JPS6031829A - High purity refining method of aqueous non-electrolytic organic substance solution - Google Patents

High purity refining method of aqueous non-electrolytic organic substance solution

Info

Publication number
JPS6031829A
JPS6031829A JP58140512A JP14051283A JPS6031829A JP S6031829 A JPS6031829 A JP S6031829A JP 58140512 A JP58140512 A JP 58140512A JP 14051283 A JP14051283 A JP 14051283A JP S6031829 A JPS6031829 A JP S6031829A
Authority
JP
Japan
Prior art keywords
exchange resin
resin
basic anion
anion exchange
free base
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.)
Granted
Application number
JP58140512A
Other languages
Japanese (ja)
Other versions
JPH0426840B2 (en
Inventor
Akira Matsumoto
明 松本
Masayuki Morohashi
諸橋 正行
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Chemical Japan Ltd
Original Assignee
Dow Chemical Japan Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dow Chemical Japan Ltd filed Critical Dow Chemical Japan Ltd
Priority to JP58140512A priority Critical patent/JPS6031829A/en
Publication of JPS6031829A publication Critical patent/JPS6031829A/en
Publication of JPH0426840B2 publication Critical patent/JPH0426840B2/ja
Granted legal-status Critical Current

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  • Seasonings (AREA)
  • Treatment Of Water By Ion Exchange (AREA)

Abstract

PURPOSE:To refine the title aqueous solution to high purity, by providing dimethylhydroxyethyl-benzylammonium to a free base type weak basic ion exchange resin. CONSTITUTION:A layer comprising a free base type weak basic anion exchange resin, to which 5-50vol% of dimethylhydroxyethyl-benzylammonium is provided as an ion exchange group, is formed as an upper layer part and a layer comprising a hydroxyl type strong basic anion exchange resin having a porous resin matrix structure is formed as a lower layer part to form a resin bed. Subsequently, an aqueous non-electrolytic org. substance solution after cation removing treatment is passed through said resin bed.

Description

【発明の詳細な説明】 技術分野 本発明は、非電解有機質水溶液の高純度精製方法に関す
る。
DETAILED DESCRIPTION OF THE INVENTION Technical Field The present invention relates to a method for purifying a non-electrolytic organic aqueous solution to high purity.

従来技術 ブドウ糖、異性化糖、水飴、ンルビトール、キシロース
、イノシトール、マルトース、 せ蔗糖、ハチミツ、グ
リオキザール、グリセリン、ゼラチンなどの非電解有機
質の水溶液の水溶液には、不純物として色素、塩類、有
機酸類などが含有されておシ、これら水溶液の精製には
骨炭、活性炭々どの吸着剤が使用されるとともに、イオ
ン交換樹脂も盛んに使用されている。これらの水溶液の
精製に広く用いられている従来のイオン交換方式として
は、先ず水素型強酸性陽イオン交換樹脂の単独樹脂塔で
、次いで遊離塩基型弱塩基性陰イオン交換樹脂の単独樹
脂塔で、そして更に水素型強酸性陽イオン交換樹脂と水
酸基型強塩基性陰イオン交換樹脂との混床樹脂塔で順次
に処理することによって脱色脱塩精製するものがある。
Conventional technology Aqueous solutions of non-electrolytic organic substances such as glucose, high fructose sugar, starch syrup, nlubitol, xylose, inositol, maltose, sucrose, honey, glyoxal, glycerin, and gelatin contain impurities such as pigments, salts, and organic acids. In order to purify these aqueous solutions, adsorbents such as bone char and activated carbon are used, and ion exchange resins are also widely used. The conventional ion exchange method widely used for the purification of these aqueous solutions is to first use a single resin column of a hydrogen-type strongly acidic cation exchange resin, and then to use a single resin column of a free base-type weakly basic anion exchange resin. There are also products that undergo decolorization and desalination purification by sequential treatment in a mixed bed resin column containing a hydrogen type strongly acidic cation exchange resin and a hydroxyl group type strongly basic anion exchange resin.

しかし、この方法では、イオン交換樹脂を通過後の液が
、時間の経過とともに−の低下を生じたシ、加熱濃縮に
際して漸次着色したシする等の問題があり、そのため製
品の品質が低下し、生産性が悪化することが多かった。
However, with this method, there are problems such as the liquid after passing through the ion exchange resin decreasing in - value over time and gradually becoming colored during heating and concentration, resulting in a decrease in product quality. Productivity often deteriorated.

発明の目的 本発明の目的は、非電解有機質水溶液をイオン交換樹脂
を用いて高純匪にF#製することができ、高品質の処理
製品を提供することのできる方法を提供することにある
OBJECTS OF THE INVENTION An object of the present invention is to provide a method that can produce high-purity F# from a non-electrolyzed organic aqueous solution using an ion exchange resin and provide a high-quality treated product. .

発明の構成 本発明は即ち非電解有機質水溶液の高純度精製方法を提
供するものであって、この方法は、非電解有機質水溶液
t1水素型強酸性陽イオン交換樹脂で脱カチオン処理し
た後、遊離塩基型弱塩基性陰イオン交換樹脂を上層部に
充填し、そしてこの遊離塩基型弱塩基性陰イオン交換樹
脂に対して5〜5(ljj%の、ジメチルハイドロキシ
エチルベンジルアンモニウムを交換基としかつ多孔質の
樹脂母体構造を有する。水酸基型強塩基性陰イオン交換
樹脂ケ下層部に充填したカラムを通過せしめることを含
んでなる。
Components of the Invention The present invention provides a method for purifying a non-electrolytic organic aqueous solution to high purity, and this method comprises decationizing the non-electrolytic organic aqueous solution t1 with a hydrogen-type strongly acidic cation exchange resin, and then converting the free base into A type of weakly basic anion exchange resin is filled in the upper layer, and a porous resin containing 5 to 5% (ljj%) of dimethyl hydroxyethylbenzyl ammonium as an exchange group to the free base type weakly basic anion exchange resin is used. It has a resin matrix structure of: hydroxyl group-type strongly basic anion exchange resin and is passed through a column packed in the lower layer.

本発明者らは、種々の非電解有機質水溶液の精製方法に
ついて鋭意研究した結果、水素型強酸性陽イオン交換樹
脂で脱カチオン処理後の非電解有機質水溶液を、遊離塩
基型弱塩基性陰イオン交換樹脂にジメチルハイドロキシ
エチルベンジルアンモニウムをイオン交換基として有し
かつ多孔質の樹脂母体構造を有する水酸基型強塩基性陰
イオン交換樹脂5〜50容量チ、を層状に添加したカラ
ムを通過せしめることにより、極めて優れた脱塩効果が
得られることを見出し、本発明に到達したものである。
As a result of intensive research into purification methods for various non-electrolytic organic aqueous solutions, the present inventors have discovered that a non-electrolytic aqueous solution that has been decationized using a hydrogen-type strongly acidic cation exchange resin can be purified using a free base-type weakly basic anion exchange resin. By passing through a column in which 5 to 50 volumes of a hydroxyl group-type strongly basic anion exchange resin having dimethyl hydroxyethylbenzylammonium as an ion exchange group and a porous resin matrix structure is added to the resin in a layered manner, The present invention was achieved based on the discovery that an extremely excellent desalting effect can be obtained.

上記遊離塩基型弱塩基性陰イオン交換樹脂と水酸基型強
塩基性陰イオン交換樹脂とは、両者の比重差を利用して
、後者が前者の下部に層状に充填された状態のカラムを
形成するのが好ましい。本発明の方法によれば、従来の
弱塩基性陰イオン交換樹脂では容易に除去することがで
きなかった非電解有機質水溶液中の不純物をイオン交換
によ如有効に除去することができるため、前述の如き問
題を生ずることなく、理想的な脱塩精製ができる。
The free base-type weakly basic anion exchange resin and the hydroxyl group-type strongly basic anion exchange resin utilize the difference in specific gravity between the two to form a column in which the latter is packed under the former in a layered manner. is preferable. According to the method of the present invention, impurities in a non-electrolytic organic aqueous solution that could not be easily removed using conventional weakly basic anion exchange resins can be effectively removed by ion exchange. Ideal desalting and purification can be performed without causing problems such as.

本発明の方法においては、上記水酸基型強塩基性陰イオ
ン交換樹脂は、上記遊離塩基型弱塩基性陰イオン交換樹
脂に対して5〜20容量係の量で添加されるのが好まし
い。
In the method of the present invention, the hydroxyl group type strongly basic anion exchange resin is preferably added in an amount of 5 to 20 volume parts relative to the free base type weakly basic anion exchange resin.

本発明に有用な遊離塩基型弱塩基性陰イオン交換樹脂と
しては、例えば、ダウエックス(DOWEX。
Examples of free base type weakly basic anion exchange resins useful in the present invention include DOWEX.

デ・ダウケミカルカンパニーの登録商標)66、アンバ
ーライト(A(1b@rlite 、米国、ローム・ア
ンド・ハース社の登録商標)IRA−93、ダイヤイオ
ン(三菱化成工業株式会社の登録商標)WA−30等の
スチレン系陰イオン交換樹脂があシ、また交換基として
ジメチルハイドロキシエチルベンジルアンモニウムを有
する多孔性水酸基型強塩基性陰イオン交換樹脂としては
、例えば、ダウエックスMSA −2、アンバーライト
IRA−910、等の陰イオン交換樹脂がある。また、
水素型強酸性陽イオン交換樹脂としては、例えば、/”
71−ックス88、アンバーライトIR−200等があ
る。
66 (registered trademark of De Dow Chemical Company), Amberlite (A (1b@rlite, registered trademark of Rohm and Haas Company, USA) IRA-93, Diaion (registered trademark of Mitsubishi Chemical Corporation) WA- Examples of porous hydroxyl group-type strongly basic anion exchange resins having dimethyl hydroxyethyl benzyl ammonium as an exchange group include DOWEX MSA-2 and Amberlite IRA-2. There are anion exchange resins such as 910.
Examples of hydrogen-type strongly acidic cation exchange resins include /”
71-x88, Amberlite IR-200, etc.

実施例 下記の例により本発明を更に説明するが、本発明はこれ
らの例によって限定されるものではない。
EXAMPLES The present invention will be further illustrated by the following examples, but the invention is not limited by these examples.

例1 水素型強酸性陽イオン樹脂によシ脱カチオン処理された
甜菜糖水溶液を次いで脱アニオン処理するため、同一樹
脂塔内においてその上層部に遊離塩基型のダウエックス
66(デ・ダウケミカルカン・臂ニー製多孔性スチレン
系陰イオン交換樹脂)2mlf充填し、下層部に水酸基
型のダウエックスMSA −2(ザ・ダウケミカルカン
/f ニー 実長孔性スチレン系陰イオン交換樹脂)0
.2mNr充填したカラムを用いて、本発明の方法を実
施し、これを従来法による処理と比較した。
Example 1 In order to subsequently deanionize a beet sugar aqueous solution that has been decationized using a hydrogen-type strongly acidic cation resin, free base type DOWEX 66 (de Dow Chemical Can) is added to the upper layer of the same resin column.・Filled with 2 ml of porous styrenic anion exchange resin (manufactured by the Dow Chemical Company) and 0 ml of hydroxyl group-type DOWEX MSA-2 (The Dow Chemical Can/F Ni Real long-porous styrenic anion exchange resin) in the lower layer.
.. The method of the present invention was carried out using a column packed with 2 mNr and compared with conventional treatment.

即ち、上記樹脂カラムに、脱カチオン処理後の甜菜糖水
溶液(BXI5.1、PH2,1,電気伝導度2200
μV)t−1空間速度6で導入し、流出液の−と電気伝
導度を連続的に測定したところ、第1図の実線によシ示
すグラフを得た。図において、縦軸は−と電気伝導度を
示し、横軸は時間と流量を示す。
That is, a beet sugar aqueous solution (BXI 5.1, PH 2.1, electrical conductivity 2200) after decationization was added to the resin column.
When the effluent was introduced at a space velocity of 6 μV) and the electrical conductivity of the effluent was continuously measured, the graph shown by the solid line in FIG. 1 was obtained. In the figure, the vertical axis indicates - and electrical conductivity, and the horizontal axis indicates time and flow rate.

また、樹脂塔内にダウエックス66のみを充填した樹脂
カラムを用いて、上記と同一の条件下に流出液の声と電
気伝導度を測定したところ、第1図の破線によシ示すグ
ラフを得た。
In addition, when we measured the voice and electrical conductivity of the effluent under the same conditions as above using a resin column filled only with DOWEX 66, the graph shown by the broken line in Figure 1 was obtained. Obtained.

これらのグラフにより明らかな如く、本発明の方法によ
れば、従来法に比較して、はるかに優れた脱塩効果が得
られ、処理量も大きくなる。
As is clear from these graphs, the method of the present invention provides a much better desalting effect and a larger throughput than the conventional method.

例2 水素型強酸性陽イオン交換樹脂によシ脱カチオン処理し
た異性化糖水溶液(BX37.2、p)(2,0、電気
伝導度1000μv)1、例1で用いたと同一の構成の
カラムに導入し、流出液の声と電気伝導度を連続的に測
定したところ、第2図の実線により示すグラフを得た。
Example 2 Aqueous isomerized sugar solution (BX37.2, p) (2,0, electrical conductivity 1000 μv) decationized with hydrogen type strongly acidic cation exchange resin 1, column with the same configuration as used in Example 1 When the sound and electrical conductivity of the effluent were continuously measured, the graph shown by the solid line in FIG. 2 was obtained.

また、例1と全く同様にして従来法による処理を行い、
流出液の11と電気伝導度を測定した。結果を第2図に
破線によるグラフにより示す。
In addition, treatment was performed using the conventional method in exactly the same manner as in Example 1,
The electrical conductivity of the effluent was measured. The results are shown graphically in FIG. 2 with broken lines.

これらのグラフから、本発明の方法によれば、従来法に
比較して、はるかに優れた脱塩効果が得られ、処理量も
大きくなることがわかる。
From these graphs, it can be seen that the method of the present invention provides a much better desalting effect and a larger throughput than the conventional method.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図及びag2図は、それぞれ、本発明の例において
得られた流出液のpl(と電気伝導度のグラフである。 特許出願人 ダワ・ケミカル日本株式会社 特許出願代理人 弁理士 青 木 朗 弁理士西舘和之 弁理士 吉 1)維 夫 弁理士 山 口 昭 之 弁理士 西 山 雅 也
Figures 1 and 2 are graphs of PL (and electrical conductivity) of the effluent obtained in the example of the present invention, respectively. Patent applicant: Akira Aoki, patent attorney, Dawa Chemical Japan Co., Ltd. Patent Attorney Kazuyuki Nishidate Patent Attorney Yoshi 1) Patent Attorney Akio Yamaguchi Patent Attorney Masaya Nishiyama

Claims (1)

【特許請求の範囲】[Claims] 1、非電解有機質水溶液を、水素型強酸性陽イオン交換
樹脂で脱カチオン処理した後、遊離塩基型弱塩基性陰イ
オン交換樹脂を上層部に充填し、そしてこの遊離塩基型
弱塩基性陰イオン交換樹脂に対して5〜50容量係の、
ジメチルハイドロキシエチルベンジルアンモニウムを交
換基トシカつ多孔質の樹脂母体構造を有する、水酸基型
強塩基性陰イオン交換樹脂を下層部に充填したカラムを
通過せしめることを含んでなる非電解有機質水溶液の高
純度精製方法。
1. After decationizing the non-electrolytic organic aqueous solution with a hydrogen type strongly acidic cation exchange resin, the upper layer is filled with a free base type weakly basic anion exchange resin, and this free base type weakly basic anion 5 to 50 volumes per exchange resin,
High purity of a non-electrolytic organic aqueous solution comprising passing it through a column packed in the lower layer with a hydroxyl group-type strongly basic anion exchange resin having a porous resin matrix structure with an exchange group of dimethyl hydroxyethyl benzyl ammonium. Purification method.
JP58140512A 1983-08-02 1983-08-02 High purity refining method of aqueous non-electrolytic organic substance solution Granted JPS6031829A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58140512A JPS6031829A (en) 1983-08-02 1983-08-02 High purity refining method of aqueous non-electrolytic organic substance solution

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58140512A JPS6031829A (en) 1983-08-02 1983-08-02 High purity refining method of aqueous non-electrolytic organic substance solution

Publications (2)

Publication Number Publication Date
JPS6031829A true JPS6031829A (en) 1985-02-18
JPH0426840B2 JPH0426840B2 (en) 1992-05-08

Family

ID=15270367

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58140512A Granted JPS6031829A (en) 1983-08-02 1983-08-02 High purity refining method of aqueous non-electrolytic organic substance solution

Country Status (1)

Country Link
JP (1) JPS6031829A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10176532A (en) * 1996-12-16 1998-06-30 Sanshin Seisakusho:Kk Regenerating method for engine cooling liquid

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5419759A (en) * 1977-07-13 1979-02-14 Fujitsu Ltd Production of optically transmitting fibers
JPS565511A (en) * 1979-06-26 1981-01-21 Sumitomo Electric Ind Ltd Production of multicore fiber

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5419759A (en) * 1977-07-13 1979-02-14 Fujitsu Ltd Production of optically transmitting fibers
JPS565511A (en) * 1979-06-26 1981-01-21 Sumitomo Electric Ind Ltd Production of multicore fiber

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10176532A (en) * 1996-12-16 1998-06-30 Sanshin Seisakusho:Kk Regenerating method for engine cooling liquid

Also Published As

Publication number Publication date
JPH0426840B2 (en) 1992-05-08

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