Crystal growth,optical and thermal studies of nonlinear optical γ-glycine single crystal grown from lithium nitrate

Single crystals of the nonlinear material γ-glycine have been grown in the presence of lithium nitrate by slow-evaporation method. Structural characterization of the grown crystals was carried out by powder and single crystal X-ray diffraction (XRD) methods and it is observed that the samples crystallize in hexagonal system with non-centrosymmetric space groups. The modes of vibrations of different molecular groups present in glycine have been identified by spectral analyses. UV–visible transmittance study was performed to analyze optical transparency of γ-glycine crystals and found that the crystal was transparent in the entire visible-NIR region. Second harmonic generation (SHG) conversion efficiency has been estimated as 62 mV and the output power by the crystal was 1.72 times that of potassium dihydrogen phosphate (KDP) crystal. The thermal stability and decomposition of the sample have been studied by thermal analysis and it is observed that the γ-glycine crystal have good thermal stability.     

Inverse acoustical characterization of natural jute sound absorbing material by the particle swarm optimization method

For modeling of jute as acoustic material, knowledge of its non-acoustical parameters like porosity, tortuosity, air flow resistivity, thermal and viscous characteristic lengths is a prime requisite. Measurement of these non-acoustical parameters is not straightforward and involves a dedicated measurement setup. So in order to overcome this issue, the inverse acoustical characterization can be used. In this paper, the particle swarm optimization method (PSO) is used as an optimization method. This method estimates the non-acoustical parameters of jute material in felt form by minimizing the error between experimental and theoretical sound absorption data. In this work, the impedance prediction models for fibrous materials like Johnson–Champoux–Allard model with rigid and limp frame and Garai–Pompoli model is used for sound absorption coefficient calculation by the transfer matrix method along with the PSO. The inverse estimated non-acoustical parameters for jute material are then compared with estimated and experimentally measured parameters for jute felts. Using these inversely predicted parameters, sound absorption of multilayer sound absorbers is also studied.     

Physical properties and processing conditions correlations of the ldpe/lldpe tubular blown films

Experiments are carried out to verify a theory developed to correlate the strain history of the polymer during film blowing to the ultimate physical properties of the film. The theory predicts that the amount of strain put into the film once it starts to freeze, defined as strain in the amorphous region and the plastic strain, has a dominant effect on the film properties. Two grades of low and linear low density polyethylene, experimental resins supplied by Mobil chemical company, were used to produce the blown film yielding a 1.25 mil film at the for all experimental runs. Film surface and bulk temperatures, along the machine direction and around the bubble, were measured using the infra-red techniques to identify the points where film starts to crystallize. A video digitization technique was used to measure the bubble kinematics. Film properties were measured using standard ASTM methods. The results indicate a correlation between the amount of strain and a measure of stress with ultimate physical properties of the blown film. This principle leads to the correlation of both the machine and transverse film properties on the same surface. The results obtained can potentially be exploited by designing the blown-film equipment and processing conditions such that optimal bubble stretching produces desired film properties.     

Ni(II) selective sensors based on Schiff bases membranes in poly(vinyl chloride)

The two nickel chelates of Schiff bases, 3-hydroxy-N-{2-[(3-hydroxy-N-phenylbutyrimidoyl)-amino]-phenyl}-N′-phenylbutyramidine (M₁) and bis-4-(ethyliminomethyl)naphthalene-1-ol (M₂), have been synthesized and explored as ionophores for preparing PVC-based membrane sensors selective to nickel ion. The influences of membrane compositions on the potentiometric response of the electrodes have been found to substantially improve the performance characteristics. The best performance was obtained with the electrode having a membrane composition (w/w; mg) of (M₁): PVC:NaTPB:CN in the ratio 5:150:5:150. The sensor shows a linear potential response for Ni²⁺ over a wide concentration range 1.6 × 10⁻⁷ to 1.0 × 10⁻² M with Nernstian compliance (30.0 ± 0.2 mV/decade of activity) within pH range 2.5-9.5 and a fast response time of 10 s. The sensor has been found to work satisfactorily in partially non-aqueous media up to 20% (v/v) content of methanol, ethanol, and acetonitrile and could be used for a period of 4 months. The analytical usefulness of the proposed electrode has been evaluated by its application in the determination of nickel in real samples. The practical utility of the membrane electrode has also been observed in the presence of surfactants.     

Elastin-calmodulin scaffold for protein microarray fabrication

In this work, we report a new method to reversibly immobilize proteins to a surface in a functionally active orientation directly from cell lysate by employing a fusion protein consisting of a thermal-responsive elastin (ELP) domain as the surface anchor and a calcium-responsive calmodulin (CalM) domain for protein capturing. Incorporation of an M13 tag into recombinant proteins enables not only easy surface immobilization but also direct purification from cell lysates. The feasibility of concept was demonstrated using the M13-tagged yellow fluorescent protein (M13-YFP). The ELP-CalM functionalized surfaces were shown to capture M13-YFP directly from cell lysate through the specific calmodulin-M13 association in a calcium-dependent manner. We also demonstrated that immobilization is reversible; the bound proteins were released from the surface in the presence of EDTA.     

Fly ash supported NiO as an efficient catalyst for the synthesis of xanthene and its molecular docking study against plasmodium glutathione reductase

A novel fly ash supported NiO (FA–NiO) nanocomposite solid heterogeneous catalyst has been prepared by impregnation of Ni(NO₃)₂ · 6H₂O on thermally activated fly ash (FA) support. FT-IR spectroscopy, X-ray diffraction analysis, scanning electron microscopy, TEM and BET techniques were employed to characterize the catalyst. The catalytic adeptness of FA–NiO was tested and optimized in xanthene formation. Catalyst gave very high yield and good purity. Stability of the catalyst could be promising as it easily recovered and reused giving a similar yield up to four cycles. FA–NiO is an efficient catalyst providing an environmentally clean process for xanthene formation and for developing a revolutionary way to use the majority of waste fly ash. Further, we have also performed docking simulation between 1ONF and a xanthene molecule to evaluate binding orientation and affinity of the ligand.     

Liquid crystals alignment with PbS nanosculptured thin films

Lead sulphide (PbS) nano-sculptured thin films (nSTFs) are prepared for the first time using glancing angle deposition technique by physical vapour deposition process. An anisotropic morphology is obtained, which provides an orientational effect. Due to this anisotropic nature of PbS nSTF an attempt has been made to check its effect on the alignment of nematic liquid crystals (LCs). Two different LC devices were fabricated, that is, anti-parallel aligned or electrically-controlled birefringence and hybrid twisted nematic. It is noticed that in both types of devices, good alignment is obtained with high extinction and contrast. A significant effect of these alignments on the electro-optic properties of the LC is reported such as the threshold voltage, response time and contrast ratio.     

Furfuroxides of lanthanum,praseodymium, neodymium,and samarium

Ln(R)₃, Ln(R)₂(OPrⁱ), and Ln(R)(OPrⁱ)₂ (where Ln = La, Pr, Nd, and Sm; R = deprotonated furfuryl alcohol, RH) were prepared from lanthanide isopropoxide and furfuryl alcohol in 1:3, 1:2 and 1:1 stoichiometric ratios respectively in anhydrous benzene under reflux. Ln(R)₂-(OPrⁱ) and Ln(R)(OPrⁱ)₂ were also obtained at room temperature. The isopropoxy group(s) of these derivatives were replaced by tertiary butoxy group(s) during the alcohol exchange reactions with tertiary butanol. All these derivatives are soluble in benzene except the tertiary butoxy derivatives which are only sparingly soluble. However, they become insoluble on standing. These furfuroxides did not distil at ～300°C/10² torr but decomposed. Isopropoxy/butoxy furfuroxides were characterized by the elemental analysis and also by estimating the liberated isopropanol. The i.r. spectra of Ln(R)₃ clearly supports the presence of furfuroxide groups in these derivatives.