JPS6142623B2 - - Google Patents
Info
- Publication number
- JPS6142623B2 JPS6142623B2 JP54018222A JP1822279A JPS6142623B2 JP S6142623 B2 JPS6142623 B2 JP S6142623B2 JP 54018222 A JP54018222 A JP 54018222A JP 1822279 A JP1822279 A JP 1822279A JP S6142623 B2 JPS6142623 B2 JP S6142623B2
- Authority
- JP
- Japan
- Prior art keywords
- foam
- powder
- synthetic resin
- water
- resin
- 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
Links
- 239000006260 foam Substances 0.000 claims description 42
- 239000000843 powder Substances 0.000 claims description 30
- 239000011148 porous material Substances 0.000 claims description 10
- 229920003002 synthetic resin Polymers 0.000 claims description 10
- 239000000057 synthetic resin Substances 0.000 claims description 10
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 3
- -1 and then dried Substances 0.000 claims description 2
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- 239000004416 thermosoftening plastic Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims 1
- 239000000463 material Substances 0.000 description 19
- 238000000034 method Methods 0.000 description 14
- 239000008187 granular material Substances 0.000 description 9
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 5
- 239000005038 ethylene vinyl acetate Substances 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 239000012943 hotmelt Substances 0.000 description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 5
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 4
- 229920005830 Polyurethane Foam Polymers 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 4
- 239000001768 carboxy methyl cellulose Substances 0.000 description 4
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 4
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 239000011496 polyurethane foam Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 239000002537 cosmetic Substances 0.000 description 3
- 239000004088 foaming agent Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 239000011358 absorbing material Substances 0.000 description 2
- 239000012814 acoustic material Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000012805 post-processing Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- JIQNZSFCZNGYEW-UHFFFAOYSA-N 2-methylprop-1-en-1-ol;urea Chemical compound NC(N)=O.CC(C)=CO JIQNZSFCZNGYEW-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004687 Nylon copolymer Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000006757 chemical reactions by type Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
Landscapes
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はポリウレタン等の発泡体からなる圧縮
多孔質素材の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for manufacturing a compressed porous material made of a foam such as polyurethane.
一般的に発泡体の製造にあたつては、成形時点
で発泡薬剤や発泡倍率を予め設定して所望の発泡
倍率としている。
Generally, when manufacturing a foam, the foaming agent and foaming ratio are set in advance at the time of molding to obtain a desired foaming ratio.
すなわち、多孔質材として仕上げる前に、条件
が設定され、その条件によつて所望の発泡密度の
発泡体を製造するという方法が取られている。こ
の方法の典型的なものとしてキヤスト成形法が上
げられる。 That is, a method is used in which conditions are set before finishing the material as a porous material, and a foam having a desired foam density is manufactured based on the conditions. A typical example of this method is cast molding.
しかしながら、上述のように発泡処理前に発泡
剤や機械の条件を設定する方法では、条件に応じ
て成形用鋳型を製作する必要があり、この鋳型の
作成に多くの経費や労力を費すことが多々ある。
また、設備的に最適な条件を見出すために多くの
日数を要したりして、不利な面が多い。加えて、
上記の成形方法では相当な熟練を必要とするとい
う難点もある。更に、品質面について言えば、上
述の方法では、複合機能を有し且つ所望密度の発
泡体を得ることが非常に難しい。
However, with the above-mentioned method of setting the foaming agent and machine conditions before the foaming process, it is necessary to create a mold for molding according to the conditions, which requires a lot of expense and effort. There are many.
In addition, there are many disadvantages in that it takes many days to find the optimum conditions in terms of equipment. In addition,
The above molding method also has the disadvantage of requiring considerable skill. Furthermore, in terms of quality, it is very difficult to obtain a foam with multiple functions and a desired density using the methods described above.
例えば、発泡ウレタンに柔軟弾性機能とともに
強吸水保水機能を具備させようとすると、上述の
方法では、発泡剤とともに吸水性素材をウレタン
樹脂に配合して発泡させる。しかし、吸水性素材
を配合して所望密度、すなわち所望の発泡倍率の
発泡体を得るためには発泡時に微妙なコントロー
ルが必要であり、実際問題として所望の発泡倍率
の発泡体を得ることは非常に困難である。 For example, in order to provide urethane foam with a strong water-absorbing and water-retaining function as well as a flexible and elastic function, the above-mentioned method involves blending a water-absorbing material with a foaming agent into a urethane resin and foaming the resin. However, in order to obtain a foam with a desired density, that is, a desired expansion ratio by blending a water-absorbing material, delicate control is required at the time of foaming, and as a practical matter, it is very difficult to obtain a foam with a desired expansion ratio. It is difficult to
なお、柔軟で且つ弾性を有する発泡体に、上述
の強吸水保水機能に限らず、研磨機能や吸油機能
を併せて具備させることができれば、拭き具、化
粧用塗布具、衛生材料または衣料雑貨等に、極め
て広範な用途が期待できる。 In addition, if a flexible and elastic foam can be provided with polishing and oil-absorbing functions in addition to the above-mentioned strong water-absorbing and water-retaining functions, it can be used as wipes, cosmetic applicators, sanitary materials, clothing miscellaneous goods, etc. An extremely wide range of applications can be expected.
本発明は上述した問題点に鑑み開発されたもの
であり、その目的は、単一素材の柔軟な発泡体に
後加工を施すことにより、発泡体を所望の見掛密
度とすることができ、また発泡体に所望の機能を
具備させることも可能な方法を提供することにあ
る。
The present invention was developed in view of the above-mentioned problems, and its purpose is to provide a foam with a desired apparent density by post-processing a flexible foam made of a single material. Another object of the present invention is to provide a method that allows a foam to have desired functions.
本発明においては、上記の目的を、通気性を有
する発泡体に合成樹脂液または合成樹脂原料液を
付着させた後乾燥し、更に前記発泡体に前記発泡
体の孔径よりも小さな熱可塑性合成樹脂粉粒体を
付着させ、その後前記発泡体と合成樹脂粉粒体の
融点温度の中間温度で加熱圧縮しつつ固定化処理
を行う圧縮多孔質素材の製造方法により達成す
る。
In the present invention, the above object is achieved by attaching a synthetic resin liquid or a synthetic resin raw material liquid to an air-permeable foam, and then drying the foam, and then applying a thermoplastic synthetic resin smaller than the pore diameter of the foam to the foam. This is achieved by a method for manufacturing a compressed porous material, in which a powder is attached and then a fixation process is performed while heating and compressing at a temperature intermediate between the melting points of the foam and the synthetic resin powder.
本発明の基本的な構成を述べると、ポリエステ
ルベースもしくはポリエーテルベースのウレタン
等の連続気泡の発泡体またはその他の通気性を有
する発泡体の骨格部表面に、その骨格素材よりも
融点が低い熱可塑性樹脂またはブロツクされたイ
ソシアネート類の如く、加熱、解離により接着機
能を有する合成樹脂原料を含浸または塗布した
後、乾燥する。次いで、発泡体の孔径よりも小さ
なナイロンもしくはエチレン酢酸ビニル共重合体
等のホツトメルト性を有する粉粒体単体、または
前記粉粒体と海綿末、皮粉、炭酸カルシウム粉、
木粉末等の有機もしくは無機物の粉粒体との混合
物を、振動もしくは散布等の方法により、または
溶液媒体とともに、前記発泡体の孔内に付着させ
た後、加熱圧縮を行い発泡体を所望の見掛密度と
する。
To describe the basic structure of the present invention, heat having a melting point lower than that of the skeleton material is applied to the surface of the skeleton of an open-cell foam such as polyester-based or polyether-based urethane or other breathable foam. After impregnating or applying a synthetic resin raw material such as a plastic resin or blocked isocyanate that has an adhesive function by heating and dissociation, it is dried. Next, a single powder or granule having hot-melt properties such as nylon or ethylene vinyl acetate copolymer having a smaller pore size than the pore size of the foam, or the powder and granule together with sponge powder, skin powder, calcium carbonate powder,
A mixture of organic or inorganic powder such as wood powder is deposited into the pores of the foam by vibration or scattering, or together with a solution medium, and then heated and compressed to form the foam into the desired shape. Apparent density.
換言すれば、所望の密度よりも小さな密度に仕
上げた発泡体の骨格表皮部に反応性または溶融性
の強接着性の素材を付着させておき、更に接着機
能を有するホツトメルト性粉粒体のみ、またはホ
ツトメルト性粉粒体とともに所望機能を有する素
材の粉粒体を発泡体に付着させ、加熱圧縮により
発泡体の密度を所望の密度まで高めるものであ
る。また、所望機能を有する素材の粉粒体を入れ
た場合には、これら粉粒体により吸水性、研磨性
等の機能が付与された改質発泡体が得られる。 In other words, a reactive or meltable strongly adhesive material is attached to the skeletal skin part of the foam finished at a density lower than the desired density, and only hot-melt granular material having an adhesive function is used. Alternatively, powder and granules of a material having a desired function are attached to a foam together with hot-melt powder, and the density of the foam is increased to a desired density by heating and compression. In addition, when granules of a material having desired functions are added, a modified foam having functions such as water absorption and abrasive properties can be obtained by these granules.
以下、実施例に基づき本発明を詳細に説明す
る。なお、言うまでもなく本発明はこれらの実施
例に限定されるものではない。
Hereinafter, the present invention will be explained in detail based on Examples. It goes without saying that the present invention is not limited to these examples.
実施例 1
発泡倍率が8倍で厚さが6mmのポリエステル系
ポリウレタンフオームシートを、フエノールでブ
ロツクされたメチレンビス4フエニールイソシア
ネートを2%およびジブチル錫ジラウレートを
0.1%含むメチルエチルケトン(MEK)とメチル
アルコールの1:1の混合液中に浸漬し、50%絞
りになるように脱液した後、60℃で乾燥した。次
に、融点が120℃の100メツシユ通過のナイロン樹
脂粉末と100メツシユ通過の海綿粉末とが3:1
の割合で混合された混合物を、前記ポリウレタン
フオームシートに散布し、振動板上で振動させて
フオームシートの孔内にできるだけ均一に付着さ
せた。次いで表面が波形になつたプレス板の板面
を180℃にセツトしたプレス機により厚さ4mmの
状態で約5分間加熱圧縮処理し、厚さが4mmに固
定化され且つ表面に波形を有する柔軟で且つ弾性
および吸水性を有するシートを得た。Example 1 A polyester polyurethane foam sheet with an expansion ratio of 8 times and a thickness of 6 mm was prepared by adding 2% of phenol-blocked methylene bis-4 phenyl isocyanate and dibutyltin dilaurate.
It was immersed in a 1:1 mixture of 0.1% methyl ethyl ketone (MEK) and methyl alcohol, removed to a 50% reduction, and then dried at 60°C. Next, nylon resin powder with a melting point of 120°C and passed through 100 meshes and sponge powder passed through 100 meshes were mixed in a ratio of 3:1.
The mixture mixed in the proportions of 1 to 3 was spread on the polyurethane foam sheet, and was vibrated on a diaphragm to adhere as uniformly as possible within the holes of the foam sheet. Next, the surface of the pressed plate with the corrugated surface was heated and compressed for about 5 minutes to a thickness of 4 mm using a press machine set at 180°C to form a flexible sheet with a fixed thickness of 4 mm and a corrugated surface. A sheet having elasticity and water absorbency was obtained.
実施例 2
発泡倍率が12倍で厚さが35mmのポリウレタンフ
オームに、ジメチルヒドロキシエチレン尿素(ベ
ツカミンNF−1第日本インキ(株)製)がウレタン
フオームの重量の7%、塩化マグネシウムがウレ
タンフオームの重量の0.7%になるように水溶液
に含浸させた後、50%絞りになるように脱液し、
80℃で乾燥した。次に、塩化ビニル・酢酸ビニル
共重合体樹脂粉末、炭酸カルシウム50メツシユ通
過粉末およびCMC(カルボキシメチルセルロー
ス)の架橋生成体粉末の適量を混合し、前記ポリ
ウレタンフオーム上に散布し、振動させてフオー
ムの孔内に付着させた。次いで板面温度が180℃
のプレス機により厚さ10mmにセツトし7分間加熱
圧縮し、厚さが10mmの柔軟で吸水性を有し、表面
が粗面の圧縮多孔質シートを得た。Example 2 A polyurethane foam with an expansion ratio of 12 times and a thickness of 35 mm was mixed with dimethyl hydroxyethylene urea (Betsukamine NF-1 manufactured by Dai-Nippon Ink Co., Ltd.) in an amount of 7% of the weight of the urethane foam, and with magnesium chloride in an amount of 7% by weight of the urethane foam. After impregnating it in an aqueous solution to a concentration of 0.7% of the weight, it is dehydrated to a concentration of 50%.
Dry at 80°C. Next, appropriate amounts of vinyl chloride/vinyl acetate copolymer resin powder, calcium carbonate powder passed through 50 meshes, and CMC (carboxymethyl cellulose) crosslinked product powder are mixed, sprinkled on the polyurethane foam, and shaken to form a foam. It was attached inside the hole. Next, the board surface temperature is 180℃
The sheet was set to a thickness of 10 mm using a press machine, and heated and compressed for 7 minutes to obtain a compressed porous sheet with a thickness of 10 mm, which was flexible, had water absorption properties, and had a rough surface.
実施例1では、多孔質骨格表皮部に付着したブ
ロツクイソシアネートが最終の加熱圧縮工程で解
離し、反応して、骨格の接着現象を呈するもので
あり、同時にホツトメルト性を有する粉粒体が孔
内の改質材を接合するように作用する。この実施
例においては、プレス板表面の凹凸模様を発泡体
の表面に転写している。 In Example 1, the block isocyanate adhering to the porous skeletal skin dissociates and reacts in the final heat compression process, resulting in a skeletal adhesion phenomenon. It acts to bond the modified materials. In this example, the uneven pattern on the surface of the press plate is transferred to the surface of the foam.
実施例2においては、ホツトメルト性の樹脂お
よびホツトメルト性の粉粒体を骨格の表皮部およ
び孔内に付着させているが、実施例1と同様の効
果を奏することができる。 In Example 2, hot-melt resin and hot-melt powder are adhered to the skin of the skeleton and inside the pores, but the same effects as in Example 1 can be achieved.
上記実施例では、特に発泡ウレタンフオームを
用いていたが、接着剤および改質のための粉粒体
を適宜選定することにより、他の発泡体も同様に
処理することができる。 In the above embodiments, urethane foam was particularly used, but other foams can be treated in the same way by appropriately selecting the adhesive and the powder for modification.
骨格表皮部に付着させる樹脂としては次のよう
なものが好ましい。 The following resins are preferred as the resin to be attached to the skeletal skin.
反応タイプとしては、予めフエノールまたは3
級アルコールでブロツクされた2官能基以上のイ
ソシアネート基を含む各種化合物が良好である。 As for the reaction type, phenol or 3
Various compounds containing two or more functional isocyanate groups blocked with an alcohol are suitable.
また、低温度溶融樹脂としては、ナイロン、
EVA(エチレンビニル・アセテート)、ポリエス
テル、アクリル、ポリウレタン樹脂等が良い。 In addition, low-temperature melting resins include nylon,
Good materials include EVA (ethylene vinyl acetate), polyester, acrylic, and polyurethane resin.
また、接着のために使用する粉粒体としては次
のようなものが好ましい。 Further, as the powder or granular material used for adhesion, the following are preferable.
補強、すなわち、強度の向上を目的とする場合
には、ナイロン、ポリエステル、アクリル、ポリ
ウレタンEVA(エチレンビニル・アセテート)
等の樹脂粉粒体等が良い。 For reinforcement, that is, to improve strength, use nylon, polyester, acrylic, polyurethane EVA (ethylene vinyl acetate)
Resin powder and granules such as .
これらの合成樹脂粉粒体とともに混合される改
質材としては、研磨性を高める場合には、炭酸カ
ルシウム粉末、酸化珪素粉末、テフロン粉末等を
混入すると良い。 As the modifier to be mixed with these synthetic resin powders, calcium carbonate powder, silicon oxide powder, Teflon powder, etc. may be mixed in order to improve the abrasiveness.
更に、吸水保水性を高める場合には、CMC
(カルボキシメチルセルロース)の架橋生成体、
澱粉ポリアクリロニトリルグラフト重合体のアル
カリ金属カルボキシレート塩等の超吸水保水性素
材、海綿、ビニロン、レーヨン粉末等も良い。こ
れらの無機、有機の粉粒体は吸油効果もある。 Furthermore, when increasing water absorption and water retention, CMC
(carboxymethylcellulose) crosslinked product,
Super-absorbent and water-retentive materials such as alkali metal carboxylate salts of starch polyacrylonitrile graft polymers, sponges, vinylon, rayon powders, etc. are also suitable. These inorganic and organic powders also have an oil-absorbing effect.
また、得られた発泡体の外観を向上したり風合
を良好にする場合には、木粉または馬皮、牛皮も
しくは各種合皮の粉末等を混合配合することが好
ましく、このようにすることにより衣料雑貨等の
用途に最適な発泡体が得られる。 In addition, in order to improve the appearance or feel of the obtained foam, it is preferable to mix and blend wood flour, horsehide, cowhide, or various synthetic leather powders, etc. As a result, a foam suitable for use in clothing and miscellaneous goods etc. can be obtained.
前述した実施例1の素材に上述のような粉粒体
を併用することにより、弾性柔軟性に加えて吸水
性を具備し、且つ素材強度も向上した。この素材
を化粧用パフに仕上げた結果、弾性柔軟性、吸水
性、強度等において従来にない機能を持つ優れた
ものが得られた。更に、この素材は小児用オムツ
カバー等の衛生材分野にも使用できるものであつ
た。 By using the above-mentioned granular material in combination with the material of Example 1, the material was provided with water absorbency in addition to elastic flexibility, and the strength of the material was also improved. As a result of making this material into a cosmetic puff, we were able to obtain an excellent product with unprecedented functions such as elasticity, flexibility, water absorption, and strength. Furthermore, this material could also be used in the field of sanitary materials such as diaper covers for children.
また、上述の実施例2に無機粉末および吸水剤
を配合することにより、拭き具や洗滌用具等の雑
貨分野での広範な応用が可能となつた。 Further, by blending inorganic powder and a water absorbing agent into the above-mentioned Example 2, it became possible to apply it widely in the field of miscellaneous goods such as wiping tools and cleaning tools.
更に、部分圧縮、表面凹凸模様圧縮により音響
面での可変化が簡単にできるので音響材としての
用途がある。 Furthermore, it can be used as an acoustic material because it can be easily varied in terms of acoustics by partial compression and compression of surface unevenness patterns.
以上のように、本発明の方法によれば、発泡体
を後加工することにより、容易に所望の発泡密度
とすることができる。しかも本発明の方法は少量
の場合にも簡単に実施でき、設備、経費も節約で
きる。また改質材を用いることにより、発泡体の
有する柔軟弾性という利点を損ねることなく、更
に付加価値の高い所望の品質とすることもでき
る。本発明の方法では改質材を選定することによ
り、種々の改質が可能であり、衣料、洗滌雑貨、
化粧用具、衛生材、音響材等の種々の広範な分野
に使用可能であり、業界の発展に大きく寄与する
ものである。
As described above, according to the method of the present invention, a desired foam density can be easily achieved by post-processing the foam. Moreover, the method of the present invention can be easily carried out even in small quantities, and equipment and costs can be saved. Furthermore, by using a modifying material, it is possible to obtain a desired quality with even higher added value without impairing the advantage of flexibility and elasticity that the foam has. In the method of the present invention, various modifications can be made by selecting the modification material, and various modifications can be made to clothing, laundry miscellaneous goods,
It can be used in a wide variety of fields such as cosmetic tools, sanitary materials, and acoustic materials, and will greatly contribute to the development of the industry.
Claims (1)
成樹脂原料液を付着させた後乾燥し、更に前記発
泡体に前記発泡体の孔径よりも小さな熱可塑性合
成樹脂粉粒体を付着させ、その後前記発泡体と合
成樹脂粉粒体の融点温度の中間温度で加熱圧縮し
つつ固定化処理を行うことを特徴とする圧縮多孔
質素材の製造方法。1. A synthetic resin liquid or a synthetic resin raw material liquid is attached to an air-permeable foam, and then dried, and thermoplastic synthetic resin powder particles smaller than the pore diameter of the foam are attached to the foam, and then the A method for producing a compressed porous material, characterized in that a fixing treatment is performed while heating and compressing at a temperature intermediate between the melting points of a foam and a synthetic resin powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1822279A JPS55111237A (en) | 1979-02-20 | 1979-02-20 | Production of compressed porous material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1822279A JPS55111237A (en) | 1979-02-20 | 1979-02-20 | Production of compressed porous material |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9752286A Division JPS61258843A (en) | 1986-04-26 | 1986-04-26 | Compressed porous material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS55111237A JPS55111237A (en) | 1980-08-27 |
JPS6142623B2 true JPS6142623B2 (en) | 1986-09-22 |
Family
ID=11965608
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1822279A Granted JPS55111237A (en) | 1979-02-20 | 1979-02-20 | Production of compressed porous material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55111237A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS496263A (en) * | 1972-05-10 | 1974-01-19 | ||
JPS50154579A (en) * | 1974-06-05 | 1975-12-12 |
-
1979
- 1979-02-20 JP JP1822279A patent/JPS55111237A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS496263A (en) * | 1972-05-10 | 1974-01-19 | ||
JPS50154579A (en) * | 1974-06-05 | 1975-12-12 |
Also Published As
Publication number | Publication date |
---|---|
JPS55111237A (en) | 1980-08-27 |
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