Thermally reversible light scattering (TRLS) films were synthesized by the reaction-induced phase separation of solutions of N -4-ethoxybenzylidene-4‘- n -butylaniline (EBBA; 20−50 wt %) and polystyrene (PS; 1−5 wt %) in diglycidyl ether of bisphenol A (DGEBA), using benzyldimethylamine (BDMA) (0.06 mol with respect to epoxy groups), to initiate the polymerization. The material obtained after complete reaction consisted of a dispersion of EBBA/PS droplets in the epoxy network partially swollen by EBBA. The fractionation of EBBA between both phases was estimated using a simple thermodynamic model. Due to the matching of refractive indices of the three components, the multiphasic material was transparent above the nematic−isotropic transition temperature ( T NI ) of the EBBA/PS droplets. Below T NI the material exhibited a sharp transition to an opaque state due to the mismatching of refractive indices when EBBA was segregated as a nematic phase inside the droplets. The PS addition produced a significant decrease of the cloud-point conversion with respect to formulations devoid of PS. This led to relatively large domains that behave efficiently as light scattering centers in the PS-modified material, enabling high contrast ratios between transparent and opaque states to be obtained. The morphologies generated, and the corresponding optical properties of the TRLS films, did not change in the course of successive cooling/heating cycles.
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Hoppe et al. (2004) studied this question.
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