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Published March 16, 2020 | Version v1
Journal article

Single site MIL-101 for novel low-temperature liquid-phase toluene methylation

  • 1. Egyptian Petroleum Research Institute. Analysis and Evaluation Division (Egypt)
  • 2. Egyptian Petroleum Research Institute. Catalysis Department, Petroleum Refining Division (Egypt)

Description

P-xylene is one of petrochemical products eagerly in demand. Until recently, the process for preparing of p-xylene was done via gas-phase toluene methylation reaction at high temperature using a strong acid catalyst. In this work, high surface area, shape-selective and single-site MIL-101(Cr) was used as a catalyst to perform toluene methylation reaction in a liquid phase at low reaction temperature (60-120 °C). Toluene conversion and p-xylene selectivity are up to 50% and 90%, respectively. Under the optimum operating conditions; 1:1 toluene: methanol molar ratio, the reaction temperature is 120 °C. The catalyst was synthesized via the hydrothermal method and the MIL-101 structure was confirmed by different analytical techniques: TGA, XRD, FTIR and BET surface area. The remarkably high toluene conversion and xylene selectivity at a low reaction temperature, in comparison to previous research, was attributed to the suppression of side reactions that could convert methanol to linear hydrocarbons, and to the inhibition of p-xylene isomerization. This suppression can be attributed to the single site properties and to the uniform pore size distribution of the prepared MIL 101 catalyst.

Graphic abstract

Synthesis and characterization of single-site MIL-101(Cr) were used as a catalyst for toluene methylation reaction in a liquid phase at low reaction temperature (60–120 °C). The results suggest that toluene conversion and p-xylene selectivity are up to 50% and 90%, respectively, under the optimum operating conditions; 1:1 toluene: methanol molar ratio, the reaction temperature is 120 °C.

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Publishing Information

Journal Title
Journal of Chemical Sciences (Online)
Journal Volume
132
Journal Issue
1
Journal Page Range
vp.
ISSN
0973-7103

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Copyright (c) 2020 © Indian Academy of Sciences 2020