Oxidation Of Bisphenol A Research Articles

Revealing the essence of anion ligands in regulating amorphous MnOx to activate peracetic acid for micropollutant removal

How the anion ligands of manganese precursors affect the catalytic activity of amorphous manganese oxides (MnOx) in Fenton-like process is poorly understood. Here, five amorphous MnOx synthesized by Mn(II) precursors with different ligands were characterized and adopted to activate peracetic acid (PAA) for bisphenol A (BPA) degradation. Although > 90 % BPA removal was achieved in the five MnOx/PAA processes via both adsorption and oxidation, the oxidation kobs greatly differentiates by the ligands types with the order of MnOx-N > MnOx-S > MnOx-Cl > MnOx-AA > MnOx-OA. Ligands types would affect the specific surface area of MnOx and their ability to adsorb BPA, however which is not the decisive factor in determining the contaminant oxidation efficiency. Multiple experimental results indicate that the generation of oxygen vacancies induced by the ligands alters the Mn(III)/Mn(IV) ratio, ultimately contributing to the different efficiency of BPA oxidation driven by the direct electron transfer mechanism. Moreover, amorphous MnOx holds the promise of practical applications in catalytic PAA of various micropollutants with good stability. This study advances the fundamental understanding of ligand-regulated amorphous MnOx-catalyzed PAA process.

Periodate activation with polyaniline-derived carbon for bisphenol A degradation: Insight into the roles of nitrogen dopants and non-radical species formation

Periodate-based advanced oxidation processes (PI-AOPs) activated by carbon catalysts have shown promising application prospects in the removal of emerging contaminants. Herein, a series of N-doped carbon catalysts (NC) were prepared by in-situ pyrolysis of N-containing polymers (polyaniline) to unveil the potential mechanism of N dopants on PI activation. The optimized sample NC700 showed a satisfying degradation performance, achieving 100 % removal of bisphenol A (BPA) at a concentration of 10 mg/L within 90 min in the presence of 0.1 mM PI. The impacts of various N types on PI activation were systematically investigated by dynamic fitting and density functional theory computations. These analyses highlighted the crucial role of graphitic N configuration on carbon surface, which exhibited the highest adsorption energy and a positive correlation with the normalized degradation efficiency. The chemical quenching experiments and electrochemical experiments confirmed that the BPA oxidation mechanism was primarily mediated electron transfer by [NC-PI]* complex, with singlet oxygen (1O2) /superoxide radicals (O2•–) playing a supplementary role. In situ ATR-SERAS measurement strengthened the understanding of PI activation by carbon catalyst based on electron transfer pathway. Owing to the non-radical oxidation mechanism, the NC/PI system had a broad pH adaptability and great anti-interference ability against typical wastewater components. This study provides mechanistic insights into the carbon-driven PI activation process for wastewater treatment, advancing the practical application of PI-AOPs.

Role of quercetin in permanganate oxidation of bisphenol A: Kinetics and mechanism

Potassium permanganate (Mn (VII)) oxidation, a green advanced oxidation technology, is widely used as an in-situ remediation method for groundwater contamination. Based on the complexity of organic substances in aquatic environments, many novel organic components, whose processes and mechanisms affecting the oxidative efficacy of Mn (VII), remain unknown and need to be studied systematically. Therefore, using the reducing macromolecular quercetin as the organic matter, the efficiency and mechanism of quercetin-bound, low-valent Mn enhanced Mn (VII) oxidation of bisphenol A (BPA) were studied. The pH and concentration of quercetin strongly influenced its performance. Under pH 4.0–6.0, quercetin evidently promoted the BPA degradation rate in the Mn (VII)/quercetin (Mn (VII)/Q) system. However, the presence of quercetin had little effect on the degradation efficiency of Mn (VII) at pH ≥ 7.0. This study found that at pH 4.0–5.0, quercetin could act as both a reductant and complexing ligand in the process of BPA oxidation. As a complexing ligand, quercetin stabilized the intermediate states of Mn (III) to form complexes. These stable complexes could efficiently oxidize BPA. While low concentrations of quercetin were insufficient to complex and stabilize Mn (III), Mn (III) was reduced to Mn (II). Mn (II) then reacted with Mn (VII) to form MnO2, enhancing the degradation efficiency of the Mn (VII)/Q system for BPA through its catalytic and oxidative properties. This study provides a better understanding of the degradation of organic pollutants by KMnO4 in groundwater treatment.

Multi-win situation of wastewater purification, carbon emission reduction and resource utilization: Conversion of refractory organics and nitrate to urea and ammonia in a flow-through electrochemical integrated system

The advanced oxidation process is an efficient technology for the degradation and detoxification of refractory organics to ensure water safety. However, most researches focus on improving pollutant degradation but overlook carbon emission and resource utilization. In this study, a flow-through electrochemical integrated system was constructed to simultaneously realize bisphenol A (BPA) oxidation into small non-toxic organics and CO2, and generated CO2 coupled with nitrate-containing wastewater conversion to urea and ammonia on a porous cathode (Zr-Fe/CN). The synergistic effect between anodic BPA oxidation with cathodic CO2 and NO3−reduction improves the electron utilization efficiency and thus increasing the BPA degradation, urea yield rate (UYR) and NH3 yield rate (NYR) by 13.4 % 18.4 % and 8.3 %, respectively. Furthermore, the flow-through operation mode significantly increased the mass transfer efficiency and quickly carried generated CO2 from the anode into the cathode to improve CO2 utilization efficiency. Compared to the parallel plate electrode reactor, the BPA degradation efficiency, UYR and NYR in the flow-through reactor increased from 59.46 % to 84.49 % (the initial concentration of BPA was 40 mg/L), 9.94 mmol h−1g−1 to 19.55 mmol h−1g−1, and 80.31 mmol h−1g−1 to 106.06 mmol h−1g−1 within 60 min, respectively. Moreover, the total carbon conversion efficiency (from BPA to urea) increased from 20.2 % to 42.4 % and the total Faraday efficiency (FE) increased from 78.6 % to 96.3 %. This work provides a multi-win strategy of harmless, resource-based and carbon emission reduction for wastewater treatment.

Selective degradation of pollutants in the Mn-NG/PMS system: The crucial role of surface reactive Mn(IV) species

The combination of transition metal oxides with carbon-based materials is a promising strategy for constructing efficient catalysts for peroxymonosulfate (PMS) activation to degrade aqueous organic contaminants. However, the complex heterostructure of the composites often hinders the identification of the actual reactive species responsible for pollutant degradation. In this study, we integrate Mn3O4 into N-doped graphite (NG) to elucidate the mechanisms involved in the Mn-NG composite mediated PMS activation process. The Mn-NG/PMS system shows excellent performance in oxidizing bisphenol A (BPA) over a wide pH range (3.4 to 9.4) and in the presence of co-existing substrates. Mn sites in Mn3O4 are responsible for the activation of PMS, and the NG matrix enhances the dispersion of Mn in the Mn-NG composite. Multiple experimental results indicate that free radicals (i.e., hydroxyl radicals (HO•) and sulfate radicals (SO4•−)) are not generated, and surface reactive Mn(IV) is proposed as the primary reactive species for BPA oxidation. This study provides new insights into understanding the role of Mn oxides in carbon-based composites in PMS activation for degradation of organic pollutants.

One-step electrochemical preparation of platinum nanoparticle decorated self-healing reduced graphene oxide three-dimensional nanoarray for portable detection of bisphenol A

Highly selective and sensitive analysis of bisphenol A (BPA) in many plastic products remains its significance. We explored a simple, highly sensitive, and inexpensive electrochemical sensor based on a self-healing three-dimensional nanoarray (3DN) via a single-step electrochemical preparation of both platinum nanoparticles (PtNPs) and reduced graphene oxide (rGO) on a glassy carbon electrode for the portable detection of bisphenol (BPA) in plastic bottled waters. The structure of PtNPs/3DNrGO was confirmed by electron microscope and spectroscopic characterization. Electrochemical characteristics indicated that PtNPs/3DNrGO could decrease the oxidation overpotential due to the self-healing effect of the physical interaction between PtNPs and hydroxyl groups of rGO with an increase in the active surface area. The PtNPs/3DNrGO exhibited remarkably efficient electrocatalytic performance for the oxidation of BPA. The PtNPs/3DNrGO sensor for BPA demonstrated a wide linear range from 0.7 to 20 µM with a low limit of detection of 6 nM (S/N = 3) and effective performance including high sensitivity, high repeatability, and excellent selectivity. The developed sensor had been effectively implemented to assess BPA in plastic samples with desirable impacts. The interaction mechanism of both PtNPs and rGO was inferred by density functional theory. The proposed electrochemical sensor enabled the development of a portable, low-cost, and user-friendly monitoring of water quality, which will offer theoretical support for environmental monitoring.

Enhanced mineralization of bisphenol A by electric arc furnace slag: Fenton-like oxidation

Bisphenol A (BPA) aqueous solution was treated through a heterogeneous Fenton-like oxidation process with electric arc furnace slag (EAFS), a waste product from an Argentinian steel processing plant, as the catalyst. SEM/EDS, XRD, and Mössbauer spectroscopy characterization revealed a significant presence of Fe and minor amounts of Cu and Mn in EAFS, known to play active roles in the Fenton-like reactions. The predominant crystalline form of iron in EAFS was magnesiowüstite, accompanied by minor amounts of hematite, magnetite, maghemite, and metallic iron. Batch Fenton-like oxidation experiments were conducted under acidic conditions (pH 2.8–3), examining the effect of temperature (25, 50, and 70 °C) and catalyst load (0.1, 0.5, and 1 g/L) on BPA degradation and mineralization over 180 min. BPA was completely degraded within the first minutes, while mineralization levels improved from 40% to an outstanding 70% as the temperature increased from 25 to 70 °C. The catalyst gradually lost its activity after five cycles at 25 °C, but raising the temperature up to 70 °C allowed maintaining mineralization levels between 70 and 50% over ten cycles. The oxidation process involved a combined Fenton-like homogeneous/heterogeneous mechanism, and deactivation was linked to a lower leaching of active cations over the cycles, reduction of the Fe(II)/Fe(III) ratio in the iron phases, and blocking of active sites by adsorption of reaction intermediates. EAFS demonstrated an exceptional performance in the Fenton-like oxidation of BPA. The utilization of this type of industrial waste materials represents a promising technological alternative that could benefit both steel processing and water treatment plants.

Integrating detection and degradation of bisphenol A by photocatalytic fuel cell-driven photoelectrochemical sensor

To ensure food safety and environmental protection, it is crucial to rapidly identify and remove bisphenol A (BPA), a plasticizer commonly used in the inner lining of food containers and beverage packaging. Here, a photocatalytic fuel cell (PFC)-integrated self-powered photoelectrochemical (PEC) sensor is constructed. Unlike conventional single PEC or PFC sensors, this PFC-integrated PEC sensor relies on not only the difference in Fermi energy levels between photoanode and photocathode but also charge accumulation resulted from the oxidation of BPA by photogenerated holes. Consequently, this sensor achieved a remarkable maximum output power (Pmax) of 8.58 μW cm−2, as well as a high sensitivity, wide linear detection range (0.1–200 μM), low detection limit (0.05 μM), great stability, reproducibility, and real sample detection capability. This work integrates PFC and PEC technologies successfully for the rapid identification and efficient removal of BPA.

Eco-friendly fabrication of silver nanoparticle-decorated electrodes for aqueous bisphenol A sensing

This work fabricated an electrochemical sensor for detecting bisphenol A (BPA) by employing silver nanoparticles (AgNPs) synthesized through an eco-friendly approach. The AgNPs were produced using parsley leaf extract, which acted as a reducing and stabilizing agent in the synthesis process. The AgNPs synthesized using the green approach exhibited an average size of 15.2 ± 2.1 nm. The AgNP-modified screen-printed electrode (SPE) exhibited excellent electrocatalytic activity towards BPA oxidation, with an enhanced peak current of 28.6 μA compared to 5.2 μA for the bare SPE. The optimized sensor exhibited impressive analytical performance, boasting a broad linear range spanning 0.05–5 μM for BPA detection. Remarkably, it achieved a low limit of detection of 0.02 μM, coupled with high sensitivity. Furthermore, the sensor demonstrated commendable reproducibility, with a RSD of 3.6%, and exceptional repeatability, evidenced by an RSD of 2.4%. Upon evaluating the sensor's performance in analyzing real water specimens, the recoveries oscillated between 95.8% and 103.5%, accompanied by RSDs not exceeding 4.2%, thereby demonstrating its successful application for BPA detection. The eco-friendly synthesis approach and superior analytical performance make the AgNP-modified SPE a promising tool for on-site environmental monitoring and drinking water analysis.

Overlooked interaction between redox-mediator and bisphenol-A in permanganate oxidation

Research efforts on permanganate (Mn(VII)) combined with redox-mediator (RM), have received increasing attention due to their significant performance for bisphenol-A (BPA) removal. However, the mechanisms underpinning BPA degradation remain underexplored. Here we show the overlooked interactions between RM and BPA during permanganate oxidation by introducing an RM—N-hydroxyphthalimide (NHPI). We discovered that the concurrent generation of MnO2 and phthalimide-N-oxyl (PINO) radical significantly enhances BPA oxidation within the pH range of 5.0–6.0. The detection of radical cross-coupling products between PINO radicals and BPA or its derivatives corroborates the pivotal role of radical cross-coupling in BPA oxidation. Intriguingly, we observed the formation of an NHPI-BPA complex, which undergoes preferential oxidation by Mn(VII), marked by the emergence of an electron-rich domain in NHPI. These findings unveil the underlying mechanisms in the Mn(VII)/RM system and bridge the knowledge gap concerning BPA transformation via complexation. This research paves the way for further exploration into optimizing complexation sites and RM dosage, significantly enhancing the system's efficiency in water treatment applications.

Simultaneous determination of environmental endocrine disruptors bisphenol A and 4-nitrophenol bleached from food-contacting materials using the spin-ladder compound La2Cu2O5 modified glassy carbon electrode

Environmental endocrine-disrupting chemicals, Bisphenol A (BPA) and 4-Nitrophenol (4-NP), pose significant risks to reproductive health in both animals and humans. Here, we introduce the first utilization of the 4-leg spin ladder compound La2Cu2O5 as an electrode material for electrochemical sensor. Nanostructured La2Cu2O5 was synthesized via a straightforward Sol-Gel method and thoroughly characterized using X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy, and powder X-ray diffraction. La2Cu2O5 nanoparticles modified glassy carbon electrode (GCE) exhibited a significant electrocatalytic activity towards the oxidation of BPA and 4-NP in phosphate buffer saline (pH 7.0). Square wave voltammetry studies revealed lowest detection limits of 3 nM for BPA and 2.6 nM for 4-NP over a wider concentration range of 0.01–500 μM. Notably, this study marks the first utilization of La2Cu2O5 for simultaneous electrochemical detection of BPA and 4-NP, demonstrating its potential in this field. Furthermore, the sensor exhibited good sensitivity, reproducibility, and selectivity towards BPA and 4-NP, even in the presence of similar potential organic and inorganic interferents. Additionally, the newly developed sensor enabled simultaneous quantification of BPA and 4-NP in real samples such as packaged milk, river water, and plastic bottles, achieving recovery rates above 95%. Importantly, our results underscore the leaching of BPA into water from thin and thick plastics at elevated temperatures (40 °C–80 °C), emphasizing the utility of the proposed sensor for rapid and simultaneous detection of BPA and 4-NP in environmental and food matrices.

Voltammetric determination of bisphenol A using modified carbon paste electrode

ABSTRACT Designing effective and accurate methods to determine bisphenol A (BPA) residues is crucial for safeguarding food safety and preserving the environment. The main objective of the present work is to develop a simple and sensitive electrochemical sensor to detect BPA based on a modified carbon paste electrode (CPE). For this, CeO2 nanoparticles (CeO2 NPs) and ionic liquid (IL) were used to modify CPE. Cyclic voltammetry (CV) was utilised as the technique to investigate the electrochemical behaviour of BPA at the surface of various electrodes (unmodified CPE, CeO2 NPs/CPE, ILCPE, and CeO2 NPs/ILCPE). The obtained result showed that the CeO2 NPs/ILCPE exhibited better electrocatalytic performance to BPA oxidation than that observed at other CPEs. For quantification of BPA, differential pulse voltammetry (DPV) was utilised. Under the optimum detection conditions, the CeO2 NPs/ILCPE sensor showed good linearity in the detection of BPA within range 0.02–460.0 µM with a limit of detection (LOD) of 0.01 µM. Finally, the enhanced electrochemical response from CeO2 NPs/IL-modified CPE towards BPA has been used to evaluate the practical application of this sensor. The obtained results (recovery and relative standard deviation (RSD) values) confirmed the applicability of the modified CPE to detect BPA in real samples. Based on the findings, the CeO2 NPs/ILCPE sensor appears to be a suitable platform for BPA determination.

From e-waste to eco-sensors: synthesis of reduced graphene oxide/ZnO from discarded batteries for a rapid electrochemical bisphenol A sensor.

Improper disposal of used dry cell batteries and the leaching of bisphenol A (BPA), a prevalent endocrine disruptor present in food packaging, into surface water pose a significant threat to both the environment and drinking water, threatening the sustainability of the ecosystem. Thus, it is imperative to manage detrimental e-waste and regularly monitor BPA using a sensitive and reliable technique. This study proposes a cost-effective reduced graphene oxide/zinc oxide (rGO/ZnO) nanohybrid, entirely synthesized from electronic waste, for electrochemically detecting BPA in an aqueous medium. Graphite and metallic Zn precursors obtained from discarded batteries were employed to synthesize rGO/ZnO. The successful characterization of the prepared rGO and rGO/ZnO nanohybrid was conducted through different state-of-the-art techniques. An rGO/ZnO-modified glassy carbon electrode (GCE) exhibited superior conductivity and a larger surface area. Voltammetric study at the rGO/ZnO-modified GCE successfully detected BPA in an aqueous medium, demonstrating a one-electron and proton pathway for BPA oxidation. The sensor demonstrated a linear response within the concentration range of 1-30 μM, with a limit of detection of 0.98 nM and sensitivity of 0.055 μA μM-1. The developed electrode could also detect BPA in real water samples with reasonable recovery. These findings imply that the developed sensor has the potential to be a sensitive, practical, and economical monitoring system for BPA in water.

Activation of periodate by ABTS as an electron shuttle for degradation of aqueous organic pollutants and enhancement effect of phosphate

Periodate (PI) based advanced oxidation processes (AOPs) have recently attracted much attention due to their high application potential in water purification through production of reactive species. In the study, 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) was used as a representative electron shuttle, and its reaction with PI was investigated in detail. It was found that PI can be activated by ABTS via one-electron transfer to produce ABTS•+ and IO3•, cooperatively promoting oxidation of organic contaminants such as bisphenol A (BPA). Their contribution in BPA oxidation at pH 7 was estimated as 81.9% and 18.1%, respectively. With phosphate, BPA oxidation rate in the PI/ABTS process increased linearly with raised phosphate concentrations from 0 to 10 mM. The enhancement effect of phosphate is attributed to formation of PI-phosphate complexes, which facilitate PI activation by ABTS, and production of more ABTS•+ and IO3•, and additional phosphate radicals. Accordingly, the contribution of IO3• and phosphate radicals in BPA oxidation raised to 57.7% in the process with 4 mM phosphate, while that of ABTS•+ decreased to 42.3%. The reaction stoichiometry ratio of ABTS to PI was measured as 1.1 at pH 7, suggesting the little involvement of IO3• and phosphate radicals in production of ABTS•+ due to their high self-quenching. The PI/ABTS process exhibited excellent anti-interference capacity towards water matrix components (e.g. Cl−, HCO3− and natural organic matters). Moreover, an immobilized ABTS (ABTS/ZnAl-LDH) was successfully developed as a heterogeneous electron shuttle for PI oxidation, which resultantly exhibited the good catalytic activity and stability in degradation of BPA, further improving feasibility of the process in treatment of actual water. This work advances understanding on reaction of PI with ABTS from stoichiometric and kinetic aspects, and provides a high performance AOP for selective oxidation of trace organic contaminants.

Hydroxyl radical-driven transformations of bisphenol A and 2,4-dinitroanisole: Experimental and computational analysis.

This study used experimental and computational analysis to investigate the advanced oxidation of bisphenol A (BPA) and 2,4-dinitroanisole (DNAN). The pseudo first-order reaction rate constants depended on the molar peroxide ratio and were between 0.13 and 0.28 min-1 for BPA and between 0.018 and 0.032 min-1 for DNAN. The kinetic differences appear to be due in part to the energy requirements for oxidation, which depended on the reaction mechanism but were typically lower for BPA than they were for DNAN. Density functional theory (DFT) was used to develop transformation pathways that included experimentally-detected byproducts. The most energetically favored pathway for BPA oxidation begins with the formation of hydroxylated derivatives, while for DNAN, the most energetically favorable degradation pathway begins with the substitution of the methoxy group. Overall, these findings demonstrate the power of combining experimental and computational tools to reveal transformation mechanisms during water treatment. PRACTITIONER POINTS: Advanced oxidation transformations for two emerging water pollutants, bisphenol A and dinitroanisole, was investigated. The observed reaction kinetics depended on molar peroxide ratio in a manner that is in keeping with previous findings. Density functional theory-based analysis revealed reaction energy requirements and degradation pathways.

PH-dependent bisphenol A transformation and iodine disinfection byproduct generation by peracetic acid: Kinetic and mechanistic explorations

Peracetic acid (PAA) is regarded as an environmentally friendly oxidant because of its low formation of toxic byproducts. However, this study revealed the potential risk of generating disinfection byproducts (DBPs) when treating iodine-containing wastewater with PAA. The transformation efficiency of bisphenol A (BPA), a commonly detected phenolic contaminant and a surrogate for phenolic moieties in dissolved organic matter, by PAA increased rapidly in the presence of I−, which was primarily attributed to the formation of active iodine (HOI/I2) in the system. Kinetic model simulations demonstrated that the second-order rate constant between PAA and HOI was 54.0 M−1 s−1 at pH 7.0, which was lower than the generation rate of HOI via the reaction between PAA and I−. Therefore, HOI can combine with BPA to produce iodine disinfection byproducts (I-DBPs). The transformation of BPA and the generation of I-DBPs in the I−/PAA system were highly pH-dependent. Specifically, acidic conditions were more favorable for BPA degradation because of the higher reaction rates of BPA and HOI. More iodinated aromatic products were detected after 5 min of the reaction under acidic and neutral conditions, resulting in higher toxicity towards E. coli. After 12 h of the reaction, more adsorbable organic iodine (AOI) was generated at alkaline conditions because HOI was not able to efficiency transform to IO3−. The presence of H2O2 in the PAA solution played a role in the reaction with HOI, particularly under alkaline conditions. This study significantly advances the understanding of the role of I− in BPA oxidation by PAA and provides a warning to further evaluate the potential environmental risk during the treatment of iodine-bearing wastewater with PAA.

Green polyaspartic acid as a novel permanganate activator for enhanced degradation of organic contaminants: Role of reactive Mn(III) species

Attention has been long focused on enhancing permanganate (Mn(VII)) oxidation capacity for eliminating organic contaminants via generating active manganese intermediates (AMnIs). Nevertheless, limited consideration has been given to the unnecessary consumption of Mn(VII) due to the spontaneous disproportionation of AMnIs during their formation. In this work, we innovatively introduced green polyaspartic acid (PASP) as both reducing and chelating agents to activate Mn(VII) to enhance the oxidation capacity and utilization efficiency of Mn(VII). Multiple lines of evidence suggest that Mn(III), existing as Mn(III)-PASP complex, was generated and dominated the degradation of bisphenol A (BPA) in the Mn(VII)/PASP system. The stabilized Mn(III) species enabled Mn(VII) utilization efficiency in the Mn(VII)/PASP system to be higher than that in Mn(VII) alone. Moreover, the electrophilic Mn(III) species was verified to mainly attack the inclusive benzene ring and isopropyl group to realize BPA oxidation and its toxicity reduction in the Mn(VII)/PASP system. In addition, the Mn(VII)/PASP system showed the potential for selectively oxidizing organic contaminants bearing phenol and aniline moieties in real waters without interference from most of coexisting water matrices. This work brightens an overlooked route to both high oxidation capacity and efficient Mn(VII) utilization in the Mn(VII)-based oxidation processes.

Facile Chemical Synthesis of Co-Ru-Based Heterometallic Supramolecular Polymer for Electrochemical Oxidation of Bisphenol A: Kinetics Study at the Electrode/Electrolyte Interface.

Regardless of the adverse effects of Bisphenol A (BPA), its use in industry and in day-to-day life is increasing at a higher rate every year. In the present study, a simple and reliable chemical approach was used to develop an efficient BPA sensor based on a Co-Ru-based heterometallic supramolecular polymer (polyCoRu). Surface morphology and elemental analysis were examined using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). Furthermore, functional group analysis was accomplished by Fourier transform infrared spectroscopy (FT-IR). UV-vis spectroscopy was used to confirm the complexation in the ratio of 0.5:0.5:1 (metal 1/metal 2/ligand). Electrochemical characterization of the synthesized polyCoRu was conducted using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) analyses. The study identified two distinct linear dynamic ranges for the detection of BPA, 0.197-2.94 and 3.5-17.72 μM. The regression equation was utilized to determine the sensitivity and limit of detection (LOD), resulting in values of 0.6 μA cm-2 μM-1 and 0.02 μM (S/N = 3), respectively. The kinetics of BPA oxidation at the polyCoRu/GCE were investigated to evaluate the heterogeneous rate constant (k), charge transfer coefficient (α), and the number of electrons transferred during the oxidation and rate-determining step. A probable electrochemical reaction mechanism has been presented for further comprehending the phenomena occurring at the electrode surface. The practical applicability of the fabricated electrode was analyzed using tap water, resulting in a high percentage of recovery ranging from 96 to 105%. Furthermore, the reproducibility and stability data demonstrated the excellent performance of polyCoRu/GCE.

Sensitive Electrochemical Determination of Bisphenol a Using a Disposable, Electrodeposited Antimony-Graphene Nanocomposite Pencil Graphite Electrode (PGE) and Differential Pulse Voltammetry (DPV)

Herein the synergistic properties of electrochemically reduced graphene oxide–antimony nanoparticles (ERGO-SbNPs) were leveraged for the ultrasensitive determination of bisphenol A (BPA) in water samples using disposable pencil graphite rods. A novel pencil-graphite multi-electrode array was utilized as the coating tool resulting in the production of highly reproducible and disposable single-use ERGO-SbNP-coated pencil graphite rods. This coating method effectively mitigated the fouling caused by BPA by-products during oxidation. The analytical determination of BPA oxidation on the single-use ERGO-SbNP-coated pencil graphite rods demonstrated an impressive 0.0,125 µM detection limit, surpassing the USEPA drinking water standard of 0.087 µM. Furthermore, the developed electrochemical sensor exhibited exceptional reproducibility for BPA in tap water samples from Western Cape, South Africa with few interferences. The study’s findings not only highlight the sensor’s superior performance but also present a promising alternative to existing anti-fouling measures.

Cu-MOF/Pd derived oxide nanoparticles based carbon composite - An innovative electrochemical sensing platform for Bisphenol A

Bisphenol A (BPA), an endocrine disrupting chemical, had been used worldwide as a raw material in water bottles and food packages. It leaches into food products and water sources and hence, it should be monitored effectively. Herein, an electrochemical sensing platform based on Cu-MOF@Pd-500 modified glassy carbon (GC) electrode was fabricated for the sensing of BPA. The material was synthesized by a simple solvothermal method, carbonized at 500 ⁰C, and characterized by various surface analytical techniques. Cyclic voltammetric (CV) analysis reveals that the Cu-MOF@Pd-500 modified GCE exhibits 1.5 folds hike in peak current and a considerable shift in peak potential towards the anodic side when compared to Cu-MOF@ 500, suggesting the higher electrocatalytic activity of the former than that of the later. The electrochemical oxidation of BPA provides an irreversible diffusion-controlled process involving two electrons and two protons. Differential pulse voltammetric (DPV) analysis reveals that the constructed sensor material provides a linear response over BPA concentration of 1 − 150 µM with a low detection limit (LOD) of 0.06 µM, (S/N = 3) and amperometric studies deliver a linear range of 1–22 µM with a LOD of 0.025 µM in 0.1 M PBS at a pH 7.0. Additionally, the Cu-MOF@Pd-500 delivers good repeatability, stability, and anti-interference capabilities. The results obtained also support the effectiveness of Cu-MOF@Pd-500 for quantifying and identifying BPA in real sample analysis (plastic water bottles) with an average recovery of the ratio of 101.93 having a relative standard deviation (RSD) of 0.42%.