Thermodynamic potentials The four ways to say energy

2018 ◽  
pp. 53-66
Author(s):  
James H. Luscombe
1998 ◽  
Vol 538 ◽  
Author(s):  
Raúl A. Enrique ◽  
Pascal Bellon

AbstractPhase stability in alloys under irradiation is studied considering effective thermodynamic potentials. A simple kinetic model of a binary alloy with phase separation is investigated. Time evolution in the alloy results from two competing dynamics: thermal diffusion, and irradiation induced ballistic exchanges. The dynamical (steady state) phase diagram is evaluated exactly performing Kinetic Monte Carlo simulations. The solution is then compared to two theoretical frameworks: the effective quasi-interactions model as proposed by Vaks and Kamishenko, and the effective free energy model as proposed by Martin. New developments of these models are proposed to allow for quantitative comparisons. Both theoretical frameworks yield fairly good approximations to the dynamical phase diagram.


Author(s):  
Jochen Rau

Thermodynamic processes involve energy exchanges in the forms of work, heat, or particles. Such exchanges might be reversible or irreversible, and they might be controlled by barriers or reservoirs. A cyclic process takes a system through several states and eventually back to its initial state; it may convert heat into work (engine) or vice versa (heat pump). This chapter defines work and heat mathematically and investigates their respective properties, in particular their impact on entropy. It discusses the roles of barriers and reservoirs and introduces cyclic processes. Basic constraints imposed by the laws of thermodynamics are considered, in particular on the efficiency of a heat engine. The chapter also introduces the thermodynamic potentials: free energy, enthalpy, free enthalpy, and grand potential. These are used to describe energy exchanges and equilibrium in the presence of reservoirs. Finally, this chapter considers thermodynamic coefficients which characterize the response of a system to heating, compression, and other external actions.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Antonio Sabatini ◽  
Marco Borsari ◽  
Gerard P. Moss ◽  
Stefano Iotti

AbstractAccording to the 1994 IUBMB-IUPAC Joint Commission on Biochemical Nomenclature (JCBN) on chemical and biochemical reactions, two categories of thermodynamics, based on different concepts and different formalisms, are established: (i) chemical thermodynamics, which employ conventional thermodynamic potentials to deal with chemical reactions [1], [2], [3]; and (ii) biochemical thermodynamics, which employ transformed thermodynamic quantities to deal with biochemical reactions based on the formalism proposed by Alberty [4], [5], [6], [7]. We showed that the two worlds of chemical and biochemical thermodynamics, which so far have been treated separately, can be reunified within the same thermodynamic framework. The thermodynamics of chemical reactions, in which all species are explicitly considered with their atoms and charge balanced, are compared with the transformed thermodynamics generally used to treat biochemical reactions where atoms and charges are not balanced. The transformed thermodynamic quantities suggested by Alberty are obtained by a mathematical transformation of the usual thermodynamic quantities. The present analysis demonstrates that the transformed values for ΔrG′0 and ΔrH′0 can be obtained directly, without performing any transformation, by simply writing the chemical reactions with all the pseudoisomers explicitly included and the elements and charges balanced. The appropriate procedures for computing the stoichiometric coefficients for the pseudoisomers are fully explained by means of an example calculation for the biochemical ATP hydrolysis reaction. It is concluded that the analysis reunifies the “two separate worlds” of conventional thermodynamics and transformed thermodynamics.


2014 ◽  
Vol 89 (6) ◽  
Author(s):  
Yu Rim Lim ◽  
Seong Jun Park ◽  
Sanggeun Song ◽  
Gil-Suk Yang ◽  
Young-Gui Yoon ◽  
...  

Author(s):  
Jonathan Skipp ◽  
Sergey Nazarenko

Abstract We study the thermodynamic equilibrium spectra of the Charney- Hasegawa-Mima (CHM) equation in its weakly nonlinear limit. In this limit, the equation has three adiabatic invariants, in contrast to the two invariants of the 2D Euler or Gross-Pitaevskii equations, which are examples for comparison. We explore how the third invariant considerably enriches the variety of equilibrium spectra that the CHM system can access. In particular we characterise the singular limits of these spectra in which condensates occur, i.e. a single Fourier mode (or pair of modes) accumulate(s) a macroscopic fraction of the total invariants. We show that these equilibrium condensates provide a simple explanation for the characteristic structures observed in CHM systems of finite size: highly anisotropic zonal flows, large-scale isotropic vortices, and vortices at small scale. We show how these condensates are associated with combinations of negative thermodynamic potentials (e.g. temperature).


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