Supramolecular π–π assembly of a neutral [Cu(salen)] complex via the templating effect of an ionic inorganic complex Na2[Cu(mnt)2] forming a framework type material having well-defined channels

A classical ionic inorganic complex Na₂[Cu(mnt)₂] (mnt²⁻ = maleonitriledithiolate = 1,2-dicyanoethylenedithiolate), that acts as a template in assembling neutral [Cu(salen)] (salen = bis(salicylidene)ethylenediamine) complexes forming a framework type arrangement, is accommodated in the channel formed in the crystal structure of a new type of host–guest compound [Cu(salen)]₄ · Na₂[Cu(mnt)₂] (1). The non-covalent supramolecular interactions among [Cu(salen)] complexes and between [Cu(salen)] and [Cu(mnt)₂]²⁻ complexes in the crystal lattice of 1 result in weak antiferromagnetic coupling.     

Flux measurements for a DD neutron generator using neutron activation analysis

The fast and maximum thermal neutron fluxes from the DD-109 neutron generator at the University of Sharjah were experimentally measured by the activation technique using different neutron reactions. The thermal and fast neutron fluxes were found to be 2.960 × 10~6 and6.186 × 10~7 n/cm~2 s, respectively. This was done to verify the modeling results for the optimum moderator thickness needed to maximize the thermal neutron flux. The optimum moderator thickness was found to be between 3.5 and4 cm. The present data were compared with the detailed MCNP model-based calculation performed in earlier work to simulate the generator.     

The Structure And Properties of a Thermo‐mechanically Processed Low Carbon High Strength Steel

Research efforts were given towards development of low carbon high strength steels since recent past. The present study deals with the development of a low carbon high strength steel alloyed with Mn, Ni, Mo, Cu and microalloyed with Ti and Nb. The steel was subjected to three stage controlled rolling operation followed by accelerated cooling. The structure and properties of the steel at various processing conditions were evaluated. Microstructural observation reveals predominantly lath martensite along with twinned martensite structure at all processing conditions. High strength values at higher finish rolling temperatures have been obtained due to fine martensitic structure along with tiny precipitates of microalloying carbide and carbonitride. The strength value increases marginally at lower finishing temperature due to comparatively finer lath size of martensite and increased precipitation density of carbides, carbonitrides along with Cu particles. The variation in impact toughness properties at different finish rolling temperatures is found to be negligible at ambient and subambient temperatures. The formation of stable and large TiN/TiCN particles during casting have impaired the impact toughness values at ambient and at ‐40°C temperatures.     

Twinning-induced sluggish evolution of texture during recrystallization in AISI 316L stainless steel after cold rolling

This paper deals with the evolution of texture in AISI 316L austenitic stainless steel during annealing after 95 pct cold rolling. After 95 pct cold rolling, the texture is mainly of the brass type {110}〈112〉, along with a scatter toward the S orientation {123}〈634〉 and Goss orientation {011}〈100〉. Weak evidence of Cu component is observed at this high deformation level. During annealing, recovery is observed before any detectable recrystallization. Recrystallization proceeds through nucleation of subgrain by twinning within the deformed matrix and, later, preferential growth of those to consume the deformed matrix. After recrystallization, the overall texture intensity was weak; however, there are some discernible texture components. There was no existence of the brass component at this stage. Major components are centered on Goss orientation and Cu component {112}〈111〉 as well as the BR component {236}〈385〉. Also, a few orientations come up after recrystallization (i.e., {142}〈2−11〉 and {012}〈221〉). With increase in annealing temperature, the textural evolution shows emergence of weak texture with another new component, {197}〈211〉. The evolution of texture was correlated with the deformation texture through twin chain reaction.     

Neural network optimized with evolutionary computing technique for solving the 2-dimensional Bratu problem

In this paper, a stochastic technique is developed to solve 2-dimensional Bratu equations using feed-forward artificial neural networks, optimized with genetic and interior-point algorithms. The 2-dimensional equations are first transformed into a 1-dimensional boundary value problem, and a mathematical model of the transformed equation is then formulated with neural networks using an unsupervised error. Network weights are optimized to minimize the error. Evolutionary computing based on genetic algorithms is used as a tool for global search, integrated with an interior-point method for rapid local convergence. The methodology is applied to solve three cases of boundary value problems for the Bratu equations. The accuracy, convergence and effectiveness of the scheme is validated for a large number of simulations. Comparison of results is made with the exact solution derived using MATHEMATICA, and is found to be in good agreement.     

A copper–cyclen coordination complex associated with a polyoxometalate anion: Synthesis,crystal structure and electrochemistry of [Cu(cyclen)(MeCN)][W6O19]

The reaction between Cu(NO₃)₂·3H₂O and a tetra-aza macrocycle, more specifically, cyclen in 1:1 MeCN–MeOH solvent mixture forms a Cu²⁺–cyclen coordination complex in situ, that has been reacted with an isopolyanion [W₆O₁₉]^2? in a slow diffusion technique, resulting in the isolation of an ion-pair solid [Cu(cyclen)(MeCN)][W₆O₁₉] (1). Single crystal structural investigation on 1 shows a square pyramidal geometry around the metal centre (copper ion) with an axially bound MeCN solvent molecule. The title compound 1 is the first crystallographically characterized ion-pair compound, in which a transition metal coordination complex of a tetra-aza-crown ether (cyclen) has been associated with a polyoxometalate cluster anion. This communication deals with synthesis, spectroscopic, structural and electrochemical analyses of compound 1.     

Development of controlled strength-loss resorbable beta-tricalcium phosphate bioceramic structures

Controlling the strength-loss rate during biodegradation is a bottleneck in developing viable resorbable ceramic implants. Resorbable beta-tricalcium phosphate (β-TCP) bioceramic is known for its excellent biocompatibility. However, it exhibits poor sinterability and poor flexural strength. Here, we improved sintering behavior and biaxial flexural strength of β-TCP bioceramic without altering its biocompatibility by introducing multi-oxide sintering additives, in small quantities. These additives could also tailor the rate of resorption and hardness deterioration of β-TCP. A range of additives were prepared and introduced into β-TCP powder. Resultant powders were uniaxially pressed and sintered at 1250 °C, in air. Considerable improvement in densification (up to 33%) and biaxial flexural strength (up to 43%) were achieved. X-ray powder diffraction (XRD) analysis confirmed that the additives didn't alter the phase purity. In vitro cytotoxicity and biocompatibility analyses were performed using a prostate cancer cell-line. Results showed that the doped and pure β-TCP structures were non-toxic and biocompatible.     

The comparative study of biocomposites based on hydrochar and chitosan-modified urea-formaldehyde resins

To provide new insight into the field of urea-formaldehyde (UF) adhesives science, in this work, for the first time, UF resin was modified with hydrochar of spent mushroom substrate (HCUF) and chitosan (CHUF) to investigate the effect of these bio-fillers on the hydrolytic and thermal stability of in situ prepared UF resins. The characterization of the modified UF biocomposites was performed using X-ray diffraction analysis (XRD), Fourier transforms infrared spectroscopy (FTIR), non-isothermal thermogravimetric analysis (TG), differential thermal gravimetry (DTG), and differential thermal analysis (DTA). Scanning electron micrographs (SEM) of the CHUF and HCUF biocomposites show a spherical structure that differs from each other because the surface of the CHUF biocomposite has pronounced pores that form a network structure. With its hydroxyl and amino groups, chitosan bonding to UF resin through hydrogen bonds, which is confirmed by FTIR analysis. The content of free FA in CHUF biocomposite is 0.06%, while that of HCUF is higher and amounts to 0.48%. The content of released FA in both modified UF biocomposites was similar (2.5% and 2.8% for CHUF and HCUF, respectively). The hydrolytic stability of CHUF is slightly higher compared to the HCUF biocomposite. Thermal analysis shows that the CHUF is thermally more stable because it starts to decompose at a slightly higher temperature than the HCUF biocomposite.