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Oxygen‐plasma‐treated polypropylene interfaces with air, water, and epoxy resins: Part I. Air and water

机译:氧等离子体处理的聚丙烯与空气、水和环氧树脂的界面:第一部分。 空气和水

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AbstractOxygen plasma treatment of polypropylene (PP) surfaces led to introduction of oxygencontaining functionalities, with consequent improvement of surface wettability. A combination of X‐ray photoelectron spectroscopy (XPS), static secondary ion mass spectroscopy (SSIMS), and contact angle measurements (water‐in‐air and air‐in‐water) allowed us to characterize the behavior of the treated surface in contact with air (low‐energy surface) and water (high‐energy surface).The treated surface showed the tendency to rearrange itself to minimize its interfacial energy. When contacted with air (low‐energy surface), polar groups were buried away from the polymer/air interface, while in contact with water (high‐energy surface) polar groups remained at the polymer/water interface.When contacted with air, the polymer surface layer rearranged by macromolecular motions within itself, since interdiffusion with the bulk polymer seems forbidden. These motions are thermally activated and it was possible to obtain an apparent activation energy (58.1 kJ/mol) close to those reported for oth
机译:摘要聚丙烯(PP)表面的氧等离子体处理引入了含氧官能团,从而提高了表面润湿性。X射线光电子能谱(XPS)、静态二次离子质谱(SSIMS)和接触角测量(空气中的水和水中的空气)的结合使我们能够表征处理表面与空气(低能表面)和水(高能表面)接触的行为。经过处理的表面显示出重新排列自身以最小化其界面能量的趋势。当与空气(低能表面)接触时,极性基团被埋在远离聚合物/空气界面的地方,而与水(高能表面)接触时,极性基团仍留在聚合物/水界面。当与空气接触时,聚合物表面层通过自身内部的大分子运动重新排列,因为与块状聚合物的相互扩散似乎是被禁止的。这些运动是热活化的,并且可以获得接近其他报告的表观活化能(58.1 kJ / mol)

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