Published September 2014 | Version v1
Journal article

A recyclable and highly active Co3O4 nanoparticles/titanate nanowire catalyst for organic dyes degradation with peroxymonosulfate

  • 1. Key Laboratory of Advanced Textile Materials and Manufacturing Technology, and Engineering Research Center for Eco-Dyeing and Finishing of Textiles, Ministry of Education, Zhejiang Sci-Tech University, Hangzhou 310018 (China)
  • 2. Valparaiso Department of Water Works, 205 Billings Street, Valparaiso, IN 46383 (United States)
  • 3. Institute of Microstructure and Properties of Advanced Materials, Beijing University of Technology, Beijing 100124 (China)
  • 4. Groupe en Sciences des Radiations, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC J1H 5N4 (Canada)

Description

Sodium ions of TNWs were exchanged with hydrogen ions, and this protocol was very suitable for capturing high density of cobalt ions. Meanwhile, the fabricated Co3O4/TNWs nano-material presented a highly catalytic and stable activity for dye degradation. - Highlights: • Co3O4 nanoparticles were deposited on the pretreated TNWs surface. • The TNWs treated by hydrogen ions captures higher density of cobalt ions. • The Co3O4/TNWs catalyst possesses highly efficiency for dyes degradation with oxone. - Abstract: In this paper, we reported a recyclable and highly active porous catalyst of titanate nanowires (TNWs) coated with well-distributed Co3O4 nanoparticles (NPs) (Co3O4/TNWs). Sodium ions of TNWs were exchanged with hydrogen ions in the dilute nitric acid, and this protocol was very suitable for capturing cobalt ions. X-ray diffraction (XRD) demonstrated the existence of Co3O4 phase with unique lattice planes, such as (2 2 0), (3 1 1) and (5 1 1). Electron microscopes (FE-SEM and TEM) indicated that the Co3O4 NPs with an average diameter of 22 ± 3 nm were coated uniformly on TNWs surface (average diameter: 37 ± 5.5 nm), and the Co3O4 NPs mainly exposed their (2 2 0) and (2 2 2) active planes. XPS analysis confirms the formation of Co3O4 phase by the presence of Co 2p peaks at 780.1 eV (2p 3/2) and 795.5 eV (2p 1/2). Methylene blue (MB) and other organic dyes (rhodamine B (RhB) and methyl orange (MO)) were chosen as target compounds for catalytic degradation under indoor scattering light. Compared to the original Co3O4/TNWs catalyst, the catalytic efficiency of nanoscaled catalyst with oxone for MB was about 15 times higher, and the MB solution (10 mg L−1) was completely degraded within 8 min. The catalytic activity of recycled catalyst used in the sixth run still remained very active, and the degradation time for MB was only 16 min. The nanosized catalyst also had a high activity for dyes of RhB (10 mg L−1) and MO (10 mg L−1), as the degradation efficiencies of RhB and MO after 10 min of contact time were about 90.2% and 92.6%, respectively

Availability note (English)

Available from http://dx.doi.org/10.1016/j.materresbull.2014.05.046

Additional details

Identifiers

DOI
10.1016/j.materresbull.2014.05.046;
PII
S0025-5408(14)00322-5;

Publishing Information

Journal Title
Materials Research Bulletin
Journal Volume
57
Journal Page Range
p. 170-176
ISSN
0025-5408
CODEN
MRBUAC

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.