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首页> 外文期刊>Colloids and Surfaces, A. Physicochemical and Engineering Aspects >Watching cellulose grow - Kinetic investigations on cellulose thin film formation at the gas-solid interface using a quartz crystal microbalance with dissipation (QCM-D)
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Watching cellulose grow - Kinetic investigations on cellulose thin film formation at the gas-solid interface using a quartz crystal microbalance with dissipation (QCM-D)

机译:观察纤维素的生长-使用带耗散的石英晶体微量天平(QCM-D)在气固界面处形成纤维素薄膜的动力学研究

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摘要

The conversion of trimethylsilyl cellulose (TMSC) to cellulose films via acid vapor hydrolysis is investigated at the gas solid interface in situ, in real time and under ambient conditions using the QCM-D technique. For this purpose, a permanent flow of gaseous HCl is employed which reacts with TMSC spun on QCM sensors to form cellulose films. The kinetics behind this reaction is elucidated and reveals first order. This desilylation reaction proceeds via a fast first phase (k=3.01×10 ~(-3)s ~(-1)) and a second slower phase (k=6.29×10 ~(-5)s ~(-1)) where less accessible silyl groups are cleaved off. Besides kinetics, film thicknesses have been determined using the QCM method. Moreover, the influence of the acid concentration on the kinetics and layer thickness was studied. A comparison between the materials synthesized in the QCM chamber with those obtained by classical vapor phase hydrolysis does not show any differences in the surface characteristics and composition as proven by X-ray photoelectron spectroscopy, atomic force microscopy, and wettability studies.
机译:使用QCM-D技术,在气体固相界面上实时,实时地在环境条件下研究了三甲基硅烷基纤维素(TMSC)通过酸蒸汽水解向纤维素膜的转化。为此,使用了永久性的气态HCl,它与在QCM传感器上旋转的TMSC反应形成纤维素膜。阐明了该反应背后的动力学并揭示了一级反应。该去甲硅烷基化反应通过快速的第一阶段(k = 3.01×10〜(-3)s〜(-1))和第二较慢的阶段(k = 6.29×10〜(-5)s〜(-1))进行。其中较难获得的甲硅烷基被裂解掉。除了动力学以外,还使用QCM方法确定了膜厚度。此外,研究了酸浓度对动力学和层厚度的影响。通过X射线光电子能谱,原子力显微镜和润湿性研究证明,在QCM室中合成的材料与通过经典气相水解获得的材料之间没有任何表面特性和组成差异。

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