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RAFT Dispersion Alternating Copolymerization of Styrene with N-Phenylmaleimide: Morphology Control and Application as an Aqueous Foam Stabilizer
[Image: see text] We report a new nonaqueous polymerization-induced self-assembly (PISA) formulation based on the reversible addition–fragmentation chain transfer (RAFT) dispersion alternating copolymerization of styrene with N-phenylmaleimide using a nonionic poly(N,N-dimethylacrylamide) stabilizer...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041161/ https://www.ncbi.nlm.nih.gov/pubmed/27708458 http://dx.doi.org/10.1021/acs.macromol.6b01563 |
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author | Yang, Pengcheng Mykhaylyk, Oleksandr O. Jones, Elizabeth R. Armes, Steven P. |
author_facet | Yang, Pengcheng Mykhaylyk, Oleksandr O. Jones, Elizabeth R. Armes, Steven P. |
author_sort | Yang, Pengcheng |
collection | PubMed |
description | [Image: see text] We report a new nonaqueous polymerization-induced self-assembly (PISA) formulation based on the reversible addition–fragmentation chain transfer (RAFT) dispersion alternating copolymerization of styrene with N-phenylmaleimide using a nonionic poly(N,N-dimethylacrylamide) stabilizer in a 50/50 w/w ethanol/methyl ethyl ketone (MEK) mixture. The MEK cosolvent is significantly less toxic than the 1,4-dioxane cosolvent reported previously [ P. Yang; Macromolecules2013, 46, 8545−8556]. The core-forming alternating copolymer block has a relatively high glass transition temperature (T(g)), which leads to vesicular morphologies being observed during PISA, as well as the more typical sphere and worm phases. Each of these copolymer morphologies has been characterized by transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) studies. TEM studies reveal micrometer-sized elliptical particles with internal structure, with SAXS analysis suggesting an oligolamellar vesicle morphology. This structure differs from that previously reported for a closely related PISA formulation utilizing a poly(methacrylic acid) stabilizer block for which unilamellar platelet-like particles are observed by TEM and SAXS. This suggests that interlamellar interactions are governed by the nature of the steric stabilizer layer. Moreover, using the MEK cosolvent also enables access to a unilamellar vesicular morphology, despite the high T(g) of the alternating copolymer core-forming block. This was achieved by simply conducting the PISA synthesis at a higher temperature for a longer reaction time (80 °C for 24 h). Presumably, MEK solvates the core-forming block more than the previously utilized 1,4-dioxane cosolvent, which leads to greater chain mobility. Finally, preliminary experiments indicate that the worms are much more efficient stabilizers for aqueous foams than either the spheres or the oligolamellar elliptical vesicles. |
format | Online Article Text |
id | pubmed-5041161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50411612016-10-03 RAFT Dispersion Alternating Copolymerization of Styrene with N-Phenylmaleimide: Morphology Control and Application as an Aqueous Foam Stabilizer Yang, Pengcheng Mykhaylyk, Oleksandr O. Jones, Elizabeth R. Armes, Steven P. Macromolecules [Image: see text] We report a new nonaqueous polymerization-induced self-assembly (PISA) formulation based on the reversible addition–fragmentation chain transfer (RAFT) dispersion alternating copolymerization of styrene with N-phenylmaleimide using a nonionic poly(N,N-dimethylacrylamide) stabilizer in a 50/50 w/w ethanol/methyl ethyl ketone (MEK) mixture. The MEK cosolvent is significantly less toxic than the 1,4-dioxane cosolvent reported previously [ P. Yang; Macromolecules2013, 46, 8545−8556]. The core-forming alternating copolymer block has a relatively high glass transition temperature (T(g)), which leads to vesicular morphologies being observed during PISA, as well as the more typical sphere and worm phases. Each of these copolymer morphologies has been characterized by transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) studies. TEM studies reveal micrometer-sized elliptical particles with internal structure, with SAXS analysis suggesting an oligolamellar vesicle morphology. This structure differs from that previously reported for a closely related PISA formulation utilizing a poly(methacrylic acid) stabilizer block for which unilamellar platelet-like particles are observed by TEM and SAXS. This suggests that interlamellar interactions are governed by the nature of the steric stabilizer layer. Moreover, using the MEK cosolvent also enables access to a unilamellar vesicular morphology, despite the high T(g) of the alternating copolymer core-forming block. This was achieved by simply conducting the PISA synthesis at a higher temperature for a longer reaction time (80 °C for 24 h). Presumably, MEK solvates the core-forming block more than the previously utilized 1,4-dioxane cosolvent, which leads to greater chain mobility. Finally, preliminary experiments indicate that the worms are much more efficient stabilizers for aqueous foams than either the spheres or the oligolamellar elliptical vesicles. American Chemical Society 2016-09-02 2016-09-27 /pmc/articles/PMC5041161/ /pubmed/27708458 http://dx.doi.org/10.1021/acs.macromol.6b01563 Text en Copyright © 2016 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Yang, Pengcheng Mykhaylyk, Oleksandr O. Jones, Elizabeth R. Armes, Steven P. RAFT Dispersion Alternating Copolymerization of Styrene with N-Phenylmaleimide: Morphology Control and Application as an Aqueous Foam Stabilizer |
title | RAFT Dispersion Alternating Copolymerization of Styrene
with N-Phenylmaleimide: Morphology Control
and Application as an Aqueous Foam Stabilizer |
title_full | RAFT Dispersion Alternating Copolymerization of Styrene
with N-Phenylmaleimide: Morphology Control
and Application as an Aqueous Foam Stabilizer |
title_fullStr | RAFT Dispersion Alternating Copolymerization of Styrene
with N-Phenylmaleimide: Morphology Control
and Application as an Aqueous Foam Stabilizer |
title_full_unstemmed | RAFT Dispersion Alternating Copolymerization of Styrene
with N-Phenylmaleimide: Morphology Control
and Application as an Aqueous Foam Stabilizer |
title_short | RAFT Dispersion Alternating Copolymerization of Styrene
with N-Phenylmaleimide: Morphology Control
and Application as an Aqueous Foam Stabilizer |
title_sort | raft dispersion alternating copolymerization of styrene
with n-phenylmaleimide: morphology control
and application as an aqueous foam stabilizer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5041161/ https://www.ncbi.nlm.nih.gov/pubmed/27708458 http://dx.doi.org/10.1021/acs.macromol.6b01563 |
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