JPS614111A - Method of producing foamable plastic insulator - Google Patents

Method of producing foamable plastic insulator

Info

Publication number
JPS614111A
JPS614111A JP12392884A JP12392884A JPS614111A JP S614111 A JPS614111 A JP S614111A JP 12392884 A JP12392884 A JP 12392884A JP 12392884 A JP12392884 A JP 12392884A JP S614111 A JPS614111 A JP S614111A
Authority
JP
Japan
Prior art keywords
weight
agent
nucleating agent
group
plastic insulator
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
Application number
JP12392884A
Other languages
Japanese (ja)
Inventor
八田 敏正
嶋崎 行雄
英雄 高野
大谷 智行
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hitachi Cable Ltd
Original Assignee
Hitachi Cable Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hitachi Cable Ltd filed Critical Hitachi Cable Ltd
Priority to JP12392884A priority Critical patent/JPS614111A/en
Publication of JPS614111A publication Critical patent/JPS614111A/en
Pending legal-status Critical Current

Links

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、通信ケーブル絶縁心線あるいは同軸ケーブル
等の絶縁体として適用される発泡プラスチック絶縁体の
製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for manufacturing a foamed plastic insulator that is used as an insulator for communication cable insulated core wires, coaxial cables, and the like.

[従来の技術] 発泡プラスチック絶縁体を製造する方法としては、次に
示す3種類の方法が知られている。
[Prior Art] The following three types of methods are known as methods for manufacturing foamed plastic insulators.

(1)化学発泡剤を用いる方法。(1) A method using a chemical foaming agent.

(21気体発泡剤を用いる方法。(Method using 21 gas blowing agent.

(3)、揮発性液体発泡剤を用いる方法。(3) A method using a volatile liquid blowing agent.

(1)の方法については化学発泡剤が均一に分散される
ため、発泡剤分解時ガスが均一に分布している。さらに
化学発泡剤自身が核形成効果を有することから均一微細
な発泡プラスチック絶縁体が得られる。しかしながら、
発泡剤の分解後に残渣が残るので、誘電特性が損なわれ
るという問題がある。
In method (1), since the chemical blowing agent is uniformly dispersed, the gas is uniformly distributed when the blowing agent is decomposed. Furthermore, since the chemical foaming agent itself has a nucleation effect, a uniform and fine foamed plastic insulator can be obtained. however,
There is a problem that a residue remains after the blowing agent decomposes, which impairs the dielectric properties.

一方、(a及び(31の方法では均一微細気泡を得るた
め、無機あるいは有機の核形成剤としである種の物質を
添加する必要のあることが知られており、例えば炭酸カ
ルシウム、ホワイトカーボン、珪藻土、クレー、2,3
−ジヒドロ−1,4−7タラジオン、フタル酸ヒドラジ
ドなどである。
On the other hand, it is known that methods (a and 31) require the addition of certain substances as inorganic or organic nucleating agents in order to obtain uniform microbubbles, such as calcium carbonate, white carbon, Diatomaceous earth, clay, 2,3
-dihydro-1,4-7 talradione, phthalic acid hydrazide, and the like.

[発明が解決しようとする問題点〕 これらの物質をプラスチックに混線する場合、均−に分
散ざぜることが難しく、細かいスクリーンメツシュを使
用したスクリーニング、あるいはワックス、滑剤等の分
散剤を使用し、分散性を改良してきた。しかし、前者に
おいてはT程数の増加、後者においては効果の点で、ま
た分散剤を多量に使用する点で問題があった。また、例
え比較的良好な分散が得られても発泡体製造中2次凝集
し、スクリーンメツシュが目詰まりして発泡性能を著し
く損なうことがあり、その度ごとに押出を中止してスク
リーンメツシュを交換する必要が生じ、連続的に安定し
た製造ができないという問題がある。
[Problems to be solved by the invention] When these substances are mixed with plastic, it is difficult to disperse them evenly, so screening using a fine screen mesh or dispersing agents such as wax and lubricants are required. , the dispersibility has been improved. However, the former has problems in terms of an increase in the T number, and the latter has problems in terms of effectiveness and the use of a large amount of dispersant. Furthermore, even if relatively good dispersion is obtained, secondary agglomeration may occur during foam production, clogging the screen mesh and significantly impairing foaming performance. There is a problem that it becomes necessary to replace the housing, and continuous and stable production cannot be performed.

本発明は、核形成剤の分散性及び2次凝集を改良して発
泡プラスチック絶縁体を長時間安定して製造することが
できる製造方法の捉供を目的とするものである。
The object of the present invention is to provide a manufacturing method capable of stably manufacturing a foamed plastic insulator for a long period of time by improving the dispersibility and secondary agglomeration of a nucleating agent.

−1″l!llI*t8ThM(7)f=IU]本発明
の製造方法は、プラスチックに発泡剤及び核形成剤を含
有せしめてなる混合物を押出して発泡プラスチック絶縁
体を製造する方法にd3いて、上記混合物には一般式R
−0−Ti −(OX)s(但し、式中Rはアルキン基
、Xはアシル基、アルキンベンゼンスルボニル基、又は
ジアルキルパイロホスフェート基を示す)で表されるチ
タネート系カップリング剤が核形成剤の含有量の0.0
5〜5重量%添加されていることを特徴とするものであ
る。
-1″l!llI*t8ThM(7)f=IU] The manufacturing method of the present invention is a method for manufacturing a foamed plastic insulator by extruding a mixture of plastic containing a foaming agent and a nucleating agent. , the above mixture has the general formula R
A titanate coupling agent represented by -0-Ti-(OX)s (wherein R is an alkyne group and X is an acyl group, an alkynebenzenesulfonyl group, or a dialkylpyrophosphate group) forms a nucleus. 0.0 of agent content
It is characterized by being added in an amount of 5 to 5% by weight.

[作用J 本発明において使用されるプラスチックとしては、ポリ
エチレン、ポリプロピレン、プロピレン−エチレン共重
合体、エチレン−プロピレン共重合体、エチレン−α・
オレフィン共重合体等のポリオレフィンが代表的であり
、これらは1種あるいは2種以上の混合で使用可能であ
る。また、ポリテトラフルオロエチレン、ポリビニリデ
ンフロライド、テ1〜ラフルオロエチレンーエチレン共
重合体等のふっ素糸樹脂も使用可能である。
[Function J] Plastics used in the present invention include polyethylene, polypropylene, propylene-ethylene copolymer, ethylene-propylene copolymer, ethylene-α.
Polyolefins such as olefin copolymers are typical, and these can be used alone or in a mixture of two or more. Further, fluorine thread resins such as polytetrafluoroethylene, polyvinylidene fluoride, and Te1-rafluoroethylene-ethylene copolymers can also be used.

戸体発泡剤としては、窒素ガス、炭酸ガスが、揮発性液
体発泡剤としては、フレオンがその代表例としてあげら
れる。
Representative examples of the door body foaming agent include nitrogen gas and carbon dioxide gas, and representative examples of the volatile liquid foaming agent include Freon.

核形成剤としては、無機物質と有機物質とがあり、前者
としては炭酸カルシウム、ホワイトカーボン、珪藻土、
クレー、タルクといったものがあげられ、後者にはフタ
ル酸ヒドラジドがあげられる。核形成剤は、プラスチッ
クiooma部に対し0.5〜10重湯部の範囲で添加
するのが一般的である。
Nucleating agents include inorganic substances and organic substances, and the former include calcium carbonate, white carbon, diatomaceous earth,
Examples include clay and talc, and the latter includes phthalic acid hydrazide. The nucleating agent is generally added in an amount of 0.5 to 10 parts by weight based on the iooma part of the plastic.

一般式R−0−王i −(OX)3 ((IJし、f、
 中Rはアルキン基、Xはアシル基、アルキンベンゼン
スルホニル基、又はジアルキルパイ[」ホスフェート基
を示す)で表されるチタネート系カップリング剤として
は、インプロピルトリイソステアロイルチタネート、イ
ンプロビルトリドデシベンゼン“スルホニルチタネート
、イソプロピルトリス(ジオクチルバイ0ホスフエート
)チタネー1−、ビス(ジオクチルパイロホスフェート
)オキシアセテートチタネート、トリス(ジオクチルパ
イロホスフェート)エチレンチタネ゛−1−等である。
General formula R-0-Oi-(OX)3 ((IJ, f,
Examples of titanate coupling agents in which R is an alkyne group and X is an acyl group, an alkynebenzenesulfonyl group, or a dialkylpi [''phosphate group] include impropyl triisostearoyl titanate, impropyl tridodecibenzene; These include sulfonyl titanate, isopropyl tris(dioctyl bi-ophosphate) titanate-1-, bis(dioctyl pyrophosphate) oxyacetate titanate, tris(dioctyl pyrophosphate) ethylene titanate-1-, and the like.

これらチタネート系カップリング剤の添加量は、核形成
剤に対して0.05〜5重量%の範囲で添加する必要が
あり、0.05重量%未満では目的とする効果を達成で
きず、5M量%を越えると樹脂粘度が低下して気泡径が
大きくなり、またブリードが生じてくる。好ましい範囲
は0.5〜2重量%である。
The amount of these titanate-based coupling agents added must be in the range of 0.05 to 5% by weight relative to the nucleating agent; if it is less than 0.05% by weight, the desired effect cannot be achieved; If the amount exceeds %, the resin viscosity decreases, the bubble diameter increases, and bleeding occurs. The preferred range is 0.5-2% by weight.

チタネート系カップリング剤の添加方法は、予め核形成
剤とブレンドし、それをプラスチックに混線する方法、
プラスチックに核形成剤と共に添加して混練する方法の
どちらでもよい。
The titanate coupling agent can be added by blending it with a nucleating agent in advance and mixing it with the plastic.
Either method may be used, such as adding it to the plastic together with a nucleating agent and kneading it.

本発明においては、上記成分以外に必要に応じて酸化防
止剤、銅害防止剤、着色剤等を添加しても差し支えない
In the present invention, in addition to the above-mentioned components, antioxidants, copper damage inhibitors, colorants, etc. may be added as necessary.

[実施例] 実施例1 低密度ポリエチレン(密度:0.921、メルトインデ
ックス0.217 / 10’m in) 100重1
部に、核形成剤としてミストロンペーパータルク3重量
部、ビス(ジオクチルパイロホスフェート)オキシアセ
テートチタネート0.003重量部(核形成剤の0.1
重量%)を添加してミ主シングロールで混練し、発泡用
混和物とした。
[Example] Example 1 Low density polyethylene (density: 0.921, melt index 0.217 / 10'min) 100 weight 1
3 parts by weight of Mistron paper talc as a nucleating agent, 0.003 parts by weight of bis(dioctylpyrophosphate) oxyacetate titanate (0.1 part by weight of a nucleating agent)
% by weight) and kneaded with a main single roll to obtain a foaming mixture.

65#IIφ押出機を用い、シリンダ中央部J:り窒素
ガスを圧力2589/a/rで注入し、外径0.5mの
銅導体に押出被覆して外径0.8りlll#lの発泡絶
縁電線を製造した。なお、押出温度は225℃、線速は
2000m /min テ打つ’IC0実施例2 ポリプロピレン(密度0.890、メルトフローレート
: 2g/min ) 100重量部に、核形成剤とし
て焼成りシー3重量部、トリス(ジオクチルパイロホス
フェート)エチレンチタネート0.03重量部(核形成
剤の1重量%)を添加してミキシングロールで混練し、
発泡用混和物とした。
Using a 65#IIφ extruder, nitrogen gas was injected into the center of the cylinder at a pressure of 2589/a/r, and a copper conductor with an outer diameter of 0.5 m was extruded and coated with an outer diameter of 0.8 mm. A foam insulated wire was manufactured. The extrusion temperature was 225°C, and the linear speed was 2000 m/min. IC0 Example 2: 100 parts by weight of polypropylene (density 0.890, melt flow rate: 2 g/min), and 3 parts by weight of calcined seaweed as a nucleating agent. 1% by weight of tris(dioctylpyrophosphate) ethylene titanate (1% by weight of the nucleating agent) and kneaded with a mixing roll.
It was used as a foaming mixture.

押出温度を250℃とした以外は実施例1と同様にして
発泡絶縁電線を製造した。
A foamed insulated wire was produced in the same manner as in Example 1 except that the extrusion temperature was 250°C.

実施例3 −     、。□1.工f、ア、工、。、94318
.。
Example 3-. □1. Engineering f, a, engineering. ,94318
.. .

トインデックス:0.9g/10m 1n)100重量
部に、核形成剤としてフタル酸ヒドラジド1重量部、イ
ソプロピルトリイソステアロイチタネート0.03重酸
部(核形成剤の0.3重量%)を添加してミキシング1
コールで混練し、発泡用混和物とした。
To index: 0.9g/10m 1n), 1 part by weight of phthalic acid hydrazide and 0.03 parts by weight of isopropyl triisostearo titanate (0.3% by weight of the nucleating agent) were added as a nucleating agent. and mixing 1
The mixture was kneaded with coal to obtain a foaming mixture.

65IIIIlIφ押出機を用い、シリンダ中央部より
フレオン(R−114)を圧力15(1g/CI!で注
入し、外径2mの銅導体上に押出被覆して外径8mの発
泡絶縁電線を製造した。
Using a 65IIIIIIφ extruder, Freon (R-114) was injected from the center of the cylinder at a pressure of 15 (1 g/CI!) and extruded to coat a copper conductor with an outer diameter of 2 m to produce a foam insulated wire with an outer diameter of 8 m. .

なお、押出温度は132℃、線速は50m/1nで製造
した。
The extrusion temperature was 132° C., and the linear speed was 50 m/1n.

比較例1 核形成剤としてミストロンベーバタタルに代えて炭酸カ
ルシウムを3重量部添加し、チタネート系カップリング
剤は添加しなかった。その他は実施例1と同様にして発
泡絶縁電線を製造した。
Comparative Example 1 As a nucleating agent, 3 parts by weight of calcium carbonate was added in place of Mistronbebatatar, and no titanate coupling agent was added. A foam insulated wire was manufactured in the same manner as in Example 1 in other respects.

比較例2 核形成剤として焼成りレーに代えてフタル酸ヒドラジド
を2重量部添加し、イソプロピルトリイソステアロイル
チタネートを0.11重量部(核形成剤の5.5重量%
)添加した。その他は実施例2と同様にして発泡絶縁電
線を製造した。
Comparative Example 2 As a nucleating agent, 2 parts by weight of phthalic acid hydrazide was added instead of calcined clay, and 0.11 parts by weight of isopropyl triisostearoyl titanate (5.5% by weight of the nucleating agent) was added.
) was added. A foam insulated wire was manufactured in the same manner as in Example 2 in other respects.

各実施例及び各比較例とも2重萌間の連続押出を行い、
押出始め及び24時間経過後のヘッド部樹脂圧力、発泡
度、気泡径を測定した。その結果は第1表に示す通りで
ある。
In each example and each comparative example, continuous extrusion was carried out between two layers,
The head resin pressure, foaming degree, and cell diameter were measured at the beginning of extrusion and after 24 hours had passed. The results are shown in Table 1.

第   1   表 [発明の効果] 以上説明したきた通り、本発明は核形成剤とチタ季−ト
系カップリング剤を併用するものであり、これによって
核形成剤の2次凝集を防止でき、長時間安定した発泡体
の製造が可能となる。
Table 1 [Effects of the Invention] As explained above, the present invention uses a nucleating agent and a titanium-based coupling agent in combination, which prevents secondary aggregation of the nucleating agent and provides a long service life. It becomes possible to produce a foam that is stable over time.

−例一-Example 1

Claims (1)

【特許請求の範囲】[Claims] (1)プラスチックに発泡剤及び核形成剤を含有せしめ
てなる混合物を押出して発泡プラスチック絶縁体を製造
する方法において、上記混合物には一般式R−O−Ti
−(OX)_3(但し、式中Rはアルギン基、Xはアシ
ル基、アルキンベンゼンスルホニル基、又はジアルキル
パイロホスフェート基を示す)で表されるチタネート系
カップリング剤が核形成剤の含有量の0.05〜5重量
%添加されていることを特徴とする発泡プラスチック絶
縁体の製造方法。
(1) In a method for producing a foamed plastic insulator by extruding a mixture of plastic containing a foaming agent and a nucleating agent, the mixture has the general formula R-O-Ti.
The titanate coupling agent represented by -(OX)_3 (in the formula, R is an alginic group, X is an acyl group, an alkynebenzenesulfonyl group, or a dialkylpyrophosphate group) has a content of nucleating agent. A method for producing a foamed plastic insulator, characterized in that the additive is added in an amount of 0.05 to 5% by weight.
JP12392884A 1984-06-15 1984-06-15 Method of producing foamable plastic insulator Pending JPS614111A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12392884A JPS614111A (en) 1984-06-15 1984-06-15 Method of producing foamable plastic insulator

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12392884A JPS614111A (en) 1984-06-15 1984-06-15 Method of producing foamable plastic insulator

Publications (1)

Publication Number Publication Date
JPS614111A true JPS614111A (en) 1986-01-10

Family

ID=14872808

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12392884A Pending JPS614111A (en) 1984-06-15 1984-06-15 Method of producing foamable plastic insulator

Country Status (1)

Country Link
JP (1) JPS614111A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8193888B2 (en) 2009-01-22 2012-06-05 Murata Manufacturing Co., Ltd. Laminated inductor

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6086129A (en) * 1983-10-18 1985-05-15 Toyo Ink Mfg Co Ltd Resin composition for foam-insulated electrical wire

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6086129A (en) * 1983-10-18 1985-05-15 Toyo Ink Mfg Co Ltd Resin composition for foam-insulated electrical wire

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8193888B2 (en) 2009-01-22 2012-06-05 Murata Manufacturing Co., Ltd. Laminated inductor

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