This study reports the synthesis of graphene by oxidizing graphite to graphite oxide using H2SO4 and KMnO4 and reducing graphene oxide to graphene by using NaBH4. Graphene was then characterized using FT-IR, TEM, AFM, XRD, Raman spectroscopy and solid state NMR. Nafion-Graphene in combination with a mercury film electrode, bismuth film electrode and antimony film electrode was used as a sensing platform for trace metal analysis in 0.1 M acetate buffer (pH 4.6) at 120 s deposition time, using square-wave anodic stripping voltammetry (SWASV). Detection limits were calculated using 3σblank/slope. For practical applications recovery studies was done by spiking test samples with known concentrations of metal ions and comparing the results to inductively coupled plasma mass spectrometry (ICPMS). This was then followed by real sample analyses.

This study reports the synthesis of graphene by oxidizing graphite to graphite oxide using H2SO4 and KMnO4 and reducing graphene oxide to graphene by using NaBH4. Graphene was then characterized using FT-IR, TEM, AFM, XRD, Raman spectroscopy and solid state NMR. Nafion-Graphene in combination with a mercury film electrode, bismuth film electrode and antimony film electrode was used as a sensing platform for trace metal analysis in 0.1 M acetate buffer (pH 4.6) at 120 s deposition time, using square-wave anodic stripping voltammetry (SWASV). Detection limits were calculated using 3σblank/slope. For practical applications recovery studies was done by spiking test samples with known concentrations of metal ions and comparing the results to inductively coupled plasma mass spectrometry (ICPMS). This was then followed by real sample analyses.

Magister Scientiae - MSc (Dept. of Chemistry) / This study reports the synthesis of graphene by oxidizing graphite to graphite oxide using H2SO4 and KMnO4 and reducing graphene oxide to graphene by using NaBH4. Graphene was then characterized using FT-IR, TEM, AFM, XRD, Raman spectroscopy and solid state NMR. Nafion-Graphene in combination with a mercury film electrode, bismuth film electrode and antimony film electrode was used as a sensing platform for trace metal analysis in 0.1 M acetate buffer (pH 4.6) at 120 s deposition time, using square-wave anodic stripping voltammetry (SWASV). Detection limits were calculated using 3σblank/slope. For practical applications recovery studies was done by spiking test samples with known concentrations of metal ions and comparing the results to inductively coupled plasma mass spectrometry (ICPMS). This was then followed by real sample analyses. / South Africa

The accurate and rapid detection of clinically relevant analytes at the point-of-care (POC) is a crucial element for the increase in our quality of life. There are multiple detection techniques for sensing a target analyte in biological samples. However, electrochemical sensors excel because of their versatility, accuracy and sensitivity. Among the many challenges in the fabrication of electrochemistry-based POC sensors, the miniaturization of the working electrodes is one of the most difficult to overcome. Decreasing the size of the sensors will result in less electroactive surface area (ESA) and, therefore, lower sensitivity. Thus, the design of miniaturized electrodes with high ESA is desired in this research field. The methodology developed in our laboratory to accomplish this goal is based on the fabrication of microstructured gold electrodes (MSEs) by depositing, via sputtering, a gold thin-film onto a pre-stressed polystyrene substrate masked with adhesive vinyl stencils and thermally shrinking the substrate at high temperatures (135-160 °C). In my thesis work, I developed cost-effective sensitive electrochemical platforms using only bench-top approaches. First, the ESA and, thus, the sensitivity of the MSEs were enhanced by using a simple and rapid nano-roughening approach. The ESA of MSEs was increased 4x by applying high voltage pulsing in sulfuric acid. The resulting electrodes possessed high anti-fouling capabilities and excellent response toward the enzyme-free detection of glucose with a limit of detection (LOD) of 0.62 mM in the presence of bovine serum albumin (BSA) and ascorbic acid. Furthermore, the fabrication cost of the MSEs electrodes was decreased by 5x by replacing the sputtering deposition step with a cost-effective solution-based electroless deposition technique. In this case, the PS substrates were coated with a polydopamine adhesion layer and noble metal films (copper, silver and gold) were subsequently plated. Not only the cost of the gold electrode was substantially reduced but, due to the intrinsic roughness of the surface, the MSEs electrodes obtained via electroless deposition showed a higher ESA than those made via sputtering. Furthermore, the developed electroless method was extended for the fabrication of paper-based sensing devices. The sensing versatility of these surfaces was demonstrated by electrochemically detecting mercury with a 0.27 ppb LOD and by sensing thiophenol via surface-enhanced Raman scattering (SERS). The MSEs electrodes fabricated via electroless deposition were subjected to the nano-roughening technique to generate affordable and high ESA electrodes. These platforms were used to design enzyme-based biosensors to accurately detect glucose and urea in complex samples. Glucose was detected in four different types of wine, with matrix interference measured below 10%, and in human serum, with a measured concentration that was not statistically different from that obtained from commercially available biosensors. Urea was detected in human urine and plasma with matrix interferences measured to be below 8% in both cases. We envision that the fabrication techniques developed in this thesis will rapidly grow in the scientific community for the prompt and accurate design of POC electrochemical devices. / Thesis / Doctor of Philosophy (PhD)

Gegenstand der vorliegenden Arbeit ist die Synthese und Charakterisierung neuer chromophorer Catecholderivate mit ausgeprägten push-pull-pi-Systemen. Die solvatochromen Eigenschaften dieser Verbindungen werden in Abhängigkeit der Wasserstoffbrückenbindungsdonor- und -akzeptorfähigkeit sowie Lösungsmitteldipolarität diskutiert. Mit entsprechenden methoxy- und dimethoxyfunktionalisierten Catecholderivaten ist es möglich, vergleichende Struktur-Eigenschaftsbeziehungen aufzustellen. Durch Untersuchungen zu den Wechselwirkungen der chromophoren Catechole mit Schwermetallionen kann gezeigt werden, dass die synthetisierten Verbindungen als Sensoren eingesetzt werden können. In der vorliegenden Arbeit wird des Weiteren die Adsorption der Catecholderivate an Metalloxide beschrieben. Mit Farbstoffen sensibilisierte Oberflächen stellen derzeit ein interessantes Forschunggebiet dar. Ferner wird über die Umsetzung der Catecholderivate mit Trialkoxysilanen zu zwitterionischen, spirozyklischen, pentakoordinierten lambda5Si-Silicaten sowie mit Tetraalkoxysilanen zu dianionischen, hexakoordinierten lambda6Si-Silicaten berichtet. Besonderes Augenmerk lag dabei auf UV/vis-spektroskopischen Untersuchungen.

Gegenstand der vorliegenden Arbeit ist die Synthese und Charakterisierung neuer chromophorer Catecholderivate mit ausgeprägten push-pull-pi-Systemen. Die solvatochromen Eigenschaften dieser Verbindungen werden in Abhängigkeit der Wasserstoffbrückenbindungsdonor- und -akzeptorfähigkeit sowie Lösungsmitteldipolarität diskutiert. Mit entsprechenden methoxy- und dimethoxyfunktionalisierten Catecholderivaten ist es möglich, vergleichende Struktur-Eigenschaftsbeziehungen aufzustellen. Durch Untersuchungen zu den Wechselwirkungen der chromophoren Catechole mit Schwermetallionen kann gezeigt werden, dass die synthetisierten Verbindungen als Sensoren eingesetzt werden können. In der vorliegenden Arbeit wird des Weiteren die Adsorption der Catecholderivate an Metalloxide beschrieben. Mit Farbstoffen sensibilisierte Oberflächen stellen derzeit ein interessantes Forschunggebiet dar. Ferner wird über die Umsetzung der Catecholderivate mit Trialkoxysilanen zu zwitterionischen, spirozyklischen, pentakoordinierten lambda5Si-Silicaten sowie mit Tetraalkoxysilanen zu dianionischen, hexakoordinierten lambda6Si-Silicaten berichtet. Besonderes Augenmerk lag dabei auf UV/vis-spektroskopischen Untersuchungen.

<p>Cadmium (Cd) is a highly mobile and toxic heavy metal that negatively affects plants, soil biota, animals and humans, even in very low concentrations. Currently, Cd contamination of cocoa produced in Latin American countries is a significant problem, as concentrations can exceed acceptable levels set by the European Union (0.5 mg/kg), sometimes by more than 10 times allowable levels. In South America, <i>Theobroma cacao</i> is an essential component of the basic market basket. This crop contributes to the Latin-American trade balance, as these countries export cacao and chocolate-based products to major consumer countries such as the United States and Europe. Some soil amendments can alter the bioavailability and uptake of Cd into edible plant tissues, though cacao plants can accumulate Cd without displaying any visible symptoms of phytotoxicity, which makes it difficult to determine if potential remediation strategies are successful. Currently, the only effective way to quantify Cd accumulation in plant tissues is via destructive post-harvest practices that are time-consuming and expensive. New hyperspectral imaging (HSI) technologies developed for use in high-throughput plant phenotyping are powerful tools for monitoring environmental stress and predicting the nutritional status in plants. Consequently, the experiments described in this thesis were conducted to determine if HSI technologies could be adapted for monitoring plant stress caused by Cd, and estimating its concentration in vegetative plant tissues. Two leafy green crops were used in these experiments, basil (<i>Ocimum basilicum L.</i> var. Genovese) and kale (<i>Brassica oleracea L</i>. var. Lacinato), because they are fast growing, and therefore, could serve as indicator crops on cacao farms. In addition, we expected these two leafy green crops would differ in their morphological responses to Cd stress. Specifically, we predicted that stress responses would be visible in basil, but not kale, which is known to be a hyperaccumulator. The plants were subject to four levels of soil Cd (0, 5, 10 and 15 ppm), and half of the pots were amended with biochar at a rate of 3% (v/v), as this amendment has previously been demonstrated to improve plant health and reduce Cd uptake. The experiments were conducted at Purdue’s new Controlled Environment Phenotyping Center (CEPF). The plants were imaged weekly and manual measurements of plant growth and development were collected at the same times, and concentrations of Cd as well as many other elements were determined after harvest. Fourteen vegetation indices generated using HSI images collected from the side and top view of plants were evaluated for their potential to identify subtle signs of plant stress due soil Cd and the biochar amendment. In addition, three mathematical models were evaluated for their potential to estimate Cd concentrations in the plant biomass and determine if they exceed safe standards (0.28 mg/kg) set by the Food and Agriculture Organization (FAO) for leafy greens. Results of these studies confirm that like many plants, these leafy green crops can accumulate Cd levels that are well above safety thresholds for human health, but exhibit few visible symptoms of stress. The normalized difference vegetation index (NDVI) and the chlorophyll index at the red edge (CI_RE) were the best indices for detecting Cd stress in these crops, and the plant senescence and reflectance index (PSRI) and anthocyanin reflectance index (ARI) were the best at detecting subtle changes in plant physiology due to the biochar amendment. The heavy metal stress index (HMSSI), developed exclusively for detecting heavy metal stress, was only able to detect Cd stress in basil when images were taken from the top view. Results of the mathematical models indicated that principal components analysis (PCA) and partial least squares (PLS) models overfit despite efforts to transform the data, indicating that they are not capable of predicting Cd concentrations in these crops at these levels. However, the artificial neural networks (ANN) was able to predict whether leafy greens had levels of Cd that were above or below critical thresholds suggested by the FAO, indicating that HSI could be further developed to predict Cd concentrations in plant tissues. Further research conducted in the field and in the presence of other environmental stress factors are needed to confirm the utility of these tools, and determine whether they can be adapted to monitor Cd uptake in cacao plants.</p>