Carbon nitrides can form coordination compounds or metallic oxides in the presence of transition metals, depending on the reaction conditions. By adjusting the pH to basic levels for mild synthesis with metals, composites like g-C₃N₄-M(OH)_x (where M represents metals) were obtained for nickel (II) and manganese (II), while copper (II) yielded coordination compounds such as Cu-g-C₃N₄. These materials underwent spectroscopic and electrochemical characterization, revealing their photocatalytic potential to generate superoxide anion radicals—a feature consistent across all metals. Notably, the copper coordination compound also produced significant hydroxyl radicals. Leveraging this catalytic advantage, with band gap energy in the visible region, all compounds were activated to disinfect E. coli bacteria, achieving total disinfection with Cu-g-C₃N₄. The textural properties influence the catalytic performance, with copper’s stabilization as a coordination compound enabling more efficient activity compared to the other metals. Additionally, the determination of radicals generated under light in the presence of dicloxacillin supported the proposed mechanism and highlighted the potential for degrading organic molecules with this new material, alongside its disinfectant properties.

The antibacterial activity of g-C₃N₄ and Cu-g-C₃N₄ was evaluated against E. coli, with their disinfection capabilities influenced by structural characteristics, photocatalytic properties, and modulation under a static magnetic field. The incorporation of Cu²⁺ does not significantly affect the (210) reflection in XRD analysis, indicating that the alignment of aromatic layers remains stable. However, the presence of copper enables complete disinfection, in contrast to graphitic carbon nitride, which achieves only partial disinfection. Cu²⁺ is likely positioned at N-aliphatic sites and coexists with hydroxylated species, which may influence photocatalytic performance by modifying reactant adsorption and ROS generation. SEM-EDS analysis confirmed that Cu²⁺ modification did not significantly alter the material’s morphology, although a 3% copper content was detected, suggesting a heterogeneous surface distribution. Thermodynamic analysis showed that exposure to a magnetic field increased the Gibbs free energy of adsorption from 6.34 J/m² to 10.52 J/m², reducing interactions with key reactants essential for ROS formation. As a result, both disinfection and photodegradation efficiency were significantly diminished. Additionally, the presence of a magnetic field was found to modify the surface properties of the material, affecting its photocatalytic performance. In Cu-C₃N₄ materials, a decrease in the contact angle suggests enhanced hydrophilicity, while an increase in surface tension may influence the adsorption of water and hydroxyl radicals. This study underscores the effect of a magnetic field on the photocatalytic behavior of materials deposited on polymeric substrates with intrinsic electronic properties, ultimately impacting overall disinfection efficiency.

A carbon-based material was synthesized using potato peels (BPP) and banana pseudo-stems (BPS), both of which were modified with manganese to produce BPP-Mn and BPS-Mn, respectively. These materials were assessed for their ability to activate peroxymonosulfate (PMS) in the presence of MnCO₃ to degrade acetaminophen (ACE), an emerging water contaminant. The materials underwent characterization using spectroscopic, textural, and electrochemical techniques. Manganese served a dual function: enhancing adsorption properties and facilitating the breaking of peroxide bonds. Additionally, carbonate ions played a structural role in the materials, transforming into CO₂ at high temperatures and thereby increasing material porosity, which improved adsorption capabilities. This presents a notable advantage for materials that have not undergone de-lignification. Among the materials tested, BPS exhibited the highest efficiency in the carbocatalytic degradation of ACE, achieving a synergy index of 1.31 within just 5 min, with 42% ACE degradation in BPS compared to BPS-Mn, which achieved 100% ACE removal through adsorption. Reactive oxygen species such as sulfate, hydroxyl, and superoxide anion radicals were identified as the primary contributors to pollutant degradation. In contrast, no degradation was observed for BPP and BPP-Mn, which is likely linked to the lower lignin content in their precursor material. This work addressed the challenge of revalorizing lignocellulosic waste by highlighting its potential as an oxidant for emerging pollutants. Furthermore, the study demonstrated the coexistence of various reactive oxygen species, confirming the capacity of carbon-based matrices to activate PMS.