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Voltage-Induced Sample Release from Anion Exchange Supports in Capillary Electrochromatography
https://nitech.repo.nii.ac.jp/records/4564
https://nitech.repo.nii.ac.jp/records/4564b7384e8b-d13a-4060-ab4c-5998ebd323ce
| 名前 / ファイル | ライセンス | アクション |
|---|---|---|
本文_fulltext (47.0 kB)
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1998 c The Japan Society for Analytical Chemistry
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| Item type | 学術雑誌論文 / Journal Article(1) | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| 公開日 | 2012-11-06 | |||||||||
| タイトル | ||||||||||
| タイトル | Voltage-Induced Sample Release from Anion Exchange Supports in Capillary Electrochromatography | |||||||||
| 言語 | en | |||||||||
| 言語 | ||||||||||
| 言語 | eng | |||||||||
| 資源タイプ | ||||||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||||||
| 資源タイプ | journal article | |||||||||
| 著者 |
Kitagawa, Shinya
× Kitagawa, Shinya
× Tsuda, Takao
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| 著者別名 | ||||||||||
| 姓名 | 北川, 慎也 | |||||||||
| 書誌情報 |
en : Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 巻 14, 号 3, p. 571-575, 発行日 1998-06 |
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| 出版者 | ||||||||||
| 出版者 | The Japan Society for Analytical Chemistry | |||||||||
| 言語 | en | |||||||||
| ISSN | ||||||||||
| 収録物識別子タイプ | ISSN | |||||||||
| 収録物識別子 | 0910-6340 | |||||||||
| item_10001_source_id_32 | ||||||||||
| 収録物識別子タイプ | NCID | |||||||||
| 収録物識別子 | AA10500785 | |||||||||
| 出版タイプ | ||||||||||
| 出版タイプ | VoR | |||||||||
| 出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||||||
| item_10001_relation_34 | ||||||||||
| 関連タイプ | isIdenticalTo | |||||||||
| 識別子タイプ | DOI | |||||||||
| 関連識別子 | http://dx.doi.org/10.2116/analsci.14.571 | |||||||||
| 関連名称 | 10.2116/analsci.14.571 | |||||||||
| 内容記述 | ||||||||||
| 内容記述タイプ | Other | |||||||||
| 内容記述 | An electric field application on ion exchange packing supports induced the release of sample solutes from the supports. When the electric field was applied temporary on the column, this phenomenon was observed as an increase in the pulsed concentration in the mobile phase. Namely a peak emerges on a chromatogram. The effect of the applied voltage on the ion exchange resin was examined by using a tiny mini-column. The sample solution was continuously passed through and the variations of effluent composition with and without application of electric field were analyzed. It was observed that amounts of increments of molar concentration of both benzoic acid and benzenesulfonic acid in mobile phase depended on the strength of the electric field. A theory of variation of distribution constant due to the electric field is proposed. | |||||||||
| 言語 | en | |||||||||
