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Shape-selective catalysts of Mg2+ ion exchange modified SAPO-11 molecular sieves for alkylation of 2-methylnaphthalene

  • Runping Ye
  • , Qinghua Liu
  • , Zhihui Wen
  • , Lejie Jiang
  • , Chengkai Jin
  • , Birong Gao
  • , Bin Zhang
  • , Rongbin Zhang
  • , Yong Qin
  • , Gang Feng
  • Nanchang University
  • CAS - Institute of Coal Chemistry

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

The conversion of 2-methylnaphthalene (2-MN) and methanol by molecular zeolites to 2,6-dimethylnaphthalene (2,6-DMN) is significant for the preparation of polyethylene naphthalate. However, there is still a challenge to develop catalysts with efficient selectivity and activity. In this work, the hydrothermally synthesized SAPO-11 samples were modified by ion-exchange of Mg2+ for the catalytic alkylation of 2-MN, and thus the selectivity of 2,6-DMN was greatly improved. The results show that the Mg2+ ion-exchanged SAPO-11 molecular sieves could maintain the original main structure and morphology. However, the introduction of Mg2+ regulated the pore structure, acid content, acid strength and the distribution ratio of Brönsted acid and Lewis acid sites in the molecular sieves, and thus the Mg/SAPO-11 catalyst presented better catalytic performance than the pure SAPO-11. After 6 h of reaction, the selectivity of 2,6-DMN could still maintain 41.3% and the ratio of 2,6-/2,7-DMN was 1.87 over 0.06M-Mg/SAPO-11 sample. The deep isomerization of methylnaphthalene was reduced due to the Mg2+ ion exchange resulting in a shape-selective effect from passivation of the outer surface of the catalyst and adjustment of the open pore size. Therefore, this work presents a shape-selective catalysis in zeolites using Mg2+ ion exchange strategy for the alkylation of 2-MN.

Original languageEnglish
Article number112291
JournalMicroporous and Mesoporous Materials
Volume346
DOIs
StatePublished - Dec 2022
Externally publishedYes

Keywords

  • 2-Methylnaphthalene
  • Alkylation
  • Mg/SAPO-11
  • Shape-selective catalysis

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