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China Surfactant Detergent & Cosmetics ›› 2024, Vol. 54 ›› Issue (6): 669-676.doi: 10.3969/j.issn.2097-2806.2024.06.007

• Development and application • Previous Articles     Next Articles

Synthesis and photocatalytic activity of a CaMoO4 photocatalyst modified with C-O functional groups

Lei Wang*(),Jun Tian   

  1. Schoo of Chemistry and Bioengineering, Yinchuan Energy College, Yinchuan, Ningxia 750000, China
  • Received:2023-06-08 Revised:2024-05-21 Online:2024-06-22 Published:2024-06-24
  • Contact: * E-mail: 13709511472@163.com.

Abstract:

A CaMoO4 photocatalyst with high activity for degradation of aureomycin hydrochloride was prepared by sol-gel method. The phase structure, purity, functional group, surface morphology, optical properties and photocatalytic activity of the CaMoO4 photocatalyst were investigated by various characterization methods. The results showed that the CaMoO4 photocatalyst was tetragonal phase, and a small amount of C-O functional groups were present in the sample. The particles were approximately spherical, which consisted of large particles and fine particles. It had high visible-light response with an optical band gap value of 3.21 eV. The photocatalytic activity of CaMoO4 photocatalyst was studied at different drug concentrations, catalyst dosages and pH values using aureomycin hydrochloride as the target for degradation. The results showed that the degradation percentage reached 94% at the drug mass concentration of 200 mg/L, photocatalyst dosage of 1 g/L and pH of 7. The photocatalytic mechanism of the CaMoO4 photocatalyst was proposed based on experimental results and band theory. The mechanism study showed that the C-O functional groups provided extra energy for electron transition to the conduction band of the CaMoO4 photocatalyst and promoted the generation of electron hole pairs. Holes, hydroxyl radicals and superoxide radicals were the key factors to promote the degradation of aureomycin hydrochloride.

Key words: sol-gel method, CaMoO4, photocatalytic mechanism, conduction band, free radical

CLC Number: 

  • O469