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dc.contributor.authorBourque, Alexander
dc.date.accessioned2014-04-04T14:57:37Z
dc.date.available2014-04-04T14:57:37Z
dc.date.issued2014-04-04
dc.identifier.urihttp://hdl.handle.net/10222/49088
dc.descriptionAn assessment of the thermochromic behaviour of three-component chemical systems comprising a colour-changing leuco dye, an electron-accepting phenolic developer, and a long-chain alkyl alcohol solid solvent.en_US
dc.description.abstractThermochromic materials undergo temperature-dependent colour changes. Although there are several origins of thermochromism, two distinct types of thermochromism are common in thermochromic mixtures. Melt-lightened thermochromism occurs when the colour density of a mixture decreases with increasing temperature, and is usually associated with colour loss upon mixture melting. Melt-darkened thermochromism occurs when the colour density of a mixture increases with increasing temperature, and is usually associated conversion from a decoloured solid state to a coloured melt. Three-component thermochromic systems generally consist of a leuco dye (minor component), a phenolic colour developer (intermediate component), and a high melting-point organic solvent (dominant component). In these systems, the colouring behaviour is controlled by competing binary interactions, with the dye:developer interaction responsible for colour formation and the developer:solvent interaction responsible for colour erasure. In the present study, three-component mixtures composed of CVL (dye), long-chain alkyl gallates (phenolic developer), and long-chain alkyl alcohols (long-chain solvent) were examined. The thermochromic behaviour (i.e., melt-lightened vs. melt-darkened thermochromism) of these mixtures was examined as a function of the matching of the alkyl chain length of the gallate developer and alcohol solvent. When the alkyl chain lengths were well matched, the developer:solvent interaction dominated in the solid state and melt-darkened thermochromism was observed. When the alkyl chain lengths were poorly matched, the dye:developer interaction dominated in the solid state, and melt-lightened thermochromism was observed. The colour density of the molten state was determined by the developer:dye molar ratio, with high molar ratios yielding coloured melts and low molar ratios yielding decoloured melts. Additional studies employing chemically dissimilar developers and solvents (e.g., bisphenol A with 1-hexadecanol) yielded mixtures that displayed optimal melt-lightened thermochromism. The high solid-state colour density due to weak developer:solvent interactions provides further evidence that competing binary interactions are responsible for the colouring behaviour observed for three-component thermochromic systems. Ternary thermochromic phase diagrams were used to define compositional regions of optimal thermochromic behaviour (i.e., high colour contrast), providing a useful experimental tool for the rapid identification of ideal sample compositions. Additionally, an examination of the properties of thermally erasable ink-jet printer inks was carried out during the present study.en_US
dc.language.isoenen_US
dc.subjectThermochromismen_US
dc.subjectLeuco Dyesen_US
dc.subjectColour chemistryen_US
dc.subjectPolymorphismen_US
dc.titleInvestigations of Reversible Thermochromism in Three-Component Systemsen_US
dc.date.defence2014-03-27
dc.contributor.departmentDepartment of Chemistryen_US
dc.contributor.degreeDoctor of Philosophyen_US
dc.contributor.external-examinerDr. Bart Kahren_US
dc.contributor.graduate-coordinatorDr. Mark Stradiottoen_US
dc.contributor.thesis-readerDr. D. Jean Burnellen_US
dc.contributor.thesis-readerDr. Jeff. R. Dahnen_US
dc.contributor.thesis-readerDr. Peng Zhangen_US
dc.contributor.thesis-supervisorDr. Mary Anne Whiteen_US
dc.contributor.ethics-approvalNot Applicableen_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.copyright-releaseYesen_US
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