JPS5811140A - High water-absorbing laminate - Google Patents

High water-absorbing laminate

Info

Publication number
JPS5811140A
JPS5811140A JP56108571A JP10857181A JPS5811140A JP S5811140 A JPS5811140 A JP S5811140A JP 56108571 A JP56108571 A JP 56108571A JP 10857181 A JP10857181 A JP 10857181A JP S5811140 A JPS5811140 A JP S5811140A
Authority
JP
Japan
Prior art keywords
water
polyvinyl alcohol
laminate
film
high 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.)
Granted
Application number
JP56108571A
Other languages
Japanese (ja)
Other versions
JPH0159108B2 (en
Inventor
本郷 正春
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.)
Nippon Synthetic Chemical Industry Co Ltd
Original Assignee
Nippon Synthetic Chemical Industry 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 Nippon Synthetic Chemical Industry Co Ltd filed Critical Nippon Synthetic Chemical Industry Co Ltd
Priority to JP56108571A priority Critical patent/JPS5811140A/en
Publication of JPS5811140A publication Critical patent/JPS5811140A/en
Publication of JPH0159108B2 publication Critical patent/JPH0159108B2/ja
Granted legal-status Critical Current

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  • Laminated Bodies (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】 本発明は、高吸水性高分子層を含む積層物に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a laminate including a superabsorbent polymer layer.

高吸水性を有する高分子から作ったフィルムを細巾に裁
断したものは、植物用保水剤即ち水ボケ代替物としての
用途が期待できるが、形状が平板なためこれを吸水させ
て鉢などに充填したときの通気性が小さく、又感触的に
も不満足で、天然の水ゴブに類似しているとは言いがた
い。
Films made from highly water-absorbent polymers are cut into thin strips and are expected to be used as water retention agents for plants, i.e., as a substitute for water stains, but since they are flat in shape, they can be used to absorb water and used in pots, etc. When filled, the air permeability is low, and the feel is also unsatisfactory, making it hard to say that it resembles a natural water gob.

本発明はこのような難点を解決したものでおる。The present invention solves these difficulties.

本発明の高吸水性積層物は、第1図に示したように、薄
層基材(Al及び高吸水性高分子層像)よりなり、次の
ようなすぐれた効果を奏する。
As shown in FIG. 1, the superabsorbent laminate of the present invention is made of a thin layer base material (image of Al and superabsorbent polymer layers), and has the following excellent effects.

(イ)その裁断物に水を含ませると渦巻状(@2図参照
)、らせん状(第3図参照)にカールし、見かけ体積が
顕著に増加する。
(b) When the cut material is soaked with water, it curls into a spiral shape (see Figure 2) or a spiral shape (see Figure 3), and its apparent volume increases significantly.

仲)そのためこれをおさえても復元力を生じていわゆる
腰をもつようになる。
(Naka) Therefore, even if you suppress this, you will develop a resilience and have what is called a waist.

(ハ)そのカール形状に起因して保水性のみならず通気
性もすぐれているので、植物用蒸発防止材、植物輸送資
材、植物育成培土、土壌保水材として極めて好適である
(c) Due to its curled shape, it has excellent not only water retention but also air permeability, so it is extremely suitable as an evaporation prevention material for plants, a plant transportation material, a plant growing soil, and a soil water retention material.

に)吸水時でも強度が大きい。2) High strength even when water is absorbed.

(ホ)外観、感触が好ましい。(e) Favorable appearance and feel.

というすぐれた効果を奏すること、そして高吸水性高分
子層の)として無機質又は有機質資材を配合したものを
用いるときは、上記効果に加え一段と外観、感触、風合
いが向上することを見出し、本発明を完成するに至った
It has been discovered that when a super absorbent polymer layer () containing an inorganic or organic material is used, the appearance, feel, and texture are further improved in addition to the above effects, and the present invention has been made. I was able to complete it.

本発明において用いられる薄層基材(A)としては、ポ
リオレフィン系フィルム、ナイロン系フィルム、ポリエ
ステル系フィルム、ポリビニルアルコール系フィルム、
エチレン−ビニルアルコール共重合体系フィルム、ポリ
塩化ビニル系フィルム、セルロース系フィルムなどのフ
ィルムがあげられ、そのほかフィルムの割繊物を縦横方
向に重ねて接着したスプリットクロス、繊布、不織布、
ネット、紙、アルミニウム箔なども用いられる。これら
の中ではポリビニルアルコール(変性ポリビニルアルコ
ールを含む)系フィルム、々かんづく一軸又は二軸に延
伸したポリビニルアルコール系フィルムが高吸水性高分
子層(A)との接着性がすぐれている点、吸水させたと
きの感触、風合いの点などで特に好捷しい。
The thin layer base material (A) used in the present invention includes a polyolefin film, a nylon film, a polyester film, a polyvinyl alcohol film,
Films such as ethylene-vinyl alcohol copolymer film, polyvinyl chloride film, and cellulose film are mentioned, as well as split cloth, textile fabric, nonwoven fabric, which is made by stacking split films vertically and horizontally and bonding them together.
Net, paper, aluminum foil, etc. are also used. Among these, polyvinyl alcohol (including modified polyvinyl alcohol) films and uniaxially or biaxially stretched polyvinyl alcohol films have excellent adhesion with the superabsorbent polymer layer (A); It is especially good in terms of feel and texture when water is absorbed.

高吸水性高分子層@)を構成する高分子としては従来公
知の任意の高吸水性高分子があげられるが、層形成時に
は未だ水溶性を有しかつ層形成後の熱処理等の手段によ
り高吸水性を有するに至るような高分子が特に好ましい
。このような高分子としてはビニルエステルー不飽和カ
ルボン酸(又はその誘導体)共重合体ケシ化物、即ちア
クリル酸、メタクリル酸、クロトン酸などの不飽和モノ
カルボン酸又はそのエステル・塩、マレイン酸、フマー
ル酸、イタコン酸などの不飽和ジカルボン酸又はその部
分又は完全エステル・塩・無水物等で変性されたポリビ
ニルアルコールが典型的なものとしてあげられる。不飽
和カルボン酸(又はその誘導体)の変性量は0.5〜5
0モル%、特に1〜10モル%とするのが適当である。
Any conventionally known superabsorbent polymers can be used as the polymer constituting the superabsorbent polymer layer (@), but they are still water-soluble at the time of layer formation and are highly Particularly preferred are polymers that exhibit water absorption properties. Examples of such polymers include vinyl ester-unsaturated carboxylic acid (or derivatives thereof) copolymer silicide, that is, unsaturated monocarboxylic acids such as acrylic acid, methacrylic acid, and crotonic acid, or esters and salts thereof, maleic acid, Typical examples include polyvinyl alcohol modified with unsaturated dicarboxylic acids such as fumaric acid and itaconic acid, or their partial or complete esters, salts, anhydrides, and the like. The amount of modification of unsaturated carboxylic acid (or its derivative) is 0.5 to 5
A suitable content is 0 mol%, especially 1 to 10 mol%.

なおこの変性ポリビニルアルコールはポリビニルアルコ
ールド併用することも多い、たとえば上記変性ポリビニ
ルアルコールとポリビニルアルコールド?i=’flt
f99〜20:1〜80程度の比率で用いる如くである
Note that this modified polyvinyl alcohol is often used in combination with polyvinyl alcohol, for example, the above-mentioned modified polyvinyl alcohol and polyvinyl alcohol? i='flt
It seems to be used at a ratio of about f99-20:1-80.

その他の高分子として鰹[、ポリエチレンオキシド、ポ
リビニルピロリドン、スルホン化ポリエチレン、デンプ
ン−(メタ)アクリロニトリル共重合体ケン化物、加水
分解されたポリアクリルアミド、ポリアクリル酸塩、デ
ンプン−(メタ)アクリル酸塩共重合体、エチレンービ
ニルエステルー不飽和カルボン酸(又はその誘導体)共
重合体ケン化物、ヒドロキシアクリレート−アクリルア
ミド共重合体ケシ化物など、或いはこれらの架橋体があ
げられる。
Other polymers include bonito [, polyethylene oxide, polyvinylpyrrolidone, sulfonated polyethylene, saponified starch-(meth)acrylonitrile copolymer, hydrolyzed polyacrylamide, polyacrylate, starch-(meth)acrylate] Examples include copolymers, saponified ethylene-vinyl ester-unsaturated carboxylic acid (or derivatives thereof) copolymers, pycnized hydroxyacrylate-acrylamide copolymers, and crosslinked products thereof.

薄層基材(4)上に高吸水性高分子層(I3)を設ける
方法としては、 (1)薄層基材(3)上に潜在的に高吸水能を有する高
分子の溶液を塗布、流延、押出しコートした後、高吸水
能付与処理(熱I18!理、酸処理、放射線。
The method of providing the highly water-absorbing polymer layer (I3) on the thin-layer base material (4) is as follows: (1) Applying a solution of a polymer that potentially has high water-absorbing capacity on the thin-layer base material (3). After , casting and extrusion coating, high water absorption ability imparting treatment (thermal I18! treatment, acid treatment, radiation.

電子線照射など)を行う。electron beam irradiation, etc.).

(2)潜在的に高吸水能を有する高分子のフィルムを作
成し、これと薄層基材η)とを接着剤、ヒートシール等
の手段により接着し、ついで高吸水能付与処理を行う。
(2) A polymer film potentially having high water absorption capacity is prepared, and this and the thin layer base material η) are adhered by means such as an adhesive or heat sealing, and then a high water absorption capacity imparting treatment is performed.

(3)高吸水能を有する高分子のフィルムを薄層基材(
4)と接着する。
(3) A thin layer of a polymer film with high water absorption capacity (
4) Glue.

などの方法が採用される。Methods such as these are adopted.

高吸水性高分子層ω)には、その製造に際し種々の無機
質又は有機質資材を配合することが極めて望ましい。そ
れにより一段と外観、感触、風合いの点で好ましいもの
が得られるからである。
It is extremely desirable to incorporate various inorganic or organic materials into the superabsorbent polymer layer ω) during its manufacture. This is because a more favorable appearance, touch, and texture can be obtained.

無機質資材としてはパーライト、ゼオライト、砂、軽石
、鉱さい、火山灰、バーミキュライト、培土、無水ケイ
酸、炭酸カルシウム、炭酸マグネシウム、炭酸パリクム
、クレー、珪藻土、タルク、長石粉、酸化チタン、アル
ミナ、石コク、鉱物質繊維などがあげられる。
Inorganic materials include perlite, zeolite, sand, pumice, slag, volcanic ash, vermiculite, culture soil, silicic anhydride, calcium carbonate, magnesium carbonate, paricum carbonate, clay, diatomaceous earth, talc, feldspar powder, titanium oxide, alumina, stone base, Examples include mineral fibers.

有機質資材としてはピートモス、バルブ、繊維、腐葉土
、植物裁断物などがあげられる。
Examples of organic materials include peat moss, bulbs, fibers, leaf mold, and shredded plants.

高吸水性高分子に対する有機質又は無機質資材の配合量
は広い範囲から選択されるが、後者を前者の約20倍以
下、特に0.01〜15倍とすることが望ましい。
The amount of organic or inorganic material added to the superabsorbent polymer can be selected from a wide range, but it is desirable that the latter be about 20 times or less, particularly 0.01 to 15 times the former.

薄層基材囚及び高吸水性高分子俤)よりなる積層物はそ
のままで或いは適当な大きさに裁断して用、いられる。
The laminate consisting of the thin base material and the super absorbent polymer can be used as is or cut into appropriate sizes.

細巾に裁断したものけこれを水と接触させるとらせん状
、渦巻状などの形状にカールするという県味ある挙動を
示すので、水ボケ代替用、保水材、土壌改良材、野菜や
魚貝類の鮮度保持材、擬似餌などの用途に特に有用であ
る。小片に裁断したものも、水と接触するとカールして
かさを増し空気を包含するので、保水材、土壌改良材な
どの用途に有用である。
When cut into thin strips and brought into contact with water, it curls into a spiral or spiral shape, which is typical of the prefecture, so it can be used as a substitute for water stains, as a water retention material, as a soil improvement material, and for vegetables, fish, and shellfish. It is particularly useful for applications such as freshness-preserving materials and artificial baits. When cut into small pieces, they curl and increase in bulk when they come into contact with water and enclose air, making them useful for applications such as water retention materials and soil improvement materials.

次に例をあげて本発明の積層体をさらに説明する。以下
1部」、「96」とあるのは特にことわりのない限り重
量基準で表わしたものである。
Next, the laminate of the present invention will be further explained by giving an example. "1 part" and "96" below are expressed on a weight basis unless otherwise specified.

例1 マレイン酸モノメチル含量5モル%のマレイン酸モノメ
チル−酢酸ビニル共重合体の酢酸ビニル成分の98モル
%をケン化して得られたマレイン酸モノメチル変性ポリ
ビニルアルコール1750部及び重合度1700、ケン
化度99.7モル%のポリビニルアルコール750部を
水10000部に溶解して20%水溶液を調製し、これ
にパーライト500部を加えて混合した。
Example 1 1750 parts of monomethyl maleate-modified polyvinyl alcohol obtained by saponifying 98 mol% of the vinyl acetate component of a monomethyl maleate-vinyl acetate copolymer with a monomethyl maleate content of 5 mol%, a polymerization degree of 1700, and a saponification degree of A 20% aqueous solution was prepared by dissolving 750 parts of 99.7 mol% polyvinyl alcohol in 10,000 parts of water, and 500 parts of perlite was added thereto and mixed.

剥離紙の上に厚み14μの二輪延伸ポリビニルアルコー
ルフィルムを置き、この上から前記混合物を流延し、1
00℃の乾燥機中に約10分同人れて、厚み0.5 m
のシート状の積層物を得、はぼ乾燥が終了した時点でこ
の積層物を155℃の乾燥機中に1.5時間入れて熱処
理することによ妙高吸水性付与を行い、その後蒸気槽を
約1分間通して柔軟化した。
A two-wheeled stretched polyvinyl alcohol film with a thickness of 14 μm was placed on the release paper, and the mixture was cast onto it.
After being placed in the dryer at 00℃ for about 10 minutes, it became 0.5 m thick.
A sheet-like laminate was obtained, and when drying was completed, the laminate was heat-treated in a dryer at 155°C for 1.5 hours to give it a high water absorption property, and then placed in a steam tank. It softened for about 1 minute.

かくして得られた積層シートを中2〜5麿、長さ20〜
60国となるように流延方向に対し直角方向に裁断した
。この細条物を水の中に投入したところ、吸水につれ第
2図の如く渦巻状になり、これを攪拌するとしだいに第
6図の如きらせん状にカールした。
The thus obtained laminated sheet has a medium size of 2 to 5 mm and a length of 20 to 20 mm.
It was cut in a direction perpendicular to the casting direction so that 60 countries were formed. When this strip was put into water, it became spiral-shaped as shown in FIG. 2 as it absorbed water, and when it was stirred, it gradually curled into a spiral shape as shown in FIG. 6.

結果を@1表に示す。The results are shown in Table @1.

対照例 二l1lI延伸ホリビニルアルコールフイルムヲ用いる
ことなく、ガラス板上に混合物を流延したほかは例1と
同様にして単層のシートを作成し、裁断した。得られた
細条物はこれを水の中に投入しても膨潤するだけで、カ
ールは認められなかった。
Comparative Example 2 A single-layer sheet was prepared and cut in the same manner as in Example 1, except that the mixture was cast on a glass plate without using the stretched polyvinyl alcohol film. Even when the obtained strips were put into water, they only swelled and no curling was observed.

結果を第1表に合せて示す。The results are also shown in Table 1.

第  1  表 (注) 吸水後の体積は、乾燥細条toyを水中に投入して吸水
させた後手で強く絞りあげたときの見かけの体積、浸漬
絞り上げ後重量は、そのときの重置。
Table 1 (Note) The volume after water absorption is the apparent volume when the dry strip toy is placed in water and squeezed strongly after it has been soaked in water, and the weight after immersion and squeezing is the weight at that time.

40℃下での乾燥時開け、上記浸漬絞り上げ後のサンプ
ルを10a四方のガラス製容器に拡げ、40’Cの室内
に放置したとき、もとの乾燥重量になるまでの時間。
The time it takes for the sample to return to its original dry weight when opened during drying at 40°C, spread the sample after immersion and squeezing into a 10a square glass container, and leave it in a room at 40'C.

例2 例1において水分15%のピートモス20(1をさらに
配合したほかは例1と同様にして積層シートを作成し、
このシートを流延方向とは直角方向に中2〜5N1、長
さ20〜605+となるように裁断した。この細条物を
水の中に投入したところ、吸水につれ渦巻状にカールし
た。吸水後の体積は605匡、浸漬絞シ上は後重量は6
4.5f、40℃下での乾燥時開は12.5時間であっ
た。
Example 2 A laminated sheet was prepared in the same manner as in Example 1 except that peat moss 20 (1) with a moisture content of 15% was further blended in Example 1.
This sheet was cut in a direction perpendicular to the casting direction to have a medium size of 2 to 5N1 and a length of 20 to 605+. When this strip was put into water, it curled into a spiral shape as it absorbed water. The volume after water absorption is 605 squares, and the weight after soaking and drawing is 6
The drying time at 4.5 f and 40° C. was 12.5 hours.

例6 例1で用いたマレイン酸モノメチル変性ポリビニルアル
コール粒子600部及び水210部よりなる含水粒子を
径601WIIの押出機に供給し、1o。
Example 6 The water-containing particles consisting of 600 parts of monomethyl maleate-modified polyvinyl alcohol particles used in Example 1 and 210 parts of water were fed into an extruder having a diameter of 601 WII, and 1o.

〜145℃で混練してT−ダイから吐出すると共に、・
例1で用いた二軸延伸ポリビニルアルコールフィルム上
に0.5fl厚に押出しコートした。この積層物を14
0℃の乾燥機中に1.5時間入れて熱処理することによ
υ高吸水性を付与し、その後蒸気槽を通して柔軟化した
。。
While kneading at ~145°C and discharging from the T-die,
The biaxially oriented polyvinyl alcohol film used in Example 1 was extrusion coated to a thickness of 0.5 fl. 14 pieces of this laminate
The material was heat-treated in a dryer at 0° C. for 1.5 hours to impart high water absorption properties, and then passed through a steam bath to soften it. .

かくして得られた積層シートを中2〜6厘、長さ10σ
と々るように斜め方向に裁断した。この細条物を水の中
に投入したところ、吸水につれて第6図の如くらせん状
にカールした。吸水後の体積は200印、浸漬絞り上げ
後重量Vi+ 50.51140℃下での乾燥時聞け5
4.5時間であった。
The thus obtained laminated sheet has a medium size of 2 to 6 cm and a length of 10σ.
I cut it diagonally so that it would fit. When this strip was put into water, it curled into a spiral shape as shown in Figure 6 as it absorbed water. Volume after water absorption is 200 mark, weight after immersion and squeezing Vi+ 50.51 When drying at 40℃ 5
It took 4.5 hours.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の積層物の一例を示した断面図、第2図
、第6図は本発明の積層物の裁断物を水中に投入したと
きの形状の例を示17た見取図である。 A・・・・・・薄層基材 B・・・・・高吸水性高分子 特許出願人 日本合成化学工業株式会社第 1 司 茅21刃     隼 3 図 ぶ  6角労か
FIG. 1 is a sectional view showing an example of the laminate of the present invention, and FIGS. 2 and 6 are sketches showing an example of the shape of the cut product of the laminate of the present invention when placed in water. . A... Thin layer base material B... Super absorbent polymer patent applicant Nippon Gosei Chemical Industry Co., Ltd.

Claims (1)

【特許請求の範囲】 1、薄層基材体)及び高吸水性高分子+jp10S)よ
ねなる高吸水性積層物。 2.0)が無機質又は有機質資材を配合した高吸水性高
分子層である特許請求の範囲第1項記載の積層物。 5、(4)がフィルムである特許請求の範囲第1項記載
の積層物。 4、  (A)diポリビニルアルコール系フィルムで
ある特許請求の範囲第1項記載の81履物。 5、 網中裁断物の形状を有する特許請求の範囲第1項
記載の積層物。
[Claims] 1. A super absorbent laminate consisting of a thin layer base material) and a super absorbent polymer +jp10S). The laminate according to claim 1, wherein 2.0) is a super absorbent polymer layer containing an inorganic or organic material. 5. The laminate according to claim 1, wherein (4) is a film. 4. (A) 81 Footwear according to claim 1, which is a di-polyvinyl alcohol film. 5. The laminate according to claim 1, which has the shape of a cut product.
JP56108571A 1981-07-10 1981-07-10 High water-absorbing laminate Granted JPS5811140A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56108571A JPS5811140A (en) 1981-07-10 1981-07-10 High water-absorbing laminate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56108571A JPS5811140A (en) 1981-07-10 1981-07-10 High water-absorbing laminate

Publications (2)

Publication Number Publication Date
JPS5811140A true JPS5811140A (en) 1983-01-21
JPH0159108B2 JPH0159108B2 (en) 1989-12-14

Family

ID=14488186

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56108571A Granted JPS5811140A (en) 1981-07-10 1981-07-10 High water-absorbing laminate

Country Status (1)

Country Link
JP (1) JPS5811140A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009197853A (en) * 2008-02-20 2009-09-03 Yutaka Giken Co Ltd Brake disk and its manufacturing method
JP2010533779A (en) * 2007-07-20 2010-10-28 バイエル・イノヴェイション・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング Polymer composite film having a barrier function

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51125683A (en) * 1975-04-23 1976-11-02 Sanyo Chem Ind Ltd Method of adding water absorbring power
JPS562163A (en) * 1979-06-18 1981-01-10 Satsuki Kitani Sheett or plateeshaped water absorbing material
JPS5620679A (en) * 1979-07-28 1981-02-26 Hiraoka Shokusen Waterrproof sheet

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51125683A (en) * 1975-04-23 1976-11-02 Sanyo Chem Ind Ltd Method of adding water absorbring power
JPS562163A (en) * 1979-06-18 1981-01-10 Satsuki Kitani Sheett or plateeshaped water absorbing material
JPS5620679A (en) * 1979-07-28 1981-02-26 Hiraoka Shokusen Waterrproof sheet

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010533779A (en) * 2007-07-20 2010-10-28 バイエル・イノヴェイション・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング Polymer composite film having a barrier function
JP2009197853A (en) * 2008-02-20 2009-09-03 Yutaka Giken Co Ltd Brake disk and its manufacturing method

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