In recent years, advanced oxidation processes (AOPs) demonstrated great efficiency in eliminating emerging contaminants in aqueous media. However, a majority of scientists believe that one of the main reasons hindering their industrial application is the low efficiencies recorded. This can be partially attributed to reactive oxygen species (ROS) scavenging from real water matrix constituents. A promising strategy to cost-effectively increase efficiency is the simultaneous use of different AOPs. Herein, photocatalysis and sodium persulfate activation (SPS) were used simultaneously to decompose the antibiotic sulfamethoxazole (SMX) in ultrapure water (UPW) and real water matrices, such as bottled water (BW) and wastewater (WW). Specifically, copper-promoted BiVO₄ photocatalysts with variable CuO_x (0.75–10% wt.) content were synthesized in powder form and characterized using ΒΕΤ, XRD, DRS, SEM, and HRTEM. Results showed that under simulated solar light irradiation alone, 0.75 Cu.BVO leads to 0.5 mg/L SMX destruction in UPW in a very short treatment time, whereas higher amounts of copper loading decreased SMX degradation. In contrast, the efficiency of all photocatalytic materials dropped significantly in BW and WW. This phenomenon was surpassed using persulfate in the proposed system resulting in synergistic effects, thus significantly improving the efficiency of the combined process. Specifically, when 0.75 Cu.BVO was added in BW, only 40% SMX degradation took place in 120 min under simulated solar irradiation alone, whereas in the solar/SPS/Cu.BVO system, complete elimination was achieved after 60 min. Moreover, ~37%, 45%, and 66% synergy degrees were recorded in WW using 0.75 Cu, 3.0 Cu, and 10.0 Cu.BVO, respectively. Interestingly, experimental results highlight that catalyst screening or process/system examination must be performed in a wide window of operating parameters to avoid erroneous conclusions regarding optimal materials or process combinations for a specific application.

The solar-induced semiconductor photocatalytic process is one of the greenest and most promising technologies for the elimination of pharmaceuticals in aqueous media. In the context of this study, a bismuth oxychloride (BiOCl) photocatalyst was fabricated and characterized by its morphology, crystallographic structure, and optical properties. Its photocatalytic efficiency was tested towards the degradation of Losartan (LOS), a medication used to treat high blood pressure, in water using a solar simulator. The as-prepared BiOCl exhibited significant photocatalytic efficiency, achieving complete degradation of 0.3 mg/L LOS in short periods of irradiation (15–30 min). The examined system showed optimal efficiency using 500 mg/L of BiOCL (k_app = 0.21 min⁻¹) and pH 3 (k_app = 0.32 min⁻¹). However, LOS removal significantly decreased in environmentally relevant water matrices, including wastewater (k_app = 0.006 min⁻¹) and bottled water (k_app = 0.023 min⁻¹). Additional tests carried out in synthetic water matrices showed that the LOS degradation rate was reduced by more than 40% in the presence of humic acid (k_app = 0.016 min⁻¹) and bicarbonates (k_app = 0.029 min⁻¹), while chlorides did not affect the overall efficiency. Moreover, photogenerated holes and singlet oxygen were the dominant oxidative species. The efficiency of the BiOCl photocatalyst towards LOS degradation was further studied using a flat plate pilot-plant scale photoreactor. It was found that more than 75% of LOS was removed after 100 kJ/L of accumulated solar irradiation. The results obtained in the pilot-plant unit confirmed the suitability of BiOCl as a potential photocatalytic material.

Developing highly active and available, environmentally friendly, and low-cost photocatalytic materials is one of the most popular topics in photocatalytic degradation systems. In the present study, a series of BiOCl/Sepiolite composite photocatalysts were prepared (in the range of 5%BiOCl/Sepiolite–30%BiOCl/Sepiolite). Their characterization was conducted using X-ray diffraction, diffuse reflectance spectroscopy, scanning electron microscopy, nitrogen physical physisorption at the temperature of liquid nitrogen (77 K), and attenuated total reflectance-Fourier transform infrared spectroscopy. Results showed that composite photocatalysts possess superior efficiency than the parent materials for losartan, an antihypertensive agent, degradation in water, with the sample with only 10%wt. BiOCl shows the highest performance. The beneficial effect of the addition of sepiolite to BiOCl is derived from the increase in surface area, the prevention of particle aggregation, and the efficient separation of photogenerated species. Increasing catalyst concentration from 125 mg/L up to 500 mg/L was accompanied by an increase in the apparent kinetic constant from 0.077 min⁻¹ to 0.197 min⁻¹ while varying losartan concentration from 0.25 to 5.00 mg/L slowed down the removal efficiency. In addition, losartan degradation was only partially hampered in the case of bottled water, whereas it was practically stopped in a secondary wastewater effluent. Overall, this study serves as a useful guide for using geopolymers in photocatalytic applications.

In this work, the decomposition of bisphenol S (BPS) by biochar derived from banana peel (BPB) promoted by copper phosphide (Cu₃P) was examined. Different materials with Cu₃P loadings from 0.25 to 4.00 wt.% on biochar were synthesized, characterized using the Brunauer–Emmett–Teller (BET) method, X-ray diffraction (XRD) and a scanning electron microscope (SEM) equipped with an energy dispersive spectrometer (EDS), and evaluated. Nearly all of the synthesized materials exhibited low to moderate adsorption capacity, attributable to their limited surface area (<3.1 m²/g). However, in the presence of sodium persulfate (SPS), the 2%Cu₃P/ΒPB/SPS system was capable of removing 90% of 500 μg/L BPS in less than 10 min. The system’s performance was enhanced under inherent pH, and the reaction rate followed pseudo-first-order kinetics with respect to BPS and persulfate concentrations. Interestingly, the presence of 250 mg/L of sodium chloride had a negligible effect, while low to moderate inhibition was observed in the presence of bicarbonates and humic acid. In contrast, significant retardation was observed in experiments performed in real matrices, such as secondary effluent (WW) and bottled water (BW). According to scavenging experiments, both radical and non-radical mechanisms participated in the BPS degradation. Four transformation products were identified using the UHPLC/TOF-MS system in negative ionization mode, with two of them having higher molecular weights than BPS, while the other two TBPs involved the ring-opening reaction, and a BPS decomposition pathway was proposed.

This work examines the solar photocatalytic degradation of the antibiotic sulfamethoxazole (SMX) using molybdenum telluride (MoTe₂)-promoted bismuth oxychloride (BiOCl). Different loadings of molybdenum telluride in the 0–1% range on BiOCl were synthesized and evaluated. Although the presence of MoTe₂ did not alter either the adsorption capacity or the energy gap of BiOCl, the synthesized photocatalyst demonstrated higher photocatalytic activity due to the enhanced separation of photogenerated pairs. The 0.5MoTe₂/BiOCl photocatalyst achieved a kinetic constant nearly 2.8 times higher than that of pure BiOCl, leading to the elimination of 500 μg/L SMX within 90 min. The system’s performance was enhanced under neutral to acidic conditions and lower SMX concentrations. Based on experiments with radical scavengers, photogenerated holes appeared to be the dominant species, with the contribution of reactive species following the order ${\mathrm{h}}^{+}>{\mathrm{O}}_2^{•-}/{\mathrm{e}}^{-}>$¹${\mathrm{O}}_2{>\mathrm{H}\mathrm{O}}^{•}$. Interestingly, in different water matrices, photocatalytic activity was not diminished and even increased by 20%, likely because of the action of photogenerated holes and the selectivity of secondary generated radicals. The photocatalyst retained > 90% of its activity after three sequential experiments. Finally, four transformation products from SMX photodegradation were identified via UHPLC-TOF-MS, and a degradation pathway is proposed.

In this study, biochars (BC) from potato peel residuals were synthesized at 400, 600, and 800 °C, characterized, and evaluated for the persulfate-assisted oxidation of venlafaxine (VEN). BC pyrolyzed at 800 °C demonstrated the highest catalytic activity, resulting in the degradation of 750 μg/L of VEN in the presence of 500 mg/L persulfate in less than 90 min. Acidic conditions favored VEN destruction, while the apparent kinetic constant was reduced from 0.1136 at pH 3 to 0.0389 and 0.0352 min⁻¹ for pH 7 and 9, respectively. Interestingly, the presence of inorganic ions such as bicarbonates and chlorides, as well as humic acid, only slightly reduced process efficiency. Scavenging tests and electron paramagnetic resonance spectroscopy indicate a mixed mechanism dominated by non-radical pathways, with minor radical contributions, mediated by oxygenated surface functionalities of the 800 °C biochar. Five transformation products were identified through LC-HRMS suspect and non-target approaches, and a potential degradation pathway was proposed. Most of the identified transformation products exhibited lower toxicity levels than the parent compound. Finally, life cycle analysis revealed that, despite its superior kinetics, the 800 °C biochar carries the largest environmental footprint, underscoring the need for integrated assessments that jointly optimize removal performance and environmental impacts.