Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology

BACKGROUND: Adipate esters are used as low-temperature and low-viscosity plasticizers for polyvinyl chloride and its copolymers. In this work, optimization of lipase-catalyzed production of dilauryl adipate was carried out using response surface methodology (RSM) based on a four-factor-five-level...

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Main Authors: Abdul Rahman, Mohd Basyaruddin, Chaibakhsh, Naz, Basri, Mahiran, Raja Abdul Rahman, Raja Noor Zaliha, Salleh, Abu Bakar, Md Radzi, Salina
Format: Article
Language:English
Published: Society of Chemical Industry 2008
Online Access:http://psasir.upm.edu.my/id/eprint/4775/1/Modeling%20and%20optimization%20of%20lipase-catalyzed%20synthesis%20of%20dilauryl.pdf
http://psasir.upm.edu.my/id/eprint/4775/
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jctb.1960/abstract
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spelling my.upm.eprints.47752016-09-27T07:19:04Z http://psasir.upm.edu.my/id/eprint/4775/ Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology Abdul Rahman, Mohd Basyaruddin Chaibakhsh, Naz Basri, Mahiran Raja Abdul Rahman, Raja Noor Zaliha Salleh, Abu Bakar Md Radzi, Salina BACKGROUND: Adipate esters are used as low-temperature and low-viscosity plasticizers for polyvinyl chloride and its copolymers. In this work, optimization of lipase-catalyzed production of dilauryl adipate was carried out using response surface methodology (RSM) based on a four-factor-five-level central composite rotatable design (CCRD). Immobilized lipase from Candida antarctica (Novozym 435) was used as catalyst in this reaction. Various reaction parameters affecting the synthesis of adipate ester, including alcohol/acidmolar ratio, amount of enzyme, temperature and reaction time, were investigated. RESULTS: Statistical analysis showed that the amount of enzyme was less significant than the other three factors. The optimal conditions for the enzymatic reaction were obtained at 5.7:1 substrate molar ratio using 0.18 g of enzyme at 53.1 ◦C for 282.2min. Under these conditions the esterification percentage was 96.0%. CONCLUSIONS: The results demonstrated that response surface methodology can be applied effectively to optimize the lipase-catalyzed synthesis of adipate ester. The optimum conditions can obtained be used to scale up the process. Society of Chemical Industry 2008 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/4775/1/Modeling%20and%20optimization%20of%20lipase-catalyzed%20synthesis%20of%20dilauryl.pdf Abdul Rahman, Mohd Basyaruddin and Chaibakhsh, Naz and Basri, Mahiran and Raja Abdul Rahman, Raja Noor Zaliha and Salleh, Abu Bakar and Md Radzi, Salina (2008) Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology. Journal of Chemical Technology and Biotechnology, 83 (11). pp. 1534-1540. ISSN 0268-2575; ESSN: 1097-4660 http://onlinelibrary.wiley.com/wol1/doi/10.1002/jctb.1960/abstract 10.1002/jctb.1960
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description BACKGROUND: Adipate esters are used as low-temperature and low-viscosity plasticizers for polyvinyl chloride and its copolymers. In this work, optimization of lipase-catalyzed production of dilauryl adipate was carried out using response surface methodology (RSM) based on a four-factor-five-level central composite rotatable design (CCRD). Immobilized lipase from Candida antarctica (Novozym 435) was used as catalyst in this reaction. Various reaction parameters affecting the synthesis of adipate ester, including alcohol/acidmolar ratio, amount of enzyme, temperature and reaction time, were investigated. RESULTS: Statistical analysis showed that the amount of enzyme was less significant than the other three factors. The optimal conditions for the enzymatic reaction were obtained at 5.7:1 substrate molar ratio using 0.18 g of enzyme at 53.1 ◦C for 282.2min. Under these conditions the esterification percentage was 96.0%. CONCLUSIONS: The results demonstrated that response surface methodology can be applied effectively to optimize the lipase-catalyzed synthesis of adipate ester. The optimum conditions can obtained be used to scale up the process.
format Article
author Abdul Rahman, Mohd Basyaruddin
Chaibakhsh, Naz
Basri, Mahiran
Raja Abdul Rahman, Raja Noor Zaliha
Salleh, Abu Bakar
Md Radzi, Salina
spellingShingle Abdul Rahman, Mohd Basyaruddin
Chaibakhsh, Naz
Basri, Mahiran
Raja Abdul Rahman, Raja Noor Zaliha
Salleh, Abu Bakar
Md Radzi, Salina
Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology
author_facet Abdul Rahman, Mohd Basyaruddin
Chaibakhsh, Naz
Basri, Mahiran
Raja Abdul Rahman, Raja Noor Zaliha
Salleh, Abu Bakar
Md Radzi, Salina
author_sort Abdul Rahman, Mohd Basyaruddin
title Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology
title_short Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology
title_full Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology
title_fullStr Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology
title_full_unstemmed Modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology
title_sort modeling and optimization of lipase-catalyzed synthesis of dilauryl adipate ester by response surface methodology
publisher Society of Chemical Industry
publishDate 2008
url http://psasir.upm.edu.my/id/eprint/4775/1/Modeling%20and%20optimization%20of%20lipase-catalyzed%20synthesis%20of%20dilauryl.pdf
http://psasir.upm.edu.my/id/eprint/4775/
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jctb.1960/abstract
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