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Effects of absorbed moisture on high-performance organic fibers.

机译:吸收的水分对高性能有机纤维的影响。

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The problem addressed in this thesis is that of absorbed moisture in high-performance fibers. The goal is to determine what physical form absorbed moisture exists in as a function of environmental conditions and to obtain a better understanding of the physical state of absorbed moisture as a function of fiber chemical and physical structure. A number of different fiber systems were examined and include: three Kevlar fibers (Kevlar 29, 49, and 149), two aramid copolymer fibers (X-500 and Technora), two polybenzimidazole fibers (unmodified and sulfonated), and six poly(vinyl alcohol) fibers.; Thermogravimetric analysis studies provided information about: (1) the amount of absorbed moisture as a function of %RH, (2) the maximum rate moisture loss temperature, and (3) the weight fraction of an initial, quick moisture loss process. Nuclear magnetic resonance experiments as a function of %RH and temperature assessed chemical environment and/or mobility state differences among various fibers.; TGA measurements show that fiber chemical and physical structures have a significant effect on the amount of absorbed moisture associated with a given fiber. S-shaped moisture absorption profiles versus %RH are observed in all cases. Strong upturns in fiber moisture absorption at high %RH may be accounted for on the basis of transverse fiber swelling. NMR results suggest that water is present in an amorphous form. Mobility cessation temperatures are observed which correspond to the solidification of water into a glasslike state, but there is no evidence for ice formation in any of the fibers examined.; Factors controlling the physical structure of water in fibers are based on the potential for hydrogen bond interactions. These are directly related to fiber chemical structure and moisture accessibility to those sites. The most important parameter is accessibility to potential sites, which is controlled by fiber physical structure. Chemically related factors are evident at secondary levels.; Experimental results and model calculations suggest that water may exist in three potential states among the high-performance fibers evaluated. These include: (1) polymer-water hydrogen bond interactions, (2) water-water bridge structures between oriented, adjacent intermolecular sites or microfibrillar crystallite domains, and (3) water of hydration associated with ionic impurities.
机译:本论文解决的问题是高性能纤维中吸收水分的问题。目的是确定作为环境条件函数存在的吸收水分的物理形式,并更好地了解作为纤维化学和物理结构函数的吸收水分的物理状态。检查了许多不同的纤维系统,其中包括:三根凯夫拉纤维(凯夫拉尔29、49和149),两根芳族聚酰胺共聚物纤维(X-500和Technora),两根聚苯并咪唑纤维(未改性和磺化)和六种聚乙烯基酒精)纤维。热重分析研究提供了有关以下方面的信息:(1)所吸收水分的量与%RH的关系;(2)最大水分损失速率;以及(3)初始快速水分损失过程的重量分数。核磁共振实验是%RH和温度的函数,可评估各种纤维之间的化学环境和/或迁移率状态差异。 TGA测量表明,纤维的化学和物理结构对与给定纤维相关的吸收水分量有很大影响。在所有情况下均观察到S形吸湿曲线与%RH的关系。高纤维相对湿度下,纤维水分吸收的强烈上升可能是由于纤维横向膨胀引起的。 NMR结果表明水以无定形形式存在。观察到停止流动的温度对应于水固化成玻璃状的状态,但是没有证据表明在所检查的任何纤维中都形成冰。控制纤维中水的物理结构的因素是基于氢键相互作用的潜力。这些直接关系到纤维化学结构和湿气可及性。最重要的参数是对潜在站点的可访问性,这由光纤的物理结构控制。与化学有关的因素在中学阶段很明显。实验结果和模型计算表明,在所评估的高性能纤维中,水可能以三种潜在状态存在。这些包括:(1)聚合物-水氢键相互作用,(2)取向的相邻分子间位点或微原纤微晶畴之间的水-水桥结构,以及(3)与离子杂质相关的水合水。

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