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通过声速测量估算有机链长度。

Estimating organic chain length through sound velocity measurements.

作者信息

Povey Malcolm J W, Stec Zoe, Hindle Scott A, Kennedy John D, Taylor Richard G

机构信息

University of Leeds, Procter Department of Food Science, Leeds, LS29 JT, UK.

出版信息

Ultrasonics. 2005 Feb;43(4):219-26. doi: 10.1016/j.ultras.2004.06.011.

Abstract

The ability to measure the length of polymers while monitoring their production is evidently extremely valuable, but is also a useful tool for chemical identification purposes at other times, e.g. the analysis of waste water. A study of the relationship between velocity of sound and chain length has been carried out. Initial studies were performed on two model systems; a series of pure liquid n-alkanes (pentane to hexadecane) and 1-alcohols (methanol to 1-dodecanol). This study was extended to look at an industrially significant system of dimethylsiloxanes 200 fluid (L2, 0.65 cSt) to 200 fluid (5000 cSt). Corresponding density data have been taken from the literature and the adiabatic compressibility determined. The measured adiabatic compressibility has been compared with two molecular models of wound velocity, the Schaaffs model and a development of the Urick equation. The Urick equation approach is based on a determination of the compressibility of the methylene or siloxane repeat units which make up the chains in these linear molecules. We show that the Urick equation approach accurately predicts sound velocity and compressibility for the higher members of each series, whilst the Schaaffs approach fails for the 1-alcohols. We suggest that this is because of the influence of the hydroxyl end group through hydrogen bonding with methylene groups within the chain. This interaction modifies the derived compressibility of the methylene groups, so reducing their compressibility relative to that of the n-alkanes. The technique described provides valuable new insights into end-group, intermolecular and intra-molecular interactions in liquid linear-chain molecules. From this detailed analysis of the mechanisms involved, a model is derived. This model can give very precise estimations of the composition of a pure liquid. In the case of mixtures of polymers, it is necessary to use the modified Urick equation and then, in addition, the concentration dependence of both the velocity of sound and the density must be measured.

摘要

在监测聚合物生产过程中测量其长度的能力显然极具价值,而且在其他时候,例如在废水分析中,也是用于化学鉴定的有用工具。已经开展了一项关于声速与链长之间关系的研究。最初的研究是在两个模型系统上进行的;一系列纯液态正构烷烃(戊烷至十六烷)和一元醇(甲醇至十二醇)。这项研究扩展到考察具有工业意义的二甲基硅氧烷系统,从200流体(0.65厘沲)到200流体(5000厘沲)。相应的密度数据取自文献并测定了绝热压缩率。将测得的绝热压缩率与两个声速分子模型进行了比较,即沙夫斯模型和对乌里克方程的改进。乌里克方程方法基于对构成这些线性分子链的亚甲基或硅氧烷重复单元的压缩率的测定。我们表明,乌里克方程方法能准确预测每个系列中较高成员的声速和压缩率,而沙夫斯方法对一元醇不适用。我们认为这是由于羟基端基通过与链内亚甲基形成氢键而产生的影响。这种相互作用改变了推导出的亚甲基的压缩率,从而相对于正构烷烃降低了它们的压缩率。所描述的技术为液态线性链分子中的端基、分子间和分子内相互作用提供了有价值的新见解。通过对所涉及机制的详细分析,得出了一个模型。该模型可以非常精确地估计纯液体的组成。对于聚合物混合物的情况,有必要使用改进的乌里克方程,此外,还必须测量声速和密度的浓度依赖性。

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