4.8 Article

Rational Design of a Bifunctional Catalyst for the Oxydehydration of Glycerol: A Combined Theoretical and Experimental Study

期刊

ACS CATALYSIS
卷 5, 期 1, 页码 82-94

出版社

AMER CHEMICAL SOC
DOI: 10.1021/cs501307v

关键词

catalyst design; bifunctional catalyst; glycerol; acrylic acid; density functional theory

资金

  1. Korea Ministry of Environment as Converging technology project [202-091-001]
  2. Supercomputing Center/Korea Institute of Science and Technology Information [KSC-2013-814 C1-025]
  3. National Research Foundation of Korea (NRF) grant - Korea government (MEST) [2013R1A2A2A01067164]

向作者/读者索取更多资源

Due to its cost effectiveness and eco-friendliness, oxydehydration of glycerol is currently attracting considerable attention. In an attempt to develop an efficient catalyst for the reaction, tungsten-incorporated molybdenum vanadium mixed oxide (MoVW) catalysts were designed on the basis of computational calculations and mechanistic insights. By incorporating tungsten into molybdenum vanadium mixed oxide structure, the catalysts are active and selective not only for the dehydration of glycerol but also for the subsequent oxidation of acrolein to acrylic acid. Through DFT calculations, we confirmed that tungsten species induced a change in the electron density of neighboring atoms, which leads to selective production of acrylic acid. Structural characterization demonstrates that the structure of such MoVW catalysts is similar to that of DFT models. The incorporated tungsten species enhanced the add and redox properties of the catalyst, leading to high selectivity for acrylic acid (30.5%). It not only induced but also stabilized the reduced oxidation states of molybdenum and vanadium atoms, as confirmed by XPS and DFT calculations. Hence, a stable and selective production of acrylic add was achieved with full glycerol conversion for 110 h. The MoVW catalytic system with an additional acid catalyst bed exhibited remarkable selectivity for acrylic add (47.2%), suggesting its potential for practical applications.

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