JPS60219249A - Polyvinyl chloride resin composition - Google Patents

Polyvinyl chloride resin composition

Info

Publication number
JPS60219249A
JPS60219249A JP59076311A JP7631184A JPS60219249A JP S60219249 A JPS60219249 A JP S60219249A JP 59076311 A JP59076311 A JP 59076311A JP 7631184 A JP7631184 A JP 7631184A JP S60219249 A JPS60219249 A JP S60219249A
Authority
JP
Japan
Prior art keywords
parts
polyvinyl chloride
vinyl acetate
weight
chloride resin
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
JP59076311A
Other languages
Japanese (ja)
Inventor
Isamu Sekiguchi
勇 関口
Hideo Sunatsuka
砂塚 英夫
Hirotada Kobayashi
弘忠 小林
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.)
Fujikura Ltd
Original Assignee
Fujikura Ltd
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 Fujikura Ltd filed Critical Fujikura Ltd
Priority to JP59076311A priority Critical patent/JPS60219249A/en
Publication of JPS60219249A publication Critical patent/JPS60219249A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:The titled composition generating little poisonous gas on burning, made by incorporating an ethylene-vinyl acetate copolymer, a nitrile butadiene rubber, fine particulate CaCO3, a plasticizer, and a flame retardant containing no halogen into a PVC resin. CONSTITUTION:To 100pts.wt. PVC resin are incorporated 5-25pts.wt. ethylene- vinyl acetate copolymer containing at least 60wt% vinyl acetate, 5-20pts.wt. nitrile butadiene rubber, 55-80pts.wt. fine particulate CaCO3, 30-60pts.wt. plasticizer (e.g. dioctyl phthalate), and 5-30pts.wt. flame retardant containing no halogen (e.g. Sb2O3). EFFECT:A PVC resin composition having well-balanced properties such as processability, mechanical properties, low-temperature resistance, oil resistance, and flexibility can be obtained. USE:Coating material for wire and cable.

Description

【発明の詳細な説明】 く産業上の利用分野〉 本発明は、難燃性でかつ燃か、I、時における塩り女ガ
スなどの有毒ガス発生量の少ないポリ塩化ビニル樹脂混
和物に係り、特に、’l’i、I;線・ケーブルの被抜
材として有用な混和物に051するものである。
[Detailed description of the invention] Industrial application field> The present invention relates to a polyvinyl chloride resin mixture that is flame retardant and generates a small amount of toxic gas such as salt gas when burned. In particular, 'l'i, I; is used as an admixture useful as a material for drawing wires and cables.

〈背景技術とその問題点〉 近年、火災などの発生時、各種合成樹脂あるい′ はそ
れらの温和物などKより発生する有毒ガスの放田が大き
な問題どなってきており、各種の検討がなされている。
<Background technology and its problems> In recent years, when fires occur, the release of toxic gases from K such as various synthetic resins or their mild products has become a major problem, and various studies are being carried out. being done.

ポリ塩化ビニル樹脂混yF+3物においても、このよう
な観点から、各種の改善が施されてきているが、これら
の対策により、加工性、機械的特性、耐寒性、耐油性な
ど、他の特性が低下するなどの問題があった。
Various improvements have been made to polyvinyl chloride resin blends F+3 from this perspective, but these measures have improved other properties such as processability, mechanical properties, cold resistance, and oil resistance. There were problems such as a decline in

〈発明の目的〉 本発明は1.上述のようなポリ塩化ビニル樹脂混和物に
おいて、従来のものにあっては、塩酸ガスのような有毒
ガスの発生を抑えると、その他の諸特性が悪化する傾向
きなるのに鑑みてなされたものである。そして、その目
的とするところは、有毒ガスの発生を抑えると共に1そ
の他の諸特性においても良好なバランスのとれたポリ塩
化ビニル樹脂混和物を得ることにある。
<Object of the invention> The present invention has the following features: 1. This was done in view of the fact that in the conventional polyvinyl chloride resin mixtures mentioned above, if the generation of toxic gases such as hydrochloric acid gas is suppressed, other properties tend to deteriorate. It is. The purpose is to obtain a polyvinyl chloride resin mixture that suppresses the generation of toxic gases and also has a good balance in other properties.

ビニル樹脂混和物から発生する有毒ガス例えば塩酸ガス
(H6f)を少なくするkは、 (イ)、発生する塩酸ガスと化学反応を起して、火災時
温度でも塩酸ガス、塩素ガスなどを放出しな゛い物質を
生成する物質を添加すること、(′日)、ポリ塩化ビニ
ル樹脂に苅し6%ヒの位!脂と相溶性がよく、かつ他の
物性の低下管招かす、しかも塩酸ガスの発生のない他の
樹脂をブレンドして、ポリ塩化ビニル樹脂の相対混合、
tを低減させること、 が好ましいことに着目して発明されたものである。
K reduces toxic gases such as hydrochloric acid gas (H6f) generated from vinyl resin mixtures. Adding a substance that produces a substance that is 6% higher than the polyvinyl chloride resin! Relative mixing of polyvinyl chloride resin by blending with other resins that have good compatibility with fats and do not cause deterioration of other physical properties and do not generate hydrochloric acid gas,
This invention was developed focusing on the fact that it is preferable to reduce t.

そして、発生する塩酸ガスなどの捕獲物質としては、カ
ルシュラム(Ca)、パリウA(Ba)、カリウム(K
)、マグネシュウム(Mg )などの金属化合物も考え
られ石が“、好ましくは安価な微粒状の尿酸カルシュラ
ムを用いである。゛また、ブレンド樹脂としでは、エチ
レン−酢酸ビニル共重゛合体(以下1.EVAという)
、ニトリルブタジエンプム(以下、NB’Rという、)
を用いである。これら6両樹脂は溶解度指数(s、p値
)がポリ塩化とができる。
Capture substances such as generated hydrochloric acid gas include calcilum (Ca), paliu A (Ba), and potassium (K).
), magnesium (Mg), and other metal compounds are also considered, but it is preferable to use inexpensive fine granular uric acid calcium. .EVA)
, nitrile butadiene pum (hereinafter referred to as NB'R)
is used. Both of these six resins have solubility indexes (s, p values) that can be polychlorinated.

一方、電線・ケーブルの被覆材とした場合、適度の加工
性と可続性が必要なためC可塑剤を添加する。また、ポ
リ塩化ビニル樹脂の混合量の相対的な減少により、適量
の難燃剤(ハロゲン元素を含有しないもの)を混合する
。 −7 しかして、本発明の配合構成゛は、ポリ塩化ピニク樹脂
100主爪叩シと、EV’A(酢酸ビール含有景6〇−
以上のもの)5〜25重掃部と、N、 B R55〜8
0重量部と、可塑剤30〜60重量部と、難燃剤5〜3
0重景部主爪らなる。
On the other hand, when used as a coating material for electric wires and cables, C plasticizer is added because appropriate workability and fusibility are required. Furthermore, by relatively reducing the amount of polyvinyl chloride resin mixed, an appropriate amount of flame retardant (one that does not contain a halogen element) is mixed. -7 Therefore, the composition of the present invention consists of polychlorinated pinic resin 100 main nails and EV'A (containing acetic acid beer 60-
or above) 5-25 heavy sweeping section, N, B R55-8
0 parts by weight, 30 to 60 parts by weight of plasticizer, and 5 to 3 parts by weight of flame retardant.
0 Jukeibu Main Tsume Naru.

ことで、EVAiiポリ塩化ビニル404脂とりがなる
割合でも相溶し、生成された混和物に対して、不揮発性
および非移行性を伺与し、また無機物質の高充填化を可
能し、更に耐油、耐熱性の向上、および耐寒性の向上を
もたらす。しかし、−511重部未満では上記YAE付
与効果が得られず、罵た25重量部を越えると、!、+
C)アップになると共に混和物の溶融粘度−が高く次シ
、長時間押用しに支障をきたすようKな不ため、その混
合量は5・〜25重量部か好ましい。
As a result, EVAii polyvinyl chloride 404 and fat remover are compatible even at the same ratio, imparting non-volatile and non-migrating properties to the resulting mixture, and allowing for high loading of inorganic substances. Provides improved oil resistance, heat resistance, and cold resistance. However, if it is less than -511 parts by weight, the above-mentioned YAE imparting effect cannot be obtained, and if it exceeds 25 parts by weight,... , +
C) As the melt viscosity of the mixture becomes higher, the melt viscosity of the mixture becomes higher and the mixture becomes difficult to press for a long time, so the mixing amount is preferably 5 to 25 parts by weight.

EVAの上記範囲の混合により、混和物のM特性はかな
り改碧されるが、より好ましくは、とのEVAと同様、
ポリ塩化ビニル(!7J脂に対し゛C1良好な相溶・性
を有するN B ’Rを、E’VAと併用すると、諸物
件がより一層向上し、格め−Cバランスの七れた混和物
を得ることができる。とのNBRの混合量5〜20重量
部としたのは、5重量部では添加効果が得られず、20
重片部を越えると、コスト的に好ましくない上に、ポリ
塩化ビニル樹Jlftの基本的特性が失われるからであ
る。
By mixing EVA in the above range, the M properties of the mixture are considerably improved, but more preferably, as with EVA,
When NB'R, which has good compatibility and properties with polyvinyl chloride (!7J), is used in combination with E'VA, various properties are further improved, resulting in a mixture with a good grade-C balance. The reason for setting the mixing amount of NBR to 5 to 20 parts by weight is that 5 parts by weight does not have the effect of adding NBR, and 20 parts by weight cannot be obtained.
If it exceeds the overlapped section, it is not only unfavorable in terms of cost, but also the basic characteristics of the polyvinyl chloride tree Jlft will be lost.

また、辰酸カルシュウムを微粒状としたのは、塩酸ガス
などの捕獲時、表面積の増大によって大′@次反応効果
が得られるためである。そして、その混合量は、多いt
よど大きな捕獲効果が得られて好ましいわけであるが、
その量があまり大きくなると、低温特性、物理特性、加
工性、難燃性などに好ましくない点が表われるため、実
用上、55〜80重量部がよい。なお、555重部未満
では、十分な添加効果が表われない。
Furthermore, the reason why calcium citrate is made into fine particles is that when capturing hydrochloric acid gas, etc., a large '@ order reaction effect can be obtained by increasing the surface area. And the mixing amount is large t
This is preferable because it has a very large capture effect, but
If the amount is too large, unfavorable points will appear in low-temperature properties, physical properties, processability, flame retardance, etc., so 55 to 80 parts by weight is practically preferable. Note that if the amount is less than 555 parts by weight, sufficient addition effects will not be exhibited.

また、上記ETA、NBRば非抽用1非移行性で高分子
可塑剤としての効果も有するが、本混和物にお込ては、
この他に一般の可塑剤も耐容しである。例えば、フタル
酸エステル(D OP、 n −DOP、DIDPなど
)脂肪族2#M基酸エステル(DOA、DOS、Do 
Zなど)、リン酸エステA;(TCP、TOPなど)、
エポキシ可塑剤、その他、トリメリ=ul−酸系可塑剤
などが挙げられ、その添加量は、300重部未満では、
良好な加工性と可撓性が得られず、逆に、60重量部を
越えると“、゛機械的特性の低下による実用性に問題が
生じる丸め、30〜60重を部としである。
In addition, the above-mentioned ETA and NBR are non-extractable and non-migratory and have the effect as a polymer plasticizer, but in this mixture,
In addition, common plasticizers are also tolerated. For example, phthalate esters (DOP, n-DOP, DIDP, etc.), aliphatic 2#M base acid esters (DOA, DOS, Do
Z, etc.), Phosphate A; (TCP, TOP, etc.),
Examples include epoxy plasticizers, trimelli-ul-acid plasticizers, etc., and if the amount added is less than 300 parts by weight,
Good workability and flexibility cannot be obtained, and on the contrary, if the amount exceeds 60 parts by weight, problems arise in practicality due to deterioration of mechanical properties.

史忙、ハロゲン元素を含有しない難燃剤とし゛ては、例
えば三酸化アンチモン、硼酸亜鉛、水酸化アルミニウム
、水酸化マグネシウム、赤燐、リン系難燃剤(トリクレ
ジルフォスフェート、トリフェニルフォスフェートなど
)、メタホウ酸バリウムなどが挙げられ、ポリ塩化ビニ
ル樹脂の相対的混合量の減少による難燃性の低下を防ぐ
。このAき、5爪部部未満では十分な難燃性が得られず
、筺た30重上1部を越えると、4幾械的特性、耐油性
、耐熱性、力1江性などの低下のため、その添加量は、
5〜30重」11:部としである。
Examples of flame retardants that do not contain halogen elements include antimony trioxide, zinc borate, aluminum hydroxide, magnesium hydroxide, red phosphorus, and phosphorus flame retardants (tricresyl phosphate, triphenyl phosphate, etc.) , barium metaborate, etc., to prevent a decrease in flame retardancy due to a decrease in the relative amount of polyvinyl chloride resin mixed. If the thickness is less than 5 parts, sufficient flame retardancy cannot be obtained, and if it exceeds 30 parts, the mechanical properties, oil resistance, heat resistance, strength, etc. will deteriorate. Therefore, the amount added is
5 to 30 weights" 11: parts.

なお、必要により、その他の添力1げ1り例えばλ1色
剤、安定剤、潤滑剤、発泡剤など′(l?適宜添加する
ことができる。
If necessary, other additives such as a λ1 coloring agent, a stabilizer, a lubricant, a foaming agent, etc. can be added as appropriate.

〈笑施例〉 本発明のポリ塩化ビニル樹脂混第11物を下1.己のm
1表の配合により試作した。な3?、谷考のため、本発
明の条件を¥11ださない幌イ11物もれ考例としC試
作した。
<Example> The 11th polyvinyl chloride resin mixture of the present invention was prepared as shown in 1. my own m
A prototype was made using the formulation shown in Table 1. What 3? For Tani's consideration, a C prototype was made using the conditions of the present invention as an example of a hood with 11 items that do not cost 11 yen.

上記各釈、イ(1物について、4Vlr種の試験を行な
ったところ、次のεj′52表の如き結果金竹た。
When we conducted 4Vlr tests on each of the above-mentioned products, we obtained the results as shown in the following εj'52 table.

この結果から、酸素指数が30tj度で、FIjJ油性
、脆化温hxの向上していることが明確である、〈発明
の効果〉 本発明は、以上説明したように1ポリ塩化ビニル樹脂に
、塩酸ガスなどの右行ガスの発生を抑える微粒状のLA
 rllllカルシュラムよび耐油、耐熱性などの緒特
性を向上させるEVA、NBR,更には加工性、可撓性
などを向上させる可塑剤、難燃性を何方する負IL燃剤
を最適混合比で混和しであるため、各特性にバランスの
とれた優れた混和物、特に、11.線・ケーブルの被覆
材として最適のポリ塩化ビニル樹脂汎オロ物を得ること
ができる。
From this result, it is clear that the oxygen index is 30tj degrees, and the FIjJ oiliness and embrittlement temperature hx are improved. <Effects of the Invention> As explained above, the present invention provides polyvinyl chloride resin with Fine particle LA that suppresses the generation of right-handed gases such as hydrochloric acid gas
EVA and NBR that improve properties such as calslum, oil resistance and heat resistance, plasticizers that improve workability and flexibility, and negative IL fuel that improves flame retardance are mixed in the optimal mixing ratio. Therefore, an excellent mixture with well-balanced properties, especially 11. It is possible to obtain a polyvinyl chloride resin that is optimal as a covering material for wires and cables.

Claims (1)

【特許請求の範囲】[Claims] ポリ塩化ビニル樹脂100重量部と、エチレン−酢酸ビ
ニル共重合体(酢酸ビニル含有J6″60チ以上のもの
)5〜25重量部と、ニトリルブタジェンゴム5〜20
重量部と、微粒状の屍酸カルシュウム55〜80重量部
と、可塑剤30〜6034景部と、ハロゲン元素を含有
しない難撚剤5〜30重景部主爪らなるポリ塩化ビニル
樹脂混和物。
100 parts by weight of polyvinyl chloride resin, 5 to 25 parts by weight of ethylene-vinyl acetate copolymer (containing vinyl acetate J6" or more), and 5 to 20 parts by weight of nitrile butadiene rubber.
55 to 80 parts by weight of finely divided calcium chloride, 30 to 6034 parts of a plasticizer, and 5 to 30 parts of a twist retardant not containing a halogen element. .
JP59076311A 1984-04-16 1984-04-16 Polyvinyl chloride resin composition Pending JPS60219249A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59076311A JPS60219249A (en) 1984-04-16 1984-04-16 Polyvinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59076311A JPS60219249A (en) 1984-04-16 1984-04-16 Polyvinyl chloride resin composition

Publications (1)

Publication Number Publication Date
JPS60219249A true JPS60219249A (en) 1985-11-01

Family

ID=13601819

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59076311A Pending JPS60219249A (en) 1984-04-16 1984-04-16 Polyvinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPS60219249A (en)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS641849A (en) * 1987-06-23 1989-01-06 Nichilay Magnet Co Ltd Wall plate
JPH04164938A (en) * 1990-10-30 1992-06-10 Yazaki Corp Thermoplastic vinyl chloride elastomer
EP0732533A1 (en) * 1995-03-16 1996-09-18 KM Europa Metal Aktiengesellschaft Conduit having a thermally and/or acoustically insulating sleeve
EP0762041A1 (en) * 1995-09-08 1997-03-12 KM Europa Metal Aktiengesellschaft Use of a plastic coated copper pipe
CN103205070A (en) * 2013-04-12 2013-07-17 江苏领瑞新材料科技有限公司 Cold-resistant oilproof flame-retardant PVC (Polyvinyl Chloride) cable material and preparation method thereof
CN103275428A (en) * 2013-06-18 2013-09-04 张宇 Cold-resistant PVC cable material and preparation method thereof
CN103275427A (en) * 2013-06-18 2013-09-04 张宇 PVC cable material and preparation method thereof
CN103524928A (en) * 2013-09-29 2014-01-22 吴江海宏塑料制品有限公司 High-temperature-resistant gasket material and preparation method thereof
CN103524933A (en) * 2013-09-30 2014-01-22 芜湖航天特种电缆厂 Flame-retardant cable material and preparation method
CN103724885A (en) * 2014-01-10 2014-04-16 安徽瑞升电气科技有限公司 Compound cable material
CN103788430A (en) * 2014-01-15 2014-05-14 杜肯(武汉)绝热材料有限公司 Low-temperature resisting rubber-plastic foaming heat preservation material
CN104299708A (en) * 2014-11-05 2015-01-21 浙江秦山电缆有限公司 Flame-retardant and environment-friendly cable resisting high temperature, oil and acid
CN104558880A (en) * 2013-10-09 2015-04-29 北京化工大学 Transparent polyvinyl chloride material, and preparation and application thereof
JP2017069119A (en) * 2015-10-01 2017-04-06 株式会社オートネットワーク技術研究所 Composition for wire coating material and insulation wire
CN108047600A (en) * 2017-12-18 2018-05-18 宁波斯凯勒智能科技有限公司 A kind of polyvinyl chloride cable material of excellent fireproof performance and preparation method thereof
CN109280232A (en) * 2018-09-19 2019-01-29 铜陵市铜都特种线缆有限公司 A kind of high temperature-resistant cable protective cover material
JP2019070066A (en) * 2017-10-06 2019-05-09 古河電気工業株式会社 Flame-retardant hard vinyl chloride resin composition, corrosion prevention layer of power cable, flame-retardant power cable, and flame-retardant simple water-shielding power cable
CN110564024A (en) * 2018-06-05 2019-12-13 天龙伟业线缆有限公司 Flame-retardant and fire-resistant cable material and preparation method thereof
CN111117016A (en) * 2020-01-06 2020-05-08 神州节能科技集团有限公司 Low-corrosivity rubber and plastic product and preparation method thereof
CN111117017A (en) * 2020-01-06 2020-05-08 神州节能科技集团有限公司 Rubber-plastic product without short-chain chlorinated paraffin and preparation method thereof

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS641849A (en) * 1987-06-23 1989-01-06 Nichilay Magnet Co Ltd Wall plate
JPH04164938A (en) * 1990-10-30 1992-06-10 Yazaki Corp Thermoplastic vinyl chloride elastomer
EP0732533A1 (en) * 1995-03-16 1996-09-18 KM Europa Metal Aktiengesellschaft Conduit having a thermally and/or acoustically insulating sleeve
EP0762041A1 (en) * 1995-09-08 1997-03-12 KM Europa Metal Aktiengesellschaft Use of a plastic coated copper pipe
CN103205070A (en) * 2013-04-12 2013-07-17 江苏领瑞新材料科技有限公司 Cold-resistant oilproof flame-retardant PVC (Polyvinyl Chloride) cable material and preparation method thereof
CN103275428A (en) * 2013-06-18 2013-09-04 张宇 Cold-resistant PVC cable material and preparation method thereof
CN103275427A (en) * 2013-06-18 2013-09-04 张宇 PVC cable material and preparation method thereof
CN103524928A (en) * 2013-09-29 2014-01-22 吴江海宏塑料制品有限公司 High-temperature-resistant gasket material and preparation method thereof
CN103524933A (en) * 2013-09-30 2014-01-22 芜湖航天特种电缆厂 Flame-retardant cable material and preparation method
CN104558880A (en) * 2013-10-09 2015-04-29 北京化工大学 Transparent polyvinyl chloride material, and preparation and application thereof
CN103724885A (en) * 2014-01-10 2014-04-16 安徽瑞升电气科技有限公司 Compound cable material
CN103788430A (en) * 2014-01-15 2014-05-14 杜肯(武汉)绝热材料有限公司 Low-temperature resisting rubber-plastic foaming heat preservation material
CN104299708A (en) * 2014-11-05 2015-01-21 浙江秦山电缆有限公司 Flame-retardant and environment-friendly cable resisting high temperature, oil and acid
US10442949B2 (en) 2015-10-01 2019-10-15 Autonetworks Technologies, Ltd. Composition for electric wire coating material and insulated electric wire
WO2017057177A1 (en) * 2015-10-01 2017-04-06 株式会社オートネットワーク技術研究所 Wire coating material composition and insulated wire
CN108028093A (en) * 2015-10-01 2018-05-11 株式会社自动网络技术研究所 Wire covering materials composition and insulated electric conductor
JP2017069119A (en) * 2015-10-01 2017-04-06 株式会社オートネットワーク技術研究所 Composition for wire coating material and insulation wire
CN108028093B (en) * 2015-10-01 2020-06-05 株式会社自动网络技术研究所 Composition for wire coating material and insulated wire
JP2019070066A (en) * 2017-10-06 2019-05-09 古河電気工業株式会社 Flame-retardant hard vinyl chloride resin composition, corrosion prevention layer of power cable, flame-retardant power cable, and flame-retardant simple water-shielding power cable
CN108047600A (en) * 2017-12-18 2018-05-18 宁波斯凯勒智能科技有限公司 A kind of polyvinyl chloride cable material of excellent fireproof performance and preparation method thereof
CN110564024A (en) * 2018-06-05 2019-12-13 天龙伟业线缆有限公司 Flame-retardant and fire-resistant cable material and preparation method thereof
CN109280232A (en) * 2018-09-19 2019-01-29 铜陵市铜都特种线缆有限公司 A kind of high temperature-resistant cable protective cover material
CN111117016A (en) * 2020-01-06 2020-05-08 神州节能科技集团有限公司 Low-corrosivity rubber and plastic product and preparation method thereof
CN111117017A (en) * 2020-01-06 2020-05-08 神州节能科技集团有限公司 Rubber-plastic product without short-chain chlorinated paraffin and preparation method thereof

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