Laser Induced Liquid Phase Reaction Synthesis Assisted Joining of Metal Matrix Composites

A Laser Induced Liquid Phase Reaction Synthesis Assisted Joining technique is employed for SiC-particulate/Al-alloy composite to produce joints. Joints in SiC/Al-alloy composite are produced by synthesis of suitable material product as a result of interaction between composite and Ti (or Ti-alloy) reactive filler material induced by laser energy in the joint region. Such reaction product minimizes or eliminates the formation of deleterious aluminum carbide phase in the joint region depending upon the type and nature of die interfacial reactive filler material and also the laser processing parameters. A laser beam is utilized to both synthesize the interfacial reactant mixture and to heat the base material adjacent to the joint region to minimize the thermal stresses. The technique along with suitable filler material, further can be extended to a variety of metal matrix composite systems including combinations of Gr/Al, B/Al, B₄C/Mg, Steel/Al, W/Al, Al₂ O₃ and Gr/Cu which are excellent for use in various automotive, aerospace and electronic applications. Preliminary observations describing the proof of concept of laser induced reaction joining of metal matrix composites are reported     

A decade of clinical trial developments in postmyocardial infarction, congestive heart failure, and sustained ventricular tachyarrhythmia patients: from CAST to AVID and beyond. Cardiac Arrhythmic Suppression Trial. Antiarrhythmic Versus Implantable Defibrillators

Multiple trials using antiarrhythmic drugs, pharmacologic therapy, and implantable cardioverter defibrillators have been performed in an attempt to improve survival in patients: (1) postmyocardial infarction; (2) with congestive heart failure, with and without nonsustained ventricular tachycardia; and (3) with sustained ventricular tachycardia and those who have survived an out-of-hospital cardiac arrest. This article reviews some of the key findings and limitations of completed and ongoing trials. We also make recommendations for the current treatment of such patients based on the results of these trials.     

The synthesis of symmetrical and unsymmetrical P1/P1' cyclic ureas as HIV protease inhibitors

Cyclic urea SD146, a potent HIV protease inhibitor bearing a flat resistance profile, possessed poor solubility and bioavailability, which precluded further development of the compound. In an effort to improve upon the pharmacokinetic profile of the compound, several analogs modified at the P1/P1' residues were prepared and evaluated. Several of those compounds displayed significant improvement of physical properties.     

Consideration of conformational transitions and racemization during process development of recombinant glucagon-like peptide-1

This article summarizes the results of a combined analysis from two identical multicenter clinical trials that investigated the efficacy and safety of sertraline versus placebo for treating panic disorder. Patients with panic disorder who were treated with sertraline had a statistically significant reduction in the mean number of panic attacks per week (the primary efficacy measure) as compared with placebo (4.8 vs. 2.5, p < .001). Sertraline-treated patients also showed greater improvement that was statistically significant on several ratings of panic disorder symptomatology and functioning. The design characteristics, clinical rating measures, and outcome measures in these trials included most of the features deemed essential by Shear and Maser (1994) in their summary of the NIMH Consensus Conference for the development of standardized assessments for panic disorder. This suggests that the NIMH Consensus Conference played a key role in developing successful multicenter pharmacological treatment studies, such as this one that ultimately demonstrated that sertraline was an effective treatment for panic disorder.     

Dynamic provisioning in multi-tenant service clouds

Cloud-based systems promise an on-demand service provisioning system along with a ??pay-as-you-use?? policy. In the case of multi-tenant systems this would mean dynamic creation of a tenant by integrating existing cloud-based services on the fly. Presently, dynamic creation of a tenant is handled by building the required components from scratch. Although multi-tenant systems help providers save cost by allocating multiple tenants to the same instance of an application, they incur huge reconfiguration costs. Cost and time spent on these reconfiguration activities can be reduced by re-constructing tenants from existing tenant configurations supported by service providers. Multi-tenant cloud-based systems also lack the facility of allowing clients to specify their requirements. Giving clients the flexibility to specify requirements helps them avoid spending an excessive amount of time and effort looking through a list of services, many of which might not be relevant to them. Moreover, dynamic provisioning in the cloud requires an integrated solution across the technology stack (software, platform and infrastructure) combining functional, non-functional and resource allocation requirements. Existing research works in the area of web service matching, although numerous, still fall short, since they usually consider each requirement type in isolation and cannot provide an integrated solution. To that end, in this paper we investigate the features needed for dynamic service provisioning on the cloud. We propose a novel User Interface-Tenant Selector-Customizer (UTC) model and approach, which enables cloud-based services to be systematically modeled and provisioned as variants of existing service tenants in the cloud. Our approach considers functional, non-functional and resource allocation requirements, which are explicitly specified by the client via the user interface component of the model. To the best of our knowledge, ours is the first such integrated approach. We illustrate our ideas using a realistic running example, and also present a proof-of-concept prototype built using IBM??s Rational Software Architect modeling tool. We also present experimental results demonstrating the applicability of our matching algorithm. Our results show significant reduction in matching time with the help of an elimination process that reduces the search space needed for performing matching.     

Production of alumina fibre through jute fibre substrate

Alumina fibre has been produced using jute fibre as substrate material at temperatures lower than 1600 C in a reducing atmosphere. Processed jute fibre was chemically pretreated by saturation with Al₂Cl₆ · 12H₂O, coked and then pyrolysed to obtain alumina fibre. Chemical pretreatment conditions have been determined by following weight loss measurements of the jute fibre at 0.1 to 0.6 N solutions of NaOH, KOH, NH₄OH, Na₂CO₃, K₂CO₃, HCl and acetic acid. The effect of heat treatment on the jute fibre and jute fibre + aluminium salt has been studied from 150 to 1600 C. Trace elements present (Fe₂O₃, SiO₂, K₂O, Na₂O, CaO, MgO, ZnO, MnO, V₂O₅, P₂O₅, CuO) on heat-treated products have been determined by atomic absorption spectrometry. Optical and scanning electron micrographs of representative samples showing growth mechanism are presented. The effect of copper, nickel and platinum catalysts and fluxing agents such as K₂O and Na₂O in fibre formation has also been examined. Particle size and surface area analyses of intermediate and final products have been carried out. Changes in 2 values are plotted for various products from X-ray diffraction studies. It is conceived that the porous surface of cellulosic fibrils in the jute fibre adsorbs the AlCl₃ molecules which decompose to oxide and are gradually shaped to the fibrous form during the course of thermal treatment in a reducing atmosphere and due to the high surface area.     

Time temperature equivalence in plasticized PVC

The viscoelastic response of plasticized PVC was determined from stress-relaxation data over a wide range of time at different temperatures. The relaxation modulus as a function of time was determined from these data. The relaxation curves were then shifted horizontally to obtain a master curve at a reference temperature. The amount of shift was evaluated using the WLF equation. The coefficients C and C used in the equation for the PVC were determined according to the method of reduced variables.     

Study of viscosity of mono-, di-, and trialkylamines

Viscosities of several mono-, di-, and trialkylamines have been measured in the temperature range 298 to 333 K. It is observed that viscosities are highly dependent on shape, size, and association through H-bond or through dipole. Following the transition state theory, energy, Gibbs free energy, and entropy of activation of viscous flow have been calculated. The values of expansion energy for these liquids have also been calculated using free volume theory, and subsequently amines have been classified as volume-restrained or energy-restrained liquids. The group contribution method of Van Velzen, Cardozo, and Langenkamp for estimating viscosity has been examined with the present and literature data, and the new group contribution increments N _i and B _i for amines have been evaluated.     

Human DDX3X Unwinds Japanese Encephalitis and Zika Viral 5′ Terminal Regions

Flavivirus genus includes many deadly viruses such as the Japanese encephalitis virus (JEV) and Zika virus (ZIKV). The 5′ terminal regions (TR) of flaviviruses interact with human proteins and such interactions are critical for viral replication. One of the human proteins identified to interact with the 5′ TR of JEV is the DEAD-box helicase, DDX3X. In this study, we in vitro transcribed the 5′ TR of JEV and demonstrated its direct interaction with recombinant DDX3X (K_d of 1.66 ± 0.21 µM) using microscale thermophoresis (MST). Due to the proposed structural similarities of 5′ and 3′ TRs of flaviviruses, we investigated if the ZIKV 5′ TR could also interact with human DDX3X. Our MST studies suggested that DDX3X recognizes ZIKV 5′ TR with a K_d of 7.05 ± 0.75 µM. Next, we performed helicase assays that suggested that the binding of DDX3X leads to the unwinding of JEV and ZIKV 5′ TRs. Overall, our data indicate, for the first time, that DDX3X can directly bind and unwind in vitro transcribed flaviviral TRs. In summary, our work indicates that DDX3X could be further explored as a therapeutic target to inhibit Flaviviral replication