Impact of Processing Effects on Surface Segregation of Bottlebrush Polymer Additives

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dc.citation.firstpage8909
dc.citation.issueNumber19
dc.citation.journalTitleMacromolecules
dc.citation.lastpage8917
dc.citation.volumeNumber55
dc.contributor.authorLee, Dongjoo
dc.contributor.authorCharpota, Nilesh
dc.contributor.authorMei, Hao
dc.contributor.authorTerlier, Tanguy
dc.contributor.authorPietrzak, Danica
dc.contributor.authorStein, Gila E.
dc.contributor.authorVerduzco, Rafael
dc.date.accessioned2022-11-03T14:38:39Z
dc.date.available2022-11-03T14:38:39Z
dc.date.issued2022
dc.description.abstractThe surface properties of polymeric materials govern interactions with the surroundings and are responsible for various application-relevant properties. Recent studies have shown that bottlebrush polymers can be used to modify the surface chemistry of the polymers because they spontaneously segregate to the interfaces when they are blended with the linear polymers, driven in large part by entropic effects that arise from the unique architecture of bottlebrush polymers. However, while prior work has largely focused on equilibrium segregation profiles, kinetic and processing effects can also drive bottlebrush additives to surfaces and interfaces. In solution-cast blends of polymers and colloids, vertical stratification is controlled by the relative Péclet (Pe) numbers of the constituents, i.e., the relative rates of solvent evaporation and solute diffusion. Herein, we studied processing effects that drive bottlebrush additives to interfaces when blended with linear polymers. We prepared blends of bottlebrush polystyrene (BBPS) and linear perdeuterated polystyrene (dPS), where the BBPS side-chain length was fixed at Nsc = 48, the BBPS backbone length ranged from Nb = 30–260, and the dPS chain length ranged from Nm = 40–548. The relative Pe numbers of BBPS and dPS were varied by changing the solvent and sizes of BBPS and dPS. In contrast to other binary blends where the constituents have disparate sizes (e.g., colloid/colloid, polymer/colloid, and polymer/polymer), we found that the relative Pe number cannot account for the degree of segregation observed in these bottlebrush and linear polymer blends. For a fixed BBPS side-chain length, we observe stronger surface segregation of bottlebrush additives when the blend is cast using lower boiling point solvents and/or for blends with longer bottlebrush polymers. We further show that solvent annealing of the film can increase the enrichment of bottlebrush additives near surfaces. This study provides insight into the interplay of processing effects and blend thermodynamics that govern surface segregation of bottlebrush polymer additives.
dc.identifier.citationLee, Dongjoo, Charpota, Nilesh, Mei, Hao, et al.. "Impact of Processing Effects on Surface Segregation of Bottlebrush Polymer Additives." <i>Macromolecules,</i> 55, no. 19 (2022) American Chemical Society: 8909-8917. https://doi.org/10.1021/acs.macromol.2c01418.
dc.identifier.doihttps://doi.org/10.1021/acs.macromol.2c01418
dc.identifier.urihttps://hdl.handle.net/1911/113792
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.rightsThis is an author's peer-reviewed final manuscript, as accepted by the publisher. The published article is copyrighted by the American Chemical Society.
dc.titleImpact of Processing Effects on Surface Segregation of Bottlebrush Polymer Additives
dc.typeJournal article
dc.type.dcmiText
dc.type.publicationpost-print
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