The thesis examines for the first time the supercapacitive properties of three different nickel (II) phthalocyanine complexes, nickel (II) tetraamino phthalocyanine (NiTAPc), nickel (II) phthalocyanine and nickel (II) tetra tert-butylphthalocyanine as a) nanocomposites with multiwalled carbon nanotubes and as (b) an electropolymer supported on multiwalled carbon nanotube platform (MWCNT-polyNiTAPc). The supercapacitive properties of nickel (II) tetraaminophthalocyanine (NiTAPc)/multi-walled carbon nanotube (MWCNT) nanocomposite films have been found to possess a maximum specific capacitance of 981 F g-1 (200 mF cm-2), a maximum power density of 700 Wkg -1, a maximum specific energy of 134 Wh kg-1 and excellent stability of over 1500 chargedischarge continuous cycling. When compared to MWCNTs modified with unsubstituted nickel (II) phthalocyanine (MWCNT-NiPc) or nickel (II) tetra tert-butylphthalocyanine (MWCNT-tBuNiPc), MWCNT-NiTAPc exhibited superior supercapacitive behaviour, possibly due to the influence of nitrogen-containing groups on the phthalocyanine. The MWCNTpolyNiTAPc electrode had a maximum (112 mF cm-2) capacitance which was higher than that observed for MWCNT-polyNi(OH)TAPc (84.9 mFcm-2) but lower that of the MWCNT-NiTAPc (200 mF cm-2). Copyright / Dissertation (MSc)--University of Pretoria, 2010. / Chemistry / unrestricted

Amid a growing world population and diminishing living space, the discerning and beneficial use of steel plant slag as liming material in agriculture has become a viable option. However, until the potentially detrimental effect on human health and environmental quality of heavy metals contained within the matrixes of slag has been assessed, the use of slag in agriculture cannot be deemed sustainable. This study aims to correlate the mechanisms by which chromium(III) and nickel are sorbed in Eastern Highveld soils to easily classifiable soil constituents. In addition, the influence of an external source of silicon, as would be the case in dissolving slag, on Cr(III) and Ni mobility was investigated. The study consisted of an investigation into the mechanisms by which Cr(III) and Ni are sequestered in soil within a single wetting and drying cycle, as well as over a period of five rewetting and drying cycles. The effect of Si was observed for the latter and a detailed mineralogical study conducted as part of the former. Additionally, the reactivity of and heavy metal (Cr and Ni) release from two commercially available slag samples used as liming material in a highly buffered soil was investigated. Five main conclusions were drawn: (i) whereas Cr(III) is effectively sorbed (even at near water saturated conditions) and precipitation ascribed to bulk-solution saturation, Ni is not sequestered as effectively, and initially precipitates owing to the influence of soil mineralogy; (ii) conclusive evidence could not be gathered for the further immobilisation after sorption of Cr(III) and Ni over a short time period; (iii) both Cr(III) and Ni associate mainly with the amorphous Fe oxide mineral phase; (iv) an external source of Si renders Ni less mobile in soil that does not sequester the element effectively, but more mobile in soil that does tend to sequester the element to some degree; and (v) although neither Cr(III) nor Ni mobility could be explained using field classifiable soil characteristics (soil colour and texture), soil mineralogical and detailed surface charge characterisation did provide explanations for sorption behaviour. Copyright / Dissertation (MSc(Agric))--University of Pretoria, 2009. / Plant Production and Soil Science / unrestricted

M. Tech. (Department of Chemistry, Faculty of Applied and Computer Sciences), Vaal University of Technology. / Lead, nickel and cobalt dithiocarbamates complexes were synthesized using methanol and water as solvents. All complexes were refluxed at 60 °C, cooled at room temperature, washed with methanol to remove the impurities and dried under the fume hood. A combination of Fourier transformer infrared (FTIR), elemental analysis (EA) and thermogravimetric analysis (TGA) were used to characterize these complexes. There was shifting of bands from low to high frequencies of the dithiocarbamates complexes compared to benzimidazole derivatives. The absence of the N-H band and the presence of new C=S bands confirmed that the complexes can be used in the preparation of metal sulphide nanoparticles. Elemental analysis showed that there was a percentage mismatch for the complexes I, III, IV and V. Complexes II and VI calculated percentages were within the limits with the found percentages except for sulphur which was low. The TGA curves decomposed to form a mixture of metal and metal sulphides for complex I, II, III and IV except for complex VI which gave metal sulphide only. All benzimidazole complexes decomposed at higher temperatures and were considered as stable complexes. Lead sulphide (PbS) is an important group IV-VI metal chalcogenide semiconductor. It has a direct narrow band gap of 0.41 eV at 300K and a large excitonic Bohr radius of 18 nm. Lead sulphide absorption band can be tuned to anywhere between near IR to UV (0.4μm) covering the entire visible spectrum, while achieving the quantum confinement region. The synthesis of lead sulphide nanoparticles was conducted by varying the effect of the reaction conditions such as the type of capping agents and temperature. Lead dithiocarbamate complex derived from benzimidazole, [Pb(S2N2C8H5)2] was thermolysed in hexadecylamine (HDA) and trioctylphosphine oxide (TOPO) at different reaction temperatures (140, 160 and 180 °C) to produce HDA and TOPO capped PbS nanoparticles. The nanoparticles were characterized using X-ray diffraction (XRD) for structural analysis, transmission electron microscopy (TEM) for shape and size, Ultraviolet visible (UV/Vis) and Photoluminescence (PL) spectroscopy for optical properties. An increase in temperature gave a decrease in the sizes of the nanoparticles when using the HDA capped lead benzimidazole dithiocarbamate complex. The observed morphology was cubes. TOPO capped lead benzimidazole dithiocarbamate complex gave no specific trend when temperature was varied. A cross-like layer with quasi spherical particles on top was observed at 160 °C. At 180 °C, the cross-like layer decomposed into rods- like materials with quasi spherical particles on top for TOPO capped PbS nanoparticles. For lead 2-methylbenzimidazole [Pb(S2N2C9H7)2] dithiocarbamate complex, TOPO capped PbS produced agglomerated cubic morphology at low temperature but as the temperature was increased agglomerated cylindrical shapes were observed. HDA capped PbS produced polydispersed nanocubes which were increasing in size when the temperature was increased. Nanoparticles displayed a blue shift in band edges with good photoluminescence behaviour which was red shifted from their respective band edges all temperatures and capping agents. XRD confirmed the crystal structure of cubic phase (galena) of PbS at all temperatures except for HDA capped PbS nanoparticles at 140 °C from lead benzimidazole dithiocarbamate complex which confirmed the crystal structure of face-centred cubic phase of PbS nanoparticles. Nickel sulphide has much more complicated phase diagram than cobalt sulfides and iron sulfides. Their chemical composition has many crystalline phases such as α-NiS, β=NiS, NiS2, Ni3S2, Ni3S4, Ni7S6 and Ni9S8. Ni3S2 phase has shown potential as a low-cost counter electrode material in dye sensitised solar cells, while the α-NiS phase has been applied as a cathode Material in lithium-ion batteries. The synthesis of nickel sulphide nanoparticles was done by varying the effect of the reaction conditions such concentration and temperature. Nickel benzimidazole dithiocarbamate [Ni(S2N2C8H5)2] and nickel 2-methylbenzimidazole [Ni (S2N2C9H7)2] dithiocarbamates complexes were thermolysed in hexadecylamine (HDA) at different reaction temperatures (140, 160 and 180 °C) and precursor concentrations (0.30, 0.35 and 0.40 g) to produce HDA capped NiS nanoparticles. It was observed that increasing both temperature and precursor concentration increased the size of the nanoparticles. Anisotropic particles were observed for both complexes when varying precursor concentration and temperature. Nickel benzimidazole dithiocarbamate complex produced stable shapes (spheres and cubes) of nickel sulphide nanoparticles. Nickel 2-methylbenzimidazole dithiocarbamate complex produced a mixture of spheres, cubes, triangles and rods nickel sulphide nanoparticles at all concentrations. But when varying temperature, it only produced that mixture at 160 °C. The optical measurements supported the presence of smaller particles at all temperatures and concentrations. XRD showed the presence of C7OS8 and pure nickel as impurities. However, the crystal structure of cubic Ni3S4 was observed at low temperatures and an introduction of monoclinic NixS6 at high temperature (180 °C) when varying temperature for both complexes. When varying concentration using nickel benzimidazole dithiocarbamate complex, XRD showed the presence of NiSO4.6H2O impurities at high temperatures. At 160 °C a mixture of hexagonal NiS and cubic Ni3S4 was observed. At low temperatures only nickel as a metal was found as an impurity and the crystal structure of cubic Ni3S4 was observed. When nickel 2-methylbenzimidazole complex was used, C7OS8 and pure nickel were found as impurities but the crystal structure of cubic Ni3S4 was observed. Cobalt sulphide (CoS) belongs to the family of group II-IV compounds with considerable potential for application in electronic devices. They have a complex phase diagram and their chemical composition have many phases such as Co4S3, Co9S8, CoS, Co1-xS, Co3S4, Co2S3 and CoS2. The synthesis of cobalt sulphide nanoparticles was conducted by varying the effect of temperature on size and shape of the nanoparticles. Nickel benzimidazole dithiocarbamate, [Ni(S2N2C8H5)2] and nickel 2-methylbenzimidazole [Ni(S2N2C9H7)2] complexes were thermolysed in hexadecylamine (HDA) at different reaction temperatures (140, 160 and 180 °C) to produce HDA capped CoS nanoparticles. Cobalt benzimidazole dithiocarbamate complex produced close to spherical shapes nanoparticles at all temperatures. The images showed that as temperature was increased, the size of the particles decreased. All the main reflection peaks were indexed to face-centred cubic Co3S4 and there were some impurities of C7OS8 at all temperatures. The optical measurements supported the presence of smaller particles at all temperatures. Cobalt 2-methylbenzimidazole dithiocarbamate complex produced big and undefined morphology. The optical properties were also featureless and XRD only showed impurities of C7OS8. The impurity is thought to be generated from a side reaction between benzimidazole and carbon disulphide to give this persistent organic moiety.

Die vorliegende Arbeit beschäftigt sich mit der Entwicklung einer Synthesestrategie einphasiger intermetallischer Verbindungen des Systems Molybdän-Nickel als Volumenmaterial. Anhand dieser Materialien soll aufgeklärt werden, ob geordnete intermetallische Verbindungen eine höhere Aktivität in der elektrokatalytischen Wasserstoffbildung aus Wasser besitzen als nicht geordnete Substitutionslegierungen. Des Weiteren soll der Grund für die veränderte Aktivität identifiziert werden. Dazu wurden die Verbindungen mittels elektrochemischer Charakterisierungsmethoden und zwei verschiedenen Stabilitätstests in der Wasserstoffbildungsreaktion untersucht. Die Ergebnisse legen nahe, dass die Verbindungen unter den Reaktionsbedingungen nicht stabil sind. Bei Molybdängehalten ≤25 At.-% und Potentialen unterhalb des reversiblen Wasserstoffpotentials kann sich jedoch eine passivierende Nickelhydroxidschicht ausbilden, sodass eine fortschreitende Korrosion unter kathodischen Stromflüssen verhindert werden kann. Diese Nickelhydroxidschicht ist jedoch auch für die Desaktivierung der Mo-Ni Materialien verantwortlich. Es konnte weiterhin festgestellt werden, dass die elektrochemisch aktive Oberfläche, in Folge der Auslaugung von Molybdän, proportional zum Molybdängehalt steigt, was sich in vermeintlich höheren Aktivitäten der Mo-Ni Materialien äußert.

Thesis (M. Sc. Agriculture (Animal Production)) -- University of Limpopo, 2021 / The study was carried out to determine the concentration levels of mercury (Hg), lead (Pb), cadmium (Cd), chromium (Cr), nickel (Ni) and zinc (Zn) in water, soil, witbuffels grass and meat of goats reared along the river banks of Middle Olifants (Mogalatsana village) and Mogalakwena (Papegaai village) rivers. The samples were collected from the river water, soils along the river banks, grass grown along the river banks and male Pedi goats reared in Mogalatsana and Papegaai villages. The samples were analysed for the selected heavy metals with an inductively coupled plasma mass spectroscopy (ICP-MS). Data was analysed as in a complete randomised design. The results of selected heavy metals in water of both rivers ranged from 0.00 mg/litre of water (Ni and Cr) to 0.04 mg/litre of water (Hg). The concentration levels of selected heavy metals in water were similar (P>0.05) for Middle Olifants and Mogalakwena rivers. The concentration levels of selected heavy metals in the soils along the banks of Middle Olifants and Mogalakwena rivers ranged from 0.00 mg/kg DM soil (Hg and Cd) to 63.70 mg/kg DM soil (Cr). There were similar (P>0.05) concentration levels of selected heavy metals in the soils along the banks of Middle Olifants and Mogalakwena rivers. Heavy metal concentration levels in the witbuffels grass grown along the banks of Middle Olifants and Mogalakwena rivers ranged from 0.00 mg/kg DM of grass (Hg and Cd) to 5.05 mg/kg DM of grass (Zn). Similar (P>0.05) concentrations of selected heavy metals were observed in witbuffels grass grown along the banks of Middle Olifants and Mogalakwena rivers. However, the concentration levels of Zn, Pb and Cd in water from both sites were above internationally maximum permissible levels, indicating that the water from these rivers was not safe for drinking by humans and animals. The concentration levels of Ni and Pb in soils from both sites were above internationally recommended maximum permissible limits. Similarly, chromium concentration levels in witbuffels grass from both sites were above the recommended maximum permissible limits for livestock, indicating that the grass was not safe for consumption by livestock. It is recommended that further studies be conducted to ascertain these findings. Blood, liver, kidney and meat samples of yearling male Pedi goats grazing along the banks of Middle Olifants river (Mogalatsana village) had similar (P>0.05) Cr, Cd, Hg, Ni and Pb concentration levels, respectively. However, goat liver samples had higher (P<0.05) Zn concentrations than meat, kidney and blood samples. Samples of goat v meat contained higher (P<0.05) Zn concentrations than those of kidneys and blood. Similarly, goat kidney samples contained more (P<0.05) Zn than blood samples. Blood, liver, kidney and meat samples of Pedi goats grazing along the banks of Mogalakwena river (Papegaai village) contained similar (P>0.05) concentration levels of Cr, Cd, Hg, Ni and Pb, respectively. However, goat meat samples contained higher (P<0.05) Zn concentrations than liver, kidney and blood samples. Samples of goat liver contained higher (P<0.05) Zn concentration levels than kidney and blood samples. Similarly, goat kidney samples contained more (P<0.05) Zn than blood samples. Meat, blood, liver and kidney samples of male Pedi goats raised in Mogalatsana and Papegaai villages had similar (P>0.05) chromium, cadmium, mercury, nickel and lead concentrations, respectively. However, liver and kidney samples of goats from Mogalatsana village had higher (P<0.05) zinc levels than those from Papegaai village. Blood and meat samples of goats from Papegaai village had higher (P<0.05) zinc levels than those from Mogalatsana village. The concentration levels of Zn, Ni, Pb, Cr and Cd in the blood, liver, kidney and meat samples of male Pedi goats reared along the banks of Middle Olifants and Mogalakwena rivers were within the maximum permissible levels for human consumption. Mercury concentration levels in liver, kidney and meat samples of the goats were within the maximum permissible levels for human consumption. However, mercury concentration levels in the blood of goats grazing along the banks of Middle Olifants and Mogalakwena rivers were above the maximum permissible limit of 0.2 mg/litre of blood. It was concluded that meat, livers and kidneys of the goats were fit for human consumption. However, blood from these goats was not fit for human consumption.

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