Degradation Of Amoxicillin Research Articles

Pulsed corona discharge: an advanced treatment method for antibiotic-contaminated water

Water pollution is one of the most significant problems of the current century. With the increase in medicine availability and use, pharmaceutical pollutants such as antibiotics become more prevalent in natural environments with potentially negative impact. In this study, a pulsed corona discharge was investigated as a possible treatment method of water contaminated with amoxicillin (AMX). Two system configurations were used: plasma and plasma-ozonation. In order to better grasp the effect of system and water matrix on degradation, different pulse widths, solutions pH and conductivity values, as well as the nature of the dissolved salts were investigated. Decreasing the pulse width from 300 ns to 106 ns (full width at half maximum) led to almost a two-fold increase in energy yield at 50% pollutant removal, and the addition of the ozonation reactor resulted six times enhancement in efficiency. While the water matrix had little impact on AMX degradation, the buffering capacity of carbonates has proven beneficial by preventing pH decrease during treatment. Under optimum conditions, the energy yield was 57 g kWh−1 at 93% removal of AMX in tap water. A number of 26 potential degradation products have been identified, resulting from hydroxylation of the benzene ring, oxidation of the thioester and amine groups, hydrolysis, and cleavage of the benzene, β-lactam and thiazole rings, along with fragmentation of the resulting compounds. All but seven degradation intermediates are completely removed by extending treatment duration to 60 min and the persistent ones are less toxic than the parent compound.

Influence of Hydrothermal Temperature on the Physical Characteristics and Photocatalytics Activity of TiO2 for Degradation of Amoxicillin

Titanium dioxide (TiO2) is a photocatalyst material widely used for environmental remediation applications. In this research, TiO2 material was synthesized using the hydrothermal method at various temperatures (150°C, 180°C, and 200°C). Based on the Fourier-transform infrared (FTIR) data, it was found that all the synthesized materials showed similar absorption peaks, and Ti-O-Ti bonds were detected, which is a characteristic of TiO2. X-ray diffraction (XRD) analysis showed that all the synthesized materials were TiO2 anatase with different crystalline sizes. The synthesized TiO2 using the hydrothermal temperature of 180°C showed the smallest crystalline size of 86.81 nm. Based on the analysis of the band gap energy, it was found that wider band gap energy was obtained at higher hydrothermal temperatures. The band gap energies of the synthesized materials are 3.18 eV, 3.19 eV, and 3.21 eV for hydrothermal temperatures of 150°C, 180°C, and 200°C, respectively. The photocatalytic activity of the three synthesized materials was tested in the photodegradation experiment of amoxicillin under ultraviolet (UV) irradiation. As a result, it was found that TiO2 synthesized at 180°C has the highest photocatalytic activity by degrading 100% of amoxicillin compounds within 120 minutes.

Effect of gold nanoparticles on SiO2@g-C3N4 catalyst for the degradation of amoxicillin

Gold nanoparticles in different proportions (0.5 and 1 %) have been grafted at the surface of a SiO2@g-C3N4 nanotube-based composite (SiO2 nanotubes obtained from halloysite clay) and also g-C3N4 (for comparison purposes) to test their degradation capacity over the antibiotic amoxicillin proving that the introduction of these nanoparticles on the catalyst modifies the degradation mechanism followed by the pollutant. Results obtained show that the introduction of the appropriate percentage of gold NPs in the composite improves amoxicillin degradation efficiency and establish a direct correlation between the presence of gold NPs and the production of ⋅O2-.

Enhanced efficiency of interfacial charge transfer in Ag3PO4/BiPO4@CNTs photocatalyst for amoxicillin degradation: Synergistic effect of p-n heterojunction and conjugated channels

Inspired by the remarkable efficiency in separating photogenerated carriers achieved through the fabrication of conjugated polymeric photocatalysts, we have developed a novel photocatalytic system. This system utilizes carbon nanotubes coated with an Ag3PO4/BiPO4 p-n heterostructure (ABCx) for the degradation of amoxicillin in aquatic environments under visible light. The ABCx conjugated photocatalysts demonstrate excellent efficiency in photogenerated charge separation, material stability, and effective amoxicillin removal. The first-order kinetic constants for ABCx (x[‰]=2, 5, 7) show enhancements of 1.40-fold, 2.53-fold, and 2.10-fold, respectively, compared to those of Ag3PO4/BiPO4 in the degradation of amoxicillin. FT-IR and photochemical conversion studies reveal the presence of delocalized π-bonds within the conjugated system (P = CC = C···C = O), which can lead to the formation of a rapidly generated and long-lived triplet state T1 rather than the lowest singlet excited state S1 generated from either direct excitation or reverse intersystem crossing. In situ XPS analysis confirms that photogenerated charges migrate from BiPO4 to Ag3PO4 through a conjugated redox pathway. Density Functional Theory (DFT) was employed to investigate the work function, determining the Fermi levels of Ag3PO4 and BiPO4 to be -4.27 eV and -5.09 eV, respectively, and further confirming the direction of charge migration. In summary, the incorporation of conjugated π bonds via an inorganic semiconductor heterojunction enhances the efficiency of photogenerated charge separation and transport.

PANI/GO and Sm co-modified Ti/PbO2 dimensionally stable anode for highly efficient amoxicillin degradation: Performance assessment, impact parameters and degradation mechanism

The abuse and uncontrolled discharge of antibiotics present a severe threat to environment and human health, necessitating the development of efficient and sustainable treatment technology. In this work, we employ a facile one-step electrodeposition method to prepare polyaniline/graphite oxide (PANI/GO) and samarium (Sm) co-modified Ti/PbO2 (Ti/PbO2-PANI/GO-Sm) electrode for the degradation of amoxicillin (AMX). Compared with traditional Ti/PbO2 electrode, Ti/PbO2-PANI/GO-Sm electrode exhibits more excellent oxygen evolution potential (2.63 V) and longer service life (56 h). In degradation experiment, under optimized conditions (50 mg L−1 AMX, 20 mA cm−2, pH 3, 0.050 M Na2SO4, 25 °C), Ti/PbO2-PANI/GO-Sm electrode achieves remarkable removal efficiencies of 88.76% for AMX and 79.92% for chemical oxygen demand at 90 min. In addition, trapping experiment confirms that ·OH plays a major role in the degradation process. Based on theoretical calculation and liquid chromatography-mass spectrometer results, the heterocyclic portion of AMX molecule is more susceptible to ·OH attacks. Thus, this novel electrode offers a sustainable and efficient solution to address environmental challenges posed by antibiotic-contaminated wastewater.

Validation and Application of a Dried Blood Spot Amoxicillin Assay

Dried blood spot (DBS) antibiotic assays can facilitate pharmacokinetic (PK) investigations in situations where venous blood sampling is logistically and/or ethically challenging. The aim of this study was to establish, validate and demonstrate the application of a DBS amoxicillin assay for PK studies in vulnerable populations. The matrix effect, process efficiency (84–104%) and recovery (85–110%) of the liquid chromatography–mass spectrometry (LC–MS/MS) assay for amoxicillin in DBS was determined at 1, 10 and 100 µg/mL, and three different haematocrits. Thermal stability studies of amoxicillin in DBS were performed and a bridging study comprising 26 paired plasma and DBS samples was conducted in four healthy individuals. The limits of detection and quantification were 0.02 and 0.05 µg/mL for plasma and DBS amoxicillin assays, respectively. Accuracy and interday precision of amoxicillin in DBS (0.1–100 µg/mL) were 88–103% and 4.5–9.2%, respectively. At room temperature (22 °C) and 4 °C, amoxicillin was stable in DBS for ≈4 and 26 h, respectively. There was no degradation of amoxicillin in DBS at −20 °C for > 6 months. When comparing DBS and plasma collected from healthy volunteers, the slope of the Deming regression was 0.74. Amoxicillin CL/F estimates from DBS and plasma concentration data were 40.8 and 30.7 L/h/70 kg, respectively; V/F was 43.2 and 37.4 L/70 kg, respectively. In conclusion, amoxicillin can be reliably assayed from DBS in research studies but may have limited application in therapeutic drug monitoring. Due to poor stability at room temperature, amoxicillin DBS samples should be promptly dried and placed in frozen storage.

Enhanced catalytic degradation of amoxicillin by phyto-mediated synthesised ZnO NPs and ZnO-rGO hybrid nanocomposite: Assessment of antioxidant activity, adsorption, and thermodynamic analysis

Abstract Antibiotics are resistant compounds that become emerging contaminants that cause hazards to human health and the ecological environment due to their wide production and consumption. The present research reveals the remediation of amoxicillin (AMX) antibiotic by catalytic degradation using fabricated zinc oxide (ZnO) and zinc oxide-reduced graphene oxide (ZnO-rGO) catalysts. The characterization of the catalyst was carried out via UV–Vis spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, energy dispersive X-ray spectroscopy, and scanning electron microscopy to evaluate the morphology and composition of synthesised catalyst. The catalytic ability of ZnO-rGO and ZnO was investigated by analysing the degradation of AMX. The ZnO-rGO nanocomposites (NCs) showed improved catalytic performance towards AMX degradation (96%) than pure ZnO nanoparticles (85%), which may be attributed to the incorporation of rGO, which enhanced the adsorption rate and changed the electron–hole recombination rate. The antioxidant potential of synthesised nanomaterials was also analysed by three different methods. The adsorption behaviour was explained through the Langmuir and Freundlich models, and the results revealed that AMX adsorption followed the Freundlich model more closely for both catalysts. The adsorption of AMX was also studied thermodynamically at different temperatures. The negative Gibbs energy change, positive enthalpy change, and entropy change showed the reaction’s spontaneity and endothermic nature. Finally, it can be assumed that the ZnO-rGO NCs could be an effective semiconductor for the degradation of AMX from wastewater.

Efficacy of an inulin-based treatment on intestinal colonization by multidrug-resistant E. coli: insight into the mechanism of action

ABSTRACT Inulin, an increasingly studied dietary fiber, alters intestinal microbiota. The aim of this study was to assess whether inulin decreases intestinal colonization by multidrug resistant E. coli and to investigate its potential mechanisms of action. Mice with amoxicillin-induced intestinal dysbiosis mice were inoculated with extended spectrum beta-lactamase producing E. coli (ESBL-E. coli). The combination of inulin and pantoprazole (IP) significantly reduced ESBL-E. coli fecal titers, whereas pantoprazole alone did not and inulin had a delayed and limited effect. Fecal microbiome was assessed using shotgun metagenomic sequencing and qPCR. The efficacy of IP was predicted by increased abundance of 74 taxa, including two species of Adlercreutzia. Preventive treatments with A. caecimuris or A. muris also reduced ESBL-E. coli fecal titers. Fecal microbiota of mice effectively treated by IP was enriched in genes involved in inulin catabolism, production of propionate and expression of beta-lactamases. They also had increased beta-lactamase activity and decreased amoxicillin concentration. These results suggest that IP act through production of propionate and degradation of amoxicillin by the microbiota. The combination of pantoprazole and inulin is a potential treatment of intestinal colonization by multidrug-resistant E. coli. The ability of prebiotics to promote propionate and/or beta-lactamase producing bacteria may be used as a screening tool to identify potential treatments of intestinal colonization by multidrug resistant Enterobacterales.

Boosting solar-driven photocatalytic degradation of organic contaminants and bacterial deactivation using marigold- like Cu2O decorated g-C3N4 nanocomposite

Keeping the high efficiency in designing photocatalysts in view, the present work was aimed at the development of a heterojunction photocatalyst with boosted efficiencies, both for degradation of organic contaminants and bacterial deactivation. Heterojunction nanocomposites of g-C3N4 (GCN) and Cu2O (Cu2O /GCN-5 %, Cu2O /GCN-15 %, Cu2O/GCN-25 %, and Cu2O /GCN-50 %) were prepared by hydrothermal method and their photocatalytic performance was evaluated. XPS result confirms the surface chemical composition of nanocomposite and consistent with EDX analysis. The BET studies of Cu2O/GCN −25 % nanocomposite reveals the larger specific surface area (128.10 m2/g), compared to intact Cu2O, which facilitates more active sites on the surface. The optical bandgap energy (2.39 eV-2.58 eV) is tuned towards the visible region by loading g-C3N4 in marigold-like Cu2O. The efficient charge transfer betwixt marigold-like Cu2O and g-C3N4 was demonstrated in PL, CV, and EIS analysis. The Cu2O/GCN-25 % nanocomposite exhibits superior photocatalytic activity towards Aniline blue dye (86.4 %) and β-lactam antibiotic amoxicillin (79 %) under 100 min of sunlight irradiation. HPLC analysis further confirmed the degradation and disintegration of Amoxicillin. The probable photocatalytic mechanism was proposed and tested through a radical scavenger experiment. It was found that ●OH radicals significantly take part in the photodegradation. In addition, the bactericidal activities of Cu2O/GCN-25 % nanocomposite was determined. The highest bactericidal activity was observed for Bacillus subtilis (26 mm). Hence, the marigold-like Cu2O/GCN-25 % nanocomposite is a feasible material for the degradation of dyeing and pharmaceutical industrial effluents as well as bacterial growth inhibition.

Metal-organic framework gel derived magnetic hierarchical porous Fe-N-C catalyst as peroxymonosulfate activator for efficient degradation of amoxicillin via singlet oxygen-dominated nonradical pathway

The rational design of transition metal and nitrogen co-doped carbon-based catalysts for the efficient removal of antibiotics through non-radical pathway of peroxymonosulfate (PMS) activation has attracted widespread attention. Herein, a magnetic hierarchical porous Fe-N-C catalyst (FeBDC-NH2-800) was successfully constructed by pyrolyzing the hierarchical porous precursor metal–organic framework gel (FeBDC-NH2) consisting of nitrogen-containing ligands. Benefiting from the defective heterojunction structure, the catalyst exhibited effective and efficient degradation towards amoxicillin (AMX) by activating PMS to produce 1O2. The degradation of AMX was up to 97.4 % within 30 min, which was 2.48 and 2.16 times more than that of FeBDC-NH2/PMS and nanosized Fe3O4/PMS respectively. The high degradation performance could be maintained toward low pollutant concentration conditions and cycle experiments, manifesting its possibility for practical application. Combining the data of quenching experiments, electron spin resonance spectra, electrochemical experiments, X-ray photoelectron spectra and density functional theory calculation, the mechanism was revealed that radical pathway contributed little during degradation while singlet oxygen played a significant role. The cleavage of lattice oxygen and defective heterogeneous structure of FeBDC-NH2-800 contributed together to promote PMS for 1O2 production.

Modeling of Mass Transfer and Reaction Kinetics in ZnO Nanoparticle Micro-Reactor Systems for AMX and DOX Degradation

This study aims to model the coupled phenomena of photocatalytic reaction and mass transfer in the degradation of Amoxicillin (AMX) and Doxycycline (DOX) using Zinc oxide (ZnO) nanoparticles within microreactor systems. The objective is to gain a comprehensive understanding of the dynamic interaction between the photocatalytic degradation kinetics and the mass transfer processes to optimize the conditions for efficient antibiotic removal from contaminated water. This involves characterizing the reaction kinetics via the Langmuir-Hinshelwood model, estimating the mass transfer coefficients, and analyzing the effects of axial dispersion to ensure the accurate determination of intrinsic kinetic constants and minimize mass transfer limitations. This study used a syringe pump to ensure a consistent flow of antibiotic solution into the microreactor. The results indicate that AMX reaches adsorption equilibrium more rapidly than DOX, corresponding to its faster photocatalytic degradation kinetics and higher final conversion rate (89% for AMX, 86% for DOX). The mass transfer coefficient (kd) was estimated using the Sherwood number, derived from three different models, with the constant Sherwood model best fitting the R1 microreactor data. An analysis of the Damköhler number (DaII) indicates that high flow rates minimize mass transfer limitations in the R1 microreactor, allowing the determination of near-intrinsic kinetic constants. On the contrary, at low flow rates, kinetic constants are apparent as a result of mass-transfer limitations. The study concludes that higher flow rates (≥ 10 mL/h) in the R1 microreactor are preferable to approach intrinsic kinetics and reduce mass transfer limitations during photocatalytic degradation of antibiotics. These findings underscore the potential of ZnO-based oxidation processes in treating antibiotic-contaminated water with optimized conditions, providing a pathway for efficient and sustainable wastewater treatment.

Photocatalytic Decomposition of Amoxicillin Using Zinc Ferrite Nanoparticles

Catalysts enriched in Zinc ferrite (ZFO) were synthesized using coprecipitation and hydrothermal methods. Mixtures of crystalline nanoparticles (ZFO and α-Fe2O3, several allotropic varieties of FeO) were characterized by various techniques such as X-ray diffraction (XRD), transmission electron microscopy (TEM, SEM), N2 sorption, UV-visible spectrophotometry (UV-Vis) and X-ray photoelectron spectroscopy (XPS). After detailed characterizations, the catalytic performance of the solids (1 g/L) in the degradation of amoxicillin (AMX) (10 mg/L) as an antibiotic pollutant in water was evaluated. In addition, we used air as the oxygen source and adjusted the pH to 5.0. Consequently, the catalysts obtained via the hydrothermal method HT-ZFO had a high activity (100% of AMX removal in less than 100 min when an LED (75 W) light was used) compared to a similar mixture of oxides with graphene HT-ZFO-GO (a longer time of 150 min) that was necessary for the complete degradation of AMX. Impregnation with an aqueous solution containing 80 mg of GO obtained using Hummer’s method, reduced into RGO by an ultrasound treatment, enhances the initial reaction rate but is associated with a prolonged time for complete AMX removal (10 ppm in water) that we attribute to its spontaneous corrosion.

Time series-based prediction of antibiotic degradation via photocatalysis using ensemble gradient boosting.

This study aims to evaluate the effectiveness of the laboratory-made catalyst Ni2P-ZrO2 (NPZ) in the degradation of an antibiotic in an aqueous suspension when exposed to ultraviolet (UV) light. The degradation of amoxicillin (AMX) was predicted using time series forecasting through the ensemble gradient boosting model. The degradation experiments were conducted utilizing two distinct photocatalyst compositions of Nickel phosphide-zirconium dioxide (NPZ) in the proportions of 1:9 and 2:8. The most effective experimental results were obtained using a natural pH, a catalyst concentration of 0.20 g/L and reaction duration of 0.5 h after testing the different catalysts. Experimental data were used for training, validating and confirming time series predictions. The use of ensemble technique highly affected the experimental findings. The model's performance was quite satisfactory in terms of correlation coefficient (94.00%), normalized mean square error (0.01) and mean square root error (0.0911) which significantly contributed to the model's accuracy. All input variables, such as pH, catalyst dose and irradiation time, had a significant impact on the degrading efficacy. The study has demonstrated that time series forecasting can be used for predicting the degradation process precisely.

Pilot plant approach combining photocatalysis and adsorption for antibiotics removal from slaughterhouse and urban wastewater treatment plant effluents

The main objective of this research is to perform a real case-study of antibiotic decontamination from real slaughterhouse and wastewater effluents by applying a sequential treatment of TiO2/UV–vis photocatalysis and adsorption. More precisely, the removal of five classes of antibiotics: enrofloxacin, sulfadiazine, trimethoprim, azithromycin, amoxicillin and amoxicillin degradation products was studied in an 80 L/h photocatalytic and adsorption pilot-scale plant over multiple cycles, operating in semi-continuous mode. The results exhibited significant removal rates, ranging from 77% to 100% for the slaughterhouse effluent, and 61–89% for the wastewater treatment plant effluent, thus demonstrating that the treatment is more effective when it is applied directly in the emission source, previous to antibiotic dilution in the municipal collector. Using the two processes sequentially results in greater efficiency than when they are used in isolation. After photocatalysis, antibiotic degradation products are easily adsorbed, since they have more affinity for the adsorbent, and the presence of competing compounds decreases considerably. After applying several cycles of treatment, the adsorption performance remains almost constant. By contrast, the photocatalysis performance decreased, which was attributed to catalyst agglomeration determined by Asymmetric Flow Field-Flow Fractionation (AF4) coupled with Dynamic Light Scattering (DLS) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS).

Synthesis of pure and Cd-doped hydroxyapatite for the photo-catalytic degradation of Amoxicillin and Ciprofloxacin: Crystallographic characterization using XRD

Nanosized hydroxyapatite (HAp) is considered an elementary material for artificial bone tissue engineering and the applications are expanding and one of them is the photocatalytic degradation of environmentally hazardous pollutants. In this research, HAp nanoparticles, in pure form and doped with cadmium (Cd), were synthesized using a conventional wet-chemical precipitation method. Additionally, the synthesized samples such as pure and Cd-doped HAp were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV–Vis spectroscopy. Moreover, the XRD analysis allowed for a detailed estimation of the crystallite size, assisting in their tailoring of increased photocatalytic activity. The crystallite sizes of the nano-crystallite Hap were evaluated using the Scherrer Method (SM), Williamson-Hall Method (WHM), Size-Strain Plot (SSP), Halder-Wagner Method (HWM), and Sahadat-Scherrer Method (SSM). The models confirmed the formation of nano crystallite hydroxyapatite in pure and doped form. Cadmium doping in HAp showed great photocatalytic activity for example at 150 min, 31 % amoxicillin and 52 % ciprofloxacin were degraded upon 1.5 wt % Cd doping in HAp crystal. The research demonstrated that doping Cd in HAp crystal improved photocatalytic activity towards antibiotic solution (ciprofloxacin and amoxicillin) under all test circumstances.

Facile Synthesis of Carbon-Based Inks to Develop Metal-Free ORR Electrocatalysts for Electro-Fenton Removal of Amoxicillin.

The electro-Fenton process is based on the generation of hydroxyl radicals (OH•) from hydroxide peroxide (H2O2) generated in situ by an oxygen reduction reaction (ORR). Catalysts based on carbon gels have aroused the interest of researchers as ORR catalysts due to their textural, chemical and even electrical properties. In this work, we synthesized metal-free electrocatalysts based on carbon gels doped with graphene oxide, which were conformed to a working electrode. The catalysts were prepared from organic-gel-based inks using painted (brush) and screen-printed methods free of binders. These new methods of electrode preparation were compared with the conventional pasted method on graphite supports using a binder. All these materials were tested for the electro-Fenton degradation of amoxicillin using a homemade magnetite coated with carbon (Fe3O4/C) as a Fenton catalyst. All catalysts showed very good behavior, but the one prepared by ink painting (brush) was the best one. The degradation of amoxicillin was close to 90% under optimal conditions ([Fe3O4/C] = 100 mg L-1, -0.55 V) with the catalyst prepared using the painted method with a brush, which had 14.59 mA cm-2 as JK and a H2O2 electrogeneration close to 100% at the optimal voltage. These results show that carbon-gel-based electrocatalysts are not only very good at this type of application but can be adhered to graphite free of binders, thus enhancing all their catalytic properties.

Photosensitizing CNTs by organotin(IV) compounds: generation of reactive oxygen species and degradation of amoxicillin.

This work is based on probing photosensitization in carbon nanotubes (CNTs) by organotin(IV) compounds to fabricate a hybrid material with excellent photocatalytic activity and generation of reactive oxygen species. Two organotin(IV) compounds (compounds 1 and 2) were synthesized and characterized by spectroscopic and spectrometric studies, elemental analysis and single crystal X-ray diffraction followed by their impregnation inside the CNTs. The so obtained hybrid materials (1@CNT and 2@CNT) were characterized by FTIR, TGA, FE-SEM, HR-TEM, PXRD and XPS analysis, and assessed for photosensitization and generation of reactive oxygen species. The enhanced photocatalytic activity of the fabricated materials in comparison to bare CNTs is attributed to the reduction of band gap and suppression of rapid recombination rates due to the encapsulation of photogenerated electrons. The generation of reactive species in photocatalyst 1@CNT was validated by the degradation of Amoxicillin (AMX) under optimized conditions for catalytic dosage, H2O2 concentration, response time and pH. The material 1@CNT could degrade ca. 83% of AMX by generating free radicals (˙OH and ˙O2-) under visible light irradiation at pH 6 as investigated by UV-visible spectroscopy and supported by EPR and DFT studies. Furthermore, the structural stability and sustained photocatalytic properties of 1@CNT over four cycles highlight its potential as an eco-friendly solution for degrading environmental toxins.

Degradation of amoxicillin residue under visible light over TiO2 doped with Cr prepared from tannery wastewater

The degradation of amoxicillin residue has been performed using TiO2 photocatalyst doped with Cr prepared from tannery wastewater under visible light exposure. The incorporation of Cr metal into TiO2 structure was conducted via hydrothermal method. From the characterization results, it is found that doping Cr from the tannery wastewater into TiO2 structure has been successfully shifted the light absorption into visible region. Among the various Cr content in the TiO2-Cr photocatalyst, TiO2-0.33Cr (medium level) shows the highest ability in the visible light absorption, suggesting it to be the best photocatalyst. It is also clearly proven that in the presence of TiO2-0.33Cr photocatalyst, the degradation of amoxicillin can reach almost 100 % after the third cycles. Furthermore, this study also investigated the optimum condition for photodegradation of amoxicillin as the prevalent antibiotic residue in batch technique. The concentration of amoxicillin after the photodegradation process was determined using a UV–visible spectrophotometer. The result identifies the optimal condition for the amoxicillin photodegradation is reached at pH 6, with 10 mg of the photocatalyst mass per 30 mL of the sample solution, and an irradiation time at 90 min. The photodegradation of amoxicillin using TiO2-0.33Cr follows the pseudo-first order kinetic model with kinetic constant (k) is high as 0.004 min−1.

Ideal Parameter Estimation of Photocatalysis Process to Boost Amoxicillin Degradation Efficiency Using Marine Predators Optimization Algorithm

This paper presents a methodology for determining the optimal parameters of a photocatalysis process for treating pharmaceutical wastewater. Three parameters are considered: pH value, catalyst dosages, and reaction time to boost the amoxicillin degradation efficiency (ADE). The proposed methodology contains two stages: fuzzy modelling and a parameter determination process using the marine predators algorithm (MPA). Firstly, based on the experimental dataset of ADE in terms of pH value, catalyst dosages, and reaction time, a robust fuzzy model is produced to model the photocatalysis/ozonation process. The target is reducing the root mean square error (RMSE) between the actual data and the experimental dataset. Using fuzzy, the RMSE decreased from 2.0248 using ANOVA to 0.3148 using fuzzy (decreased by 84%). Next, using the MPA, the optimal parameters of pH value, catalyst dosages, and reaction time corresponding to maximum ADE are determined. The suggested strategy boosted the ADE from 88.23% to a rate of 11.68% compared with the experimental and RSM approaches. Under this condition, the optimal solutions are 11, 384 mg/L, and 33.615 min, respectively, for pH, catalyst dosages, and reaction time.

A novel carbon doped CeO2/g-C3N4 heterostructure for disinfection of microorganisms and degradation of Malachite green and Amoxicillin under sunlight

The fabrication of semiconductor heterojunction with defect engineering is an efficient technique to boost photocatalytic activity. In this study, a novel step-scheme heterojunction C-CeO2/g-C3N4 nanocomposite was developed via the hydrothermal method for the degradation of aqueous dye and antibiotics in sunlight. The photocatalytic experiment of the CeO2/g-C3N4 heterojunction nanocomposite reveals superior photocatalytic activity and significant reusability. Further, 91.9 % of Malachite green (MG) and 87.5 % of Amoxicillin(AMX) were degraded by C-CeO2/g-C3N4 nanocomposite under 150 mins of sunlight irradiation, which is ∼ 1.78 folds of the photodegradation performance of C-CeO2. The decomposition of MG and AMX into non-toxic secondary compounds was verified by total organic carbon and high-performance liquid chromatography analysis. Further, the migration and separation of charge carriers due to photons were confirmed through electrochemical analysis and, photoluminescence spectroscopy. The potential S-Scheme charge transfer pathway for improved photocatalytic activity was postulated via the quenching experiment, Mott Schottky (M-S) plot, and XPS Valance band spectroscopy (VB-XPS). In addition, the C-CeO2/g-C3N4 nanocomposite displays excellent bactericidal and fungicidal activity against pathogenic microorganisms S. aureus, E. coli, and C. albican. Hence, the synthesized S-Scheme heterojunction C-CeO2/g-C3N4 nanocomposite is an ideal catalyst for the detoxification of industrial wastewater.