Solidification or Melting Initiation over a Limited Portion of an Edge in a Plate

This paper proposes a method for obtaining short-time analytical solutions to problems in pure heat conduction, and heat conduction with phase change. The method employs the notion of fictitious initial temperatures in some fictitious extensions of the original phase region. Analytical results obtained in the case of a heat conduction problem in a rectangular plate are presented first and compared with numerical solutions. This analytical solution is also required later in the determination of liquid temperature in the phase change problem. The method is then extended to a two-phase solidification problem in which solidification starts over a limited portion of one of the vertical edges of the rectangular plate. The freezing front in this case consists of spread along the vertical edge and growth towards the interior. The spread along the edge can have asymptotic behaviour not commonly found. The method is applicable to other geometries, e.g. inside and outside of a long cylinder, a three-dimensional slab, etc.     

相移电子散斑干涉测量物面形状

本文提出了一种用于测量三维物体表面形状的新方案.利用电子散斑干涉仪,通过两次图像采集之间折射率变化,获得代表等高线的相关条纹图,应用相移技术,可以获得高精度的形状测量结果.文中还讨论了自制气体相移器原理及性能。     

Rheology of semiconcentrated fibre suspension in the Oldroyd-B fluid

The constitutive equation for a semiconcentrated fibre suspension in the Oldroyd-B fluid has been derived from a statistical model of such a suspension by employing the molecular theory for polymeric liquids. To circumvent theoretical difficulties in viscoelastic fluid mechanics, several simplified models are used to account for the interactions of fibres and polymer molecules. Some of material functions are calculated in terms of the constitutive equation. The project Supported by the University of Melbourne of Australia, the National Natural Science Foundation of China and Zhejiang Province     

Geometric properties of two phase flow in geothermal reservoirs

The two phase flow equations frequently used in geothermal engineering ignore capillary pressure, which results in a singular system of equations. Analysis of these equations reveals three mechanisms for altering saturation: local boiling, the spatial dependence of flowing enthalpy due to the convective transport of fluid, and counterflow. A scalar function is associated with each of these three mechanims. At each point in space, flows are essentially two dimensional, with gravity establishing a vertical hierarchy, in that volumetric, energy and mass fluxes can never point below a lower member in this triple. With increasing liquid saturation, the characteristics associated with the saturation equation move up from below this grouping of directions, and eventually may even point above volumetric fluxes. Finally, weak shocks and the associated entropy condition are considered. The characteristics of the saturation equation coincide with the velocity of extremely weak shocks, and saturation increases with the passage of a weak shock, provided the magnitude of the characteristic speed increases with saturation.Notation C_l liquid heat capacity - C_m rock heat capacity - C_v vapour heat capacity - G counterflow energy flux - h flowing enthalpy - hl liquid enthalpy - h_v vapour enthalpy - k permeability - k downward vector - P pressure - S liquid saturation - T temperature - dT/dP derivative at saturation - z vertical coordinate - l liquid viscosity - v vapour viscosity - Pl liquid density - _m rock density - _v vapour density - porosity     

Non-isothermal kinetics of a moving phase boundary

In this paper we derive an explicit formula for a kinetic relation governing the motion of a phase boundary in a bilinear thermoelastic material capable of undergoing solid-solid phase transitions. To obtain the relation, we study traveling wave solutions of a regularized problem that includes viscosity, heat conduction and convective heat exchange with an ambient medium. Both inertia and latent heat of transformation are taken into account. We investigate the effect of material parameters on the kinetic relation and show that in a certain range of parameters the driving force becomes a non-monotone function of the interface velocity. The model also predicts a nonzero resistance to phase boundary motion, part of which is caused by the thermal trapping. Received: November 15, 2001 / Published online September 4, 2002 RID="*" ID="*" e-mail: annav@math.pitt.edu Communicated by Lev Truskinovsky, Minneapolis     

Instability of the Motion of a Drop in Filtration Flows

The behavior of an inclusion (drop) of foreign fluid in a porous medium saturated with another fluid is considered. A steady-state regime of gravity-induced drop settlement is found and the instability of this regime is demonstrated. The horizontal motion of a liquid inclusion under the action of a stationary reservoir pressure gradient is also studied.     

Phase Interaction in a Vapor-Liquid Medium in Transient Flow Regimes

A mathematical model and a numerical method are developed for studying nonlinear wave processes in two-phase liquids with gas or vapor bubbles under conditions of impact interaction with deformable media. On the basis of the proposed approach to the numerical modeling of the dynamics of the transient processes in the two-phase vapor-liquid and deformable media, the basic features of the phase behavior, the phase transitions, and the interphase heat and mass transfer, typical of liquids containing vapor bubbles, are analyzed. The results of solving problems of the dynamics of different vapor-liquid media are presented.__________Translated from Izvestiya Rossiiskoi Academii Nauk, Mekhanika Zhidkosti i Gaza, No. 3, 2005, pp. 88–102.Original Russian Text Copyright © 2005 by Petushkov.     

Homogeneous and unimolecular gas‐phase thermal decomposition kinetics of methyl benzoylformate: experimental and theoretical study

The kinetics of the gas‐phase thermal decomposition of the α‐ketoester methyl benzoylformate was carried out in a static system with reaction vessel deactivated with allyl bromide, and in the presence of the free radical inhibitor propene. The rate coefficients were determined over the temperature range of 440–481 °C and pressures from 32 to 80 Torr. The reaction was found to be homogenous, unimolecular and obey a first‐order rate law. The products are methyl benzoate and CO. The temperature dependence of the rate coefficient gives the following Arrhenius parameters: log₁₀ k (s^?1) = 13.56 ± 0.31 and E_a (kJ mol^?1) = 232.6 ± 4.4. Theoretical calculations of the kinetic and thermodynamic parameters are in good agreement with the experimental values using PBE1PBE/6‐311++g(d,p). A theoretical Arrhenius plot was constructed at this level of theory, and the good agreement with the experimental Arrhenius plot suggests that this model of transition state may describe reasonably the elimination process. These results suggest a concerted non‐synchronous semi‐polar three‐membered cyclic transition state type of mechanism. The most advanced coordinate is the bond breaking C^δ+‐‐‐^δ‐OCH₃ with an evolution of 66.7%, implying this as the limiting factor of the elimination process. Copyright © 2014 John Wiley & Sons, Ltd.     

Gas‐phase elimination kinetics of selected aliphatic α,β‐unsaturated aldehydes catalyzed by hydrogen chloride

The gas‐phase elimination of 2‐methyl‐2‐propenal catalyzed by HCl yields propene and CO gas, while E‐2‐pentenal with the same catalyst gives butene and CO gas. The kinetics determinations were carried out in a static system with the reaction vessels deactivated with allyl bromide and the presence of the free radical inhibitor toluene. Temperature and pressure ranges were 350.0–410.0 °C and 34–76 Torr. The elimination reactions are homogeneous and unimolecular, and follow a first‐order rate law. The rate coefficients for the reactions are expressible by the following Arrhenius equations: Data from the kinetic and thermodynamic parameters of these catalyzed elimination reactions implies a mechanism of a concerted five‐membered cyclic transition state structure for the formation of the corresponding olefin and carbon monoxide. Copyright © 2015 John Wiley & Sons, Ltd.     

Toward automatic evaluation of defect detectability in infrared images of composites and honeycomb structures

Non-destructive testing (NDT) refers to inspection methods employed to assess a material specimen without impairing its future usefulness. An important type of these methods is infrared (IR) for NDT (IRNDT), which employs the heat emitted by bodies/objects to rapidly and noninvasively inspect wide surfaces and to find specific defects such as delaminations, cracks, voids, and discontinuities in materials. Current advancements in sensor technology for IRNDT generate great amounts of image sequences. These data require further processing to determine the integrity of objects. Processing techniques for IRNDT data implicitly looks for defect visibility enhancement. Commonly, IRNDT community employs signal to noise ratio (SNR) to measure defect visibility. Nonetheless, current applications of SNR are local, thereby overseeing spatial information, and depend on a-priori knowledge of defect’s location. In this paper, we present a general framework to assess defect detectability based on SNR maps derived from processed IR images. The joint use of image segmentation procedures along with algorithms for filling regions of interest (ROI) estimates a reference background to compute SNR maps. Our main contributions are: (i) a method to compute SNR maps that takes into account spatial variation and are independent of a-priori knowledge of defect location in the sample, (ii) spatial background analysis in processed images, and (iii) semi-automatic calculation of segmentation algorithm parameters. We test our approach in carbon fiber and honeycomb samples with complex geometries and defects with different sizes and depths.