Isomerization of alkyl naphthalene and refining of 2-methylnaphthalene

A preparation process of 2-methylnaphthalene (2-MN) was proposed by isomerization, side-stream distillation and extractive distillation. The isomerization of alkyl naphthalene was catalyzed by acid-treated HBEA zeolites, and the 2-MN selectivity of isomerization was 92.70%. Side-stream distillation...

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Published inChinese journal of chemical engineering Vol. 25; no. 2; pp. 149 - 152
Main Authors Sun, Hao, Shi, Saijian, Gu, Zhenggui
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.02.2017
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Abstract A preparation process of 2-methylnaphthalene (2-MN) was proposed by isomerization, side-stream distillation and extractive distillation. The isomerization of alkyl naphthalene was catalyzed by acid-treated HBEA zeolites, and the 2-MN selectivity of isomerization was 92.70%. Side-stream distillation and extractive distillation were investigated by simulation, and effects of operation parameters on 2-MN were studied. Further, the simulated results were verified by experiment. Under the optimal condition, the mass fraction of 2-MN reached to 98.09%; in the oroduct, and the yield was 83.84% in refining orocess.
AbstractList A preparation process of 2-methylnaphthalene (2-MN) was proposed by isomerization, side-stream distillation and extractive distillation. The isomerization of alkyl naphthalene was catalyzed by acid-treated HBEA zeolites, and the 2-MN selectivity of isomerization was 92.70%. Side-stream distillation and extractive distillation were investigated by simulation, and effects of operation parameters on 2-MN were studied. Further, the simulated results were verified by experiment. Under the optimal condition, the mass fraction of 2-MN reached to 98.09% in the product, and the yield was 83.84% in refining process.
A preparation process of 2-methylnaphthalene (2-MN) was proposed by isomerization, side-stream distillation and extractive distillation. The isomerization of alkyl naphthalene was catalyzed by acid-treated HBEA zeolites, and the 2-MN selectivity of isomerization was 92.70%. Side-stream distillation and extractive distillation were investigated by simulation, and effects of operation parameters on 2-MN were studied. Further, the simulated results were verified by experiment. Under the optimal condition, the mass fraction of 2-MN reached to 98.09%; in the oroduct, and the yield was 83.84% in refining orocess.
Author Hao Sun saijian Shi Zhenggui Gu
AuthorAffiliation School of Chemistry and Materials Science, Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing Normal University, Nanjing 210023, China
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Keywords Extractive distillation
Simulation
2-Methylnaphthalene
Side-stream distillation
Isomerization
Catalyst
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Notes 11-3270/TQ
A preparation process of 2-methylnaphthalene (2-MN) was proposed by isomerization, side-stream distillation and extractive distillation. The isomerization of alkyl naphthalene was catalyzed by acid-treated HBEA zeolites, and the 2-MN selectivity of isomerization was 92.70%. Side-stream distillation and extractive distillation were investigated by simulation, and effects of operation parameters on 2-MN were studied. Further, the simulated results were verified by experiment. Under the optimal condition, the mass fraction of 2-MN reached to 98.09%; in the oroduct, and the yield was 83.84% in refining orocess.
Side-stream distillationExtractive distillationlsomerization2-MethylnaphthaleneSimulationCatalyst
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Snippet A preparation process of 2-methylnaphthalene (2-MN) was proposed by isomerization, side-stream distillation and extractive distillation. The isomerization of...
A preparation process of 2-methylnaphthalene (2-MN) was proposed by isomerization, side-stream distillation and extractive distillation. The isomerization of...
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elsevier
chongqing
SourceType Enrichment Source
Index Database
Publisher
StartPage 149
SubjectTerms 2-Methylnaphthalene
2-甲基萘
Catalyst
Extractive distillation
Isomerization
Side-stream distillation
Simulation
制备工艺
异构化
最佳条件
烷基萘
精制过程
萃取精馏
验证实验
Title Isomerization of alkyl naphthalene and refining of 2-methylnaphthalene
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