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Thermally conductive, super flexible and flame-retardant BN-OH/PVA composite film reinforced by lignin nanoparticles

The usage of thermally conductive materials is limited due to their low thermal conductivity, poor thermal stability and brittleness, particularly at high working temperatures. In this work, for the first time, lignin nanoparticles (LNPs) were utilized to enhance the thermal conductivity, stability,...

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Published in:Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2019, Vol.7 (45), p.14159-14169
Main Authors: Wang, Xiu, Ji, Song-Lin, Wang, Xin-Qi, Bian, Hui-Yang, Lin, Ling-Rui, Dai, Hong-Qi, Xiao, Huining
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cited_by cdi_FETCH-LOGICAL-c344t-a6b28e587224ec7696009c5ca995a625b1c42aaec9a10df8937b43104ab7d7f93
cites cdi_FETCH-LOGICAL-c344t-a6b28e587224ec7696009c5ca995a625b1c42aaec9a10df8937b43104ab7d7f93
container_end_page 14169
container_issue 45
container_start_page 14159
container_title Journal of materials chemistry. C, Materials for optical and electronic devices
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creator Wang, Xiu
Ji, Song-Lin
Wang, Xin-Qi
Bian, Hui-Yang
Lin, Ling-Rui
Dai, Hong-Qi
Xiao, Huining
description The usage of thermally conductive materials is limited due to their low thermal conductivity, poor thermal stability and brittleness, particularly at high working temperatures. In this work, for the first time, lignin nanoparticles (LNPs) were utilized to enhance the thermal conductivity, stability, flame-retardancy, and flexibility of boron nitride (BN)-OH/polyvinyl alcohol (PVA) composite film, which played an important role as reinforcements. BN-OH/PVA/LNP composite film was fabricated through vacuum filtration in conjunction with chemical cross-linking. With the loading of LNPs at 2.5 vol%, the BN-OH/PVA/LNP composite film exhibited a higher through-plane thermal conductivity (up to 1.74 W m −1 K −1 ) than the one without LNPs (1.65 W m −1 K −1 ). After cross-linking with glutaraldehyde (GA), the elongation of the composite at break was 132%, an increase of 267% compared with the non-crosslinked one. The initial decomposition temperature of the BN-OH/PVA composite film was approximately 260 °C. However, in the presence of 7.1 vol% LNPs, the BN-OH/PVA/LNP composite film started to degrade at a much higher temperature, i.e. , 310 °C, demonstrating improved thermal stability. Furthermore, the addition of LNPs enhanced the flame-retardancy of the composites according to the burn test and differential scanning calorimetry (DSC). The resulting composite film with multiple improved properties is highly promising as a thermal interface material (TIM) and packaging material for various applications. LNPs were utilized as functional fillers to enhance the thermal conductivity, flame-retardancy, and flexibility of BN-OH/PVA composite film.
doi_str_mv 10.1039/c9tc04961d
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In this work, for the first time, lignin nanoparticles (LNPs) were utilized to enhance the thermal conductivity, stability, flame-retardancy, and flexibility of boron nitride (BN)-OH/polyvinyl alcohol (PVA) composite film, which played an important role as reinforcements. BN-OH/PVA/LNP composite film was fabricated through vacuum filtration in conjunction with chemical cross-linking. With the loading of LNPs at 2.5 vol%, the BN-OH/PVA/LNP composite film exhibited a higher through-plane thermal conductivity (up to 1.74 W m −1 K −1 ) than the one without LNPs (1.65 W m −1 K −1 ). After cross-linking with glutaraldehyde (GA), the elongation of the composite at break was 132%, an increase of 267% compared with the non-crosslinked one. The initial decomposition temperature of the BN-OH/PVA composite film was approximately 260 °C. However, in the presence of 7.1 vol% LNPs, the BN-OH/PVA/LNP composite film started to degrade at a much higher temperature, i.e. , 310 °C, demonstrating improved thermal stability. Furthermore, the addition of LNPs enhanced the flame-retardancy of the composites according to the burn test and differential scanning calorimetry (DSC). The resulting composite film with multiple improved properties is highly promising as a thermal interface material (TIM) and packaging material for various applications. 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C, Materials for optical and electronic devices</title><description>The usage of thermally conductive materials is limited due to their low thermal conductivity, poor thermal stability and brittleness, particularly at high working temperatures. In this work, for the first time, lignin nanoparticles (LNPs) were utilized to enhance the thermal conductivity, stability, flame-retardancy, and flexibility of boron nitride (BN)-OH/polyvinyl alcohol (PVA) composite film, which played an important role as reinforcements. BN-OH/PVA/LNP composite film was fabricated through vacuum filtration in conjunction with chemical cross-linking. With the loading of LNPs at 2.5 vol%, the BN-OH/PVA/LNP composite film exhibited a higher through-plane thermal conductivity (up to 1.74 W m −1 K −1 ) than the one without LNPs (1.65 W m −1 K −1 ). After cross-linking with glutaraldehyde (GA), the elongation of the composite at break was 132%, an increase of 267% compared with the non-crosslinked one. The initial decomposition temperature of the BN-OH/PVA composite film was approximately 260 °C. However, in the presence of 7.1 vol% LNPs, the BN-OH/PVA/LNP composite film started to degrade at a much higher temperature, i.e. , 310 °C, demonstrating improved thermal stability. Furthermore, the addition of LNPs enhanced the flame-retardancy of the composites according to the burn test and differential scanning calorimetry (DSC). The resulting composite film with multiple improved properties is highly promising as a thermal interface material (TIM) and packaging material for various applications. 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subjects Boron nitride
Crosslinking
Elongation
Flame retardants
Glutaraldehyde
Heat conductivity
Heat transfer
Lignin
Nanoparticles
Organic chemistry
Photographic film
Polyvinyl alcohol
Thermal conductivity
Thermal stability
Vacuum filtration
title Thermally conductive, super flexible and flame-retardant BN-OH/PVA composite film reinforced by lignin nanoparticles
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