Boltzmann's Statistical Mechanics Kinetic Theory of Ideal Gases In
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Solutes and Solution
Solutes and Solution The first rule of solubility is “likes dissolve likes” Polar or ionic substances are soluble in polar solvents Non-polar substances are soluble in non- polar solvents Solutes and Solution There must be a reason why a substance is soluble in a solvent: either the solution process lowers the overall enthalpy of the system (Hrxn < 0) Or the solution process increases the overall entropy of the system (Srxn > 0) Entropy is a measure of the amount of disorder in a system—entropy must increase for any spontaneous change 1 Solutes and Solution The forces that drive the dissolution of a solute usually involve both enthalpy and entropy terms Hsoln < 0 for most species The creation of a solution takes a more ordered system (solid phase or pure liquid phase) and makes more disordered system (solute molecules are more randomly distributed throughout the solution) Saturation and Equilibrium If we have enough solute available, a solution can become saturated—the point when no more solute may be accepted into the solvent Saturation indicates an equilibrium between the pure solute and solvent and the solution solute + solvent solution KC 2 Saturation and Equilibrium solute + solvent solution KC The magnitude of KC indicates how soluble a solute is in that particular solvent If KC is large, the solute is very soluble If KC is small, the solute is only slightly soluble Saturation and Equilibrium Examples: + - NaCl(s) + H2O(l) Na (aq) + Cl (aq) KC = 37.3 A saturated solution of NaCl has a [Na+] = 6.11 M and [Cl-] = -
THE SOLUBILITY of GASES in LIQUIDS Introductory Information C
THE SOLUBILITY OF GASES IN LIQUIDS Introductory Information C. L. Young, R. Battino, and H. L. Clever INTRODUCTION The Solubility Data Project aims to make a comprehensive search of the literature for data on the solubility of gases, liquids and solids in liquids. Data of suitable accuracy are compiled into data sheets set out in a uniform format. The data for each system are evaluated and where data of sufficient accuracy are available values are recommended and in some cases a smoothing equation is given to represent the variation of solubility with pressure and/or temperature. A text giving an evaluation and recommended values and the compiled data sheets are published on consecutive pages. The following paper by E. Wilhelm gives a rigorous thermodynamic treatment on the solubility of gases in liquids. DEFINITION OF GAS SOLUBILITY The distinction between vapor-liquid equilibria and the solubility of gases in liquids is arbitrary. It is generally accepted that the equilibrium set up at 300K between a typical gas such as argon and a liquid such as water is gas-liquid solubility whereas the equilibrium set up between hexane and cyclohexane at 350K is an example of vapor-liquid equilibrium. However, the distinction between gas-liquid solubility and vapor-liquid equilibrium is often not so clear. The equilibria set up between methane and propane above the critical temperature of methane and below the criti cal temperature of propane may be classed as vapor-liquid equilibrium or as gas-liquid solubility depending on the particular range of pressure considered and the particular worker concerned. -
Blackbody Radiation: (Vibrational Energies of Atoms in Solid Produce BB Radiation)
Independent study in physics The Thermodynamic Interaction of Light with Matter Mirna Alhanash Project in Physics Uppsala University Contents Abstract ................................................................................................................................................................................ 3 Introduction ......................................................................................................................................................................... 3 Blackbody Radiation: (vibrational energies of atoms in solid produce BB radiation) .................................... 4 Stefan-Boltzmann .............................................................................................................................................................. 6 Wien displacement law..................................................................................................................................................... 7 Photoelectric effect ......................................................................................................................................................... 12 Frequency dependence/Atom model & electron excitation .................................................................................. 12 Why we see colours ....................................................................................................................................................... 14 Optical properties of materials: .................................................................................................................................. -
Ludwig Boltzmann Was Born in Vienna, Austria. He Received His Early Education from a Private Tutor at Home
Ludwig Boltzmann (1844-1906) Ludwig Boltzmann was born in Vienna, Austria. He received his early education from a private tutor at home. In 1863 he entered the University of Vienna, and was awarded his doctorate in 1866. His thesis was on the kinetic theory of gases under the supervision of Josef Stefan. Boltzmann moved to the University of Graz in 1869 where he was appointed chair of the department of theoretical physics. He would move six more times, occupying chairs in mathematics and experimental physics. Boltzmann was one of the most highly regarded scientists, and universities wishing to increase their prestige would lure him to their institutions with high salaries and prestigious posts. Boltzmann himself was subject to mood swings and he joked that this was due to his being born on the night between Shrove Tuesday and Ash Wednesday (or between Carnival and Lent). Traveling and relocating would temporarily provide relief from his depression. He married Henriette von Aigentler in 1876. They had three daughters and two sons. Boltzmann is best known for pioneering the field of statistical mechanics. This work was done independently of J. Willard Gibbs (who never moved from his home in Connecticut). Together their theories connected the seemingly wide gap between the macroscopic properties and behavior of substances with the microscopic properties and behavior of atoms and molecules. Interestingly, the history of statistical mechanics begins with a mathematical prize at Cambridge in 1855 on the subject of evaluating the motions of Saturn’s rings. (Laplace had developed a mechanical theory of the rings concluding that their stability was due to irregularities in mass distribution.) The prize was won by James Clerk Maxwell who then went on to develop the theory that, without knowing the individual motions of particles (or molecules), it was possible to use their statistical behavior to calculate properties of a gas such as viscosity, collision rate, diffusion rate and the ability to conduct heat. -
AP Chemistry Chapter 5 Gases Ch
AP Chemistry Chapter 5 Gases Ch. 5 Gases Agenda 23 September 2017 Per 3 & 5 ○ 5.1 Pressure ○ 5.2 The Gas Laws ○ 5.3 The Ideal Gas Law ○ 5.4 Gas Stoichiometry ○ 5.5 Dalton’s Law of Partial Pressures ○ 5.6 The Kinetic Molecular Theory of Gases ○ 5.7 Effusion and Diffusion ○ 5.8 Real Gases ○ 5.9 Characteristics of Several Real Gases ○ 5.10 Chemistry in the Atmosphere 5.1 Units of Pressure 760 mm Hg = 760 Torr = 1 atm Pressure = Force = Newton = pascal (Pa) Area m2 5.2 Gas Laws of Boyle, Charles and Avogadro PV = k Slope = k V = k P y = k(1/P) + 0 5.2 Gas Laws of Boyle - use the actual data from Boyle’s Experiment Table 5.1 And Desmos to plot Volume vs. Pressure And then Pressure vs 1/V. And PV vs. V And PV vs. P Boyle’s Law 3 centuries later? Boyle’s law only holds precisely at very low pressures.Measurements at higher pressures reveal PV is not constant, but varies as pressure varies. Deviations slight at pressures close to 1 atm we assume gases obey Boyle’s law in our calcs. A gas that strictly obeys Boyle’s Law is called an Ideal gas. Extrapolate (extend the line beyond the experimental points) back to zero pressure to find “ideal” value for k, 22.41 L atm Look Extrapolatefamiliar? (extend the line beyond the experimental points) back to zero pressure to find “ideal” value for k, 22.41 L atm The volume of a gas at constant pressure increases linearly with the Charles’ Law temperature of the gas. -
THE SOLUBILITY of GASES in LIQUIDS INTRODUCTION the Solubility Data Project Aims to Make a Comprehensive Search of the Lit- Erat
THE SOLUBILITY OF GASES IN LIQUIDS R. Battino, H. L. Clever and C. L. Young INTRODUCTION The Solubility Data Project aims to make a comprehensive search of the lit erature for data on the solubility of gases, liquids and solids in liquids. Data of suitable accuracy are compiled into data sheets set out in a uni form format. The data for each system are evaluated and where data of suf ficient accuracy are available values recommended and in some cases a smoothing equation suggested to represent the variation of solubility with pressure and/or temperature. A text giving an evaluation and recommended values and the compiled data sheets are pUblished on consecutive pages. DEFINITION OF GAS SOLUBILITY The distinction between vapor-liquid equilibria and the solUbility of gases in liquids is arbitrary. It is generally accepted that the equilibrium set up at 300K between a typical gas such as argon and a liquid such as water is gas liquid solubility whereas the equilibrium set up between hexane and cyclohexane at 350K is an example of vapor-liquid equilibrium. However, the distinction between gas-liquid solUbility and vapor-liquid equilibrium is often not so clear. The equilibria set up between methane and propane above the critical temperature of methane and below the critical temperature of propane may be classed as vapor-liquid equilibrium or as gas-liquid solu bility depending on the particular range of pressure considered and the par ticular worker concerned. The difficulty partly stems from our inability to rigorously distinguish between a gas, a vapor, and a liquid, which has been discussed in numerous textbooks. -
The Philosophy and Physics of Time Travel: the Possibility of Time Travel
University of Minnesota Morris Digital Well University of Minnesota Morris Digital Well Honors Capstone Projects Student Scholarship 2017 The Philosophy and Physics of Time Travel: The Possibility of Time Travel Ramitha Rupasinghe University of Minnesota, Morris, [email protected] Follow this and additional works at: https://digitalcommons.morris.umn.edu/honors Part of the Philosophy Commons, and the Physics Commons Recommended Citation Rupasinghe, Ramitha, "The Philosophy and Physics of Time Travel: The Possibility of Time Travel" (2017). Honors Capstone Projects. 1. https://digitalcommons.morris.umn.edu/honors/1 This Paper is brought to you for free and open access by the Student Scholarship at University of Minnesota Morris Digital Well. It has been accepted for inclusion in Honors Capstone Projects by an authorized administrator of University of Minnesota Morris Digital Well. For more information, please contact [email protected]. The Philosophy and Physics of Time Travel: The possibility of time travel Ramitha Rupasinghe IS 4994H - Honors Capstone Project Defense Panel – Pieranna Garavaso, Michael Korth, James Togeas University of Minnesota, Morris Spring 2017 1. Introduction Time is mysterious. Philosophers and scientists have pondered the question of what time might be for centuries and yet till this day, we don’t know what it is. Everyone talks about time, in fact, it’s the most common noun per the Oxford Dictionary. It’s in everything from history to music to culture. Despite time’s mysterious nature there are a lot of things that we can discuss in a logical manner. Time travel on the other hand is even more mysterious. -
Useful Constants
Appendix A Useful Constants A.1 Physical Constants Table A.1 Physical constants in SI units Symbol Constant Value c Speed of light 2.997925 × 108 m/s −19 e Elementary charge 1.602191 × 10 C −12 2 2 3 ε0 Permittivity 8.854 × 10 C s / kgm −7 2 μ0 Permeability 4π × 10 kgm/C −27 mH Atomic mass unit 1.660531 × 10 kg −31 me Electron mass 9.109558 × 10 kg −27 mp Proton mass 1.672614 × 10 kg −27 mn Neutron mass 1.674920 × 10 kg h Planck constant 6.626196 × 10−34 Js h¯ Planck constant 1.054591 × 10−34 Js R Gas constant 8.314510 × 103 J/(kgK) −23 k Boltzmann constant 1.380622 × 10 J/K −8 2 4 σ Stefan–Boltzmann constant 5.66961 × 10 W/ m K G Gravitational constant 6.6732 × 10−11 m3/ kgs2 M. Benacquista, An Introduction to the Evolution of Single and Binary Stars, 223 Undergraduate Lecture Notes in Physics, DOI 10.1007/978-1-4419-9991-7, © Springer Science+Business Media New York 2013 224 A Useful Constants Table A.2 Useful combinations and alternate units Symbol Constant Value 2 mHc Atomic mass unit 931.50MeV 2 mec Electron rest mass energy 511.00keV 2 mpc Proton rest mass energy 938.28MeV 2 mnc Neutron rest mass energy 939.57MeV h Planck constant 4.136 × 10−15 eVs h¯ Planck constant 6.582 × 10−16 eVs k Boltzmann constant 8.617 × 10−5 eV/K hc 1,240eVnm hc¯ 197.3eVnm 2 e /(4πε0) 1.440eVnm A.2 Astronomical Constants Table A.3 Astronomical units Symbol Constant Value AU Astronomical unit 1.4959787066 × 1011 m ly Light year 9.460730472 × 1015 m pc Parsec 2.0624806 × 105 AU 3.2615638ly 3.0856776 × 1016 m d Sidereal day 23h 56m 04.0905309s 8.61640905309 -
Josiah Willard Gibbs
GENERAL ARTICLE Josiah Willard Gibbs V Kumaran The foundations of classical thermodynamics, as taught in V Kumaran is a professor textbooks today, were laid down in nearly complete form by of chemical engineering at the Indian Institute of Josiah Willard Gibbs more than a century ago. This article Science, Bangalore. His presentsaportraitofGibbs,aquietandmodestmanwhowas research interests include responsible for some of the most important advances in the statistical mechanics and history of science. fluid mechanics. Thermodynamics, the science of the interconversion of heat and work, originated from the necessity of designing efficient engines in the late 18th and early 19th centuries. Engines are machines that convert heat energy obtained by combustion of coal, wood or other types of fuel into useful work for running trains, ships, etc. The efficiency of an engine is determined by the amount of useful work obtained for a given amount of heat input. There are two laws related to the efficiency of an engine. The first law of thermodynamics states that heat and work are inter-convertible, and it is not possible to obtain more work than the amount of heat input into the machine. The formulation of this law can be traced back to the work of Leibniz, Dalton, Joule, Clausius, and a host of other scientists in the late 17th and early 18th century. The more subtle second law of thermodynamics states that it is not possible to convert all heat into work; all engines have to ‘waste’ some of the heat input by transferring it to a heat sink. The second law also established the minimum amount of heat that has to be wasted based on the absolute temperatures of the heat source and the heat sink. -
Episode 1: Phis Wants to Be a Physicist
Episode 1: Phis wants to be a physicist Illustration: Xia Hong Script: Xia Hong 12/2012 Phis is 14 years old. Like most kids of her age, she’s a bit anxious about finding the person inside her… She tried singing. Hmm… “You are very talented, Phis!” Her best friend Lizzy told her. Sports are also not her cup of tea… Episode 1: Phis wants to be a physicist 1 “I wish I could But why I’m short, but does height I’m very be as confident She’s smart. She’s pretty. matter?! confident! as Lizzy!” Phis And she is told her little taller than me! sister Chemi. No wonder she’s “Then I would so confident! know what I can do.” “Who says size doesn’t matter?” Phis is not convinced. “Just read the newspaper…” “It’s always good to be either really small or really big, not in between!” Even her name sounds sharp — it is the same as the Lizzy in Pride and Prejudice ! Chemi, don’t you think our names are a bit strange? Episode 1: Phis wants to be a physicist 2 Phis’s self-search reached a conclusion after a monthly Science Day event in school hosted by Ms. Allen. What I’ll show you today is the It is our fascinating pleasure world of to have quantum Prof. Lee mechanics. here. Imagine, we live in the quantum world. Quantum We have to comply to its rules, and behave very We no longer have a differently from certain answer for things our normal life. -
Ideal Gas Law PV = Nrt R = Universal Gas Constant R = 0.08206 L-Atm R = 8.314 J Mol-K Mol-K Example
Ideal gas law PV = nRT R = universal gas constant R = 0.08206 L-atm R = 8.314 J mol-K mol-K Example: In the reaction of oxygen with carbon to produce carbon dioxide, how many liters of oxygen at 747 mm Hg and 21.0 °C are needed to react with 24.022 g of carbon? CHEM 102 Winter 2011 Practice: In the reaction of oxygen and hydrogen to make water, how many liters of hydrogen at exactly 0 °C and 1 atm are needed to react with 10.0 g of oxygen? 2 CHEM 102 Winter 2011 Combined gas law V decreases with pressure (V α 1/P). V increases with temperature (V α T). V increases with particles (V α n). Combining these ideas: V α n x T P For a given amount of gas (constant number of particles, ninitial = nafter) that changes in volume, temperature, or pressure: Vinitial α ninitial x Tinitial Pinitial Vafter α nafter x Tafter Pafter ninitial = n after Vinitial x Pinitial = Vafter x Pafter Tinitial Tafter 3 CHEM 102 Winter 2011 Example: A sample of gas is pressurized to 1.80 atm and volume of 90.0 cm3. What volume would the gas have if it were pressurized to 4.00 atm without a change in temperature? 4 CHEM 102 Winter 2011 Example: A 2547-mL sample of gas is at 421 °C. What is the new gas temperature if the gas is cooled at constant pressure until it has a volume of 1616 mL? 5 CHEM 102 Winter 2011 Practice: A balloon is filled with helium. -
CEE 370 Environmental Engineering Principles Henry's
CEE 370 Lecture #7 9/18/2019 Updated: 18 September 2019 Print version CEE 370 Environmental Engineering Principles Lecture #7 Environmental Chemistry V: Thermodynamics, Henry’s Law, Acids-bases II Reading: Mihelcic & Zimmerman, Chapter 3 Davis & Masten, Chapter 2 Mihelcic, Chapt 3 David Reckhow CEE 370 L#7 1 Henry’s Law Henry's Law states that the amount of a gas that dissolves into a liquid is proportional to the partial pressure that gas exerts on the surface of the liquid. In equation form, that is: C AH = K p A where, CA = concentration of A, [mol/L] or [mg/L] KH = equilibrium constant (often called Henry's Law constant), [mol/L-atm] or [mg/L-atm] pA = partial pressure of A, [atm] David Reckhow CEE 370 L#7 2 Lecture #7 Dave Reckhow 1 CEE 370 Lecture #7 9/18/2019 Henry’s Law Constants Reaction Name Kh, mol/L-atm pKh = -log Kh -2 CO2(g) _ CO2(aq) Carbon 3.41 x 10 1.47 dioxide NH3(g) _ NH3(aq) Ammonia 57.6 -1.76 -1 H2S(g) _ H2S(aq) Hydrogen 1.02 x 10 0.99 sulfide -3 CH4(g) _ CH4(aq) Methane 1.50 x 10 2.82 -3 O2(g) _ O2(aq) Oxygen 1.26 x 10 2.90 David Reckhow CEE 370 L#7 3 Example: Solubility of O2 in Water Background Although the atmosphere we breathe is comprised of approximately 20.9 percent oxygen, oxygen is only slightly soluble in water. In addition, the solubility decreases as the temperature increases.