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Atomic force microscopy characterization of ultrathin polystyrene films formed by admicellar polymerization on silica disks

机译:硅胶圆盘上通过原子聚合形成的超薄聚苯乙烯薄膜的原子力显微镜表征

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Atomic force microscopy was used to study the characteristics of polymer films formed via admicellar polymerization (the polymerization of monomers solubilized in adsorbed surfactant aggregates). The investigated system included cetyltrimethylammonium bromide (C(16)TAB) as a cationic surfactant, styrene, 2,2'-azobisisobutyrilnitrile as an initiator, and polished silica disk substrates. Our goal was to examine changes in the properties and morphology of the formed polymer films due to changes in the surfactant and monomer feed levels. Normal tapping and phase-contrast modes in air were used to image the nanoscopic and microscopic morphologies of the polystyrene-modified silica. The root-mean-square roughness of the surface before and after modification was statistically analyzed and compared. The images were captured with loading-force set-point ratios of 0.2-0.9, and this allowed us to examine the stability of the polystyrene films. In the first series, for which the feed ratio of C(16)TAB to styrene was kept constant and the total feed concentration was varied, a uniform layer of a polystyrene film was observed along with some nanometersize aggregates at high feed concentrations of both C(16)TAB and styrene. These droplets eventually agglomerated with the film beneath and formed larger macrodroplets in a ring arrangement. At lower concentrations, droplets and holes were observed that eventually agglomerated to form a bi-continuous thin film. In the second experimental series, the concentration of C(16)TAB was kept constant, and the feed ratio of C(16)TAB to styrene was varied. A smooth thin film was observed at high concentrations of styrene. This film could be deformed and/or removed to expose the silica surface beneath. At lower styrene loadings, the polystyrene film became unstable and formed dropletlike aggregates, possibly because of either the uneven adsolubilization of the styrene monomer within the admicelle or the dewetting effect during washing and drying. The structure of the polystyrene film formed on a smooth silica disk was very dependent on the amount of the surfactant fed to the system; this contrasted with the results on precipitated silica. (C) 2003 Wiley Periodicals, Inc. [References: 24]
机译:原子力显微镜用于研究通过原子聚合(溶解在吸附的表面活性剂聚集体中的单体的聚合反应)形成的聚合物薄膜的特性。所研究的系统包括十六烷基三甲基溴化铵(C(16)TAB)作为阳离子表面活性剂,苯乙烯,2,2'-偶氮二异丁腈作为引发剂和抛光的二氧化硅圆盘基材。我们的目标是检查由于表面活性剂和单体进料量的变化而导致形成的聚合物薄膜的性质和形态的变化。空气中的正常拍打和相衬模式用于成像聚苯乙烯改性二氧化硅的纳米和微观形态。统计分析和比较改性前后表面的均方根粗糙度。以0.2-0.9的加载力设定点比率捕获图像,这使我们能够检查聚苯乙烯薄膜的稳定性。在第一个系列中,C(16)TAB与苯乙烯的进料比保持恒定并且总进料浓度变化,在两种进料浓度较高的情况下,观察到均匀的聚苯乙烯薄膜层以及一些纳米级聚集体(16)TAB和苯乙烯。这些液滴最终与下面的膜团聚,并以环形排列形成较大的大液滴。在较低的浓度下,观察到液滴和孔洞,这些液滴和孔洞最终凝结形成双连续薄膜。在第二个实验系列中,C(16)TAB的浓度保持恒定,并且C(16)TAB与苯乙烯的进料比变化。在高浓度的苯乙烯下观察到光滑的薄膜。该膜可以变形和/或去除以暴露下面的二氧化硅表面。在较低的苯乙烯负载量下,聚苯乙烯薄膜变得不稳定并形成液滴状的聚集体,这可能是由于苯乙烯单体在胶束内不均匀的增溶作用或在洗涤和干燥过程中的去湿作用所致。在光滑的二氧化硅盘上形成的聚苯乙烯薄膜的结构非常取决于进料到系统中的表面活性剂的量;这取决于表面活性剂的量。这与沉淀二氧化硅的结果相反。 (C)2003 Wiley Periodicals,Inc. [参考:24]

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