镁含量对Ni/MgAl2O4催化剂甲烷干重整反应性能的影响

Effect of Mg content in Ni/MgAl2O4 catalysts on catalytic performance during methane dry reforming reaction

  • 摘要: 本研究采用溶剂蒸发自组装法制备了不同Mg含量的镁铝尖晶石(MgAl2O4)载体,随后负载了金属Ni,并将该催化剂(Ni/x-MAO)应用于甲烷干重整制合成气反应。结合X射线衍射、氮气物理吸附-脱附和透射电镜等表征对催化剂的结构性质进行了分析,发现适量Mg的加入(10%−15%)有利于提高载体的比表面积,并形成耐高温的有序介孔结构。该结构可以将Ni颗粒限域在孔道内,有利于形成高分散、小晶粒的活性物种,其在高温反应下不易烧结。同时,H2-TPR和XPS结果表明,10%−15%的Mg含量有利于增强Ni与MgAl2O4的金属-载体相互作用,有效抑制Ni烧结,且其表面的活性氧物种有效抑制了积炭生成。在性能评价中,10%−15%Mg含量的Ni/MgAl2O4催化剂呈现出优异的CH4和CO2转化率,在180 h的长周期活性评价期间,Ni/15-MAO催化剂的CH4和CO2转化率分别保持在92.6%和92.5%左右,同时积炭量仅为0.89%,且反应后的Ni颗粒尺寸变化不大。

     

    Abstract: Methane dry reforming reaction is a promising route for the valorization of both CO2 and CH4. However, the catalysts usually suffered from the coking deactivation and the sintering of active phase under the harsh reaction conditions. In this paper, the Mg-Al spinel support with different Mg content prepared by the solvent evaporation-induced self-assembly method was investigated. With this support, Ni/MgAl2O4 was used as the catalyst for methane dry reforming to syngas. XRD, BET and TEM results showed that the addition of appropriate amount of magnesium (10%−15%) was beneficial to the formation of highly stable ordered mesoporous magnesia spinel support with large specific surface area, which can confine the Ni particles in the pore structure and thus enhance the nickel dispersion and improve the resistance of coke formation under high temperature. H2-TPR and XPS analysis indicated the addition of 10%−15% magnesium can promote the interaction between Ni and MgAl2O4, inhibiting the agglomeration of Ni and the coke formation with the active surface-adsorbed oxygen species. Detailed activity tests showed that Ni/MgAl2O4 catalysts with 10%−15% magnesium content has high CH4 and CO2 conversion. During the long-term test for 180 h, the Ni/15-MAO catalyst exihibited the CH4 and CO2 conversions of 92.6% and 92.5%, respectively. The coke deposition percentage was only 0.89% and the grain size of Ni was maintained after reaction.

     

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