JPH07161230A - Flame retardant composition, electric wire, and cable - Google Patents
Flame retardant composition, electric wire, and cableInfo
- Publication number
- JPH07161230A JPH07161230A JP34144093A JP34144093A JPH07161230A JP H07161230 A JPH07161230 A JP H07161230A JP 34144093 A JP34144093 A JP 34144093A JP 34144093 A JP34144093 A JP 34144093A JP H07161230 A JPH07161230 A JP H07161230A
- Authority
- JP
- Japan
- Prior art keywords
- retardant composition
- natural mineral
- electric wire
- flame
- magnesium hydroxide
- 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
【0001】[0001]
【産業上の利用分野】本発明は燃焼時にハロゲン化水素
ガスを発生せず、かつ吸湿性を抑えた難燃性組成物、及
び該難燃性組成物の被覆層を具えた電線、ケーブルに関
するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a flame-retardant composition which does not generate hydrogen halide gas at the time of combustion and has suppressed hygroscopicity, and an electric wire and a cable provided with a coating layer of the flame-retardant composition. It is a thing.
【0002】[0002]
【従来の技術】電線、ケーブルの燃焼時の発煙、毒性、
腐食等の二次災害を防止する目的から、例えば特開平1-
141929号公報に示されるように、被覆材に難燃性を付与
する難燃剤の一つとして、水酸化マグネシウムが使用さ
れている。2. Description of the Related Art Smoke generation, toxicity when burning electric wires and cables,
For the purpose of preventing secondary disasters such as corrosion, for example, JP-A-1-
As disclosed in Japanese Patent No. 141929, magnesium hydroxide is used as one of the flame retardants that impart flame retardancy to the coating material.
【0003】[0003]
【発明が解決しようとする課題】従来から使用されてい
る水酸化マグネシウムは、海水中のマグネシウムを原料
とするものである。これを難燃剤として使用した難燃性
組成物は、高湿度空気中に放置すると水分を吸湿し、電
線、ケーブルに被覆する際、押出機内で吸湿した水分が
発泡し、外観不良になるという問題があった。Magnesium hydroxide conventionally used is made from magnesium in seawater as a raw material. The flame-retardant composition using this as a flame retardant absorbs moisture when left in high-humidity air, and when covering electric wires and cables, moisture absorbed in the extruder foams, resulting in poor appearance. was there.
【0004】[0004]
【課題を解決するための手段】本発明は上述の問題点を
解消し、吸湿性を抑えた難燃性組成物及びそれを用いた
電線、ケーブルを提供するもので、その特徴は、水酸化
マグネシウムを主成分とする天然鉱物を粉砕し、脂肪
酸、脂肪酸金属塩、シランカップリング剤、チタネート
カップリング剤より選ばれた少なくとも1種類を主成分
とする表面処理剤を、上記天然鉱物に対して 0.5〜5重
量%添加して表面処理を施してプラスチック又はゴムに
添加し、難燃性を付与するとともに吸湿性を抑えた難燃
性組成物、及び該難燃性組成物の被覆層を具えている電
線、ケーブルにある。The present invention solves the above-mentioned problems and provides a flame-retardant composition having suppressed hygroscopicity, and an electric wire and cable using the same. A natural mineral containing magnesium as a main component is ground, and a surface treatment agent containing at least one selected from fatty acids, fatty acid metal salts, silane coupling agents, and titanate coupling agents as a main component is added to the above natural mineral. A flame-retardant composition which is added to plastic or rubber after surface treatment by adding 0.5 to 5% by weight to impart flame retardancy and suppress hygroscopicity, and a coating layer of the flame retardant composition There are electric wires and cables on the wire.
【0005】[0005]
【作用】上述の問題を解決するため、種々の水酸化マグ
ネシウムを用いて検討を行ったところ、水酸化マグネシ
ウムを主成分とする天然鉱物を原料とした水酸化マグネ
シウムが吸湿性を抑えるのにすぐれていることを見出し
た。このメカニズムに関しては不明であるが、結晶構造
等が従来品と異なっているためではないかと思われる。
なお、表面処理剤の添加量を 0.5〜5重量%と規定した
のは、 0.5重量%未満では表面処理の効果を示さず、5
重量%を越えるとコスト面で好ましくないからである。[Function] In order to solve the above-mentioned problems, studies were conducted using various magnesium hydroxides. Magnesium hydroxide made from a natural mineral containing magnesium hydroxide as a main component was excellent in suppressing hygroscopicity. I found that. Although this mechanism is unclear, it may be because the crystal structure is different from that of conventional products.
The amount of the surface treatment agent added was defined as 0.5 to 5% by weight, because the effect of the surface treatment is not shown when the amount is less than 0.5% by weight.
This is because if it exceeds the weight percentage, it is not preferable in terms of cost.
【0006】[0006]
【実施例】表1に示す各種材料を6インチオープンロー
ルで15分混練した後、ペレタイザーにて約3mm×3mm×
3mmのペレットに加工し、吸湿性を評価した。結果は表
1の通りである。[Examples] Various materials shown in Table 1 were kneaded with a 6-inch open roll for 15 minutes, and then mixed with a pelletizer to about 3 mm x 3 mm x
The pellets were processed into 3 mm pellets and the hygroscopicity was evaluated. The results are shown in Table 1.
【0007】表面処理の方法は次のように行った。 (1)スーパーミキサー内で水酸化マグネシウムを攪拌
する。 (2)水酸化マグネシウムを攪拌しながら、表面処理剤
を約5分間にわたって徐々に投入する。 (3)表面処理剤を全量投入した後、さらに約20分間攪
拌する。The surface treatment method was performed as follows. (1) Stir magnesium hydroxide in a super mixer. (2) While stirring magnesium hydroxide, the surface treatment agent is gradually added over about 5 minutes. (3) After adding all of the surface treatment agent, stir for about 20 minutes.
【0008】用いたプラスチック材及び水酸化マグネシ
ウム表面処理剤の銘柄等は次の通りである。 EEA:日本ユニカーWN−170 水酸化マグネシウム A:従来(海水法)の水酸化マグネシウム 例、協和化学キスマ5 B:従来(海水法)の水酸化マグネシウム 例、協和化学キスマ5B C:天然鉱物(ブルーサイト)を原料としてシランカッ
プリング剤で表面処理した水酸化マグネシウム 例、神島化学マグシーズN−1 シランカップリング剤=信越化学 添加量 0.1重量% D:同上をシランカップリング剤で表面処理した水酸化
マグネシウム 例、シランカップリング剤=信越化学 添加量= 0.5重
量% E:同上を脂肪酸で表面処理した水酸化マグネシウム 脂肪酸=ステアリン酸 添加量= 0.5重量% F:同上を脂肪酸金属塩で表面処理した水酸化マグネシ
ウム 例、脂肪酸金属塩=ステアリン酸亜鉛 添加量= 0.5重量%The brands of the plastic material and the magnesium hydroxide surface treatment agent used are as follows. EEA: Nippon Unicar WN-170 Magnesium hydroxide A: Conventional (seawater method) magnesium hydroxide Example, Kyowa Chemical Kisuma 5B: Conventional (seawater method) magnesium hydroxide Example, Kyowa Chemical Kisuma 5B C: Natural mineral (blue) Magnesium hydroxide surface-treated with silane coupling agent as raw material (Example), Kamijima Chemical Magsee's N-1 Silane coupling agent = Shin-Etsu Chemical 0.1 wt% D: Same as above, hydroxylated with silane coupling agent Magnesium Example, silane coupling agent = Shin-Etsu Chemical Addition amount = 0.5% by weight E: Magnesium hydroxide surface-treated with fatty acid Fatty acid = stearic acid Addition amount = 0.5% by weight F: Water surface-treated with fatty acid metal salt Magnesium oxide Example, fatty acid metal salt = zinc stearate Addition amount = 0.5% by weight
【0009】[0009]
【表1】 [Table 1]
【0010】吸湿量の測定は以下のようにして行った。
ペレット 100gを上述の試料より採取し、湿度70%のデ
シケータ中に放置し、各時間毎の水分量を測定した。水
分量はカールフィッシャー水分計にて測定した。比較例
1,2に示す従来の水酸化マグネシウムを使用したもの
は、1日後でも水分量が約300ppmと多く、30日後では約
1400ppmまで増加した。比較例は天然鉱物を用い表面処
理を施した例であるが、表面処理剤の量が少ないため、
比較例1,2と同様の傾向を示した。これに対して、実
施例1〜3は1日後の水分量が約100ppm前後と少なく、
30日後でも 350〜400ppm程度までしか水分量が増えてお
らず、吸湿性が少ないことが確認できた。The moisture absorption amount was measured as follows.
100 g of the pellet was sampled from the above sample, left in a desiccator having a humidity of 70%, and the water content at each time was measured. The water content was measured with a Karl Fischer water content meter. The ones using the conventional magnesium hydroxide shown in Comparative Examples 1 and 2 have a large water content of about 300 ppm even after 1 day, and about 30 days after about 30 ppm.
It increased to 1400ppm. The comparative example is an example where the surface treatment is performed using a natural mineral, but since the amount of the surface treatment agent is small,
The same tendency as Comparative Examples 1 and 2 was shown. On the other hand, in Examples 1 to 3, the water content after one day was as small as about 100 ppm,
Even after 30 days, the amount of water increased only up to about 350 to 400 ppm, and it was confirmed that the hygroscopicity was low.
【0011】以上は材料としてEEAを使用した場合を
示したが、エチレンプロピレンゴム、アクリルゴム、超
低密度ポリエチレン、直鎖状低密度ポリエチレン、エチ
レンビニルアセテート、エチレンメタアクリレート、エ
チレンメチルメタアクリレート等のゴム、プラスチック
材料においても、又これらの混合物に対しても同様の効
果が認められ、天然鉱物を原料とした水酸化マグネシウ
ムが吸湿性が少ないことが確認された。The case where EEA is used as the material has been shown above, but ethylene propylene rubber, acrylic rubber, ultra low density polyethylene, linear low density polyethylene, ethylene vinyl acetate, ethylene methacrylate, ethylene methyl methacrylate, etc. Similar effects were observed in rubber and plastic materials, and also in a mixture thereof, and it was confirmed that magnesium hydroxide made from a natural mineral had a low hygroscopic property.
【0012】[0012]
【発明の効果】以上説明したように、本発明の難燃性組
成物によれば、吸湿性が少なく、電線、ケーブルの製造
時に特に乾燥工程を必要としないで、外観良好な電線、
ケーブルを作成することができる。As described above, according to the flame-retardant composition of the present invention, an electric wire having a low hygroscopicity, a good appearance without requiring a drying step during the production of the electric wire or cable,
Cables can be made.
Claims (2)
鉱物を粉砕し、脂肪酸、脂肪酸金属塩、シランカップリ
ング剤、チタネートカップリング剤より選ばれた少なく
とも1種類を主成分とする表面処理剤を、上記天然鉱物
に対して 0.5〜5重量%添加して表面処理を施してプラ
スチック又はゴムに添加し難燃性を付与するとともに吸
湿性を抑えたことを特徴とする難燃性組成物。1. A surface-treating agent containing at least one selected from fatty acids, fatty acid metal salts, silane coupling agents and titanate coupling agents as a main component, which is obtained by crushing a natural mineral containing magnesium hydroxide as a main component. A flame-retardant composition comprising 0.5 to 5 wt% of the above-mentioned natural mineral, surface-treated and added to plastic or rubber to impart flame retardancy and suppress hygroscopicity.
具えていることを特徴とする電線、ケーブル。2. An electric wire or cable comprising a coating layer of the flame-retardant composition according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34144093A JP3339154B2 (en) | 1993-12-10 | 1993-12-10 | Flame retardant composition and electric wire and cable |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34144093A JP3339154B2 (en) | 1993-12-10 | 1993-12-10 | Flame retardant composition and electric wire and cable |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH07161230A true JPH07161230A (en) | 1995-06-23 |
JP3339154B2 JP3339154B2 (en) | 2002-10-28 |
Family
ID=18346102
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP34144093A Expired - Lifetime JP3339154B2 (en) | 1993-12-10 | 1993-12-10 | Flame retardant composition and electric wire and cable |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3339154B2 (en) |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998046673A1 (en) * | 1997-04-17 | 1998-10-22 | Duslo, A.S. S^¿Ala | A polymeric composite material with improved flame resistance |
US6162548A (en) * | 1997-07-23 | 2000-12-19 | Pirelli Cavi E Sistemi S.P.A. | Cables with a halogen-free recyclable coating comprising polypropylene and an ethylene copolymer having high elastic recovery |
US6255399B1 (en) | 1997-07-23 | 2001-07-03 | Pirelli Cavi E Sistemi S.P.A. | Cables with a halogen-free recyclable coating comprising polypropylene and an ethylene copolymer having high structural uniformity |
US6372344B1 (en) | 1997-07-23 | 2002-04-16 | Pirelli Cavi E Sistemi S.P.A. | Cables with a halogen-free recyclable coating comprising polypropylene and an ethylene copolymer having high elastic recovery |
US6410651B1 (en) | 1997-07-23 | 2002-06-25 | Pirelli Cavi E Sistemi S.P.A. | Cables with a halogen-free recyclable coating comprising polypropylene and an ethylene copolymer having high structural uniformity |
WO2003000822A1 (en) * | 2001-06-22 | 2003-01-03 | Asahi Kasei Kabushiki Kaisha | Particulate coated flame-retardant for polymer |
US6552112B1 (en) | 1997-07-23 | 2003-04-22 | Pirelli Cavi E Sistemi S.P.A. | Cable with self-extinguishing properties and flame-retardant composition |
JP2006111678A (en) * | 2004-10-13 | 2006-04-27 | Nippon Unicar Co Ltd | Surface-treated magnesium hydroxide, whitening-resistant flame-retardant resin composition compounded with the same, and extrusion-molded article obtained from the composition |
JP2007284702A (en) * | 2007-08-09 | 2007-11-01 | Nippon Unicar Co Ltd | Method for improving flexibility of flame retardant resin composition and extrusion-molded product improved in flexibility |
JP2008069296A (en) * | 2006-09-15 | 2008-03-27 | Jfe Mineral Co Ltd | Surface-treating agent for preparing flame retardant composition having nucleus of magnesium hydroxide grain, method for preparing flame retardant composition and flame retardant composition |
EP1942173A1 (en) * | 2005-10-25 | 2008-07-09 | Konoshima Chemical Co., Ltd. | Flame retardant, flame-retardant resin composition and molded body |
DE112007003027T5 (en) | 2006-12-12 | 2009-10-22 | AUTONETWORKS Technologies, LTD., Yokkaichi | Flame retardant resin composition, insulated wire and wiring harness |
JP2010509430A (en) * | 2006-11-10 | 2010-03-25 | セルヴィシオス インダストリアレス ペニョーレス,ソシエダッド アノニマ デ キャピタル ヴァリアブル | Method for preparing flame retardant additives used in coatings, and preparations prepared by said method |
CN102741378A (en) * | 2010-02-03 | 2012-10-17 | 株式会社自动网络技术研究所 | Fire retardant, fire retardant resin composition, and insulated electrical wire |
US8901233B2 (en) | 2010-02-03 | 2014-12-02 | Autonetworks Technologies, Ltd. | Flame retardant, flame-retardant resin composition, and insulated wire |
US20160177120A1 (en) * | 2014-12-22 | 2016-06-23 | Bridgestone Sports Co., Ltd. | Resin composition for golf balls |
JP2017002213A (en) * | 2015-06-12 | 2017-01-05 | 信越化学工業株式会社 | Fire retardant room temperature curable organopolysiloxane composition and electric and electronic component |
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JP5481917B2 (en) | 2008-06-27 | 2014-04-23 | 株式会社オートネットワーク技術研究所 | Flame retardant composition and insulated wire and wire harness using the same |
JP2010111718A (en) | 2008-11-04 | 2010-05-20 | Autonetworks Technologies Ltd | Flame retardant, flame-retardant composition, and insulated electric wire |
JP5604789B2 (en) | 2009-01-29 | 2014-10-15 | 株式会社オートネットワーク技術研究所 | Flame retardant, flame retardant resin composition and insulated wire |
JP5444740B2 (en) | 2009-02-02 | 2014-03-19 | 株式会社オートネットワーク技術研究所 | Flame retardant resin composition and insulated wire |
-
1993
- 1993-12-10 JP JP34144093A patent/JP3339154B2/en not_active Expired - Lifetime
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998046673A1 (en) * | 1997-04-17 | 1998-10-22 | Duslo, A.S. S^¿Ala | A polymeric composite material with improved flame resistance |
US6162548A (en) * | 1997-07-23 | 2000-12-19 | Pirelli Cavi E Sistemi S.P.A. | Cables with a halogen-free recyclable coating comprising polypropylene and an ethylene copolymer having high elastic recovery |
US6255399B1 (en) | 1997-07-23 | 2001-07-03 | Pirelli Cavi E Sistemi S.P.A. | Cables with a halogen-free recyclable coating comprising polypropylene and an ethylene copolymer having high structural uniformity |
US6372344B1 (en) | 1997-07-23 | 2002-04-16 | Pirelli Cavi E Sistemi S.P.A. | Cables with a halogen-free recyclable coating comprising polypropylene and an ethylene copolymer having high elastic recovery |
US6410651B1 (en) | 1997-07-23 | 2002-06-25 | Pirelli Cavi E Sistemi S.P.A. | Cables with a halogen-free recyclable coating comprising polypropylene and an ethylene copolymer having high structural uniformity |
US6552112B1 (en) | 1997-07-23 | 2003-04-22 | Pirelli Cavi E Sistemi S.P.A. | Cable with self-extinguishing properties and flame-retardant composition |
US6756447B2 (en) | 1997-07-23 | 2004-06-29 | Pierelli Cavi E Sistemi.S.P.A. | Flame-retardant polymer composition comprising polypropylene and an ethylene copolymer having high structural uniformity |
WO2003000822A1 (en) * | 2001-06-22 | 2003-01-03 | Asahi Kasei Kabushiki Kaisha | Particulate coated flame-retardant for polymer |
JP2006111678A (en) * | 2004-10-13 | 2006-04-27 | Nippon Unicar Co Ltd | Surface-treated magnesium hydroxide, whitening-resistant flame-retardant resin composition compounded with the same, and extrusion-molded article obtained from the composition |
EP1942173A1 (en) * | 2005-10-25 | 2008-07-09 | Konoshima Chemical Co., Ltd. | Flame retardant, flame-retardant resin composition and molded body |
EP1942173A4 (en) * | 2005-10-25 | 2012-04-04 | Konoshima Chemical | Flame retardant, flame-retardant resin composition and molded body |
JP2008069296A (en) * | 2006-09-15 | 2008-03-27 | Jfe Mineral Co Ltd | Surface-treating agent for preparing flame retardant composition having nucleus of magnesium hydroxide grain, method for preparing flame retardant composition and flame retardant composition |
JP2010509430A (en) * | 2006-11-10 | 2010-03-25 | セルヴィシオス インダストリアレス ペニョーレス,ソシエダッド アノニマ デ キャピタル ヴァリアブル | Method for preparing flame retardant additives used in coatings, and preparations prepared by said method |
DE112007003027T5 (en) | 2006-12-12 | 2009-10-22 | AUTONETWORKS Technologies, LTD., Yokkaichi | Flame retardant resin composition, insulated wire and wiring harness |
JP2007284702A (en) * | 2007-08-09 | 2007-11-01 | Nippon Unicar Co Ltd | Method for improving flexibility of flame retardant resin composition and extrusion-molded product improved in flexibility |
CN102741378A (en) * | 2010-02-03 | 2012-10-17 | 株式会社自动网络技术研究所 | Fire retardant, fire retardant resin composition, and insulated electrical wire |
US8901233B2 (en) | 2010-02-03 | 2014-12-02 | Autonetworks Technologies, Ltd. | Flame retardant, flame-retardant resin composition, and insulated wire |
US8907003B2 (en) | 2010-02-03 | 2014-12-09 | Autonetworks Technologies, Ltd. | Flame retardant, flame-retardant resin composition, and insulated wire |
US20160177120A1 (en) * | 2014-12-22 | 2016-06-23 | Bridgestone Sports Co., Ltd. | Resin composition for golf balls |
US9593253B2 (en) * | 2014-12-22 | 2017-03-14 | Bridgestone Sports Co., Ltd. | Resin composition for golf balls |
JP2017002213A (en) * | 2015-06-12 | 2017-01-05 | 信越化学工業株式会社 | Fire retardant room temperature curable organopolysiloxane composition and electric and electronic component |
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