Phase Behavior in Blends of Asymmetrical Polyolefins

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dc.contributor.advisor Balsara, NP en Nedoma, Alisyn en 2017-10-12T22:28:19Z en 2010-12-17 en 2010-06-15 en
dc.identifier.citation Sub type: PhD Thesis. Supervisors: Balsara NP. University of California, Berkeley, 17 Dec 2010 en
dc.identifier.uri en
dc.description.abstract Polymer composites combine the physical properties of two or more distinct chemical species into a single material. Blends of two homopolymers, mixed homogeneously or structured on the nanoscale, are particularly useful nanocomposite materials because ordering occurs via thermodynamic equilibration rather than costly nanofabrication. However, the majority of homopolymer pairs are immiscible, leading to mechanically unstable materials. This work explores one route for compatibilizing two immiscible homopolymers (components A and B) via the addition of a tailored diblock copolymer surfactant (component A-C). The A-block of the copolymer was selected on the basis of having a neutral interaction with the A homopolymer, and the C-block had a favorable interaction with the B homopolymer. The favorable interaction between species B and C was first examined by preparing binary blends of B and C homopolymers. A detailed thermodynamic study explored the effects of blend composition and homopolymer chain length on the thermodynamic phase behavior of binary B/C blends. The results were used to design A/B/A-C ternary blends where the favorable interaction between homopolymer B and the C-block enabled the copolymer surfactant to efficiently stabilize the interface between nanoscale-ordered domains of A and B. The phase behavior of the resulting polymer nanocomposites was studied as a function of the composition of the blend and the chain lengths of the A and B homopolymers. These studies provide new insight into the tunability of of polymer nanocomposite materials by controlling parameters that have not been studied previously. Polymer pairs that are miscible over a large range of chain lengths, N B and N C , are interesting to thermodynamic studies because the Flory-Huggins interaction parameter, χ , can be measured using scattering techniques and the theoretical framework of the Random Phase Approximation. Most tabulated χ values have been measured over a limited range of chain lengths small enough for the polymers to homogenize; such studies are largely constrained to the vicinity of N B ≈ N C . This dissertation presents the most comprehensive study of χ to date for a single pair of homopolymers. Polyisobutylene (component B) and deuterated polybutadiene with 63 % 1,2 addition (component C) were selected for this study because they exhibit a large window of miscibility and may be tailored to cross the spinodal at experimentally accessible temperatures. Binary blends were designed across a range of values for N B / N C and the composition of the blend, φ B , to study the effect of these parameters on the measured value, χ sc . In addition to the strict temperature dependence presumed for χ , this study documented a composition and molecular weight dependence. The empirical expression for χ sc , measured 2 using small angle neutron scattering, was three times more dependent on composition then the expression for χ used to predict thermodynamic behavior. Despite this three-fold diminished dependence on φ B , the composition-dependent χ profoundly affected the phase behavior of binary blends. Binary B/C blends exhibited macrophase separation upon heating (above a threshold chain length), enabling experimental determination of the binodal and spinodal. These measured quantities were compared to predictions using Flory-Huggins Theory with the composition- and molecular weight-dependent χ . Phase diagrams are expected to be symmetric in the vicinity of N B ≈ N C , with the critical point located at φ B,crit = 0.5. However, both the measured and predicted phase diagrams were asymmetric in the vicinity of N B ≈ N C , and increasingly symmetric as the value of N B / N C was decreased. A range of values was studied for N B / N C ≤ 1, a nd in all cases φ B,crit was found to be < 0.5, in stark contrast to the expectation of Flory-Huggins Theory that φ B,crit ≥ 0.5. This effect was shown to result from the comb ined effects of a composition-dependent χ and N B / N C removed from values of 1. Remarkable agreement was obtained between the predicted phase diagrams and measured phase transitions, over a range of values for N B / N C and φ B , by accounting for the composition and molecular weight dependence of χ . The miscibility of binary B/C blends was used as the basis for designing a diblock copolymer (component A-C) to order immiscible binary blends of polyisobutylene and deuterated polybutadiene with 89 % 1,2 addition (component A). The copolymer comprised one block chemically identical to component C (miscible in component B) and one block chemically identical to component A. This is in contrast to the majority of ternary blend studies which comprise A/B/A-B polymer systems with neutral interactions between each homopolymer and the corresponding block of the diblock copolymer. Ternary A/B/A-C blends exhibit a favorable interaction between the B homopolymer and C block, demonstrated by the miscibility of B/C blends. The A-C diblock copolymer surfactant can produce microstructures when added to A/B blends at much lower concentrations of copolymer than for an analagous A-B copolymer. Previous studies have only considered the case N A ≈ N B and a symmetric diblock copolymer ( N A-block ≈ N C-block ). In the present work, symmetric diblock copolymers were added to critical A/B blends. The values of N A / N B were varied over two orders of magnitude. For each blend, the ratio of A:B was fixed by the Flory-Huggins Theory prediction for the critical point (which depends only on N A / N B ), and a constant amount of copolymer was used for all blends. By creating blends with a wide range of values for N A / N B , the study accessed critical compositions, φ A,crit , well removed from the typical value of 0.5 (on a copolymer-free basis). The resulting phase behavior correlated directly with N A / N B , suggesting that the microstructures observed in a blend could be tuned not only by the conventional method of changing the amount of copolymer, but also by adjusting the ratio N A / N B . Lamellar or microemulsion phases were observed over a temperature window for nearly all of the A/B/A-C blends studied. The former represent an ordered microphase and the latter a disordered microphase, each with unique applications. Previous work has attempted to distinguish the scattering profiles of lamellar phases from those of microemulsions by fitting both with the Teubner-Strey equation for microemulsions. The lamellar phase was judged to exist when the microemulsion fit did not capture the entire range of the scattering profile, otherwise the phase was presumed to be a microemulsion. This dissertation introduces the use of 3 lamellar structure factor that fits scattering profiles unsuitable for the microemulsion fit. In addition, the lamellar fits include as adjustable parameters the size of each microdomain and corresponding interfacial width. These fit values agree quantitatively with independently generated predictions using self-consistent field theory, indicating a broad understanding of the physical parameters that affect thermodynamic behavior in the A/B/A-C system studied. The composition of a blend, in particular the concentration of diblock copolymer, is known to affect the phase behavior, however most studies have only considered blends where equal amounts of A and B are blended with copolymer and φ A,crit = 0.5 (on a copolymer-free basis). This dissertation presents a study for which the concentration of diblock copolymer was fixed and the composition of the A and B homopolymers was systematically varied across a range of compositions including φ A,crit . The experiment corresponded to tracing the copolymer isopleth on a ternary phase prism. Theoretical groups have predicted a rich phase behavior along the isopleth for similar ternary systems, however, the observed phase behavior was quantitatively identical for all blends studied. Self-consistent field theory predictions agreed with fit values of the domain spacing and microdomain widths. There was no discernible correlation between φ A and phase behavior. This finding, and that of the study with critical A/B/A-C blends, together suggest that N A / N B correlates strongly with the phase behavior of a blend, while φ A does not. This relationship, captured by mean-field theory, provides a simple method for tuning the phase behavior of polymer nanocomposites without using additional surfactant. en
dc.publisher ProQuest en
dc.relation.ispartof PhD Thesis - University of Auckland en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
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dc.title Phase Behavior in Blends of Asymmetrical Polyolefins en
dc.type Thesis en Chemical Engineering en University of California, Berkeley en Doctoral en PhD en
dc.rights.holder Copyright: The author en en
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pubs.elements-id 639432 en
pubs.record-created-at-source-date 2017-07-24 en

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