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Porous SiOC/SiC ceramics via an active-filler- catalyzed polymer-derived method

机译:通过一个活性填料——多孔SiOC /碳化硅陶瓷催化polymer-derived方法

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摘要

In this study, bulk and porous SiOC materials were synthesized via a polymer-derived ceramic (PDC) method from a base polysiloxane (PSO) precursor and an iron (Fe) catalyst under an inert pyrolytic atmosphere. Fe catalyzes not only the formation and nucleation of b-SiC at lower temperatures but also promotes phase separation of the amorphous SiOxCy phase, compared to PDCs without the Fe catalyst. Samples with Fe pyrolyzed at 1100 1C have an appreciable b-SiC content compared to a negligible/ unobservable b-SiC content in the corresponding Fe-less samples. Selective etching of the SiO2 phase shows that Fe also induces segregation of the amorphous SiOxCy phase, yielding larger specific surface areas and gas sorption capability below 1300 1C. At 1500 1C, the pore structure changes to form interconnected networks due to the highly phase separated SiO2 and b-SiC microstructure. A Gibbs free energy minimization method was used to determine the relative phase content of the pyrolyzed samples, with the effect of Fe quantified with simplified vapor–liquid–solid (VLS), solid–liquid–solid (SLS), and classical nucleation theories.
机译:在这项研究中,大部分和多孔SiOC材料通过polymer-derived合成陶瓷(PDC)方法从基聚硅氧烷(PSO)的前体和铁(Fe)催化剂在惰性热解气氛。形成和成核的b-SiC低气温也促进相分离的无定形SiOxCy阶段,而髓没有铁催化剂。正交1100 1 c有明显的b-SiC内容相比可以忽略不计/不可见的在相应的Fe-less b-SiC内容样本。显示,菲也引发种族隔离的非晶态SiOxCy阶段,产生更大的具体下面的表面区域和气体吸附能力1300 1 c。由于高度形成互联网络相分离的二氧化硅和b-SiC微观结构。吉布斯自由能最小化方法确定的相对相位内容正交样本,与铁的影响量化与简化vapor-liquid-solid(VLS)、solid-liquid-solid (SLS)和经典成核理论。

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