Phase Transitions Affected by Molecular Interconversion

dc.contributor.advisorAnisimov, Mikhailen_US
dc.contributor.authorLongo, Thomasen_US
dc.contributor.departmentChemical Physicsen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2023-06-25T05:47:51Z
dc.date.available2023-06-25T05:47:51Z
dc.date.issued2023en_US
dc.description.abstractTypically, pure substances may be found with only one gaseous or liquid state, while their solid state may exist in various polymorphic states. The existence of two distinct liquid forms in a single component substance is more unusual since liquids lack the long-range order common to crystals. Yet, the existence of multiple amorphous states in a single component substance, a phenomenon known as "liquid polyamorphism," has been observed or predicted in a wide variety of substances. In contrast to standard phase transitions, it has been suggested that polyamorphic liquid-liquid transitions are caused by the interconversion of molecular or supramolecular states. To investigate this phenomenon, a nonequilibrium thermodynamic model was developed to quantitatively describe the interplay between the dynamics of molecular interconversion and fluid-phase separation. The theory has been compared to a variety of interconverting systems, and has demonstrated a quantitative agreement with the results of Monte Carlo and Molecular Dynamics simulations. In this thesis, it is shown that there are two major effects of molecular interconversion on the thermodynamics and the kinetics of fluid-phase separation: if the system evolves to an equilibrium state, then the growth of one of the alternative phases may result in the destruction of phase coexistence - a phenomenon referred to as "phase amplification." It is demonstrated that depending on the experimental or simulation conditions, either phase separation or phase amplification would be observed. Previous studies of polyamorphic substances report conflicting observations of phase formation, which may be explained by the possibility of phase amplification occurring. Alternatively, if the system evolves to a nonequilibrium steady state, the phase domain growth could be restricted at a mesoscopic length scale. This phenomenon (referred to as "microphase separation") is one of the simplest examples of steady-state dissipative structures, and may be applicable to active matter systems, hydrodynamic instabilities, and bifurcations in chemical reactions, in which the nonequilibrium conditions could be imposed by an external flux of matter or energy.en_US
dc.identifierhttps://doi.org/10.13016/dspace/a9eg-hxcd
dc.identifier.urihttp://hdl.handle.net/1903/30157
dc.language.isoenen_US
dc.subject.pqcontrolledThermodynamicsen_US
dc.subject.pqcontrolledPhysicsen_US
dc.subject.pqcontrolledChemistryen_US
dc.subject.pquncontrolledDissipative Structuresen_US
dc.subject.pquncontrolledPhase Amplificationen_US
dc.subject.pquncontrolledPhase Separationen_US
dc.subject.pquncontrolledPhase Transitionen_US
dc.subject.pquncontrolledSpecies Interconversionen_US
dc.titlePhase Transitions Affected by Molecular Interconversionen_US
dc.typeDissertationen_US

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