Abstract:A new poly(methylsilane-carbosilane) (PMSCS) for silicon carbide precursor was prepared using Wurtz-type copolymerization of methyldichlorosilane (MeHSiCl 2 ), chloromethyldichloromethylsilane (ClCH 2 MeSiCl 2 ), and (dichloromethyl)methylsilane (Cl 2 CHMeSiH 2 ), with (chloromethyl)methylsilane (ClCH 2 MeSiH 2 ) or trimethylchlorosilane (Me 3 SiCl) as terminated reagent. The ceramic yield of PMSCS was markedly increased by introduction of Cl 2 CHMeSiH 2 comonomer and capped with ClCH 2 MeSiH 2 . The H 2 MeSiC… Show more
“…33 Sawai et al and Whitmarsh et al assigned the peak at $2 ppm to -CH 2units in the scaffold and SiCH 2 Cl units, respectively. 34,35 Herein, based on the 1 H NMR spectra of (CH 3 ) 3 -SiCH 2 Cl and (CH 3 )SiOCH 2 CH 3 , 36,37 we conrmed that the peaks observed at 1.5-4 ppm originate from Si-O-alkyl and -SiCH 2 Cl units (Fig. 4).…”
Section: Spectroscopic Analysis Of Vhpcsmentioning
Polymerization of VHPCS by the Grignard coupling reaction depended on the type of starting material. In the case of Cl3SiCH2Cl starting material, a stepwise growth manner was shown, due to a coupling between –CH2Cl and the Si–Cl sites.
“…33 Sawai et al and Whitmarsh et al assigned the peak at $2 ppm to -CH 2units in the scaffold and SiCH 2 Cl units, respectively. 34,35 Herein, based on the 1 H NMR spectra of (CH 3 ) 3 -SiCH 2 Cl and (CH 3 )SiOCH 2 CH 3 , 36,37 we conrmed that the peaks observed at 1.5-4 ppm originate from Si-O-alkyl and -SiCH 2 Cl units (Fig. 4).…”
Section: Spectroscopic Analysis Of Vhpcsmentioning
Polymerization of VHPCS by the Grignard coupling reaction depended on the type of starting material. In the case of Cl3SiCH2Cl starting material, a stepwise growth manner was shown, due to a coupling between –CH2Cl and the Si–Cl sites.
“…Commonly used types include solid polycarbosilanes (PCSs), perhydrogen PCSs (HPCSs), polymethylsilane (PMS), etc. 18,[21][22][23] Among others, PCS remains the most commercialized SiC ceramic precursor. However, the ceramic products derived from PCS contain more free carbon.…”
Section: Introductionmentioning
confidence: 99%
“…In recent decades, extensive research has been conducted to prepare SiC ceramic polymer precursors. Commonly used types include solid polycarbosilanes (PCSs), perhydrogen PCSs (HPCSs), polymethylsilane (PMS), etc 18,21–23 . Among others, PCS remains the most commercialized SiC ceramic precursor.…”
A series of SiC/SiC composites were fabricated through the precursor infiltration and pyrolysis (PIP) process, using solid polycarbosilane (PCS) and liquid vinyl perhydrogen PCS (VHPCS) solutions as impregnating agents. The physicochemical characteristics of the SiC matrices derived from PCS and VHPCS were investigated and compared. The impact of the PCS composition on the microstructure, density, flexural strength, and modulus of the resulting SiC/SiC composites was also examined. As the VHPCS content increased to 60 wt%, the flexural strength of the composites gradually rose to a peak of 490.9 MPa before decreasing as the VHPCS proportion continued to increase. Meanwhile, the flexural modulus increased continually with the introduction of VHPCS. A possible mechanism is proposed to explain the different variations in flexural strength and modulus, taking into account the ceramic toughening principle and the distinct properties of PCS and VHPCS.
“…However, the high melting point of PCS makes it difficult to prepare C/C–SiC ceramic composites. Various functional groups were introduced into the main chain of PCS in an attempt to solve processing difficulties, but this effort did not produce the desired outcome 18 …”
Section: Introductionmentioning
confidence: 99%
“…Various functional groups were introduced into the main chain of PCS in an attempt to solve processing difficulties, but this effort did not produce the desired outcome. 18 Advanced PCPs have also attracted the attention of researchers. Chemistry plays a major role in the precise control of the chemical compositions and microstructure of ceramics at low processing temperatures using welldefined single-source precursors.…”
Carbon-fiber-reinforced carbon-silicon carbide (C/C-SiC) composites were prepared by impregnating carbon fibers with ethynylphenyl-terminated poly(silylene-acetylene) (EPTSA) as a single-source precursor with subsequent hot pressing and pyrolysis. The structural evolution, crystallization behavior, and graphitization of bulk C-SiC ceramics, as well as their mechanical properties and ablation behavior, were investigated. The EPTSA precursor starts to transform into inorganic SiC ceramic materials at 800 • C, which is characterized by an amorphous structure with weight loss, shrinkage, and densification between 800 and 1000 • C. The formation of SiC crystals inhibited the growth of the graphitic structure between 1000 and 1200 • C. As the temperature was raised, both graphite and SiC crystals continued to grow, and the crystalline forms became more complete. The carbon-fiber cloth (T300CF)-reinforced C-SiC composite (T300CF/C-SiC) prepared using polymer infiltration and pyrolysis (PIP) exhibited excellent mechanical properties. After five PIP cycles, the flexural strength, flexural modulus, and interlaminar shear strength of the T300CF/C-SiC composite reached 169 MPa, 32.5 GPa, and 9.38 MPa, respectively. In addition, the chopped-carbon-fiber-reinforced C-SiC composite fabricated using the PIP process demonstrated good oxyacetylene-torch ablation properties.
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