Solution Rheology and Microstructure of Associative Polymers

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dc.contributor.advisor Alan E. Tonelli, Committee Co-Chair en_US
dc.contributor.advisor John van Zanten, Committee Member en_US
dc.contributor.advisor Richard J. Spontak, Committee Member en_US
dc.contributor.advisor Sam S. Hudson, Committee Member en_US
dc.contributor.advisor Saad A. Khan, Committee Chair en_US
dc.contributor.author Abdala, Ahmed AbdelHay Ahmed en_US
dc.date.accessioned 2010-04-02T18:26:05Z
dc.date.available 2010-04-02T18:26:05Z
dc.date.issued 2003-07-28 en_US
dc.identifier.other etd-12062002-001230 en_US
dc.identifier.uri http://www.lib.ncsu.edu/resolver/1840.16/3032
dc.description.abstract Water-soluble associative polymers are widely used in a variety of applications because of their ability to modulate rheology and material microstructures. This study focuses on understanding the structure-property relationship for hydrophobically modified alkali soluble emulsion (HASE) polymers with emphasis on their microstructure and rheological properties. These polymers have a complex comb-like structure that is a polyelectrolyte backbone, a copolymer of acrylic or methacrylic acid and alkyl acrylate, with a few hydrophobic macromonomers randomly grafted to this backbone. The hydrophobic macromonomer consists of hydrophobic groups that are separated from the polymer chains by polyethylene oxide (PEO) spacers. Upon neutralization, the polymer backbone adopts a more extended conformation allowing the hydrophobic groups to associate forming a transient network structure that enhances the solution rheological properties. In the first part of this study, we investigate the effect of the polymer composition on their microstructures and rheological properties. In particular, the effects of the concentrations of methacrylic acid (MAA) and macromonomers on the solution rheology are examined. We find that polymers with low MAA content have smaller hydrodynamic size and weaker network structures compared to larger hydrodynamic size and stronger network structure for polymers with high MAA content. However, due to chain increased stiffness at higher MAA and the lower contribution from the aggregation of ethyl-acrylate groups, a broad maximum in the viscoelastic properties of the polymer solution is observed at about 40 mole% MAA. Moreover, the material functions of polymers with different MAA content show different concentration dependences. In the second part of this study, co-solvents of water and propylene glycol (PG) in different proportions are used to investigate the effect of the solvent quality on the solution rheology of these polymers. The steady and dynamic properties show the presence of two regimes with respect to the solvent composition. In "water-rich" solvents, the hydrophobic association dominates the solution rheology. In contrast, in "PG-rich" solvents, the hydrophobic association is suppressed due to the lower tendency of the hydrophobes to aggregate, the smaller coil size of the polymer chains and changes in the PEO spacer conformations. These two different types of behavior are discussed and confirmed by the different concentration dependences in each regime. In the third part of the study, the ability of using diffusing wave spectroscopy (DWS) to probe the dynamics of HASE polymers is examined. We find that DWS accurately probes the structural changes induced by the change in the solvent quality or the polymer concentration. Moreover, comparison with conventional mechanical rheometry data reveals excellent qualitative agreement between the data obtained from the two techniques. Quantitatively, however, there is a discrepancy between the data obtained from each technique. Several reasons for the discrepancy are discussed, including the possibility that the dynamics at the micro-level could be different from the bulk properties. The scaling of the creep compliance, high–frequency elastic modulus and relaxation time with polymer concentration show power-law dependences. The power-law exponents are discussed in light of theoretical predictions and available experimental data. An approach to modulate the hydrophobic association is presented in the last part of the study. The first step in this approach involves the addition of inclusion compound forming hosts (α- or β- cyclodextrin) to the polymer solution. The encapsulation of the hydrophobic groups leads to significant reduction in the solution viscosity and viscoelastic properties The second step requires the addition of surfactants to reactivate the hydrophobic groups and thus recover the solution rheological properties. We are able to recover the solution properties using different nonionic surfactants. en_US
dc.rights I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to NC State University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. en_US
dc.subject TGA en_US
dc.subject thermal gravimetric analysis en_US
dc.subject creep compliance en_US
dc.subject Clarase en_US
dc.subject steady shear viscosity en_US
dc.subject sticky Reptation en_US
dc.subject sticky Rouse en_US
dc.subject time dependent diffusion coefficient en_US
dc.subject mean square displacement en_US
dc.subject solubility parameter en_US
dc.subject Nuclear magnetic resonance en_US
dc.subject NMR en_US
dc.subject NP surfactants en_US
dc.subject cyclodextrinase enzymes en_US
dc.subject Anti-icing fluids en_US
dc.subject microrheology en_US
dc.subject Brownian motion en_US
dc.subject Associating polymers en_US
dc.subject Tracer microrheology en_US
dc.subject DSC en_US
dc.subject differential scanning calorimetry en_US
dc.subject dynamic frequency spectrum en_US
dc.subject Stokes-Einstein relation en_US
dc.subject Stokes-Einstein equation en_US
dc.subject intrinsic viscosity en_US
dc.title Solution Rheology and Microstructure of Associative Polymers en_US
dc.degree.name PhD en_US
dc.degree.level dissertation en_US
dc.degree.discipline Chemical Engineering en_US


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