thermodynamics of materials

21
Thermodynamics of Materials 9th Lecture 2008. 3. 31 (Mon.) A rigid container is divided into two compartments of equal volume by a partition. One compartment contains 1 mole of ideal gas A at 1 atm, and the other contains 1 mole of ideal gas B at 1 atm. Calculate the increase in entropy which occurs when the partition between the two compartments is removed. 1 mol (1 atm) A 1 mol (1 atm) B

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Page 1: Thermodynamics of Materials

Thermodynamics of Materials

9th Lecture2008. 3. 31 (Mon.)

A rigid container is divided into two compartments of equal volume by a partition. One compartmentcontains 1 mole of ideal gas A at 1 atm, and the other contains 1 mole of ideal gas B at 1 atm.Calculate the increase in entropy which occurs when the partition between the two compartments is removed.

1 mol(1 atm)

A

1 mol(1 atm)

B

Page 2: Thermodynamics of Materials

Calculate the increase in entropy

1)by Boltzman’s way 2)by volume change of each gas3)by pressure change of each gas

1 mol(1 atm)

A

1 mol(1 atm)

B

12

1221

PlnkPlnkSSS

−=−=Δ →

121

21

2

1

=

⎟⎠⎞

⎜⎝⎛

⎟⎠⎞

⎜⎝⎛=

P

PNN

볼츠만 엔트로피로 구하는 법

42222

22221

2

lnRlnRlnRlnR

lnklnklnkPPlnk NNNN

==+=

+==⎟⎟⎠

⎞⎜⎜⎝

⎛=

Page 3: Thermodynamics of Materials

1 mol(1 atm)

A

1 mol(1 atm)

B

21

2 lnRVVlnRdV

VR

VR

TPRTPVdV

TP

TqSA

===

=→===Δ

∫ ∫δ

4lnRSSS BA =Δ+Δ=Δ∴

Isothermal mixing→ No change in E

PdVwqwqdE ==−== δδδδ0

21

2 lnRVVlnRdV

VRdV

TP

TqSB =====Δ ∫ ∫ ∫δ

Volume 변화로 생각해서 구하는 법

1 mol(1 atm)

A

1 mol(1 atm)

B

( )T constant at VPVPPPlnR

VVlnRdV

VRdV

TP

TqS

22112

1

1

2

==

====Δ ∫∫ ∫

δ

4lnRSSS BA =Δ+Δ=Δ∴

Isothermal mixing→ No change in E

250

1

250

1

2

1

2

1

lnR.

lnRPPlnRS

lnR.

lnRPPlnRS

B

A

===Δ

===Δ

Pressure 변화로 생각해서 구하는 법

A,1 A,2

B,1 B,2

P 1, P 0.5P 1, P 0.5

= =

= =

Page 4: Thermodynamics of Materials

If the first compartment has contained2 moles of ideal gas A, what would have been the increase in entropy when the partition was removed?

2 mol(2 atm)

A

1 mol(1 atm)

B

2 mol(2 atm)

A

1 mol(1 atm)

B

Calculate the change in entropy in three ways(Boltzman, volume change, pressure change).

( ) ( )NNlnkS 22 221 =Δ →

2 mol(2 atm)

A

1 mol(1 atm)

B

( ) 823 lnRlnR ==

821 lnRS =Δ∴ →

1

21221

2

2

1 121

21

PPlnkTSSS

PPNN

=−=Δ

=⎟⎠⎞

⎜⎝⎛

⎟⎠⎞

⎜⎝⎛=

볼츠만 엔트로피로 구하는 법

Page 5: Thermodynamics of Materials

222221

1

1

2 lnRVVlnR

VVlnRSA ===Δ

21

2 lnRVVlnRSB ==Δ

823 lnRlnRSSS BA ==Δ+Δ=Δ∴

1

2

VVlnnRTdV

VnRTPdVwq ==== δδ

2 mol(2 atm)

A

1 mol(1 atm)

B

2 mol(2 atm)

A

1 mol(1 atm)

B Isothermal mixing→ No change in E

PdVwqwqdE ==−== δδδδ0

Volume 변화로 생각해서 구하는 법

2212222

2

1

1

2 lnRlnRPPlnR

VVlnRSA ====Δ

250

1

2

1 lnR.

lnRPPlnRSB ===Δ

23 lnRSSS BA =Δ+Δ=Δ∴

1

2

VVlnnRTdV

VnRTPdVwq ==== δδ

2 mol(2 atm)

A

1 mol(1 atm)

B

2 mol(2 atm)

A

1 mol(1 atm)

B Isothermal mixing→ No change in E

Pressure 변화로 생각해서 구하는 법

2

1

1

221 P

PVVVPVP T 21 =→=때일정할가

A,1 A,2

B,1 B,2

P 2, P 1P 1, P 0.5

= =

= =

Page 6: Thermodynamics of Materials

Calculate the corresponding increase in entropy in each of the above two situations if both compartments had contained ideal gas A.

2 mol(2 atm)

A

2 mol(2 atm)

A

1 mol(1 atm)

A

3 molA

Calculate the change in entropy in three ways(Boltzman, Volume Change, Pressure Change).

2 mol(2 atm)

A

2 mol(2 atm)

A

1 mol(1 atm)

A

3 molA

NNNN

NN

ClnR

Clnk

PPlnkS

2323

2

1

221

822===Δ → !N!N

!NC NN 23

23 =

( )N Nln C N ln N N( N ln N N N lnN N )

= −

− − + −3 2 3 3 3

2 2 2

4272233 lnRlnNlnN =−= 27

3221 lnRS =Δ∴ →

121

21

2

2

231 =⎟⎠⎞

⎜⎝⎛

⎟⎠⎞

⎜⎝⎛= PCP

NN

NN

볼츠만 엔트로피로 구하는 법

Page 7: Thermodynamics of Materials

3422

1

2 lnRVVlnRSA ==Δ

2732lnRSSS AA =Δ+Δ=Δ∴ ′

A, A,

A , A ,

2V , V ( )3

2V , V ( )3′ ′

= = →

= = →

1 2

1 2

1 2 32 3

2 21 13 3

몰이 2개의부피 1몰은 부피

몰은 부피에해당

32

1

2 lnRVVlnRSA ==Δ ′

2 mol(2 atm)

A

1 mol(1 atm)

A

3 molA

Volume 변화로 생각해서 구하는 법

3422

2

1 lnRPPlnRSA ==Δ

2732lnRSSS AA =Δ+Δ=Δ∴ ′

32

231

34

232

2

1

12

11

2

1

12

11

=⇒==

=⇒==

′′ PPRT

VP,RT

VP

PPRT

VP,RT

VP

,A,A

,A,A

2 mol(2 atm)

A

1 mol(1 atm)

A

3 molA

Pressure 변화로 생각해서 구하는 법

32

2

1 lnRPPlnRSA ==Δ ′

Page 8: Thermodynamics of Materials

Statistical Thermodynamics(D.R. Gaskell Chap. 4 and R.T. DeHoff, Chap. 6)

Atomic description of thermodynamics in contrast withphenomenological description

microstate vs macrostate

Fundamental assumption or principle in ST

→ All microstates are equally probable.

→The probability of occurrence of any given macrostate (nj), which is macroscopically observable phenomenon, is proportional to the number of possible microstates.

A postulate of the quantum theory is that, if a particle is confined to move within a given fixed volume, then its energy is quantized, i.e., the particle may only have certain discrete allowed values of energy, which are separated by “forbidden energy bands.”

Page 9: Thermodynamics of Materials

http://www.2ndlaw.com/entropy.html

http://www.2ndlaw.com/entropy.html

Quantized Energy → Energy Levels

Page 10: Thermodynamics of Materials

The most probable distribution of molecules on various accessibleenergy levels

The maximum number of microstates

Equilibrium

one mole = 6 ×1023 molecules

Microstate

One arrangement in which the total energy of the system is distributed among energylevels and in space.

Irreversibility → change from less number of microstatesto more number of microstates.

Page 11: Thermodynamics of Materials

W = number of microstates

S = k ln W

1

2

121221

WWlnk

WlnkWlnkSSS

=

−=−=Δ →

⎟⎟⎠

⎞⎜⎜⎝

⎛=Δ →

1

221 smicrostate of .no

smicrostate of .nolnkS

How many microstates are there in one mole of ice or water at 273 K?

Page 12: Thermodynamics of Materials

How many microstates are there in one mole of ice or water at 273 K?

273 41 /Δ =KS for ice J K

273 63 /Δ =KS for water J K

Hint)

KK WlnkWlnk 273

273

1==

ice of mole one for s microstate of number→

K

KK W

WlnkS0

2732730 =Δ →

K/J ice for S K 412730 =Δ →

KK Wln.WlnkK/J 27323

273 104141 −×==

24273 1092 ×=→ .Wln K

2424 10311092273 10 ×× ==→ ..

K eW

Page 13: Thermodynamics of Materials

water of mole one for s microstate of number→

K/J water for S K 632730 =Δ →

KK Wln.WlnkK/J 27323

273 104163 −×==

.KW ×→ =

242 0 10273 10

ice .Kcf . W ×=

241 3 10273 10

The solution’s entropy is greater than that of the puresolvent because solution has a higher density of states.

Solvent molecules less tend to “escape” from theirgreater entropy state in the solution to a vaporphase or to a solid phase than they “escape” from the pure solvent.

This lessened tendency to leave the solution results in a higher boiling point and lower freezing point for the solution compared to the pure solvent.

Colligative Effects (비점상승, 융점강하)

http://www.2ndlaw.com/entropy.html

Page 14: Thermodynamics of Materials

Atomistic View

- What is pressure?- What is temperature?- What is internal energy?- What is heat or heat capacity?- What is entropy?

Kinetic Theory

http://hyperphysics.phy-astr.gsu.edu/hbase/hframe.html

Page 15: Thermodynamics of Materials

Maxwell-Boltzmann Velocity Distribution of Gas

Newton's Laws and Collisions

http://hyperphysics.phy-astr.gsu.edu/hbase/hframe.html

Page 16: Thermodynamics of Materials

What is Gas Pressure?

http://hyperphysics.phy-astr.gsu.edu/hbase/hframe.html

= ⋅ = =2N 3 kN RTP kT T3V 2 V V

=PV RT

⎡ ⎤=⎢ ⎥

⎣ ⎦

21 3mv kT2 2

What is Temperature? → translational K.E.

http://hyperphysics.phy-astr.gsu.edu/hbase/hframe.html

Page 17: Thermodynamics of Materials

What is Internal Energy?

http://hyperphysics.phy-astr.gsu.edu/hbase/hframe.html

What is Heat Capacity?

http://hyperphysics.phy-astr.gsu.edu/hbase/hframe.html

→ capacity to store energy (heat)

CV =7/2 R

CV > 7/2 R

Page 18: Thermodynamics of Materials

http://www.2ndlaw.com/entropy.html

단원자 기체 : translation다원자 기체 : translation, rotation, vibration

액체 : translation, rotation, vibration고체 : constrained vibration

vibration frequency ≅ 1012/sec

→ 물질이 에너지를 저장하는 방법

Page 19: Thermodynamics of Materials

Vibration : large energy difference between levels

→ difficult to be excited.→ high E levels are not accessible.

Most liquid water molecules and gas phase water are in the lowest vibrational state.

Rotation : small energy difference between levels

→ easy to be excited

Water molecules rotate faster and faster with increasing temperature.

Page 20: Thermodynamics of Materials

Translation : very small energy difference between levels

→ very easily excited

그림에서 첫번째 rotation level 근처

At RT, ~ 1000 miles an hour

http://www.2ndlaw.com/entropy.html

Quantized Energy → Energy Levels

Page 21: Thermodynamics of Materials

Energy Difference between the Ground State and the First excited State

(CO at 300K in a box 10 cm on a side )

• Average thermal energy, kT = 0.59 kcal/mole• Translational energy, ΔEt = 1.7×10-20 kcal/mole• Rotational energy, ΔEr = 0.01104 kcal/mole• Vibrational energy, ΔEv = 6.21 kcal/mole• Electronic energy, ΔEe = 186.0 kcal/mole

Wavelengths to measure changes in the various modes of energy

(CO at 300K in a box 10 cm on a side )

• Translational energy, λt = 0.2 light years, none• Rotational energy, λr = 0.26 cm, far IR or Microwave• Vibration energy, λv = 4,610 μ, near IR• Electronic energy, λe = 0.154 μ, UV

Mode Wavelength Portion of spectrum