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Development of photoactive ZnS-SiO2 composites on biogenic silica matrix for organic pollutant degradation
Sulfide ZnS-SiO 2 composite photocatalysts with biogenic silica matrix were prepared by sol–gel method based on wet gel and xerogel. FT-IR, SEM, XRD, EDXRF, UV–Vis, and XPS methods were systematically used to characterize the obtained materials. The use of support allowed to obtain stable porous (S...
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Published in: | Environmental science and pollution research international 2024-11, Vol.31 (52), p.61612-61628 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Sulfide ZnS-SiO
2
composite photocatalysts with biogenic silica matrix were prepared by sol–gel method based on wet gel and xerogel. FT-IR, SEM, XRD, EDXRF, UV–Vis, and XPS methods were systematically used to characterize the obtained materials. The use of support allowed to obtain stable porous (S
BET
= 79–105 m
2
g
−1
; V
pore
= 0.25–0.17 cm
3
·g
−1
) ZnS-SiO
2
photocatalysts in aqueous solutions. Zn
2+
content in methyl orange solution after its degradation was 0.4 MPC. ZnS-SiO
2
composites had 3.68–3.70 eV band gap. The obtained materials were photoactive under different irradiation conditions (sunlight, UV-light, Xenon light, visible light) due to effective separation of charge carriers (e
−
and h
+
). Methyl orange degradation degree under UV light excitation was 35–88%, under sunlight – 11–30%. ZnS-SiO
2
composite synthesized using silica xerogel showed a greater photoactivity due to a presence of cone-shaped or cylindrical pores with one open end in its structure and a higher content of ZnS photoactive component. A comparative study of photocatalytic performance of methyl orange degradation by ZnS-SiO
2
under UV irradiation was investigated using radical scavengers.
•
O
2
−
was main active species during MO degradation under UV irradiation, and electrons played additional role during the photocatalytic process. |
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ISSN: | 1614-7499 0944-1344 1614-7499 |
DOI: | 10.1007/s11356-024-35357-5 |