Structural characterization and oxidative dehydrogenation activity of V2O5/Ce(x)Zr(1-x)O2/SiO2 catalysts

The thermal stability of a nanosized Ce(x)Zr(1-x)O2 solid solution on a silica surface and the dispersion behavior of V2O5 over Ce(x)Zr(1-x)O2/SiO2 have been investigated using XRD, Raman spectroscopy, XPS, HREM, and BET surface area techniques. Oxidative dehydrogenation of ethylbenzene to styrene was performed as a test reaction to assess the usefulness of the VOx/Ce(x)Zr(1-x)O2/SiO2 catalyst. Ce(x)Zr(1-x)O2/SiO2 (1:1:2 mol ratio based on oxides) was synthesized through a soft-chemical route from ultrahigh dilute solutions by adopting a deposition coprecipitation technique. A theoretical monolayer equivalent to 10 wt % V2O5 was impregnated over the calcined Ce(x)Zr(1-x)O2/SiO2 sample (773 K) by an aqueous wet impregnation technique. The prepared V2O5/Ce(x)Zr(1-x)O2/SiO2 sample was subjected to thermal treatments from 773 to 1073 K. The XRD measurements indicate the presence of cubic Ce0.75Zr0.25O2 in the case of Ce(x)Zr(1-x)O2/SiO2, while cubic Ce0.5Zr0.5O2 and tetragonal Ce0.16Zr0.84O2 in the case of V2O5/Ce(x)Zr(1-x)O2/SiO2 when calcined at various temperatures. Dispersed vanadium oxide induces more incorporation of zirconium into the ceria lattice, thereby decreasing its lattice size and also accelerating the crystallization of Ce-Zr-O solid solutions at higher calcination temperatures. Further, it interacts selectively with the ceria portion of the composite oxide to form CeVO4. The RS measurements provide good evidence about the dispersed form of vanadium oxide and the CeVO4 compound. The HREM studies show the presence of small Ce-Zr-oxide particles of approximately 5 nm size over the surface of amorphous silica and corroborate with the results obtained from other techniques. The catalytic activity studies reveal the ability of vanadium oxide supported on Ce(x)Zr(1-x)O2/SiO2 to efficiently catalyze the ODH of ethylbenzene at normal atmospheric pressure. The remarkable ability of Ce(x)Zr(1-x)O2 to prevent the deactivation of supported vanadium oxide leading to stable activity in the time-on-stream experiments and high selectivity to styrene are other important observations.     

Short-range interactions between non-ionic surfactant layers

Short-range interactions between surfactant and lipid layers are of great importance in technical applications in complex fluids such as foams, dispersions and emulsions, as well as in the formulation and performance of dispersants, detergents and flocculants. It is also of utmost importance in biological systems where interactions between biomembranes influence a range of processes. The field of short-range interactions has been thoroughly investigated during the past 30 years, following the emergence of a number of techniques to measure interaction forces. Thus, our understanding has increased considerably and it is timely to summarize relevant knowledge accumulated in this area. In this review we focus on the nature of short-range interactions between non-ionic and zwitterionic surfactant and lipid layers exposing their polar groups to the surrounding medium. We discuss the complex interplay of short-range (van der Waals, hydration, steric and other) forces based on recent theoretical and experimental results.     

Critical properties of the paramagnetic-to-ferromagnetic transition in nanocrystalline Gd diluted with Fe

Nanocrystalline Gd_0.946Fe_0.054 of average grain size 68 nm was prepared by melt-spinning. The magnetic behavior in the vicinity of the paramagnetic to ferromagnetic transition was investigated via dc magnetization and ac susceptibility measurements. The transition temperature and effective critical exponents for the order parameter and zero-field susceptibility were determined using Arrott-Noakes and Kouvel-Fisher analyses. The values obtained were T_C=291.71±0.07 K, β_eff=0.385±0.009, and γ_eff=1.24±0.03, respectively. Correction to scaling analysis indicated that the asymptotic exponents were both smaller than the effective ones within the reduced-temperature range investigated, contrary to the behavior seen in monocrystalline Gd. This behavior can be explained in terms of a crossover from 3D short-range Heisenberg universality class to the 3D Ising universality class due to increased anisotropy induced by the high magnetic fields used in the measurements and also possibly due to strain.     

Continuous opinion model in small-world directed networks

In the compromise model of continuous opinions proposed by Deffuant et al., the states of two agents in a network can start to converge if they are neighbors and if their opinions are sufficiently close to each other, below a given threshold of tolerance ?. In directed networks, if agent i is a neighbor of agent j,j need not be a neighbor of i. In Watts-Strogatz networks we performed simulations to find the averaged number of final opinions 〈F〉 and their distribution as a function of ? and of the network structural disorder. In directed networks 〈F〉 exhibits a rich structure, being larger than in undirected networks for higher values of ?, and smaller for lower values of ?.     

Background field method at finite temperature and density

In this Letter we make use of the Background Field Method (BFM) to compute the effective potential of an SU(2)$\mathit{SU}(2)$ gauge field theory, in the presence of chemical potential and temperature. The main idea is to consider the chemical potential as the background field. The gauge fixing condition required by the BFM turns out to be exactly the one we found in a previous article in a different context.     

Smectic A-Nematic and Nematic-Isotropic Liquid Transitions in 8CB Liquid Crystal: Comparative Analysis

A differential heat flux calorimeter has been used to study the Smectic A-Nematic and Nematic-Isotropic Liquid transitions in 8CB liquid crystal. The Faktor and Hanks model under our working conditions enables us to distinguish first-order from second-order transitions by analysis of differential signal. The critical exponent values obtained justify the proportionality between Cp evolution and the normalized differential signal (differential signal divided by the scanning rate).     

Flexible semi‐transparent silicon (100) fabric with high‐k/metal gate devices

Can we build a flexible and transparent truly high performance computer? High‐k/metal gate stack based metal–oxide–semiconductor capacitor devices are monolithically fabricated on industry's most widely used low‐cost bulk single‐crystalline silicon (100) wafers and then released as continuous, mechanically flexible, optically semi‐transparent and high thermal budget compatible silicon fabric with devices. This is the first ever demonstration with this set of materials which allows full degree of freedom to fabricate nanoelectronics devices using state‐of‐the‐art CMOS compatible processes and then to utilize them in an unprecedented way for wide deployment over nearly any kind of shape and architecture surfaces. Electrical characterization shows uncompromising performance of post release devices. Mechanical characterization shows extra‐ordinary flexibility (minimum bending radius of 1 cm) making this generic process attractive to extend the horizon of flexible electronics for truly high performance computers.

     

Nature of halogen-centered intermolecular interactions in crystal growth and design: Fluorine-centered interactions in dimers in crystalline hexafluoropropylene as a prototype

The wide occurrence of halogen-centered noncovalent interactions in crystal growth and design prompted this study, which includes a mini review of recent advances in the field. Particular emphasis is placed on providing compelling theoretical evidence of the formation of these interactions between sites of positive electrostatic potential, as well as between sites of negative electrostatic potential, localized on the electrostatic surfaces of the bound fluorine atoms in a prototypical system, hexafluoropropylene (C₃F₆), upon its interaction with another same molecule to form (C₃F₆)₂ dimers. The existence of σ- and π-hole interactions is shown for the stable dimers. Even so, weakly bound interactions locally responsible in holding the molecular fragments together cannot and should not be overlooked since they are partly responsible for determining the overall geometry of the crystal. The results of combined quantum theory of atoms in molecules, molecular electrostatic surface potential, and reduced density gradient noncovalent interaction analyses showed that these latter interactions do indeed play a role in the stability and growth of crystalline C₃F₆ itself and the (C₃F₆)₂ dimers. A symmetry adapted perturbation theory energy decomposition analysis leads to the conclusion that a great majority of the (C₃F₆)₂ dimers examined are the consequence of dispersion (and electrostatics), with nonnegligible contribution from polarization, which together competes with an exchange repulsion component to determine the equilibrium geometries. In a few structures of the (C₃F₆)₂ dimer, the fluorine is found to serve as a six-center five-bond donor/acceptor, as found for carbon in other systems (Malischewski and Seppelt, Angew. Chem. Int. Ed. 2017, 56, 368). © 2019 Wiley Periodicals, Inc.     

Transmission of macroeconomic shocks to risk parameters: Their uses in stress testing

In this paper, we are interested in evaluating the resilience of financial portfolios under extreme economic conditions. Therefore, we use empirical measures to characterize the transmission process of macroeconomic shocks to risk parameters. We propose the use of an extensive family of models, called General Transfer Function Models, which condense well the characteristics of the transmission described by the impact measures. The procedure for estimating the parameters of these models is described employing the Bayesian approach and using the prior information provided by the impact measures. In addition, we illustrate the use of the estimated models from the credit risk data of a portfolio.     

A Review of Cellulose and Cellulose Blends for Preparation of Bio-derived and Conventional Membranes,Nanostructured Thin Films,and Composites

Cellulose has been used as a raw material for the manufacture of membranes and fibers for many years. This review gives the background of the most recent methods of treating or dissolving cellulose, and its derivatives to form polymer films or membranes for a variety of applications. Indeed, some potential applications of bacterial cellulose, nanofibrillar cellulose (NFC) for films showing enhanced barrier characteristics are reviewed as well as the utilization of cellulose nanonocrystals (CNC) for production of highly oriented super strong films or thin films is discussed. Because of the success of the Lyocell process as well as the amine/metal thiocyanate solvent blends of cellulose and other polysaccharides like starch, chitosan, and other natural polymers. Consequently, the use of cellulose (or its derivatives) and another polysaccharide dissolved as a blend is also elaborated. It is our hope that the reader will want to follow up and investigate these new systems and use them to develop end use materials for all sorts of applications, from medical to water filtration, or electrogels for use in batteries.