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dc.contributor.authorMoradi, Sasan
dc.contributor.authorRomán Concha, Frida Rosario
dc.contributor.authorCalventus Solé, Yolanda
dc.contributor.authorHutchinson, John M.
dc.contributor.otherUniversitat Politècnica de Catalunya. Doctorat en Polímers i Biopolímers
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament de Màquines i Motors Tèrmics
dc.date.accessioned2021-05-19T07:25:30Z
dc.date.available2021-05-19T07:25:30Z
dc.date.issued2021-01
dc.identifier.citationMoradi, S. [et al.]. Densification: A route towards enhanced thermal conductivity of epoxy composites. "Polymers", 2021, vol. 13, núm. 2, p. 286/1-286/12.
dc.identifier.issn2073-4360
dc.identifier.urihttp://hdl.handle.net/2117/345880
dc.description.abstractWhen an amorphous polymer is cooled under pressure from above its glass transition temperature to room temperature, and then the pressure is released, this results in a densified state of the glass. This procedure applied to an epoxy composite system filled with boron nitride (BN) particles has been shown to increase the density of the composite, reduce its enthalpy, and, most importantly, significantly enhance its thermal conductivity. An epoxy-BN composite with 58 wt% BN platelets of average size 30 µm has been densified by curing under pressures of up to 2.0 MPa and then cooling the cured sample to room temperature before releasing the pressure. It is found that the thermal conductivity is increased from approximately 3 W/mK for a sample cured at ambient pressure to approximately 7 W/mK; in parallel, the density increases from 1.55 to 1.72 ± 0.01 g/cm3. This densification process is much more effective in enhancing the thermal conductivity than is either simply applying pressure to consolidate the epoxy composite mixture before curing or applying pressure during cure but then removing the pressure before cooling to room temperature; this last procedure results in a thermal conductivity of approximately 5 W/mK. Furthermore, it has been shown that the densification and corresponding effect on the thermal conductivity is reversible; it can be removed by heating above the glass transition temperature and then cooling without pressure and can be reinstated by again heating above the glass transition temperature and then cooling under pressure. This implies that a densified state and an enhanced thermal conductivity can be induced even in a composite prepared without the use of pressure.
dc.description.sponsorshipThis research was funded by a grant from the Spanish Ministerio de Economia y Competitividad, grant number MAT2017-82849-C2-2-R. The APC was funded by the research group’s contract research funds.
dc.language.isoeng
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.rightsAttribution 4.0
dc.rights.urihttps:// creativecommons.org/licenses/by/ 4.0/
dc.subjectÀrees temàtiques de la UPC::Física::Termodinàmica
dc.subjectÀrees temàtiques de la UPC::Enginyeria dels materials
dc.subject.lcshCalorimetry
dc.subject.lcshThermal conductivity
dc.subject.lcshEpoxy compounds
dc.subject.lcshHeat -- Transmission
dc.subject.otherThermal conductivity
dc.subject.otherEpoxy composites
dc.subject.otherBoron nitride
dc.subject.otherDensification
dc.subject.otherGlass transition
dc.subject.otherDifferential scanning calorimetry (DSC)
dc.titleDensification: A route towards enhanced thermal conductivity of epoxy composites
dc.typeArticle
dc.subject.lemacCalorimetria
dc.subject.lemacEpòxids
dc.subject.lemacCalor -- Transmissió
dc.contributor.groupUniversitat Politècnica de Catalunya. POLTEPO - Polímers Termoestables Epoxídics
dc.identifier.doi10.3390/polym13020286
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttps://www.mdpi.com/2073-4360/13/2/286
dc.rights.accessOpen Access
local.identifier.drac30882393
dc.description.versionPostprint (published version)
dc.relation.projectidinfo:eu-repo/grantAgreement/MICINN/1PE/ MAT2017-82849-C2-2-R
local.citation.authorMoradi, S.; Roman, F.; Calventus, Y.; Hutchinson, J.M.
local.citation.publicationNamePolymers
local.citation.volume13
local.citation.number2
local.citation.startingPage286/1
local.citation.endingPage286/12


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