Effects of Grafting Maleic Anhydride onto Poly‐ɛ‐caprolactone on Facilitative Enzymatic Hydrolysis

Abstract Plastic waste is a global issue because it causes overflowing landfills and pollution, leading to environmental concerns. To address this crisis, materials that can be decomposed in the natural environment are introduced to replace conventional plastics. Poly‐ɛ‐caprolactone (PCL) is a commo...

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Main Authors: Kotchaporn Thangunpai, Donghao Hu, Mikio Kajiyama, Marcos A. Neves, Toshiharu Enomae
Format: Article
Language:English
Published: Wiley-VCH 2023-12-01
Series:Macromolecular Materials and Engineering
Subjects:
Online Access:https://doi.org/10.1002/mame.202300067
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author Kotchaporn Thangunpai
Donghao Hu
Mikio Kajiyama
Marcos A. Neves
Toshiharu Enomae
author_facet Kotchaporn Thangunpai
Donghao Hu
Mikio Kajiyama
Marcos A. Neves
Toshiharu Enomae
author_sort Kotchaporn Thangunpai
collection DOAJ
description Abstract Plastic waste is a global issue because it causes overflowing landfills and pollution, leading to environmental concerns. To address this crisis, materials that can be decomposed in the natural environment are introduced to replace conventional plastics. Poly‐ɛ‐caprolactone (PCL) is a commonly used plastic that can degrade in natural environments. However, owing to its hydrophobicity, its natural decomposition rate is low. In this study, PCL is modified with maleic anhydride (MA) (PCL‐g‐MA) to increase hydrophilicity and amorphous region for faster decomposition. To assess the hydrolysis in seawater, lipase hydrolysis is performed to compare the decomposition of PCL‐g‐MA and PCL. Consequently, in a Pseudomonas lipase‐containing PBS solution, it takes 72 and 120 h for complete hydrolyze of PCL‐g‐MA and PCL, respectively. MA grafted onto PCL increases the amorphous region, where lipase can easily diffuse into PCL‐g‐MA. Morphological (FESEM and POM images), thermal (TGA and DSC), and structural (FTIR, XRD, and XPS) analyzes support the hydrolysis reaction. The mechanisms proposed in this study confirm that lipase hydrolysis starts in the amorphous regions and then transfers to the crystal regions. This hydrolysis progress is expected to facilitate the creation of eco‐friendly low‐cost PCL‐g‐MA composites with high‐rate hydrolysis, such as bio‐plastics and bio‐fibers.
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spelling doaj.art-8ee3b679a4a74dbb903d6e0ccaf707572023-12-14T03:52:31ZengWiley-VCHMacromolecular Materials and Engineering1438-74921439-20542023-12-0130812n/an/a10.1002/mame.202300067Effects of Grafting Maleic Anhydride onto Poly‐ɛ‐caprolactone on Facilitative Enzymatic HydrolysisKotchaporn Thangunpai0Donghao Hu1Mikio Kajiyama2Marcos A. Neves3Toshiharu Enomae4Graduate School of Science and Technology University of Tsukuba 1‐1‐1 Tennodai Tsukuba Ibaraki 305‐8572 JapanDepartment of Chemistry & State Key Laboratory of Molecular Engineering of Polymers Fudan University Shanghai 200433 P. R. ChinaFaculty of Life and Environmental Sciences University of Tsukuba 1‐1‐1 Tennodai Tsukuba Ibaraki 305‐8572 JapanFaculty of Life and Environmental Sciences University of Tsukuba 1‐1‐1 Tennodai Tsukuba Ibaraki 305‐8572 JapanFaculty of Life and Environmental Sciences University of Tsukuba 1‐1‐1 Tennodai Tsukuba Ibaraki 305‐8572 JapanAbstract Plastic waste is a global issue because it causes overflowing landfills and pollution, leading to environmental concerns. To address this crisis, materials that can be decomposed in the natural environment are introduced to replace conventional plastics. Poly‐ɛ‐caprolactone (PCL) is a commonly used plastic that can degrade in natural environments. However, owing to its hydrophobicity, its natural decomposition rate is low. In this study, PCL is modified with maleic anhydride (MA) (PCL‐g‐MA) to increase hydrophilicity and amorphous region for faster decomposition. To assess the hydrolysis in seawater, lipase hydrolysis is performed to compare the decomposition of PCL‐g‐MA and PCL. Consequently, in a Pseudomonas lipase‐containing PBS solution, it takes 72 and 120 h for complete hydrolyze of PCL‐g‐MA and PCL, respectively. MA grafted onto PCL increases the amorphous region, where lipase can easily diffuse into PCL‐g‐MA. Morphological (FESEM and POM images), thermal (TGA and DSC), and structural (FTIR, XRD, and XPS) analyzes support the hydrolysis reaction. The mechanisms proposed in this study confirm that lipase hydrolysis starts in the amorphous regions and then transfers to the crystal regions. This hydrolysis progress is expected to facilitate the creation of eco‐friendly low‐cost PCL‐g‐MA composites with high‐rate hydrolysis, such as bio‐plastics and bio‐fibers.https://doi.org/10.1002/mame.202300067enzymatic hydrolysisgraftinglipasesmaleic anhydridepoly‐ɛ‐caprolactone
spellingShingle Kotchaporn Thangunpai
Donghao Hu
Mikio Kajiyama
Marcos A. Neves
Toshiharu Enomae
Effects of Grafting Maleic Anhydride onto Poly‐ɛ‐caprolactone on Facilitative Enzymatic Hydrolysis
Macromolecular Materials and Engineering
enzymatic hydrolysis
grafting
lipases
maleic anhydride
poly‐ɛ‐caprolactone
title Effects of Grafting Maleic Anhydride onto Poly‐ɛ‐caprolactone on Facilitative Enzymatic Hydrolysis
title_full Effects of Grafting Maleic Anhydride onto Poly‐ɛ‐caprolactone on Facilitative Enzymatic Hydrolysis
title_fullStr Effects of Grafting Maleic Anhydride onto Poly‐ɛ‐caprolactone on Facilitative Enzymatic Hydrolysis
title_full_unstemmed Effects of Grafting Maleic Anhydride onto Poly‐ɛ‐caprolactone on Facilitative Enzymatic Hydrolysis
title_short Effects of Grafting Maleic Anhydride onto Poly‐ɛ‐caprolactone on Facilitative Enzymatic Hydrolysis
title_sort effects of grafting maleic anhydride onto poly e caprolactone on facilitative enzymatic hydrolysis
topic enzymatic hydrolysis
grafting
lipases
maleic anhydride
poly‐ɛ‐caprolactone
url https://doi.org/10.1002/mame.202300067
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