Flyback-based high-side gate driver for a 10-kV SiC MOSFET
2016 10TH INTERNATIONAL CONFERENCE ON COMPATIBILITY, POWER ELECTRONICS AND POWER ENGINEERING (CPE-POWERENG)
Authors: Wolski, Kornel; Grzejszczak, Piotr; Barlik, Roman
Abstract
Aside from providing voltage and current of sufficient values, a gate driver of a SiC MOSFET must also be durable enough to keep operating properly in given place of a main circuit of a converter. A high-side SiC MOSFET constitutes a challenge to being driven properly, since a high-voltage potential becomes repetitively applied at an output of the gate driver. In order to limit a resulting flow of parasitic current Cdv/dt to ground of the driver, a low-capacitance isolation must be implemented. Presented in this paper is a flyback-based gate driver, which is dedicated for driving a high-side 10-kV SiC MOSFET. Required properties of the gate driver such as high dielectric strength and low input-to-output stray capacitance were evaluated through a series of measurements. Switching voltage values and switching speeds of the driver were examined in an 800-V double pulse test with a 1.2 kV SiC MOSFET and compared with two other devices potentially capable of operating with the 10-kV SiC MOSFET.
EXPOSURE OF ALASKA BROWN BEARS (URSUS ARCTOS) TO BACTERIAL, VIRAL, AND PARASITIC AGENTS VARIES SPATIOTEMPORALLY AND MAY BE INFLUENCED BY AGE
JOURNAL OF WILDLIFE DISEASES
Authors: Ramey, Andrew M.; Cleveland, Christopher A.; Hilderbrand, Grant, V; Joly, Kyle; Gustine, David D.; Mangipane, Buck; Leacock, William B.; Crupi, Anthony P.; Hill, Dolores E.; Dubey, Jitender P.; Yabsley, Michael J.
Abstract
We collected blood and serum from 155 brown bears (Ursus arctos) inhabiting five locations in Alaska, US during 2013-16 and tested samples for evidence of prior exposure to a suite of bacterial, viral, and parasitic agents. Antibody seroprevalence among Alaska brown bears was estimated to be 15% for Brucella spp., 10% for Francisella tularensis, 7% for Leptospira spp., 18% for canine adenovirus type 1 (CAV-1), 5% for canine distemper virus (CDV), 5% for canine parvovirus, 5% for influenza A virus (IAV), and 44% for Toxoplasma gondii. No samples were seropositive for antibodies to Trichinella spp. Point estimates of prior exposure to pathogens among brown bears at previously unsampled locations generally fell within the range of estimates for previously or contemporaneously sampled bears in Alaska. Statistical support was found for variation in antibody seroprevalence among bears by location or age cohort for CAV-1, CDV, IAV, and T. gondii. There was limited concordance in comparisons between our results and previous serosurveys regarding spatial and age-related trends in antibody seroprevalence among Alaska brown bears suggestive of temporal variation. However, we found evidence that the seroprevalence of CAV-1 antibodies is consistently high in bears inhabiting southwest Alaska and the cumulative probability of exposure may increase with age. We found evidence for seroconversion or seroreversion to six different infectious agents in one or more bears. Results of this study increase our collective understanding of disease risk to both Alaska brown bear populations and humans that utilize this resource.