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具有疏水性成分的、纳米结构形态可调的超薄纤维素薄膜。

Ultrathin cellulose films of tunable nanostructured morphology with a hydrophobic component.

作者信息

Nyfors Laura, Suchy Miro, Laine Janne, Kontturi Eero

机构信息

Department of Forest Products Technology, Helsinki University of Technology, P.O. Box 6300, FIN-02015 TKK, Finland.

出版信息

Biomacromolecules. 2009 May 11;10(5):1276-81. doi: 10.1021/bm900099e.

Abstract

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 degrees to 71 degrees 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 achieved. 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.

摘要

近年来,人们开发了多种在表面植入纳米尺寸图案的不同方法。旋涂互不相溶的二元聚合物共混物是在薄膜上制备微结构和纳米结构的一种直接方法。本研究利用二元共混物轻松制备出稳定的、表面功能化的纤维素薄膜。将三甲基硅烷基纤维素(TMSC)主相和聚苯乙烯(PS)次相在甲苯中的共混物旋涂成超薄膜,然后将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天平(QCM-D)对薄膜进行表征和定量分析。AFM显示,在旋涂过程中形成了水平相分离结构:TMSC水解为纤维素后,PS从纤维素中突出形成明显的斑块。这些斑块是盘状结构,具有圆形径向横截面,高度约为5-20纳米。原始旋涂溶液中PS的含量越少,薄膜中PS岛的尺寸越小。XPS测量结果支持了AFM的结果。当疏水性PS的相对含量从1:100增加到1:5时,PS/纤维素薄膜的水接触角从61度增加到71度。因此,通过简单地改变薄膜组分的比例,可以实现精细调整的疏水性能。通过QCM-D研究了薄膜在接触水时的溶胀情况。溶胀不受共混物中PS含量的影响,在纤维素含量相等的情况下,共混物薄膜和纯纤维素薄膜表现出相似的溶胀特性。此外,QCM-D评估表明,这些薄膜在较长时间内是稳定的,适合用QCM-D进行基础研究。

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