JP2543384B2 - Flame retardant resin composition - Google Patents
Flame retardant resin compositionInfo
- Publication number
- JP2543384B2 JP2543384B2 JP62333280A JP33328087A JP2543384B2 JP 2543384 B2 JP2543384 B2 JP 2543384B2 JP 62333280 A JP62333280 A JP 62333280A JP 33328087 A JP33328087 A JP 33328087A JP 2543384 B2 JP2543384 B2 JP 2543384B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- flame
- resin composition
- flame retardant
- 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.)
- Expired - Lifetime
Links
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は柔軟材料、特にポリエーテルブロックアミド
の難燃化に関し、更に詳しくは、ポリエーテルブロック
アミドの弾性および柔軟性を損なわず、優れた難燃性を
有する樹脂組成物に関する。TECHNICAL FIELD The present invention relates to a flame-retardant material for a flexible material, in particular, a polyether block amide, and more specifically, it does not impair the elasticity and flexibility of the polyether block amide and is excellent. The present invention relates to a flame-retardant resin composition.
〔従来の技術〕 ポリエーテルブロックアミド樹脂は、組成中のナイロ
ン成分、ポリエーテル成分の比率を変化させる事により
柔軟性や諸性質を自在に変化せしめる事のできる、優れ
た共重合樹脂であり、この優れた特徴を生かして多分野
に使用されている。しかし、難燃性が劣るため、難燃性
を要求する分野、例えば、自動車、電線被覆、チューブ
への適用が困難であった。現在、この分野に対応してい
る難燃化樹脂は、ポリ塩化ビニル、ポリエチレンを主体
とするもので、弾性の点で劣るものであった。[Prior Art] Polyether block amide resin is an excellent copolymer resin that can be freely changed in flexibility and various properties by changing the ratio of the nylon component and the polyether component in the composition, It is used in various fields by taking advantage of this excellent feature. However, since it has poor flame retardancy, it has been difficult to apply it to fields requiring flame retardancy, such as automobiles, wire coatings, and tubes. At present, flame-retardant resins compatible with this field are mainly composed of polyvinyl chloride and polyethylene, and have poor elasticity.
ポリエーテルブロックアミド樹脂を難燃化する試みと
して、通常のポリアミド、ポリエステル等に用いられる
難燃剤、例えば、メラミン系、シアヌル酸系、臭素系あ
るいはアンチモン系の難燃剤を添加することが行なわれ
ているが、いずれも難燃効果が小さかったり、また難燃
性は得られても、ポリエーテルブロックアミド樹脂の弾
性や柔軟性が損なわれる欠点があった。As an attempt to make the polyether block amide resin flame-retardant, it is common to add flame retardants used for polyamide, polyester, etc., for example, melamine-based, cyanuric acid-based, bromine-based or antimony-based flame retardants. However, all of them have a drawback that the flame-retardant effect is small, or even if the flame-retardant property is obtained, the elasticity and flexibility of the polyether block amide resin are impaired.
本発明はかかる従来技術の問題点を解決するものであ
る。The present invention solves the problems of the prior art.
上記問題点を解決するため、本発明は次の手段をと
る。In order to solve the above problems, the present invention takes the following means.
即ち、本発明の難燃性樹脂組成物は、ショア硬度25〜
80Dのポリエーテルブロックアミド50〜80重量%および
分子量50,000〜200,000のポリエチレンを主鎖とする塩
素含量30〜40重量%の塩素化ポリエチレン20〜50重量%
からなる樹脂組成物100重量部に対し、安定剤0.5〜10重
量部、臭素系難燃剤10〜50重量部および三酸化アンチモ
ン10〜30重量部を溶融混練することを特徴とするもので
ある。That is, the flame-retardant resin composition of the present invention has a Shore hardness of 25 to
80D polyether block amide 50 to 80% by weight and polyethylene having a molecular weight of 50,000 to 200,000 as the main chain and chlorine content of 30 to 40% by weight chlorinated polyethylene 20 to 50% by weight
0.5 to 10 parts by weight of a stabilizer, 10 to 50 parts by weight of a brominated flame retardant, and 10 to 30 parts by weight of antimony trioxide are melt-kneaded with 100 parts by weight of a resin composition consisting of.
以下、本発明の構成を具体的に説明する。 Hereinafter, the configuration of the present invention will be specifically described.
本発明で言うポリエーテルブロックアミドとはポリア
ミドとポリエーテルをエステル結合でフロック共重合し
たものであり、ポリアミドとしてはナイロン6,ナイロン
66,ナイロン11,ナイロン12等が用いられ、ポリエーテル
としてはポリエチレングリコール、ポリプロピレングリ
コール、ポリテトラメチレングリコール等を用いること
ができる。また、ポリアミドとポリエーテルをブロック
共重合させる方法としては末端カルボン酸のポリアミド
プレポリマーとポリエーテルを反応させる方法、あるい
はポリアミド形成原料、ジカルボン酸およびポリエーテ
ルを一括反応させる方法等、種々あるが、本発明におい
てはいずれのものでもよい。このポリエーテルブロック
アミド樹脂はポリアミド成分の種類、量、およびポリエ
ーテルの種類、量によって硬さが異なるが本発明におい
てはショアDが25〜80のものを対象とする。The polyether block amide referred to in the present invention is a block copolymer of polyamide and polyether with an ester bond, and examples of polyamide include nylon 6 and nylon.
66, nylon 11, nylon 12, etc. are used, and as the polyether, polyethylene glycol, polypropylene glycol, polytetramethylene glycol, etc. can be used. Further, as a method of block-copolymerizing polyamide and polyether, there are various methods such as a method of reacting a polyamide prepolymer of a terminal carboxylic acid with a polyether, or a method of collectively reacting a polyamide-forming raw material, a dicarboxylic acid and a polyether, In the present invention, any one may be used. The hardness of the polyether block amide resin varies depending on the type and amount of the polyamide component and the type and amount of the polyether, but the Shore D of the present invention is 25-80.
本発明における塩素化ポリエチレンは分子量が50,000
〜200,000のポリエチレンを主鎖とし、塩素含量が30〜4
0重量%である必要がある。この塩素化ポリエチレンは
柔軟性を有するものである。The chlorinated polyethylene in the present invention has a molecular weight of 50,000.
~ 200,000 polyethylene main chain, chlorine content 30 ~ 4
Must be 0% by weight. This chlorinated polyethylene has flexibility.
ポリエーテルブロックアミドと塩素化ポリエチレンの
配合割合は50〜80/50〜20であり、ポリエーテルブロッ
クアミドが50重量%未満では弾性に欠け、80重量%を越
えると難燃化が困難となる。The blending ratio of the polyether block amide and the chlorinated polyethylene is 50-80 / 50-20. When the polyether block amide is less than 50% by weight, elasticity is lacking, and when it exceeds 80% by weight, flame retardancy becomes difficult.
安定剤としては特にエポキシ化大豆油、あるいは12−
ヒドロキシステアリン酸マグネシウムあるいはこれらの
混合物が好ましい。これらの安定剤はアミド基と塩素の
反応を抑制し、安定な樹脂組成物を与える。Epoxidized soybean oil, or 12-
Magnesium hydroxystearate or mixtures thereof are preferred. These stabilizers suppress the reaction between amide groups and chlorine and give a stable resin composition.
難燃剤としては臭素系の化合物が必要で、例えばデカ
ブロムジフェニルエーテル、臭素化オリゴカーボネー
ト、臭素化ビスフェノールA型難燃剤を用いることがで
きる。A bromine-based compound is necessary as the flame retardant, and for example, decabrom diphenyl ether, brominated oligocarbonate, brominated bisphenol A type flame retardant can be used.
また、難燃助剤として三酸化アンチモンを添加する必
要がある。Further, it is necessary to add antimony trioxide as a flame retardant aid.
これら添加剤の添加量は前記樹脂100重量部に対し、
安定剤0.5〜10重量部、好ましくは1〜5重量部、難燃
材10〜50重量部、好ましくは20〜40重量部、三酸化アン
チモン10〜30重量部、好ましくは15〜25重量部である。The amount of these additives added is 100 parts by weight of the resin,
Stabilizer 0.5 to 10 parts by weight, preferably 1 to 5 parts by weight, flame retardant 10 to 50 parts by weight, preferably 20 to 40 parts by weight, antimony trioxide 10 to 30 parts by weight, preferably 15 to 25 parts by weight is there.
なお、本発明においては、上記の他、本発明の効果を
損なわない程度に他の樹脂、補強剤、充填剤、着色等を
添加してもよい。In the present invention, other than the above, other resins, reinforcing agents, fillers, colorings and the like may be added to the extent that the effects of the present invention are not impaired.
以下、実施例を挙げて本発明を具体的に説明する。 Hereinafter, the present invention will be described specifically with reference to examples.
実施例1 ポリエーテルブロックアミド樹脂として“PEBAX"6333
(ショアD63,ATO社製)を用い、塩素化ポリエチレンと
してはショアA57、分子量約150,000〜200,000、Cl分40
%のものAとショアD67、分子量50,000〜100,000、Cl分
40%のものBを用いた。Example 1 "PEBAX" 6333 as a polyether block amide resin
(Shore D63, manufactured by ATO), as chlorinated polyethylene, Shore A57, molecular weight about 150,000-200,000, Cl content 40
% A and Shore D67, molecular weight 50,000-100,000, Cl content
40% B was used.
添加剤は下記のものを用いた。 The following additives were used.
臭素系難燃剤:臭素化オリゴカーボネート 難燃助剤:Sb2O3 安定剤:エポキシ化大豆油 上記の混合物を所定量、2軸混練機で溶融混練しペレ
ットにした後、所定の厚みのシートを作り、難燃テスト
を行ない表1の結果を得た。Brominated flame retardant: Brominated oligocarbonate Flame retardant aid: Sb 2 O 3 Stabilizer: Epoxidized soybean oil The above mixture is melt kneaded with a twin-screw kneader to form pellets, and then a sheet with a predetermined thickness A flame retardant test was conducted and the results shown in Table 1 were obtained.
なお、難燃性テストはUL94の値で示した。 In addition, the flame retardancy test was shown by the value of UL94.
実施例2 実施例1のNo.8の組成物100重量部に対し、ナイロン1
1を10,20,25部を混練した組成物の厚さ1/32inのシート
で難燃性テストを行なった結果、いずれもUL94のV−0
に合格した。 Example 2 To 100 parts by weight of the composition No. 8 of Example 1, 1 part of nylon was used.
As a result of a flame retardancy test using a 1 / 32-in thick sheet of a composition obtained by kneading 10, 20, and 25 parts of 1 with each other, UL94 V-0
Passed.
本発明はポリエーテルブロックアミドに塩素化ポリエ
チレンをブレンドし、これに所定の難燃化剤を添加する
ものであり、その結果、弾性を損なうことなく、難燃性
を向上させることができる。According to the present invention, polyether block amide is blended with chlorinated polyethylene and a predetermined flame retardant is added to the blend, and as a result, flame retardancy can be improved without impairing elasticity.
Claims (1)
クアミド50〜80重量%および分子量50,000〜200,000の
ポリエチレンを主鎖とする塩素含量30〜40重量%の塩素
化ポリエチレン20〜50重量%からなる樹脂組成物100重
量部に対し、安定剤0.5〜10重量部、臭素系難燃剤10〜5
0重量部および三酸化アンチモン10〜30重量部を溶融混
練してなる難燃性樹脂組成物。1. Consists of 50 to 80% by weight of a polyether block amide having a Shore hardness of 25 to 80D, and 20 to 50% by weight of chlorinated polyethylene having a chlorine content of 30 to 40% by weight with polyethylene having a molecular weight of 50,000 to 200,000 as a main chain. Stabilizer 0.5 to 10 parts by weight, brominated flame retardant 10 to 5 per 100 parts by weight of the resin composition.
A flame-retardant resin composition obtained by melt-kneading 0 parts by weight and 10 to 30 parts by weight of antimony trioxide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62333280A JP2543384B2 (en) | 1987-12-29 | 1987-12-29 | Flame retardant resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62333280A JP2543384B2 (en) | 1987-12-29 | 1987-12-29 | Flame retardant resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01174558A JPH01174558A (en) | 1989-07-11 |
JP2543384B2 true JP2543384B2 (en) | 1996-10-16 |
Family
ID=18264332
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62333280A Expired - Lifetime JP2543384B2 (en) | 1987-12-29 | 1987-12-29 | Flame retardant resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2543384B2 (en) |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5693740A (en) * | 1979-12-27 | 1981-07-29 | Dainichi Nippon Cables Ltd | Flame-retarding rubber composition |
JPS59206460A (en) * | 1983-05-11 | 1984-11-22 | Dainippon Ink & Chem Inc | Flame-retardant polyamide resin composition |
-
1987
- 1987-12-29 JP JP62333280A patent/JP2543384B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH01174558A (en) | 1989-07-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6924825B2 (en) | Flame-retardant polyester composition | |
JP2003510396A (en) | Flame retardant thermoplastic composition with improved properties | |
GB1602692A (en) | Thermoplastic moulding compositions based on polyamides obtained from w-aminocarboxylic acids or lactams of more than 10 carbon atoms and possessing flexibility and low temperature impact strength | |
JP3264773B2 (en) | Thermoplastic resin composition | |
JPH08333511A (en) | Heat-stable and weather-resistant polyamide molding composition | |
JP2543384B2 (en) | Flame retardant resin composition | |
JPH0411647A (en) | Vinyl chloride resin composition | |
JPH064755B2 (en) | Flame-retardant aromatic polyester composition | |
JP3235378B2 (en) | PBT resin molding material | |
EP0639623B1 (en) | Thermoplastic resin composition | |
JP3801656B2 (en) | Flame retardant polypropylene resin composition | |
JP3388649B2 (en) | Polyester resin composition | |
JPH0329822B2 (en) | ||
JPS62252454A (en) | Fire retardant polyamide material | |
JPH08245875A (en) | Flame-retardant polyamide resin composition and its production | |
JP2669921B2 (en) | Surface mount compatible electronic components made of flame retardant resin composition | |
JP4034831B2 (en) | Flame retardant polyester resin composition with improved tracking resistance | |
JPS5817150A (en) | Flame-retardant polyester composition | |
JP3801657B2 (en) | Flame retardant polypropylene resin composition | |
JP3010455B2 (en) | Resin composition with excellent antistatic properties | |
JPH0428762A (en) | New composition | |
JPS60260646A (en) | Polyester resin composition | |
JPS60149644A (en) | Flame-retardant resin composition | |
JPH0678476B2 (en) | Polybutylene terephthalate resin composition | |
JPH0220551A (en) | Injection-moldable polyester resin composition |