JPH02195604A - Foam insulating electric wire - Google Patents
Foam insulating electric wireInfo
- Publication number
- JPH02195604A JPH02195604A JP1483189A JP1483189A JPH02195604A JP H02195604 A JPH02195604 A JP H02195604A JP 1483189 A JP1483189 A JP 1483189A JP 1483189 A JP1483189 A JP 1483189A JP H02195604 A JPH02195604 A JP H02195604A
- Authority
- JP
- Japan
- Prior art keywords
- polypropylene
- density polyethylene
- melt index
- block copolymer
- insulating film
- 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
- 239000006260 foam Substances 0.000 title claims description 14
- 239000004743 Polypropylene Substances 0.000 claims abstract description 46
- 229920001155 polypropylene Polymers 0.000 claims abstract description 42
- -1 polypropylene Polymers 0.000 claims abstract description 38
- 239000000463 material Substances 0.000 claims abstract description 19
- 239000004698 Polyethylene Substances 0.000 claims abstract description 17
- 229920001400 block copolymer Polymers 0.000 claims abstract description 16
- 229920001903 high density polyethylene Polymers 0.000 claims abstract description 15
- 239000004700 high-density polyethylene Substances 0.000 claims abstract description 15
- 229920000181 Ethylene propylene rubber Polymers 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 4
- 229920000573 polyethylene Polymers 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 11
- 238000000576 coating method Methods 0.000 claims description 11
- 238000005187 foaming Methods 0.000 abstract description 10
- 230000006866 deterioration Effects 0.000 abstract description 5
- 239000004020 conductor Substances 0.000 abstract description 4
- 239000013078 crystal Substances 0.000 abstract description 4
- 229920001684 low density polyethylene Polymers 0.000 abstract description 4
- 239000004702 low-density polyethylene Substances 0.000 abstract description 4
- 238000002425 crystallisation Methods 0.000 abstract description 2
- 230000008025 crystallization Effects 0.000 abstract description 2
- 230000007423 decrease Effects 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 238000009413 insulation Methods 0.000 description 8
- 238000001125 extrusion Methods 0.000 description 5
- 239000000155 melt Substances 0.000 description 4
- 230000008054 signal transmission Effects 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 230000003712 anti-aging effect Effects 0.000 description 2
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 2
- 235000019399 azodicarbonamide Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- NBOCQTNZUPTTEI-UHFFFAOYSA-N 4-[4-(hydrazinesulfonyl)phenoxy]benzenesulfonohydrazide Chemical compound C1=CC(S(=O)(=O)NN)=CC=C1OC1=CC=C(S(=O)(=O)NN)C=C1 NBOCQTNZUPTTEI-UHFFFAOYSA-N 0.000 description 1
- UNPLRYRWJLTVAE-UHFFFAOYSA-N Cloperastine hydrochloride Chemical compound Cl.C1=CC(Cl)=CC=C1C(C=1C=CC=CC=1)OCCN1CCCCC1 UNPLRYRWJLTVAE-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
- 230000005540 biological transmission Effects 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000011162 core material Substances 0.000 description 1
- 229920006038 crystalline resin Polymers 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
Landscapes
- Organic Insulating Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は1例えば、電子計算機の架間または架内の配線
に用いられる高速信号伝送用同軸ケーブルに使用される
発泡絶縁電線に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a foam insulated wire used, for example, in a coaxial cable for high-speed signal transmission used for wiring between or within a computer rack. .
(従来の技術〕
この種の発泡絶縁電線に要求される特性の中に高速信号
伝送特性と外力に対する耐変形性があるが、特に高速信
号伝送特性は伝送時間の一層の短縮化の要求から益々要
求される傾向にある。このため、電線の被覆材料として
比誘電率が小さいものを用い、且つ発泡率を高くするこ
とが要求されるが、発泡率を高くすると、外力に対する
耐変形性が低くなる。これらの要求を満足する材料とし
て通常ポリエチレン(PE)、ポリプロピレン(PP)
及び弗素樹脂等が掲げられる。(Prior Art) Among the characteristics required of this type of foam insulated wire are high-speed signal transmission characteristics and deformation resistance against external forces.In particular, high-speed signal transmission characteristics are becoming increasingly important due to the demand for further shortening of transmission time. For this reason, it is necessary to use a material with a low dielectric constant as the covering material for electric wires, and to increase the foaming rate. Polyethylene (PE) and polypropylene (PP) are usually used as materials that meet these requirements.
and fluororesins, etc.
これらの3つの材料のうちポリエチレンは最も特性が悪
く、特に発泡率がおおむね50%を越えると、アンダー
カーペットケーブルの如き高度の耐変形性が要求される
ケーブルには使用することができなかった。また、弗素
樹脂は材料費が極端に高く、一方ボリブロビレンは高い
発泡率でも外力に対する耐変形性が高く安価な材料とし
て最も使用されている。Of these three materials, polyethylene has the worst properties, and especially when the foaming ratio exceeds approximately 50%, it cannot be used for cables that require a high degree of deformation resistance, such as undercarpet cables. In addition, fluororesin has an extremely high material cost, while polypropylene is most used as an inexpensive material that has high resistance to deformation against external forces even at a high foaming rate.
しかし、ポリプロピレンは代表的な結晶性の樹脂であり
、押出機等で溶融径電線形状に成形すると、伸びが経時
的に低下する特性を有しており、この傾向は発泡率か高
くなるほど、また肉厚が小さくなるほど顕著となる。こ
のような欠点を改善する材料として低密度ポリエチレン
やエチレン・プロピレンゴム(EPR)とポリプロピレ
ンとのブロックコポリマーが知られているか、これでも
特性を著しく改善することができなかった。However, polypropylene is a typical crystalline resin, and when it is molded into the shape of a molten wire using an extruder, its elongation decreases over time, and this tendency decreases as the foaming rate increases. This becomes more noticeable as the wall thickness decreases. Low-density polyethylene and block copolymers of ethylene-propylene rubber (EPR) and polypropylene are known as materials that can improve these drawbacks, but even these have not been able to significantly improve the properties.
本発明の目的は、上記の欠点を回避し、伸びの低下を抑
制することかでき、且つ機械的強度がすぐれた絶縁被覆
を有する安価な発泡絶縁電線を提供することにある。An object of the present invention is to provide an inexpensive foam insulated wire that avoids the above-mentioned drawbacks, can suppress a decrease in elongation, and has an insulation coating with excellent mechanical strength.
本発明は、上記の課題を解決するために、ポリプロピレ
ンとポリプロピレン/ポリエチレンのブロックコポリマ
ーとポリプロピレン/エチレン・プロピレンゴムのブロ
ックコポリマーとのいずれかの材料とこの材料よりもメ
ルトインデックスが大きい高密度ポリエチレンとの混合
物の発泡体から成る絶縁被覆を有することな特徴とする
発泡絶縁電線を提供するものである。In order to solve the above-mentioned problems, the present invention combines a material consisting of polypropylene, a polypropylene/polyethylene block copolymer, and a polypropylene/ethylene-propylene rubber block copolymer, and a high-density polyethylene having a larger melt index than this material. The present invention provides a foam insulated wire characterized in that it has an insulation coating made of a foam of a mixture of.
〔作用〕
このように、ポリプロピレン、ポリプロピレン/ポリエ
チレンのブロックコポリマー、ポリプロピレン/エチレ
ン・プロピレンゴムのブロックコポリマーに、この材料
よりもメルトインデックスか大きい高密度ポリエチレン
を混合すると、絶縁被覆の伸びの経時的低下を抑制する
ことができる上に機械的強度か向上する。[Effect] In this way, when high-density polyethylene, which has a higher melt index than this material, is mixed with polypropylene, a block copolymer of polypropylene/polyethylene, or a block copolymer of polypropylene/ethylene propylene rubber, the elongation of the insulation coating decreases over time. In addition to being able to suppress this, it also improves mechanical strength.
次に1本発明の発泡絶縁電線を詳細に説明すると1本発
明の発泡絶縁電線は、導体とこの導体の上に押出被覆さ
れた絶縁被覆とから成っているが、この絶縁被覆は、先
にのべたように、ポリプロピレン(pp)単独あるいは
ポリプロピレン(pp)と低密度ポリエチレン(PE)
とのブロックコポリマーまたはポリプロピレン(PP)
とエチレン・プロピレンゴム(EPR)とのブロックコ
ポリマーのいずれかの材料と、これらの材料よりもメル
トインデックスが大きい高密度ポリエチレン(PE)と
の混合物の発泡体から成っている。Next, the foam insulated wire of the present invention will be explained in detail. The foam insulated wire of the present invention consists of a conductor and an insulating coating extruded on the conductor. As mentioned above, polypropylene (PP) alone or polypropylene (PP) and low density polyethylene (PE)
block copolymer or polypropylene (PP) with
and ethylene propylene rubber (EPR), and high-density polyethylene (PE), which has a higher melt index than these materials.
高密度ポリエチレンのメルトインデックスがポリプロピ
レン単独またはこのポリプロピレンと低密度ポリエチレ
ンまたはエチレン・プロピレンゴムとのブロックコポリ
マーのメルトインデックスよりも小さいと、機械的強度
がよくなるか、樹脂同志の相溶性が悪く、伸びの経時的
低下か抑えられない上に電線の外観が著しく悪くなる。If the melt index of high-density polyethylene is smaller than the melt index of polypropylene alone or a block copolymer of polypropylene and low-density polyethylene or ethylene-propylene rubber, the mechanical strength may be good, or the compatibility between the resins may be poor, resulting in poor elongation. In addition to the uncontrollable deterioration over time, the appearance of the wires deteriorates significantly.
逆に、高密度ポリエチレンのメルトインデックスがポリ
プロピレン等の材料のインデックスよりも大きすぎる場
合には伸びの経時的低下は著しく抑制されるが、機械的
強度、耐衝撃性等が著しく悪くなるので高密度ポリエチ
レンのメルトインデックスは10g710分以下が適当
である。尚、ポリプロピレン及びそのブロックコポリマ
ーと高密度ポリエチレンとの混合率はいかなる場合でも
効果かある。On the other hand, if the melt index of high-density polyethylene is larger than the index of materials such as polypropylene, the decline in elongation over time will be significantly suppressed, but mechanical strength, impact resistance, etc. will deteriorate significantly, so high-density polyethylene The appropriate melt index of polyethylene is 10 g, 710 minutes or less. Incidentally, the mixing ratio of polypropylene or its block copolymer with high density polyethylene is effective in any case.
本発明に用いられる発泡材料としては、アゾジカルボン
アミド(ADCA)、アゾビスイソブチロニトリル(A
IBN)、ジニトロソペンタメチレンテトラミン(DP
T)、p−)ルエンスルホニルヒドラジド(TSH)、
p、p−オキシビス(ベンゼンスルホニルヒドラジド)
(OBSH)等の熱分解型有機発泡材、窒素、炭酸ガス
、クロロフルオロカーボン(フロン)等のガス類または
これらの組み合わせを用いることができる。押出しに際
してはその外に発泡核材、老化防止剤、銅害防止剤1着
色剤等を添加してもよいことはもちろんである。Foamed materials used in the present invention include azodicarbonamide (ADCA), azobisisobutyronitrile (A
IBN), dinitrosopentamethylenetetramine (DP
T), p-) luenesulfonyl hydrazide (TSH),
p,p-oxybis(benzenesulfonylhydrazide)
A pyrolyzable organic foaming material such as (OBSH), gases such as nitrogen, carbon dioxide, chlorofluorocarbon (fluorocarbon), or a combination thereof can be used. Of course, during extrusion, a foaming core material, an anti-aging agent, a copper damage inhibitor, a coloring agent, etc. may also be added.
ポリプロピレンの伸びの経時的低下は、ポリプロピレン
が溶融し、凝固した後の結晶の成長によるものであり、
発泡絶縁電線では結晶の成長の仕方が不均一となり、更
に絶縁被覆が薄肉である場合には加工時の残留歪が加わ
って伸びの低下が促進されると考えられる。The decrease in elongation of polypropylene over time is due to the growth of crystals after the polypropylene melts and solidifies;
In foam insulated wires, crystals grow unevenly, and if the insulation coating is thin, it is thought that residual strain during processing is added, accelerating the decline in elongation.
これに対して、メルトインデックスがポリプロピレンま
たはブロックコポリマーより大きい高密度ポリエチレン
は、ポリプロピレンとの相溶性にすぐれているため、ポ
リプロピレンにこのような高密度ポリエチレンを混合す
ると、ポリプロピレンか高密度ポリエチレンに分散し。On the other hand, high-density polyethylene, which has a higher melt index than polypropylene or block copolymers, has excellent compatibility with polypropylene, so if such high-density polyethylene is mixed with polypropylene, it will disperse into the polypropylene or high-density polyethylene. .
ポリプロピレンの結晶も全体的に分散するのてポリプロ
ピレンの結晶化が抑制されて伸びの低下が抑えられると
考えられる。It is thought that since the polypropylene crystals are also dispersed throughout, crystallization of the polypropylene is suppressed and a decrease in elongation is suppressed.
次に、本発明の発泡絶縁電線の具体例と比較例とを表1
に示す、いずれの例も発泡絶縁電線は、直径が40 m
mの押出機を用いて製造したが、押出機内で表1に示
す材料に発泡核剤、老化防止剤及び銅害防止剤を添加し
たものを溶融混練し、更に押出機バレルの途中から発泡
剤としてクロロフルオロカーボン500(通称フロン5
00;CCl2F2/CH3−C)(F、=73.8/
26.2重量比)を注入し、直径が0.226mmの軟
鋼単線導体の上に仕上り径約1.35mmとなるように
発泡率が約55%の絶縁被覆を施した。また、各個の伸
び試験の結果は表2に示されているが、この伸び試験は
J I 5C3005に基き管状のサンプルを用いてテ
ンシロン型引張り試験機によって引張り速度50mm/
分で求め、その測定は常温放置で押出し当日と7日目と
300日目100日目0で行った。更に、常温変形率は
JISC3005の加熱変形試験機の装置、方法を用い
、測定温度のみ常温(23℃)で行なった。尚、荷重は
750gとした。Next, Table 1 shows specific examples and comparative examples of the foam insulated wire of the present invention.
The foam insulated wires shown in both examples have a diameter of 40 m.
The material shown in Table 1 was melt-kneaded in the extruder with a foaming nucleating agent, an anti-aging agent, and a copper damage inhibitor added, and the foaming agent was added from the middle of the extruder barrel. Chlorofluorocarbon 500 (commonly known as Freon 5)
00; CCl2F2/CH3-C) (F, = 73.8/
26.2 weight ratio), and an insulating coating with a foaming rate of about 55% was applied on a mild steel single wire conductor with a diameter of 0.226 mm so that the finished diameter was about 1.35 mm. In addition, the results of each elongation test are shown in Table 2, and this elongation test was conducted using a tubular sample according to J I 5C3005 using a Tensilon type tensile tester at a tensile speed of 50 mm/
The measurement was performed on the day of extrusion, on the 7th day, on the 300th day, and on the 100th day 0 after being left at room temperature. Further, the room temperature deformation rate was measured using the apparatus and method of a JISC3005 heating deformation tester, and the measurement temperature was only at room temperature (23° C.). Note that the load was 750 g.
具体例1.2は、ノーブレンBC8D (三菱油化製P
PとPEのブロックコポリマー:メルトインデックス1
.2g/lo分、密度0.89g/Cm″″)に、レク
スロンE750 (C)(日石化学製高密度PE;メル
トインデックス5.3g/lo分、密度0.963g/
cm’) (具体例1)、レクスロンE780 (C)
(0石化学製高密度PE、メルトインデックス8.0g
/10分、密度0.963g/cm’ )をそれぞれ重
量比で80 : 20で混合した材料を使用した。Specific example 1.2 is Noblen BC8D (Mitsubishi Yuka P
Block copolymer of P and PE: melt index 1
.. 2g/lomin, density 0.89g/Cm''''), Lexron E750 (C) (Nisseki Chemical high density PE; melt index 5.3g/lomin, density 0.963g/
cm') (Example 1), Rexron E780 (C)
(High-density PE made by 0 Rock Chemical, melt index 8.0g
/10 minutes, density 0.963 g/cm') were mixed at a weight ratio of 80:20.
また、具体例3.4は、UBE C211(宇部興産
製PPとPEのブロックコポリマー;メルトインデック
ス2.7g710分、密度0.90g/cm″′)にレ
クスロンE750 (C)(具体例3)及びレクスロン
E780 (C)(具体例4)をそれぞれ重量比80
: 20で混合した材料を使用した。Further, in Specific Example 3.4, LEXRON E750 (C) (Specific Example 3) and Rexron E780 (C) (Specific Example 4) at a weight ratio of 80
: Materials mixed in step 20 were used.
一方、比較例1はノーブレンBC8Dのみを使用し、比
較例2.3はノーブレンBC8DにHizex5305
E (三井石油化学製高密度PE:メルトインデックス
0.8g710分、密度0.945g/cm’ )(比
較例2)及びレクスロンM41(0石化学製低密度PE
:メルトインデックス6.0g/10分、密度0゜92
2g/cm:l)をそれぞれ重量比で8020で混合し
た材料を使用した。On the other hand, Comparative Example 1 uses only Noblen BC8D, and Comparative Example 2.3 uses Noblen BC8D and Hizex5305.
E (high-density PE made by Mitsui Petrochemicals: melt index 0.8 g 710 minutes, density 0.945 g/cm') (Comparative Example 2) and Rexron M41 (low-density PE made by 0 Seki Kagaku)
: Melt index 6.0g/10min, density 0°92
2g/cm:l) were mixed at a weight ratio of 8020.
比較例4はUBE C211のみを使用し、また比較
例5.6はUBE C211にHizex5305E
(比較例5)及びUBE C180(比較例6)を
それぞれ重量比で80:20で混合した材料を使用した
。Comparative example 4 uses only UBE C211, and comparative example 5.6 uses Hizex5305E in UBE C211.
(Comparative Example 5) and UBE C180 (Comparative Example 6) were mixed at a weight ratio of 80:20.
表1
表
表2から明らかなように、比較例1.2及び4.5では
E数の経過と共に絶縁被覆の伸びか低下し、押出し後l
OO日目下ば絶対値で100%以下、残率(押出し当日
との比)で20%以下となった。また、比較例3.6は
日数の経過による絶縁被覆の伸びの低下は小さく、10
0日目0も残率で90%以上あるが、常温変形率が著し
く悪くなって機械的強度が低下する。これに対して本発
明の具体例では押出し当日の当初の絶縁被覆の伸びが比
較例1〜6に比べて大きく、且lOO日経過しても絶対
値で350%以上、残率で90%以上伸びが保持され、
且つ常温変形率も極めて小さいことか解る。Table 1 As is clear from Table 2, in Comparative Examples 1.2 and 4.5, the elongation of the insulation coating decreased as the E number increased, and after extrusion
On day OO, the absolute value was 100% or less, and the residual rate (ratio to the day of extrusion) was 20% or less. In addition, in Comparative Example 3.6, the decrease in elongation of the insulation coating with the passage of days was small, and 10
On the 0th day, the residual ratio is 90% or more, but the room temperature deformation rate becomes significantly worse and the mechanical strength decreases. On the other hand, in the specific example of the present invention, the initial elongation of the insulation coating on the day of extrusion is larger than that in Comparative Examples 1 to 6, and even after 100 days, the absolute value is 350% or more and the residual rate is 90% or more. Elongation is maintained,
It can also be seen that the deformation rate at room temperature is extremely small.
本発明によれば、上記のように、ポリプロピレンあるい
はポリプロピレン/ポリエチレンのブロックコポリマー
またはポリプロピレン/エチレン・プロピレンゴムのプ
ロウクコボリマーにこれらの材料よりもメルトインデッ
クスが大きい高密度ポリエチレンを混合するだけで絶縁
被覆の伸びの経時的な低下を抑制することができ、且つ
機械的強度が低下することかない安価な発泡絶縁電線を
提供することができる実益かある。According to the present invention, as described above, insulation can be achieved by simply mixing polypropylene, a block copolymer of polypropylene/polyethylene, or a block copolymer of polypropylene/ethylene-propylene rubber with high-density polyethylene having a higher melt index than these materials. There is a practical benefit in that it is possible to suppress the deterioration of the elongation of the coating over time and to provide an inexpensive foam insulated wire that does not have a decrease in mechanical strength.
じ−ざf四声。Ji-za f four tones.
Claims (1)
ックコポリマーとポリプロピレン/エチレン・プロピレ
ンゴムのブロックコポリマーとのいずれかの材料とこの
材料よりもメルトインデックスが大きい高密度ポリエチ
レンとの混合物の発泡体から成る絶縁被覆を有すること
を特徴とする発泡絶縁電線。having an insulating coating consisting of a foam of a mixture of polypropylene, a block copolymer of polypropylene/polyethylene, a block copolymer of polypropylene/ethylene-propylene rubber, and a high-density polyethylene having a higher melt index than this material; Features foam insulated wire.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1014831A JP2618464B2 (en) | 1989-01-24 | 1989-01-24 | Foam insulated wire |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1014831A JP2618464B2 (en) | 1989-01-24 | 1989-01-24 | Foam insulated wire |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02195604A true JPH02195604A (en) | 1990-08-02 |
JP2618464B2 JP2618464B2 (en) | 1997-06-11 |
Family
ID=11871984
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1014831A Expired - Lifetime JP2618464B2 (en) | 1989-01-24 | 1989-01-24 | Foam insulated wire |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2618464B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5532434A (en) * | 1993-07-26 | 1996-07-02 | Mitsubishi Denki Kabushiki Kaisha | Insulated wire |
KR20120092076A (en) * | 2011-02-10 | 2012-08-20 | 엘에스전선 주식회사 | Cable including insulation layer with non-crosslinking resin |
KR20120095309A (en) * | 2011-02-18 | 2012-08-28 | 엘에스전선 주식회사 | Cable including insulation layer with non-crosslinking resin |
KR101957049B1 (en) * | 2017-10-11 | 2019-03-11 | 한화토탈 주식회사 | Polypropylene for insulation layer of power cable |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS505224A (en) * | 1972-12-01 | 1975-01-20 |
-
1989
- 1989-01-24 JP JP1014831A patent/JP2618464B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS505224A (en) * | 1972-12-01 | 1975-01-20 |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5532434A (en) * | 1993-07-26 | 1996-07-02 | Mitsubishi Denki Kabushiki Kaisha | Insulated wire |
KR20120092076A (en) * | 2011-02-10 | 2012-08-20 | 엘에스전선 주식회사 | Cable including insulation layer with non-crosslinking resin |
KR20200058334A (en) * | 2011-02-10 | 2020-05-27 | 엘에스전선 주식회사 | Mixture with non-crosslinking resin for preparing insulation layer of power cable |
KR20120095309A (en) * | 2011-02-18 | 2012-08-28 | 엘에스전선 주식회사 | Cable including insulation layer with non-crosslinking resin |
KR20200060306A (en) * | 2011-02-18 | 2020-05-29 | 엘에스전선 주식회사 | Mixture with non-crosslinking resin for preparing insulation layer of power cable |
KR101957049B1 (en) * | 2017-10-11 | 2019-03-11 | 한화토탈 주식회사 | Polypropylene for insulation layer of power cable |
Also Published As
Publication number | Publication date |
---|---|
JP2618464B2 (en) | 1997-06-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3267228B2 (en) | Foam wire | |
US6335490B1 (en) | Insulating material for coaxial cable, coaxial cable and method for producing coaxial cable | |
US8723041B2 (en) | Electric cable comprising a foamed polyolefine insulation and manufacturing process thereof | |
US4683166A (en) | Foamed plastic insulated wire and method for producing same | |
US6130385A (en) | Coaxial high-frequency cable and dielectric material thereof | |
EP1440119B1 (en) | Insulating foam composition | |
US5346926A (en) | Small diameter electric wire insulated with highly expanded cellular polyethylene and production thereof | |
US5180754A (en) | Polymer composition for foam molding | |
CA1124950A (en) | Foamed plastic insulated wire and method for producing the same | |
US4547328A (en) | Method for producing foamed plastic insulator | |
JPH02195604A (en) | Foam insulating electric wire | |
JP2006022276A (en) | Composition for insulator and high-foaming insulator and coaxial cable for high frequency using the composition | |
JPH02195603A (en) | Foam insulating electric wire | |
US8766096B2 (en) | Production method of foamed electric wire | |
JP3241126B2 (en) | Small diameter high foam polyethylene insulated cable and method of manufacturing the same | |
JP2007237645A (en) | Foam molding method, foamed coaxial cable, and manufacturing method therefor | |
JPH11213759A (en) | Thin foamed electric wire and manufacture of electric wire | |
JPH03146532A (en) | Polyolefin resin composition for expansion | |
US6613983B1 (en) | Thin-conductor foamed-polyolefin-insulated wire and manufacturing method thereof | |
JP2597299B2 (en) | Foam and method for producing foam | |
JPH087672A (en) | Communication cable | |
JPH04146940A (en) | Expandable polyethylene resin composition for communication cable | |
JPH08203349A (en) | Foam-insulated wire | |
JPH02210722A (en) | Formation of highly foamed propylene series resin insulating cover | |
JPH08185720A (en) | Electric wire insulated with foamed plastic and manufacture thereof |