Polydimethylsiloxane thermal degradation - Part 1. Kinetic aspects

Citation
G. Camino et al., Polydimethylsiloxane thermal degradation - Part 1. Kinetic aspects, POLYMER, 42(6), 2001, pp. 2395-2402
Citations number
16
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
POLYMER
ISSN journal
00323861 → ACNP
Volume
42
Issue
6
Year of publication
2001
Pages
2395 - 2402
Database
ISI
SICI code
0032-3861(200103)42:6<2395:PTD-P1>2.0.ZU;2-9
Abstract
A combination of traditional kinetic formal treatments and computer simulat ion has been made to analyze polydimethylsiloxane (PDMS) thermal degradatio n. It was shown that PDMS thermally decomposes to cyclic oligomers through Si-O bond scission in a chain-folded cyclic conformation energetically favo red by overlapping of empty silicon d-orbitals with orbitals of oxygen and carbon atoms. Kinetic treatment shows that PDMS thermal volatilization, as rate of heating increases, becomes dominated by rate of diffusion and evapo ration of oligomers produced on its decomposition. At high heating rate (e. g. 100 degreesC min(-1).) thermal decomposition in nitrogen and in air tend to overlap because the rate of reaction between the material and oxygen is strongly reduced by low-oxygen solubility and high-thermal degradation rat e. In nitrogen a small black residue is formed (silicon oxycarbide) which i s produced by an alternative decomposition path leading to cyclic oligomers , made possible at high heating rate. (C) 2000 Elsevier Science Ltd. All ri ghts reserved.