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Call number: LD2668 .T4 1950 O2 / Master of Science

A dissertation submitted to the Faculty of Science, University of the Witwatersrand, Johannesburg, in fulfillment of the requirements for the degree of Master of Science Johannesburg September 2012 / Electron spin resonance (ESR) was used to characterize a suite of carbon nanospheres (CNS) samples with varying nitrogen concentrations at room temperature. The CNS were produced using two different reactors (vertical and horizontal) under different preparatory conditions. Resonance spectra of samples produced from the vertical reactor showed resonance lines- a narrow paramagnetic component, and broader component. They were attributed to nitrogen paramagnetic impurities and carrier spins, respectively. Samples produced in the horizontal reactor revealed stronger line spectra that were narrower and Dysonian in shape. The nitrogen content of the samples produced by the horizontal reactor was determined through ESR analysis which involves integration of the resonance peak, and normalizing to the mass of the sample. The relative g-shift was also measured by using a DPPH reference sample. Room temperature power saturation experiments were performed on samples produced from the horizontal reactor with the aim of estimating the spin relaxation times. Two samples from the horizontal reactor were further investigated at low temperatures (4 K- 320 K) at a constant microwave power. The resonance parameters investigated were linewidth, asymmetry ratio and amplitude, and possible spin-lattice relaxation mechanisms were investigated. The variation of the amplitude with temperature was investigated using two models: (1) a model based on lattice vibrations, and (2) a model based on nanographites assembly (considered interaction between carrier and localized spins). At low temperatures both models have amplitude that changes inversely with temperature in accordance with Curie law. At high temperatures (T > 200 K) a model based on nanographites assembly provide an alternative; it describes the rise in the signal amplitude in terms of thermally activated paramagnetic electrons from non-magnetic ground state to excited state at energy . Analysis of linewidth and asymmetry ratio data confirmed that the spin-lattice relaxation governed by thermal activated electrons is a dominant relaxation mechanism at high temperatures.

The NRT2 (high affinity nitrate transporter 2) family is a part of the iHATS (inducible high affinity system) that studies have shown is responsible for the influx of nitrate into the plant cell after provision of nitrate. The ZmNRT2.1 from Zea mays was constitutively expressed in Nicotiana tabacum. To assess how over-expression of this foreign NRT2.1 affects nitrate influx by plants, nitrate content in leaf and root tissue, gene expression, and vegetal growth were analyzed in media with deficient or high nitrate concentrations (0.1, 1, or 10 mM). Compared to wild type plants: the transgenic lines had a significantly larger fresh weight in all nitrate conditions; primary root length was significantly longer in the 0.1 and 1 mM nitrate conditions; both the fresh weight and the primary root length were significantly higher when 50 mM NaCl was applied as a stress factor to medias containing 0.1 and 10 mM nitrate. / Includes bibliography. / Thesis (M.S.)--Florida Atlantic University, 2015. / FAU Electronic Theses and Dissertations Collection

by Kwok Chun-kiu. / Thesis (M.Ph.)--Chinese University of Hong Kong, 1987. / Bibliography: leaves 69-74.

Wheat (Triticum aestivum L. cv Minaret) was grown long-term under CO₂ partial pressures of 36 and 70 or 100 Pa with various N applications (4 to 23 g m-2 N), to test hypotheses of N re-allocation: 1) a decrease in N from leaves to other organs, 2) a relative decrease in N from Rubisco to other photosynthetic components. Elevated CO₂ did not affect phenology, main stem leaf appearance, the pattern of N allocation throughout the plant, or the fraction of crop N in grain at harvest, but 1) stimulated biomass and yield by 5 to 20% over the N range used, and 2) caused a faster loss of N and components from flag leaves during grain-fill. Responses of photosynthesis to varying pCi were fitted, and rates of maximal carboxylation and non-photorespiratory respiration estimated. The former, was proportional to Rubisco content, and light-saturated photosynthetic rate at 70 Pa CO₂ was proportional to A TP-synthase. Potential photosynthetic rates at 70 Pa CO₂ were calculated, compared with observed, and used to estimate excess investment in Rubisco. The excess was greater in high N treatments than low, declining as leaves senesced. The fraction of Rubisco estimated to be in excess, was strongly dependent on leaf N content, increasing from - 5% in leaves with 1 g N m-2 to -40% in leaves with 2 g N m-2. Growth at elevated CO₂ usually decreased the excess somewhat, but only as a consequence of a general decrease in leaf N, given that relationships of components to leaf N content were independent of CO₂ and N treatment, demonstrating that no direct CO₂ effect on N allocation within leaves had occurred. It is concluded that there is scope for improving the N-use efficiency of C₃ crop plants in elevated CO₂ conditions, by genetic manipulation to decrease the amount of Rubisco.

Leung Cheuk-wan. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2006. / Includes bibliographical references. / Abstracts in English and Chinese. / Abstract --- p.i / Abstract (Chinese) --- p.ii / Acknowledgement --- p.iii / Table of Contents --- p.v / Lists of Tables --- p.ix / Lists of Figures --- p.x / Chapter Chapter 1 --- Introduction --- p.1 / Chapter 1.1 --- TiO2 Photocatalysis --- p.1 / Chapter 1.1.1 --- Mechanisms of TiO2 Photocatalysis --- p.1 / Chapter 1.2 --- Visible Light Photocatalyst --- p.4 / Chapter 1.2.1 --- Preparation of Visible Light Ti02 Photocatalysts --- p.5 / Chapter 1.2.1.1 --- Dye Sensitization --- p.5 / Chapter 1.2.1.2 --- Metal Doping --- p.6 / Chapter 1.2.1.3 --- Coupling of Semiconductors --- p.6 / Chapter 1.2.1.4 --- Nonmetal Doping --- p.7 / Chapter 1.3 --- Enhanced TiO2 Photocatalytic Activity under UV Light --- p.8 / Chapter 1.3.1 --- Preparation of TiO2 Photocatalyst with Enhanced Activity in UV Light --- p.8 / Chapter 1.3.1.1 --- Loading of Metal --- p.8 / Chapter 1.3.1.2 --- Impurity Co-doping --- p.9 / Chapter 1.3.1.3 --- Morphological Control --- p.10 / Chapter 1.3.1.4 --- Increasing Surface Area --- p.10 / Chapter 1.4 --- Summary --- p.11 / Chapter 1.6 --- Aim of This Research and its Significance --- p.12 / Chapter 1.7 --- References --- p.13 / Chapter Chapter 2 --- Preparation of N-doped TiO2 with Enhanced Surface Area: A Detailed Characterization and Mechanism --- p.19 / Chapter 2.1 --- Introduction --- p.19 / Chapter 2.2 --- Experimental --- p.21 / Chapter 2.2.1 --- Materials and Catalyst Preparation --- p.21 / Chapter 2.2.2 --- Characterization --- p.21 / Chapter 2.2.3 --- Photocatalytic Activity --- p.23 / Chapter 2.3 --- Results and Discussion --- p.24 / Chapter 2.3.1 --- XRD Analysis --- p.24 / Chapter 2.3.2 --- UV-Vis Absorption Spectroscopy and Bandgap Energies --- p.27 / Chapter 2.3.3 --- N2 Sorption Analysis --- p.29 / Chapter 2.3.4 --- SEM Analysis --- p.33 / Chapter 2.3.5 --- TEM Analysis --- p.35 / Chapter 2.3.6 --- FT-IR Spectroscopy --- p.36 / Chapter 2.3.7 --- Raman Spectroscopy --- p.39 / Chapter 2.3.8 --- XPS Studies --- p.44 / Chapter 2.3.9 --- PL Measurements --- p.49 / Chapter 2.3.10 --- Photocatalytic Activity Measurements --- p.50 / Chapter 2.3.11 --- Advantages of Using Urea as a N-doping Source --- p.54 / Chapter 2.3.12 --- Mechanisms for N-doping --- p.56 / Chapter 2.4 --- Conclusions --- p.58 / Chapter 2.5 --- References --- p.59 / Chapter Chapter 3 --- Preparation of Nanoporous Interstitial B-doped TiCO2 with Enhanced Photocatalytic Activity --- p.63 / Chapter 3.1 --- Introduction --- p.63 / Chapter 3.2 --- Experimental --- p.65 / Chapter 3.2.1 --- Materials and Catalyst Preparation --- p.65 / Chapter 3.2.2 --- Characterization --- p.66 / Chapter 3.2.3 --- Photocatalytic Activity --- p.67 / Chapter 3.3 --- Results and Discussion --- p.68 / Chapter 3.3.1 --- XRD Analysis --- p.68 / Chapter 3.3.2 --- UV-Vis Absorption Spectroscopy and Bandgap Energies --- p.71 / Chapter 3.3.3 --- N2 Sorption Analysis --- p.73 / Chapter 3.3.4 --- SEM and TEM --- p.76 / Chapter 3.3.5 --- FT-IR Spectroscopy --- p.80 / Chapter 3.3.6 --- Raman Spectroscopy --- p.82 / Chapter 3.3.7 --- PL Measurements --- p.84 / Chapter 3.3.8 --- XPS Studies --- p.85 / Chapter 3.3.9 --- Photocatalytic Activity Measurements --- p.89 / Chapter 3.3.10 --- State and Form of Boron in TiO2 Lattice and its Effects --- p.91 / Chapter 3.4 --- Conclusions --- p.93 / Chapter 3.5 --- References --- p.94 / Chapter Chapter 4 --- Conclusions --- p.97

Vita. / Digitized by Kansas Correctional Industries

Digitized by Kansas Correctional Industries

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