Cha Seunghee, Kim Heewon, Choi Hyunkyung, Kim Chul Sung, Ha Kyoung-Su
Department of Chemical and Biomolecular Engineering, Sogang University, 35 Baekbeom-ro, Mapo-gu, Seoul 04107, Korea.
Department of Physics, Kookmin University, 77 Jeongneung-ro, Seongbuk-gu, Seoul 02707, Korea.
Nanomaterials (Basel). 2022 Oct 21;12(20):3704. doi: 10.3390/nano12203704.
Among various iron carbide phases, χ-FeC, a highly active phase in Fischer-Tropsch synthesis, was directly synthesized using a wet-chemical route, which makes a pre-activation step unnecessary. In addition, χ-FeC nanoparticles were encapsulated with mesoporous silica for protection from deactivation. Further structural analysis showed that the protective silica shell had a partially ordered mesoporous structure with a short range. According to the XRD result, the sintering of χ-FeC crystals did not seem to be significant, which was believed to be the beneficial effect of the protective shell providing restrictive geometrical space for nanoparticles. More interestingly, the protective silica shell was also found to be effective in maintaining the phase of χ-FeC against re-oxidation and transformation to other iron carbide phases. Fischer-Tropsch activity of χ-FeC in this study was comparable to or higher than those from previous reports. In addition, CO selectivity was found to be very low after stabilization.
在各种碳化铁相中,χ-FeC是费托合成中的高活性相,采用湿化学路线直接合成,无需预活化步骤。此外,χ-FeC纳米颗粒被介孔二氧化硅包裹以防止失活。进一步的结构分析表明,保护性二氧化硅壳层具有部分有序的短程介孔结构。根据XRD结果,χ-FeC晶体的烧结似乎并不显著,这被认为是保护壳层为纳米颗粒提供限制性几何空间的有益效果。更有趣的是,还发现保护性二氧化硅壳层在保持χ-FeC相抵抗再氧化和转化为其他碳化铁相方面是有效的。本研究中χ-FeC的费托活性与先前报道的相当或更高。此外,稳定后发现CO选择性非常低。