Effect of substrate bias in amorphous carbon films having embedded nanocrystallites

The effect of substrate bias on the structural, morphological, electrical and mechanical properties of amorphous carbon (a―C) films having embedded nanocrystallites deposited by filtered cathodic jet carbon arc technique has been investigated. X-ray diffraction exhibits predominantly an amorphous nature of the film. High resolution transmission electron microscope investigations reveal largely an amorphous structure. However, an ultra-fine nanograined microstructure with the average grain size between 20 and 50 nm was observed throughout the entire film and the majority of the individual grains were single crystallites with the preferred interplanar spacing of about 0.2 nm. All the parameters evaluated were seen to depend strongly on the negative substrate bias and exhibit maxima or minima in the properties of the films deposited at − 150 V substrate bias. These a-C films having embedded nanocrystallites act as hard coating materials.     

PBT/Thermoplastic Elastomer Blends—Mechanical,Morphological, and Rheological Characterization

The blends of poly(butylene terephthalate) (PBT) with thermoplastic elastomer (TPE) at a blending composition of 10–30 wt.% TPE were prepared with an objective to enhance impact toughness of PBT. Two different grades of PBT were selected based on carboxyl end group and viscosity. Melting behavior, mechanical properties, morphology, and rheology of the blends were studied. At all levels of TPE, PBT showed negligible changes in its melting and crystallization temperature; however, percentage crystallinity decreased with an increase in the amount of thermoplastic elastomer. The notched as well as unnotched Izod impact strength of PBT increased with the incorporation of TPE, the increase being about 47% (unnotched) and 54% (notched) with low molecular weight PBT and 18% (unnotched) and 70% (notched) with high molecular weight PBT at 10% TPE level. The tensile strength and tensile modulus of the blends decreased steadily as the weight percent of TPE increased. Analysis of the tensile data using predicted theories indicated that at TPE levels of 30 wt.%, the blends cannot take excessive stress because the interfacial adhesion is lowered. Small angle light scattering (SALS) studies of the samples indicated the decreased rate of crystallization and, hence, an increase in spherulitic radius in the presence of TPE. The increasing incorporation of TPE in PBT/TPE blends increased the shear thinning behavior and hence eased processability.     

Room temperature amorphous to nanocrystalline transformation in ultra-thin films under tensile stress: an in situ TEM study

The amorphous to crystalline phase transformation process is typically known to take place at very high temperatures and facilitated by very high compressive stresses. In this study, we demonstrate crystallization of amorphous ultra-thin platinum films at room temperature under tensile stresses. Using a micro-electro-mechanical device, we applied up to 3% uniaxial tensile strain in 3-5 nm thick focused ion beam deposited platinum films supported by another 3-5 nm thick amorphous carbon film. The experiments were performed in situ inside a transmission electron microscope to acquire the bright field and selected area diffraction patterns. The platinum films were observed to crystallize irreversibly from an amorphous phase to face-centered cubic nanocrystals with average grain size of about 10 nm. Measurement of crystal spacing from electron diffraction patterns confirms large tensile residual stress in the platinum specimens. We propose that addition of the externally applied stress provides the activation energy needed to nucleate crystallization, while subsequent grain growth takes place through enhanced atomic and vacancy diffusion as an energetically favorable route towards stress relaxation at the nanoscale.     

Nanoscale Densification Creep in Polymer-Derived Silicon Carbonitrides at 1350°C

The measurement of axial and radial strains during uniaxial compression creep of SiCN shows the deformation to be entirely volumetric (as opposed to shear). Phenomenologically, the densification strain rate shows a good fit to an exponential stress dependence. This result is explained by the large volume of the diffusing molecular units in the oligomeric amorphous structure of SiCN, which causes the driving force to become nonlinear in stress. The size of the diffusing unit is estimated to be 1.2 nm.     

Empirical analysis of anticipatory standardization processes: a case study

The processes followed for developing anticipatory standards such as those for web services are still not well-understood. In spite of the openness of the process, there are few analyses that shed light on the roles that different participants play or the actions they engage in during the development of these standards. We analyze archival documents that capture development of SOAP, a core web service standard. Our analysis shows that participants spend a bulk of their time discussing technical issues, identifying action items, and engaging in discussion to reach consensus. These activities reveal prototypical roles that participants take on such as: Advocate, Architect, Bystander, Critic, Facilitator, Guru, and Procrastinator. Together, the findings support the existence of three clusters in standards development processes: design activities performed by Architects, sense-making activities performed by Critics, and managerial activities performed by Facilitators; along with the important activity of coordinating the work of multiple participants. We discuss implications of our findings and identify opportunities for future work.     

Setup for in situ deep level transient spectroscopy of semiconductors during swift heavy ion irradiation

A computerized system for in situ deep level characterization during irradiation in semiconductors has been set up and tested in the beam line for materials science studies of the 15 MV Pelletron accelerator at the Inter-University Accelerator Centre, New Delhi. This is a new facility for in situ irradiation-induced deep level studies, available in the beam line of an accelerator laboratory. It is based on the well-known deep level transient spectroscopy (DLTS) technique. High versatility for data manipulation is achieved through multifunction data acquisition card and LABVIEW. In situ DLTS studies of deep levels produced by impact of 100 MeV Si ions on Aun-Si(100) Schottky barrier diode are presented to illustrate performance of the automated DLTS facility in the beam line.     

Methacrylic acid and dodecyl methacrylate (MAc‐DMA) hydrogel for enhanced catalytic activity of lipase of Bacillus coagulans MTCC‐6375

An alkaline thermotolerant bacterial lipase of Bacillus coagulans MTCC‐6375 was purified and immobilized on a methacrylic acid and dodecyl methacrylate (MAc‐DMA) hydrogel. The lipase was optimally bound to the matrix after 20 min of incubation at 55°C and pH 9 under shaking conditions. The matrix‐bound lipase retained approximately 50% of its initial activity at 70–80°C after 3 h of incubation. The immobilized lipase was highly active on medium chain length p‐nitrophenyl acyl ester (C: 8, p‐nitrophenyl caprylate) than other p‐nitrophenyl acyl esters. The presence of Fe³⁺, NH₄⁺, K⁺, and Zn²⁺ ions at 1 mM concentration in the reaction mixture resulted in a profound increase in the activity of immobilized lipase. Most of the detergents partially reduced the activity of the immobilized lipase. The immobilized lipase performed ～62% conversion in 12 h at temperature 55°C. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1420–1426, 2006     

A study of the synthesis,kinetics, and characterization of reactive graft copolymers of poly(vinyl imidazole) and cellulose for use as supports in enzyme immobilization and metal ion uptake

In continuation to our earlier work to use bioresource for developing alternate materials for use at the interface of biotechnology and polymer science, we have utilized pine needles as a renewable stock of cellulose to synthesize graft copolymers of vinyl imidazole. Kinetics of N‐VIm by simultaneous γ‐irradiation method has been investigated as a function of total dose, monomer concentration, and amount of water. Effect of water–methanol solvent composition on graft yields and polymerization kinetics has also been studied at the optimum grafting conditions of the total dose and monomer concentration. Effect of some additives such as ZnCl₂, Mohr salt, tetramethylethylene diamine, potassium persulfate, ammonium persulfate as grafting accelerators and promoters has also been studied. Graft copolymers have been characterized by elemental analysis, FTIR, and swelling studies. The graft copolymers have been used as supports for metal ions sorption, enzyme immobilization, and as potential biomimicking catalysts. Sorption behavior of Fe²⁺ ions and Cu²⁺ ions and the immobilization of bovine serum albumin and protease as a function of graft yield has been reported. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1522–1530, 2006     

Structure–property relationships for sulfonated poly(butylene terephthalate)

Structure–property relationships have been developed for sulfonated poly(butylene terephthalate) copolymers. The compositional variables investigated were sulfonate content, molecular weight, and polymer endgroup composition, and the fundamental polymer properties evaluated were melt viscosity, crystallization kinetics, and impact strength. It was found that all compositional variables significantly affect all of the polymer properties of interest. The most interesting effect is the influence of polymer endgroup composition on polymer properties. The trends indicate that the carboxylic acid endgroups form intermolecular interactions with sodium sulfonate groups, resulting in a decrease in the strength of intermolecular ionic interactions between sodium sulfonate groups. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4662–4771, 2006     

Development of Diaminoquinazoline Histone Lysine Methyltransferase Inhibitors as Potent Blood‐Stage Antimalarial Compounds

Modulating epigenetic mechanisms in malarial parasites is an emerging avenue for the discovery of novel antimalarial drugs. Previously we demonstrated the potent in vitro and in vivo antimalarial activity of (1‐benzyl‐4‐piperidyl)[6,7‐dimethoxy‐2‐(4‐methyl‐1,4‐diazepin‐1‐yl)‐4‐quinazolinyl]amine (BIX01294; 1 ), a known human G9a inhibitor, together with its dose‐dependent effects on histone methylation in the malarial parasite. This work describes our initial medicinal chemistry efforts to optimise the diaminoquinazoline chemotype for antimalarial activity. A variety of analogues were designed by substituting the 2 and 4 positions of the quinazoline core, and these molecules were tested against Plasmodium falciparum (3D7 strain). Several analogues with IC₅₀ values as low as 18.5 nM and with low mammalian cell toxicity (HepG2) were identified. Certain pharmacophoric features required for antimalarial activity were found to be analogous to the previously published SAR of these analogues for G9a inhibition, thereby suggesting potential similarities between the malarial and human HKMT targets of this chemotype. Physiochemical, in vitro activity, and in vitro metabolism studies were also performed for a select set of potent analogues to evaluate their potential as antimalarial leads.