Electrokinetics in Salt-Free Non-aqueous Solution

碩士 === 國立中央大學 === 化學工程與材料工程研究所 === 98 === In general, the dissociation of counterion from charged particle is difficult in a medium with low dielectric constant due to strong Coulomb attraction. However, in electronic paper, charged particles exist in low dielectric medium and migrate by application...

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Main Authors: Wei-Sheng Yun, 雲惟勝
Other Authors: Heng-kwong Tsao
Format: Others
Language:zh-TW
Published: 2010
Online Access:http://ndltd.ncl.edu.tw/handle/53123748948791186407
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spelling ndltd-TW-098NCU050630182016-04-20T04:17:46Z http://ndltd.ncl.edu.tw/handle/53123748948791186407 Electrokinetics in Salt-Free Non-aqueous Solution 不含離子非水溶液之電動力學行為 Wei-Sheng Yun 雲惟勝 碩士 國立中央大學 化學工程與材料工程研究所 98 In general, the dissociation of counterion from charged particle is difficult in a medium with low dielectric constant due to strong Coulomb attraction. However, in electronic paper, charged particles exist in low dielectric medium and migrate by application of an electric filed, so called electrophoresis. In this work, the electrophoretic mobility and the origin of counterion dissociation from charged particle are investigated by using capillary electrophoresis system through electro-osmosis in a salt-free and low dielectric constant medium, in which the Joule heat effect is insignificant under strong electric field due to low electric current. Owing to strong Coulomb interaction, the surface charge density (?) of silica particles in a salt-free and low dielectric constant medium is very small compared to that in water. Therefore, the electrophoretic mobility is essentially zero. Intuitively, it is anticipated that the electro-osmotic flow (EOF) is absent in a fused silica capillary because of the lack of counterions. We consider organic solvents with low dielectric constant (?), including ethanol (? = 24), propanol (? = 20), butanol (? = 19), tetrahydrofuran (? = 7), and dioxane (? = 2), and their mixtures with water. The dielectric constant of the mixture can be controlled by tuning the concentrations (c). It is interesting to find that EOF always occurs regardless of the dielectric constant. The mobility generally declines with increasing viscosity or decreasing dielectric constant. The relationship between surface charge density and dielectric constant can be described by surface charge decsity ~ exp(-ac) ~ (dielectric constant)^b. In conclusion, even in a salt-free and low dielectric constant medium, counterion dissociation always takes place and thus electrokinetic phenomena occur, as long as particles’ sizes are large enough. An example is EOF, which involves a very large surface area of an inner tube wall. Consequently, in order to increase the response time in e-paper applications, the electrophoretic mobility can be increased by increasing the surface charge density or particle size. Heng-kwong Tsao 曹恒光 2010 學位論文 ; thesis 91 zh-TW
collection NDLTD
language zh-TW
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description 碩士 === 國立中央大學 === 化學工程與材料工程研究所 === 98 === In general, the dissociation of counterion from charged particle is difficult in a medium with low dielectric constant due to strong Coulomb attraction. However, in electronic paper, charged particles exist in low dielectric medium and migrate by application of an electric filed, so called electrophoresis. In this work, the electrophoretic mobility and the origin of counterion dissociation from charged particle are investigated by using capillary electrophoresis system through electro-osmosis in a salt-free and low dielectric constant medium, in which the Joule heat effect is insignificant under strong electric field due to low electric current. Owing to strong Coulomb interaction, the surface charge density (?) of silica particles in a salt-free and low dielectric constant medium is very small compared to that in water. Therefore, the electrophoretic mobility is essentially zero. Intuitively, it is anticipated that the electro-osmotic flow (EOF) is absent in a fused silica capillary because of the lack of counterions. We consider organic solvents with low dielectric constant (?), including ethanol (? = 24), propanol (? = 20), butanol (? = 19), tetrahydrofuran (? = 7), and dioxane (? = 2), and their mixtures with water. The dielectric constant of the mixture can be controlled by tuning the concentrations (c). It is interesting to find that EOF always occurs regardless of the dielectric constant. The mobility generally declines with increasing viscosity or decreasing dielectric constant. The relationship between surface charge density and dielectric constant can be described by surface charge decsity ~ exp(-ac) ~ (dielectric constant)^b. In conclusion, even in a salt-free and low dielectric constant medium, counterion dissociation always takes place and thus electrokinetic phenomena occur, as long as particles’ sizes are large enough. An example is EOF, which involves a very large surface area of an inner tube wall. Consequently, in order to increase the response time in e-paper applications, the electrophoretic mobility can be increased by increasing the surface charge density or particle size.
author2 Heng-kwong Tsao
author_facet Heng-kwong Tsao
Wei-Sheng Yun
雲惟勝
author Wei-Sheng Yun
雲惟勝
spellingShingle Wei-Sheng Yun
雲惟勝
Electrokinetics in Salt-Free Non-aqueous Solution
author_sort Wei-Sheng Yun
title Electrokinetics in Salt-Free Non-aqueous Solution
title_short Electrokinetics in Salt-Free Non-aqueous Solution
title_full Electrokinetics in Salt-Free Non-aqueous Solution
title_fullStr Electrokinetics in Salt-Free Non-aqueous Solution
title_full_unstemmed Electrokinetics in Salt-Free Non-aqueous Solution
title_sort electrokinetics in salt-free non-aqueous solution
publishDate 2010
url http://ndltd.ncl.edu.tw/handle/53123748948791186407
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