Total Organic Carbon Removal Research Articles

Enhancing degradation of sulfapyridine by magnetic Fe2O3-CoFe2O4@NC prepared through a facile solid phase coordination-calcination method for peroxymonosulfate activation

In this study, a facile and environmentally friendly solid phase coordination combined with calcination method was designed and ultra-efficient nitrogen carbon coated bimetallic composites (Fe2O3-CoFe2O4@NC) was fabricated to activate PMS for sulfapyridine (SPY) antibiotic elimination. A series of materials after calcined under different temperature and with different metal ratios were synthesized and Co/Fe carbon-based material calcined under 500 °C with 2:1 Co/Fe molar ratios (Fe2O3-CoFe2O4@NC) was demonstrated to be superior to rapidly remove 10 mg L−1 SPY within 10 min by activating 0.6 mM PMS. Meanwhile, the main reasons why different catalysts possessed different degradation efficiency were explored. The magnetic Fe2O3-CoFe2O4@NC showed a superior catalytic activity with kobs of 0.5314 min−1, which was 13.5-, 18.5- and 12.6 times than that of Co3O4@NC/PMS, Fe2O3@NC/PMS and CoFe/PMS systems, respectively. This was attributed to the synergistic effect of Co and Fe and accelerated electron transfer, which resulted in the generation of SO4−, 1O2, O2− and OH. The Fe2O3-CoFe2O4@NC/PMS system exhibited strong environment tolerance to most anions and humic acid, as well as high stability and recyclability. In detail, Cl−, NO3−, H2PO4− and humic acid (HA) showed promoting effect on SPY degradation, and the excellent removal efficiency maintained in actual water matrix. Moreover, the SPY degradation rate could reach 90 % after the fifth cycle and the mineralization rate was preferable, with 56.4 % of total organic carbon (TOC) removal rate. Generally, the degradation of SPY mainly involved bonds cleavage and hydroxyl addition, and five possible degradation pathways were proposed. This work provided an environmentally friendly, facile and promising route to synthesize nitrogen carbon coated bimetallic catalysts with sufficient properties for pollutant removal.

Integrated AI-driven optimization of Fenton process for the treatment of antibiotic sulfamethoxazole: Insights into mechanistic approach

Antibiotics, as a class of environmental pollutants, pose a significant challenge due to their persistent nature and resistance to easy degradation. This study delves into modeling and optimizing conventional Fenton degradation of antibiotic sulfamethoxazole (SMX) and total organic carbon (TOC) under varying levels of H2O2, Fe2+ concentration, pH, and temperature using statistical and artificial intelligence techniques including Multiple Regression Analysis (MRA), Support Vector Regression (SVR) and Artificial Neural Network (ANN). In statistical metrics, the ANN model demonstrated superior predictive accuracy compared to its counterparts, with lowest RMSE values of 0.986 and 1.173 for SMX and TOC removal, respectively. Sensitivity showcased H2O2/Fe2+ ratio, time and pH as pivotal for SMX degradation, while in simultaneous SMX and TOC reduction, fine tuning the time, pH, and temperature was essential. Leveraging a Hybrid Genetic Algorithm-Desirability Optimization approach, the trained ANN model revealed an optimal desirability of 0.941 out of 1000 solutions which yielded a 91.18% SMX degradation and 87.90% TOC removal under following specific conditions: treatment time of 48.5 min, Fe2+: 7.05 mg L−1, H2O2: 128.82 mg L−1, pH: 5.1, initial SMX: 97.6 mg L−1, and a temperature: 29.8 °C. LC/MS analysis reveals multiple intermediates with higher m/z (242, 270 and 288) and lower m/z (98, 108, 156 and 173) values identified, however no aliphatic hydrocarbon was isolated, because of the low mineralization performance of Fenton process. Furthermore, some inorganic fragments like NH4+ and NO3− were also determined in solution. This comprehensive research enriches AI modeling for intricate Fenton-based contaminant degradation, advancing sustainable antibiotic removal strategies.

Effect of small-molecule phenolic compounds on the removal of triclosan (TCS) by heat/persulfate process: Formation of cross-coupling products and implications for wastewater treatment

In this study, the effect of three small molecule phenolic compounds (SMPCs) (Phenol (PHOH), p-hydroxybenzoic acid (PHBA) and 3,5-dihydroxytoluene (DHT)) on the transformation of triclosan (TCS) in heat activated persulfate (heat/PS) process was investigated. TCS in single and mixed solutions were almost completely removed after 120 min of heat/PS treatment. Compared with single TCS system, the generation of cross-coupling products in the mixed system was beneficial for the removal of total organic carbon (TOC). Overall cytotoxicity and genotoxicity tests on mammalian cells showed that the reaction products in mixed phenol system was less toxic than those in the single TCS system, which confirmed the low toxicity of cross-coupling products. Product analysis was combined with theoretical calculations to propose a mechanism for the cross-coupling of coexisting phenolic pollutants that hydrogen on the phenolic hydroxyl groups of different pollutants was extracted by SO4•- to form phenoxy radicals, which coupled with each other to form cross-coupling products. Lowering the pH of the reaction solution can promote the occurrence of cross-coupling reaction, favoring the removal of TOC and the reduction of toxicity. These results will provide insights into the transformation of phenolic pollutants in water treatment for further control of environmental risks.

Oxidation of organics in water by active chlorine performed in microfluidic electrochemical reactors: a new way to improve the performances of the process

Wastewater polluted by organics can be treated by using electro-generated active chlorine, even if this promising route presents some important drawbacks such as the production of chlorinated by-products. Here, for the first time, this process was studied in a microfluidic electrochemical reactor with a very small inter-electrode distance (145 μm) using a water solution of NaCl and phenol and a BDD anode. The potential production of chloroacetic acids, chlorophenols, carboxylic acids, chlorate and perchlorate was carefully evaluated. It was shown, for the first time, up to our knowledge, that the use of the microfluidic device allows to perform the treatment under a continuous mode and to achieve higher current efficiencies and a lower generation of some important by-products such as chlorate and perchlorate. As an example, the use of the microfluidic apparatus equipped with an Ag cathode allowed to achieve a high removal of total organic carbon (about 76%) coupled with a current efficiency of 17% and the production of a small amount of chlorate (about 30 ppm) and no perchlorate. The effect of many parameters (namely, flow rate, current density and nature of cathode) was also investigated.

Mechanism and application of enhanced degradation of phenol through peroxymonosulfate activation by sulfur-doped biochar prepared with sodium thiosulfate as activator and sulfur dopant

Na2S2O3 was used as activator and sulfur dopant for preparation of sulfur-doped biochar (SBC) with high specific surface area and sulfur content, and its performance to activate peroxymonosulfate (PMS) for phenol degradation was studied. In the presence of 0.3 g/L S4BC-800 and 1 g/L PMS, 20 mg/L phenol could be removed completely in 30 min. S doping improved the electron transfer performance of the composite and enhanced the activation property of PMS for phenol degradation. Free radical quenching experiment and electron paramagnetic resonance analysis indicated that SO4•−, •OH, and 1O2 were involved in phenol degradation. In addition, the current oxidation process confirmed that there was also direct oxidation based on electron transfer between PMS and phenol with S4BC-800 as mediator. The S4BC-800/PMS system could effectively decompose the recalcitrant organic pollutants in the effluent of sewage treatment plant, achieving the total organic carbon removal rate of 83.26 %.

Nitrogen-doped carbon-coated Cu0 activates molecular oxygen for norfloxacin degradation over a wide pH range

The Fenton-like activated molecular oxygen technology demonstrates significant potential in the treatment of refractory organic pollutants in wastewater, offering promising development prospects. We prepared a N-doped C-coated copper-based catalyst Cu0/NC3-600 through the pyrolysis of Mel-modified Cu-based metal–organic framework (MOF). The results indicate that the degradation of 20 mg/L norfloxacin (NOR) was achieved using 1.0 g/L Cu0/NC3-600 across a wide pH range, with a removal rate exceeding 95 % and total organic carbon (TOC) removals approaching 70 % after 60 min at pH 5–11. The nitrogen doping enhances the electronic structure of the carbon material, facilitating the adsorption of molecular oxygen. Additionally, the formed carbon layer effectively prevent copper leaching,contributing to increased stability to a certain extent. Subsequently, we propose the catalytic reaction mechanism for the Cu0/NC/air system. Under acidic conditions, Cu0/NC3-600 activates molecular oxygen to produce the •O2–, which serves as the primary active species for NOR degradation. While in alkaline conditions, the high-valent copper species Cu3+ is generated in conjunction with •O2–, both working simultaneously for NOR degradation. Furthermore, based on the LC-MS results, we deduced four possible degradation pathways. This work offers a novel perspective on expanding the pH range of copper-based catalysts with excellent ability to activate molecular oxygen for environmental water treatment.

Exploring effects of carbon, nitrogen, and phosphorus on greywater treatment by polyculture microalgae using response surface methodology and machine learning

The microalgae-based wastewater treatment is a promising technique that contribute to achieving sustainable development goals (SDGs), such as SDG-6, “Clean Water and Sanitation”. However, it is strongly influenced by the initial composition of wastewater. In this study, the impact of initial organics and nutrient concentration on the removal of total organic carbon (TOC), total carbon (TC), ammonium (NH4+), total nitrogen (TN), and phosphate (PO43−) from greywater using native polyculture microalgae was explored. Response surface methodology was employed along with two machine learning approaches, AdaBoost and XGBoost, to evaluate the interactions among three main factors: TOC, NH4+, and PO43−, and their effects on treatment efficiency. The C/N ratios for achieving maximum TOC and TC removal efficiency of 99.2% and 97.7% were determined to be 10.3, and 65.4–73.6, respectively. Notably, the N/P ratio did not significantly affect their removal. The highest NH4+ removal efficiency, reaching 96.2%, was attained at C/N ratios of 4.3, 24.0, 38.2, and 212.9, coupled with N/P ratios of 0.3, 2.6, and 23.4. Highest TN removal efficiency of 77.2% was achieved at C/N and N/P ratios of 12.2 and 2.0, respectively. Highest PO43− removal of 78.8% was obtained at N/P ratio 12.8. However, C/N ratio did not affect the removal efficiency. Maintaining these specified C/N and N/P ratios in the influent greywater would ensure that the treated greywater meets the required standards for various reuse applications, including flushing, groundwater recharge, and surface water discharge. The integration of RSM with AdaBoost and XGBoost provided accurate predictions of removal efficiencies. For all the models, XGBoost had the highest R2, and lowest MAE and MSE values. The cross validation of RSM models with AdaBoost and XGBoost further reinforced the reliability of these models in predicting treatment outcomes.

A novel continuous-flow photocatalytic device for antibiotic degradation

The presence of antibiotic contaminants in water reservoirs and aquatic environments poses considerable risks to public and ecosystem health. Despite its high mineralization efficiency and environmental friendliness, photocatalytic technology has limited practical applications due to low energy efficiency, intermittent operation, and inconvenient catalyst recovery. Here, we developed a continuous-flow photocatalytic device (CFP-D) with outstanding activity, stability, and university towards antibiotic wastewater degradation. Complete removal of total organic carbon was achieved for multiple antibiotic wastewaters using CFP-D in a continuous flow process. The unique combination of continuous-flow reactor and highly photo-permeable F-Ti-SiO2 aerogel with abundant TiO5 active sites overcomes the limitations of conventional photocatalytic devices. This study provides new insights for the design of highly efficient monolithic catalysts and continuous flow reaction devices, and showcases the immense potential of CFP-D in medical and organic wastewater treatment.

Integrated Electrochemical Oxidation and Biodegradation for Remediation of a Neonicotinoid Insecticide Pollutant.

A novel integrated electrochemical oxidation (EO) and bacterial degradation (BD) technique was employed for the remediation of the chloropyridinyl and chlorothiazolyl classes of neonicotinoid (NEO) insecticides in the environment. Imidacloprid (IM), clothianidin (CL), acetamiprid (AC), and thiamethoxam (TH) were chosen as the target NEOs. Pseudomonas oleovorans SA2, identified through 16S rRNA gene analysis, exhibited the potential for BD. In EO, for the selected NEOs, the total percentage of chemical oxygen demand (COD) was noted in a range of 58-69%, respectively. Subsequently, in the biodegradation of EO-treated NEOs (BEO) phase, a higher percentage (80%) of total organic carbon removal was achieved. The optimum concentration of NEOs was found to be 200 ppm (62%) for EO, while for BEO, the COD efficiency was increased up to 79%. Fourier-transform infrared spectroscopy confirms that the heterocyclic group and aromatic ring were degraded in the EO and further utilized by SA2. Gas chromatography-mass spectroscopy indicated up to 96% degradation of IM and other NEOs in BD (BEO) compared to that of EO (73%). New intermediate molecules such as silanediamine, 1,1-dimethyl-n,n'-diphenyl produced during the EO process served as carbon sources for bacterial growth and further mineralized. As a result, BEO enhanced the removal of NEOs with a higher efficiency of COD and a lower consumption of energy. The removal efficiency of the NEOs by the integrated approach was achieved in the order of AC > CL > IM > TH. This synergistic EO and BD approach holds promise for the efficient detoxification of NEOs from polluted environments.

Enhanced treatment of p-nitrophenol and coking wastewater through electrochemical and electrochemical-ozonation coupling process utilizing a novel Ti4O7 reactive electrochemical membrane anode

Organic pollutants in water could be removed by electrochemical treatment using a reactive electrochemical membrane (REM) with Magnéli phase Ti4O7, yet it is challenging to design suitable porosity to realize effective mass transfer and enhance the reactivity. Here, a novel Ti4O7 REM was prepared by a spark plasma sintering (SPS) method, which showed excellent electrochemical reactivity and mass transfer rate for organic pollutants in water. Compared to other Ti4O7 REMs, the novel Ti4O7 REM achieved a 140–9000-fold decrease in charge transfer resistance and a 5–110-fold increase in mass transfer rate. The p-nitrophenol in water can be completely removed in the REM system, with a maximum total organic carbon (TOC) removal rate of 85%. Then the REM system obtained an amazing removal rate of TOC (50.1%) and UV254 (89.6%) in the electrochemical treatment of real coking wastewater. In addition, to further enhance the removal efficiency, a coupled oxidation process with the novel Ti4O7 REM and O3 aeration was investigated. The TOC removal rate and energy consumption were 57.1% and 165.2 kWh (kg TOC)−1 at the optimal conditions within a short treating time. Our findings highlighted an innovative REM for a broad range of potential environmental applications.

Synthesis, Characterization, and Photocatalytic Performance of ZnFe2O4-g-C3N4 Composites for Tetracycline Removal from Contaminated Water

The presence of emerging contaminants in wastewater like tetracycline poses a significant challenge in water reuse worldwide. The implementation of a p-n heterojunction and dye-sensitized techniques in the enhancement of graphite carbon nitride provides a promising alternative for visible light-driven degradation of emerging contaminants present in wastewater. The present study investigated dye-sensitized and plain composites in degrading tetracycline using natural sunlight in a parabolic trough reactor. The study synthesized four composites of ZnFe2O4-g-C3N4 at 5, 15, and 25 wt% loading of the ferrite by direct annealing of melamine, followed by thermal and ultrasonic exfoliation of bulk graphite carbon nitride and in situ precipitation with zinc ferrites to yield a composite photocatalyst. The photocatalysts were characterized using X-ray diffraction (XRD) analyses which confirmed that all the spinel ferrite phases of ZnFe2O4 were well bonded with g-C3N4 nanosheets to form a composite. The crystallite sizes were calculated by the Debye–Scherrer equation indicating crystal sizes of between 4.63 and 8.61 nm confirming the nanostructures. The scanning electron microscope-energy dispersive spectroscopy (SEM-EDX) tests verified that the spherical globules of ZnFe2O4 were well attached to the mesoporous layers of g-C3N4 and absence of contaminant phases. The UV-Vis analysis for 25% ZF-GCN revealed a band gap reduction from 2.67 eV to 2.03 eV. The PL intensity for all the composites decreased at excitation of 266 nm and 550 nm which was evidence for suppressed charge recombination. A 25% ferrite loading resulted in the best photocatalytic performance with tetracycline degradation of 93.64% and total organic carbon (TOC) removal of 51.89%. The sensitization of the 25% ZF-GCN composite with Eosin Y further improved its performance for degradation of tetracycline to 94.62% and TOC removal to 68.29%. Therefore, dye sensitization is an efficient way of improving the photocatalytic activity of a multicomponent photocatalyst for the removal of emerging pollutants.

Harmonizing the cyano-group and Na to enhance selective photocatalytic O2 activation on carbon nitride for refractory pollutant degradation

Manipulating exciton dissociation and charge-carrier transfer processes to selectively generate free radicals of more robust photocatalytic oxidation capacity for mineralizing refractory pollutants remains challenging. Herein, we propose a strategy by simultaneously introducing the cyano-group and Na into graphitic carbon nitride (CN) to obtain CN-Cy-Na, which makes the charge-carrier transfer pathways the dominant process and consequently achieves the selective generation of free radicals. Briefly, the cyano-group intensifies the local charge density of CN, offering a potential well to attract the hole of exciton, which accelerates the exciton dissociation. Meanwhile, the separated electron transfers efficiently under the robust built-in electric field induced by the cyano-group and Na, and eventually accumulates in the heptazine ring of CN for the following O2 reduction due to the reinforced electron sink effect caused by Na. As a result, CN-Cy-Na exhibits 4.42 mmol L-1 h-1 productivity with 97.6% selectivity for free radicals and achieves 82.1% total organic carbon removal efficiency in the tetracycline photodegradation within 6 h. Additionally, CN-Cy-Na also shows outstanding photodegradation efficiency of refractory pollutants, including antibiotics, pesticide plastic additives, and dyes. This work presents an innovative approach to manipulating the exciton effect and enhancing charge-carrier mobility within two-dimensional photocatalysts, opening an avenue for precise control of free radical generation.

Oxygen vacancy based WO3/SnO2-x promote electrochemical H2O2 accumulation by two-electron water oxidation reaction and toxic uniform dimethylhydrazine degradation

The key to constructing an anodic electro-Fenton system hinges on two pivotal criteria: enhancing the catalyst activity and selectivity in water oxidation reaction (WOR), while simultaneously inhibiting the decomposition of hydrogen peroxide (H2O2) which is on-site electrosynthesized at the anode. To address the issues, we synthesized novel WO3/SnO2-x electrocatalysts, enriched with oxygen vacancies, capitalize on the combined activity and selectivity advantages of both WO3 and SnO2-x for the two-electron pathway electrocatalytic production of H2O2. Moreover, the introduction of oxygen vacancies plays a critical role in impeding the decomposition of H2O2. This innovative design ensures that the Faraday efficiency and yield of H2O2 are maintained at over 80 %, with a noteworthy production rate of 0.2 mmol h−1 cm−2. We constructed a novel electro-Fenton system that operates using only H2O as its feedstock and applied it to treat highly toxic uniform dimethylhydrazine (UDMH) from rocket launch effluent. Our experiments revealed a substantial total organic carbon (TOC) removal, achieving approximately 90 % after 120 mins of treatment. Additionally, the toxicity of N-nitrosodimethylamine (NDMA), a byproduct of great concern, was shown to be effectively mitigated, as evidenced by acute toxicity evaluations using zebrafish embryos. The degradation mechanism of UDMH is predominantly characterized by the advanced oxidative action of H2O2 and hydroxyl radicals, as well as by complex electron transfer processes that warrant further investigation.

Remediation of oil-drilling cuttings by ozonation in a bubble flow reactor

Oil-drilling cuttings (ODCs) are the major wastes generated during oil/gas exploration and extraction. In the present work, a new method based on ozonation is suggested for the remediation of ODCs at ambient conditions, without pre-drying. During the ozonation process, the pressure drop across the gas phase along with the pH, redox potential, and temperature of liquid phase are monitored with the aid of built-in sensors. Occasionally, solid and liquid samples are collected to measure the total organic carbon (TOC) of each phase as a function of time, while the concentration of the total petroleum hydrocarbons (TPH) is measured before and after the completion of treatment. The maximum TOC removal efficiency for the solid phase reached ∼60% and that of TPH ∼ 40% whereas the energy efficiency was ∼ 0.1 kWh/g-TOC. The main mechanisms of ODC remediation are the mass-transfer of organic species from the solid to aqueous phase, and the direct oxidation by dissolved ozone, whereas their synergistic action is reflected in fluctuations of TOC concentration in liquid phase. The TOC removal efficiency of the solid phase increases with the flow rate decreasing, the ozone concentration increasing, and the mass ratio of ODC to seawater (SW) increasing. Ozonation in the liquid phase after its separation from treated ODC proceeds very fast through the direct oxidation by ozone. The process energy efficiency is favoured for low ozone concentration, low gas flow rate, high ODC to SW mass ratio, oxygen as feed gas, and without the addition of sodium dodecyl sulphate (SDS) as surfactant.

Photocatalytic degradation of enrofloxacin with CoAl-LDH mediated persulfate system: Efficiency evaluations and reaction pathways

Residual enrofloxacin (ENR) exposed in aqueous environments is challenging to the ecosphere. In this work, a layered double hydroxide CoAl-LDH was used to activate the common oxidizing agent persulfate (PS) for photodegradation of ENR, and the degradation pathways of ENR were scrutinized and elucidated. The results indicated that, under the optimal conditions obtained through orthogonal experiments, even though the degradation rate of ENR was as high as 97.72%, the removal of total organic carbon (TOC) from the system was only about 30%. Eleven probable reaction pathways were categorized, and thirty-one types of intermediates were identified in participating in the complex degradation process. The major products of ENR were P4 (C17H20FN3O3), P22 (C19H22FN3O4), P19 (C17H18FN3O3), which are mainly derived from the cleavage of the piperazine groups and quinolone rings. Density functional theory (DFT) calculations of the Fukui index for ENR revealed that the two N atoms in the piperazine ring were the core reactive sites in triggering the degradation chains, which were sensitive for electrophilic attack by the dominant radicals (•OH and SO4•-) generated from the composite PS-UV-CoAl-LDH system.

Preparation, characterization and photocatalysis performances of superparamagnetic MgFe2O4@CeO2 nanocomposites: Synthesized via an easy and green sol–gel method

The characterization of MgFe2O4@CeO2 superparamagnetic nanocomposites was thoroughly investigated using powder X-ray diffraction (XRD), a vibrating sample magnetometer (VSM), scanning electron microscopy (SEM), dispersive X-ray analysis (EDX), elemental mapping (MAP), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET) and UV–Vis diffuse reflectance spectroscopy (DRS) analyses. The photocatalytic activity of the synthesized samples was evaluated as a novel magnetic nanocatalyst for degrading Congo red (CR) dye in an aqueous solution under visible light at room conditions. The results demonstrate that the efficiency of photocatalytic degradation is higher than that of absorbance and photolysis. The degradation efficiency of photodegradation is 93% within 49% of total organic carbon removal performance. The prepared MgFe2O4@CeO2 magnetic nanocomposites (MNCs) can be easily recovered and recycled for five repeated cycles, demonstrating potential extensive efficiency in magnetic nanocomposites in wastewater and water treatment. The nanoscale morphology of MgFe2O4@CeO2 MNCs was characterized as spherical, with a size range of 35–40 nm, utilizing SEM and TEM techniques. The saturation magnetization (Ms) of the resulting nanocomposites was analyzed by VSM, revealing a value of 3.58 emu/g. Furthermore, the surface area was determined to be 27.194 m2/g using BET analysis, and the band gap was identified as 2.85 eV through DRS analysis.

Insights into behaviors of functional groups in biomass derived products during aqueous phase reforming over Ni/α-MoO3 catalysts

Aqueous phase reforming (APR) of biomass-derived products has been widely applied for hydrogen generation, chemicals production, and wastewater treatment. Despite its widespread application, the complexity of the raw materials and reaction mechanisms significantly complicates the APR process, impeding its development. This study investigated the APR performance of biomass-derived products using Ni/α-MoO3 catalysts toward hydrogen production and pollutant control, conducted at a temperature of 225 °C and a residence time of 30 min, thus comprehensively understanding the effect of different functional groups. The results showed that the amide (R–HCON) exhibited superior hydrogen production potential during APR. In terms of total organic carbon (TOC) removal, ether showed a 98.10% removal efficiency without a catalyst, whereas the presence of catalyst greatly enhanced the TOC removal efficiency of acetaldehyde (-CHO) from 62.26% to 86.68%. The performed APR of biomass-derived products on Ni/α-MoO3 catalysts primary resulted in the presence of N, N-Dimethylformamide (HCON-(CH3)2), and aminobenzene (Ph-NH2) for Ni leaching with a lower concentration. The carbon deposition on the catalyst primarily resulted from the combined effects of various compounds and the oxygen vacancies within the catalysts. This study aims to provide novel insights into the APR process for both biomass and biomass-derived materials.

Optimization of Vancomycin Antibiotic Removal from Synthetic and Real Wastewater Using UV/Fe3 O4 @Alg-ZnO Nanocomposite Photocatalysis: Response Surface Methodology Based on a Box-Behnken Design

Background: Vancomycin (VCM) is a critical antibiotic due to its high consumption and side effects, including increased bacterial resistance affecting treatment processes. This research investigated the efficiency of VCM antibiotic removal from an aqueous solution using a UV/Fe3 O4 @Alg-ZnO integrated process. Methods: Response surface methodology (RSM) and a Box-Behnken design were applied using Design-Expert software to optimize the number of samples and simultaneously understand the interactive effects between variables. X-ray diffraction (XRD), a vibrating-sample magnetometer (VSM), field effect scanning electron microscopy (FE-SEM), and Fourier transform infrared (FTIR) analyses were used to check the structural characteristics. The effects of initial catalyst concentration (0.1, 0.3, and 0.5 g/L), initial pollutant concentration (10, 30, and 50 mg/L), contact time (10, 30, and 50 minutes), and pH (3, 7, and 11) on VCM decomposition rate were investigated. Spectrophotometry, total organic carbon (TOC), and GC-MS analyses were used to check the efficiency of the process. Results: In this study, VCM and TOC removal efficiency was 92.64% and 85.38%, respectively, under optimal conditions. The reason for the reduction in the efficiency of the combined UV/Fe3 O4 @Alg-ZnO process in real raw sewage, after activated sludge (13%) and after activated sludge and stabilization ponds (24%), is the high COD, which causes the active radicals produced to be spent on other species instead of the VCM antibiotic. Conclusion: The current study showed that the UV/Fe3 O4 @Alg-ZnO process performs well in removing VCM and TOC. In real wastewater, this efficiency was significantly reduced.

Assembling an S-type heterojunction comprising vacancy-rich CeO2-x and CuBi2O4 for improved photocatalytic oxidation of gaseous toluene

The exploration of highly efficient methods for degrading VOCs, with concurrent low energy consumption and lasting reusability, holds significant appeal. In this regard, an S-type CuBi2O4/CeO2-x heterojunction with the robust interfacial interactions is presented as an active photocatalyst for the efficient decomposition of gaseous toluene under full-spectrum irradiation. The optimal sample CC15 effectively degrades gaseous toluene at a high concentration of 1800 ppm within 2 h, achieving a notable CO2 yield of 87.05 %, and a TOC (total organic carbon) removal rate of 89.33 %. Furthermore, CuBi2O4/CeO2-x exhibits exceptional stability, maintaining its 100 % degradation capability over 32 cycles for nearly 64 h. Comparative characterization reveals that the superior performance derives from an abundance of oxygen vacancies and effective pre-adsorption capabilities, which facilitate rapid adsorption of VOCs on the catalyst surface, thereby increasing the likelihood of degradation reactions. Additionally, the formation of an S-type heterojunction, valence pairing between Bi3+ and Ce3+/4+ ions, and strong interfacial interactions serve as the primary pathways for the efficient separation of photogenerated carriers, contributing to the high CO2 production rate and prolonged cycle stability. The present investigation underscores the significant potential of vacancy-rich S-type heterojunctions and interfacial interactions between composite components, offering excellent activity and long-term availability for VOCs removal.

Cobalt-doped iron-based metal–organic gels as efficient visible-light-driven peroxymonosulfate activators for the efficient degradation of norfloxacin with simultaneous antibacterial activity

A strategically fabricated cobalt-doped iron-based metal–organic gel (CFM) synergistically promotes peroxymonosulfate (PMS) activation and visible light-induced photocatalysis to remove norfloxacin (NOR). Cobalt incorporation into the metal–organic gel significantly optimizes its electronic structure, leading to the exceptional performance of CFM in synergistically activating PMS, amplifying visible light absorption, and enhancing photoinduced charge separation efficiency. The Vis/50 %-CFM/PMS system enables a NOR removal rate of up to 96.8 % within 60 min and a total organic carbon (TOC) removal rate of 78.3 %, signifying excellent decontamination performance. Exhibiting robust mineralization potential, the Vis/CFM/PMS system has undergone comprehensive analysis of the intermediary degradation process using Density Functional Theory (DFT) calculations. The toxicity of degradation intermediates was assessed employing the quantitative structure–activity relationship (QSAR) model. In addition, the Vis/CFM/PMS system showed antibacterial effects against E. coli and S. aureus. This investigation furnishes a novel perspective toward developing innovative PMS activation photocatalyst coupling systems for environmental remediation.