催化作用
介孔材料
选择性
沸石
化学
浸出(土壤学)
ZSM-5型
布朗斯特德-洛瑞酸碱理论
化学工程
无机化学
有机化学
环境科学
土壤科学
工程类
土壤水分
作者
Jipeng Meng,Tianyun Cui,Di Bai,Chuang Li,Xiao Chen,Changhai Liang
出处
期刊:Fuel
[Elsevier BV]
日期:2022-05-14
卷期号:324: 124589-124589
被引量:40
标识
DOI:10.1016/j.fuel.2022.124589
摘要
Hydroisomerization has been considered as an effective and efficient route for production of transportation fuels and lubricants with superior cold-flow properties. In current work, n-hexadecane (n-C16) hydroisomerization was investigated over Pt catalysts supported on hierarchical ZSM-48, which was post-treated by multi-step procedures including alkaline-acid, acid-alkaline-acid, steaming-alkaline-acid, and fluorination-alkaline-acid leaching. This work was purposed to construct the secondary mesoporous network, enhance the accessible acid sites in hierarchical ZSM-48 zeolite, and investigate their cooperative effects on hydroisomerization performance. The results demonstrated that the microporosity and the crystallinity were preserved after the controllable leaching, coupled with more exposed accessible acidity and enhanced mesoporosity. High dispersion of Pt particles and quantitative metal-acid balance were unable to be the threats for the sequential acid-catalyzed reaction. The cooperative effects of enhanced mesoporosity and highly-accessible acidity accelerated the diffusion and promoted the proximity of metal sites and acid sites, thereby persuading the treated ZSM-48 samples to exhibit excellent activity and iso-selectivity. The i-C16 yield over Pt/ZSM-48(H) catalyst could reach around 86 wt% at conversion rates of 90 wt% with iso-selectivity of 96 wt%. However, the excessively accessible acid sites in Pt/ZSM-48(F) could induce further skeletal transformation and deteriorate the iso-selectivity, although the mesoporous structure was as well established.
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