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Tato práce se zabývá studiem termooxidační stability kompozitů polymethylmethakrylátu (PMMA) plněného mikro a nanočásticemi siliky. V připravených vzorcích byly použity různé objemové zlomky a různé velikosti částic siliky. Studium stability bylo prováděno pomocí termogravimetrie, která umožňuje simulovat podmínky termooxidační degradace. Indukční perioda byla stanovena za použití různých rychlostí ohřevu a aplikací izokonverzních metod. Závislosti teplot degradací na rychlostech ohřevu sloužily pro určení parametrů odvozených ze čtyř různých teplotních funkcí, které dovolují předpověď stability materiálu (indukční periody) při zvoleném rozsahu teplot. Zjištěné výsledky ukazují, že větší částice siliky snižuji stabilitu PMMA, zatímco nanočástice v nízkých koncentracích ji nijak neovlivňují.

M. Tech. (Department of Chemistry, Faculty of Applied and Computer Sciences), Vaal University of Technology. / Water scarcity due to limited resources and pollution of the little available water by organic and inorganic contaminants remains as one of the critical issues of the 21st century. Several treatment methods have been developed, with some being used successfully at industrial scale but many challenges including secondary sludge generation, high operation costs, high maintenance costs and high energy input were observed. In this study, the adsorption process was explored as an effective means for the removal of Cr(VI) ions from aqueous solution due to its economic feasibility and use of abundantly available adsorbents. Amongst the many available adsorbents, this work focused on exploring functionalized activated carbons (ACs) as adsorbents for Cr(VI) ions due to their favorable adsorption characteristics which involve large surface area, high porosity, and high radiant stability. The iron oxide functionalized polyethyleneimine activated carbon-silica composites were prepared through co-precipitation of Fe(II) and Fe(III) over Macadamia activated carbon to form the AC-Fe3O4 co-shell which was reacted with tetraethylorthosilicate (TEOS) and the polyethyleneimine (PEI). The different adsorbents prepared were labelled AC-Fe3O4, AC-Fe3O4-SiO2 and AC-Fe3O4-SiO2-PEI. The adsorbents were further characterized using elemental analysis (CHNS), thermo gravimetric analysis (TGA), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), Fourier transform infrared (FTIR) spectroscopy, Brunauer-Emmett-Teller (BET), transmission electron spectroscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). FTIR displayed successful attachment of Fe3O4 and SiO2 with bands at 404 and 786 cm-1 being assigned to the asymmetric vibration of Fe-O and Si-O-Si while the asymmetric stretch of Si-OH is observed at 1066 cm-1. XRD showed the presence of magnetite particles in the adsorbents confirmed by the JCPDS 00-019-0629. EDS revealed the presence of Fe, Si, and N atoms which can relate to successful incorporation of the desired functional groups. Each of these materials were evaluated for their Cr(VI) ion removal through batch adsorption experiments where one parameter at a time was varied while all others were fixed. The parameters investigated included the effect of pH, contact time, initials Cr(VI) concentration, adsorbent dosage concentration and temperature. The optimum conditions were obtained at pH 3, initial concentration 2.5 mg/L, contact time of 120 min for AC-Fe3O4-SiO2-PEI. The optimization of each parameter was done in order to determine the conditions in which the adsorbents work best in the uptake of Cr(VI). All the three studied adsorbents showed acceptable adsorption performance for the removal of Cr(VI) from aqueous solutions. Adsorption isotherms studied confirmed that the adsorption data in all the three adsorbents fitted well into the Langmuir isotherm, demonstrating a homogeneous monolayer coverage. Regarding the kinetic studies, the adsorption data were best described by the pseudo-second order rate model with R2 values of 0.974, 0.974 and 0.962 for AC-Fe3O4, AC-Fe3O4-SiO2 and AC-Fe3O4-SiO2-PEI, respectively. The adsorption capacity observed from the present study (6.62, 3.92 and 5.48 for AC-Fe3O4, AC-Fe3O4-SiO2 and AC-Fe3O4-SiO2-PEI, respectively) were satisfactory and suitable as compared to those reported in literature. Thermodynamics data of the adsorption processes revealed a feasible spontaneous endothermic adsorption process which also confirmed that the reaction process occurred through chemisorption.

A porous silica –silica composite was processed with varying fiber diameters using the slurry moulding technique. The advantage of the process was that the density of the composite could be processed to the required levels. The reinforcements used were fibers obtained by leaching E-glass cloth, imported silica fibers with diameter <1.8µ and hollow silica fibers processed using sol-gel method. All the properties depend on the density of the composite. The compressive strength was measured in the perpendicular and parallel directions. Strength was high when the load axis was along the fiber direction. The composite with fine fibers (< 1.8 µ pure silica fibers) showed higher strength compared to the leached silica fibers. The thermal conductivity measurement on these composites showed an increase with temperature owing to the domination of radiation at high temperatures. As the vacuum level was approached, the thermal conductivity showed a decrease due to the absence of the convective part of the thermal transfer process. For use as a thermal protection system, it is important to measure the thermal response of these tiles in a simulated re-entry environment. Tests were done to measure this response for a given heat flux conditions at 38W/cm2 to 75W/cm2 and the backwall temperature was measured for various types of silica -silica composites. The role of impurities like sodium and B2O3 was also studied with respect to the conversion from amorphous to crystalline forms of SiO2. The severe increase in the coefficient of thermal expansion when SiO2 converted from amorphous to α– crystoballite was also measured. CSZP CSZP which belongs to the NZP family was processed using the co-precipitation technique. The influence of substituting the ‘P’ site with ‘Si’ atom was studied for its influence on thermal expansion – both at the bulk level by dilatometry and at the intrinsic level using high temperature XRD. For many anisotropic materials micro-cracking is a serious issue while cooling from the sintering temperature. It has been previously proved that this extent of micro-cracking depends on the particle size. Smaller the particle size is therefore preferred. One of the significant results obtained in this study was the successful use of microwaves to process crack free CSZP with fine grain size. CSZP with 95% density having a grain size as small as 1µ have been processed using microwave sintering. Dielectric property evaluation namely dielectric constant, dielectric loss and temperature coefficient of resonant frequency which are vital parameters required if this material is to be used as a candidate TPS have also been measured. The thermal conductivity of the sample was measured using Laser flash apparatus and was found to be 0.9 W/mk which provides an indication that this material can be used as a successful material for TPS. Finally a composite consisting of silica fiber with CSZP as matrix was processed and tested for heat flux. The low back wall temperature indicates that this material is a potential replacement for silica tile.