ES 202 Fluid and Thermal Systems Lecture 20: Isentropic Processes (1/28/2003)

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Presentation transcript:

ES 202 Fluid and Thermal Systems Lecture 20: Isentropic Processes (1/28/2003)

Lecture 20ES 202 Fluid & Thermal Systems2 Assignments Homework: –7-35, 7-40 in Cengel & Turner Reading assignment –7-12 in Cengel & Turner –ES 201 notes

Lecture 20ES 202 Fluid & Thermal Systems3 Announcements Homework due today at 5 pm in my office Check the revised course syllabus on the course web page again. There are more changes.

Lecture 20ES 202 Fluid & Thermal Systems4 Road Map of Lecture 20 Comments on Quiz 3 –saturated liquid (x = 0) and saturated vapor (x = 1) –good job on interpolation problem –weak on Compressed Liquid Approximation (quality is undefined in compressed liquid region) –constant pressure and temperature curves on phase diagrams (shape and direction) Supplement to Lecture 19 Property variation in an ideal gas: variable specific heats –Gibbs equation –graphical interpretation –newly defined variables Isentropic processes –When is “constant entropy” a good assumption? –entropy change for an ideal gas with constant specific heats (special case) –entropy change for an ideal gas with variable specific heats (general case) Examples

Lecture 20ES 202 Fluid & Thermal Systems5 Interpretation of CLA on Phase Diagrams exact state approximate state constant temperature line P-v diagram Constant pressure line exact state approximate state T-v diagram CLA stands for Compressed Liquid Approximation

Lecture 20ES 202 Fluid & Thermal Systems6 Critical-point properties: SubstanceTemperaturePressure Air132.5 K3.77 MPa Water647.3 K22.09 MPa (extracted from Table A-1 in Cengel & Turner) Relationship between c v and c p –Which one has a higher value? –What is the reason for the difference? –Apply your reasoning to the Ideal Gas Model and Incompressible Substance Model Supplement to Lecture 19

Lecture 20ES 202 Fluid & Thermal Systems7 Property Variation in an Ideal Gas Recall the Gibbs equation (relationship between changes in properties) For an ideal gas with finite temperature change: How to evaluate the integrals? (graphical interpretation) or, c v or c p T  u or  h would be a straight horizontal line for constant specific heats

Lecture 20ES 202 Fluid & Thermal Systems8 An Easy Way Out For variable specific heats, due to the frequent usage of the integrals, its value (from a common reference point) is tabulated (e.g. Table A- 17 in Cengel & Turner) A new variable is defined: which is the temperature dependent part in entropy change By making use of this newly defined variable, the entropy difference between any two states can be easily expressed as:

Lecture 20ES 202 Fluid & Thermal Systems9 Constant Property Processes constant pressure (isobaric; piston-cylinder model) constant volume (rigid system boundaries) constant temperature (sufficient time for heat transfer with environment) constant entropy (reversible, adiabatic) They serve as good models for complex problems. When is “constant entropy” a good assumption? –process time scale short compared with heat transfer time scale (i.e. heat transfer rate much slower than other processes in the problem) –for example, rapid compression/expansion process

Lecture 20ES 202 Fluid & Thermal Systems10 Isentropic Processes Recall the Gibbs equation for an ideal gas: For an isentropic proces (ds = 0), –you only need to know one more thermodynamic property to fix the state –the Gibbs equation can be reduced to: The relationship between temperature, pressure and specific volume can be obtained by direct integration of the above equations. or

Lecture 20ES 202 Fluid & Thermal Systems11 Isentropic Processes (II) For the special case of constant specific heats, direct integration yields: where k = c p / c v > 1 The results confirm the previous claim that if you know one more thermodynamic property (temperature, pressure or specific volume), you know everything else!

Lecture 20ES 202 Fluid & Thermal Systems12 Isentropic Processes (III) For the general case of variable specific heats, we can recall the newly defined variable s 0 : which further defines two new variables (useful for isentropic analysis): Relative pressure Relative specific volume: