JPS59226049A - Polyvinyl chloride composition - Google Patents

Polyvinyl chloride composition

Info

Publication number
JPS59226049A
JPS59226049A JP10232683A JP10232683A JPS59226049A JP S59226049 A JPS59226049 A JP S59226049A JP 10232683 A JP10232683 A JP 10232683A JP 10232683 A JP10232683 A JP 10232683A JP S59226049 A JPS59226049 A JP S59226049A
Authority
JP
Japan
Prior art keywords
polyvinyl chloride
chlorinated
flame
antimony oxide
olefin
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
Application number
JP10232683A
Other languages
Japanese (ja)
Inventor
Tetsuo Hinoma
日野間 哲夫
Taku Zama
座間 卓
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP10232683A priority Critical patent/JPS59226049A/en
Publication of JPS59226049A publication Critical patent/JPS59226049A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:The titled composition having effectively flame retardance without damaging low voltaility and freeze resistance, obtained by blending polyvinyl chloride with a straight-chain alcohol phthalic ester and a chlorinated alpha-olefin as plasticizers, and antimony oxide as a flame-retardant. CONSTITUTION:100pts.wt. polyvinyl chloride is blended with 40-70pts.wt. 9-12C straight-chain alcohol phthalic ester and 5-25pts.wt. chlorinated 20-30C alpha-olefin containing 38-42wt% chlorine as plasticizers and 2-20pts.wt. antimony oxide as a flame-retardant. USE:Suitable for synchetic leather substitute for cars.

Description

【発明の詳細な説明】 本発明は、ポリ塩化ビニルに可塑剤として炭素数9〜1
2の直鎖アルコールフタル酸エステルと長鎖α−オレフ
ィンの塩素化物、難燃剤として酸化アンチモンを配合し
てなるポリ塩化ビニル組成物に関し、その目的とすると
ころは車輛用合成皮革に要求される可塑剤の特性つまシ
、低揮発性、耐寒性に極力悪影響を与えずに、塩素化炭
化水素−酸化アンチモン系で効果的に難燃化されたポリ
塩化ビニル組成物を提供することにある◎ポリ塩化ビニ
ル組成物の主なる用途に、車幅用合成皮革が挙げられる
が、いわゆる車輛用塩ビレザーは、難燃性であることは
勿論のこと、その使用される温度条件が真夏では、80
℃以上、真冬では、−40℃以下に達する場合でもフォ
ギング(可塑剤の揮発による窓ガラスの曇υ)の問題が
発生せず1゛しかも柔軟性(耐寒性)が保持されている
ことが必要である。然して低揮発性能として、120℃
×400時間の揮発減量が15−以下であることが望ま
れ、耐寒性能としては、クラッシュパーグ柔軟温度で一
40℃以下が望まれている。そのため、車輪用塩ビレザ
ーの製造に際して通常低揮発性で、耐寒性の良好な炭素
数9〜12の直鎖7/l/コール7タル酸エステルを可
塑剤として用イ、酸化アンチモンを添加することによシ
難燃化する方法が行なわれている。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides polyvinyl chloride with 9 to 1 carbon atoms as a plasticizer.
Concerning a polyvinyl chloride composition containing a linear alcohol phthalate ester (2), a chlorinated product of a long-chain α-olefin, and antimony oxide as a flame retardant, its purpose is to improve the plasticity required for synthetic leather for vehicles. Our objective is to provide a polyvinyl chloride composition that is effectively flame-retardant using a chlorinated hydrocarbon-antimony oxide system while minimizing adverse effects on properties, low volatility, and cold resistance. The main use of vinyl chloride compositions is synthetic leather for car widths, but so-called PVC leather for cars is not only flame retardant, but also has temperatures up to 80% in midsummer.
℃ or above, and even when the temperature reaches -40℃ or below, the problem of fogging (fogging of window glass due to volatilization of plasticizer) does not occur, and flexibility (cold resistance) must be maintained. It is. However, as a low volatility performance, 120℃
It is desired that the volatilization loss after 400 hours is 15 or less, and as for the cold resistance, a crushed purg softening temperature of -40°C or less is desired. Therefore, when manufacturing PVC leather for wheels, a linear 7/l/coal 7 tarate ester with a carbon number of 9 to 12, which has low volatility and good cold resistance, is usually used as a plasticizer, and antimony oxide is added. Various methods are being used to make it flame retardant.

通常、塩ビレザー等の軟質塩化ビニル樹脂組成物を難燃
化するには、可塑剤の一部を、塩素化パラフィン等の汎
用のハロゲン系緘燃性二次可塑剤に置き替え、三酸化ア
ンチモンを添加して、三酸化アンチモンとハロゲンの相
乗難燃効果によシ達成されている。
Normally, in order to make soft PVC resin compositions such as PVC leather flame retardant, part of the plasticizer is replaced with a general-purpose halogen-based flammable secondary plasticizer such as chlorinated paraffin, and antimony trioxide This is achieved through the synergistic flame retardant effect of antimony trioxide and halogen.

然るに、塩素化ノ母ラフインとして揮発性の少ない、炭
素数20〜30のツク・・ラフインワックスを原料とし
た品種にあっては、耐寒性が悪く、他方耐寒性の良好な
炭素#!ilO〜18のn−パラフィンを原料とした品
種にあっては、揮発性が大きいという欠点がある。その
ため、車輛用レゾ−のように特に低揮発性、耐寒性を要
求される分野において使用するのに不適当であった。
However, varieties made from rough-in wax with a carbon number of 20 to 30, which has low volatility as a chlorinated rough-in, have poor cold resistance, while carbon #!, which has good cold resistance, has poor cold resistance. Varieties made from n-paraffin of ilO~18 have the disadvantage of high volatility. Therefore, it was unsuitable for use in fields where low volatility and cold resistance are particularly required, such as automotive resols.

本発明者はポリ塩化ビニル組成物の難燃化を炭F[9〜
12(7[j鎖アルコールフタル酸エステル、塩素化炭
化水素、酸化アンチモン系で種々検討した結果、二次可
塑剤として炭素数20〜30のα−オレフィンを塩素含
有量38〜42チに塩素化して得られるα−オレフィン
塩素化物を用い、酸化アンチモンを配合することによシ
、可塑剤として使用される炭素数9〜12の直鎖アルコ
ールフタル酸エステルの持つ低揮発性で耐寒性にすぐれ
ているという特性を損うことなく、難燃性の優れたポリ
塩化ビニル組成物が得られることを見い出した。又ポリ
塩化ビニルに可塑剤として炭素数9〜12の直鎖アルコ
ールフタル酸エステルを配合してなる7]?す塩化ビニ
ル組成物を酸化アンチモン単独で難燃化する方法と比較
して、上記α−オレフィン塩素化物を二次可塑剤として
更に配合することによって′高価な炭素数9〜12の直
鎖アルコールフタル酸エステル及び酸化アンチモン夫々
の使用量を減少することも可能である。
The present inventors have proposed flame retardant polyvinyl chloride compositions using charcoal F[9-
12 (7 [As a result of various studies on J-chain alcohol phthalate esters, chlorinated hydrocarbons, and antimony oxide systems, we found that α-olefins having 20 to 30 carbon atoms were chlorinated to have a chlorine content of 38 to 42% as a secondary plasticizer. By using a chlorinated α-olefin obtained by adding antimony oxide, it is possible to achieve the low volatility and cold resistance of linear alcohol phthalate esters with 9 to 12 carbon atoms, which are used as plasticizers. It has been discovered that a polyvinyl chloride composition with excellent flame retardancy can be obtained without impairing the properties of polyvinyl chloride.Also, by blending linear alcohol phthalate ester having 9 to 12 carbon atoms as a plasticizer with polyvinyl chloride. Compared to the method of making a vinyl chloride composition flame retardant using antimony oxide alone, by further blending the above-mentioned α-olefin chloride as a secondary plasticizer, it is possible to make the vinyl chloride composition flame retardant. It is also possible to reduce the amounts of each of the 12 linear alcohol phthalates and antimony oxide used.

α−オレフィンにあっても炭素数が18以下のもの及び
炭素数20〜30で塩素含有量38%未満のものは揮発
性が大きく、共用される要素数9〜12の直鎖アルコー
ルフタル酸エステルの偽れた低揮発性を損う。又炭素数
20〜3oのものにあっても塩素含有量が43g6以上
のもの及び炭素数32以上のものにあってはその塩素含
有量にかかわりなく、炭素数9〜12の直鎖アルコール
フタル酸エステルの優れた耐寒性を損うため、低揮発性
で、耐寒性の要求される車輛用d?す塩化ビニル組成物
の難燃化に適さない。
Even among α-olefins, those with 18 or less carbon atoms and those with 20 to 30 carbon atoms and less than 38% chlorine content are highly volatile, and linear alcohol phthalate esters with 9 to 12 elements are commonly used. Impairs the false low volatility of. In addition, even if the carbon number is 20 to 3 o, the chlorine content is 43g6 or more, and if the carbon number is 32 or more, regardless of the chlorine content, linear alcohol phthalic acid with a carbon number of 9 to 12 Because it impairs the excellent cold resistance of ester, d? is used for vehicles that require low volatility and cold resistance. It is not suitable for making flame retardant vinyl chloride compositions.

本発明は、かかる知見に基づいてなされたもので、ポリ
塩化ビニル100重量部に対して、(4)可塑剤として
炭素数9〜12の直鎖アルコールフタル酸エステル40
〜70重量部、炭素数20〜30で塩素含有量38〜4
2%のα−オレフィン塩素化物5〜25重量部、(B)
 m燃剤として酸化アンチモン2〜20重量部を配合し
てなる低揮発性で、耐寒性に優れ、かつ難燃化されたポ
リ塩化ビニル組成物である。
The present invention was made based on such knowledge, and (4) 40 parts by weight of linear alcohol phthalate having 9 to 12 carbon atoms as a plasticizer to 100 parts by weight of polyvinyl chloride.
~70 parts by weight, carbon number 20-30, chlorine content 38-4
5 to 25 parts by weight of 2% α-olefin chloride, (B)
This is a low volatility, excellent cold resistance, and flame retardant polyvinyl chloride composition which contains 2 to 20 parts by weight of antimony oxide as a flame agent.

本発明に使用する炭素数9〜12の直鎖アルコールフタ
ル酸エステルとしては、ジノニルフタレート、ジデシル
フタレート、ジラウリルフタレート、ジラウリルフタレ
ート及びこれらの混合物が挙げられる。これらに適合す
る製品としてrDUPJ(新日本理化■製)、rPL2
00J (三菱瓦斯化学■製)、rPL911PJ  
(シェル化学展)及び「ビニサイザー124J (花王
石鹸■製)が挙げられる。
Examples of the linear alcohol phthalate having 9 to 12 carbon atoms used in the present invention include dinonyl phthalate, didecyl phthalate, dilauryl phthalate, dilauryl phthalate, and mixtures thereof. Products that meet these requirements include rDUPJ (manufactured by New Japan Chemical Co., Ltd.) and rPL2.
00J (manufactured by Mitsubishi Gas Chemical), rPL911PJ
(Shell Chemical Exhibition) and Vinicizer 124J (manufactured by Kao Soap).

又、本発明において使用される炭素数20〜30のα−
オレフィン塩素化物の原料α−オレフィンとしては、合
成洗剤用に製造されるα−オレフィンの副産物として得
られ、単品又は混合物として使用される。例えば、混合
物としては三菱化成工業■製「ダイヤレフ208」が挙
げられる。α−オレフィン塩素化物はα−オレフィンを
加熱溶融せしめた状態で塩素によ938〜42%塩素化
させることによシ容易に製造取得することができる。
Further, α- having 20 to 30 carbon atoms used in the present invention
α-olefin, a raw material for chlorinated olefins, is obtained as a by-product of α-olefin produced for synthetic detergents, and is used singly or as a mixture. For example, examples of the mixture include "Diaref 208" manufactured by Mitsubishi Chemical Corporation. The α-olefin chloride can be easily produced by chlorinating 938 to 42% of α-olefin in a heated and melted state with chlorine.

本発明における酸化アンチモンとは三酸化アンチモン又
は五酸化アンチモンをいう。
Antimony oxide in the present invention refers to antimony trioxide or antimony pentoxide.

又、上述の成分の他に、更に必要に応じて顔料、充填剤
、帯電防止剤、表面処理剤、紫外線吸収剤、発泡剤、安
定剤、抗酸化剤等を配合することは何等差支えない。
In addition to the above-mentioned components, there is no problem in adding pigments, fillers, antistatic agents, surface treatment agents, ultraviolet absorbers, foaming agents, stabilizers, antioxidants, etc. as necessary.

本発明において各成分の配合量を限定したのは、この範
囲をはずれると、充分な低揮発性、1岨寒性、難燃性が
得られなくなるからである。
The reason why the amount of each component is limited in the present invention is that if it deviates from this range, sufficient low volatility, cold resistance, and flame retardance cannot be obtained.

次に実施例によシ具体的に説明する。Next, a detailed explanation will be given using an example.

実施例 下表に示す各成分を160℃の混線ロールにて混練し、
プレス成型して、1鰐厚のシートを得た。
Example Each component shown in the table below was kneaded using a mixed wire roll at 160°C.
Press molding was performed to obtain a sheet with a thickness of one crocodile.

このシートについて難燃性(酸素指数)、揮発性(12
0℃、400時間の揮発域:1t)、機械特性、熱老化
特性等の試験を行ない、その結果を同表に示した。
Regarding this sheet, flame retardancy (oxygen index), volatility (12
Tests were conducted on the volatile range (1t), mechanical properties, heat aging properties, etc. at 0°C for 400 hours, and the results are shown in the table.

上表から明らかなように、本発明によれば、シートの揮
発減量を増大させることなく、かつ耐寒性や機械特性を
低下させることなく、難燃性(酸素指数)を向上させる
ことができる上に炭素数9〜12の直鎖アルコールフタ
ル酸エステル及び三酸化アンチモンの使用量を減少させ
ても良好な難燃性が維持されることから、車輛用合成皮
革として、供するのに極めて好適であることが了解され
よう。
As is clear from the table above, according to the present invention, the flame retardance (oxygen index) can be improved without increasing the volatilization loss of the sheet and without reducing the cold resistance or mechanical properties. Good flame retardancy is maintained even if the amount of linear alcohol phthalate having 9 to 12 carbon atoms and antimony trioxide is reduced, making it extremely suitable for use as synthetic leather for vehicles. That will be understood.

特許出願人 味の素株式会社Patent applicant: Ajinomoto Co., Inc.

Claims (1)

【特許請求の範囲】[Claims] ポリ塩化ビニル100重量部に対して、(4)可塑剤と
して炭素数9〜12の直鎖アルコールフタル酸エステル
40〜70重量部と炭素数20〜30で塩素含有量38
〜42チのα−オレフィン塩素化物5〜25重量部、及
び(B) M燃剤として酸化アンチモン2〜20重量部
を配合してなるポリ塩化ビニル組成物。
With respect to 100 parts by weight of polyvinyl chloride, (4) 40 to 70 parts by weight of linear alcohol phthalate ester having 9 to 12 carbon atoms as a plasticizer and chlorine content of 38 parts by weight with 20 to 30 carbon atoms.
A polyvinyl chloride composition comprising 5 to 25 parts by weight of a chlorinated α-olefin of 1 to 42%, and 2 to 20 parts by weight of antimony oxide as the (B) M refueling agent.
JP10232683A 1983-06-08 1983-06-08 Polyvinyl chloride composition Pending JPS59226049A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10232683A JPS59226049A (en) 1983-06-08 1983-06-08 Polyvinyl chloride composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10232683A JPS59226049A (en) 1983-06-08 1983-06-08 Polyvinyl chloride composition

Publications (1)

Publication Number Publication Date
JPS59226049A true JPS59226049A (en) 1984-12-19

Family

ID=14324417

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10232683A Pending JPS59226049A (en) 1983-06-08 1983-06-08 Polyvinyl chloride composition

Country Status (1)

Country Link
JP (1) JPS59226049A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017206635A (en) * 2016-05-20 2017-11-24 矢崎総業株式会社 Resin composition and insulated wire using the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017206635A (en) * 2016-05-20 2017-11-24 矢崎総業株式会社 Resin composition and insulated wire using the same
CN107400305A (en) * 2016-05-20 2017-11-28 矢崎总业株式会社 Resin combination and the insulated electric conductor using the resin combination

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