JPH1045812A - Production of fiber-containing water absorbing resin - Google Patents

Production of fiber-containing water absorbing resin

Info

Publication number
JPH1045812A
JPH1045812A JP20241996A JP20241996A JPH1045812A JP H1045812 A JPH1045812 A JP H1045812A JP 20241996 A JP20241996 A JP 20241996A JP 20241996 A JP20241996 A JP 20241996A JP H1045812 A JPH1045812 A JP H1045812A
Authority
JP
Japan
Prior art keywords
polymerization
fiber
acrylic acid
water
monomer
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
Application number
JP20241996A
Other languages
Japanese (ja)
Inventor
Fumito Yamai
二三人 山井
Hisashi Ike
寿 池
Takashi Senda
隆 千田
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.)
Sekisui Kasei Co Ltd
Original Assignee
Sekisui Plastics Co 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 Sekisui Plastics Co Ltd filed Critical Sekisui Plastics Co Ltd
Priority to JP20241996A priority Critical patent/JPH1045812A/en
Publication of JPH1045812A publication Critical patent/JPH1045812A/en
Pending legal-status Critical Current

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  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

PROBLEM TO BE SOLVED: To suppress a phenomenon such as bumping at the time of an exothermic reaction, facilitate the polymerization control and enable the efficient production of the subject resin by including prescribed staple fibers in an acrylic acid- based monomer before polymerization when carrying out the stationary polymerization. SOLUTION: (C) Staple fibers having 1-100μm average fiber diameter and 0.5-10mm length are contained in (A) an aqueous solution of an acrylic acid- based monomer to carry out the stationary polymerization when adding (B) a polymerization initiator to the component A and conducting the stationary polymerization without stirring the resultant reactional mixture. Furthermore, the component A is preferably contained in an amount of 0.1-5 pts.wt. based on 100 pts.wt. component A and, e.g. conjugated fibers such as a polyester/ polyethylene are preferably used as the component C.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、重合前に短繊維を
含有させて重合することにより突沸を防ぐ繊維含有吸水
性樹脂組成物の製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a fiber-containing water-absorbent resin composition in which short fibers are contained before polymerization to prevent bumping by polymerization.

【0002】[0002]

【従来の技術】近年、衛生用品、農園芸用土壌改良剤、
吸着剤等のさまざまなところで吸水性樹脂が盛んに使わ
れるようになった。特に使い捨てオムツ、生理用ナプキ
ンへの使用量は年々増加している。通常の吸水性樹脂は
主にアクリル酸塩を重合させたものであり、その製造方
法には逆相懸濁重合、静置重合等が知られている。
BACKGROUND OF THE INVENTION In recent years, sanitary goods, soil improvers for agriculture and horticulture,
Water-absorbing resins have come into widespread use in various places such as adsorbents. In particular, the amount used for disposable diapers and sanitary napkins is increasing year by year. Ordinary water-absorbing resins are mainly those obtained by polymerizing acrylates, and known methods for producing such resins include reversed-phase suspension polymerization and static polymerization.

【0003】このうち、逆相懸濁重合は重合熱の除去が
容易という利点があるものの、シクロへキサン等の溶媒
を用いるためコストがかかるという欠点がある。これに
対して、静置重合は、モノマーの水溶液に重合開始剤を
加え、加熱下で攪拌せずに重合を行わせるものであっ
て、安価なコストでシート状の吸水性樹脂を製造できる
が、重合熱の除去が困難であり、そのため突沸による過
大な発泡、波打ち、シートの変形などが生じやすい。そ
の結果、重合工程から乾燥工程への搬送コンベア間の受
け渡しに支障をきたしたり、シートを裁断するのが困難
になる。また品質的にもむらが生じてしまい好ましくな
い。
[0003] Among these, reversed-phase suspension polymerization has the advantage that heat of polymerization is easily removed, but has the disadvantage that it is costly because a solvent such as cyclohexane is used. On the other hand, static polymerization is a method in which a polymerization initiator is added to an aqueous solution of a monomer and polymerization is performed without stirring under heating, and a sheet-like water-absorbing resin can be produced at low cost. However, it is difficult to remove the heat of polymerization, so that excessive foaming, waving, and sheet deformation due to bumping are likely to occur. As a result, the transfer between the conveyors from the polymerization step to the drying step is hindered, and it becomes difficult to cut the sheet. Further, the quality is not uniform, which is not preferable.

【0004】[0004]

【発明が解決しようとする課題】静置重合の急激な反応
を抑制する方法としては、特開平4−175319号公
報に開示の重合方法が挙げられる。この方法は、ビニル
系モノマーを含む水溶液を攪拌せずに、比較的低温度で
重合を行わせ、重合率が70%以上の段階で必要により
重合温度を上げて重合を完結させるものである。
As a method for suppressing a rapid reaction of static polymerization, there is a polymerization method disclosed in Japanese Patent Application Laid-Open No. 4-175319. In this method, polymerization is carried out at a relatively low temperature without stirring an aqueous solution containing a vinyl monomer, and the polymerization temperature is raised as needed at a stage where the conversion is 70% or more to complete the polymerization.

【0005】しかし、この方法は、比較的低温度で重合
を行わせるために生産効率が低く、かつ温度管理のため
に複雑な設備を必要とし、しかも製造できるシートの厚
みにも制限があり、さらに得られるシート状の吸水性樹
脂は品質上残存モノマーが高くなるという欠点がある。
本発明の目的は、静置重合における突沸を抑えて、シー
トの波打ちや変形などのない吸水性樹脂を効率よく製造
できる繊維含有吸水性樹脂の製造方法を提供することで
ある。
However, this method has a low production efficiency because polymerization is performed at a relatively low temperature, requires complicated equipment for temperature control, and has a limitation in the thickness of a sheet that can be produced. Further, the obtained sheet-like water-absorbent resin has a disadvantage that the residual monomer is high in quality.
An object of the present invention is to provide a method for producing a fiber-containing water-absorbent resin capable of efficiently producing a water-absorbent resin without waving or deformation of a sheet by suppressing bumping in static polymerization.

【0006】[0006]

【課題を解決するための手段】本発明者らは、上記の課
題を解決するため鋭意研究を重ねた結果、アクリル酸系
モノマーの水溶液に短繊維を含有させて静置重合すると
きは、発熱反応時にゲル相内部からの水蒸気の逸散が容
易になり、前記のような突沸等の現象を抑えることがで
き、その結果、特別な温度管理を必要としないので、重
合コントロールが容易になり、効率よく繊維含有吸水性
樹脂を製造できるという新たな知見を得て、本発明を完
成するに到った。
Means for Solving the Problems The inventors of the present invention have conducted intensive studies to solve the above-mentioned problems. As a result, when static polymerization is carried out by containing short fibers in an aqueous solution of an acrylic acid monomer, an exothermic reaction occurs. Evaporation of water vapor from the inside of the gel phase during the reaction is facilitated, and the above-described phenomenon such as bumping can be suppressed. The present inventors have obtained a new finding that a fiber-containing water-absorbent resin can be efficiently produced, and have completed the present invention.

【0007】本発明の方法によって得られる繊維含有吸
水性樹脂は短繊維が重合当初から添加されているので、
吸水性樹脂から繊維が剥離しにくいという作用もある。
また、この繊維含有吸水性樹脂は、表面から繊維が出て
いるため、おむつ等の吸収体内で吸水性樹脂が移動、脱
落するのを阻止することができる。即ち、本発明の繊維
含有吸水性樹脂の製造方法は、アクリル酸系モノマーの
水溶液に重合開始剤を加えて、攪拌することなく静置重
合するものであって、平均繊維径1〜100μmで長さ
0.5〜10mmの短繊維を前記アクリル酸系モノマー
の水溶液に含有させて静置重合することを特徴とする。
In the fiber-containing water-absorbent resin obtained by the method of the present invention, since short fibers are added from the beginning of polymerization,
There is also an effect that the fibers are hardly peeled off from the water absorbent resin.
In addition, since the fiber-containing water-absorbent resin has fibers protruding from the surface, it is possible to prevent the water-absorbent resin from moving and falling off in an absorbent body such as a diaper. That is, the method for producing a fiber-containing water-absorbent resin of the present invention is a method in which a polymerization initiator is added to an aqueous solution of an acrylic acid-based monomer, and the mixture is allowed to stand for polymerization without stirring. It is characterized in that short fibers having a length of 0.5 to 10 mm are contained in an aqueous solution of the acrylic acid-based monomer and subjected to static polymerization.

【0008】このとき、短繊維は、前記アクリル酸系モ
ノマー100重量部に対して0.1〜5重量部の割合で
含有させるのが好ましい。なお、繊維含有吸水性樹脂
は、特開平56−65630号公報、特公平3−456
55号公報、特公平8−19609号公報に記載されて
いるように、従来より公知であるが、これらの公報に記
載の方法は、重合した吸水性樹脂と繊維とを混合するも
のであり、重合前から短繊維を加えて静置重合したもの
は知られていない。
In this case, it is preferable that the short fibers are contained in a proportion of 0.1 to 5 parts by weight based on 100 parts by weight of the acrylic acid monomer. The fiber-containing water-absorbing resin is disclosed in JP-A-56-65630, Japanese Patent Publication No. 3-456.
No. 55, as disclosed in Japanese Patent Publication No. Hei 8-19609, conventionally known, the method described in these publications is to mix a polymerized water-absorbing resin and fiber, There is no known polymer obtained by adding a short fiber before polymerization and performing static polymerization.

【0009】[0009]

【発明の実施の形態】本発明におけるアクリル酸系モノ
マーとしては、例えばアクリル酸またはメタクリル酸
と、その中和物とを主成分とするものである。中和物と
しては、例えば(メタ)アクリル酸のナトリウム塩、カ
リウム塩、アンモニウム塩から選ばれる1種または2種
以上が挙げられ、好ましくはナトリウム塩、カリウム塩
などのアルカリ金属塩である。アクリル酸モノマーをア
ルカリ金属塩へ中和するときのアルカリ剤としては、例
えば水酸化ナトリウム、水酸化カリウム等のアルカリ金
属の水酸化物等が挙げられる。
BEST MODE FOR CARRYING OUT THE INVENTION The acrylic acid monomer in the present invention is, for example, one containing acrylic acid or methacrylic acid and its neutralized product as main components. Examples of the neutralized product include one or more selected from a sodium salt, a potassium salt, and an ammonium salt of (meth) acrylic acid, and an alkali metal salt such as a sodium salt and a potassium salt is preferable. Examples of the alkali agent for neutralizing the acrylic acid monomer into an alkali metal salt include hydroxides of alkali metals such as sodium hydroxide and potassium hydroxide.

【0010】また、(メタ)アクリル酸以外の他のモノ
マーを(メタ)アクリル酸と併用してもよい。このよう
な他のモノマーとしては、従来より吸水性樹脂の製造に
用いられているものであれば、特別な制限なしに使用可
能であり、例えばクロトン酸、(無水)マレイン酸、フ
マル酸、イタコン酸およびこれらの中和物から選ばれる
1種以上の水溶性エチレン性不飽和単量体が挙げられ
る。
A monomer other than (meth) acrylic acid may be used in combination with (meth) acrylic acid. As such other monomers, those which have been conventionally used in the production of water-absorbent resins can be used without any particular limitation. One or more water-soluble ethylenically unsaturated monomers selected from acids and neutralized products thereof are exemplified.

【0011】上記部分中和(メタ)アクリル酸の中和度
は、通常、50〜95モル%、好ましくは60〜90モ
ル%である。上記モノマーに架橋剤を併用することがで
きる。このような架橋剤としては、例えばメチレンビス
アクリルアミド、ポリエチレングリコールジアクリレー
ト等の2重結合が2個以上ありかつアクリル酸系モノマ
ーと共重合性を示すもの、エチレングリコールジグリシ
ジルエーテル等のアクリル酸系モノマー中のカルボキシ
ル基と反応する官能基を2個以上有する化合物等が使用
可能である。
The degree of neutralization of the partially neutralized (meth) acrylic acid is usually 50 to 95 mol%, preferably 60 to 90 mol%. A crosslinking agent can be used in combination with the above monomers. Examples of such a crosslinking agent include those having two or more double bonds such as methylenebisacrylamide and polyethylene glycol diacrylate and exhibiting copolymerizability with an acrylic acid monomer, and acrylic acid such as ethylene glycol diglycidyl ether. Compounds having two or more functional groups that react with the carboxyl group in the monomer can be used.

【0012】本発明における短繊維は、平均繊維径が1
〜100μm、長さが0.5〜10mmの粉末繊維であ
る。平均繊維径が1μm未満または繊維長が0.5mm
未満では、発熱反応時にゲル相内部から水蒸気が抜けに
くく突沸を起こしてしまう。一方、平均繊維径が100
μmを超えるか、繊維長が10mmを超えると、吸水量
が落ちる等の品質面に影響を及ぼす。
In the present invention, the short fibers have an average fiber diameter of 1
It is a powder fiber having a length of 0.5 to 100 mm and a length of 0.5 to 10 mm. Average fiber diameter is less than 1μm or fiber length is 0.5mm
If it is less than 3, water vapor hardly escapes from the inside of the gel phase during the exothermic reaction, causing bumping. On the other hand, if the average fiber diameter is 100
If it exceeds μm or if the fiber length exceeds 10 mm, the quality is affected, such as a decrease in water absorption.

【0013】前記短繊維としては、例えばポリエステル
/ポリエチレン、ポリエステル/酢酸ビニル共重合体等
の複合繊維、ポリプロピレン等の疎水性繊維、パルプ、
レーヨン等の親水性繊維等が挙げられる。本発明におけ
る短繊維の使用量は、アクリル酸系モノマー100重量
部に対して0.1〜5重量部が好ましい。短繊維の使用
量が0.1重量部未満であると、突沸を起こすおそれが
ある。一方、使用量が5重量部を超えると、アクリル酸
系モノマーの粘度が高くなり過ぎてモノマーの取扱いが
困難になるばかりでなく、繊維がきれいに分散しなくな
り好ましくない。
Examples of the short fibers include conjugate fibers such as polyester / polyethylene and polyester / vinyl acetate copolymer, hydrophobic fibers such as polypropylene, pulp, and the like.
And hydrophilic fibers such as rayon. The amount of the short fiber used in the present invention is preferably 0.1 to 5 parts by weight based on 100 parts by weight of the acrylic acid monomer. If the amount of short fibers used is less than 0.1 parts by weight, bumping may occur. On the other hand, if the used amount exceeds 5 parts by weight, the viscosity of the acrylic acid monomer becomes too high, which makes the handling of the monomer difficult and undesirably prevents the fibers from being finely dispersed.

【0014】本発明における重合開始剤としては、一般
に使用される水溶性ラジカル重合開始剤を用いることが
できる。このようなラジカル重合開始剤としては、例え
ば過硫酸カリウム、過硫酸アンモニウム等の過硫酸塩、
過酸化水素、クメンハイドロパーオキシド等のハイドロ
パ−オキシド、2.2−アゾビス−2−アミジノプロパ
ン塩酸塩等のアゾ化合物が挙げられる。
As the polymerization initiator in the present invention, a commonly used water-soluble radical polymerization initiator can be used. As such a radical polymerization initiator, for example, potassium persulfate, persulfates such as ammonium persulfate,
Hydroperoxides such as hydrogen peroxide and cumene hydroperoxide, and azo compounds such as 2.2-azobis-2-amidinopropane hydrochloride are exemplified.

【0015】これらのラジカル重合開始剤は1種類を単
独で使用してもよいし、2種類以上を混合して使用する
ことも可能であり、さらには亜硫酸塩、L−アスコルビ
ン酸等の還元剤との組み合わせによるレドックス開始剤
系も使用可能である。重合温度は、使用するラジカル重
合開始剤の種類等によって種々変えることができるが、
通常0〜150℃、好ましくは10〜100℃である。
One of these radical polymerization initiators may be used alone, or two or more of them may be used in combination. Further, a reducing agent such as sulfite or L-ascorbic acid may be used. Redox initiator systems in combination with are also possible. The polymerization temperature can be variously changed depending on the type of the radical polymerization initiator used,
It is usually 0 to 150 ° C, preferably 10 to 100 ° C.

【0016】重合により吸水樹脂の含水ゲル・シートが
得られる。これを乾燥、粉砕、分級することにより製品
が得られる。その際、本発明の方法では、重合時に多量
の水蒸気を発生するためゲルシートの水分値が低く、従
って乾燥工程の時間が大幅に短縮されるという利点もあ
る。
By the polymerization, a hydrogel sheet of a water-absorbing resin is obtained. The product is obtained by drying, pulverizing and classifying the product. At that time, the method of the present invention has an advantage that a large amount of water vapor is generated at the time of polymerization, so that the water value of the gel sheet is low, and thus the time of the drying step is greatly reduced.

【0017】[0017]

【実施例】【Example】

実施例1 アクリル酸ナトリウム75モル%およびアクリル酸25
モル%からなる単量体成分の水溶液1000g(単量体
成分45重量%)にN.Nーメチレンビスアクリルアミ
ド0.2gを加えて溶解後、窒素ガスを吹き込んで溶存
酸素を追い出し液温を10℃とした。
Example 1 75 mol% of sodium acrylate and 25 of acrylic acid
The amount of N.O.M. After adding and dissolving 0.2 g of N-methylenebisacrylamide, nitrogen gas was blown out to expel dissolved oxygen and the liquid temperature was set to 10 ° C.

【0018】次にポリプロピレン短織維(長さ5mm、
平均繊維径25μm)10gを単量体溶液に投入し撹件
した。5分後、イオン交換水130gに過硫酸カリウム
1.3g,チオ硫酸カリウム0.3gを加えた水溶液
(A)を、攪拌下で単量体溶液に投入し、それを70℃
の温水に浸したテフロンコートのステンレスバット(3
70mm×470mm×50mm)中に注入した。
Next, polypropylene short weave fiber (length 5 mm,
10 g of an average fiber diameter (25 μm) was charged into the monomer solution and stirred. Five minutes later, an aqueous solution (A) obtained by adding 1.3 g of potassium persulfate and 0.3 g of potassium thiosulfate to 130 g of ion-exchanged water was added to the monomer solution with stirring, and the mixture was heated to 70 ° C.
Teflon-coated stainless steel bat soaked in warm water (3
(70 mm × 470 mm × 50 mm).

【0019】得られたゲルシートの厚みは約5mmであ
った。約5分後、発熱がピークに達し、水蒸気がゲルシ
ートの表面から出てきたものの突沸による大きな気泡の
生成やゲルシートの変形は見られなかった。得られた含
水ゲルを乾燥、粉砕、分級を行って繊維含有吸水性樹脂
の製品を得た。 実施例2 実施例1においてポリプロピレン短繊維の添加量を20
gにしたほかは実施例1と同様の操作を行った。その結
果、実施例1と同様に、重合開始から5分後にゲルシー
トの表面より水蒸気が出てきたものの突沸による大きな
気泡の生成やゲルシートの変形は見られなかった。 実施例3 実施例1で使用したポリプロピレン短織維(長さ5m
m)に代えて、繊維長が2mmのポリプロピレン短繊維
を使用したほかは実施例1と同様の操作を行った。その
結果、実施例1と同様に、重合開姶から5分後にゲルシ
ートの表面より水蒸気が出てきたものの突沸による大き
な気泡の生成やゲルシートの変形は見られなかった。 実施例4 実施例1で使用したポリプロピレン短繊維に代えて、ポ
リプロピレン/ポリエチレン複合繊維(長さ5mm、平
均繊維径15μm)を使用したほかは、実施例1と同様
の操作を行った。その結果、実施例1と同様に、重合開
始から5分後にゲルシート表面より水蒸気が出てきたも
のの突沸による大きな気泡の生成やゲルシートの変形は
見られなかった。 実施例5 実施例1で使用したポリプロピレン短織維(平均繊維径
25μm)に代えて、平均繊維径5μmのポリプロピレ
ン短繊維を使用したほかは実施例1と同様の操作を行っ
た。その結果、実施例1と同様に、重合開始から5分後
にゲルンートの表面より水蒸気が出てきたものの突沸に
よる大きな気泡の生成やゲルシートの変形は見られなか
った。 比較例1 繊維を添加しなかったほかは実施例1と同様の操作を行
った。その結果、重合開始から5分後に突沸が発生し、
ゲルシートが部分的に裂けてしまった。 比較例2 繊維長0.1mmのポリプロピレン短繊維を使用したほ
かは実施例1と同様の操作を行った。その結果、重合開
始から5分後に突沸が発生し、ゲルシートが部分的に裂
けてしまった。 比較例3 ポリプロピレン短繊維に代えて、セルロース短繊維(平
均繊維径0.1μm)を使用したほかは実施例1と同様
の操作を行った。その結果、重合開姶から5分後に突沸
が発生し、ゲルシートが部分的に裂けてしまった。 比較例4 平均繊維径300μmのポリプロピレン短繊維を使用し
たほかは実施例1と同様の操作を行った。その結果、重
合開姶から5分後にゲルシート表面より水蒸気が出てき
たものの突沸による大きな気泡の生成やゲルシートの変
形は見られなかった。しかし、得られた吸水性樹脂は吸
水量においては通常の吸水性樹脂の2/3倍量しかなか
った。
The thickness of the obtained gel sheet was about 5 mm. After about 5 minutes, heat generation reached a peak, and although steam came out of the surface of the gel sheet, generation of large bubbles due to bumping and deformation of the gel sheet were not observed. The obtained hydrogel was dried, pulverized, and classified to obtain a fiber-containing water-absorbent resin product. Example 2 In Example 1, the added amount of the polypropylene short fiber was 20.
The same operation as in Example 1 was performed except for changing to g. As a result, as in Example 1, water vapor came out from the surface of the gel sheet 5 minutes after the start of polymerization, but generation of large bubbles due to bumping and deformation of the gel sheet were not observed. Example 3 Short polypropylene fiber (length 5 m) used in Example 1
The same operation as in Example 1 was performed except that polypropylene short fibers having a fiber length of 2 mm were used instead of m). As a result, as in Example 1, water vapor came out of the surface of the gel sheet 5 minutes after the polymerization was started, but generation of large bubbles due to bumping and deformation of the gel sheet were not observed. Example 4 The same operation as in Example 1 was performed, except that polypropylene / polyethylene composite fiber (length: 5 mm, average fiber diameter: 15 μm) was used instead of the polypropylene short fiber used in Example 1. As a result, as in Example 1, water vapor came out from the surface of the gel sheet 5 minutes after the start of polymerization, but generation of large bubbles due to bumping and deformation of the gel sheet were not observed. Example 5 The same operation as in Example 1 was performed except that polypropylene short fibers having an average fiber diameter of 5 μm were used instead of the polypropylene short fibers (average fiber diameter 25 μm) used in Example 1. As a result, as in Example 1, water vapor came out of the surface of the gel nut 5 minutes after the start of the polymerization, but no large bubbles were formed due to bumping and no deformation of the gel sheet was observed. Comparative Example 1 The same operation as in Example 1 was performed except that no fiber was added. As a result, bumping occurs 5 minutes after the start of polymerization,
The gel sheet has been partially torn. Comparative Example 2 The same operation as in Example 1 was performed except that polypropylene short fibers having a fiber length of 0.1 mm were used. As a result, bumping occurred 5 minutes after the start of the polymerization, and the gel sheet was partially torn. Comparative Example 3 The same operation as in Example 1 was carried out except that cellulose short fibers (average fiber diameter: 0.1 μm) were used instead of polypropylene short fibers. As a result, bumping occurred 5 minutes after the polymerization was started, and the gel sheet was partially torn. Comparative Example 4 The same operation as in Example 1 was performed except that polypropylene short fibers having an average fiber diameter of 300 μm were used. As a result, although water vapor came out from the gel sheet surface 5 minutes after the polymerization was started, generation of large bubbles due to bumping and deformation of the gel sheet were not observed. However, the obtained water-absorbent resin had only 2/3 times the amount of normal water-absorbent resin in water absorption.

【0020】[0020]

【発明の効果】本発明によれば、静置重合において、所
定の短繊維を重合前にアクリル酸系モノマーに含有させ
ることにより、発熱反応時に突沸等の現象を抑えられ、
重合コントロールが容易になり、効率よく繊維含有吸水
性樹脂を製造できるという効果がある。
According to the present invention, a phenomenon such as bumping during an exothermic reaction can be suppressed by allowing a predetermined short fiber to be contained in an acrylic acid monomer before polymerization in static polymerization.
There is an effect that the polymerization can be easily controlled and the fiber-containing water-absorbent resin can be efficiently produced.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】アクリル酸系モノマーの水溶液に重合開始
剤を加えて、攪拌することなく静置重合する吸水性樹脂
の製造方法において、 平均繊維径1〜100μmで長さ0.5〜10mmの短
繊維を前記アクリル酸系モノマーの水溶液に含有させて
静置重合することを特徴とする繊維含有吸水性樹脂の製
造方法。
1. A method for producing a water-absorbent resin, which comprises adding a polymerization initiator to an aqueous solution of an acrylic acid monomer and carrying out standing polymerization without stirring, comprising: an average fiber diameter of 1 to 100 μm and a length of 0.5 to 10 mm. A method for producing a fiber-containing water-absorbent resin, wherein a short fiber is contained in an aqueous solution of the acrylic acid-based monomer and subjected to static polymerization.
【請求項2】短繊維を前記モノマー100重量部に対し
て0.1〜5重量部の割合で前記アクリル酸系モノマー
の水溶液に含有させた請求項1記載の繊維含有吸水性樹
脂の製造方法。
2. The process for producing a fiber-containing water-absorbent resin according to claim 1, wherein the short fibers are contained in the aqueous solution of the acrylic acid monomer in a ratio of 0.1 to 5 parts by weight based on 100 parts by weight of the monomer. .
JP20241996A 1996-07-31 1996-07-31 Production of fiber-containing water absorbing resin Pending JPH1045812A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20241996A JPH1045812A (en) 1996-07-31 1996-07-31 Production of fiber-containing water absorbing resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20241996A JPH1045812A (en) 1996-07-31 1996-07-31 Production of fiber-containing water absorbing resin

Publications (1)

Publication Number Publication Date
JPH1045812A true JPH1045812A (en) 1998-02-17

Family

ID=16457201

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20241996A Pending JPH1045812A (en) 1996-07-31 1996-07-31 Production of fiber-containing water absorbing resin

Country Status (1)

Country Link
JP (1) JPH1045812A (en)

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US7091253B2 (en) 2000-08-03 2006-08-15 Nippon Shokubai Co., Ltd. Water-absorbent resin, hydropolymer, process for producing them, and uses of them
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US9062140B2 (en) 2005-04-07 2015-06-23 Nippon Shokubai Co., Ltd. Polyacrylic acid (salt) water-absorbent resin, production process thereof, and acrylic acid used in polymerization for production of water-absorbent resin
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