Novel mixed ligand complexes of Co(II), Ni(II), Cu(II), and Zn(II) with 1,10-phenanthroline and acesulfame. Synthesis,structural analysis and hydrogen adsorption study

Four novel metal organic framework (MOF) structures containing acesulfame (ace) and 1,10-phenanthroline (phen) ligands of Co²⁺, Ni²⁺, Cu²⁺ and Zn²⁺ metal cations were synthesized. The crystal structure analysis of three compounds (1, 2, and 3) was also performed. The structural formula for complex 4 is proposed based on spectroscopic and thermal analysis data. It has been determined that structures 1, 2, and 4 are in a distorted octahedral geometry. It has been suggested that the charge balance of the coordination sphere with 2+ is provided by two monoanionic ace ligands located outside the coordination sphere as counter-ion. In structure 3, there are two Cu^II metal cations, two phen ligands coordinated as bidentate to each metal cation and ace ligand that provides monoanionic-monodentate coordination. The Cu²⁺ cation has distorted bipyramidal geometry. The maximum hydrogen gas adsorption has been found 1.4575 mL/g (0.046 wt%) for the Ni complex.     

Doping of Nb to the Ba and Cu Sites in the Y0.6Gd0.4Ba2Cu3O7−δ

Polycrystalline samples of Y_0.6Gd_0.4Ba_2?x Nb _x Cu₃O_7?δ and Y_0.6Gd_0.4Ba₂Cu_3?x Nb _x O_7?δ with different Nb contents (x=0.025, 0.075, 0.125, 0.175 and 0.225) were prepared using the solid state reaction method. Structural and electrical properties of new compounds were investigated with optical microscope, scanning electron microscopy (SEM), X-ray diffraction (XRD), Four Point Probe (FPP). The results indicated that Nb constituted YBa₂NbO₆ structure instead of substituting to the Y_0.6Gd_0.4Ba₂Cu₃O_7?δ structure. YBa₂NbO₆ structures gathered between grains. Transition temperature did not change significantly, but critical current (J _c) values decreased with increase of Nb concentration. The underlying reason is that the oxygen concentration of compounds remained unchanged due to Gd; thus, T _c values did not change significantly.     

Kinetic Investigation of Reaction Between Mineral Ulexite and Citric Acid

In this study, the dissolution kinetics of ulexite, a sodium-calcium-borate hydrate (Na₂O·2CaO·5B₂O₃·16H₂O) in citric acid solutions was investigated in a batch reactor. The rate of dissolution can be expressed according to surface chemical reaction controlling with changing fluid reactant concentration. The activation energy of the process was found to be 39.4 kJ/mol.     

A theory of thin lamellar eutectic growth with anisotropic interphase boundaries

We present a semiempirical theory of the effects of an orientation dependence of the surface free energy of interphase boundaries (interphase boundary anisotropy) on lamellar eutectic growth in thin samples. We show that, to a good approximation, thin lamellar eutectic patterns with a strong interphase boundary anisotropy travel along the growth front at such a velocity – or, equivalently, at such an inclination angle of the lamellae left behind in the solid – that the surface tension force of the interphase boundary is nearly parallel to the applied thermal gradient. This explains, among other things, the crystallographic locking of lamellar eutectic patterns that occurs in those eutectic grains, which have cusp singularities in the Wulff plot of the interphase boundary. Based on this theory, we show that the rotating directional solidification method, by which a thin sample is rotated with respect to a fixed unidirectional thermal gradient, must yield eutectic lamellae whose trajectories are nearly homothetic to the two-dimensional Wulff form of the interphase boundary. This opens up new possibilities for the experimental study of interphase boundary anisotropy in eutectic alloys.     

Flow time analyses of a simulated flexible job shop by considering jockeying

It has been essential to include flexibility in manufacturing policy making since variability in demand and products are considerably increasing. However, it is important to know and to monitor the proper level and type of flexibility that is required to obtain full benefits from it. This paper analyses the effects of flexibility on flow time performance of a simulated job shop. For that purpose, several scenarios are developed under four flexibility levels with two different machine selection rule and three types of dispatching rules. Furthermore, effect of jockeying as a queuing policy on the flow time performance is also investigated through simulation modeling. Results indicated that full flexibility is a preferable state for most of the cases. However, in some cases, chain configurations perform similar results since it combines the benefits of pooling and specialization. In addition, it is observed that a queue control mechanism like jockeying is an effective way to improve performance even though it may increase complexity of controlling policy.     

Latent heat energy storage characteristics of building composites of bentonite clay and pumice sand with different organic PCMs

In the present work, six new kinds of building composite PCMs (BCPCMs), PS/octadecane, BC/octadecane, PS/CA–MA, BC/CA–MA, PS/PEG1000, and BC/PEG1000 composites, were prepared by using vacuum impregnation method. The maximum percent of PCM in the composites was assigned to be 12, 13, 18, 23, 30, and 42 wt%, respectively. The form‐stable BCPCMs were characterized using SEM, FT‐IR, DSC, and TG analysis techniques. The characterization results showed the existence of homogenous dispersion of the PCM into the PBM matrixes. The DSC measurements indicated that the melting temperatures of the form‐stable BCPCMs are in the range of 20–33°C while they have latent heats of melting in the range of about 28–55 J/g. These results make them promising BCPCMs for low temperature‐passive TES applications in buildings. Thermal cycling test indicated that the prepared BCPCMs have good thermal reliability and chemical stability. TG analysis proved that the prepared BCPCMs have good thermal durability. In addition, the thermal conductivity of BCPCMs was enhanced considerably by addition of expanded graphite (EG). The improvement in thermal conductivity of the BCPCMs caused appreciably reduction in their melting times. Copyright © 2014 John Wiley & Sons, Ltd.     

A new ship energy management algorithm to the smart electricity grid system

In this paper, a new energy management algorithm has been suggested for the ships connected with alternative energies considering the smart electricity grid features. The algorithm focuses on the use of optimum energy source on the shipboard based on the priorities of authorities such as the most economic, environmental, or both criteria at the ports. The algorithm is performed in MATLAB, and several case studies are simulated to validate the results. The 5 maritime nations, which are at different regions: United States, Belgium, Turkey, China, and Australia, are taken into account in the case studies. The actual data of a bulk carrier ship have been used to achieve tangible results in the simulations. The results of the case studies are compared to determine the changes of energy cost and released emission to meet demand of electricity on the ships. Capital cost of the proposed concept is also given to make an economic evaluation. The results show that the ship energy management algorithm provides the significant economic and environmental advantages. This paper aims to contribute to the importance of the ships in the smart electricity grid concept for the maritime and electricity sector representatives.     

Tungsten(VI) oxide supported rhodium(0) nanoparticles; highly efficient catalyst for H2 production from dimethylamine borane

It reports the preparation and characterization of tungsten(VI) oxide supported rhodium(0) nanoparticles (Rh⁰/WO₃ NPs) being used as catalysts in releasing H₂ from dimethylamine borane (DMAB). The reducible nature of WO₃ plays a significant role in the catalytic efficiency of rhodium(0) nanoparticles in the dehydrogenation of DMAB. The Rh⁰/WO₃ NPs were in-situ generated from the reduction of Rh²⁺ ions on the surface of WO₃ during the catalytic dehydrogenation of dimethylamine borane in toluene and isolated from the reaction solution after the dehydrogenation to be characterized by using SEM, TEM, XPS, ATR-IR and XRD. The results reveal the formation of Rh⁰ NPs with a mean particle size of 1.92 ± 0.34 nm dispersed on the surface of tungsten(VI) oxide. Rh⁰/WO₃ NPs are found to be very active catalyst releasing 1.0 equiv. H₂ per mole of dimethylamine borane under ambient conditions. Among the various WO₃ supported Rh⁰ NPs with different metal loadings, the sample with 0.1% wt. Rh provide the record catalytic activity (TOF = 2816 h^?1) which is one of the highest value ever reported for rhodium-based catalysts in H₂ generation from DMAB at 60.0 ± 0.5 °C. Rh⁰/WO₃ NPs were also reusable catalyst in dehydrogenation of DMAB retaining 55% of their initial catalytic activity in the 3rd run of the dehydrogenation reaction. Control experiments were performed at various catalyst concentrations and temperatures to investigate the kinetics of dehydrogenation and to calculate the activation parameters for the reaction.