The thermodynamic free energy is a concept useful in the thermodynamics of chemical or thermal processes in engineering and science. The change in the free energy is the maximum amount of work that a thermodynamic system can perform in a process at constant temperature, and its sign indicates whether a process is thermodynamically favorable or forbidden. Since free energy usually contains potential energy, it is not absolute but depends on the choice of a zero point. Therefore, only relative free energy values, or changes in free energy, are physically meaningful.
The free energy is a thermodynamic state function, like the internal energy, enthalpy, and entropy.
Hello, I am working on non linear fluid dynamics with my professor. We are trying to model multiphase flows of immiscible fluids. And my professor today asked me to look up works on 'free energy flows', but I cannot find anything on the internet that I can use, let alone understand. Can someone...
Hi. I have two questions:
1) Is -ΔG the amount of useful work a system can do while the pressure and temperature of the surroundings are constant?
2) Is exergy = -ΔG only if the pressure and temperature of the system and surroundings is constant?
thanks
In euclidean quantum field theory, the imaginary part of the free energy, defined as the logaritm of the partition function, is it connected to the decay rate?
I have a question that has puzzled me during the last couple of days. Suppose that there is a system (e.g. a small box filled with gas) that is connected to a heat bath (much larger than the system) at a constant temperature T. The studied system and the heat bath are thought to be isolated from...
This question came to mind when studying voltaic cells. In voltaic cells, for some ions (Cu2+ for example), both oxidation and reduction are possible. Given both possiblities, how do we determine which reaction will take place? I first thought that comparing the signage in voltage of both...
Hello everyone,
I am having a little difficulty understand precisely what Gibbs free energy is. I have read in my textbook that a negative change in Gibbs free energy implies that the substance under consideration will react/change spontaneously. As such, the more negative the Gibbs free...
I calculated some gibbs free energy values for a chemical reaction at 298K and 1773K both giving me negative values . the amount for the reaction at 298K is -162443J and the one at 1773K is -81147.85J.
Both shows that the reaction are spontaneous and so thermodynamically the process at 298K is...
http://en.wikipedia.org/wiki/Helmholtz_free_energy#Work_in_an_Isothermal_Process_and_Equilibrium_Conditions
Hi. In the proof that dw <= -dA for isothermal work, where is it assumed T must be constant during the whole process?
Just for kicks. I tried calculating Keq from Gibb's free energy. This should be a straight forward calculation, but the answer is no where near close.
Here is my calculations in SAGE:
sage: R=8.314; T=298; G=237000 ; Keq=var('Keq'); f=G+R*T*log(Keq)
sage: f.solve(Keq)
[Keq ==...
what is actually meant by gibbs free energy and what is the difference between gibbs free energy and activation energy?In an enthalpy diagram how can it be denoted(just like for activation energy is denoted by the energy difference between transition state and reactants' enthalpy)?I just search...
If ##ΔG_{sys} = ΔH_{sys} - TΔS_{sys}; ΔS_{sys} = \frac {-ΔH_{surr}}{T} ##
Then, doesn't this expression just simplify to:
##ΔG_{sys} = ΔH_{sys} + ΔH_{surr}## and isn't ##ΔH_{sys} = -ΔH_{surr}##?
So then ##ΔG = 0##...this does not seem correct...could anyone please clarify my mistake and...
*to moderators: i apologize about the double post, but i didn't know how to get rid of the other post and i wanted a get an answer asap and no one was answering the other post so i reposted here in the appropriate section*
enthalpy is the energy available if a system with some defined volume...
***i just realized that i posted this in the wrong section; could a moderator perhaps move this thread to the classical physics section please? Sorry for the trouble***
enthalpy is the energy available if a system with some defined volume were to be annihilated and have the atmosphere...
The problem is :
a) Find Helmholtz free energy F(V, T) of a simple solid.
b) Use the result of part a) to verify that (∂F/∂T)v and (∂F/∂V)T are consistent with S(T, V) and P(V, T) in equation P=a0T-b0ln(V/V0)
I know:
Helmholtz free energy is F=U-TS
and dF=-SdT-PdV
S=-((∂F/∂T)v)...
Homework Statement
When gaseous nitrogen and hydrogen are converted to gaseous ammonia, then delta G equals: -16.64Kj/mol
3h2+ n2=2nh3
Using the s values , calculate the delta h for the formation of ammonia
Homework Equations
Delta s for:
H2:130.6
N2:191.5
Nh3:192.5
T= 298...
the gibbs free energy is defined to be H-TS. In my thermo book, it says that if i were to create a system out from volume V=0 at constant pressure and temperature, the work that i would need to provide is G=H-TS. But for constant pressure i thought the work terms in enthalpy canceled out and...
ΔG° is the measure of Gibbs Free energy change at 1 bar but no specified temperature and also the stoichiometric amounts depending on the equation of the chemical reaction.
For example, if X ->2Y then the ΔG° would be equal to ΔG°f(2Y)-ΔG°f(X). While for ΔG it is a general term for Gibbs Free...
In reaction there is a Gibbs Free energy change. I'm still not sure what this means as in my secondary school years we just learned of one component of it which is the enthalpy change. That was simple as it just showed how much heat was released or absorbed. But with Gibbs Free energy, i don't...
Gibbs Free Energy is the appropriate potential when there is both heat exchange and mechanical work (G=E-TS+PV). On the other hand the grand potential is appropriate when there is heat exchange and chemical work (g=E-TS-μN).
Is there any issue in defining a potential of the form (E-TS-μN+PV)...
Homework Statement
I am attempting the problem below, I might have the correct answer but would appreciate if someone could confirm this (or tell me where I'm going wrong).
Consider a statement having 2 states, one at energy 0 and one at energy ε. Find an expression for the Helmholtz free...
Hi I have a 4 part question about phase changes and I hope you guys can help me out here thanks :)
The chemical equation for vaporization for water is H2O(l)-->H2O(g)
1) When ΔG is 0 during a phase change we would use the formula ΔH=TΔS and put in values to get the boiling/melting point by...
So reading on his work I stumble upon him wanting to give everyone free energy.
This video shows how it could work. But mythbusters did a program on this where they say it's not possible.
I'm not asking about creating energy but just if it's possible like how Tesla wanted to get energy...
I'm wondering why the Gibbs function is related to the equation of state as follows (supposedly):
V=(\frac{∂G}{∂P})_T
I found a thread on here that mentions this relationship, but doesn't explain it at all. Any help understanding this would be appreciated, this is my first introduction to...
Hi thanks for reading. I have 2 questions regarding the topics mentioned that I'm having trouble with. Hope you guys can help me out here :)
1) The first law is ΔU=Q+W so we can rearrange this to get ΔH=ΔU+PΔV so would this indicate that ΔH only measures the heat given out at constant...
In the expression defining Gibbs free energy,
G = U - TS +pV,
are T and p the temperature and pressure of the environment, or of the system itself? Or is it a requirement that the system has the same temperature and pressure as the environment for the Gibbs free energy to be defined?
Dear all,
I have been spending 12 hours on this and cannot seem to come up with a solution.
We derive Helmholtz Free Energy (A) from the second law of thermodynamics.
dS(Total) = dS(system) + dS(surrounds)
we try to express dS(surrounds) with properties of the system.
Assuming...
I am study chapter 5 of An Introduction to Thermal Physics by Schroeder and I am having trouble understanding his explanation of the differences between enthaply, Helmholtz free energy, and Gibbs free energy.
Schroeder defines enthalpy of a system as its energy plus the work needed to make...
Hi,
Suppose I have a dissociative adsorption reaction and want to find the free energy change ΔF, this can be written at constant temperature:
\Delta F = \Delta E -T\Delta S
Now given the adsorption energy \Delta E_{ads} I would like to extrapolate the Free energy assuming that the adsorbate...
If or when magnetic charges (magnetic monopoles) are found, would a magnetic current create an electric field? If so, would you be able to generate an electric current with an applied field?
Hi,Im just beginner and I m trying to learn integrals.I m just in starting phase,but still in few tences,not details...How or why we get logarithm in gibbs free energy equation?Because of integration of this equation or due to probability and statistics laws?
Thanks
Compute the coefficient of expansion α in terms of P and V...
Homework Statement
Compute the coefficient of expansion α in terms of P and V for an ideal Van der Waals
gas
Homework Equations
(p+a/v^2)(v-b)=RT
The Attempt at a Solution
Is this as simple as solving for a? How...
Hi,
As I understand, during the process of phase change from a liquid to solid (or any phase change for that matter,) the temperature of the substance remains constant as the energy being applied to the substance is used in changing phase.
How does this relate to Gibbs free energy? I read that...
If this isn't the correct place to ask this, please point me to where I should. I feel there are quite a few guidelines to what can be posted and what cannot, so I hope I don't break any rules!
I'm working on a problem, that deals with a superheated steam, that goes from an initial state to...
Hi there:
When using ΔG=ΔG°+RT ln Q to calculate the energy yield of a reaction, does it matter if I use ΔG° calculated at 1°C or 25°C? Also, why are there two choices and when are they each applicable? Finally, I have also seen ΔG°' written (note the prime). What does this mean and how does...
Homework Statement
The following reaction takes place at standard conditions
4NH3(g)+6NO(g)----->5N2(g)+6H20
A)calculate reaction enthalpy and Gibbs reaction energy
B)Calculate Kp
Homework Equations
the table gives the following values for deltaG0f[X]
NH3(g)=-16.5 Kj/mol...
Homework Statement
In the previous question, you had to calculate the the standard Free Energy Change (Go) in order to solve for the equilibrium constant, K, for the reaction:
N2(g) + 3H2(g) → 2NH3(g)
This is the Free Energy measured under standard conditions, when the reaction is...
1. Homework Statement [/b]
Consider a Van der Waals gas.
Consider a recipient of volume 2V, with a mobile wall (with no friction) that divides the recipient in two, each part having exactally N particles. The system is at equilibrium and the mobile wall is exactally in the middle of the...
Homework Statement
Consider a Van der Waals gas.
Consider a recipient of volume 2V, with a mobile wall (with no friction) that divides the recipient in two, each part having exactally N particles. The system is at equilibrium and the mobile wall is exactally in the middle of the recipient...
Thermodynamics--Gibbs free energy: what can we actually measure in the lab?
Hi everyone:
I am getting back into thermodynamics after a long absence and have realized that there are basics I have never understood. If a patient person could either explain or direct me to an online resource...
hello
This is a section from Callen, Herbert B - Thermodynamics and an Introduction to Thermostatistics
"Any equilibrium state can be characterized either as a state of maximum entropy for given energy or as a state of minimum energy for given entropy. But these two criteria nevertheless...
The Gibbs energy is used to determine the spontaneity of a thermodynamic process under isobaric conditions.
The Helmholtz energy is used to determine the spontaneity of a thermodynamic process under isovolumetric conditions.
I was curious: is there an energy used to determine the spontaneity...
Homework Statement
Consider a mixture of hard spheres of diameter σ. The potential energy
for a hard sphere system is given by
\beta U(r) = 0 (r > \sigma)
∞ (r ≤ \sigma)
The packing fraction (η) of the system is the amount of space occupied
by the particles.
(b) The...
I'm looking at the free energy of a body (theory of elasticity) but I can't really square the general expression with the one usually used for isotropic bodies.
According to wikipedia (http://en.wikipedia.org/wiki/Elastic_energy), Landau & Lifgarbagez etc the general expression for the free...
Homework Statement
From Hill's "Introduction to Statistical Thermodynamics", question 3-4 reads:
(note "STR" denotes the case of most probable distribution and should be read as C*)
Homework Equations
The most probable distribution for a system of independent indistinguishable...
I'm trying to figure out if the Helmholtz & Gibbs free energy are ever used outside of chemical reactions (I suppose they could be used in nuclear reactions in a plasma as well.) It seems to me that they are not, as I can only recall using them for chemical reactions in my thermodynamics course...