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Preparation of low carbon olefins on a core–shell K–Fe5C2@ZSM-5 catalyst by Fischer–Tropsch synthesis

机译:用Fischer-Tropsch合成制备核心壳K-Fe5C2上核 - 壳K-Fe5C2 @ ZSM-5催化剂的低碳烯烃

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In this study, a core–shell catalyst based on Fe _(5) C _(2) @ZSM-5 (ZSM-5 capped Fe _(5) C _(2) as active phase) is prepared by the coating-carbonization method for Fischer–Tropsch synthesis (FTS). Further, the designed ZSM-5 zeolites are utilized to screen the low carbon hydrocarbons from the products generated on the iron carbide active centre, and for catalytic disassembly of the long-chain hydrocarbons into low carbon olefins. Prior to utilization, the physical–chemical properties of the prepared catalysts are systematically characterized by various techniques of X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), Fourier transform infrared (FT-IR), and scanning electron microscopy (SEM) as well as transmission electron microscopy (TEM) observations, in addition to the effects of coating-carbonization, molecular sieve coating amount, and K-doping on core–shell iron-based catalysts. Next, the performance of Fischer–Tropsch synthesis is investigated in a micro-fixed bed reactor. The results manifest that, comparing with Fe _(5) C _(2) and a supported Fe/ZSM-5 catalyst prepared by the traditional impregnation method, the core–shell Fe _(5) C _(2) @ZSM-5 catalysts show higher CO conversion rate, reaction activity and selectivity to low-carbon olefins. Comparatively, the Fe _(5) C _(2) @ZSM-5C catalyst prepared by carbonization after the coating method exhibited more surface area, smaller average pore size, and more reactive active sites, resulting in the improvement of screening of high carbon hydrocarbons and the enhancement of selectivity to low carbon olefins, in comparison to those prepared by the carbonization-coating method. In conclusion, the K-doping catalyst had significantly improved the reactive activity of the core–shell Fe _(5) C _(2) @ZSM-5 catalyst and the selectivity to low carbon olefins, while the CO conversion on K–Fe _(5) C _(2) @ZSM-20C still remained good.
机译:在该研究中,通过涂层制备基于Fe _(5)C _(2)+ ZSM-5(ZSM-5封端的Fe _(5)C _(2))的核 - 壳催化剂是用涂层制备的 - Fischer-Tropsch合成(FTS)的碳化方法。此外,设计的ZSM-5沸石用于将低碳烃从铁碳化物活性中心产生的产物中筛选,并用于长链烃的催化拆卸成低碳烯烃。在利用之前,通过各种X射线衍射(XRD),Brunauer-Emmett-Teller(BET),傅里叶变换红外(FT-IR)和扫描电子显微镜(Scount Electronic显微镜)系统特征在系统的物理化学性质。 (SEM)以及透射电子显微镜(TEM)观察,除了涂布 - 碳化,分子筛涂布量和K型核 - 壳铁基催化剂的影响之外。接下来,在微固定床反应器中研究了Fischer-Tropsch合成的性能。结果表明,与通过传统浸渍方法制备的Fe _(5)C _(2)和支持的Fe / ZSM-5催化剂相比,核心壳Fe _(5)C _(2)@ ZSM- 5催化剂显示出更高的CO转化率,反应活性和对低碳烯烃的选择性。相比之下,通过碳化在涂布方法中制备的Fe _(5)C _(2)+ ZSM-5C催化剂表现出更多的表面积,较小的平均孔径和更多的反应性活性位点,导致高碳筛选的改善与通过碳化涂覆方法制备的那些相比,烃和对低碳烯烃的选择性增强。总之,K掺杂催化剂显着改善了核 - 壳Fe _(5)C _(2)℃的反应活性,ZSM-5催化剂和低碳烯烃的选择性,而CO转化在K-Fe上_(5)C _(2)@ zsm-20c仍然保持不错。

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