Synthesis and characterization of polypyrrole-graft-poly(ε-caprolactone) copolymers:: new electrically conductive nanocomposites

被引:67
作者
Mecerreyes, D
Stevens, R
Nguyen, C
Pomposo, JA
Bengoetxea, M
Grande, H
机构
[1] Ctr Electrochem Res & Dev, Cidetec, Parque Tecnol Miramon, Donostia San Sebastian 20009, Spain
[2] NASA, Ames Res Ctr, Moffett Field, CA 94035 USA
[3] IBM Corp, Almaden Res Ctr, San Jose, CA USA
关键词
polypyrrole; graft copolymers; nanocomposite;
D O I
10.1016/S0379-6779(01)00503-3
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A series of polypyrrole-graft-poly(epsilon-caprolactone) (PPy-g-PCL) copolymers have been synthesized via oxidative copolymerization of pyrrole and pyrrole-end functional macromonomers. Copolymerizations were carried out in tetrahydrofuran at 0 degreesC using FeCl3 as the oxidizing and doping agent. Poly(E-caprolactone) rich copolymers (>85 wt.%) were partly soluble in common organic solvents, whereas polypyrrole-rich copolymers were completely insoluble. The composition of the PPy-g-PCL copolymers was determined by Fourier transform infra-red (FTIR) spectroscopy and thermal gravimetrical analysis (TGA). By controlling the monomer feed and molecular weight of the macromonomer, graft copolymers across a broad composition range were obtained. Both differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) show that the PPy-g-PCL copolymers phase separate into PPy and PCL rich domains. The electrical conductivity of the nanocomposites increases with the amount of polypyrrole in the copolymer between the value of pure PCL (10(-12) S/cm) and that of polypyrrole (10 S/cm). Atomic force microscopy (AFM) confirmed the presence of nanophases (15-40 nm) and hence, the preparation of new nanomaterials. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:173 / 178
页数:6
相关论文
共 17 条
[1]  
Alkan S, 1999, J POLYM SCI POL CHEM, V37, P4218, DOI 10.1002/(SICI)1099-0518(19991115)37:22<4218::AID-POLA22>3.0.CO
[2]  
2-Z
[3]   BLOCK COPOLYMER THERMODYNAMICS - THEORY AND EXPERIMENT [J].
BATES, FS ;
FREDRICKSON, GH .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 (01) :525-557
[4]   SYNTHESIS OF 1,2-DIHYDRO-3H-PYRROLO[1,2-A]PYRROLE-1-CARBOXYLIC ACIDS AND HOMOLOGOUS PYRIDINE AND AZEPINE ANALOGS THEREOF [J].
CARPIO, H ;
GALEAZZI, E ;
GREENHOUSE, R ;
GUZMAN, A ;
VELARDE, E ;
ANTONIO, Y ;
FRANCO, F ;
LEON, A ;
PEREZ, V ;
SALAS, R ;
VALDES, D ;
ACKRELL, J ;
CHO, D ;
GALLEGRA, P ;
HALPERN, O ;
KOEHLER, R ;
MADDOX, ML ;
MUCHOWSKI, JM ;
PRINCE, A ;
TEGG, D ;
THURBER, TC ;
VANHORN, AR ;
WREN, D .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1982, 60 (18) :2295-2312
[5]   Ordered bicontinuous nanoporous and nanorelief ceramic films from self assembling polymer precursors [J].
Chan, VZH ;
Hoffman, J ;
Lee, VY ;
Iatrou, H ;
Avgeropoulos, A ;
Hadjichristidis, N ;
Miller, RD ;
Thomas, EL .
SCIENCE, 1999, 286 (5445) :1716-1719
[6]   Synthesis of conductive nanocomposites by selective in situ polymerization of pyrrole within the lamellar microdomains of a block copolymer [J].
de Jesus, MC ;
Weiss, RA ;
Hahn, SF .
MACROMOLECULES, 1998, 31 (07) :2230-2235
[7]  
EGIBURU JL, 1996, POLYMER, V37, P3615
[8]   Conducting polymer nanocomposites: A brief overview [J].
Gangopadhyay, R ;
De, A .
CHEMISTRY OF MATERIALS, 2000, 12 (03) :608-622
[9]   A polystyrene-oligothiophene-polystyrene triblock copolymer [J].
Hempenius, MA ;
Langeveld-Voss, BMW ;
van Haare, JAEH ;
Janssen, RAJ ;
Sheiko, SS ;
Spatz, JP ;
Möller, M ;
Meijer, EW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (12) :2798-2804
[10]   Conducting copolymers of polypyrrole/polytetrahydrofuran [J].
Kizilyar, N ;
Toppare, L ;
Onen, A ;
Yagci, Y .
POLYMER BULLETIN, 1998, 40 (06) :639-645