碱酸处理Pt/ β分级双功能催化剂对正庚烷加氢异构反应中多支i-庚烷的选择性更高

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
Kai Guo, Aizeng Ma, Jinzhi Li, Lingjiang Kong, Hongquan Liu, Zhongwei Yu, Dadong Li
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引用次数: 0

摘要

采用在β沸石上引入Pt原子的浸渍法制备了Pt/ β催化剂,并用适当浓度的碱酸后处理。采用XRD、N2吸附解吸、SEM、TEM、Py-IR、XRF和MAS NMR等手段对催化剂的理化性质、结构特征和酸度进行表征,并以正庚烷为基体化合物,在微固定床装置上对催化剂的异构化性能进行了评价。测试和评价结果表明,改性Pt/ β催化剂通过引入层次结构和扩大β分子筛骨架通道,改善了催化剂的构效关系,使其具有更高的多支i-庚烷产率。结果表明,碱酸处理Pt/Beta催化剂的多支i-庚烷收率最高,为24.6%,比正庚烷转化率最高的母催化剂(85.0%)高9.3%。沸石对孔隙层次的调节在加氢异构化过程中具有明显的优势,可以有效地改善高辛烷值多支异构体的组成,为化工行业提供原料。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alkali-acid treated hierarchical Pt/Beta bifunctional catalyst for higher selectivity of multi-branched i-heptane in n-heptane hydroisomerization

Pt/Beta catalyst was prepared by the impregnation method of introducing Pt atoms on Beta zeolite which post-treated with appropriate concentration alkali-acid. XRD, N2 adsorption desorption, SEM, TEM, Py-IR, XRF, and MAS NMR were used to characterize the physicochemical properties including textural characters and acidity, and then the isomerization performance of the catalyst was evaluated in a micro fixed bed device using n-heptane as a medal compound. Test and evaluation results indicated that the modified Pt/beta catalyst exhibited higher multi-branched i-heptane yield than the parent sample due to the better structure activity relationship of the catalyst by introducing hierarchical structures and enlarge the channel of Beta zeolite framework. Indeed, the alkali-acid treated Pt/Beta catalysts exhibited 24.6% of the highest multi-branched i-heptane yield which was 9.3% higher than the parent catalyst at the n-heptane conversion rate of 85.0%. The regulation of zeolite on pore hierarchy has obvious advantages in the hydroisomerization process, which can improve the composition of multi-branched isomers with high octane number effectively as well as supply raw materials for the chemical industry.

Graphical Abstract

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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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