Abstract

Polyaniline (PANI) and its block copolymer (PANI-PEO2000) has been prepared under effect of Maghnite-H+ (Algerian MMT) in different weight percentage (wt %) by cationic polymerization method. The structure of PANI and PANI-PEO2000 is predicted by the FT-IR and 1HNMR spectra. The thermal stability of homopolymer and block copolymer is confirmed by difference scanning calorimetry and analysis thermogravimetry. So after this results we can suggest that our heterogeneous catalyst called maghnite (Algerian MMT) can modified the morphology and the physical chemical properties of polyaniline (PANI) and its homolog block polyaniline-b-poly ethylene oxide (PANI-b-PEO2000) in the mild conditions under microwave irradiation.

Highlights

  • Polyaniline (PANI) and its block copolymer (PANI-PEO) are the best promising material in conducting polymers, because of environmental stability, easy processing, and economical efficiency [1, 2]

  • The aim of this paper is to study the polymerization of aniline and its homolog block copolymer PANI-PEO catalyzed by Maghnite- H+ under microwave irradiation [18]

  • Polyaniline (PANI) homopolymer was prepared in laboratory of polymers chemistry (Oran University, Algeria) by standard chemical intercaled method [21]

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Summary

Introduction

Polyaniline (PANI) and its block copolymer (PANI-PEO) are the best promising material in conducting polymers, because of environmental stability, easy processing, and economical efficiency [1, 2]. Absence of solvent reduces the risk of explosions when reaction takes place in a microwave oven [12, 13]. The absence of solvent reduces the risk of Composite Materials explosions when the reaction takes place in a closed vessel in an oven [14, 15]. The aim of this paper is to study the polymerization of aniline and its homolog block copolymer PANI-PEO catalyzed by Maghnite- H+ under microwave irradiation [18]. This catalyst can be separated from the polymer product and regenerated by heating at a temperature above 100°C [19, 20]. The kinetics studies of different synthesis are discussed together with the mechanism of polymerization

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