Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol 1,3-diglycerolate diacrylate and its mechanism
Glycerol 1,3-diglycerolate diacrylate (GDD) was graft copolymerized onto poly(3-hydroxyoctanoate-co-3- hydroxyhexanoate) P(3HO-co-3HHX) to render the latter more hydrophilic. Grafting of P(3HO-co-3HHX) backbone was performed using benzoyl peroxide as free radical initiator in homogenous acetone so...
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iium-603402019-06-25T02:45:59Z http://irep.iium.edu.my/60340/ Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol 1,3-diglycerolate diacrylate and its mechanism Ansari, Nor Faezah Annuar, M. Suffian QD Chemistry QH301 Biology TP248.13 Biotechnology Glycerol 1,3-diglycerolate diacrylate (GDD) was graft copolymerized onto poly(3-hydroxyoctanoate-co-3- hydroxyhexanoate) P(3HO-co-3HHX) to render the latter more hydrophilic. Grafting of P(3HO-co-3HHX) backbone was performed using benzoyl peroxide as free radical initiator in homogenous acetone solution. The graft copolymer of P(3HO-co-3HHX)-g-GDD was characterized using spectroscopic and thermal methods. The presence of GDD monomer in the grafted P(3HO-co-3HHX) materials linked through covalent bond was indicated by spectroscopic analyses. Different parameters affecting the graft yield viz. monomer concentration, initiator concentration, temperature and reaction time were also investigated. Water uptake measurement showed that P(3HO-co-3HHX)-g-GDD copolymer became more hydrophilic as the GDD concentration in the copolymer increased. Introduction of hydroxyl groups via grafted GDD monomers improved the wettability and imparted amphiphilicity to the graft copolymer, thus potentially improving their facility for cellular interaction. Thermal stability of grafted copolymer reduced with increased grafting yield. The activation energy, Ea, for the graft copolymerization was calculated at » 51 kJ mol¡1. Mechanism of grafting reaction was also proposed. Taylor & Francis 2017-12-01 Article PeerReviewed application/pdf en http://irep.iium.edu.my/60340/1/60340_Functionalization%20of%20medium-chain-length%20_article.pdf application/pdf en http://irep.iium.edu.my/60340/2/60340_Functionalization%20of%20medium-chain-length%20_scopus.pdf Ansari, Nor Faezah and Annuar, M. Suffian (2017) Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol 1,3-diglycerolate diacrylate and its mechanism. Journal of Macromolecular Science: Pure and Applied Chemistry, 55 (1). pp. 66-74. ISSN 1060-1325 E-ISSN 1520-5738 http://www.tandfonline.com/doi/abs/10.1080/10601325.2017.1387490?journalCode=lmsa20 10.1080/10601325.2017.1387490 |
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QD Chemistry QH301 Biology TP248.13 Biotechnology Ansari, Nor Faezah Annuar, M. Suffian Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol 1,3-diglycerolate diacrylate and its mechanism |
description |
Glycerol 1,3-diglycerolate diacrylate (GDD) was graft copolymerized onto poly(3-hydroxyoctanoate-co-3-
hydroxyhexanoate) P(3HO-co-3HHX) to render the latter more hydrophilic. Grafting of P(3HO-co-3HHX)
backbone was performed using benzoyl peroxide as free radical initiator in homogenous acetone solution.
The graft copolymer of P(3HO-co-3HHX)-g-GDD was characterized using spectroscopic and thermal
methods. The presence of GDD monomer in the grafted P(3HO-co-3HHX) materials linked through
covalent bond was indicated by spectroscopic analyses. Different parameters affecting the graft yield viz.
monomer concentration, initiator concentration, temperature and reaction time were also investigated.
Water uptake measurement showed that P(3HO-co-3HHX)-g-GDD copolymer became more hydrophilic as
the GDD concentration in the copolymer increased. Introduction of hydroxyl groups via grafted GDD
monomers improved the wettability and imparted amphiphilicity to the graft copolymer, thus potentially
improving their facility for cellular interaction. Thermal stability of grafted copolymer reduced with
increased grafting yield. The activation energy, Ea, for the graft copolymerization was calculated at » 51 kJ
mol¡1. Mechanism of grafting reaction was also proposed. |
format |
Article |
author |
Ansari, Nor Faezah Annuar, M. Suffian |
author_facet |
Ansari, Nor Faezah Annuar, M. Suffian |
author_sort |
Ansari, Nor Faezah |
title |
Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol
1,3-diglycerolate diacrylate and its mechanism |
title_short |
Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol
1,3-diglycerolate diacrylate and its mechanism |
title_full |
Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol
1,3-diglycerolate diacrylate and its mechanism |
title_fullStr |
Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol
1,3-diglycerolate diacrylate and its mechanism |
title_full_unstemmed |
Functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol
1,3-diglycerolate diacrylate and its mechanism |
title_sort |
functionalization of medium-chain-length poly(3-hydroxyalkanoates) as amphiphilic material by graft copolymerization with glycerol
1,3-diglycerolate diacrylate and its mechanism |
publisher |
Taylor & Francis |
publishDate |
2017 |
url |
http://irep.iium.edu.my/60340/ http://irep.iium.edu.my/60340/ http://irep.iium.edu.my/60340/ http://irep.iium.edu.my/60340/1/60340_Functionalization%20of%20medium-chain-length%20_article.pdf http://irep.iium.edu.my/60340/2/60340_Functionalization%20of%20medium-chain-length%20_scopus.pdf |
first_indexed |
2023-09-18T21:25:32Z |
last_indexed |
2023-09-18T21:25:32Z |
_version_ |
1777412165882347520 |