Controllable tailoring of Ni-encapsulated in hollow silicalite-1 for production of cyclohexanol by hydrodeoxygenation of guaiacol

被引:0
|
作者
He, Yixin [1 ]
Hu, Yijun [1 ]
Yuan, Shen-ao [1 ]
Chen, Xiaozhou [1 ]
Deng, Longbin [1 ]
Yu, Xin [1 ]
Wang, Yutong [2 ]
Li, Yusen [3 ]
Tian, Yajie [1 ]
机构
[1] Henan Univ, Sch Energy Sci & Technol, Zhengzhou 450046, Peoples R China
[2] Shenyang Univ Chem Technol, Coll Chem Engn, Shenyang 110142, Peoples R China
[3] Henan Univ, Collaborat Innovat Ctr Nano Funct Mat & Applicat, Sch Nanosci & Mat Engn, Kaifeng 475004, Peoples R China
来源
MOLECULAR CATALYSIS | 2025年 / 572卷
基金
中国国家自然科学基金;
关键词
Ni; Hollow structure; ZSM-5; Hydrodeoxygenation; Cyclohexanol; ASSISTED SELECTIVE HYDRODEOXYGENATION; SUPPORTED NI; BIO-OIL; HYDROGENATION; CATALYST; PHENOL; ZEOLITE; SITES; ZSM-5;
D O I
10.1016/j.mcat.2024.114775
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Selective hydrodeoxygenation of guaiacol is an effective method for preparing cyclohexanol. In this study, we prepared a hollow silicalite-1 zeolite-supported Ni catalyst (Ni@HL-S1) through a sequential crystallizationdissolution-recrystallization process. The highly dispersed Ni, encapsulated within the zeolite shell, enhances the adsorption and spillover of active hydrogen. The hierarchical pores of Ni@HL-S1 expose a surface that facilitates guaiacol adsorption, accelerating its hydrogenation and producing 2-methoxycyclohexanol. Additionally, Ni interacts with Si-OH defect sites through dissolution-recrystallization, partially serving as moderate Br & oslash;nsted acid sites. This interaction improves the deoxygenation of 2-methoxycyclohexanol, resulting in the production of cyclohexanol. A yield of cyclohexanol greater than 97 wt% is achieved after a 2-hour reaction at 200 degrees C.
引用
收藏
页数:9
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