Synthesis and characterization of ZnZr composites for the photocatalytic degradation of phenolic molecules: addition effect of ZrO2over hydrozincite Zn5(OH)6(CO3)2

Autor: R. Pérez-Hernández, Francisco Tzompantzi, C.E. Santolalla-Vargas, Verónica De la Luz Tlapaya, Clara Tzompantzi-Flores, Ricardo Gómez, J.C. Castillo-Rodríguez
Rok vydání: 2019
Předmět:
Zdroj: Journal of Chemical Technology & Biotechnology. 94:3428-3439
ISSN: 1097-4660
0268-2575
Popis: BACKGROUND: The composite materials ZrO₂/Zn₅(OH)₆(CO₃)₂ were prepared in only one step by chemical co‐precipitation and thermal hydrolysis of urea. ZrO₂ was added at 5, 8 and 10 mol%. The samples were dried at 80 °C and characterized by adsorption–desorption of N₂ isotherms, X‐ray diffraction (XRD) and scanning electron microscopy (SEM) techniques, and diffuse reflectance (DRS), UV–visible, Fourier‐transform infrared (FTIR) and X‐ray photoelectron (XPS) spectroscopies. The materials were assessed in the photodegradation of phenol and polychlorinated phenolic molecules under UV‐light irradiation. The possible mechanism was discussed from studies that corroborated or discarded the formation of the species •OH, •O₂⁻ and h⁺. RESULTS: The addition of ZrO₂ to Zn₅(OH)₆(CO₃)₂ resulted in a composite material with high photoactivity. The material containing 8 mol% of ZrO₂ (ZnZr‐8.0%) was the sample with the best percentages of photodegradation and mineralization. The photodegradation enhancement was achieved partly by an increment in the specific surface area and principally due to localized states originating in the composite interphase which improved charge transfer. XPS study revealed that the ZrO₂ addition increases the oxygen vacancies which enhanced the organic molecule photodegradation via direct hole attack. CONCLUSION: The ZnZr composite system constitutes an excellent alternative for the photodegradation of persistent organic pollutants due to the low cost, high stability and null toxicity of the support Zn₅(OH)₆(CO₃)₂. © 2019 Society of Chemical Industry
Databáze: OpenAIRE