Inherently flame retardant vinyl bearing hyperbranched polysiloxanes having improved thermal stability-Ceramization and analysis of associated thermal properties. (January 2018)

• Record Type: Journal Article
• Authors: Indulekha, K.; Thomas, Deepthi; Supriya, N.; Rajeev, R.S.; Mathew, Dona; Ninan, K.N.; Gouri, C.
• Is Part Of: Polymer degradation and stability. Volume 147(2018)
• Page Start: 12
• Page End: 24
• Publication Date: 2018-01
• Subjects: Hyper-branched silicones -- Inherently flame retardant polymer -- Vinyl polysiloxane -- Silicone terpolymer -- Thermal stability; Polymers -- Deterioration -- Periodicals; Stabilizing agents -- Periodicals; Polymères -- Dégradation -- Périodiques; Stabilisants -- Périodiques; 668.9
• DOI: 10.1016/j.polymdegradstab.2017.11.007
• Languages: English
• ISSNs: 0141-3910

Abstract

Abstract: This study describes the synthesis and characterization of novel hyperbranched silicone polymers having high thermal stability and inherent flame retardancy achieved purely by molecular architecture, without the incorporation of any specific additive or filler. A series of hyper-branched terpolymers ( Me D Ph D Vi T) containing vinyl, phenyl and methyl moieties were synthesized by the acid catalysed copolymerization of vinyltriethoxysilane (VTES), diphenyldimethoxysilane (DPDMS) and dimethyldiethoxysilane (DMDES). Curing of these polymers is effected through condensation of the hydroxyl groups triggered by dibutyltindiluarate (DBTDL) catalyst. Glass to rubber transition temperature (Tg )of the cured polymers vary systematically from −110 °C to +50 °C with the increase in the content of vinyl T ( Vi T) units in the polymer backbone. The terpolymer with maximum Vi T-unit content shows an onset of thermal decomposition above 540 °C and leaves 86% char residue at 900 °C, attributed to the retardation of depolymerisation by Vi T unit. The limiting oxygen index (LOI) of the terpolymers increases from 26 to 37% with increase in Vi T unit content alone, from 13.4 to 53.3 mol% and the terpolymer with 53.3 mol % Vi T unit rates as V-0, the best in the UL-94 flame test. The ceramic residue from the cured elastomer comprises of free carbon and silica/Si-O-C ceramics. A probable mechanism has been proposed for the rearrangement of vinyl groups to carbonaceous ceramics under high temperature environment. The vinyl groups promote the formation of a carbonized, in particular graphitized, layer and SiOC phases during pyrolysis, as evidenced by TG-MS, pyrolysis GC-MS, Raman spectroscopy and FESEM analysis. Comparative study with a non-phenylated silicone elastomer confirms the mechanism of formation of carbon rich residue by the thermal rearrangement of vinyl groups. Highlights: Novel hyperbranched polysiloxanes having inherent flame retardancy syntheisized. Flame retardancy and thermal stability achieved without any additives. Detailed thermal decomposition studies carried out and probable mechanism proposed. These are promising pre-ceramic polymers for Si-O-C type ceramics.