• Journal of the Korean Chemical Society
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• v.35 no.4
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• pp.308-315
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• 1991

The structure and thermodynamic properties of body centered cubic structure of simple Coulombic liquids are computed from the perturbation theory for one-component plasma. A comparison of perturbation theory (PT) and Monte Carlo (MC) simulation shows excellent agreement. The hardsphere perturbation theory is applicable to a long-range attractive system, such as the one-component plasma. A comparison of the radial distribution function (g(r)) and the structure factor (S(q)) for PT data and MC data shows agreement. Thus the perturbation theory is an applicable method to explain the structure and thermodynamic properties of Coulomb liquids.

• Korean Journal of Air-Conditioning and Refrigeration Engineering
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• v.23 no.10
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• pp.662-669
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• 2011

A numerical study was performed for thermodynamic efficiencies of a basic ORC (Organic Rankine Cycle), ORC with a FLH (Feed Liquid Heater), and ORC with a regenerator. The efficiencies of the basic ORC were higher in the order of R113, R123, R245ca, and R245fa for its working fluids. It was confirmed that an optimal FLH pressure existed to maximize efficiency of the ORC with a FLH. A correlation was developed to predict the optimal FLH pressure as a function of evaporation and condensation pressure and its average absolute deviation was 0.505%. The efficiency enhancement of the basic ORC with a FLH was higher than that with a regenerator. It was presented that the basic ORC efficiency could be improved more than 10% by a FLH with $30^{\circ}C$ condensation and over $110^{\circ}C$ evaporation temperatures.

• Korean Journal of Metals and Materials
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• v.50 no.1
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• pp.45-51
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• 2012

Thermodynamics of carbon in manganese alloy melts is important in manufacturing low carbon ferromanganese and silico-manganese alloys. In order to predict the carbon solubility in liquid $Mn-Si-Fe-C_{sat}$ alloys as a function of melt composition and temperature, thermodynamic interactions among carbon, silicon and iron in carbon saturated liquid manganese should be known. In the present study, the effects of silicon and iron on the carbon solubility in Mn-Si, Mn-Fe and Mn-Si-Fe melts were measured in the temperature range from 1673 to 1773 K. The carbon solubility decreases significantly as silicon and iron contents increase in liquid manganese alloy. The interaction parameters among carbon, silicon and iron in carbon saturated liquid manganese were determined from the carbon solubility data and the Lupis' relation for the interaction coefficient at constant activity.

• The Korean Journal of Ceramics
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• v.4 no.2
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• pp.61-67
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• 1998

The significance of point defects as relevant centers concerning electrochemical function is highlighted. Starting from the most simple case of dilute equilibrium bulk defect chemistry, influence of defect interaction and in particular the impact of interfaces on point defect redistribution are considered. Then recent progress in the field of kinetics in bulk and at boundaries is discussed. Finally, selected applications with emphasis on battery and sensor technology are presented.

• Journal of the korean Society of Automotive Engineers
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• v.6 no.1
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• pp.46-54
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• 1984

We applies Molecular Dynamics simulation technics to a system of Lennard-Jones potential interacting Argon liquid to study shear flow behavior. The thermodynamic state of the system is .rho.=35.54 Kg, mole/m$^{3}$, T=86.5.deg. K which is the triple point of Argon liquid. We applies shear rate : .epsilon.=9.26*10$^{9}$ 1/sec in the system. We find the response function, shear viscosity changes, and shear rate build-up as a function of time. We also find the thermal conductivity in a soft-sphere system.

• Journal of the Korean Chemical Society
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• v.7 no.2
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• pp.179-181
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• 1963

The partition function of liquid halogens is developed applying the significant liquid structure theory proposed by H. Eyring and co-workers. The parameters in the partition function are determined by triple point technique which was proposed by the authors in the previous paper, and also the thermodynamic properties and the surface tension are calculated by the method therein.

• Journal of the Korean Chemical Society
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• v.7 no.2
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• pp.174-178
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• 1963

The new method to determine the parameters in the liquid partition function of H. Eyring and co-workers is proposed, in which method the equilibrium condition of the three phases and the boundary condition of the liquid partition function at the triple point are used. The calculated thermodynamic properties using the new determined parameters are agreed well with the observed values.

• Bulletin of the Korean Chemical Society
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• v.30 no.7
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• pp.1667-1670
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• 2009

• Proceedings of the SAREK Conference
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• 2007.11a
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• pp.652-657
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• 2007

This paper is an interim report on the investigation of thermodynamic properties of $CO_2$/oil mixture refrigerant. First, liquid density of POE (poly-ol ester) and PAG (poly alkylene glycol) were measured and expressed as a function of temperature. Then, a solubility equation was developed which enables us to calculate the weight fraction of $CO_2$ for the mixture in a liquid state. An experimental apparatus with a cell was constructed to measure P-$\upsilon$-T-$\chi$ data for $CO_2$/oil mixture. The volume of the cell was determined using a certain formula considering change in volume as a function of temperature and pressure. Then, experimental data were obtained over the temperatures $40^{\circ}C$, $50^{\circ}C$, $60^{\circ}C$, $70^{\circ}C$ and $80^{\circ}C$ with various mole fractions. Finally, assuming a primitive model of ideal gas, the volume of $CO_2$/oil mixture was predicted with a relatively larger error of 5.05% for $CO_2$/PAG and 8.81% for $CO_2$/POE. The volume of $CO_2$/oil mixtures would be better predicted using an appropriate equation of state, of which results will be reported soon.

• Korean Chemical Engineering Research
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• v.61 no.1
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• pp.116-122
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• 2023

We study the relationship of entropy with the properties of molecules and also with the macroscopic specifications of the system, i.e., component and phase. Understanding different viewpoints of classical mechanics and quantum mechanics for the indistinguishability of molecules belonging to the same component, we discuss a few thermodynamic systems in which the properties of molecules are to be consistent with the component as a macroscopic term of classifying the molecules. With a clear definition of thermodynamic microstate, the drawback of the Boltzmann statistics caused by the distinguishability of molecules is avoided, and the Gibbs paradox of entropy consequently disappears. Corresponding to the characteristics of fluid and solid phases, we investigated the effects of the indistinguishability and the symmetry number of molecules and the number of microstates realized in time on the partition function and the entropy. In particular, we show that crystalline solid can be regarded as a system which does not satisfy the ergodic hypothesis.