4.7 Article

One-pot synthesis of phosphorylated mesoporous carbon heterogeneous catalysts with tailored surface acidity

期刊

CATALYSIS TODAY
卷 186, 期 1, 页码 12-19

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cattod.2011.08.004

关键词

Soft-templating; Mesoporous carbon; Phosphorylation; Ammonia-TPD; Isopropanol dehydration

资金

  1. Fluid Interface Reactions, Structures and Transport (FIRST) Center, an Energy Frontier Research Center
  2. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [ERKCC61]
  3. U.S. Dept. of Energy, Office of Energy Efficiency and Renewable Energy
  4. Materials Sciences & Engineering Division, Office of Basic Energy Sciences
  5. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences, U.S. Dept. of Energy [DE-AC05-OR22725]
  6. Oak Ridge National Laboratory

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Soft-templated phosphorylated mesoporous carbons with homogeneous distributions of phosphate groups were prepared by a one-pot synthesis method using mixtures of phosphoric acid with hydrochloric, or nitric acids in the presence of Pluronic F127 triblock copolymer. Adjusting the various ratios of phosphoric acid used in these mixtures resulted in carbons with distinct adsorption, structural and surface acidity properties. The pore size distributions (PSDs) from nitrogen adsorption at -196 degrees C showed that mesoporous carbons exhibit specific surface areas as high as 551 m(2)/g and mesopores as large as 13 nm. Both structural ordering of the mesopores and the final phosphate contents were strongly dependent on the ratios of H3PO4 in the synthesis gels, as shown by transmission electron microscopy (TEM), X-ray photoelectron (XPS) and energy dispersive X-ray spectroscopy (EDS). The number of surface acid sites determined from temperature programmed desorption of ammonia (NH3-TPD) were in the range of 0.3-1.5 mmol/g while the active surface areas are estimated to comprise 5-54% of the total surface areas. Finally, the conversion temperatures for the isopropanol dehydration were lowered by as much as 100 degrees C by transitioning from the least acidic to the most acidic catalysts surface. Published by Elsevier B.V.

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