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Ionomeric polymer metal composites can be used as transducers characterized by high strain and low force. They are created by bonding a thin conductive electrode to the surfaces of an ionomeric polymer. Much of the work in the past has focused on using a voltage across the thickness of the polymer to produce mechanical motion. That work has often demonstrated that the mechanism of transduction within the polymer was associated with the accumulation of charge in the polymer. This thesis will discuss the use of current as a means to better control the accumulation of charge. Better control of the charge will provide more reliable control of the mechanical motion of the polymer. The data presented in this thesis demonstrates that the response of an ionomeric polymer to a current input is repeatable. The repeatability is a desirable result; however, using current to actuate the polymers also produces back relaxation in the response. Examination of the back relaxation reveals a low frequency non-linearity. The nonlinearity is quantified by the fact that the gain associated with the back relaxation does not increase linearly with an increase in input current. There is also a change in the response at certain voltage thresholds. For example, when the voltage across the polymer exceeds 3 V, the rate of back relaxation increases. The repeatability of the response will aid in implementing reliable control of the polymer, but the non-linearities in the back relaxation will provide a considerable challenge in developing a model to be used in control. / Master of Science

DNA sequences containing contiguous AA or TT mismatches, as well as sequences containing a 3-deazacytidine analogue were synthesized. Irradiation of anthraquinone abstracts an electron from the DNA. The loss of an electron from double-stranded DNA results in the formation of a radical cation that migrates through the DNA where it reacts irreversibly with H2O or O2 at GG steps. Subsequent treatment with piperidine or Fpg enzyme cleaves the backbone of the DNA at the site of reaction. DNA oligomers were designed to contain contiguous AA, TT, or G3-deazacytidine mismatches. It was revealed that the mismatches destabilize the duplex DNA; however, there is no measurable effect on the overall secondary structure of the DNA. The contiguous (AA)n mismatch, where n lt 7, was shown to have no effect on charge migration efficiency. In contrast, the contiguous (TT)n mismatch, where n gt 2, was shown to have near complete inhibition of charge migration through the mismatch region. Charge migration through the G3-deazacytidine mismatch was shown to have no effect on charge migration efficiency as well. Interestingly, reaction at the (G3-deazacytidine)2 base pairs revealed a change in the ratio of oxidative damage at the Gs. In (GC)2 base pairs, the ratio of damage at the two Gs is 10:1 with the majority of damage occurring at the 5-G. However, the (G3-deazacytidine)2 base pairs had an equal distribution of damage at the 5 and 3-Gs, with the amount of total reactivity equaling the (GC)2 base pairs. These findings indicate that the base composition in mismatched DNA determines the effect on charge migration efficiency and trapping reactivity.

Due to the continuous power supply reduction, Charge Pumps, also referred to as DC-DC converters, circuits are widely used in integrated circuits (ICs) to generate high voltages for many applications, such as EEP-ROMs, Flash memories for programming and erasing of the floating gate, switched capacitor circuits, operational amplifiers, voltage regulators, LCD drivers, piezoelectricactuators, etc. A charge pump is a kind of DC to DC converter that uses capacitors as energy storage elements to create either a higher or lower voltage power source. The development of the charge pumps is motivated by ever increasing the needs for the small form factor (i.e small size and low weight), high-conversion-efficiency and low costpower management system, which is the best candidate suitable to meet the needs of continuosly shrinking portable electronic devices like MP3 players, cellular phones, PDA's. / text

The problem with which this investigation is concerned is that of measuring the rate coefficients for termolecular charge transfer reactions of He2+ in atmospheric pressure afterglows with the minority reacting species. Of particular interest was the discovery that the presence of a third body can change an improbable charge transfer reaction involving He+2 into a very probable one, as in the case of the reaction with argon. For example, in Tables II and II it was shown that less than a 300 torr pressure of helium was required to double the effective rate of reaction of argon with He2+ while over 3000 torr was required for CH4. The sensitivity of the method has been sufficient to detect termolecular components as small as 2 x 10-30 cm /sec and values were found to range widely from 2 x 10 for Ne to 67 x 10-30 cm6/sec for CO2. The size of these termolecular rates not only served to explain specific anomalous efficiencies of the charge transfer process observed in atmospheric pressure lasers but also suggested the general importance of three-body ion-molecule reactions in higher pressure plasmas.

No description available.

Mémoire (M.Sc.)--Université du Québec à Chicoutimi, 1978. / Document électronique également accessible en format PDF. CaQCU

No description available.

Call number: LD2668 .T4 1978 M42 / Master of Science

Il y a beaucoup de mystères entourant les cuprates supraconducteurs. Certaines expériences montrent que de l'ordre de charge serait présent dans les mêmes conditions que la supraconductivité. Les phénomènes seraient peut-être en compétition. On tentera de modéliser l'ordre de charge à l'aide du modèle de Hubbard. Des méthodes d'amas seront utilisées pour résoudre approximativement le modèle. Ensuite, on tente de mettre l'ordre de charge en compétition avec la supraconductivité pour en voir les effets.