JPS59202243A - Flame-retardant polyolefin resin composition - Google Patents
Flame-retardant polyolefin resin compositionInfo
- Publication number
- JPS59202243A JPS59202243A JP58078087A JP7808783A JPS59202243A JP S59202243 A JPS59202243 A JP S59202243A JP 58078087 A JP58078087 A JP 58078087A JP 7808783 A JP7808783 A JP 7808783A JP S59202243 A JPS59202243 A JP S59202243A
- Authority
- JP
- Japan
- Prior art keywords
- molybdenum
- polyolefin resin
- flame
- weight
- parts
- 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
Abstract
Description
【発明の詳細な説明】
本発明は新規な難燃性ポリオレフィン樹脂組成物に関す
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel flame retardant polyolefin resin composition.
従来よりポリオレフィン樹脂の難燃化にはノ・ロゲン系
雉燃剤が一般に用いられているか、このハロゲン系、;
jI燃剤配合の組成物シま燃焼の際に多1jにの煙を発
生させたり・・ロゲン化水素のような有毒な腐食性ガス
を発生するため、火災時に人身事故や機器腐食を発生す
るおそれが高かった。Traditionally, halogen-based flame retardants have been commonly used to make polyolefin resins flame retardant;
Compositions containing refueling agents generate a large amount of smoke when burned, and generate toxic and corrosive gases such as hydrogen chloride, so there is a risk of personal injury or equipment corrosion in the event of a fire. it was high.
燃焼時に有毒で1に食性ガスが発生しない樹脂の難燃化
方法としては、結晶水な有する無機化合物を用いる方法
か提案されているが、この場合含水無機物の難燃付与効
果か極めて倣弱であるため極く多量配合しないと所望の
難燃性が得られなかった。そのために含水無機物による
高難燃樹脂組成物には含水無機物の多量配合の際の諸問
題、即ち配合作業性、成形加工性などの低下、(幾械的
強度などの緒特性の低下かあった。As a flame retardant method for resins that does not generate poisonous or edible gases when burned, it has been proposed to use inorganic compounds containing water of crystallization, but in this case, the flame retardant effect of water-containing inorganics is extremely weak. Therefore, the desired flame retardancy could not be obtained unless a very large amount was blended. For this reason, highly flame-retardant resin compositions made of hydrated inorganic substances suffer from various problems when blending a large amount of hydrated inorganic substances, such as a decrease in compounding workability, moldability, etc., and a decrease in mechanical properties such as mechanical strength. .
本発明はかかる点に着目し、鋭意検討した結果、添加剤
の好ましい相乗作用により難燃性が向上し、よって難燃
剤の認配合量を減じ、そのことにより上記のごとき填料
の多量配合の諸問題を解決することかで゛、きたもので
、その要旨はポリオレフィン樹脂100重量部に対して
水酸化アルミニウム、水酸化マグ坏シウム、ハイドロタ
ルサイトより選ばれる含水無機物1種もし。The present invention has focused on this point, and as a result of intensive studies, it has been found that flame retardancy is improved due to the favorable synergistic effect of additives, thereby reducing the approved blending amount of flame retardant. The idea was to solve the problem, and the gist of this was to use one hydrated inorganic substance selected from aluminum hydroxide, magnesium hydroxide, and hydrotalcite per 100 parts by weight of polyolefin resin.
くは2種以上の混合物50〜200重量部、三酸化アン
チモン10〜150重量部、モリブデン化合物1〜50
重量部を配合してなることを特徴とするチI燃性ポリオ
レフィン樹脂組成物である。50 to 200 parts by weight of a mixture of two or more types, 10 to 150 parts by weight of antimony trioxide, 1 to 50 parts by weight of a molybdenum compound
This is a flammable polyolefin resin composition characterized in that it contains parts by weight.
本発明で言うポリオレフィン樹脂とは、例えばポリエチ
レン、ポリプロピレン、ポリブテン、4−メチルペンテ
ン−1重合体、エチレン・酢酸ビニル共重合体、エチレ
ン・エチルアクリレート共重合体、エチレン・プロピレ
ン共重合体、エチレン・プロピレン・ジエン三元共重合
体などの1種もしくは2種以上のブレンドであり、その
架橋化物も含む。The polyolefin resin referred to in the present invention includes, for example, polyethylene, polypropylene, polybutene, 4-methylpentene-1 polymer, ethylene/vinyl acetate copolymer, ethylene/ethyl acrylate copolymer, ethylene/propylene copolymer, ethylene/ It is a blend of one or more types of propylene/diene terpolymer, and also includes crosslinked products thereof.
またモリブデン化合物としては、特に限定されないが、
例えば三酸化モリブデン、水酸化モリブテン(Vl)
、二硫化モリブデン、酸化モリブデンアセチルアセ]・
ネート、モリブデン酸アンモニウム、モリブデン酸カリ
ウム、モリブテンカルシウム、モリブデン酸ナトリウム
などが入手しやすく一般的である。In addition, molybdenum compounds are not particularly limited, but include
For example, molybdenum trioxide, molybdenum hydroxide (Vl)
, molybdenum disulfide, molybdenum oxide acetylacetate]・
Nate, ammonium molybdate, potassium molybdate, calcium molybdate, sodium molybdate, etc. are easily available and common.
本発明において、ポリオレフィン樹脂100重量部に対
して添加物の配合量を該含水無機物を50〜200重量
部、三酸化アンチモン10〜150重量部、モリブデン
化合物1〜50重量部と夫々限定した理由はこれらの添
加物の配合量が下限量より少量の場合には、ポリオレフ
ィン樹脂への難燃付与効果が薄(、また上限量以上配合
してもその効果は飽和し経済的にメリットかないばかり
でなく、組成物の機械的強度の低下が顕著になるためで
ある。In the present invention, the content of the additives is limited to 50 to 200 parts by weight of the hydrated inorganic substance, 10 to 150 parts by weight of antimony trioxide, and 1 to 50 parts by weight of the molybdenum compound, based on 100 parts by weight of the polyolefin resin. If the amount of these additives is less than the lower limit, the flame retardant effect on the polyolefin resin will be weak (and if the amount exceeds the upper limit, the effect will be saturated and there will be no economic benefit). This is because the mechanical strength of the composition decreases significantly.
本発明の樹脂組成物にはこれらの各成分の他に、必要に
応じて架橋剤、滑剤、酸化防止剤、紫外線吸収剤、着色
剤、充填剤等を配合し得るものである。In addition to these components, the resin composition of the present invention may contain crosslinking agents, lubricants, antioxidants, ultraviolet absorbers, colorants, fillers, and the like, if necessary.
以下に本発明離燃樹脂組成物の実施例を比較例と共に示
す。Examples of the flame retardant resin composition of the present invention are shown below together with comparative examples.
表−1に記載した配合比につい−(夫々をオープンロー
ルにて100℃にて約30発温合し、帯状のシートをつ
くり、さらに160°Cにて5分プレス成形して組成物
シートをつくり所定の形状に切断し、UL−94の燃焼
試験用試料及びJISK 6301低温衝撃ぜい化試験
用試料をつくったっ
それらの試料について得られた試験結果を表−]に併0
己した。Regarding the compounding ratios listed in Table 1, each was heated in an open roll at 100°C for about 30 minutes to form a belt-shaped sheet, and then press-molded at 160°C for 5 minutes to obtain a composition sheet. UL-94 combustion test samples and JISK 6301 low-temperature impact embrittlement test samples were prepared and cut into specified shapes.The test results obtained for these samples are also shown in Table 0.
I did it myself.
表から明らかなように水酸化マダイ・シウム、水酸化ア
ルミニウムの単独配合の場合(比較例I及び2)ベース
樹脂100重量部に対して250重量部配合してもUL
−94の規定に基づ< Min燃度はV−Oにはならな
い。またこれら含水無機物&t1m三酸化アンチモンも
しくは三酸化モリブデンを単独で添加しても(比較例3
,4)やばり蕪燃度はV−Oにはならない。しかしなが
ら実施例1.2.3. sで示されるように樹脂に対す
る添加物の総和量が比較例1.2.3.4の場合よりず
っと少ないにもかかわらず実施例組成物の難燃度はいず
れも■−〇にランクされる。このことは規定した添加物
である含水無機物、三酸化アンチモノ、モリブデン化合
物の三者間に好まし7い相乗効果あることを示している
。ただし比較例5が示すように三酸化アンチモン、モリ
ブテン化合物の配合量か少ないと充分な難燃性は得られ
ない。一方衝撃ぜい化温度に注目すると実施例1.2.
3.5の衝撃ぜい化温度はいずれも一15℃Jユ下で良
好であった。さらに水酸化アルミニウムもしくは水酸化
マグネシウムを樹脂100重量部に対して250重量部
配合した比較例1,2の衝撃せい化温度は+I O”C
に対して、樹脂に対する添加物の配合量の総和の多い実
施例4の衝撃ぜい化温度の方が低いというメリットがあ
る。この理由は詳らかでないが、三酸化アンチモン、三
酸化モリブデン、二硫化モリブデンの比重か水酸化アル
ミニウム、水酸化マグネシウムの比重に比べてがなり大
きいことによる配合剤のボリューム効果によるものと推
定される。As is clear from the table, when red sea bream sium hydroxide and aluminum hydroxide are used alone (Comparative Examples I and 2), even when 250 parts by weight are added to 100 parts by weight of the base resin, the UL is still high.
Based on the provisions of -94, <Min fuel level will not become V-O. Moreover, even if these hydrated inorganic substances &t1m antimony trioxide or molybdenum trioxide are added alone (Comparative Example 3
, 4) The degree of burnout does not become V-O. However, Example 1.2.3. Although the total amount of additives to the resin is much smaller than that of Comparative Example 1.2.3.4 as shown by s, the flame retardance of the example compositions is ranked ■-〇. . This indicates that there is a favorable synergistic effect among the three specified additives, namely the hydrated inorganic substance, antimono trioxide, and the molybdenum compound. However, as shown in Comparative Example 5, sufficient flame retardancy cannot be obtained if the amounts of antimony trioxide and molybdenum compounds are too small. On the other hand, focusing on the impact embrittlement temperature, Example 1.2.
The impact embrittlement temperature of 3.5 was all good at -15°C. Furthermore, the impact hardening temperature of Comparative Examples 1 and 2, in which 250 parts by weight of aluminum hydroxide or magnesium hydroxide was added to 100 parts by weight of the resin, was +IO"C.
On the other hand, there is an advantage that the impact embrittlement temperature of Example 4, which has a larger total amount of additives to the resin, is lower. The reason for this is not clear, but it is presumed to be due to the volume effect of the compounding agents, which is caused by the specific gravity of antimony trioxide, molybdenum trioxide, and molybdenum disulfide being larger than that of aluminum hydroxide and magnesium hydroxide.
以上実施例から明らかなように、本発明の難燃性ポリオ
レフィン樹脂組成物・シまポリオレフィン樹脂本来の機
械的強度を損うことなく、しかも従来の如くハロゲン系
難燃剤を全く使用しないため燃焼時に腐食性ガスや多量
の煙を発生することもなくしかも従来にない高難燃性の
ポリオレフィン樹脂組成物であり、その工業的価値は極
めて犬なるものがある。As is clear from the examples above, the flame-retardant polyolefin resin composition of the present invention does not impair the inherent mechanical strength of the striped polyolefin resin, and because it does not use any halogen-based flame retardant as in the past, It is a polyolefin resin composition that does not generate corrosive gas or large amounts of smoke, and has unprecedented flame retardancy, and its industrial value is extremely high.
第1頁の続き 0発 明 者 藤村俊− 平塚市東へ幡5丁目1番9号古 河電気工業株式会社平塚電線製 造所内Continuation of page 1 0 shots by Shun Fujimura Hiratsuka City Higashihe Hata 5-1-9 Old Manufactured by Kawa Denki Kogyo Co., Ltd. Hiratsuka Electric Wire Co., Ltd. Inside the factory
Claims (1)
水酸化アルミニウム、水酸化マグネシウム及びハイドロ
タルサイトのいずれかの含水無機物の単独もしくは混合
物50〜200重量部、二酸化アンチモン10〜150
重量部、モリブデン化合物1〜50重量部を配合したこ
とを特徴とする難燃性ポリオレフづン樹脂組成物。(1) For 100 parts by weight of polyolefin resin,
50 to 200 parts by weight of a hydrated inorganic substance such as aluminum hydroxide, magnesium hydroxide, or hydrotalcite, 10 to 150 parts by weight of antimony dioxide
1. A flame-retardant polyolefin resin composition comprising 1 to 50 parts by weight of a molybdenum compound.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58078087A JPS59202243A (en) | 1983-05-02 | 1983-05-02 | Flame-retardant polyolefin resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58078087A JPS59202243A (en) | 1983-05-02 | 1983-05-02 | Flame-retardant polyolefin resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59202243A true JPS59202243A (en) | 1984-11-16 |
Family
ID=13652059
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58078087A Pending JPS59202243A (en) | 1983-05-02 | 1983-05-02 | Flame-retardant polyolefin resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59202243A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04175353A (en) * | 1990-07-18 | 1992-06-23 | Chisso Corp | Composite polypr0pylene material for automobile |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53104650A (en) * | 1977-02-24 | 1978-09-12 | Kyowa Kagaku Kougiyou Kk | Noncombustible thermoplastic resin composition |
JPS55104336A (en) * | 1979-02-02 | 1980-08-09 | Sumitomo Bakelite Co Ltd | Fire-retardant resin composition |
JPS5667363A (en) * | 1979-11-05 | 1981-06-06 | Furukawa Electric Co Ltd:The | Highly inorganic substance-filled flame retardant resin composition |
-
1983
- 1983-05-02 JP JP58078087A patent/JPS59202243A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53104650A (en) * | 1977-02-24 | 1978-09-12 | Kyowa Kagaku Kougiyou Kk | Noncombustible thermoplastic resin composition |
JPS55104336A (en) * | 1979-02-02 | 1980-08-09 | Sumitomo Bakelite Co Ltd | Fire-retardant resin composition |
JPS5667363A (en) * | 1979-11-05 | 1981-06-06 | Furukawa Electric Co Ltd:The | Highly inorganic substance-filled flame retardant resin composition |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04175353A (en) * | 1990-07-18 | 1992-06-23 | Chisso Corp | Composite polypr0pylene material for automobile |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4791160A (en) | Flame-retardant resin compositions | |
JPS59202243A (en) | Flame-retardant polyolefin resin composition | |
WO2002052059A1 (en) | Flame retardant polypropylene resin composition | |
JPH0118118B2 (en) | ||
JPH05509122A (en) | flame retardant composition | |
JPH046215B2 (en) | ||
JPS6327543A (en) | Flame-retardant resin composition | |
JP2898859B2 (en) | Flame retardant resin composition | |
JPS59217741A (en) | Flame-retardant polyolefin resin composition | |
JPH07149965A (en) | Flame-retardant resin composition | |
JP2717269B2 (en) | Flame retardant resin composition | |
JPS6013832A (en) | Flame-retardant ethylene-ethyl acrylate copolymer composition | |
JPH11158329A (en) | Flame-retardant resin composition | |
JPS6097510A (en) | Flame resistant electrically insulating composition | |
JPS6212005A (en) | Flame resisting electric insulator compositioin | |
JPS5971346A (en) | Flame-retardant, low-smoking polyolefin resin composition | |
JPH06220264A (en) | Flame-retardant resin composition and frame-retardant insulated wire | |
JPS624734A (en) | Flame-retarding composition | |
JPS6088048A (en) | Low-smoking flame-retardant resin composition | |
JPH01201347A (en) | Flame-retarding polyolefin resin composition | |
JPH0668928B2 (en) | Flame-retardant wire / cable | |
JPH04253747A (en) | Flame-retarding electrical-insulating composition | |
JPS5618636A (en) | Flame-retarding resin composition | |
JPH03212453A (en) | Fire-retardant resin composition | |
JPS59221345A (en) | Flame-retardant polyolefin resin composition |