Synthesis and interfacial properties of montmorillonite/polypyrrole nanocomposites

被引:94
作者
Boukerma, K
Piquemal, JY
Chehimi, MM
Mravcáková, M
Omastová, M
Beaunier, P
机构
[1] Univ Paris 07, ITODYS, F-75005 Paris, France
[2] CNRS, UMR 7086, F-75005 Paris, France
[3] Slovak Acad Sci, Inst Polymer, Bratislava 84236, Slovakia
[4] Univ Paris 06, Lab React Surface, F-75252 Paris 05, France
关键词
polypyrrole; montmorillonite; nanocomposites;
D O I
10.1016/j.polymer.2005.11.065
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Montmorillonite/polypyrrole (MMT/PPy) nanocomposites were prepared by the in situ polymerization of pyrrole in the presence of MMT. The morphology of the MMT/PPy nanocomposites as examined by scanning electron microscopy differs slightly from that of the untreated MMT but markedly from that of polypyrrole. X-ray photoelectron spectroscopy (XPS) showed that the materials have MMT-rich surfaces, an indication that polypyrrole is essentially intercalated in the host clay galleries. The transmission electron microscopy showed, that the interlamellar spacing of the untreated MMT increased from 1.25 to 18.9 nm, when compared to nanocomposite MMT/10.8% PPy. Moreover, XPS highlighted the cation exchange of Na+ from montmorillonite by K+ (from the oxidant) and by the positively charged polypyrrole chains. Inverse gas chromatography indicated that the nanocomposites are high surface energy materials with a dispersive contribution to the surface energy (gamma(d)(s)) reaching 200 mJ/m(2) at 150 degrees C, for a PPy loading of 21.4 wt%. The (gamma(d)(s)) values of the MMT/PPy nanocomposites were correlated to the changes in the specific surface area of the MMT induced by the intercalation of polypyrrole. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:569 / 576
页数:8
相关论文
共 49 条
[1]   Adsorption of poly(methyl methacrylate) and poly(vinyl chloride) blends onto polypyrrole - Study by X-ray photoelectron spectroscopy, time-of-flight static secondary ion mass spectroscopy, and inverse gas chromatography [J].
Abel, ML ;
Chehimi, MM ;
Fricker, F ;
Delamar, M ;
Brown, AM ;
Watts, JF .
JOURNAL OF CHROMATOGRAPHY A, 2002, 969 (1-2) :273-285
[2]   Polymer-layered silicate nanocomposites: Preparation, properties and uses of a new class of materials [J].
Alexandre, Michael ;
Dubois, Philippe .
Materials Science and Engineering: R: Reports, 2000, 28 (1-2) :1-63
[3]  
[Anonymous], INTRINSICALLY CONDUC
[4]   Correlation of mechanical properties of clay filled polyamide mouldings with chromatographically measured surface energies [J].
Ansari, DM ;
Price, GJ .
POLYMER, 2004, 45 (11) :3663-3670
[5]  
ARMES SP, 1998, HDB CONDUCTING POLYM, P423
[6]   Synthesis and characterization of active ester-functionalized polypyrrole-silica nanoparticles: Application to the covalent attachment of proteins [J].
Azioune, A ;
Ben Slimane, A ;
Hamou, LA ;
Pleuvy, A ;
Chehimi, MM ;
Perruchot, C ;
Armes, SP .
LANGMUIR, 2004, 20 (08) :3350-3356
[7]   A conducting nanocomposite via intercalative polymerisation of thiophene in montmorillonite clay [J].
Ballav, N ;
Biswas, M .
SYNTHETIC METALS, 2004, 142 (1-3) :309-315
[8]   APPLICATION OF INVERSE GAS-CHROMATOGRAPHY TO THE STUDY OF THE SURFACE-PROPERTIES OF MODIFIED LAYERED MINERALS [J].
BANDOSZ, TJ ;
PUTYERA, K ;
JAGIELLO, J ;
SCHWARZ, JA .
MICROPOROUS MATERIALS, 1993, 1 (01) :73-79
[9]  
Belgacem MN, 1999, SURF SCI SERIES, V80, P41
[10]   Polypyrrole-coated poly(vinyl chloride) powder particles: surface chemical and morphological characterisation by means of X-ray photoelectron spectroscopy and scanning electron microscopy [J].
Ben Slimane, A ;
Chehimi, MM ;
Vaulay, MJ .
COLLOID AND POLYMER SCIENCE, 2004, 282 (04) :314-323