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非离子聚合物和氨基酸辅助合成ZSM-5纳米晶体及其在2-甲基萘烷基化反应中的催化应用

Nonionic polymer and amino acid-assisted synthesis of ZSM-5 nanocrystals and their catalytic application in the alkylation of 2-methylnaphthalene.

作者信息

Zhan Junling, Wang Ying, He Tengfei, Sheng Luyang, Wu Banghao, Liu Qun, Jia Mingjun, Zhang Yu

机构信息

College of Chemistry, Jilin University, Changchun, Jilin, 130012, China.

College of Petrochemical Technology, Jilin Institute of Chemical Technology, Jilin, Jilin, 132022, China.

出版信息

Dalton Trans. 2024 Apr 30;53(17):7384-7396. doi: 10.1039/d4dt00096j.

Abstract

The synthesis of nanosized ZSM-5 zeolites with high crystallinity and suitable acidity is very significant for their great potential in various catalytic applications. Herein, a series of zeolite ZSM-5 crystals with different particle sizes and SiO/AlO ratios (10-30) were synthesized by a temperature-varying two-step crystallization method in a concentrated gel system containing L-lysine and/or polyvinylpyrrolidone (PVP) additives. By optimizing the addition amounts of the two additives, the crystal size of the ZSM-5 zeolite could be reduced to less than 100 nm. Meanwhile, relatively high crystallinity and framework Al incorporation rates could be achieved, resulting in the generation of high-quality ZSM-5 nanocrystals. The nanosized H-form ZSM-5 zeolite with a SiO/AlO ratio of 20 showed enhanced catalytic efficiency and stability for the alkylation of 2-methylnaphthalene (2-MN) with methanol to produce an important intermediate, 2,6-dimethylnaphthalene (2,6-DMN). A relatively high and steady yield of 2,6-DMN (above 7.2%) could be achieved during 20 h time-on-stream at 400 °C. The smaller crystal size, higher crystallinity and framework Al content could provide more accessible Brønsted acid sites in the 10-membered ring channel of the ZSM-5 nanocrystals, which are the main active sites responsible for the shape-selectivity of the targeted product of 2,6-DMN. As a result, the formation of other side products like 1-MN and poly-MN could be effectively inhibited, thus leading to an improved 2,6-DMN yield and coke resistance over the nanosized ZSM-5 catalyst.

摘要

合成具有高结晶度和适宜酸度的纳米ZSM-5沸石对于其在各种催化应用中的巨大潜力而言非常重要。在此,通过在含有L-赖氨酸和/或聚乙烯吡咯烷酮(PVP)添加剂的浓凝胶体系中采用变温两步结晶法,合成了一系列具有不同粒径和SiO/AlO比(10 - 30)的ZSM-5沸石晶体。通过优化两种添加剂的添加量,ZSM-5沸石的晶体尺寸可减小至小于100 nm。同时,可实现相对较高的结晶度和骨架铝掺入率,从而生成高质量的ZSM-5纳米晶体。SiO/AlO比为20的纳米H型ZSM-5沸石在2-甲基萘(2-MN)与甲醇烷基化制备重要中间体2,6-二甲基萘(2,6-DMN)的反应中表现出增强的催化效率和稳定性。在400℃下连续反应20 h期间,2,6-DMN可实现相对较高且稳定的产率(高于7.2%)。较小的晶体尺寸、较高的结晶度和骨架铝含量可在ZSM-5纳米晶体的十元环通道中提供更多可及的布朗斯台德酸位点,这些是负责目标产物2,6-DMN形状选择性的主要活性位点。结果,可有效抑制其他副产物如1-MN和多甲基萘的形成,从而在纳米ZSM-5催化剂上提高2,6-DMN产率和抗积炭性能。

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