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Dynamics of One Laser Pulse Surface Nanofoaming of Biopolymers

机译:一种生物聚合物激光脉冲表面纳米发泡的动力学

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Self standing films of the biopolymers gelatine, collagen, chitosan, irradiated with single nanosecond and femtosecond laser pulses easily yield on their surface, a nanofoam layer, formed by a cavitation and bubble growth mechanism. The laser foam has interesting properties that challenge the molecular features of the natural extracellular matrix and which make them good candidates for artificial matrix fabrication (nanoscopic fibers, large availability of cell adhesion sites, permeability to fluids due to open cell structure). As part of the mechanistic study, the dynamics of the process has been measured in the ns timescale by recording the optical transmission of the films at 632 nm during and after the foaming laser pulse. A rapid drop 100 . 0% taking place within the first 100 ns supports the cavitation mechanism as described by the previous negative pressure wave model. As modeled a strong pressure rise (~several thousands of bar) first takes place in the absorption volume due to pressure confinement and finite sound velocity, and then upon relaxation after some delay equal to the pressure transit time gives rise to a rarefaction wave (negative pressure) in which nucleation and bubble growth are very fast.
机译:用单纳秒和飞秒激光脉冲辐照的生物聚合物明胶,胶原蛋白,脱乙酰壳多糖的自立膜很容易在其表面产生由空化和气泡生长机制形成的纳米泡沫层。激光泡沫具有有趣的特性,这些特性挑战了天然细胞外基质的分子特征,使其成为人造基质制造的良好候选者(纳米纤维,大量的细胞粘附位点,由于开放的细胞结构而对液体的渗透性)。作为机理研究的一部分,通过在发泡激光脉冲期间和之后记录薄膜在632 nm处的光透射率,在ns时标中测量了该过程的动力学。急跌100。在前100 ns内发生的0%支持空化机制,如先前的负压波模型所述。如模型所示,由于压力限制和有限的声速,首先在吸收体积中发生了很大的压力上升(约几千巴),然后在松弛之后,等于压力传递时间的一定延迟,产生了稀疏波(负值)。压力),其中成核和气泡生长非常快。

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