4.7 Article

Rapid degradation of azo dye methyl orange using hollow cobalt nanoparticles

期刊

CHEMOSPHERE
卷 144, 期 -, 页码 1530-1535

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2015.10.040

关键词

Azo dye; Methyl orange; Reductive degradation; Cobalt; Hollow particles; Magnetic separation

资金

  1. UMass CVIP Technology Development Fund
  2. NSF [CMMI-1031532]

向作者/读者索取更多资源

A rapid and efficient method for methyl orange degradation using hollow cobalt (Co) nanoparticles is reported. Hollow Co nanoparticles were fabricated by a galvanic replacement reaction using aluminum (Al) nanoparticles as the template material. The methyl orange degradation characteristics were investigated by measuring the time dependent UV-Vis absorption of the dye solution, which showed a very fast degradation rate under acidic conditions. At an initial methyl orange concentration of 100 mg/L (pH = 2.5) and Co nanoparticle dosage of 0.5 g/L, the azo dye degradation efficiency reached up to 99% within 4 min, and the degradation constant rate was up to 2.444 min(-1), which is the highest value among other studies. A comparison of the decolorization rates at similar conditions with several other azo dyes, including Congo red, Amaranth, and Orange G, showed that the dye with a simpler structure and lower molecular mass decolorized considerably faster than the ones having a more complicated structure (higher molecular mass). The methyl orange degradation was also conducted using hollow nickel (Ni) nanoparticles and commercially available solid spherical Co and Ni nanoparticles. The results showed that Cobased nanoparticles outperformed Ni-based nanoparticles, with the hollow Co nanoparticles exhibiting the fastest degradation rate. Using the hollow Co nanoparticles is a very promising approach for the remediation of methyl orange dye containing wastewater due to the fast degradation rate and high degradation efficiency. In addition, these hollow Co nanoparticles are easily recycled because of their magnetic property. (C) 2015 Elsevier Ltd. All rights reserved.

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