4.7 Article

Optimization of TiO2/ZSM-5 photocatalysts: Energy band engineering by solid state diffusion method with calcination

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2021.105563

关键词

Calcination; TiO2; ZSM-5; Photocatalysis; Solid phase diffusion method; Pigments and dyeing wastewater

资金

  1. National Natural Science Foundation of China [51974049, 51904045]
  2. Key Technology Innovation Projects of Key Industries in Chongqing [cstc2016zdcyztzx0020-03]
  3. China Postdoctoral Science Foundation [2019M663436]
  4. Chongqing Postdoctoral Science Foundation [cstc2019jcyjbshX0011]

向作者/读者索取更多资源

In this study, TiO2/ZSM-5 hybrids were developed for the photodegradation of methyl orange in water under UV light using a calcination strategy. The optimal sample, Z-T (450), calcined at 450 degrees Celsius, showed nearly 99% degradation rate for methyl orange due to its uniform distribution, high specific surface area, and efficient charge separation/transfer. The use of calcination not only provides a clean, low-cost, and efficient method for azo dye degradation, but also opens up opportunities for industrial applications of photocatalytic technology.
In this work, based on a type of energy band engineering strategy as calcination, TiO2/ZSM-5 hybrids for photodegradation of methyl orange (MO) in water under UV light have been developed via a facile solid state diffusion method. Effects of varied calcination temperatures on TiO2/ZSM-5 hybrids have been systematically characterized including XRD, FT-IR, SEM, TEM, EDX mapping, BET, PL, EIS, UV-vis DRS, active species trapping experiments and Mott-Schottky curves. It was found that the calcination temperature influenced photocatalytic activity, typically on physicochemical properties of materials and adjustment for the energy gap and band position of TiO2. The XRD analysis revealed that hybridization of ZSM-5 kept the crystal phase of TiO2 as anatase unchanged with the high-rising calcined temperature. The optimum sample calcined at 450 degrees C named as Z-T (450) presented nearly 99% degradation rate for MO, owing to optimal uniform distribution, highest specific surface area and best charge separation/transfer efficiency. The FT-IR comparison result that the functional groups and peak strength of the used catalyst were alike as before, showed the stability of photocatalyst. Adoption of calcination strategy does provide not only a clean, low-cost and highly efficient path to approach the complete degradation of azo dyes, but also a chance for photocatalytic technology to fulfill the implementation in industrial applications.

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