结晶
产量(工程)
三元运算
双功能
粒径
热液循环
Crystal(编程语言)
材料科学
水热合成
化学工程
化学
分数(化学)
双功能催化剂
晶体生长
比表面积
粒子(生态学)
催化作用
多相催化
反应条件
矿物学
无机化学
作文(语言)
形态学(生物学)
晶体结构
晶种
作者
Bangjian Liu,Hong Yang,Limin Ren,Zhaoyang Song,Quanjie Liu,Shuandi Hou,Anfeng Zhang,Xinwen Guo
标识
DOI:10.1021/acs.chemmater.5c00735
摘要
In this study, a rapid synthesis of ZSM-50 zeolites is achieved by a two-step aging–crystallization hydrothermal method. By optimizing the temperature/time for aging (393 K/48 h) and crystallization (423 K/72 h), the synthesis time for obtaining pure-phase ZSM-50 zeolites has been significantly shortened to 4 days from typically weeks. The gel compositions to form pure-phase ZSM-50 have also been mapped out in the ternary composition diagram of 5Al2O3/SiO2–OSDA/SiO2–OH–/SiO2 under the optimized aging–crystallization conditions. Furthermore, three ZSM-50 samples are synthesized using different gel compositions and/or crystallization conditions. The samples have different acidity characteristics and average crystal sizes from 5 to 17 μm. As catalysts for n-heptane hydroisomerization, the three Pt-loaded ZSM-50 catalysts deliver the maximum iso-heptane yield directly correlated to their surface weak Brönsted acid sites on the external surface. The ZSM-50 (5 μm) catalyst has a superior catalytic activity, achieving a maximum iso-heptane yield of 71.4% at 543 K, along with a high fraction of multibranched isomers of 29.1%. This study highlights the pivotal role of particle size in modulating acid properties and pore accessibility in ZSM-50 and offers a facile strategy for designing effective bifunctional catalysts for n-alkane isomerization.
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