JPH02190126A - Absorbing sheet for pet animal - Google Patents
Absorbing sheet for pet animalInfo
- Publication number
- JPH02190126A JPH02190126A JP1039689A JP1039689A JPH02190126A JP H02190126 A JPH02190126 A JP H02190126A JP 1039689 A JP1039689 A JP 1039689A JP 1039689 A JP1039689 A JP 1039689A JP H02190126 A JPH02190126 A JP H02190126A
- Authority
- JP
- Japan
- Prior art keywords
- sheet
- water
- liquid
- sponge
- absorbing
- 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
Links
- 241001465754 Metazoa Species 0.000 title claims abstract description 12
- 229920000642 polymer Polymers 0.000 claims abstract description 30
- 239000012783 reinforcing fiber Substances 0.000 claims abstract description 14
- 230000008961 swelling Effects 0.000 claims abstract description 12
- 239000005871 repellent Substances 0.000 claims abstract description 7
- 230000002745 absorbent Effects 0.000 claims description 27
- 239000002250 absorbent Substances 0.000 claims description 27
- 229920002678 cellulose Polymers 0.000 claims description 23
- 239000001913 cellulose Substances 0.000 claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 230000002940 repellent Effects 0.000 claims description 5
- 229920000297 Rayon Polymers 0.000 abstract description 24
- -1 polypropylene Polymers 0.000 abstract description 15
- 239000000463 material Substances 0.000 abstract description 7
- 239000000835 fiber Substances 0.000 abstract description 6
- 239000004698 Polyethylene Substances 0.000 abstract description 5
- 229920000573 polyethylene Polymers 0.000 abstract description 5
- 239000004743 Polypropylene Substances 0.000 abstract description 4
- 229920001155 polypropylene Polymers 0.000 abstract description 4
- 240000008564 Boehmeria nivea Species 0.000 abstract description 3
- 238000005304 joining Methods 0.000 abstract description 3
- 229920000728 polyester Polymers 0.000 abstract description 3
- 229920000742 Cotton Polymers 0.000 abstract description 2
- 229920001296 polysiloxane Polymers 0.000 abstract description 2
- 229920000915 polyvinyl chloride Polymers 0.000 abstract description 2
- 239000004800 polyvinyl chloride Substances 0.000 abstract description 2
- 239000002964 rayon Substances 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000001846 repelling effect Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 210000002700 urine Anatomy 0.000 description 10
- 239000000839 emulsion Substances 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 239000000178 monomer Substances 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 6
- 230000009477 glass transition Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 229920003002 synthetic resin Polymers 0.000 description 4
- 239000000057 synthetic resin Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000001733 carboxylic acid esters Chemical class 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000010446 mirabilite Substances 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 241000282472 Canis lupus familiaris Species 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 230000001112 coagulating effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 2
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Laminated Bodies (AREA)
- Housing For Livestock And Birds (AREA)
Abstract
Description
【発明の詳細な説明】
(技術分野)
本発明は、液吸収能及び湿潤時の保形性(強度)にすぐ
れたペット動物用吸収シートに関するものである。DETAILED DESCRIPTION OF THE INVENTION (Technical Field) The present invention relates to an absorbent sheet for pet animals that has excellent liquid absorption ability and shape retention (strength) when wet.
(従来技術及びその問題点) 犬や猫等のペット動物の排尿を吸収処理ために。(Prior art and its problems) For absorbing and processing the urine of pet animals such as dogs and cats.
吸収体シートが用いられている。従来の吸収シートとし
ては、吸収紙を主体とし、これに吸水膨潤性ポリマーを
含有させたものが用いられている。An absorbent sheet is used. Conventional absorbent sheets are mainly made of absorbent paper and contain water-absorbing and swelling polymers.
しかしながら、このような吸収シートは、湿潤強度が弱
いために、ペット動物が排尿後、その上で動いた時に、
吸収シートに切れや破れを生じたり、あるいはよれて塊
となることがあり、その結果、排尿が吸収シートから漏
れる等の問題がある。However, such absorbent sheets have low wet strength, so when a pet animal moves on it after urinating,
The absorbent sheet may be cut, torn, or twisted into clumps, resulting in problems such as urine leaking from the absorbent sheet.
このような問題は、吸収紙として湿潤強度の大きい吸収
紙を用いて一応解決することができる。しかし、吸収紙
の湿潤強度を大きくすると、液吸収速度及び液吸収能が
悪化するため、ペット動物の効果的な排尿処理ができな
くなるという不都合を生じる。Such problems can be solved to some extent by using absorbent paper with high wet strength as the absorbent paper. However, when the wet strength of the absorbent paper is increased, the liquid absorption speed and liquid absorption capacity deteriorate, resulting in the inconvenience that it becomes impossible to effectively treat the urine of pet animals.
(発明の課題)
本発明は、液吸収速度及び液吸収能にすぐれるとともに
、湿潤強度にすぐれたペット動物用吸収シートを提供す
ることをその課題とする。(Problem of the Invention) An object of the present invention is to provide an absorbent sheet for pet animals that is excellent in liquid absorption speed and ability, and also has excellent wet strength.
(課題を解決するための手段)
本発明者らは2前記課題を解決すべく鋭意研究を重ねた
結果1本発明を完成するに至った。(Means for Solving the Problems) The present inventors have conducted extensive research to solve the above-mentioned problems, and as a result, they have completed the present invention.
すなわち、本発明によれば、セルロース系スポンジ圧縮
体からなるシートの一方の面に、撥水処理を施すか又は
液不透過性フィルムを接合させてなるペット動物用吸収
シートが提供される。That is, according to the present invention, there is provided an absorbent sheet for pet animals, which is formed by subjecting one side of a sheet made of a compressed cellulose sponge to a water-repellent treatment or bonding a liquid-impermeable film to the sheet.
本発明で用いるセルロース系スポンジは、セルロース骨
格を有するスポンジを意味する。このようなものとして
は、セルロース自体からなるスポンジの他、セルロース
誘導体、例えば、ビスコース、セルロースエーテル、セ
ルロースエステル等からなるスポンジあるいはそれらの
混合物からなるスポンジを挙げることができる。また、
このセルロース系スポンジは、例えば、補強繊維を含む
ことができる。このセルロース系スポンジは1通常、0
.01−0.8g/aJ、好ましくは0.03−0.6
g/a+?という低密度のものである。The cellulose sponge used in the present invention means a sponge having a cellulose skeleton. Examples of such materials include sponges made of cellulose itself, sponges made of cellulose derivatives such as viscose, cellulose ether, cellulose ester, etc., and sponges made of mixtures thereof. Also,
The cellulosic sponge can include reinforcing fibers, for example. This cellulose sponge is usually 1,0
.. 01-0.8g/aJ, preferably 0.03-0.6
g/a+? It has a low density.
次に、ビスコースを原料とするセルロース系スポンジの
製造例を示すと、ビスコースに対して、補強繊維、その
他の補助成分を加え、さらに慣用の結晶芒硝を加えて混
合し、得られた混合物を所要形状に成形し、これを加熱
凝固させた後、酸性水溶液と接触させてセルロースを再
生し、次いで、水洗乾燥し、スポンジを得る。Next, an example of manufacturing a cellulose sponge using viscose as a raw material is a mixture obtained by adding reinforcing fibers and other auxiliary ingredients to viscose, and adding and mixing commonly used crystalline sulfate. After molding into a desired shape and coagulating it by heating, it is brought into contact with an acidic aqueous solution to regenerate cellulose, and then washed with water and dried to obtain a sponge.
前記原料ビスコース中のセルロース濃度は特に限定され
ないが、通常、8〜10重量%に規定するのが好ましい
、ビスコース中のアルカリ濃度は、3〜15重量%、好
ましくは5〜10重量%に規定するのがよい、ビスコー
スに加える補強繊維の量は、一般に、スポンジ中のその
割合が10〜50重量%となるような割合量である。即
ち、ビスコース中のセルロースと補強繊維との合計量に
対して、10〜50重量%である。The cellulose concentration in the raw material viscose is not particularly limited, but it is usually preferably set to 8 to 10% by weight.The alkali concentration in the viscose is 3 to 15% by weight, preferably 5 to 10% by weight. The amount of reinforcing fibers added to the viscose which may be defined is generally such that its proportion in the sponge is 10-50% by weight. That is, it is 10 to 50% by weight based on the total amount of cellulose and reinforcing fibers in the viscose.
補強繊維としては、例えば、ラミー麻、綿、パルプ等の
天然繊維の他、各種合成繊維、例えば、レーヨン系、ポ
リプロピレン系、ポリエステル系のもの等が挙げられる
。これらのものは、単独又は2種以上の混合物の形で用
いられる。乾燥時の柔軟性にすぐれ、乾燥した時の収縮
性の小さなスポンジを得る点からは、捲縮率(JIS
L 1015(7,12゜2))が10〜30重量%の
範囲にある合成繊維や異形断面(円又は楕円以外の形状
の断面)を有する合成繊維の使用が好ましい、補強繊維
の長さは5〜20mmの範囲及び繊維の太さは0.5〜
15d(デニール)、好ましくは1〜6dの範囲に規定
するのが好ましい。Examples of reinforcing fibers include natural fibers such as ramie hemp, cotton, and pulp, as well as various synthetic fibers such as rayon, polypropylene, and polyester fibers. These materials may be used alone or in the form of a mixture of two or more. The crimp rate (JIS
It is preferable to use synthetic fibers with L 1015 (7,12°2)) in the range of 10 to 30% by weight or synthetic fibers with irregular cross sections (cross sections of shapes other than circles or ellipses).The length of the reinforcing fibers is The range is 5-20mm and the fiber thickness is 0.5-20mm.
It is preferable to define the denier to be 15 d (denier), preferably in the range of 1 to 6 d.
結晶芒硝としては、一般に、平均粒径1〜5IIIlの
ものが用いられ、その添加量は、ビスコース中のセルロ
ースと補強繊維の合計量に対して20〜80倍重量であ
る。ビスコースに添加した結晶芒硝は、凝固、再生工程
や水洗工程でスポンジから溶出除去される。Generally, crystalline Glauber's salt having an average particle size of 1 to 5III is used, and the amount added is 20 to 80 times the total amount of cellulose and reinforcing fibers in the viscose. The crystalline mirabilite added to viscose is eluted and removed from the sponge during the coagulation, regeneration process, and water washing process.
前記原料ビスコースに対しては、さらに、得られるスポ
ンジの物性を改良するために種々の添加剤を加えること
ができる。このような添加剤としては、補強繊維の分散
や、ビスコースの補強繊維への浸透を助長するために各
種界面活性剤を分散剤として添加することができる。ま
た、スポンジの性能向上や柔軟性向上のためにポリオー
ル化合物や、化学修飾セルロース、尿素等を改良剤とし
て添加することができる0分散剤として用いる界面活性
剤の添加量は、ビスコースに対し0.1〜2重量2の範
囲にするのが好ましい。ポリオール化合物等の改良剤の
添加量は、ビスコースに対し1〜10重量での範囲にす
るのが好ましい。Various additives can be added to the raw material viscose in order to improve the physical properties of the resulting sponge. As such additives, various surfactants can be added as dispersants in order to promote dispersion of reinforcing fibers and penetration of viscose into reinforcing fibers. In addition, to improve the performance and flexibility of the sponge, polyol compounds, chemically modified cellulose, urea, etc. can be added as modifiers.The amount of surfactant used as a dispersant is A range of .1 to 2 weight 2 is preferred. The amount of the modifier such as a polyol compound is preferably in the range of 1 to 10% by weight based on viscose.
前記界面活性剤としては、例えば、炭素数14のα−オ
レフィンスルホン酸ナトリウム、ラウリル硫酸ナトリウ
ム、ポリオキシエチレンラウリルエーテル硫酸ナトリウ
ム(エチレンオキシド付加モル数3)等の水溶性の陰イ
オン性界面活性剤や、トウィーン(丁ween)8Q、
炭素数12のジェタノールアマイド、ポリオキシエチレ
ンラウリルエーテル(エチレンオキシド付加モル数8)
等のHLBIO以上の非イオン性界面活性剤が挙げられ
る。Examples of the surfactant include water-soluble anionic surfactants such as sodium α-olefin sulfonate having 14 carbon atoms, sodium lauryl sulfate, and sodium polyoxyethylene lauryl ether sulfate (3 moles of ethylene oxide added); , Tween 8Q,
Jetanolamide with 12 carbon atoms, polyoxyethylene lauryl ether (8 moles of ethylene oxide added)
Examples include nonionic surfactants of HLBIO or higher.
また、ポリオール化合物としては、例えば、グリセリン
の他、ポリエチレングリコール、ポリプロピレングリコ
ール等のポリアルキレンゲリコールが挙げられる。ポリ
オール化合物の平均分子量は、90〜toooo、好ま
しくは600〜6000の範囲である。Examples of the polyol compound include glycerin and polyalkylene gelylcols such as polyethylene glycol and polypropylene glycol. The average molecular weight of the polyol compound ranges from 90 to too much, preferably from 600 to 6,000.
さらに、スポンジの強度を改善するために、下記一般式
で表わされる不飽和カルボン酸エステルを単量体成分の
少なくとも1種として用いて得られたガラス転移温度が
−15〜20℃の範囲にある重合体の水性エマルジョン
を添加することができる。Furthermore, in order to improve the strength of the sponge, an unsaturated carboxylic acid ester represented by the following general formula is used as at least one monomer component, and the glass transition temperature obtained is in the range of -15 to 20°C. Aqueous emulsions of polymers can be added.
CHR”=CH” C0OR’ 前記式中、R1及びR2は水素又はメチル基を示す。CHR”=CH” C0OR' In the above formula, R1 and R2 represent hydrogen or a methyl group.
R3はアルキル基を示し、特に炭素数2〜5の低級アル
キル基が好ましい。R3 represents an alkyl group, particularly preferably a lower alkyl group having 2 to 5 carbon atoms.
前記不飽和カルボン酸エステルの具体例としては、例え
ば、アクリル酸やメタクリル酸のエチル。Specific examples of the unsaturated carboxylic acid ester include ethyl acrylic acid and methacrylic acid.
プロピル又はブチルエステル等を挙げることができる。Examples include propyl or butyl esters.
前記重合体において、ガラス転移温度が一15℃より低
い重合体を用いると、得られるビスコーススポンジにベ
タツキが生じるので好ましくなく、一方、20℃を超え
るようになると、得られるビスコーススポンジの柔軟性
が損われるようになるので好ましくない、ガラス転移湿
度は、重合体がガラス状の硬い状態からゴム状に変化す
る温度であり、重合体の構造因子によって影響される。Among the above polymers, if a polymer with a glass transition temperature lower than 115°C is used, the resulting viscose sponge will become sticky, which is undesirable.On the other hand, if it exceeds 20°C, the flexibility of the resulting viscose sponge will decrease. The glass transition humidity, which is undesirable because properties become impaired, is the temperature at which a polymer changes from a glassy, hard state to a rubbery state, and is influenced by structural factors of the polymer.
一般に、ガラス転移温度は、架橋構造を有する重合体で
は高くなり、架橋の度合により変化する。また。Generally, the glass transition temperature is higher for polymers having a crosslinked structure, and changes depending on the degree of crosslinking. Also.
重合体に可塑剤を添加すると低下する。従って。It decreases when plasticizers are added to the polymer. Therefore.
重合体のガラス転移温度は、重合体の架橋度合や可塑剤
の添加量等を調節してコントロールすることができる。The glass transition temperature of a polymer can be controlled by adjusting the degree of crosslinking of the polymer, the amount of plasticizer added, and the like.
重合体の水性エマルジョンは、前記不飽和カルボン酸エ
ステルを水媒体中で乳化剤の存在下で乳化重合すること
によって得ることができる。この重合体の水性エマルジ
ョンの製造については1例えば、特公昭62−4588
2号公報及び特開昭57−109803号公報等に詳述
されている。水性エマルジョン中の重合体粒子の平均粒
径は、通常、0.01〜5.0.であるが、重合体粒子
は、小さくなるにつれて比表面積が増加し、接着力が向
上するので、その平均粒径は小さいほど好ましい。The aqueous emulsion of the polymer can be obtained by emulsion polymerization of the unsaturated carboxylic acid ester in an aqueous medium in the presence of an emulsifier. Regarding the production of aqueous emulsions of this polymer, see 1, for example, Japanese Patent Publication No. 62-4588.
This method is described in detail in Publication No. 2 and Japanese Patent Application Laid-open No. 109803/1983. The average particle size of the polymer particles in the aqueous emulsion is usually 0.01 to 5.0. However, as the polymer particles become smaller, the specific surface area increases and the adhesive force improves, so it is preferable that the average particle size is smaller.
なお、前記重合体は、前記した一般式(1)で表わされ
る単量体のホモ重合体又は共重合体であることができる
他、他の不飽和単量体との共重合体であることができる
。この場合、不飽和単量体としては、塩化ビニル、酢酸
ビニル、スチレン、アクリルアミド、ジビニルベンゼン
等が挙げられるが、その重合体中の含有量は、10モル
%以下、好ましくは5モルで以下である。In addition, the polymer may be a homopolymer or a copolymer of the monomer represented by the general formula (1) described above, or it may be a copolymer with another unsaturated monomer. Can be done. In this case, unsaturated monomers include vinyl chloride, vinyl acetate, styrene, acrylamide, divinylbenzene, etc., but the content in the polymer is 10 mol% or less, preferably 5 mol% or less. be.
さらに、セルロース系スポンジには1着色剤、脱臭剤、
抗菌剤、殺菌剤等の補助成分を添加することができる。In addition, cellulose sponge has 1 colorant, deodorizer,
Auxiliary ingredients such as antibacterial agents and bactericidal agents can be added.
ビスコース混合物を凝固させるための加熱温度は、90
〜100℃の温度が一般に採用され、その処理時間は約
2時間程度である。この場合、加熱処理時間を短縮する
ために、ビスコース混合物の加熱処理に際し、あらかじ
め硫酸又は硫酸/硫酸亜鉛処理することもできる。The heating temperature for coagulating the viscose mixture is 90
Temperatures of ˜100° C. are generally employed and treatment times are on the order of about 2 hours. In this case, in order to shorten the heat treatment time, the viscose mixture may be treated with sulfuric acid or sulfuric acid/zinc sulfate in advance during the heat treatment.
本発明で用いるセルロース系スポンジ圧縮体は、前記の
ようにして得られた低密度のスポンジを圧縮加工し、そ
の密度を0.1〜Ig/ad、好ましくは0.3〜0
、5g/ dに増加させることによって得ることができ
る。圧縮スポンジは、その密度が前記範囲より小さくな
ると強度が小さくなり、一方、前記範囲より大きくなる
と、柔軟性(風合)が悪くなるので。The compressed cellulose sponge used in the present invention is obtained by compressing the low-density sponge obtained as described above, and the density thereof is 0.1 to Ig/ad, preferably 0.3 to 0.
, can be obtained by increasing to 5 g/d. If the density of compressed sponge is less than the above range, the strength will be low, while if it is larger than the above range, the flexibility (hand) will be poor.
前記範囲の密度になるように圧縮するのがよい。It is preferable to compress the material to a density within the above range.
セルロース系スポンジ圧縮体には、吸水膨潤性ポリマー
を含有させるのが好ましい。吸水膨潤ポリマーとしては
、従来公知のもの、例えば、アクリロニトリルグラフト
化澱粉の加水分解物、ポリアクリル酸塩架橋体の他、ポ
リアクリルアミド系。It is preferable that the compressed cellulose sponge contains a water-absorbing and swelling polymer. Examples of water-absorbing swelling polymers include conventionally known ones, such as hydrolysates of acrylonitrile-grafted starch, crosslinked polyacrylates, and polyacrylamide-based polymers.
酢酸ビニル/アクリル酸メチルコポリマー系のもの等が
ある。このような吸水膨潤性ポリマーは、粒状、粉末状
あるいは繊維状等の形状で用いられ、その形状は特に制
限されない、また、吸水膨潤性ポリマーをスポンジに含
有させる方法としては、スポンジの表面に分散させる方
法、スポンジとスポンジとの間にサンドインチ状に介在
させる方法の他、スポンジ中に含有させることができる
。さらに、吸水膨潤性ポリマーの原料であるモノマーを
、スポンジ中に含浸させ、この状態で重合反応及び架橋
反応を行ってスポンジ中に含有させることもできる。吸
水膨潤性ポリマーの使用量は、スポンジと吸水膨潤性ポ
リマーとの合計量に対して。There are vinyl acetate/methyl acrylate copolymer types. Such water-absorbing and swelling polymers are used in the form of granules, powders, fibers, etc., and the shape is not particularly limited. In addition to the method of interposing it in the form of a sandwich between two sponges, it can also be incorporated into the sponge. Furthermore, the monomer that is the raw material for the water-absorbing and swelling polymer can be impregnated into a sponge, and in this state, a polymerization reaction and a crosslinking reaction can be performed to contain it in the sponge. The amount of water-absorbing swelling polymer used is based on the total amount of the sponge and water-absorbing swelling polymer.
5〜70重量算の割合である。The ratio is 5-70% by weight.
本発明の吸収シートを製造するには、セルロース系スポ
ンジ圧縮体のシートの一方の面(裏面)に撥水処理を施
すか又は液不透過性フィルムを接合させる。撥水処理剤
としては、慣用のシリコーン系又はフッ素系の撥水処理
剤が用いられる。液不透過性フィルムとしては、ポリエ
チレン、ポリプロビレン、ポリエステル、ポリアミド、
ポリ塩化ビニル等の各種合成樹脂からなるフィルムを用
いることができる1合成樹脂フィルムをスポンジ圧縮体
シート面に対する接合方法としては、接着剤を用いる方
法や、溶融合成樹脂フィルムを積層接着させる方法等が
ある。また、スポンジ圧縮体の表面には、液透過性シー
ト、例えば、不織布や、細孔を穿設した合成樹脂フィル
ムを接合させることもできる。さらに、スポンジ圧縮体
シートの裏面に接合した液不透過性フィルムの外面には
、使用に際してのシートの固定化を容易にするために、
粘着剤層を形成することもできる。To produce the absorbent sheet of the present invention, one side (back side) of the compressed cellulose sponge sheet is subjected to water repellent treatment or a liquid-impermeable film is bonded to it. As the water repellent, a conventional silicone-based or fluorine-based water repellent is used. Liquid-impermeable films include polyethylene, polypropylene, polyester, polyamide,
Films made of various synthetic resins such as polyvinyl chloride can be used.1 Methods of joining the synthetic resin film to the sheet surface of the compressed sponge body include a method using an adhesive, a method of laminating and bonding molten synthetic resin films, etc. be. Further, a liquid permeable sheet such as a nonwoven fabric or a synthetic resin film having pores can be bonded to the surface of the compressed sponge body. Furthermore, on the outer surface of the liquid-impermeable film bonded to the back surface of the compressed sponge sheet, in order to facilitate immobilization of the sheet during use,
An adhesive layer can also be formed.
(発明の効果)
本発明のペット動物用吸収シートは、液吸収体として、
セルロース系スポンジ圧縮体を用いたことから非常にコ
ンパクト化された製品として用いることができる。従っ
て、その保管、陳列に場所をとらない、しかも、圧縮体
でありながら、その保形性はすぐれている。その上、液
吸収性にすぐれ、排尿を吸収した時には迅速にこれを吸
収し、体積増加を示し1元の非圧縮体の体積に復元する
特性を有する。しかも、スポンジ圧縮体は湿潤強度にす
ぐれており、排尿を吸収した時に、その上をペット動物
が踏み付けても、切れや破れを生じるようなこともなく
、また、その動物の足に排尿が付着することも少ない。(Effect of the invention) The absorbent sheet for pet animals of the present invention, as a liquid absorber,
Since a compressed cellulose sponge is used, it can be used as a very compact product. Therefore, it does not take up much space to store or display, and even though it is a compressed body, it has excellent shape retention. Furthermore, it has excellent liquid absorption properties, and when it absorbs urine, it quickly absorbs it, shows an increase in volume, and has the property of returning to its original volume of an incompressible body. In addition, the compressed sponge material has excellent wet strength, so even if a pet animal steps on it when it absorbs urine, it will not cut or tear, and the urine will stick to the animal's paws. There's not much to do.
(実施例) 次に本発明を実施例によりさらに詳細に説明する。(Example) Next, the present invention will be explained in more detail with reference to Examples.
実施例
〔スポンジの製造〕
セルロース9重量%及びアルカリ5重量%を含むビスコ
ースに対し、補強繊維として長さ10mmのラミー麻を
ビスコース中のセルロースの40重量%になる割合で添
加し、結晶芒硝(平均粒径:3+am)をビスコース中
のセルロースの50倍重量になるように添加し1次いで
重合体の水性エマルジョンを添加し、混合した後、この
混合物をブロック状に成形し、95〜100℃で3時間
煮沸処理した後、4%硫酸中に浸漬してセルロースを再
生し、水洗後、乾燥してビスコーススポンジを得た。Example [Production of sponge] To viscose containing 9% by weight of cellulose and 5% by weight of alkali, ramie hemp with a length of 10 mm was added as a reinforcing fiber at a ratio of 40% by weight of the cellulose in the viscose, and crystallized. Glauber's salt (average particle size: 3+am) was added in an amount 50 times the weight of cellulose in the viscose, then an aqueous emulsion of the polymer was added, mixed, and the mixture was shaped into a block. After boiling at 100° C. for 3 hours, it was immersed in 4% sulfuric acid to regenerate cellulose, washed with water, and dried to obtain a viscose sponge.
以上のようにして得たビスコーススポンジの性能評価を
以下のようにして行った。その結果を表−1に示す。The performance of the viscose sponge obtained as described above was evaluated as follows. The results are shown in Table-1.
(1)柔軟性(風合い)
乾燥スポンジを、厚さ10mm、縦100+sm、横1
00+mmの方形体に切断したものについて、女性5人
による官能テストを行い、評価した。(1) Flexibility (texture) Dry sponge with thickness 10mm, length 100+sm, width 1
A sensory test was conducted on the pieces cut into square pieces of 00+ mm and evaluated by five women.
O・・・非常に良い 0・・・良 いΔ・・・普
通 X・・・良くない(2)強度
乾燥スポンジを、厚さ2■、巾25m+a、長さ150
m5+に切断したものを試料として用い、これを水に浸
漬後、引張試験機にて、チャック間隔100mm、引張
速度200+++m/分の条件で引張強度を測定した。0...Very good 0...Good Δ...Fair
Passive
A sample cut to m5+ was used as a sample, and after being immersed in water, the tensile strength was measured using a tensile tester at a chuck interval of 100 mm and a tensile speed of 200 m/min.
表−1
なお、前記で用いた重合体の水性エマルジョンは、単量
体として、ブチルメタクリレートを用いて得られたもの
である。すなわち、常法に従い、水の中に乳化剤と水溶
性触媒を溶かし、これを撹拌しながら、単量体と界面活
性剤を加えて加熱することにより、表−1に示す種々の
ガラス転移温度を有する濃度40重量%、平均粒径0.
174の水性エマルジョンを得た。Table 1 Note that the aqueous emulsion of the polymer used above was obtained using butyl methacrylate as a monomer. That is, by dissolving an emulsifier and a water-soluble catalyst in water according to a conventional method, adding a monomer and a surfactant while stirring, and heating, various glass transition temperatures shown in Table 1 can be achieved. with a concentration of 40% by weight and an average particle size of 0.
An aqueous emulsion of 174 was obtained.
前記実験番号3のブロック状スポンジを厚さ3■朧のシ
ートに切断し、ローラで圧縮してスポンジ圧縮体(嵩密
度0.45g/cd)とし、この圧縮体シートの裏面に
ポリエチレンフィルムをホットメルト法で接合して吸収
シートを得た。The block-shaped sponge of Experiment No. 3 was cut into sheets with a thickness of 3 mm and compressed with a roller to form a compressed sponge body (bulk density 0.45 g/cd). A hot polyethylene film was placed on the back of the compressed sheet. An absorbent sheet was obtained by joining using a melt method.
一方、比較のために、厚さ3−履の綿状バルブシート(
嵩密度0.1g/aj)を、不織布とポリエチレンフィ
ルムとの間に挾持し、周縁を接合して比較用の吸収シー
トを得た。On the other hand, for comparison, a cotton-like valve seat with a thickness of 3 mm (
(bulk density: 0.1 g/aj) was sandwiched between a nonwoven fabric and a polyethylene film, and the peripheral edges were joined to obtain a comparative absorbent sheet.
次に、前記のようにして得た各吸収シートを実用試験に
供し、以下のようにしてその評価を行った。その結果を
表−2に示す。Next, each absorbent sheet obtained as described above was subjected to a practical test and evaluated as follows. The results are shown in Table-2.
(1)ヨレ、キレの発生
ヨークシャテリヤを飼っている5家庭において使用し、
使用後の吸収シートを官能テストによる総合平均点によ
り評価した。評価基準は下記の通りとし、5家庭の平均
点を評価点とした。(1) Occurrence of twisting and cracking.Used in 5 households that keep Yorkshire terriers.
The absorbent sheet after use was evaluated based on the overall average score based on a sensory test. The evaluation criteria were as follows, and the average score of the five households was used as the evaluation score.
ヨレ、キレが非常に多い ・・・ 1点ヨレ、キレが若
干ある ・・・ 3点ヨレ、キレがない ・・
・ 5点(2)足跡の付着
犬が排尿を吸収したシートの上を踏み付けた後。There is a lot of twisting and sharpness... There is some twisting and sharpness at one point... There is no twisting and sharpness at three points...
・5 points (2) Footprints after a dog steps on a sheet that has absorbed urine.
板間及び畳の上を歩いた時に、尿の付着による足跡が付
くかどうかを総合平均点により評価した。When walking on wooden floors and tatami mats, whether or not footprints were left due to urine was evaluated based on the overall average score.
評価基準は下記の通りとし、5家庭の平均点を評価点と
した。The evaluation criteria were as follows, and the average score of the five households was used as the evaluation score.
足跡が非常に付く ・・・ 1点足跡が若干付く
・・・ 3点足跡が全く付かない ・・
・ 5点表−2
実施例2
実施例1において、ビスコースに対して水性エマルジョ
ンを添加しない以外は同様にしてスポンジを製造した。There are a lot of footprints... There are a few 1-point footprints... There are no 3-point footprints...
- 5-Point Table-2 Example 2 A sponge was produced in the same manner as in Example 1 except that no aqueous emulsion was added to the viscose.
得られたスポンジを厚さ3鳳■のシートに切断し、ロー
ル加工してスポンジ圧縮体(嵩密度0.45g/cd)
を得た。この圧縮体シートの裏面にポリエチレンフィル
ムをホットメルト法で接合して吸収シートを得た。この
吸収シートを実用試験に供したところ、実施例1と同様
に良好な結果が得られた。The obtained sponge was cut into sheets with a thickness of 3 mm and rolled to form compressed sponge bodies (bulk density 0.45 g/cd).
I got it. A polyethylene film was bonded to the back surface of this compressed sheet using a hot melt method to obtain an absorbent sheet. When this absorbent sheet was subjected to a practical test, similar good results as in Example 1 were obtained.
実施例3
実施例2で得られた圧縮体シートの裏面に、撥水剤とし
て、シリコン樹脂系、フッ素樹脂系、金属せっけん系等
からなる塗布液を塗布、乾燥して吸収シートを得た。こ
の吸収シートにおいては、表面から吸収した排尿の裏面
からの漏れが防止されることが確認された。Example 3 On the back side of the compressed sheet obtained in Example 2, a coating liquid made of silicone resin, fluororesin, metal soap, etc. was applied as a water repellent and dried to obtain an absorbent sheet. It was confirmed that this absorbent sheet prevents urine absorbed from the front surface from leaking from the back surface.
実施例4
実施例2で得た吸収シートの表面に、吸水膨潤性ポリマ
ー粒子を分散させ、その上に不織布を積層し、周縁を接
着して吸水膨潤性ポリマーを含む吸収シートを得た。こ
の吸収シートは、その吸水膨潤性ポリマーの作用により
、排尿吸収能の著しく高められたものであった。Example 4 Water-absorbing and swelling polymer particles were dispersed on the surface of the absorbent sheet obtained in Example 2, a nonwoven fabric was layered thereon, and the periphery was adhered to obtain an absorbent sheet containing the water-absorbing and swelling polymer. This absorbent sheet had significantly improved urine absorption ability due to the action of the water-absorbing and swelling polymer.
Claims (2)
からなるシートの一方の面に、撥水処理を施すか又は液
不透過性フィルムを接合させてなるペット動物用吸収シ
ート。(1) An absorbent sheet for pet animals, which is made of a sheet made of a compressed cellulose sponge containing reinforcing fibers, and one side of which is treated with water repellent treatment or bonded with a liquid-impermeable film.
1のシート。(2) The sheet according to claim 1, wherein the compressed body contains a water-absorbing and swelling polymer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1039689A JPH02190126A (en) | 1989-01-18 | 1989-01-18 | Absorbing sheet for pet animal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1039689A JPH02190126A (en) | 1989-01-18 | 1989-01-18 | Absorbing sheet for pet animal |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02190126A true JPH02190126A (en) | 1990-07-26 |
Family
ID=11748969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1039689A Pending JPH02190126A (en) | 1989-01-18 | 1989-01-18 | Absorbing sheet for pet animal |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02190126A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20050087310A (en) * | 2004-02-26 | 2005-08-31 | 이광훈 | Pet for bedpan |
WO2006090942A1 (en) * | 2005-02-28 | 2006-08-31 | Kwang Hun Lee | Stool for pet |
JP2013225678A (en) * | 2006-03-30 | 2013-10-31 | Konica Minolta Inc | Organic electroluminescent element, lighting device and display device |
JP2016128256A (en) * | 2015-01-05 | 2016-07-14 | 内山工業株式会社 | Composite molded article and method for manufacturing the same |
-
1989
- 1989-01-18 JP JP1039689A patent/JPH02190126A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20050087310A (en) * | 2004-02-26 | 2005-08-31 | 이광훈 | Pet for bedpan |
WO2006090942A1 (en) * | 2005-02-28 | 2006-08-31 | Kwang Hun Lee | Stool for pet |
JP2013225678A (en) * | 2006-03-30 | 2013-10-31 | Konica Minolta Inc | Organic electroluminescent element, lighting device and display device |
JP2016128256A (en) * | 2015-01-05 | 2016-07-14 | 内山工業株式会社 | Composite molded article and method for manufacturing the same |
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