Gibbs free energy Definition and 124 Threads

I've seen a lot of articles, where people calculate free Gibbs energy of system using several methods in some sense indirect methods, but I've never seen it is being calculated using its definition: $$ \Phi=U+pV-TS $$ Imagine a big MD system at its equilibrium in a box with periodic boundary...

Before we prove this, consider a thought experiment. We have the following setup We break the left partition so that the gases on the left mix. What happens next is that due to a chemical potential difference, gas flows from the right compartment to the mixture. Note that - the partial...

I have a rather basic question regarding the chemical potential (##\mu##) in thermodynamics and its relation to the Gibbs free energy (##G##). All thermodynamics textbooks I've looked at (Landau & Lifshitz, Kittel...) derive the fact that, at constant temperature ##T## and pressure ##p##, the...

So I had to find change in entropy of system in reversible isothermal process. $$T\Delta S_{sys.}=Q\implies \Delta S_{sys.}=nRln\left(\frac{V_2}{V_1}\right)$$ This was good because for isothermal process ##\Delta U=0\implies Q=W## Then I read this Throughout an entire reversible process, the...

Hello, is someone able to explain why these two are wrong. I am not sure how to figure out the enthalpy direction as the reaction is not changing state of matter, nor is it changing temperature. (Please solve without calculating anything) Thank you

Hey all, On page 446 in Peskin, he provides 2 different ways of writing the Gibbs Free Energy: $$\textbf{G}(M,t) = M^{1+\delta}h(tM^{-1/\beta})$$, and $$\textbf{G}(M,t) = t^{\beta(1+\delta)}f(Mt^{-\beta})$$ where ##h## and ##f## are some initial condition functions that have a smooth limit as...

Hi everybody, I don't understand what changes between these two graphs. In particular, why does free energy reach a minimum in one graph and a maximum in the other? Shouldn't a chemical reaction always have an energy maximum, represented by the activation energy?

SO2(g)+1/2O2(g)⇌SO3(g);ΔHo=-98.32KJ/mole,ΔSo=-95J/(mole-K). find Kp at 298 Kelvin? In given question at first Δ G will be calculated using formula ΔG = Δ H – T x ΔS, by putting the given values in formula we get ΔG = -70.01 kJ/mol. Then Keq will be calculated using equation = Δ G = -RT ln Keq...

Will the presence of attractive interactions between gas molecules raise or lower the molar Gibbs energy of a gas relative to its ‘perfect’ value? I would think that these attracting forces result in a lower energy state. A decrease in the energy state implies a decrease in the enthalpy. A...

Hello , we learned in thermodynamics that to calculate ΔHr °(of the reaction ) using ΔHf °(standard heat of formation ), we have to respect that ΔHf °=ΔHr ° of a reaction forming 1 mol of compound from pure elements in their most stable form at standard state . the problem is when we want to...

we assume that we have an exergonic reaction , a substrate going to a product , is the negative ΔG′° the principal reason that the equilibrium favors the product (there is more product than substrate at equilibrium )?, or it is not and that depends on other factors? , thanks .

In chemical reactions generally ΔG < 0 , but if we were to consider a reversible path between pure reactants and products at 1 bar pressure , shouldn't the ΔG = 0 for every reaction ? and if it is due to non-pv work , I don't see any non pv work being done in reactions happing in a closed...

hi guys I am trying to derive the Gibbs free energy for a superconductor in the intermediate state , the book(Introduction to Superconductivity by A.C. Rose-Innes) just stated the equation as its : $$ G(Ha) = Vgs(0)+\frac{V\mu_{o}H_{c}}{2n}[H_{a}(2-\frac{H_{a}}{H_{c}})-H_{c}(1-n))] $$ I am not...

Summary:: Gibbs and Helmholtz energies calculations for heating an ideal gas at constant volume I am solving a problem involving an ideal gas that undergoes several chained changes of state. One of the steps asks to calculate the change in Gibbs Energy (DeltaG) and Helmholtz energy (Delta A)...

I know that when it is ΔG>0 , it means there is no spontaneity, when ΔG=0 there is equilibrium, and when ΔG<0, there is spontaneity. But what happens when this is in the context of partial molar properties, when G is molar? I suppose molar ΔG is referred to a solution. Right? In that case, is...

#Can somebody please explain what is the difference between single phase and homogeneous phase in context with thermodynamics? #Also in the fundamental relations in thermodynamics like dg=vdp-sdT , it says this is applicable to homogeneous phase of constant composition. Isn't this equation...

Where have I gone wrong? According to the key, the right option is a.

In the textbook Thermal Physics by Daniel Schroeder he says the following: However, I don't follow this argument. Let's say that G was the following: $$G(T, P, N) = (TPN)^{1/3}$$ Then $$G(\lambda T, \lambda P, \lambda N) = \lambda G$$ So $$G$$ is extensive, but $$G \not \propto N.$$

Summary: Please help me with this problem ,I can't do it The normal boiling point of liquid bromine is 58.2°C. At 9.3°C the equilibrium vapor pressure of liquid bromine is 100 torr. From this data, calculate the standard state Gibbs energy of formation of bromine vapor at room temperature...

I was thinking about giving the bond energy to calculate the enthalpy change of some exothermic and spontaneous reaction. Than using that exothermic enthalpy to heat the own products and reagents. That would change the Gibbs free energy of the equation (as the elements will be in a different...

If this belongs in classical physics, please move it there. But it seems like the kind of question chemistry people would know so I'm putting it here. I was reading a textbook on chemical thermodynamics, and it says to raise the partial molar Gibbs free energy of n moles a substance from...

What is the entropy change of the system in the Gibbs Free Energy Equation? The general expression for entropy change is ΔS=q/T The only exchange between the system and the surroundings is ΔH done reversibly, with no PV work and no matter transfer, therefore q(syst) = ΔH(syst) therefore surely...

At equilibrium, we know that deltaG = 0. But what about deltaG_zero, i.e. the standard Gibbs free energy? When is deltaG_zero = 0? In the solution manual it says that it means that K = 1, but by calculating an equilibrium constant you are already stating that we are at equilibrium? I.e. that...

Calculate deltaG for the reaction: H2O(l) = H2O(g). 100 degrees celsius, water is clean. P(H2O) = 0.1 bar. Given that it is an equilibrium, I'd think that deltaG would be zero. But the answer is in fact negative. How is that possible?

Advanced Problems textbook. (It's on pages 212-213). I'll post the question and following it the solution in the book: The question: The Solution: What I don't understand is how did they arrive at the identities with ##\frac{\bar{G}_1''-\bar{G}_1'}{0}## and...

Hello. I'd like to ask a question about meaning of Gibbs free energy. In undergraduate school, I learned that Gibbs free energy is "available" energy we can extract from system at constant pressure and temperature. G=H-TS=U+PV-TS In above expression, however, I can't understand why "TS term" is...

Homework Statement By means of a Maxwell relation derived from the Gibbs free energy and making use of the third law of thermodynamics, prove that the thermal expansion coefficient β must be zero at T = 0. I tried but I got something funny. Homework Equations $$G=U-TS+PV$$ $$dG=\mu...

By means of a Maxwell relation derived from the Gibbs free energy and making use of the third law of thermodynamics, prove that the thermal expansion coefficient β must be zero at T = 0. I tried but I got something funny. My working:

Homework Statement For a Particular system the following expression for Gibbs free energy is known: G = -kTN ln (a T^(5/2) / P) where a is a constant (whose dimensions make the argument of the logarithm dimensionless). Obtain expressions for a) The entropy, S b) The connection between V, P...

Homework Statement Calculate changes in A and G of one mole of an ideal gas that undergoes the following processes respectively. 1. adiabatic expansion from (T1, P1) to (T2, P2) 2. isobaric expansion from (P, V1, T1) to (P, V2, T2) (if it is not isothermal) 3. isochoric expansion from (V, P1...

Homework Statement I am needing to graph the Gibbs free energy of mixed gases to determine the range when the gases will form an ideal mixture The two gases have the same Gibbs free energy. Homework Equations ##G = (1-X)G_A + XG_B## for unmixed ##G = (1-X)G_A + (X)G_B + RT(x*ln(x) +...

Homework Statement the isothermal compressibility of graphite is about ##3*10^{-6} bar^{-1}##, while that of diamond is more than ten times less and hence negligible in comparison. (isothermal compressibility is the fractional reduction in volume per unit increase in pressure, as defined in...

Hi, I'm preparing for my exams in a few weeks, of which one covers Thermodynamics. I was trying to solve a question, where I noticed the Gibb's free energy had to equal the (negative) work. I kind of came to an answer, but was not sure if I did it the right way. All steps are reversible...

When I studied chemistry in high school, I learned that if the change of enthalpy of a reaction ΔH > 0 , the reaction is endothermic, and if ΔH<0, it is exothermic. However in thermodynamic class, I learnt: $$ ΔG = ΔH - TΔS $$ For a reaction of a battery, the data reads ΔG = -394kJ/mol. (which...

I am learning physics on khan academy and they do a proof to show that delta G for a reversible reaction is negative and how for a irreversible reaction it is positive. However in the proof, they assume that the heat put in by the isotherm is less for an irreversible reaction compared with a...

I understand that the change in Gibbs Free Energy at equillibrium is 0 and this leads to the equation -deltaH=TdeltaS. My questions here is that if a reaction is at equillibrium, how can there be any change in enthalpy or entropy at all? Why wouldn't these terms be 0?

Hello. A known equation that is useful for calculating equilbrium constants is: ΔG° = -RT * ln(K) This is all well and good. Given a standard gibbs free energy of reaction for some given reaction, the equilibrium constant for the reaction can be found. My trouble is in which ΔG° to use. For...

Say I have an exothermic reaction, whose change in Entropy is positive. (not the most common of reactions, but it can still happen) If I increase the temperature, by La Chatlier's principle, the reaction should move to the left. However, by Gibbs free energy, if I increase the temperature, the...

So I know that things in the Universe tend to move toward a state of least potential energy. This is why forces point in the direction of decreasing potential energy, as everything is trying to minimize its potential energy. So my main question is: does Gibb's free energy basically just...

We were learning about the change in free energy in class, but I was wondering since the Gibbs free energy decreases as a system becomes more stable, is the minimum absolute free energy for a material the same for every material, or can other materials be more stable than others?

Homework Statement Estimate the vapor pressure of mercury at 25 ∘C (use data from Appendix D from the textbook). Homework Equations Using the appendix I can find ΔG, ΔH, and ΔS. The Attempt at a Solution I have no idea where to start. I think that maybe vapor pressure would be found when...

I am not able to understand the mathematical expression of "change in Gibbs free energy", For a chemical reaction occurring at constant temperature and constant pressure, (ΔS)total = (ΔS)system + (ΔS)surrounding Considering that reaction is exothermic, ΔH be the heat supplied by system to...

So I understand that enthalpy is energy. But what energy specifically? Is enthalpy heat energy? Is it the energy that bonds atoms together and that's why it can either be released or absorbed? Or is that what Gibbs free energy is? I'm trying to make sense of the equation: ΔG=ΔH-TΔS...

1. Surfactant molecule is made from water-loving head and grease-loving tail (Figure 1). http://tinypic.com/r/2j2gdah/9 (Figure 1) My question: How do we measure the cross-sectional area of the alkyl chain of surfactant? Do we measure it vertically (refer to GREEN DOUBLE ARROWS of Figure 1) or...

Homework Statement We have a Gibbs Free Energy function G=G(P, T, N1, N2) I am not writing the whole function because I just want a push in the right direction. Find expressions for the entropy, volume, internal energy, enthalpy and chemical potential. Homework Equations Maxwell Relations...

Hello, I get that ΔG measures the spontaneity/capacity of a system to do non-mechanical work, and that if: ΔG>0, the reaction is not spontaneous ΔG<0, the reaction is spontaneous ΔG=0, the reaction is at equilibrium So why is Gibbs free energy zero for phase changes at constant temperature and...

Hello, PF! Days ago, while playing Batman: Arkham Origins, I was wandering through the Batcave when I noticed something that caught my eye immediately. There's a nice, cozy lab in there which includes a blackboard where Bruce Wayne apparently did some kind of thermodynamic calculations, which...

Hi everybody! Lately I tried to overcome some problems with understanding thermodynamics laws, and unfortunately I couldn't find anything about my question:nb) and I really hope someone can help me here... My question is: This version of Gibbs formula dG= VdP-SdT, can be applied to any close...

Hello, Gibbs free energy describes the maximum of useful work that can be done by a chemical reaction. My question is(Sorry I am not into chemistry and biochemistry) : during a chemical reaction that creates ATP, we say that ATP stores energy between its chemical bonds . For exemple this is the...

Hello, The Gibbs free energy is the maximum amount of non-expansion work that can be extracted from a closed system; this maximum can be attained only in a completely reversible process. This maximum work is equal to H-TS. My question is this TS energy is what kind of energy? and from where it...