JPH022982B2 - - Google Patents

Info

Publication number
JPH022982B2
JPH022982B2 JP56007276A JP727681A JPH022982B2 JP H022982 B2 JPH022982 B2 JP H022982B2 JP 56007276 A JP56007276 A JP 56007276A JP 727681 A JP727681 A JP 727681A JP H022982 B2 JPH022982 B2 JP H022982B2
Authority
JP
Japan
Prior art keywords
pulp
thermoplastic resin
weight
nonionic surfactant
water
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.)
Expired - Lifetime
Application number
JP56007276A
Other languages
Japanese (ja)
Other versions
JPS57121657A (en
Inventor
Koji Horimoto
Yoshinori Morita
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.)
Mitsui Petrochemical Industries Ltd
Original Assignee
Mitsui Petrochemical Industries 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 Mitsui Petrochemical Industries Ltd filed Critical Mitsui Petrochemical Industries Ltd
Priority to JP56007276A priority Critical patent/JPS57121657A/en
Publication of JPS57121657A publication Critical patent/JPS57121657A/en
Publication of JPH022982B2 publication Critical patent/JPH022982B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Nonwoven Fabrics (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は吸収用材料の製法に関するものであ
り、より詳細には、水性液体の吸収性等に優れた
吸収用材料の製法に関する。 〔従来技術〕 木材パルプ等を細かく粉砕した植物性繊維素材
に熱可塑性樹脂繊維を混合して、熱を加えながら
適度に加圧し、立体形状の繊維質吸収体とし、紙
おむつ等の用途に用いることは特開昭53−17455
号公報に開示されている。 また、特開昭55−16611号公報には、木材パル
プ、熱可塑性樹脂繊維に、更にポリグルコース又
はサツカロースのアクリル酸グラフト重合物など
の保水性高分子物質の粉末を併用して乾式抄紙に
より得られる吸水性シートが紙おむつ等の用途に
用いられることを開示している。 これらの技術において、熱可塑性樹脂繊維素材
は、木材パルプ中に、より均一に混合されること
が望ましく、また加熱処理によつて熱可塑性樹脂
繊維が、溶融し、木材パルプは各所で係留され
る。このような吸収用材料は、繊維相互の絡み合
いが強化されており、弾力性、復元性などの形状
安定性に優れた製品となることが知られている。 〔発明が解決しようとする問題点〕 しかしながら、熱可塑性樹脂繊維を多量に配合
すると、吸収用材料の機械的強度は改良される
が、吸水性の低下は避けることができない。従つ
て、熱可塑性樹脂繊維の使用割合は、用途に応じ
て機械的強度と吸水性能を勘案して決められてい
る。 一方、熱可塑性樹脂の親水性を改善するため、
表面をポリビニルアルコール、ポリアクリル酸等
の種々の界面活性剤で処理することが特公昭52−
47049号公報で知られている。しかるにこれらの
繊維を併用して作成された吸収用材料は、界面活
性剤の種類により吸収性能が著しく異なり、中に
は水を吸収させるために圧縮、復元等を繰り返し
て強制的に水を吸収させなければならず、表面に
水を滴下させただけでは水が吸収浸透しないもの
もある。 また、特開昭54−59466号公報には、ポリプロ
ピレン樹脂に10重量%の界面活性剤を配合した物
をパルプ状物に形成し、それを植物性繊維素材に
使用したものが開示されている。しかし、このよ
うな吸収用材料はパルプ状物の内部に大部分の界
面活性剤が存在するため、その配合量の多量にも
かかわらず親水性への寄与が低く却つて熱融着処
理時に低温で簡単に繊維形態が失われる虞があ
り、吸収用材料として好ましくない。本発明は、
このような事情に鑑みてなされたもので、上記の
ような熱可塑性樹脂繊維を併用した吸収用材料の
製法に関するものであり、特に、水性液体の浸透
性に優れると共に、その保水性に優れた吸収用材
料の製法を提供することを目的としている。 〔問題点を解決するための手段〕 前記目的を達成するために、本発明に係る吸収
用材料の製法では、HLB値が3乃至20の範囲に
ある非イオン性界面活性剤で表面又は表層部を処
理した、前記非イオン性界面活性剤の保持量が
0.5重量%以上4重量%以下である熱可塑性樹脂
パルプ状物5乃至50重量%と、植物性繊維素材95
乃至50重量%とを混合し、流体性熱媒体を介して
熱融着処理することを特徴としている。 〔発明の好ましい実施態様〕 以下、本発明に係る吸収用材料の製法の好まし
い態様を説明する。 (1) 使用される熱可塑性樹脂パルプ状物(以下、
「合成パルプ」と略称することがある。)として
は、ポリエチレン、ポリプロピレン、エチレン
−プロピレン共重合体、エチレン−1−ブテン
共重合体、エチレン−4−メチル−1−ペンテ
ン共重合体等のα−オレフインの1種または2
種以上からなるポリオレフイン樹脂の微細繊維
状物が好適であり、例えば特公昭52−47049号
公報等に開示されているフラツシユ紡糸法によ
つて得られるものが好ましい。 (2) 使用される非イオン性界面活性剤としては、
例えば、ポリオキシエチレンアルキルエーテ
ル、ポリオキシエチレンアルキルフエニルエー
テル、ポリオキシエチレン脂肪酸エステル等が
ある。中でも、1,5−ソルビタン、3,4−
ソルビタン、1,4−ソルビタン等のソルビタ
ンのモノ脂肪酸エステル、或いはソルビタンモ
ノ脂肪酸に更にポリエチレンオキサイド等のポ
リアルキレンオキサイドを反応させた化合物、
グリセリンジ脂肪酸エチレン等の多価アルコー
ルの部分エステルが好適である。 これ等の非イオン性界面活性剤は熱可塑性樹
脂パルプ状物の表面及び表層部(後述のフラツ
シユ紡糸による場合)を予め処理するものであ
り、その後に植物性繊維素材と混合し、これを
熱融着処理することによつて、熱可塑性樹脂パ
ルプ状物の表面のみが溶融し、熱可塑性樹脂パ
ルプ状物の形態を維持したまま、植物性繊維素
材と結合され、吸収用材料となるものである。
この際、非イオン性界面活性剤は、熱可塑性樹
脂パルプ状物の表面及び表層部に0.5重量%以
上4重量%以下、好ましくは0.7乃至3重量%
の割合で保持される。非イオン性界面活性剤の
量が多かつたり、又は熱可塑性樹脂パルプ状物
の内部に多く含まれると機械的強度が低下し、
吸収用材料としての商品価値が劣るものとな
る。 これ等の非イオン性界面活性剤を用いて得ら
れる吸収用材料は水性液体の浸透性に特に優れ
ており、また浸透した水性液体の保持性にも優
れている。 本発明で用いられる非イオン性界面活性剤は
通常水溶性でないものが多く、種々のHLBの
値をとり得る。中でもHLBの値の大きなもの
は比較的少量で水性液体浸透性を改良すると共
に、吸収用材料に水性液体が浸透した後も、吸
収用材料は水性液体を有効に保持し続けること
ができる。また、HLB値が大きすぎると、親
油性が低下して熱可塑性樹脂との相溶性が悪く
なり、非イオン性界面活性剤は処理時の熱可塑
性樹脂への吸着性及び熱融着処理後の樹脂への
保持性が悪くなる。 従つて、このような要件に適合するために、
非イオン性界面活性剤のHLB値は3乃至20の
範囲にあり、より好ましくは4乃至17の範囲で
ある。合成パルプに非イオン性界面活性剤処理
を行うには、以下の種々の方法が採用される。 非イオン性界面活性剤を添加した水スリラ
ーに合成パルプを浸漬する湿式法。尚、熱可
塑性樹脂をフラツシユ紡糸方法等によつて合
成パルプ状物に形成する場合に、非イオン性
界面活性剤を添加した溶液中に熱可塑性樹脂
の高温溶液又は融解液等を噴出して、熱可塑
性樹脂の合成パルプを形成させると同時に合
成パルプの表層部に非イオン性界面活性剤を
含浸させるのが好ましい。 合成パルプの表面に予め非イオン性界面活
性剤を噴霧等の方法でコーテングする乾式
法。 中でも、本発明においてはHLB値が3乃
至20の非イオン性界面活性剤を合成パルプの
水スラリー中に添加撹拌するだけで、効率よ
く、ほぼ全量を合成パルプに吸着させること
ができるので、好ましい処理方法として推奨
される。 (3) 植物性繊維素材(以下「木材パルプ」と略称
することがある。)としては、各種木材パルプ、
レーヨン短繊維が例示される。 (4) 吸収用材料は、予め非イオン性界面活性剤で
処理した合成パルプ5乃至50重量%と木材パル
プ95乃至50重量%とを混合し、ウエブ状に形成
したものを流体性熱媒体を介して加熱融着する
ことによつて製造される。合成パルプと木材パ
ルプの混合物を得るには湿式抄造法、乾式抄造
法の何れをも採用することができる。 合成パルプの割合が5重量%未満であると、
融着処理による機械的強度の改善は殆ど見られ
ず、また、50重量%を超えると、吸収性能の低
下は避けることができない。 また、合成パルプを融着処理するには、エア
ーオーブン、赤外線ヒータ等の間接加熱が行わ
れる。間接加熱とは気体、液体等の流体性熱媒
体によつて加熱されることを意味する。このよ
うな間接加熱は無圧状態で吸収用材料の表面と
内部とにおいて同時に均一な熱融着処理を行う
ことができ、この為、合成パルプの形態を維持
させた状態で嵩高な吸収用材料を得ることがで
きる。加熱温度は合成パルプの素材である熱可
塑性樹脂の種類にもよるが、使用熱可塑性樹脂
の融点以上乃至融点よりも約50℃高い温度の範
囲が好ましい。 本発明の吸収用材料は通常、ウエブ状であり加
熱温度や加圧条件によつて、ある程度の嵩密度を
調節することができ、必要に応じて融着処理と同
時にプレス処理を行い。種々の嵩密度の製品とす
ることができる。 本発明の吸収用材料には、その吸収性能を更に
改善する為に他の保水性物質が併用されていても
よい。このような保水性物質としては、例えば前
記特開昭56−16611号公報に開示されているよう
に種々の高分子電解質の微粒子を例示することが
できる。中でも好適な併用物質は木材パルプ、木
綿、デンプンのようなポリグリコース或いはサツ
カロース、アクリル酸やアクリロニトリルのよう
な親水性の基又は加水分解物である。 〔発明の効果〕 本発明の製法によつて得られる吸収用材料は、
水性液体の吸収性、保持性に優れると共に、機械
的強度に優れ、簡単に製造することができ、生理
用ナプキン、医療用スポンジ、傷当てパツド、タ
オル等に使用され、用途に応じて保水性の小さい
外装材や不透水性の裏打材を積層することが行わ
れる。 〔実施例〕 以下実施例を示す。 実施例 1 高密度ポリエチレン製合成パルプ(繊維平均長
さ0.9ミリ)20gを水1中に投入し、グリセリ
ンモノステアレート150mgを投入して撹拌後、分
離採取した。この合成パルプにはグリセリンモノ
ステアレートが0.75重量%含まれていた。 この合成パルプ12g及び紙綿48gを均一に混合
し、乾式抄造によつて目付け375g/m2のウエブ
状物を成形した。このウエブ状物を150℃のエア
ーオーブン中に10分間入れて合成パルプの融着処
理を行つた。 得られた吸収用材料の吸収性能を見る為に、水
平に静置された吸収用材料の表面にスポイトで水
道水を1c.c.滴下し、水滴が吸収用材料の表面上か
ら内部に浸透し終わるまでの所要時間を測定した
結果、0.7秒であつた。 実施例 2及び3 実施例1において、合成パルプに対するグリセ
リンモノステアレートの使用量を変える以外には
同様に行つた。結果を第1表に示す。 【表】
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for producing an absorbent material, and more particularly, to a method for producing an absorbent material having excellent absorbency for aqueous liquids. [Prior art] Thermoplastic resin fibers are mixed with a vegetable fiber material made by finely pulverizing wood pulp, etc., and moderately pressurized while applying heat to form a three-dimensional fibrous absorbent material, which is used for purposes such as disposable diapers. is Japanese Patent Publication No. 53-17455
It is disclosed in the publication No. In addition, JP-A No. 55-16611 discloses that wood pulp, thermoplastic resin fibers, and powders of water-retentive polymers such as polyglucose or sutucarose grafted with acrylic acid are used in combination to obtain paper by dry papermaking. It is disclosed that the water-absorbent sheet is used for purposes such as disposable diapers. In these technologies, it is desirable that the thermoplastic resin fiber material is mixed more uniformly into the wood pulp, and the thermoplastic resin fibers are melted by heat treatment and the wood pulp is moored at various locations. . It is known that such absorbent materials have strengthened intertwining of fibers, resulting in products with excellent shape stability such as elasticity and restorability. [Problems to be Solved by the Invention] However, when a large amount of thermoplastic resin fiber is blended, although the mechanical strength of the absorbent material is improved, a decrease in water absorbency cannot be avoided. Therefore, the proportion of thermoplastic resin fibers used is determined depending on the application, taking into consideration mechanical strength and water absorption performance. On the other hand, to improve the hydrophilicity of thermoplastic resin,
The surface was treated with various surfactants such as polyvinyl alcohol and polyacrylic acid.
It is known from Publication No. 47049. However, the absorption performance of absorbent materials made by using these fibers in combination differs markedly depending on the type of surfactant, and some require repeated compression and restoration to absorb water forcibly. For some products, simply dropping water on the surface will not absorb the water. Furthermore, JP-A-54-59466 discloses a pulp-like material prepared by blending a polypropylene resin with 10% by weight of a surfactant, which is then used as a vegetable fiber material. . However, since most of the surfactant in such absorbent materials is present inside the pulp-like material, its contribution to hydrophilicity is low despite the large amount of surfactant contained within the pulp, and on the contrary, it is difficult to maintain low temperatures during heat fusion processing. There is a risk that the fiber form will be easily lost, making it undesirable as an absorbent material. The present invention
This was developed in view of these circumstances, and relates to a method for producing an absorbent material that uses thermoplastic resin fibers as described above. The purpose is to provide a method for producing absorbent materials. [Means for solving the problem] In order to achieve the above object, in the method for producing an absorbent material according to the present invention, the surface or surface layer is coated with a nonionic surfactant having an HLB value in the range of 3 to 20. The retained amount of the nonionic surfactant was treated with
5 to 50% by weight of thermoplastic resin pulp which is 0.5% to 4% by weight and vegetable fiber material 95
It is characterized in that it is mixed with 50% by weight and subjected to heat fusion treatment via a fluid heat medium. [Preferred Embodiments of the Invention] Preferred embodiments of the method for producing an absorbent material according to the present invention will be described below. (1) Thermoplastic resin pulp used (hereinafter referred to as
It is sometimes abbreviated as "synthetic pulp." ) is one or two α-olefins such as polyethylene, polypropylene, ethylene-propylene copolymer, ethylene-1-butene copolymer, and ethylene-4-methyl-1-pentene copolymer.
A fine fibrous material of a polyolefin resin consisting of at least one type of polyolefin resin is suitable, and one obtained, for example, by the flash spinning method disclosed in Japanese Patent Publication No. 52-47049 is preferred. (2) The nonionic surfactants used are:
Examples include polyoxyethylene alkyl ether, polyoxyethylene alkyl phenyl ether, polyoxyethylene fatty acid ester, and the like. Among them, 1,5-sorbitan, 3,4-
Sorbitan, sorbitan monofatty acid ester such as 1,4-sorbitan, or a compound obtained by reacting sorbitan monofatty acid with polyalkylene oxide such as polyethylene oxide,
Partial esters of polyhydric alcohols such as glycerine difatty acid ethylene are preferred. These nonionic surfactants are used to pre-treat the surface and surface layer of thermoplastic resin pulp (in the case of flash spinning described below), and then mix it with vegetable fiber material and heat it. By fusion treatment, only the surface of the thermoplastic resin pulp is melted, and while maintaining the form of the thermoplastic resin pulp, it is combined with the vegetable fiber material and becomes an absorbent material. be.
At this time, the nonionic surfactant is added to the surface and surface layer of the thermoplastic resin pulp in an amount of 0.5% by weight or more and 4% by weight or less, preferably 0.7 to 3% by weight.
retained at a rate of If the amount of nonionic surfactant is large or contained in a large amount inside the thermoplastic resin pulp, the mechanical strength will decrease.
The commercial value as an absorbent material will be inferior. Absorbent materials obtained using these nonionic surfactants have particularly excellent permeability to aqueous liquids, and also excellent retention of permeated aqueous liquids. The nonionic surfactants used in the present invention are generally not water-soluble and can have various HLB values. Among them, those with a large HLB value improve the aqueous liquid permeability even in a relatively small amount, and even after the aqueous liquid has penetrated into the absorbent material, the absorbent material can continue to effectively retain the aqueous liquid. In addition, if the HLB value is too large, the lipophilicity will decrease and the compatibility with the thermoplastic resin will deteriorate, and the nonionic surfactant will have poor adsorption to the thermoplastic resin during processing and Retention to resin deteriorates. Therefore, in order to meet these requirements,
The HLB value of the nonionic surfactant is in the range of 3 to 20, more preferably in the range of 4 to 17. The following various methods are employed to treat synthetic pulp with a nonionic surfactant. A wet method in which synthetic pulp is immersed in a water chiller containing a nonionic surfactant. In addition, when forming a thermoplastic resin into a synthetic pulp-like material by a flash spinning method or the like, a high-temperature solution or melt of the thermoplastic resin is spouted into a solution containing a nonionic surfactant. It is preferable to impregnate the surface layer of the synthetic pulp with a nonionic surfactant at the same time as forming the synthetic pulp of the thermoplastic resin. A dry method in which the surface of synthetic pulp is coated with a nonionic surfactant by spraying or other methods. Among these, in the present invention, a nonionic surfactant with an HLB value of 3 to 20 is preferable because almost the entire amount can be efficiently adsorbed to the synthetic pulp by simply adding and stirring it to the water slurry of the synthetic pulp. Recommended treatment method. (3) Vegetable fiber materials (hereinafter sometimes abbreviated as "wood pulp") include various wood pulps,
Rayon short fibers are exemplified. (4) The absorption material is a mixture of 5 to 50% by weight of synthetic pulp previously treated with a nonionic surfactant and 95 to 50% by weight of wood pulp, formed into a web, and then heated with a fluid heat medium. It is manufactured by heat-sealing the material through a heat-sealing method. To obtain a mixture of synthetic pulp and wood pulp, either a wet papermaking method or a dry papermaking method can be employed. When the proportion of synthetic pulp is less than 5% by weight,
There is almost no improvement in mechanical strength due to fusing treatment, and if the content exceeds 50% by weight, a decline in absorption performance is unavoidable. Further, in order to fuse the synthetic pulp, indirect heating using an air oven, an infrared heater, etc. is performed. Indirect heating means heating by a fluid heat medium such as gas or liquid. This type of indirect heating can uniformly heat-fuse the surface and interior of the absorbent material at the same time in a pressureless state. Therefore, it is possible to create bulky absorbent materials while maintaining the form of synthetic pulp. can be obtained. Although the heating temperature depends on the type of thermoplastic resin that is the raw material for the synthetic pulp, it is preferably in the range of at least the melting point of the thermoplastic resin used to about 50° C. higher than the melting point. The absorbent material of the present invention is usually in the form of a web, and its bulk density can be adjusted to a certain extent by adjusting the heating temperature and pressurizing conditions, and if necessary, press treatment is performed simultaneously with fusing treatment. Products can be made of various bulk densities. The absorbent material of the present invention may contain other water-retaining substances in order to further improve its absorbent performance. Examples of such water-retentive substances include fine particles of various polymer electrolytes as disclosed in the above-mentioned Japanese Patent Application Laid-Open No. 16611/1983. Among these, suitable concomitant materials are wood pulp, cotton, polyglycose or succalose such as starch, and hydrophilic groups or hydrolysates such as acrylic acid and acrylonitrile. [Effects of the invention] The absorbent material obtained by the production method of the present invention is
It has excellent absorbency and retention of water-based liquids, has excellent mechanical strength, and can be easily manufactured.It is used for sanitary napkins, medical sponges, wound dressing pads, towels, etc., and has water retention properties depending on the purpose. Lamination of a small exterior material or water-impermeable backing material is carried out. [Example] Examples are shown below. Example 1 20 g of high-density polyethylene synthetic pulp (average fiber length: 0.9 mm) was put into 1 water, 150 mg of glycerin monostearate was added, stirred, and then separated and collected. This synthetic pulp contained 0.75% by weight of glycerin monostearate. 12 g of this synthetic pulp and 48 g of paper cotton were uniformly mixed and formed into a web-like product with a basis weight of 375 g/m 2 by dry papermaking. This web-like material was placed in an air oven at 150° C. for 10 minutes to perform a synthetic pulp fusing treatment. In order to check the absorption performance of the obtained absorbent material, 1 c.c. of tap water was dropped with a dropper onto the surface of the absorbent material placed horizontally, and the water droplets penetrated into the interior of the absorbent material from the surface. As a result of measuring the time required to complete the process, it was 0.7 seconds. Examples 2 and 3 The same procedure as in Example 1 was carried out except that the amount of glycerin monostearate used for the synthetic pulp was changed. The results are shown in Table 1. 【table】

Claims (1)

【特許請求の範囲】[Claims] 1 HLB値が3乃至20の範囲にある非イオン性
界面活性剤で表面又は表層部を処理した、前記非
イオン性界面活性剤の保持量が0.5重量%以上4
重量%以下である熱可塑性樹脂パルプ状物5乃至
50重量%と、植物性繊維素材95乃至50重量%とを
混合し、流体性熱媒体を介して熱融着処理するこ
とを特徴とする吸収用材料の製法。
1 The surface or surface layer is treated with a nonionic surfactant with an HLB value in the range of 3 to 20, and the retained amount of the nonionic surfactant is 0.5% by weight or more 4
Thermoplastic resin pulp-like material that is not more than 5% by weight
1. A method for producing an absorbent material, which comprises mixing 50% by weight of a vegetable fiber material and 95 to 50% by weight of a vegetable fiber material, and subjecting the mixture to heat fusion treatment via a fluid heat medium.
JP56007276A 1981-01-22 1981-01-22 Absorbing material Granted JPS57121657A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56007276A JPS57121657A (en) 1981-01-22 1981-01-22 Absorbing material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56007276A JPS57121657A (en) 1981-01-22 1981-01-22 Absorbing material

Publications (2)

Publication Number Publication Date
JPS57121657A JPS57121657A (en) 1982-07-29
JPH022982B2 true JPH022982B2 (en) 1990-01-22

Family

ID=11661499

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56007276A Granted JPS57121657A (en) 1981-01-22 1981-01-22 Absorbing material

Country Status (1)

Country Link
JP (1) JPS57121657A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU588057B2 (en) * 1985-10-07 1989-09-07 Kimberly-Clark Worldwide, Inc. Multilayer nonwoven fabric
JP2584495B2 (en) * 1988-07-27 1997-02-26 花王株式会社 Method for producing super absorbent fiber sheet
JP2622744B2 (en) * 1989-02-20 1997-06-18 チッソ株式会社 Water-retaining nonwoven

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5111919A (en) * 1974-07-17 1976-01-30 Kuraray Co Setsuchakuseisenino seizoho
JPS5459466A (en) * 1977-10-18 1979-05-14 Kimberly Clark Co Nowoven fabric and production thereof

Also Published As

Publication number Publication date
JPS57121657A (en) 1982-07-29

Similar Documents

Publication Publication Date Title
EP0123414B1 (en) Absorbent material
US4655877A (en) Absorbent web structure
KR960004688B1 (en) Synthetic pulp and absorbent comprising the same
EP0095917B1 (en) Hydrophilic microfibrous absorbent webs, methods for their manufacture and use thereof in disposable absorbent articles
CA1065294A (en) Absorbent articles and methods for their preparation
TWI288645B (en) Superabsorbent polymers having a slow rate of absorption
US5599763A (en) Absorbent material, absorbent body, and method for production thereof
US6300275B1 (en) Resilient superabsorbent compositions
US8741427B2 (en) Microcavity-containing resilient, thermoplastic foam; composite of such foam and particles; methods of preparing and articles prepared from same
EP1858998B1 (en) Superabsorbing foam, method for the production and use thereof
KR20000069445A (en) Highly absorbent composite compositions, absorbent sheets provided with the compositions, and process for producing the same
NL8602749A (en) PROCESS FOR PREPARING A POROUS POLYMER AND ABSORBENT ARTICLES MADE THEREFROM.
KR20000069765A (en) Methylated Hydroxypropylcellulose and Temperature Responsive Products Made Therefrom
JP2004535842A (en) Synthetic fiber blended with absorbent material and method for producing the material
JPWO2002085959A1 (en) Water-absorbing resin suitable for absorbing high-molecular-weight-containing viscous liquid, and absorber and absorbent article using the same
MXPA00010975A (en) Absorbent fibrous material and methods to make me
HU218107B (en) Superabsorbent polymer foam
EP1347790A1 (en) Absorbent compositions
JPWO2017200085A1 (en) Water-absorbent resin particles, method for producing the same, absorbent comprising the same and absorbent article
CN116084087A (en) Method for producing high-hydroscopicity cloned-spun non-woven fabric by adding SAP (super absorbent polymer) on cloned-spinning production line
JPH022982B2 (en)
KR20010014432A (en) Process for manufacturing wet laid fibrous structures comprising substantially non swellable particles added to the wet fibre web
EP0099428B1 (en) Absorbent web structure
JPS5825499B2 (en) water absorbing agent
US20250025857A1 (en) Absorbent article