高分子体系中的菲克式和非菲克式扩散

G. Rehage, O. Ernst, J. Fuhrmann
{"title":"高分子体系中的菲克式和非菲克式扩散","authors":"G. Rehage, O. Ernst, J. Fuhrmann","doi":"10.1039/DF9704900208","DOIUrl":null,"url":null,"abstract":"The normal and the anomalous diffusion in binary polymer solutions are considered. After a survey of the theory of diffusion it is demonstrated which criteria must be fulfilled so that the Fickian diffusion occurs. For transport between the solvent and a solution, or between two solutions, normal diffusion is found. Experimental results with polystyrene + solvent systems are given. With good solvents the diffusion coefficient increases strongly with increasing polymer concentration, passes through a maximum at medium concentrations and decreases by several decades at high polymer concentrations. This concentration dependence arises because the diffusion coefficient is not only a transport coefficient, but also contains a thermodynamic factor. With poor solvents, which show a phase separation of the polymer at low temperatures, the concentration dependence of the diffusion coefficient is even more complicated. With increasing concentration of polymer the diffusion coefficient first decreases, passes through a minimum and the increases again. In this case there is also a maximum at medium concentrations and a strong decrease at high polymer concentrations. The minimum for a binary system is located at the critical point of the system.Normally ln D is a linear function of 1/T. Deviations from the linear course can be explained by the temperature dependence of the thermodynamic factor.For anomalous diffusion the √t-relations are no longer valid, since the diffusion coefficient depends not only on concentration, but also explicitly on time. The anomalous diffusion is due to the fact that superimposed on the normal diffusion is another process. If a solvent penetrates into a glassy polymer, then relaxation processes are superimposed on the diffusion process. The polymer changes from the glassy state into a state of internal thermodynamic equilibrium. Experimentally the continuous range between the pure glassy polymer and the pure solvent can be divided into three parts of an open system. In the first and the third part only diffusion occurs, while in the second part diffusion and structural relaxation are superimposed.","PeriodicalId":11262,"journal":{"name":"Discussions of The Faraday Society","volume":"42 1","pages":"208-221"},"PeriodicalIF":0.0000,"publicationDate":"1970-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"59","resultStr":"{\"title\":\"Fickian and non-Fickian diffusion in high polymer systems\",\"authors\":\"G. Rehage, O. Ernst, J. Fuhrmann\",\"doi\":\"10.1039/DF9704900208\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The normal and the anomalous diffusion in binary polymer solutions are considered. After a survey of the theory of diffusion it is demonstrated which criteria must be fulfilled so that the Fickian diffusion occurs. For transport between the solvent and a solution, or between two solutions, normal diffusion is found. Experimental results with polystyrene + solvent systems are given. With good solvents the diffusion coefficient increases strongly with increasing polymer concentration, passes through a maximum at medium concentrations and decreases by several decades at high polymer concentrations. This concentration dependence arises because the diffusion coefficient is not only a transport coefficient, but also contains a thermodynamic factor. With poor solvents, which show a phase separation of the polymer at low temperatures, the concentration dependence of the diffusion coefficient is even more complicated. With increasing concentration of polymer the diffusion coefficient first decreases, passes through a minimum and the increases again. In this case there is also a maximum at medium concentrations and a strong decrease at high polymer concentrations. The minimum for a binary system is located at the critical point of the system.Normally ln D is a linear function of 1/T. Deviations from the linear course can be explained by the temperature dependence of the thermodynamic factor.For anomalous diffusion the √t-relations are no longer valid, since the diffusion coefficient depends not only on concentration, but also explicitly on time. The anomalous diffusion is due to the fact that superimposed on the normal diffusion is another process. If a solvent penetrates into a glassy polymer, then relaxation processes are superimposed on the diffusion process. The polymer changes from the glassy state into a state of internal thermodynamic equilibrium. Experimentally the continuous range between the pure glassy polymer and the pure solvent can be divided into three parts of an open system. In the first and the third part only diffusion occurs, while in the second part diffusion and structural relaxation are superimposed.\",\"PeriodicalId\":11262,\"journal\":{\"name\":\"Discussions of The Faraday Society\",\"volume\":\"42 1\",\"pages\":\"208-221\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1970-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"59\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Discussions of The Faraday Society\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/DF9704900208\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Discussions of The Faraday Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/DF9704900208","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 59

摘要

研究了二元聚合物溶液中的正常扩散和异常扩散。在对扩散理论进行综述之后,论证了必须满足哪些条件才能发生菲克式扩散。对于溶剂和溶液之间或两个溶液之间的传输,发现正常扩散。给出了聚苯乙烯+溶剂体系的实验结果。在良好的溶剂中,扩散系数随着聚合物浓度的增加而强烈增加,在中等浓度时达到最大值,在高浓度时减小几十年。这种浓度依赖性的产生是因为扩散系数不仅是一个输运系数,而且还包含一个热力学因素。在较差的溶剂条件下,聚合物在低温下表现为相分离,扩散系数的浓度依赖关系更加复杂。随着聚合物浓度的增加,扩散系数先减小,经过最小值后又增大。在这种情况下,在中等浓度下也有一个最大值,在高聚合物浓度下有一个强烈的下降。二元系统的最小值位于系统的临界点。通常ln D是1/T的线性函数。偏离线性过程可以用热力学因素对温度的依赖性来解释。对于反常扩散,√t关系不再有效,因为扩散系数不仅取决于浓度,而且明确地取决于时间。反常扩散是由于在正常扩散上叠加了另一个过程。如果溶剂渗透到玻璃聚合物中,那么弛豫过程就会叠加在扩散过程上。聚合物由玻璃态变为内部热力学平衡态。在实验中,纯玻璃聚合物和纯溶剂之间的连续范围可以分为三个部分的开放体系。在第一部分和第三部分中只发生扩散,而在第二部分中扩散和结构弛豫是叠加的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fickian and non-Fickian diffusion in high polymer systems
The normal and the anomalous diffusion in binary polymer solutions are considered. After a survey of the theory of diffusion it is demonstrated which criteria must be fulfilled so that the Fickian diffusion occurs. For transport between the solvent and a solution, or between two solutions, normal diffusion is found. Experimental results with polystyrene + solvent systems are given. With good solvents the diffusion coefficient increases strongly with increasing polymer concentration, passes through a maximum at medium concentrations and decreases by several decades at high polymer concentrations. This concentration dependence arises because the diffusion coefficient is not only a transport coefficient, but also contains a thermodynamic factor. With poor solvents, which show a phase separation of the polymer at low temperatures, the concentration dependence of the diffusion coefficient is even more complicated. With increasing concentration of polymer the diffusion coefficient first decreases, passes through a minimum and the increases again. In this case there is also a maximum at medium concentrations and a strong decrease at high polymer concentrations. The minimum for a binary system is located at the critical point of the system.Normally ln D is a linear function of 1/T. Deviations from the linear course can be explained by the temperature dependence of the thermodynamic factor.For anomalous diffusion the √t-relations are no longer valid, since the diffusion coefficient depends not only on concentration, but also explicitly on time. The anomalous diffusion is due to the fact that superimposed on the normal diffusion is another process. If a solvent penetrates into a glassy polymer, then relaxation processes are superimposed on the diffusion process. The polymer changes from the glassy state into a state of internal thermodynamic equilibrium. Experimentally the continuous range between the pure glassy polymer and the pure solvent can be divided into three parts of an open system. In the first and the third part only diffusion occurs, while in the second part diffusion and structural relaxation are superimposed.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信