2017
DOI: 10.1021/acsmacrolett.6b00941
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Highly Insulating Polyethylene Blends for High-Voltage Direct-Current Power Cables

Abstract: The insulation of state-of-the-art extruded highvoltage direct-current (HVDC) power cables is composed of cross-linked low-density polyethylene. Driven by the search for sustainable energy solutions, concepts that improve the ability to withstand high electrical fields and, ultimately, the power transmission efficiency are in high demand. The performance of a HVDC insulation material is limited by its residual electrical conductivity. Here, we demonstrate that the addition of small amounts of high-density poly… Show more

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Cited by 79 publications
(67 citation statements)
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“…Also, the mixing of polymers in small amounts will not change the total crystallinity of the material but lead to distinct changes in the nanostructure. This will result in charge trapping and then reduce the mobility of charge carriers [10].…”
Section: Differential Scanning Calorimetry (Dsc) Resultsmentioning
confidence: 99%
“…Also, the mixing of polymers in small amounts will not change the total crystallinity of the material but lead to distinct changes in the nanostructure. This will result in charge trapping and then reduce the mobility of charge carriers [10].…”
Section: Differential Scanning Calorimetry (Dsc) Resultsmentioning
confidence: 99%
“…In literature where the morphology of LDPE specimens for HVDC cable applications have been studied, no banded spherulites are seen in the extruded samples [5]. However, when pellets have been directly compression moulded to plaque specimens banded spherulite morphologies have been observed [14,15].…”
Section: Resultsmentioning
confidence: 99%
“…Especially DC conductivity characterization can be affected by many parameters that may lead to erroneous conclusions, e.g. changes in morphology, oxidation, protective pressing film used during compression moulding, additives and moisture [4][5][6][7].…”
Section: Introductionmentioning
confidence: 99%
“…The samples were cooled down in liquid nitrogen and then fractured. Thereafter all samples were etched for one hour using solution of 1wt% potassium permanganate in a mixture of sulfuric acid, ortho-phosphoric acid and water [3]. The process was stopped by washing in a mixture of sulfuric acid and water, thereafter in hydrogen peroxide and finally in isopropanol.…”
Section: Scanning Electron Microscopymentioning
confidence: 99%