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In order to study the generation mechanism of electrochemical migration in a printed wiring board, paper/phenol‐resin composites with and without an adhesive layer, epoxy resin, and a laminate of epoxy resin and a paper/phenol‐resin composite were aged at 85 °C and 85% relative humidity (RH) with and without application of a DC voltage, and the space charge distributions in the samples were observed by the pulsed electroacoustic method. In the case of the composite with the adhesive layer, a large amount of negative charge is induced at the interface between the composite and the adhesive layer on the anode. It was found that such formation of space charge enhances the electric field intensity at the anode. The reason for this is because the conductivity is much lower in the adhesive layer than in the composite. Electrochemical migration does not occur when the same electric field is applied to the composite without the adhesive layer, whereas it does occur if the adhesive layer was replaced by epoxy resin with a similar conductivity to the adhesive layer. These results clearly indicate that electrochemical migration generates because the electric field at the anode surface is enhanced due to the low conductivity of the adhesive layer. © 2011 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.

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SUMMARYMore and more electronics are intended for use in adverse environments at high temperatures with high humidity. The spatial distributions of internal charge carriers, mainly due to ionic impurities that appear in hot and humid environments, are considered to affect the reliability of bulk insulation. Therefore, the authors examined space charge behavior inside paper/phenol-resin composites for printed circuit boards under DC voltages, focusing on the effect of the water absorption temperature. Both the sample weight and thickness were increased monotonically by immersion in water with an increase in the water temperature from 24°C to 85 °C, indicating that the water absorption by the sample was temperature dependent. In the early periods of water absorption (up to 10 hours), the electric field decreased near the two electrodes and increased in the other regions. Furthermore, heterocharge formation was observed near the cathode as the water absorption progressed, becoming more significant at higher water temperatures. Ion chromatography analyses detected numerous ions such as Na + , NH 4 + , and Cl -from the water, in which the sample had been immersed for 100 hours at various temperatures. It is highly possible that these ions are responsible for the heterocharge formation.

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