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Lect# 7: Thermodynamics and Entropy Reading: Zumdahl 10.2, 10.3 Outline: Isothermal processes (∆T = 0) Isothermal gas expansion and work(w) Reversible and irreversible processes
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Isothermal Processes Recall: Isothermal means T = 0. Since E = nC v T, then E = 0 for an isothermal process. Since E = q + w, then q = -w (isothermal process)
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Example: Isothermal Expansion Consider a mass (M) connected to a ideal gas confined by a piston. The piston is submerged in a constant T bath, so T = 0.
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Initially, V = V 1 P = P 1 Pressure of gas is equal to that created by the pull of the hanging mass: P 1 = force/area = M 1 g/A A = piston area g = gravitational acceleration (9.8 m/s 2 ) Note : kg m -1 s -2 = 1 Pa
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One-Step Expansion: If we change the weight to M 1 /4, then the pressure becomes P ext = (M 1 /4)g/A = P 1 /4 The mass will be lifted until the internal pressure equals the external pressure, at which point V final = 4V 1 What work is done in this expansion? w = -P ext V = -P 1 /4 (4V 1 - V 1 ) = -3/4 P 1 V 1
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What if we expand in two steps? In this expansion we go in two steps: Step 1: M 1 to M 1 /2 Step 2: M 1 /2 to M 1 /4 In first step: P ext = P 1 /2, V final = 2V 1 w 1 = -P ext V = -P 1 /2 (2V 1 - V 1 ) = -1/2 P 1 V 1
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In Step 2 (M 1 /2 to M 1 /4 ): P ext = P 1 /4, V final = 4V 1 w 2 = -P ext V =- P 1 /4 (4V 1 - 2V 1 ) = -1/2 P 1 V 1 w total = w 1 + w 2 = -P 1 V 1 /2 - P 1 V 1 /2 = -P 1 V 1 Note: w total,2 step > w total,1 step More work was done in the two-step expansion
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Graphically, we can envision this two-step process on a PV diagram: Work is given by the area under the “PV” curve.
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Infinite Step Expansion Imagine that we perform a process in which we decrease the weight very slightly (∆M) between an infinite number of (reversible) expansions. Instead of determining the sum of work performed at each step to get w total, we can integrate:
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Graphically, see how much more work is done in the infinite-step expansion (red area) Two Step Reversible
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If we perform the integration from V 1 to V 2:
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Two Step Compression Now we will do the opposite, compress the fully expanded gas: V init = 4V 1 P init = P 1 /4 Compress in two steps: first put on mass = M 1 /2, Then, in step two, replace mass M 1 /2 with a bigger mass M 1
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In first step: w 1 = -P ext V = -P 1 /2 (2V 1 - 4V 1 ) = P 1 V 1 w total = w 1 + w 2 = 2P 1 V 1 (see table 10.3) In second step: w 2 = -P ext V = -P 1 (V 1 - 2V 1 ) = P 1 V 1
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Compression/Expansion In two-step example: w expan. = -P 1 V 1 w comp. = 2P 1 V 1 w total = P 1 V 1 q total = -P 1 V 1 We have undergone a “cycle” where the system returns to the starting state. Since isothermal ( T = 0) then, E = 0 but, q = -w ≠ 0
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Entropy: A Thermodynamic Definition Let’s consider the four- step cycle illustrated: 1: Isothermal expansion 2: Const V cooling 3: Isothermal compression 4: Const V heating
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Step 1: Isothermal Expansion at T = T high from V 1 to V 2 T = 0, so E = 0 and q = -w Do this expansion reversibly, so that
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Step 2: Const V cooling to T = T low. V = 0, therefore, w = 0 q 2 = E = nC v T = nC v (T low -T high )
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Step 3: Isothermal compression at T = T low from V 2 to V 1. Since T = 0, then E = 0 and q = -w Do compression reversibly, then
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Step 4: Const-V heating to T = T high. V = 0, so, w = 0, and q 4 = E = nC v T = nC v (T high -T low ) = -q 2
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The thermodynamic definition of entropy(finally!)
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Calculating Entropy: summary T = 0 V = 0 P = 0
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Calculating Entropy: simple example Example: What is S for the heating of a mole of a monatomic gas @constant volume from 298 K to 350 K? 3/2R
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Connecting with Lecture 6 From this lecture: Exactly the same as derived in the previous lecture!
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