GPELab,a Matlab toolbox to solve Gross–Pitaevskii equations I: Computation of stationary solutions

This paper presents GPELab (Gross–Pitaevskii Equation Laboratory), an advanced easy-to-use and flexible Matlab toolbox for numerically simulating many complex physics situations related to Bose–Einstein condensation. The model equation that GPELab solves is the Gross–Pitaevskii equation. The aim of this first part is to present the physical problems and the robust and accurate numerical schemes that are implemented for computing stationary solutions, to show a few computational examples and to explain how the basic GPELab functions work. Problems that can be solved include: 1d, 2d and 3d situations, general potentials, large classes of local and nonlocal nonlinearities, multi-components problems, and fast rotating gases. The toolbox is developed in such a way that other physics applications that require the numerical solution of general Schrödinger-type equations can be considered.     

Curing of mixtures of epoxy resins and 4‐methyl‐1,3‐dioxolan‐2‐one with several initiators

Diglycidyl ether of bisphenol A or 3,4‐epoxycyclohexylmethyl 3,4‐epoxycyclohexane carboxylate were mixed with different proportions of 4‐methyl‐1,3‐dioxolan‐2‐one and cured using lanthanide triflates as initiators. In order to compare the materials obtained, conventional initiators such as boron trifluoride complexes and N,N‐dimethylaminopyridine were also tested. The curing process was followed by differential scanning calorimetry (DSC) and Fourier transform IR in attenuated total reflectance mode. This technique proved that the carbonate accelerates the curing process because it helps to form the active initiating species, although it was not chemically incorporated into the network and remained entrapped in the material. The DSC kinetic study was also reported. © 2006 Wiley Periodicals Inc. J Appl Polym Sci 102: 2086–2093, 2006     

Decomposition de l'acetylene,de l'ethylene et du benzene sur le carbone aux tres hautes temperatures et sous de basses pressions

At high temperatures (1000–2000°C) and low pressures (10^?5?10^?2 Torr) ethylene, acetylene and benzene decompose helerogeneously on pyrolytic carbon giving mainly hydrogen and deposited carbon, with collision yields of the order of 10^?4. The kinetics of these carbon deposition reactions show some striking similarities with carbon removal reactions by oxygen or oxygenated compounds.The true reaction order of these decomposition reactions is one above 1400°C, but becomes smaller at lower temperatures. This behaviour, common in gas-solid reactions, is generally interpreted as an inhibition due to chemisorption of some intermediate or reaction product. Evidence is also obtained that decomposition of the hydrocarbon molecules only occurs on peculiar sites of the carbon surface, i.e. the decomposition is not a purely thermal process, but involves a specific chemical interaction with the surface.Moreover, the behaviour of the pyrocarbon surface in carbon deposition reactions is similar to that observed in gasification reactions, i.e. the reactivity of the surface accommodates itself to the temperature and pressure conditions, as revealed by the observation of “transitory” and “stationary rates”. Transitory rates show that the surface deactivates with increasing temperatures (Figs. 4 and 5) [from which a maximum in the stationary rate results (Figs. 1–3)] and decreasing pressures (Figs. 7 and 8). The interpretation assumes that reaction sites are continuously created as an effect of carbon atoms deposition, but also deactivated by a thermal healing process.A main difference between carbon deposition reactions from hydrocarbons and carbon gasification reactions concerns the temperature range where reactivity is temperature dependent: in carbon deposition reactions, deactivation of the pyrocarbon surface is still effective up to much higher temperatures (Fig. 12).     

Bubble nucleation and growth in fluids

The nucleation and growth of CO₂ bubbles in non-Newtonian and Newtonian fluids that were initially supersaturated under different pressures are investigated in the present work. Quantitative information by means of two cameras reveals that at an immobile nucleation site the bubble grows rapidly followed by a linear increase in bubble diameter with time. After reaching a critical size, the bubble detaches from the stagnant site to rise in liquids with an exponential temporary increase for both the diameter and distance. A simple physical reasoning was proposed to qualitatively explain these observed phenomena. Recently, the growth rate and flow fields around a CO₂ micro-bubble were measured in a microdevice by a micro-Particle Image Velocimetry in water. This information at microscale gives new insight into the complex mechanism of bubble nucleation and growth in fluids and could help to develop a rigorous theoretical modelling and numerical simulation such as the Lattice Boltzmann approach.     

Incremental inconsistency detection with low memory overhead

Ensuring models’ consistency is a key concern when using a model‐based development approach. Therefore, model inconsistency detection has received significant attention over the last years. To be useful, inconsistency detection has to be sound, efficient, and scalable. Incremental detection is one way to achieve efficiency in the presence of large models. In most of the existing approaches, incrementalization is carried out at the expense of the memory consumption that becomes proportional to the model size and the number of consistency rules. In this paper, we propose a new incremental inconsistency detection approach that only consumes a small and model size‐independent amount of memory. It will therefore scale better to projects using large models and many consistency rules. Copyright © 2012 John Wiley & Sons, Ltd.     

High styrene–rubber ionomers,an alternative to thermoplastic elastomers

High styrene rubber ionomers were prepared by sulfonating styrene–butadiene rubber of high styrene content (high styrene rubber) in 1,2‐dichloroethane using acetyl sulfate reagent, followed by neutralization of the precursor acids using methanolic zinc acetate. The ionomers were characterized using X‐ray fluorescence spectroscopy, Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (NMR), dynamic mechanical analysis (DMA), and also by the evaluation of mechanical properties. The FTIR studies of the ionomer reveal that the sulfonate groups are attached to the benzene ring. The NMR spectra give credence to this observation. Results of DMA show an ionic transition (T_i) in addition to glass–rubber transition (T_g). Incorporation of ionic groups results in improved mechanical properties as well as retention of properties after three cycles of processing. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2294–2300, 2002     

Optimizing BRDF orientations for the manipulation of anisotropic highlights

This paper introduces a system for the direct editing of highlights produced by anisotropic BRDFs, which we call anisotropic highlights. We first provide a comprehensive analysis of the link between the direction of anisotropy and the shape of highlight curves for arbitrary object surfaces. The gained insights provide the required ingredients to infer BRDF orientations from a prescribed highlight tangent field. This amounts to a non‐linear optimization problem, which is solved at interactive framerates during manipulation. Taking inspiration from sculpting software, we provide tools that give the impression of manipulating highlight curves while actually modifying their tangents. Our solver produces desired highlight shapes for a host of lighting environments and anisotropic BRDFs.     

Improving retrieval accuracy of Hierarchical Cellular Trees for generic metric spaces

Metric Access Methods (MAMs) are indexing techniques which allow working in generic metric spaces. Therefore, MAMs are specially useful for Content-Based Image Retrieval systems based on features which use non L _p norms as similarity measures. MAMs naturally allow the design of image browsers due to their inherent hierarchical structure. The Hierarchical Cellular Tree (HCT), a MAM-based indexing technique, provides the starting point of our work. In this paper, we describe some limitations detected in the original formulation of the HCT and propose some modifications to both the index building and the search algorithm. First, the covering radius, which is defined as the distance from the representative to the furthest element in a node, may not cover all the elements belonging to the node’s subtree. Therefore, we propose to redefine the covering radius as the distance from the representative to the furthest element in the node’s subtree. This new definition is essential to guarantee a correct construction of the HCT. Second, the proposed Progressive Query retrieval scheme can be redesigned to perform the nearest neighbor operation in a more efficient way. We propose a new retrieval scheme which takes advantage of the benefits of the search algorithm used in the index building. Furthermore, while the evaluation of the HCT in the original work was only subjective, we propose an objective evaluation based on two aspects which are crucial in any approximate search algorithm: the retrieval time and the retrieval accuracy. Finally, we illustrate the usefulness of the proposal by presenting some actual applications.     

New thermosets obtained by cationic copolymerization of DGEBA with γ‐caprolactone with improvement in the shrinkage. II. Time–temperature–transformation (TTT) cure diagram

Mixtures of diglycidylether of bisphenol A (DGEBA) with different proportions of γ‐caprolactone (γ‐CL) were cured with ytterbium triflate as initiator. The curing was studied with differential scanning calorimetry (DSC) and thermo mechanical analysis (TMA). The results are presented in the form of a time–temperature–transformation diagram. The kinetic analysis was performed by means of the isoconversional integral procedure and the kinetic model was also determined using the Coats–Redfern method. Gelation was determined by means of combined experiences of DSC and TMA. The relationship between the glass transition temperature (T_g) and the degree of conversion α was determined by DSC. Using the isoconversional lines and the T_g‐α relationship, the vitrificacion curve was obtained. The methodology developed makes it possible to obtain the TTT diagram using only no‐isothermal experiments with equivalent results to those using classical isothermal procedures. The addition of γ‐CL accelerates the curing and reduces the shrinkage after gelation and consequently the internal stresses in the material. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

The biodrying process of sewage sludge – a review

Abstract

Sewage treatment can be classified into three phases: liquid, gaseous, and solid. Treatment of solids is performed in several steps, and the greatest difficulty in removing water from sewage sludge is due to the bound water present in the sludge. Thus, biodrying, a drying method that can be classified as biological, has been recently applied to treat this type of waste. This review paper aims to report and compile data from 49 biodrying assays of sewage sludge found in the literature (through the present, 2019) into one synthesis table, to discuss and compare the numerous variables found in these papers and their implications for biodrying, and to suggest possibilities for future research. This paper additionally intends to improve knowledge of biodrying and to consequently contribute to the monitoring and understanding of the process.