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Tailoring Photoprotection of Polylactide with New Isobornyl Derivatives of Phenol and Aniline

This article is devoted to the development of new photostabilizers for polylactide (PLA), a polymer that is an environmentally friendly alternative to polymers and is based on fossil raw materials. We have elucidated the role of the reaction center of two potential PLA photoprotectors: N-isobornylan...

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Autores principales: Belyi, Vladimir A., Kuzivanov, Ivan M., Fedorova, Irina V., Shumova, Olga A., Tropnikov, Evgeniy M., Istomina, Elena I., Chukicheva, Irina Yu., Kuchin, Aleksandr V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10180735/
https://www.ncbi.nlm.nih.gov/pubmed/37177288
http://dx.doi.org/10.3390/polym15092141
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author Belyi, Vladimir A.
Kuzivanov, Ivan M.
Fedorova, Irina V.
Shumova, Olga A.
Tropnikov, Evgeniy M.
Istomina, Elena I.
Chukicheva, Irina Yu.
Kuchin, Aleksandr V.
author_facet Belyi, Vladimir A.
Kuzivanov, Ivan M.
Fedorova, Irina V.
Shumova, Olga A.
Tropnikov, Evgeniy M.
Istomina, Elena I.
Chukicheva, Irina Yu.
Kuchin, Aleksandr V.
author_sort Belyi, Vladimir A.
collection PubMed
description This article is devoted to the development of new photostabilizers for polylactide (PLA), a polymer that is an environmentally friendly alternative to polymers and is based on fossil raw materials. We have elucidated the role of the reaction center of two potential PLA photoprotectors: N-isobornylaniline and 2-isobornylphenol, in reactions occurring in a polymer matrix under the action of UV-C radiation. PLA samples with the photostabilizers were irradiated under a wavelength of 253.7 nm for 4, 8 and 12 h. The effectiveness of the photostabilizers was evaluated based on FTIR spectrometric data, (1)H and (13)C NMR, scanning electron microscopy and simultaneous thermal analysis (TG-DSC). Both stabilizers led to the protection of ester bonds between monomer units of PLA. However, 2-isobornylphenol proved to be more effective at a concentration of 0.05 wt.%, while the optimal concentration of N-isobornylaniline was 0.5 wt.% by weight. TG-DSC showed that the addition of N-isobornylaniline led to an increase in PLA resistance to thermal decomposition; the temperature of the onset of weight loss increased by 2.8 °C at 0.05 wt.% and by 8.1 °C at 0.5 wt.% of N-isobornylaniline. The photoprotector 2-isobornylphenol, on the contrary, reduced the thermal stability of PLA.
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spelling pubmed-101807352023-05-13 Tailoring Photoprotection of Polylactide with New Isobornyl Derivatives of Phenol and Aniline Belyi, Vladimir A. Kuzivanov, Ivan M. Fedorova, Irina V. Shumova, Olga A. Tropnikov, Evgeniy M. Istomina, Elena I. Chukicheva, Irina Yu. Kuchin, Aleksandr V. Polymers (Basel) Article This article is devoted to the development of new photostabilizers for polylactide (PLA), a polymer that is an environmentally friendly alternative to polymers and is based on fossil raw materials. We have elucidated the role of the reaction center of two potential PLA photoprotectors: N-isobornylaniline and 2-isobornylphenol, in reactions occurring in a polymer matrix under the action of UV-C radiation. PLA samples with the photostabilizers were irradiated under a wavelength of 253.7 nm for 4, 8 and 12 h. The effectiveness of the photostabilizers was evaluated based on FTIR spectrometric data, (1)H and (13)C NMR, scanning electron microscopy and simultaneous thermal analysis (TG-DSC). Both stabilizers led to the protection of ester bonds between monomer units of PLA. However, 2-isobornylphenol proved to be more effective at a concentration of 0.05 wt.%, while the optimal concentration of N-isobornylaniline was 0.5 wt.% by weight. TG-DSC showed that the addition of N-isobornylaniline led to an increase in PLA resistance to thermal decomposition; the temperature of the onset of weight loss increased by 2.8 °C at 0.05 wt.% and by 8.1 °C at 0.5 wt.% of N-isobornylaniline. The photoprotector 2-isobornylphenol, on the contrary, reduced the thermal stability of PLA. MDPI 2023-04-29 /pmc/articles/PMC10180735/ /pubmed/37177288 http://dx.doi.org/10.3390/polym15092141 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Belyi, Vladimir A.
Kuzivanov, Ivan M.
Fedorova, Irina V.
Shumova, Olga A.
Tropnikov, Evgeniy M.
Istomina, Elena I.
Chukicheva, Irina Yu.
Kuchin, Aleksandr V.
Tailoring Photoprotection of Polylactide with New Isobornyl Derivatives of Phenol and Aniline
title Tailoring Photoprotection of Polylactide with New Isobornyl Derivatives of Phenol and Aniline
title_full Tailoring Photoprotection of Polylactide with New Isobornyl Derivatives of Phenol and Aniline
title_fullStr Tailoring Photoprotection of Polylactide with New Isobornyl Derivatives of Phenol and Aniline
title_full_unstemmed Tailoring Photoprotection of Polylactide with New Isobornyl Derivatives of Phenol and Aniline
title_short Tailoring Photoprotection of Polylactide with New Isobornyl Derivatives of Phenol and Aniline
title_sort tailoring photoprotection of polylactide with new isobornyl derivatives of phenol and aniline
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10180735/
https://www.ncbi.nlm.nih.gov/pubmed/37177288
http://dx.doi.org/10.3390/polym15092141
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