photolytic, acidic, basic, oxidative, and thermal degradation. The peaks from the degradation products did not interfere with that from dutasteride. The method was used to quantify dutasteride in pharmaceutical preparations.     

Synthesis,antitubercular evaluation and molecular docking studies of phthalimide bearing 1,2,3-triazoles

In a search for safer and potent antitubercular agents, here a library of newly substituted dioxoisoindolinylmethyl-triazolyl-N-phenylacetamide derivatives (5a–l) has been synthesized via click chemistry approach. All synthesized compounds were evaluated for their antitubercular activity against Mycobacterium tuberculosis H₃₇Rv (MTB). Among the screened compounds, 5d, 5e, 5h, and 5l showed good antitubercular activity. The compounds 5d and 5l have shown very effective antitubercular activity against Mycobacterium tuberculosis H₃₇Rv (MTB) with MIC 12.5?μg/mL. All the newly synthesized compounds were thoroughly characterized by ¹H NMR, ¹³C NMR, and HRMS spectral data. We further performed exploratory docking studies on the crystal structure of Mycobacterium tuberculosis enoyl reductase to demonstrate the mechanism of antitubercular activity.     

Polyoxometalates as chemically and structurally versatile components in self-assembled materials

Polyoxometalates (POMs) are anionic molecular metal oxides with expansive diversity in terms of their composition, structure, nuclearity and charge. Within this vast collection of compounds are dominant structural motifs (POM platforms), that are amenable to significant chemical tuning with minimal perturbation of the inorganic oxide molecular structure. Consequently, this enables the systematic investigation of these compounds as inorganic additives within materials whereby structure and charge can be tuned independently i.e. [PW₁₂O₄₀]³⁻vs. [SiW₁₂O₄₀]⁴⁻ while also investigating the impact of varying the charge balancing cations on self-assembly. The rich surface chemistry of POMs also supports their functionalisation by organic components to yield so-called inorganic–organic hybrids which will be the key focus of this perspective. We will introduce the modifications possible for each POM platform, as well as discussing the range of nanoparticles, microparticles and surfaces that have been developed using both surfactant and polymer building blocks. We will also illustrate important examples of POM-hybrids alongside their potential utility in applications such as imaging, therapeutic delivery and energy storage.

Polyoxometalates are anionic molecular metal oxides with diversity in composition, structure, nuclearity and charge. Their adaptable chemistry leads to potential for self-assembly with other building blocks into a variety of hybrid structures.     

Hydrothermal Synthesis of Zeolite Crystals Using Natural Scolecite

Natural scolecite is converted into analcime type zeolite by hydrothemal method at 180 °C at autogeneous pressure for 24 to 160 hours growth runs. Mordenite is detected in the final product. Cube and spheroid crystals of the products are illustrated and described. Crystals synthesized are characterized by X-ray diffraction, infrared spectroscopy EDAX and scanning electron microscopy. Particle size is estimated as 20–60 microns, induction period for nucleation as 12 hrs, and lattice parameter of cube crystals as 13.70 Å. Mechanism of growth, influence of anions and duration of growth etc. are discussed. It is established that the crystals grow in the system Na₂O Al₂O₃ SiO₂ H₂O.     

Synthesis of analcime-type zeolite from natural stilbite by hydrothermal method

Using calcined stilbite, aluminium hydroxide and sodium hydroxide as ingradients, the procedure to synthesize a zeolite by hydrothermal method is described. Studies on characterisation (of crystals grown) by X-rays and by infrared spectroscopy, and their morphology by a scanning electron microscope are reported. That the crystals grown have cubic symmetry with a = 13.66 Å and that they are analcime type is established. From infrared spectral studies it is confirmed that the crystals are zeolites. Needle, prismatic, and layer crystals obtained are illustrated and described.