Thesis (Ph. D.)--Michigan State University. Electrical Engineering, 2008. / Title from PDF t.p. (Proquest, viewed on Aug. 17, 2009) Includes bibliographical references (p. 120-135). Also issued in print.

Thesis (DTech (Science))--Peninsula Technikon, Cape Town, 2003. / The impetus for the refinement and renewal of daily-used products has spurred international interest in investigating the small in homogeneities that might exist in these products. This interest has become an important part in the design philosophy, which is based on structural information gained by the analysis of these products. It is this drive that initiated the study to investigate the simultaneous use of novel nuclear analytical techniques such as micro proton induced X-ray emission( u-PlXE), micro proton induced gamma-ray emission (u-PlGE) and micro proton backscattering (u-RBS) to achieved a broader and yet deeper insight into the fine structure of products. The fundamental underlying physical principles of these techniques are discussed to gain in-depth knowledge on how to them to obtain the desired information. Also determined was the degree of accuracy that could be attained in the application of this knowledge. These principles were evaluated in conjunction with the instrumentation with which the applicability of these techniques could then be further extended. More so is the use of sophisticated software that facilitated the use of both physical and instrumental parameters. After describing the necessary implements to achieve this further know-how, products of industrial origin were investigated to determine in homogeneities that existed in those products and compared those theoretical values. The first application was made to ceramic-based sorption electrodes to be used in the purification of wastewater.

Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Earth and Planetary Sciences, 1981. / Microfiche copy available in Archives and Science. / Includes bibliographies. / by Glenn Lamar Ray. / Ph.D.

A nuclear microprobe, typically consisting of 2 - 4 quadrupole magnetic lenses and apertures serving as objective and a collimating divergence slits, focuses MeV ions to approximately 1 x 1 μm for modification and analysis of materials. Although far less utilized, electrostatic quadrupole fields similarly afford strong focusing of ions and have the added benefit of doing so independent of ion mass. Instead, electrostatic quadrupole focusing exhibits energy dependence on focusing ions. A heavy ion microprobe could extend the spatial resolution of conventional microprobe techniques to masses untenable by quadrupole magnetic fields. An electrostatic quadrupole doublet focusing system has been designed and constructed using several non-conventional methods and materials for a wide range of microprobe applications. The system was modeled using the software package "Propagate Rays and Aberrations by Matrices" which quantifies system specific parameters such as demagnification and intrinsic aberrations. Direct experimental verification was obtained for several of the parameters associated with the system. Details of the project and with specific applications of the system are presented.

Thesis: Ph. D., Massachusetts Institute of Technology, Department of Physics, 1977 / Includes bibliographical references. / Ph. D. / Ph. D. Massachusetts Institute of Technology, Department of Physics

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Hemihedrite from the Florence Lead-Silver mine in Pinal County, Arizona, USA was first described and assigned the ideal chemical formula Pb10Zn(CrO4)(6)(SiO4)(2)F-2, based upon a variety of chemical and crystal-structure analyses. The primary methods used to determine the fluorine content for hemihedrite were colorimetry, which resulted in values of F that were too high and inconsistent with the structural data, and infrared (IR) spectroscopic analysis that failed to detect OH or H2O. Our reinvestigation using electron microprobe analysis of the type material, and additional samples from the type locality, the Rat Tail claim, Arizona, and Nevada, reveals the absence of fluorine, while the presence of OH is confirmed by Raman spectroscopy. These findings suggest that the colorimetric determination of fluorine in the original description of hemihedrite probably misidentified F due to the interferences from PO4 and SO4, both found in our chemical analyses. As a consequence of these results, the study presented here proposes a redefinition of the chemical composition of hemihedrite to the ideal chemical formula Pb10Zn(CrO4)(6)(SiO4)(2)(OH)(2). Hemihedrite is isotypic with iranite with substitution of Zn for Cu, and raygrantite with substitution of Cr for S. Structural data from a sample from the Rat Tail claim, Arizona, indicate that hemihedrite is triclinic in space group P (1) over bar, a = 9.4891(7), b = 11.4242(8), c = 10.8155(7) angstrom, alpha = 120.368(2)degrees, ss = 92.017(3)degrees, gamma = 55.857(2)degrees, V = 784.88(9) angstrom(3), Z = 1, consistent with previous investigations. The structure was refined from single-crystal X-ray diffraction data to R-1 = 0.022 for 5705 unique observed reflections, and the ideal chemical formula Pb10Zn(CrO4)(6)(SiO4)(2)(OH)(2) was assumed during the refinement. Electron microprobe analyses of this sample yielded the empirical chemical formula Pb-10.05(Zn0.91Mg0.02)(Sigma) (= 0.93) (Cr5.98S0.01P0.01)(Sigma = 6.00) Si1.97O34 H-2.16 based on 34 O atoms and six (Cr + S + P) per unit cell.

No description available.