Redefining water purification: gC3N4-CLDH's electrochemical SMX eradication.
Chemosphere
; 362: 142921, 2024 Aug.
Article
in En
| MEDLINE
| ID: mdl-39053778
ABSTRACT
The contamination of water sources by pharmaceutical compounds presents global environmental and health risks, necessitating the development of efficient water treatment technologies. In this study, the synthesis, characterization, and evaluation of a novel graphitic carbon nitride-calcined (Fe-Ca) layered double hydroxide (gC3N4-CLDH) composite for electrochemical degradation of sulfamethoxazole (SMX) in water yielded significant outcomes are reported. SEM, XRD, FTIR, and XPS analyses confirmed well-defined composite structures with unique morphology and crystalline properties. Electrochemical degradation experiments demonstrated >98% SMX removal and >75% TOC removal under optimized conditions, highlighting its effectiveness. The composite exhibited excellent mineralization efficiency across various pH levels, with superoxide radicals (O2â-) and hydroxyl radicals (âOH) identified as primary reactive oxygen species. With remarkable regeneration capability for up to 7 cycles, the gC3N4-CLDH composite emerges as a highly promising solution for sustainable water treatment. Humic acid (HA) in water significantly slows SMX degradation, suggests complicating SMX degradation with natural organic matter. Despite this, the gC3N4-CLDH composite effectively degrades SMX in groundwater and industrial wastewater, with slight efficiency reduction in the latter due to higher impurity levels. These findings highlight the complexities of treating pharmaceutical pollutants in various water types. Overall, gC3N4-CLDH's high removal efficiency, broad pH applicability, sustainability, and mechanistic insights provide a solid foundation for future research and real-world environmental applications.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Sulfamethoxazole
/
Water Pollutants, Chemical
/
Water Purification
/
Graphite
Language:
En
Journal:
Chemosphere
Year:
2024
Document type:
Article
Country of publication:
United kingdom