89 research outputs found
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Electroluminescence excitation mechanisms in an epoxy resin under divergent and uniform field
Electroluminescence excitation mechanisms have been investigated in epoxy resin under divergent and uniform field situations. Metallic wires embedded in the resin were used to produce field divergence whereas film samples were metallised to obtain a uniform field. Electroluminescence under divergent field was stimulated by an impulse voltage. Light was emitted on the positive and negative fronts of the square pulses when the field exceeded 20 kV/mm at the wire surface, with equal intensity and without polarity dependence. There was evidence of space charge accumulation around the wires in multiple-pulse experiments. Charge injection and extraction occurring at both fronts of the pulse provide the condition for EL excitation. Further excitation of the EL during the plateau of the voltage pulse is prevented by the opposite field of the trapped charge. Field computation with and without space charge supports the proposed interpretation. A DC voltage was used for the uniform field experiments. A continuous level of electroluminescence is found at 175 kV/mm. Charging/discharging current measurements and space charge profile analyses using the pulsed electro-acoustic (PEA) technique were performed at different fields up to the EL level. Dipolar orientation generates a long lasting transient current that prevents the conduction level being reached within the experimental protocol (one hour poling time). The continuous EL emission is nevertheless associated with a regime where the conduction becomes dominant over the orientational polarization. Polarization and space charge contribute to the PEA charge profiles. Homo-charge injection at anode and cathode is seen at 20 kV/mm and a penetration of positive space charge in the bulk is detected above 100 kV/mm, suggesting an excitation of the continuous EL by bipolar charge recombination
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Space charge induced luminescence in epoxy resin
Dielectric breakdown of epoxies is preceded by a light emission from the solid state material, so-called electroluminescence. Very little is known however on the luminescence properties of epoxy. 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
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The relationship between charge distribution, charge packet formation and electroluminescence in XLPE under DC
Different reports describing the internal distribution of space charge in cross-linked polyethylene (XLPE) under DC field have been published recently. The most striking fact observed is the organization of the space charge into charge packets that cross the insulation. All models for charge packet formation imply that carrier recombination will occur. As the recombination region is potentially a luminescence one it is of interest to record the electroluminescence in this regime. This topic is addressed in this paper
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Evaluation of the onset of space charge and electroluminescence as a marker for cross linked polyethylene ageing
The aim of the “ARTEMIS” project is to investigate the ageing mechanisms for cross-linked polyethylene under thermo-electrical stress and to identify ageing markers, which can be used to carry out diagnostic procedures. A carefully selected set of techniques which can give cross-correlated information on space charge phenomenology and material degradation were used to investigate specimens peeled from reference and aged cables. The paper shows that ageing induces a change in the density and depth of trapping levels, and an increase in the number and size of mesovoids. Interpretation of these results is discussed in terms of physico-chemical modifications, which can affect trap distribution and microstructure
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Characterizing HV XLPE cables by electrical, chemical and microstructural measurements on cable peeling: Effects of surface roughness, thermal treatment and peeling location
Characterization of the electrical, chemical, and microstructural properties of high voltage cables was the first step of the European project “ARTEMIS”, which has the aim of investigating degradation processes and constructing aging models for the diagnosis of cross-linked polyethylene (XLPE) cables. Cables produced by two different manufacturers were subjected to a large number of electrical, microstructural, and chemical characterizations, using cable peelings, instead of lengths of whole cables, as specimens for the measurements. Here the effect of surface deformation and roughness due to peeling and the relevance and significance of thermal pre-treatment prior to electrical and other measurements is discussed. Special emphasis is put on space charge, conduction current and luminescence measurements. We also consider the dependence of these properties on the spatial position of the specimen within the cable. It is shown that even though the two faces of the cable peel specimens have different roughness, the low-field electrical properties seem quite insensitive to surface roughness, while significant differences are detectable at high fields. Thermal pre-treatment is required to stabilize the insulating material to enable us to obtain reproducible results and reliable inter-comparisons throughout the whole project. The spatial position of the specimens along the cable radius can also have a non-negligible influence on the measured properties, due to differential microstructure and chemical composition
A linear CO chemistry parameterization in a chemistry-transport model: evaluation and application to data assimilation
This paper presents an evaluation of a new linear parameterization valid for the troposphere and the stratosphere, based on a first order approximation of the carbon monoxide (CO) continuity equation. This linear scheme (hereinafter noted LINCO) has been implemented in the 3-D Chemical Transport Model (CTM) MOCAGE (MOdèle de Chimie Atmospherique Grande Echelle). First, a one and a half years of LINCO simulation has been compared to output obtained from a detailed chemical scheme output. The mean differences between both schemes are about ±25 ppbv (part per billion by volume) or 15% in the troposphere and ±10 ppbv or 100% in the stratosphere. Second, LINCO has been compared to diverse observations from satellite instruments covering the troposphere (Measurements Of Pollution In The Troposphere: MOPITT) and the stratosphere (Microwave Limb Sounder: MLS) and also from aircraft (Measurements of ozone and water vapour by Airbus in-service aircraft: MOZAIC programme) mostly flying in the upper troposphere and lower stratosphere (UTLS). In the troposphere, the LINCO seasonal variations as well as the vertical and horizontal distributions are quite close to MOPITT CO observations. However, a bias of ~−40 ppbv is observed at 700 Pa between LINCO and MOPITT. In the stratosphere, MLS and LINCO present similar large-scale patterns, except over the poles where the CO concentration is underestimated by the model. In the UTLS, LINCO presents small biases less than 2% compared to independent MOZAIC profiles. Third, we assimilated MOPITT CO using a variational 3D-FGAT (First Guess at Appropriate Time) method in conjunction with MOCAGE for a long run of one and a half years. The data assimilation greatly improves the vertical CO distribution in the troposphere from 700 to 350 hPa compared to independent MOZAIC profiles. At 146 hPa, the assimilated CO distribution is also improved compared to MLS observations by reducing the bias up to a factor of 2 in the tropics. This study confirms that the linear scheme is able to simulate reasonably well the CO distribution in the troposphere and in the lower stratosphere. Therefore, the low computing cost of the linear scheme opens new perspectives to make free runs and CO data assimilation runs at high resolution and over periods of several years
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Space charge and associated electroluminescence processes in XLPE cable peelings
The intent of this paper is to cross-correlate the information obtained by space charge profile analysis and electroluminescence (EL) detection in cross-linked polyethylene samples submitted to dc fields, with the objective to make a link between space charge phenomena and energy release as revealed by detection of visible photons. Space charge measurements carried out at different electrical fields by the pulsed electro-acoustic method show the presence of a low-field threshold, close to 15 to 20 kV/mm, above which space charge begins to accumulate considerably in the insulation. Charges are seen to cross the insulation thickness through a packet-like behavior at higher fields, starting at about 60 to 70 kV/mm. EL measurements show the existence of two distinct thresholds, one related to the permanent excitation of EL under voltage, the other being transient EL detected upon specimen short-circuit. The former occurs at values of field corresponding to space charge packet formation, and the latter to the onset of space charge accumulation. The two techniques give therefore consistent information on space charge phenomena and associated energy release in the optical EM spectrum
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Photoluminescence, recombination induced luminescence and electroluminescence in epoxy resin
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
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Charge distribution and electroluminescence in cross-linked polyethylene under dc field
The intent of this paper is to cross-correlate the information obtained by space charge distribution analysis and electroluminescence (EL) detection in cross-linked polyethylene samples submitted to dc fields, with the objective to make a link between space charge phenomena and energy release as revealed by the detection of visible photons. Space charge measurements carried out at different field levels by the pulsed electro-acoustic method show the presence of a low-field threshold, close to 15-20 kV mm-1, above which considerable space charge begins to accumulate in the insulation. Charges are seen to cross the insulation thickness through a packet-like behaviour at higher fields, starting at about 60-70 kV mm-1. EL measurements show the existence of two distinct thresholds, one related to the continuous excitation of EL under voltage, the other being transient EL detected upon specimen short circuit. The former occurs at values of field corresponding to charge packet formation and the latter to the onset of space charge accumulation. The correspondence between pertinent values of the electric field obtained through space charge and EL analyses provides support for the existence of degradation thresholds in insulating materials. Special emphasis is given to the relationship between charge packet formation and propagation, and EL. 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 processes associated with charge packet propagation, EL 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. The mechanisms underlying EL and charge packets are further considered on the basis of these results
Dielectric relaxations in PEEK by combined dynamic dielectric spectroscopy and thermally stimulated current
The molecular dynamics of a quenched poly (ether ether ketone) (PEEK) was studied over a broad frequency range from 10-3 to 106 Hz by combining dynamic dielectric spectroscopy (DDS) and thermo-stimulated current (TSC) analysis. The dielectric relaxation losses e00 KK has been determined from the real part e0 T(x) thanks to Kramers–Kronig transform. In this way, conduction and relaxation processes can be analyzed independently. Two secondary dipolar relaxations, the c and the b modes, corresponding to non-cooperative localized molecular mobility have been pointed out. The main a relaxation appeared close to the glass transition temperature as determined by DSC; it has been attributed to the delocalized cooperative mobility of the free amorphous phase. The relaxation times of dielectric relaxations determined with TSC at low frequency converge with relaxation times extracted from DDS at high frequency. This correlation emphasized continuity of mobility kinetics between vitreous and liquid state. The dielectric spectroscopy exhibits the ac relaxation, near 443 K, which has been associated with the rigid amorphous phase confined by crystallites. This present experiment demonstrates coherence of the dynamics of the PEEK heterogeneous amorphous phase between glassy and liquid state and significantly improve the knowledge of molecular/dynamic structure relationships
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