(621h) The One Step Oxidation of Methanol to Dimethoxymethane on V2O5/CeO2 Catalysts
AIChE Annual Meeting
2015
2015 AIChE Annual Meeting Proceedings
Catalysis and Reaction Engineering Division
Poster Session: Catalysis and Reaction Engineering (CRE) Division
Wednesday, November 11, 2015 - 6:00pm to 8:00pm
The One Step Oxidation of Methanol to
Dimethoxymethane on V2O5/CeO2 Catalysts
Heqin Guoa, Bo Houa,
Litao Jiaa, Debao Lia*
a State Key Laboratory of Coal
Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan,
030001, China.
*Corresponding author: Tel. /Fax: +86
351 4040410. E-mail addresses: dbli@sxicc.ac.cn
Dimethoxymethane
(CH3OCH2OCH3), as an important chemical
intermediate, was widely used as diesel additive and building block in organic
synthesis. Generally, DMM is produced by the
two-stage synthesis. Such a flow chart could lead to a high cost, which
inhibits the application of DMM. Compared with
the two-step technique, the one-stage technique can synthesize DMM on the bi-founctional (employing redox sites and acidic sites) catalysts (3CH3OH + 1/2O2 °úCH3OCH2OCH3
+ 2H2O). This technique is expected to avoid the drawback of the
two-stage production.
In the present study, the V2O5/CeO2
catalysts with different V2O5
content were prepared by the Sol-Gel method and characterized by XRD, BET,
Raman, NH3-TPD and H2-TPR
techniques. The catalytic properties were evaluated by the one-step oxidation
of methanol to dimethoxymethane. The results showed that the vanadium was
monolayer dispersed as V2O5 content was 15 wt%, aggregated as V2O5 crystalline
above 20 wt% and formed CeVO4 at 30 wt%. The higher dispersion of vanadium can lead to
stronger reducibility and more acidic sites, which were closely
related to the higher methanol conversion and
dimethoxymethane (DMM) selectivity.
Keywords: Vanadia-cerium catalyst; Methanol oxidation reaction;
Acidity; Redox; Dimethoxymethane