Degradation and Quality of Energy
6. Degradation and Quality of Energy
Consider a Carnot cycle operating between thermal energy reservoirs at the high and low temperatures T H and T L , respectively. The term (1– T 0 /T H ) represents the quality of the energy or the work potential per unit energy that can be extracted in the form of heat from a thermal energy reservoir at a temperature T H . Therefore, the heat Q H extracted from the ther-
mal energy reservoir at T H has the potential to perform work equal to Q H × quality = Q H
(1– T 0 /T H ) where quality of energy at T H is
given by (1– T 0 /T H ). It is seen that at a specified temperature, the quality equals the efficiency of a Carnot engine that is operated between TERs at temperatures T
and T 0 . Assume that it is possible to re- move 100 kJ of heat from hot gases that are at 1000 K (and which constitute a thermal energy reservoir) using a Carnot engine operating between 1000 K and the ambient temperature of 300 K (cf. Figure 22a ). Us- ing the engine under these conditions, it is possible to produce a work output of
Figure 21: The heating of a coffee pot using a Carnot heat pump.
Figure 22: a. Carnot engine operating between hot gases and the ambient; b. Carnot engine operating between water and the ambient.
100 ×(1 – 298÷1000) ≈ 70 kJ, as illustrated in Figure 22a . Therefore, the quality of energy at 1000 K is 70%. The entropy change of the hot gases is –0.1 kJ K –1
(= –100 ÷ 1000), while the entropy gain for the ambient is 0.1 kJ K (i.e., 30 kJ÷300 K). Alternatively, we can cool the hot gases using water to transfer the 100 kJ of energy. Assume that during this process the water temperature rises by 2 K from 399 K to 401 K (with the average water temperature being 400 K, as shown in Figure 22b ). If a Carnot engine is placed between the water at 400 K and the ambient at 300 K, then for the same 100 kJ of heat removed from radiator water, we can extract only 100 ×(1 – 298÷400) ≈ 25 kJ, and 75 kJ is
rejected to the ambient. In this case, the energy quality is only 25% of the extracted heat. Figure 23 illustrates the processes depicted in Figure 22a and b using a T–S diagram. The cy- cle A–B–C–D–A in Figure 23 represents the Carnot engine (CE) of Figure 22a , while area ABJIA and EGKIE represent heat transfer from engine and to hot water, respectively, for Figure 22b , while the area C–D–I–H represents the rejected heat of CE for the first case, and the area D-C-H–K–J–I–D that for the latter case. Since more heat is rejected for the second case, the work potential or the quality of the thermal energy is degraded to a smaller value at the lower temperature. This is due to the irreversible heat transfer or the temperature gradients between hot gases and radiator water (as shown in Figure 22b ). In general property gradients cause entropy generation.
Now, one might ask about the Maxwell-Boltzmann distribution of molecular veloci- ties. Consider a monatomic gas within a container with rigid adiabatic walls. A “pseudo” tem- perature distribution exists for the monatomic gas. The question is whether with collision and transfer of energy, there can be degradation of energy or generation of entropy. First, tem- perature is a continuum property and the temperature cannot be associated with a group of molecules. Secondly, after frequent collisions, at that location where frequent transfers occur, the intensive state is not altered over a time period much larger than collision time. Thus, no gradient exists and there is no entropy generation.
a. Adiabatic Reversible Processes Recall that for any process within a closed or fixed mass system, dS = δQ/T b + δσ.
For any reversible process δσ =0 so that dS = δQ/T. For an adiabatic reversible process, δQ = δσ = 0, so that
dS = 0. Consequently, the entropy remains unchanged for an adiabatic reversible process. These
processes are also known as isentropic processes.
Parts
» COMPUTATIONAL MECHANICS and APPLIED ANALYSIS
» Explicit and Implicit Functions and Total Differentiation
» Exact (Perfect) and Inexact (Imperfect) Differentials
» Intermolecular Forces and Potential Energy
» Internal Energy, Temperature, Collision Number and Mean Free Path
» Vector or Cross Product r The area A due to a vector product
» First Law for a Closed System
» First Law For an Open System
» STATEMENTS OF THE SECOND LAW
» Cyclical Integral for a Reversible Heat Engine
» Irreversibility and Entropy of an Isolated System
» Degradation and Quality of Energy
» SINGLE–COMPONENT INCOMPRESSIBLE FLUIDS
» Evaluation of Entropy for a Control Volume
» Internally Reversible Work for an Open System
» MAXIMUM ENTROPY AND MINIMUM ENERGY
» Generalized Derivation for a Single Phase
» LaGrange Multiplier Method for Equilibrium
» Absolute and Relative Availability Under Interactions with Ambient
» Irreversibility or Lost Work
» Applications of the Availability Balance Equation
» Closed System (Non–Flow Systems)
» Heat Pumps and Refrigerators
» Work Producing and Consumption Devices
» Graphical Illustration of Lost, Isentropic, and Optimum Work
» Flow Processes or Heat Exchangers
» CLASSICAL RATIONALE FOR POSTULATORY APPROACH
» Generalized Legendre Transform
» Van der Waals (VW) Equation of State
» Other Two–Parameter Equations of State
» Compressibility Charts (Principle of Corresponding States)
» Boyle Temperature and Boyle Curves
» Three Parameter Equations of State
» Empirical Equations Of State
» State Equations for Liquids/Solids
» Internal Energy (du) Relation
» EXPERIMENTS TO MEASURE (u O – u)
» Vapor Pressure and the Clapeyron Equation
» Saturation Relations with Surface Tension Effects
» Temperature Change During Throttling
» Throttling in Closed Systems
» Procedure for Determining Thermodynamic Properties
» Euler and Gibbs–Duhem Equations
» Relationship Between Molal and Pure Properties
» Relations between Partial Molal and Pure Properties
» Mixing Rules for Equations of State
» Partial Molal Properties Using Mixture State Equations
» Ideal Solution and Raoult’s Law
» Completely Miscible Mixtures
» DEVIATIONS FROM RAOULT’S LAW
» Mathematical Criterion for Stability
» APPLICATION TO BOILING AND CONDENSATION
» Physical Processes and Stability
» Constant Temperature and Volume
» Equivalence Ratio, Stoichiometric Ratio
» Entropy, Gibbs Function, and Gibbs Function of Formation
» Entropy Generated During an Adiabatic Chemical Reaction
» MASS CONSERVATION AND MOLE BALANCE EQUATIONS
» Evaluation of Properties During an Irreversible Chemical Reaction
» Criteria in Terms of Chemical Force Potential
» Generalized Relation for the Chemical Potential
» Nonideal Mixtures and Solutions
» Gas, Liquid and Solid Mixtures
» Availability Balance Equation
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