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Enhanced High Thermal Conductivity Cellulose Filaments via Hydrodynamic Focusing
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2022 (English)In: Nano Letters, ISSN 1530-6984, E-ISSN 1530-6992, Vol. 22, no 21, p. 8406-8412Article in journal (Refereed) Published
Abstract [en]

Nanocellulose is regarded as a green and renewable nanomaterial that has attracted increased attention. In this study, we demonstrate that nanocellulose materials can exhibit high thermal conductivity when their nanofibrils are highly aligned and bonded in the form of filaments. The thermal conductivity of individual filaments, consisting of highly aligned cellulose nanofibrils, fabricated by the flow-focusing method is measured in dried condition using a T-type measurement technique. The maximum thermal conductivity of the nanocellulose filaments obtained is 14.5 W/m-K, which is approximately five times higher than those of cellulose nanopaper and cellulose nanocrystals. Structural investigations suggest that the crystallinity of the filament remarkably influence their thermal conductivity. Smaller diameter filaments with higher crystallinity, that is, more internanofibril hydrogen bonds and less intrananofibril disorder, tend to have higher thermal conductivity. Temperature-dependence measurements also reveal that the filaments exhibit phonon transport at effective dimension between 2D and 3D. 

Place, publisher, year, edition, pages
American Chemical Society (ACS) , 2022. Vol. 22, no 21, p. 8406-8412
Keywords [en]
crystallinity, filament, flow focusing, Nanocellulose, thermal conductivity, Cellulose, Diameter, Dimensions, Filaments, Hydrogen Bonds, Transport, Hydrodynamics, Nanoparticles, Nanostructures, Focusing, Nanofibers, Temperature distribution, nanomaterial, nanoparticle, Cellulose nanofibrils, Condition, Cristallinity, High thermal conductivity, Hydrodynamic focusing, Measurement techniques, Nano-cellulose, Nano-fibrils, chemistry
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Chemical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-328881DOI: 10.1021/acs.nanolett.2c02057ISI: 000877600400001PubMedID: 36283691Scopus ID: 2-s2.0-85140957245OAI: oai:DiVA.org:kth-328881DiVA, id: diva2:1766717
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QC 20230613

Available from: 2023-06-13 Created: 2023-06-13 Last updated: 2023-06-13Bibliographically approved

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Lundell, FredrikSöderberg, L. Daniel

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