Acta Phys. -Chim. Sin. ›› 2010, Vol. 26 ›› Issue (02): 373-377.doi: 10.3866/PKU.WHXB20100222

• CATALYSIS AND SURFACE STRUCTURE • Previous Articles     Next Articles

Incorporation of CuO into Mesoporous Carbon CMK-3 and Its Adsorption and Catalytic Oxidation of Phenol

HU Long-Xing, DANG Song-Tao, YANG Xia-Ping   

  1. School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, P. R. China
  • Received:2009-07-17 Revised:2009-11-28 Published:2010-01-26
  • Contact: DANG Song-Tao E-mail:yanlingjz@gmail.com

Abstract:

Copper (II) oxide nanoparticles were incorporated into the pore systemof mesoporous carbon CMK-3 by a facile method, forming the composite Cu/CMK-3. Cu/CMK-3 was characterized by powder X-ray diffraction, nitrogen physisorption, and transmission electron microscopy. Results showed that Cu/CMK-3 preserved the ordered mesoporous structure of CMK-3 and copper (II) oxide was dispersed within the CMK-3 channels as small nanoparticles. CMK-3 still had a large surface area after copper (II) oxide was incorporated. The adsorption and catalytic dry oxidation ability of Cu/CMK-3 for phenol was determined. The adsorption and recycle results indicate that Cu/CMK-3 adsorbs aqueous phenol well because of its large surface area. Most of the phenol adsorbed on CMK-3 was catalytically dry-oxidized at relatively low temperature. We demonstrate that Cu/CMK-3 can be used as a sorbent-catalyst for aqueous phenol. After seven cycles, Cu/CMK-3 retained a substantial fraction of its adsorption ability for phenol. A combined thermogravimetry-mass spectroscopy (TG-MS) instrument was used to investigate the catalytic activity and ignition behavior of Cu/CMK-3. Results show that CuO is the active component during the catalytic dry oxidization of phenol. The adsorbed phenol is catalytically dry-oxidized into carbon dioxide and water at the relatively low temperature of about 180 ℃, where no phenol desorption or CMK-3 ignition occurred.

Key words: Adsorption, Mesoporous carbon CMK-3, Copper (II) oxide, Catalytic dry oxidation