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Postsynthesis of hierarchical core/shell ZSM-5 as an efficient catalyst in ketalation and acetalization reactions
Frontiers of Chemical Science and Engineering ( IF 4.5 ) Pub Date : 2020-01-15 , DOI: 10.1007/s11705-019-1878-0
Peng Luo , Yejun Guan , Hao Xu , Mingyuan He , Peng Wu

Hierarchical core/shell Zeolite Socony Mobil-five (ZSM-5) zeolite was hydrothermally postsythesized in the solution of NaOH and diammonium surfactant via a dissolution-reassembly strategy. The silica and alumina species were firstly dissolved partially from the bulky ZSM-5 crystals and then were in situ reassembled into the MFI-type nanosheets with the structure-directing effect of diammonium surfactant, attaching to the out-surface of ZSM-5 core crystals. The mesopores thus were generated in both the core and shell part, giving rise to a micropore/mesopore composite material. The micropore volume and the acidity of the resultant hybrid were well-preserved during this in situ recrystallization process. Possessing the multiple mesopores and enlarged external surface area, the core/shell ZSM-5 zeolite exhibited higher activity in the ketalation and acetalization reactions involving bulky molecules in comparison to the pristine ZSM-5.



中文翻译:

后合成核/壳ZSM-5分层化合物作为缩酮化和缩醛化反应的有效催化剂

通过溶解-重组策略,在NaOH和二铵表面活性剂溶液中水热后合成了分级核/壳沸石美孚五型(ZSM-5)沸石。首先从庞大的ZSM-5晶体中部分溶解二氧化硅和氧化铝,然后原位重组装成MFI型纳米片,并具有二铵表面活性剂的结构导向作用,并附着在ZSM-5核心晶体的外表面。因此,在核和壳部分都产生了中孔,从而产生了微孔/中孔复合材料。在此原位过程中,得到的杂种的微孔体积和酸度得到了很好的保存重结晶过程。与原始ZSM-5相比,具有多个中孔和更大的外部表面积,核/壳ZSM-5沸石在涉及大分子的缩酮化和缩醛化反应中显示出更高的活性。

更新日期:2020-04-21
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