Efimov-Driven Phase Transitions of the Unitary Bose
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Equation of State for Benzene for Temperatures from the Melting Line up to 725 K with Pressures up to 500 Mpa†
High Temperatures-High Pressures, Vol. 41, pp. 81–97 ©2012 Old City Publishing, Inc. Reprints available directly from the publisher Published by license under the OCP Science imprint, Photocopying permitted by license only a member of the Old City Publishing Group Equation of state for benzene for temperatures from the melting line up to 725 K with pressures up to 500 MPa† MONIKA THOL ,1,2,* ERIC W. Lemm ON 2 AND ROLAND SPAN 1 1Thermodynamics, Ruhr-University Bochum, Universitaetsstrasse 150, 44801 Bochum, Germany 2National Institute of Standards and Technology, 325 Broadway, Boulder, Colorado 80305, USA Received: December 23, 2010. Accepted: April 17, 2011. An equation of state (EOS) is presented for the thermodynamic properties of benzene that is valid from the triple point temperature (278.674 K) to 725 K with pressures up to 500 MPa. The equation is expressed in terms of the Helmholtz energy as a function of temperature and density. This for- mulation can be used for the calculation of all thermodynamic properties. Comparisons to experimental data are given to establish the accuracy of the EOS. The approximate uncertainties (k = 2) of properties calculated with the new equation are 0.1% below T = 350 K and 0.2% above T = 350 K for vapor pressure and liquid density, 1% for saturated vapor density, 0.1% for density up to T = 350 K and p = 100 MPa, 0.1 – 0.5% in density above T = 350 K, 1% for the isobaric and saturated heat capaci- ties, and 0.5% in speed of sound. Deviations in the critical region are higher for all properties except vapor pressure. -
Geometrical Vortex Lattice Pinning and Melting in Ybacuo Submicron Bridges Received: 10 August 2016 G
www.nature.com/scientificreports OPEN Geometrical vortex lattice pinning and melting in YBaCuO submicron bridges Received: 10 August 2016 G. P. Papari1,*, A. Glatz2,3,*, F. Carillo4, D. Stornaiuolo1,5, D. Massarotti5,6, V. Rouco1, Accepted: 11 November 2016 L. Longobardi6,7, F. Beltram2, V. M. Vinokur2 & F. Tafuri5,6 Published: 23 December 2016 Since the discovery of high-temperature superconductors (HTSs), most efforts of researchers have been focused on the fabrication of superconducting devices capable of immobilizing vortices, hence of operating at enhanced temperatures and magnetic fields. Recent findings that geometric restrictions may induce self-arresting hypervortices recovering the dissipation-free state at high fields and temperatures made superconducting strips a mainstream of superconductivity studies. Here we report on the geometrical melting of the vortex lattice in a wide YBCO submicron bridge preceded by magnetoresistance (MR) oscillations fingerprinting the underlying regular vortex structure. Combined magnetoresistance measurements and numerical simulations unambiguously relate the resistance oscillations to the penetration of vortex rows with intermediate geometrical pinning and uncover the details of geometrical melting. Our findings offer a reliable and reproducible pathway for controlling vortices in geometrically restricted nanodevices and introduce a novel technique of geometrical spectroscopy, inferring detailed information of the structure of the vortex system through a combined use of MR curves and large-scale simulations. Superconductors are materials in which below the superconducting transition temperature, Tc, electrons form so-called Cooper pairs, which are bosons, hence occupying the same lowest quantum state1. The wave function of this Cooper condensate has a fixed phase. Hence, by virtue of the uncertainty principle, the number of Cooper pairs in the condensate is undefined. -
Phase Diagrams and Phase Separation
Phase Diagrams and Phase Separation Books MF Ashby and DA Jones, Engineering Materials Vol 2, Pergamon P Haasen, Physical Metallurgy, G Strobl, The Physics of Polymers, Springer Introduction Mixing two (or more) components together can lead to new properties: Metal alloys e.g. steel, bronze, brass…. Polymers e.g. rubber toughened systems. Can either get complete mixing on the atomic/molecular level, or phase separation. Phase Diagrams allow us to map out what happens under different conditions (specifically of concentration and temperature). Free Energy of Mixing Entropy of Mixing nA atoms of A nB atoms of B AM Donald 1 Phase Diagrams Total atoms N = nA + nB Then Smix = k ln W N! = k ln nA!nb! This can be rewritten in terms of concentrations of the two types of atoms: nA/N = cA nB/N = cB and using Stirling's approximation Smix = -Nk (cAln cA + cBln cB) / kN mix S AB0.5 This is a parabolic curve. There is always a positive entropy gain on mixing (note the logarithms are negative) – so that entropic considerations alone will lead to a homogeneous mixture. The infinite slope at cA=0 and 1 means that it is very hard to remove final few impurities from a mixture. AM Donald 2 Phase Diagrams This is the situation if no molecular interactions to lead to enthalpic contribution to the free energy (this corresponds to the athermal or ideal mixing case). Enthalpic Contribution Assume a coordination number Z. Within a mean field approximation there are 2 nAA bonds of A-A type = 1/2 NcAZcA = 1/2 NZcA nBB bonds of B-B type = 1/2 NcBZcB = 1/2 NZ(1- 2 cA) and nAB bonds of A-B type = NZcA(1-cA) where the factor 1/2 comes in to avoid double counting and cB = (1-cA). -
Two-Dimensional Vortex Lattice Melting Superconducting Length
Two-Dimensional Vortex Lattice Melting Superconducting Length-Scales and Vortex Lattices Flux Motion Melting Concepts Journal Paper Presentation: “Melting of the Vortex Lattice Through the Hexatic Phase in an MoGe3 Thin Film” 1 Repulsive Interaction Between Vortices Vortex Lattice 2 Vortex Melting in Superconducting Nb 3 (For 3D clean Type II superconductor) Vortex Lattice Expands on Freezing (Like Ice) Jump in the Magnetization 4 Melting Concepts 3D Solid Liquid Lindemann Criterion (∆r)2 ↵a 1st Order Transition ⇡ p 5 6 Journal Presentation Motivation/Context Results Interpretation Questions/Ideas for Future Work (aim for 30-45 mins) Please check the course site about the presentation schedule No class on The April 8, 15 Make-Ups on Ms April 12, 19 (Weekly Discussion to be Rescheduled) 7 First Definitive Observation of the Hexatic Phase in a Superconducting Film (with 8 thanks to Indranil Roy and Pratap Raychaudhuri) Two Dimensional Melting (BKT + HNY theory) 9 10 Hexatics have been observed in 2D colloidal systems Why not in the Melting of the Vortex Phase of Superconducting Films ?? 11 Quest for the Hexatic Liquid Phase in ↵ MoGe − Why Not Before ?? Orientational Coupling Hexatic Glass !! between Atomic and Vortex Lattices Solution: Amorphous Superconductor (no lattice effect) Very Weak Pinning BCS-Type Superconductor 12 Scanning Tunneling Spectroscopy (STS) Magnetotransport 13 14 15 16 17 The Resulting Phase Diagram 18 Summary First Observation of Hexatic Fluid Phase in a 2D Superconducting Film Pinning Significantly Weaker than in Previous Studies STS (imaging) Magnetotransport (“shear”) Questions/Ideas for the Future Size-Dependence of Hexatic Order Parameter ?? Low T limit of the Hexatic Fluid: Quantum Vortex Fluid ?? What happens in Layered Films ?? 19 20. -
Suppression of Phase Separation in Lifepo4 Nanoparticles
Suppression of Phase Separation in LiFePO4 Nanoparticles During Battery Discharge Peng Bai,†,§ Daniel A. Cogswell† and Martin Z. Bazant*,†,‡ †Department of Chemical Engineering and ‡Department of Mathematics, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA §State Key Laboratory of Automotive Safety and Energy, Department of Automotive Engineering, Tsinghua University, Beijing 100084, P. R. China *Corresponding author: Dr. Martin Z. Bazant. Tel: (617)258-7039; Fax: (617)258-5766; Email: [email protected] August 8, 2011 ABSTRACT: Using a novel electrochemical phase-field model, we question the common belief that LixFePO4 nanoparticles separate into Li-rich and Li-poor phases during battery discharge. For small currents, spinodal decomposition or nucleation leads to moving phase boundaries. Above a critical current density (in the Tafel regime), the spinodal disappears, and particles fill homogeneously, which may explain the superior rate capability and long cycle life of nano-LiFePO4 cathodes. KEYWORDS: Li-ion battery, LiFePO4, phase-field model, Butler-Volmer equation, spinodal decomposition, intercalation waves. 1 Introduction. – LiFePO4-based electrochemical energy storage is one of the most promising developments for electric vehicle power systems and other high-rate applications such as power tools 2,3 and renewable energy storage. Nanoparticles of LiFePO4 have recently been used to demonstrate ultrafast battery discharge4 and high power density carbon pseudocapacitors.5 However, the -
Sodium Spinor Bose-Einstein Condensates
SODIUM SPINOR BOSE-EINSTEIN CONDENSATES: ALL-OPTICAL PRODUCTION AND SPIN DYNAMICS By JIEJIANG BachelorofScienceinOpticalInformationScience UniversityofShanghaiforScienceandTechnology Shanghai,China 2009 SubmittedtotheFacultyofthe GraduateCollegeof OklahomaStateUniversity inpartialfulfillmentof therequirementsfor theDegreeof DOCTOROFPHILOSOPHY December,2015 COPYRIGHT c By JIE JIANG December, 2015 SODIUM SPINOR BOSE-EINSTEIN CONDENSATES: ALL-OPTICAL PRODUCTION AND SPIN DYNAMICS Dissertation Approved: Dr. Yingmei Liu Dissertation Advisor Dr. Albert T. Rosenberger Dr. Gil Summy Dr. Weili Zhang iii ACKNOWLEDGMENTS I would like to first express my sincere gratitude to my thesis advisor Dr. Yingmei Liu, who introduced ultracold quantum gases to me and guided me throughout my PhD study. I am greatly impressed by her profound knowledge, persistent enthusiasm and love in BEC research. It has been a truly rewarding and privilege experience to perform my PhD study under her guidance. I also want to thank my committee members, Dr. Albert Rosenberger, Dr. Gil Summy, and Dr. Weili Zhang for their advice and support during my PhD study. I thank Dr. Rosenberger for the knowledge in lasers and laser spectroscopy I learnt from him. I thank Dr. Summy for his support in the department and the academic exchange with his lab. Dr. Zhang offered me a unique opportunity to perform microfabrication in a cleanroom, which greatly extended my research experience. During my more than six years study at OSU, I had opportunities to work with many wonderful people and the team members in Liu’s lab have been providing endless help for me which is important to my work. Many thanks extend to my current colleagues Lichao Zhao, Tao Tang, Zihe Chen, and Micah Webb as well as our former members Zongkai Tian, Jared Austin, and Alex Behlen. -
1504.05850V4.Pdf
Compact Stars in the QCD Phase Diagram IV (CSQCD IV) September 26-30, 2014, Prerow, Germany http://www.ift.uni.wroc.pl/˜csqcdiv Entropic and enthalpic phase transitions in high energy density nuclear matter Igor Iosilevskiy1,2 1 Joint Institute for High Temperatures (Russian Academy of Sciences), Izhorskaya Str. 13/2, 125412 Moscow, Russia 2 Moscow Institute of Physics and Technology (State Research University), Dolgoprudny, 141700, Moscow Region, Russia 1 Abstract Features of Gas-Liquid (GL) and Quark-Hadron (QH) phase transitions (PT) in dense nuclear matter are under discussion in comparison with their terrestrial coun- terparts, e.g. so-called ”plasma” PT in shock-compressed hydrogen, nitrogen etc. Both, GLPT and QHPT, when being represented in widely accepted temperature – baryonic chemical potential plane, are often considered as similar, i.e. amenable to one-to-one mapping by simple scaling. It is argued that this impression is illusive and that GLPT and QHPT belong to different classes: GLPT is typical enthalpic PT (Van-der-Waals-like) while QHPT (”deconfinement-driven”) is typical entropic PT. Subdivision of 1st-order fluid-fluid phase transitions into enthalpic and entropic subclasses was proposed in [arXiv:1403.8053]. Properties of enthalpic and entropic PTs differ significantly. Entropic PT is always internal part of more general and ex- tended thermodynamic anomaly – domains with abnormal (negative) sign for the set of (usually positive) second derivatives of thermodynamic potential, e.g. Gruneizen and thermal expansion and thermal pressure coefficients etc. Negative sign of these derivatives lead to violation of standard behavior and relative order for many iso-lines in P –V plane, e.g. -
Melting of Lamellar Phases in Temperature Sensitive Colloid-Polymer Suspensions
PHYSICAL REVIEW LETTERS week ending VOLUME 93, NUMBER 5 30 JULY 2004 Melting of Lamellar Phases in Temperature Sensitive Colloid-Polymer Suspensions A. M. Alsayed, Z. Dogic, and A. G. Yodh Department of Physics and Astronomy, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6396, USA (Received 10 March 2004; published 29 July 2004) We prepare a novel suspension composed of rodlike fd virus and thermosensitive polymer poly(N-isopropylacrylamide) whose phase diagram is temperature and concentration dependent. The system exhibits a rich variety of stable and metastable phases, and provides a unique opportunity to directly observe melting of lamellar phases and single lamellae. Typically, lamellar phases swell with increasing temperature before melting into the nematic phase. The highly swollen lamellae can be superheated as a result of topological nucleation barriers that slow the formation of the nematic phase. DOI: 10.1103/PhysRevLett.93.057801 PACS numbers: 64.70.Md, 61.30.–v, 64.60.My Melting of three-dimensional (3D) crystals is among lamellar phases and coexisting isotropic or nematic the most ubiquitous phase transitions in nature [1]. In phases. contrast to freezing, melting of 3D crystals usually has The fd=NIPA solutions are unusual new materials no associated energy barrier. Bulk melting is initiated at a whose lamellar phases differ from those of amphiphilic premelted surface, which then acts as a heterogeneous molecules. The lamellar phase can swell considerably and nucleation site and eliminates the nucleation barrier for melt into a nematic phase, a transition almost never the phase transition [2]. In this Letter, we investigate observed in block-copolymer lamellar systems. -
Arxiv:2010.01933V2 [Cond-Mat.Quant-Gas] 18 Feb 2021 Tigated in Refs
Finite temperature spin dynamics of a two-dimensional Bose-Bose atomic mixture Arko Roy,1, ∗ Miki Ota,1, ∗ Alessio Recati,1, 2 and Franco Dalfovo1 1INO-CNR BEC Center and Universit`adi Trento, via Sommarive 14, I-38123 Trento, Italy 2Trento Institute for Fundamental Physics and Applications, INFN, 38123 Povo, Italy We examine the role of thermal fluctuations in uniform two-dimensional binary Bose mixtures of dilute ultracold atomic gases. We use a mean-field Hartree-Fock theory to derive analytical predictions for the miscible-immiscible transition. A nontrivial result of this theory is that a fully miscible phase at T = 0 may become unstable at T 6= 0, as a consequence of a divergent behaviour in the spin susceptibility. We test this prediction by performing numerical simulations with the Stochastic (Projected) Gross-Pitaevskii equation, which includes beyond mean-field effects. We calculate the equilibrium configurations at different temperatures and interaction strengths and we simulate spin oscillations produced by a weak external perturbation. Despite some qualitative agreement, the comparison between the two theories shows that the mean-field approximation is not able to properly describe the behavior of the two-dimensional mixture near the miscible-immiscible transition, as thermal fluctuations smoothen all sharp features both in the phase diagram and in spin dynamics, except for temperature well below the critical temperature for superfluidity. I. INTRODUCTION ing the Popov theory. It is then natural to ask whether such a phase-transition also exists in 2D. The study of phase-separation in two-component clas- It is worth stressing that, in 2D Bose gases, thermal sical fluids is of paramount importance and the role of fluctuations are much more important than in 3D, as they temperature can be rather nontrivial. -
Physical Changes
How Matter Changes By Cindy Grigg Changes in matter happen around you every day. Some changes make matter look different. Other changes make one kind of matter become another kind of matter. When you scrunch a sheet of paper up into a ball, it is still paper. It only changed shape. You can cut a large, rectangular piece of paper into many small triangles. It changed shape and size, but it is still paper. These kinds of changes are called physical changes. Physical changes are changes in the way matter looks. Changes in size and shape, like the changes in the cut pieces of paper, are physical changes. Physical changes are changes in the size, shape, state, or appearance of matter. Another kind of physical change happens when matter changes from one state to another state. When water freezes and makes ice, it is still water. It has only changed its state of matter from a liquid to a solid. It has changed its appearance and shape, but it is still water. You can change the ice back into water by letting it melt. Matter looks different when it changes states, but it stays the same kind of matter. Solids like ice can change into liquids. Heat speeds up the moving particles in ice. The particles move apart. Heat melts ice and changes it to liquid water. Metals can be changed from a solid to a liquid state also. Metals must be heated to a high temperature to melt. Melting is changing from a solid state to a liquid state. -
Nucleation Initiated Spinodal Decomposition in a Polymerizing System Thein Yk U University of Akron Main Campus, [email protected]
The University of Akron IdeaExchange@UAkron College of Polymer Science and Polymer Engineering 5-1996 Nucleation Initiated Spinodal Decomposition in a Polymerizing System Thein yK u University of Akron Main Campus, [email protected] Jae Hyung Lee University of Akron Main Campus Please take a moment to share how this work helps you through this survey. Your feedback will be important as we plan further development of our repository. Follow this and additional works at: http://ideaexchange.uakron.edu/polymer_ideas Part of the Polymer Science Commons Recommended Citation Kyu, Thein nda Lee, Jae Hyung, "Nucleation Initiated Spinodal Decomposition in a Polymerizing System" (1996). College of Polymer Science and Polymer Engineering. 67. http://ideaexchange.uakron.edu/polymer_ideas/67 This Article is brought to you for free and open access by IdeaExchange@UAkron, the institutional repository of The nivU ersity of Akron in Akron, Ohio, USA. It has been accepted for inclusion in College of Polymer Science and Polymer Engineering by an authorized administrator of IdeaExchange@UAkron. For more information, please contact [email protected], [email protected]. VOLUME 76, NUMBER 20 PHYSICAL REVIEW LETTERS 13MAY 1996 Nucleation Initiated Spinodal Decomposition in a Polymerizing System Thein Kyu and Jae-Hyung Lee Institute of Polymer Engineering, The University of Akron, Akron, Ohio 44325 (Received 29 September 1995) Dynamics of phase separation in a polymerizing system, consisting of carboxyl terminated polybutadiene acrylonitrile/epoxy/methylene dianiline, was investigated by means of time-resolved light scattering. The initial length scale was found to decrease for some early periods of the reaction which has been explained in the context of nucleation initiated spinodal decomposition. -
Spinodal Lines and Equations of State: a Review
10 l Nuclear Engineering and Design 95 (1986) 297-314 297 North-Holland, Amsterdam SPINODAL LINES AND EQUATIONS OF STATE: A REVIEW John H. LIENHARD, N, SHAMSUNDAR and PaulO, BINEY * Heat Transfer/ Phase-Change Laboratory, Mechanical Engineering Department, University of Houston, Houston, TX 77004, USA The importance of knowing superheated liquid properties, and of locating the liquid spinodal line, is discussed, The measurement and prediction of the spinodal line, and the limits of isentropic pressure undershoot, are reviewed, Means are presented for formulating equations of state and fundamental equations to predict superheated liquid properties and spinodal limits, It is shown how the temperature dependence of surface tension can be used to verify p - v - T equations of state, or how this dependence can be predicted if the equation of state is known. 1. Scope methods for making simplified predictions of property information, which can be applied to the full range of Today's technology, with its emphasis on miniaturiz fluids - water, mercury, nitrogen, etc. [3-5]; and predic ing and intensifying thennal processes, steadily de tions of the depressurizations that might occur in ther mands higher heat fluxes and poses greater dangers of mohydraulic accidents. (See e.g. refs. [6,7].) sending liquids beyond their boiling points into the metastable, or superheated, state. This state poses the threat of serious thermohydraulic explosions. Yet we 2. The spinodal limit of liquid superheat know little about its thermal properties, and cannot predict process behavior after a liquid becomes super heated. Some of the practical situations that require a 2.1. The role of the equation of state in defining the spinodal line knowledge the limits of liquid superheat, and the physi cal properties of superheated liquids, include: - Thennohydraulic explosions as might occur in nuclear Fig.