Loading…
Photocatalytic efficiency of Ag2Te on ZnTe quantum dots: preparation, characterisation and application of response surface methodology
Photodegradation of ampicillin (AMP) over illuminated Ag 2 Te/ZnTe was investigated with the influence of physico-chemical attributes of the nano-catalyst. The Ag 2 Te content was increased in the hybrid catalyst. The photodegradation performance was enhanced due to decrease in the band gap of the c...
Saved in:
Published in: | International journal of environmental analytical chemistry 2022-11, Vol.102 (13), p.3069-3082 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Photodegradation of ampicillin (AMP) over illuminated Ag
2
Te/ZnTe was investigated with the influence of physico-chemical attributes of the nano-catalyst. The Ag
2
Te content was increased in the hybrid catalyst. The photodegradation performance was enhanced due to decrease in the band gap of the catalyst. This was further enhanced by adding Ag
2
Te to ZnTe quantum dots (QDs). The prepared catalyst was studied using analytic techniques such as X-ray diffraction, ultraviolet-visible spectroscopy, field emission scanning electron microscope and dynamic light scattering. The crystallite sizes are distinguished to be 8.62, 14.45, 17.28 and 21.44 nm for ZnTe QDs, Ag
2
Te/ZnTe-0, Ag
2
Te/ZnTe-1 and Ag
2
Te/ZnTe-2, respectively. The effect of three factors such as pH, nano-catalyst dose and AMP concentration was studied for photodecomposition of AMP. Study of reaction optimisation was performed by using the response surface methodology with Box-Behnken design. High correlation was found for the actual and the predicted amount (R
2
= 0.9907, Adj. R
2
= 0.9787 and Pred.R
2
= 0.9657). Optimisation outcome indicated that the maximum efficiency of photodegradation was found at neutral pH, with nano-catalyst dose of 1.0 g/L and AMP concentration 10 mg/L. |
---|---|
ISSN: | 0306-7319 1029-0397 |
DOI: | 10.1080/03067319.2020.1763970 |