JPH062822B2 - Antistatic treatment method for water absorbent resin powder - Google Patents
Antistatic treatment method for water absorbent resin powderInfo
- Publication number
- JPH062822B2 JPH062822B2 JP63331835A JP33183588A JPH062822B2 JP H062822 B2 JPH062822 B2 JP H062822B2 JP 63331835 A JP63331835 A JP 63331835A JP 33183588 A JP33183588 A JP 33183588A JP H062822 B2 JPH062822 B2 JP H062822B2
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- JP
- Japan
- Prior art keywords
- water
- absorbent resin
- resin powder
- antistatic treatment
- treatment method
- 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.)
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- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Description
【発明の詳細な説明】 <産業上の利用分野> 本発明は吸水性樹脂粉末の帯電防止処理法に関する。The present invention relates to an antistatic treatment method for water-absorbent resin powder.
<従来の技術> 吸水性樹脂粉末は、優れた給水能力および多少の圧力を
受けても一度吸水した液は離水しないという優れた保持
力から、パルパや吸水紙に代わる液吸収素材として、お
むつ、生理用品等の衛生用品メーカーを中心に注目を集
め実用化されてきたものであり、近年、その用途は農
業、園芸、食品、メディカル等に幅広く拡がりつつあ
る。<Prior Art> Water-absorbent resin powder is a liquid absorbent material that replaces pulpers and water-absorbent paper because of its excellent water-supplying ability and the excellent holding power that it does not separate the liquid that has once absorbed water even if it receives some pressure. It has been put to practical use with a focus on manufacturers of sanitary products such as sanitary products, and in recent years, its applications have been widely spread to agriculture, horticulture, food, medical and the like.
ところで、吸水性樹脂粉末は親水性ではあっても、本
来、非導電性物質であるため、粉末同士の摩擦により静
電気を蓄積して帯電しやすい性質を有している。By the way, even though the water-absorbent resin powder is hydrophilic, it is essentially a non-conductive substance, and therefore has a property of easily accumulating due to accumulation of static electricity due to friction between powders.
このため、帯電した場合、吸水性樹脂の製造工程におい
てその中間品または最終仕上品を空気輸送する際に、帯
電による粉塵爆発を引き起こす危険性があった。Therefore, when charged, there is a risk of causing dust explosion due to charging when pneumatically transporting the intermediate product or the final finished product in the manufacturing process of the water absorbent resin.
また、吸水性樹脂粉末は、通常、防湿性のプラスチック
フィルム製の内装を有する紙袋に15〜20kg単位で包
装・出荷されているが、吸水性樹脂粉末が帯電した場
合、内装にかなりの量の吸水性樹脂粉末が付着するた
め、包装内の吸水性樹脂粉末を余すことなく使用するこ
とができないという不経済があった。The water-absorbent resin powder is usually packaged and shipped in 15 to 20 kg units in a paper bag having a moisture-proof plastic film interior, but when the water-absorbent resin powder is charged, a considerable amount of the water-absorbent resin powder is added to the interior. Since the water-absorbent resin powder adheres, it is uneconomical that the water-absorbent resin powder in the package cannot be used completely.
さらに、吸水性樹脂粉末を用いて、おむつ、生理用品等
を製造する場合においても、帯電によって生じた静電気
が放電して装置が損傷したり、塵やほこりが付着したり
して火災が発生する等、種々の設備上のトラブルが発生
する虞があった。Furthermore, even when diapers, sanitary products, etc. are manufactured using water-absorbent resin powder, static electricity generated by electrification discharges the device and damages the device, and dust or dust adheres to cause a fire. There is a possibility that various equipment troubles may occur.
かかる吸水性樹脂粉末が静電気を蓄積するのを防止する
ための帯電防止処理法としては、従来、界面活性剤を用
いる処理法が一般に用いられてきた。この界面活性剤を
用いる処理法は、帯電防止能を有する界面活性剤を吸水
性樹脂の内部に練り込んだり、外部に塗布したりして、
静電気の蓄積を防止する処理法である。As an antistatic treatment method for preventing the water absorbent resin powder from accumulating static electricity, a treatment method using a surfactant has been generally used conventionally. The treatment method using this surfactant is to knead a surfactant having an antistatic ability into the water-absorbent resin or to coat it outside.
This is a processing method that prevents the accumulation of static electricity.
<発明が解決しようとする課題> しかしながら、上記従来の帯電防止処理法は、一時的な
除電法であるため、永久的な帯電防止効果を期待できな
いとともに、界面活性剤が一般に油状であるため、吸水
性樹脂粉末に付着させて界面活性剤層を形成させた場
合、べとつきにより粉体流動性が低下して作業性が悪く
なるという問題があった。<Problems to be Solved by the Invention> However, since the above-mentioned conventional antistatic treatment method is a temporary charge removal method, a permanent antistatic effect cannot be expected, and since the surfactant is generally oily, When the surface-active agent layer is formed by adhering it to the water-absorbent resin powder, there is a problem that the fluidity of the powder is lowered due to stickiness and the workability is deteriorated.
本発明は以上の事情に鑑みてなされたものであって、そ
の目的とするところは、優れた処理効果を有するととも
に、処理後も優れた粉体流動性を有し、作業性が低下す
ることのない吸水性樹脂粉末の帯電防止処理法を提供す
るにある。The present invention has been made in view of the above circumstances, and it is an object of the present invention to have not only excellent treatment effects but also excellent powder fluidity even after treatment, resulting in reduced workability. Another object of the present invention is to provide an antistatic treatment method for a water-absorbent resin powder that does not have the above.
<課題を解決するための手段> 上記目的を達成するための本発明に係る吸水性樹脂粉末
の帯電防止処理法(以下、「本発明方法」という)にお
いては、吸水性樹脂粉末に、所定の無機化合物の粉末
を、該吸水性樹脂粉末100重量部に対して、0.01
〜5重量部添加する。<Means for Solving the Problems> In the antistatic treatment method for a water-absorbent resin powder according to the present invention for achieving the above object (hereinafter, referred to as “method of the present invention”), a predetermined amount of water-absorbent resin powder is added. The amount of the inorganic compound powder is 0.01% with respect to 100 parts by weight of the water absorbent resin powder.
Add ~ 5 parts by weight.
本発明方法において用いられる無機化合物の粉末は、亜
鉛またはカルシウムを構成元素として有する無機化合物
の粉末である。The inorganic compound powder used in the method of the present invention is an inorganic compound powder having zinc or calcium as a constituent element.
以下、本発明方法を詳細に説明する。Hereinafter, the method of the present invention will be described in detail.
本発明方法を用いて帯電防止処理し得る粉末状の吸水性
樹脂としては、水に溶解せず、水中において自重の50
倍程度以上の水を吸収して膨潤し、ヒドロゲルを形成す
る樹脂であればよく、例えばアクリル酸のアルカリ金属
による部分的中和物の重合体架橋物、澱粉−アクリロニ
トリルグラフト重合体の加水分解物、澱粉−アクリル酸
グラフト重合体の中和物、架橋カルボキシメチルセルロ
ース、アクリル酸メチル−酢酸ビニル共重合体の加水分
解物、架橋ポリビニルアルコール変成物などが挙げられ
る。The powdery water-absorbent resin which can be subjected to antistatic treatment using the method of the present invention does not dissolve in water and has a weight of 50 in water.
It may be a resin that absorbs about twice or more of water and swells to form a hydrogel, for example, a polymer cross-linked product of a partially neutralized acrylic acid with an alkali metal, a hydrolyzate of a starch-acrylonitrile graft polymer. , A starch-acrylic acid graft polymer neutralized product, a crosslinked carboxymethyl cellulose, a hydrolyzed product of a methyl acrylate-vinyl acetate copolymer, a crosslinked polyvinyl alcohol modified product, and the like.
本発明方法は、粉末状の吸水性樹脂の帯電防止処理に適
用される。処理対象の粉末の大きさは、通常10〜20
0メッシュであり、これらの粉末同士の摩擦により帯電
しやすいものである。なお、上記粒度範囲のものを用い
るのは、10メッシュ未満の場合、吸水速度が小さくな
るからであり、200メッシュを越えた場合、ままこ現
象が生じるからである。The method of the present invention is applied to the antistatic treatment of powdery water-absorbent resin. The size of the powder to be treated is usually 10 to 20.
It is 0 mesh and is easily charged by friction between these powders. The reason why the particles having the above-mentioned particle size range is used is that the water absorption rate becomes small when the particle size is less than 10 mesh, and the litter phenomenon occurs when the particle size exceeds 200 mesh.
本発明方法において用いられる無機化合物としては、具
体的には、亜鉛華、炭酸亜鉛などの亜鉛の酸化物または
炭酸塩;炭酸カルシウム、酸化カルシウム、硫酸カルシ
ウム、水酸化カルシウムなどのカルシウムの炭酸塩、酸
化物、硫酸塩または水酸化物が例示される。Specific examples of the inorganic compound used in the method of the present invention include zinc oxides and carbonates such as zinc white and zinc carbonate; calcium carbonates such as calcium carbonate, calcium oxide, calcium sulfate and calcium hydroxide; Examples are oxides, sulfates or hydroxides.
また、用いる無機化合物は、含水物か無水物かを限定さ
れず、また含水物の含水量もまた限定されない。The inorganic compound used is not limited to a hydrous substance or an anhydrous substance, and the water content of the hydrous substance is also not limited.
なお、上記無機化合物は、一種または二種以上の粉末を
混合して用いてよい。The inorganic compound may be used alone or as a mixture of two or more kinds.
上記無機化合物の粒径は、小さい方が本発明方法を実施
する上で適しており、平均粒径50μm以下のものが好
ましい。平均粒径が50μmを越えた場合、吸水性樹脂
粉末から無機化合物が分離して好ましくないからであ
る。A smaller particle size of the above-mentioned inorganic compound is more suitable for carrying out the method of the present invention, and an average particle size of 50 μm or less is preferable. When the average particle size exceeds 50 μm, the inorganic compound is separated from the water absorbent resin powder, which is not preferable.
本発明方法においては、粉末状の上記無機化合物を、吸
水性樹脂粉末100重量部に対して、0.01〜5重量
部用いる必要がある。このように添加量を限定したの
は、0.01重量部未満の場合、帯電防止のための有意
な添加効果が期待できないからであり、5重量部を越え
た場合、増量に相応した添加効果が得られないのみなら
ず、飛散の問題が生じるからである。In the method of the present invention, it is necessary to use the powdery inorganic compound in an amount of 0.01 to 5 parts by weight based on 100 parts by weight of the water absorbent resin powder. The reason why the addition amount is limited in this way is that if it is less than 0.01 part by weight, a significant addition effect for antistatic cannot be expected, and if it exceeds 5 parts by weight, the addition effect corresponding to the increase in amount is obtained. Is not only obtained, but also the problem of scattering occurs.
吸水性樹脂粉末と上記無機化合物とを混合することによ
り、該吸水性樹脂に帯電防止処理が施される。By mixing the water-absorbent resin powder and the inorganic compound, the water-absorbent resin is subjected to antistatic treatment.
混合方法としては、従来公知の種々の方法を用いること
ができ、例えばタンブラー、Vブレンダー、スーパーミ
キサー、ナウターミキサー、リボンブレンダー、コニカ
ルブレンダー、ヘンシェルミキサー、レディゲミキサー
などの種々の混合機を用いて混合することができる。As a mixing method, various conventionally known methods can be used. For example, various mixers such as a tumbler, a V blender, a super mixer, a Nauter mixer, a ribbon blender, a conical blender, a Henschel mixer, and a Loedige mixer are used. Can be mixed.
無機化合物の粉末が、吸水性樹脂粉末から分離するのを
防止するために、両者を混合する前に、吸水性樹脂粉末
の吸水性能に悪影響を与えない程度の量および種類の展
着剤を混合して粉末の表面にコーティングしてもよい。In order to prevent the powder of the inorganic compound from separating from the water-absorbent resin powder, before spreading the two, mix a spreading agent in an amount and kind that does not adversely affect the water-absorbing performance of the water-absorbent resin powder. Then, the surface of the powder may be coated.
コーティングに用い得る展着剤としては、液状ポリブテ
ン、液状ポリエチレングリコール、多価アルコール、グ
リコールエーテル化合物などが挙げられる。Spreading agents that can be used for coating include liquid polybutene, liquid polyethylene glycol, polyhydric alcohols, glycol ether compounds and the like.
<実施例> 以下、本発明を実施例に基いて、より詳細に説明する。
なお、本発明方法は、下記の実施例に示す処理法に限定
されるものではなく、本発明の要旨を変更しない範囲
で、適宜変更を加え得ることは勿論である。<Examples> Hereinafter, the present invention will be described in more detail with reference to Examples.
The method of the present invention is not limited to the processing method shown in the following examples, and it goes without saying that appropriate modifications can be made without departing from the scope of the present invention.
(A)吸水性樹脂粉末の調製 80%アクリル酸75重量部、48.6%水酸化ナトリ
ウム48.0重量部およびイオン交換水48.6重量部
を混合して中和度70%のアクリル酸塩水溶液を調製し
た。このアクリル酸塩水溶液1029gに、1%N,N
−メチレンビスアクリルアミド水溶液5gを添加して窒
素置換した後、2%ペルオキソ二硫酸塩K2S2O8水
溶液36g、2%ピロ亜硫酸塩K2S2O5水溶液2
1.6gおよび40%グリオキサール水溶液を水で50
倍に薄めた希釈液14.4gを添加して混合液を得た。
次いで、この混合液を、縦48cm、横37cmのバット
(内面テフロンコーテイング)に注入し、乾燥温度42
℃の熱風循環乾燥器内で20分間重合して縦48cm、横
37cm、厚さ5〜6mmの板状の含水ゲルを得た。得られ
た含水ゲルを表面温度130℃のドラムドライヤで乾燥
してフレーク状の樹脂とし、この樹脂をピンミルで粉砕
した後、分級し、60〜120メッシュの吸水性樹脂粉
末を得た。(A) Preparation of Water-Absorbent Resin Powder 75% by weight of 80% acrylic acid, 48.0% by weight of 48.6% sodium hydroxide and 48.6 parts by weight of deionized water are mixed to obtain acrylic acid having a neutralization degree of 70%. An aqueous salt solution was prepared. To 1029 g of this aqueous acrylate solution, 1% N, N
After adding 5 g of a methylenebisacrylamide aqueous solution and performing nitrogen substitution, 36 g of a 2% peroxodisulfate K 2 S 2 O 8 aqueous solution, and 2% of a 2% pyrosulfite K 2 S 2 O 5 aqueous solution 2
50 g of 1.6 g and 40% aqueous glyoxal solution in water
14.4 g of the diluted solution diluted twice was added to obtain a mixed solution.
Then, this mixed solution is poured into a bat (inner Teflon coating) having a length of 48 cm and a width of 37 cm, and the drying temperature is 42
Polymerization was carried out for 20 minutes in a hot air circulation dryer at ℃ to obtain a plate-shaped hydrogel having a length of 48 cm, a width of 37 cm and a thickness of 5 to 6 mm. The obtained water-containing gel was dried with a drum dryer having a surface temperature of 130 ° C. to give a flake-like resin, which was crushed with a pin mill and then classified to obtain a water-absorbent resin powder of 60 to 120 mesh.
上記吸水性樹脂粉末を、温度22℃、相対湿度60%の
恒温・恒湿室内の、シリカゲルを収容したデシケーター
内で一昼夜乾燥した。The water-absorbent resin powder was dried overnight in a desiccator containing silica gel in a constant temperature / humidity chamber having a temperature of 22 ° C. and a relative humidity of 60%.
(B)吸水性樹脂粉末の帯電防止処理 (実施例1) 上記(A)で得た吸水性樹脂粉末100gと、無機化合
物としての粉末状の炭酸亜鉛(正同化学社製)0.5g
とを、前記恒温・恒湿室内で、小型攪拌機にて均一に撹
拌混合することにより、帯電防止処理を行ない試料1を
得た。(B) Antistatic treatment of water-absorbent resin powder (Example 1) 100 g of the water-absorbent resin powder obtained in (A) above, and 0.5 g of powdered zinc carbonate (manufactured by Shodo Chemical Co., Ltd.) as an inorganic compound
And were uniformly stirred and mixed in the constant temperature and constant humidity chamber with a small stirrer, and antistatic treatment was performed to obtain Sample 1.
(実施例2) 炭酸亜鉛に代えて、亜鉛華1号(堺化学工業社製)を同
量用いたこと以外は実施例1と同様にして、帯電防止処
理を行い試料2を得た。(Example 2) A sample 2 was obtained in the same manner as in Example 1 except that Zinc Hua No. 1 (manufactured by Sakai Chemical Industry Co., Ltd.) was used in place of zinc carbonate.
(実施例3) 炭酸亜鉛に代えて、軽質の炭酸カルシウム(竹原化学工
業社製)を同量用いたこと以外は実施例1と同様にし
て、帯電防止処理を行い試料3を得た。(Example 3) Sample 3 was obtained in the same manner as in Example 1 except that the same amount of light calcium carbonate (manufactured by Takehara Chemical Industry Co., Ltd.) was used instead of zinc carbonate.
(比較例1) 帯電防止処理を行わなかった吸水性樹脂粉末を比較試料
1とした。(Comparative Example 1) A water absorbent resin powder that was not subjected to antistatic treatment was used as Comparative Sample 1.
(比較例2) 炭酸亜鉛に代えて、タルク(竹原化学工業社製)を同量
用いたこと以外は実施例1と同様にして、帯電防止処理
を行い比較試料2を得た。Comparative Example 2 Comparative sample 2 was obtained by performing antistatic treatment in the same manner as in Example 1 except that the same amount of talc (manufactured by Takehara Chemical Industry Co., Ltd.) was used instead of zinc carbonate.
(比較例3) 炭酸亜鉛に代えて、シリカ(東洋曹達社製、商品名「ト
クシール」)を同量用いたこと以外は実施例1と同様に
して、帯電防止処理を行い比較試料3を得た。(Comparative Example 3) Comparative sample 3 was obtained by performing an antistatic treatment in the same manner as in Example 1 except that the same amount of silica (manufactured by Toyo Soda Co., Ltd., trade name "TOKUSIL") was used instead of zinc carbonate. It was
(C)帯電防止能の評価試験 上記試料1〜3および比較試料1〜3から各10gを分
取して、内面が厚さ0.03mm、縦100mm、横150
mmのポリエチレン製フィルムでできている袋に入れ、袋
の開口部を手で絞って閉じた後、袋を30秒間強く手で
上下左右に振って、吸水性樹脂粉末のフィルムへの付着
状態を目視にて観察し、各試料または比較試料について
の帯電防止能を下記の基準で評価した。(C) Antistatic Evaluation Test 10 g of each of the above Samples 1 to 3 and Comparative Samples 1 to 3 was sampled so that the inner surface had a thickness of 0.03 mm, a length of 100 mm and a width of 150.
After putting it in the bag made of polyethylene film of mm, squeezing the opening of the bag by hand, shake the bag strongly up and down, left and right for 30 seconds to check the adhesion state of the water-absorbent resin powder to the film. It was visually observed and the antistatic ability of each sample or comparative sample was evaluated according to the following criteria.
(評価基準) 評価A………全く付着しない。(Evaluation Criteria) Evaluation A: No adherence at all.
評価B………少し付着するだけである。Evaluation B: Only a little adhered.
評価C………かなり付着する。Evaluation C ... Adheres considerably.
評価D………ほとんど全面に付着する。Evaluation D: Adhesion almost all over the surface.
下記表に、上記評価結果を示す。The evaluation results are shown in the table below.
上記表に示すように、本発明方法を用いて帯電防止処理
した吸水性樹脂粉末(試料1〜3)は、ポリエチレン製
フィルムに全く付着しないか、少し付着したのに過ぎな
いのに対して、帯電防止処理を行わなかったもの(比較
試料1)および本発明方法によらないで帯電防止処理を
行ったもの(比較試料2および3)は、付着の程度が激
しかった。 As shown in the above table, the water-absorbent resin powder (samples 1 to 3) subjected to antistatic treatment using the method of the present invention does not adhere to the polyethylene film at all, or only slightly adheres to it, whereas The degree of adhesion was high in the case where the antistatic treatment was not performed (Comparative Sample 1) and the case where the antistatic treatment was not performed by the method of the present invention (Comparative Samples 2 and 3).
以上より、従来公知の帯電防止処理法に比べて、本発明
方法は優れた帯電防止処理法であることが分った。From the above, it was found that the method of the present invention is an excellent antistatic treatment method as compared with conventionally known antistatic treatment methods.
<発明の効果> 以上説明したように、本発明に係る吸水性樹脂粉末の帯
電防止処理法は、優れた帯電防止処理を可能にする等、
本発明は優れた特有の効果を奏する。<Effects of the Invention> As described above, the antistatic treatment method for the water absorbent resin powder according to the present invention enables an excellent antistatic treatment.
The present invention has excellent unique effects.
Claims (1)
を構成元素として有する無機化合物の粉末を、該吸水性
樹脂粉末100重量部に対して、0.01〜5重量部添
加することを特徴とする吸水性樹脂粉末の帯電防止処理
法。1. A water-absorbent resin powder comprising 0.01 to 5 parts by weight of an inorganic compound powder containing zinc or calcium as a constituent element, relative to 100 parts by weight of the water-absorbent resin powder. Antistatic treatment method for water absorbent resin powder.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63331835A JPH062822B2 (en) | 1988-12-29 | 1988-12-29 | Antistatic treatment method for water absorbent resin powder |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63331835A JPH062822B2 (en) | 1988-12-29 | 1988-12-29 | Antistatic treatment method for water absorbent resin powder |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02178332A JPH02178332A (en) | 1990-07-11 |
| JPH062822B2 true JPH062822B2 (en) | 1994-01-12 |
Family
ID=18248179
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63331835A Expired - Fee Related JPH062822B2 (en) | 1988-12-29 | 1988-12-29 | Antistatic treatment method for water absorbent resin powder |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH062822B2 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0516026A1 (en) * | 1991-05-28 | 1992-12-02 | Takeda Chemical Industries, Ltd. | Hydrogel and method of producing same |
| JP4163538B2 (en) * | 2003-03-20 | 2008-10-08 | 株式会社日本触媒 | Water absorbent resin composition |
| WO2005053381A1 (en) * | 2003-12-05 | 2005-06-16 | Nippon Shokubai Co., Ltd. | Particulate water retaining material for cultivating plant having water absorbent resin as main component |
| JP4694810B2 (en) * | 2004-09-08 | 2011-06-08 | 株式会社日本触媒 | Water-retaining material for plant growth mainly composed of water-absorbent resin |
| JP4694809B2 (en) * | 2004-09-08 | 2011-06-08 | 株式会社日本触媒 | Water retention material for plant growth mainly composed of biodegradable water-absorbent resin |
| JP5290727B2 (en) * | 2008-12-11 | 2013-09-18 | 花王株式会社 | Method for producing water absorbent resin composite |
| TWI424007B (en) | 2011-12-22 | 2014-01-21 | Ind Tech Res Inst | Method for crosslinking a colloid, and crosslinked colloid therefrom |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61257235A (en) * | 1985-05-08 | 1986-11-14 | Sanyo Chem Ind Ltd | Water absorbent resin composition, its preparation and water absorbent-water retention agent |
| JP3208489B2 (en) * | 1991-07-30 | 2001-09-10 | セイコープレシジョン株式会社 | Camera with battery check device |
-
1988
- 1988-12-29 JP JP63331835A patent/JPH062822B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02178332A (en) | 1990-07-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |