∆U=Q+W S, A, G.

Slides:



Advertisements
Similar presentations
Lecture 24 Chemical equilibrium Equilibrium constant Dissociation of diatomic molecule Heterophase reactions.
Advertisements

We will call μ the Chemical Potential Right now we will think of it as the molar free energy, but we will refine this definition later… Free Energy.
Phase transitions Qualitative discussion: the 1-component system water specific volume.
Physical Transformations of Pure Substances
Phase Transformations - Vocabulary
Liquid-Vapor Equilibrium (Intermolecular Forces and Liquids and Solids) Green/Damji: 17.1 Chang: Chapter 11 Copyright © The McGraw-Hill Companies, Inc.
Gibbs Free Energy Gibbs free energy is a measure of chemical energy All chemical systems tend naturally toward states of minimum Gibbs free energy G =
Second law of Thermodyna mics - 2. If an irreversible process occurs in a closed system, the entropy S of the system always increase; it never decreases.
The Advanced Chemical Engineering Thermodynamics The variables (thermodynamic properties) and the equations in thermodynamics Q&A -2- 9/22/2005(2) Ji-Sheng.
Chapter 18 Entropy, Free Energy and Equilibrium
Copyright McGraw-Hill 2009 Chapter 18 Entropy, Free Energy and Equilibrium.
Ch. 9 K&K: Gibbs Free Energy and Chemical Reactions Recall (ch. 8): Free energyconditions. Helmholtz F isothermal Enthalpy H constant pressure Gibbs G.
Thermodynamics Mr. Leavings. Objectives Use the laws of thermodynamics to solve problems, identify energy flow within a system, determine the classification.
Question of the Day: 1. Is an endo or exo reaction more likely to be spontaneous? 2. Use the diagram below: If 1 mol of water is produced in the combustion,
System strives for minimum Free Energy. aA + bB cC + dD G0G0 rxn d  G 0 (D) f c  G 0 (C) f = [+] - b  G 0 (B) f a  G 0 (A) f [+] G0G0 rxn n 
Byeong-Joo Lee Byeong-Joo Lee POSTECH - MSE Phase Equilibria in a Single- Component System.
Chem. 412 – Phys. Chem. I. Free Energy Comparisons Helmholtz F.E. (A)Gibbs F.E. (G) A = U - TSG = H -  A sys =  U sys - T  S
Reaction Mechanisms in Inorganic Chemistry. Elementary Reaction Kinetics: A Review of the Fundamentals.
where Q is the reaction quotient
Topic 4 The thermodynamics of mixtures
General Phase Equilibrium
ERT 108/3 PHYSICAL CHEMISTRY SECOND LAW OF THERMODYNAMICS Prepared by: Pn. Hairul Nazirah Abdul Halim.
Standard Enthalpy Change of Reaction
Entropy and Free Energy. Learning Objectives  Use the Gibbs free-energy equation to determine whether a reaction is spontaneous or not.  Understand.
A science that includes the study of energy transformations and the relationships among the physical properties of substances which are affected by.
Entropy Changes in Chemical Reactions.  Because entropy is a state function, the property is what it is regardless of pathway, the entropy change for.
A science that includes the study of energy transformations and the relationships among the physical properties of substances which are affected by.
Stoichiometry Review 1.Write the equation for a reaction between Ca(OH) 2 and NaCl Unbalanced: Ca(OH) 2 + NaCl  CaCl 2 + NaOH Balanced: 1 Ca(OH)
Spontaneity, Entropy and Free Energy. Spontaneous Processes and Entropy  First Law “Energy can neither be created nor destroyed" The energy of the universe.
Ch. 19: Spontaneity (“Thermodynamically Favored”), Entropy and Free Energy.
OBJECTIVE 3 Students will identify that density is a fundamental property of matter. Changes in pressure and temperature can change the density of a material.
Equilibrium Expressions. Equilibrium When the rate of the forward and reverse reactions are equal. The equilibrium constant K eq is a value that shows.
Hess’s Law.
A First Course on Kinetics and Reaction Engineering
Solution of Thermodynamics: Theory and applications
Chemical and Phase Equilibrium (2)
Figure 6.2 Comparison among the Debye heat capacity, the Einstein heat capacity, and the actual heat capacity of aluminum.
Lecture 6 Defining the equilibrium by minimizing the Gibbs energy Acid dew point temperature of flue gases.
Chemical Thermodynamics – Gibbs Free Energy and Spontaneity
Free Energy Review: MgO + C(graph)  Mg + CO ∆Ho = KJ/mol ∆So = J/K a. Is the reaction thermodynamically favorable under standard.
Draw the resonance structures of: NO2- NNO HCO2-
Peter Atkins • Julio de Paula Atkins’ Physical Chemistry
Spontaneity (ΔG) Free Energy (Gibb's) Entropy (ΔS)
Universe = system (Ur) and reservoir (Ur,Tr) constrained by U0=Ur+Us
الاحتراق.
Liquid-Vapor Equilibrium
Phase Changes.
Stoichiometry w/Volume
Entropy changes in irreversible Processes
Typical Reaction: reactants  products
Stoichiometry w/Volume
Free Energy and Chemical Reactions
Free Energy Also called Gibbs Free Energy
Entropy and Free Energy
Why does an ice cube melt in the mouth?
Stoichiometry w/Volume
General Chemistry CHEM 101 (3+1+0).
Consider a gas phase reaction
Entropy & Chemical Reactions
THE EQUILIBRIUM CONSTANT
Natural systems tend toward states of minimum energy
Thermochemistry Lesson # 4: Hess’s Law.
(∆S)U,V≥0 Pending! Can happen spontaneously or not mol, g
Thermodynamics Lecture 3
Ch. 17: Reaction Energy and Reaction Kinetics
Entropy.
Enthalpy, Entropy, Free Energy, and Spontaneity Thermodynamic Favorability* *New College Board jargon which replaces “spontaneous” and should be used in.
Enthalpy Nature is lazy Nature loves decreases in heat
Chemical Equilibrium Mass transfer takes place from higher chemical potential to lower chemical potential. If the chemical potential of reactants are.
Natural systems tend toward states of minimum energy
Presentation transcript:

∆U=Q+W S, A, G

T, P, V A CP, CV U, H, S, A, G A’ Closed system State variation

The drive force ? ? Equilibrium A Nonequilibrium Direction of variation and the limitation The drive force ? A B How to judge? What could be got from the variation? Q, W, Wf

The justification at constant temperature and pressure Phase variation liquid gas water G(l) G(g) δmol, Water(Liquid) ↔Water (Gas) Phase equilibrium: Phase variation direction: For chemical reaction:

Phase transformation or reaction: AB G = GB – GA The variation of the Gibbs energy with pressure at constant temperature The variation of the Gibbs energy with temperature at constant pressure Gibbs-helmholtz equation

Example 1: 1/2N2+3/2H2 NH3 25℃,PΘ: 600℃,PΘ: 25℃,10PΘ: Gibbs-helmholtz equation 600℃,PΘ: 25℃,10PΘ:

Example 2: Diamond Graphite 25℃,Py Smy/JK-1  mol-1 CHmy/kJmol-1  /g  cm-3 C(graphite) 5.6940 – 353.514 2.260 C(diamond) 2.4388 – 355.410 3.513 How about increase temperature? 1000℃, p0: How about increase pressure?