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이 병 주 포항공과대학교 신소재공학과 calphad@postech.ac.kr. Thermodynamics. Gibbs energy, Enthalpy. Gibbs Energy for a Unary System - from dG = – SdT + VdP. Gibbs Energy as a function of T and P. @ constant P. @ constant T. Gibbs Energy for a Unary System - from G = H – ST.
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이 병 주 포항공과대학교 신소재공학과 calphad@postech.ac.kr Thermodynamics Gibbs energy, Enthalpy ...
Gibbs Energy for a Unary System - from dG = –SdT + VdP Gibbs Energy as a function of T and P @ constant P @ constant T
Gibbs Energy for a Unary System - from G = H – ST Gibbs Energy as a function of T and P @ constant P @ constant T
Gibbs Energy for a Unary System - Temperature Dependency 서로 다른 출발점에서 유도된 위의 두 식은 같은 식인가? Empirical Representation of Heat Capacities 를 이용하여 위의 두 식이 동일한 것임을 증명하라.
Gibbs Energy for a Unary System - Effect of Pressure Molar volume of Fe = 7.1 cm3 Expansivity = 0.3 × 10-4 K-1 ∆H(1→100atm,298) = 17 cal ※ The same enthalpy increase is obtained by heating from 298 to 301 K at 1atm Molar volume of Al = 10 cm3 Expansivity = 0.69 × 10-4 K-1 ∆H(1→100atm,298) = 23.7 cal ※ The same enthalpy increase is obtained by heating from 298 to 302 K at 1atm ∆S(1→100atm,298) = -0.00052 e.u. for Fe -0.00167 e.u. for Al ※ The same entropy decrease is obtained by lowering the temperature from 298 by 0.27 and 0.09 K at 1 atm. ※ The molar enthalpies and entropies of condensed phases are relatively insensitive to pressure change
Gibbs Energy for a Unary System - absolute value available ? • V(T,P) based on expansivity and compressibility • Cp(T) • S298: by integrating Cp/T from 0 to 298 K and using 3rd law of thermodynamics • (the entropy of any homogeneous substance in complete internal • equilibrium may be taken as zero at 0 K) • H298: from first principles calculations, but generally unknown • ※ H298 becomes a reference value for GT • ※ Introduction of Standard State
Gibbs Energy change of a reaction • Neumann-Kopp rule: heat capacity of a solid compound is equal to the • sum of the heat capacities of its constituent elements. • Richards’ rule: cal/degree • Trouton’s rule: cal/degree • In reactions in which a gas reacts with a condensed phase to produce • a condensed phase, the entropy change is that corresponding to the • disappearance of the gas.
First Approximations Richards’ rule: Trouton’s rule: cal/degree cal/degree
Numerical Example • A quantity of supercooled liquid Tin is adiabatically contained at 495 K. • Calculate the fraction of the Tin which spontaneously freezes. Given J at Tm = 505 K 505 K 495 K x moles of solid (1-x) moles of liquid 1 mole of liquid
Thermodynamics 교과과정 이해에 대한 Check Point - I
First Law of thermodynamics • Microscopic vs. Macroscopic View Point의 이해 • State function vs. Process variable, 기타 용어의 이해 • 열역학 1법칙의 탄생 과정, 1법칙 중요성의 이해 • Special processes의 중요성 이해, 응용력 • Constant-Volume Process: ΔU = qv • Constant-Pressure Process: ΔH = qp • 3. Reversible Adiabatic Process: q = 0 • 4. Reversible Isothermal Process: ΔU = ΔH = 0
Second Law of thermodynamics • (Mechanical, Thermal, Chemical) Irreversibility • Irreversibility vs. Creation of Irreversible Entropy • Maximum Entropy, Minimum Internal Energy as a Criterion of Equilibrium
Statistical Thermodynamics • Statistical Thermodynamics 의 개본 개념 이해 • Ideal Gas에 대한 Statistical Thermodynamics의 응용력 • 통계열역학 개념을 통한 엔트로피의 이해 • Heat capacity 계산에의 응용 • Heat capacity at low temperature
Criterion of Thermodynamic Equilibrium, Thermodynamic Relations • Helmholtz Free Energy, Gibbs Free Energy의 탄생 배경 • Free energy minimum과 equilibrium 간의 상관관계 • Chemical Potential의 정의, Gibbs energy와의 관계 • Chemical Work으로서의 term • Thermodynamic Relation 들의 응용력, 중요성 이해
Application of Criterion • 1기압하Pb의melting point 는600K이다. • 1기압하590K로과냉된액상Pb가응고하는것은 • 자발적인반응이라는것을 • (1) maximum-entropy criterion과 • (2) minimum-Gibbs-Energy criterion을이용하여보이시오. 2. 1번문제에서의Pb가단열된용기에보관되어있었다면 용기내부는결국어떠한(평형)상태가될것인지예측하시오.
Numerical Example • A quantity of supercooled liquid Tin is adiabatically contained at 495 K. • Calculate the fraction of the Tin which spontaneously freezes. Given J at Tm = 505 K 505 K 495 K x moles of solid (1-x) moles of liquid 1 mole of liquid
Example - Phase Transformation of Graphite to Diamond • Calculate graphite→diamond transformation pressure at 298 K, given • H298,gra – H298,dia = -1900 J • S298,gra = 5.74 J/K • S298,dia = 2.37 J/K • density of graphite at 298 K = 2.22 g/cm3 • density of diamond at 298 K = 3.515 g/cm3
Gibbs Energy for a Unary System • V(T,P) based on expansivity and compressibility • Cp(T) • S298: by integrating Cp/T from 0 to 298 K and using 3rd law of thermodynamics • (the entropy of any homogeneous substance in complete internal • equilibrium may be taken as zero at 0 K) • H298: from first principles calculations, but generally unknown • ※ H298 becomes a reference value for GT • ※ Introduction of Standard State