Surface properties and catalytic activity of TiO2-ZrO 2 mixed oxides in dehydration of methanol to dimethyl ether

V. Vishwanathan, Hyun Seog Roh, Jae Woo Kim, Ki Won Jun

Research output: Contribution to journalArticlepeer-review

129 Citations (Scopus)


A series of TiO2-ZrO2 mixed oxides with varying molar ratio of TiO2 to ZrO2 were prepared by the co-precipitation method. The crystalline phases of the oxides were characterized by XRD and their acid-base properties by TPD of NH3 and CO 2 and IR of adsorbed pyridine. The catalytic activities were investigated for the vapor phase dehydration of methanol to dimethyl ether (DME) in a fixed-bed reactor under atmospheric pressure. The mixed oxides are highly amorphous in nature. The acid-base properties and CH3OH conversion activity are increasing with TiO2 content and an optimum value is achieved for a molar ratio of Ti/Zr in the vicinity of 1/1. At lower reaction temperature (< 300°C), the selectivity for DME is nearly 100%. A good correlation is observed between dehydration activity and the acid-base properties of the TiO2-ZrO2 catalysts. It is significant to note that TiO2-ZrO2 catalysts show high stability against water during dehydration reaction. Based on our results, a surface mechanism involving both acid-base sites has been proposed for DME formation.

Original languageEnglish
Pages (from-to)23-28
Number of pages6
JournalCatalysis Letters
Issue number1-2
Publication statusPublished - 2004 Jul

Bibliographical note

Funding Information:
The present work was performed as a CP Transfer & Dissemination program of Korean National Cleaner Production Center (KNCPC) and the fellowship for V. Vishwanathan is supported by the Brain Pool program of Korea Science and Engineering Foundation (KO-SEF).

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)


Dive into the research topics of 'Surface properties and catalytic activity of TiO2-ZrO 2 mixed oxides in dehydration of methanol to dimethyl ether'. Together they form a unique fingerprint.

Cite this