The stability of poly (m-carborane-siloxane) elastomers exposed to heat and gamma radiation

Poly(m-carboranyl-siloxatie) elastomers containing a mixture of di-methyl- and methylphenyl-silyl units were synthesised using the ferric chloride catalysed condensation reaction between di-chloro-diorganosilane and bis(di-methylmethoxysilyl)-m-carborane. These elastomeric materials were originally developed to have greater stability to extreme thermal environments and retain tailorable physical and chemical properties relative to comparable non-carborane containing elastomers. Prepared samples were aged either by heating in air at elevated temperatures or by gamma irradiation from a Co-60 source. Multinuclear (H-1, C-13 and B-11) solid and solution state nuclear magnetic resonance (NMR) was used to assess degradation. This included measurements of segmental chain dynamics using a solid-echo pulse sequence reflecting changes in crosslink density and assessing changes to the carborane fragment by B-11 and H-1 Magic Angle Spinning (MAS) methods. Thermogravimetric measurements were also performed to assess thermal stability. Gamma radiation (to a dose of 1 MGy) was found to induce only a small degree of elastomer hardening as evidenced by a reduction in segmental chain dynamics. The carborane cage however, remained intact at these dose levels. Thermal degradation was observed to lead to oxidative crosslinking, the degree of which is dependent on temperature. At temperatures below 350 degrees C, only small changes in segmental dynamics were observed commensurate with only minor weight loss at this temperature. At temperatures above 350 degrees C, the degradation of the elastomer increased dramatically with decreased segmental dynamics and presumed partial oxidation of the carborane cage. The integrity of the in-carborane cage and the segmental dynamics were found to be significantly reduced at temperatures above 580 degrees C, in line with the known cage rearrangement temperature for icosahedral carboranes. Crown Copyright (c) 2005 Published by Elsevier Ltd. All rights reserved.