Browsing by Author "Baker, Priscilla"

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    Actuation behaviour of a derivatized pyrrole accordion type polymer
    (ESG, 2014) Ward, Meryck; Botha, Shanielle; Iwuoha, Emmanuel I.; Baker, Priscilla
    A monomer (Phenazine-2,3-diimino(pyrrole-2-yl)–PDP) derived from the condensation reaction between 2,3-diaminophenazine and a pyrrole derivative has been synthesized as a hinge molecule in the design of a zig-zag polymer. The monomer was polymerized both chemically and electrochemically in order to produce the polymer material, phenazine-2,3-diimino(pyrrole-2-yl (PPDP). During electrochemical polymerization the system was doped using 1,4-napthaquinone sulphonic acid (NQSA) and polyvinylsulfonic acid (PVSA) respectively, to improve conductivity. Characterization of the materials by Fourier transform infrared spectroscopy (FTIR) confirmed the successful linking of the starting materials to produce the hinge molecule and nuclear magnetic resonance spectroscopy (NMR) supported the FTIR data. The electrochemistry of the polymer in the doped and undoped state was evaluated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS).
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    Amperometric biosensor systems prepared on poly (aniline-ferrocenium hexafluorophosphate) composites doped with poly(vinyl sulfonic acid sodium salt)
    (University of the Western Cape, 2008) Ndangili, Peter Munyao; Iwuoha, Emmanuel; Baker, Priscilla; Dept. of Chemistry; Faculty of Science
    The main hypothesis in this study is the development of a nanocomposite mediated amperometric biosensor for detection of hydrogen peroxide. The aim is to combine the electrochemical properties of both polyaniline and ferrocenium hexafluorophosphate into highly conductive nano composites capable of exhibiting electrochemistry in non acidic media; shuttling electrons between HRP and GCE for biosensor applications.
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    Application of Sutherlandia flutescens in cosmetic skin industry (phytochemical fingerprinting and its activity against skin immune diseases.
    (University of the Western Cape, 2019) Msebele, Bongiwe; Baker, Priscilla
    Hyperpigmentation disorders such as melasma, freckles and black-pigmented spots on the surface of the skin are often a result of increased over production and accumulation of melanin pigments in the skin. In melanin biogenesis, tyrosinase is the key enzyme that catalysis the synthesis of melanin, thus the most effective and easiest way to reduce melanin synthesis is by inhibiting tyrosinase. There are a large number of reported tyrosinase inhibitors, their identification and isolation from natural sources is highly important because when natural tyrosinase inhibitors are identified in natural sources, their production is relatively low in cost. Tyrosinase inhibitors are highly sought in the cosmetic industry because of their skin – whitening effects. Most common used tyrosinase inhibitors are kojic acid (KA), arbutin, hydroquinone and ascorbic acid. However, these inhibitors have side effects and lack clinical efficiency. These facts led us to focus our research work on the exploration of natural tyrosinase inhibitors. Due to the therapeutic potential of medical plants researchers are not only concerned with validating ethnopharmacological usage of plants, but also with identification, isolation and characterization of bioactive components. Sutherlandia frutescens and Psoralea aphylla are both examples of indigenous fynbos species, which have been applied by indigenous people for the benefit of their medicinal properties.
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    Application on gold nanoparticles-dotted 4-nitrophenylazo graphene in a label-free impedimetric deoxynivalenol immunosensor
    (MDPI, 2015) Sunday, Christopher Edozie; Masikini, Malua; Wilson, Lindsay; Rassie, Candice; Waryo, Tesfaye T.; Baker, Priscilla; Iwuoha, Emmanuel I.
    In this paper, we report a new concept to construct a label-free electrochemical inhibition-based immunosensor for the detection of the mycotoxin deoxynivalenol (DON) in cereal samples. The electrochemical impedance spectroscopy of tris(bipyridine) ruthenium (II) chloride was used as a marker enhanced with gold nanoparticles-dotted 4-nitrophenylazo functionalized graphene (AuNp/G/PhNO2) nanocatalyst mediated in Nafion on a glassy carbon electrode. Under the optimized conditions, the formation of immunocomplexes inhibited electron flow and increased the charge transfer resistance of the sensing interface linearly. The change in impedance was proportional to DON concentrations in the range of 6–30 ng/mL with a sensitivity and detection limit of 32.14 ΩL/ng and 0.3 µg/mL, respectively, which compares favorably with the ELISA result. The proposed sensor had a stability of 80.3%, good precision and selectivity in DON standard solution containing different interfering agents, indicating promising application prospect for this strategy in designing impedimetric, electrochemiluminescent, voltammetric or amperometric sensors.
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    Aptameric recognition-modulated electroactivity of poly(4-styrenesolfonic acid)-doped polyaniline films for single-shot detection of tetrodotoxin
    (MDPI, 2015) Fomo, Gertrude; Waryo, Tesfaye T.; Sunday, Christopher Edozie; Baleg, Abd A.; Baker, Priscilla; Iwuoha, Emmanuel I.
    The work being reported is the first electrochemical sensor for tetrodotoxin (TTX). It was developed on a glassy carbon electrodes (C) that was modified with poly(4-styrenesolfonic acid)-doped polyaniline film (PANI/PSSA). An amine-end functionalized TTX-binding aptamer, 5′-NH2-AAAAATTTCACACGGGTGCCTCGGCTGTCC-3′ (NH2-Apt), was grafted via covalent glutaraldehyde (glu) cross-linking. The resulting aptasensor (C//PANI+/PSSA-glu-NH2-Apt) was interrogated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) in sodium acetate buffer (NaOAc, pH 4.8) before and after 30 min incubation in standard TTX solutions. Both CV and EIS results confirmed that the binding of the analyte to the immobilized aptamer modulated the electrochemical properties of the sensor: particularly the charge transfer resistance (Rct) of the PANI+/PSSA film, which served as a signal reporter. Based on the Rct calibration curve of the TTX aptasensor, the values of the dynamic linear range (DLR), sensitivity and limit of detection (LOD) of the sensor were determined to be 0.23–1.07 ng·mL−1 TTX, 134.88 ± 11.42 Ω·ng·mL−1 and 0.199 ng·mL−1 , respectively. Further studies are being planned to improve the DLR as well as to evaluate selectivity and matrix effects in real samples.
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    Boron-doped Diamond Sensors for the Determination of Organic Compounds in Aqueous Media
    (University of the Western Cape, 2010) Hess, Euodia; Baker, Priscilla; Iwuoha, Emmanuel; Dept. of Chemistry; Faculty of Science
    In electrochemical oxidation treatment of wastewater, the electrode material is an important parameter in optimizing oxidative electrochemical processes, since the mechanism and products of several anodic reactions are known to depend on the anode material. The electrochemical oxidation of benzaldehyde, nitrobenzene and m-cresol on bare boron-doped diamond (BDD) electrode was investigated. Cytochrome c was then electrochemically immobilsed onto the functionalized BDD electrode by cyclic voltammetry. Oxidation and reduction reaction mechanism of each flavonoid was studied. There was one oxidation and reduction peaks for quercitin and catechin respectively, and two oxidation and two reduction peaks for rutin. The cytochrome c modified BDD electrode showed good sensitivity for all three flavonoids and low detection limits i.e. 0.42 to 11.24 M as evaluated at oxidation and reduction peaks, respectively.
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    Carcinoembryonic antigen immunosensor developed with organoclay nanogold composite film
    (ESG, 2014) Kemmegne-Mbouguen, Justin Claude; Ngameni, Emmanuel; Baker, Priscilla; Waryo, Tesfaye T.; Kgarebe, Boitumelo; Iwuoha, Emmanuel I.
    Organoclay nanogold composite were prepared using gold nanoparticles and the natural Cameroonian clay grafted with amino organosilane. The functionnalization of clay provided abundant amino group to assemble gold nanoparticles. A label-free electrochemical immunosensor for the sensitive determination of carcinoembryonic antigen (CEA) was fabricated by immobilizing anti-CEA onto organoclay nanogold composite film modified electrode by the cross-linking method using glutaraldehyde. In addition, the preparation procedure of the immunosensor was investigated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Under optimal conditions, the resulting immunosensor displayed a high sensitivity for the detection of CEA, and responded to the CEA concentration in two ranges from 0.05 to 5.0 ng/mL (R = 0.991) and from 5.0 to 120.0 ng/mL (R = 0.998) with a detection limit of 0.01 ng/mL.
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    Charge Transfer and Capacitive Properties of Polyaniline/ Polyamide Thin Films
    (University of the Western Cape, 2018) Abrahams, Dhielnawaaz; Baker, Priscilla
    Blending polymers together offers researchers the ability to create novel materials that have a combination of desired properties of the individual polymers for a variety of functions as well as improving specific properties. The behaviour of the resulting blended polymer or blend is determined by the interactions between the two polymers. The resultant synergy from blending an intrinsically conducting polymer like polyaniline (PANI), is that it possesses the electrical, electronic, magnetic and optical properties of a metal while retaining the poor mechanical properties, solubility and processibility commonly associated with a conventional polymer. Aromatic polyamic acid has outstanding thermal, mechanical, electrical, and solvent resistance properties that can overcome the poor mechanical properties and instability of the conventional conducting polymers, such as polyaniline.
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    Correction: Baker, P. et al. electrochemical aptasensor for endocrine disrupting 17β-estradiol based on a poly(3,4-ethylenedioxylthiopene)-gold nanocomposite platform. Sensors 2010, 10, 9872-9890
    (MDPI, 2011) Olowu, Rasaq A.; Arotiba, Omotayo A.; Mailu, Stephen N.; Waryo, Tesfaye T.; Baker, Priscilla; Iwuoha, Emmanuel I.
    Herewith please find corrected structures for Figure 8 in our paper published in Sensors in 2010.
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    Determination of anthracene on Ag-Au alloy nanoparticles/overoxidized-polypyrrole composite modified glassy carbon electrodes
    (MDPI, 2010) Mailu, Stephen N.; Waryo, Tesfaye T.; Ndangili, Peter M.; Ngece, Fanelwa R.; Baleg, Abd A.; Baker, Priscilla; Iwuoha, Emmanuel I.
    A novel electrochemical sensor for the detection of anthracene was prepared by modifying a glassy carbon electrode (GCE) with over-oxidized polypyrrole (PPyox) and Ag-Au (1:3) bimetallic nanoparticles (Ag-AuNPs). The composite electrode (PPyox/Ag-AuNPs/GCE) was prepared by potentiodynamic polymerization of pyrrole on GCE followed by its overoxidation in 0.1 M NaOH. Ag-Au bimetallic nanoparticles were chemically prepared by the reduction of AgNO3 and HAuCl4 using C6H5O7Na3 as the reducing agent as well as the capping agent and then immobilized on the surface of the PPyox/GCE. The nanoparticles were characterized by UV-visible spectroscopy technique which confirmed the homogeneous formation of the bimetallic alloy nanoparticles. Transmission electron microscopy showed that the synthesized bimetallic nanoparticles were in the range of 20–50 nm. The electrochemical behaviour of anthracene at the PPyox/Ag-AuNPs/GCE with Ag: Au atomic ratio 25:75 (1:3) exhibited a higher electrocatalytic effect compared to that observed when GCE was modified with each constituent of the composite (i.e., PPyox, Ag-AuNPs) and bare GCE. A linear relationship between anodic current and anthracene concentration was attained over the range of 3.0 × 10−6 to 3.56 × 10−4 M with a detection limit of 1.69 × 10−7 M. The proposed method was simple, less time consuming and showed a high sensitivity.
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    Determination of Chromium(VI), Vanadium(V), Selenium(IV) and Zinc(II) in the City of Cape Town's potable water by stripping voltammetry at boron doped diamond electrodes
    (University of the Western Cape, 2011) Fillis, Ismarelda Rosaline; Baker, Priscilla
    The main aim of this study is to investigate theelectrochemical determination of two beneficial (selenium and zinc) and two toxic (chromium and vanadium) metals in the potable water within the City of Cape Town's distribution area. The Water Laboratory of the City's Scientific Services Branch analyses for these metals in their elemental state, using the Inductively Coupled Plasma Optical Emission Spectrometer (ICP-OES). This is a standard method used for the detection of trace metals. The most sensitive voltammetric method for determining these metals is by adsorptive stripping voltammetry, using a thin mercury film electrode with a glassy carbon support. This voltammetric method is used for quantitative determination of specific ionic species. Because of mercury's toxicity it is not really favoured for trace metals anymore. Many other possibilities are under investigation, e.g. bismuth-film, modified glassy carbon and antimony electrodes. The boron-doped diamond (BDD) electrode has distinct advantages when used to determine metal concentrations. Advantages of BDD electrodes include lower detection limit, speciation and wider potential window. In this study cyclic voltammetry (CV) was used to determine the copper, cadmium and lead concentrations in potable water by means of square wave voltammetry (SWV) and a bare glassy carbon electrode (GCE). Furthermore, a boron-doped diamond electrode (BDDE) was used to investigate the possibilities of determining selenium, chromium and vanadium by SWV. Real samples (potable water samples) were analysed electrochemically to qualify and quantify these metals and determine whether they comply with the SANS 241:2006 drinking water guidelines.The copper, cadmium, lead and selenium peaks appear very close to the theoretical values, which indicate that these metals can be detected by SWV method, but further analysis with more samples is advised. Even though responses were observed for vanadium and chromium, it was not reliable and requires further investigation. Further studies into the analyses of zinc are also advised.
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    Development of amperometric biosensor with cyclopentadienylruthenium (II) thiolato schiff base self-assembled monolayer (SAM) on gold
    (University of the Western Cape, 2007) Ticha, Lawrence Awa; Baker, Priscilla; Iwuoha, Emmanuel; Dept. of Chemistry; Faculty of Science
    A novel cyclopentadienylruthenium(II) thiolato Schiff base, [Ru(SC6H4NC(H)C6H4OCH2CH2SMe)(η5-C2H5]2 was synthesized and deposited as a selfassembled monolayer (SAM) on a gold electrode. Effective electronic communication between the Ru(II) centers and the gold electrode was established by electrostatically cycling the Shiff base-doped gold electrode in 0.1 M NaOH from -200 mV to +600 mV. The SAMmodified gold electrode (Au/SAM) exhibited quasi-reversible electrochemistry. The integrity of this electro-catalytic SAM, with respect to its ability to block and electro-catalyze certain Faradaic processes, was interrogated using Cyclic and Osteryoung Square Wave voltammetric experiments. The formal potential, E0', varied with pH to give a slope of about - 34 mV pH-1. The surface concentration, Γ, of the ruthenium redox centers was found to be 1.591 x 10-11 mol cm-2. By electrostatically doping the Au/SAM/Horseradish peroxidase at an applied potential of +700 mV vs Ag/AgCl, a biosensor was produced for the amperometric analysis of hydrogen peroxide, cumene hydroperoxide and tert-butylhydroperoxide. The electrocatalytic-type biosensors displayed typical Michaelis-Menten kinetics with their limits of detection of 6.45 M, 6.92 M and 7.01 M for hydrogen peroxide, cumene hydroperoxide and tert-butylhydroperoxide respectively.
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    Electro-analytical protocols for quantitative assessment of phenols in South African rooibos, green and black tea samples
    (University of Western Cape, 2022) Abrahams, Dhielnawaaz; Baker, Priscilla
    The worldwide tea market was estimated at almost 200 billion U.S. dollars in 2020. It is perceived to rise to 318 billion dollars by 2025. Tea has a long history of prominence around the world. Increases in tea production in Africa over the past decade have aggravated the pressure the industry exerts on natural resources such as water, soil, and vegetation. The increasing numbers of tea production factories coupled with the increased global demand for tea are adding to the growing problem. The growing conflicts over water resources are set to worsen in the context of climate change. This increase has occurred at a time when regional and national legislation is becoming increasingly stringent. These controls have been taken to offset environmental damage. Tea has probably the most elevated substance of polyphenols among food and refreshment items.
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    Electrochemical actuation potential of diaminophenazine linked pyrrole derivatives
    (2013) Ward, Meryck; Baker, Priscilla
    A novel monomer (Phenazine-2,3-diimino(pyrrole-2-yl)–PDP) derived from the condensation reaction between 2,3-diaminophenazine and a pyrrole derivative has been synthesized as a hinge molecule in the design of a zig-zag polymer with actuation possibility. The monomer was polymerized chemically and electrochemically to produce the new polymer material – polymerized Phenazine-2,3-diimino(pyrrole-2-yl) PPDP. Two very crucial properties of a good actuator material, relate specifically to its solubility testing and electrical conductivity. The hinged polymer material was studied intensively in terms of its spectroscopy; Fourier Transform Infrared - FTIR, 1H’NMR, thermal properties (Differential Scanning Calorimetry-DSC and Thermogravimetric Analysis-TGA) as well as voltammetry and conductivity. Conductivity was evaluated using three different approaches including; 4 probe measurements, plotting of I/V curves based on potentiostatic measurements and an electrochemical impedance experiment using a dielectric Solartron interface. Electrochemical kinetics of the polymer prepared as a thin film at glassy carbon electrode (GCE) was also done and it was clear that the thin film conductivity was vastly different from the compressed pellet conductivity (thick film). The zig-zag polymer was then further modified by homogeneous inclusion of gold nanoparticles to improve conductivity and solubility, in the thick film arrangement. Conductivity of the thin film was studied by electrochemical impedance spectroscopy with the relative charge transfer values being determined for unmodified and modified polymer systems. The solubility testing of the material plays an important role as it is required for a wide range of experimental applications. The zig-zag polymer showed great promise for applications; in dye sensitized solar cells and free standing interpenetrating polymer network (IPN), solubility testing and electrical conductivity would need to be improved in order to be used in these applications.
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    Electrochemical aptasensor for endocrine disrupting 17β-estradiol based on a poly(3,4-ethylenedioxylthiopene)-gold nanocomposite platform
    (MDPI, 2010) Olowu, Rasaq A.; Mailu, Stephen N.; Waryo, Tesfaye T.; Baker, Priscilla; Iwuoha, Emmanuel I.; Arotiba, Omotayo A.
    A simple and highly sensitive electrochemical DNA aptasensor with high affinity for endocrine disrupting 17β-estradiol, was developed. Poly(3,4-ethylenedioxylthiophene) (PEDOT) doped with gold nanoparticles (AuNPs) was electrochemically synthesized and employed for the immobilization of biotinylated aptamer towards the detection of the target. The diffusion coefficient of the nanocomposite was 6.50 × 10−7 cm2 s−1, which showed that the nanocomposite was highly conducting. Electrochemical impedance investigation also revealed the catalytic properties of the nanocomposite with an exchange current value of 2.16 × 10−4 A, compared to 2.14 × 10−5 A obtained for the bare electrode. Streptavidin was covalently attached to the platform using carbodiimide chemistry and the aptamer immobilized via streptavidin—biotin interaction. The electrochemical signal generated from the aptamer–target molecule interaction was monitored electrochemically using cyclic voltammetry and square wave voltammetry in the presence of [Fe(CN)6]−3/−4 as a redox probe. The signal observed shows a current decrease due to interference of the bound 17β-estradiol. The current drop was proportional to the concentration of 17β-estradiol. The PEDOT/AuNP platform exhibited high electroactivity, with increased peak current. The platform was found suitable for the immobilization of the DNAaptamer. The aptasensor was able to distinguish 17β-estradiol from structurally similar endocrine disrupting chemicals denoting its specificity to 17β-estradiol. The detectable concentration range of the 17β-estradiol was 0.1 nM–100 nM, with a detection limit of 0.02 nM.
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    An electrochemical DNA biosensor developed on a nanocomposite platform of gold and poly(propyleneimine) dendrimer
    (MDPI, 2008) Arotiba, Omotayo A.; Owino, Joseph; Songa, Everlyne; Hendricks, Nicolette; Waryo, Tesfaye T.; Jahed, Nazeem; Baker, Priscilla; Iwuoha, Emmanuel I.
    An electrochemical DNA nanobiosensor was prepared by immobilization of a 20mer thiolated probe DNA on electro-deposited generation 4 (G4) poly(propyleneimine) dendrimer (PPI) doped with gold nanoparticles (AuNP) as platform, on a glassy carbon electrode (GCE). Field emission scanning electron microscopy results confirmed the codeposition of PPI (which was linked to the carbon electrode surface by C-N covalent bonds) and AuNP ca 60 nm. Voltammetric interrogations showed that the platform (GCE/PPI-AuNP) was conducting and exhibited reversible electrochemistry (E°′ = 235 mV) in pH 7.2 phosphate buffer saline solution (PBS) due to the PPI component. The redox chemistry of PPI was pH dependent and involves a two electron, one proton process, as interpreted from a 28 mV/pH value obtained from pH studies. The charge transfer resistance (Rct) from the electrochemical impedance spectroscopy (EIS) profiles of GCE/PPI-AuNP monitored with ferro/ferricyanide (Fe(CN)6 3-/4-) redox probe, decreased by 81% compared to bare GCE. The conductivity (in PBS) and reduced Rct (in Fe(CN)6 3-/4-) values confirmed PPI-AuNP as a suitable electron transfer mediator platform for voltammetric and impedimetric DNA biosensor. The DNA probe was effectively wired onto the GCE/PPI-AuNP via Au-S linkage and electrostatic interactions. The nanobiosensor responses to target DNA which gave a dynamic linear range of 0.01 - 5 nM in PBS was based on the changes in Rct values using Fe(CN)6 3-/4- redox probe.
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    Electrochemical immunosensor based on polythionine/gold nanoparticles for the determination of Aflatoxin B1
    (MDPI, 2008) Owino, Joseph H.O.; Arotiba, Omotayo A.; Hendricks, Nicolette; Songa, Everlyne; Jahed, Nazeem; Waryo, Tesfaye T.; Ngece, Rachel F.; Baker, Priscilla; Iwuoha, Emmanuel I.
    An aflatoxin B1 (AFB1) electrochemical immunosensor was developed by the immobilisation of aflatoxin B1-bovine serum albumin (AFB1-BSA) conjugate on a polythionine (PTH)/gold nanoparticles (AuNP)-modified glassy carbon electrode (GCE). The surface of the AFB1-BSA conjugate was covered with horseradish peroxidase (HRP), in order to prevent non-specific binding of the immunosensors with ions in the test solution. The AFB1 immunosensor exhibited a quasi-reversible electrochemistry as indicated by a cyclic voltammetric (CV) peak separation (ΔEp) value of 62 mV. The experimental procedure for the detection of AFB1 involved the setting up of a competition between free AFB1 and the immobilised AFB1-BSA conjugate for the binding sites of free anti-aflatoxin B1 (anti-AFB1) antibody. The immunosensor’s differential pulse voltammetry (DPV) responses (peak currents) decreased as the concentration of free AFB1 increased within a dynamic linear range (DLR) of 0.6 - 2.4 ng/mL AFB1 and a limit of detection (LOD) of 0.07 ng/mL AFB1. This immunosensing procedure eliminates the need for enzyme-labeled secondary antibodies normally used in conventional ELISA–based immunosensors.
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    Electrochemical impedance modelling of the reactivities of dendrimeric poly(propylene imine) DNA nanobiosensors
    (University of the Western Cape, 2008) Arotiba, Omotayo Ademola; Baker, Priscilla; Dept. of Chemistry; Faculty of Science
    In this thesis, I present the electrochemical studies of three dendrimeric polypropylene imine (PPI) nanomaterials and their applications as a platform in the development of a novel label free DNA nanobiosensor based on electrochemical impedance spectroscopy. Cyclic voltammetry (CV), differentia pulse voltammetry (DPV), square wave voltammetry (SWV) and electrochemical impedance spectroscopy (EIS) techniques were used to study and model the electrochemical reactivities of the nanomaterials on glassy carbon electrode (GCE) as the working electrode.
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    Electrochemically reduced graphene oxide pencil-graphite in situ plated bismuth-film electrode for the determination of trace metals by anodic stripping voltammetry
    (ESG, 2014) Pokpas, Keagan; Zbeda, Salma; Jahed, Nazeem; Mohamed, Nuralli; Baker, Priscilla; Iwuoha, Emmanuel I.
    An electrochemical platform was developed based on a pencil-graphite electrode (PGE) modified with electrochemically reduced graphene oxide (ERGO) sheets and in conjunction with an in situ plated bismuth-film (ERGO-PG-BiE). The ERGO-PG-BiE was used as a sensing platform for determining Zn2+, Cd2+ and Pb2+ by square wave anodic stripping voltammetry (SWASV). ERGO sheets were deposited on to pencil-graphite electrodes by cyclic voltammetric reduction from a graphene oxide (GO) solution. The GO, with flake thicknesses varying between 1.78 to 2.10 nm (2 sheets) was characterized using FT-IR, HR-SEM, HR-TEM, AFM, XRD and Raman spectroscopy. Parameters influencing the electroanalytical response of the ERGO-PG-BiE such as, bismuth-film concentration, deposition potential, deposition time and rotation speed were investigated and optimized. The ERGO-PG-BiE gave well-defined, reproducible peaks with detection limits of 0.19 μg L-1, 0.09 μg L-1 and 0.12 μg L-1 for Zn2+, Cd2+ and Pb2+ respectively, at a deposition time of 120 seconds. For real sample analysis, the enhanced voltammetric sensor proved to be suitable for the detection and quantitation of heavy metals below the US EPA prescribed drinking water standards of 5 mg L-1, 5 μg L-1 and 15 μg L-1 for Zn2+, Cd2+ and Pb2+ respectively.
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    Encapsulating of humic acid in hydrogel matrix for the complexation of heavy metals in aqueous solutions
    (University of Western Cape, 2020) Sithi, Rabelani Leonard; Baker, Priscilla; Muya, Francis
    Rapid industrialization growth without appropriate emission standards for discharging environmental pollutants had exposed the ecosystem to detrimental effect. Due to their bioaccumulation propensity in organisms, toxicity and non-biodegradable aspect, heavy metal spoliation is currently a significant ecological obligation. Owing to their natural abundance and extensive use, cadmium (Cd) and lead (Pb), among different heavy metals, are the predominant toxic metals. The intrusion of Cd and Pb metal ions into the ecosystem is accomplished by widely accepted methods such as anticorrosive coating of steel, electronic circuit and batteries.