Download - Gibbs Energy
![Page 1: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/1.jpg)
Chemistry 433Chemistry 433
Lecture 14Lecture 14Gibbs Free Energy
and Chemical Potential
NC State University
![Page 2: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/2.jpg)
The internal energy expressed in terms of its natural variables
We can use the combination of the first and second laws to derive an expression for the internal energy in terms of its natural variables. If we consider a reversible process:
dU = δq + δwδw = -PdV (definition of work)
S ( )δq = TdS (second law rearranged)Therefore, dU = TdS - PdV
This expression expresses the fact that the internal energyU has a T when the entropy changes and a slope -P whenthe volume changes We will use this expression to derivethe volume changes. We will use this expression to derivethe P and T dependence of the free energy functions.
![Page 3: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/3.jpg)
The Gibbs energy expressed in terms of its natural variables
To find the natural variables for the Gibbs energy we beginTo find the natural variables for the Gibbs energy we beginwith the internal energy:dU = TdS - PdV
d b i iand substitute into:dH = dU + PdV + VdPto find:dH = TdS + VdP (S and P are natural variables of enthalpy)and using:dG = dH - TdS - SdTdG = dH - TdS - SdTwe find:dG = -SdT + VdP (T and P are natural variables of G)O i h G i f l It t l i blOnce again we see why G is so useful. Its natural variablesare ones that we commonly experience: T and P.
![Page 4: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/4.jpg)
The variation of the Gibbs energy with pressure
We shown that dG = VdP - SdT. This differential can be used to determine both the pressure and temperature dependence of the free energy. At constant temperature:p gy pSdT = 0 and dG = VdP. The integrated form of this equation is:
For one mole of an ideal gas we have:ΔG = VdP
P1
P2
ΔGm = RT dPPP1
P2
= RT ln P2
P1
Note that we have expressed G as a molar quantity Gm = G/n.
![Page 5: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/5.jpg)
The variation of the Gibbs energy with pressure
We can use the above expression to indicate the pfree energy at some pressure P relative to the pressure of the standard state P = 1 bar.
P
G0(T) is the standard molar Gibb’s free energy for a gas. G ’ f
Gm T = G0 T + RT ln P1 bar
As discussed above the standard molar Gibb’s free energy is the free energy of one mole of the gas at 1 bar of pressure. The Gibb’s free energy increases logarithmically with pressure. gy g y pThis is entirely an entropic effect.Note that the 1 bar can be omitted since we can write:
RT ln P1 bar = RT ln P – RT ln 1 = RT ln P
![Page 6: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/6.jpg)
The pressure dependence of G for liquids and solids
If we are dealing with a liquid or a solid the molar volume g qis more or less a constant as a function of pressure. Actually, it depends on the isothermal compressibility, κ = 1/V(∂V/∂P) but κ is very small It is a number of theκ = -1/V(∂V/∂P)T, but κ is very small. It is a number of the order 10-4 atm-1 for liquids and 10-6 atm-1 for solids. Wehave discussed the fact that the density of liquids is
t t l ff t d b Th ll l fnot strongly affected by pressure. The small value of κis another way of saying the same thing.For our purposes we can treat the volume as a constant p pand we obtain
Gm T = G0 T + Vm P – 1m m
![Page 7: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/7.jpg)
QuestionWhat is the isothermal compressibility κ = -1/V(∂V/∂P)T for an ideal gas?
A. κ = -1/VB. κ = 1/PC. κ = 1/TD. κ = nRT/P
![Page 8: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/8.jpg)
QuestionWhat is the isothermal compressibility κ = -1/V(∂V/∂P)T for an ideal gas?
A. κ = -1/VB. κ = 1/PC. κ = 1/TD. κ = nRT/P
![Page 9: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/9.jpg)
QuestionCompare the following two equations for the pressure dependence of the Gibbs free energy. Which one applies t th f ti f di d f hit ?to the formation of diamond from graphite?
PA. Gm T = G0 T + RT ln P1 bar
B. Gm T = G0 T + Vm P – 1
![Page 10: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/10.jpg)
QuestionCompare the following two equations for the pressure dependence of the Gibbs free energy. Which one applies t th f ti f di d f hit ?to the formation of diamond from graphite?
PA. Gm T = G0 T + RT ln P1 bar
B. Gm T = G0 T + Vm P – 1
![Page 11: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/11.jpg)
Systems with more than one component
Up to this point we have derived state functions for pure p p psystems. (The one exception is the entropy of mixing).However, in order for a chemical change to occur we musthave more than one component present We need generalizehave more than one component present. We need generalizethe methods to account for the presence of more than onetype of molecule. In the introduction we stated that we wouldd thi i tit ll d th h i l t ti l Thdo this using a quantity called the chemical potential. Thechemical potential is nothing more than the molar Gibbsfree energy of a particular component. Formally we write itgy p p ythis way:
μ = ∂G Rate of change of G as number ofmoles of i changes with all otherμ i = ∂ni T,P, j ≠ i
moles of i changes with all othervariables held constant.
![Page 12: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/12.jpg)
Example: a gas phase reactionp g p
Let’s consider a gas phase reaction as an example. We willt tb k luse a textbook example:
N2O4 (g) = 2 NO2 (g)We know how to write the equilibrium constant for this reaction.q
K =PNO2
2
PN2O4
At constant T and P we will write the total Gibbs energy as:
dG = μ dn + μ dn
N2O4
dG = μNO2dnNO2
+ μN2O4dnN2O4
dG = 2μNO2dn – μN2O4
dnWe use the reaction stoichiometry to obtain the factor 2 for NO2.
![Page 13: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/13.jpg)
Definition of the Gibbs free energy change for chemical reactionchange for chemical reaction
We now define ΔrxnG:
Δ rxnG = dGdn T,P
This is ΔrxnG but it is not ΔrxnGo! Note that we will use ΔrxnGand ΔG interchangably.If we now apply the pressure dependence for one componentIf we now apply the pressure dependence for one component,
t lti t t
Gm T = G0 T + RT ln P1 bar
to a multicomponent system:μ i T = μ i
0 T + RT ln Pi
1 bar
These two expressions are essentially identical. The chemical potential, μi, is nothing more than a molar free energy.
![Page 14: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/14.jpg)
QuestionHow should one think of the chemical potential, μof component j?of component j?
A. It is the potential energy of that componentB It i l f f th t tB. It is a molar free energy of that componentC. It is potential entropy of that componentD. It is a molar entropy of that component
![Page 15: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/15.jpg)
QuestionHow should one think of the chemical potential, μof component j?of component j?
A. It is the potential energy of that componentB It i l f f th t tB. It is a molar free energy of that componentC. It is potential entropy of that componentD. It is a molar entropy of that component
Single component:G T = G0 T + RT ln P
Multiple components each have a μj:
Gm T = G T + RT ln 1 bar
Pμ i T = μ i0 T + RT ln Pi
1 bar
![Page 16: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/16.jpg)
Application of definitions to the chemical reactionchemical reaction
We can write the Gibbs energy as:
and use the chemical potentials:ΔG = 2μNO2
– μN2O4
p
μNO2= μNO2
0 + RT ln PNO2
μ = μ0 + RT ln P
to obtain the following:
μN2O4= μN2O4
+ RT ln PN2O4
ΔG = 2μNO20 – μN2O4
0 + 2RT ln PNO2– RT ln PN2O4
ΔG = ΔG0 + RT lnPNO2
2
ΔG0 = 2 0 0ΔG = ΔG0 + RT ln 2
PN2O4
, ΔG0 = 2μNO20 – μN2O4
0
![Page 17: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/17.jpg)
Note the significance of ΔG and ΔGog
The change ΔG is the change in the Gibbs energy function.It h th ibl f lIt has three possible ranges of value:ΔG < 0 (process is spontaneous)ΔG = 0 (system is at equilibrium)( y q )ΔG > 0 (reverse process is spontaneous)
On the other hand ΔGo is the standard molar Gibbs energyOn the other hand ΔG is the standard molar Gibbs energychange for the reaction. It is a constant for a given chemicalreaction. We will develop these ideas for a general reactionl t i th F l t’ id th t tlater in the course. For now, let’s consider the system atequilibrium. Equilibrium means ΔG = 0 so:
PNO2
0 = ΔG0 + RT ln K , ΔG0 = –RT ln K , K =PNO2
PN2O4
![Page 18: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/18.jpg)
QuestionWhich statement is true at equilibrium if K = 2?
A ΔG RT l (2) ΔGo 0A. ΔG = -RT ln(2), ΔGo = 0B. ΔG = 0, ΔGo = -RT ln(2)C. ΔG = ΔGo = -RT ln(2)B. ΔG = 0, ΔGo = 0
![Page 19: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/19.jpg)
QuestionWhich statement is true at equilibrium if K = 2?
A ΔG RT l (2) ΔGo 0A. ΔG = -RT ln(2), ΔGo = 0B. ΔG = 0, ΔGo = -RT ln(2)C. ΔG = ΔGo = -RT ln(2)B. ΔG = 0, ΔGo = 0
![Page 20: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/20.jpg)
Temperature dependence of ΔGo
The van’t Hoff equationThe van t Hoff equation We use two facts that we have derived to determine thet t d d f th f Htemperature dependence of the free energy. Here are weare skipping some derivations that are not often used andderiving a very useful expression in biology.
ΔG0 = –RT ln(K)ΔG0 = ΔH0 – TΔS0
ln(K) = – ΔH0
RT + ΔS0
RΔH0 1 1ln(K2) – ln(K1) = ΔH0
R1T1
– 1T2
If we plot ln(K) vs 1/T the slope is -ΔHo/R. This is a useful expression for determining the standard enthalpy change.
![Page 21: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/21.jpg)
Example: the formation of diamond p
Graphite and diamond are two forms of carbon. Given that th f f f ti f di d ithe free energy of formation of diamond is:C(s, graphite) C(s, diamond) ΔrGo = + 2.90 kJ/moland the densities are:ρ(graphite) = 2.26 and ρ(diamond) = 3.51calculate the pressure required to transform carbon intodiamonddiamond.
Solution: Graphite will be in equilibrium with diamond when:
0 = ΔG0 + ΔVm P – 1
P = 1 – ΔG0
= 1 – ΔG0
P = 1 –ΔVm
= 1 – Mρd
– Mρgr
![Page 22: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/22.jpg)
Example: the formation of diamond p
Plugging the values we find:
0 = ΔG0 + ΔVm P – 1ΔG0 ΔG0
P = 1 – ΔGΔVm
= 1 – ΔGMρd
– Mρgr
2900 J/ l= 1 – 2900 J/mol
0.012 kg/mol 13510 – 1
22603510 2260= 1.5 x 109 Pa = 15000 bar
![Page 23: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/23.jpg)
Protein folding example:T t t d lTwo state model
kf
U Fku
Unfolded Foldedku
K = [F]/[U]
K = ff/(1-ff)( )Fraction folded ff Fraction unfolded 1-ff
![Page 24: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/24.jpg)
Thermodynamic modelyff = 1/(1+K)K ΔGo/RTK = e-ΔGo/RT
ff = 1/(1 + e-ΔGo/RT)ff = 1/(1 + e-ΔHo/RTeΔSo/R)
The temperature at which the protein is 50% folded can be defined as Tis 50% folded can be defined as Tmthe melt temperature. At Tm , ΔGo = 0 or Tm = ΔHo/ΔSo.At Tm , ΔG 0 or Tm ΔH /ΔS .
![Page 25: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/25.jpg)
Equilibrium melt curvesq
Mostly folded o o
Mostly unfoldedTm
Mostly unfolded
In this case: Tm = 300 K = ΔHo/ΔSo
![Page 26: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/26.jpg)
Van’t Hoff plotsp
Slope = -ΔHo/R
The standard method for obtaining theThe standard method for obtaining the reaction enthalpy is a plot of ln K vs. 1/T
![Page 27: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/27.jpg)
QuestionWhat determines the steepness of the equilibrium melt curve?A. The melt temperatureB. The equilibrium constantC. The ratio of the enthalpy to the entropyD. The magnitude of the enthalpy and entropy
![Page 28: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/28.jpg)
QuestionWhat determines the steepness of the equilibrium melt curve?A. The melt temperatureB. The equilibrium constantC. The ratio of the enthalpy to the entropyD. The magnitude of the enthalpy and entropy
![Page 29: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/29.jpg)
QuestionWhat can you say about the enthalpy of reaction for the process shown in the figure below?p gA. The reaction is exothermic.B. The reaction is endothermic.C. The reaction is spontaneous.D. None of the above.
![Page 30: Gibbs Energy](https://reader033.vdocuments.pub/reader033/viewer/2022042503/55cf97da550346d03393fdd9/html5/thumbnails/30.jpg)
QuestionWhat can you say about the enthalpy of reaction for the process shown in the figure below?p gA. The reaction is exothermic.B. The reaction is endothermic.C. The reaction is spontaneous.D. None of the above.