Synthesis and morphological characterization of PMMA/polyaniline nanofiber composites

被引:41
|
作者
Araújo, PLB
Araújo, ES
Santos, RFS
Pacheco, APL
机构
[1] Univ Fed Pernambuco, Dept Nucl Engn, BR-50740540 Recife, PE, Brazil
[2] Univ Fed Pernambuco, Dept Quim, BR-50740540 Recife, PE, Brazil
[3] Ctr Reg Ciencias Nucl, Recife, PE, Brazil
关键词
PANI composites; PMMA; ultrasound; self-assembly nanofiber;
D O I
10.1016/j.mejo.2005.04.024
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Poly (methyl methacrylate) (PMMA)/Polyaniline nanofibers composite films were prepared by solution casting. Doped polyanifine self-assembled nanofibers (PANFs) were synthesized by interfacial polymerization performed in an aqueous HCI/dichloromethane biphasic system in the presence of ammonium peroxydisulfate as oxidant agent. Sodium dodecyl sulfate (SDS) was added to the organic phase in order to verify possible modification the morphology the nanostrucutures when compared with previous reports. Treatment in an ultrasonic bath of PANFs on butanone resulted in a green dispersion (up to 250 mg/dL). Dispersed PANFs were then combined with PMMA/butanone solution. Additional sonication and posterior film cast from solution procedures resulted in slight green PMMA/PANFs 0.15-0.30% (wt/wt) composite films. Film composites were characterized by UV-Vis spectroscopy and Scanning Electron Microscopy (SEM). PANFs powder was investioated by (SEM). An investigation by viscosity method on molecular structure of neat PMMA exposed to ultrasonic irradiation up to 2 h showed small change (<5%) in the viscosity-average molar mass, Mv (approximate to 100 kg/mol). It suggests that mechanical degradation by, cavitation does not occur on PMMA under those conditions. Thus, ultrasonic bath treatment is a simple, accessible method for mitigating solubility problems of PANI doped with inorganic acids and improving quality of low concentration PMMA/PANI composites. Application of these composites relies on the radiolytic stabilization effects of PANI on PMMA matrix. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1055 / 1057
页数:3
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