Volume 39 Issue 12
Dec.  2011
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WANG Wei-Yan, Yang-Yun-Quan, Luo-He-An, Yang-Yan-Song, Hu- Tao, Liu-Wen-Yang, He- Bing, Qin-Bai-Hao. Preparation of TiO2-Al2O3composite support and its performance in catalystic hydrodeoxygenation[J]. Journal of Fuel Chemistry and Technology, 2011, 39(12): 924-929.
Citation: WANG Wei-Yan, Yang-Yun-Quan, Luo-He-An, Yang-Yan-Song, Hu- Tao, Liu-Wen-Yang, He- Bing, Qin-Bai-Hao. Preparation of TiO2-Al2O3composite support and its performance in catalystic hydrodeoxygenation[J]. Journal of Fuel Chemistry and Technology, 2011, 39(12): 924-929.

Preparation of TiO2-Al2O3composite support and its performance in catalystic hydrodeoxygenation

  • Received Date: 2010-12-27
  • Rev Recd Date: 2011-04-06
  • Publish Date: 2011-12-31
  • TiO2-Al2O3 composite supports were prepared by co-precipitation method and characterized by N2 physisorption, X-ray diffraction (XRD) and pyridine adsorption FT-IR spectroscopy. Ni-Mo-S/TiO2-Al2O3 supported catalysts were prepared with in-situ sulfidation method and their hydrodeoxygenation (HDO) properties were tested using phenol as model compound. The effects of aluminum sources and precipitants on the properties of TiO2-Al2O3 composite supports and the effects of support properties on the HDO properties of Ni-Mo-S/TiO2-Al2O3 catalysts were studied. The results showed that the pore volume and average pore diameter of the support prepared using aluminum chloride as aluminum source were as high as 1.12cm3/g and 18.0nm, respectively. The support prepared using aluminum sulfate and ammonium bicarbonate as initial materials had high specific surface area (295m2/g). Among three precipitants, the support precipitated using ammonia solution had the most L-acid sites while the support prepared using aluminum sulfate had a little of B-acid sites. The primary factors of supports which affected the HDO properties of Ni-Mo-S/TiO2-Al2O3 catalysts were the acidity and specific surface area of supports. In the HDO of phenol on Ni-Mo-S/TiO2-Al2O3 catalyst, the conversion, the deoxygenation reaction rate and the total oxygen-free compound were as high as 81.9%, 79.4% and 100%, respectively.
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