JPH03267172A - Production of foam - Google Patents
Production of foamInfo
- Publication number
- JPH03267172A JPH03267172A JP6779190A JP6779190A JPH03267172A JP H03267172 A JPH03267172 A JP H03267172A JP 6779190 A JP6779190 A JP 6779190A JP 6779190 A JP6779190 A JP 6779190A JP H03267172 A JPH03267172 A JP H03267172A
- Authority
- JP
- Japan
- Prior art keywords
- type
- compsn
- fine pores
- foam
- liquid
- 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 9
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000007788 liquid Substances 0.000 claims abstract description 9
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims description 9
- 239000003973 paint Substances 0.000 claims description 5
- 239000000758 substrate Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 abstract description 16
- 238000000034 method Methods 0.000 abstract description 14
- 239000011248 coating agent Substances 0.000 abstract description 13
- 239000011347 resin Substances 0.000 abstract description 13
- 229920005989 resin Polymers 0.000 abstract description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 5
- 239000004593 Epoxy Substances 0.000 abstract description 4
- 239000000178 monomer Substances 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 3
- 229920000728 polyester Polymers 0.000 abstract description 3
- 238000003756 stirring Methods 0.000 abstract description 3
- 239000003054 catalyst Substances 0.000 abstract description 2
- 238000009833 condensation Methods 0.000 abstract description 2
- 230000005494 condensation Effects 0.000 abstract description 2
- 239000003431 cross linking reagent Substances 0.000 abstract description 2
- 239000011148 porous material Substances 0.000 abstract 4
- 238000003848 UV Light-Curing Methods 0.000 abstract 3
- 238000005187 foaming Methods 0.000 description 17
- 239000007789 gas Substances 0.000 description 11
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 6
- 238000001723 curing Methods 0.000 description 4
- 239000004088 foaming agent Substances 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 125000003396 thiol group Chemical class [H]S* 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 150000004808 allyl alcohols Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- SOGFHWHHBILCSX-UHFFFAOYSA-J prop-2-enoate silicon(4+) Chemical compound [Si+4].[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C SOGFHWHHBILCSX-UHFFFAOYSA-J 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 230000008054 signal transmission Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、薄肉細径高発泡電線・ケーブルの絶縁被覆あ
るいはその他の発泡シート、フィルムなどの発泡体を簡
易かつ効率よく製造するための方法に関するものである
。[Detailed Description of the Invention] [Industrial Application Field] The present invention provides a method for simply and efficiently producing insulation coatings for thin-walled, small-diameter, highly foamed electric wires and cables, and other foamed materials such as foamed sheets and films. It is related to.
[従来の技術]
近年、通信機器類や精密電子機器類は小型化あるいは高
密度実装化の傾向が著しく、その要請に対応するために
、ケーブル線心もますます細径化される傾向にあり、外
径が1.0−以下といった細径の絶縁電線も使用される
ようになった。[Conventional technology] In recent years, communication equipment and precision electronic equipment have shown a remarkable trend toward miniaturization and high-density packaging, and to meet this demand, cable cores are also becoming smaller and smaller in diameter. Insulated wires with small diameters, such as those with an outer diameter of 1.0 mm or less, have also come to be used.
一方、コンピュータなどにおいては、伝送信号の一層の
高速化を求める傾向が顕著であり、これに使用される上
記細径絶縁電線の絶縁体層を高発泡化し、可能な限り低
誘電率化することにより伝送信号の高速化を図った所謂
ハイスピードケーブルへの要望が高まっている。On the other hand, in computers and other devices, there is a remarkable tendency to require even faster transmission signals, and the insulator layer of the above-mentioned thin insulated wires used for this purpose is highly foamed and has a dielectric constant as low as possible. Therefore, there is an increasing demand for so-called high-speed cables that increase the speed of transmission signals.
コンピュータ等の信号伝送用電線・ケーブルに発泡絶縁
体を被覆する方法として、予め発泡させたフィルムを導
体上に巻付ける方法もとられているが、発泡絶縁体被覆
の形成には押出方式が用いられる場合が多い。A method of covering wires and cables for signal transmission in computers, etc. with foam insulation is to wrap a pre-foamed film around the conductor, but an extrusion method is used to form the foam insulation coating. This is often the case.
このような絶縁体の発泡手段としては、ガスにより発泡
させる物理的なガス発泡法と化学反応を利用した化学発
泡法が知られている。As means for foaming such an insulator, there are known a physical gas foaming method in which foaming is performed using gas, and a chemical foaming method that utilizes a chemical reaction.
前者のガス発泡法には、液体フロンのような揮発性発泡
用液体を溶融樹脂中に強制注入させ、その気化圧により
発泡させる方法、あるいは押出機中の溶融樹脂中に直接
気泡形成用ガスを圧入させることにより一様に分布した
細胞状の微細な独立気泡体を樹脂中に発生させる方法な
どがある。The former gas foaming method involves forcibly injecting a volatile foaming liquid such as liquid chlorofluorocarbon into the molten resin and causing foaming by its vaporization pressure, or directly injecting the foaming gas into the molten resin in an extruder. There is a method of generating uniformly distributed cellular fine closed cells in a resin by press-fitting the resin.
後者の化学発泡法は、樹脂中に発泡剤を分散混大した状
態で成形し、その後熱を加えることにより発泡剤を化学
的に反応分解させることによりガスを発生させ、発泡さ
せるものである。The latter chemical foaming method involves molding a resin with a foaming agent dispersed therein, and then applying heat to chemically decompose the foaming agent to generate gas and foam.
[発明か解決しようとする課題]
上記したガス発泡の前者の方法は、樹脂をいったん溶融
させその中に揮発性発泡用液体を強制注入するものであ
り、強い圧力を必要とする場合が多い。また、このよう
な液化ガスは気化圧が強く、微細な発泡構造体を得るこ
とが難しい上、良好な製品外観を得ることも困難である
。さらに、液化ガスの注入速度が遅いために高速化が難
しく、生産性に劣るという問題もある。[Problems to be Solved by the Invention] The former method of gas foaming described above involves once melting the resin and forcibly injecting a volatile foaming liquid into it, which often requires strong pressure. Furthermore, such liquefied gas has a strong vaporization pressure, making it difficult to obtain a fine foamed structure and also difficult to obtain a good product appearance. Furthermore, since the injection speed of the liquefied gas is slow, it is difficult to increase the speed, resulting in poor productivity.
また、押出機中で直接ガスを圧入する方法は、そのため
の特別な設備が必要であり、また特別の技術をも必要と
する。Further, the method of directly pressurizing gas into an extruder requires special equipment and special techniques.
一方、化学発泡の場合には、前述したように予め樹脂中
に発泡剤を混練し分散混合しておく必要があり、この発
泡剤を成形加工後に熱により反応分解させて生したガス
により発泡を行なわせるものである。従って、この際の
樹脂の成形加工温度は、発泡剤が成形加工中に分解しな
いようにするために当該発泡剤の分解温度より低く保持
されねばならないという問題があり、使用する発泡剤そ
のものが大巾に制約されるという問題がある。On the other hand, in the case of chemical foaming, as mentioned above, it is necessary to knead and disperse the foaming agent into the resin in advance, and after the molding process, this foaming agent is reacted and decomposed by heat, and the gas generated is used to cause foaming. It is something you can do. Therefore, there is a problem in that the molding temperature of the resin in this case must be kept lower than the decomposition temperature of the blowing agent in order to prevent the blowing agent from decomposing during the molding process, and the blowing agent used itself has a large There is a problem in that it is limited in width.
さらに、押出被覆方式の場合には、素線の径が細くなる
と、プレッシャーにより断線が起り易く高速化が難しく
なるという別な問題もあり、先に説明した導体の細径化
という今日的要請に対応しにくいという問題もある。Furthermore, in the case of the extrusion coating method, there is another problem in that as the diameter of the wire becomes smaller, it is more likely to break due to pressure, making it difficult to increase the speed. There are also problems that are difficult to deal with.
本発明の目的は、上記したような従来技術の問題点を解
消し、容易かつ高速に良好な外観を有する薄肉細径発泡
絶縁電線・ケーブルあるいは発泡シートやフィルムを入
手することができる発泡体の製造方法を提供しようとす
るものである。An object of the present invention is to solve the problems of the prior art as described above, and to easily and quickly obtain thin-walled, small-diameter foamed insulated wires/cables or foamed sheets or films with a good appearance. The purpose is to provide a manufacturing method.
[課題を解決するための手段]
本発明は、微細気泡を内在する液状の紫外線硬化型組成
物あるいは熱硬化型組成物を塗料として基体に塗布し、
これを硬化させるものであり、それによって硬化と同時
に発泡体を得ることができ、生産性を著しく向上させる
ことを可能としたものである。[Means for Solving the Problems] The present invention involves applying a liquid ultraviolet curable composition or thermosetting composition containing microbubbles to a substrate as a paint,
By curing this, a foam can be obtained at the same time as curing, making it possible to significantly improve productivity.
微細気泡を内在させるには、空気、酸素、窒素など任意
の気体を液状の前記組成物中に注入し、これを高速撹拌
すれば容易に微細気泡を分散させることができる。その
ための分散撹拌装置としては、微細な気泡を均一に分散
させることができればよいのであり、例えばジューサー
ミキサー等の汎用的撹拌機をそのまま使用しても差支え
ない。In order to incorporate fine bubbles, any gas such as air, oxygen, or nitrogen may be injected into the liquid composition, and the mixture may be stirred at high speed to easily disperse the fine bubbles. As a dispersion stirring device for this purpose, it is sufficient as long as it can uniformly disperse fine air bubbles, and for example, a general purpose stirring device such as a juicer mixer may be used as is.
本発明に使用する紫外線硬化型樹脂塗料としては、ラジ
カル重合型、カチオン重合型、エン/チオール重合型な
ど、紫外線によって硬化する塗料であればよく、ペース
オリゴマーとしては、例えばポリエステルアクリレート
、ウレタンアクリレート、エポキシアクリレート、ポリ
エーテルアクリレート、ポリブタジェンアクリレート、
エポキシウレタンアクリレート、シリコンアクリレート
、ポリエステルウレタンアクリレート、ポリエーテルウ
レタンアクリレート、ビニル/アクリルオリゴマー ポ
リエン/チオール、ポリスチリルエチルメタクリレート
などを挙げることができ、これらを塩素化あるいはふっ
素化したものでもよく、2種以上を組合せて使用しても
よい。The ultraviolet curable resin coating used in the present invention may be any coating that is cured by ultraviolet rays, such as radical polymerization type, cationic polymerization type, ene/thiol polymerization type, etc. Examples of the pace oligomer include polyester acrylate, urethane acrylate, Epoxy acrylate, polyether acrylate, polybutadiene acrylate,
Examples include epoxy urethane acrylate, silicon acrylate, polyester urethane acrylate, polyether urethane acrylate, vinyl/acrylic oligomer, polyene/thiol, polystyrylethyl methacrylate, etc. Chlorinated or fluorinated versions of these may also be used, and two or more types of these may be used. may be used in combination.
また、モノマーとしては、光重合性モノマー(反応性希
釈剤)としてビニルモノマー、単官能アクリレート、多
官能アクリレート、アリルアルコール誘導体などのほか
に、非反応性希釈剤を必要に応じて用いることができる
。In addition, as monomers, in addition to photopolymerizable monomers (reactive diluents) such as vinyl monomers, monofunctional acrylates, polyfunctional acrylates, allyl alcohol derivatives, non-reactive diluents can be used as necessary. .
光開始剤としてはアセトフェノン系、ベンゾイン系、ベ
ンゾフェノン系、チオキサンソン系、その他任意の光開
始剤を組合せることができる。また、光開始助剤を組合
せてもよい。As the photoinitiator, acetophenone type, benzoin type, benzophenone type, thioxanthone type, and other arbitrary photoinitiators can be combined. A photoinitiation aid may also be used in combination.
また、本発明に使用する熱硬化型樹脂塗料としては、微
細気泡を内在できるものであって、縮合型、付加重合型
など架橋剤や触媒の存在下において常温または加熱硬化
するものであればよく、エポキシ系、ポリウレタン系、
アクリル系など一液型や二液型あるいはそれ以上の組合
せてあってもよい。In addition, the thermosetting resin coating used in the present invention may contain fine bubbles and may be a condensation type, addition polymerization type, or other type that cures at room temperature or by heating in the presence of a crosslinking agent or catalyst. , epoxy type, polyurethane type,
It may be a one-component type, a two-component type, such as an acrylic type, or a combination of more.
この他必要に応じて熱重合禁止剤、充填剤、接着付与剤
、チクソ付与剤、可塑剤、非反応性ボリマー、着色剤、
難燃剤、難燃助剤、酸化防止剤、離型剤などを用いても
よい。In addition, thermal polymerization inhibitors, fillers, adhesion promoters, thixotropic agents, plasticizers, non-reactive polymers, colorants,
Flame retardants, flame retardant aids, antioxidants, mold release agents, etc. may also be used.
塗布する方法としてはスプレー ロールコータ、ディッ
ピングなど目的、用途、製品形状によって選択組合せす
ればよい。Coating methods such as spray, roll coater, and dipping may be selected and combined depending on the purpose, application, and product shape.
硬化方法としては必要とする紫外線を放出するものであ
ればよく、たとえば高圧水銀灯、メタルハライドランプ
などがある。Any curing method may be used as long as it emits the necessary ultraviolet rays, such as a high-pressure mercury lamp or a metal halide lamp.
この発泡架橋組成物は、フィルム、シートにすることも
でき、またプラスチック、金属物に塗布することも可能
である。また、金属線に塗布硬化させることで発泡電線
・ケーブルを容易につくることができる。This foamed crosslinked composition can be made into a film or sheet, and can also be applied to plastic or metal objects. In addition, foamed electric wires and cables can be easily made by coating and curing metal wires.
[実施例] 以下に、本発明について実施例を参照し説明する。[Example] The present invention will be described below with reference to Examples.
なお、下記それぞれの実施例における発泡度は次式によ
って計算した数値である。Note that the degree of foaming in each of the following examples is a value calculated using the following formula.
ここに
A・・・気泡を内在硬化させた組成物
B・・・気泡を内在せずに硬化させた組成物実施例1
微細気泡を内在させた紫外線硬化型ウレタンアクリレー
ト系塗料を、ガラス板上に流し厚さ3m1l (55
μm)のドクターブレード(東洋精機型 参考規格JI
S−に、−5101、JISK−5400ほか)を用い
て、被膜(フィルム状)を形成し、これを窒素雰囲気中
で紫外線を照射(ランプ強度80W/am、照射距離1
00mm、積算照射量100mJ/aIr)シ硬化させ
発泡架橋体を得、発泡度を測定したところ65〜73%
もの高発泡フィルムを得た。Here, A: Composition cured with internal bubbles B: Composition cured without internal bubbles Example 1 An ultraviolet curable urethane acrylate paint containing internal microbubbles was applied onto a glass plate. Pour into a thickness of 3ml (55
μm) doctor blade (Toyo Seiki type reference standard JI
A coating (film) was formed on S- using -5101, JISK-5400, etc.), and this was irradiated with ultraviolet rays in a nitrogen atmosphere (lamp intensity 80 W/am, irradiation distance 1).
00mm, cumulative irradiation dose 100mJ/aIr) was cured to obtain a foamed crosslinked product, and the foaming degree was measured to be 65 to 73%.
A highly foamed film was obtained.
実施例2
微細気泡を内在させた紫外線硬化型ウレタンアクリレー
ト系塗料を導体径127μmの金属線(スズメツキ線)
を線速200 m/minで塗布した後、紫外線を均一
に照射し硬化させ被覆厚50μmの発泡電線を得、発泡
度を測定したところ60〜71%もの高発泡架橋電線を
得た。Example 2 A metal wire (Suzmetsuki wire) with a conductor diameter of 127 μm was coated with ultraviolet curable urethane acrylate paint containing microbubbles.
was coated at a line speed of 200 m/min, and then uniformly irradiated with ultraviolet rays to cure the wire to obtain a foamed wire with a coating thickness of 50 μm.The degree of foaming was measured, and a highly foamed crosslinked wire of 60 to 71% was obtained.
実施例3
微細気泡を内在させた熱硬化型エポキシ系塗料を導体径
127μmの金属線(銀メツキ線)に線速100 m/
minで塗布した後、加熱炉(800°C)を通して硬
化させ、被覆厚50μmの発泡電線を得、発泡度を測定
したところ、65〜80%もの高発泡架橋電線を得た。Example 3 A thermosetting epoxy paint containing microbubbles was applied to a metal wire (silver-plated wire) with a conductor diameter of 127 μm at a line speed of 100 m/
After coating at min., it was cured in a heating oven (800°C) to obtain a foamed wire with a coating thickness of 50 μm.The degree of foaming was measured, and a highly foamed crosslinked wire of 65 to 80% was obtained.
斯界における今日的要請に応え得る意義は大きなものが
ある。It has great significance in meeting the contemporary demands of this field.
Claims (1)
るいは熱硬化型組成物を塗料として基体に塗布し、これ
を硬化させる発泡体の製造方法。(1) A method for producing a foam, in which a liquid ultraviolet curable composition or thermosetting composition containing microbubbles is applied as a paint to a substrate, and then cured.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6779190A JPH03267172A (en) | 1990-03-16 | 1990-03-16 | Production of foam |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6779190A JPH03267172A (en) | 1990-03-16 | 1990-03-16 | Production of foam |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03267172A true JPH03267172A (en) | 1991-11-28 |
Family
ID=13355128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6779190A Pending JPH03267172A (en) | 1990-03-16 | 1990-03-16 | Production of foam |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03267172A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100264342B1 (en) * | 1998-01-14 | 2000-08-16 | 김병수 | Electric wire for a ship |
US6353037B1 (en) | 2000-07-12 | 2002-03-05 | 3M Innovative Properties Company | Foams containing functionalized metal oxide nanoparticles and methods of making same |
US6573305B1 (en) | 1999-09-17 | 2003-06-03 | 3M Innovative Properties Company | Foams made by photopolymerization of emulsions |
US7138436B2 (en) | 2001-06-13 | 2006-11-21 | 3M Innovative Properties Company | Uncrosslinked foams made from emulsions |
-
1990
- 1990-03-16 JP JP6779190A patent/JPH03267172A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100264342B1 (en) * | 1998-01-14 | 2000-08-16 | 김병수 | Electric wire for a ship |
US6573305B1 (en) | 1999-09-17 | 2003-06-03 | 3M Innovative Properties Company | Foams made by photopolymerization of emulsions |
US6759080B2 (en) | 1999-09-17 | 2004-07-06 | 3M Innovative Properties Company | Process for making foams by photopolymerization of emulsions |
US6353037B1 (en) | 2000-07-12 | 2002-03-05 | 3M Innovative Properties Company | Foams containing functionalized metal oxide nanoparticles and methods of making same |
US6462100B1 (en) | 2000-07-12 | 2002-10-08 | 3M Innovative Properties Company | Foams containing functionalized metal oxide nanoparticles and methods of making same |
US7138436B2 (en) | 2001-06-13 | 2006-11-21 | 3M Innovative Properties Company | Uncrosslinked foams made from emulsions |
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