Alexandra A. Ioannidi

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.

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 (2/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.

Biochar derived from pomegranate peel at different pyrolysis temperatures (450, 600, and 850 °C) was synthesized and characterized by BET, XRD, FTIR, and SEM-EDX. Its catalytic efficiency in the degradation of the antihypertensive losartan (LOS) in the presence of sodium persulfate was examined. The biochar pyrolyzed at 850 °C exhibited higher catalytic activity, which was correlated with the greater surface area and higher concentration of minerals on its surface. Interestingly, despite adsorption being favored at alkaline pH, pH 3 showed the highest LOS degradation. LOS decomposition followed pseudo-first-order kinetics. The addition of persulfate significantly increased LOS reduction, while the presence of inorganic and organic water matrix constituents such as sodium chloride, bicarbonate, and humic acid inhibited the oxidation. Experiments conducted with radical scavengers revealed that both hydroxyl and sulfate radicals, as well as singlet oxygen, participated in LOS decomposition, with the former being the dominant species. Using a continuous flow reactor, the system exhibited a satisfactory steady-state performance of 90% LOS removal for 114 h. Afterward, a moderate decrease in performance was observed, which can be attributed to the alteration of the catalyst’s surface and mineral dissolution due to acidity.

This work examines the use of pristine Mo₂C as an intriguing sodium persulfate (SPS) activator for the degradation of the drug losartan (LOS). Using 500 mg/L Mo₂C and 250 mg/L SPS, 500 μg/L LOS was degraded in less than 45 min. LOS decomposition was enhanced in acidic pH, while the apparent kinetic constant decreased with higher LOS concentrations. According to experiments conducted in the presence of scavengers of reactive species, sulfate radicals, hydroxyl radicals, and singlet oxygen participated in LOS oxidation, with the latter being the predominant reactive species. The presence of competitors such as bicarbonate and organic matter reduced the observed efficiency in actual matrices, while, interestingly, the addition of chloride accelerated the degradation rate. The catalyst showed remarkable stability, with complete LOS removal being retained after five sequential experiments. The system was examined for simultaneous LOS decomposition and elimination of Escherichia coli. The presence of E. coli retarded LOS destruction, resulting in only 30% removal after 3 h, while the system was capable of reducing E. coli concentration by 1.23 log. However, in the presence of simulated solar irradiation, E. coli was reduced by almost 4 log and LOS was completely degraded in 45 min, revealing a significant synergistic effect of the solar/Mo₂C/SPS system.

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.

The pursuit of low-cost, high-efficiency co-catalysts that are free of noble metals has become an area of considerable interest in the field of photocatalysis over the past few years. In this work, a series of cobalt phosphide (CoP 0.125–1.00 wt.%)-promoted bismuth vanadate (BiVO₄) photocatalysts was synthesized and physicochemical characterized by means of X-Ray diffraction, nitrogen isotherm absorption diffuse-reflectance spectroscopy, and high-resolution transmission electron microscopy. The efficiency of the as prepared photocatalytic materials was investigated for sulfamethoxazole (SMX) destruction in ultrapure water under simulated solar light irradiation. Results showed that the deposition of small amounts (0.50 wt.%) of CoP on BiVO₄ enhances SMX degradation. Moreover, SMX removal increased by increasing 0.50 CoP/BiVO₄ loading (up to 1 g/L) and decreasing SMX loading (1000–250 μg/L). Further tests were carried out in real and synthetic matrices, such as wastewater secondary effluent and bottled water, revealing the existence of hindering effects on SMX removal. The efficiency of 0.50 CoP/BiVO₄ photocatalyst was further investigated in a pilot plant configuration where the examined system was able to remove >99% of 300 μg/L SMX in deionized water utilizing 80 kJ/L of solar irradiation.

In this study, spent malt rootlet-derived biochar was modified by a friendly eco-method using a low temperature (100 °C) and dilute acid, base, or water. The modification significantly enhanced the surface area from 100 to 308–428 m²g⁻¹ and changed the morphology and the carbon phase. In addition, the mineral’s percentage and zero-point charge were significantly affected. Among the examined materials, the acid-treated biochar exhibited higher degradation of the drug losartan in the presence of persulfate. Interestingly, the biochar acted as an adsorbent at pH 3, whereas at pH = 5.6 and 10, the apparent kinetic constant’s ratio k_oxidation/k_adsorption was 3.73 ± 0.03, demonstrating losartan oxidation. Scavenging experiments indirectly demonstrated that the role of the non-radical mechanism (singlet oxygen) was crucial; however, sulfate and hydroxyl radicals also significantly participated in the oxidation of losartan. Experiments in secondary effluent resulted in decreased efficiency in comparison to pure water; this is ascribed to the competition between the actual water matrix constituents and the target compound for the active biochar sites and reactive species.