Abstract

Energetic O+ ions were implanted into polyurethane (PU) fiber filaments, at 60 and 100keV with doses of 5×1014 and 1×1015ions/cm2, to modify the near-surface fiber morphology. The implantations were performed at room temperature and at −197°C, a temperature well below the glass transition temperature for this system. At room temperature, the lower energy implantation heats the fibers primarily near their surface, causing the fiber surface to smoothen and to develop a flattened shape. At the higher energy, the ion beam deposits its energy closer to the fiber core, heating the fiber more uniformly and causing them to re-solidify slowly. This favors a cylindrical equilibrium shape with a smooth fiber surface and no crack lines. The average fiber diameter reduced during 100keV implantation from 3.1 to 2.3μm. At −197°C, the ion implantation does not provide enough heat to cause notable physical modifications, but the fibers crack and break during subsequent warming to room temperature. The dose dependence of the crack formation along the fiber intersections is presented. The ion beams further cause near-surface chemical modifications in the fibers, particularly introducing two new chemical functional groups (C–(CO)–C and C–N–C).

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