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The incorporation of 23 nm titanium dioxide nanoparticles into an epoxy matrix to form a nanocomposite structure is described. It is shown that the use of nanometric particles results in a substantial change in the behaviour of the composite, which can be traced to the mitigation of internal charge when a comparison is made with conventional TiO 2 fillers. A variety of diagnostic techniques (including dielectric spectroscopy, electroluminescence, thermally stimulated current and photoluminescence) have been used to augment pulsed electro-acoustic space charge measurement to provide a basis for understanding the underlying physics of the phenomenon. It would appear that, when the size of the inclusions becomes small enough, they act cooperatively with the host structure and cease to exhibit interfacial properties, leading to Maxwell-Wagner polarization. It is postulated that the particles are surrounded by high charge concentrations in the Gouy-Chapman-Stern layer. Since nanoparticles have very high specific areas, these regions allow limited charge percolation through nano-filled dielectrics.The practical consequences of this have also been explored in terms of the electric strength exhibited. It would appear that there was a window in which real advantages accrue from the nano-formulated material. An optimum loading of about 10% (by weight) is indicated.

This is the unspecified version of the paper.This version of the publication may differ from the final published version. Permanent repository link ABSTRACTIn this research, the influence of water absorption on the dielectric properties of epoxy resin and epoxy micro-composites and nano-composites filled with silica has been studied. Nanocomposites were found to absorb significantly more water than unfilled epoxy. However, the microcomposite absorbed less water than unfilled epoxy: corresponding to reduced proportion of the epoxy in this composite. The glass transition temperatures of all the samples were measured by both differential scanning calorimetry and dielectric spectroscopy. The T g decreased as the water absorption increased and, in all cases, corresponded to a drop of approximately 20K as the humidity was increased from 0% to 100%. This implied that for all the samples, the amount of water in the resin component of the composites was almost identical. It was concluded that the extra water found in the nanocomposites was located around the surface of the nanoparticles. This was confirmed by measuring the water uptake, and the swelling and density change, as a function of humidity as water was absorbed. The water shell model, originally proposed by Lewis and developed by Tanaka, has been further developed to explain low frequency dielectric spectroscopy results in which percolation of charge carriers through overlapping water shells was shown to occur. This has been discussed in terms of a percolation model. At 100% relative humidity, water is believed to surround the nanoparticles to a depth of approximately 5 monolayers. A second layer of water is proposed that is dispersed by sufficiently concentrated to be conductive; this may extend for approximately 25 nm. If all the water had existed in a single layer surrounding a nanoparticle, this layer would have been approximately 3 to 4 nm thick at 100%. This "characteristic thickness" of water surrounding a given size of nanoparticle appeared to be independent of the concentration of nanoparticles but approximately proportional to water uptake. Filler particles that have surfaces that are functionalized to be hydrophobic considerably reduce the amount of water absorbed in nanocomposites under the same conditions of humidity. Comments are made on the possible effect on electrical aging.

Dielectric studies are described aimed at providing an understanding of the charge storage and transport of an epoxy resin containing TiO 2 nanoparticles. Comparative results for conventionally filled composites are given, and the results discussed in terms of the underlying physics. It is shown that nanometric fillers mitigate the interfacial polarization characteristic of conventional materials with a reduction in the internal field accumulations. Background and Vision

The results of space charge evolution in cross-linked polyethylene power cables under dc electrical field at a uniform temperature and during external voltage polarity reversal are presented in the paper. A mirror image charge distribution was observed in the steady state, but the pre-existing field altered the way in which the steady state charge distribution was formed from that obtaining when the cable was first polarized. Polarity reversing charge was generated in the middle of the insulation and moved towards the appropriate electrodes under the influence of a field in excess of the maximum applied field. Our results show that the mirror effect is a steady state effect that is due to crossinterface currents that depend only on the interface field and not its polarity. Measurements on cable sections with an elevated mean temperature and temperature gradient show that the interface currents are temperature dependent, and that differences between the activation energies of the interface and bulk currents can eliminate and possibly even invert the polarity of the space charge distribution.Index Terms -Space charge, PEA, XLPE insulated power cables, voltage polarity reversal, temperature gradient, "mirror image effect".

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This is the unspecified version of the paper.This version of the publication may differ from the final published version. between charge packet formation and propagation, and electroluminescence. Although the two phenomena are observed in the same field range, it is found that the onset of continuous EL follows the formation at the electrodes of positive and negative space charge regions that extend into the bulk prior to the propagation of charge packets. Charge recombination appears to be the excitation process of EL since oppositely charged domains meet in the material bulk. To gain an insight into specific light excitation process associated with charge packet propagation, electroluminescence has been recorded for several hours under fields at which charge packet dynamics were evidenced. It is shown that current and luminescence oscillations are detected during charge packet propagation, and that they are in phase. Mechanisms underlying EL and charge packets are further considered on the basis of these results. Permanent repository link2

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