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Department of Chemical and Biological Engineering

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https://hdl.handle.net/10217/100365
These digital collections include theses, dissertations, and faculty publications from the Department of Chemical and Biological Engineering. Due to departmental name changes, materials from the following historical departments are also included here: Agricultural Engineering; Agricultural and Chemical Engineering; Chemical and Bioresource Engineering; Chemical Engineering.

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Browsing Department of Chemical and Biological Engineering by Author "Bailey, Travis S., advisor"

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    Development of tethered micelle hydrogel networks through sphere-forming AB/ABA block copolymer melts
    (Colorado State University. Libraries, 2013) Guo, Chen, author; Bailey, Travis S., advisor; Kipper, Matt J., committee member; Chen, Eugene, committee member; Wickramasinghe, S. Ranil, committee member
    The overriding theme of the work contained in this thesis is concerned with the preparation of tethered micelle hydrogel networks through the melt-state self-assembly of sphere-forming AB diblock and ABA triblock copolymer blends. The first chapter of this dissertation introduces the various projects pursued and provides background information for the reader. The second chapter of this thesis contains the initial demonstration of this novel strategy using polystyrene-poly(ethylene oxide) (PS-PEO, SO) diblock and PS-PEO-PS (SOS) triblock copolymers. Included in this chapter is a discussion of the synthetic polymerization techniques used to produce the SO and SOS block copolymers, the basic melt-state fabrication and characterization strategies used to pre-structure the tethered micelle networks, and the impact of changing both the SOS concentration and temperature on the resultant properties of the hydrogels produced. In these initial studies, the SOS triblock copolymer was constructed to be exactly double the SO diblock copolymer molecular weight, such that the preferred lattice dimensions during self-assembly were "matched". These "matched" hydrogels produced equilibrium swelling ratios (3.8-36.9 g water/g polymer) and dynamic elastic moduli (G' = 1.7-160 kPa) tunable across an impressive range of values using only temperature (10-50 °C) and SOS concentration (3.3-72.0 mol%). The third chapter of this thesis describes our efforts to influence the swelling and mechanical properties exhibited by simply modifying the PEO midblock molecular weight in the SOS tethering molecules. In doing so, we were able to show that the degree of coronal layer overlap between adjacent micelles was the primary contributing factor determining the dynamic mechanical response of the hydrogel. That is, the changes in mechanical properties produced due to altering tether concentration, tether length, or temperature, could all be understood in terms of their impact on the degree of coronal layer overlap in the system. In addition to these findings, we also discovered an interesting relationship between swelling and tether length. Increases in tether length by a factor of 1.6 compared to that of the matched system, resulted in higher swelling ratios and smaller elastic moduli (due to reduced coronal layer overlap). However, increases in tether length by a factor of 2.3 produced swelling behavior and mechanical properties nearly identical to that of the matched system. We concluded that the increase in tether length by a factor of 2.3 was sufficient to allow bridging into the second shell of the nearest neighbor micelles, negating the swelling advantage anticipated for the system. The fourth chapter of this thesis concerns our efforts to demonstrate the modification potential of the swollen hydrogel systems of Chapters 2 and 3. In this study, the terminal hydroxyl functionality present in the aforementioned SO diblock copolymers was substituted with either an azide or alkyne functionality. Cu(I) catalyzed coupling of the azide/alkyne functional diblock copolymer was then performed in the swollen state, producing a secondary network of tethers in the system. Installation of the secondary network produced dramatic improvements in the hydrogel tensile modulus, strain at break, stress at break, and toughness, while permitting swelling ratios, small strain rheological properties, and response in unconfined compression to remain largely unchanged. The fifth and final chapter of this thesis concerns a discussion of preliminary data supporting several promising directions for future work involving the further development of these tethered micelle networks.
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    Elastic free-standing RTIL composite membranes for CO2/N2 separation based on sphere-forming triblock/diblock copolymer blends
    (Colorado State University. Libraries, 2016) Wijayasekara, Dilanji B., author; Bailey, Travis S., advisor; Fisk, John D., committee member; Kipper, Matthew, committee member; James, Susan, committee member
    The main focus of this dissertation was the development of a robust polymeric membrane material for separating CO2 from a gas mixture of CO2 and N2. Flu gas, which is mainly a mixture CO2 and N2, is the single largest form of anthropogenic CO2 emissions to the atmosphere. Capturing CO2 from flu gas is considered as a measure of controlling anthropogenic CO2 emissions. Existing CO2 capturing technologies for flu gas suffer from low efficiency and the low cost effectiveness. Adoption of membrane technology is comparatively the best route towards the economical separations. Challenges faced by existing CO2 separation membrane materials are the lack of high mechanical robustness and the processability required for fabrication of membrane units while maximizing their gas separation properties. We were able to form a novel membrane material that addresses each of these challenges. These novel membranes are based on highly swollen, self-standing films produced using sphere-forming PS-PEO diblock and PS-PEO-PS triblock copolymer blends. The intricate connectivity among spherical domains produced during melt-state assembly (prior to swelling), provides a framework that remains elastically tough even in the presence of large quantities of 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIMTf2N) - a room temperature ionic liquid (RTIL) that has high selectivity for CO2 over N2. Further investigations on improving the robustness of these membranes and the gas separation properties were carried out based on two scenarios. First, potential of improving the thermal stability of these membranes by replacing the thermoplastic polystyrene with a thermoset moiety such as a chemically cross-linked polyisoprene (PI) was researched. Cross-linking chemistry utilized required a post-polymerization modification of PI and it was found that this oxidation modification of olefins on PI caused the decoupling of triblock copolymer in the blend and also substantially hindered melt-state self assembly. The membranes formed with this modification turned out to have inferior mechanical properties compared to the polystyrene based ones, most likely due to the above mentioned complications. Due to the time restrictions, this study was limited to just the identification of the existing challenges in the proposed strategy. Recommendations for addressing the challenges identified are also presented later in the dissertation. The second scenario for improving the performance of these membranes was to increase their productivity by improving both the CO2 permeability and maximizing the trans-membrane pressure differentials possible during operation. To accomplish this we focused on the development of an alternative matrix material (alternative for PEO) enriched with ionic groups. The goal was to increase matrix solubility in the RTIL (improved CO2 permeability) while simultaneously strengthening matrix-RTIL interactions for reduced leaching under higher pressure differentials. Synthetic routes to achieve this task involved a sequential polymerization of isoprene and ethoxy ethyl glycidyl ether (EEGE) monomers. Polymerization of EEGE to yield high molecular weight linear blocks proved to be extremely challenging due to the undesirable chain transfer reaction tendency of EEGE monomer. A great deal of research effort was spent characterizing various anionic reaction conditions and developing measures aimed at suppressing chain transfer. While ultimately unsuccessful, the results of these studies provide significant insight into the challenges of forming high molecular weight linear polyglycidols and will hopefully provide inspiration for the development of future synthetically successful strategies. A series of proof of concept experiments for transforming alcohol functionalities on this polymer system to imidazolium was also completed successfully. The dissertation concludes with a final project completed outside the main objective of the dissertation - a morphological characterization of a series of thermoplastic elastomers with unique molecular architectures. This work is reported separately in the appendix I.
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    Phototunable block copolymer hydrogels
    (Colorado State University. Libraries, 2017) Huq, Nabila A., author; Bailey, Travis S., advisor; Kipper, Matthew J., committee member; Reynolds, Melissa M., committee member; Snow, Christopher D., committee member
    Thermoplastic elastomer (TPE) hydrogel networks, based on swelling of nanostructured blends of amphiphilic, sphere-forming AB diblock and ABA triblock copolymers, provide direct access to thermally processable plastics that exhibit exceptional elastic recovery and fatigue resistance even after hydration. In such two-component systems, the ratio of ABA to AB block copolymer (BCP) is used to control the resultant swelling ratio, system modulus, and overall mechanical response. This dissertation focuses on developing material strategies through which adjustment of such AB/ABA ratios, and thus the resultant properties, can be accomplished using light. The chapters within capture the manipulation of a photoreactive AB diblock copolymer micelle-like spheres to controllably generate ABA triblock copolymer and the network nanostructure in situ, both in the melt state and after dispersal in solution. This was accomplished using efficient photoinduced [4 + 4]cycloaddition (λ = 365 nm) between terminal anthracene units on a ω-anthracenylpolystyrene-b-poly(ethylene oxide) diblock copolymer precursor to produce the desired amount of polystyrene-b-poly(ethylene oxide)-b-polystyrene triblock copolymer. This direct, UV-mediated handle on tethering between adjacent micelles in the BCP matrix was found to be capable of controllably manipulating hydrogel material properties using (1) duration of irradiation, (2) hydration level and consequent micelle spacing upon exposure, and (3) photopatterning strategies to spatially direct swelling and mechanics. This level of control yielded an array of hydrogels, ranging from those irradiated in the dry melt to produce high-modulus, elastic materials suited for fibrocartilage repair and replacement, to moldable or injectable precursor solutions irradiated into soft, conformally shaped TPE hydrogels ideal for use in high contact applications such as wound healing. The development and scope of this versatile new photoactive BCP system is enclosed.