JPS61254A - Fluoroelastomer composition - Google Patents
Fluoroelastomer compositionInfo
- Publication number
- JPS61254A JPS61254A JP12156784A JP12156784A JPS61254A JP S61254 A JPS61254 A JP S61254A JP 12156784 A JP12156784 A JP 12156784A JP 12156784 A JP12156784 A JP 12156784A JP S61254 A JPS61254 A JP S61254A
- Authority
- JP
- Japan
- Prior art keywords
- tetrafluoroethylene
- compound
- propylene
- propylene copolymer
- perylene
- 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
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、赤色に着色可能な四ふつ化]ニチレンープロ
ピレン系共重合体組成物に関するもので゛ある。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a red-colorable tetrafluorinated nethylene-propylene copolymer composition.
[従来の技術]
四ふっ化エチレン−プロピレン系共重合体は、耐熱性、
耐油性1.′耐薬品性に加え、電気的にも優れた性能を
有することからガスケット、パツキン、ホース等積々の
用途に使用されており、特に耐熱可撓電線の被覆材料と
しくの期待の高い材料である。[Prior art] Tetrafluoroethylene-propylene copolymer has heat resistance,
Oil resistance 1. 'In addition to its chemical resistance, it has excellent electrical performance, so it is used in a variety of applications such as gaskets, packing, and hoses, and is particularly promising as a coating material for heat-resistant flexible electric wires. be.
電線用被覆相別に適用するに際しては、識別を行うこと
の必要性から着色できることが不可欠の条f1どなる。When applying wire coatings to different phases, it is essential to be able to color them because of the need for identification.
しかるに、従来、電線・ケーブル用としC使用されてき
/、:W色剤をそのまま四ふつ化エチレン−プロピレン
共重合体に適用覆るには、以下に述べるような問題を生
じることが発明者の検討結果用らかにな−)lこ。However, the inventors have considered that applying the W coloring agent, which has conventionally been used for electric wires and cables, directly to the tetrafluoroethylene-propylene copolymer will cause the following problems. The result is easy-)lko.
づなわら、ふっ素樹脂用として使用され(いる耐熱性の
無機系着色剤は多桁に混和しないと鮮明な色を出1こと
ができず、その場合、電気特性、特に絶縁抵抗が大幅に
低下づる問題を生じた。一方、一般のゴム、プラスチッ
ク用として使用されている汎用の着色剤は1〜2phr
と少量でも鮮明な色を出1ことが可能であるが、耐熱性
に劣るため200℃を越える高温雰囲気上においては極
めて、1 短時間で退色づるごとになる。However, the heat-resistant inorganic colorants used for fluororesin cannot produce vivid colors unless they are mixed in large quantities, and in that case, the electrical properties, especially the insulation resistance, decrease significantly. On the other hand, general-purpose colorants used for general rubber and plastics contain 1 to 2 phr.
Although it is possible to produce vivid colors even with a small amount of 1, it has poor heat resistance and will fade in an extremely short time in a high temperature atmosphere exceeding 200°C.
[発明が解決しにうとする問題点1
本発明は、上記に基いてなされた1つのであって、電気
特性に優れ、しかも高温に長時間さらされても退色しな
い黄色の成形体を実現できる四ふつ化二[チレンープロ
ピレン系共重合体組成物の提供を目的とするものである
。[Problem to be solved by the invention 1 The present invention has been made based on the above, and is capable of realizing a yellow molded product that has excellent electrical properties and does not fade even when exposed to high temperatures for a long time. The purpose of the present invention is to provide a tetrafluoride-propylene copolymer composition.
し問題点を解決するための手段1
本発明の組成物は、四ふつ化エチレン−プロピレン系共
重合体100重量部に対し、上記一般式で示されるペリ
レン系、ポリアゾ系、キナクリドン系、アンスラキノン
系の少なくとし1種を0.5重量部以上添加してなるこ
とを特徴と7るものである。Means for Solving the Problem 1 The composition of the present invention contains perylene, polyazo, quinacridone, and anthraquinone represented by the above general formula, based on 100 parts by weight of the tetrafluoroethylene-propylene copolymer. It is characterized in that it contains at least 0.5 parts by weight of at least one of the following.
(A) ペリレン系
(C) キナクリドン系
■ アンスラキノン系
1作用+ NHq Q
本発明tJ、 a3いて、四ふ−)化工ヂレンープロビ
レン系」4.ii会合体()(は、主成分の四ふつ化エ
チレンとゾ[1ピ1ノンに加えて、これらと共重合可能
な成分、例え(J−1ヂレン、プラン−1、イソブチン
、アクリル酸および−でのアルキル1スプル、メタクリ
ル酸およびそのアルキル1スプル、ぶつ化ビニル、ふっ
化ビニリデン、ベキ1ノフルオ・ロプロペン、クロロエ
チルビニルエーテル、グリシジルビニルエーテル、クロ
ロトリフルオロエチレン、パーフルオロアルキルビニル
エーテル等を適用に含右ゼしめたものであってもよい。(A) Perylene type (C) Quinacridone type ■ Anthraquinone type 1 action + NHq Q Present invention tJ, a3, 4-) Chemically modified dylene-propylene type 4. ii aggregate (2) (in addition to the main components of tetrafluoroethylene and Applications include alkyl 1 sprue, methacrylic acid and its alkyl 1 sprue, vinyl buttride, vinylidene fluoride, monofluoropropene, chloroethyl vinyl ether, glycidyl vinyl ether, chlorotrifluoroethylene, perfluoroalkyl vinyl ether, etc. It may be angled to the right.
かかる共重合体においC1四ぶつ化エチレン/プロピレ
ンの含有モル負としては9515〜30/70、特に9
0/10〜45155の範囲から選定づることが耐熱性
、成形性等の面から好ましく、また、適宜加えられる主
成分以外の成分の含有量としては通常50モル%以下、
特に30モル%以下の範囲から選定することが好ましい
。In such a copolymer, the molar content of C1 tetrabutylene/propylene is 9515 to 30/70, especially 9
It is preferable to select from the range of 0/10 to 45155 from the viewpoint of heat resistance, moldability, etc., and the content of components other than the main component, which may be added as appropriate, is usually 50 mol% or less,
In particular, it is preferable to select from a range of 30 mol% or less.
かかる四ふっ化エヂレンープロピレン系共重合体に添加
される着色剤は、ペリレン系、ポリアゾ系、キナクリド
ン系、゛アンスラキノン系から選ばれる赤色用耐熱性顔
料である。The coloring agent added to the tetrafluoroedylene-propylene copolymer is a red heat-resistant pigment selected from perylene, polyazo, quinacridone, and anthraquinone.
着色剤の添加量は、四ふっ化エヂレンープロピレン系共
重合体100重量部に対しUo、5宙吊部以上とする必
要があり、でれ以干では着色が不モ分である。その上限
は特に限定しないが、耐熱名化特性の低下を招かない範
囲である20重量部が適切である。The amount of the coloring agent added must be at least 5 parts by weight per 100 parts by weight of the polyethylene tetrafluoride-propylene copolymer, and if the coloring is less than that, the coloring will be insignificant. The upper limit is not particularly limited, but a suitable range is 20 parts by weight, which is within a range that does not cause a decrease in heat resistance properties.
四ふっ化エチレン−プロピレン系共重合体と着色剤を含
イ1りる組成物は所定形状【J成]゛!された後、架橋
2\れる。A composition containing a tetrafluoroethylene-propylene copolymer and a colorant has a predetermined shape [J-formation]! After that, cross-linking 2\ is carried out.
架橋15 fi、としては、有機化酸化物やアミン類等
の添加に、J、る化学架橋、あるいはγ線や電f線等の
電1illIft放射線の前用による照射架m等が採用
され、限定されない。For cross-linking, chemical cross-linking with J, or irradiation with electric radiation such as γ-rays or electric f-rays is used to add organic oxides, amines, etc., and limited Not done.
有機化酸化物の具体例としては、ジー【−ブチルパーオ
キザイド、t−ブチルクミルパーオキ4ノ゛イト、ジク
ミルバーオキ1ノイド、2,5−ジメチル−2,5−ジ
(t−ブチルパーオキシ)−ヘキシン−3,1,3−ビ
ス−(t−ブチルパーオキシ−イソプロビル)ベンゼン
等があげられる。Specific examples of organic oxides include di[-butyl peroxide, t-butylcumyl peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-di(t-butyl peroxide), )-hexyne-3,1,3-bis-(t-butylperoxy-isoprobyl)benzene and the like.
アミン類の具体例としては、ヘキサメチレンジアミン、
デトラエチレンペンタミン、トリエチレンテトラミン等
のいわゆるアルキルポリアミンあるいはそ−のカルバミ
ン酸、シンナミリデン酸等の塩またはピペラジン、ピペ
リジン、ピリジン、ノ7二1リ リ′・7
”す″。“1′等17) 70 ? 7” −(y ’
) M ’)アミンおよびその塩等があげられる。Specific examples of amines include hexamethylene diamine,
So-called alkyl polyamines such as detraethylenepentamine and triethylenetetramine, or their salts such as carbamic acid and cinnamylidenic acid, or piperazine, piperidine, pyridine, and the like.
"vinegar". "1' etc. 17) 70? 7"-(y'
) M') Amines and their salts, etc.
また、アリル化合物、硫黄、有機アミン類、マレイミド
、メタクリレート類、ジじニル化合物等の架橋助剤の採
用も可能であり、好ましくは、フタル酸ジアリル、l・
リアリルtS、t−リアリルイソシアヌレート、トリノ
7リルシアヌレート等のアリル化合物が採用可能である
。It is also possible to employ crosslinking aids such as allyl compounds, sulfur, organic amines, maleimide, methacrylates, and didinyl compounds, and preferably diallyl phthalate, l.
Allyl compounds such as realyl tS, t-lylyl isocyanurate, and trino7lyl cyanurate can be employed.
本発明においては、上記成分以外にポリぶつ化ビニリデ
ン、エチレンテトラフルAロエヂレン、ポリテトラフル
オロエチレン等のふっそ樹脂、ぶつ化ビニリデン−へキ
リフルオロプロピレン共重合体に代表されるふっ素ゴム
を適宜混合しCもよい。また、MTカーボンやFTカー
ボン等のカーボンブラック、炭酸カルシウム、タルり、
クレー、無水ケイ酸といった充填剤、その他補強剤、滑
剤、酸化防止剤、安定剤等を配合して−bよい。In the present invention, in addition to the above-mentioned components, fluorocarbon resins such as polyvinylidene buttomide, ethylenetetrafluoroethylene, polytetrafluoroethylene, and fluororubbers such as vinylidenebutylidene-hekylyfluoropropylene copolymer are appropriately mixed. ShiC is also good. In addition, carbon black such as MT carbon and FT carbon, calcium carbonate, tartar,
Fillers such as clay and silicic anhydride, other reinforcing agents, lubricants, antioxidants, stabilizers, etc. may be added.
[実施例1
(a )四ふつ化エチレン−プロピレン共重合体(四ふ
っ化エチレン/プロピレン含有モル費−54/46、数
平均分子量5万)
100重量部
(b)1.3−ヒス(t−プチルパーオキシーイソプ「
1ピル)ベンゼン 1重量部(C)トリアリルイソ
シアヌレート 5重量部(iスデノ7リン酸ナトリウ
lx 1重量部(e )チタン白
5重量部および([)成分として第1表の
各個に示すような顔料を配合し、60℃に加熱した8イ
ンチロールで混練した。次に、これをヘッド:100’
C、シリンダー1:100℃、シリンダー2:80℃に
設定した40m/m押出機(L/D=22)により、外
径1.6mmφのスズメッキ銅撚線外周に0.5mmの
厚さに押出被覆し、13気圧のスチーム(温度:195
℃)中に3分間保持することにより電線を作成した。[Example 1 (a) Tetrafluoroethylene-propylene copolymer (tetrafluoroethylene/propylene content molar cost - 54/46, number average molecular weight 50,000) 100 parts by weight (b) 1.3-His (t) -butylperoxyisopropylene
1 pill) Benzene 1 part by weight (C) Triallylisocyanurate 5 parts by weight (i Sodium heptaphosphate lx 1 part by weight (e) Titanium white
5 parts by weight and the pigments shown in Table 1 as components ([) were blended and kneaded using an 8-inch roll heated to 60°C. Next, add this to the head: 100'
C, Cylinder 1: Extruded to a thickness of 0.5 mm on the outer circumference of a tin-plated copper stranded wire with an outer diameter of 1.6 mmφ using a 40 m/m extruder (L/D = 22) set at 100 °C and cylinder 2 at 80 °C. covered with steam at 13 atm (temperature: 195
℃) for 3 minutes to prepare an electric wire.
このようにして作成した電線の絶縁抵抗並びに色相の熱
安定性についての評価結果を第1表の下欄に示づ。The evaluation results of the insulation resistance and thermal stability of the hue of the electric wire thus prepared are shown in the lower column of Table 1.
第1表
(/1) ペリレン系
OO
O0
NH,Q
(5) クロモフタルレット
第1表から明らかな通り、本発明の範囲にある実施例1
〜4ではいずれも良好な絶縁抵抗、色相および色相の熱
安定性を示ず。Table 1 (/1) Perylene-based OO 00 NH,Q (5) Chromophthalet As is clear from Table 1, Example 1 within the scope of the present invention
- 4 did not exhibit good insulation resistance, hue, or thermal stability of hue.
これに対し、比較例1および2は汎用の赤色着色剤を添
加したものであるが、絶縁抵抗および初期の色相は良好
であったが、耐熱性が悪く、250℃で4日熱劣化する
と脱色してしまった。On the other hand, in Comparative Examples 1 and 2, a general-purpose red colorant was added, but the insulation resistance and initial hue were good, but the heat resistance was poor, and the color faded after 4 days of heat deterioration at 250°C. have done.
比較例363よひ4は、無機系の力1−ミウム系レッド
を添加したものであるが、添加量が2 ph+・では良
好な色相が冑られず、10pt+rと多昂添加覆ると絶
縁抵抗が大ぎく低下してしまう。Comparative Example 363 Yohi 4 has inorganic power 1-mium-based red added, but when the addition amount is 2 ph+, a good hue is not achieved, and when the amount of addition is 10 pt+r, the insulation resistance increases. It will drop significantly.
[発明の効果コ[Effects of invention
Claims (1)
重量部に対し、下記一般式で示されるペリレン系、ポリ
アゾ系、キナクリドン系、アンスラキノン系の少なくと
も1種を0.5重量部以上添加してなることを特徴とす
る含ふっ素エラストマ組成物。 (A)ペリレン系 ▲数式、化学式、表等があります▼ (B)ポリアゾ系 ▲数式、化学式、表等があります▼ (c)キナクリドン系 ▲数式、化学式、表等があります▼ (D)アンスラキノン系 ▲数式、化学式、表等があります▼(1) Tetrafluoroethylene-propylene copolymer 100
1. A fluorine-containing elastomer composition comprising at least 0.5 part by weight of at least one of perylene, polyazo, quinacridone, and anthraquinone represented by the following general formula, based on part by weight. (A) Perylene series ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (B) Polyazo series ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (c) Quinacridone series ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (D) Anthraquinone System ▲ Contains mathematical formulas, chemical formulas, tables, etc. ▼
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12156784A JPS61254A (en) | 1984-06-13 | 1984-06-13 | Fluoroelastomer composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12156784A JPS61254A (en) | 1984-06-13 | 1984-06-13 | Fluoroelastomer composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61254A true JPS61254A (en) | 1986-01-06 |
JPH0117497B2 JPH0117497B2 (en) | 1989-03-30 |
Family
ID=14814427
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12156784A Granted JPS61254A (en) | 1984-06-13 | 1984-06-13 | Fluoroelastomer composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61254A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01181666A (en) * | 1988-01-13 | 1989-07-19 | Sanyo Kokusaku Pulp Co Ltd | Band takeup stopping method |
EP0807668A2 (en) * | 1996-05-13 | 1997-11-19 | Bayer Corporation | Crystal growth modifiers for perylene pigments |
JPWO2016043100A1 (en) * | 2014-09-16 | 2017-04-27 | ダイキン工業株式会社 | Fluorine-containing elastomer composition and molded article |
JP2017214555A (en) * | 2016-05-30 | 2017-12-07 | 日本バルカー工業株式会社 | Perfluoroelastomer composition and seal material |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4920055A (en) * | 1972-06-15 | 1974-02-22 | ||
JPS4920054A (en) * | 1972-06-16 | 1974-02-22 | ||
JPS56166251A (en) * | 1980-04-23 | 1981-12-21 | Du Pont | Fluoroelastomer composition |
-
1984
- 1984-06-13 JP JP12156784A patent/JPS61254A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4920055A (en) * | 1972-06-15 | 1974-02-22 | ||
JPS4920054A (en) * | 1972-06-16 | 1974-02-22 | ||
JPS56166251A (en) * | 1980-04-23 | 1981-12-21 | Du Pont | Fluoroelastomer composition |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01181666A (en) * | 1988-01-13 | 1989-07-19 | Sanyo Kokusaku Pulp Co Ltd | Band takeup stopping method |
JPH0524062B2 (en) * | 1988-01-13 | 1993-04-06 | Sanyo Kokusaku Pulp Co | |
EP0807668A2 (en) * | 1996-05-13 | 1997-11-19 | Bayer Corporation | Crystal growth modifiers for perylene pigments |
EP0807668A3 (en) * | 1996-05-13 | 1998-08-19 | Bayer Corporation | Crystal growth modifiers for perylene pigments |
EP1634927A2 (en) * | 1996-05-13 | 2006-03-15 | Sun Chemical Corporation | Crystal growth modifiers for perylene pigments |
EP1634927A3 (en) * | 1996-05-13 | 2006-03-22 | Sun Chemical Corporation | Crystal growth modifiers for perylene pigments |
JPWO2016043100A1 (en) * | 2014-09-16 | 2017-04-27 | ダイキン工業株式会社 | Fluorine-containing elastomer composition and molded article |
JP2017214555A (en) * | 2016-05-30 | 2017-12-07 | 日本バルカー工業株式会社 | Perfluoroelastomer composition and seal material |
WO2017208927A1 (en) * | 2016-05-30 | 2017-12-07 | 日本バルカー工業株式会社 | Perfluoroelastomer composition and sealing material |
CN109153835A (en) * | 2016-05-30 | 2019-01-04 | 日本华尔卡工业株式会社 | Perfluoroelastomer composition and sealing material |
KR20190013809A (en) * | 2016-05-30 | 2019-02-11 | 주식회사 발카 | The perfluoroelastomer composition and the sealing material |
EP3467025A4 (en) * | 2016-05-30 | 2020-02-19 | Valqua, Ltd. | Perfluoroelastomer composition and sealing material |
CN109153835B (en) * | 2016-05-30 | 2021-04-06 | 株式会社华尔卡 | Perfluoroelastomer composition and sealing material |
US11118045B2 (en) | 2016-05-30 | 2021-09-14 | Valqua, Ltd. | Perfluoroelastomer composition and sealing material |
Also Published As
Publication number | Publication date |
---|---|
JPH0117497B2 (en) | 1989-03-30 |
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