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JPS588082B2 - Densen - Google Patents
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JPS588082B2 - Densen - Google Patents

Densen

Info

Publication number
JPS588082B2
JPS588082B2 JP50086642A JP8664275A JPS588082B2 JP S588082 B2 JPS588082 B2 JP S588082B2 JP 50086642 A JP50086642 A JP 50086642A JP 8664275 A JP8664275 A JP 8664275A JP S588082 B2 JPS588082 B2 JP S588082B2
Authority
JP
Japan
Prior art keywords
acid
glycol
present
wire
polymer
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
Application number
JP50086642A
Other languages
Japanese (ja)
Other versions
JPS5212483A (en
Inventor
川瀬昭治
中村芳嗣
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.)
Teijin Ltd
Original Assignee
Teijin 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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP50086642A priority Critical patent/JPS588082B2/en
Publication of JPS5212483A publication Critical patent/JPS5212483A/en
Publication of JPS588082B2 publication Critical patent/JPS588082B2/en
Expired legal-status Critical Current

Links

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  • Organic Insulating Materials (AREA)
  • Insulated Conductors (AREA)

Description

【発明の詳細な説明】 本発明は、ポリへキサメチレンテレフタレートを主成分
とするポリエステルを被覆材とする電線に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an electric wire whose covering material is polyester containing polyhexamethylene terephthalate as a main component.

被覆材により被覆された電線(以下、単に被覆電線とも
いう)の用途として、例えば線状形伏の一般配線用や螺
旋状に形態保持性を持たせた所謂カールコード等がある
Electric wires covered with a covering material (hereinafter also simply referred to as covered electric wires) are used, for example, for general wiring in a linear shape, and so-called curl cords in which a spiral shape has shape retention properties.

一般的被覆材としてのゴム類は、被覆電線の製造時に硬
化工程が必要とされ、その繁雑さやコスト面から他の熱
可塑性樹脂(例えばポリ塩化ビニル、ポリエチレン、ポ
リプロピレン、ナイロン等)が使用されている。
Rubbers, which are commonly used as covering materials, require a curing process when manufacturing covered wires, and due to the complexity and cost of this process, other thermoplastic resins (e.g., polyvinyl chloride, polyethylene, polypropylene, nylon, etc.) are used. There is.

ところが、これらの代替樹脂であっても高速被覆が円滑
に行なわれ難かったり、好ましくない影響を多方面に及
ぼす可塑剤の使用が必須であったり、あるいは耐熱性や
耐薬品性がその用途に要求されるレベルに達していない
等の欠点がある。
However, even with these alternative resins, high-speed coating is difficult to perform smoothly, the use of plasticizers that have undesirable effects in many areas is essential, or heat resistance and chemical resistance are required for the application. There are some drawbacks, such as not reaching the level expected.

本発明者は、かかる欠点が実用上殆んど有しない電線被
覆用素材を有する電線について鋭意研究した結果、特定
のポリエステルを被覆用素材とする電線がかかる要件を
満足することを見出し、本発明に到達したものである。
As a result of intensive research into electric wires having wire sheathing materials that practically do not have such drawbacks, the present inventors have found that electric wires whose sheathing material is a specific polyester satisfy these requirements, and the present invention has been made. has been reached.

すなわち本発明は、熱可塑性樹脂の素材により被覆され
た電線において、該被覆素材が極限粘度0.4以上のポ
リへキサメチレンテレフタレートであることを特徴とす
る電線である。
That is, the present invention provides an electric wire coated with a thermoplastic resin material, characterized in that the covering material is polyhexamethylene terephthalate having an intrinsic viscosity of 0.4 or more.

本発明でいうポリへキサメチレンテレフタレートとは、
ポリへキサメチレンテレフタレートのホモポリマーは勿
論のこと、そのテレフタル酸成分及び/又はへキサメチ
レングリコール成分の一部例えば30モル受以下、特に
20モル係以下を他の二官能性カルボン酸及び/又はグ
リコールで置き換えたコポリエステルをも包含する。
Polyhexamethylene terephthalate as used in the present invention is
Not only a homopolymer of polyhexamethylene terephthalate, but also a part of its terephthalic acid component and/or hexamethylene glycol component, for example, 30 molar or less, especially 20 molar or less, may be mixed with other difunctional carboxylic acids and/or Also included are copolyesters substituted with glycols.

かかる他の二官能性カルボン酸としては、例えばイソフ
タル酸、メチルテレフタル酸、ナフタリン酸ジカルボン
酸、ジフエニルジカルボン酸、ジフエノキシエタンジカ
ルボン酸、シフエニルエーテルジカルボン酸、シフエニ
ルスルホンジカルボン酸、ヘキサヒドロテレフタル酸、
アジピン酸、セバチン酸等の如き芳香族、脂肪族ジカル
ボン酸、オキシ安息香酸、ヒドロキシエトキシ安息香酸
、ε−オキシカプロン酸等の如きオキシ酸等を挙げるこ
とができる。
Such other difunctional carboxylic acids include, for example, isophthalic acid, methyl terephthalic acid, naphthalic dicarboxylic acid, diphenyl dicarboxylic acid, diphenoxyethane dicarboxylic acid, cyphenyl ether dicarboxylic acid, cyphenyl sulfonic dicarboxylic acid, and hexahydrocarbonic acid. Terephthalic acid,
Examples include aromatic and aliphatic dicarboxylic acids such as adipic acid and sebacic acid, oxyacids such as oxybenzoic acid, hydroxyethoxybenzoic acid, and ε-oxycaproic acid.

また他のグリコールとしては、例えばエチレングリコー
ル、フロピレングリコール、トリメチレングリコール、
テトラメチレングリコールペンタメチレングリコール、
デカメチレングリコール、ネオペンチレングリコール、
シクロヘキサンジメチロール、トリシクロデカンジメチ
ロール、2.2−ヒス(β−ヒドロキシエトキシフニエ
ル)プロパン、ジエチレングリコール、ポリエチレング
リコール、ポリテトラメチレングリコール等を挙げるこ
とができる。
Other glycols include, for example, ethylene glycol, fluoropylene glycol, trimethylene glycol,
Tetramethylene glycol pentamethylene glycol,
decamethylene glycol, neopentylene glycol,
Examples include cyclohexane dimethylol, tricyclodecane dimethylol, 2,2-his(β-hydroxyethoxyphenyl)propane, diethylene glycol, polyethylene glycol, polytetramethylene glycol, and the like.

また上記ポリへキサメチレンテレフタレートには、ピロ
メリット酸、トリメリット酸、ペンタエリスリトール等
の如き3官能以上の多官能性化合物及び/又は安息香酸
の如き単官能性化合物も得られるポリマーが実質的に線
状である範囲内で共重合せしめても良い。
In addition, the above-mentioned polyhexamethylene terephthalate includes polymers that can also obtain polyfunctional compounds of trifunctional or higher functionality such as pyromellitic acid, trimellitic acid, pentaerythritol, etc. and/or monofunctional compounds such as benzoic acid. Copolymerization may be carried out within a linear range.

本発明に用いられるポリへキサメチレンチレフタレート
の極限粘度(オルソクロロフェノール中35℃で測定)
が0.4以上であることが必要である。
Intrinsic viscosity of polyhexamethylene ethylene phthalate used in the present invention (measured at 35°C in orthochlorophenol)
is required to be 0.4 or more.

0.4未満ではポリマーがもろく屈曲性が不充分である
ため、電線の被覆材として不適当である。
If it is less than 0.4, the polymer will be brittle and have insufficient flexibility, making it unsuitable as a coating material for electric wires.

極限粘度が2,5を超えるもの、特に30を超えるもの
は溶融粘度が高過ぎて加工しにくいので不適当である。
Those having an intrinsic viscosity exceeding 2.5, especially those exceeding 30, are unsuitable because their melt viscosity is too high and processing is difficult.

本発明の電線において、導体である金属部分については
その種類、大きさ(径)については特に限定は々いが、
通常の室内配線用や電話線用(カールコード)には特に
好適に用いられる。
In the electric wire of the present invention, there are no particular limitations on the type and size (diameter) of the metal portion that is a conductor;
It is particularly suitable for use in normal indoor wiring and telephone lines (curl cords).

本発明に用いられるポリへキサメチレンテレフタレート
には安定剤(例えば紫外線吸収剤、抗酸化剤等)、螢光
増白剤、核剤、顔料、滑剤、難燃剤、難燃助剤等の1種
以上を配合しても良い。
Polyhexamethylene terephthalate used in the present invention includes one type of stabilizer (e.g. ultraviolet absorber, antioxidant, etc.), fluorescent brightener, nucleating agent, pigment, lubricant, flame retardant, flame retardant aid, etc. The above may be combined.

本発明の電線被覆材に用いる上記の如き特定の組成を有
するコポリエステルエーテルは溶融成形が可能であり、
しかも硬化特性が優れており、電線被覆材として有用な
素材である。
The copolyester ether having the above-mentioned specific composition used in the wire coating material of the present invention can be melt-molded,
Moreover, it has excellent curing properties and is a useful material as a wire coating material.

電線の被覆は従来公知のモールド成形等がそのまま利用
でき、かつ高速生産可能な利点を有する。
The wire coating has the advantage that conventionally known molding and the like can be used as is, and high-speed production is possible.

以下、実施例により本発明を詳述する。Hereinafter, the present invention will be explained in detail with reference to Examples.

例中において「部」は重量部を意味する。In the examples, "parts" mean parts by weight.

また極限粘度〔η〕はO−クロロフェノール10rnl
に試料ポリマー120〜を溶解し、35°Cで測定した
In addition, the intrinsic viscosity [η] is O-chlorophenol 10rnl
Sample polymer 120 ~ was dissolved in and measured at 35°C.

実施例 1 ジメチルテレフタレート194部、ヘキサメチレングリ
コール236部、チタニウムテトラブトキシド0.17
部を攪拌機付反応容器に仕込み窒素範囲気中で徐々に加
熱した。
Example 1 194 parts of dimethyl terephthalate, 236 parts of hexamethylene glycol, 0.17 parts of titanium tetrabutoxide
A portion of the mixture was placed in a reaction vessel equipped with a stirrer and gradually heated in a nitrogen atmosphere.

反応の結果、生成するメタノールは精留塔を介して系外
へ留出せしめた。
As a result of the reaction, methanol produced was distilled out of the system via a rectification column.

系外に留出するメタノールが理論量の約94係に達した
ところで系内の温度を240℃にし、徐々に系内を減圧
にし、30分後に30mmHg、更に30分後に0.
5 mmH g以下にし約3時間重縮合せしめて得られ
たポリマーの〔η)−1.01、軟化点148.0°C
であった。
When the amount of methanol distilled out of the system reached about 94% of the theoretical amount, the temperature inside the system was raised to 240°C, and the pressure inside the system was gradually reduced to 30 mmHg after 30 minutes, and 0.5 mmHg after another 30 minutes.
[η)-1.01, softening point of the polymer obtained by polycondensation for about 3 hours at 5 mmHg or less, 148.0°C
Met.

このポリマーを110℃、3時間乾燥した後30闘押出
し機で太さが1.8mm(4本より合せたもの)の電線
を厚さ04mmに被覆しだ。
After drying this polymer at 110° C. for 3 hours, it was coated with a wire having a thickness of 1.8 mm (combined of 4 wires) to a thickness of 04 mm using a 30 mm extruder.

この電線の耐電圧は13.000ボルト以上であった。The electric wire had a withstand voltage of 13,000 volts or more.

比較例 l 実施例1と同じ厚さの可塑化ポリ塩化ビニール被覆電線
の耐電比は2.000ボルトであった。
Comparative Example 1 A plasticized polyvinyl chloride coated wire having the same thickness as in Example 1 had a dielectric strength ratio of 2.000 volts.

実施例 2 実施例1において、酸成分をジメチルテレフタレート8
5モル係、ジメチルデカン−1.10−ジカルボキシレ
ート15モル受の共重合体とする以外は同じ操作により
、〔η)一0.94であるポリマーを得た。
Example 2 In Example 1, the acid component was dimethyl terephthalate 8
A polymer having [η) -0.94 was obtained by the same procedure except that a copolymer containing 5 moles of dimethyldecane-1,10-dicarboxylate and 15 moles of dimethyldecane-1,10-dicarboxylate was used.

このポリマーを70℃で12時間乾燥し、径0. 6
mmの電線を被覆速度150m/分で0.08mmの厚
みに被覆できた。
This polymer was dried at 70°C for 12 hours, and the diameter was 0. 6
It was possible to coat an electric wire with a thickness of 0.08 mm at a coating speed of 150 m/min.

この耐電圧は11.000ボルトであった。This withstand voltage was 11,000 volts.

比較例 2 可塑化ポリ塩化ビニル、ポリエチレン、ポリプロピレン
を被覆用素材として実施例2の様な操作を行なったとこ
ろ、0.08mm厚みの一様な被覆はできなかった。
Comparative Example 2 When the same operation as in Example 2 was carried out using plasticized polyvinyl chloride, polyethylene, and polypropylene as coating materials, a uniform coating with a thickness of 0.08 mm could not be obtained.

Claims (1)

【特許請求の範囲】[Claims] 1 熱可塑性樹脂の素材により被覆された電線において
、該被覆素材が極限粘度0.4以上のポリへキサメチレ
ンテレフタレートであることを特徴とする電線。
1. An electric wire coated with a thermoplastic resin material, characterized in that the covering material is polyhexamethylene terephthalate having an intrinsic viscosity of 0.4 or more.
JP50086642A 1975-07-17 1975-07-17 Densen Expired JPS588082B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50086642A JPS588082B2 (en) 1975-07-17 1975-07-17 Densen

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50086642A JPS588082B2 (en) 1975-07-17 1975-07-17 Densen

Publications (2)

Publication Number Publication Date
JPS5212483A JPS5212483A (en) 1977-01-31
JPS588082B2 true JPS588082B2 (en) 1983-02-14

Family

ID=13892670

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50086642A Expired JPS588082B2 (en) 1975-07-17 1975-07-17 Densen

Country Status (1)

Country Link
JP (1) JPS588082B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53133908A (en) * 1977-01-26 1978-11-22 Nippon Telegraph & Telephone Method of drawing pile out by casing with spiral frame
JPS59140342U (en) * 1983-03-10 1984-09-19 三谷セキサン株式会社 Edge cutting device for removed piles
JPS61169150U (en) * 1985-04-08 1986-10-20

Also Published As

Publication number Publication date
JPS5212483A (en) 1977-01-31

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