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Hydrogen-bonding athermal lattice chains compared with associating hard-sphere chains

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dc.contributor.authorLee, Chul Soo-
dc.contributor.authorKang, Jeong Won-
dc.contributor.authorLee, Ju Ho-
dc.contributor.authorYoo, Ki-Pung-
dc.date.accessioned2021-09-09T09:59:59Z-
dc.date.available2021-09-09T09:59:59Z-
dc.date.created2021-06-10-
dc.date.issued2008-03-25-
dc.identifier.issn0378-3812-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/123880-
dc.description.abstractWith its flexibility and simplicity in derivation, the Veytsman statistics is proved to provide a powerful tool for representing association contributions to Helmholtz free energy of lattice fluids. However, based on a heuristic argument the probability function in the statistics is in need of a critical review as to its accuracy and parameter characteristics. For these purposes different probability functions were compared with molecular simulation data of associating hard-sphere chains in this work. Association energy of lattice fluids was found to be equal to the square-well depth of off-lattice fluids. The form and parameter value for probability functions were reviewed and a new probability function was proposed for the best agreements with molecular simulation data. The proposed probability function with optimized parameter yielded the average absolute deviations of monomer fractions and compressibility factors less than 0.04 and 7%, respectively. (c) 2008 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectPHASE-EQUILIBRIA-
dc.subjectPURE FLUIDS-
dc.subjectSTATE-
dc.subjectEQUATION-
dc.subjectSIMULATION-
dc.subjectSYSTEMS-
dc.subjectMODEL-
dc.subjectMOLECULES-
dc.subjectMIXTURES-
dc.subjectSITES-
dc.titleHydrogen-bonding athermal lattice chains compared with associating hard-sphere chains-
dc.typeArticle-
dc.contributor.affiliatedAuthorKang, Jeong Won-
dc.identifier.doi10.1016/j.fluid.2008.01.005-
dc.identifier.scopusid2-s2.0-39749116143-
dc.identifier.wosid000254815800024-
dc.identifier.bibliographicCitationFLUID PHASE EQUILIBRIA, v.265, no.1-2, pp.215 - 222-
dc.relation.isPartOfFLUID PHASE EQUILIBRIA-
dc.citation.titleFLUID PHASE EQUILIBRIA-
dc.citation.volume265-
dc.citation.number1-2-
dc.citation.startPage215-
dc.citation.endPage222-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaThermodynamics-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryThermodynamics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusPHASE-EQUILIBRIA-
dc.subject.keywordPlusPURE FLUIDS-
dc.subject.keywordPlusSTATE-
dc.subject.keywordPlusEQUATION-
dc.subject.keywordPlusSIMULATION-
dc.subject.keywordPlusSYSTEMS-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusMOLECULES-
dc.subject.keywordPlusMIXTURES-
dc.subject.keywordPlusSITES-
dc.subject.keywordAuthorequations of state-
dc.subject.keywordAuthorathermal lattice chains-
dc.subject.keywordAuthorassociation-
dc.subject.keywordAuthormolecular simulation-
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