Klein Robert J, Fischer Daniel A, Lenhart Joseph L
Organic Materials Department (1821), Sandia National Laboratories, Albuquerque, New Mexico 87185, USA.
Langmuir. 2008 Aug 5;24(15):8187-97. doi: 10.1021/la800134u. Epub 2008 Jun 27.
The process of implanting oxygen in polystyrene (PS) via exposure to ultraviolet-ozone (UV-O) was systematically investigated using the characterization technique of near-edge X-ray absorption fine structure (NEXAFS). Samples of PS exposed to UV-O for 10-300 s and washed with isopropanol were analyzed using the carbon and oxygen K-edge NEXAFS partial electron yields, using various retarding bias voltages to depth-profile the oxygen penetration into the surface. Evaluation of reference polymers provided a scale to quantify the oxygen concentration implanted by UV-O treatment. We find that ozone initially reacts with the double bonds on the phenyl rings, forming carbonyl groups, but within 1 min of exposure, the ratio of double to single oxygen bonds stabilizes at a lower value. Oxygen penetrates the film with relative ease, creating a fairly uniform distribution of oxygen within at least the first 4 nm (the effective depth probed by NEXAFS here). Before oxygen accumulates in large concentrations, however, it preferentially degrades the uppermost layer of the film by removing oxygenated low-molecular-weight oligomers. The failure to accumulate high concentrations of oxygen is seen in the nearly constant carbon edge jump, the low concentration of oxygen even at 5 min exposure (58% of that in poly(4-acetoxystyrene), the polymer with the most similarities to UV-O-treated PS), and the relatively high contact angles. At 5 min exposure the oxygen concentration contains ca. 7 atomic % oxygen. The oxygen species that are implanted consist predominantly of single O-C bonds and double O=C bonds but also include a small fraction of O-H. UV-O treatment leads a plateau after 2 min exposure in the water contact angle hysteresis, at a value of 67 +/- 2 degrees , due primarily to chemical heterogeneity. Annealing above T(g) allows oxygenated species to move short distances away from the surface but not diffuse further than 1-2 nm.
通过近边X射线吸收精细结构(NEXAFS)表征技术,系统研究了聚苯乙烯(PS)通过暴露于紫外臭氧(UV - O)来注入氧的过程。使用碳和氧K边NEXAFS部分电子产率分析了暴露于UV - O 10 - 300秒并用异丙醇洗涤的PS样品,使用各种减速偏置电压对氧渗入表面的深度进行剖析。对参考聚合物的评估提供了一个尺度,用于量化通过UV - O处理注入的氧浓度。我们发现,臭氧最初与苯环上的双键反应,形成羰基,但在暴露1分钟内,双键与单键氧键的比例稳定在较低值。氧相对容易地穿透薄膜,在至少前4纳米(此处NEXAFS探测的有效深度)内形成相当均匀的氧分布。然而,在氧大量积累之前,它会优先通过去除氧化的低分子量低聚物来降解薄膜的最上层。在几乎恒定的碳边跃变、即使暴露5分钟时氧浓度仍较低(仅为聚(4 - 乙酰氧基苯乙烯)中氧浓度的58%,聚(4 - 乙酰氧基苯乙烯)是与UV - O处理的PS最相似的聚合物)以及相对较高的接触角中,可以看出未能积累高浓度的氧。在暴露5分钟时,氧浓度约为7原子%。注入的氧物种主要由单O - C键和双O = C键组成,但也包括一小部分O - H。由于化学不均匀性,UV - O处理在暴露2分钟后导致水接触角滞后出现一个平台期,其值为67±2度。高于玻璃化转变温度(Tg)进行退火,使氧化物种能够从表面短距离移动,但扩散不超过1 - 2纳米。