Phase Behavior of Polymer-Grafted Nanoparticles

dc.contributor.advisorKrishnamoorti, Ramanan
dc.contributor.committeeMemberRobertson, Megan L.
dc.contributor.committeeMemberConrad, Jacinta C.
dc.contributor.committeeMemberArdebili, Haleh
dc.contributor.committeeMemberHu, Yandi
dc.creatorMongcopa, Katrina Irene
dc.creator.orcid0000-0001-5393-6871
dc.date.accessioned2020-01-03T23:55:47Z
dc.date.available2020-01-03T23:55:47Z
dc.date.createdAugust 2015
dc.date.issued2015-08
dc.date.submittedAugust 2015
dc.date.updated2020-01-03T23:55:48Z
dc.description.abstractThe fundamental thermodynamic interactions between polymer-grafted nanoparticles and their surroundings—whether in a polymer matrix or a solvent—are crucial to the properties and performance of the resulting material. The phase behavior and conformations of the grafted polymer are governed by both entropic and enthalpic effects that in turn, drive dispersion and aggregation in the system. Although the dispersion-aggregation transition in the athermal case is largely entropic in nature, significant enthalpic interactions exist in many chemically dissimilar graft-matrix and graft-solvent systems that influence their phase transition. In this work, the phase behavior and conformational transitions of polystyrene (PS)-grafted silica nanoparticles in a poly(vinyl methyl ether) (PVME) matrix and cyclohexane are investigated—both systems exhibit conformational changes in the brush as a function of temperature. Through a combination of transmission electron microscopy imaging, small angle x-ray and neutron scattering techniques, a gradual wetting-dewetting transition in the silica-PS/PVME composite is elucidated and found to be distinct from the dispersion-aggregation transition. This is in stark contrast to athermal systems of chemically similar brush and matrix chains where the two transition events are analogous. Moreover, using light and neutron scattering, a coil-to-globule transition of the grafted PS chains in cyclohexane is probed as the solvent quality changes from good to poor. Measurements of the hydrodynamic size reveal a continuous change from a highly-swollen brush to a globule-like configuration before particle aggregation occurs. These observations are consistent with changes in the brush thickness and radius of gyration measured from neutron scattering experiments. This work presents key insights into the thermodynamic behavior of polymer-grafted nanoparticles unique to dissimilar graft-matrix and graft-solvent systems. Furthermore, it highlights fundamentally important concepts crucial to the design and functionality of advanced materials.
dc.description.departmentMechanical Engineering, Department of
dc.format.digitalOriginborn digital
dc.format.mimetypeapplication/pdf
dc.identifier.citationPortions of this document appear in: Cao, Peng-Fei, Ajaykumar Bunha, Joey Mangadlao, Mary Jane Felipe, Katrina Irene Mongcopa, and Rigoberto Advincula. "A supramolecularly templated catenane initiator and a controlled ring expansion strategy." Chemical Communications 48, no. 99 (2012): 12094-12096. And in: Martin, Tyler B., Katrina Irene S. Mongcopa, Rana Ashkar, Paul Butler, Ramanan Krishnamoorti, and Arthi Jayaraman. "Wetting–dewetting and dispersion–aggregation transitions are distinct for polymer grafted nanoparticles in chemically dissimilar polymer matrix." Journal of the American Chemical Society 137, no. 33 (2015): 10624-10631.
dc.identifier.urihttps://hdl.handle.net/10657/5700
dc.language.isoeng
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.subjectPolymers
dc.subjectHybrid nanoparticles
dc.subjectPhase behavior
dc.titlePhase Behavior of Polymer-Grafted Nanoparticles
dc.type.dcmiText
dc.type.genreThesis
thesis.degree.collegeCullen College of Engineering
thesis.degree.departmentMechanical Engineering, Department of
thesis.degree.disciplineMaterials Engineering
thesis.degree.grantorUniversity of Houston
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy

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