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PLGA Barrier Materials from CO(2). The influence of Lactide Co-monomer on Glycolic Acid Polyesters

[Image: see text] The combination of the predicted polymer market growth and the emergence of renewable feedstocks creates a fantastic opportunity for sustainable polymers. To replace fossil-based feedstock, there are only three alternative sustainable carbon sources: biomass, CO(2), and existing pl...

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Autores principales: Murcia Valderrama, Maria A., van Putten, Robert-Jan, Gruter, Gert-Jan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493221/
https://www.ncbi.nlm.nih.gov/pubmed/32954354
http://dx.doi.org/10.1021/acsapm.0c00315
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author Murcia Valderrama, Maria A.
van Putten, Robert-Jan
Gruter, Gert-Jan M.
author_facet Murcia Valderrama, Maria A.
van Putten, Robert-Jan
Gruter, Gert-Jan M.
author_sort Murcia Valderrama, Maria A.
collection PubMed
description [Image: see text] The combination of the predicted polymer market growth and the emergence of renewable feedstocks creates a fantastic opportunity for sustainable polymers. To replace fossil-based feedstock, there are only three alternative sustainable carbon sources: biomass, CO(2), and existing plastics (via mechanical and/or chemical recycling). The ultimate circular feedstock would be CO(2): it can be electrochemically reduced to formic acid derivatives that subsequently can be converted into useful monomers such as glycolic acid. This work is part of the European Horizon 2020 project “Ocean” in which the steps from CO(2) to glycolic acid are developed. Polyglycolic acid (PGA) and poly(lactide-co-glycolide) (PLGA) copolyesters with high lactic acid (LA) content are well-known. PGA is very difficult to handle due to its high crystallinity. On the other hand, PLGAs with high LA content lack good oxygen and moisture barriers. The aim of this work is to understand the structure–property relationships for the mostly unexplored glycolic acid rich PLGA copolymer series and to assess their suitability as barrier materials. Thus, PLGA copolymers with between 50 and 91 mol % glycolic acid were synthesized and their properties were evaluated. Increased thermal stability was observed with increasing glycolic acid content. Only those containing 87 and 91 mol % glycolic acid were semicrystalline. A crystallization study under non-isothermal conditions revealed that copolymerization reduces the crystallization rate for PLGA compared to polylactic acid (PLA) and PGA. While PGA homopolymer crystallizes completely when cooled at 10 °C·min(–1), the copolymers with 9 and 13% lactic acid show almost 10 times slower crystallization, which is a huge advantage vis-à-vis PGA for processing. The kinetics of this process, modeled with the Jeziorny-modified Avrami method, confirmed those observations. Barrier property assessment revealed great potential for these copolymers for application in barrier films. Increasing glycolic acid content in PLGA copolymers enhances the barrier to both oxygen and water vapor. At room temperature and a relative humidity below 70% the PLGA copolymers with high glycolic acid content outperform the barrier properties of polyethylene terephthalate.
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spelling pubmed-74932212020-09-16 PLGA Barrier Materials from CO(2). The influence of Lactide Co-monomer on Glycolic Acid Polyesters Murcia Valderrama, Maria A. van Putten, Robert-Jan Gruter, Gert-Jan M. ACS Appl Polym Mater [Image: see text] The combination of the predicted polymer market growth and the emergence of renewable feedstocks creates a fantastic opportunity for sustainable polymers. To replace fossil-based feedstock, there are only three alternative sustainable carbon sources: biomass, CO(2), and existing plastics (via mechanical and/or chemical recycling). The ultimate circular feedstock would be CO(2): it can be electrochemically reduced to formic acid derivatives that subsequently can be converted into useful monomers such as glycolic acid. This work is part of the European Horizon 2020 project “Ocean” in which the steps from CO(2) to glycolic acid are developed. Polyglycolic acid (PGA) and poly(lactide-co-glycolide) (PLGA) copolyesters with high lactic acid (LA) content are well-known. PGA is very difficult to handle due to its high crystallinity. On the other hand, PLGAs with high LA content lack good oxygen and moisture barriers. The aim of this work is to understand the structure–property relationships for the mostly unexplored glycolic acid rich PLGA copolymer series and to assess their suitability as barrier materials. Thus, PLGA copolymers with between 50 and 91 mol % glycolic acid were synthesized and their properties were evaluated. Increased thermal stability was observed with increasing glycolic acid content. Only those containing 87 and 91 mol % glycolic acid were semicrystalline. A crystallization study under non-isothermal conditions revealed that copolymerization reduces the crystallization rate for PLGA compared to polylactic acid (PLA) and PGA. While PGA homopolymer crystallizes completely when cooled at 10 °C·min(–1), the copolymers with 9 and 13% lactic acid show almost 10 times slower crystallization, which is a huge advantage vis-à-vis PGA for processing. The kinetics of this process, modeled with the Jeziorny-modified Avrami method, confirmed those observations. Barrier property assessment revealed great potential for these copolymers for application in barrier films. Increasing glycolic acid content in PLGA copolymers enhances the barrier to both oxygen and water vapor. At room temperature and a relative humidity below 70% the PLGA copolymers with high glycolic acid content outperform the barrier properties of polyethylene terephthalate. American Chemical Society 2020-06-24 2020-07-10 /pmc/articles/PMC7493221/ /pubmed/32954354 http://dx.doi.org/10.1021/acsapm.0c00315 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Murcia Valderrama, Maria A.
van Putten, Robert-Jan
Gruter, Gert-Jan M.
PLGA Barrier Materials from CO(2). The influence of Lactide Co-monomer on Glycolic Acid Polyesters
title PLGA Barrier Materials from CO(2). The influence of Lactide Co-monomer on Glycolic Acid Polyesters
title_full PLGA Barrier Materials from CO(2). The influence of Lactide Co-monomer on Glycolic Acid Polyesters
title_fullStr PLGA Barrier Materials from CO(2). The influence of Lactide Co-monomer on Glycolic Acid Polyesters
title_full_unstemmed PLGA Barrier Materials from CO(2). The influence of Lactide Co-monomer on Glycolic Acid Polyesters
title_short PLGA Barrier Materials from CO(2). The influence of Lactide Co-monomer on Glycolic Acid Polyesters
title_sort plga barrier materials from co(2). the influence of lactide co-monomer on glycolic acid polyesters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493221/
https://www.ncbi.nlm.nih.gov/pubmed/32954354
http://dx.doi.org/10.1021/acsapm.0c00315
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