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Photocatalytic degradation of Rhodamine B dye using low‐cost pyrofabricated titanium dioxide quantum dots‐kaolinite nanocomposite.

Authors :
Awad, Mahmoud E.
Farrag, Amr M.
El‐Bindary, Ashraf A.
El‐Bindary, Mohamed A.
Kiwaan, Hala A.
Source :
Applied Organometallic Chemistry; Jul2023, Vol. 37 Issue 7, p1-17, 17p
Publication Year :
2023

Abstract

In this study, we report a simple technique for the pyrofabrication of a novel photocatalyst of titanium dioxide quantum dots‐kaolinite nanocomposite (TiO2‐QDs‐Kao) used for rhodamine B (RhB) dye degradation. The photocatalyst was characterized by using different analytical techniques, including XRD, XRF, XPS, FTIR, DTA/TGA, SEM–EDX, TEM, BET, BJH, ZP and UV–Vis DRS. The photocatalytic degradation of RhB was performed in aqueous solutions using the sustainable sunlight energy under atmospheric conditions and fixed neutral medium (pH = 7). The produced photocatalyst exhibited optical band gap energy of 2.85 eV, an improved large specific surface area of 107.724 m2/g with pore radius of 1.45 nm and total pore volume of 0.123 cm3/g. The study indicated a maximum 91% degradation efficiency of RhB after 120 min using the optimum dose 1,400 mg/l of the TiO2‐QDs‐Kao photocatalyst. The degradation of RhB dye fitted the Langmuir first‐order kinetics with rate constant 0.0151 min−1. The radical trapping experiments based on scavengers confirmed that the mechanism of photocatalytic degradation activity was potentially based on electron (e−) and hole (h+) conduction band. The potential energy of the valence and conduction bands EVB and ECB were calculated 2.73 and −0.12 eV, respectively. A triple reusability study confirmed a high stability of TiO2‐QDs‐Kao photocatalyst with detected degradation efficiencies of 91.0, 89.9, 88.8 and 87.5%, respectively. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02682605
Volume :
37
Issue :
7
Database :
Complementary Index
Journal :
Applied Organometallic Chemistry
Publication Type :
Academic Journal
Accession number :
164488038
Full Text :
https://doi.org/10.1002/aoc.7113