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Preparation and Performances of ZIF-67-Derived FeCo Bimetallic Catalysts for CO 2 Hydrogenation to Light Olefins

机译:ZIF-67-衍生的FECO双金属催化剂的制备和性能用于CO 2氢化至轻质烯烃

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A novel sodium-promoted Fe-Co/NC catalyst prepared by incipient-wet-impregnation method using ZIF-67 as a support was employed to convert CO 2 to light olefins through hydrogenation reaction. Properties of the synthesized catalysts calcinated at various temperatures (from 400 to 700 °C) were investigated by XRD, SEM, TEM and M?ssbauer spectroscopy. Characterization results showed that the support could be fully converted into carbon support above 500 °C, which could anchor metal particles, thus resulting in a uniform dispersion of active components. Furthermore, the Fe-Co alloy was formed during N 2 calcination, and was converted into active components, such as Fe 3 O 4 , Fe 5 C 2 , and Co 2 C during the reaction. The reaction result indicated that FeCo/NC-600 catalyst exhibited the highest selectivity of light olefins (C 2 = ? C 4 =, 27%) and CO 2 conversion could reach around 37% when this catalyst pyrolyzed at 600 °C in N 2 . The highest selectivity for light olefins may be related to the combination of suitable particle size and sufficient active sites of iron carbide.
机译:使用ZIF-67作为载体的初期湿浸渍法制备的新型促进的Fe-Co / Nc催化剂作为载体,通过氢化反应将CO 2转化为轻烯烃。通过XRD,SEM,TEM和M≥Ssbauer光谱研究在各种温度(400至700℃)下煅烧的合成催化剂的性质。表征结果表明,载体可以完全转化为500℃的碳载体,这可以锚定金属颗粒,从而导致活性组分的均匀分散。此外,在N 2煅烧期间形成Fe-Co合金,并在反应过程中转化为活性组分,例如Fe 3 O 4,Fe 5 C 2和CO 2 C.反应结果表明,当该催化剂在600℃下在N 2中热解热时,FECO / NC-600催化剂表现出最高选择性的光烯烃(C 2 =ΔC4 =,27%),CO 2转化率达到约37% 。光烯烃的最高选择性可能与合适的粒度和碳化铁的充分活性位点的组合有关。

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