JP2002309126A - Release agent for flame spread prevention coating - Google Patents
Release agent for flame spread prevention coatingInfo
- Publication number
- JP2002309126A JP2002309126A JP2001113474A JP2001113474A JP2002309126A JP 2002309126 A JP2002309126 A JP 2002309126A JP 2001113474 A JP2001113474 A JP 2001113474A JP 2001113474 A JP2001113474 A JP 2001113474A JP 2002309126 A JP2002309126 A JP 2002309126A
- Authority
- JP
- Japan
- Prior art keywords
- release agent
- flame retardant
- fire spread
- weight
- spread prevention
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 50
- 239000011248 coating agent Substances 0.000 title claims abstract description 49
- 238000000576 coating method Methods 0.000 title claims abstract description 49
- 230000002265 prevention Effects 0.000 title claims abstract description 34
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000003063 flame retardant Substances 0.000 claims abstract description 30
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims abstract description 28
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 claims abstract description 24
- 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 claims abstract description 22
- 239000000839 emulsion Substances 0.000 claims abstract description 21
- 239000012046 mixed solvent Substances 0.000 claims abstract description 15
- 239000012796 inorganic flame retardant Substances 0.000 claims abstract description 14
- 239000007788 liquid Substances 0.000 claims abstract description 14
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims abstract description 14
- 235000019445 benzyl alcohol Nutrition 0.000 claims abstract description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 230000000694 effects Effects 0.000 description 12
- 230000008961 swelling Effects 0.000 description 9
- 238000010276 construction Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 7
- 239000000835 fiber Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 230000035515 penetration Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000002985 plastic film Substances 0.000 description 4
- 229920006255 plastic film Polymers 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- HQUQLFOMPYWACS-UHFFFAOYSA-N tris(2-chloroethyl) phosphate Chemical compound ClCCOP(=O)(OCCCl)OCCCl HQUQLFOMPYWACS-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 206010000369 Accident Diseases 0.000 description 2
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 2
- 235000017491 Bambusa tulda Nutrition 0.000 description 2
- 241001330002 Bambuseae Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000011425 bamboo Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 2
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 2
- YAOMHRRYSRRRKP-UHFFFAOYSA-N 1,2-dichloropropyl 2,3-dichloropropyl 3,3-dichloropropyl phosphate Chemical compound ClC(Cl)CCOP(=O)(OC(Cl)C(Cl)C)OCC(Cl)CCl YAOMHRRYSRRRKP-UHFFFAOYSA-N 0.000 description 1
- ANHAEBWRQNIPEV-UHFFFAOYSA-N 2-chloroethyl dihydrogen phosphate Chemical compound OP(O)(=O)OCCCl ANHAEBWRQNIPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004114 Ammonium polyphosphate Substances 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical compound BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 1
- 229920001276 ammonium polyphosphate Polymers 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、電線・ケーブルの
外周に設けられた延焼防止剤の硬化被覆を効率的に剥離
するための剥離剤に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a stripping agent for efficiently stripping a cured coating of a fire spreader provided on the outer periphery of an electric wire or cable.
【0002】[0002]
【従来の技術】従来より、大量の非難燃性の電線・ケー
ブルが布設されている原子力発電所や火力発電所などの
施設においては、万一の火災事故の発生に備えて、電線
・ケーブルの外周に、延焼防止剤を塗布することが行わ
れている。塗布された延焼防止剤は、時間の経過ととも
に硬化して電線・ケーブルシースと密着し、延焼防止効
果の高い被覆が形成される。2. Description of the Related Art Conventionally, in a facility such as a nuclear power plant or a thermal power plant in which a large amount of non-flammable electric wires and cables are laid, in order to prepare for a possible fire accident, the use of electric wires and cables is required. Application of a fire spread inhibitor to the outer periphery is performed. The applied fire retardant hardens with the passage of time and adheres to the electric wire / cable sheath, forming a coating having a high fire spread prevention effect.
【0003】ところで、近時、このような施設において
は、システムの変更や電線・ケーブルの劣化などから、
布設された電線・ケーブルをラダートレイなどから取り
外す機会が増えてきており、それにともなって次のよう
な問題が生じている。[0003] Recently, in such facilities, due to system changes and deterioration of electric wires and cables, etc.,
Opportunities to remove laid wires and cables from ladder trays and the like have increased, and the following problems have arisen accordingly.
【0004】すなわち、上記延焼防止剤には、従来、エ
チレン−アクリル酸エステル重合体(EEA)や、エチ
レン−酢酸ビニル共重合体(EVA)の水性エマルジョ
ンに、無機水和物などの難燃剤を多量に添加したものが
多用されているが、これらは極めて硬い硬化体を形成し
て電線・ケーブルに密着しているため、剥ぎ取りが困難
で、無理に機械的に破砕して除去しようとすると、電線
・ケーブルやラダートレイなどを損傷させてしまうおそ
れがあった。[0004] That is, a flame retardant such as an inorganic hydrate is conventionally added to an aqueous emulsion of an ethylene-acrylic acid ester polymer (EEA) or an ethylene-vinyl acetate copolymer (EVA) as the fire spread inhibitor. A large amount is added, but they form an extremely hard cured body and are in close contact with the wires and cables, making it difficult to peel them off. There is a possibility that the wires, cables, ladder trays and the like may be damaged.
【0005】このため、このような施工済みの延焼防止
剤を周囲を損傷させることなく容易に剥ぎ取ることがで
きる技術が求められ、例えば、発泡ウレタンなどに水を
含ませ、これを加熱体とともに硬化した延焼防止剤の上
に置き、加温軟化させた後、竹べらなどで剥ぎ取る方法
や、ジクロロメタンのような有機溶剤を含む剥離液によ
り延焼防止被覆を膨潤軟化させた後、同様に竹べらなど
で剥ぎ取る方法などが提案されてきている。[0005] For this reason, there is a demand for a technique capable of easily peeling off such an applied fire spread preventing agent without damaging the surroundings. For example, water is contained in urethane foam or the like, and this is mixed with a heating element. Place it on the cured fire retardant, soften it by heating, then peel it off with a bamboo spatula, or after swelling and softening the anti-fire spread coating with a stripping solution containing an organic solvent such as dichloromethane, likewise a bamboo spatula There has been proposed a method of stripping the film.
【0006】[0006]
【発明が解決しようとする課題】しかしながら、水を用
い加温軟化させる方法では、軟化に要する時間が長いう
えに、延焼防止剤の種類によっては十分に軟化しないも
のがあり、さらに、施工面が垂直の場合には適用できな
いという問題がある。However, in the method of heating and softening using water, the time required for softening is long, and depending on the type of fire spread preventing agent, there are some which do not soften sufficiently. There is a problem that it cannot be applied in the case of vertical.
【0007】また、ジクロロメタンのような有機溶剤を
含む剥離液を用いる方法では、延焼防止被覆を膨潤させ
るだけでなく、電線・ケーブルシースをも膨潤させると
いう問題がある。The method using a stripping solution containing an organic solvent such as dichloromethane has a problem that not only does the fire spread coating swell, but also the wire and cable sheaths swell.
【0008】さらに、原子力発電所などの施設において
は、防火の観点から難燃性に乏しい材料の使用は好まし
くない。Further, in a facility such as a nuclear power plant, it is not preferable to use a material having poor flame retardancy from the viewpoint of fire prevention.
【0009】本発明はこのような点に対処してなされた
もので、電線・ケーブル上に設けられた延焼防止被覆
を、施工面の形態に関係なく短時間に膨潤軟化させるこ
とができ、しかも電線・ケーブルシースに悪影響を及ぼ
すことがなく、またそれ自体優れた難燃性を有する延焼
防止被覆用剥離剤を提供することを目的とする。[0009] The present invention has been made in view of such a point, it is possible to swell and soften the fire prevention coating provided on the wires and cables in a short time irrespective of the form of the construction surface. An object of the present invention is to provide a release agent for fire spread prevention coating which does not adversely affect electric wire / cable sheaths and has excellent flame retardancy itself.
【0010】[0010]
【課題を解決するための手段】上記目的を達成するため
に、本発明の延焼防止被覆用剥離剤は、電線・ケーブル
上に設けられた延焼防止被覆に用いる剥離剤であって、
ベンズアルデヒドまたはアセチルアセトン10〜30重量%
とベンジルアルコール70〜90重量%とからなる混合溶
剤、水性エマルジョン、液状有機難燃剤および無機難燃
剤を含有することを特徴としている。Means for Solving the Problems In order to achieve the above object, a release agent for fire spread prevention coating of the present invention is a release agent used for a fire spread prevention coating provided on electric wires and cables,
10-30% by weight of benzaldehyde or acetylacetone
And a benzyl alcohol of 70 to 90% by weight, an aqueous emulsion, a liquid organic flame retardant and an inorganic flame retardant.
【0011】上記構成の剥離剤においては、溶剤とし
て、ベンズアルデヒドまたはアセチルアセトンとベンジ
ルアルコールを特定の割合で混合した混合溶剤を用いる
とともに、これらの溶剤に、水性エマルジョン、液状有
機難燃剤および無機難燃剤を配合するようにしたので、
電線・ケーブル上に設けられた延焼防止被覆を施工面の
形態などに関わりなく短時間に膨潤軟化させることがで
き、しかも電線・ケーブルシースに悪影響を及ぼすこと
がなく、またそれ自体優れた難燃性を有している。In the release agent having the above constitution, a mixed solvent of benzaldehyde or acetylacetone and benzyl alcohol mixed at a specific ratio is used as a solvent, and an aqueous emulsion, a liquid organic flame retardant and an inorganic flame retardant are added to these solvents. I decided to mix
It can swell and soften in a short time regardless of the type of construction surface, etc., the fire-prevention coating provided on the wires and cables, and it does not adversely affect the wires and cable sheaths, and is itself excellent flame retardant It has nature.
【0012】本発明においては、請求項2に記載したよ
うに、混合溶剤100重量部に対して、水性エマルジョン1
重量部〜30重量部、液状有機難燃剤20重量部〜60重量
部、無機難燃剤20重量部〜80重量部を含有することが好
ましい。このように構成することにより、上述した効果
がさらに向上かつ安定したものとなる。In the present invention, as described in claim 2, 100 parts by weight of the mixed solvent is added to the aqueous emulsion 1
It is preferable to contain 30 parts by weight, 20 to 60 parts by weight of a liquid organic flame retardant, and 20 to 80 parts by weight of an inorganic flame retardant. With this configuration, the above-described effects are further improved and stabilized.
【0013】本発明の延焼防止被覆用剥離剤は、請求項
3に記載したように、延焼防止被覆が、アクリル系延焼
防止剤からなる硬化被覆である場合に、特に顕著な効果
を得ることができる。As described in claim 3, the release agent for fire spread prevention coating of the present invention can obtain a particularly remarkable effect when the fire spread prevention coating is a cured coating made of an acrylic fire prevention agent. it can.
【0014】[0014]
【発明の実施の形態】以下、本発明の実施の形態を説明
する。Embodiments of the present invention will be described below.
【0015】本発明の延焼防止被覆用剥離剤において
は、溶剤として、ベンズアルデヒドまたはアセチルアセ
トンと、ベンジルアルコールとを、重量比で10:90〜3
0:70となるように混合した混合溶剤を用いる。ベンズ
アルデヒドまたはアセチルアセトンの割合が前記範囲よ
り少ないと、延焼防止被覆に対する膨潤軟化作用が不十
分となり、延焼防止被覆を短時間に膨潤軟化させること
が困難になる。また、ベンズアルデヒドまたはアセチル
アセトンの割合が前記範囲より多くなると、電線・ケー
ブルのシース(特にPVCシース)を膨潤させ、機械的
強度などが低下して実用に供し得なくなる。ベンズアル
デヒドまたはアセチルアセトンと、ベンジルアルコール
のより好ましい混合比は、15:85〜25:75の範囲であ
る。In the release agent for preventing fire spread according to the present invention, benzaldehyde or acetylacetone and benzyl alcohol are used as solvents in a weight ratio of 10:90 to 3: 3.
Use a mixed solvent that is mixed to be 0:70. If the proportion of benzaldehyde or acetylacetone is less than the above range, the swelling / softening effect on the fire spread prevention coating becomes insufficient, and it becomes difficult to swell and soften the fire spread prevention coating in a short time. On the other hand, if the ratio of benzaldehyde or acetylacetone is more than the above range, the sheath (especially, PVC sheath) of the electric wire / cable swells, and the mechanical strength and the like are reduced, and it cannot be put to practical use. A more preferred mixing ratio of benzaldehyde or acetylacetone to benzyl alcohol is in the range of 15:85 to 25:75.
【0016】なお、図1は、ベンズアルデヒド、アセチ
ルアセトン、ベンジルアルコールおよび燐酸トリエチル
をそれぞれ単独で使用した場合の延焼防止剤(FBシー
ル)の硬化体に対する膨潤軟化効果を調べるために行っ
た試験結果をグラフに示したもので、横軸が浸漬時間、
縦軸が溶剤の膨潤軟化効果の指標となる重量変化率であ
る。図1からも明らかなように、ベンズアルデヒドおよ
びアセチルアセトンは、ベンジルアルコールや燐酸トリ
エチルなどの溶剤に比べ、延焼防止剤の硬化体に対し優
れた膨潤軟化作用を有している。FIG. 1 is a graph showing the results of a test conducted to examine the swelling / softening effect of a fire retardant (FB seal) on a cured product when benzaldehyde, acetylacetone, benzyl alcohol and triethyl phosphate are used alone. The horizontal axis is the immersion time,
The vertical axis represents the weight change rate which is an index of the swelling / softening effect of the solvent. As is clear from FIG. 1, benzaldehyde and acetylacetone have an excellent swelling / softening effect on the cured product of the fire spread inhibitor as compared with solvents such as benzyl alcohol and triethyl phosphate.
【0017】本発明においては、このようなベンズアル
デヒドまたはアセチルアセトンとベンジルアルコールと
の混合溶剤とともに、水性エマルジョン、液状有機難燃
剤および無機難燃剤を配合する。In the present invention, an aqueous emulsion, a liquid organic flame retardant and an inorganic flame retardant are blended together with such a mixed solvent of benzaldehyde or acetylacetone and benzyl alcohol.
【0018】水性エマルジョンは、主として、施工面の
形態や施工方法などに応じて剥離剤の粘度を調整すると
ともに、前記溶剤が延焼防止被覆に浸透して吸収された
後に塗膜を形成して、残留する成分を延焼防止被覆の外
周に付着させるために配合されるものである。このよう
な水性エマルジョンしては、EEAなどのアクリル系水
性エマルジョンやEVAなどの酢酸ビニル系水性エマル
ジョンなどが挙げられ、その配合量は、通常、前記混合
溶剤100重量部に対して1重量部〜30重量部の範囲であ
る。The aqueous emulsion mainly adjusts the viscosity of the release agent according to the form of the construction surface, the construction method, and the like, and forms a coating film after the solvent has penetrated and absorbed into the anti-fire spread coating. It is blended in order to make the remaining components adhere to the outer periphery of the fire spread prevention coating. Examples of such an aqueous emulsion include an acrylic aqueous emulsion such as EEA and a vinyl acetate aqueous emulsion such as EVA. The amount of the aqueous emulsion is usually 1 part by weight to 100 parts by weight of the mixed solvent. It is in the range of 30 parts by weight.
【0019】また、液状有機難燃剤および無機難燃剤
は、剥離作業時の安全性を考慮して剥離剤に難燃性を付
与するために配合されるもので、液状有機難燃剤は、プ
ラスチックなどの分子(炭化水素)が高温酸化して発生
するOHフリーラジカルを捕捉して連鎖反応を停止する
と同時に、プラスチックなどの炭化を促進し分解により
低分子量可燃性物質が生じないようにする機構により、
あるいは不燃性のガスを発生する機構により、燃焼の継
続を抑える働きをする。本発明においては、常温で液状
の、トリス(クロロエチル)ホスフェート、トリス(ジ
クロロプロピル)ホスフェート、トリス(ジブロモプロ
ピル)ホスフェートなどの含ハロゲンリン酸エステル
や、塩素化パラフィンなどが使用され、なかでも、トリ
ス(クロロエチル)ホスフェートの使用が好ましい。The liquid organic flame retardant and the inorganic flame retardant are compounded in order to impart flame retardancy to the release agent in consideration of safety at the time of the release operation. By stopping the chain reaction by capturing the OH free radicals generated by high temperature oxidation of the molecules (hydrocarbons), it promotes the carbonization of plastics and the like to prevent the generation of low molecular weight combustible substances by decomposition.
Alternatively, the mechanism that suppresses the continuation of combustion is provided by a mechanism that generates nonflammable gas. In the present invention, a halogen-containing phosphoric acid ester such as tris (chloroethyl) phosphate, tris (dichloropropyl) phosphate and tris (dibromopropyl) phosphate, which is liquid at ordinary temperature, and chlorinated paraffin are used. The use of (chloroethyl) phosphate is preferred.
【0020】また、無機難燃剤は、加熱により分解揮発
する構造水が冷却剤として作用することにより、あるい
はそれ自身の吸熱分解反応により、燃焼を抑え自己消化
性を付与する働きをする。本発明においては、水酸化ア
ルミニウム、水酸化マグネシウム、炭酸水素ナトリウム
などが使用され、なかでも水酸化アルミニウムの使用が
好ましい。The inorganic flame retardant functions to suppress combustion and impart self-extinguishing property by the structure water which decomposes and volatilizes by heating as a cooling agent or by its own endothermic decomposition reaction. In the present invention, aluminum hydroxide, magnesium hydroxide, sodium hydrogen carbonate and the like are used, and among them, the use of aluminum hydroxide is preferred.
【0021】これらの難燃剤の配合量は、前記混合溶剤
100重量部に対して、液状の有機難燃剤が20重量部〜60
重量部、無機難燃剤が20重量部〜80重量部の範囲が好ま
しい。液状有機難燃剤および無機難燃剤の配合量のいず
れか一方でも前記範囲未満になると、難燃効果が不十分
になる。また、有機難燃剤が60重量部を越えると、剥離
剤の延焼防止被覆を膨潤軟化させる効果が低下し、へら
で剥離可能となるまでに時間がかかる。一方、無機難燃
剤が80重量部を越えると、剥離剤の粘度が高くなりすぎ
て施工が困難になる。The amount of these flame retardants is based on the mixed solvent
20 parts by weight to 60 parts by weight of liquid organic flame retardant per 100 parts by weight
It is preferable that the inorganic flame retardant be in the range of 20 to 80 parts by weight. If any one of the amounts of the liquid organic flame retardant and the inorganic flame retardant is less than the above range, the flame retardant effect becomes insufficient. On the other hand, when the amount of the organic flame retardant exceeds 60 parts by weight, the effect of the release agent to swell and soften the anti-fire spread coating is reduced, and it takes a long time before the release can be performed with a spatula. On the other hand, when the amount of the inorganic flame retardant exceeds 80 parts by weight, the viscosity of the release agent becomes too high, and the application becomes difficult.
【0022】本発明においては、剥離剤の施工面の形態
(例えば水平面や垂直面など)や施工方法などによっ
て、前記水性エマルジョン、有機難燃剤、無機難燃剤の
配合量をそれぞれ変化させ、剥離剤の粘度を調整するこ
とができる。In the present invention, the amounts of the aqueous emulsion, the organic flame retardant, and the inorganic flame retardant are varied depending on the form (for example, a horizontal plane or a vertical plane) of the construction surface of the release agent and the construction method. Can be adjusted.
【0023】本発明の剥離剤には、本発明の効果を阻害
しない範囲で、上記成分の他に必要に応じて、充填剤、
顔料、香料その他の添加剤を配合してもよい。例えば充
填剤としては、フェノール樹脂繊維、カーボン繊維、セ
ルロースパウダなどが例示される。The release agent of the present invention may further include a filler, if necessary, in addition to the above components, as long as the effects of the present invention are not impaired.
Pigments, fragrances and other additives may be blended. For example, examples of the filler include phenol resin fibers, carbon fibers, and cellulose powder.
【0024】本発明の剥離剤は、ベンズアルデヒドまた
はアセチルアセトンとベンジルアルコールとの混合溶剤
に、液状の有機難燃剤を添加混合し、さらに、水性エマ
ルジョンを加えて十分に撹拌混合した後、無機難燃剤そ
の他の必要に応じて配合される各成分を添加混合するこ
とにより得られる。The release agent of the present invention is obtained by adding and mixing a liquid organic flame retardant to a mixed solvent of benzaldehyde or acetylacetone and benzyl alcohol, further adding an aqueous emulsion, and sufficiently stirring and mixing. Can be obtained by adding and mixing each component blended as required.
【0025】このようにして得られる本発明の剥離剤を
用いて、電線・ケーブル上に設けられた延焼防止被覆を
剥離除去するには、剥離剤を電線・ケーブル上に設けら
れた延焼防止被覆の表面に直接塗布し、剥離剤中の溶剤
が浸透して延焼防止被覆が膨潤軟化するのを待って、そ
の軟化した延焼防止被覆を剥離剤の塗付層とともに木製
のへらなどを用いて剥ぎ取るようにすればよい。In order to remove the anti-fire spread coating provided on the electric wire / cable using the release agent of the present invention thus obtained, the release agent is applied to the anti-fire spread coating provided on the electric wire / cable. After the solvent in the release agent has penetrated and the fire-prevention coating has swelled and softened, peel off the softened fire-prevention coating together with the release agent coating layer using a wooden spatula. You should take it.
【0026】剥離剤は、延焼防止被覆の表面に直接塗布
する代わりに、ポリエチレンやポリプロピレンなどのプ
ラスチックフィルムの片面に予め塗布しておき、その剥
離剤層側を延焼防止被覆側に向けて貼り付けるようにし
てもよい。この方法では、プラスチックフィルムが剥離
剤中の混合溶剤の揮発を抑える効果を有するため、膨潤
軟化がより促進される。なお、したがって、剥離剤を直
接塗布する場合にも、その上をプラスチックフィルムな
どで覆うことが望ましい。The release agent is applied to one surface of a plastic film such as polyethylene or polypropylene in advance, instead of being directly applied to the surface of the fire spread prevention coating, and the release agent layer side is attached to the fire spread prevention side. You may do so. In this method, since the plastic film has an effect of suppressing volatilization of the mixed solvent in the release agent, swelling and softening are further promoted. Therefore, even when the release agent is directly applied, it is desirable to cover the release agent with a plastic film or the like.
【0027】また、剥離剤の塗布層の上あるいは上記プ
ラスチックフィルムの上からバンドヒータのような面状
ヒータ、赤外線ヒータ、温風機などを用いて20℃〜50℃
に加温してもよい。このように加温することにより、剥
離剤の延焼防止被覆への浸透と膨潤軟化が促進され、剥
離効率をさらに高めることができる。Further, a surface heater such as a band heater, an infrared heater, a hot air blower, or the like is used to cover the release agent coating layer or the plastic film.
May be heated. By heating in this manner, penetration of the release agent into the fire spread prevention coating and swelling and softening are promoted, and the release efficiency can be further increased.
【0028】なお、延焼防止被覆が厚い場合には、前記
の一連の操作を繰り返すようにすればよいが、床や壁な
どのケーブル貫通部に施工された延焼防止被覆のよう
に、塗布面積が限られしかも被覆が非常に厚い場合に
は、図2に示すように、ケーブル貫通部10に施工され
た延焼防止被覆11に、ケーブル12を取り囲むように
複数の孔13を設け、これらの孔13に剥離剤14を充
填するようにすればよい。1回の作業で効率良く延焼防
止被覆11を剥離除去することができる。この方法は、
ケーブル貫通部の延焼防止被覆に限らず、通常のケーブ
ル線路に施工された延焼防止被覆にも適用できることは
いうまでもなく、厚い延焼防止被覆であっても容易にか
つ短時間に剥離除去することが可能となる。なお、この
方法には、充填性も考慮して、前記の混合溶剤100重量
部に対して、水性エマルジョン1重量部〜5重量部、液状
有機難燃剤20重量部〜50重量部、無機難燃剤20重量部〜
50重量部を配合した剥離剤が好ましく使用される。When the fire-prevention coating is thick, the above-mentioned series of operations may be repeated. However, as in the case of a fire-prevention coating applied to a cable penetration portion such as a floor or a wall, the application area is limited. In addition, when the coating is very thick, as shown in FIG. 2, a plurality of holes 13 are provided around the cable 12 in the fire spread prevention coating 11 applied to the cable penetration portion 10, and these holes 13 are formed. The release agent 14 may be filled. The fire spread prevention coating 11 can be efficiently removed and removed in one operation. This method
It can be applied not only to the fire spread prevention coating of the cable penetration part but also to the fire spread prevention coating applied to the ordinary cable line. Becomes possible. In this method, taking into account the filling properties, 100 parts by weight of the above mixed solvent, 1 part by weight to 5 parts by weight of the aqueous emulsion, 20 parts by weight to 50 parts by weight of the liquid organic flame retardant, and the inorganic flame retardant 20 parts by weight
A release agent containing 50 parts by weight is preferably used.
【0029】本発明の剥離剤が適用される延焼防止被覆
は、EEAエマルジョンなどのアクリル系もしくはEV
Aエマルジョンなどの酢酸ビニル系水性エマルジョンを
ベースに、有機難燃剤、難燃助剤、無機充填剤、不燃性
繊維、可塑剤などを添加した延焼防止剤を、電線・ケー
ブル上に被覆し硬化させたものである。有機難燃剤とし
ては、塩素化パラフィン、塩素化ナフタリン、デカブロ
モジフェニルオキサイド、ポリリン酸アンモニウムなど
が、難燃助剤としては、三酸化アンチモン、ホウ酸亜
鉛、酸化亜鉛などが、無機充填剤としては、水酸化アル
ミニウム、炭酸カルシウム、含水珪酸マグネシウム、二
酸化チタン、クレー、タルクなどが、不燃性繊維として
は、アスベスト、セラミック繊維、ガラス繊維、フェノ
ール樹脂繊維などが、可塑剤としては、トリス(クロロ
エチル)ホスフェートなどのリン酸エステル、塩素化ビ
フェニル、フタル酸ジブチルなどがそれぞれ挙げられ
る。The anti-fire spread coating to which the release agent of the present invention is applied may be an acrylic or EV such as an EEA emulsion.
Based on a vinyl acetate-based aqueous emulsion such as emulsion A, an organic fire retardant, a flame retardant aid, an inorganic filler, a non-flammable fiber, a plasticizer, etc., and a fire retardant added to the wire and cable and cured. It is a thing. As organic flame retardants, chlorinated paraffin, chlorinated naphthalene, decabromodiphenyl oxide, ammonium polyphosphate, etc., as flame retardant aids, antimony trioxide, zinc borate, zinc oxide, etc., as inorganic fillers , Aluminum hydroxide, calcium carbonate, hydrous magnesium silicate, titanium dioxide, clay, talc, etc., as non-combustible fibers, asbestos, ceramic fibers, glass fibers, phenol resin fibers, etc., and as a plasticizer, tris (chloroethyl) Phosphate such as phosphate, chlorinated biphenyl, dibutyl phthalate and the like can be mentioned.
【0030】本発明においては、なかでも、アクリル系
水性エマルジョンに、有機難燃剤として塩素化パラフィ
ン、難燃助剤として水酸化アルミニウムおよびホウ酸亜
鉛、無機充填剤として水酸化アルミニウム、二酸化チタ
ンおよびクレー、不燃性繊維としてフェノール樹脂繊
維、可塑剤としてトリス(クロロエチル)ホスフェート
を混合した延焼防止剤の硬化被覆に適用した場合に顕著
な効果が得られる。このような延焼防止剤の市販品とし
ては、鐘淵化学社製のFBシール(商品名)が例示され
る。In the present invention, chlorinated paraffin is used as an organic flame retardant, aluminum hydroxide and zinc borate are used as flame retardants, aluminum hydroxide, titanium dioxide and clay are used as inorganic fillers. A remarkable effect can be obtained when applied to the cured coating of a fire retardant mixed with phenol resin fibers as non-combustible fibers and tris (chloroethyl) phosphate as a plasticizer. An example of a commercially available product of such a fire spread agent is FB seal (trade name) manufactured by Kanegafuchi Chemical Co., Ltd.
【0031】[0031]
【実施例】次に、本発明を実施例によりさらに詳細に説
明するが、本発明はこれらの実施例に限定されるもので
はない。なお、以下の記載において「部」は「重量部」
を意味する。Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples. In the following description, “parts” means “parts by weight”.
Means
【0032】実施例1 ベンジルアルコール80部とベンズアルデヒド20部を混合
した混合溶剤に、液状有機難燃剤であるトリスクロロエ
チルホスフェート40部を添加し、さらにアクリル系水性
エマルジョン25部を添加し、十分に撹拌した。次いで、
撹拌しながら水酸化アルミニウム40部およびセルロース
パウダ5部を添加し混合して、剥離剤を調製した。Example 1 To a mixed solvent in which 80 parts of benzyl alcohol and 20 parts of benzaldehyde were mixed, 40 parts of trischloroethyl phosphate, which is a liquid organic flame retardant, was added, and 25 parts of an aqueous acrylic emulsion was added. Stirred. Then
While stirring, 40 parts of aluminum hydroxide and 5 parts of cellulose powder were added and mixed to prepare a release agent.
【0033】実施例2〜4、比較例1〜4 配合組成を表1に示すように変えた以外は、実施例1と
同様にして剥離剤を調製した。Examples 2 to 4 and Comparative Examples 1 to 4 Release agents were prepared in the same manner as in Example 1 except that the composition was changed as shown in Table 1.
【0034】上記各実施例および比較例で得られた剥離
剤の特性を調べるため、以下に示すような特性評価試験
を行なった。In order to examine the properties of the release agents obtained in the above Examples and Comparative Examples, the following property evaluation tests were performed.
【0035】[軟化試験]鐘淵化学社製のFBシール
(延焼防止剤)を内径30mmの環状の金型に6mm厚に充填
し、乾燥硬化させた後、この硬化体の表面に剥離剤を約
20mm厚に塗布し、硬化体裏面の硬度(JIS A)の変化を
測定した。[Softening test] An annular mold having an inner diameter of 30 mm was filled with an FB seal (fire spreader) manufactured by Kanegabuchi Chemical Co., Ltd. to a thickness of 6 mm, dried and cured, and then a release agent was applied to the surface of the cured product. about
It was applied to a thickness of 20 mm, and the change in hardness (JIS A) on the back surface of the cured product was measured.
【0036】[引張試験]CVケーブルシース用PVC
を用いて作製した2mm厚のシートを、剥離剤とは別に混
合した混合溶剤中に室温で1週間浸漬し、強度および伸
びの変化を調べた。なお、強度および伸びはJIS K 6723
に準拠して測定した。これらの測定結果を表1下欄に示
す。[Tensile test] PVC for CV cable sheath
Was immersed in a mixed solvent separately from the release agent at room temperature for 1 week, and changes in strength and elongation were examined. The strength and elongation are based on JIS K 6723
It measured according to. The results of these measurements are shown in the lower column of Table 1.
【0037】[0037]
【表1】 [Table 1]
【0038】実施例5 ベンジルアルコール80部とベンズアルデヒド20部を混合
した混合溶剤に、トリスクロロエチルホスフェート40部
を添加し、さらにアクリル系水性エマルジョン3部を添
加し十分に撹拌した。次いで、撹拌しながら水酸化アル
ミニウム40部およびセルロースパウダ5部を添加し混合
して、剥離剤を調製した。Example 5 To a mixed solvent obtained by mixing 80 parts of benzyl alcohol and 20 parts of benzaldehyde, 40 parts of trischloroethyl phosphate was added, and 3 parts of an acrylic aqueous emulsion was further added, followed by sufficient stirring. Next, 40 parts of aluminum hydroxide and 5 parts of cellulose powder were added and mixed with stirring to prepare a release agent.
【0039】得られた剥離剤を、ケーブル貫通部の延焼
防止被覆を模擬して作製したFBシールの硬化ブロック
(25cm×20cm×20cm、ほぼ中央に外径10mmのケーブル20
本を埋設)のケーブル群の周囲にほぼ等間隔で設けた5
個の断面円形状の孔(直径1cm、深さ15cm)に充填し、
そのまま常温で放置した。7日後、延焼防止被覆の剥離
除去を試みたところ、全体が十分に軟化しており、ほぼ
完全にケーブルから除去することができた。The obtained release agent was applied to a cured block (25 cm × 20 cm × 20 cm, approximately 10 mm in outer diameter of a cable 20) at the center of an FB seal prepared by simulating a fire spread prevention coating at the cable penetration portion.
5) are installed at approximately equal intervals around the cable group
Filled into circular holes (diameter 1cm, depth 15cm)
It was left at room temperature. After 7 days, an attempt was made to peel and remove the fire spread prevention coating. As a result, the whole was sufficiently softened and could be almost completely removed from the cable.
【0040】[0040]
【発明の効果】以上説明したように、本発明の剥離剤に
よれば、電線・ケーブル外周に被覆された延焼防止被覆
を、施工場所や施工面の形態などに制約されることな
く、短時間に膨潤軟化させて効率良く剥離することがで
き、しかも、電線・ケーブルシースの特性を低下させる
こともない。また、十分な難燃性を有しているので、万
一延焼防止被覆の剥離作業中に火災事故等が発生した場
合でも引火して燃焼することもない。As described above, according to the release agent of the present invention, the fire spread prevention coating applied to the outer periphery of the electric wire / cable can be applied in a short time without being restricted by the construction place or construction form. Swelling and softening, and can be peeled off efficiently, and without deteriorating the characteristics of the electric wire / cable sheath. Further, since it has sufficient flame retardancy, even if a fire accident or the like occurs during the peeling operation of the fire spread prevention coating, it does not catch fire and burn.
【図1】各種有機溶剤の延焼防止被覆に対する膨潤軟化
特性を示すグラフ。FIG. 1 is a graph showing swelling and softening characteristics of various organic solvents with respect to a fire spread prevention coating.
【図2】本発明の剥離剤による延焼防止被覆の剥離方法
の一例を説明するための断面図。FIG. 2 is a cross-sectional view for explaining an example of a method for removing a fire spread prevention coating using a release agent of the present invention.
10………ケーブル貫通部 11………延焼防止被覆 12………ケーブル 13………孔 14………剥離剤 10 Cable penetration part 11 Fire spread prevention coating 12 Cable 13 Hole 14 Release agent
───────────────────────────────────────────────────── フロントページの続き (72)発明者 守屋 彰 大阪府大阪市北区中之島3丁目3番22号 関西電力株式会社内 (72)発明者 新舘 均 神奈川県川崎市川崎区小田栄2丁目1番1 号 昭和電線電纜株式会社内 (72)発明者 岡下 稔 神奈川県川崎市川崎区小田栄2丁目1番1 号 昭和電線電纜株式会社内 (72)発明者 平井 進 神奈川県川崎市川崎区小田栄2丁目1番1 号 昭和電線電纜株式会社内 Fターム(参考) 4J038 RA02 RA05 RA06 RA09 RA15 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Akira Moriya 3-3-22 Nakanoshima, Kita-ku, Osaka City, Osaka Prefecture Inside Kansai Electric Power Company (72) Inventor Hitoshi Shintate 2-1-1 Sakae Oda, Kawasaki-ku, Kawasaki-ku, Kanagawa Prefecture No. 1 Inside Showa Electric Wire & Cable Co., Ltd. (72) Inventor Minoru Okashita 2-1-1 Oda Sakae, Kawasaki-ku, Kawasaki City, Kanagawa Prefecture Inside of Showa Electric Wire & Cable Co., Ltd. (72) Inventor Susumu Hirai Oda, Kawasaki-ku, Kawasaki City, Kanagawa Prefecture 2-1-1 Sakae Showa Electric Wire & Cable Co., Ltd. F-term (reference) 4J038 RA02 RA05 RA06 RA09 RA15
Claims (3)
被覆に用いる剥離剤であって、ベンズアルデヒドまたは
アセチルアセトン10重量%〜30重量%とベンジルアルコ
ール70重量%〜90重量%とからなる混合溶剤、水性エマ
ルジョン、液状有機難燃剤および無機難燃剤を含有する
ことを特徴とする延焼防止被覆用剥離剤。1. A release agent used for a fire spread prevention coating provided on an electric wire or cable, comprising a mixed solvent of 10% to 30% by weight of benzaldehyde or acetylacetone and 70% to 90% by weight of benzyl alcohol. A release agent for anti-fire spread coating, comprising an aqueous emulsion, a liquid organic flame retardant and an inorganic flame retardant.
ルジョン1重量部〜30重量部、液状有機難燃剤20重量部
〜60重量部、無機難燃剤20重量部〜80重量部を含有する
ことを特徴とする請求項1記載の延焼防止被覆用剥離
剤。2. 100 parts by weight of a mixed solvent, 1 to 30 parts by weight of an aqueous emulsion, 20 to 60 parts by weight of a liquid organic flame retardant, and 20 to 80 parts by weight of an inorganic flame retardant. The release agent for fire spread prevention coating according to claim 1, characterized in that:
からなる硬化被覆であることを特徴とする請求項1また
は2記載の延焼防止被覆用剥離剤。3. The release agent for fire spread prevention coating according to claim 1, wherein the fire spread prevention coating is a cured coating comprising an acrylic fire spread prevention agent.
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JP2001113474A JP4570807B2 (en) | 2001-04-12 | 2001-04-12 | Release agent for fire spread prevention coating |
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JP2001113474A JP4570807B2 (en) | 2001-04-12 | 2001-04-12 | Release agent for fire spread prevention coating |
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JP2002309126A true JP2002309126A (en) | 2002-10-23 |
JP4570807B2 JP4570807B2 (en) | 2010-10-27 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4457206B1 (en) * | 2009-05-13 | 2010-04-28 | 国立大学法人 岡山大学 | Coating film removing agent and coating film removing method using the same |
CN111029887A (en) * | 2019-12-19 | 2020-04-17 | 北京航天控制仪器研究所 | Device and method for stripping polyimide copper-clad wire coating layer |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09183922A (en) * | 1995-12-28 | 1997-07-15 | Showa Electric Wire & Cable Co Ltd | Release agent for flame spread preventing cover |
JPH10152633A (en) * | 1996-11-25 | 1998-06-09 | Showa Electric Wire & Cable Co Ltd | Release agent for fire spread preventive coating |
JPH10168363A (en) * | 1996-12-06 | 1998-06-23 | Elf Atochem Sa | Aqueous composition for peeling paint and primer having high cross-linking degree |
-
2001
- 2001-04-12 JP JP2001113474A patent/JP4570807B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09183922A (en) * | 1995-12-28 | 1997-07-15 | Showa Electric Wire & Cable Co Ltd | Release agent for flame spread preventing cover |
JPH10152633A (en) * | 1996-11-25 | 1998-06-09 | Showa Electric Wire & Cable Co Ltd | Release agent for fire spread preventive coating |
JPH10168363A (en) * | 1996-12-06 | 1998-06-23 | Elf Atochem Sa | Aqueous composition for peeling paint and primer having high cross-linking degree |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4457206B1 (en) * | 2009-05-13 | 2010-04-28 | 国立大学法人 岡山大学 | Coating film removing agent and coating film removing method using the same |
WO2010131539A1 (en) * | 2009-05-13 | 2010-11-18 | 国立大学法人岡山大学 | Coating film remover and method for removing coating film using same |
JP2010285592A (en) * | 2009-05-13 | 2010-12-24 | Okayama Univ | Coating film-removing agent and coating film-removing method using the same |
JP2010285590A (en) * | 2009-05-13 | 2010-12-24 | Okayama Univ | Coating film-removing agent and coating film-removing method using the same |
CN111029887A (en) * | 2019-12-19 | 2020-04-17 | 北京航天控制仪器研究所 | Device and method for stripping polyimide copper-clad wire coating layer |
CN111029887B (en) * | 2019-12-19 | 2021-12-07 | 北京航天控制仪器研究所 | Device and method for stripping polyimide copper-clad wire coating layer |
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