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Synthesis of mesoporous benzoxazine by combination of amphiphilic block copolymers and reaction-induced microphase separation

A series of immiscible crystalline-crystalline diblock copolymers, poly(ethylene oxide)-b-(£`-caprolactone) (PEO-b-PCL), were blended with (3-phenyl-3,4-dihydro-2H-1,3-benzoxazin-6-yl) methanol (Pa-OH). FT-IR analyses provide that the ether group of PEO is a stronger hydrogen bond acceptor than the carbonyl group of PCL with the hydroxyl group of Pa-OH. Pa-OH after curing results in the excluded and confined PCL phase based on differential scanning calorimeter (DSC) analyses. In addition, the mesoporous structure was proved with the increasing the ratio of PCL to PEO in block copolymers by small angle X-ray scattering (SAXS), transmission electron microscopy (TEM) analyses and N2 adsorption-desorption isotherms (BET)
The poly(styrene-b-4-vinyl pyridine) diblock copolymer was blended with Pa-OH monomer. FT-IR analyses demonstrate the intermolecular hydrogen bonding interaction between the pyridine group of P4VP and the hydroxyl group of Pa-OH. After curing, the block copolymers were incorporated into polybenzoxazine resin to access the nanostructure through the reaction induced microphase separation mechanism by TEM and SAXS analyses.

Identiferoai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0727112-121439
Date27 July 2012
CreatorsChu, Wei-cheng
ContributorsChih-Feng Wang, Shiao-Wei Kuo, Ching-Hsuan Lin, Chih-Feng Huang, Ming Chen
PublisherNSYSU
Source SetsNSYSU Electronic Thesis and Dissertation Archive
LanguageCholon
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0727112-121439
Rightsuser_define, Copyright information available at source archive

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