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Ultrathin Cellulose Films of Tunable Nanostructured Morphology with a Hydrophobic Component

机译:具有疏水成分的可调节纳米结构的超薄纤维素膜

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摘要

In recent years, a wide range of different methods to implant nanosized patterns on surfaces have been developed. Spin coating immiscible binary polymer blends is a straightforward method to prepare micro- and nanostructures on thin films. This study utilizes binary blends to effortlessly prepare stable, surface-functionalized cellulose films. Blends of trimethylsilyl cellulose (TMSC) majority phase and polystyrene (PS) minority phase in toluene were spin coated into an ultrathin film, and TMSC was hydrolyzed to cellulose. The films were characterized and quantified using atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), contact angle measurements, and quartz crystal microbalance (QCM-D). AFM revealed that horizontally phase-separated structures form during spin coating; after the hydrolyzation of TMSC to cellulose, PS protrudes from cellulose as distinct patches. The patches are disk-like structures with a circular radial cross-section and a height of ca. 5-20 nanometers.The smaller the amount of PS in the original spin coating solution, the smaller the PS island dimensions in the films. The results obtained from the XPS measurements support the AFM results. Water contact angle of the PS/cellulose films increases from 61? to 71? when the relative amount of hydrophobic PS is increased from 1:100 to 1:5. Thus by simply varying the ratio of the film components subtly tailored hydrophobic properties can be chieved. The swelling of the films due to exposure to water was studied by QCM-D. The swelling was not affected by the amount of PS in the blend, and at equivalent cellulose content the blends and pure cellulose films exhibited similar swelling characteristics. In addition, the QCM-D evaluation demonstrated that the films are stable over extended periods of time and are suitable for fundamental studies by QCM-D.
机译:近年来,已经开发了各种各样的在表面上植入纳米尺寸图案的不同方法。旋涂不混溶的二元聚合物共混物是在薄膜上制备微米和纳米结构的直接方法。这项研究利用二元共混物轻松制备了稳定的,表面功能化的纤维素膜。将三甲基硅烷基纤维素(TMSC)多数相和聚苯乙烯(PS)少数相在甲苯中的混合物旋涂成超薄薄膜,并将TMSC水解为纤维素。使用原子力显微镜(AFM),X射线光电子能谱(XPS),接触角测量和石英晶体微量天平(QCM-D)对膜进行表征和定量。原子力显微镜显示在旋涂过程中形成了水平相分离的结构。在TMSC水解为纤维素后,PS从纤维素突出,成为不同的斑块。所述补片是具有圆形径向横截面且高度为约1μm的盘状结构。 5-20纳米。原始旋涂溶液中的PS量越小,薄膜中的PS岛尺寸越小。从XPS测量获得的结果支持AFM结果。 PS /纤维素膜的水接触角从61°增加。到71?当疏水性PS的相对量从1:100增加到1:5时。因此,通过简单地改变膜组分的比例,可以实现微调的疏水性能。通过QCM-D研究了由于暴露于水而引起的膜溶胀。溶胀不受共混物中PS的量的影响,并且在相等的纤维素含量下,共混物和纯纤维素膜表现出相似的溶胀特性。此外,QCM-D评估表明该膜在较长的时间内是稳定的,并且适合QCM-D进行基础研究。

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