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首页> 外文期刊>Petroleum Science and Technology >Catalytic cracking of isopropylbenzene over hybrid HZSM-12/M41S (M41S=MCM-41 or MCM-48) micro-mesoporous materials
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Catalytic cracking of isopropylbenzene over hybrid HZSM-12/M41S (M41S=MCM-41 or MCM-48) micro-mesoporous materials

机译:异丙基苯催化裂化杂交HZSM-12 / M41S(M41S = MCM-41或MCM-48)微介孔材料

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摘要

The catalytic cracking of isopropylbenzene was investigaded over hybrid ZSM-12/MCM-41 and HZSM-12/MCM-48 micro-mesoporous materials, in order to verify the effect of the acid site of the accessibility of mesoporous channels combined with the acid sites into the zeolite. The hybrid materials were synthesized by the hydrothermal method using the template mechanism. The obtained materials were characterized by X-ray diffraction and BET isotherms using nitrogen adsorption-desorption at 77K. The X-ray diffraction patterns presented characteristic peaks of the microporous and mesoporous phases. These analysis revealed the formation of ordered hexagonal MCM-41 or cubic MCM-48 mesoporous phases, associated with the ZSM-12 structure. In order to generate acid sites, the materials were ion exchanged with ammonium chloride solution. The calcined hybrid materials were tested as catalyst for cracking of isopropyl-benzene, using a fixed bed reactor at 450 C-o and nitrogen gas. The catalytic tests showed that the HZSM-12/AlMCM-41 and HZSM-12/MCM-48 hybrid materials have potential for use in cracking reactions, bening more active than the zeolite or the M41S alone. The catalytic activities of the hybrid materials can be associated with a synergistic effect between the acid sites present on the zeolitic phase and the mesoporous phase. In order to verify how the structure of the hybrid materials may affect and control their catalytic performances, the results were compared with HZSM-12 physically mixed with MCM-41 and MCM-48.
机译:在杂交ZSM-12 / MCM-41和HZSM-12 / MCM-48微介孔材料上研究异丙基苯的催化裂化,以验证酸部位与酸部位结合的酸部位的酸部位的影响进入沸石。使用模板机制通过水热法合成杂化材料。所得物质的特征在于X射线衍射和BET等温,在77K处使用氮吸附 - 解吸剂。 X射线衍射图案呈现微孔和中孔阶段的特征峰。这些分析表明,与ZSM-12结构相关的有序六方MCM-41或立方MCM-48中孔相的形成。为了产生酸性位点,将材料与氯化铵溶液进行离子交换。在450个C-O和氮气下,将煅烧的杂交材料作为异丙基 - 苯的催化剂进行催化剂。催化试验表明,HZSM-12 / ALMCM-41和HZSM-12 / MCM-48杂化材料具有在裂化反应中使用的可能性,因此单独比沸石或M41S更活跃。杂化材料的催化活性可以与沸石相和中孔相的酸位点之间的协同效应相关。为了验证混合材料的结构如何影响和控制其催化性能,将结果与与MCM-41和MCM-48物理混合的HZSM-12进行比较。

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