ENERGY ANALYSIS OF CLOSED SYSTEMS

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Thermodynamics: An Engineering Approach Seventh Edition in SI Units Yunus A. Cengel, Michael A. Boles McGraw-Hill, 2011 Chapter 4 ENERGY ANALYSIS OF CLOSED SYSTEMS Mehmet Kanoglu University of Gaziantep Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

Objectives Examine the moving boundary work or P dv work commonly encountered in reciprocating devices such as automotive engines and compressors. Identify the first law of thermodynamics as simply a statement of the conservation of energy principle for closed (fixed mass) systems. Develop the general energy balance applied to closed systems. Define the specific heat at constant volume and the specific heat at constant pressure. Relate the specific heats to the calculation of the changes in internal energy and enthalpy of ideal gases. Describe incompressible substances and determine the changes in their internal energy and enthalpy. Solve energy balance problems for closed (fixed mass) systems that involve heat and work interactions for general pure substances, ideal gases, and incompressible substances. 2

MOVING BOUNDARY WORK Moving boundary work (P dv work): The expansion and compression work in a piston-cylinder device. Quasi-equilibrium process: A process during which the system remains nearly in equilibrium at all times. W b is positive for expansion W b is negative for compression The work associated with a moving boundary is called boundary work. A gas does a differential amount of work δw b as it forces the piston to move by a differential amount ds. 3

The boundary work done during a process depends on the path followed as well as the end states. The area under the process curve on a P-V diagram is equal, in magnitude, to the work done during a quasi-equilibrium expansion or compression process of a closed system. 4

Polytropic, Isothermal, and Isobaric processes Polytropic process: C, n (polytropic exponent) constants Polytropic process Polytropic and for ideal gas When n = 1 (isothermal process) Constant pressure process What is the boundary work for a constantvolume process? Schematic and P-V diagram for a polytropic process. 5

Example 4-2 Boundary work for a constant-pressure process Example 4-3 Isothemal compression of an ideal gas 6

ENERGY BALANCE FOR CLOSED SYSTEMS Energy balance for any system undergoing any process Energy balance intherateform The total quantities are related to the quantities per unit time is Energy balance per unit mass basis Energy balance for a cycle Energy balance in differential form 7

Energy balance when sign convention is used: (i.e., heat input and work output are positive; heat output and work input are negative). Various forms of the first-law relation for closed systems when sign convention is used. The first law cannot be proven mathematically, ti but no process in nature is known to have violated the first law, and this should be taken as sufficient proof. 8

Energy balance for a constant-pressure expansion or compression process General analysis for a closed system undergoing a quasi-equilibrium constant-pressure process. Q is to the system and W is from the system. For a constant-pressure expansion or compression process: ΔU + W = ΔH b An example of constant-pressure process 9

10

Example 4-5 Electric heating of a gas at constant pressure Example 4-6 Unrestrained expansion of water 11

Energy balance for closed systems Q W other = Δ U + W b = Δ H Q W = m ( h 2 h other 1 ) other 2 <moving boundary> Q W = m ( u 2 u other 1 ) <fixed boundary> 12

SPECIFIC HEATS Specific heat at constant volume, c v : The energy required to raise the temperature of the unit mass of a substance by one degree as the volume is maintained constant. Specific heat at constant pressure, c p : The energy required to raise the temperature of the unit mass of a substance by one degree as the pressure is maintained constant. Constant- volume and constantpressure specific heats c v and c p (values are for helium gas). 13

True or False? c p is always greater than c v The equations in the figure are valid for any substance undergoing any process. c v and c p are properties. c v is related to the changes in internal energy and c p to the changes in enthalpy. A common unit for specific heats is kj/kg C or kj/kg K. Are these units identical? Formal definitions of c v and c p. 14

INTERNAL ENERGY, ENTHALPY, AND SPECIFIC HEATS OF IDEAL GASES Joule showed using this experimental apparatus that u=u(t) Internal energy and For ideal gases, enthalpy change of u, h, c v, and c p an ideal gas vary with temperature only. 15

At low pressures, all real gases approach ideal-gas behavior, and therefore their specific heats depend on temperature only. The specific heats of real gases at low pressures are called ideal-gas specific heats, or zero-pressure specific heats, and are often denoted c p0 and c v0. u and h data for a number of gases have been tabulated. These tables are obtained by choosing an arbitrary reference point and performing the integrations by treating state 1 as the reference state. Ideal-gas constant- pressure specific heats for some gases (see Table A 2c for c p equations). In the preparation of ideal-gas tables, 0 K is chosen as the reference temperature. 16

Internal energy and enthalpy change when specific heat is taken constant at an average value (kj/kg) 17

Three ways of calculating Δu and Δh 1. By using the tabulated u and h data. This is the easiest and most accurate way when tables are readily available. 2. By using the c v or c p relations (Table A-2c) as a function of temperature and performing the integrations. This is very inconvenient for hand calculations but quite desirable for computerized calculations. The results obtained are very accurate. 3. By using average specific heats. This is very simple and certainly very convenient when property tables are not available. The results obtained are reasonably accurate if the temperature t interval is not very large. Three ways of calculating Δu. 18

Specific Heat Relations of Ideal Gases The relationship between c p, c v and R dh = c p dt and du = c v dt On a molar basis Specific heat ratio The c p of an ideal gas can be determined from a knowledge of c v and R. The specific ratio varies with temperature, but this variation is very mild. For monatomic gases (helium, argon, etc.), its value is essentially constant at 1.667. Many diatomic gases, including air, have a specific heat ratio of about 1.4 at room temperature. 19

Example 4-9 Heating of a gas by a resistance heater Example 4-10 Heating of a gas at Constant pressure 20

INTERNAL ENERGY, ENTHALPY, AND SPECIFIC HEATS OF SOLIDS AND LIQUIDS Incompressible substance: A substance whose specific volume (or density) is constant. Solids and liquidsid are incompressible ibl substances. 21

Internal Energy Changes Enthalpy Changes Usually a more accurate relation than The enthalpy of a compressed liquid 22

Example 4-12 Cooling of an iron block by Water Example 4-13 Heating of aluminum rods in a furnace 23

Summary Moving boundary work W b for an isothermal process W b for a constant-pressure process W b for a polytropic process Energy balance for closed systems Energy balance for a constant-pressure expansion or compression process Specific heats Constant-pressure specific heat, c p Constant-volume t specific heat, c v Internal energy, enthalpy, and specific heats of ideal gases Specific heat relations of ideal gases Internal energy, enthalpy, and specific heats of incompressible ibl substances (solids and liquids) id 24