JPS6140524Y2 - - Google Patents
Info
- Publication number
- JPS6140524Y2 JPS6140524Y2 JP11171681U JP11171681U JPS6140524Y2 JP S6140524 Y2 JPS6140524 Y2 JP S6140524Y2 JP 11171681 U JP11171681 U JP 11171681U JP 11171681 U JP11171681 U JP 11171681U JP S6140524 Y2 JPS6140524 Y2 JP S6140524Y2
- Authority
- JP
- Japan
- Prior art keywords
- zinc
- parts
- weight
- heat
- cover
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- 239000012779 reinforcing material Substances 0.000 claims description 9
- 239000011701 zinc Substances 0.000 claims description 9
- 229920005601 base polymer Polymers 0.000 claims description 8
- 229910052725 zinc Inorganic materials 0.000 claims description 8
- 150000003752 zinc compounds Chemical class 0.000 claims description 7
- 239000004604 Blowing Agent Substances 0.000 claims description 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 5
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 5
- 239000000203 mixture Substances 0.000 description 12
- 230000001681 protective effect Effects 0.000 description 9
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 8
- 239000004745 nonwoven fabric Substances 0.000 description 8
- -1 nitrososulfonamide Chemical class 0.000 description 7
- 239000002759 woven fabric Substances 0.000 description 6
- 238000004891 communication Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000011787 zinc oxide Substances 0.000 description 4
- 239000003063 flame retardant Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 230000009993 protective function Effects 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- MXMMCUUTDVVBBT-UHFFFAOYSA-N 1-amino-3-(sulfonylamino)urea Chemical class NNC(=O)NN=S(=O)=O MXMMCUUTDVVBBT-UHFFFAOYSA-N 0.000 description 1
- CMQUQOHNANGDOR-UHFFFAOYSA-N 2,3-dibromo-4-(2,4-dibromo-5-hydroxyphenyl)phenol Chemical compound BrC1=C(Br)C(O)=CC=C1C1=CC(O)=C(Br)C=C1Br CMQUQOHNANGDOR-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000004114 Ammonium polyphosphate Substances 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- CYEGIZYXCXGFSX-UHFFFAOYSA-N NS(=O)(=O)N=O Chemical compound NS(=O)(=O)N=O CYEGIZYXCXGFSX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- VRFNYSYURHAPFL-UHFFFAOYSA-N [(4-methylphenyl)sulfonylamino]urea Chemical compound CC1=CC=C(S(=O)(=O)NNC(N)=O)C=C1 VRFNYSYURHAPFL-UHFFFAOYSA-N 0.000 description 1
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 description 1
- YGCOKJWKWLYHTG-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical compound OCN(CO)C1=NC(N(CO)CO)=NC(N(CO)CO)=N1 YGCOKJWKWLYHTG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 1
- 229920001276 ammonium polyphosphate Polymers 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- CNWSQCLBDWYLAN-UHFFFAOYSA-N butylurea Chemical compound CCCCNC(N)=O CNWSQCLBDWYLAN-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper 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
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000004079 fireproofing Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229960002449 glycine Drugs 0.000 description 1
- 235000013905 glycine and its sodium salt Nutrition 0.000 description 1
- 239000012796 inorganic flame retardant Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- GVYLCNUFSHDAAW-UHFFFAOYSA-N mirex Chemical compound ClC12C(Cl)(Cl)C3(Cl)C4(Cl)C1(Cl)C1(Cl)C2(Cl)C3(Cl)C4(Cl)C1(Cl)Cl GVYLCNUFSHDAAW-UHFFFAOYSA-N 0.000 description 1
- 150000002752 molybdenum compounds Chemical class 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000008093 supporting effect Effects 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Laminated Bodies (AREA)
- Organic Insulating Materials (AREA)
- Insulated Conductors (AREA)
Description
本考案は、物体を火炎から防護するために用い
る防護カバに関し、特に架空配線された通信ケー
ブルのような高所に露出状態で存する物体の防護
に適した防護カバに関するものである。
上記した高所に露出状態で存する物体の防護す
るカバには次の種々の諸特性を満足することが要
求される。
火炎時、下から火焔にてあぶられても溶融滴
下することなく物体を火焔から保護し得るこ
と。
日光、雨水に長時間曝されても火災に際して
防護機能を維持すること。
大量生産可能とするために優れた成形加工性
を有すること。
上記諸要求項目のうち、特にの要求が厳し
い。その理由は、既設の物体を防護カバで覆つた
とき、通常、物体には凹凸があるから、防護カバ
の内面のある部分は物質の表面と接触し、ある部
分は非接触のまゝとなる。かゝる状態において防
護カバが火焔にて高温度に加熱されるとその構成
材料がたとえ熱硬化性樹脂であつても、多くの熱
硬化性樹脂は解重合、架橋の切断などのため、低
分子化して溶融滴下し易くなり殊に上記非接触部
分からの滴下が顕著となるからである。滴下によ
りカバに孔があくと、カバはその防護機能を低下
乃至喪失することとなること云うまでもない。
上記に鑑み、本考案は、上記諸要求を満足する
新規な防護カバを提案するものであつて、エチレ
ン−酢酸ビニル共重合成分と塩化ビニル成分とを
含むベースポリマーと、該ポリマー100重量部あ
たり、5〜70重量部の有機発泡剤と、亜鉛量に換
算して3〜50重量部の亜鉛又は亜鉛化合物とから
なり、かつ耐熱性補強材により補強されてなるこ
とを特徴とするものである。
ベースポリマーとしては、エチレン−酢酸ビニ
ル共重合体と塩化ビニルとのグラフト重合体、エ
チレン−酢酸ビニル共重合体とポリ塩化ビニル及
び/又は上記グラフト重合体との混合物などが用
いられる。ベースポリマー中の酢酸ビニル成分の
含有量は20〜50重量%程度が好ましく、一方塩化
ビニル成分の含有量は、40〜70重量%程度が好ま
しい。
有機発泡剤としては、100〜400℃の温度で分解
して窒素ガス、一酸化炭素、炭酸ガス、アンモニ
アガスなどを放出して有機高分子類を発泡させ得
るものが用いられる。たとえば、メラミン、尿素
ホルムアルデヒド、アミノ酢酸、トリメチロール
メラミン、ヘキサメチロールメラミン、メラミン
樹脂、N,N′−ジニトロソーペンタメチレンテ
トラミン、グアニジン等の有機アミン類、ジシア
ンジアミド、ブチルウレア、ポリアミド樹脂、ア
ゾジカルボンアミド、ニトロソスルホンアミド等
の有機アミド類、p−トルエンスルホニルセミカ
ルバジド、p,p′−オキシベンゼンスルホニルカ
ルバジド等のスルホニルカルバジド類を例示する
ことができる。
亜鉛又は亜鉛化合物としては、亜鉛粉未、
3ZnO・2B2O2・3H2O,2ZnO・3B2O2・31/2H2O
などの硼酸亜鉛化合物類、ZnO・ZnMoO4,
CaO・ZnMoO4などのモリブデン・亜鉛化合物
類、ZnO,ZnCO3、Zn3(PO4)3・4H2Oなどであ
る。
本発明のカバは火焔にて加熱されると生成した
酸化亜鉛の作用によりベースポリマーの脱塩酸反
応が生じてベースポリマーが炭化し、かつ上記有
機発泡剤及びエチレン−酢酸ビニル成分の発泡作
用により速かに断熱性の発泡炭化層を形成して物
体を火焔から保護する機能を果す。従つて、亜鉛
化合物としては上記の例示のものに限らず、火災
時の高温度で分解して酸化亜鉛を生成するもので
あれば好適に使用することができる。
有機発泡剤、亜鉛又は亜鉛化合物の使用量が少
ないと発泡炭化層の形成作用が乏しくなり、一
方、使用量が過剰であると組成物の成形加工性が
乏しくなるので、それら成分の使用量は、ベース
ポリマー100部(重量部、以下同様)あたり、有
機発泡剤は5〜70部程度、亜鉛又は亜鉛化合物は
亜鉛量に換算して3〜50部程度が好ましい。な
お、有機発泡剤、亜鉛又は亜鉛化合物とも成形加
工性を向上させる観点から可及的微粉未のもの、
特に300メツシユの篩を通過するものが好まし
い。
上記した成分からなるポリマー組成物には必要
に応じて通常の難燃剤、老化防止剤、可塑剤充填
剤など、通常のゴム、プラスチツク用の配合剤を
通常量程度であれば配合してさしつかえない。こ
とに、難燃剤の使用は好ましく、たとえば三酸化
アンチモン、水和アルミナ、ポリリン酸アンモニ
ウムなどの無機難燃剤、テトラブロモビスフエノ
ール、デカブロモジフエニルオキサイド、パーク
ロロペンタシクロデカン、トリス、ブロモクロロ
プロピルホスフエートなどの有機難燃剤などが例
示される。
耐熱補強材としては、ガラス、アスベスト、カ
ーボン、セラミツク、各種金属などの無機物質の
繊維、ウール、織布、不織布などが用いられ、ま
た、フエノール樹脂、ポリイミド、ポリ4弗化エ
チレンなどの耐熱性有機樹脂の繊維(たとえばカ
イノール:商品名)、織布、不織布などが用いら
れる。耐熱補強材として繊維を用いるときは所謂
FRPの場合と同様にして、たとえば長さ3〜15
mmの短繊維を前記したポリマー組成物100部あた
り5〜100部程度混合して、所望のカバ形状に成
形する。また、織布、不織布を用いる場合は、た
とえば厚さ0.1〜1.0mmの織布、不織布の1層乃至
多数層の片面、両面、あるいは中間に上記ポリマ
ー組成物を施す、あるいは該組成物の層中に織
布、不織布の層をうめこむなどの方法で用いてよ
い。ウールを用いる場合には、ウールを抑圧して
不織布のごとき状態として不織布と同様に使用し
てよくまたポリマーと混合可能なものについては
上記ポリマー組成物と一緒に混合して使用しても
よい。さらに耐熱補強材として鋼、軟鋼、ステン
レス、アルミニウム、銅、黄銅、等の金属線から
なる網状体を用いてもよい。かゝる網状体は外径
0.1〜1.0mm程度の金属線からなり、網目の大きさ
は5〜100メツシユ程度のものである。
かゝる耐熱補強材の存在によつて、本発明のカ
バは常態における形態保持性、機械的特性におい
て優れ、しかも火災に際しては、本発明で用いる
ポリマー組成物自体の速やかな発泡防火性能に加
えて耐熱補強材による発泡炭化物層の支持作用に
よつて、部分的な孔あきが防止される。なお、耐
熱補強材はシート又は箔状あるいは孔あきシート
又は箔状として上記した織布、不織布使用の場合
と同様の方法で用いてもよい。本考案は厚さは、
たとえば0.5〜10mm程度であつて単なるシート状
として用いて防護の必要な物品をシートにて覆う
かたちで用いてよく、また、次に述べる実施例の
ように半割形のチユーブ、パイプとして用いても
よい。
以下、実施例、比較例により本考案を一層詳細
に説明する。
付図は本考案実施例の半割形防護カバを架空配
線された通信ケーブルに適用した例を断面図で示
すものであり、1は半割形の防護カバであり、カ
バ1は、その上下半割部材がボルト、ナツト2に
より結合されている。3,4はそれぞれ通信ケー
ブル、メツセンジヤーワイヤであり5はハンガで
ある。カバ1を下表に示す材料で構成し、各構成
組成物の特性、カバの防護特性を評価して同様に
示した。
The present invention relates to a protective cover used to protect objects from flames, and more particularly to a protective cover suitable for protecting objects that are exposed at high places, such as overhead communication cables. The cover that protects the object that is exposed at a high place is required to satisfy the following various characteristics. To protect an object from flames without dripping melt even if it is scorched by flames from below. To maintain the protective function in the event of a fire even if exposed to sunlight or rainwater for a long time. It must have excellent moldability to enable mass production. Among the above requirements, some are particularly demanding. The reason is that when an existing object is covered with a protective cover, the object usually has unevenness, so some parts of the inner surface of the protective cover will come into contact with the surface of the material, and some parts will remain out of contact. . If the protective cover is heated to a high temperature with a flame under such conditions, even if its constituent material is a thermosetting resin, many thermosetting resins will depolymerize, break crosslinks, etc. This is because it becomes molecularized and easily melts and drips, particularly from the non-contact portions. Needless to say, if a hole is created in the cover due to dripping, the cover will deteriorate or lose its protective function. In view of the above, the present invention proposes a new protective cover that satisfies the above requirements, which comprises a base polymer containing an ethylene-vinyl acetate copolymer component and a vinyl chloride component, and a base polymer containing an ethylene-vinyl acetate copolymer component and a vinyl chloride component, and , consisting of 5 to 70 parts by weight of an organic blowing agent and 3 to 50 parts by weight of zinc or a zinc compound in terms of zinc amount, and is reinforced with a heat-resistant reinforcing material. . As the base polymer, a graft polymer of ethylene-vinyl acetate copolymer and vinyl chloride, a mixture of ethylene-vinyl acetate copolymer and polyvinyl chloride and/or the above graft polymer, etc. are used. The content of the vinyl acetate component in the base polymer is preferably about 20 to 50% by weight, while the content of the vinyl chloride component is preferably about 40 to 70% by weight. As the organic foaming agent, one that can decompose at a temperature of 100 to 400°C and release nitrogen gas, carbon monoxide, carbon dioxide gas, ammonia gas, etc. to foam the organic polymers is used. For example, organic amines such as melamine, urea formaldehyde, aminoacetic acid, trimethylolmelamine, hexamethylolmelamine, melamine resin, N,N'-dinitrosopentamethylenetetramine, guanidine, dicyandiamide, butylurea, polyamide resin, azodicarbonamide, Examples include organic amides such as nitrososulfonamide, and sulfonylcarbazides such as p-toluenesulfonyl semicarbazide and p,p'-oxybenzenesulfonylcarbazide. Zinc or zinc compounds include zinc powder,
3ZnO・2B 2 O 2・3H 2 O, 2ZnO・3B 2 O 2・31/2H 2 O
Zinc borate compounds such as ZnO・ZnMoO 4 ,
These include molybdenum/zinc compounds such as CaO/ZnMoO 4 , ZnO, ZnCO 3 , Zn 3 (PO 4 ) 3 /4H 2 O, etc. When the Kaba of the present invention is heated with a flame, a dehydrochloric acid reaction occurs in the base polymer due to the action of the generated zinc oxide, and the base polymer is carbonized. It forms an insulating carbonized foam layer that protects objects from flames. Therefore, the zinc compound is not limited to the above-mentioned examples, but any compound that decomposes at high temperatures during a fire to produce zinc oxide can be suitably used. If the amount of organic blowing agent, zinc or zinc compound used is small, the foamed carbonized layer formation effect will be poor, while if the amount used is excessive, the moldability of the composition will be poor, so the amount of these components used is The organic blowing agent is preferably about 5 to 70 parts, and the zinc or zinc compound is preferably about 3 to 50 parts in terms of zinc amount, per 100 parts (by weight, hereinafter the same) of the base polymer. In addition, from the viewpoint of improving molding processability, the organic blowing agent, zinc or zinc compound should be used as finely powdered as possible.
Particularly preferred is one that passes through a 300 mesh sieve. If necessary, the polymer composition consisting of the above-mentioned components may contain ordinary compounding agents for rubber and plastics, such as ordinary flame retardants, anti-aging agents, plasticizer fillers, etc., in ordinary amounts. . In particular, the use of flame retardants is preferred, for example inorganic flame retardants such as antimony trioxide, hydrated alumina, ammonium polyphosphate, tetrabromobisphenol, decabromodiphenyl oxide, perchloropentacyclodecane, tris, bromochloropropyl. Examples include organic flame retardants such as phosphates. As heat-resistant reinforcing materials, fibers of inorganic materials such as glass, asbestos, carbon, ceramics, various metals, wool, woven fabrics, non-woven fabrics, etc. are used, and heat-resistant reinforcing materials such as phenolic resin, polyimide, polytetrafluoroethylene, etc. Organic resin fibers (for example, Kynol: trade name), woven fabrics, non-woven fabrics, etc. are used. When using fiber as a heat-resistant reinforcing material, the so-called
In the same way as for FRP, for example, length 3 to 15
About 5 to 100 parts of short fibers of mm in diameter are mixed with 100 parts of the above-mentioned polymer composition and formed into a desired cover shape. In addition, when using a woven fabric or a non-woven fabric, for example, the above-mentioned polymer composition is applied to one side, both sides, or an intermediate layer of one or multiple layers of a woven fabric or non-woven fabric with a thickness of 0.1 to 1.0 mm, or a layer of the composition is applied. It may be used by embedding a layer of woven fabric or non-woven fabric therein. When wool is used, it may be compressed to form a nonwoven fabric and used in the same manner as a nonwoven fabric, and those that can be mixed with a polymer may be used by mixing with the above polymer composition. Further, as a heat-resistant reinforcing material, a mesh body made of metal wires of steel, mild steel, stainless steel, aluminum, copper, brass, etc. may be used. Such a net-like body has an outer diameter
It is made of metal wire of about 0.1 to 1.0 mm, and the mesh size is about 5 to 100 meshes. Due to the presence of such a heat-resistant reinforcing material, the cover of the present invention has excellent shape retention and mechanical properties under normal conditions, and in the event of a fire, in addition to the rapid foaming fireproofing performance of the polymer composition itself used in the present invention. The supporting action of the foamed carbide layer by the heat-resistant reinforcing material prevents local porosity. Note that the heat-resistant reinforcing material may be used in the form of a sheet, a foil, or a perforated sheet or foil in the same manner as in the case of using a woven fabric or a nonwoven fabric as described above. The thickness of this invention is
For example, it is about 0.5 to 10 mm and can be used as a simple sheet to cover items that require protection, or as a half-split tube or pipe as shown in the following example. Good too. Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples. The attached figure shows a cross-sectional view of an example in which the half-split protective cover according to the embodiment of the present invention is applied to an overhead-wired communication cable. The split members are connected by bolts and nuts 2. 3 and 4 are a communication cable and messenger wire, respectively, and 5 is a hanger. Cover 1 was constructed from the materials shown in the table below, and the characteristics of each component composition and the protective properties of Cover were evaluated and shown in the same manner.
【表】
特性評価
(1) ポリマー組成物の加工性
実施例、比較例に示す組成物を実験用2本ロ
ールで混練し、コンパウンドを作製する。次に
ステンレス金網(0.48mm径、10メツシユ)とコ
ンパウンドを積層し厚さ4mmの成形シートを作
製する。成形後の外観からきわめて平滑で均一
な成形物を得たものを可、流れが悪く表面に凹
凸があり不均一に成形されるものを不可と判定
する。
(2) ポリマー組成物の耐候性
(1)で混練されたコンパウンドを厚さ2mmのプ
レス成形シートに作製し、幅20mm、長さ100mm
の短冊片に切り、それを外径30mmのマンドレル
上に巻きつけ試片とする。
これをJIS A 1415によるウエーザーメータ
ー曝露1000時間行ない亀裂の発生有無を観察し
亀裂を生じたものを不可とし、生じないものを
可と判定する。
(3) 耐熱カバの耐火テスト
表中の試料を被保護ケーブル〔導体径0.65、
100対ゴムシート(0.5mm厚)、LAPテープ、ポ
リエチレン絶縁被覆(0.3mm厚)を有し外径40
mmの市外PEF−LAPケーブル〕及びメツセン
ジヤーワイヤーに外嵌しこれを耐火試験炉に装
入してJIS A 1301屋外2級加熱曲線に準じて
加熱を行なう。30分加熱する間の各線芯の短絡
時間と30分後の未短絡の線芯を百分率で表わし
た。尚無処理のケーブルのみでは8分で短絡が
開始し14分20秒で全線芯が短絡してしまう。[Table] Characteristic evaluation (1) Processability of polymer composition The compositions shown in Examples and Comparative Examples were kneaded using two experimental rolls to prepare a compound. Next, a stainless wire mesh (0.48 mm diameter, 10 meshes) and the compound are laminated to form a 4 mm thick molded sheet. Based on the appearance after molding, a molded product that is extremely smooth and uniform is determined to be acceptable, and a molded product that has poor flow and unevenness on the surface and is molded unevenly is determined to be unacceptable. (2) Weather resistance of polymer composition The compound kneaded in (1) was made into a press-molded sheet with a thickness of 2 mm, and a width of 20 mm and a length of 100 mm.
Cut it into strips and wrap it around a mandrel with an outer diameter of 30 mm to make a test piece. This is exposed to a weather meter according to JIS A 1415 for 1000 hours, and the presence or absence of cracks is observed. Those with cracks are judged as unacceptable, and those with no cracks are judged as acceptable. (3) Fire resistance test of heat-resistant cover The samples in the table were tested on the protected cable [conductor diameter 0.65,
100 pairs rubber sheet (0.5mm thick), LAP tape, polyethylene insulation coating (0.3mm thick), outer diameter 40
2 mm long-distance PEF-LAP cable] and messenger wire, and put this into a fireproof test furnace and heat it according to the JIS A 1301 outdoor class 2 heating curve. The short-circuiting time of each wire core during 30 minutes of heating and the unshorted wire core after 30 minutes were expressed as a percentage. If only the untreated cable was used, short circuits would start in 8 minutes, and all wire cores would short circuit in 14 minutes and 20 seconds.
付図は本考案実施例の半割形防護カバを架空配
線された通信ケーブルに適用した例を断面図にて
示すものであつて、1は半割形の防護カバであ
り、カバ1はその上下半割部材がボルト、ナツト
2により結合されている。3,4はそれぞれ通信
ケーブル、メツセンジヤーワイヤーであり、5は
ハンガである。
The attached figure is a cross-sectional view of an example in which the half-split type protective cover according to the embodiment of the present invention is applied to an overhead wired communication cable. The half members are connected by bolts and nuts 2. 3 and 4 are a communication cable and messenger wire, respectively, and 5 is a hanger.
Claims (1)
成分とを含むベースポリマーと、該ポリマー100
重量部あたり、5〜70重量部の有機発泡剤と亜鉛
量に換算して3〜50重量部の亜鉛又は亜鉛化合物
とからなり、かつ耐熱性補強材により補強されて
なることを特徴とする防護カバ。 A base polymer containing an ethylene-vinyl acetate copolymer component and a vinyl chloride component, and the polymer 100
Protection characterized by comprising 5 to 70 parts by weight of an organic blowing agent and 3 to 50 parts by weight of zinc or a zinc compound per part by weight, and reinforced with a heat-resistant reinforcing material. Hippo.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11171681U JPS5817129U (en) | 1981-07-27 | 1981-07-27 | protective cover |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11171681U JPS5817129U (en) | 1981-07-27 | 1981-07-27 | protective cover |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5817129U JPS5817129U (en) | 1983-02-02 |
JPS6140524Y2 true JPS6140524Y2 (en) | 1986-11-19 |
Family
ID=29906058
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11171681U Granted JPS5817129U (en) | 1981-07-27 | 1981-07-27 | protective cover |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5817129U (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60122032U (en) * | 1984-01-27 | 1985-08-17 | 本田技研工業株式会社 | Friction clutch release mechanism |
JP5992589B1 (en) * | 2015-09-04 | 2016-09-14 | 株式会社レグルス | Thermally expandable vinyl chloride resin material and method for producing thermally expandable vinyl chloride resin material |
-
1981
- 1981-07-27 JP JP11171681U patent/JPS5817129U/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5817129U (en) | 1983-02-02 |
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