Liu H, Da Costa P, Hadj Taief H Bel, Benzina M, Gálvez M E
Sorbonne Université, CNRS, Institut Jean Le Rond d'Alembert F-78210 St Cyr L'Ecole France
Laboratoire Eau, Energie et Environnement (LR3E), Code: AD-10-02, Ecole Nationale d'Ingénieurs de Sfax, Université de Sfax B.P1173.W.3038 Sfax Tunisia.
RSC Adv. 2018 May 29;8(35):19627-19634. doi: 10.1039/c8ra02615g. eCollection 2018 May 25.
Mg-promotion of natural clay based Ni-catalysts was considered, as a way of boosting the dry reforming of methane (DRM) activity of these materials. The results of the DRM experiments performed at temperatures from 600 °C to 850 °C evidenced much higher methane and CO conversions for the Mg-promoted catalysts. Mg-promotion led of course to a significant increase of CO-adsorption ability (basicity). However, the increased catalytic activity of the Mg-promoted materials was rather linked to increased Ni-dispersion and Ni crystallite size. Indeed, independent of the physico-chemical properties of the support, the presence of Mg led to the formation of a MgNiO mixed phase that, upon reduction, resulted in the formation of metallic Ni clusters having sizes around 7-9 nm, considerably smaller than in any of the non-promoted catalysts. Carbon formation was found to take place to a greater extent in the presence of the Mg-promoted catalysts, due to C-H bond activation leading also to favored direct methane decomposition (DMD). In spite of this, the activity of the Mg-promoted catalysts was well maintained over 5 hour DRM experiments performed at 750 °C.
人们考虑对天然粘土基镍催化剂进行镁促进,以此提高这些材料的甲烷干重整(DRM)活性。在600℃至850℃温度下进行的DRM实验结果表明,镁促进的催化剂具有更高的甲烷和一氧化碳转化率。镁促进当然会导致一氧化碳吸附能力(碱度)显著提高。然而,镁促进材料催化活性的提高与镍分散度的增加和镍微晶尺寸的增加有关。事实上,无论载体的物理化学性质如何,镁的存在都会导致形成MgNiO混合相,该混合相在还原后会形成尺寸约为7-9nm的金属镍簇,比任何未促进的催化剂中的镍簇都要小得多。由于C-H键活化也有利于直接甲烷分解(DMD),发现在镁促进的催化剂存在下会更大量地形成碳。尽管如此,在750℃下进行的5小时DRM实验中,镁促进催化剂的活性仍能得到很好的维持。