Abstract
Thermal conductivity of polymer fibers in the axial direction has been extensively studied while thermal conductivity in the radial direction λ remains unknown. In this work, polymer fibers with different molecular arrangements (crystalline, liquid crystalline, and amorphous) were plastically deformed. λ was measured at engineering strains ϵ = 0.2-2.3 using time-domain thermoreflectance. λ decreases with increasing strains for polyethylene (PE) and poly(p-phenylene-2,6-benzobisoxazole) (PBO) fibers and is independent of strain for poly(methyl methacrylate) (PMMA) fibers. The extrapolated thermal conductivity at zero strain is λ0 ≈ 0.27 Wm-1 K-1 for crystalline PE, λ0 ≈ 0.29 Wm-1 K-1 for liquid crystalline PBO, and λ0 ≈ 0.18 Wm-1 K-1 for amorphous PMMA. λ of PE drops to λ ≈ 0.14 Wm-1 K-1 at ϵ = 1.9; λ of PBO drops to λ ≈ 0.12 Wm-1 K-1 at ϵ = 2.1. We attribute the decrease of λ with ϵ in crystalline and liquid crystalline fibers to structural disorder induced by plastic deformation. The combination of structural disorder and phonon focusing effects produces a thermal conductivity in deformed PE and PBO fibers that is lower than amorphous PMMA.
Original language | English (US) |
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Pages (from-to) | 646-650 |
Number of pages | 5 |
Journal | ACS Macro Letters |
Volume | 5 |
Issue number | 6 |
DOIs | |
State | Published - Jun 21 2016 |
ASJC Scopus subject areas
- Organic Chemistry
- Polymers and Plastics
- Inorganic Chemistry
- Materials Chemistry