JPH02142006A - Flame retardant electrical insulation composition - Google Patents
Flame retardant electrical insulation compositionInfo
- Publication number
- JPH02142006A JPH02142006A JP29687588A JP29687588A JPH02142006A JP H02142006 A JPH02142006 A JP H02142006A JP 29687588 A JP29687588 A JP 29687588A JP 29687588 A JP29687588 A JP 29687588A JP H02142006 A JPH02142006 A JP H02142006A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- electrical insulation
- derivative
- ethyl acrylate
- organic acid
- 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
Links
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims description 10
- 239000003063 flame retardant Substances 0.000 title claims description 10
- 239000000203 mixture Substances 0.000 title claims description 10
- 238000010292 electrical insulation Methods 0.000 title claims description 5
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 claims description 10
- 150000007524 organic acids Chemical class 0.000 claims description 10
- 229910001853 inorganic hydroxide Inorganic materials 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
- 230000000052 comparative effect Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 3
- CGPRUXZTHGTMKW-UHFFFAOYSA-N ethene;ethyl prop-2-enoate Chemical class C=C.CCOC(=O)C=C CGPRUXZTHGTMKW-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- 229910052751 metal Chemical class 0.000 description 2
- 239000002184 metal Chemical class 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 230000008733 trauma Effects 0.000 description 2
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical class [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- -1 softener Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Landscapes
- Organic Insulating Materials (AREA)
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]
この発明は、発煙性および毒性が少なく、腐食性のない
難燃性電気組成物に係り、電気・ケーブルの絶縁体やシ
ース材料として好適なものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a flame-retardant electrical composition with low smoke emission, low toxicity, and no corrosion, which is suitable as an insulator or sheath material for electrical cables. It is something.
[従来の技術]
ポリマーの難燃化処理法として、従来のハロゲン系化合
物やりん化合物を混和する方法に代わり、最近では火災
時の安全性を重要視する観点から水酸化マグネシウム等
の無機水酸化物を混和する方法が注目されている。これ
らのものは、ハロゲン系化合物やりん系のものに比べ発
煙性や毒性が少なく、また、腐食性もないという特徴を
もっている。[Prior art] In place of the conventional method of mixing halogen compounds or phosphorous compounds as a flame retardant treatment method for polymers, inorganic hydroxides such as magnesium hydroxide have recently been used from the perspective of placing importance on safety in the event of a fire. The method of mixing things is attracting attention. These materials have the characteristics of being less smoke-producing and toxic than halogen-based compounds and phosphorus-based materials, and are also non-corrosive.
[発明が解決しようとする課題〕
ところが、無機水酸化物は、前述のハロゲン系やりん系
化合物に比べて難燃性が劣るため、同等の効果を得るた
めには多量に混和しなければならない、その結果、引張
特性や耐外傷性等の機械的特性が著しく低下してしまう
という問題がある。[Problem to be solved by the invention] However, inorganic hydroxides have inferior flame retardancy compared to the above-mentioned halogen-based and phosphorus-based compounds, so they must be mixed in large amounts in order to obtain the same effect. As a result, there is a problem in that mechanical properties such as tensile properties and trauma resistance are significantly reduced.
この発明は、このような点に鑑みてなされたもので、従
来の技術の欠点を解消し、機械的特性を向上させた難燃
性電気絶縁組成物を提供することを目的とする。The present invention has been made in view of these points, and aims to provide a flame-retardant electrical insulating composition that eliminates the drawbacks of the conventional techniques and has improved mechanical properties.
[課題を解決するための手段および作用]この発明は、
不飽和有機酸またはその誘導体で変性したエチレンエチ
ルアクリレート共重合体100重量部に無機水酸化物を
50〜300重量部混和したことを特徴とする難燃性電
気絶縁組成物に関する。[Means and effects for solving the problem] This invention has the following features:
The present invention relates to a flame-retardant electrical insulation composition characterized in that 50 to 300 parts by weight of an inorganic hydroxide is mixed with 100 parts by weight of an ethylene ethyl acrylate copolymer modified with an unsaturated organic acid or a derivative thereof.
これにより難燃性を維持しながら機械的特性を大幅に向
上させることができる。This makes it possible to significantly improve mechanical properties while maintaining flame retardancy.
[実 施 例]
この発明では、不飽和有機酸またはその誘導体で変性し
たエチレンエチルアクリレート共重合体とは、エチレン
エチルアクリレート共重合体に有機過酸化物の存在下で
不飽和有機酸またはその誘導体を加熱によりグラフト反
応させたものである。[Example] In the present invention, an ethylene ethyl acrylate copolymer modified with an unsaturated organic acid or its derivative refers to an ethylene ethyl acrylate copolymer modified with an unsaturated organic acid or its derivative in the presence of an organic peroxide. is obtained by grafting reaction by heating.
不飽和有機酸としては、マレイン酸、フマル酸、イクコ
ン酸、シトラコン酸等があり、これらの誘導体とは無水
物、金属塩等が挙げられる。Examples of unsaturated organic acids include maleic acid, fumaric acid, ichconic acid, and citraconic acid, and examples of derivatives thereof include anhydrides and metal salts.
不飽和有機酸またはその誘導体の含有量は、ポリマー1
00に対し0.01〜1重量%が望ましく、これが0.
01重量%未満では目的とする機械的特性を向上できず
、また1重1%以上では金属への粘着が大きくなり混練
加工が難しくなるためである。The content of unsaturated organic acid or its derivative is
0.01 to 1% by weight based on 0.00.
This is because if it is less than 0.1% by weight, the desired mechanical properties cannot be improved, and if it is more than 1% by weight, the adhesion to metal becomes large and kneading becomes difficult.
この発明において、上記の変性したエチレンエチルアク
リレート共重合体としてはメルトフロレー)−MFRo
、1〜10g/10分、エチルアクリレート含有15〜
40重量%が望ましく、これらの範囲外では引張特性等
の機械的特性の低下が大きい。In this invention, the above-mentioned modified ethylene ethyl acrylate copolymer is melt flow)-MFRo.
, 1~10g/10min, ethyl acrylate content 15~
A content of 40% by weight is desirable; outside this range, mechanical properties such as tensile properties are significantly reduced.
また、この発明にお番づる無機水酸化物としては水酸化
アルミニアム、水酸化マグネシウム、水酸化カルシウム
、ハイドロタルサイト類等が挙げられる。この無機水酸
化物は、前述の変性したエチレンエチルアクリレート共
重合体]、 O0重量部に対して50〜300重量部の
範囲で混和させる必要があり、50重1部未満では目的
とする難燃性を伺与できず、また300重量部を越える
と押出加工性が著しく低下して成形が難しくなってしま
う。Inorganic hydroxides suitable for this invention include aluminum hydroxide, magnesium hydroxide, calcium hydroxide, hydrotalcites, and the like. This inorganic hydroxide needs to be mixed in a range of 50 to 300 parts by weight with respect to the above-mentioned modified ethylene ethyl acrylate copolymer], O0 parts by weight, and if it is less than 50 parts by weight, it will not achieve the desired flame retardancy. Moreover, if it exceeds 300 parts by weight, extrusion processability will be significantly reduced and molding will become difficult.
この発明では」二記成分に加えて架橋剤、酸化防止剤、
滑剤、軟化剤、カップリング剤等を添加してもよい。In this invention, in addition to the above two components, a crosslinking agent, an antioxidant,
A lubricant, softener, coupling agent, etc. may be added.
以下、この発明の具体的な実施例を比較例とともに説明
する。第1表の実施例1〜6および比較例1〜4に示し
た変性エチレンエチルアクリレ−]・共重合体は210
℃の温度に保持した40m / m押出機(L/D=2
5)により、無水マレイン酸を開始剤ジクミルパーオキ
サイドの存在下でエチレンエチルアクリレート共重合体
にグラフトさせたものである。Hereinafter, specific examples of the present invention will be described together with comparative examples. The modified ethylene ethyl acrylate copolymers shown in Examples 1 to 6 and Comparative Examples 1 to 4 in Table 1 were 210
A 40 m/m extruder (L/D=2
5), maleic anhydride is grafted onto an ethylene ethyl acrylate copolymer in the presence of an initiator dicumyl peroxide.
各種成分を第1表の実施例1〜6および比較例1〜4に
示すような配合割合でパンバリ混練した後、160°C
の温度に保持した8 0 m / m押出機(L/D=
20)を用い、外径3mmのエチレンプロピレンゴム絶
縁線心を3本撚り合せた外周上に2 m m厚で押出被
覆し、各種ケーブルを作製して各試料とした。After panburi kneading various ingredients in the mixing ratios shown in Examples 1 to 6 and Comparative Examples 1 to 4 in Table 1, the mixture was heated at 160°C.
An 80 m/m extruder (L/D=
20), the outer periphery of three twisted ethylene propylene rubber insulated wire cores with an outer diameter of 3 mm was coated by extrusion to a thickness of 2 mm, and various cables were prepared and used as samples.
各側で得られたケーブルの評価結果は、第1表の下欄に
纏めて示す。The evaluation results of the cables obtained on each side are summarized in the lower column of Table 1.
引張特性は、190℃の温度で1mm厚にプレス成形後
、JISダンベル3号試験片を作製し、ショツパー型別
り試験機により200111 m /分の速度で引張試
験を行なった。For tensile properties, JIS dumbbell No. 3 test pieces were prepared after press molding to a thickness of 1 mm at a temperature of 190° C., and tensile tests were conducted using a Schopper type testing machine at a speed of 200111 m /min.
耐傷性の評価は、JIS C3003に41:1処し
、エンピッ硬度法で行なった。エンピッでケーブル表面
を擦り、白化するところのエンピッ硬度を求めた。The scratch resistance was evaluated using the 41:1 JIS C3003 hardness method. The surface of the cable was rubbed with empi and the hardness of the empi was determined at the point where it turned white.
難燃性の評価は、I EEE規格383に準拠し2.4
m長のケーブルを8本垂直に並べ、下方から70 、0
00 B T U / l〕rの炎を20分間当て、そ
の後炎を取り去り1.8m未満で自己消炎すれば合格、
1.8m以上に延焼したものは不合格とした。The flame retardant evaluation is 2.4 in accordance with IEEE standard 383.
Eight m-long cables are lined up vertically, 70 and 0 from the bottom.
00 B T U / l]r for 20 minutes, then remove the flame and pass if the flame self-extinguishes at a distance of less than 1.8 m.
Those whose fire spread over 1.8 m were rejected.
これに対し、無機水酸化物の含有量が少ない比較例1は
、難燃性が不合格であり、含有量が300重量部を越え
る比較例2は押出性が悪い。On the other hand, Comparative Example 1 with a small content of inorganic hydroxide failed in flame retardancy, and Comparative Example 2 with a content of more than 300 parts by weight had poor extrudability.
前記の変性を施していない比較例3は耐傷性が劣り、ま
た規定外のポリマーを用いた比較例4は難燃性が不合格
である。Comparative Example 3, in which the above modification was not performed, had poor scratch resistance, and Comparative Example 4, in which a non-specified polymer was used, failed in terms of flame retardancy.
第1表から明らかなように、この発明J係る実施例1〜
6に示す組成物は、引張特性および耐傷性に優れ、垂直
トレイ燃焼試験に合格するものである。As is clear from Table 1, Examples 1 to 1 according to this invention J
The composition shown in No. 6 has excellent tensile properties and scratch resistance, and passes the vertical tray burn test.
(以下余白)
[発明の効果]
この発明によれば、引張特性、耐外傷性等の機械的特性
に優れたノンハロゲン難燃性電気絶縁組成物を得ること
ができる。(The following is a blank space) [Effects of the Invention] According to the present invention, a halogen-free flame-retardant electrical insulating composition having excellent mechanical properties such as tensile properties and trauma resistance can be obtained.
Claims (3)
エチルアクリレート共重合体100重量部に無機水酸化
物を50〜300重量部を混和してなる難燃性電気絶縁
組成物。1. A flame-retardant electrical insulation composition prepared by mixing 50 to 300 parts by weight of an inorganic hydroxide with 100 parts by weight of an ethylene ethyl acrylate copolymer modified with an unsaturated organic acid or a derivative thereof.
エチルアクリレート共重合体中の不飽和有機酸またはそ
の誘導体中の不飽和有機酸またはその誘導体の含有量が
ポリマーに対し0.01〜1重量%である請求項1記載
の難燃性電気絶縁組成物。2. The content of the unsaturated organic acid or its derivative in the unsaturated organic acid or its derivative in the ethylene ethyl acrylate copolymer modified with the unsaturated organic acid or its derivative is 0.01 to 1% by weight based on the polymer. The flame retardant electrical insulation composition according to claim 1.
エチルアクリレート共重合体のMFR(メルトフローレ
ート)が0.1〜10g/10分,エチルアクリレート
含有量が5〜40重量%である請求項1記載の難燃性電
気絶縁組成物。3. 2. The ethylene ethyl acrylate copolymer modified with an unsaturated organic acid or its derivative has an MFR (melt flow rate) of 0.1 to 10 g/10 min and an ethyl acrylate content of 5 to 40% by weight. Flame retardant electrical insulation composition.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29687588A JPH02142006A (en) | 1988-11-22 | 1988-11-22 | Flame retardant electrical insulation composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29687588A JPH02142006A (en) | 1988-11-22 | 1988-11-22 | Flame retardant electrical insulation composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02142006A true JPH02142006A (en) | 1990-05-31 |
Family
ID=17839297
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP29687588A Pending JPH02142006A (en) | 1988-11-22 | 1988-11-22 | Flame retardant electrical insulation composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02142006A (en) |
-
1988
- 1988-11-22 JP JP29687588A patent/JPH02142006A/en active Pending
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