{"title":"修正Onsager-Kirkwood-Fröhlich理论对水介电特性的理论研究","authors":"D. Putintsev, N. M. Putintsev","doi":"10.1109/ICDL.2019.8796591","DOIUrl":null,"url":null,"abstract":"In the work, we present the new method for calculation dielectric properties for Water in the wide temperature range. We use the modified Onsager-Kirkwood-Fröhlich theory, which makes it possible to calculate the polarization characteristics without using the static permittivity. We assumed that the dielectric is an isotropic medium consisting of molecules that do not interact with each other and are located in molecular electric fields. It allows us to use the average cosine of the angle between local electric field vectors and the dipole moment vectors of molecules in a medium as the average measure of the local orientation of the dipoles. This approach also makes it possible to equate the value of the energy of the interaction of dipoles with molecular fields to the value of the internal interaction energy if the energy of the interaction of the dipoles with external fields used for the experimental determination of the value of static permittivity is much less than the energy of the interaction. The calculated values of the dipole moment agree with the modern quantum mechanical calculations, and the results of calculating the values of permittivity are in practical agreement with experiment in the wide range of123.15K-573.15K. The method allows to calculate the static permittivity of water in various aggregate states: ice Ih in the range from 123K to melting point, supercooled water in the range from 238K to melting point, water at the saturation line from the melting point to the precritical region.","PeriodicalId":102217,"journal":{"name":"2019 IEEE 20th International Conference on Dielectric Liquids (ICDL)","volume":"19 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The theoretical study of dielectric properties of water using the modified Onsager-Kirkwood-Fröhlich theory\",\"authors\":\"D. Putintsev, N. M. Putintsev\",\"doi\":\"10.1109/ICDL.2019.8796591\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In the work, we present the new method for calculation dielectric properties for Water in the wide temperature range. We use the modified Onsager-Kirkwood-Fröhlich theory, which makes it possible to calculate the polarization characteristics without using the static permittivity. We assumed that the dielectric is an isotropic medium consisting of molecules that do not interact with each other and are located in molecular electric fields. It allows us to use the average cosine of the angle between local electric field vectors and the dipole moment vectors of molecules in a medium as the average measure of the local orientation of the dipoles. This approach also makes it possible to equate the value of the energy of the interaction of dipoles with molecular fields to the value of the internal interaction energy if the energy of the interaction of the dipoles with external fields used for the experimental determination of the value of static permittivity is much less than the energy of the interaction. The calculated values of the dipole moment agree with the modern quantum mechanical calculations, and the results of calculating the values of permittivity are in practical agreement with experiment in the wide range of123.15K-573.15K. The method allows to calculate the static permittivity of water in various aggregate states: ice Ih in the range from 123K to melting point, supercooled water in the range from 238K to melting point, water at the saturation line from the melting point to the precritical region.\",\"PeriodicalId\":102217,\"journal\":{\"name\":\"2019 IEEE 20th International Conference on Dielectric Liquids (ICDL)\",\"volume\":\"19 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2019 IEEE 20th International Conference on Dielectric Liquids (ICDL)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ICDL.2019.8796591\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2019 IEEE 20th International Conference on Dielectric Liquids (ICDL)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICDL.2019.8796591","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
在工作中,我们提出了计算水在宽温度范围内介电特性的新方法。我们使用了修正的Onsager-Kirkwood-Fröhlich理论,使得在不使用静态介电常数的情况下计算极化特性成为可能。我们假设电介质是一种各向同性介质,由互不相互作用的分子组成,并且位于分子电场中。它允许我们使用局部电场矢量和介质中分子偶极矩矢量之间夹角的平均余弦值作为偶极子局部取向的平均度量。如果用于测定静态介电常数值的实验用的偶极子与外场的相互作用的能量远小于相互作用的能量,那么这种方法也使偶极子与分子场相互作用的能量等于内部相互作用能的值成为可能。偶极矩的计算值与现代量子力学计算结果一致,介电常数的计算结果在123.15 k -573.15 k范围内与实验结果基本一致。该方法可以计算水在各种聚集状态下的静态介电常数:冰Ih在123K到熔点范围内,过冷水在238K到熔点范围内,水在熔点到临界区域的饱和线上。
The theoretical study of dielectric properties of water using the modified Onsager-Kirkwood-Fröhlich theory
In the work, we present the new method for calculation dielectric properties for Water in the wide temperature range. We use the modified Onsager-Kirkwood-Fröhlich theory, which makes it possible to calculate the polarization characteristics without using the static permittivity. We assumed that the dielectric is an isotropic medium consisting of molecules that do not interact with each other and are located in molecular electric fields. It allows us to use the average cosine of the angle between local electric field vectors and the dipole moment vectors of molecules in a medium as the average measure of the local orientation of the dipoles. This approach also makes it possible to equate the value of the energy of the interaction of dipoles with molecular fields to the value of the internal interaction energy if the energy of the interaction of the dipoles with external fields used for the experimental determination of the value of static permittivity is much less than the energy of the interaction. The calculated values of the dipole moment agree with the modern quantum mechanical calculations, and the results of calculating the values of permittivity are in practical agreement with experiment in the wide range of123.15K-573.15K. The method allows to calculate the static permittivity of water in various aggregate states: ice Ih in the range from 123K to melting point, supercooled water in the range from 238K to melting point, water at the saturation line from the melting point to the precritical region.