4.6 Article

Modification of small-crystal titanium silicalite-1 with organic bases: Recrystallization and catalytic properties in the hydroxylation of phenol

Journal

APPLIED CATALYSIS A-GENERAL
Volume 453, Issue -, Pages 272-279

Publisher

ELSEVIER
DOI: 10.1016/j.apcata.2012.12.027

Keywords

Titanium silicalite-1; Organic base; Recrystallization; Hydroxylation of phenol; Modification

Funding

  1. program for New Century Excellent Talent in University [NCET-04-0268]
  2. Ministry of Education of China

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Small-crystal titanium silicalite-1 (TS-1) with a crystal size of about 600 nm x 400 nm x 250 nm, was treated with different organic bases, including ethylamine, diethylamine, tetramethyl ammonium hydroxide, tetrapropyl ammonium hydroxide and tetrabutyl ammonium hydroxide. The treated TS-1 was characterized by X-ray powder diffraction (XRD), Fourier-transform infrared spectrum (FTIR), ultraviolet-visible diffuse reflectance spectrum (UV-vis), X-ray photoelectron spectrum (XPS), n-hexane and cyclohexane physical adsorption, nitrogen physisorption, inductive coupled plasma emission (ICP), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Modification with different bases led to different molar ratios of Si/Ti on the external surface, according to the XPS data. The TEM images showed that many irregular hollows were generated during modification, due to the random dissolution of framework silicon and titanium. The dissolved amorphous silica and titania recrystallize on the external surface of the TS-1 crystals in the presence of template, and different axis-oriented recrystallization occurred for different templates. Tetrapropyl ammonium favored a-orientation and tetrabutyl ammonium favored b-orientation. Especially the modification with tetrapropyl ammonium hydroxide improved the catalytic properties of small-crystal TS-1 for the hydroxylation of phenol. The conversion of phenol reached 32.6% over small-crystal TS-1 modified with 0.06 mol/L tetrapropyl ammonium hydroxide for 72 h. (C) 2013 Elsevier B.V. All rights reserved.

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