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JPS6046762B2 - Resin composition for DC electrical insulation - Google Patents
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JPS6046762B2 - Resin composition for DC electrical insulation - Google Patents

Resin composition for DC electrical insulation

Info

Publication number
JPS6046762B2
JPS6046762B2 JP6775078A JP6775078A JPS6046762B2 JP S6046762 B2 JPS6046762 B2 JP S6046762B2 JP 6775078 A JP6775078 A JP 6775078A JP 6775078 A JP6775078 A JP 6775078A JP S6046762 B2 JPS6046762 B2 JP S6046762B2
Authority
JP
Japan
Prior art keywords
resin composition
electrical insulation
voltage
tree
crosslinking
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
JP6775078A
Other languages
Japanese (ja)
Other versions
JPS54159680A (en
Inventor
陽一 川崎
清峰 谷口
義孝 新田
正人 縄田
英昭 河村
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.)
NUC Corp
Denryoku Chuo Kenkyusho
Original Assignee
Denryoku Chuo Kenkyusho
Nippon Unicar Co 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 Denryoku Chuo Kenkyusho, Nippon Unicar Co Ltd filed Critical Denryoku Chuo Kenkyusho
Priority to JP6775078A priority Critical patent/JPS6046762B2/en
Publication of JPS54159680A publication Critical patent/JPS54159680A/en
Publication of JPS6046762B2 publication Critical patent/JPS6046762B2/en
Expired legal-status Critical Current

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  • Organic Insulating Materials (AREA)
  • Insulated Conductors (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 本発明は直流高圧用電線、ケーブルあるいはこれらの
接続部、端末部およびその他の直流回路の絶縁に用いる
直流電気絶縁用樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a resin composition for direct current electrical insulation used for insulating high voltage direct current wires, cables, their connections, terminals, and other direct current circuits.

ポリエチレンおよび架橋ポリエチレン等のポリオレフ
ィン重合体を主成分とした絶縁体を有する 電線・ケー
ブルはその保守の容易さから交流高圧送電用として広く
使われている。
Electric wires and cables with insulators mainly composed of polyolefin polymers such as polyethylene and cross-linked polyethylene are widely used for AC high-voltage power transmission because of their ease of maintenance.

しかし、交流送電は誘電損失があるので線路充電電流の
補償が必要とされ、遠距離・大電流の送電には直流送電
の方が有利である事は広く知られている。ところが、架
橋ポリエチレンを絶縁体としたケーブルを250KVの
直流送電に使用する実験において、絶縁性能の安定性に
欠けるとの結果が発表された(電気学会電力技術合同研
究会資料PE−76−1ホ直’流ケーブルの絶縁性能と
試験法、1976年12月14日)。したがつて、これ
らの欠点を改良し、直流送電に適した絶縁用樹脂組成物
の開発か望まれていた。絶縁性能の安定性に欠ける原因
は直流によ り発生する絶縁体中の空間電荷の蓄積がト
リ−状・の放電劣化を起こさせる事にあるとの観点から
、一つの解決策として従来の絶縁材層の中にもう一層以
上の電荷が注入されにくい合成樹脂材料層をもうける事
によつて或る程度問題は解決できる事が知られている(
特開昭51−110678号)。しかフし、従来よりこ
れら超高圧電力ケーブルはΞ層から成る構成のものが多
く、これにさらにもう一層空間電荷解消のための新しい
樹脂層を設ける事は押出機の新規が必要となる事、層の
増加は不良率増加の危険がある事などから現有設備が有
効に利用てきる技術の開発につとめた。そして従来のポ
リオレフィン組成物にポリアミドを添加して絶縁物中に
電荷が注入されにくい合成樹脂材料を均等に分散させる
実験を行つたところ、意外にも絶縁性を損なう事なしに
、この空間電荷の蓄積を緩和てきることを発見し、直流
送電に適した絶縁用樹脂組成物の開発に成功した。この
発明はトリー放電による劣化を抑制する効果を有する直
流電気絶縁用樹脂組成物に関する。電荷が注入されにく
い樹脂としてはポリエチレンテレフタレート等のポリエ
ステル類も有用である事が知られているが(特開昭51
−110678号)、一般に入手し得るポリエステル樹
脂は融点が高く(ポリエチレンテレフタレートで260
℃)、混練、押出し、および架橋のいずれの温度でも溶
融しないので好ましくないと考える。本発明によれば、
ポリオレフィン100重量部にポリアミドおよびポリア
ミド共重合体群から選ばれた1種または数種の混合物1
0〜5鍾量部を配合し、必要に応じて酸化防止剤、熱劣
化防止剤、紫外線安定剤、架橋剤、架橋助剤、発泡剤等
を所要量配合−した樹脂組成物を用いることによつて、
ポ3りオレフィン絶縁直流ケーブルおよび直流高圧用絶
縁材料の安定性を向上させることに成功した。
However, since AC power transmission has dielectric loss, it is necessary to compensate for the line charging current, and it is widely known that DC power transmission is more advantageous for transmitting large currents over long distances. However, in an experiment in which a cable with cross-linked polyethylene as an insulator was used for 250KV DC power transmission, it was announced that the insulation performance lacked stability (IEEJ Electric Power Technology Joint Study Group Material PE-76-1) Insulation performance and testing methods for DC cables, December 14, 1976). Therefore, it has been desired to develop an insulating resin composition suitable for direct current power transmission by improving these drawbacks. The reason for the lack of stability in insulation performance is that the accumulation of space charge in the insulator caused by direct current causes tree-shaped discharge deterioration, so one solution is to use conventional insulation. It is known that the problem can be solved to some extent by creating a synthetic resin material layer that is difficult to inject into the material layer (
JP-A-51-110678). However, conventionally, many of these ultra-high voltage power cables have a structure consisting of a Ξ layer, and adding a new resin layer to eliminate space charges would require a new extruder. Since increasing the number of layers risks increasing the defective rate, we worked to develop technology that would make effective use of existing equipment. Then, when we conducted an experiment in which we added polyamide to a conventional polyolefin composition to evenly disperse a synthetic resin material that is difficult to inject charge into an insulator, we surprisingly succeeded in reducing this space charge without impairing the insulation properties. They discovered that the accumulation can be alleviated and succeeded in developing an insulating resin composition suitable for DC power transmission. The present invention relates to a resin composition for direct current electrical insulation that has the effect of suppressing deterioration due to tree discharge. It is known that polyesters such as polyethylene terephthalate are also useful as resins that are difficult to inject charges into (Japanese Unexamined Patent Publication No. 51
-110678), commonly available polyester resins have a high melting point (polyethylene terephthalate has a high melting point of 260
℃), kneading, extrusion, and crosslinking, and therefore it is considered unfavorable. According to the invention,
1 or a mixture of polyamides and polyamide copolymers selected from the group 1 to 100 parts by weight of polyolefin
A resin composition containing 0 to 5 parts by weight and, if necessary, a required amount of an antioxidant, a heat deterioration inhibitor, an ultraviolet stabilizer, a crosslinking agent, a crosslinking aid, a blowing agent, etc., is used. Then,
We succeeded in improving the stability of polyolefin-insulated DC cables and DC high-voltage insulation materials.

ここで言うポリオレフィンとは低密度ポリエチレン、高
密度ポリエチレンのみなら゛ずエチレン成分が50%以
上のエチレン共重合体、例えばエチレン.一ビニルエス
テル共重合体、エチレン−アルキルアクリレート共重合
体、エチレン−プロピレン共重合体等と、ポリエチレン
を一部改質した各種の変成ポリエチレン等の電気絶縁用
として使用可能なポリオレフィン重合体すべてを指すも
のとすこる。ポリアミド、ポリアミド共重合体について
は、その融点がポリオレフィンの押出温度以下にあるも
のが成形上望ましく、特に架橋ポリエチレン用に配合す
る場合にはポリアミド共重合体が取扱い易いが、融点が
架橋温度以下のポリアミドのク場合には粉末化し、ポリ
オレフィンに混練する事によつて使用可能となる。また
、その配合量については1呼量部未満では耐トリー性の
効果が不足し、5唾量部以上では成形性の低下と電線・
ケーブル用として必要な曲げ特性、伸長度などの機械的
特性の面で制約を受ける。この発明の組成物に適用可能
な安定剤としては4−4″チオビス(6−t−ブチルー
3−メチルフェノール)や2,6−ジーt−ブチルーp
−クレ)ゾール等であるが、これに限定される事はなく
、通常ポリオレフィンに有効な安定剤はそのまま使用て
きる。
The polyolefins mentioned here include not only low-density polyethylene and high-density polyethylene, but also ethylene copolymers containing 50% or more of ethylene, such as ethylene. Refers to all polyolefin polymers that can be used for electrical insulation, such as monovinyl ester copolymers, ethylene-alkyl acrylate copolymers, ethylene-propylene copolymers, and various modified polyethylenes that are partially modified from polyethylene. It's so cold. Regarding polyamides and polyamide copolymers, those whose melting points are below the extrusion temperature of polyolefins are desirable for molding purposes. Polyamide copolymers are easy to handle especially when blended for crosslinked polyethylene, but polyamides whose melting points are below the crosslinking temperature are preferred. In the case of polyamide, it can be used by powdering it and kneading it into polyolefin. In addition, if the blending amount is less than 1 part by volume, the tree resistance effect will be insufficient, and if it is more than 5 parts by volume, the moldability will decrease and the wire
There are restrictions on mechanical properties such as bending properties and elongation required for cables. Stabilizers applicable to the compositions of this invention include 4-4'' thiobis(6-t-butyl-3-methylphenol) and 2,6-di-t-butyl-p
-cresol, etc., but the stabilizer is not limited thereto, and any stabilizer that is usually effective for polyolefins can be used as is.

この発明に適用できる架橋剤としてはジクミル・パーオ
キサイド、2,5−ジメチルー2,5、−ビス(tーブ
チルパーオキシ)ヘキサン、t一ブチルクミルパーオキ
サイドなど分解速度が半減期1分間で100〜200℃
のものが望ましい。
Examples of crosslinking agents that can be applied to this invention include dicumyl peroxide, 2,5-dimethyl-2,5,-bis(t-butylperoxy)hexane, and t-butylcumyl peroxide, which have a half-life of 100% per minute. ~200℃
Preferably.

以下実施例及び比較例を第1表にもとついて説明する。
第1表に示す各種の配合物をブレス成形により5T!r
l!l厚のシートとし、25Tfn角に試料1を打抜き
、第1図に示すように先端曲率半径を5×10−3Tm
I!l以下に研磨した針状電極2をそう入して、針端と
対向する試料の面に銀ペイントを塗付し、その間の絶縁
厚さを5Tmに設定したものに、第2図で示す装置にて
直流電圧を印加してトリーの発生を観察した。シリコン
オイルを満した槽8に試料1を入れ、直流電圧発生装置
3て発生した直流電圧を試料に印加し、トリーの長さを
顕微鏡5により測定した。4は光源、6はフィルター、
7は真空スイッチである。
Examples and comparative examples will be explained below based on Table 1.
5T! by breath molding various compounds shown in Table 1! r
l! Sample 1 was punched into a 25Tfn square sheet with a thickness of l, and the radius of curvature at the tip was 5 x 10-3Tm as shown in Figure 1.
I! A needle-like electrode 2 polished to a thickness of 1 or less is inserted, silver paint is applied to the surface of the sample facing the needle end, and the insulation thickness between the two is set to 5Tm.The apparatus shown in FIG. The generation of trees was observed by applying a DC voltage. Sample 1 was placed in a tank 8 filled with silicone oil, a DC voltage generated by DC voltage generator 3 was applied to the sample, and the length of the tree was measured using microscope 5. 4 is a light source, 6 is a filter,
7 is a vacuum switch.

直流ケーブル等の直流用絶縁材料に固有な現象である極
性反転の影響は、−40KVの負極性を1紛間印加後、
印加を停止し、1秒後に+40KVの正極性インパルス
電圧を印加した時に針端に発生したトリーの長さを測定
して判定した。50%直流トリー発生電圧及び50%イ
ンパルストリー発生電圧は印加時間1時間後に試料の5
0%にトリーが発生する電圧である。
The effect of polarity reversal, which is a phenomenon unique to DC insulation materials such as DC cables, is that after applying negative polarity of -40KV for one time,
The application was stopped, and after 1 second, a positive impulse voltage of +40 KV was applied, and the length of the tree generated at the needle end was measured and determined. The 50% DC tree generation voltage and the 50% impulse tree generation voltage are 50% of the sample voltage after 1 hour of application.
This is the voltage at which tree occurs at 0%.

機械特性はブレス成形により1?厚のシートとしJIS
K676Oに準拠して引張り伸びを測定して判定した。
Mechanical properties are 1 due to press molding? Thick sheet JIS
Judgment was made by measuring tensile elongation in accordance with K676O.

比較例1及び4に示すとおり、ポリエチレンは極性効果
がある為、正極性と負極性とては50%直流トリー発生
電圧及び50%インパルストリー発生電圧の差が大きく
、又極性反転させた場合のトリーの伸び長さも大きいの
で直流送電においてその絶縁性能の安定性に欠ける事を
裏付けているが、実施例1から9に示すとおりポリオレ
フィンにポリアミド及びポリアミド共重合体の両方又は
どちらか一方を配合することによりこの極性効果を減少
させトリーの発生及び伸長の要因と考えられる空間電荷
の蓄積を緩和し直流電気絶縁材料として優れたものを得
ることができた。
As shown in Comparative Examples 1 and 4, polyethylene has a polarity effect, so there is a large difference between the 50% DC tree generation voltage and the 50% impulse tree generation voltage between positive and negative polarities, and when the polarity is reversed, The extended length of the tree is also large, which confirms that its insulation performance lacks stability in DC power transmission, but as shown in Examples 1 to 9, polyamide and/or polyamide copolymer are blended with polyolefin. By doing so, we were able to reduce this polarity effect and alleviate the accumulation of space charge, which is thought to be a factor in the generation and elongation of trees, making it possible to obtain an excellent DC electrical insulating material.

尚比較例2では空間電荷の蓄積の緩和は不充分であり又
比較例3ては機械特性の低下が著しく絶縁材料としての
機能をはたし得ない。実施例9及び比較例4は2重量部
のジクミルパーオキサイドを添加して化学架橋をさせた
が、実施例2及び9に示すとおり架橋の有無はこのポリ
アミド等の添加の効果には悪い影響を与えない。又実施
例1から9はいずれも50%交流トリー発生電圧が上昇
していることを認められたが、誘電率、誘電体損の増加
により誘電損失が増加する為、遠距離高電圧、大電流等
の場合交流送電ては、この組成の応用は有利ではない。
また、HDPE,EVA,EEAのみてポリアミド類の
添加がない場合にはLDPEのみの場合(比較例1〜3
)と同様の傾向を示した。これらの直流電気絶縁用樹脂
組成物による直流高圧用ケーブルおよび直流高圧用絶縁
材の製造方法については従来の方法によつて可能であり
、押出し加工条件を一部修正する程の変更でよい。
In Comparative Example 2, the relaxation of space charge accumulation was insufficient, and in Comparative Example 3, the mechanical properties were significantly deteriorated and the material could not function as an insulating material. In Example 9 and Comparative Example 4, 2 parts by weight of dicumyl peroxide was added to cause chemical crosslinking, but as shown in Examples 2 and 9, the presence or absence of crosslinking had a negative effect on the effect of adding polyamide, etc. not give. Furthermore, in all of Examples 1 to 9, it was observed that the AC tree generation voltage increased by 50%, but since the dielectric loss increases due to the increase in dielectric constant and dielectric loss, it is difficult to use long-distance high voltages and large currents. For AC power transmission, the application of this composition is not advantageous.
In addition, when only HDPE, EVA, and EEA are used without the addition of polyamides, when only LDPE is used (Comparative Examples 1 to 3)
) showed a similar trend. The method for producing DC high voltage cables and DC high voltage insulation materials using these DC electrical insulation resin compositions can be carried out by conventional methods, and only a partial modification of the extrusion processing conditions is sufficient.

ケーブルの構造についても従来の絶縁材層を本発明の組
成物に置換する事によるものとする。
The structure of the cable is also based on replacing the conventional insulating material layer with the composition of the present invention.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はトリー発生状況の観察に使用する試料の形状お
よび電極の配置を示す図であり、第2図はトリー観察の
ための実験装置の概略図である。
FIG. 1 is a diagram showing the shape of a sample and the arrangement of electrodes used for observing the state of tree formation, and FIG. 2 is a schematic diagram of an experimental apparatus for tree observation.

Claims (1)

【特許請求の範囲】 1 ポリオレフィン100重量部にポリアミドおよびポ
リアミド共重合体から選ばれた1種またはそれらの中の
数種からなる混合物10〜50重量部を配合した事を特
徴とする直流電気絶縁用樹脂組成物。 2 酸化防止剤、熱劣化防止剤、紫外線安定剤および/
または他の安定剤を所要量配合した特許請求の範囲第1
項記載の組成物。 3 架橋剤、架橋助剤および/または発泡剤を所要量配
合した特許請求の範囲第1、2項記載の組成物。 4 第1〜3項の組成物にカーボン・ブラックを配合し
た組成物。
[Claims] 1. A direct current electrical insulation characterized by blending 100 parts by weight of polyolefin with 10 to 50 parts by weight of one selected from polyamides and polyamide copolymers or a mixture of several of them. Resin composition for use. 2 Antioxidants, thermal deterioration inhibitors, ultraviolet stabilizers and/or
or other stabilizers in the required amount.
Compositions as described in Section. 3. The composition according to claims 1 and 2, which contains a crosslinking agent, a crosslinking aid, and/or a blowing agent in required amounts. 4. A composition in which carbon black is blended with the compositions of items 1 to 3.
JP6775078A 1978-06-07 1978-06-07 Resin composition for DC electrical insulation Expired JPS6046762B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6775078A JPS6046762B2 (en) 1978-06-07 1978-06-07 Resin composition for DC electrical insulation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6775078A JPS6046762B2 (en) 1978-06-07 1978-06-07 Resin composition for DC electrical insulation

Publications (2)

Publication Number Publication Date
JPS54159680A JPS54159680A (en) 1979-12-17
JPS6046762B2 true JPS6046762B2 (en) 1985-10-17

Family

ID=13353924

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6775078A Expired JPS6046762B2 (en) 1978-06-07 1978-06-07 Resin composition for DC electrical insulation

Country Status (1)

Country Link
JP (1) JPS6046762B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05505634A (en) * 1990-03-23 1993-08-19 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Polymer foam containing gas barrier resin

Also Published As

Publication number Publication date
JPS54159680A (en) 1979-12-17

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