Pyrolysis, silicon organic compounds

A great potential for new compounds is provided by structures with two carbon and two silicon atoms around the central silicon. These polysilanes with organic groups lead to silicon-carbide ceramics. A wide field of application would be opened up if one could make a polysilane as a plastic mass which could be extruded and modeled and if after pyrolysis silicon-carbide is formed without a strong contraction (this means a high ceramic yield). Polysilane fibers are only one product in a range of many... 

Another MS technique used in connection to pyrolysis is MIMS (membrane introduction mass spectrometry). MIMS is in fact a special inlet for the mass spectrometer, where a membrane (usually silicone, non-polar) lets only certain molecule types enter the Ionization chamber of the MS. This allows, for example, direct analysis of certain volatile organic compounds from air. The system makes possible the coupling of atmospheric pyrolysis to a mass spectrometer [61a] allowing direct sampling of the pyrolysate. Other parts of the mass spectrometer do not need to be changed when using MIMS. 

The presence of amorphous oxycarbide (Si-O-C) phase was also revealed in the Nicalon fibers at the interface between SiC core and surface SiOa layer (Pumpuck, 1980 Lipowitz, 1987 Laffon, 1989 Porte, 1989), although any thermodynamically stable compounds have not been found in the Si-O-C system. The formation of such an amorphous silicon oxycarbide phase was also suggested during the pyrolysis of organics-substituted polysiloxane gels to form SiC (Zhang, 1990 Babonneau, 1990 Bums, 1992). 

Although silicon nanocrystals are now more commonly prepared by a variety of means which are easier to scale up, e.g., pyrolysis of silanes (Xuegeng et al. 2004), thermal treatment of silsesquioxanes (Hessel et al. 2006, 2010), and from reactions of molecular silicon compounds (Wilcoxon et al. 1999 Bley and Kauzlarich 1996), this review will concentrate on routes which proceed via the formation of porous silicon. More general reviews of silicon nanocrystals Irom physics and chemistry perspectives are available (Shirahata 2011 Kang et al. 2011 Heitmann et al. 2005). Derivatization of porous silicon and SiNCs usually relies on the chemistry of the hydrogen-terminated silicon surface, which shares some of the organic reactivity of hydrosilanes (Buriak 2002). Reaction with alcohols results in Si-O-C bonded monolayers (Sweryda-Krawiec et al. 1999), but these are suseeptible to hydrolysis under ambient conditions. Alternately, addition of surface Si-H aeross a C = C double bond produces Si-C bonded monolayers, which are very stable. 

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