17 research outputs found

    Simulation of electrical ageing in insulating polymers using a quantitative physical model

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    Simulation of electrical ageing in insulating polymers using a quantitative physical mode

    The Role of Local Space Charge Concentrations in Producing Branched Tree Structures

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    Electrical trees are branched damage structures produced in polymeric insulation subject to high divergent fields. The density of branching ranges from a sparse form like a tree in winter to a dense compact form like a bush. This variation in form is significant as the bush structure occurs at higher voltages but grows slower. We present here a deterministic model for the formation of electrical trees based on damage produced by charges injected into the polymer from discharges taking place within the gas-filled tubules of the tree. A number of processes within the mechanism cause the space charge fields to fluctuate chaotically, and this is held to be responsible for the branching that is observed. Different tree shapes are found depending on whether or not injected/extracted charges reach a kinetic energy high enough for damage only at a few tree tips or everywhere around the tree periphery

    Percolation model for electrical breakdown in insulating polymers

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    It is suggested that an electric field above a given value eliminates the barriers to the transport of trapped charge carriers so as to produce an extended state in the form of a percolation cluster, and that the consequent current multiplication results in electrical breakdown. This model provides an estimated value of intrinsic breakdown strength close to the actual value. By considering the interactions between trap barrier potentials, the effect of electrical aging can be explained in terms of an increase in trap density. Many phenomena, such as the effect of weak points and the change of breakdown strength with the content of co-monomers or additives, can also be explained using this model

    Fast soliton-like charge pulses in insulating polymers

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    A previously unknown mode of conduction is identified in insulating polymers at moderate fields (40-50 MV/m). This takes the form of coherent charged pulses with a mobility (similar to 10(-10) m(2)V(-1)s(-1)) several orders of magnitude larger than that traditionally associated with independent charge carriers (similar to 10(-14) m(2)V(-1)s(-1)). It is shown that this phenomenon is consistent with a mechanism in which a charged compression boundary is formed electro-mechanically during injection and thereafter travels as a coherent solitary wave (soliton) through the polymer

    Electric field criteria for charge packet formation and movement in XLPE.

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    The formation of space charge packets in XLPE (Cross-linked polyethylene) tapes from unaged cable insulation has been studied utilising the pulsed electro-acoustic (PEA) technique. The 150 m thick sheets were studied under constant applied dc field of 120 kV/mm at a temperature of 20 C for a period of 48 hours. After an inception period of about 3.5 hours, during which heterocharge accumulates at the anode and increases the local field there, a sequence of positive charge packets were observed to transit the sample starting from near the anode. Calculation of the internal field showed that the packets required a field of 140 kV/mm for their initiation. Reduction of the applied field step-wise from 120 kV/mm to 80 kV/mm indicated that the charge packet would keep moving as long as the local field at its front exceeded 100 kV/mm, but with a reducing magnitude. A return to an applied field of 120 kV/mm confirmed that the local field required to initiate a new packet was in excess of 135 kV/mm. The results are discussed in terms of current theories of charge packet formation. The first packet appears to be a moving front of field ionisation. The generation of subsequent packets is governed by the field at the anode and the balance of charge injection and extraction process, which occur there. The nature of the negative charges produced at the ionisation front is not clear, but they are unlikely to be electrons

    Photoluminescence, recombination induced luminescence and electroluminescence in epoxy resin.

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    Dielectric breakdown of epoxies is preceded by light emission, or so-called electroluminescence, from the solid-state material. Very little is known about the luminescence properties of epoxies. The aim of this paper is to derive information that can be used as a basis to understand the nature of the excited states and their involvement in electrical degradation processes. Three different kinds of stimulation were used to excite the material luminescence. Photoluminescence was performed on the base resin, the hardener and the cured resin. Luminescence excited by a silent discharge has been analysed to identify which of the luminescent centres are optically active upon the recombination of electrical charges and could therefore act as charge traps. Finally, the electroluminescence spectrum has been acquired and compared with the previous ones. Although the identification of the origin of these emissions is far from being complete, it has been found that the photoluminescence from the cured resin is due to in-chain chromophores, which acts as trapping centres. The excited states involved in photoluminescence also seems to be involved in electroluminescence, but other components are detected as well, which could be due to the degradation of the resin molecule under the effect of the electric stress

    Erratum: 'Percolation model for electrical breakdown in insulating polymers' (vol 85, pg 4454, 2004)

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    Erratum: 'Percolation model for electrical breakdown in insulating polymers' (vol 85, pg 4454, 2004

    'Sub-Hertz' Dielectric Spectroscopy

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    Dielectric spectroscopy measurements below 1 Hz are often dominated by “conduction-like” effects. For this reason, they often appear to be dismissed as being of little interest. In this paper two “sub-hertz” responses are considered that give insights into the insulating sys-tems concerned. The first system is that of cross-linked polyethylene, taken from a power cable system. Measurements at temperatures between 60°C and close to melting at 100°C show a change in characteristic from a percolation process to a “true” DC conduction at close to the melting point. Using DC conductivities, it appears to be possible to show whether the cable has been subjected to thermo-electric ageing. This might give insights into where the conduction and hence the ageing in the XLPE is occurring. The second system is an epoxy composite. By considering the sub-hertz response, it is possible to demonstrate the effect of the interface between the filler and the epoxy matrix. In this system, ageing, resulting in delamination between the glass fiber filler and the epoxy, is clearly detected by sub-hertz dielectric spectroscopy. This process is likely to be facilitated by the presence of water, which is known to lead to mechanical failure in such systems, and which can also be detected by "sub-hertz" dielectric spectroscopy. The implications for nano-dielectrics are then briefly considered

    Influence of thermal treatment and residues on space charge accumulation in XLPE for DC power cable application

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    Effects of cross-linking by-products (residues) of polyethylene on space charge accumulation and decay are investigated in the paper using the pulsed electro-acoustic technique. Space charge profiles have shown a great variation both in the charge initiation over the voltage ramping up process and later on long term stressing and decay (volts off) among the samples subjected to different conditioning, which results in diverse residues content (fresh, 0.5% residue and thoroughly degassed). The results show that by-products of cross-linking or the residual impurities play a key role in the space charge accumulation in cross-linked polyethylene. On the removal of impurities by degassing, small homocharge was built up in the vicinity of the electrode. It is concluded that space charge accumulation is governed by the charge injection through dielectric/electrode interface when sample is thoroughly degassed
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