DocumentCode :
3371553
Title :
Electrical Breakdown and Recovery of Water and Propylene Carbonate
Author :
Xiao, S. ; Kolb, J. ; Lu, XP ; Laroussi, M. ; Joshi, R.P. ; Schoenbach, K.H. ; Schamiloglu, Edl
Author_Institution :
ECE Dept., Old Dominion Univ., Norfolk, VA
fYear :
2005
fDate :
13-17 June 2005
Firstpage :
742
Lastpage :
745
Abstract :
Polar liquids, especially water, offer the advantages of high permittivity, a high dielectric strength and a fast dielectric recovery. These benefits make them appealing dielectrics for use in high-energy storage systems and as high-power switching media. In certain applications, however, the use of water is limited by its relatively high freezing point of 0degC and low boiling point 100degC. In comparison, propylene carbonate (C4H6O3) has a freezing temperature of -55degC and boiling point of 243degC in addition to its high permittivity of 65. The dielectric strength was found to be 2.3 MV/cm, slightly higher than that of water tested under the same conditions. As an alternative to water in high repetition rate systems we studied the dielectric recovery of propylene carbonate after breakdown. We found the recovery time to be more than one order of magnitude longer than for water. Moreover, the breakdown in propylene carbonate gives rise to a polymer formation in the liquid.
Keywords :
electric breakdown; electric strength; permittivity; water; dielectric recovery; electrical breakdown; high dielectric strength; high permittivity; high repetition rate systems; high-energy storage systems; high-power switching media; polar liquids; propylene carbonate; water; Bioelectric phenomena; Breakdown voltage; Dielectric breakdown; Dielectric liquids; Electric breakdown; Electrodes; Pulse power systems; Switches; Temperature; Water storage;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Pulsed Power Conference, 2005 IEEE
Conference_Location :
Monterey, CA
Print_ISBN :
0-7803-9189-6
Electronic_ISBN :
0-7803-9190-x
Type :
conf
DOI :
10.1109/PPC.2005.300768
Filename :
4084324
Link To Document :
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