氧化镁填充环氧纳米复合材料在不同温度和电场强度下的空间电荷行为

T. Andritsch, R. Kochetov, B. Lennon, P. Morshuis, J. Smit
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引用次数: 29

摘要

空间电荷积累是高压直流绝缘的一种典型现象。这对聚合物特别重要,因为它们不具有自愈特性。因此,与老化有关的空间电荷积累被证明是HVDC应用的限制因素。研究了环氧基纳米复合材料在氧化镁填充下的性能。纳米级氧化镁已经被证明可以降低高场强下的空间电荷密度。此外,当填料浓度较低时,氧化镁纳米复合材料的短期直流击穿强度有所提高。所有样品的基础材料是市售双酚a环氧树脂。通过透射电镜对MgO的粒径和分散性进行了验证,结果表明MgO的平均粒径为22 nm。用pea法获得了空间电荷分布,并与纯环氧树脂进行了比较。在直流场强为10 ~ 18 kV/mm的条件下,进行了剖面测量。为了观察温度对电荷分布的影响,在室温和60℃下进行了测量。计算了纯环氧树脂和纳米复合材料在不同场强和温度下的场增强系数。结果表明,与未填充的环氧树脂相比,MgO纳米复合材料在更高场强和更高温度下表现出更好的空间电荷行为。当电场强度或温度升高时,空间电荷积累和场增强因子均降低。对观测到的空间电荷行为给出了可能的解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Space charge behavior of magnesium oxide filled epoxy nanocomposites at different temperatures and electric field strengths
Space charge accumulation is a phenomenon, which is typical for high voltage dc insulation. It is of special importance for polymers, since they do not possess self-healing properties. Thus, the accumulation of space charges, which is linked to ageing, proved to be a limiting factor for HVDC applications. The focus of this paper is the behavior of epoxy based nanocomposites with magnesium oxide filler material. Nanoscale magnesium oxide has already been shown to decrease the space charge density for high field strengths. Additionally, MgO-nanocomposites showed an increase in the short term dc breakdown strength for low filler concentrations. Base material for all samples is commercially available bisphenol-A epoxy resin. Transmission electron microscopy was performed to validate the particle size and dispersion and showed that MgO has an average particle size of 22 nm. Space Charge profiles were obtained with the PEA-method and compared to neat epoxy. The profiles were taken under dc field strengths between 10 and 18 kV/mm. To see the influence of temperature on the charge distribution, the measurement was performed both at room temperature and at 60°C. The field enhancement factor of both the neat epoxy and the nanocomposite for different field strengths and temperatures has been calculated. It turned out that MgO nanocomposites show overall better space charge behavior at higher field strengths and at higher temperatures, compared to the unfilled epoxy. Both the space charge accumulation and the field enhancement factor are reduced, when going to higher electric field strengths or temperatures. Possible explanations for the observed space charge behavior are given.
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