Thesis (Ph. D.)--University of Wisconsin--Madison, 1956. / Typescript. Vita. Abstracted in Dissertation abstracts, v. 16 (1956) no. 5, p. 883-884. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 179-184).

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Antimony trioxide (Sb2O3) is a common additive in flame retardant formulations and a study has been made to determine the effects of adding it alone, or with four commercial brominated materials (OBDPO, BTBPE, TBBA and PDBS80) to ABS polymer. The results focus upon mechanical, rheological, microscopical and flame retardant properties, and the effects of different Sb2O3 grades with average particle sizes ranging from 0.1 to 11.8 μm. The Sb2O3 was mainly studied up to 12 wt% loading in ABS, since this is considered to be the maximum level used in commercial flame retardant formulations.

Student Number : 0420699F - MSc Dissertation - School of Physics - Faculty of Science / This dissertation presents for the first time the conditions for the synthesis of VO2 by ultrasonic nebula-spray pyrolysis (UNSP) from a precursor solution of NH4VO3+VCl3 optimized as follows: a carrier gas of argon at a flow rate of 11 liters per minute, a furnace temperature of 400 to 700oC. This work also incorporates thermodynamic variables of Tpr-P-V into the equations that relate the mean diameter of droplets, D, to frequency of the exciting ultrasound waves, f, the density of the precursor solution, #26; and the surface tension, #27;, previously worked on independently by Lang and Jokanovic. The incorporation results in the diameters of the droplets (and consequently the collected grains) being smaller as p and Tpr are increased in a non- linear form. The variable V, however, increases the diameter of the droplets as it is allowed to increase. This study shows the departures many authors find of the theory from experiment but it also shows that the departure does not lie in the equations but rather on post- synthesis and annealing effects. From X-ray diffraction, scanning electron microscopy (SEM) and Raman spectroscopy, this study shows that as furnace temperature is increased the morphology of the sample surfaces for both VO2 and WO3 transforms from amorphous to crystalline, from spherical grains to plate-like structures, with grain mean diameter increasing non-linearly in some cases and decreasing non-linearly in other cases confirming previous findings, the latter enjoying the majority vote. In Raman spectra of the as- obtained WO3, asymmetric broadening of the Raman peaks was observed in some samples and a phonon confinement model was employed in the size distribution prediction. These findings prompted the re- workout of the phonon confinement model. In this dissertation an equation has been derived based on the Faucet-Campbell equation of the PC model. The new equation relates the ratio of neighboring peaks in a material’s Raman spectrum to the mean diameter of the grains. The present modification allows the PCM model to predict the grain size beyond the current limiting range of 0 to 100 nm. Analysis of the experimental data using this equation unveils two different equations- one for particles of size below 100 nm and the other equation for particles with larger that 100 nm. Also this analysis has enabled the present study to evaluate the phonon dispersion relations for WO3.

Call number: LD2668 .T4 1959 R46

Thesis (M.Sc.(Biochemistry)) -- University of Limpopo, 2019. / Retinoblastoma binding protein 6 (RBBP6) is the protein encoded by the Retinoblastoma Binding Protein 6 (RBBP6) gene that is located in chromosome 16p12.2. There is a growing list of newly discovered RBBP6 hypothetical splice variants but there are only three RBBP6 splice variants that are well documented. RBBP6 has been previously implicated in the regulation of cell cycle and apoptosis but little is known about the expression and regulation of the human RBBP6 splice variants during cell cycle progression and breast cancer development. This study was aimed at determining the expression pattern of RBBP6 alternatively spliced variants during arsenic trioxide-induced cell cycle arrest and apoptosis in breast cancer MCF-7 cells. It was also aimed at determining RBBP6 specific microRNAs and how they are regulated in MCF-7 breast cancer cells. MCF-7 cells were maintained and subjected to arsenic trioxide-induced cell cycle arrest and apoptosis. The MTT (3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide) and the Muse™ Count & Viability assays were used to evaluate the effect of arsenic trioxide on the viability of MCF-7 cells. Cell cycle arrest using 11 μM arsenic trioxide and apoptosis using 32 μM arsenic trioxide were analysed using the MUSE® Cell Analyzer, light and fluorescence microscopy. Arsenic triode-induced apoptosis was analysed using the Muse™ Annexin V & Dead Cell Kit, MultiCaspase and MitoPotential assays using the Muse™ MultiCaspase Kit and Muse™ MitoPotential Kit. Arsenic trioxide-induced cell cycle arrest was analysed using the Muse™ Cell Cycle Kit. Semi-quantitative analysis of RBBP6 variants was carried out using the conventional Polymerase Chain Reaction (PCR), while the quantitative analysis was done using the Real-Time Quantitative PCR. The localization of RBBP6 isoforms was done using Immunocytochemistry (ICC). Web based Bioinformatics tools were used to identify RBBP6-specific microRNAs. The MTT results showed that arsenic trioxide decreased the viability of the MCF-7 cells in a dose-dependent manner. The Muse™ Cell Cycle analysis showed that 11 μM of arsenic trioxide induced G2/M cell cycle arrest in MCF-7 cells, while the Muse™ Annexin V & Dead Cell assay showed that 32 μM of arsenic trioxide induced the extrinsic apoptotic pathway in MCF-7 breast cancer cells. Using the conventional PCR, the MCF-7 cells were found to express the RBBP6 variant 1 transcript but lacks the expression of variant 2 and 3 transcripts, contrary to the kidney embryonic Hek 293 cells that exhibited the expression of RBBP6 variant 1, 2 and 3. Additionally, arsenic trioxide downregulated RBBP6 variant 1 in breast cancer cells during cell cycle arrest and apoptosis. The Real-Time PCR confirmed that MCF-7 cells lowly express RBBP6 variant 3. On the other hand, the ICC analysis showed that RBBP6 isoform 1 is localized and highly expressed in MCF-7 breast cancer cells. The Web based Bioinformatics tools showed that RBBP6 variant 1 specific microRNAs are down regulated in MCF-7 breast cancer cells. These results together showed that As2O3 is effective against MCF-7 cells and also regulated the expression of RBBP6 variants, especially, variant 1. This study showed that there are RBBP6 variants that are involved in breast cancer progression and there are those that may be involved in breast cancer suppression. Targeting these RBBP6 variants for therapeutic development is a promising strategy. In conjunction with RBBP6 expression, arsenic trioxide should be further explored as a breast cancer drug.

Graduation date: 2003

Thesis (M.S.)--Ohio University, November, 2000. / Title from PDF t.p.

Thesis (M.S.)--Ohio University, August, 1999. / Title from PDF t.p.