JPH02189809A - Flame retardant wire/cable - Google Patents
Flame retardant wire/cableInfo
- Publication number
- JPH02189809A JPH02189809A JP1007918A JP791889A JPH02189809A JP H02189809 A JPH02189809 A JP H02189809A JP 1007918 A JP1007918 A JP 1007918A JP 791889 A JP791889 A JP 791889A JP H02189809 A JPH02189809 A JP H02189809A
- Authority
- JP
- Japan
- Prior art keywords
- flame retardant
- flame
- polyolefine
- foaming agent
- retardant
- 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
- 239000003063 flame retardant Substances 0.000 title claims abstract description 23
- 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 title claims abstract description 22
- 229920000098 polyolefin Polymers 0.000 claims abstract description 20
- 239000004088 foaming agent Substances 0.000 claims abstract description 8
- 229910052751 metal Inorganic materials 0.000 claims abstract description 8
- 239000002184 metal Substances 0.000 claims abstract description 8
- 239000004020 conductor Substances 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 abstract description 6
- 239000007789 gas Substances 0.000 abstract description 5
- 239000006260 foam Substances 0.000 abstract description 4
- 238000005187 foaming Methods 0.000 abstract description 4
- 229910000039 hydrogen halide Inorganic materials 0.000 abstract description 4
- 239000012433 hydrogen halide Substances 0.000 abstract description 4
- 239000000779 smoke Substances 0.000 abstract description 4
- 230000001473 noxious effect Effects 0.000 abstract 1
- 238000002485 combustion reaction Methods 0.000 description 11
- 229910052736 halogen Inorganic materials 0.000 description 7
- 150000002367 halogens Chemical class 0.000 description 7
- -1 polyethylene Polymers 0.000 description 7
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000004604 Blowing Agent Substances 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 4
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 3
- 235000019399 azodicarbonamide Nutrition 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000007765 extrusion coating Methods 0.000 description 3
- 239000012212 insulator Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000004156 Azodicarbonamide Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 2
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920013639 polyalphaolefin Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- HGTUJZTUQFXBIH-UHFFFAOYSA-N (2,3-dimethyl-3-phenylbutan-2-yl)benzene Chemical group C=1C=CC=CC=1C(C)(C)C(C)(C)C1=CC=CC=C1 HGTUJZTUQFXBIH-UHFFFAOYSA-N 0.000 description 1
- MEJAPGGFIJZHEJ-UHFFFAOYSA-N 5-acetamido-1,3,4-thiadiazole-2-sulfonyl chloride Chemical compound CC(=O)NC1=NN=C(S(Cl)(=O)=O)S1 MEJAPGGFIJZHEJ-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 241000252233 Cyprinus carpio Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- VCNTUJWBXWAWEJ-UHFFFAOYSA-J aluminum;sodium;dicarbonate Chemical compound [Na+].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O VCNTUJWBXWAWEJ-UHFFFAOYSA-J 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 229910001647 dawsonite Inorganic materials 0.000 description 1
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 1
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000000314 lubricant 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
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- XJKVPKYVPCWHFO-UHFFFAOYSA-N silicon;hydrate Chemical compound O.[Si] XJKVPKYVPCWHFO-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 230000037351 starvation Effects 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 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 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Insulated Conductors (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Abstract
Description
【発明の詳細な説明】
1産業上の利用分野]
本発明は燃焼時にハロゲンを放出せず、且つ断熱性の優
れた難燃性電線・ケーブルに関するものである。DETAILED DESCRIPTION OF THE INVENTION 1. Field of Industrial Application] The present invention relates to flame-retardant wires and cables that do not emit halogen during combustion and have excellent heat insulation properties.
[従来の技術1
近年、防災思想が高まるにつれ、難燃月利についでもq
lに燃えにくいというだけでなく、有毒ガス、1渇食1
′11ガス、黒煙の発生の少ないものが要求されるよう
になってきている。[Conventional technology 1] In recent years, as the idea of disaster prevention has increased,
Not only is it difficult to burn, but it also contains toxic gas, 1 starvation, 1
'11 There is a growing demand for products that generate less gas and black smoke.
例えば、分子内にハ[Jゲンを内在するポリ塩化ビニル
、ボリク[コロブレンゴム、或いは各種のふっ素ポリマ
ー、ふっ素ゴムといったハ[コゲン含右ポリマーが勤燃
性に優れたものとして重宝されてぎたが、これらは燃焼
時に有ifで且つIl!食性のハロゲン化水素ガスを多
量に発生し問題となっている。For example, polyvinyl chloride, borikolobrene rubber, and various fluoropolymers and fluororubbers, which contain hydrogen in the molecule, have been prized for their excellent combustibility. These are present at the time of combustion and Il! It generates a large amount of edible hydrogen halide gas, which is a problem.
一方、ポリマー自体はハロゲンを含まないポリエチレン
等のポリオレフィンについても、塩素や臭素を含むハロ
ゲン系難燃剤を用いて難燃化されているため、やはりハ
[]ゲン化水素ガスを発生や煙の多量発生は避けられな
い。On the other hand, even polyolefins such as polyethylene, which do not contain halogens, are flame-retardant using halogen-based flame retardants containing chlorine and bromine. Its occurrence is inevitable.
そこで最近は、ポリエチレン等の分子内にハ[1ゲンを
含まないポリマーをベースとし、これに例えば水酸化ア
ルミニウム等の分子内に結晶水を多く含み、且つハロゲ
ンを含まない吸熱型の無機化合物を難燃剤として添加す
る、いわゆるノンハ1−1ゲンボリオレフイン材料が、
燃焼時に有毒な腐食性カスを発生Iず、しかし煙の発生
4も少ない難燃月別とじで注1」され、特に電線・ケー
ブルの分野で絶縁体又はシース材料どして脚光を浴びつ
つある。Therefore, recently, polymers such as polyethylene that do not contain a halogen in the molecule are used as base materials, and endothermic inorganic compounds that contain a large amount of water of crystallization in the molecule and do not contain halogens, such as aluminum hydroxide, have recently been added. The so-called non-HA 1-1 polyolefin material added as a flame retardant is
It is known for its flame-retardant binding, which does not produce toxic corrosive scum when burned, but also produces little smoke, and is attracting attention as an insulator or sheath material, especially in the field of electric wires and cables.
[発明が解決しようとする課題]
しかしながら、例えばケーブル線心の絶縁体として…燃
f’l I、J 13+を使用し、ぞの土に一1記のノ
ンハ[−1ゲンポリオレフイン拐籾を施したケーブルに
ついて考察すると、単に該ノンハ【−1ゲンボリオレフ
イン材IIは、燃えにくいだ(ブでは不十分で゛あり、
内在づ−る可燃性月利の温度上譬に伴う液化、ガス化、
着火の防止作用、即し断熱作用を右しでいることが必要
であり、そうでな(プれば電線・クープルへの適用範囲
が制限されるという問題がある。[Problems to be Solved by the Invention] However, for example, when insulators for cable cores are used...F'l I, J 13+, and the soil is coated with the non-ha[-1] polyolefin grains. When we consider the cables that were used, we found that the non-ha[-1 Gemboriolefin material II is simply flammable;
Liquefaction, gasification, and
It is necessary to have an ignition prevention effect, that is, a heat insulation effect; otherwise, there is a problem that the scope of application to electric wires and couples will be limited.
又、燃焼時の炭化層の形成についても考慮すべきC゛あ
り、割れやクシツク、落F等が生じても役立たない。こ
れらの問題を解決づるためには、必要以−トに難燃剤を
多く用いるか、或いは被覆厚を厚くづることが必要であ
るが、それらの対策は電線・ケーブルにd3りる各種の
性能低下、経済性、スペース等の点から好ましくないも
のである。Also, the formation of a carbonized layer during combustion must be taken into account, and it is not helpful if cracks, cracks, or falling F occur. In order to solve these problems, it is necessary to use more flame retardant than necessary or to increase the thickness of the coating, but these measures will reduce the performance of wires and cables. , which is undesirable from the viewpoint of economy, space, etc.
本発明の目的は、前記した従来技術の欠点を解消し、上
記のノンハロゲン材料の長所を全く損なわずに燃焼時に
断熱効果を発揮する勤燃月利を被覆した電線・ケーブル
を提供することにある。An object of the present invention is to eliminate the drawbacks of the prior art mentioned above and to provide wires and cables coated with a heat-insulating material that exhibits a heat insulating effect during combustion without impairing the advantages of the non-halogen materials mentioned above. .
し課題を解決するだめの手段及び作用コ本発明の要旨は
、ポリオレフィンに金属水和物ど発泡剤、更に必要に応
じ−C[燃助剤を加えてなる難燃性ポリオレフィン組成
物を導体又は絶縁線心−[−に被覆したことにあり、そ
れによって燃焼時に発泡剤が分解発泡してノンハ[]ゲ
ン被膜を膨張さ[強固な発泡断熱層を形成り−るように
したものである。Means and operation for solving the problem The gist of the present invention is to prepare a flame-retardant polyolefin composition prepared by adding a blowing agent such as a metal hydrate to a polyolefin and, if necessary, a combustion aid. The insulated wire core is coated with the foam so that the foaming agent decomposes and foams during combustion, expanding the non-hazardous coating to form a strong foamed heat insulating layer.
上記のポリオレフィンとしては、低、中、高密度のポリ
エチレン、ボリア]」ピレン、ポリブテン1等のポリ−
α−オレフィン;ブラン−1,プ[]ピレン等とエチレ
ンとのブ[lツクランジノ1具重合体等のポリ−α−オ
レフィン共重合体:二1ニチレン 酢酸ビニル共重合体
、]ニチレンーコーチルアクリレート共重合体、エブレ
ンープロピレンージ」ンJラス1〜マー等が挙げられ、
これらの2種以」−のiI′A合物を用い(も差し支え
ない、。The above-mentioned polyolefins include low, medium, and high density polyethylenes, polyolefins such as boria, pyrene, and polybutene 1.
α-olefin; poly-α-olefin copolymer such as bran-1, p[]pyrene, etc. and ethylene; poly-α-olefin copolymer such as b[l-crandyno-1] polymer; 21-nytylene vinyl acetate copolymer; Examples include acrylate copolymers, Eblene-propylene resins, etc.
Two or more of these iI'A compounds may also be used.
金属水和物としては、水酸化アルミニウム、水酸化マグ
ネシウム、硼酸亜鉛、ハイド[]タルザイ1〜、ドーソ
ナイト等が代表的なものであるが、これらに限定される
訳ではない。金属水和物の添加(至)は特に制限されな
いが、ポリオレフィン100重gB部に対しで50重量
部未満では難燃性が小さく、200重量部を越えると物
性、加工性等に問題が生じてくるので、一般的には50
〜200重量部が好ましい1゜
発泡剤は、有機系及び無機系のいずれの発泡剤でもよい
が、実用的には、ノンハ[」ケン難燃性ポリオレフィン
の成形加工温度、例えば150℃以下で分解、発泡しな
いことが必要である。代表的な発泡剤どしては、)!ゾ
ジカルボンアミド、アゾビスホルムアミド、N、N’
−ジニ1−ロンペンタメヂレンデトラミン、オキシビ
スベンげンスルホルヒドラジッド、等のアゾ系、二1へ
1]ン系、スルボニルヒドラジッド系等が挙げられる。Typical examples of metal hydrates include aluminum hydroxide, magnesium hydroxide, zinc borate, Hyde[]Talzai 1~, Dawsonite, etc., but are not limited to these. There are no particular restrictions on the amount of metal hydrate added, but if it is less than 50 parts by weight per 100 parts by weight of polyolefin, the flame retardancy will be low, and if it exceeds 200 parts by weight, problems will occur in physical properties, processability, etc. generally 50
The 1° blowing agent, which is preferably 200 parts by weight, may be either an organic or an inorganic blowing agent, but in practical terms, it decomposes at a temperature below the molding temperature of the flame-retardant polyolefin, for example 150°C. , it is necessary that no foaming occurs. What are the typical blowing agents?)! Zodicarbonamide, azobisformamide, N, N'
Examples include azo-based compounds such as -dini-1-lone pentamedylene detramine, oxybisbenzene sulfohydrazide, etc., 21-1]one-based compounds, and sulfonyl hydrazide-based compounds.
これらの発泡剤の分解速度や分解温度を調節するために
、例えば酸化亜鉛等の無機塩、ステアリン酸鉛哲の金属
石鹸等の助剤を使用してもよい。又、良好な発泡を得る
ために、分解温度の異なる2種以上の発泡剤を併用する
こともできる。In order to adjust the decomposition rate and decomposition temperature of these blowing agents, auxiliary agents such as inorganic salts such as zinc oxide and metal soaps such as lead stearate may be used. Moreover, in order to obtain good foaming, two or more foaming agents having different decomposition temperatures can be used in combination.
上記の組成物に必要に応じて添加される難燃助剤として
は、赤りん、カーボンブラック等が代表的なものである
が、特に発火点260℃以上、粒径10μ以下の赤りん
は難燃性即ち酸素指数を著しく高めることができる点で
好ましく、更に取扱の安全性のために粒子表面を例えば
メラミン樹脂、フェノール樹脂等で被覆したものが一層
好ましい。Typical flame retardant additives added to the above composition as needed are red phosphorus, carbon black, etc., but red phosphorus with an ignition point of 260°C or higher and a particle size of 10μ or less is particularly difficult to use. It is preferable in that the flammability, that is, the oxygen index, can be significantly increased, and it is even more preferable to coat the particle surface with, for example, melamine resin, phenol resin, etc. for safety in handling.
この他、五酸化りんやりん酸メラミン等のりん化合物も
有用である。カーボンブラックは燃焼時の灰の強化に有
効であり、又ノンハロの欠点である表面キズ発生時のキ
ズのつきやすさの防止や耐候性にも有効である。ノJ−
ボンブンツクとしてはブ17ンネル、ファ・−ネス、ザ
ーマル、アセチレンのいずれでもよい。In addition, phosphorus compounds such as phosphorus pentoxide and melamine phosphate are also useful. Carbon black is effective in strengthening ash during combustion, and is also effective in preventing surface scratches, which are disadvantages of non-halogen materials, and in improving weather resistance. No J-
As the bomb, any one of 17-channel, fluorescein, thermal, and acetylene may be used.
尚、難燃助剤の添加量は、ポリオ−レノイン100重量
部に対し、夫々赤りん10重量部以下、カーボンブラッ
ク550重14部以下が好ましい。The addition amount of the flame retardant aid is preferably 10 parts by weight or less of red phosphorus and 14 parts by weight or less of 550 parts of carbon black, respectively, per 100 parts by weight of polyolenoin.
その他、酸化防11−剤、滑剤、着色剤等、ノン八[1
ゲンボリオレフィン難燃性組成物において通常用いられ
ている添加剤はそのまま01用り−ることができる。In addition, antioxidant 11-agents, lubricants, colorants, etc.
Additives commonly used in gemboriolefin flame retardant compositions can be used as they are.
」−記の発泡性鯉燃性ポリオレフィン組成物は、架橋網
状化処理されていてもJ:い。架橋方法としては、ジク
ミルパーオニ1リ−イド等の有機過酸化物を用い(加熱
架橋する化学架橋法、電子線やα線等のJネルギーリッ
チ線を照射づる放射線照射架橋法、及びビニルシランを
バーΔキリーイドと共にポリオレフィンに加えてシラン
グラフ1へポリオレフィンを作り、これを水雰囲気中で
架[するシラン−水架橋法がある0、これらの架橋払を
用い−て本発明の組成物を架橋することによって、ポリ
マー粘度が非架橋ポリマーのそれに比べて大きくなり、
−層有効な発泡断熱層を形成することができる。The foamable carp retardant polyolefin composition described in "-" may be subjected to crosslinking and reticulation treatment. Crosslinking methods include using an organic peroxide such as dicumyl perionide (chemical crosslinking method using heat crosslinking, radiation crosslinking method using J energy rich rays such as electron beams and alpha rays, and vinyl silane with bar Δ There is a silane-water crosslinking method in which a polyolefin is added to Silangraph 1 with Kyrieid and crosslinked in a water atmosphere.By crosslinking the composition of the present invention using these crosslinkers, , the polymer viscosity becomes larger compared to that of non-crosslinked polymers,
- It is possible to form an effective foam insulation layer.
[実 施 例]
以下、本発明を、図面を参照しつつ、実施例及び比較例
に端づいて更に詳しく説明する。[Examples] Hereinafter, the present invention will be described in more detail with reference to the drawings, starting with Examples and Comparative Examples.
実施例1
エチレン−エチルアクリレート共重合体100重量部に
水酸化アルミニウム100重間部、アゾジカルボンアミ
ド1重量部を加えてなる組成物を、外径1.2mmの導
体上に厚さ1.4mmにポリエチレン絶縁体を被覆して
なる外径4.0mmの絶縁線心上に1.0mmの厚さに
なるように押出被覆して電線を製造した。Example 1 A composition prepared by adding 100 parts by weight of ethylene-ethyl acrylate copolymer, 100 parts by weight of aluminum hydroxide, and 1 part by weight of azodicarbonamide was applied to a conductor having an outer diameter of 1.2 mm to a thickness of 1.4 mm. An electric wire was manufactured by extrusion coating an insulated wire core having an outer diameter of 4.0 mm to a thickness of 1.0 mm, which was made by coating a polyethylene insulator.
実施例2
エヂレンーエチルアクリレー1へ共重合体100重量部
に水酸化アルミニウム100重h1部、赤りん2重量部
、アゾジカルボンアミド1重hi sl+を加えてなる
組成物を、実施例1と同じ絶縁線心上に1.0#の厚さ
になるように押出被覆して電線を製造した。Example 2 A composition obtained by adding 1 part by weight of aluminum hydroxide, 2 parts by weight of red phosphorus, and 1 part by weight of azodicarbonamide to 100 parts by weight of the copolymer was prepared in Example 1. An electric wire was manufactured by extrusion coating onto the same insulated wire core to a thickness of 1.0#.
実施例3
実施例1及び2で得られた各電線に30 M radの
電子線を照射して架橋処理した。Example 3 Each of the electric wires obtained in Examples 1 and 2 was crosslinked by irradiating it with an electron beam of 30 Mrad.
比較例1
丁チレンーエチルアクリレート共重合体100重量部に
水酸化アルミニウム100重量部を加えてなる組成物を
、実施例1と同じ絶縁線心上に1.0Mの厚さになるよ
うに押出被覆して電線を製 )告 し Iこ 。Comparative Example 1 A composition prepared by adding 100 parts by weight of aluminum hydroxide to 100 parts by weight of ethylene-ethyl acrylate copolymer was extruded onto the same insulated wire core as in Example 1 to a thickness of 1.0M. (I coated wires to make electric wires.)
比較例2
エチレン 」デルアクリレート共重合体100重量部に
水酸化アルミニウム100重尾部、赤りん2型組部を加
えてなる組成物を、実施例1と同じ絶縁線心−)=に1
.0mmの厚さになるように押出被覆して電線を製造し
た。Comparative Example 2 A composition obtained by adding 100 parts by weight of ethylene delacrylate copolymer, 100 parts by weight of aluminum hydroxide, and 2 parts of red phosphorus was added to the same insulated wire core as in Example 1.
.. An electric wire was manufactured by extrusion coating to a thickness of 0 mm.
く燃焼試験)
実施例1・〜3及び比較例の電線について、Ul−サツ
シ]りh (5ubject)785に記載されている
I’R−1燃焼試験を行った。そして15秒間隔の接炎
を5回行った時の延焼状態を調べ、延焼時間が60秒未
満のものを合格とした。Combustion Test) The electric wires of Examples 1 to 3 and Comparative Example were subjected to the I'R-1 combustion test described in U.L. Then, the state of fire spread was examined when flame contact was performed five times at intervals of 15 seconds, and those with a fire spread time of less than 60 seconds were judged to have passed.
その結果、実施例1へ・3の電線はいずれも合格し、し
かもシース被覆物の燃焼時の発泡状態は良好で断熱効果
が大きかった。尚、燃焼時の発泡断熱層は実施例3の電
線が最も優れていた。As a result, all the electric wires of Examples 1 and 3 passed the test, and the foaming state of the sheath coating during combustion was good, and the heat insulation effect was large. Note that the electric wire of Example 3 had the best foamed heat insulating layer during combustion.
これに対し、比較例1の電線は4回目の接炎で内層のポ
リエチレンに着火し、60秒以上延焼しつづけ、又比較
例2の電線は5回目の接炎で内層のポリエチレンに着火
し、60秒以上延焼し・つづけ、いずれも不合格であっ
た。On the other hand, the electric wire of Comparative Example 1 ignited the inner layer of polyethylene on the fourth flame contact and continued to spread for more than 60 seconds, and the electric wire of Comparative Example 2 ignited the inner layer of polyethylene on the fifth flame contact. The fire spread and continued for more than 60 seconds, and all were rejected.
[発明の効果]
以上説明したように本発明によれば、ノン八1」ケン難
燃性ポリオレフィンのもつ、燃焼時に有毒で腐食性のハ
ロゲン化水素ガスを発生づることなく、且つ煙の発生量
も少ないという長所を損なうことなく、接炎時に発泡剤
が有効に分解して膨張した発泡断熱層を形成する難燃性
電線・ケーブルが得られる効果がある。[Effects of the Invention] As explained above, according to the present invention, the flame-retardant polyolefin does not generate toxic and corrosive hydrogen halide gas when burned, and the amount of smoke generated can be reduced. This has the effect of providing flame-retardant wires and cables in which the foaming agent effectively decomposes and expands when exposed to flame, forming an expanded foamed heat insulating layer, without sacrificing the advantage of having a small amount of heat.
Claims (2)
難燃性ポリオレフィン組成物を導体又は絶縁線心上に被
覆したことを特徴とする難燃性電線・ケーブル。1. A flame-retardant electric wire/cable characterized in that a conductor or an insulated wire core is coated with a flame-retardant polyolefin composition made by adding a metal hydrate and a foaming agent to polyolefin.
加えてなる難燃性ポリオレフィン組成物を導体又は絶縁
線心上に被覆したことを特徴とする難燃性電線・ケーブ
ル。2. A flame-retardant electric wire/cable characterized in that a conductor or an insulated wire core is coated with a flame-retardant polyolefin composition made by adding a metal hydrate, a flame retardant aid, and a foaming agent to polyolefin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1007918A JPH02189809A (en) | 1989-01-17 | 1989-01-17 | Flame retardant wire/cable |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1007918A JPH02189809A (en) | 1989-01-17 | 1989-01-17 | Flame retardant wire/cable |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02189809A true JPH02189809A (en) | 1990-07-25 |
Family
ID=11678909
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1007918A Pending JPH02189809A (en) | 1989-01-17 | 1989-01-17 | Flame retardant wire/cable |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02189809A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001052537A (en) * | 1999-08-09 | 2001-02-23 | Sumitomo Electric Ind Ltd | Non-halogen flame retardant shield cable |
FR2858458A1 (en) * | 2003-08-01 | 2005-02-04 | Sagem | FLAME RETARDANT ELECTRICAL CABLE WITH A MULTILAYER EXTERNAL SHEATH |
US7700679B2 (en) | 2005-02-18 | 2010-04-20 | Tyco Electronics Corporation | Heat-recoverable article and composition therefor |
-
1989
- 1989-01-17 JP JP1007918A patent/JPH02189809A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001052537A (en) * | 1999-08-09 | 2001-02-23 | Sumitomo Electric Ind Ltd | Non-halogen flame retardant shield cable |
FR2858458A1 (en) * | 2003-08-01 | 2005-02-04 | Sagem | FLAME RETARDANT ELECTRICAL CABLE WITH A MULTILAYER EXTERNAL SHEATH |
EP1504887A1 (en) * | 2003-08-01 | 2005-02-09 | Sagem SA | Electrical cable rendered fire-proof by the use of an outer multilayered sheath |
US7700679B2 (en) | 2005-02-18 | 2010-04-20 | Tyco Electronics Corporation | Heat-recoverable article and composition therefor |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4549041A (en) | Flame-retardant cross-linked composition and flame-retardant cable using same | |
CN103642118B (en) | Tube wall bubble-tight irradiation crosslinking halogen-free fire proofing and application during heat shrinkable | |
AU629876B2 (en) | Flame retardant compositions | |
JPH02189809A (en) | Flame retardant wire/cable | |
US4014770A (en) | Electron beam cured intumescent coating composition | |
JP2919277B2 (en) | Crosslinked polyolefin resin foam and heat insulating pipe cover using the same | |
JPH02187434A (en) | Flame-resistant foamed sheet | |
JP2508130B2 (en) | Flame-retardant wire / cable | |
JPS5928574Y2 (en) | flame retardant cable | |
JPS5928573Y2 (en) | flame retardant cable | |
JPS6348890B2 (en) | ||
JPS6241367B2 (en) | ||
JPS60202163A (en) | Expandable fireproofing composition | |
JPS60202165A (en) | Expandable fireproofing composition | |
JPH0320908A (en) | Flame retardant electric wire and cable | |
JP3276169B2 (en) | Foamable polyolefin resin composition and flame-retardant polyolefin resin foam | |
JPH0337909A (en) | Incombustible coated electric wire/cable | |
JP2887965B2 (en) | Flame retardant wires and cables | |
JPH0119690B2 (en) | ||
JPS6339018B2 (en) | ||
JPH0515011B2 (en) | ||
JPS6134036A (en) | Flame-retarding electrical insulating composition | |
JPH02182449A (en) | Resin coated metal plate for building material | |
JPH07119323B2 (en) | Flame retardant electrical insulation composition | |
JPH03190013A (en) | Flame resistant electrical insulating compound |