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Tailoring Dielectric Properties using Designed Polymer-Grafted ZnO Nanoparticles in Silicone Rubber
KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Ytbehandlingsteknik.ORCID-id: 0000-0002-3310-9964
KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Polymera material.
KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Polymera material.ORCID-id: 0000-0002-0236-5420
KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Ytbehandlingsteknik.
Vise andre og tillknytning
2017 (engelsk)Inngår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 5, s. 14241-14258, artikkel-id C6TA11237DArtikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Polymer grafts were used to tailor the interphases between ZnO nanoparticles (NPs) and silicone matrices. The final electrical properties of the nanocomposites were tuned by the grafted interphases, by controlling the inter-particle distance and the NP-morphology. The nanocomposites can be used in electrical applications where control of the resistivity is desired. Hansen's solubility parameters were used to select a semi-compatible polymer for grafting to obtain anisotropic NP morphologies in silicone, and the grafted NPs self-assembled into various morphologies inside the silicone matrices. The morphologies in the semi-compatible nanocomposites could be tuned by steering the graft length of poly(n-butyl methacrylate) via entropic matrix-graft wetting using surface-initiated atom-transfer radical polymerization. Image analysis models were developed to calculate the radius of primary NPs, the fraction of aggregates, the dispersion, and the face-to-face distance of NPs. The dielectric properties of the nanocomposites were related to the morphology and the face-to-face distance of the NPs. The dielectric losses, above 100 Hz, for nanocomposites with grafted NPs were approximately one decade lower than those of pristine NPs. The isotropic nanocomposites increased the resistivity up to 100 times compared to that of neat silicone rubber, due to the trapping of charge carriers by the interphase of dispersed NPs and nanoclusters. On the other hand, the resistivity of anisotropic nanocomposites decreased 10–100 times when the inter-particle distance in continuous agglomerates was close to the hopping distance of charge carriers. The electrical breakdown strength increased for compatible isotropic nanocomposites, and the temperature dependence of the resistivity and the activation energy were ∼50% lower in the nanocomposites with grafted NPs. These flexible dielectric nanocomposites are promising candidates for low-loss high-voltage transmission cable accessories, mobile electronic devices, wearables and sensors.

sted, utgiver, år, opplag, sider
RSC Publishing, 2017. Vol. 5, s. 14241-14258, artikkel-id C6TA11237D
Emneord [en]
tailoring nanoparticle arrangement, polymer grafting, tuning of dielectric properties
HSV kategori
Forskningsprogram
Fiber- och polymervetenskap
Identifikatorer
URN: urn:nbn:se:kth:diva-204038DOI: 10.1039/C6TA11237DISI: 000405190000036Scopus ID: 2-s2.0-85023756284OAI: oai:DiVA.org:kth-204038DiVA, id: diva2:1084014
Forskningsfinansiär
SweGRIDS - Swedish Centre for Smart Grids and Energy StorageSwedish Foundation for Strategic Research , SM14-0034
Merknad

QC 20170323

Tilgjengelig fra: 2017-03-23 Laget: 2017-03-23 Sist oppdatert: 2017-08-15bibliografisk kontrollert
Inngår i avhandling
1. Controlled Polymer Grafting from Nanoparticles for the Design of Dielectric Nanocomposites
Åpne denne publikasjonen i ny fane eller vindu >>Controlled Polymer Grafting from Nanoparticles for the Design of Dielectric Nanocomposites
2017 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

The interest for polymeric nanocomposites has rapidly grown during the last decades, fuelled by the great potential and superior properties of nanoparticles (NPs). The production volumes of commercial NPs have increased exponentially during the last ten years, and the quality has been significantly improved. The aim of this study was to design polymer grafted commercially available metal-oxide NPs, and graphene oxide (GO), to develop isotropic (homogeneous) and anisotropic (heterogeneous) polymer nanocomposites for dielectric applications. The motivation was to formulate functional insulation materials for compact components in future power-grid systems using high-voltage direct-current (HVDC) or high-voltage alternating-current (HVAC), and to fabricate responsive sensor materials for monitoring e.g. temperature and voltage fluctuations in so called “Smart Grids”.

Aluminium oxide (Al2O3), zinc oxide (ZnO) and reduced GO (rGO) NPs were modified with sparse polymer grafts via a controlled “covalent route” and were mixed with silicone (PDMS) or polyethylene matrices (EBA and LDPE) commonly used in HV-cable systems. The graft length and the graft-to-matrix compatibility were tailored to obtain nanocomposites with various self-assembled NP-morphologies, including well-dispersed, connected and phase-separated structures. The graft length was used to adjust the inter-particle distance of nanocomposites with continuous morphologies or connected (percolated) NPs. It was found that nanocomposites with percolated NPs and short inter-particle distances exhibited 10-100 times higher conductivity than the unfilled (neat) polymer, or displayed a rapid non-linear increase in conductivity (~1 million times) with increasingelectric field, while well-dispersed NPs with long inter-particle distances exhibited 10-100 times lower conductivity (i.e. higher resistivity) as an effect of their trapping of charge carriers. These tunable and functional properties are desirable for HV-insulation, field-grading applications, and flexible electronics.

In addition it was shown that GO modified with dense polymer grafts via a “physisorption route” formed suspensions with liquid crystals, or matrix-free GO-composites with well-dispersed GO in isotropic or nematic states. These materials were reinforced by the GO, and exhibited elevated glass transition temperatures and a rapid thermo-responsive shape-memory effect, and are thus proposed to have a great potential as sensor materials and responsive separation membranes.

Abstract [sv]

Intresset för polymera nanokompositer har snabbt ökat under de senaste decennierna, drivet av den stora potentialen och de överlägsna egenskaperna hos nanopartiklar (NPs). Produktionsvolymerna för kommersiella NP har ökat exponentiellt under de senaste tio åren, och kvaliteten har förbättrats avsevärt. Syftet med denna studie var att polymer-ympa kommersiellt tillgängliga metalloxid-NPs, och grafenoxid (GO), för att designa isotropa (homogena) och anisotropa (heterogena) polymera nanokompositer för dielektriska tillämpningar. Motiveringen var att formulera funktionella isoleringsmaterial för kompakta komponenter i framtida kraftnätssystem som använder högspänd likström (HVDC) eller högspänd växelström (HVAC), samt att tillverka responsiva sensormaterial för övervakning av t.ex. temperatur- and spänningsvariationer i så kallade "Smart Grids".

Aluminiumoxid (Al2O3), zinkoxid (ZnO) och reducerad GO (rGO) NPs modifierades med glesa polymerympar via en kontrollerad "kovalent väg" och blandades med silikon (PDMS) eller polyeten matriser (EBA och LDPE) som är vanliga i HV-kabelsystem. Ymplängden och ymp-till-matrix kompatibiliteten skräddarsyddes för att erhålla nanokompositer med olika självordnande NP-morfologier, inklusive väldispergerade, länkade och fasseparerade strukturer. Ymplängden användes för att justera partikelavståndet i nanokompositer med förbundna morfologier eller länkade NPs. Man fann att nanokompositer med länkade NPs och korta interpartikelavstånd uppvisade 10-100 gånger högre konduktivitet än den ofyllda (rena) polymeren, eller erhöll en snabb icke-linjär ökning i konduktivitet (~1 miljon gånger) med ökande elektriskt fält, medan väldispergerade NPs med långa interpartikelavstånd uppvisade 10-100 gånger lägre ledningsförmåga (dvs. högre resistivitet) som en effekt av deras infångande av laddningsbärare. Dessa inställbara och funktionella egenskaper är önskvärda för HV-isolering, fältstyrande applikationer och flexibel elektronik.

Dessutom visades att GO, som modifierats med täta polymerympar via en "fysisorptionsväg", bildade suspensioner med flytande kristaller, eller matrisfria GO-kompositer med väldispergerad GO i isotropa eller nematiska tillstånd. Dessa material armerades av GO och uppvisade förhöjda glastransitionstemperaturer och en snabb värmeresponsiv form-minneseffekt, och föreslås därigenom ha en stor potential som sensor-material och responsiva separationsmembran.

sted, utgiver, år, opplag, sider
Stockholm: KTH Royal Institute of Technology, 2017. s. 96
Serie
TRITA-CHE-Report, ISSN 1654-1081 ; 2017:16
HSV kategori
Forskningsprogram
Fiber- och polymervetenskap
Identifikatorer
urn:nbn:se:kth:diva-204036 (URN)
Disputas
2017-04-28, Kollegiesalen, Brinellvägen 8, KTH-huset, KTH Campus, Stockholm, 10:00 (engelsk)
Opponent
Veileder
Forskningsfinansiär
SweGRIDS - Swedish Centre for Smart Grids and Energy Storage
Merknad

QC 20170323

Tilgjengelig fra: 2017-03-23 Laget: 2017-03-23 Sist oppdatert: 2017-08-10bibliografisk kontrollert

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