JPS5966424A - Preparation of water absorbing resin - Google Patents
Preparation of water absorbing resinInfo
- Publication number
- JPS5966424A JPS5966424A JP17739382A JP17739382A JPS5966424A JP S5966424 A JPS5966424 A JP S5966424A JP 17739382 A JP17739382 A JP 17739382A JP 17739382 A JP17739382 A JP 17739382A JP S5966424 A JPS5966424 A JP S5966424A
- Authority
- JP
- Japan
- Prior art keywords
- aqueous solution
- polyacrylic acid
- water absorbing
- neutralization degree
- added
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Description
【発明の詳細な説明】
ポリアクリル酸をアルミニウムイオンで架橋した吸水性
樹脂は既に提案されているが、本発明はそれ等に関する
工業的製法と性能の改善に関するものである。DETAILED DESCRIPTION OF THE INVENTION Water-absorbing resins made by crosslinking polyacrylic acid with aluminum ions have already been proposed, and the present invention relates to industrial production methods and improvements in performance thereof.
工業的にポリアクリル酸塩を製造する場合、その均質な
中和度を得ることは、使用原料の成分比や重合度の不均
質等の原因で正確には不可能である。然し乍ら中和度の
不均質は樹脂の性能等に影響する。吸水性樹脂に於ては
、適量のアルミニウドイオンで架橋された残余の水素イ
オンの100%は1価の陽イオンで置換されることが望
ましく、又、アルカリ等が過剰に存在することも好まし
くないが、特にイ]ン水溶液の吸水性能や安定性に著し
い相違が生じる。陽イオンが1価の炭酸水素塩は、酸の
存在により容易に分解して炭酸ガスを発生ずるが、本発
明はその現象に着目し、ポリアクリル酸の1価の陽イオ
ンによる中和度を100%未満として加えた後、中和度
が100%となるよりやや過剰の量の炭酸水素塩を加え
ることにより、自動的に100%中和のポリアクリル酸
塩が得られることが判明した。又、やや過剰に加えた炭
酸水素塩はそのまま樹脂中に存在するが、イオン性溶液
中に於ては残存する炭酸水素塩が緩衝作用を示し、吸水
性能が向上することも判明した尚、使用する炭酸水素塩
は水溶液中及び大気中で安定なものが望ましく、アルカ
リ金属の塩は好ましいものであり、以下に述べる本発明
の好適実流側に於ては炭酸水素ナトリウムを使用した。When polyacrylic acid salts are produced industrially, it is impossible to obtain a uniform degree of neutralization due to the non-uniformity of the component ratio of the raw materials used and the degree of polymerization. However, non-uniformity in the degree of neutralization affects the performance of the resin. In the water-absorbing resin, it is preferable that 100% of the remaining hydrogen ions cross-linked with an appropriate amount of aluminum oxide ions be replaced with monovalent cations, and it is also preferable that an alkali etc. be present in excess. However, there is a significant difference in the water absorption performance and stability of the ion aqueous solution. Hydrogen carbonates with monovalent cations easily decompose in the presence of acids and generate carbon dioxide gas, but the present invention focused on this phenomenon and investigated the degree of neutralization of polyacrylic acid with monovalent cations. It has been found that by adding less than 100% and then adding a slightly excess amount of bicarbonate to achieve a degree of neutralization of 100%, a 100% neutralized polyacrylate can automatically be obtained. In addition, it has been found that although hydrogen carbonate added in a slight excess remains in the resin as it is, the remaining hydrogen carbonate exhibits a buffering effect in ionic solutions, improving water absorption performance. The hydrogen carbonate to be used is preferably one that is stable in an aqueous solution and in the atmosphere, and an alkali metal salt is preferred, and sodium hydrogen carbonate was used in the preferred practical implementation of the present invention described below.
(実施例)
過硫酸塩を触媒として重合したポリアクリル酸10%水
溶液を稀釈して1%溶液とし、水酸化ナトリウムを加え
てP H6程度に中和した後、ポリアクリル酸固形分に
対する4%重量部のアルミン酸ナトリウムを水に溶解し
て加え、充分混合し、10時間以−ト放置後PHが一定
するまでの量よりやや過剰の量の炭酸水素ナトリウムを
加えて乾燥するが、一定するP H域は9前後であり、
これはポリアクリル酸ナトリウムのPHと略一致する。(Example) A 10% aqueous solution of polyacrylic acid polymerized using persulfate as a catalyst was diluted to make a 1% solution, and after neutralizing it to about pH 6 by adding sodium hydroxide, the solution was 4% based on the solid content of polyacrylic acid. Add part by weight of sodium aluminate dissolved in water, mix thoroughly, and after leaving for 10 hours or more, add a slightly excess amount of sodium bicarbonate until the pH becomes constant, then dry. The PH range is around 9,
This approximately matches the pH of sodium polyacrylate.
このようにして得られた吸水性樹脂の1%食塩水中に於
ける吸水量は、従来のものが自重の100〜120倍程
であるのに比較し、約2倍の220倍の性能を有し、略
一定である。又、高濃度のイオン水中に於ては炭酸水素
ナトリウムの添加量の多い方が高い吸水性能を得られた
が、これはその緩衝作用によるものと思われる。The amount of water absorbed by the water-absorbing resin obtained in this way in 1% saline is about 100 to 120 times its own weight, while the performance of the conventional resin is 220 times its own weight. However, it remains approximately constant. Furthermore, in highly concentrated ionized water, higher water absorption performance was obtained with a larger amount of sodium bicarbonate added, which is thought to be due to its buffering effect.
以上のように本発明の吸水性樹脂の製造方法は工業的製
法として好適であり、しかも性能及び経済性に優れたも
のである。As described above, the method for producing a water-absorbing resin of the present invention is suitable as an industrial production method, and has excellent performance and economical efficiency.
特許出願人 エスレン化工株式会社Patent applicant Eslen Kako Co., Ltd.
Claims (1)
100%未満のポリアクリル酸水溶液に前記陽イオンの
炭酸水素塩を加えることを特徴とする吸水性樹脂の製造
方法。 ■前記1価の陽イオンを水酸化ナトリウムとし、炭酸水
素塩を炭酸水素ナトリウムとする前記第0項記載の方法
。[Scope of Claims] A method for producing a water-absorbing resin, which comprises adding a hydrogen carbonate of the cation to an aqueous polyacrylic acid solution in which the degree of neutralization by the 01-valent cation and aluminum ion is less than 100%. (2) The method according to item 0, wherein the monovalent cation is sodium hydroxide and the hydrogen carbonate is sodium hydrogen carbonate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17739382A JPS604842B2 (en) | 1982-10-08 | 1982-10-08 | Manufacturing method of water absorbent resin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17739382A JPS604842B2 (en) | 1982-10-08 | 1982-10-08 | Manufacturing method of water absorbent resin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5966424A true JPS5966424A (en) | 1984-04-14 |
| JPS604842B2 JPS604842B2 (en) | 1985-02-07 |
Family
ID=16030145
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17739382A Expired JPS604842B2 (en) | 1982-10-08 | 1982-10-08 | Manufacturing method of water absorbent resin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS604842B2 (en) |
-
1982
- 1982-10-08 JP JP17739382A patent/JPS604842B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS604842B2 (en) | 1985-02-07 |
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