Fenton's Reagent Research Articles

Source identification, characteristics, and spatial distribution of airborne microplastic deposition in Lahore City, Pakistan.

A large volume of atmospheric microplastics (MPs) has been observed worldwide and is considered an emerging global environmental issue. Nevertheless, no significant assessment of the atmospheric deposition of MPs in Pakistan has been reported yet. The present study was designed to highlight the source, type, and spatial distribution of MPs in atmospheric fallout in Lahore, Pakistan. A total of 23 sites were sampled in Lahore with a heterogeneous background of human activities. All samples were collected in a box with a one-foot depth fitted with a steel tray of 0.1 m2 at the bottom. Fenton's reagent and hydrogen peroxide were used to remove organic matter, and sodium chloride for density separation, while the MPs were quantified through a stereomicroscope, and polymers were identified through ATR-FTIR spectroscopy. The highest deposition rate (particles/m2/day) was observed at Badami Bagh, i.e., 6819, followed by Mall Road 4414, and Chung 4263, while the lowest was in Sabzazaar (i.e., 524) and Township (1047) with an average deposition rate of 2340 ± 1392. Among the MPs, the major portion was fiber, i.e., 96%, while fragment was 1.9%, sheets 0.78%, foams 1.12%, beads 0.04%, and other MPs 0.06%. At all sampling sites, 20 different types of polymers were identified with different percentages, of which polyester fibers were predominant with an abundance of 96.09% associated with clothes and textiles. A high frequency of MPs was found in populated areas with dense traffic, plastic wastes, household plastic materials, and mismanagement of wastes, which accelerates the atmospheric deposition of airborne microplastics. Evaluation and characterization of MP help assess health and environmental impacts, cleanup efforts, and guiding regulations. It also provides valuable information for waste management innovation to reduce plastic pollution.

A High-Methanol-Permeation Resistivity Polyamide-Based Proton Exchange Membrane Fabricated via a Hyperbranching Design.

Four non-fluorinated sulfonimide polyamides (s-PAs) were successfully synthesized and a series of membranes were prepared by blending s-PA with polyvinylidene fluoride (PVDF) to achieve high-methanol-permeation resistivity for direct methanol fuel cell (DMFC) applications. Four membranes were fabricated by blending 50 wt% PVDF with s-PA, named BPD-101, BPD-102, BPD-111 and BPD-211, respectively. The s-PA/PVDF membranes exhibit high methanol resistivity, especially for the BPD-111 membrane with methanol resistivity of 8.13 × 10-7 cm2/s, which is one order of magnitude smaller than that of the Nafion 117 membrane. The tensile strength of the BPD-111 membrane is 15 MPa, comparable to that of the Nafion 117 membrane. Moreover, the four membranes also show good thermal stability up to 230 °C. The BPD-x membrane exhibits good oxidative stability, and the measured residual weights of the BPD-111 membrane are 97% and 93% after treating in Fenton's reagent (80 °C) for 1 h and 24 h, respectively. By considering the mechanical, thermal and dimensional properties, the polyamide proton-exchange membrane exhibits promising application potential for direct methanol fuel cells.

Purification and tailored functionalities in detonation nanodiamond

Abstract Nanodiamonds (NDs) offer immense potential in various fields, but graphitic or metal-based impurities hinder their widespread adoption. Conventional purification methods often employ harsh chemicals or high temperatures, raising concerns about ND integrity and surface properties. Herein, we compared various strategies to purify and tailor the surface functional groups in the detonation-derived NDs. A facile 2-step purification strategy combining salt-assisted air oxidation (SAAO) and Fenton chemistry is particularly interesting for efficient and selective removal of graphitic impurities while preserving the diamond lattice structure. SAAO selectively burns off graphitic impurities at 450 °C under controlled oxygen flow, minimizing damage to the diamond core. Subsequently, Fenton's reagent (H2O2/Fe2+) introduces hydrophilic functional groups onto the ND surface, further enhancing diamond purity and promoting subsequent functionalization. This synergistic approach enables (i) highly efficient removal of graphitic impurities while preserving ND morphology and crystal structure, (ii) controlled introduction of surface functionalities, and (iii) improved colloidal stability of purified NDs. This green and efficient purification protocol is beneficial for tailoring ND properties and unlocking their full potential in diverse applications ranging from biomedicine and electronics to catalysis and quantum technologies.

Degradation of Procion Golden Yellow H-R Dye Using Ultrasound Combined with Advanced Oxidation Process

The current study aims to degrade Procion Golden Yellow H-R through ultrasound-induced cavitation coupled with various oxidants. A comprehensive investigation was conducted to examine the impact of parameters, specifically pH, power, and frequency, on the extent of degradation. The primary aim was to optimize degradation by solely utilizing a cavitation reactor where only 23.8% degradation was observed under the established optimum conditions of pH 2.5, frequency of 22 kHz, and power of 200 W. The investigation of the combined process of cavitation with H2O2, Fenton reagent (H2O2/Fe2+), NaOCl, and potassium persulphate (KPS) was subsequently conducted under optimized conditions. The combined operations greatly enhanced degradation with the use of H2O2 loading of 0.1 g/L leading to 53.3% degradation and the H2O2/Fe2+ ratio of 1:0.25 resulting in 94.6% degradation, while the NaOCl quantum of 0.075 g/L yielded 90% degradation and the KPS quantity of 2 g/L resulted in 97.5% degradation in the specific combinations. A toxicity test on two bacterial strains, Staphylococcus aureus and Escherichia coli, was carried out using the original dye solution and after treatment. The various individual and combination processes were compared using the parameters of cavitational yield and total treatment cost. The study elucidates that combining ultrasonic cavitation with KPS is an effective method for treating wastewater containing Procion Golden Yellow H-R dye, especially when implemented at a larger scale of operation.

Innovating Ferro-sonication approach for extracting microplastics from wastewater

For accurate and reliable analysis of microplastics (MPs) in wastewater (WW), it is imperative to comprehend the significance of pre-treating WW before analysis. The suspended solids (SS) in the matrix tend to adhere to the MPs during filtration, which interferes with the detection of the MPs. In this regard, the present study aims to develop and optimize a pretreatment method to improve the extraction efficiency of MPs from WW by reducing the SS. A combination of the Fenton reaction and ultrasonication, ferro-sonication (Fe-UlS), was proposed to digest and eliminate the SS from WW. This hybrid pretreatment, Fe-UlS, was optimized for ultrasonication amplitude, treatment time, and hydrogen peroxide dose using response surface methodology (RSM) with a Box-Behnken design, achieving a desirability of 0.984. The optimum conditions for the Fe-UlS, such as the (1:1) Fenton reagent ratio (0.05 M FeSO4: 30 % H2O2), ultrasonication amplitude (31 %), and total process time (30 min) were found to be statistically significant (p < 0.05). The developed method was then employed for the extraction of spiked polyethylene (PE), polypropylene (PP) and polyethylene terephthalate (PET) MPs in real WW and found efficient in removing 83 % of the TSS present in the primary influent were in 30 min at a temperature of 45 °C. Also, the method did not affect the physio-chemical characteristics of the MPs; however, the thermal analysis of PE and PP MPs showed a statistically significant decrease in the melting temperature, as proven by paired t-test analysis. Further, a non-targeted liquid chromatography-mass spectrometry (LC-MS) analysis proved that Fe-UlS is a stable process, as it did not cause any leaching of MPs under the optimum pretreatment conditions. Finally, Laser Direct-Infrared Imaging (LD-IR) analysis was conducted to validate the developed Fe-UlS pretreatment approach for MP analysis in real WW. About 3434 MPs were detected in 100 mL of WW primary influent, within the size range of 9 to 500 μm. This hybrid pretreatment approach not only streamlines WW sample processing but also reduces the required concentration of Fenton reagent and processing time, yielding accurate and reliable results for monitoring MPs in WW.

A comparative study on the influences of sulfonated- and phosphorated-graphene oxide on polyvinylidene fluoride cation-exchange membranes for electrodialysis

The –SO3H and –PO3H2 groups were grafted on graphene oxide (GO) by adding sulfuric acid and phosphoric acid at the same weight percentage, respectively. The physicochemical properties of the sulfonated GO (SGO) and phosphorated GO (PGO) were compared using different techniques. SGO and PGO were individually incorporated into the PVDF matrix (at the same wt%) to compare their effects on the properties of the resulting PVDF/SGO and PVDF/PGO cation-exchange membranes (CEMs). Membranes' characteristics including ionic conductivity and water content, area resistance, and the rate at which Na+ ions diffuse throughout the membranes changed considerably by altering the type of ion exchange sites, and more desirable values were obtained using PGO. Nevertheless, PVDF/SGO provided an ion exchange capacity (IEC) of 5.5 meq g−1, while it was about 1.7 times lower than PVDF/PGO (9.4 meq g−1). It also provided a promising ionic conductivity (17.24 mS cm−1), transport number (93.65 %), permselectivity (89.58 %), and low area resistance (2.7 Ω cm2), which exceeded those of the commercial CEMs such as Ralex. Moreover, PVDF/SGO exhibited desirable mechanical characteristics, and a low weight loss (2.4 %) and low resistance change (22.2 %) after 9 h being submerged in the Fenton reagent, however, these parameters were better for PVDF/PGO.

An “all-in-one” and confined self-enhancing Fenton-like membrane reactor for multiple antibiotic treatment in aquatic environment at natural pH

Conventional Fenton oxidation technique utilized for the treatment of antibiotics is plagued by issues such as extra H2O2 requirement and harsh reaction conditions. In this work, an “all-in-one” membrane reactor with H2O2 self-supply and self-catalysis at natural pH conditions for multiplex antibiotic residues degradation was developed by loading bifunctional composite Pt/CuO2 Janus nanoparticles (Pt/CuO2 JNPs) on the surface of the PVDF membrane. Specifically, the Fenton reagents H2O2, which was generated from the decomposition of the functional material CuO2 NPs in a near natural pH condition without extra addition, was synergistic activated by nano-enzyme Pt NPs and Cu2+. This, in turn, greatly improves the practicability of the reactor. Notably, the large number of nanopores present on the surface of the reactor endows it with a confined self-enhancing effect, which could greatly improve its catalytic degradation efficiency of antibiotics. The developed membrane reactor is capable of degradation 97.6 % of chloramphenicol (CAP) residues after several cycles of filtration. The apparent rate constant of the developed membrane reactor for CAP is approximately folded for the bulk reaction system. What’s more, the developed membrane reactor features favorable usability and preservability and superior universality for common antibiotics.

Injectable Dual Fenton/Enzymatically Cross-Linked Double-Network Hydrogels Based on Acrylic/Phenolic Polymers with Highly Reinforced and Tunable Mechanical Properties.

Injectable hydrogels have been extensively used as promising therapeutic scaffolds for a wide range of biomedical applications, such as tissue regeneration and drug delivery. However, their low fracture toughness and brittleness often limit their scope of application. Double-network (DN) hydrogel, which is composed of independently cross-linked rigid and ductile polymer networks, has been proposed as an alternative technique to compensate for the weak mechanical properties of hydrogels. Nevertheless, some challenges still remain, such as the complicated and time-consuming process for DN formation, and the difficulty in controlling the mechanical properties of DN hydrogels. In this study, we introduce a simple, rapid, and controllable method to prepare in situ cross-linkable injectable DN hydrogels composed of acrylamide (AAm) and 4-arm-PPO-PEO-tyramine (TTA) via dual Fenton- and enzyme-mediated reactions. By varying the concentration of Fenton's reagent, the DN hydrogels were rapidly formed with controllable gelation rate. Importantly, the DN hydrogels showed a 13-fold increase in compressive strength and a 14-fold increase in tensile strength, compared to the single network hydrogels. The mechanical properties, elasticity, and plasticity of DN hydrogels could also be modulated by simply varying the preparation conditions, including the cross-linking density and reagent concentrations. At low cross-linker concentration (<0.05 wt %), the plastic DN hydrogel stretched to over 6,500%, whereas high cross-linker concentration (≥0.05 wt %) induced fully elastic hydrogels, without hysteresis. Besides, DN hydrogels were endowed with rapid self-recovery and highly enhanced adhesion, which can be further applied to wearable devices. Moreover, human dermal fibroblasts treated with DN hydrogels retained viability, demonstrating the biocompatibility of the cross-linking system. Therefore, we expect that the dual Fenton-/enzyme-mediated cross-linkable DN hydrogels offer great potential as advanced biomaterials applied for hard tissue regeneration and replacement.

Study on the treatment of oil production wastewater by corona discharge coupling Fenton reagent

As the main by-product of oil production, oil production wastewater has the characteristics of high organic content and poor biodegradability, which makes the low temperature plasma wastewater treatment technology get new development. The Ground electrode atomization negative corona discharge（GEANCD） technology increases the discharge current on the basis of traditional corona discharge, but the uneven atomization of liquid is a key challenge at present, which will have a great impact on the degradation of wastewater pollutants. In this study, the GEANCD reactor was redesigned and a self-developed spiral wire hole electrode (SWHE) was used to replace the conventional wire electrode (WE). The discharge characteristics of the reactor under the two electrode structures were investigated and the optimal discharge parameters were determined. Under the optimum discharge parameters, the treatment effect of the two electrode structures with or without coupling Fenton reagent on oil production wastewater was also compared. The experimental results show that under the optimal discharge parameters of flow rate of 25 mL/min, plate electrode distance of 50 mm and discharge voltage of 14 kV, the reactor equipped with SWHE has higher discharge current, and the treatment effect of oil production wastewater is better when coupled with Fenton reagent.

Analysis of factors influencing on Electro-Fenton and research on combination technology (II): a review.

The principle of Fenton reagent is to produce ·OH by mixing H2O2 and Fe2+ to realize the oxidation of organic pollutants, although Fenton reagent has the advantages of non-toxicity and short reaction time, but there are its related defects. The Fenton-like technology has been widely studied because of its various forms and better results than the traditional Fenton technology in terms of pollutant degradation efficiency. This paper reviews the electro-Fenton technology among the Fenton-like technologies and provides an overview of the homogeneous electro-Fenton. It also focuses on summarizing the effects of factors such as H2O2, reactant concentration, reactor volume and electrode quality, reaction time and voltage (potential) on the efficiency of electro-Fenton process. It is shown that appropriate enhancement of H2O2 concentration, voltage (potential) and reaction volume can help to improve the process efficiency; the process efficiency also can be improved by increasing the reaction time and electrode quality. Feeding modes of H2O2 have different effects on process efficiency. Finally, a considerable number of experimental studies have shown that the combination of electro-Fenton with ultrasound, anodic oxidation and electrocoagulation technologies is superior to the single electro-Fenton process in terms of pollutant degradation.

Experimental and DFT studies on using Fenton reagent as oxidant to enhance the leaching of cuprite in sulfuric acid system

The utilization of a Fenton reagent was implemented within this investigation to facilitate the oxidation of cuprite with the purpose of enhancing its leaching efficacy in sulfuric acid. The concentration of 0.007 mol/L Fenton reagent increased the extraction rate of cuprite from 69.43 to 91.53 %, which increased by 22.1 %. The XPS, AFM, SEM–EDS, and ToF-SIMS results showed that the leaching process of cuprite significantly enhanced its oxidation and the conversion of Cu(I) species to Cu(II) species by the Fenton reagent；Electrochemical tests revealed that as the concentration of the Fenton reagent increased, the strength of the oxidation reaction increased. After the adsorption of hydroxyl radicals (•OH) onto the cuprite surface, the population of Cu12-O12 decreased notably from 0.45 to 0.26, concomitantly with an expansion in bond length from 1.824 Å to 1.930 Å. As the population of Cu12-O7 decreased from 0.39 to 0.05, the bond length exhibited a notable increase from 1.849 Å to 2.241 Å. The findings indicated that following the adsorption of •OH on the cuprite (111) surface, structural instability ensued. The EPR test confirmed that the introduction of Fenton reagent into the reaction system generated •OH. Simultaneously, with the extension of reaction time, the concentration of •OH in the system decreased, resulting in a reduction of the signal peak intensity.

First-ever study uncovers microplastic contamination in Nepalese table salt

Despite numerous studies on microplastic contamination in table salt worldwide, research focusing on Nepalese table salts is remarkably lacking. This study aims to address this gap by investigating microplastic contamination in salt samples collected from all seven provincial zones of Nepal. Our objective is to comprehensively assess the presence and characteristics of microplastics in salt sold within local markets across the country. Five salt packaging companies utilized by Nepalese consumers were identified. The collected salt samples were digested with Fenton's reagent to extract microplastics, which were then observed under a digital microscope. Using an OMAX stereomicroscope at 30× magnification and an OMAX A3503S digital camera, each microplastic was carefully identified and quantified. FTIR analysis was conducted to identify the polymer types. All tested salt samples (100 %) from both Nepalese and Indian packaging companies contained microplastics. Microplastic abundance exhibits variability among the samples, ranging from 80 to 1040 microplastics per kilogram of salt. The average value stands at 381 ± 219 microplastics per kilogram of salt sample. The distribution of microplastic concentrations within the salt samples reveals that the majority fall within the 301–400 microplastics per kilogram salt range, constituting 33 % of the total samples. Color analysis showed diverse contamination sources, while microplastic shapes included fibers (56 %), films (17 %), fragments (16 %) and pellets (11 %). Polymer type analysis confirmed the presence of polyethylene and polypropylene in tested microplastics. The study estimated that Nepalese individuals ingest an average of 1853 microplastics annually, indicating significant exposure from salt consumption. Surprisingly, factors such as storage conditions, date of salt packaging and thickness of packaging material did not significantly affect microplastic presence in the samples, suspecting manufacturing processes as the primary contributors to contamination. Therefore, the raw materials and purification practices for salt need improvement, as existing methods are insufficient to eliminate microplastics. These findings emphasize the need for further research and mitigation efforts to address microplastic contamination in Nepalese salt and its potential health impacts.

Degradation of reactive violet 1 using innovative approach of hydrodynamic cavitation coupled with oxidants

The study explores use of hydrodynamic cavitation and various oxidants for treating wastewater containing Reactive Violet 1 dye. Study of impact of operational variables demonstrated that most favorable conditions for maximum degradation of 70.9 % were pH of 2.5, pressure of 4 bar, and use of dual slit venturi. When the optimized conditions were employed in combination with hydrogen peroxide (75 ppm i.e. 2.2 mM as optimum loading), Fenton reagent (H2O2/Fe2+ ratio of 1:0.125), KPS (100 ppm i.e. 0.037 mM) and NaOCl (100 ppm i.e. 1.343 mM), enhanced degradation as 93.7 %, 97.5 %, 92.3 % and 85.1 % respectively were seen. The decolorization of the dye exhibited second-order kinetics in each approach. Analysis for toxicity assessment, cavitational yield and treatment cost, elucidated that HC + Fenton method is the most effective giving 97.5 % of degradation at an operating cost of 1.78 Rs/L (0.021 $/L) within 30 min treatment.

Targeting Bacterial Persisters via Reactive Oxygen Species‐Generating Hydrogel Microspheres

AbstractThe presence of bacterial persisters is a key factor contributing to chronic infection. However, no effective treatment methods are currently available. Thus, a platform is developed, called reactive oxygen species (ROS) bomb, based on microenvironment‐adaptive hydrogel microspheres, to oxidize the cell membranes of persisters in chronic periprosthetic joint infection (PJI). Fenton reagent hydroxy iron oxide (FeOOH) and a glucose oxidase (GOx)/calcium phosphate (CaP) acid‐responsive shell are sequentially induced on the surface of mesoporous polydopamine (PDA) nanoparticles by the PDA‐mediated ion precipitation and interfacial adhesion, followed by the coloaded with glucose into microfluidic hyaluronic acid hydrogel microspheres. Hydroxyl radicals are explosively generated through GOx‐mediated glucose oxidase, H2O2 production, and its Fenton‐like reactions with FeOOH, which also benefit from the weakly acidic microenvironment around persisters, result in the destruction of bacterial cell membrane, and subsequent overflow of cellular contents such as dsDNA, proteins, and K+. The bactericidal rates of methicillin‐resistant Staphylococcus aureus and Staphylococcus epidermidis persisters are up to 99.14% and 98.96%, and the bacterial loads in lesion location are significantly decreased after ROS bombs treated, effectively alleviated the inflammation and bone resorption damage. This work provides a new strategy toward persisters clearance and shows great application potential in other chronic infection‐related diseases.

Investigating the Removal Efficiency of Fenton Reaction for Drugs in Municipal Wastewater

AbstractDrugs and their metabolites have become new types of pollutants, the presence of which constitutes a serious environmental problem. This article applies the established LC–MS/MS method to investigate the removal efficiency of different ratios of Fenton reagents for common drugs in wastewater. The results showed that the linearity of the 10 common drugs was good in the dynamic range of 1–100 ng/L, and the R2&gt;0.99. The LODs and LOQs ranged from 0.01–0.443 ng/L and 0.04–1.44 ng/L, respectively. The average relative recoveries ranged from 72.99–117 %. In addition, considering the economic and application effects of chemical reagents, the optimal test dose of H2O2 in Fenton reagent was determined to be 12.5 mL. This experiment provides a simple, rapid and low‐cost LC–MS/MS method for the detection of drugs in wastewater. It also provides data reference for effective management of drug production sites and domestic wastewater pollution.

Fenton-reactive groundwater circulation well for groundwater remediation of a toluene-contaminated site

ABSTRACT In order to improve the remediation efficiency of the groundwater circulation well (GCW) on toluene-contaminated soil, we used a combination of GCW and Fenton reagent for remediation. Taking a toluene-contaminated site in Suzhou City, Jiangsu Province, China, as an example, Fenton reagent with a molar ratio of H2O2/contaminant = 10:1 and H2O2/Fe2+ = 2:1 was added to GCW at an aeration rate of 0.005 m3/s. After 216 h of remediation, the toluene concentrations at the site were reduced to the remediation target values. In this study, the Fenton reagent was rapidly delivered to the influence radius of GCW, which reduced the time required for remediation and provided a new model for the application of GCW.

Evaluation of an Electrocoagulation Process Modified by Fenton Reagent

This article is oriented to the degradation of nickel in an ionic state at laboratory level from synthetic water made with nickel sulfate, using the electrocoagulation process with aluminum cathodes and modifying this process by the addition of the Fenton reagent, which results from the combination of hydrogen peroxide (H2O2) and ferrous sulfate (FeSO4) being this reagent a catalyst and oxo-coagulant agent, The efficiency of this reagent will be compared with the typical treatment with aluminum sulfate, which is a typical process based on ion exchange/coagulation at the same percentage concentrations as the Fenton reagent. For this purpose, the optimum conditions of the advanced electrocoagulation process were determined, which consisted of determining the concentrations of Fenton’s reagent at concentrations of 150 ppm, 300 ppm, and 450 ppm, in addition to the operating variables such as pH of 8 and 10, voltage of 17.5 V and 19 V and their reaction time, which were compared with aluminum sulfate at 300 ppm, 600 ppm, and 900 ppm. The results obtained with respect to the typical treatment were 0% nickel degradation. However, with the advanced oxidation treatment, an average reduction of 97.5% was found at the conditions of 19 V, pH 10, and Fenton 150 ppm in a time of 30 min.

Highly Crystalline Copper Aluminum-Layered Double Hydroxides with Intrinsic Fenton-Like Catalytic Activity for Robust Oral Health Management.

As the main challenge of dental healthcare, oral infectious diseases are highly associated with the colonization of pathogenic microbes. However, current antibacterial treatments in the field of stomatology still lack a facile, safe, and universal approach. Herein, we report the controllable synthesis of copper aluminum-layered double hydroxides (CuAl-LDHs) with high Fenton-like catalytic activity, which can be utilized in the treatment of oral infectious diseases with negligible side effects. Our strategy can efficiently avoid the unwanted doping of other divalent metal ions in the synthesis of Cu-contained LDHs and result in the formation of binary CuAl-LDHs with high crystallinity and purity. Evidenced by experimental and theoretical results, CuAl-LDHs exhibit excellent catalytic ability toward the ·OH generation in the presence of H2O2 and hold strong affinity toward bacteria, endowing them with great catalytic sterilization against both Gram-positive and Gram-negative bacteria. As expected, these CuAl-LDHs provide outstanding treatments for mucosal infection and periodontitis by promoting wound healing and remodeling of the periodontal microenvironment. Moreover, toxicity investigation demonstrates the overall safety. Accordingly, the current study not only provides a convenient and economic strategy for treating oral infectious diseases but also extends the development of novel LDH-based Fenton or Fenton-like antibacterial reagents for further biomedical applications.

Comparative study on graphene oxide and sulfonated graphene oxide reinforced polyethersulfone-based cation-exchange membrane

In this research, polyethersulfone/sulfonated graphene oxide (PES/SGO) heterogeneous cation exchange membranes were fabricated by the mold casting method. The sulfonation of GO was carried out using the diazonium salt of sulfanilic acid. The properties of the synthesized GO and SGO were compared in terms of chemical structure, morphology, surface charge, crystallinity, and thermal stability. The variations in surface morphology and roughness, hydrophilicity, dimensional stability, and ionic conductivity of the PES-based membranes as a function of GO and SGO content were investigated. Results revealed that SGO enjoyed a higher level of oxygenated groups contributing to its higher surface charge. SGO also tolerated a higher temperature before being fully decomposed due to the presence of the sulfur-containing groups. A finer nanostructured morphology was observed in the SGO-containing membranes, resulting in a considerably lower surface roughness of these membranes than the corresponding GO-based membranes. The membrane comprising 10 wt% SGO showed the lowest surface roughness of 88 nm, and the highest water uptake of 16.66 %, ion-exchange capacity of 1.12 meq g-1, and the lowest charge transfer resistance of 3.6 Ω and area resistance of 0.9 Ωcm2. This was accompanied with a considerable increment in the permselectivity and cation (Na+) transport number of this membrane to 95.9 % and 97.5 %, respectively, due to the higher surface adhesion energy of 94.57 J m-2 and higher Na+ flux of 4.43×10-7 mol m-2 s-1, which were significantly higher than that obtained for the corresponding PES-based membrane containing 10 wt% GO. Furthermore, a lower weight loss and resistance change were observed for PES/SGO after being exposed to the Fenton reagent for 9 h, indicating the impact of the sulfonated groups on the oxidative stability enhancement of the membrane.

Unintended polyhalogenated carbazole production during advanced oxidation of coking wastewater

Polyhalogenated carbazoles (PHCZs) are emerging as dioxin-like global pollutants, yet their environmental origins are not fully understood. This study investigates the application of the Fenton process in coking wastewater treatment, focusing on its dual role in carbazole removal and unintended PHCZ formation. The common halide ions (Cl– and Br–) in coking wastewater, especially Br– ions, exerted a notable impact on carbazole removal. Particularly, the influence of Br– ions was more significant, not only enhancing carbazole removal but also shaping the congener composition of PHCZ formation. Elevated halide ion concentrations were associated with the heightened formation of higher halogenated carbazoles. The Fenton reagent dosage ratio was identified as a crucial factor affecting the congener composition of PHCZs and their toxic equivalency value. The coexisting organic substance (i.e., phenol) in coking wastewater was observed to inhibit PHCZ formation, likely through competitive reactions with carbazole. Intriguingly, ammonium (NH4+) facilitated the generation of higher and mixed halogenated carbazoles, possibly due to the generation of nitrogen-containing brominating agents with stronger bromination capacity. This study underscores the importance of a comprehensive assessment, considering both substrate removal and potential byproduct formation, when employing the Fenton process for saline wastewater treatment.