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Spontaneous Patterning during Frontal Polymerization
[Image: see text] Complex patterns integral to the structure and function of biological materials arise spontaneously during morphogenesis. In contrast, functional patterns in synthetic materials are typically created through multistep manufacturing processes, limiting accessibility to spatially var...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155460/ https://www.ncbi.nlm.nih.gov/pubmed/34056090 http://dx.doi.org/10.1021/acscentsci.1c00110 |
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author | Lloyd, Evan M. Feinberg, Elizabeth C. Gao, Yuan Peterson, Suzanne R. Soman, Bhaskar Hemmer, Julie Dean, Leon M. Wu, Qiong Geubelle, Philippe H. Sottos, Nancy R. Moore, Jeffrey S. |
author_facet | Lloyd, Evan M. Feinberg, Elizabeth C. Gao, Yuan Peterson, Suzanne R. Soman, Bhaskar Hemmer, Julie Dean, Leon M. Wu, Qiong Geubelle, Philippe H. Sottos, Nancy R. Moore, Jeffrey S. |
author_sort | Lloyd, Evan M. |
collection | PubMed |
description | [Image: see text] Complex patterns integral to the structure and function of biological materials arise spontaneously during morphogenesis. In contrast, functional patterns in synthetic materials are typically created through multistep manufacturing processes, limiting accessibility to spatially varying materials systems. Here, we harness rapid reaction-thermal transport during frontal polymerization to drive the emergence of spatially varying patterns during the synthesis of engineering polymers. Tuning of the reaction kinetics and thermal transport enables internal feedback control over thermal gradients to spontaneously pattern morphological, chemical, optical, and mechanical properties of structural materials. We achieve patterned regions with two orders of magnitude change in modulus in poly(cyclooctadiene) and 20 °C change in glass transition temperature in poly(dicyclopentadiene). Our results suggest a facile route to patterned structural materials with complex microstructures without the need for masks, molds, or printers utilized in conventional manufacturing. Moreover, we envision that more sophisticated control of reaction-transport driven fronts may enable spontaneous growth of structures and patterns in synthetic materials, inaccessible by traditional manufacturing approaches. |
format | Online Article Text |
id | pubmed-8155460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-81554602021-05-28 Spontaneous Patterning during Frontal Polymerization Lloyd, Evan M. Feinberg, Elizabeth C. Gao, Yuan Peterson, Suzanne R. Soman, Bhaskar Hemmer, Julie Dean, Leon M. Wu, Qiong Geubelle, Philippe H. Sottos, Nancy R. Moore, Jeffrey S. ACS Cent Sci [Image: see text] Complex patterns integral to the structure and function of biological materials arise spontaneously during morphogenesis. In contrast, functional patterns in synthetic materials are typically created through multistep manufacturing processes, limiting accessibility to spatially varying materials systems. Here, we harness rapid reaction-thermal transport during frontal polymerization to drive the emergence of spatially varying patterns during the synthesis of engineering polymers. Tuning of the reaction kinetics and thermal transport enables internal feedback control over thermal gradients to spontaneously pattern morphological, chemical, optical, and mechanical properties of structural materials. We achieve patterned regions with two orders of magnitude change in modulus in poly(cyclooctadiene) and 20 °C change in glass transition temperature in poly(dicyclopentadiene). Our results suggest a facile route to patterned structural materials with complex microstructures without the need for masks, molds, or printers utilized in conventional manufacturing. Moreover, we envision that more sophisticated control of reaction-transport driven fronts may enable spontaneous growth of structures and patterns in synthetic materials, inaccessible by traditional manufacturing approaches. American Chemical Society 2021-03-24 2021-04-28 /pmc/articles/PMC8155460/ /pubmed/34056090 http://dx.doi.org/10.1021/acscentsci.1c00110 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Lloyd, Evan M. Feinberg, Elizabeth C. Gao, Yuan Peterson, Suzanne R. Soman, Bhaskar Hemmer, Julie Dean, Leon M. Wu, Qiong Geubelle, Philippe H. Sottos, Nancy R. Moore, Jeffrey S. Spontaneous Patterning during Frontal Polymerization |
title | Spontaneous Patterning during Frontal Polymerization |
title_full | Spontaneous Patterning during Frontal Polymerization |
title_fullStr | Spontaneous Patterning during Frontal Polymerization |
title_full_unstemmed | Spontaneous Patterning during Frontal Polymerization |
title_short | Spontaneous Patterning during Frontal Polymerization |
title_sort | spontaneous patterning during frontal polymerization |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155460/ https://www.ncbi.nlm.nih.gov/pubmed/34056090 http://dx.doi.org/10.1021/acscentsci.1c00110 |
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