Entropy Variation in Isothermal Fluid Flow Considering Real Gas Effects
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Entropy Stable Numerical Approximations for the Isothermal and Polytropic Euler Equations
ENTROPY STABLE NUMERICAL APPROXIMATIONS FOR THE ISOTHERMAL AND POLYTROPIC EULER EQUATIONS ANDREW R. WINTERS1;∗, CHRISTOF CZERNIK, MORITZ B. SCHILY, AND GREGOR J. GASSNER3 Abstract. In this work we analyze the entropic properties of the Euler equations when the system is closed with the assumption of a polytropic gas. In this case, the pressure solely depends upon the density of the fluid and the energy equation is not necessary anymore as the mass conservation and momentum conservation then form a closed system. Further, the total energy acts as a convex mathematical entropy function for the polytropic Euler equations. The polytropic equation of state gives the pressure as a scaled power law of the density in terms of the adiabatic index γ. As such, there are important limiting cases contained within the polytropic model like the isothermal Euler equations (γ = 1) and the shallow water equations (γ = 2). We first mimic the continuous entropy analysis on the discrete level in a finite volume context to get special numerical flux functions. Next, these numerical fluxes are incorporated into a particular discontinuous Galerkin (DG) spectral element framework where derivatives are approximated with summation-by-parts operators. This guarantees a high-order accurate DG numerical approximation to the polytropic Euler equations that is also consistent to its auxiliary total energy behavior. Numerical examples are provided to verify the theoretical derivations, i.e., the entropic properties of the high order DG scheme. Keywords: Isothermal Euler, Polytropic Euler, Entropy stability, Finite volume, Summation- by-parts, Nodal discontinuous Galerkin spectral element method 1. Introduction The compressible Euler equations of gas dynamics ! ! %t + r · (%v ) = 0; ! ! ! ! ! ! (1.1) (%v )t + r · (%v ⊗ v ) + rp = 0; ! ! Et + r · (v [E + p]) = 0; are a system of partial differential equations (PDEs) where the conserved quantities are the mass ! % ! 2 %, the momenta %v, and the total energy E = 2 kvk + %e. -
Thermal Properties and the Prospects of Thermal Energy Storage of Mg–25%Cu–15%Zn Eutectic Alloy As Phasechange Material
materials Article Thermal Properties and the Prospects of Thermal Energy Storage of Mg–25%Cu–15%Zn Eutectic Alloy as Phase Change Material Zheng Sun , Linfeng Li, Xiaomin Cheng *, Jiaoqun Zhu, Yuanyuan Li and Weibing Zhou School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070, China; [email protected] (Z.S.); [email protected] (L.L.); [email protected] (J.Z.); [email protected] (Y.L.); [email protected] (W.Z.) * Correspondence: [email protected]; Tel.: +86-13507117513 Abstract: This study focuses on the characterization of eutectic alloy, Mg–25%Cu–15%Zn with a phase change temperature of 452.6 ◦C, as a phase change material (PCM) for thermal energy storage (TES). The phase composition, microstructure, phase change temperature and enthalpy of the alloy were investigated after 100, 200, 400 and 500 thermal cycles. The results indicate that no considerable phase transformation and structural change occurred, and only a small decrease in phase transition temperature and enthalpy appeared in the alloy after 500 thermal cycles, which implied that the Mg–25%Cu–15%Zn eutectic alloy had thermal reliability with respect to repeated thermal cycling, which can provide a theoretical basis for industrial application. Thermal expansion and thermal Citation: Sun, Z.; Li, L.; Cheng, X.; conductivity of the alloy between room temperature and melting temperature were also determined. Zhu, J.; Li, Y.; Zhou, W. Thermal The thermophysical properties demonstrated that the Mg–25%Cu–15%Zn eutectic alloy can be Properties and the Prospects of considered a potential PCM for TES. -
Temperature & Thermal Expansion
Temperature & Thermal Expansion Temperature Zeroth Law of Thermodynamics Temperature Measurement Thermal Expansion Homework Temperature & Thermal Equilibrium Temperature – Fundamental physical quantity – Measure of average kinetic energy of molecular motion Thermal equilibrium – Two objects in thermal contact cease to have an exchange of energy The Zeroth Law of Thermodynamics If objects A and B are separately in thermal equilibrium with a third object C (the thermometer), the A and B are in thermal equilibrium with each other. Temperature Measurement In principle, any system whose physical properties change with tempera- ture can be used as a thermometer Some physical properties commonly used are – The volume of a liquid – The length of a solid – The electrical resistance of a conductor – The pressure of a gas held at constant volume – The volume of a gas held at constant pressure The Glass-Bulb Thermometer Common thermometer in everyday use Physical property that changes is the volume of a liquid - usually mercury or alcohol Since the cross-sectional area of the capillary tube is constant, the change in volume varies linearly with its length along the tube Calibrating the Thermometer The thermometer can be calibrated by putting it in thermal equilibrium with environments at known temperatures and marking the end of the liquid column Commonly used environments are – Ice-water mixture in equilibrium at the freezing point of water – Water-steam mixture in equilibrium at the boiling point of water Once the ends of the liquid column have -
Thermal Expansion
Protection from Protect Your Thermal Expansion Water Heater from Protection from thermal expansion is provided in a For further plumbing system by the installation of a thermal expansion tank and a temperature and information Thermal pressure relief valve (T & P Valve) at the top of the tank. contact your Expansion The thermal expansion tank controls the increased local water pressure generated within the normal operating temperature range of the water heater. The small purveyor, tank with a sealed compressible air cushion Without a functioning provides a space to store and hold the additional expanded water volume. City or County Temperature & building The T & P Valve is the primary safety feature for the water heater. The temperature portion of the Pressure Relief Valve T & P Valve is designed to open and vent water department, to the atmosphere whenever the water your water heater can temperature within the tank reaches approxi- licensed plumber º º mately 210 F (99 C). Venting allows cold water to enter the tank. or the The pressure portion of a T & P Valve is designed PNWS/AWWA to open and vent to the atmosphere whenever water pressure within the tank exceeds the Cross-Connection pressure setting on the valve. The T & P Valve is normally pre-set at 125 psi or 150 psi. Control Committee through the Water heaters installed in compliance with the current plumbing code will have the required T & P PNWS office at Valve and thermal expansion tank. For public health protection, the water purveyor may require (877) 767-2992 the installation of a check valve or backflow preventer downstream of the water meter. -
Muddiest Point – Entropy and Reversible I Am Confused About Entropy and How It Is Different in a Reversible Versus Irreversible Case
1 Muddiest Point { Entropy and Reversible I am confused about entropy and how it is different in a reversible versus irreversible case. Note: Some of the discussion below follows from the previous muddiest points comment on the general idea of a reversible and an irreversible process. You may wish to have a look at that comment before reading this one. Let's talk about entropy first, and then we will consider how \reversible" gets involved. Generally we divide the universe into two parts, a system (what we are studying) and the surrounding (everything else). In the end the total change in the entropy will be the sum of the change in both, dStotal = dSsystem + dSsurrounding: This total change of entropy has only two possibilities: Either there is no spontaneous change (equilibrium) and dStotal = 0, or there is a spontaneous change because we are not at equilibrium, and dStotal > 0. Of course the entropy change of each piece, system or surroundings, can be positive or negative. However, the second law says the sum must be zero or positive. Let's start by thinking about the entropy change in the system and then we will add the entropy change in the surroundings. Entropy change in the system: When you consider the change in entropy for a process you should first consider whether or not you are looking at an isolated system. Start with an isolated system. An isolated system is not able to exchange energy with anything else (the surroundings) via heat or work. Think of surrounding the system with a perfect, rigid insulating blanket. -
Non-Steady, Isothermal Gas Pipeline Flow
RICE UNIVERSITY NON-STEADY, ISOTHERMAL GAS PIPELINE FLOW Hsiang-Yun Lu A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENT FOR THE DEGREE OF MASTER OF SCIENCE Thesis Director's Signature Houston, Texas May 1963 ABSTRACT What has been done in this thesis is to derive a numerical method to solve approximately the non-steady gas pipeline flow problem by assum¬ ing that the flow is isothermal. Under this assumption, the application of this method is restricted to the following conditions: (1) A variable rate of heat transfer through the pipeline is assumed possible to make the flow isothermal; (2) The pipeline is very long as compared with its diameter, the skin friction exists in the pipe, and the velocity and the change of ve¬ locity aYe small. (3) No shock is permitted. 1 The isothermal assumption takes the advantage that the temperature of the entire flow is constant and therefore the problem is solved with¬ out introducing the energy equation. After a few transformations the governing differential equations are reduced to only two simultaneous ones containing the pressure and mass flow rate as functions of time and distance. The solution is carried out by a step-by-step method. First, the simultaneous equations are transformed into three sets of simultaneous difference equations, and then, solve them by computer (e.g., IBM 1620 ; l Computer which has been used to solve the examples in this thesis). Once the pressure and the mass flow rate of the flow have been found, all the other properties of the flow can be determined. -
Compressible Flow
94 c 2004 Faith A. Morrison, all rights reserved. Compressible Fluids Faith A. Morrison Associate Professor of Chemical Engineering Michigan Technological University November 4, 2004 Chemical engineering is mostly concerned with incompressible flows in pipes, reactors, mixers, and other process equipment. Gases may be modeled as incompressible fluids in both microscopic and macroscopic calculations as long as the pressure changes are less than about 20% of the mean pressure (Geankoplis, Denn). The friction-factor/Reynolds-number correlation for incompressible fluids is found to apply to compressible fluids in this regime of pressure variation (Perry and Chilton, Denn). Compressible flow is important in selected application, however, including high-speed flow of gasses in pipes, through nozzles, in tur- bines, and especially in relief valves. We include here a brief discussion of issues related to the flow of compressible fluids; for more information the reader is encouraged to consult the literature. A compressible fluid is one in which the fluid density changes when it is subjected to high pressure-gradients. For gasses, changes in density are accompanied by changes in temperature, and this complicates considerably the analysis of compressible flow. The key difference between compressible and incompressible flow is the way that forces are transmitted through the fluid. Consider the flow of water in a straw. When a thirsty child applies suction to one end of a straw submerged in water, the water moves - both the water close to her mouth moves and the water at the far end moves towards the lower- pressure area created in the mouth. Likewise, in a long, completely filled piping system, if a pump is turned on at one end, the water will immediately begin to flow out of the other end of the pipe. -
Lecture 15 November 7, 2019 1 / 26 Counting
...Thermodynamics Positive specific heats and compressibility Negative elastic moduli and auxetic materials Clausius Clapeyron Relation for Phase boundary \Phase" defined by discontinuities in state variables Gibbs-Helmholtz equation to calculate G Lecture 15 November 7, 2019 1 / 26 Counting There are five laws of Thermodynamics. 5,4,3,2 ... ? Laws of Thermodynamics 2, 1, 0, 3, and ? Lecture 15 November 7, 2019 2 / 26 Third Law What is the entropy at absolute zero? Z T dQ S = + S0 0 T Unless S = 0 defined, ratios of entropies S1=S2 are meaningless. Lecture 15 November 7, 2019 3 / 26 The Nernst Heat Theorem (1926) Consider a system undergoing a pro- cess between initial and final equilibrium states as a result of external influences, such as pressure. The system experiences a change in entropy, and the change tends to zero as the temperature char- acterising the process tends to zero. Lecture 15 November 7, 2019 4 / 26 Nernst Heat Theorem: based on Experimental observation For any exothermic isothermal chemical process. ∆H increases with T, ∆G decreases with T. He postulated that at T=0, ∆G = ∆H ∆G = Gf − Gi = ∆H − ∆(TS) = Hf − Hi − T (Sf − Si ) = ∆H − T ∆S So from Nernst's observation d (∆H − ∆G) ! 0 =) ∆S ! 0 As T ! 0, observed that dT ∆G ! ∆H asymptotically Lecture 15 November 7, 2019 5 / 26 ITMA Planck statement of the Third Law: The entropy of all perfect crystals is the same at absolute zero, and may be taken to be zero. Lecture 15 November 7, 2019 6 / 26 Planck Third Law All perfect crystals have the same entropy at T = 0. -
The Coefficient of Thermal Expansion and Your Heating System By: Admin - May 06, 2021
The Coefficient of Thermal Expansion and your Heating System By: Admin - May 06, 2021 We’ve all been there. The lid on pickle jar is impossibly tight, but when you run hot water over the jar you can easily unscrew the lid. The metal lid expands more than the glass jar, which is a simple illustration of how materials, when heated, expand at different rates. The relationship of how materials expand or contract through temperature change is driven by the coefficient of thermal expansion or CTE of those materials and is a critical factor when designing a heater. Determining the appropriate materials for the heater is not as simple as running warm water over a metal lid. The coefficient of thermal expansion is a critical factor when pairing dissimilar materials in a system. With the help of Watlow representatives, you can make sure your system is designed for success, efficiency and a long lifespan. What is the coefficient of thermal expansion? To understand the science behind the coefficient of thermal expansion (CTE), one must first understand the basics of thermal expansion. Physical property changes, such as shape, area, volume and density, occur during thermal expansion. Every material or metal/metal alloy will have a slightly different expansion rate. CTE, then, is the relative expansion or contraction of materials driven by a change in temperature. Metals, ceramics and other materials have unique coefficients of thermal expansion and do not expand and contract at equal rates. For example, if the volume of a section of aluminum and a section of ceramic are equal and are heated from X to Y degrees, the aluminum could increase in dimension by a factor of four compared to the ceramic. -
Entropy 2006, 8, 143-168 Entropy ISSN 1099-4300
Entropy 2006, 8, 143-168 entropy ISSN 1099-4300 www.mdpi.org/entropy/ Full paper On the Propagation of Blast Wave in Earth′s Atmosphere: Adiabatic and Isothermal Flow R.P.Yadav1, P.K.Agarwal2 and Atul Sharma3, * 1. Department of Physics, Govt. P.G. College, Bisalpur (Pilibhit), U.P., India Email: [email protected] 2. Department of Physics, D.A.V. College, Muzaffarnagar, U.P., India Email: [email protected] 3. Department of Physics, V.S.P. Govt. College, Kairana (Muzaffarnagar), U.P., India Email:[email protected] Received: 11 April 2006 / Accepted: 21 August 2006 / Published: 21 August 2006 __________________________________________________________________________________ Abstract Adiabatic and isothermal propagations of spherical blast wave produced due to a nuclear explosion have been studied using the Energy hypothesis of Thomas, in the nonuniform atmosphere of the earth. The explosion is considered at different heights. Entropy production is also calculated along with the strength and velocity of the shock. In both the cases; for adiabatic and isothermal flows, it has been found that shock strength and shock velocity are larger at larger heights of explosion, in comparison to smaller heights of explosion. Isothermal propagation leads to a smaller value of shock strength and shock velocity in comparison to the adiabatic propagation. For the adiabatic case, the production of entropy is higher at higher heights of explosion, which goes on decreasing as the shock moves away from the point of explosion. However for the isothermal shock, the calculation of entropy production shows negative values. With negative values for the isothermal case, the production of entropy is smaller at higher heights of explosion, which goes on increasing as the shock moves away from the point of explosion. -
Isothermal Process It Is the Process in Which Other Physical Quantities Might Change but the Temperature of the System Remains Or Is Forced to Remain Constant
Sajit Chandra Shakya Department of Physics Kathmandu Don Bosco College New Baneshwor, Kathmandu Isothermal process It is the process in which other physical quantities might change but the temperature of the system remains or is forced to remain constant. For example, the constant temperature of human body. Under constant temperature, the volume of a gas system is inversely proportional to the pressure applied, the phenomena being called Boyle's Law, written in symbols as 1 V ∝ P 1 Or, V = KB× where KB is a constant quantity. P Or, PV = KB …………….. (i) This means whatever be the values of volume and pressure, their product will be constant. So, P1V1 = KB, P2V2 = KB, P3V3 = KB, etc, Or, P1V1 = P2V2 = P3V3, etc. The requirements for an isothermal process are as follows: 1. The process should be carried very slowly so that there is an ample time for compensation of heat in case of any loss or addition. 2. The boundaries of the system should be highly conducting so that there is a path for heat to flow into or flow away from a closed space in case of any energy loss or oversupply. 3. The boundaries should be made very thin because the resistance of the substance for heat conduction will be less for thin boundaries. Since in an isothermal change, the temperature remains constant, the internal energy also does not change, i.e. dU = 0. So if dQ amount of heat is given to a system which undergoes isothermal change, the relation for the first law of thermodynamics would be dQ = dU + dW Or, dQ = 0 + PdV Or, dQ = PdV This means all the heat supplied will be utilized for performing external work and consequently its value will be very high compared to other processes. -
Maximum Thermodynamic Power Coefficient of a Wind Turbine
Received: 17 April 2019 Revised: 22 November 2019 Accepted: 10 December 2019 DOI: 10.1002/we.2474 RESEARCH ARTICLE Maximum thermodynamic power coefficient of a wind turbine J. M. Tavares1,2 P. Patrício1,2 1ISEL—Instituto Superior de Engenharia de Lisboa, Instituto Politécnico de Lisboa, Avenida Abstract Conselheiro Emído Navarro, Lisboa, Portugal According to the centenary Betz-Joukowsky law, the power extracted from a wind turbine in 2Centro de Física Teórica e Computacional, Universidade de Lisboa, Lisboa, Portugal open flow cannot exceed 16/27 of the wind transported kinetic energy rate. This limit is usually interpreted as an absolute theoretical upper bound for the power coefficient of all wind turbines, Correspondence but it was derived in the special case of incompressible fluids. Following the same steps of Betz J. M. Tavares, ISEL—Instituto Superior de Engenharia de Lisboa, Instituto Politécnico de classical derivation, we model the turbine as an actuator disk in a one dimensional fluid flow Lisboa, Avenida Conselheiro Emído Navarro, but consider the general case of a compressible reversible fluid, such as air. In doing so, we are Lisboa, Portugal. obliged to use not only the laws of mechanics but also and explicitly the laws of thermodynamics. Email: [email protected] We show that the power coefficient depends on the inlet wind Mach number M0,andthatits Funding information maximum value exceeds the Betz-Joukowsky limit. We have developed a series expansion for Fundação para a Ciência e a Tecnologia, the maximum power coefficient in powers of the Mach number M0 that unifies all the cases Grant/Award Number: UID/FIS/00618/2019 2 (compressible and incompressible) in the same simple expression: max = 16∕27 + 8∕243M0.