Total Organic Carbon Reduction Research Articles

Pd/UiO‐66(Zr)‐2OH as a High‐Performance Catalyst for Hydrogen‐Enhanced Fenton Oxidation of Trimethoprim

ABSTRACTA novel catalyst material named Pd/UiO‐66(Zr)‐2OH was successfully developed and applied in a hydrogen‐promoted Fenton system for the efficient catalytic oxidation of the widely used antibiotic trimethoprim (TMP). The UiO‐66(Zr)‐2OH, as the carrier of catalyst in this work, was synthesized through a solvothermal method. The Pd0 nanoparticle, as the active center of the catalyst, was loaded onto its surface by the “ship‐in‐a‐bottle” strategy. The results showed that the composite Pd/UiO‐66(Zr)‐2OH demonstrated excellent catalytic performance during the reaction, achieving over 97% of TMP removal efficiency within 180 min under optimal conditions under the condition of only trace of iron without adding H2O2. This may be attributed to the fact that the [H], as a clean and efficient reducing agent, can be utilized to accelerate the regeneration of Fe2+ in the Fenton reaction, as well as in the in‐situ regeneration of H2O2. The key parameters affecting the removal efficiency of TMP, including the initial pH and concentration of Fe2+, the dosage of the synthesized material, the flow rate of H2 and the stirring speed were investigated systematically. The Pd/UiO‐66(Zr)‐2OH exhibited high stability and reusability, maintaining over 82% of its initial degradation efficiency of TMP after six reaction cycles. The mechanistic insight revealed that the system primarily relied on the generation of hydroxyl radical (·OH) and singlet oxygen (1O2) for the degradation of TMP, which was verified through quenching experiments and electron spin resonance (ESR). The degradation pathway of TMP was elucidated by analyzing intermediates and the reduction in total organic carbon (TOC). This research offers novel conceptual insights into the evolution and application of advanced oxidation technologies, efficient degradation of emerging pollutants, and expansion of pathways for hydrogen resource utilization.

Breakdown cost and recycling processes of Bentonite/TiO2 quantum dots of photo and solar degradation of Congo Red dye and industrial dyes wastes

This research presents the preparation, characterization, and application of a novel bentonite- TiO2 quantum dot (Bent/TQ) nanocomposite for the efficient photodegradation of Congo Red dye, a common pollutant in industrial wastewater. The composite was prepared via a co-precipitation method followed by calcination, which facilitated the uniform dispersion of TiO2 quantum dots within the bentonite matrix. The resulting material exhibited a high specific surface area of 205.45 m2/g and an optimized band gap of 3.15 eV, making it suitable for visible light photocatalysis. The photocatalytic efficiency of Bent/TQ was evaluated under both xenon lamp irradiation and natural sunlight. The composite demonstrated a significant degradation rate constant of 23.35 × 10⁻³ s⁻1, which is comparable to that of pure TiO2 quantum dots (28.86 × 10⁻³ s⁻1). Mechanistic studies revealed that the primary active species responsible for the degradation were hydroxyl radicals (•OH), generated through the interaction of photogenerated electron-hole pairs with H2O molecules and molecular oxygen. Total Organic Carbon (TOC) and Chemical Oxygen Demand (COD) analyses were employed to assess the mineralization efficiency of the composite. The Bent/TQ catalyst achieved a COD removal efficiency of 84.5% and a TOC reduction of 76.2% after 240 minutes of irradiation under natural sunlight. Reusability tests indicated that the photocatalyst retained approximately 80% of its original efficiency after seven consecutive cycles, though a slight decline was observed due to particle agglomeration under prolonged light exposure. The economic analysis suggested that the use of Bent/TQ nanocomposites could reduce operational costs by 29.12% compared to conventional TiO2-based systems, making it a cost-effective solution for large-scale wastewater treatment. This work highlights the potential of Bent/TQ nanocomposites as sustainable and efficient photocatalysts for environmental remediation, with future efforts aimed at enhancing their long-term stability and expanding their applicability to a broader range of pollutants.

Exploration of Bacterial Community Structure Profiling and Functional Characteristics in the Vermicomposting of Wasted Sludge and Kitchen Waste

Nowadays, the enormously growing amount of kitchen waste and wasted sludge has greatly received global attention. Vermicomposting has been represented as an eco-friendly and sustainable alternative for organic waste management. This study utilized kitchen waste generated by the university canteen and excess sludge from municipal wastewater treatment to collaboratively realize waste to resource through vermicomposting with a composting control. The results indicated that the treatment utilizing an equal mass ratio of wasted sludge and kitchen waste (T3) exhibited the greatest reduction in total organic carbon and the highest increase in total nitrogen. Furthermore, the predominant phyla observed were Proteobacteria, Actinobacteriota, Bacteroidetes, and Firmicutes. Functional prediction analysis demonstrated higher relative abundances of β-glucosidase (ascF) and 6-phospho-β-glucosidase (bglA, celF) in the vermicomposting, suggesting that the earthworms essentially enhanced the cellulose degradation. More importantly, the co-occurrence network analysis demonstrated that the vermicomposting showed a stronger interaction between Gordonia and other bacteria, thereby enhancing its ability to degrade macromolecular compounds. In general, the vermicomposting can smoothly and remarkably stabilize the kitchen waste, assisted by excess sludge and sawdust.

Integrating azo dye degradation and lipid accumulation by Candida tropicalis and Pichia kudriavzevii along with insights into underlying metabolomics for treatment of textile effluents

Azo compounds, extensively utilized across various industries, contribute to the release of toxic effluents that are detrimental to both the environment and human health. Traditional methods for azo dye removal often result in harmful byproducts or concentrated sludge, complicating disposal efforts. This study explores the potential of two yeast strains, Candida tropicalis and Pichia kudriavzevii, to effectively decolorize azo dyes (TD4, TD5, and TD6) while simultaneously accumulating lipids. The cultures achieved 80–90 % decolorization of the selected dyes during incubation, with Pichia showing higher efficiency across multiple dyes compared to Candida. Lipid profiling identified valuable fatty acids, such as palmitic acid and oleic acid, with potential applications in biofuels and other industries. Total Organic Carbon (TOC) analysis revealed a reduction in TOC, indicating degradation and mineralization of the dyes by the yeasts. Metabolic profiling via LC-MS confirmed the degradation, showing the presence of intermediates such as azoles, azolines, isoquinolines, pyridines, and benzopyrans in dye-supplemented cultures. Additionally, pathways related to energy metabolism, amino acid metabolism, drug metabolism (cytochrome P450), degradation of aromatic compounds, and steroid biosynthesis were enriched in the dye-treated cultures. Lipid output in the presence of dyes ranged from 40 % to 90 %. The study thus demonstrates a proof of concept for economically viable lipid production combined with efficient dye removal, presenting a sustainable solution to environmental and industrial challenges.

In-Vessel Aerobic Composting of Organic Waste Using Synthetic and Natural Bulking Agents

The escalating growth in municipal solid waste production underscores the imperative need for efficient waste management, especially given that a substantial portion of MSW comprises biodegradable materials suitable for composting. This study investigates the impacts of using a synthetic bulking agent (perforated plastic balls) in conjunction with biochar, a natural bulking agent, on the aerobic composting of kitchen waste. The study aim to evaluate the effectiveness of this combined approach in optimizing the composting process. Four trials, each spanning 30 days, were conducted to assess the effects of different combinations of synthetic and natural bulking agents. The study uses a uniform-size perforated synthetic bulking agent in combination with biochar to enhance the composting process. Results indicate that incorporating the perforated plastic balls (8% by weight) alongside biochar significantly influenced key composting parameters. This approach accelerated the initial rise in temperature to 55°C, enhanced the reduction of total organic carbon, improved total Kjeldahl nitrogen retention, and facilitated the achievement of optimal carbon-nitrogen (C/N) ratios ranging from 19 to 20. Furthermore, the analysis of phosphorus (P) and potassium (K) loss during composting revealed that potassium is more susceptible to leaching than phosphorus due to its higher mobility. The study concludes that the addition of a uniform-size perforated synthetic bulking agent, constituting 8% (by weight), in conjunction with a natural bulking agent, effectively enhances the composting process.

Reduction of organic matter and disinfection by products formation at surface water treatment plants in Egypt

ABSTRACT Although the removal of colloidal particles continues to be an important reason for using coagulation, currently a newer approach, the removal of organic matter to reduce the formation of disinfection byproducts (DBPs) such as trihalomethanes (THMs) are suspected carcinogens. Inefficient removal of total organic carbon (TOC) leads to the formation of carcinogenic THMs. This motivates the research efforts to find a way to reduce them in potable water. The first objective of this research is monitoring the water quality (raw and produced) for selected three water treatment plants within Giza Governorate to reveal the most polluted site (high TOC in the raw water and THMs in the treated water) in the study areas. The second objective of this study is enhancing coagulation to reduce TOC and THMs from surface water treating. In this study, two different coagulants aluminum sulfate (alum), and ferric chloride were tested under different conditions of pH and coagulant concentration to determine their effectiveness for removal of TOC, THMs and turbidity. Optimum values for the mentioned conditions were used to achieve the maximum reduction for TOC and THMs in Al-Ayat drinking water treatment plant (DWTP) which recorded the highest concentration of TOC and THMs. Ferric chloride as a coagulant achieved the maximum removal percentage % of TOC, THMs and turbidity as 79%, 82% and 94%, respectively, at ferric chloride dose 100 mg/L, while alum as a coagulant recorded the maximum removal percentage % of TOC, THMs and turbidity as 46%, 52% and 91%, respectively, at alum dose 100 mg/L. The results indicated that ferric chloride as a coagulant has the highest efficiency reduction of TOC, THMs and turbidity if compared to alum with the same dose added.

Application of a laccase-catalyzed oxidative coupling for the removal and detoxification of typical flotation reagent salicylhydroxamic acid

Residual organic flotation reagents in mineral processing wastewater (MPW) can pose environmental hazards and hinder the sustainable development of the mining industry. Laccase as a versatile biocatalyst can eliminate various recalcitrant contaminants from the environment, but its potential applications for the removal and detoxification of organic flotation reagents have until now been overlooked. Herein, the influence of superparamagnetic immobilized laccase (SPM-IMLac) on the enzymatic removal of salicylhydroxamic acid (SHA), a typical mineral flotation reagent, as well as the mechanism of this process have been explored for the first time. The results indicated that SPM-IMLac can effectively remove SHA over a broad pH range and this process follows the pseudo-first-order reaction kinetics. A methodology which combined high resolution mass spectrometry (HRMS) and a solid phase extraction (SPE) technique revealed that SPM-IMLac could catalyze a single-electron oxidation of SHA to generate self/cross-oligomers via radical-driven C-C and/or C-O-C covalent coupling pathways. The Vibrio fischeri bioluminescence inhibition assay and a total organic carbon (TOC) analysis corroborated that the SHA transformation was accompanied by detoxification and by a reduction in TOC of the reaction solution, the extent of which correlated with the extent of the oxidative coupling. Moreover, SPM-IMLac could be easily recovered and reused, while keeping its high removal efficiency of SHA in the actual MPW matrices. This study not only provides fascinating insights into the transformation mechanisms and environmental fate of SHA mediated by SPM-IMLac, but it also exploits a viable and sustainable approach for the remediation of organic flotation reagents-contaminated MPW.

Innovative RGO-bridged S-scheme CuFe2O4@Ag2S heterojunction for efficient Sun-light-driven photocatalytic disintegration of Ciprofloxacin

Antibiotics contamination in water bodies poses a significant threat to public health and the environment, necessitating advanced methods for their removal from wastewater. In response to this issue, developing a novel magnetic nanocomposite (RGO/CuFe2O4@Ag2S) as an efficient photocatalyst for the degradation of pharmaceuticals like ciprofloxacin (CIP) is of great importance. The synthesized nanocomposite underwent comprehensive characterization to elucidate its crystalline structure, chemical bonding, surface morphology, elemental composition, internal structure, optical properties, surface area, particle size distribution, and magnetic properties. Under optimized conditions (pH=9, nanocomposite dose =0.5 g/L, CIP concentration of 20 mg/L, and duration of 200 minutes), the nanocomposite demonstrated complete degradation of CIP. Moreover, post-treatment analysis revealed significant reductions in total organic carbon (TOC) and chemical oxygen demand (COD) of 70.08% and 85.08%, respectively, indicating extensive mineralization of the antibiotic. Mechanistic investigations revealed a unique S-scheme heterojunction in the RGO/CuFe2O4@Ag2S nanocomposite, where RGO acts as an electronic bridge between CuFe2O4 and Ag2S. This innovative architecture facilitates efficient charge separation and transfer, significantly enhancing the photocatalytic activity. Reusability tests demonstrated the robust nature of the photocatalyst, with only a modest 6% decline in efficiency after six consecutive cycles. To further assess the system's effectiveness in real-world applications, its performance was evaluated in treating pharmaceutical wastewater. The biodegradation efficiency was quantified by measuring the Average Oxidation State (AOS) and Carbon Oxidation State (COS) of the wastewater samples before and after treatment.

Magnetic activated carbon for the removal of methyl orange from water via adsorption and Fenton-like degradation

Water pollution caused by organic dyes is a critical environmental issue. Although activated carbon (AC) is commonly used for dye adsorption, its effectiveness is limited by challenges in separation and regeneration. To address these limitations, a convenient recyclable magnetic activated carbon (MAC) was fabricated via co-precipitation and calcination method, serving as adsorbent and catalyst for methyl orange (MO) removal through a Fenton-like degradation process. Characterization techniques, including XRD, FTIR, SEM and TEM, confirmed that Fe3O4 nanoparticles (10–20 nm) were uniformly dispersed on AC surface. The MAC maintaining a high surface area (997 m2/g) and pore volume (0.795 cm3/g) and exhibited superparamagnetic properties with a saturated magnetization of 5.52 emu/g, enabling effective separation from aqueous solutions by magnet. Batch adsorption studies revealed that MO adsorption onto MAC followed pseudo-second-order kinetic and Freundlich isotherm model, with a maximum adsorption capacity of 205 mg/g at 25 °C. Thermodynamic analysis showed that the adsorption process was spontaneous and endothermic. Simultaneous degradation of MO and in-situ regeneration of MAC were achieved via Fenton-like reaction using sodium persulfate (PS). Under a PS concentration of 9 mmol/L, the MO removal efficiency near 95% after 60 min, with a total organic carbon (TOC) reduction of 83.1%. The reaction of Fe3O4 and oxygen functional groups on AC surface with PS facilitated the generation of SO4•-, thereby enhancing catalytic degradation of MO. The degradation efficiency improved as the temperature increased from 25 °C to 45 °C. Cycle tests demonstrated that the MO removal efficiency of MAC remained above 90% after 5 cycles of regeneration. Overall, this study highlights the potential of MAC for efficient removal of organic dyes from water through the coupling of adsorption and Fenton-like degradation, providing a promising solution for addressing water pollution challenges.

Performance evaluation of hybrid electrochemical oxidation and ultraviolet light-based persulfate process for the abatement of sodium dodecyl sulfate from wastewater.

The application of hybrid advanced oxidation processes (AOPs) is an efficacious way to remediate emerging contaminants from wastewater. In the present research work, a hybrid electrochemical oxidation and ultraviolet light-based persulfate activation processes (EO-UV/PS) were used to efficiently degrade sodium dodecyl sulfate (SDS) surfactant from synthetic and municipal wastewater. By operating the EO-UV/PS at optimum operating conditions at pH of 7.0, NaCl of 0.02M, current density of 6.4mA/cm2, persulfate dose of 2.5mM, and operating period of 180min, about 94.5 ± 2.8% of SDS (20mg/L) removal was achieved from synthetic wastewater. The abetment of SDS in both EO and UV/PS obeyed pseudo-first-order kinetics with a rate constant of 0.012 and 0.019min-1, respectively. Moreover, the economic analysis revealed 0.23 $ m-3order-1 as the operating cost for degrading SDS in EO-UV/PS. The degradation pathway experimentation suggested the generation of lauric acid by-product during SDS abatement. Besides, nearly 89.3 ± 2.9% of SDS and 58.7 ± 2.4% of total organic carbon reduction was also achieved from real municipal wastewater. Phytotoxicity test on Vigna radiata affirms the non-toxic nature of the EO-UV/PS effluent.

Aerobic granular sludge inoculant for enhancing high salinity wastewater treatment: Performance and value-added biopolymer recovery

In this study, two lab-scale aerobic granular sludge (AGS) systems, seeded with intertidal wetland sediment (IWS) and activated sludge (AS), were constructed to compare their treatment performances and alginate-like exopolymers (ALE) recovery potential in high salinity wastewater treatment. Both reactors (RIWS and RAS) exhibited excellent total organic carbon (TOC) reduction rates > 95.0 %, while RIWS exhibited an improved total nitrogen (TN) removal than RAS (84.4 % vs 75.7 %). The presence of several inorganic particulates (acted as nucleus) in IWS accelerated the formation of granules in RIWS. The ALE yield of RIWS reached 466.6 ± 52.2 mg/g VSS, which was 1.6 times higher than that of RAS (286.2 ± 5.2 mg/g VSS). Moreover, to illustrate the different ALE recovery potentials, the proposed ALE biosynthesis pathway was also assessed. It was observed that the abundance of function genes encoding ALE biosynthesis of RIWS was significantly higher than that of RAS, revealing its superior ALE recovery potential. This study proposed a novel and effective treatment method for high-salinity wastewater with high potential resource recovery.

Global meta‐analysis of demersal fishing impacts on organic carbon and associated biogeochemistry

AbstractThe potential threat of fisheries on seabed carbon is a topic of growing concern, yet existing literature presents inconsistencies leaving experts divided on the topic. We conducted a global meta‐analysis to synthesize the current knowledge and quantify how demersal fishing impacts various biogeochemical properties. Direct impact studies revealed overall reductions in chlorophyll‐a (Chl‐a, 17%), phaeopigments (24%), and proteins (32%). Effects on these reactive compounds were more pronounced on surface sediment (0–2 cm), where the impact on total organic carbon (TOC) also became significant, demonstrating the effect of gear penetration, and highlighting that sampling strategies combining sediment layers can mask observed effects. Current velocity and primary productivity significantly influenced the direction and magnitude of fishing impacts. Trawling‐induced subsurface reductions of TOC in low‐energy habitats may affect carbon sequestration due to the preferential removal of semi‐reactive carbon. Intriguingly, fishing intensity gradient studies showed an average increase in TOC in chronically fished areas, possibly reflecting fishing preferences for meso‐eutrophic grounds. We estimate a ~300‐day recovery period post‐fishing for Chl‐a, though values for other parameters are less certain. Limited data on seasonality, gear types, and an under‐representation of studies in tropical and deep‐sea areas pose challenges to quantifying global scale geochemical impacts of demersal fisheries. Knowledge gaps persist in understanding the fate of disturbed organic matter including its mineralization, transport, and sequestration. Nonetheless, our insights and estimates provide foundational knowledge that can contribute to science‐based approaches for spatial fisheries management while preserving natural carbon dynamics on the seabed.

Bio-stabilization of toxic weeds (Xanthium strumarium and Lantana camara) implementing mono- and polyculture of Eisenia fetida and Eudrilus eugeniae.

The present study investigates the synergistic impact of earthworms (Eisenia fetida and Eudrilus eugeniae) and microbes during vermicomposting of invasive weed phytomass (Xanthium strumarium and Lantana camara). This study aims introducing an onsite solution for weed control while producing valuable organic manure. Vermitransformation and detailed characterization of mono- (VC1, VC2, VC4, VC5) and polyculture (VC3, VC6) of X. strumarium and L. camara has been reported for the first time employing E. fetida and E. eugeniae. The study achieved 45.16 ± 2.48-76.73 ± 1.37% vermiconvertion rate. The pH, conductivity, and concentration of heavy metals are effectively stabilized. Furthermore, it observed a significant reduction in total organic carbon (TOC) alongside the augmentation of nitrogen, phosphorus, potassium, calcium, and other trace elements (Zn, Ni, Fe). The ash content, humification index, and C/N ratio analysis established the maturity of the vermicompost. The macronutrient enhancement in the vermicompost samples was recorded 1.5- to 2.47-fold for total N, 1.19- to 1.48-fold in available P, 1.1- to 1.2-fold in total K, and 1.1- to 1.18-fold in total Ca. The germination index reveals a significant reduction in phytotoxicity, suggesting the production of mature and suitable vermicompost for agricultural use. Evaluating mono- and polyculture techniques, the research highlights the superiority of E. fetida over E. eugeniae. Further, the earthworm population and biomass have significantly increased by the end of 60-day experimental trial.

Visible light-boosted photodegradation activity of Ag–AgVO3/Zn0.5Mn0.5Fe2O4 supported heterojunctions for effective degradation of organic contaminates

Abstract One of the most important concerns in developing efficient heterojunction photocatalysts for the photodegradation of environmental contaminants is the enhancement and acceleration of photocarrier separation. In this study, novel nanocomposite photocatalysts of Ag–AgVO3 nanorods grafted with Zn0.5Mn0.5Fe2O4 metal ferrites nanoparticles were developed by using facial hydrothermal and coprecipitation techniques for the effective photodegradation of Rhodamine B (Rh B) under visible light exposure. The fabricated materials were analyzed in detail using scanning electron microscopy, energy-dispersive X-ray spectroscopy (EDS), nitrogen adsorption/desorption, transmission electron microscopy (TEM), photoluminescence spectroscopy (PL), vibrating sample magnetometer, and ultraviolet–visible diffuse reflectance spectroscopy (DRS). The results showed an efficient contribution when compared to the earlier research. The TEM showed a hybrid of nanorods of supported composite with metal ferrite and Ag attached on the surface, consistent with field emission scanning electron microscopy and EDS results. The DRS expressed a lower band gap for supported nanocomposites (1.5 eV), which, arranged with PL, showed a lower recombination rate of supported nanocomposites. The surface properties showed that the supported hybrid might be as small as 45.42 nm or as large as 20.33 nm compared with others. When comparing the photocatalytic activity of pure AgVO3, Ag/AgVO3, and Zn0.5Mn0.5Fe2O4 photocatalysts, the performance of Ag–AgVO3/Zn0.5Mn0.5Fe2O4 nanocomposite photocatalyst was clearly superior (more than 99.9% degradation efficiency was achieved). The boosted activity the Ag–AgVO3/Zn0.5Mn0.5Fe2O4 photocatalyst system was justified by Z-system heterojunction induced by the plasmonic effect, and the suggested mechanism was investigated by quenching of reactive species by scavengers. The degradation performance was achieved under optimum conditions (pH = 2, 20 ppm of pollutant concentration, 120 mM of hydrogen peroxide, 1 g/L of catalysts dose). The results showed that after 240 min of visible irradiation resulted in the high (chemical oxygen demand) and (total organic carbon) reductions with a removal efficiency of (85) to (90%) for Rh B dye. The fabricated Ag–AgVO3/Zn0.5Mn0.5Fe2O4 nanocomposites were effective in the degradation of organic pollutants in wastewater treatment.

Solar light driven degradation of piroxicam and paracetamol by heterogeneous photocatalytic fenton system: Process optimization, mechanistic studies and toxicity assessment

The widespread occurence of pharmaceutical pollutants seriously threatens the environment and human well-being. In the present study, zinc ferrite nanoparticles (ZnFe2O4 NPs) have been synthesized by co-precipitation method and used as photocatalyst for the degradation of two most commonly prescribed painkillers, piroxicam (PXM) and paracetamol (PCM), via heterogeneous Fenton process under the solar light. The synthesized ZnFe2O4 NPs showed a narrower band gap i.e. 1.87 eV, signifying the ability to efficiently work in visible light range. In context of photocatalytic applications, the operational conditions were optimized to achieve maximum degradation. PCM and PXM were completely degraded (100%) at the optimized photocatalytic dose (20 mg L−1), reaction time (180 min), initial drug concentration (10 mg L−1), and pH (6.0), which is close to the natural environment. The extent of mineralization as estimated by the reduction of total organic carbon (TOC) was observed to be ∼91 and 82% for PCM and PXM respectively. Kinetic studies revealed that photocatalytic degradation followed pseudo-first-order kinetics. Moreover, the ZnFe2O4 NPs retained ∼90 % of photocatalytic activity after five consecutive reaction cycles, showing remarkable reusability and stability of catalyst.

Integration of coagulation–flocculation and photolysis processes for treating reverse osmosis concentrate (ROC) of pharmaceutical wastewater management

ABSTRACT This study provides novel insights into optimizing the integral treatment process, contributing to ROC treatment strategies. A comprehensive treatment approach for reverse osmosis concentrate (ROC) from pharmaceutical wastewater was investigated using an integral system consisting of a coagulation-flocculation and photolysis process. Ferric chloride (FC) and poly-aluminum chloride (PAC) are examined as coagulants within the range (0.1–1) gL−1, focusing on turbidity, chemical oxygen demand (COD), and total organic carbon (TOC) removal. The findings show that the optimal FeCl3 dosage is 0.4 gL−1, achieving significant turbidity reduction to 1 NTU. PAC at 0.2 gL−1 is optimal, reducing turbidity to 1 NTU and exhibiting non-linear behavior in COD and TOC removal, introducing them as a starting point to the post-treatment. Photolysis of treated samples at pH 7 yields COD reductions of 60.5% for PAC and 79.5% for FC, with respective TOC reductions of 79.5% and 75.23% over 360 min. At (pH 3.5) showed a significant reduction in the COD and TOC of treated ROC. The FC coagulant could decrease the COD from 261 to 5 mgL−1 (98% COD removal) and the TOC from 143.9 to 5 mgL−1 (74.8% TOC removal). The FAC coagulant could decrease the COD from 675 to 39 mgL−1 (93% COD removal) and the TOC from 186 to 13.1 mgL−1 (69.7% TOC removal). The conventional oxidant (H2O2) at optimal dosages enhanced COD and TOC removal at pH 7, with treated PAC and FeCl3 achieving 81.8% and 97.2% COD reduction and 89% and 98% TOC reduction at 360 minutes. These results were supported by the cost analysis in which this system was cost effective manner. This system can offer a solution for the efficient treatment of other types of industrial wastewater and open the door to new applications for water reuse on a broad scale, contributing to global water sustainability.

Synthesis, structure and photocatalytic performance of {[Bi6(tza)5(NO3)2(OH)5O3]·H2O}n and its derivatives

A polynuclear metal-organic framework, {[Bi6(tza)5(NO3)2(OH)5O3]·H2O}n (Htza=1H-tetrazole-1-acetic acid), was successfully synthesized and characterized, and its photocatalytic properties, along with those of its derivatives, were investigated. The crystal structure of the compound was determined to belong to the orthorhombic space group Pn ma, featuring a 3D framework comprising cage-like [Bi6(µ3-O)3(µ3-OH)5]7+ clusters. {[Bi6(tza)5(NO3)2(OH)5O3]·H2O}n demonstrated significant photocatalytic activity with UV light response within the pH range of 6.0–8.0 and a band gap energy of 3.32 eV. Under optimal conditions, a reduction in chemical oxygen demand (COD) and total organic carbon (TOC) (from 126.90 mg/L to 4.57 mg/L) clearly validated the efficient methyl orange degradation. The main active groups in the degradation process were h+, ·O2− and ·OH, and the catalyst demonstrated reusability for up to six cycles. Moreover, it was hydrolyzed to Bi2O2CO3 and BiOCl under alkaline (pH=9.0–11.0) and acidic (pH=1.0–5.0) conditions, respectively, thus serving as a valuable precursor. Notably, the Bi2O2CO3 and BiOCl derivatives exhibited higher catalytic activities than catalysts synthesized using alternative methods under the same experimental conditions. Therefore, within the pH range of 1.0–11.0, {[Bi6(tza)5(NO3)2(OH)5O3]·H2O}n, along with its in situ derivatives BiOCl and Bi2O2CO3, were highly efficient UV light-driven photocatalysts.

The Bioremediation of Industrial Effluents by Phanerochaete chrysosporium: The COD, TOC Removal Efficiency and Biochemical Assessment for Dreissena polymorpha

AbstractBioremediation is one of the cheapest and easy method for biological treatment for most kind of industial wastewater. Bioremediation potential of the Phanerochaete chrysosporium for industrial wastewater from Industrial Zone Wastewater plant in Mardin, Turkey, was evaluated. The chemical oxygen demand (COD) and total organic carbon (TOC) reduction efficiencies of P. chrysoporium of on wastewater studied using biomarkers such as catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), Thiobarbituric Acid (TBARS) and reduced glutathione (GSH) levels in Dreissena polymorpha. The level of TBARS, a marker of lipid peroxidation was found to be high because of wastewater exposure after treatment. TBARS levels decreased (from 20.2 to 31.6 and from 20.8 to 37.5). GSH levels (from 52.3 to 15.9), CAT levels (from, 119.7 to 15.3 and from 91.1 to 13.4) SOD levels (from 3.8 to 0.9 and from 3.4 to 1.2) and GPX activity (from 177.2 to 104.4 and 174.2 to 100.5) decreased in the wastewater exposure groups during 24 and 96th hour compared to the control groups. GSH levels, CAT, SOD and GPX activity increased after treatment by P. chrysosporium. Results indicate that industrial wastewater caused oxidative stress in Dreissena polymorpha. The findings revealed that the highest removal efficiency for COD and TOC, at 86.3 % and 80.3 % respectively, occurred in the 1/20 diluted medium. P. chrysosporium has proven to be effective in the bioremediation of wastewater from the Industrial Zone Changes in biochemical parameters before and after bioremediation showed that antioxidant parameters such as CAT, SOD, GPx activities and GSH and TBARS levels can be used as biomarker to evaluate bioremediation efficiency.

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.

Synthesis and characterization of bi-functional Cu and Ni co-doped ZnO photocatalysts for organic pollutant degradation and antimicrobial activity

The study of visible light active photocatalysts for organic pollutants degradation and antimicrobial activity has gained significant attention in recent years. Herein, we report the synthesis of pure ZnO, Ni-doped ZnO (Ni-ZnO), Cu-doped ZnO (Cu-ZnO), and Cu and Ni co-doped ZnO (CuNi-ZnO) photocatalysts via a facile coprecipitation method. These photocatalyst materials were characterized using various analytical techniques, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscope (HR-TEM), Fourier transform infrared spectroscopy (FTIR), UV–visible spectroscopy (UV–Vis), photoluminescence (PL), and total organic carbon (TOC) analysis. XRD patterns confirm the presence of a mixed phase in the CuNi-ZnO sample. The presence of Cu, Ni, and Zn in CuNi-ZnO was verified through the XPS spectra. The nanoparticle-like morphology of the CuNi-ZnO photocatalyst was confirmed using HRTEM analysis. The FTIR spectra reveal the chemical bonds present in the materials. UV–visible spectroscopy was employed to determine the band gap of the materials, revealing a value of 3.10 eV for CuNi-ZnO. The mitigation in recombination of excited electrons (e−) and holes (h+) in CuNi-ZnO is validated through photoluminescence (PL) studies. The synthesized materials were used for the degradation of Indigo carmine (IC) dye and antimicrobial activity. The results showed that the optimized CuNi-ZnO sample displayed a better visible light photocatalytic performance (93.32 % IC dye degradation efficiency in 60 min) than the other samples. A notable degree of mineralization was observed with a reduction in total organic carbon (TOC) reaching 65.91 %. Additionally, the photocatalyst showed antimicrobial activity against both S. aureus and E. coli. Furthermore, a plausible visible light photocatalytic mechanism was proposed for the degradation of IC dye using the CuNi-ZnO photocatalyst.