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首页> 外文期刊>Ultrasonics sonochemistry >Fe3O4 nanocubes assembled on RGO nanosheets: Ultrasound induced in-situ and eco-friendly synthesis, characterization and their excellent catalytic performance for the production of liquid fuel in Fischer-tropsch synthesis
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Fe3O4 nanocubes assembled on RGO nanosheets: Ultrasound induced in-situ and eco-friendly synthesis, characterization and their excellent catalytic performance for the production of liquid fuel in Fischer-tropsch synthesis

机译:FE3O4纳米尺组装在RGO Nanosheets上:超声波诱导原位和生态友好的合成,表征及其优异的催化性能,用于生产Fischer-Tropsch合成中的液体燃料

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In this study, Fe3O4 nanocubes (NCs) decorated on RGO nanosheets (NSs) structures were successfully synthesized through an innovative and environmentally-friendly rapid sonochemical method. More importantly, iron (II) sulfate heptahydrate and GO were employed as precursors and water as reaction medium, meanwhile, NaOH within the generated free radicals from the high intensity ultrasound were sufficient as reducing and base agent in our clean synthesis. Moreover, the hydrothermal method as a conventional approach was employed to synthesize the same catalysts for the comparison with the ultrasonocation technique. The as-synthesized Fe3O4 and RGO/Fe3O4 NSs catalysts were exposed to industrially relevant Fischer-tropsch synthesis (FTS) conditions at various reaction temperatures (250-290 degrees C), and they subjected to fully characterization before and after FTS reaction using XRD, TEM, HRTEM, EDS mapping, XPS, FTIR, BET, H-2-TPR, H2-TPD and CO-TPD to understand the structure-performance relationships. Notably, the catalysts produced using the sonochemical method had a better CO conversion rate (Fe3O4 (80%), RGO/Fe3O4 (82%)] than the hydrothermally synthesized catalysts. However, compared to the naked-Fe3O4 catalysts, the sonochemically and hydrothermally synthesized RGO-supported Fe3O4 catalysts had higher long chain hydrocarbon (C5 +) selectivity values (72% and 67%) and C-2-C-4 olefin/paraffin selectivity ratio (3.2 and 2) and low CH4 selectivity values (6% and 8.5%), respectively. This can be attributed to their high surface area, the degree of reducibility, and content of Hagg iron carbide (chi-Fe5C2) as the most active phase of the FTS reaction. Proposed reaction mechanisms for the sonochemical and hydrothermal reaction synthesis of Fe3O4 and RGO/Fe3O4 nanoparticles are discussed. In conclusion, our developed surfactantless-sonochemical method holds promise for the eco-friendly synthesis of highly efficient catalysts materials for FTS reaction.
机译:在本研究中,通过创新和环境友好的快速超级化学方法成功地合成了在RGO纳米片(NSS)结构上装饰的Fe3O4纳米孔(NCS)。更重要的是,铁(II)硫酸铁庚酸氢盐和去作为前体和水作为反应介质,同时,在我们的清洁合成中的还原和基础试剂中,NaOH在来自高强度超声中的产生是充分的。此外,采用作为常规方法的水热法合成相同的催化剂,以与超声波定位技术进行比较。在各种反应温度(250-290℃)下暴露于工业相关的Fischer-Tropsch合成(FTS)条件下暴露于工业上的Fe3O4和Rgo / Fe3O4,并且它们在使用XRD的FTS反应之前和之后进行全面表征, TEM,HRTEM,EDS映射,XPS,FTIR,BET,H-2-TPR,H2-TPD和CO-TPD,以了解结构性能关系。值得注意的是,使用SONOPEMICAL方法产生的催化剂比水热合成催化剂具有更好的CO转化率(Fe3O4(80%),Rgo / Fe3O4(82%)]。然而,与裸料Fe3O4催化剂相比,多交脑化学和水热相比合成的RGO负载的Fe3O4催化剂具有较高的长链烃(C5 +)选择性值(72%和67%)和C-2-C-4烯烃/石蜡选择性比(3.2和2)和低CH 4选择性值(6%分别为8.5%)。这可以归因于它们的高表面积,哈格碳化铁(CHI-FE5C2)作为FTS反应最活跃的阶段的高表面积,还原性程度和含量。提出了多个化素和谐的反应机制讨论了Fe3O4和Rgo / Fe3O4纳米颗粒的水热反应合成。总之,我们发育的表面活性剂 - 儿化学方法具有对FTS反应的高效催化剂材料的环保合成的承担能力。

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