Thesis (Ph. D.)--University of Pennsylvania, 1926. / "Reprinted from Journal of the American Chemical Society, Vol. 48, no. 5." eContent provider-neutral record in process. Description based on print version record.

Thesis (Ph. D.)--University of Pennsylvania, 1926. / "Reprinted from Journal of the American Chemical Society, Vol. 48, no. 5."

Thesis (M. Sc.)--University of Hong Kong, 2005.

Thesis (MTech (Electrical Engineering))--Cape Peninsula University of Technology, 2011 / The purpose of this thesis was to design and develop a measurement system that would allow accurate measurement of individual cell voltages in a series cell stack. The system was initially proposed to be used in conjunction with an active cell balancer. This would allow for the efficient equalising of cells as well as provide detailed information on the cell stack and how the stack operates over time. Having a system that measures voltages accurately, with which the active cell balancer can be controlled would allow for peak cell lifetime and performance. Current battery management systems are large, complex and inefficient and a new way of battery management had to be investigated. To accurately measure individual cells in a series stack, the high common mode voltage must be negated. Different techniques that are currently used to create galvanic isolation were reviewed; circuits were designed and were simulated to find the most suitable design. The traditional methods used to create galvanic isolation did not provide adequate results. The methods were too inefficient and not accurate enough to be used. The methods that had the required accuracy were too complicated to connect in a useable system. This led to the investigation of integrated circuits created to measure voltages in large cell stacks. An integrated circuit from Linear Technology was chosen and a system was built. A system was thus designed that fulfilled the most desirable design specifications while delivering excellent results. The system allowed accurate, individual voltages to be measured in the presence of high common mode voltages. Accuracies and measurement time were well below the required system specification. Power consumption was high, but different component choice will lower power consumption to within specification. Excellent results were obtained overall with most, although not all results well below the design specifications. By including current measurements, as well as other technologies such as wireless communication, USB connectivity and a better data processor, this system will be at the forefront of current battery management technology.

published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy

In the global search for renewable sources of energy, hydrogen is a promising candidate in transportation and electronic applications. Carbon nanotubes (CNTs) have the largest hydrogen storage capacity among the hydrogen storage materials known at present. The Ni-MH battery can be used to store and then discharge large amounts of hydrogen reversibly by using hydrogen storage materials as negative electrode. The electrochemical hydrogen storage performances of metal hydride electrodes with different levels of multi wall carbon nanotubes (20%, 15%, 10%, 5% and 2% of Ni-MH battery's active materials) has been investigated under similar charge-discharge conditions. Electrochemical test cell consisted of a single hydrogen storage negative electrode sandwiched between two NiOOH/Ni(OH)2 positive electrodes. A 6M aqueous KOH solution was used as electrolyte. Electrochemical properties such as specific discharge capacity, high rate charge-discharge capability and cycle life stability have been investigated. The morphology and structure of negative electrode material were examined by scanning electron microscopy, transmission electron microscopy and X-ray diffraction analysis. Chemical analysis of the hydrogen storage alloy was performed using electron probe microanalysis, electron diffraction spectroscopy and induced coupled plasma spectroscopy analysis. Hydrogen absorption-desorption properties were measured in terms of pressure-composition-isotherm curves. It has been found in this study that the presences of CNTs significantly enhanced the overall electrochemical properties of the Ni-MH battery. Maximum specific discharge capacity was observed for 5% CNTs electrode reaching 243 mAh/g, whereas 0% CNTs could only reach 229 mAh/g. High rate charge and discharge capabilities of 5% CNTs electrodes were ~ 241% and 250% higher than the corresponding values for 0% CNTs electrode. Furthermore, the differences in electrochemical hydrogen storage of CNTs with different diameters of 10-20 nm, 20-40 nm, 40-60 nm, and 60-100 nm were investigated. Electrochemical results demonstrated that CNTs with different diameters showed a large variation in the electrochemical hydrogen storage capability under the similar experimental condition. A comparison between electrodes with different CNTs studies was carried out in order to optimize nanotubes choices for Ni-MH battery. It was found that smaller tube diameters, 20-40 nm and 5% CNTs negative electrode showed the best electrochemical properties of Ni-MH battery system.

Thesis (Ph. D.)--State University of New York at Binghamton, Materials Science and Engineering Program, 2009. / Includes bibliographical references.

Thesis (Ph. D.)--University of Hong Kong, 2002. / Includes bibliographical references (leaves 281-283).

abstract / Chemistry / Doctoral / Doctor of Philosophy

Thesis (Ph.D.)--Tufts University, 1996. / Adviser: Ronald B. Goldner. Submitted to the Dept. of Electrical Engineering. Includes bibliographical references. Access restricted to members of the Tufts University community. Also available via the World Wide Web;