4.7 Article

Synthesis, characterization and activity of an immobilized photocatalyst: Natural porous diatomite supported titania nanoparticles

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 438, Issue -, Pages 204-211

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2014.09.064

Keywords

Diatomite; TiO2; Adsorption; Photocatalysis

Funding

  1. National Technology R&D Program in the 12th five years plan of China [2011BABO3B07]
  2. China Scholarship Council (CSC)

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Diatomite, a porous non-metal mineral, was used as support to prepare TiO2/diatomite composites by a modified sol-gel method. The as-prepared composites were calcined at temperatures ranging from 450 to 950 degrees C. The characterization tests included X-ray powder diffraction (XRD), scanning electron microscopy (SEM) with an energy-dispersive X-ray spectrometer (EDS), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption/desorption measurements. The XRD analysis indicated that the binary mixtures of anatase and rutile exist in the composites. The morphology analysis confirmed the TiO2 particles were uniformly immobilized on the surface of diatom with a strong interfacial anchoring strength, which leads to few drain of photocatalytic components during practical applications. In further XPS studies of hybrid catalyst, we found the evidence of the presence of Ti-O-Si bond and increased percentage of surface hydroxyl. In addition, the adsorption capacity and photocatalytic activity of synthesized TiO2/diatomite composites were evaluated by studying the degradation kinetics of aqueous Rhodamine B under UV-light irradiation. The photocatalytic degradation was found to follow pseudo-first order kinetics according to the Langmuir-Hinshelwood model. The preferable removal efficiency was observed in composites by 750 degrees C calcination, which is attributed to a relatively appropriate anatase/rutile mixing ratio of 90/10. (C)2014 Elsevier Inc. All rights reserved.

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