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Visible light driven photoelectrocatalysis on a FTO/BiVO4/BiOI anode for water treatment involving emerging pharmaceutical pollutants
摘要: Contamination of water bodies by harmful and recalcitrant organic substances is a global challenge. A promising technique for removing these organics from water/wastewater is photoelectrocatalytic oxidation which combines electrolytic and photocatalytic processes. Herein, we report the degradation of emerging pharmaceutical pollutants e acetaminophen and cipro?oxacin e at a BiVO4/BiOI photoanode under visible irradiation via photoelectrocatalytic process. The BiVO4/BiOI was electrodeposited on a FTO glass and characterised with XRD, SEM, EDS and diffusive re?ectance UVeVis. The results con?rmed the successful electrodeposition of BiVO4/BiOI on the glass substrate. Mott-Schotty plots con?rmed the formation of p-n heterojunction between the two electrodeposited semiconductors. The calculated charge carrier density of BiVO4/BiOI was higher than those of pristine BiVO4 and BiOI. The binary electrode also gave improved photocurrent response compared with unitary electrodes. Degradation ef?ciencies of 68% and 62% were achieved upon the application of the prepared photoanode (FTO/BiVO4/BiOI) in PEC degradation of acetaminophen and cipro?oxacin respectively using a bias potential of 1.5 V within 2 h. A synthetic pharmaceutical wastewater containing a mixture acetaminophen and cipro?oxacin was also treated with the photoanode. The photoanode was also effective in the degradation of dye. The ?ndings of this study suggest the suitability of the prepared photoanode for the photoelectrocatalytic degradation of organic pharmaceutical pollutants in wastewater.
关键词: Cipro?oxacin,p-n heterojunction photoanode,Photoelectrocatalytic degradation,Bismuth oxyiodide,Acetaminophen,Bismuth vanadate
更新于2025-11-14 14:48:53
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Comparison of acetaminophen degradation in UV-LED-based advance oxidation processes: Reaction kinetics, radicals contribution, degradation pathways and acute toxicity assessment
摘要: Ultraviolet light emitting diode (UV-LED)-based advanced oxidation processes (AOPs) including UV-LED/chloramine (UV-LED/NH2Cl), UV-LED/hydrogen peroxide (UV-LED/H2O2) and UV-LED/persulfate (UV-LED/PS), were adopted for acetaminophen (AAP) removal. Results showed that AAP could be effectively degraded by the hybrid processes compared to solely using with UV irradiation and oxidants. The AAP degradation in the three UV-LED-based AOPs were in the order of UV-LED/PS N UV-LED/H2O2 N UV-LED/NH2Cl and followed a pseudo-?rst-order kinetics. The degradation rate constant (kobs) increased with increasing oxidant dosage, whereas overdosing lowered the AAP degradation. The second-order rate constants of HO?, SO4??, and Cl? with AAP were calculated as 5.15 × 109, 7.66 × 109 and 1.08 × 1010 M?1 s?1, respectively. Under neutral conditions, the contributions of UV-LED, HO?, and Cl? to AAP degradation were 4.21%, 60.15% and 35.64% in the UV-LED/NH2Cl system, whereas the respective contributions of UV-LED, HO? and SO4?? to AAP degradation were 2.09%, 22.84% and 75.07% in UV-LED/PS system, respectively. Meanwhile, the corresponding contributions of the involved reactive species were found to be pH-dependence. The natural organic materials (NOM) inhibited the ? had different effects on AAP degradation in the ?, and NO3 AAP degradation, and the presence of Cl?, HCO3 three hybrid processes. The AAP degradation was signi?cantly inhibited in the three UV-LED-based AOPs in real water. In addition, the intermediate products were also identi?ed, and possible degradation pathways were proposed in the three UV-LED-based AOPs. The acute toxicity bioassay using bacterium Vibrio ?scheri suggested that the UV-LED/PS process was more effective than the UV-LED/H2O2 and UV-LED/NH2Cl processes in reducing the acute toxicity of the reacted AAP solution. Among the three UV-LED-based AOPs, the UV-LED/PS was found to be the most ef?cient process for AAP degradation.
关键词: Acute toxicity,Rate constants,UV-LED-based AOPs,Degradation pathways,Acetaminophen
更新于2025-09-23 15:21:01
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Photocatalytic degradation of acetaminophen over Ag, Au and Pt loaded TiO2 using solar light
摘要: The sustainability and feasibility of using solar irradiation instead of UV light in photocatalysis is a promising approach for water remediation. In this study, photocatalytic degradation (PCD) of a widely used analgesic and antipyretic drug, acetaminophen (AP), with noble metal loaded TiO2 photocatalysts (Ag/TiO2, Au/TiO2 and Pt/TiO2) was investigated in aqueous suspension using solar light. The deposition of noble metals (Ag, Au and Pt) onto the TiO2 surface enhanced the PCD of AP under different operating conditions including pH, surfactants and drug excipients. However, lower degradation rate constants of AP were obtained under simulated and direct solar light as compared to UV light. The degradation mechanism of AP under UV as well as simulated solar light was found to follow similar, though not identical, reaction pathways leading to hydroxylated intermediates (e.g. 4-acetamidoresorcinol (4-AR), 4-acetamidocatechol (4-AC) and hydroquinone (HQ)) through competitive routes. The PCD of AP followed a pseudo first order kinetics according to Langmiur-Hinshelwood model. Noble metal (Ag, Au and Pt) loaded TiO2 photocatalysts can be used effectively to degrade AP in water under both solar and UV light.
关键词: Solar light,Hydroxyl radical,Noble metal,Acetaminophen,TiO2
更新于2025-09-19 17:15:36
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Sunlight-induced photocatalytic degradation of acetaminophen over efficient carbon doped TiO2 (CTiO2) nanoparticles
摘要: Carbon doped titanium oxide (CTiO2) photocatalyst was successfully synthesized by the sol–gel method. The crystal structure, surface morphology, and optical properties of CTiO2 have been characterized by X-ray diffraction, Brunauer–Emmett–Teller surface area (SBET), scanning electron microscope, UV–Vis, X-ray spectroscopy (EDS), Fourier transform infrared and X-ray photoelectron spectroscopy. The photocatalytic degradation of acetaminophen (AMP) in aqueous solution, seawater, and polluted seawater has been investigated by using the synthesized photocatalyst under irradiation of UV and natural sunlight. The effectiveness of CTiO2 compared to pure TiO2 toward the photocatalytic removal of AMP was significantly observed. The optimized conditions including catalyst dose, initial concentration of AMP and solution pH were also studied for effective photocatalytic removal. The highest degradation rate was obtained when 2.0 g L?1 of the catalyst was used at pH 7. The kinetic results revealed that the photocatalytic degradation of AMP using CTiO2 obeyed a pseudo-first-order reaction kinetics.
关键词: Photocatalytic degradation,Seawater,CTiO2,Nanoparticles,Acetaminophen,Sunlight
更新于2025-09-19 17:15:36
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SILICA a?? CARBON QUANTUM DOTS DECORATED TITANIUM DIOXIDE AS SUNLIGHT-DRIVEN PHOTOCATALYST TO DIMINISH ACETAMINOPHEN FROM AQUATIC ENVIRONMENT
摘要: The presence of pharmaceutical compound (i.e., acetaminophen) in aquatic environment has been declared as environmental issue since researchers found that it has potential risk to human health. Photocatalytic process as a promising method for waste degradation commonly employs titanium dioxide, TiO2. However, TiO2 has narrow light absorption and rapid charge recombination resulting in ineffective photocatalytic activity. In this study, silica – carbon quantum dots (Si-CQDs) from rice husk are decorated into TiO2 matrix through facile mixing approach to minimize the limitations of TiO2. Preliminary studies regarding TiO2 transformation and Si-CQDs incorporation in various amount were systematically investigated. It is observed that 1 wt% is the optimum amount of Si-CQDs in composite in order to maximize the photocatalytic ability of TiO2. Under sunlight irradiation, 1 wt% Si-CQDs/TiO2 composite is able to completely degrade 5 mg/L of acetaminophen within 240 min (33.3% faster than pure TiO2). The excellent performance of the composite is attributed to synergistic effect of Si-CQDs addition on TiO2 surface, which acted as photo sensitizer and electron trapper. Si-CQDs extend light absorption of TiO2 by reducing band gap energy from 3.20 to 3.12 eV, as confirmed by UV-Vis Diffuse Reflectance Spectroscopy (DRS) spectra. Photoluminescence (PL) spectra and N2 sorption isotherm reveal that Si-CQDs addition prolongs the lifetime of charge separation and improves surface area (17% larger than TiO2), respectively. The composite of Si-CQDs/TiO2 also demonstrates good stability which is beneficial for pharmaceutical waste removal in the future.
关键词: sunlight,photocatalyst,Titanium dioxide,acetaminophen,carbon quantum dots,pharmaceutical
更新于2025-09-19 17:13:59
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Degradation of acetaminophen in aqueous solution by UV and UV-activated sludge processes
摘要: Acetaminophen (N-acetyl-p-aminophenol, APAP) is one of the most common antipyretic analgesics used to treat common ailments throughout the world. Recently, APAP has been frequently detected in wastewater effluent and groundwater, resulting in potential risks to the environment. Current methods for eliminating APAP are complicated and cost-prohibitive. This study examined APAP degradation by ultraviolet-C (UV-C) and UV-C irradiation combined with activated sludge (UV/AS) to evaluate potential applications in wastewater treatment. The results of this study indicate that UV-C irradiation reached an APAP degradation efficiency of more than 52% and a degradation rate of 0.0012–0.0013 min?1 during 720 min of exposure, while the initial APAP concentration exhibited only a nominal effect on the degradation rate. However, the UV/AS treatment demonstrated an APAP degradation rate that was 9.6 times the rate of the UV-C-only treatment, with a degradation efficiency of 99% over the same UV irradiation period. The results further indicated that APAP photolysis efficiency was more effective when applied to sterilized AS than when applied to unsterilized AS. Finally, excessive dosage of both AS and humic acid inhibited APAP photolysis efficiency.
关键词: acetaminophen,photolysis,ultraviolet/activated sludge,ultraviolet-C,pharmaceuticals and personal care products
更新于2025-09-11 14:15:04
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Fabrication of Gd-La codoped TiO2 composite via a liquid phase plasma method and its application as visible-light photocatalysts
摘要: TiO2 was doped simultaneously with Gd and La using a liquid phase plasma (LPP) reaction to produce a photocatalyst with excellent photoactivity in the visible light region. Gadolinium chloride hexahydrate and lanthanum chloride heptahydrate precursors were used to dope the TiO2 powder with polycrystalline Gd2O3 and La2O3 particles. The doping of TiO2 with rare earth elements using LPP reaction decreased the band gap; the band gap of Gd-La codoped TiO2 photocatalysts (GLTP) was the lowest. The photodegradation efficiency of the TiO2 photocatalysts doped with either Gd or La was superior that of bare TiO2 but the photodegradation efficiency of GLTP was highest in both ultraviolet and visible light sources. Acetaminophen (Acetyl-para-aminophen, APAP) was ultimately decomposed to CO2 and H2O via intermediates, such as p-nitrophenol, hydroquinone and hydroxylhydroquinone, by hydroxyl radicals (HO?) formed on the surface of GLTP.
关键词: Liquid phase plasma,Gd-La codoped TiO2 photocatalysts,Band gap energy,Acetaminophen,Photocatalytic activity
更新于2025-09-10 09:29:36