...
首页> 外文期刊>ACS catalysis >Pyrolysis of Metal-Organic Frameworks to Fe3O4@Fe5C2 Core-Shell Nanoparticles for Fischer-Tropsch Synthesis
【24h】

Pyrolysis of Metal-Organic Frameworks to Fe3O4@Fe5C2 Core-Shell Nanoparticles for Fischer-Tropsch Synthesis

机译:金属有机骨架热解为Fe3O4 @ Fe5C2核壳纳米粒子的费托合成

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

We prepared highly active catalysts for Fischer Tropsch (FT) synthesis through the pyrolysis of iron-containing metal organic frameworks (MOFs). The Fe time yields of the nitrogen-doped catalyst were as high as 720 pmolco gFe(-1) s(-1) under the conditions of 300 degrees C, 2 MPa, and H-2/CO = 1, which is a value that surpasses that of most FT catalysts reported in the literature. The pyrolysis of the MOFs yielded nanoparticles with a unique iron oxide@iron carbide core shell structure dispersed on carbon supports. Such a structure is favorable for FT synthesis and has never been reported previously. Our strategy resolved the problem that the strong metal support interactions that are usually required to stabilize dispersed particles in calcination compromise the catalytic activity, because of the difficulty of reducing metal oxides. Moreover, we found full coverage of carbonates on the particle surfaces, which likely result from decarboxylation of the MOFs and further stabilize the particles before decomposing to CO2, leaving an active surface rich with dangling bonds for catalytic turnover.
机译:我们通过热解含铁金属有机骨架(MOF),制备了用于费托(FT)合成的高活性催化剂。在300℃,2 MPa和H-2 / CO = 1的条件下,氮掺杂催化剂的Fe时间收率高达720 pmolco gFe(-1)s(-1)。超过了文献中报道的大多数FT催化剂。 MOF的热解产生具有分散在碳载体上的独特的氧化铁@碳化铁核壳结构的纳米颗粒。这种结构对于FT合成是有利的,并且以前没有报道过。我们的策略解决了以下问题:由于难以还原金属氧化物,通常在煅烧中稳定分散的颗粒所需的强金属载体相互作用会损害催化活性。此外,我们发现颗粒表面上的碳酸盐被完全覆盖,这可能是由于MOF的脱羧作用所致,并在分解为CO2之前进一步稳定了颗粒,从而留下了一个带有悬空键的活性表面,用于催化转化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号