LIMMS/CNRS-IIS UMI 2820, Institute of Industrial Science, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8505, Japan.
Anal Chem. 2012 Mar 6;84(5):2557-61. doi: 10.1021/ac3000804. Epub 2012 Feb 24.
The properties of fluid interfaces increase in importance as the physical scale decreases and, hence, characterization of surface tension becomes all the more critical. However, there is to date no method to characterize this parameter on microscale surfaces. We propose here a simple method based on the resonance of capillary waves, which are naturally excited by thermal fluctuations, under one-dimensional spatial restrictions using single-beam dynamic light scattering. The principle was verified at methanol/air interfaces in polydimethylsiloxane (PDMS) microchannels having various widths. Characteristic comb-shape power spectra were experimentally obtained. Theoretical analysis showed that the spectral peaks correspond to the first or higher modes of the capillary wave resonance in the restricted space between the parallel channel walls. A useful relation between successive modes was derived to eliminate the effects of damping at the soft PDMS walls. Thus, for methanol, two values were calculated from three successive modes (24.8 and 21.2 mN/m); the literature value is 22.02 mN/m. For acetonitrile, the value obtained was 28.2 ± 5 mN/m, close to the literature value of 28.6 mN/m. Although accuracy and precision require further elucidation, this novel method is expected to become a powerful tool at the micro/nanoscale.
随着物理尺度的减小,流体界面的性质变得越来越重要,因此表面张力的特性变得更加关键。然而,迄今为止,还没有一种方法可以在微尺度表面上描述这个参数。在这里,我们提出了一种基于毛细波共振的简单方法,该方法利用单光束动态光散射在一维空间限制下,通过热波动自然激发毛细波共振。该原理在具有不同宽度的聚二甲基硅氧烷(PDMS)微通道中的甲醇/空气界面上得到了验证。实验得到了特征梳状功率谱。理论分析表明,谱峰对应于平行通道壁之间受限空间中毛细波共振的第一或更高模式。推导出了连续模式之间的有用关系,以消除在软 PDMS 壁处的阻尼影响。因此,对于甲醇,从三个连续模式(24.8 和 21.2 mN/m)中计算出两个值;文献值为 22.02 mN/m。对于乙腈,得到的值为 28.2 ± 5 mN/m,接近文献值 28.6 mN/m。虽然准确性和精密度需要进一步阐明,但这种新方法有望成为微/纳米尺度的有力工具。