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Photocatalyst production from wasted sediment and quality improvement with titanium dioxide to remove cephalexin in the presence of hydrogen peroxide and ultrasonic waves: A cost-effective technique.
- Source :
-
Chemosphere . Dec2021, Vol. 284, pN.PAG-N.PAG. 1p. - Publication Year :
- 2021
-
Abstract
- In this study, wasted sediment (sludge waste from shipping docks) was coupled with titanium isopropoxide by the thermal and sol-gel method as a new photocatalyst. The sediment-titanate catalyst alongside ultrasonic and UV was activated hydrogen peroxide to produce OH radicals and decompose cephalexin (CEP). The photocatalyst was crystalline with 52.29 m2/g BET area. The best destruction rate of 87.01% based on COD test was achieved at optimal conditions (pH: 8, cephalexin concentration: 100 mg/L, H 2 O 2 : 1.63 mg/L, UV: 15 W/m2, ultrasonication time: 100 min at 40 kHz, photocatalyst quantity: 1.5 g/L). The trend of anions effect was NO 3 − ≤ SO 4 2− ≤ Cl−. Decomposition of cephalexin in water solution followed the first-order kinetics (k > 0.01 min−1, R2 > 0.9). The percentage of cephalexin removal from urban water (76%) and hospital wastewater (63%) has decreased compared to the distilled water solution (87%), which is probably due to the presence of radical inhibitors. The consumed electrical energy of the studied system was calculated by 0.031 kW/h. The developed system is a promising and economical method to remove cephalexin. [Display omitted] • Disposable sediments of shipping docks were decorated with TiO 2 to activate H 2 O 2. • UV and ultrasonic waves synergized the decomposition of cephalexin by the catalyst. • Under optimal conditions, 87% of 100 mg/L cephalexin was removed within 100 min. • The anions affected the cephalexin removal by the order of NO 3 − ≤ SO 4 2− ≤ Cl−. • Hospital wastewater was treated by 63% with the electrical energy of 0.031 kW/h. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00456535
- Volume :
- 284
- Database :
- Academic Search Index
- Journal :
- Chemosphere
- Publication Type :
- Academic Journal
- Accession number :
- 152631904
- Full Text :
- https://doi.org/10.1016/j.chemosphere.2021.131337