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Controlling the morphology of polyurethane/polystyrene interpenetrating polymer networks for enhanced blood compatibility

机译:控制聚氨酯/聚苯乙烯互穿聚合物网络的形态以增强血液相容性

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摘要

Polyurethane (PU)/polystyrene (PS) IPNs were simultaneously synthesized at 80degreesC, controlling the reaction kinetics to change the morphology. Polymerization kinetics of styrene was controlled by the content of initiator, and that of polyurethane by the catalyst concentration. The effect of the initiator and the catalyst on the polymerization rate was analyzed by NMR spectroscopy and FTIR. Gelation time was also measured by using the advanced rheometric expansion system (ARES). Samples with sea-and-island morphology were obtained, when the polymerization rate of PS was relatively slow, and the phase separation time was long. When the polymerization rate of PS was relatively fast, and the phase separation time was short, cocontinuous morphology was obtained. The degree of phase separation and surface roughness decreased, as the rate of PU network formation was increased, and the phase-continuity was increased. The in vitro blood-compatibility tests showed that the surface roughness was an important factor on the adsorption of fibrinogens and platelets. A large amount of fibrinogens and platelets were adsorbed on the relatively rough surface of samples showing sea-island morphology. (C) 2002 John Wiley Sons, Inc. [References: 28]
机译:聚氨酯(PU)/聚苯乙烯(PS)IPN在80℃同时合成,控制反应动力学以改变形态。苯乙烯的聚合动力学由引发剂的含量控制,聚氨酯的聚合动力学由催化剂的浓度控制。通过NMR光谱和FTIR分析了引发剂和催化剂对聚合速率的影响。胶凝时间也通过使用先进的流变膨胀系统(ARES)进行测量。当聚苯乙烯的聚合速度相对较慢,相分离时间较长时,可获得具有海岛形的样品。当PS的聚合速率相对较快且相分离时间较短时,可获得共连续形态。随着PU网络形成速率的增加和相连续性的增加,相分离度和表面粗糙度降低。体外血液相容性测试表明,表面粗糙度是纤维蛋白原和血小板吸附的重要因素。大量的纤维蛋白原和血小板吸附在显示出海岛形态的相对粗糙的表面上。 (C)2002 John Wiley Sons,Inc. [参考:28]

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