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On Entropy, Information, and Conservation of Information
entropy Article On Entropy, Information, and Conservation of Information Yunus A. Çengel Department of Mechanical Engineering, University of Nevada, Reno, NV 89557, USA; [email protected] Abstract: The term entropy is used in different meanings in different contexts, sometimes in contradic- tory ways, resulting in misunderstandings and confusion. The root cause of the problem is the close resemblance of the defining mathematical expressions of entropy in statistical thermodynamics and information in the communications field, also called entropy, differing only by a constant factor with the unit ‘J/K’ in thermodynamics and ‘bits’ in the information theory. The thermodynamic property entropy is closely associated with the physical quantities of thermal energy and temperature, while the entropy used in the communications field is a mathematical abstraction based on probabilities of messages. The terms information and entropy are often used interchangeably in several branches of sciences. This practice gives rise to the phrase conservation of entropy in the sense of conservation of information, which is in contradiction to the fundamental increase of entropy principle in thermody- namics as an expression of the second law. The aim of this paper is to clarify matters and eliminate confusion by putting things into their rightful places within their domains. The notion of conservation of information is also put into a proper perspective. Keywords: entropy; information; conservation of information; creation of information; destruction of information; Boltzmann relation Citation: Çengel, Y.A. On Entropy, 1. Introduction Information, and Conservation of One needs to be cautious when dealing with information since it is defined differently Information. Entropy 2021, 23, 779. -
ENERGY, ENTROPY, and INFORMATION Jean Thoma June
ENERGY, ENTROPY, AND INFORMATION Jean Thoma June 1977 Research Memoranda are interim reports on research being conducted by the International Institute for Applied Systems Analysis, and as such receive only limited scientific review. Views or opinions contained herein do not necessarily represent those of the Institute or of the National Member Organizations supporting the Institute. PREFACE This Research Memorandum contains the work done during the stay of Professor Dr.Sc. Jean Thoma, Zug, Switzerland, at IIASA in November 1976. It is based on extensive discussions with Professor HAfele and other members of the Energy Program. Al- though the content of this report is not yet very uniform because of the different starting points on the subject under consideration, its publication is considered a necessary step in fostering the related discussion at IIASA evolving around th.e problem of energy demand. ABSTRACT Thermodynamical considerations of energy and entropy are being pursued in order to arrive at a general starting point for relating entropy, negentropy, and information. Thus one hopes to ultimately arrive at a common denominator for quanti- ties of a more general nature, including economic parameters. The report closes with the description of various heating appli- cation.~and related efficiencies. Such considerations are important in order to understand in greater depth the nature and composition of energy demand. This may be highlighted by the observation that it is, of course, not the energy that is consumed or demanded for but the informa- tion that goes along with it. TABLE 'OF 'CONTENTS Introduction ..................................... 1 2 . Various Aspects of Entropy ........................2 2.1 i he no me no logical Entropy ........................ -
James Clerk Maxwell
James Clerk Maxwell JAMES CLERK MAXWELL Perspectives on his Life and Work Edited by raymond flood mark mccartney and andrew whitaker 3 3 Great Clarendon Street, Oxford, OX2 6DP, United Kingdom Oxford University Press is a department of the University of Oxford. It furthers the University’s objective of excellence in research, scholarship, and education by publishing worldwide. Oxford is a registered trade mark of Oxford University Press in the UK and in certain other countries c Oxford University Press 2014 The moral rights of the authors have been asserted First Edition published in 2014 Impression: 1 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, without the prior permission in writing of Oxford University Press, or as expressly permitted by law, by licence or under terms agreed with the appropriate reprographics rights organization. Enquiries concerning reproduction outside the scope of the above should be sent to the Rights Department, Oxford University Press, at the address above You must not circulate this work in any other form and you must impose this same condition on any acquirer Published in the United States of America by Oxford University Press 198 Madison Avenue, New York, NY 10016, United States of America British Library Cataloguing in Publication Data Data available Library of Congress Control Number: 2013942195 ISBN 978–0–19–966437–5 Printed and bound by CPI Group (UK) Ltd, Croydon, CR0 4YY Links to third party websites are provided by Oxford in good faith and for information only. -
Bluff Your Way in the Second Law of Thermodynamics
Bluff your way in the Second Law of Thermodynamics Jos Uffink Department of History and Foundations of Science Utrecht University, P.O.Box 80.000, 3508 TA Utrecht, The Netherlands e-mail: uffi[email protected] 5th July 2001 ABSTRACT The aim of this article is to analyse the relation between the second law of thermodynamics and the so-called arrow of time. For this purpose, a number of different aspects in this arrow of time are distinguished, in particular those of time-(a)symmetry and of (ir)reversibility. Next I review versions of the second law in the work of Carnot, Clausius, Kelvin, Planck, Gibbs, Caratheodory´ and Lieb and Yngvason, and investigate their connection with these aspects of the arrow of time. It is shown that this connection varies a great deal along with these formulations of the second law. According to the famous formulation by Planck, the second law expresses the irreversibility of natural processes. But in many other formulations irreversibility or even time-asymmetry plays no role. I therefore argue for the view that the second law has nothing to do with the arrow of time. KEY WORDS: Thermodynamics, Second Law, Irreversibility, Time-asymmetry, Arrow of Time. 1 INTRODUCTION There is a famous lecture by the British physicist/novelist C. P. Snow about the cul- tural abyss between two types of intellectuals: those who have been educated in literary arts and those in the exact sciences. This lecture, the Two Cultures (1959), characterises the lack of mutual respect between them in a passage: A good many times I have been present at gatherings of people who, by the standards of the traditional culture, are thought highly educated and who have 1 with considerable gusto been expressing their incredulity at the illiteracy of sci- entists. -
Arxiv:1806.08325V1 [Quant-Ph] 21 Jun 2018 Between Particle Number and Energy, in the Same Way That Temperature T Acts As an Exchange Rate Between Entropy and Energy
Quantum Thermodynamics book Quantum thermodynamics with multiple conserved quantities Erick Hinds-Mingo,1 Yelena Guryanova,2 Philippe Faist,3 and David Jennings4, 1 1QOLS, Blackett Laboratory, Imperial College London, London SW7 2AZ, United Kingdom 2Institute for Quantum Optics and Quantum Information (IQOQI), Boltzmanngasse 3 1090, Vienna, Austria 3Institute for Quantum Information and Matter, Caltech, Pasadena CA, 91125 USA 4Department of Physics, University of Oxford, Oxford, OX1 3PU, United Kingdom (Dated: June 22, 2018) In this chapter we address the topic of quantum thermodynamics in the presence of additional observables beyond the energy of the system. In particular we discuss the special role that the generalized Gibbs ensemble plays in this theory, and derive this state from the perspectives of a micro-canonical ensemble, dynamical typicality and a resource-theory formulation. A notable obsta- cle occurs when some of the observables do not commute, and so it is impossible for the observables to simultaneously take on sharp microscopic values. We show how this can be circumvented, discuss information-theoretic aspects of the setting, and explain how thermodynamic costs can be traded between the different observables. Finally, we discuss open problems and future directions for the topic. INTRODUCTION Thermodynamics has been remarkable in its applicability to a vast array of systems. Indeed, the laws of macroscopic thermodynamics have been successfully applied to the studies of magnetization [1, 2], superconductivity [3], cosmology [4], chemical reactions [5] and biological phenomena [6, 7], to name a few fields. In thermodynamics, energy plays a key role as a thermodynamic potential, that is, as a function of the other thermodynamic variables which characterizes all the thermodynamic properties of the system. -
31 Jan 2021 Laws of Thermodynamics . L01–1 Review of Thermodynamics. 1
31 jan 2021 laws of thermodynamics . L01{1 Review of Thermodynamics. 1: The Basic Laws What is Thermodynamics? • Idea: The study of states of physical systems that can be characterized by macroscopic variables, usu- ally equilibrium states (mechanical, thermal or chemical), and possible transformations between them. It started as a phenomenological subject motivated by practical applications, but it gradually developed into a coherent framework that we will view here as the macroscopic counterpart to the statistical mechanics of the microscopic constituents, and provides the observational context in which to verify many of its predictions. • Plan: We will mostly be interested in internal states, so the allowed processes will include heat exchanges and the main variables will always include the internal energy and temperature. We will recall the main facts (definitions, laws and relationships) of thermodynamics and discuss physical properties that characterize different substances, rather than practical applications such as properties of specific engines. The connection with statistical mechanics, based on a microscopic model of each system, will be established later. States and State Variables for a Thermodynamical System • Energy: The internal energy E is the central quantity in the theory, and is seen as a function of some complete set of variables characterizing each state. Notice that often energy is the only relevant macroscopic conservation law, while momentum, angular momentum or other quantities may not need to be considered. • Extensive variables: For each system one can choose a set of extensive variables (S; X~ ) whose values specify ~ the equilibrium states of the system; S is the entropy and the X are quantities that may include V , fNig, ~ ~ q, M, ~p, L, .. -
Lecture 4: 09.16.05 Temperature, Heat, and Entropy
3.012 Fundamentals of Materials Science Fall 2005 Lecture 4: 09.16.05 Temperature, heat, and entropy Today: LAST TIME .........................................................................................................................................................................................2� State functions ..............................................................................................................................................................................2� Path dependent variables: heat and work..................................................................................................................................2� DEFINING TEMPERATURE ...................................................................................................................................................................4� The zeroth law of thermodynamics .............................................................................................................................................4� The absolute temperature scale ..................................................................................................................................................5� CONSEQUENCES OF THE RELATION BETWEEN TEMPERATURE, HEAT, AND ENTROPY: HEAT CAPACITY .......................................6� The difference between heat and temperature ...........................................................................................................................6� Defining heat capacity.................................................................................................................................................................6� -
HEAT and TEMPERATURE Heat Is a Type of ENERGY. When Absorbed
HEAT AND TEMPERATURE Heat is a type of ENERGY. When absorbed by a substance, heat causes inter-particle bonds to weaken and break which leads to a change of state (solid to liquid for example). Heat causing a phase change is NOT sufficient to cause an increase in temperature. Heat also causes an increase of kinetic energy (motion, friction) of the particles in a substance. This WILL cause an increase in TEMPERATURE. Temperature is NOT energy, only a measure of KINETIC ENERGY The reason why there is no change in temperature at a phase change is because the substance is using the heat only to change the way the particles interact (“stick together”). There is no increase in the particle motion and hence no rise in temperature. THERMAL ENERGY is one type of INTERNAL ENERGY possessed by an object. It is the KINETIC ENERGY component of the object’s internal energy. When thermal energy is transferred from a hot to a cold body, the term HEAT is used to describe the transferred energy. The hot body will decrease in temperature and hence in thermal energy. The cold body will increase in temperature and hence in thermal energy. Temperature Scales: The K scale is the absolute temperature scale. The lowest K temperature, 0 K, is absolute zero, the temperature at which an object possesses no thermal energy. The Celsius scale is based upon the melting point and boiling point of water at 1 atm pressure (0, 100o C) K = oC + 273.13 UNITS OF HEAT ENERGY The unit of heat energy we will use in this lesson is called the JOULE (J). -
Statistical Physics Problem Sets 5–8: Statistical Mechanics
Statistical Physics xford hysics Second year physics course A. A. Schekochihin and A. Boothroyd (with thanks to S. J. Blundell) Problem Sets 5{8: Statistical Mechanics Hilary Term 2014 Some Useful Constants −23 −1 Boltzmann's constant kB 1:3807 × 10 JK −27 Proton rest mass mp 1:6726 × 10 kg 23 −1 Avogadro's number NA 6:022 × 10 mol Standard molar volume 22:414 × 10−3 m3 mol−1 Molar gas constant R 8:315 J mol−1 K−1 1 pascal (Pa) 1 N m−2 1 standard atmosphere 1:0132 × 105 Pa (N m−2) 1 bar (= 1000 mbar) 105 N m−2 Stefan{Boltzmann constant σ 5:67 × 10−8 Wm−2K−4 2 PROBLEM SET 5: Foundations of Statistical Mechanics If you want to try your hand at some practical calculations first, start with the Ideal Gas questions Maximum Entropy Inference 5.1 Factorials. a) Use your calculator to work out ln 15! Compare your answer with the simple version of Stirling's formula (ln N! ≈ N ln N − N). How big must N be for the simple version of Stirling's formula to be correct to within 2%? b∗) Derive Stirling's formula (you can look this up in a book). If you figure out this derivation, you will know how to calculate the next term in the approximation (after N ln N − N) and therefore how to estimate the precision of ln N! ≈ N ln N − N for any given N without calculating the factorials on a calculator. Check the result of (a) using this method. -
Influence of Boundary Conditions on Statistical Properties of Ideal Bose
PHYSICAL REVIEW E, VOLUME 65, 036129 Influence of boundary conditions on statistical properties of ideal Bose-Einstein condensates Martin Holthaus* Fachbereich Physik, Carl von Ossietzky Universita¨t, D-26111 Oldenburg, Germany Kishore T. Kapale and Marlan O. Scully Max-Planck-Institut fu¨r Quantenoptik, D-85748 Garching, Germany and Department of Physics and Institute for Quantum Studies, Texas A&M University, College Station, Texas 77843 ͑Received 23 October 2001; published 27 February 2002͒ We investigate the probability distribution that governs the number of ground-state particles in a partially condensed ideal Bose gas confined to a cubic volume within the canonical ensemble. Imposing either periodic or Dirichlet boundary conditions, we derive asymptotic expressions for all its cumulants. Whereas the conden- sation temperature becomes independent of the boundary conditions in the large-system limit, as implied by Weyl’s theorem, the fluctuation of the number of condensate particles and all higher cumulants remain sensi- tive to the boundary conditions even in that limit. The implications of these findings for weakly interacting Bose gases are briefly discussed. DOI: 10.1103/PhysRevE.65.036129 PACS number͑s͒: 05.30.Ch, 05.30.Jp, 03.75.Fi ϭ When London, in 1938, wrote his now-famous papers on with 1/(kBT), where kB denotes Boltzmann’s constant. Bose-Einstein condensation of an ideal gas ͓1,2͔, he simply Note that the product runs over the excited states only, ex- considered a free system of N noninteracting Bose particles cluding the ground state ϭ0; the frequencies of the indi- without an external trapping potential, imposing periodic vidual oscillators being given by the excited-states energies boundary conditions on a cubic volume V. -
Restricted Agents in Thermodynamics and Quantum Information Theory
Research Collection Doctoral Thesis Restricted agents in thermodynamics and quantum information theory Author(s): Krämer Gabriel, Lea Philomena Publication Date: 2016 Permanent Link: https://doi.org/10.3929/ethz-a-010858172 Rights / License: In Copyright - Non-Commercial Use Permitted This page was generated automatically upon download from the ETH Zurich Research Collection. For more information please consult the Terms of use. ETH Library Diss. ETH No. 23972 Restricted agents in thermodynamics and quantum information theory A thesis submitted to attain the degree of DOCTOR OF SCIENCES of ETH ZURICH (Dr. sc. ETH Zurich) presented by Lea Philomena Kr¨amer Gabriel MPhysPhil, University of Oxford born on 18th July 1990 citizen of Germany accepted on the recommendation of Renato Renner, examiner Giulio Chiribella, co-examiner Jakob Yngvason, co-examiner 2016 To my family Acknowledgements First and foremost, I would like to thank my thesis supervisor, Prof. Renato Renner, for placing his trust in me from the beginning, and giving me the opportunity to work in his group. I am grateful for his continuous support and guidance, and I have always benefited greatly from the discussions we had | Renato without doubt has a clear vision, a powerful intuition, and a deep understanding of physics and information theory. Perhaps even more importantly, he has an exceptional gift for explaining complex subjects in a simple and understandable way. I would also like to thank my co-examiners Giulio Chiribella and Jakob Yngvason for agreeing to be part of my thesis committee, and for their input and critical questions in the discussions and conversations we had. -
Nonequilibrium Thermodynamics and Scale Invariance
Article Nonequilibrium Thermodynamics and Scale Invariance Leonid M. Martyushev 1,2,* and Vladimir Celezneff 3 1 Technical Physics Department, Ural Federal University, 19 Mira St., Ekaterinburg 620002, Russia 2 Institute of Industrial Ecology, Russian Academy of Sciences, 20 S. Kovalevskaya St., Ekaterinburg 620219, Russia 3 The Racah Institute of Physics, Hebrew University of Jerusalem, Jerusalem 91904, Israel; [email protected] * Correspondence: [email protected]; Tel.: +7-92-222-77-425 Academic Editors: Milivoje M. Kostic, Miguel Rubi and Kevin H. Knuth Received: 30 January 2017; Accepted: 14 March 2017; Published: 16 March 2017 Abstract: A variant of continuous nonequilibrium thermodynamic theory based on the postulate of the scale invariance of the local relation between generalized fluxes and forces is proposed here. This single postulate replaces the assumptions on local equilibrium and on the known relation between thermodynamic fluxes and forces, which are widely used in classical nonequilibrium thermodynamics. It is shown here that such a modification not only makes it possible to deductively obtain the main results of classical linear nonequilibrium thermodynamics, but also provides evidence for a number of statements for a nonlinear case (the maximum entropy production principle, the macroscopic reversibility principle, and generalized reciprocity relations) that are under discussion in the literature. Keywords: dissipation function; nonequilibrium thermodynamics; generalized fluxes and forces 1. Introduction Classical nonequilibrium thermodynamics is an important field of modern physics that was developed for more than a century [1–5]. It is fundamentally based on thermodynamics and statistical physics (including kinetic theory and theory of random processes) and is widely applied in biophysics, geophysics, chemistry, economics, etc.