Thesis (Master)--İzmir Institute of Technology, İzmir, 2005 / Includes bibliographical references (leaves 35-37).

Thesis (M.S.)--Brigham Young University. Dept. of Electrical and Computer Engineering, 2007. / Includes bibliographical references (p. 55-58).

This thesis includes a description of modifications of the Hilger atomic absorption apparatus, which was used for most of the work. These modifications were restricted to the atomiser and burner, which were replaced by a modified "Eel" flame. photometer atomiser-burner and resulted in improved sensitivity and instrumental stability for the atomic absorption of magnesium. A comparison of the performance of this unit with that of the unmodified Hilger apparatus is given. A "Handigas" butane-propane mixture)-air flame was used for most of this work, but a coal-gas-air flame was also studied and found to give slightly greater sensitivity. The method was found to be subject to interference from many elements. Strontium salts, employed as releasing agents to overcome the effect of other elements, were not completely effective as milligram amounts of several elements interfered even when strontium was present. Among the more serious interfering elements are: aluminium, iron, manganese and zirconium (less than 20 p.p.m. interfere); the alkali and alkaline earth metal salts (more than 200-500 p.p.m. interfere); phosphate (more than 100 p.p.m. P₂0₅ uranium (more than 4,000 p.p.m.); arsenate and vanadate. An attempt is made to explain the mechanism of some of these interfering effects. A combination of strontium salt and acetyl acetone was found to over-come the effects of small amounts of several elements that form complexes with acetyl acetone (e.g. iron and aluminium) far more effectively than strontium alone. Larger amounts of many interfering elements are removed by a solvent extraction procedure employing acetyl acetone and chloroform. Elements which cannot be removed by this means may be separated by anion-exchange, volatilisation, electrolysis or precipitation. A spiking technique, which compensates JT/GB for the effects of small amounts of interfering elements, is described and enables many samples to be analysed without prior separations. The method described has good sensitivity (the limit of determination is approximately 1 microgram of magnesium in 50 ml. of solution). It has been applied to the analysis of clay samples, iron ore, limestone and uranium metal, oxides and processing solutions. The coefficient of variation of the method was determined using two clay samples and results of 2.0 and 4.6 percent, at magnesium oxide concentrations of 0.65 and 0.22 percent respectively, wore obtained. The speed of the method compares favourably with others described for the determination of microgram amounts of magnesium, but increases if large amounts of interfering elements are present.

This research is for the implementation of non-intrusive measurement techniques in the study of high temperature pipe flow. A low pressure, laboratory scale hybrid rocket motor simulator was built to achieve high temperatures with various gases. A quartz test section was designed, built, and implemented into the existing test setup to accommodate the laser beam of the existing Tunable Diode Laser Absorption Spectrometer (TDLAS) system which was designed to observe water vapor. A super-heated water vapor injector was designed to obtain the desired water vapor concentrations. Flow characteristics were simultaneously recorded using the existing TDLAS system and the DAQ system for temperatures for later comparison. A numerical study using a commercial CFD package was used to predict the flow characteristics at certain locations for experimental comparison. Based on this study, it is concluded that the TDLAS can be used to make real time temperature measurements of heated internal gas flows.

Thesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2016. / Boron concentration analysis is an important and critical analysis performed by the Analytical Chemistry Laboratory at Koeberg Nuclear Power Station (KNPS), because boron controls reactivity and the concentration determination is a Technical Specification Parameter (safety parameter). Hence accurate, precise results for boron concentration produced by laboratories and on-line analysers are important because of their operational implications associated with reactivity control and also for nuclear safety. The project focused on comparing the quality of chemical analysis results of boron produced by analysis techniques/ methods used at Koeberg Nuclear Power Station namely; Potentiometric Titration, Atomic Absorption Spectrophotometry (Flame) and UV-VIS Azomethine-H method. The methods were described, optimised, evaluated and compared in terms of uncertainty of measurement, accuracy, precision, analysis range, limitations, appropriateness and applicability for boron analysis in 2500 mg B/kg concentration range. For Potentiometric Titration method, the measurement uncertainty = 2500 ±16 mg B/kg, accuracy= 0.2%, precision= 0.08% the range of analysis= 5-800 mg B/kg. For Atomic Absorption Spectrophotometry (Flame) the measurement uncertainty= 2500 ±51 mg B/kg, accuracy= 0.12%, precision= 0.44% the range of analysis= 0 -500 mg B/kg. For UV-VIS Azomethine-H the measurement uncertainty= 2500 ±72 mg B/kg, accuracy= 0.08%, precision= 0.44% the range of analysis= 0 -10 mg B/kg. The INPOs 95% accuracy and precision criteria for boron is ± 1%. So these techniques could be used for boron analysis in PWR. Based on the evaluation and assessments mentioned above; the Potentiometric Titration was found to be the most preferred method for boron analysis for Pressurised Water Reactors followed by Atomic Absorption Spectrophotometry (Flame) that can be of good use in determining boron especially in waste samples and samples with complex matrices. The UV-VIS Azomethine-H methods can only be used when it is really necessary to determine very low levels of boron between 0- 10mg B/kg of which it was never required before. Since it is specifically the B-10 isotope that is responsible for the ability to control reactivity, the implementation of isotopic boron analysis (by Inductively Coupled Plasma – Mass Spectrometry) at KNPS is explained and the advantage of the programme is illustrated. Although the current state of instrumental capabilities is adequate for 10B isotope determination, further work of optimising the methodology for even better results is recommended.

Cheung Wai-che. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1978. / Bibliography: leaves 134-135.

Chronic arsenic poisoning due to arsenic contamination of groundwater is a serious public health problem in Bangladesh and neighboring countries. Severe health effects associated with chronic exposure to arsenic include melanosis and several kinds of cancer. It is now generally agreed that the arsenic contamination of groundwater in Bangladesh is of geological origin. Arsenic naturally present in aquifers may be mobilized into drinking water by microbial action.<p> The formation of a novel arsenic-selenium compound: seleno-bis (S-glutathionyl) arsinium ion, [(GS)2AsSe]-, and its subsequent excretion in rabbit bile has been demonstrated previously. This molecular basis for the in vivo antagonism between arsenic and selenium was discovered using X-ray absorption spectroscopy. There is growing evidence that, in Bangladeshi people who are suffering long term chronic lowlevel arsenic poisoning, this antagonism is causing a selenium deficiency. Administering selenium supplements might provide a simple but highly effective treatment of the Bangladeshi arsenic poisoning.<p> In order to examine the disposition of [(GS)2AsSe]-, a set of rabbits were intravenously injected with selenite, arsenite or both. Whole blood, red blood cell and plasma samples were collected at different time intervals within 2hrs after injection and cecotrope samples 24hr after injection. Samples were examined using X-ray absorption spectroscopy and both arsenic and selenium K-near edge spectra were recorded.<p> iii Speciation of arsenic and selenium will be discussed in this thesis. Results indicate that [(GS)2AsSe]- is formed in blood very rapidly after injection of both arsenite and selenite, and then is removed from blood stream within 2hrs post injection. Results also show that [(GS)2AsSe]- is assembled in red blood cells, with no [(GS)2AsSe]- detected in plasma samples. [(GS)2AsSe]- is also found in cecotrope samples after injection of both arsenite and selenite.<p> The results of this study in rabbits will contribute to the understanding of chronic arsenic poisoning in humans.

Chronic arsenic poisoning due to arsenic contamination of groundwater is a serious public health problem in Bangladesh and neighboring countries. Severe health effects associated with chronic exposure to arsenic include melanosis and several kinds of cancer. It is now generally agreed that the arsenic contamination of groundwater in Bangladesh is of geological origin. Arsenic naturally present in aquifers may be mobilized into drinking water by microbial action.<p> The formation of a novel arsenic-selenium compound: seleno-bis (S-glutathionyl) arsinium ion, [(GS)2AsSe]-, and its subsequent excretion in rabbit bile has been demonstrated previously. This molecular basis for the in vivo antagonism between arsenic and selenium was discovered using X-ray absorption spectroscopy. There is growing evidence that, in Bangladeshi people who are suffering long term chronic lowlevel arsenic poisoning, this antagonism is causing a selenium deficiency. Administering selenium supplements might provide a simple but highly effective treatment of the Bangladeshi arsenic poisoning.<p> In order to examine the disposition of [(GS)2AsSe]-, a set of rabbits were intravenously injected with selenite, arsenite or both. Whole blood, red blood cell and plasma samples were collected at different time intervals within 2hrs after injection and cecotrope samples 24hr after injection. Samples were examined using X-ray absorption spectroscopy and both arsenic and selenium K-near edge spectra were recorded.<p> iii Speciation of arsenic and selenium will be discussed in this thesis. Results indicate that [(GS)2AsSe]- is formed in blood very rapidly after injection of both arsenite and selenite, and then is removed from blood stream within 2hrs post injection. Results also show that [(GS)2AsSe]- is assembled in red blood cells, with no [(GS)2AsSe]- detected in plasma samples. [(GS)2AsSe]- is also found in cecotrope samples after injection of both arsenite and selenite.<p> The results of this study in rabbits will contribute to the understanding of chronic arsenic poisoning in humans.

No description available.

The hydroxyl (OH) radical is a common intermediate species in any hydrogen- or hydrocarbon-based flame. Investigating OH at elevated temperatures and pressures is not a trivial task, and many considerations must be made to fully study the molecule. Shock tubes can provide the experimenter with a wide range of temperatures and pressures to investigate a variety of combustion characteristics including, but not limited to, OH kinetic profiles. Described in this dissertation is the diagnostic used to measure OH within a shock tube using UV absorption spectroscopy from an enhanced UV Xenon lamp passed through a spectrometer. OH absorption was made over a narrow range of wavelengths around 309.551 nm within the widely studied OH X→A ground vibrational transition region. Experiments have been performed in the shock-tube facility at Texas A&M University using this OH absorption diagnostic. A calibration mixture of stoichiometric H2/O2 diluted in 98% argon by volume was tested initially and compared with a well-known hydrogen-based kinetics mechanism to generate an absorption coefficient correlation. This correlation is valid over the range of conditions observed in the experiments at two pressures near 2 and 13 atm and temperatures from 1182 to 2017 K. Tests were completed using the absorption coefficient correlation on stoichiometric mixtures of methane, methane and water, ethane, ethylene, and acetylene to compare against a comprehensive, detailed chemical kinetics mechanism which considers up through C5 hydrocarbons. Measurements of methane show good agreement in peak OH formation and ignition delay time when compared with the mechanism. Improvements can be made in the shape of the methane-oxygen OH profile, and sensitivity and rate of production analyses were performed with the mechanism to identify key reactions for tuning. Similar results were found for methane-water-oxygen mixtures with no difference in profile shape or ignition delay time noted. There is room for improvement between the mechanism and measured values of OH for ethane-, ethylene-, and acetylene-based mixtures, although interesting pre-ignition features are nonetheless captured relatively well by the mechanism. Uncertainty in the measurement comes from the inherent noise in the photomultiplier tube signal and is ±25-150 ppm for the 2-atm experiments and ±6-25 ppm for the 13-atm experiments.