JPH0193353A - Preparation of foam - Google Patents
Preparation of foamInfo
- Publication number
- JPH0193353A JPH0193353A JP62251304A JP25130487A JPH0193353A JP H0193353 A JPH0193353 A JP H0193353A JP 62251304 A JP62251304 A JP 62251304A JP 25130487 A JP25130487 A JP 25130487A JP H0193353 A JPH0193353 A JP H0193353A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- foam
- support liner
- closed system
- substance
- 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
- 239000006260 foam Substances 0.000 title claims abstract description 40
- 239000000203 mixture Substances 0.000 claims abstract description 34
- 239000000839 emulsion Substances 0.000 claims abstract description 12
- 239000000126 substance Substances 0.000 claims abstract description 9
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 6
- 239000004088 foaming agent Substances 0.000 claims abstract description 6
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 4
- 238000010907 mechanical stirring Methods 0.000 claims description 4
- 239000010410 layer Substances 0.000 abstract description 20
- 150000001875 compounds Chemical class 0.000 abstract description 10
- 238000000576 coating method Methods 0.000 abstract description 7
- 238000000034 method Methods 0.000 abstract description 7
- 239000011248 coating agent Substances 0.000 abstract description 5
- 238000003756 stirring Methods 0.000 abstract description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 4
- 229920001971 elastomer Polymers 0.000 abstract description 4
- 239000005060 rubber Substances 0.000 abstract description 4
- 239000011593 sulfur Substances 0.000 abstract description 4
- 229910052717 sulfur Inorganic materials 0.000 abstract description 4
- 239000004640 Melamine resin Substances 0.000 abstract description 3
- 229920000877 Melamine resin Polymers 0.000 abstract description 3
- 239000002280 amphoteric surfactant Substances 0.000 abstract description 2
- 239000003945 anionic surfactant Substances 0.000 abstract description 2
- 230000001804 emulsifying effect Effects 0.000 abstract description 2
- 239000003822 epoxy resin Substances 0.000 abstract description 2
- 239000002736 nonionic surfactant Substances 0.000 abstract description 2
- 229920000647 polyepoxide Polymers 0.000 abstract description 2
- 239000005056 polyisocyanate Substances 0.000 abstract description 2
- 229920001228 polyisocyanate Polymers 0.000 abstract description 2
- 229920003002 synthetic resin Polymers 0.000 abstract description 2
- 239000000057 synthetic resin Substances 0.000 abstract description 2
- 229940126062 Compound A Drugs 0.000 abstract 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000129 anionic group Chemical group 0.000 abstract 1
- 239000011247 coating layer Substances 0.000 abstract 1
- 238000009472 formulation Methods 0.000 description 18
- 239000000123 paper Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 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 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000010345 tape casting Methods 0.000 description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229940096992 potassium oleate Drugs 0.000 description 2
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940088990 ammonium stearate Drugs 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229940094506 lauryl betaine Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- -1 polyoxyethylene Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は発泡体の製法に関するもので、さらに詳しくは
支持ライナーと一体化した薄層状態で積層されているか
、或いは支持ライナーから剥離された薄手発泡体フィル
ムの状態で得られる発泡体の製法及び該製法から得られ
る薄手発泡体フィルムを提供するものである。[Detailed Description of the Invention] <Industrial Application Field> The present invention relates to a method for producing a foam, and more particularly, the present invention relates to a method for producing a foam, and more specifically, a foam that is laminated in a thin layer integrated with a support liner or peeled from a support liner. The present invention provides a method for producing a foam obtained in the form of a thin foam film, and a thin foam film obtained from the method.
〈従来技術とその問題点〉
従来、ゴム状物質エマルジョンを主成分とする配合物を
機械的に撹拌した微細泡含有配合物を用いて発泡体を製
造する方法としては、型への流し込み法、ロールコート
法、ナイフコート法などが知られている。<Prior art and its problems> Conventionally, methods for producing foam using a microfoam-containing composition obtained by mechanically stirring a composition containing a rubber-like substance emulsion as a main component include a method of pouring into a mold; Roll coating methods, knife coating methods, etc. are known.
しかして、型への流し込み法は、長尺の発泡体シートが
得られないばかりか、生産に時間がかかるという問題が
あった。However, the casting method has the problem that not only is it impossible to obtain a long foam sheet, but also that it takes a long time to produce.
一方、ロールコート法、ナイフコート法などのコート法
は、微細泡含有配合物がコータ一部分に一時的に溜られ
て支持ライナーに塗布されるが。On the other hand, in coating methods such as roll coating and knife coating, the fine bubble-containing compound is temporarily accumulated in a portion of the coater and applied to the support liner.
空気と接触している部分が外的条件などによって部分的
にゲル化したりすることがあり、このゲルがコータ一部
分に付着したり、塗布した配合物膜、の内部或いは表面
に付着したりするために、支持ライナー上の配合物膜に
スジが付いたり、厚みが不均一になったりするという問
題があった。Parts that are in contact with air may partially gel due to external conditions, and this gel may adhere to a portion of the coater or adhere to the inside or surface of the applied compound film. Another problem was that the compound film on the support liner was streaked and had an uneven thickness.
く問題点を解決するための手段〉
本発明はかかる従来技術の問題点を解決した新規な発泡
体の製法を提供するもので、その要旨とするところは、
ゴム様物質エマルジョン、架橋剤及び起泡剤を必須成分
とする配合物を機械的撹拌にて微細泡含有配合物とし、
該含有配合物を密閉系より支持ライナー上に供給塗布し
乾燥すること′ である。Means for Solving the Problems> The present invention provides a novel method for producing a foam that solves the problems of the prior art, and its gist is as follows:
A mixture containing a rubber-like substance emulsion, a crosslinking agent, and a foaming agent as essential components is mechanically stirred to form a fine foam-containing formulation,
The containing formulation is supplied and coated onto the support liner from a closed system and dried.
本発明の製法によれば、微細泡含有配合物は。According to the process of the invention, the microfoam-containing formulation is.
支持ライナー上に供給塗布される直前まで空気等の外的
制約を受けることなく密閉系とされているので配合物の
ゲル化や消泡がなく、従ってスジが付いたり、厚みが不
均一となることがなく、シかも均一な気泡を有する発泡
体層又は発泡体フィルムが得られるものである。Since it is a closed system without external restrictions such as air until just before it is supplied onto the support liner, there is no gelling or defoaming of the compound, resulting in streaks or uneven thickness. It is possible to obtain a foam layer or a foam film having uniform cells without any problems.
本発明の実施に当って用いられるゴム様物質エマルジョ
ンとしては、天然ゴム、ウレタンゴム。Rubber-like substance emulsions used in the practice of the present invention include natural rubber and urethane rubber.
シリコーンゴム、フッ素ゴム、クロロプレンゴム。Silicone rubber, fluorine rubber, chloroprene rubber.
ニトリルゴム、スチレンブタジェンゴム、スチレン−イ
ンブレン−スチレン共重合体ゴムの如きゴム類及び(又
は)エチレン−酢酸ビニル共重合体。Rubbers such as nitrile rubber, styrene-butadiene rubber, styrene-imbrene-styrene copolymer rubber, and/or ethylene-vinyl acetate copolymers.
アクリル酸エステルを主体とする重合体又は共重合体な
どの合成樹脂類を常法に従ってエマルジョン化したもの
が挙げられる。該エマルジョンは。Examples include those obtained by emulsifying synthetic resins such as polymers or copolymers mainly composed of acrylic esters according to conventional methods. The emulsion is.
固型分が30〜70重祉%、好ましくは50〜65重量
%に調整したものが使用される。The solid content is adjusted to 30 to 70% by weight, preferably 50 to 65% by weight.
架橋剤としては、イオウ、メラミン系樹脂、エポキシ系
樹脂、ポリイソシネートなどが使用され。As the crosslinking agent, sulfur, melamine resin, epoxy resin, polyisocyanate, etc. are used.
起泡剤としては、ステアリン酸アンモン、ラウリル酸硫
酸ナトリウム、オレイン酸カリ石けんなどのアニオン系
、ポリオキシエチレン誘導体などのノニオン系、ラウリ
ルベタインなどの両性系などの界面活性剤が用いられる
。As the foaming agent, surfactants such as anionic surfactants such as ammonium stearate, sodium lauryl sulfate, and potassium oleate soap, nonionic surfactants such as polyoxyethylene derivatives, and amphoteric surfactants such as lauryl betaine are used.
これらの架橋剤及び起泡剤は、前記エマルジョンの固型
分100重量部に対してそれぞれ0.3〜7重量部及び
0.1〜10重量部の範囲で添加されて配合物とされる
。These crosslinking agents and foaming agents are added in amounts of 0.3 to 7 parts by weight and 0.1 to 10 parts by weight, respectively, to 100 parts by weight of the solid content of the emulsion to form a blend.
該配合物には、必要に応じてカルボキシル化エチルアク
リレート、メセルセルローズ、アルギン酸ナトリウムの
如き増粘剤、アンモニア、苛性ソーダの如きPH調整剤
、ポリエチレングリコール。The formulation may optionally contain carboxylated ethyl acrylate, mecellulose, thickeners such as sodium alginate, PH adjusters such as ammonia, caustic soda, polyethylene glycol.
ポリメチルビニルエーテル、ケイフッ化ソーダの如きゲ
ル化剤などの配合剤を、前記エマルジョンの固型分10
0重量部に対して合計で0.1〜20重量部の範囲で添
加することができる。A gelling agent such as polymethyl vinyl ether or sodium fluorosilicide is added to the solid content of the emulsion.
It can be added in a total amount of 0.1 to 20 parts by weight based on 0 parts by weight.
このように配合され念配合物は通常10〜300ボイズ
(at 20℃)の粘度に調整され、均一に撹拌混合さ
れる。The thus blended mixture is usually adjusted to a viscosity of 10 to 300 voids (at 20 DEG C.) and stirred and mixed uniformly.
このように撹拌混合された配合物は、オークスミキサ−
、ファインフオーム、ハイミキサーの如き撹拌機にて、
気体を配合物に強制的に導入しながら撹拌(撹拌速度5
00〜3000r、 p、m 20℃)して、気泡径約
30〜100.coxで、粘度30〜1000ボイズ(
at 20℃)に調整された1、5〜10倍の微細泡含
有配合物とされる。The mixture thus stirred and mixed is processed using an oak mixer.
, fine form, high mixer, etc.
Stir while forcing gas into the formulation (stirring speed 5
00-3000r, p, m 20℃), and the bubble diameter is about 30-100. cox, viscosity 30 to 1000 boise (
at 20° C.) to form a formulation containing 1,5 to 10 times as many microbubbles.
調整された抱含有配合物Aは1例えば図示する如き密閉
系の容器に注入され、支持ライナーに供給塗布される直
前まで空気に触れることがないように設計されていてゲ
ル化が防止されている。図面において、】は密閉系容器
で、左端に吐出口2を有する。3は支持ライナーで、容
器1の吐出口2の外端はライナー3と接触することがな
いように所定の間隙が設けられている。ライナー上に吐
出口2から供給塗布された配合物1m Aの厚みは。The prepared formulation A is poured into a closed container, for example as shown in the figure, and is designed not to come into contact with air until immediately before being supplied to the support liner to prevent gelation. . In the drawings, ] is a closed container, which has a discharge port 2 at the left end. 3 is a support liner, and a predetermined gap is provided so that the outer end of the discharge port 2 of the container 1 does not come into contact with the liner 3. The thickness of 1 mA of the formulation supplied from the discharge port 2 onto the liner is:
吐出口2の幅を調整することによって自在に変えること
ができるが1通常は30〜2000μm の範囲とされ
る。Although the width of the discharge port 2 can be freely changed by adjusting the width, it is usually in the range of 30 to 2000 μm.
支持ライナーは1発泡体薄層を有する積層物を得るか、
或いは薄手発泡体フィルムを得るか、その目的によって
選択される。即ち1発泡体薄層企有する積層物を得る場
合は、支持ライナー自体を発泡体層l−を構成する前記
抱含有配合物と親和性を有する材質のものから選択する
か、或いは支持ライナー自体は低親和性であるが表面を
活性化処理するか又は表面に親和性物質を塗設又はラミ
ネートなどして前記配合物と親和性を有するように調整
し1発泡体薄層が支持ライナー上に強固に接着一体化さ
せる。このようにして得られるシート状の積8j4物は
1例えばその緩衝性を活かして包装材料などに使用でき
る。The supporting liner obtains a laminate with one foam layer or
Alternatively, the choice is made depending on the purpose of obtaining a thin foam film. That is, if a laminate with one foam layer is to be obtained, the support liner itself is selected from a material having an affinity with the formulation comprising the foam layer l-, or the support liner itself is Although the foam has a low affinity, the surface is activated or coated or laminated with an affinity substance to make it compatible with the above-mentioned formulation, and a thin foam layer is firmly attached to the support liner. Glue and integrate. The sheet-like product thus obtained can be used, for example, as a packaging material by taking advantage of its cushioning properties.
一方、薄手発泡体フィルムを得る場合は、支持ライナー
上で乾燥硬化させた発泡体1層が、ライナーから簡単に
剥離できることが必要でメジ、そのためにはライナーの
少なくとも表面が前記配合物に対して低親和性であるこ
とが必要である。これらのライナーとしては1紙、不&
lI布、織布1編布。On the other hand, if thin foam films are to be obtained, it is necessary that a single layer of foam dried and cured on a supporting liner can be easily peeled from the liner, so that at least the surface of the liner is free from the formulation. It is necessary to have low affinity. These liners include 1 paper, non &
1I cloth, 1 knitted woven cloth.
プラスチックフィルム、金属箔などが用いられ。Plastic films, metal foils, etc. are used.
また表面をシリコーン系、フッ素、長鎖アルキル系など
で処理したものも使用できる。Also, those whose surfaces have been treated with silicone, fluorine, long-chain alkyl, etc. can also be used.
このようなライナー上に塗布された抱含有配合物層¥′
i2通常70〜95℃で10〜300秒予備乾燥させて
層面が約80℃前後になるように調整して水分を蒸散さ
せ、次いで100〜200℃で100〜500秒加熱し
て架橋硬化させ、約30−100μmの気泡径を有する
発泡体薄層を得る。A layer of a curing formulation applied onto such a liner
i2 Normally pre-dry at 70-95°C for 10-300 seconds to adjust the layer surface to about 80°C to evaporate moisture, then heat at 100-200°C for 100-500 seconds to crosslink and cure, A thin foam layer with a cell diameter of approximately 30-100 μm is obtained.
〈効果〉
本発明の製法によれば、@細泡含有配合物は密閉系容器
から層重直前に支持ライナー上に供給されるためにゲル
化することがなく、従ってゲル化物によって発泡体薄層
にスジが付いたり、不均一な厚みとなったりすることが
なく、均一な厚みの発泡体薄層又は薄手発泡体フィルム
が得られるという特徴を有する。<Effects> According to the manufacturing method of the present invention, the fine foam-containing formulation is supplied from a closed container onto the support liner immediately before layering, so it does not gel, and therefore the gelled product does not form a foam thin layer. It has the characteristic that a thin foam layer or thin foam film with a uniform thickness can be obtained without streaks or non-uniform thickness.
〈実施例〉
以下に本発明の実施例を示す。文中部とあるのは重量部
を意味する。<Example> Examples of the present invention are shown below. The text middle part means the weight part.
実7M@1
アクリル酸エテル−アクリル酸ブチル−アクリロニトリ
ル共重合体(重量比で63:28:9)からなる固型分
59fflt%のアクリル系共重合体エマルジョン16
9.5部、メラミン樹脂2部、 スfアリン酸アンモ7
ン1部、カルボキシル化エテルアクリレート2部及びア
ンモニア水2部からなる配合物(粘度 80ボイズat
20℃)全オークスミキサ−(1500r、p、 m
at 20℃)で機械撹拌して1発泡倍率約2倍、気泡
径約30〜50μmの微細泡含有配合物(粘度150ボ
イズat20℃)を得る。Fruit 7M@1 Acrylic copolymer emulsion 16 with a solid content of 59 fflt% consisting of acrylic acid ether-butyl acrylate-acrylonitrile copolymer (63:28:9 by weight)
9.5 parts, 2 parts of melamine resin, 7 parts of ammonium sulfate
A formulation consisting of 1 part of carboxylated ether acrylate, 2 parts of aqueous ammonia (viscosity 80 voids
20℃) All oak mixer (1500r, p, m
A microfoam-containing formulation (viscosity 150 voids at 20°C) with a foaming ratio of about 2 times and a cell diameter of about 30 to 50 μm is obtained by mechanical stirring at 20°C.
該抱含有配合物を図示する形状の密閉系容器に注入し、
吐出口から支持ライナー(紙)上に厚さ約200μ惰で
吐出塗工し1次いで予備乾燥及び本乾燥を行って紙と発
泡体層I−とが一体化された積JflJ物を得た。Injecting the conjugate-containing formulation into a closed container of the shape shown in the figure,
The product was discharged from the discharge port onto a support liner (paper) to a thickness of about 200 μm, and then pre-dried and main-dried to obtain a product in which the paper and the foam layer I- were integrated.
得られた発泡体薄層は厚みが均一で且つ表面は平滑であ
り、約30〜50μmの均一な気泡径を有する。The resulting thin foam layer has a uniform thickness, a smooth surface, and a uniform cell diameter of approximately 30-50 μm.
実施例2
固型分60重量%の天然ゴムエマルジョン100部
イオウ 2部オレイ
ン酸カリ石けん 3部メチルセルロー
ズ 1部アンモニア水
2部ケイフッ化ソーダ
0.5部上記配合組成からなる配合物(粘度50
ボイズat20℃)をオークスミキサ−(500r、p
、 mat20℃)で機械撹拌して1発泡倍率3倍、気
泡径約50〜80μ鶏の微細泡含有配合物(粘度150
ボイズat20℃)を得る。Example 2 Natural rubber emulsion with a solid content of 60% by weight 100 parts sulfur 2 parts potassium oleate soap 3 parts methyl cellulose 1 part aqueous ammonia
2 parts Sodium fluorosilicide
0.5 part A blend consisting of the above composition (viscosity 50
Boise at 20℃) in an oak mixer (500r, p
, mat 20℃) with mechanical stirring to obtain a foaming ratio of 3 times and a bubble diameter of about 50 to 80μ (viscosity 150μ).
Boise at 20°C) is obtained.
該配合物を図示する形状の密閉系容器に注入し。Pour the mixture into a closed container of the shape shown.
吐出口から支持ライナー(表面を接着処理したポリエス
テルフィルム)上に厚さ約80μmで吐出塗工し2次い
で予備乾燥及び本乾燥を行ってポリエステルフィルムと
発泡体#fiとが一体化された積層物を得た。A laminate in which the polyester film and the foam #fi are integrated by discharging and coating from the discharge port onto a support liner (polyester film whose surface has been treated with adhesive) to a thickness of about 80 μm, and then pre-drying and main drying. I got it.
得られた発泡体薄層は厚みが均一で表面は緻密で平滑で
あシ、約50〜80μmの均一な気泡径を有する。The resulting thin foam layer has a uniform thickness, a dense and smooth surface, and a uniform cell diameter of approximately 50-80 μm.
冥施例3
dn分53重量%のニトリルゴムエマルジョン188.
5部
イオウ 3部ラウリ
ル硫酸ナトリウム 2部アルギン酸ナ
トリウム 0.5部アンモニア水
1部ケイフッ化ソーダ
0.3部上記配合組成からなる配合物(粘
度200ボイズat20℃)をオークスミキサ−(30
00r、p0mat20℃)で機械撹拌して1発泡倍率
3倍、気泡径約80〜100μmの微細泡含有配合物(
粘度500ボイズat20°C)?得る。Example 3 Nitrile rubber emulsion with dn content of 53% by weight 188.
5 parts sulfur 3 parts sodium lauryl sulfate 2 parts sodium alginate 0.5 parts ammonia water
1 part Sodium fluorosilicide
0.3 parts A mixture (viscosity: 200 voise at 20°C) having the above composition was mixed in an oak mixer (30°C).
00r, p0mat 20°C) with mechanical stirring to create a microfoam-containing formulation with a foaming ratio of 3 times and a bubble diameter of approximately 80 to 100 μm (
Viscosity 500voices at 20°C)? obtain.
該配合物を図示する形状の密閉系容器に注入し。Pour the mixture into a closed container of the shape shown.
吐出口から支持ライナー(クラフト紙の表面にポリオレ
フインをラミネートシ、この上にシリコーン糸剥離層を
形成した剥離紙)の剥J!il! 1m面に厚さ約11
00μmで吐出塗ニレ、次いで予備及び不乾燥を行い、
ライナー面から発泡体薄層を剥離して厚さ約1100μ
慣の薄手発泡体フィルムを得た。Peel off the support liner (a release paper made by laminating polyolefin on the surface of kraft paper and forming a silicone thread release layer on top of it) from the discharge port J! Il! Approximately 11cm thick on 1m surface
00μm discharge coating elm, then preliminary and non-drying,
Peel the foam thin layer from the liner surface to a thickness of approximately 1100μ
A conventional thin foam film was obtained.
この薄手発泡体フィルムは表裏面共に平滑で緻密な面を
有し、約80〜100μ偽の均一な気泡径′jk有する
。This thin foam film has smooth and dense surfaces on both the front and back surfaces, and has a uniform cell diameter 'jk of approximately 80 to 100 μm.
比較例
実施例1の微細泡含有配合物をロールコート法及びナイ
フコート法により、支持ライナー(紙)に塗布乾燥して
1紙と発泡体薄層とが一体化された槓I!1物を得た。Comparative Example The microfoam-containing formulation of Example 1 was coated on a support liner (paper) by roll coating and knife coating and dried to form a single paper and foam thin layer. I got one thing.
得られた積層物の発泡体薄層は、気泡径が約30〜20
0μ惰と不均一で1表面には肉眼で目視できるスジが無
数に与られた。The foam thin layer of the resulting laminate has a cell diameter of about 30-20
It was non-uniform with 0μ inertia, and there were countless streaks visible to the naked eye on one surface.
図面は本発明の製法に用いられる装置の概略説明図であ
る。
■・・・密閉系容器 2・・・吐出口3・・・支持ラ
イナーThe drawing is a schematic explanatory diagram of an apparatus used in the manufacturing method of the present invention. ■...Closed container 2...Discharge port 3...Support liner
Claims (1)
成分とする配合物を機械的撹拌にて微細泡含有配合物と
し、該含有配合物を密閉系より支持ライナー上に供給塗
布し乾燥することを特徴とする発泡体の製法。 2)支持ライナーの少なくとも表面が低親和性である特
許請求の範囲第1項記載の発泡体の製法。[Claims] 1) A blend containing a rubber-like substance emulsion, a crosslinking agent, and a foaming agent as essential components is made into a microfoam-containing blend by mechanical stirring, and the blend is transferred from a closed system onto a support liner. A method for producing a foam, which is characterized by supplying, applying and drying the foam. 2) The method for producing a foam according to claim 1, wherein at least the surface of the support liner has low affinity.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62251304A JPH0193353A (en) | 1987-10-05 | 1987-10-05 | Preparation of foam |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62251304A JPH0193353A (en) | 1987-10-05 | 1987-10-05 | Preparation of foam |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0193353A true JPH0193353A (en) | 1989-04-12 |
Family
ID=17220816
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62251304A Pending JPH0193353A (en) | 1987-10-05 | 1987-10-05 | Preparation of foam |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0193353A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05214156A (en) * | 1991-10-15 | 1993-08-24 | Merck & Co Inc | Gel-like foam |
JPH10324808A (en) * | 1996-08-23 | 1998-12-08 | Toray Ind Inc | Antifouling resin composition and coating material and underwater life antideposition dirt-preventing film |
JP2004202403A (en) * | 2002-12-26 | 2004-07-22 | Nippon Tokushu Toryo Co Ltd | Application method for coating type dumping material and coating type dumping material |
JP2006131779A (en) * | 2004-11-08 | 2006-05-25 | Sumitomo Chemical Co Ltd | Aqueous emulsion composition and foamed wall paper |
KR101240047B1 (en) * | 2010-12-15 | 2013-03-06 | 권순남 | Method for foaming rubber sheet of low milli thickness |
WO2016047612A1 (en) * | 2014-09-24 | 2016-03-31 | 日東電工株式会社 | Foam sheet |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5789942A (en) * | 1980-11-26 | 1982-06-04 | Bridgestone Corp | Production of non-gel latex foamed rubber |
-
1987
- 1987-10-05 JP JP62251304A patent/JPH0193353A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5789942A (en) * | 1980-11-26 | 1982-06-04 | Bridgestone Corp | Production of non-gel latex foamed rubber |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05214156A (en) * | 1991-10-15 | 1993-08-24 | Merck & Co Inc | Gel-like foam |
JPH10324808A (en) * | 1996-08-23 | 1998-12-08 | Toray Ind Inc | Antifouling resin composition and coating material and underwater life antideposition dirt-preventing film |
JP2004202403A (en) * | 2002-12-26 | 2004-07-22 | Nippon Tokushu Toryo Co Ltd | Application method for coating type dumping material and coating type dumping material |
JP2006131779A (en) * | 2004-11-08 | 2006-05-25 | Sumitomo Chemical Co Ltd | Aqueous emulsion composition and foamed wall paper |
KR101240047B1 (en) * | 2010-12-15 | 2013-03-06 | 권순남 | Method for foaming rubber sheet of low milli thickness |
WO2016047612A1 (en) * | 2014-09-24 | 2016-03-31 | 日東電工株式会社 | Foam sheet |
WO2016047611A1 (en) * | 2014-09-24 | 2016-03-31 | 日東電工株式会社 | Foam sheet |
JP6082498B2 (en) * | 2014-09-24 | 2017-02-15 | 日東電工株式会社 | Foam sheet |
JPWO2016047612A1 (en) * | 2014-09-24 | 2017-04-27 | 日東電工株式会社 | Foam sheet |
JPWO2016047611A1 (en) * | 2014-09-24 | 2017-07-06 | 日東電工株式会社 | Foam sheet |
US10316156B2 (en) | 2014-09-24 | 2019-06-11 | Nitto Denko Corporation | Foamed sheet |
JP2021008636A (en) * | 2014-09-24 | 2021-01-28 | 日東電工株式会社 | Foamed sheet |
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