JPS5898347A - Heat-resistant, fire-retardant crosslinking blend - Google Patents
Heat-resistant, fire-retardant crosslinking blendInfo
- Publication number
- JPS5898347A JPS5898347A JP19573781A JP19573781A JPS5898347A JP S5898347 A JPS5898347 A JP S5898347A JP 19573781 A JP19573781 A JP 19573781A JP 19573781 A JP19573781 A JP 19573781A JP S5898347 A JPS5898347 A JP S5898347A
- Authority
- JP
- Japan
- Prior art keywords
- polypropylene
- styrene
- fire retardant
- heat
- fire
- 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】
本発明は、耐熱離燃性架1iIa混和物、特に、ポリグ
ロビレy(Pア)t−ベースとし九S和物に関するもの
である〇
一般に、ポリプロピレンを架橋させた場合、ポリエチレ
ン(PI)の架橋物に比較して、高度の耐熱性や優れ九
機械的特性tM費することができるが、しかし、ポリプ
ロピレンの場合、その分子構造上、架橋と同時に劣化も
進行することから、未だ十分な架橋法は確立されておら
ず、その反応において、櫨々oitt+約f:受けてい
るのが現状である。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a heat-resistant flame-retardant cross-linked 1iIa mixture, particularly a polyglobuly(P-a)t-based nine-S hydrate. In general, when polypropylene is crosslinked, Compared to crosslinked polyethylene (PI), polypropylene has a high degree of heat resistance and excellent mechanical properties, but due to its molecular structure, polypropylene deteriorates at the same time as crosslinking. However, a sufficient cross-linking method has not yet been established, and the current situation is that the reaction involves a reaction of 0.
そこで、本発明者等は、耐熱性を有しかつ十分なal1
1燃度t−有する架橋混和−を得べく、ポリプロピレン
の架橋について、檜々検討したところ、次のような結果
を得た。Therefore, the present inventors have developed a method that has heat resistance and sufficient al1.
When cross-linking of polypropylene was extensively studied in order to obtain a cross-linking compound having a flame temperature of 1, the following results were obtained.
すなわち、本角−,msは、先ず、劣化の指標として、
1lAIll物の伸びに着目し、この伸びと秦1m&と
の関係を関べたところ、ゲル分率(m定条件、120℃
、xyl・n・、詞時間浸漬、架橋され九部分がゲル化
して残留する、ため、このゲル分率がお\よその架橋度
に対応する)が(資)〜4oXで、初期値としての伸び
が300〜400 Nという満足できる架橋物を得るこ
とかでtA次。That is, the main angle −,ms is first used as an index of deterioration,
Focusing on the elongation of the 1l AIll product, we looked at the relationship between this elongation and Hata 1m&, and found that the gel fraction (m constant conditions, 120°C
, xyl・n・, after being immersed for a period of time, is crosslinked and the nine portions gel and remain, so this gel fraction (corresponding to the approximate degree of crosslinking) is ~4oX, which is the initial value. The next step is to obtain a crosslinked product with a satisfactory elongation of 300 to 400 N.
ところが、このものに燃焼試験(ULal直燃焼試験:
VW−1)に合格するまでm燃剤ta加すると、伸びは
100 !X以下に低下してしまう。However, this product underwent a combustion test (ULal direct combustion test:
If m fuel ta is added until it passes VW-1), the elongation will be 100! It will drop below X.
そこで、ポリプロピレンKJII燃剤の他に、種々の熱
可履性エラストマーを加え次ところ、架橋後の伸びt
aoo〜500 %とすることができ九〇しかし、これ
らの混和物について、耐熱性t−gべる九め、180℃
×7日の熱死J11 (OL耐熱試験の150℃級試験
に和尚する)t−行なうと、種々の熱可塑性エラストマ
ーにおいて、分子鎖に二Jl1MI合tVするものや軟
化温度の比較的低いものでは、伸び残本がθ〜3oXで
あり、伸び残率t7ON以上とするには、特定の熱可塑
性エラストマーすなワチステレジーエチレンーブチレン
ースチレンという構造tvするブロック共重合体を主成
分とする熱可塑性エラストマー(以下、ammsという
)を使用する必要があることを見い出し虎。Therefore, in addition to polypropylene KJII fuel, various thermoplastic elastomers were added, and the elongation t after crosslinking was
aoo~500%90 However, for these mixtures, the heat resistance
× 7 days heat death , the residual elongation is θ~3o We discovered that it was necessary to use plastic elastomers (hereinafter referred to as AMMS).
本発明は、このような親点に立りてなされ九もので、そ
の目的とするところは、上述のようにポリプロピレンを
ベースとし次耐熱性でかつ十分な繻燃度を有する未備混
和物を提供することにある◇
かかる本la明の峙倣燻、ポリプロピレンに離燃剤の他
に、BIAB8t−添加することにある。The present invention has been made based on the above-mentioned points, and the object thereof is to create a polypropylene-based compound having heat resistance and sufficient flammability as described above. The object of this invention is to add BIAB8T to polypropylene in addition to a flame retardant.
本発明において用いるスチレン−エチレン−ブチレン−
スチレンの構造tVする1311B8としては、特に限
にされないが、例えばクレイトン01652(商品名、
シェル化学社11)t−挙げることができる。また、J
IIm剤としては、例えは塩素系−燃剤、臭素系離燃剤
、二酸化アンチモン、硼峨匪蛤などt−使用することが
で龜る0そして、これら各組成の配合比としては、ポリ
プロピレン団〜8oムを部に対し、離燃剤はω〜120
重量部、811BBはに〜団重量部が好ましい。すなわ
ち、llAl1la剤が一重を部未満では十分な一燃性
が得られず、また120重aS會越える場合に社、その
他の骨性、例えば伸びなどが看しく低下するからである
。一方、813IO場合、20x量部未満では伸び残率
170X以上とすることができず、また5011盪藻を
越えても、それほど伸び残本の向上が期待できないから
である0
尚、本fh明においては、上記の一&組成物O他に、必
I!に応じて、酸化防止剤及び銅害防止剤等の安定剤、
果II#刑などt−配合する0そして、その場合の配合
比としては、上述のポリプロピレン、−燃剤、81BE
lの重量部数に対し、酸化防止剤および安定剤は2〜2
0重量部、架橋助剤も2〜20重量部が望宜しい。Styrene-ethylene-butylene used in the present invention
Examples of 1311B8 having the structure tV of styrene include, but are not limited to, Kraton 01652 (trade name,
Shell Chemical Co., Ltd. 11) t- can be mentioned. Also, J
As the IIm agent, for example, chlorine-based retardant, bromine-based retardant, antimony dioxide, and soybean chloride can be used.And the blending ratio of each of these compositions is polypropylene groups ~800 The retardant is ω~120
Parts by weight, 811BB, are preferably parts by weight. That is, if the llAl1la agent is less than 1 part per 1 part, sufficient flammability cannot be obtained, and if it exceeds 120 parts by part, the bone properties and other bone properties such as elongation will deteriorate undesirably. On the other hand, in the case of 813IO, if it is less than 20x parts, it is not possible to achieve a residual elongation ratio of 170x or more, and even if it exceeds 5011 parts, it is not expected to improve the elongation ratio much. In addition to the above one & composition O, it is a must! Depending on the situation, stabilizers such as antioxidants and copper inhibitors,
In that case, the blending ratio is the above-mentioned polypropylene, fuel, 81BE
2 to 2 parts by weight of antioxidants and stabilizers
0 parts by weight, and the crosslinking aid is also preferably 2 to 20 parts by weight.
また本発明の混和物の架橋手段としては、電子線照射、
化学架橋等公知の如何なるものをも利用し得るが、例え
は薄物では電子線照射による果備でよいが、厚物で線化
学的な架橋の方が好ましい〇
このようにして得られる本発明の耐熱重態性架橋混和物
の用途は骨に限定されないが、電線畿覆材などとして利
用できる他、熱収縮性チューブ、通常の成形品、シート
などとしても使用することができる。Further, as a means for crosslinking the mixture of the present invention, electron beam irradiation,
Any known chemical crosslinking may be used, but for example, for thin materials, electron beam irradiation may be used, but for thick materials, beam chemical crosslinking is preferable. The use of the heat-resistant heavy-state crosslinked mixture is not limited to bones, but it can also be used as a covering material for electric wires, as well as heat-shrinkable tubes, ordinary molded products, sheets, etc.
次に、本発明の実施例について述べる。Next, examples of the present invention will be described.
本発明の各実施例の配合比を示すと、第1表の即くで、
七のfr’ie性は#!2狭の如くである。The compounding ratio of each example of the present invention is shown in Table 1 below.
Seven's fr'ie sex is #! It is like 2 narrow.
尚、比較の喪め、ポリプロピレンのみの場合、エチレン
−α−オレフィン共重合体またはイソプレゴムを絵加し
次場合の各混和物を比較例として併示しである。For comparison, in the case of only polypropylene, the following mixtures with ethylene-α-olefin copolymer or isopre rubber added are also shown as comparative examples.
上記各機によると、本発明の各実施例において、8]l
B8を添加しであるため、伸び残率の低下が殆んどない
ことがわかる。すなわち、VW−IK合格する十分なS
撚度を有する他に、使用可能温度が150℃という高度
の耐熱性を有する混和物を得ることができる。これに対
し、ポリプロピレンのみの場合には伸びが殆んどなく、
tた、エチレン−α−オレフイy共重合体ま九はイソプ
レンゴムを添加し穴場合、熱@It試験後の伸び残率が
著しく低下することがわかる0
以上のii!明から明らかなように本発明によれば、ポ
リブーピレンに難熱剤の他に、BIIIB8七添加して
架橋させであるため、十分な廟熱度を有すると同時に、
^[40耐熱性、さらに優れ九機械的特性などを有する
ポリプロピレンをベースとした耐熱難熱性架橋混和物を
得ることがで龜る。According to each of the above-mentioned machines, in each embodiment of the present invention, 8]l
It can be seen that since B8 was added, there was almost no decrease in the residual elongation rate. That is, enough S to pass VW-IK.
In addition to having a high degree of twist, it is possible to obtain a mixture that has a high degree of heat resistance with a usable temperature of 150°C. On the other hand, when using only polypropylene, there is almost no elongation,
Furthermore, it can be seen that when isoprene rubber is added to the ethylene-α-olefin copolymer, the residual elongation after the heat test is significantly reduced. As is clear from the description, according to the present invention, in addition to the heat retardant, polybupylene is crosslinked by adding BIIIB87, so that it has a sufficient degree of heat, and at the same time,
^[40 It is now possible to obtain a heat-resistant and heat-retardant crosslinked mixture based on polypropylene that has excellent heat resistance and excellent mechanical properties.
Claims (1)
レンの構造t−有するブロック共重合体を主成分とした
熱可畿性エラストマーと、難燃剤とよりなることを特徴
とする耐熱離燃性熾lI混和物。1. A heat-resistant, flame-retardant mixture comprising a thermoplastic elastomer mainly composed of a block copolymer having the structure t- of polyethylene, styrene-ethylene-butylene-styrene, and a flame retardant.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19573781A JPS5930738B2 (en) | 1981-12-07 | 1981-12-07 | Mixture for heat-resistant and flame-retardant cross-linked polypropylene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19573781A JPS5930738B2 (en) | 1981-12-07 | 1981-12-07 | Mixture for heat-resistant and flame-retardant cross-linked polypropylene |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5898347A true JPS5898347A (en) | 1983-06-11 |
JPS5930738B2 JPS5930738B2 (en) | 1984-07-28 |
Family
ID=16346120
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19573781A Expired JPS5930738B2 (en) | 1981-12-07 | 1981-12-07 | Mixture for heat-resistant and flame-retardant cross-linked polypropylene |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5930738B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0184296A2 (en) * | 1984-11-08 | 1986-06-11 | Mobil Oil Corporation | Blends of polypropylene, polycarbonate and a saturated styrene-ethylene-butylene-styrene rubber |
KR100506756B1 (en) * | 2002-09-13 | 2005-08-08 | 현대자동차주식회사 | Composition for automobile interior materials with a high scratch-resistance |
JP2007197040A (en) * | 2006-01-25 | 2007-08-09 | Aicello Chemical Co Ltd | Stackable plastic container |
CN102492225A (en) * | 2011-11-29 | 2012-06-13 | 南京鸿瑞塑料制品有限公司 | Transparent cold resistance high melt-strength polypropylene material used for automobile expansion water tank and its preparation method |
US8956706B2 (en) | 2009-12-29 | 2015-02-17 | Saint-Gobain Performance Plastics Corporation | Flexible tubing material and method of forming the material |
CN105315603A (en) * | 2015-10-27 | 2016-02-10 | 嘉兴市博尔塑胶有限公司 | Flame-retardant thermoplastic elastomer composition |
US9987784B2 (en) | 2012-06-06 | 2018-06-05 | Saint-Gobain Performance Plastics Corporation | Thermoplastic elastomer tubing and method to make and use same |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01176539U (en) * | 1988-06-02 | 1989-12-15 | ||
JPH0332532U (en) * | 1989-08-01 | 1991-03-29 | ||
JPH03100308U (en) * | 1990-01-31 | 1991-10-21 | ||
CN107936439A (en) * | 2017-10-17 | 2018-04-20 | 国网江苏省电力公司盐城供电公司 | A kind of high tenacity flame retardant cable and its preparation process for power circuit |
-
1981
- 1981-12-07 JP JP19573781A patent/JPS5930738B2/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0184296A2 (en) * | 1984-11-08 | 1986-06-11 | Mobil Oil Corporation | Blends of polypropylene, polycarbonate and a saturated styrene-ethylene-butylene-styrene rubber |
KR100506756B1 (en) * | 2002-09-13 | 2005-08-08 | 현대자동차주식회사 | Composition for automobile interior materials with a high scratch-resistance |
JP2007197040A (en) * | 2006-01-25 | 2007-08-09 | Aicello Chemical Co Ltd | Stackable plastic container |
US8956706B2 (en) | 2009-12-29 | 2015-02-17 | Saint-Gobain Performance Plastics Corporation | Flexible tubing material and method of forming the material |
US9133332B2 (en) | 2009-12-29 | 2015-09-15 | Saint-Gobain Performance Plastics Corporation | Flexible tubing material and method of forming the material |
US9670351B2 (en) | 2009-12-29 | 2017-06-06 | Saint-Gobain Performance Plastics Corporation | Flexible tubing material and method of forming the material |
CN102492225A (en) * | 2011-11-29 | 2012-06-13 | 南京鸿瑞塑料制品有限公司 | Transparent cold resistance high melt-strength polypropylene material used for automobile expansion water tank and its preparation method |
US9987784B2 (en) | 2012-06-06 | 2018-06-05 | Saint-Gobain Performance Plastics Corporation | Thermoplastic elastomer tubing and method to make and use same |
CN105315603A (en) * | 2015-10-27 | 2016-02-10 | 嘉兴市博尔塑胶有限公司 | Flame-retardant thermoplastic elastomer composition |
Also Published As
Publication number | Publication date |
---|---|
JPS5930738B2 (en) | 1984-07-28 |
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