Industrial effluents with high concentrations of heavy metals are widespread pollutants of great concerns as they are known to be persistent and non-degradable. Continuous monitoring and treatment of the effluents become pertinent because of their impacts on wastewater treatment plants. The aim of this study is to determine the correlation between heavy metal pollution in water and the location of industries in order to ascertain the effectiveness of the municipal waste water treatment plant. Heavy metal identification and physico-chemical analysis were done using Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) and multi-parameter probe respectively. Correlation coefficients of the measured values were done to investigate the effect of the industrial effluents on the treatment plants. Heavy metal resistant bacteria were identified and characterised by polymerase chain reaction and sequencing. Leeuwkuil wastewater treatment plants were effective in maintaining temperature, pH, and chemical oxygen demand within South Africa green drop and SAGG Standards whereas the purification plant was effective in maintaining the values of Cu, Zn, Al, temperature, BOD, COD, and TDS within the SANS and WHO standard for potable water. This findings indicated the need for the treatment plants to be reviewed.The industrial wastewater were identified as a point source of heavy metal pollution that influenced Leeuwkuil wastewater treatment plants and the purification plants in Vaal, Vereenining South Africa. Pseudomonas aeruginosa, Serratia marcescens, Bacillus sp. strain and Bacillus toyonensis that showed 100% similarity were found to be resistant to Al, Cu, Pb and Zn. These identified bacteria can be considered for further study in bioremediation. / Environmental Sciences / M. Sc. (Environmental Science)

The main aim of this thesis was the development of conjugation of existing methods for analysis of arsenic-glutathione complexes (As-GS complexes) together with simple arsenic species (iAs, MMAs, DMAs) during simple run. The basic technique for analysis of As-GS complexes was the HPLC-ICP-MS method with a reverse phase separation column (C18). The separation problem of simple species has been overcome by extending of system by postcolumn hydride generation with cryotrapping system (HG-CT). The resulting HPLC/HG-CT-ICP-MS system provides a complex analysis of all the above-mentioned analytes. According to the currently available resources, it is an innovative system, where for the first time all the simple arsenic species (iAs, MMAs, DMAs) and the As-GS complexes were separated. Under the given conditions, the detection limit for the As-GS complexes of 1.9 pg cm-3 in the RP-HPLC-ICP-MS system (a quantification limit of 6.5 pg cm-3 ) was achieved at a sensitivity of 468 CPS s pg-1 . The HG-CT-ICP-MS system provided a detection limit for iAs of 1.2 pg cm-3 at a sensitivity of 1121 CPS s pg-1 , for MMAs of 0.043 pg cm-3 at a sensitivity of 895 CPS s pg-1 and for DMAs of 0.076 pg.cm-3 at a sensitivity of 926 CPS s pg-1 . This method was applied to achieve another aim, studying the pathways of enzymatic...

Die vorliegende Arbeit stellt die Ergebnisse der methodologischen Entwicklung räumlich aufgelöster Analyse mittels Scanning Laserablation-ICP-Massenspektrometrie dar. Eine neue Behandlung zur Quantifizierung transienter analytischer Signale wurde für die Wiederherstellung von Konzentrationsprofilen vorgeschlagen. Die Anwendung der entwickelten Modelle auf die räumlich aufgelöste Analyse mittels LA-ICP-MS ermöglicht verbesserten Informationsgewinn und lässt dadurch eine höhere räumliche Auflösung erreichen. Die Anwendbarkeit der LA-ICP-MS für die räumlich aufgelöste Bestimmung der Stöchiometrie in supraleitenden Borokarbiden wurde untersucht. Der Einfluss apparativer Größen auf das analytische Signal wurde aufgeklärt, um die Messbedingungen zu optimieren. Zusätzlich wurden Fraktionierungseffekte untersucht, um die Ursache und deren Auswirkung auf die Analyse supraleitender Borokarbiden zu erklären. / This work represents the results of the methodological development of spatially resolved analysis by scanning laser ablation ICP mass spectrometry. A new approach to the quantification of transient analytical signals was proposed to reveal the concentration profile. An application of the developed models on spatially resolved analysis by LA-ICP-MS allows to gain more information from experimental data and hence to achieve better spatial resolution. The applicability of LA-ICP-MS to the spatially resolved determination of the stoichiometry of superconducting borocarbides was investigated. The effect of experimental parameters on analytical signals was elucidated in order to optimize the experimental conditions. In addition, fractionation effects were investigated to identify the causes for fractionation and their influence on the analysis of superconducting borocarbides.

This thesis describes two different sample preparation strategies for inductively coupled plasma atomic emission spectrometry (ICP-AES), and their ability regarding multi element quantification in complex samples. Sensitivity, repeatability, reproducibility and accuracy were investigated. The aim was to increase the over all efficiency, the speed of analysis, and/or the sensitivity of the analytical method. The intention was to measure analytes with concentrations ranging from ng/g to mg/g simultaneously. The aim was additionally to study chemical and physical processes occurring during the sample preparation, the sample transport to the plasma, and the atomization therein. In the first sample preparation strategy, a hydrophilic highly cross-linked iminodiacetate-agarose adsorbent, IDA-Novarose, was used for preconcentration of metal ions, and matrix elimination in natural water samples. The sorbent was synthesized with different binding capacities. The effect of the capacity on preconcentration, matrix elimination, and uptake capability at high flow rates was studied. For a high capacity IDA-Novarose (≥ 45 µmole/ml) quantitative uptake was seen even at high flow rates (100 ml/min) for Cu2+ with a high affinity to the adsorbent, and for Cd2+ with a moderate affinity. For lower capacities the uptake of Cd2+ was affected by the sample matrix and the flow rate. A method based on the determination of the conditional stability constant of the metal sorbent complex was suggested for the prediction of the sorbent capacity needed to obtain quantitative recovery and optimal matrix elimination. The sorbent was used in a flow system with online buffering for the analysis of a certified riverine water (SLRS-3), tap water and lake water. With few exceptions the results obtained by ICP-AES after preconcentration agreed well with the certified concentrations and results obtained by ICP-MS. The other sample preparation strategy discussed is a method for non digested biological samples from different animal organs for the multi element analysis by ICP-AES. This “mix and measure method” consists of a simple homogenization of the sample with a mixing rod in a small amount of neutral media, followed by dilution and direct measurement with ICP-AES. The total time of analysis is only a few minutes. The ability of this fast method to accurately quantify some elements of toxic, environmental, and/or physiological concern with the lowest possible sample dilution and the highest possible plasma load was evaluated. In 10 % liver slurry Cd, Co, and Sr, at concentration levels around 0.05 µg/g were quantified simultaneously with P and K around 2000 µg/g and with several other elements in between (Al, Ca, Cu, Fe, Mg, Mn, Pb, and Zn). The relative standard deviation of repeated measurements of samples was around 5 - 6 % for regardless of the concentration of the element. The method was also used for fast screening of the elemental distribution in mice organs (brain, heart, kidney, liver, lung and spleen).

Οι πηγές πλάσματος επαγωγικής ζεύξης (Inductively Coupled Plasma Sources – ICP’s), παρέχουν πλάσμα υψηλής πυκνότητας ηλεκτρονίων σε χαμηλή πίεση και έχουν ευρεία εφαρμογή στη σύγχρονη βιομηχανία ημιαγωγών και την κατεργασία επιφανειών. Σε πολύ χαμηλές πιέσεις, (~mTorr), οι εκκενώσεις πλάσματος παρουσιάζουν ιδιαίτερη συμπεριφορά όσον αφορά τη διείσδυση του ηλεκτρομαγνητικού πεδίου και την αλληλεπίδραση κύματος-σωματιδίου: Η ανώμαλη επιδερμική διείσδυση (anomalous skin effect) και η συντονισμένη αλληλεπίδραση κύματος-σωματιδίου όταν υπερτίθεται στατικό μαγνητικό πεδίο (resonant wave-particle interaction) είναι δύο φαινόμενα τυπικά σε αυτές τις εκκενώσεις. Η κατανόηση και μαθηματική ανάλυση αυτών των ιδιαίτερα περίπλοκων φαινομένων, ώστε να προσομοιωθούν με ακρίβεια αλλά και χωρίς χρονοβόρες υπολογιστικά διαδικασίες οι πηγές πλάσματος επαγωγικής ζεύξης, αποτελεί μια σύγχρονη επιστημονική και υπολογιστική πρόκληση. Στα πλαίσια αυτά, στην παρούσα διατριβή τέθηκε ως στόχος η αξιοποίηση της υπάρχουσας επιστημονικής γνώσης στον τομέα της υπολογιστικής προσομοίωσης πλάσματος, για την ανάπτυξη ταχύτατων προσομοιώσεων των πηγών πλάσματος επαγωγικής ζεύξης, διασφαλίζοντας ταυτόχρονα την εξαγωγή έγκυρων συμπερασμάτων: Η προσέγγιση αυτή συνίσταται στη διατύπωση υπόθεσης (μοντέλου), τον έλεγχό της σε σχέση με υπάρχοντα δεδομένα και την επαναδιατύπωσή της μέχρις ότου το μοντέλο να κριθεί επαρκές. Αρχικά αναπτύχθηκε ένα ρευστοδυναμικό μοντέλο πλάσματος βασισμένο στην υπόθεση ψευδουδετερότητας και αμφιπολικής διάχυσης των φορέων φορτίου, προκειμένου να προσομοιωθεί η ενισχυμένης μαγνητικής διαπερατότητας πηγή επαγωγικής ζεύξης MaPE–ICP. Τα αποτελέσματα της προσομοίωσης συγκρίνονται με τα πειραματικά στοιχεία προηγούμενων ερευνητών για εκκενώσεις Αργού και εξετάζεται η ικανότητα του ρευστοδυναμικού μοντέλου να παρέχει μια στοιχειώδη ποσοτική περιγραφή πλάσματος επαγωγικής ζεύξης σε χαμηλή πίεση. Η αξιοπιστία του ρευστοδυναμικού μοντέλου εξελίσσεται περεταίρω, με την ενσωμάτωση μιας αποτελεσματικής αριθμητικής επίλυσης της κινητικής εξίσωσης Boltzmann για τα ηλεκτρόνια. Τα αποτελέσματα της υβριδικής προσομοίωσης για εκκένωση Αργού πίεσης 30 mTorr στον αντιδραστήρα MaPE–ICP συγκρίνονται τόσο με αντίστοιχα πειραματικά δεδομένα όσο και με τα προηγούμενα αποτελέσματα της ρευστοδυναμικής προσομοίωσης και εξετάζεται η βελτίωση της ποιοτικής συμφωνίας όσον αφορά την επίδραση των παραμέτρων με ιδιαίτερο ενδιαφέρον. Στη συνέχεια αναπτύχθηκε ένα ρευστοδυναμικό μοντέλο εκκενώσεων αίγλης τύπου ECWR (Electron Cyclotron Wave Resonance) βασισμένο σε προκαθορισμένες οριακές συνθήκες για το ηλεκτρομαγνητικό πεδίο. Προσομοιώθηκε ένα διάκενο με πλάσμα Αργού σε πίεση 15 mTorr (μονοδιάστατο μοντέλο) και τα αποτελέσματα ελέγχθηκαν έναντι αναλυτικής θεωρίας, πειραματικών δεδομένων και αποτελεσμάτων προσομοίωσης Particle In Cell/Monte Carlo (PIC/MC). Επιπρόσθετα, τα αποτελέσματα προσομοίωσης για μια εκκένωση Αργού σε πίεση 1 mTorr εντός κυλινδρικού αντιδραστήρα τύπου ECWR (δισδιάστατο μοντέλο), συγκρίνονται με τα αποτελέσματα προσομοίωσης και πειραματικά στοιχεία. Τέλος, το μοντέλο έχει επεκταθεί για να περιλάβει την διάδοση του πλάσματος που παράγεται από μια τυπική πηγή πλάσματος τύπου ECWR σε μια περιοχή διάχυσης. Τα αποτελέσματα για εκκένωση Αργού πίεσης 5 mTorr συγκρίνονται με τα αντίστοιχα αποτελέσματα ενός μοντέλου σφαιρικής διάχυσης πλάσματος και εν προκειμένω εξετάζεται η πλήρης επεκτασιμότητα του εισαχθέντος ρευστοδυναμικού μοντέλου ECWR σε διεργασίες πλάσματος. / Inductively Coupled Plasma Sources (ICP’s) are capable of producing high density-low pressure plasmas in a variety of applications for the semiconductor and material processing industry. In the mTorr range, ICP discharges exhibit an extraordinary behaviour concerning the electromagnetic field propagation and wave-particle interaction: Anomalous skin effect and resonant wave-particle interaction within a superimposed static magnetic field consist two of the most typical phenomena. The efficient comprehension and mathematical description of such a complex gas discharge in order to fast and accurately simulate ICP sources, is still a challenging task. Within this context, the thesis focuses on evaluating the existing scientific knowledge in plasma computational modeling in order to develop not only rapidly converging but reliable ICP simulations: The implementation methodology consists on formulating an hypothesis (model) and repetitively inquiring its accuracy by checking the simulation results against existing experimental and/or other simulation data. The continuation of the model re-formulation process depends on the accuracy of the simulation results. Initally a simulation of a Magnetic Pole Enhanced (MaPE)-ICP plasma source was developed, under the assumptions of plasma quasineutrality and ambipolar diffusion. The simulation results were checked against the experimental data of previous workers for Argon discharges and the ability of the model to provide an elementary quantitative description of low pressure ICP sources was scrutinized. The validity of the fluid model was enhanced with the incorporation of a time effective numerical solution of the Boltzmann transport equation for electrons. Simulation results of the hybrid model were compared to the previous fluid simulation results and existing experimental data, for a 30 mTorr Argon discharge in the MaPE–ICP reactor. The major improvements of the qualitative agreement in regard to the effect of parameters with particular interest are discussed. Moreover, a fluid model of ECWR (Electron Cyclotron Wave Resonance) discharges, based on predefined boundary conditions for the electromagnetic field, was developed: The simulation results for a 15 mTorr Argon plasma within a slab (1-dimensional model) were checked against the particle in cell/Monte Carlo (PIC/MC) simulation results that can be found in the literature and also compared to the analytical theory and experimental data. In addition, the model was further developed to simulate realistic geometries as a cylindrical ECWR reactor (2-D) and the data were also compared to both simulation results and experimental data of other researchers. Finally, the model was extended in order to simulate plasma propagation from a typical ECWR plasma source to a diffusion region. The simulation results for an Argon plasma generated from a cylindrical ECWR source in a processing chamber at 5 mTorr were presented in order to verify the feasibility of model application in ECWR plasma processes.

Předkládaná diplomová práce se zabývá extrakcí nanočástic oxidu titaničitého z produktů osobní péče, konkrétně opalovacích krémů a následnou charakterizací těchto částic. Počet komerčně dostupných produktů s obsahem nanočástic TiO2 se neustále zvyšuje a to se sebou přináší potřebu vyhodnotit potenciální osud a nepřímou expozici TiO2 nanošástic o různých velikostí a tvarů a zkoumat jejich celý životní cyklus. Bylo zkoumáno použití ultrafiltrace a ultracentrifugace jako extrakční metody. Dvě metody pro extrakci TiO2 nanočástic byly vyvinuty a aplikovány na vzorky opalovacích krémů. Extrahované částice mohou být použity pro ekotoxikologické studie, případně experimenty v mesokosmu. Velikost částic byla stanovena pomocí metody dynamického rozptylu světla a transmisní elektronové mikroskopie.

MSc (Chemistry / Department of Chemistry / In this study, three sampling sites (Tshipise thermal spring, Mphephu thermal spring and Siloam borehole) in Limpopo Province South Africa were considered for an investigation into the mineral composition of their water and soil samples. Tshipise and Mphephu thermal springs are well developed and located within tourist resorts. On the other hand, Siloam is a borehole on the grounds of a private household. The water is used for various domestic purposes such as laundry, general cleaning of the household and bathing. Water and soil samples from the three sites were collected once per week every week in February 2018. The sampling bottles were spiked with 1M HNO3 before sampling to keep any metal ions present in the water samples in solution. The soil and water samples were analysed for their chemical composition using X-ray fluorescence (XRF) and inductively coupled plasma mass spectrometry (ICP-MS) respectively. XRF analysis of the soil samples found many major oxides of which SiO2 made up 63.67%, 85.37% and 46.28% by mass of Tshipise, Mphephu and Siloam soil samples respectively. XRF analysis also showed the presence of dangerous levels of heavy metals such as As, Tl, Pb and V. The analysis of the water samples by ICP-MS found that Tshipise, Mphephu and Siloam mineral water were soft, soft-moderately hard and soft-hard respectively with regards to the water hardness scale according to the United States Geological Survey (USGS) and the Water Quality Association (WQA). Analysis of water samples also found the presence of As, Cd, Cr and V. Arsenic was found to occur at concentrations above the Maximum Allowable Concentration (MAC) set by the World Health Organisation (WHO) (10 μg L-1) for Tshipise, Mphephu and Siloam mineral water (13.63 μg L-1, 15.83 μg L-1 and 20.97 μg L-1 respectively). Water temperatures for the three sites ranged from 38°C (Siloam borehole) to 64°C (Tshipise thermal spring). The pH values were 7.25 (Siloam borehole), 7.40 (Mphephu thermal spring) and 8.67 (Tshipise thermal spring). Due to the presence of As, Tl, Pb, V, Cd and Cr, the mineral water from all three thermal springs is unsafe to consume as it would lead to serious negative health effects some of which are outlined in this study. / NRF

This diploma thesis is focused on the study of electrochemical generation volatile species of gold and silver. Two non-membrane electrolytic cells were constructed for electrochemical generation volatile species. These cells differ in the volume of electrode chamber. An atomic absorption spectrometry with quartz tube atomizer was used in most experiments. The equipment was performed in flow continuous mode. Experiments confirmed, that it is possible to use an atomic absorption spectrometry with quartz tube atomizer for generate volatile species of gold and silver by using two non-membrane electrolytic cells. The main part of this thesis was to find optimal conditions for the electrochemical generation of volatile species of gold and silver. These optimized parameters were: the cathode material, the type of electrolyte, the flow rate of the carrier gas, the generation current and the electrolyte flow rate. The calibration curves for both analytes were measured for both non-membrane electrolytic cells and the basic characteristics of the measurement were observed. Detection limit for electrochemical generation of gold was 1,61mg dm 3 and repeatability 3,93 %, detection limit for electrochemical generation of silver was 0,20 mg dm 3 and repeatability 7,33 %. Thanks to the experiments with a...

Die vorliegende Arbeit stellt die Ergebnisse der methodologischen Entwicklung räumlich aufgelöster Analyse mittels Scanning Laserablation-ICP-Massenspektrometrie dar. Eine neue Behandlung zur Quantifizierung transienter analytischer Signale wurde für die Wiederherstellung von Konzentrationsprofilen vorgeschlagen. Die Anwendung der entwickelten Modelle auf die räumlich aufgelöste Analyse mittels LA-ICP-MS ermöglicht verbesserten Informationsgewinn und lässt dadurch eine höhere räumliche Auflösung erreichen. Die Anwendbarkeit der LA-ICP-MS für die räumlich aufgelöste Bestimmung der Stöchiometrie in supraleitenden Borokarbiden wurde untersucht. Der Einfluss apparativer Größen auf das analytische Signal wurde aufgeklärt, um die Messbedingungen zu optimieren. Zusätzlich wurden Fraktionierungseffekte untersucht, um die Ursache und deren Auswirkung auf die Analyse supraleitender Borokarbiden zu erklären. / This work represents the results of the methodological development of spatially resolved analysis by scanning laser ablation ICP mass spectrometry. A new approach to the quantification of transient analytical signals was proposed to reveal the concentration profile. An application of the developed models on spatially resolved analysis by LA-ICP-MS allows to gain more information from experimental data and hence to achieve better spatial resolution. The applicability of LA-ICP-MS to the spatially resolved determination of the stoichiometry of superconducting borocarbides was investigated. The effect of experimental parameters on analytical signals was elucidated in order to optimize the experimental conditions. In addition, fractionation effects were investigated to identify the causes for fractionation and their influence on the analysis of superconducting borocarbides.

Nanopartiklar är partiklar med storlekar i området 1 till 100 nm, och som uppvisar nanospecifika egenskaper. Egenskaperna kan variera helt mellan olika typer av nanopartiklar, även bland partiklarna och deras respektive material i bulk format på grund av deras unika storlekar, former och strukturer. I denna studie har vi analyserat storlekarna och den kolloidal stabiliteten på tre nanopartiklar, Co, Y2O3, CeO2 i färskvatten och färskvatten med naturligt organiskt material med hjälp av sonifikation, NTA, AAS och ICP analys. Nanopartiklarna lät vara utsatta i lösningarna i upp till six timmar, där analys med hand av NTA skedde efter den nollte, första och sjätte timmen. Partiklarna uppvisade olika egenskaper, och alla tre partiklar varierade i storlek under experimentet. Kobalt hade tendensen att minska i storlek i bägge lösningar, medan storlekarna på yttrium- och cerium oxid tenderade att variera. För att främja vår förståelse av nanopartiklar, behövs fler studier för att få en full förståelse för de unika egenskaperna hos dessa partiklar. / Nanoparticles are particles with sizes in the range of 1 to 100 nm, which also have nanospecific properties. Their properties vary wildly between different types of nanoparticles, even among nanoparticles and their respective particles in bulk format heeding to their highly individual shapes, sizes and structures. In this study we analyzed the sizes and colloidal stability of three different nanoparticles, Co, Y2O3 and CeO2 in freshwater and freshwater with natural organic matter solutions using sonication, NTA-, AAS-, and ICP analysis. The nanoparticles were exposed to the solutions for up to six hours, with analysis being performed at the zero, first and sixth hour. The particles indeed showed different properties, as all three particles varied in size throughout the experiment. Cobalt had the tendency to decrease in size as time progressed in both solutions, while the mean size of yttrium- and cerium oxide varied. To further our understanding of nanoparticles, more studies need to be performed to properly understand the individual properties of these nanoparticles.