Journal
INTERNATIONAL JOURNAL OF ENVIRONMENTAL SCIENCE AND TECHNOLOGY
Volume 19, Issue 1, Pages 173-188Publisher
SPRINGER
DOI: 10.1007/s13762-021-03160-1
Keywords
Photodegradation; Nanomaterials; Zinc oxide; Surfactants; C12E10; Triton X-100; Central fission
Categories
Funding
- Ministry of Science and Higher Education, Poland [0911/SBAD/0398, 0912/SBAD/2006]
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This study evaluated the performance of zinc oxide nanoparticles as a photocatalyst for the photodegradation of two non-ionic surfactants. The synthesis and characterization of the nanoparticles were conducted, followed by spectrophotometric assessment of the photodegradation process. The results showed efficient degradation of the surfactants using the nanoparticles, with the reaction kinetics described by the Langmuir-Hinshelwood mechanism.
The aim of this study was to evaluate the performance of zinc oxide nanoparticles as a photocatalyst for photodegradation of two model non-ionic surfactants (Triton X-100 and C12E10). The first part of the investigation was focused on the synthesis and characterization of ZnO nanoparticles, since its crystalline structure strongly impacts its photocatalytic properties. Based on the results of the XRD analysis, it was concluded that the obtained material occurred in the form of hexagonal wurtzite with a polycrystalline structure. FT-IR and XPS analyses were used to elucidate and confirm the nanomaterial structure, whereas investigation of N-2 adsorption/desorption and SEM/TEM imaging allowed to establish that the synthesized ZnO was characterized as a mesoporous material with uniform, spherical shape and particle size fluctuating between 90 and 130 nm. The second part of the study included spectrophotometric assessment of the photodegradation process. The use of the obtained ZnO nanoparticles allowed to achieve efficient photodegradation of both C12E10 (92%) and Triton X-100 (82%) after 1 h of UV irradiation. The Langmuir-Hinshelwood mechanism was used to describe the reaction kinetics. Subsequent LC-MS/MS analysis of the residues indicated that the degradation mechanism is most likely based on both central fission of the surfactant molecules with further terminal oxidation of poly(ethylene glycol) and terminal oxidation leading to carboxylic derivatives of surfactants.
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