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Improved performance of hierarchical porous Mo/H-IM-5 catalyst in methane non-oxidative aromatization

机译:甲烷/非氧化芳构化中分级多孔Mo / H-IM-5催化剂的改进性能

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Two novel hierarchical porous IM-5-S and IM-5-M materials were synthesized using mesoporous silica SBA-15 and MCM-48 as the silica sources, and for comparison conventional IM-5-C zeolite was also synthesized with the same synthesis composition. IM-5-S and IM-5-M samples exhibited larger crystal sizes and different textural properties than the conventional IM-5-C zeolite. Moreover, Mo-modified catalysts, Mo-IM-5-S, Mo-IM-5-M, and Mo-IM-5-C, were prepared for the non-oxidative aromatization of methane. The physical properties and acidities of the samples were characterized by XRD, SEM, TEM, BET, and NH3-TPD. Compared with Mo-IM-5-C, the Mo-IM-5-S and Mo-IM-5-M catalysts showed higher yields of aromatics and better stabilities. The preferable catalytic behaviors of Mo-modified mesoporous IM-5 catalysts may be attributed to the generation of secondary mesoporous systems within the zeolite crystals, which may influence the location and state of the active Mo species, simultaneously lead to easier access to the active sites for reactants and be favorable for the diffusion of products formed in the microporous channels during the methane aromatization reaction.
机译:以中孔二氧化硅SBA-15和MCM-48为二氧化硅源,合成了两种新型的多孔IM-5-S和IM-5-M材料,为了进行比较,还用相同的合成方法合成了常规IM-5-C沸石组成。与传统的IM-5-C沸石相比,IM-5-S和IM-5-M样品具有更大的晶体尺寸和不同的组织特性。此外,制备了Mo-改性催化剂Mo-IM-5-S,Mo-IM-5-M和Mo-IM-5-C,用于甲烷的非氧化芳构化。通过XRD,SEM,TEM,BET和NH3-TPD表征了样品的物理性质和酸度。与Mo-IM-5-C相比,Mo-IM-5-S和Mo-IM-5-M催化剂显示出更高的芳烃收率和更好的稳定性。 Mo改性介孔IM-5催化剂的优选催化行为可归因于沸石晶体内次级介孔体系的生成,这可能会影响活性Mo物种的位置和状态,同时导致更容易进入活性位点在甲烷芳构化反应过程中,其对于反应物是有利的并且有利于微孔通道中形成的产物的扩散。

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