Anisotropic polymers fabricated via additive manufacturing exhibit complex thermal transport profiles that are challenging to characterize using steady-state techniques. We present a transient thermal method utilizing a short rectangular current pulse excitation to determine the directional thermal diffusivity and conductivity of anisotropic materials. The measurement is conducted on finite specimens, where the low diffusivity of the polymer media results in a highly attenuated and dispersed rear-side temperature profile over an extended transient window. Conduction losses to the adjacent coolers are accounted for by solving the one-dimensional heat conduction equation on an asymmetric multi-layer sandwich structure using the implicit Crank–Nicolson method. Because thermal diffusivity and conductivity are not independent quantities (λ=aρc), the inverse problem is deliberately formulated to estimate the diffusivity alone: the volumetric heat capacity is predetermined and held fixed, and the conductivity follows directly as λ=aρc. This removes the ill-conditioning that would otherwise arise from treating λ and a as free, independent parameters in the fit. A two-parameter non-linear least-squares fit is applied to the rear-side temperature rise following Savitzky–Golay noise filtering to estimate the directional diffusivity and effective heat flux. The method is validated using an isotropic reference standard to rule out false system anisotropy, and is subsequently applied to additively manufactured polymer specimens to resolve print-induced directionality through sequential, axis-aligned (unidirectional) measurements along the axial and transverse printing directions. The validity of the one-dimensional reduction is confirmed quantitatively by two- and three-dimensional anisotropic simulations of the exact geometry, which bound the lateral-spreading bias below 0.01% even for the highest-anisotropy specimen, and the robustness of the method to sensor thermal response, signal filtering, and effective-flux estimation is quantified. A rigorous evaluation of the expanded metrological uncertainty demonstrates the high accuracy and reliability of this low-energy excitation technique for highly dispersing media, making it a viable and highly accessible alternative for evaluating material anisotropy.
Janek et al. (Thu,) studied this question.
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