Thesis (Ph. D.)--University of Texas at Austin, 2000. / Vita. Includes bibliographical references (leaf 115). Available also in a digital version from Dissertation Abstracts.

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Aqueous polyuethane (PU) colloids, like many other water-borne polymer colloids, have become an increasingly important class of materials in the surface coating industry. Three processing stages, the pre-dispersion, dispersion and postdispersion stages, are generally involved in the production of aqueous PU colloids. However, existing researches have neglected the importance of the dispersion stage. The present study aims to develop better understanding of the dispersion stage during the production of aqueous PU colloids. Non chain-extendable PU pre-polymer (PUp) is used to enable independent study of the dispersion stage and the phase inversion process is chosen due to its widespread industrial usage. Valid drop size characterisation techniques and phase inversion detection methods have been developed in this project. Three different dispersion regions have also been identified by changing the ionic group content of PUp. Each dispersion region is associated with a particular dispersion type. Those are (I) Stable aqueous emulsions that contain small PUp-in-water drops. They were produced using PUp with more than 0.2 mmole/g of ionic groups. (2) Aqueous PUp colloids with 0.05 ~ 0.2 mmole/g of ionic groups. These emulsions contain a mixture of drop structures, including simple drops and different multiple drops. (3) Aqueous PUp dispersions containing less than 0.05 mmole/g of ionic groups. These dispersions are not stable and the resultant dispersions separated when agitation was stopped. Modified phase inversion maps are introduced to represent the occurrence of all three dispersion regions. The modified phase inversion maps are partly analogous to those of conventional non-ionic-surfactant-water (nSOW) systems. The three dispersion regions have also been "reproduced" successfully using external surfactants as substitutes for the internal stabilising groups. A new catastrophic phase inversion mechanism is proposed to explain the existence of all three dispersion regions. Other variables studied during this project include different neutralising agents. different amount of carboxylic acid groups, operating temperatures and material addition rates. In conclusion, this project shows that the phase inversion process is a feasible route for producing aqueous polymer dispersions with little or no added external surfactants. Stable PUp-W dispersions can also be produced below the minimum ionic group content reported in existing literatures.

This study has highlighted the role of emulsion droplet cross-linking (deformability and penetrability) on droplet surface chemistry, droplet colloidal stability and adsorption at the droplet-water interface and provides insight into methods for enhancing the performance of emulsion formulations. / Thesis (PhD)--University of South Australia, 2003.

This study has highlighted the role of emulsion droplet cross-linking (deformability and penetrability) on droplet surface chemistry, droplet colloidal stability and adsorption at the droplet-water interface and provides insight into methods for enhancing the performance of emulsion formulations.

This study has highlighted the role of emulsion droplet cross-linking (deformability and penetrability) on droplet surface chemistry, droplet colloidal stability and adsorption at the droplet-water interface and provides insight into methods for enhancing the performance of emulsion formulations. / Thesis (PhD)--University of South Australia, 2003.

Thesis (Ph. D.)--Drexel University, 2005. / Includes abstract and vita. Includes bibliographical references (leaves 303-307).

In this work a finite element model is proposed to describe the swelling of poly(acrylic acid) hydrogels under the influence of an external electric field. The specific application of this model is for optical applications, but the design could be used equally well for other applications such as sensors and actuators.The model is proposed as five individual modules, which work in conjunction with each other but which can also function independently. This independence allows the model to provide intermediate results to the user, and also permits each module to be improved or adjusted individually without affecting the operation of the overall model. The first module is the Electrical module, which calculates the external electric field present in the hydrogel by solving Laplace's equation. The second module is the Chemical module, which uses the electric field to calculate the diffusion and migration of ions through the hydrogel/solvent regions. The third module is the Force module, which uses the change in ion concentrations to calculate the resulting change in osmotic pressure (force). This force is then used in the Mechanical module to calculate the deformation of the hydrogel, based on the assumption of linear elasticity. Finally, the fifth module is the Optical module, which uses the deformation to calculate the theoretical change in focal length.To verify the operation of the model, numerous experiments were conducted with the deformation of a poly(acrylic acid) hydrogel being measured under various external voltages with different electrode configurations. Overall, the model agrees quite well with the experimental results, but also highlights some interesting discrepancies that will need to be considered in future work. There is also some scope for improvement in the experimental method used, but again this is left for future work.

Thesis (M. Sc.)--University of Alberta, 2009. / Title from pdf file main screen (viewed on Jan. 8, 2010). "A thesis submitted to the Faculty of Graduate Studies and Research in partial fulfillment of the requirements for the degree of Master of Science, Department of Mechanical Engineering, University of Alberta." Includes bibliographical references.

Thesis (Ph. D.)--University of Texas at Austin, 2000. / Vita. Includes bibliographical references (leaves 180-187). Available also in a digital version from Dissertation Abstracts.