If I spend more than 45 minutes on it, you have permission to take a nap.

Slides:



Advertisements
Similar presentations
Aka the Law of conservation of energy, Gibbs in 1873 stated energy cannot be created or destroyed, only transferred by any process The net change in energy.
Advertisements

AP CHEMISTRY CHAPTER 6 NOTES THERMOCHEMISTRY
CAUSES OF CHANGE Order and Spontaneity. Enthalpy and Reactions Some reactions happen easily, but some others do not. Sodium and chlorine readily react.
Chapter 16 Chemical and Phase Equilibrium Study Guide in PowerPoint to accompany Thermodynamics: An Engineering Approach, 5th edition by Yunus.
Standard Enthalpy (Ch_6.6) The heat change that results when 1 mole of a compound is formed from its elements at a pressure of 1 Atm.
Slide 1 of The First Law of Thermodynamics  Internal Energy, U.  Total energy (potential and kinetic) in a system. Translational kinetic energy.
Microstates of Entropy
Chapter 19 Chemical Thermodynamics
Thermochemistry Chapter 6 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Equilibrium Equilibrium Constant, K (or K eq ) describes conditions AT equilibrium CaCO 3(calcite) + H +  Ca 2+ + HCO 3 -
Thermodynamics Chapter 19 Liquid benzene Production of quicklime Solid benzene ⇅ CaCO 3 (s) ⇌ CaO + CO 2.
Thermal Physics Chapter 10. Zeroth Law of Thermodynamics If objects A and B are in thermal equilibrium with a third object, C, then A and B are in thermal.
System. surroundings. universe.
Thermodynamics Chapter 19 Liquid benzene Production of quicklime Solid benzene ⇅ CaCO 3 (s) ⇌ CaO + CO 2.
© 2006 Brooks/Cole - Thomson Some Thermodynamic Terms Notice that the energy change in moving from the top to the bottom is independent of pathway but.
Chemical Thermodynamics © 2009, Prentice-Hall, Inc. Chapter 19 Chemical Thermodynamics Chemistry, The Central Science, 11th edition Theodore L. Brown;
ME 475/675 Introduction to Combustion
Section 1.3.  Limiting reactant  Excess reactant  Yields:  Theoretical yield  Percentage yield  Experimental yield  Avogadro’s law  Molar volume.
Pressure Volume Work Heats of reaction can be measured either at constant pressure, giving q P or ∆H values, or at constant volume, giving q V or ∆U values.
Chemical Thermodynamics Chapter 19 (except 19.7!).
Thermodynamics Chapter st Law of Thermodynamics Energy is conserved.  E = q + w.
CHAPTER 15 : KINETIC THEORY OF GASSES
Chapter 10 Energy 10.1 The Nature of Energy Energy- the ability to do work or produce heat Potential energy- energy due to position or composition Kinetic.
Chapter 19 Chemical Thermodynamics Lecture Presentation John D. Bookstaver St. Charles Community College Cottleville, MO © 2012 Pearson Education, Inc.
Chapter 19 Chemical Thermodynamics John D. Bookstaver St. Charles Community College St. Peters, MO 2006, Prentice Hall, Inc. Modified by S.A. Green, 2006.
Spontaneity, Entropy, and Free Energy
Chapter 19 Chemical Thermodynamics. First Law of Thermodynamics Energy cannot be created nor destroyed. Therefore, the total energy of the universe is.
Thermodynamics Chapter 18.
Chapter 20: Thermodynamics
First Law of Thermodynamics  You will recall from Chapter 5 that energy cannot be created nor destroyed.  Therefore, the total energy of the universe.
THERMODYNAMICS!!!! Nick Fox Dan Voicu.
Chapter 19 Chemical Thermodynamics HW:
Chapter 8 Thermochemistry. Thermodynamics  Study of the changes in energy and transfers of energy that accompany chemical and physical processes.  address.
1 Thermal Physics Chapter Thermodynamics Concerned with the concepts of energy transfers between a system and its environment and the resulting.
Gibbs and the Law of Entropy
ENTHALPY, HESS’ LAW, AND THERMOCHEMICAL EQUATIONS.
Chemical Thermodynamics © 2009, Prentice-Hall, Inc. Topic 9 Chapter 18 Chemical Thermodynamics.
General Chemistry M. R. Naimi-Jamal Faculty of Chemistry Iran University of Science & Technology.
Dr Ku Syahidah Ku Ismail CHAPTER 5 STANDARD THERMODYNAMIC FUNCTIONS OF REACTION.
By HANN ILYANI ZULHAIMI ERT 108 PHYSICAL CHEMISTRY THE FIRST LAW OF THERMODYNAMICS.
Thermochemistry Chapter 6 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Thermochemistry! AP Chapter 5. Temperature vs. Heat Temperature is the average kinetic energy of the particles in a substance. Heat is the energy that.
Thermodynamics Thermodynamics Thermodynamics Way to calculate if a reaction will occur Way to calculate if a reaction will occur Kinetics Kinetics Way.
Thermodynamics. study of energy changes that accompany physical and chemical processes. Thermochemistry is one component of thermodynamics which focuses.
Chemistry 231 Thermodynamics in Reacting Systems.
Chapter 10 Thermal Physics. Thermal physics is the study of Temperature Heat How these affect matter.
Thermodynamics Chapter 15. Part I Measuring Energy Changes.
1 Material was developed by combining Janusa’s material with the lecture outline provided with Ebbing, D. D.; Gammon, S. D. General Chemistry, 8th ed.,
Is this your room? Then you already know about entropy.
Theory of dilute electrolyte solutions and ionized gases
3 Enthalpy. Units SI unit = joule 1KJ = 1000J = cal 1st law of Thermodynamics The total energy of the universe is constant i.e energy cannot be.
Energy Basics. Part 1: The Relationship Between Matter and Energy 1.Define matter and energy Matter is anything that occupies space and has mass. Energy.
Energy The capacity to do work or to produce heat.
Chemical Thermodynamics © 2009, Prentice-Hall, Inc. Chapter 19 Chemical Thermodynamics Chemistry, The Central Science, 11th edition Theodore L. Brown;
1. Which of the following is NOT a conversion factor for 1 mole of a substance? A. 1.0 g B. molar mass C X particles D L E. Avogadro’s.
CHAPTER 19 CHEMICAL THERMODYNAMICS SECTION 3 THE MOLECULAR INTERPRETATION OF ENTROPY.
Heat and Energy of Ractions Chapter 10 Energy World of Chemistry Zumdahl Last revision Fall 2009.
Entropy Review  Determine whether the entropy is increasing or decreasing for each of the following and why?  Loading the dishwasher  Condensation of.
Chemical Thermodynamics First Law of Thermodynamics You will recall from earlier this year that energy cannot be created nor destroyed. Therefore, the.
Thermal Physics Chapter 10. Thermodynamics Concerned with the concepts of energy transfers between a system and its environment and the resulting temperature.
Chemical Equilibrium Reactants Products Reactants Products As the time increases… [Reactants] decrease, so the rate of forward reaction decreases; [Products]
If I spend more than 45 minutes on it, you have permission to take a nap.
Thermodynamics Thermodynamics Thermodynamics Way to calculate if a reaction will occur Way to calculate if a reaction will occur Kinetics Kinetics Way.
Thermodynamics Chander Gupta and Matt Hagopian. Introduction into Thermo Thermodynamics is the study of energy and its transformations Thermochemistry.
Solution of Thermodynamics: Theory and applications
Calculating gas volumes and concentrations of solutions
Presentation transcript:

If I spend more than 45 minutes on it, you have permission to take a nap

* To provide a self-consistent way of predicting the “thermo-physical” properties of matter at a known temperature and pressure * To calculate if a chemical reaction will absorb or release heat * To calculate if a reaction will occur spontaneously * To calculate the efficiency of an engine * To calculate the volume of a gas * To calculate the equilibrium partitioning of a species among various phases

* The energy (U) contained within an atom, molecule, or group of molecules can be defined in absolute or relative terms * Absolute terms (from macro to micro) – the energy within a O2 gas molecule in earth’s atmosphere * Velocity of the Milky-way galaxy (translation energy) + * Velocity of the Solar system (translation energy) + * Velocity of the Earth orbit (translation energy) + * Velocity of the Earth rotation (translation energy) + * Velocity of the O 2 molecule in X-Y-Z motion (translation) + * Rotation of the O 2 molecule around its axis (rotational energy) + * Vibration of the O 2 molecule (vibrational energy)) * Orbital energy of the bonding electrons (electronic energy) * Intrinsic energy of the O 2 molecule (mC 2 )

* Eliminate the external energy’s applied to the atom. Set those values to zero and work from there. * Relative energy of an O2 molecule * Energy of 1 mole O2 at 0C and 1atm = 0 * Likewise for other elements/molecules at a given reference point * Energy of 1 mole H2 at 0C and 1atm = 0 OK – but before we get there, let’s start from the beginning

* Back as early as the 166o’s, Robert Boyle, using a novel J-tube manometer, measured the property of a gas and concluded that the pressure and volume vary inversely:

* Guillaume Amontons ( ), * qualitatively identified that gas volumes increased linearly with temperature. * proposed a gas volume extinction point (an absolute zero) * Jaques Charles ( ) * Gas volume and temperature are proportional (unpublished) * Joseph Louis Gay-Lussac ( ) * If a gas mass and pressure are held constant then the volume varies linearly with temperature. This is an equation of state. K is an equilibrium constant

Represent equilibrium for every chemical reaction “=“ sets equilibrium. Activities (concentration) of products and reactants are linked to system energy

* Knowing the energy of each component (species) will enable us to predict it relative activity (or concentration) * Therefore, a species energy is the ultimate property, not the equilibrium constant

The energies of each species at 25 C and 1 atm in pure water (G 25C,1atm ). These values can be found in reference books. If 1.0 mole of calcite reacts (dissolves) to form 1.0 mole of Ca +2 and CO 3 -2, the energy difference is: That is: KJ of energy must be added to the system in the form of heat, work, or entropy to dissolve one mole of CaCO 3 at 25C and 1atm.

The energies of each species at 100 C and 100 atm in pure water. These values must be computed from an equation of state. If 1.0 mole of calcite reacts (dissolves) to form 1.0 mole of Ca +2 and CO 3 -2, the energy difference is: KJ of energy must be added to dissolve one mole of CaCO 3 at 100C and 100atm.

The energies of each species at 25 C and 1 atm in pure water (G 25C,1atm ). These values can be found in reference books. If 1.0 mole of halite reacts (dissolves) to form 1.0 mole of Na +2 and Cl -, the energy difference is: That is: KJ of energy must be added to the system in the form of heat, work, or entropy to dissolve one mole of halite at 25C and 1atm.

* There are two ∆G’s * The Standard State ∆G o, which is a function of temperature and pressure * Chemical bonding * Work, Potential Energy * Entropy * The excess ∆G E, which is a function of other factors * Concentration * Electric fields * Solvent Dielectric constants Used to calculate the equilibrium constants Used to calculate the activity coefficients We are interested in G 0. G E is discussed in the Activity coefficient section

What is the standard State? The standard state refers to a thermodynamic value at a defined state (temperature, pressure and concentration) Aqueous: The hypothetical 1.0 molal solution extrapolated from infinite dilution 1 molal PropertyProperty

General Thermodynamic Equations Vapor-Aqueous

General Thermodynamic Equations Non-Aqueous Liquid-Aqueous

The evaluation of the following equation is central to any chemical modeling: This value is our goal This is true at 25 C only

Effects of Temperature

The energies of each species at 25 C and 1 atm in pure water (G 25C,1atm ). These values can be found in reference books. If 1.0 mole of halite reacts (dissolves) to form 1.0 mole of Na +2 and Cl -, the energy difference is: That is: KJ of energy must be added to the system in the form of heat, work, or entropy to dissolve one mole of halite at 25C and 1atm.

At 25C, At 100C,

Working since 1968, Helgeson, et.al., have found that the standard-state thermodynamic property of any species in water can be represented by a function with seven terms which have specific values for each species. These seven terms (a 1-4, c 1-2, and  ) are integration constants for volume (a), heat capacity (c ) and temperature and pressure properties of water (  ). They are independent of the data system used to obtain them.