Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism
Lipase-catalyzed hydrolysis of poly(ɛ-caprolactone) (PCL) in toulene was investigated. PCL with number-average molecular weight (Mn) 10,000 g mol−1 was hydrolyzed using immobilized Candida antarctica lipase B (CALB). The increase in PCL concentration led to a decrease in degradation rate. Enhanced r...
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my.um.eprints.177762017-09-08T10:08:42Z http://eprints.um.edu.my/17776/ Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism Aris, M.H. Annuar, M.S.M. Ling, T.C. QH301 Biology Lipase-catalyzed hydrolysis of poly(ɛ-caprolactone) (PCL) in toulene was investigated. PCL with number-average molecular weight (Mn) 10,000 g mol−1 was hydrolyzed using immobilized Candida antarctica lipase B (CALB). The increase in PCL concentration led to a decrease in degradation rate. Enhanced rate was observed when reaction temperature was increased from 30 to 50 °C. Enzymatic chain scission of PCL yielded cyclic dicaprolactone, tricaprolactone, tetracaprolactone and oligomers with Mn less than ∼1000 g mol−1. Catalytic formation of cyclic lactones via back-biting mechanism in low water content environment was attributed to CALB. Its hydrolysis of PCL displayed consecutive random- and chain-end scission with time from detailed thermal, molecular weight and structural analyses. Apparent activation energy, Ea for hydrolysis was 45 kJ mol−1 i.e. half of that reverse reaction. Dicaprolactone and oligomers from hydrolysis readily re-polymerized to produce mid-range polymer with Mn 1400 g mol−1 after 36 h in the same reaction medium. Elsevier 2016 Article PeerReviewed Aris, M.H. and Annuar, M.S.M. and Ling, T.C. (2016) Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism. Polymer Degradation and Stability, 133. pp. 182-191. ISSN 0141-3910 http://dx.doi.org/10.1016/j.polymdegradstab.2016.08.015 doi:10.1016/j.polymdegradstab.2016.08.015 |
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QH301 Biology Aris, M.H. Annuar, M.S.M. Ling, T.C. Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism |
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Lipase-catalyzed hydrolysis of poly(ɛ-caprolactone) (PCL) in toulene was investigated. PCL with number-average molecular weight (Mn) 10,000 g mol−1 was hydrolyzed using immobilized Candida antarctica lipase B (CALB). The increase in PCL concentration led to a decrease in degradation rate. Enhanced rate was observed when reaction temperature was increased from 30 to 50 °C. Enzymatic chain scission of PCL yielded cyclic dicaprolactone, tricaprolactone, tetracaprolactone and oligomers with Mn less than ∼1000 g mol−1. Catalytic formation of cyclic lactones via back-biting mechanism in low water content environment was attributed to CALB. Its hydrolysis of PCL displayed consecutive random- and chain-end scission with time from detailed thermal, molecular weight and structural analyses. Apparent activation energy, Ea for hydrolysis was 45 kJ mol−1 i.e. half of that reverse reaction. Dicaprolactone and oligomers from hydrolysis readily re-polymerized to produce mid-range polymer with Mn 1400 g mol−1 after 36 h in the same reaction medium. |
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Article |
author |
Aris, M.H. Annuar, M.S.M. Ling, T.C. |
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Aris, M.H. Annuar, M.S.M. Ling, T.C. |
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Aris, M.H. |
title |
Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism |
title_short |
Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism |
title_full |
Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism |
title_fullStr |
Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism |
title_full_unstemmed |
Lipase-mediated degradation of poly-ε-caprolactone in toluene: Behavior and its action mechanism |
title_sort |
lipase-mediated degradation of poly-ε-caprolactone in toluene: behavior and its action mechanism |
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Elsevier |
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2016 |
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http://eprints.um.edu.my/17776/ http://dx.doi.org/10.1016/j.polymdegradstab.2016.08.015 |
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1643690515945750528 |