Selective hydrogenation of 1,4-butynediol to 1,4-butenediol over platinum encapsulated in ZSM-48 with one-pot synthesis method

被引:4
|
作者
Zhang, Miao [1 ]
Long, Houang [1 ]
Lu, Jing [2 ]
Zhang, Mingming [3 ]
机构
[1] Yantai Univ, Shandong Appl Res Ctr Gold Nanotechnol Au SDARC, Sch Chem & Chem Engn, Yantai 264005, Peoples R China
[2] Wuhan Text Univ, Hubei Key Lab Adv Text Mat & Applicat, Hubei Int Sci & Technol Cooperat Base Intelligent, Wuhan 430200, Peoples R China
[3] Tangshan Coll, Dept Environm & Chem Engn, Tangshan 06300, Peoples R China
基金
中国国家自然科学基金;
关键词
ZSM-48; Selective hydrogenation; 1,4-butynediol; 1,4-butenediol; METAL-CLUSTERS; ZEOLITE CRYSTALS; CORE-SHELL; NANOPARTICLES; CATALYSTS; CONSEQUENCES; STABILITY; DESIGN; SILICA; EXCESS;
D O I
10.1016/j.fuel.2022.125201
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
This work presents a simple and effective strategy to prepare zeolite encapsulated Pt nanoparticles through one-pot method at high crystallization temperature. The obtained Pt@ZSM-48 combines the advantages of both highly active sites of Pt particle and controllable reactants diffusion of ZSM-48 miropores and exhibits high stability and catalytic activity even after calcination at 550 degrees C. The obtained Pt@ZSM-48 exhibited high activity for hydrogenation of 1,4-butynediol and high selectivity for 1,4-butenediol. After alkaline treatment, the diffusion obstruction of Pt@ZSM-48 can be greatly reduced, thereby increasing the conversion of 1,4-butynediol while maintaining high 1,4-butenediol selectivity. The diffusion obstruction and catalytic activity of Pt@ZSM-48 can be adjusted by post-treatment.
引用
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页数:7
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