Issue 8, 2015

A novel tin-based imidazolium-modified montmorillonite catalyst for the preparation of poly(butylene terephthalate)-based nanocomposites using in situ entropically-driven ring-opening polymerization

Abstract

A novel alkylimidazolium salt incorporating a 2,2-di-n-butyl[1,3,2]dioxastannolane moiety was synthesized and characterized. Its effectiveness as a transesterification catalyst in the entropically-driven ring-opening polymerization (ED-ROP) of macrocyclic oligomers of butylene terephthalate (BT-MCOs) was comparable to that of other tin-based transesterification catalysts. A supported version of the catalyst was prepared by ion exchange with the sodium cations present in montmorillonite. X-Ray analysis indicated the imidazolium species entered the galleries between the silicate layers. The supported catalyst was significantly more thermally stable than the non-supported catalyst. Poly(butylene terephthalate)–clay nanocomposites were obtained by the in situ ED-ROP of BT-MCOs intercalated between the clay layers, catalyzed by either the supported tin-based catalyst or by a catalyst prepared in situ from a supported imidazolium salt with diol moieties and di-n-butyldimethoxytin. X-Ray diffraction and transmission electron microscopy indicated that the ensuing nanocomposites exhibit a mix of intercalated and exfoliated silicate nanolayers.

Graphical abstract: A novel tin-based imidazolium-modified montmorillonite catalyst for the preparation of poly(butylene terephthalate)-based nanocomposites using in situ entropically-driven ring-opening polymerization

Supplementary files

Article information

Article type
Paper
Submitted
23 Oct 2014
Accepted
15 Dec 2014
First published
15 Dec 2014

RSC Adv., 2015,5, 6222-6231

Author version available

A novel tin-based imidazolium-modified montmorillonite catalyst for the preparation of poly(butylene terephthalate)-based nanocomposites using in situ entropically-driven ring-opening polymerization

L. Conzatti, R. Utzeri, P. Hodge and P. Stagnaro, RSC Adv., 2015, 5, 6222 DOI: 10.1039/C4RA12983K

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