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Visible-light-driven removal of tetracycline antibiotics and reclamation of hydrogen energy from natural water matrices and wastewater by polymeric carbon nitride foam
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A polymeric carbon nitride foam photocatalyst was used to simultaneously remove tetracycline antibiotics from water and produce hydrogen fuel under visible light, achieving efficient degradation in natural water matrices and wastewater. The study demonstrates a dual-function photocatalytic system that addresses both water pollution remediation and renewable energy generation from a single solar-driven process.
Water and energy are key sustainability issues that need to be addressed. Photocatalysis represents an attractive means to not only remediate polluted waters, but also harness solar energy. Unfortunately, the employment of photocatalysts remains a practical challenge in terms of high cost, low efficiency, secondary pollution and unexploited water matrices influence. This study investigated the feasibility of photocatalysis to both treat water and produce hydrogen with practical water systems. Polymeric carbon nitride foam (CNF) with large surface area and mesoporous structure was successfully prepared via the bubble-template effect of ammonium chloride decomposition during thermal condensation. The reaction kinetics, mechanisms, and effect of natural water matrices and wastewater on CNF-based photocatalytic removal of tetracycline hydrochloride (TC-HCl) were systematically investigated. Furthermore, the efficiency of clean hydrogen energy from natural water matrices and wastewater was also evaluated. It was found that the photocatalytic performance of CNF for TC-HCl removal was principally affected by calcination temperature in the presence of NHCl. The degradation rates of CNF-4 (calcined at 550 °C) were approximately 1.84, 2.49 and 7.47 times than that of the CNF-2 (calcined at 600 °C), CNF-1 (calcined at 500 °C) and GCN (without NHCl), respectively. Results indicate that the improved photocatalytic performance was predominantly ascribed to the large specific surface area, increased availability of exposed active sites, and enhanced transport and separation efficiency of the photogenerated carrier. Based on electron spin resonance, chemical trapping experiment and density functional theory calculation, photoinduced oxidizing species (·O and holes) initially attacked the C-N-C fragment of TC molecules, which were finally mineralized to CO, water and inorganic matters. Under the synergistic influence of water constituents (including acidity and alkalinity, ion species and dissolved organic substances), various water matrices greatly affected the degradation rate of TC-HCl, with the highest removal efficiency of 78.9% in natural seawater, followed by reservoir water (75.0%), tap water (62.3%), deionized water (49.8%), reverse osmosis concentrate (32.7%) and pharmaceutical wastewater (18.9%). Interestingly, low amounts of the emerging microplastics slightly improved TC-HCl removal, whereas high amounts (1.428 × 10 P/cm) restricted removal due to light absorption and the intrinsic adsorption interaction. Moreover, the photocatalysts were able over repeated usage. Notably, the hydrogen yields rates of polymeric carbon nitride foam were 352.2, 299.8, 184.9 and 94.3 μmol/g/h in natural seawater, pharmaceutical wastewater, water from reservoir and tap water, respectively. This study proves the potential of novel nonmetal porous photocatalyst to simultaneously treat wastewater while converting solar energy into clean hydrogen energy.
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