Interfacial Synthesis of Chiral Polyaniline Using Immobilized Enzymes in Ionic Liquid

碩士 === 國立東華大學 === 化學系 === 96 === A new interfacial enzymatic method for chiral polyaniline was developed using 1-butyl -3-methyl imidazolium hexafluorophosphate (BMIM-PF6) water immiscible ionic liquid(IL) to aqueous/ionic liquid interface and to protect the enzymes under acidic reaction conditions....

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Main Authors: Chun-Kai Huang, 黃軍凱
Other Authors: Hun-Chi Shu
Format: Others
Language:zh-TW
Published: 2008
Online Access:http://ndltd.ncl.edu.tw/handle/mfk347
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spelling ndltd-TW-096NDHU50650232019-05-15T19:39:22Z http://ndltd.ncl.edu.tw/handle/mfk347 Interfacial Synthesis of Chiral Polyaniline Using Immobilized Enzymes in Ionic Liquid 水相/離子液體兩相西每催化聚合法合成掌性聚苯胺 Chun-Kai Huang 黃軍凱 碩士 國立東華大學 化學系 96 A new interfacial enzymatic method for chiral polyaniline was developed using 1-butyl -3-methyl imidazolium hexafluorophosphate (BMIM-PF6) water immiscible ionic liquid(IL) to aqueous/ionic liquid interface and to protect the enzymes under acidic reaction conditions. The better chirality of polyaniline was obtained in lower temperature, such as the 4 oC . The optimal conditions were as follow: 0.0016mole aniline monomer mixed with 1 mL 2M camphorsulfonic acid as aqueous layer and 6mg peroxidase dissolve in 1mL BMIM PF6 as IL layer and then incubated 36 hours statically at 4oC. The different optical spectrums were found under the same optical activity camphorsulfonic acid as dopant. It shows that the peroxidase is the main factor to induce the optical activity. IL could be reused repeatly for at least 5 times . however, the chirality of polyaniline will decrease comparing with the first time using of IL. Hun-Chi Shu 蘇宏基 2008 學位論文 ; thesis 65 zh-TW
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language zh-TW
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description 碩士 === 國立東華大學 === 化學系 === 96 === A new interfacial enzymatic method for chiral polyaniline was developed using 1-butyl -3-methyl imidazolium hexafluorophosphate (BMIM-PF6) water immiscible ionic liquid(IL) to aqueous/ionic liquid interface and to protect the enzymes under acidic reaction conditions. The better chirality of polyaniline was obtained in lower temperature, such as the 4 oC . The optimal conditions were as follow: 0.0016mole aniline monomer mixed with 1 mL 2M camphorsulfonic acid as aqueous layer and 6mg peroxidase dissolve in 1mL BMIM PF6 as IL layer and then incubated 36 hours statically at 4oC. The different optical spectrums were found under the same optical activity camphorsulfonic acid as dopant. It shows that the peroxidase is the main factor to induce the optical activity. IL could be reused repeatly for at least 5 times . however, the chirality of polyaniline will decrease comparing with the first time using of IL.
author2 Hun-Chi Shu
author_facet Hun-Chi Shu
Chun-Kai Huang
黃軍凱
author Chun-Kai Huang
黃軍凱
spellingShingle Chun-Kai Huang
黃軍凱
Interfacial Synthesis of Chiral Polyaniline Using Immobilized Enzymes in Ionic Liquid
author_sort Chun-Kai Huang
title Interfacial Synthesis of Chiral Polyaniline Using Immobilized Enzymes in Ionic Liquid
title_short Interfacial Synthesis of Chiral Polyaniline Using Immobilized Enzymes in Ionic Liquid
title_full Interfacial Synthesis of Chiral Polyaniline Using Immobilized Enzymes in Ionic Liquid
title_fullStr Interfacial Synthesis of Chiral Polyaniline Using Immobilized Enzymes in Ionic Liquid
title_full_unstemmed Interfacial Synthesis of Chiral Polyaniline Using Immobilized Enzymes in Ionic Liquid
title_sort interfacial synthesis of chiral polyaniline using immobilized enzymes in ionic liquid
publishDate 2008
url http://ndltd.ncl.edu.tw/handle/mfk347
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