JPS6253479A - Fiber material having water absorbability imparted thereto - Google Patents

Fiber material having water absorbability imparted thereto

Info

Publication number
JPS6253479A
JPS6253479A JP60194125A JP19412585A JPS6253479A JP S6253479 A JPS6253479 A JP S6253479A JP 60194125 A JP60194125 A JP 60194125A JP 19412585 A JP19412585 A JP 19412585A JP S6253479 A JPS6253479 A JP S6253479A
Authority
JP
Japan
Prior art keywords
water
stock solution
resin
fiber material
super
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
JP60194125A
Other languages
Japanese (ja)
Other versions
JPS64505B2 (en
Inventor
早乙女 和雄
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.)
Hayashikane Shipbuilding and Engineering Co Ltd
Original Assignee
Hayashikane Shipbuilding and Engineering 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 Hayashikane Shipbuilding and Engineering Co Ltd filed Critical Hayashikane Shipbuilding and Engineering Co Ltd
Priority to JP60194125A priority Critical patent/JPS6253479A/en
Publication of JPS6253479A publication Critical patent/JPS6253479A/en
Publication of JPS64505B2 publication Critical patent/JPS64505B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Absorbent Articles And Supports Therefor (AREA)
  • Polymerisation Methods In General (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は高度の吸水性を有する繊維材料に関する。繊維
材料の形態として、紙、不織布、布あるいはウェブ、マ
ット、フェルト、綿状物などがあげられる。また繊維と
して、パルプ、綿、麻、羊毛などの天然繊維およびポリ
オレフィン、ナイロン、ポリエステルなどの合成繊維お
よびそれらの混合物が含まれる。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to fibrous materials with a high degree of water absorption. Examples of the form of the fibrous material include paper, nonwoven fabric, cloth or web, mat, felt, cotton-like material, and the like. Fibers include natural fibers such as pulp, cotton, linen, and wool, synthetic fibers such as polyolefin, nylon, and polyester, and mixtures thereof.

高吸水性樹脂粉末を紙あるいはパルプ錦に散布してなる
吸水性繊維材料が生理用ナプキンおよび紙おむつなどの
衛生材料に用いられている。
BACKGROUND OF THE INVENTION Water-absorbing fiber materials made by dispersing super-absorbent resin powder onto paper or pulp brocade are used in sanitary materials such as sanitary napkins and paper diapers.

従来の技術 高吸水性樹脂は自重の数百倍の水を吸収する性質を有し
、アクリル酸重合体および酢酸ビニル−アクリル酸エス
テル共重合体加水分解物などの高吸水性樹脂粉末が市販
されている。
Conventional technology Super-absorbent resins have the property of absorbing water hundreds of times their own weight, and super-absorbent resin powders such as acrylic acid polymers and vinyl acetate-acrylic acid ester copolymer hydrolysates are commercially available. ing.

ポリアクリル酸系高吸水性間脳の構造は、水に不溶で膨
潤する適度の架橋を有するポリアクリル酸の部分アルカ
リ金属塩で、水利ゲルのpHが中性域にあるように中和
度が調節される。装造法に関しては多数の出願特許が公
開されている。
The structure of the polyacrylic acid-based superabsorbent diencephalon is a partially alkali metal salt of polyacrylic acid with moderate crosslinks that is insoluble and swells in water, and the degree of neutralization is so that the pH of the water gel is in the neutral range. adjusted. A large number of patent applications regarding the mounting method have been published.

ポリマーの骨格はアクリル酸単独あるいはそれにメタク
リル酸、マレイン酸、アクリルアミドなどの水溶性共重
合単量体を加えた単量体の水溶液のラジカル重合によっ
て構成される。架橋の導入は、高濃度水溶液の重合によ
る自己架橋、メチレンビスアクリルアミドなどの多官能
性単量体あるいはポリマーの官能基と反応して架橋を形
成する官能基を有するN−メチロールアクリルアミドな
どの架橋性単量体の共重合、およびポリマーのカルボキ
シル基と反応性を有するエチレングリコールビスグリシ
ジルエーテルなどの架橋剤の添加などの方法によって行
なわれる。これらの方法によって、重合反応時あるいは
重合物の加熱乾燥時に適度の架橋が導入され、ポリマー
に高度の吸水性が付与される。上記の成分のほかにデン
プンあるいは多糖類を添加してグラフト重合体を生成さ
せる方法も知られている。
The polymer skeleton is constructed by radical polymerization of an aqueous solution of acrylic acid alone or a monomer containing a water-soluble comonomer such as methacrylic acid, maleic acid, or acrylamide. Crosslinking can be introduced by self-crosslinking by polymerization of a highly concentrated aqueous solution, or by crosslinking using polyfunctional monomers such as methylenebisacrylamide or N-methylolacrylamide, which has a functional group that reacts with the functional group of the polymer to form a crosslink. This is carried out by methods such as copolymerization of monomers and addition of a crosslinking agent such as ethylene glycol bisglycidyl ether that is reactive with the carboxyl group of the polymer. By these methods, a suitable amount of crosslinking is introduced during the polymerization reaction or during heating and drying of the polymer, thereby imparting a high degree of water absorption to the polymer. A method of producing a graft polymer by adding starch or polysaccharide in addition to the above-mentioned components is also known.

重合に供される水性原液は苛性アルカリによってpHが
中性域に中和され、水溶性ラジカル開始剤によって反応
が開始される。重合反応は烈しく生じ、多量の重合熱が
発生する。
The pH of the aqueous stock solution to be subjected to polymerization is neutralized to a neutral range with caustic alkali, and the reaction is initiated with a water-soluble radical initiator. The polymerization reaction occurs vigorously and a large amount of polymerization heat is generated.

重合反応を制御して工業的規模で実施する方法として、
水性原液を油相KM濁分散させる逆相懸濁重合法1重合
熱の除去を容易にする薄層重合法あるいは重合時の架橋
生成を抑制し、高粘度水溶液として攪拌流動処理し、重
合物の加熱乾燥時に架橋剤と反応する方法などが知られ
ている。
As a method to control the polymerization reaction and carry it out on an industrial scale,
Reverse-phase suspension polymerization method in which the aqueous stock solution is dispersed in the oil phase (1) Thin layer polymerization method that facilitates the removal of polymerization heat, or a thin layer polymerization method that suppresses the formation of crosslinks during polymerization and is subjected to agitation and fluidization treatment as a high viscosity aqueous solution. A method of reacting with a crosslinking agent during heat drying is known.

高吸水性樹脂粉末は、前記の如く、紙あるいはパルプ綿
に散布され生理用ナプキンや紙おむつの吸収材として利
用される。また脱脂綿に散布し吸水性を付与する例、そ
の他繊維材料に散布する試みがみられる。
As mentioned above, the superabsorbent resin powder is sprinkled on paper or pulp cotton and used as an absorbent material for sanitary napkins and paper diapers. There are also examples of spraying it on absorbent cotton to give it water-absorbing properties, and attempts to spray it on other textile materials.

発明が解決しようとする問題点 高吸水性樹脂粉末を繊維材料に散布して含有させ、′こ
れらの材料の吸水性を高める種々の例がみられるが、吸
水時に生成した水利ゲルが繊維から分離して、皮膚など
に付着して不快な感触を与える。これらの繊維材料は衛
生材料あるいは医療材料として使用される場合が多(、
水分、血液あるいは1垂液を吸収した膨潤ゲルが繊維基
材から分離することは避けねばならない。そのために、
高吸水性樹脂粉末を含む繊維材料を不織布で被覆して、
ゲルが外部にはみ出すのを防ぐなどの手段がとられる。
Problems to be Solved by the Invention There are various examples of increasing the water absorbency of these materials by scattering and incorporating superabsorbent resin powder into fiber materials. It adheres to the skin and gives an unpleasant sensation. These fiber materials are often used as sanitary or medical materials (
Separation of the swollen gel, which has absorbed moisture, blood or fluids, from the fiber substrate must be avoided. for that,
Covering fiber material containing super absorbent resin powder with non-woven fabric,
Measures are taken to prevent the gel from spilling out.

本発明者は、先にアクリル酸アルカリ金属塩を主成分と
し、ラジカル重合反応によって高吸水性樹脂を生成する
水性原液を紙あるいは布状物に含浸し、該含浸物を加熱
し、単量体成分を重合すること【よって、吸水性の付与
された紙および布状物を発明した(特願昭59−175
846 )。
The present inventor first impregnated a paper or cloth-like material with an aqueous stock solution containing an alkali metal acrylic acid salt as the main component and producing a superabsorbent resin through a radical polymerization reaction, heated the impregnated material, and obtained a monomer. By polymerizing the components, paper and cloth-like materials with water absorption properties were invented (Japanese Patent Application No. 59-175).
846).

ポリアクリル酸系高吸水性樹脂を生成する水性原液を繊
維材料に含浸重合して得られる製品は樹脂が繊維と一体
化され、高度の吸水性が付与される。吸水時において水
利ゲルが繊維から脱離することなく、あたかも材料を構
成する繊維自体に高度の吸水性が付与された如き挙動が
みられる。吸水試料を顕微鏡下に観察すると、繊維が高
吸水性樹脂によって均一に被覆されていることが確めら
れる。
In products obtained by impregnating and polymerizing fiber materials with an aqueous stock solution that produces polyacrylic acid-based superabsorbent resin, the resin is integrated with the fibers and a high degree of water absorption is imparted. When absorbing water, the water-use gel does not separate from the fibers, and the material behaves as if the fibers themselves had a high degree of water absorption. Observation of the water-absorbed sample under a microscope confirms that the fibers are uniformly coated with the superabsorbent resin.

このようにして製造された吸水性繊維材料は樹脂粉末を
散布した従来品に比べて著しい特長をもつが、一方問題
点として、樹脂含量が高くなると、繊維材料が乾燥時に
硬くなり、樹脂を含まない材料の柔軟性が損なわれる傾
向がみられる。
The water-absorbing fiber material produced in this way has remarkable advantages compared to conventional products that are sprayed with resin powder, but on the other hand, the problem is that when the resin content is high, the fiber material becomes hard when drying, and the resin does not contain the water-absorbing fiber material. There is a tendency for the flexibility of the material to be impaired.

従って、繊維材料の柔軟性を損なうことなく、高吸水性
樹脂含量を高めて高度の吸水性を付与することができれ
ば、その実用的効果は大である。
Therefore, if it is possible to impart a high degree of water absorption by increasing the superabsorbent resin content without impairing the flexibility of the fiber material, it would have a great practical effect.

問題点を解決するための手段 高吸水性樹脂微粉末が散布されて含まれる繊維材料に、
アクリル酸部分アルカリ金属塩を主成分とし、ラジカル
重合反応によって高吸水性樹脂を生成するpHが中性域
にある水性原液を含浸させ、該含浸物を加熱して水性原
液に含まれる単量体成分を重合して、高度の吸水性の付
与された繊維材料が得られることが判った。製品である
繊維材料に含まれる゛高吸水性樹脂の量は、あらかじめ
粉末として散布された量と水性原液の重合により生成し
た樹脂量の和で表わされる。
Means to solve the problem The fiber material containing super absorbent resin fine powder is sprinkled with it.
An aqueous stock solution containing a partial alkali metal salt of acrylic acid as a main component and having a pH in the neutral range that produces a superabsorbent resin through a radical polymerization reaction is impregnated, and the impregnated material is heated to remove the monomers contained in the aqueous stock solution. It has been found that the components can be polymerized to provide a highly water-absorbing fibrous material. The amount of superabsorbent resin contained in the fiber material that is the product is expressed as the sum of the amount sprayed in advance as a powder and the amount of resin produced by polymerization of the aqueous stock solution.

上記の方法で得られる繊維材料は、樹脂含量に相当する
高度の吸水性を示すばかりでなく、樹脂粉末が重合によ
り生成した樹脂によって強固に繊維に結合され、一体化
される結果、吸水時に水和ゲルが繊維から脱離すること
が防がれる。さらに、繊維を被覆する形で生成する樹脂
量は、該繊維材料の柔軟性を損ねない種度で、しかも樹
脂粉末を充分強固に繊維基体に結合することができる。
The fiber material obtained by the above method not only exhibits a high degree of water absorption corresponding to the resin content, but also the resin powder is strongly bonded to the fibers by the resin produced by polymerization and is integrated, so that when water is absorbed, the fiber material absorbs water. The Japanese gel is prevented from detaching from the fibers. Furthermore, the amount of resin produced to coat the fibers is at a level that does not impair the flexibility of the fiber material, and can bond the resin powder to the fiber substrate sufficiently firmly.

その結果、前掲の問題点を解決し、高度の吸水性が付与
され、吸水時に水利ゲルの脱離がなく、しかも柔軟性の
損なわれない本発明の繊維材料が得られる。
As a result, the fiber material of the present invention can be obtained which solves the above-mentioned problems, has a high degree of water absorption, does not detach the water gel when water is absorbed, and does not lose its flexibility.

本発明に適用される繊維は材質的には特に限定されず、
前述の如き各種繊維が用いられるが、セルロース系繊維
が特に好適である。繊維材料の形態も、前述の如(、用
途に応じて種々の形状が選ばれる。
The fibers applied to the present invention are not particularly limited in terms of material,
Although various fibers such as those mentioned above can be used, cellulose fibers are particularly suitable. The form of the fiber material is also as described above (various forms are selected depending on the application).

あらかじめ散布される高吸水性樹脂微粉末の粒度は10
0メツシユ以下が好ましく、200メツシユ以下の激粉
末も好適に用いられる。高吸水性樹脂を粉砕して粉末製
品を製造する際に副生ずる好ましくない200メ、シュ
以下の微粉末も本発明の製品に好適である。
The particle size of the super absorbent resin fine powder sprinkled in advance is 10
It is preferably 0 mesh or less, and a powder of 200 mesh or less is also suitably used. The undesirable fine powder of 200 mm or less, which is produced as a by-product when a super absorbent resin is pulverized to produce a powder product, is also suitable for the product of the present invention.

アクリル酸部分アルカリ金属塩を主成分とし、ラジカル
重合反応によって高吸水性樹脂を生成する水性原液は公
知の方法に準じて調製される。その概要は前述の如(で
あるが、好ましい例をあげると次のようである。
An aqueous stock solution containing a partial alkali metal salt of acrylic acid as a main component and producing a superabsorbent resin through a radical polymerization reaction is prepared according to a known method. The outline is as described above, but a preferred example is as follows.

アクリル酸水溶液に苛性ソーダを加えてカルボキシル基
の70〜80モル俤を中和した濃度20〜40重f%の
中性水溶液にラジカル開始剤と架橋剤成分を添加して水
性原液を調製する。ラジカル開始剤は通常過硫醸カリな
どの過硫竣塩が用いられる。架橋導入の手段として前述
の如き種々の方法があげられるが、メチレビスアクリル
アミドなどの多官能共重合単量体の添加、あるいは本発
明者の発明によるラジカル架橋法(特願昭6O−136
653)  の適用が適当である。
An aqueous stock solution is prepared by adding a radical initiator and a crosslinking agent component to a neutral aqueous solution having a concentration of 20 to 40% by weight, which is obtained by adding caustic soda to an acrylic acid aqueous solution to neutralize 70 to 80 moles of carboxyl groups. As the radical initiator, a persulfate salt such as persulfurized potassium is usually used. As means for introducing crosslinking, there are various methods as mentioned above, including the addition of a polyfunctional comonomer such as methylbisacrylamide, or the radical crosslinking method invented by the present inventor (Japanese Patent Application No. 6O-136).
653) is appropriate.

作用 繊維材料に散布される高吸水性樹脂微粉末量ならびに水
性原液およびそれから生成するポリアクリル酸系高吸水
性樹脂量は製品に求められる吸水性に応じて調節される
The amount of superabsorbent resin fine powder sprinkled on the working fiber material, the aqueous stock solution and the amount of polyacrylic acid-based superabsorbent resin produced therefrom are adjusted depending on the water absorbency required for the product.

水性原液から生成する樹脂量は、繊維材料に対して数多
(x量)あれば、散布された樹脂粉末を繊維に固着させ
るの罠有効である。一方、樹脂量の上限は製品および用
途によって異なり、一般に4維材料に対して半渣以下で
ある。
If the amount of resin produced from the aqueous stock solution is a large number (x amount) relative to the fiber material, it will be effective in fixing the dispersed resin powder to the fibers. On the other hand, the upper limit of the amount of resin varies depending on the product and application, and is generally less than half the amount of resin per 4-fiber material.

本発明の吸水性ra維材料はそれ自体として吸水材とし
て用いられるが、その形態がウェブ、マットあるいは綿
状物の場合、繊維を開繊し樹脂を含まない#R維と混合
して用いることもできる。たとえば、吸水性加工脱脂綿
を製品とする場合、高吸水性樹脂粉末を散布された脱脂
綿に水性原液を含浸させ、重合処理して得られる乾燥生
成物を開繊し、未処理脱脂綿と均一に混合したのち、ロ
ール綿、力、ト綿などの製品に加工する方法があげられ
る。混合綿から得られる製品は乾燥時および吸水時の感
触く優れ、高度の吸水性が付与されるばかりでなく、水
和ゲルが4#1.維から脱離することがない。
The water-absorbing RA fiber material of the present invention can be used as a water-absorbing material by itself, but when it is in the form of a web, mat, or cotton, the fibers can be spread and mixed with #R fibers that do not contain resin. You can also do it. For example, when producing water-absorbent treated absorbent cotton, absorbent cotton sprinkled with superabsorbent resin powder is impregnated with an aqueous stock solution, the dried product obtained by polymerization is opened, and then mixed uniformly with untreated absorbent cotton. After that, it can be processed into products such as rolled cotton, chikara, and tofu. Products obtained from blended cotton not only have an excellent dry and absorbent feel and are highly absorbent, but also have a hydrated gel of 4#1. There is no possibility of detachment from the fiber.

本発明の吸水性#1.維材料は異なる繊維の混合あるい
は組合せ、積層などにより多彩な製品が展開される。
Water absorbency #1 of the present invention. A wide variety of textile products are developed by mixing, combining, and laminating different fibers.

実施例1゜ 苛性ソーダ(純度93’1)34部を水230部に溶解
した水溶液に、アクリル酸72部、メチレンビスアクリ
ルアミド0.16部および過硫酸カリ0.2部を添加し
て、pHが6.8の水性原液を調製した。
Example 1 To an aqueous solution of 34 parts of caustic soda (purity 93'1) dissolved in 230 parts of water, 72 parts of acrylic acid, 0.16 parts of methylenebisacrylamide and 0.2 parts of potassium persulfate were added to adjust the pH. An aqueous stock solution of 6.8 was prepared.

マット状のパルプ綿に160メ、シュを通過したポリア
クリル酸系高吸水性樹脂微粉末をパルプ綿100 f轟
り8tを均一に散布分散させ、それに上記水性原液をパ
ルプ綿100を当り32fを噴霧して均一に含浸させた
。この水性原液含浸物を窒素気中で95℃の温度で30
分間重合した。
The polyacrylic acid-based super water absorbent resin fine powder that has passed through a 160-meter mesh was uniformly dispersed on a matte pulp cotton using 100 f/8 tons of pulp cotton, and the above aqueous stock solution was added to the pulp cotton at a rate of 32 f per 100 m/s of pulp cotton. Spray to uniformly impregnate. This aqueous stock solution impregnated product was heated at a temperature of 95°C in a nitrogen atmosphere for 30 minutes.
Polymerized for minutes.

乾燥した生成物の重量から、パルプ綿100P当り16
tの高吸水性樹脂が含まれる。その中の8fは水性原液
の重合によるものである。
From the weight of the dry product, 16 per 100P of pulp cotton
Contains t super absorbent resin. Of these, 8f is due to polymerization of the aqueous stock solution.

試料1りを水に投入し、20分後に水から引き上げて吸
水物の重量を測定し、45fであった。
One sample was put into water, and 20 minutes later, it was taken out of the water and the weight of the absorbed water was measured, and it was 45 f.

散布した樹脂の吸水率は自重の280倍、パルプ綿自体
の吸水率は自重の11倍と求められた。従って、水性原
液から生成した樹脂の吸水率は自重の240倍と計算さ
れる。
The water absorption rate of the sprayed resin was determined to be 280 times its own weight, and the water absorption rate of the pulp cotton itself was determined to be 11 times its own weight. Therefore, the water absorption rate of the resin produced from the aqueous stock solution is calculated to be 240 times its own weight.

生成物は未処理バルブ綿に比べて約4倍の吸水能を有し
、吸水物は樹脂を散布した試料にみられるような水和ゲ
ルの脱離は認められず、また柔軟な感触を与える。
The product has approximately 4 times the water absorption capacity compared to untreated valve cotton, and the water absorbent material does not exhibit the detachment of hydrated gel seen in samples sprayed with resin, and also provides a soft feel. .

実施例2゜ 実施例1の高吸水性樹脂粉末を、パルプ系不織布および
ポリエステル系不織布にそれぞれ不織布100P当り6
?の比率で散布した。これらに実施例1の水性原液を不
織布100f当り4Ctの割合で均一に噴霧含浸させた
。次に含浸試料を実施例1と同様に重合処理した。
Example 2゜The super absorbent resin powder of Example 1 was applied to a pulp-based nonwoven fabric and a polyester-based nonwoven fabric at a rate of 6 per 100P of nonwoven fabric.
? It was distributed at a ratio of These were uniformly impregnated with the aqueous stock solution of Example 1 at a rate of 4 Ct per 100 f of nonwoven fabric. Next, the impregnated sample was subjected to polymerization treatment in the same manner as in Example 1.

乾燥した生成物は、原料不織布100 ?括り樹脂粉末
6f、水性原液からの重合樹脂109を含む。
The dried product is 100% raw material nonwoven fabric. Contains binder resin powder 6f and polymerized resin 109 from an aqueous stock solution.

各試料1fの吸水物の重量は、パルプ系不織布43f、
ポリエステル系不織布32fであった。
The weight of the water absorbent of each sample 1f is as follows: 43f of pulp-based nonwoven fabric;
It was polyester nonwoven fabric 32f.

なお、吸水試料は水利ゲルの脱離がみられず、感触的に
も良好であった。
In addition, the water-absorbed sample showed no detachment of the water-use gel and had a good feel.

実施例3 アクリル酸72部、苛性ソーダ(純度93チ)34部、
メチレンビスアクリルアミド0.05部、過硫酸力IJ
 O,1部および水115部から水性原液を調製した。
Example 3 72 parts of acrylic acid, 34 parts of caustic soda (purity 93%),
Methylenebisacrylamide 0.05 part, persulfate power IJ
An aqueous stock solution was prepared from 1 part O, and 115 parts water.

脱脂綿を空気中に流動分散させ、脱脂綿1001当り、
実施例1の高吸水性樹脂微粉末10?を均一に散布し、
また上記原液201を均一に噴霧して含浸させた。含浸
物を圧縮し、窒素気中で、95℃の温度で30分間重合
処理した。
Absorbent cotton is fluidized and dispersed in the air, and per 1001 absorbent cotton,
Super absorbent resin fine powder 10 of Example 1? Spread evenly,
Further, the above stock solution 201 was uniformly sprayed to impregnate. The impregnated material was compressed and polymerized at a temperature of 95° C. for 30 minutes in a nitrogen atmosphere.

乾燥した生成物は、脱脂綿100P当り、樹脂粉末10
?および水性原液からの重合樹脂32を含む。この試料
1fの吸水物の重量は4817であった。また脱脂綿1
fの吸水物の重量は122である。
The dried product is 10 resin powder per 100 P of absorbent cotton.
? and polymerized resin 32 from an aqueous stock solution. The weight of the water absorbed material of this sample 1f was 4817. Also absorbent cotton 1
The weight of the water absorption material f is 122.

次に生成物を乾式開繊すると同時に未処理脱脂綿と混合
して、生成物1部に対して脱脂綿2部の割合からなる均
一な混合物を得た。このもの1fからの吸水物の重量は
24fであり、未処理脱脂綿の約2倍の吸水性を有する
。吸水物は水和ゲルの脱離がみられず、また感触的にも
通常の脱脂綿とほとんど変らない。
The product was then dry-opened and simultaneously mixed with untreated absorbent cotton to obtain a homogeneous mixture consisting of 1 part of product and 2 parts of absorbent cotton. The weight of the water absorbed from 1f of this product is 24f, which is about twice the water absorbency of untreated absorbent cotton. The water-absorbing material does not show any detachment of the hydrated gel, and its feel is almost the same as that of regular absorbent cotton.

発明の効果 実施例に示される如く、本発明の吸水性繊維材料は、従
来の樹脂粉末散布製品にみられる水利ゲルの基材からの
分離がみられず、高度の吸水性と良好な感触を有する。
Effects of the Invention As shown in the examples, the water-absorbing fiber material of the present invention does not exhibit separation of the water gel from the base material, which is seen in conventional resin powder spraying products, and has high water absorption and a good feel. have

吸水性繊維材料は種々の形態が可能で、他種吸水材と混
合あるいは組合せにより多彩な吸水材料製品が展開され
る。
Water-absorbing fiber materials can take various forms, and a wide variety of water-absorbing material products can be developed by mixing or combining them with other types of water-absorbing materials.

Claims (2)

【特許請求の範囲】[Claims] (1)高吸水性樹脂微粉末を含む繊維材料に、アクリル
酸部分アルカリ金属塩を主成分として含み、ラジカル重
合反応によって高吸水性樹脂を生成するpHが中性域に
ある水性原液を含浸させ、該含浸物を加熱して水性原液
に含まれる単量体成分を重合して製造される吸水性の付
与された繊維材料。
(1) A fiber material containing fine powder of a super absorbent resin is impregnated with an aqueous stock solution containing a partial alkali metal salt of acrylic acid as a main component and having a pH in the neutral range that produces a super absorbent resin through a radical polymerization reaction. A fibrous material imparted with water absorbency, which is produced by heating the impregnated material and polymerizing the monomer components contained in the aqueous stock solution.
(2)高吸水性樹脂微粉末を含む繊維材料が、高吸水性
樹脂微粉末の散布されたセルロース系繊維材料である特
許請求の範囲第一項記載の吸水性の付与された繊維材料
(2) The fibrous material imparted with water absorption properties according to claim 1, wherein the fibrous material containing the super-absorbent resin fine powder is a cellulose-based fiber material on which the super-absorbent resin fine powder is dispersed.
JP60194125A 1985-09-03 1985-09-03 Fiber material having water absorbability imparted thereto Granted JPS6253479A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60194125A JPS6253479A (en) 1985-09-03 1985-09-03 Fiber material having water absorbability imparted thereto

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60194125A JPS6253479A (en) 1985-09-03 1985-09-03 Fiber material having water absorbability imparted thereto

Publications (2)

Publication Number Publication Date
JPS6253479A true JPS6253479A (en) 1987-03-09
JPS64505B2 JPS64505B2 (en) 1989-01-06

Family

ID=16319323

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60194125A Granted JPS6253479A (en) 1985-09-03 1985-09-03 Fiber material having water absorbability imparted thereto

Country Status (1)

Country Link
JP (1) JPS6253479A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62133185A (en) * 1985-12-04 1987-06-16 マルハ株式会社 Modified cotton improved in absorbability
JPS62243606A (en) * 1986-04-15 1987-10-24 Kao Corp Production of liquid-absorbing composite
JPH02175281A (en) * 1988-12-28 1990-07-06 Ricoh Co Ltd Heat sensitive recording material
US5779737A (en) * 1994-04-15 1998-07-14 Courtaulds Fibres Holdings Limited Fibre treatment
US7338625B2 (en) 2002-09-18 2008-03-04 Kimberly-Clark Worldwide, Inc. Methods of restoring elasticity after stiffening treatments
JP2010095572A (en) * 2008-10-14 2010-04-30 Mitsubishi Rayon Co Ltd Molded product of fiber-containing resin and method for producing the same
WO2023149574A1 (en) * 2022-02-04 2023-08-10 株式会社日本触媒 Polymerization method for water absorbent resin

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9408742D0 (en) * 1994-05-03 1994-06-22 Courtaulds Fibres Holdings Ltd Fabric treatment
CN117283539A (en) 2016-09-30 2023-12-26 3Sae技术有限公司 Multi-axis relative positioning table

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62133185A (en) * 1985-12-04 1987-06-16 マルハ株式会社 Modified cotton improved in absorbability
JPH0122388B2 (en) * 1985-12-04 1989-04-26 Taiyo Fishery Co Ltd
JPS62243606A (en) * 1986-04-15 1987-10-24 Kao Corp Production of liquid-absorbing composite
JPH02175281A (en) * 1988-12-28 1990-07-06 Ricoh Co Ltd Heat sensitive recording material
US5779737A (en) * 1994-04-15 1998-07-14 Courtaulds Fibres Holdings Limited Fibre treatment
US7338625B2 (en) 2002-09-18 2008-03-04 Kimberly-Clark Worldwide, Inc. Methods of restoring elasticity after stiffening treatments
JP2010095572A (en) * 2008-10-14 2010-04-30 Mitsubishi Rayon Co Ltd Molded product of fiber-containing resin and method for producing the same
WO2023149574A1 (en) * 2022-02-04 2023-08-10 株式会社日本触媒 Polymerization method for water absorbent resin

Also Published As

Publication number Publication date
JPS64505B2 (en) 1989-01-06

Similar Documents

Publication Publication Date Title
EP0159371B1 (en) A method for preparing an absorbent fibrous fluff, the fibrous fluff prepared by the method, and an absorbent device containing the fibrous fluff
JP3205168B2 (en) Absorbent composition for disposable diapers
TWI288645B (en) Superabsorbent polymers having a slow rate of absorption
US5693707A (en) Liquid absorbent composition for nonwoven binder applications
JPH0558030B2 (en)
JPS58131133A (en) Production of absorbing material
EP0608460A1 (en) Water-decomposable non-woven fabric
MXPA00012254A (en) Absorbent structures coated with foamed superabsorbent polymer
EP1448242A1 (en) Crosslinked polyamine coating on superabsorbent hydrogels
TW200305448A (en) Superabsorbent composite and absorbent articles including the same
CN101111540A (en) Polyamine-coated superabsorbent polymers
KR950012339B1 (en) Process for the preparation of water-absorptive composite
JPS6253479A (en) Fiber material having water absorbability imparted thereto
JPH01121306A (en) Production of water absorbing complex
JP3444722B2 (en) Method for producing water-absorbing composite
DE60031560T2 (en) Aqueous Superabsorbent Polymers, and Methods of Use
JPS6328639A (en) Liquid-absorbing composite body and manufacture thereof
US3743536A (en) Nonwoven sponge fabric
JP3078049B2 (en) Manufacturing method of absorber
JPS61296162A (en) Water absorbability imparted paper and nonwoven fabric
JPS6222811A (en) Production of water-absorptive composite
JPS62133183A (en) Production of water absorbable composite
JPH051821B2 (en)
KR860001384B1 (en) Method for preparing absorbent fibrous fluff
JPS6262829A (en) Production of water-absorbing composite