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Structure of Self-Initiated Photopolymerized Films: A Comparison of Models
[Image: see text] Self-initiated photografting and photopolymerization (SI-PGP) uses UV illumination to graft polymers to surfaces without additional photoinitiators using the monomers as initiators, “inimers”. A wider use of this method is obstructed by a lack of understanding of the resulting, pre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671054/ https://www.ncbi.nlm.nih.gov/pubmed/36377414 http://dx.doi.org/10.1021/acs.langmuir.2c02396 |
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author | Nagy, Béla Ekblad, Tobias Fragneto, Giovanna Ederth, Thomas |
author_facet | Nagy, Béla Ekblad, Tobias Fragneto, Giovanna Ederth, Thomas |
author_sort | Nagy, Béla |
collection | PubMed |
description | [Image: see text] Self-initiated photografting and photopolymerization (SI-PGP) uses UV illumination to graft polymers to surfaces without additional photoinitiators using the monomers as initiators, “inimers”. A wider use of this method is obstructed by a lack of understanding of the resulting, presumably heterogeneous, polymer structure and of the parallel degradation under continuous UV illumination. We have used neutron reflectometry to investigate the structure of hydrated SI-PGP-prepared poly(HEMA-co-PEG(10)MA) (poly(2-hydroxyethyl methacrylate-co-(ethylene glycol)(10) methacrylate)) films and compared parabolic, sigmoidal, and Gaussian models for the polymer volume fraction distributions. Results from fitting these models to the data suggest that either model can be used to approximate the volume fraction profile to similar accuracy. In addition, a second layer of deuterated poly(methacrylic acid) (poly(dMAA)) was grafted over the existing poly(HEMA-co-PEG(10)MA) layer, and the resulting double-grafted films were also studied by neutron reflectometry to shed light on the UV-polymerization process and the inevitable UV-induced degradation which competes with the grafting. |
format | Online Article Text |
id | pubmed-9671054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96710542022-11-18 Structure of Self-Initiated Photopolymerized Films: A Comparison of Models Nagy, Béla Ekblad, Tobias Fragneto, Giovanna Ederth, Thomas Langmuir [Image: see text] Self-initiated photografting and photopolymerization (SI-PGP) uses UV illumination to graft polymers to surfaces without additional photoinitiators using the monomers as initiators, “inimers”. A wider use of this method is obstructed by a lack of understanding of the resulting, presumably heterogeneous, polymer structure and of the parallel degradation under continuous UV illumination. We have used neutron reflectometry to investigate the structure of hydrated SI-PGP-prepared poly(HEMA-co-PEG(10)MA) (poly(2-hydroxyethyl methacrylate-co-(ethylene glycol)(10) methacrylate)) films and compared parabolic, sigmoidal, and Gaussian models for the polymer volume fraction distributions. Results from fitting these models to the data suggest that either model can be used to approximate the volume fraction profile to similar accuracy. In addition, a second layer of deuterated poly(methacrylic acid) (poly(dMAA)) was grafted over the existing poly(HEMA-co-PEG(10)MA) layer, and the resulting double-grafted films were also studied by neutron reflectometry to shed light on the UV-polymerization process and the inevitable UV-induced degradation which competes with the grafting. American Chemical Society 2022-11-03 2022-11-15 /pmc/articles/PMC9671054/ /pubmed/36377414 http://dx.doi.org/10.1021/acs.langmuir.2c02396 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Nagy, Béla Ekblad, Tobias Fragneto, Giovanna Ederth, Thomas Structure of Self-Initiated Photopolymerized Films: A Comparison of Models |
title | Structure of Self-Initiated Photopolymerized Films:
A Comparison of Models |
title_full | Structure of Self-Initiated Photopolymerized Films:
A Comparison of Models |
title_fullStr | Structure of Self-Initiated Photopolymerized Films:
A Comparison of Models |
title_full_unstemmed | Structure of Self-Initiated Photopolymerized Films:
A Comparison of Models |
title_short | Structure of Self-Initiated Photopolymerized Films:
A Comparison of Models |
title_sort | structure of self-initiated photopolymerized films:
a comparison of models |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671054/ https://www.ncbi.nlm.nih.gov/pubmed/36377414 http://dx.doi.org/10.1021/acs.langmuir.2c02396 |
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