Selective ortho-methylation of phenol with methanol over copper manganese mixed-oxide spinel catalysts

TitleSelective ortho-methylation of phenol with methanol over copper manganese mixed-oxide spinel catalysts
Publication TypeJournal Article
Year of Publication2006
AuthorsA. Reddy, S, Gopinath, CS, Chilukuri, SV
JournalJournal of Catalysis
Volume243
Issue2
Pagination278-291
Date PublishedOCT
Type of ArticleArticle
ISSN0021-9517
Keywords2, 6-xylenol, acidity-basicity, copper-manganese oxides, ortho-alkylation, phenol methylation, Spinels
Abstract

Methylation of phenol with methanol as an alkylating agent to produce 2,6-xylenol was investigated over copper manganese mixed oxide spinels, CuxMn3-xO4 (x = 0, 0.25, 0.5, 0.75, and 1) prepared through co-precipitation. The catalytic activity strongly depends on the composition, acid-base properties, and structural stability. Various parameters, including catalyst composition, reaction temperature, feed composition, and durability of the catalyst during methylation, were investigated. Mainly o-cresol and 2,6-xylenol, along with small amounts of mesitol, were found in the product. A high ortho-selectivity of 100%, with 2,6-xylenol selectivity of 74%, was observed over Cu0.25Mn2.75O4 at 673 K. These catalysts were investigated using various techniques, including BET surface area, XRD, DRS UV-vis, TPD of NH3 and CO2, TPR, and X-ray photoemission spectroscopy (XPS). Powder XRD of the catalysts revealed the formation of copper-manganese spinels with hausmannite (Mn3O4) tetragonal structure, for x = 0-0.5, whereas an increase in copper content (x > 0.5) led to the formation of cubic Cu1.5Mn1.5O4 phase. DRS UV-vis, and FTIR further supported the changes in structural phases observed by XRD. Temperature-programmed desorption Of CO2 and NH3 showed that the catalysts have strong basicity along with weak acidity when x = 0 and 0.25. XPS and XAES analysis revealed the presence of only Cu2+ ions in fresh sample with x = 0.25, whereas for x = 1.0, both Cu1+ and Cu2+ were observed. The deactivation of the catalysts is attributed to structural changes occurring during the reaction. Catalytic activity is correlated with structure, as well as with acid-base properties. (c) 2006 Elsevier Inc. All rights reserved.

DOI10.1016/j.jcat.2006.07.014
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)3.389
Divison category: 
Catalysis and Inorganic Chemistry