Thesis (Ph. D.)--McMaster University (Canada), 1989. / Source: Dissertation Abstracts International, Volume: 62-13, Section: A, page: 0000.

Thesis (M.Sc. (Hons.)) -- University of Western Sydney, Nepean, 1998. / Includes bibliographical references (leaves 129-136).

Thesis (M. Phil.)--University of Hong Kong, 1993.

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Part 1 The coupled shock-tube/mass spectrometer apparatus is characterized in terms of its capabilities for chemical kinetic studies. Criteria for doing kinetic measurements by this experimental technique are discussed. The characterization experiments showed that our apparatus was capable of giving plausible signal shapes for non-reactive dynamic shots at P₁ = 5 torr. Measurements of ion current under static conditions showed that response of the quadrupole mass spectrometer was linear over a range of P₁ = 0-5 torr. Schlieren measurements indicated that the shock wave velocity was erratic and non-reproducible over the last 5 feet of the test section and that the velocity at the endwall could not be predicted from the schlieren data. The electron beam width was found to be ~.1" and the implications of this measurement for further studies on the free jet are outlined. The present beam width is suitable for jet studies in which bulk ionization of gas from a cross-section of the jet is performed. Design improvements needed for future reactive studies on our system are reviewed. In addition, experimental studies of jet risetime with a pulsed molecular beam apparatus showed poor agreement between the experimental and theoretical jet risetimes. The apparent discrepancy is discussed and possible explanations for it are given. Part 2 The rate constant k₁ for the reaction C₅H₁₂ → C₄H₉ + CH₃ was determined from reflected shock experiments (1100-1300°K) in which the progress of reaction was monitored by the appearance of H atoms. Atomic resonance absorption spectrophotometry at the Lyman-α line was performed on three mixtures (20 ppm, 10 ppm, 5 ppm) of neopentane in argon to give k₁ = .17 x 10¹⁸ exp (-84800±6200/RT) sec⁻¹. This result is in very good agreement with earlier single pulse shock tube experiments. In addition, calibration experiments for H atom were performed by shock-heating two mixtures (10 ppm and 5 ppm) of neopentane in argon. The results obtained were in good agreement with previous calibration data. / Doctor of Philosophy

Charge transfer at the organic/inorganic semiconductor interfaces lies at the heart of interfacial photochemistry. While decades of research have shaped the current understanding that interfacial charge transfer depends crucially on energetic driving force and electronic coupling, much less is known about the role played by the spin degree of freedom. In particular, it is not clear how spin states evolve during the charge transfer process. With the advent of group 6 transition metal dichalcogenides (TMDC), a class of two-dimensional layered materials which permits the optical generation of spin-polarized electron-hole pairs in the monolayer limit, we now have the opportunity to investigate if charge transfer at an organic/inorganic interface could enable the transfer of spin polarization. Using time-resolved Faraday rotation and transient absorption spectroscopy, it is found in the MoSe₂/H₂Pc and C60/WS₂ heterostructures that the photoinduced hole transfer from MoSe₂ to H₂Pc and electron transfer from WS₂ to C60 results in spin polarization lifetimes one order of magnitude longer than that of a monolayer. In the WS₂/MoSe₂/H₂Pc heterostructure, the addition of a WS₂ monolayer drives the dissociation of electron-hole pairs bound at the MoSe₂/H₂Pc interface and leads to the observation of nanosecond-long spin polarization at room temperature. These findings evidence the photoinduced transfer of spin polarization, a mechanism which could potentially be exploited to enhance the efficiency and selectivity of photochemical reactions involving angular momentum change, and may be generalized to other organic/inorganic interfaces composed of crystalline semiconductors with spin-momentum locking.

Kin-Fai Ho. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1999. / Includes bibliographical references (leaves [61-66]). / Abstracts in English and Chinese. / Contents / ACKNOWLEDGMENT / ABSTRACT / Chapter CHAPTER 1 --- INTRODUCTION / Chapter 1.1 --- Air Pollution in Hong Kong / Chapter 1.2 --- Brief introduction of Particulate Matter / Chapter 1.2.1 --- Total suspended particulates / Chapter 1.2.2 --- Respirable suspended particulates / Chapter 1.2.3 --- PM2.5 / Chapter 1.3 --- Lead in Air Particulate and its Harmful Effects on Human / Chapter 1.4 --- Air Sampling / Chapter 1.5 --- Sample Treatment / Chapter 1.5.1 --- Acid digestion method / Chapter 1.5.2 --- Slurry sampling method / Chapter 1.5.3 --- Comparison between acid digestion and slurry sampling method / Chapter 1.5.4 --- Chemical modification / Chapter CHAPTER 2 --- EXPERIMENTAL / Chapter 2.1 --- Apparatus / Chapter 2.2 --- Instrumental analysis / Chapter 2.2.1 --- Electrothermal atomic absorption spectrometry / Chapter 2.2.2 --- Background correction by the Zeeman effect / Chapter 2.3 --- Reagents / Chapter 2.4 --- Procedure / Chapter 2.4.1 --- Collection of air sample / Chapter 2.4.2 --- Treatment of sample collected on filter / Chapter 2.4.2.1 --- Digestion Procedure / Chapter 2.4.2.2 --- Procedure for Slurry Preparation / Chapter 2.4.3 --- Temperature program employed / Chapter 2.4.4 --- Sample introduction / Chapter 2.4.5 --- Determination of Lead in PM 2.5 by Acid Digestion Method / Chapter 2.4.6 --- Determination of Lead in PM 2.5 by Developed Method / Chapter 2.4.7 --- Study of particle size and suspension behavior of PM 2.5 in solvent / Chapter CHAPTER 3 --- RESULTS AND DISCUSSION / Chapter 3.1 --- Choice of filter for air sampling / Chapter 3.2 --- Choice of Solvents for Suspension of Air Particulates / Chapter 3.3 --- Ultrasonic agitation / Chapter 3.4 --- Effect of the sonication time / Chapter 3.5 --- Particle size and Effect of stabilization agents / Chapter 3.6 --- Effect of acid predigestion of the slurry sample / Chapter 3.7 --- Chemical Modification / Chapter 3.7.1 --- Use palladium as chemical modifier / Chapter 3.7.2 --- Amount of chemical modifier / Chapter 3.7.3 --- Effect of nitric acid / Chapter 3.8 --- Optimization of the graphite furnace temperature / Chapter 3.9 --- Effect of using platform / Chapter 3.10 --- Sample injection volume / Chapter 3.11 --- Recovery study of Lead in PM2.5 / Chapter 3.12 --- The limit of detection and precision of the developed method / Chapter CHAPTER 4 --- CONCLUSION / APPENDIX / REFERENCES

published_or_final_version / Chemistry / Master / Master of Philosophy