JPS5931442A - Electrolyte purification equipment - Google Patents
Electrolyte purification equipmentInfo
- Publication number
- JPS5931442A JPS5931442A JP57141527A JP14152782A JPS5931442A JP S5931442 A JPS5931442 A JP S5931442A JP 57141527 A JP57141527 A JP 57141527A JP 14152782 A JP14152782 A JP 14152782A JP S5931442 A JPS5931442 A JP S5931442A
- Authority
- JP
- Japan
- Prior art keywords
- liquid
- leading
- reservoir tank
- filled
- tank
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44704—Details; Accessories
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Electrolytic Production Of Metals (AREA)
Abstract
Description
【発明の詳細な説明】
この発明は電解液精製装置に関し、特に電気泳動分析で
用いるリーディング液又はターミナル液中の不純物イオ
ンを除去できる電解液精製装置に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an electrolyte purification device, and more particularly to an electrolyte purification device capable of removing impurity ions in a leading liquid or a terminal liquid used in electrophoretic analysis.
電気泳動に用いられるリーディング液又はターミナル液
番こは不純物イオンの混入する場合があり、この不純物
イオンが電気泳動分析に悪影響を与えることが多条あっ
た。特にリーディング液には、電極反応やゾーン境界面
の乱れを抑制、防止する等のため1こ、ヒドロキシエチ
ルセルロース、ヒドロキシプロピルメチルセルロース、
ヒドロキシ1ロピルセルロース、メチルセルロース、ポ
リビニルアルコール、ポリビニルピロリドン、トリトン
X−100(登録商標)などの粘性剤が添加されるが(
F.M.Everaerts他による論文”ISOTA
CHO−PHORESIS”1976年アメリカ、”J
ournal ofChromatagraphy
Library″vol4 p180〜181参照)
、これらの粘性剤は一般に純度が低(不純物イオンが混
入しやすいという問題があった。The leading liquid or terminal liquid used for electrophoresis may be contaminated with impurity ions, and these impurity ions often have an adverse effect on electrophoretic analysis. In particular, the leading liquid contains hydroxyethylcellulose, hydroxypropylmethylcellulose, etc. to suppress and prevent electrode reactions and zone boundary disturbances.
Viscous agents such as hydroxyl-lopylcellulose, methylcellulose, polyvinyl alcohol, polyvinylpyrrolidone, and Triton X-100 (registered trademark) are added (
F. M. The paper “ISOTA” by Everaerts et al.
CHO-PHORESIS” 1976 USA, “J
our own of chromatography
(Refer to Library"vol4 p180-181)
However, these viscous agents generally have low purity (there is a problem that impurity ions are easily mixed in).
この発明はこれらの事情に鑑みなされたもので、その具
体的な構成は、精製用電解液を充填するリザーバタンク
と、とのリザーバタンクにそれぞれ接続された2つの電
極槽とを備え、これらの両電極借問を通電することによ
って、リザーバタンクに充填される精製用電解液中の不
純物イオンを電気精製により除去できるよう構成してな
る電解液精製装置である。This invention was made in view of these circumstances, and its specific configuration includes a reservoir tank filled with a refining electrolyte, and two electrode tanks each connected to the reservoir tank. This is an electrolytic solution purification device configured so that impurity ions in a refining electrolytic solution filled in a reservoir tank can be removed by electrorefining by energizing both electrodes.
すなわち、この発明は情装用市解油を充填するリザーバ
タンクに電極槽を付設し、電気精製により電解液中の不
純物イオンを除去できるようにするものである。That is, in this invention, an electrode tank is attached to a reservoir tank that is filled with Ichika oil for use in the electrolytic solution, so that impurity ions in the electrolytic solution can be removed by electrorefining.
以下図に示し実施例に基づいてこの発明を詳述する。な
お、これによってこの発明が限定を受けるものではない
。The present invention will be described in detail below based on embodiments shown in the figures. Note that this invention is not limited by this.
第1図において、電解液精製装置(S)は、電気泳動装
置(E)に一体に組み込まれて構成され、リーディング
液にリザーバタンク(8)と、このリザーバタンクに中
継細管(10)(10′)を介して接続された電極槽(
9)(9)’と、これらの両電極槽に通電する直流電源
(11)とを備えている。なお、(12)(13)はリ
ーディング液リザーバタンク(8)に設置されたリーデ
ィング液導入・排出用開閉弁、(14)(14’)は電
極槽(9)(9’)にそれぞれ設置された導入用開閉弁
である。In FIG. 1, the electrolytic solution purification device (S) is configured to be integrated into the electrophoresis device (E), and includes a reservoir tank (8) for the leading liquid and a relay capillary tube (10) (10) for the reservoir tank. ’) connected through the electrode bath (
9) (9)', and a DC power supply (11) that supplies current to both of these electrode tanks. In addition, (12) and (13) are the opening/closing valves for leading liquid introduction and discharge installed in the leading liquid reservoir tank (8), and (14) and (14') are installed in the electrode tanks (9) and (9'), respectively. This is an on-off valve for introduction.
そこでリザーバタンク(8)には粘性剤を含むリーディ
ング液を充填し、中継細管(10)(10’)及び電極
槽(9)(9’)には先のリーディング液と同じ電解質
組戚で粘性剤だけを含まない液を充填する。つまりまず
導入用開閉弁(14)(14’)及び排出用開閉弁(1
3)を開放して粘性剤を含まないリーディング液を電極
槽(9)(9’)、中継細管(10)(10’)の全て
及びリザーバタンク(8)の少なくとも一部に充填する
。次いで導入用開閉弁(14)(14’)を閉じ、導入
用開閉弁(12)を開放してリザーバタンク(8)に粘
性剤を含むリーディング液を、先に充填されていた粘性
剤を含まないリーディング液を押出して充填する。Therefore, the reservoir tank (8) is filled with a leading liquid containing a viscous agent, and the relay tubes (10) (10') and electrode vessels (9) (9') are filled with the same electrolyte composition as the previous leading liquid. Fill with a liquid that does not contain only the agent. In other words, first the introduction on-off valve (14) (14') and the discharge on-off valve (1
3) is opened and a leading liquid containing no viscous agent is filled into all of the electrode vessels (9) (9'), the relay tubes (10) (10'), and at least a portion of the reservoir tank (8). Next, the introduction on-off valves (14) (14') are closed, and the introduction on-off valve (12) is opened to transfer the leading liquid containing the viscous agent to the reservoir tank (8). Fill by extruding the leading liquid.
このようにしてリーディング液リザーバタンク(8)に
粘性剤を含むリーディング液を、中継細管(10)(1
0’)及び両電極槽(9)(9’)に粘性剤を含まない
リーディング液をそれぞれ充填した後、直流電源(11
)より両電極槽(9)(9’)に通電することによって
リザーバタンク(8)内の粘性剤を含むリーディング液
中の不純物イオン(陰陽両イオン共)を電気精製により
除去できる。In this way, the leading liquid containing the viscous agent is transferred to the leading liquid reservoir tank (8).
After filling the leading liquid containing no viscous agent into the electrode chambers (9) and (9'), respectively, the DC power source (11
), impurity ions (both negative and positive ions) in the leading liquid containing the viscous agent in the reservoir tank (8) can be removed by electrical purification.
かくして精製されたリーディング液をリーディング電極
槽(2)及び泳動管(4)の試料導入部(5)までに充
填し、一方ターミナル液をターミナル液リザーバタンク
(7)からターミナル電極槽(3)及び試料導入部(5
)までの泳動管(4)に充填する。そして試料尋人部(
5)より試料を注入し両電極槽(2)(3)に高電圧電
流電源(1)より通電することによって、通常の等速電
気泳動分析かできる。この分析は、リーディング液にお
いて粘性剤と共に混入しやすい不純物イオンの影待が解
消され、粘性剤の機能(熱拡散、液の流れどによるゾー
ン境界面の乱れを防止)を十分利用して高精度に行うこ
とができる。また電気泳動分析装置(E)に電解液精製
装置(S)を一体に組み込んでいることにより、電気泳
動分析との一連の自動操作が可能になり、再汚染のおそ
れもない。The thus purified leading liquid is filled into the leading electrode tank (2) and the sample introduction part (5) of the migration tube (4), while the terminal liquid is filled from the terminal liquid reservoir tank (7) to the terminal electrode tank (3) and the sample introduction part (5) of the migration tube (4). Sample introduction part (5
) Fill the electrophoresis tube (4) up to (4). and the Sample Investigator Department (
5) By injecting the sample and applying electricity to both electrode vessels (2) and (3) from the high voltage current power source (1), normal isokinetic electrophoresis analysis can be performed. This analysis eliminates the influence of impurity ions that are likely to be mixed in with the viscous agent in the leading liquid, and takes full advantage of the viscous agent's function (preventing disturbance of the zone boundary surface due to thermal diffusion and liquid flow) to achieve high accuracy. can be done. Further, by integrating the electrolytic solution purification device (S) into the electrophoretic analysis device (E), a series of automatic operations with electrophoretic analysis becomes possible, and there is no risk of re-contamination.
もちろん夜間などの時間を利用して予め電解液の精製を
行なうことかできる。Of course, the electrolytic solution can be purified in advance using time such as nighttime.
なお、以上の構成の電解液精製装置はターミナル液リザ
ーバタンク側にも設置することかできる。Note that the electrolyte purification device having the above configuration can also be installed on the terminal liquid reservoir tank side.
また精製用電解液リ−プインク液にマグネチック・スタ
ーラーのごとき撹拌機能を持ったものを設置してもよい
。もちろん第1図の直流電源(11)と高車圧室電流電
源(1)とを共通に用いることもできる。更に上記電解
液精製装置(S)の各開閉弁の設置位置は、第2図の如
く変えることもできる。つまり排出用開閉弁をリーディ
ング液リザーバタンク(8a)ではなく電極槽(9a)
(9’a)に設置し、これによってまず導入開閉弁(1
2a)及び排出用開閉弁(15a)(15’a)を開放
し粘性剤を含むリーディング液をリーディング液リザー
バタンク(8a)及び中継細管(10a)(10’a)
、並びに電極槽(9a)(9’a)の少なくとも1部に
充蒋する。次いで導入用開閉弁(12a)を閉じ、導入
用開閉弁(14a)(14’a)を開放して、先に充填
された粘性剤を含むリーディング液を押出しながら粘性
剤を含まないリーデインク液を両電極槽(9a)(9’
a)に充填することもできる。Further, a device having a stirring function such as a magnetic stirrer may be installed in the purification electrolyte leap ink liquid. Of course, the DC power source (11) and the high vehicle pressure room current power source (1) shown in FIG. 1 can also be used in common. Furthermore, the installation positions of the on-off valves of the electrolyte purifier (S) can be changed as shown in FIG. 2. In other words, the discharge on-off valve is connected to the electrode tank (9a) instead of the leading liquid reservoir tank (8a).
(9'a).
2a) and discharge on/off valves (15a) (15'a) are opened and the leading liquid containing the viscous agent is transferred to the leading liquid reservoir tank (8a) and the relay capillary (10a) (10'a).
, and at least a portion of the electrode baths (9a) (9'a). Next, the introduction on-off valve (12a) is closed, the introduction on-off valves (14a) (14'a) are opened, and while the previously filled leading liquid containing the viscous agent is pushed out, the lead ink liquid that does not contain the viscous agent is extruded. Both electrode tanks (9a) (9'
a) can also be filled.
以下の実施例で挙げた中継細管(10)(10’)又は
(10a)(10’a)は、中継される両槽の液が混り
合わなければ、フィルタ、開閉弁などに代えることもで
きる。The relay thin tubes (10) (10') or (10a) (10'a) mentioned in the following examples may be replaced with filters, on-off valves, etc. if the liquids in both tanks to be relayed do not mix. can.
ここで参考までに第1図の電解液精製装置(S)で電気
精製したリーディング液を用いて同じく電気泳動装置(
E)で行った電気泳動分析結果を示す。Here, for reference, we used the same electrophoresis device (
The results of the electrophoretic analysis performed in E) are shown.
(イ) 装置(E)
見本細管式等速電気泳動分析装置[IP−2A](電位
勾配検出器付)
リーディング液: 0.01モル塩酸と0.02モルア
メジオール
ターミナル液:0.01モルβ−アラニンと水酸化バリ
ウム(pH10.9)
泳動管:内径1.0mmφ、長さ40mmと内径0.5
mmφ、長さ150mm
との連結管
泳動電流:200μA(6分)から100μAに切換
(ロ)装置(S)
装置(E)に付設されたリーディング液リザーバタンク
に、内径1.0mmφの中継細管を介してリーディング
電極槽と同じ寸法仕様の電極槽を接続した。(B) Apparatus (E) Sample capillary type isotachophoresis analyzer [IP-2A] (with potential gradient detector) Leading liquid: 0.01 mol Hydrochloric acid and 0.02 mol Amediol Terminal liquid: 0.01 mol β-alanine and barium hydroxide (pH 10.9) Electrophoresis tube: inner diameter 1.0 mmφ, length 40 mm, inner diameter 0.5
mmφ, length 150mm Transfer current: Switch from 200 μA (6 minutes) to 100 μA (B) Device (S) Connect a relay capillary tube with an inner diameter of 1.0 mmφ to the leading liquid reservoir tank attached to the device (E). An electrode tank with the same dimensions as the leading electrode tank was connected through the lead electrode tank.
(ハ) 実験結果(第3図参照)
A:粘性剤の一種であるPVA(ポリビニルアルコール
ンの0.2%水溶液100μlの等速電気泳動分析デー
タ。(c) Experimental results (see Figure 3) A: Isokinetic electrophoresis analysis data of 100 μl of a 0.2% aqueous solution of PVA (polyvinyl alcoholone), which is a type of viscosity agent.
B:電気的に精製したリーディング液50μlを試料と
してAと同じ条件で分析したデータ。B: Data analyzed under the same conditions as A using 50 μl of electrically purified reading liquid as a sample.
尚、Bで検出されているゾーンは電解液(試薬。The zone detected in B is the electrolyte (reagent).
溶媒、溶存二酸化炭素由来)の不純物で粘性剤由来のも
のでない。Bでは、Aで検出されている■、■、■及び
■の不純物ゾーンが消え、電気泳動によりイオン性不純
物が効果的に除去されることを示している。impurities derived from solvents and dissolved carbon dioxide) and not from viscous agents. In B, the impurity zones ■, ■, ■, and ■ detected in A disappear, indicating that ionic impurities are effectively removed by electrophoresis.
第1図はこの発明に係る電解溶液精製装置の一実施例を
示す機能説明図、第2図は他の実施例を示す要部機能説
明図、第3図は第1図の装置を用いた実験結果を示すグ
ラフである。
(S)・・・電解溶液精製装置、
(8)・・・リーディング液リザーバタンク、(9)(
9’)・・・電極槽、(10)(10’)・・・中継細
管、(11)・・直流電源。
代理人 弁理士 野河信太部Fig. 1 is a functional explanatory diagram showing one embodiment of the electrolytic solution purification device according to the present invention, Fig. 2 is a functional explanatory diagram of main parts showing another embodiment, and Fig. 3 is a functional explanatory diagram showing an embodiment of the electrolytic solution purification device according to the present invention. It is a graph showing experimental results. (S)... Electrolyte solution purification device, (8)... Leading liquid reservoir tank, (9) (
9')... Electrode tank, (10) (10')... Relay tube, (11)... DC power supply. Agent Patent Attorney Shintabu Nogawa
Claims (1)
ザーバタンクにそれぞれ接続された2つの電極槽とを備
え、これらの両電極借問を通電することによって、リザ
ーバタンクに充填される精製用電解液中の不純物イオン
を電気精製により除去できるよう構成してなる電解液精
製装置。1. Equipped with a reservoir tank filled with a purification electrolyte and two electrode tanks each connected to this reservoir tank, and by energizing both electrodes, the purification electrolyte is filled into the reservoir tank. An electrolytic solution purification device configured to remove impurity ions therein through electrical purification.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57141527A JPS5931442A (en) | 1982-08-13 | 1982-08-13 | Electrolyte purification equipment |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57141527A JPS5931442A (en) | 1982-08-13 | 1982-08-13 | Electrolyte purification equipment |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5931442A true JPS5931442A (en) | 1984-02-20 |
Family
ID=15294038
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57141527A Pending JPS5931442A (en) | 1982-08-13 | 1982-08-13 | Electrolyte purification equipment |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5931442A (en) |
-
1982
- 1982-08-13 JP JP57141527A patent/JPS5931442A/en active Pending
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