JPS5837039A - Low-smoking flexible polyvinyl chloride composition - Google Patents

Low-smoking flexible polyvinyl chloride composition

Info

Publication number
JPS5837039A
JPS5837039A JP13490181A JP13490181A JPS5837039A JP S5837039 A JPS5837039 A JP S5837039A JP 13490181 A JP13490181 A JP 13490181A JP 13490181 A JP13490181 A JP 13490181A JP S5837039 A JPS5837039 A JP S5837039A
Authority
JP
Japan
Prior art keywords
polyvinyl chloride
parts
plasticizer
low
flexible polyvinyl
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
Application number
JP13490181A
Other languages
Japanese (ja)
Other versions
JPH0155295B2 (en
Inventor
Hiroshi Kato
寛 加藤
Kazuhiko Konkouya
和彦 金光谷
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.)
Dainichi Nippon Cables Ltd
Original Assignee
Dainichi Nippon Cables 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 Dainichi Nippon Cables Ltd filed Critical Dainichi Nippon Cables Ltd
Priority to JP13490181A priority Critical patent/JPS5837039A/en
Publication of JPS5837039A publication Critical patent/JPS5837039A/en
Publication of JPH0155295B2 publication Critical patent/JPH0155295B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide a flexible PVC composition having suppressed smoking during combustion without deteriorating fire retardance, by mixing aluminum hydroxide, zinc borate, antimony trioxide and plasticizer therewith. CONSTITUTION:The titled compsn. is prepd. by mixing 30-80pts.wt. aluminum hydroxide, 1-15pts.wt. zinc borate, 3-30pts.wt. antimony trioxide and 20- 100pts.wt. plasticizer (e.g., trimellitate ester and/or adipate polyester having a viscosity of 150cps or above) with 100pts.wt. PVC. By mixing these components, especially by using said plasticizers, the compsn. having suppressed smoking during combustion can be obtained without deteriorating inherent properties and fire retardance of PVC.

Description

【発明の詳細な説明】 ′ 本発明は低発煙性軟質ポリ塩化ビニlし組成物に関
する。軟質ポリ塩化ビニル組成物は通常、難燃性に秀れ
ることから各種建材、室内調度あるいは電線被覆材料と
して汎用されているd! 。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a low-smoking flexible polyvinyl chloride coating composition. Soft polyvinyl chloride compositions usually have excellent flame retardancy, so they are widely used as various building materials, interior furnishings, and wire coating materials. .

その燃焼時の発煙量が他種ポリマー組成物番こ比ぺ多大
で、実火災時の安全性の観点からは必ず。
The amount of smoke produced when burned is much higher than that of other polymer compositions, so it is definitely important from the standpoint of safety in the event of an actual fire.

しも好ましい材料とは云えない現萩にある。It is currently in Hagi, which cannot be said to be a desirable material.

燃焼時発煙量を低減する最も直接的な方法は燃焼を完全
に行わしめることであるが、この方法では材料の初期難
燃性が損われるのが欠点であり、一方、他の方法はポリ
マー、組成物中の不燃性物(たとえば無機充填剤)を増
量することであるが、この場合該組成物の物性・加工性
を損がうのが通例である。
The most direct way to reduce the amount of smoke produced during combustion is to allow complete combustion, but this method has the disadvantage that the initial flame retardancy of the material is impaired, while other methods This involves increasing the amount of nonflammable substances (for example, inorganic fillers) in the composition, but this usually impairs the physical properties and processability of the composition.

本発明者らはかかる現状に鑑かみポリ塩化ビニル組成物
の所期の物性、および難燃性を低下させることなく、燃
焼時発煙性を低減する方法につき種々検討を重ねたとこ
ろ、特許請求の範囲に示した軟質ポリ塩化ビニル組成物
により所期の目的が達成しうろことを見出し本発明を完
成した。
In view of the current situation, the present inventors have conducted various studies on methods for reducing smoke generation during combustion without reducing the desired physical properties and flame retardance of polyvinyl chloride compositions, and have found that the patent claims The present invention was completed by discovering that the desired object could be achieved by using the flexible polyvinyl chloride composition shown in the above range.

本発明の特徴とするところは、ポリ塩化ビニル樹脂に水
酸化アルミニウムとホウ酸亜鉛および三酸化アンチモン
を添加し、さらに軟質可塑化するに当って、用いる本発
明の可塑剤とじてトリメリット酸エステルまたは粘度が
150ビpト以上のジカルボン酸ポリエステルおよびこ
れらの混合物を用いる、あるいはこれら成分が主成分で
ある、すなわち用いる可塑剤全量の少なくとも捧以上が
上記可塑剤である可塑剤を用いるところにある。
The feature of the present invention is that aluminum hydroxide, zinc borate, and antimony trioxide are added to polyvinyl chloride resin, and trimellitic acid ester is used as the plasticizer of the present invention when soft plasticizing the polyvinyl chloride resin. Alternatively, a dicarboxylic acid polyester having a viscosity of 150 bits or more and a mixture thereof is used, or a plasticizer in which these components are the main components, that is, at least a portion of the total amount of the plasticizer used is the above-mentioned plasticizer. .

通常、ポリ塩化ビニルの可塑剤としては、ジアルキルフ
タレート、ジアルキルアジペート、塩素化パラフィン、
塩素化脂肪酸エステルが著名であるが、本発明に於て、
難燃性および物性を損なうとAなく、燃焼時発煙性を低
減させるという目的の達成にはこれら通常の可塑剤は好
ましくなく、前記のトリメリット酸エステル、粘度15
0cp’a以上のジカルボン酸ポリエステルおよびこれ
らの混合物を用いることが必須であるいは少なくとも使
用全可塑剤中の捧以上をこれら本発明の可塑剤を用いる
ことが必須である。かかる本発明の可塑剤としてはトリ
メリット酸エステルとしてはトリーn−オクチルトリメ
リテート、トリイソオクチルトリメリテート、トリ(n
−オクチル−〇−グシル)トリメリテート、トリイソデ
シルトリメリテートが挙げられ市販品としてはたとえば
フ?イザーコーポレーシーン社(至)のモルフレックス
500.−510゜−525,−530,大日本インキ
化学社のモノサイザーW−700,−705,−71O
L、=715L。
Typically, plasticizers for polyvinyl chloride include dialkyl phthalates, dialkyl adipates, chlorinated paraffins,
Chlorinated fatty acid esters are well known, but in the present invention,
These common plasticizers are not preferable for achieving the purpose of reducing smoke generation during combustion, as they impair flame retardancy and physical properties, and the above-mentioned trimellitic acid ester, viscosity 15
It is essential to use dicarboxylic acid polyesters having 0 cp'a or more and mixtures thereof, or it is essential to use the plasticizers of the present invention at least in proportion to the total amount of plasticizers used. Examples of the plasticizer of the present invention include tri-n-octyl trimellitate, tri-isooctyl trimellitate, and tri-(n-octyl trimellitate) as trimellitic acid esters.
-octyl-〇-gucyl) trimellitate and triisodecyl trimellitate, and examples of commercially available products include Fu? Morflex 500 by Iser Corporation (To). -510° -525, -530, Dainippon Ink Chemical Co., Ltd. Monocizer W-700, -705, -71O
L, =715L.

−720が例示しうる。粘度150cps以上のジカル
ボン酸ポリエステVとしてはセパチン酸ポリエステル、
アジピン酸ポリエステル、フタル酸ポリエステルがあり
、市販品としては例えば大日本インキ化学社のポリサイ
ザーp−29,−p−202,−w・4000.−w−
2600+−w−2310゜−w−1200,−w−+
36DEL、−w−505FiLS等が挙げられる。
-720 is an example. Dicarboxylic acid polyester V having a viscosity of 150 cps or more includes sepatic acid polyester,
There are adipic acid polyesters and phthalic acid polyesters, and commercially available products include, for example, Polycizer p-29, -p-202, -w・4000 from Dainippon Ink Chemical Co., Ltd. -w-
2600+-w-2310°-w-1200,-w-+
Examples include 36DEL and -w-505FiLS.

これら本発明の可塑剤の使用量はポリ塩化ビニル樹脂1
00部当シ2o〜100部、好ましくは30〜70部の
範囲であシ、全可塑剤中の軸を超えない範囲での通常の
可塑剤を本発明の可塑剤と併用して用いてもよい。
The amount of these plasticizers used in the present invention is polyvinyl chloride resin 1
00 parts, the range is 20 to 100 parts, preferably 30 to 70 parts, and ordinary plasticizers may be used in combination with the plasticizer of the present invention within the range of the total plasticizer. good.

本発明で用いるホウ酸亜鉛は化学式2Zn0・3820
8・nH2O(n中2.5)で示されるものであればメ
ーカーの如何を問わず、市販品がそのまま用いうる。ホ
ウ酸亜鉛の使用量はポリ塩化ビニル樹脂100部当り1
〜15部、好ましくは3〜12部の範囲である。使用量
が前記範囲よ乏  し  く り小なる場合は添加効果が番実t、前記範囲より大なる
場合は添加量増大に伴なう発煙抑制効果の向上が認めら
れなくなるためそれぞれ好、iしくない。
Zinc borate used in the present invention has the chemical formula 2Zn0.3820
Any commercially available product can be used as is, regardless of the manufacturer, as long as it has the formula 8·nH2O (2.5 in n). The amount of zinc borate used is 1 per 100 parts of polyvinyl chloride resin.
-15 parts, preferably 3-12 parts. If the amount used is less than the above range, the effect of the addition will be unfavorable, and if it is greater than the above range, no improvement in smoke suppression effect will be observed as the amount added increases, which is respectively unfavorable and unfavorable. .

前記の水酸化アルミニウムは通常の意味での水酸化アル
ミニウムであればメーカーの如何を問わないが粒度が細
かいものの方が好ましいことは云うまでもない。水酸化
アルミニウムの使用量はポリ塩化ビニル樹脂100部当
り20〜100部、好ましくは30〜80部である。使
用量が上記範囲より少量ならば添加効果に乏しく、多量
々らば該組成物の物性低下を来たすためそれぞれ不適で
ある。本発明で用いる二酸化アンチモン本また通常の意
味での5b208であればよく例えばペースト状でも、
粉末状でもそ゛の形態には制限なく用い得、市販品とし
ては工ふ・アンド・チーケミカル社のサーモガード8、
−H,クラレモントポリケミカル社のD−55、ナシ1
ナルレッド社の0NOOR23A等の市販品であっても
よい。
The above-mentioned aluminum hydroxide may be manufactured by any manufacturer as long as it is aluminum hydroxide in the usual sense, but it goes without saying that those with fine particle size are preferable. The amount of aluminum hydroxide used is 20 to 100 parts, preferably 30 to 80 parts, per 100 parts of polyvinyl chloride resin. If the amount used is less than the above range, the effect of the addition will be poor, and if the amount is too large, the physical properties of the composition will be deteriorated, which is unsuitable. The antimony dioxide used in the present invention may also be 5b208 in the usual sense, for example, in the form of a paste,
It can be used in powdered form without any restrictions, and commercially available products include Kofu & Chi Chemical Company's Thermoguard 8,
-H, D-55 of Claremont Polychemical Co., pear 1
A commercially available product such as 0NOOR23A manufactured by Nalred may also be used.

本発明の組成物においては上記必須成分のほかに、次の
如き添加剤を補助的に用いることが全体の性能向上の意
味からも好ましい。
In the composition of the present invention, in addition to the above-mentioned essential components, it is preferable to supplementally use the following additives from the viewpoint of improving the overall performance.

シ化脂肪酸エステル、b)高級脂肪酸BンiよびC)バ
リウム−亜鉛系安定剤の王者併用が例示しうる。前記a
)の具体例としては大日本インキ化学社のエポサイザー
w  100.  w  1008゜−w−128、−
w−121が挙げられ、前記b)の具体例としてはステ
アリン酸バリウム、たトエば菊池色素社のB8.また前
記C)の具体例としてはアデカ・アーガス社製のMar
kLL、堺化学工業社製のLH2−66、日本インター
スタブ社製のインタスタブM7268A、−M7268
P、−M7268Rおよび−M7268Tが挙げられる
An example is a combination of silicified fatty acid ester, b) higher fatty acid B, and c) barium-zinc stabilizer. Said a
) is Epocizer w 100. of Dainippon Ink Chemical Co., Ltd. w 1008゜-w-128,-
w-121, and specific examples of b) include barium stearate and B8. Further, as a specific example of the above C), Mar
kLL, LH2-66 manufactured by Sakai Chemical Industry Co., Ltd., Interstub M7268A, -M7268 manufactured by Nippon Interstub Co., Ltd.
P, -M7268R and -M7268T.

さらに本発明の組成物には充填剤としての比較的少量の
クレー、スコーチ防止剤として比較的少量の水酸化マグ
ネシウムも必要基と応じて用いてもよい。これらクレー
、水酸化マグネシウムの使用量はポリ塩化ビニル100
部当り5〜50部程度である。
In addition, relatively small amounts of clay as a filler and magnesium hydroxide as a scorch inhibitor may also be used in the compositions of the present invention, as required. The amount of clay and magnesium hydroxide used is 100% of polyvinyl chloride.
It is about 5 to 50 parts per part.

本発明の低発煙性軟質ポリ塩化ビニル組成物には前記以
外にポリ塩化ビニルに通常の添加剤たとえば、安定11
、無機充填剤、滑剤、顔料、発泡剤あるいは軟化剤、可
塑剤“等を必要1こ応じて併用して用いても良い。また
本発明の低発煙性軟質ポリ塩化ビニIし組成物は通常の
混合方法、装置にて容易に製造し得、押出、力Vンダー
、射出等の加工方法にて任意の形状とせしめうるので、
シート、パイプ、テープ、フィルム等の様Aな形態で使
用し得、たとえば建材、内装用材料、電線被覆、粘着テ
ープ、その他各種工業・用品用に好適に用いうる。
In addition to the above-mentioned additives, the low-smoke flexible polyvinyl chloride composition of the present invention may contain additives commonly used in polyvinyl chloride, such as Stable 11
, an inorganic filler, a lubricant, a pigment, a blowing agent, a softener, a plasticizer, etc. may be used in combination as necessary.Furthermore, the low smoke-emitting flexible polyvinyl chloride I composition of the present invention is usually It can be easily manufactured using mixing methods and equipment, and can be formed into any shape using processing methods such as extrusion, force V-under, injection, etc.
It can be used in the form of sheets, pipes, tapes, films, etc., and can be suitably used, for example, in building materials, interior materials, electric wire coatings, adhesive tapes, and various other industrial and supplies applications.

以下、実施例、比較例に依り本発明を更にくわしく説明
する。
Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples.

実施例1〜8、比較例1〜4 樹脂基材として、ポリ塩化ビニル(三菱モンサント化成
製;ビニカ57H)を用い、第1表に示す各実施例およ
び比較例の組成を120℃にてロールミルで20分間均
一に混合した後、170℃にてプレス成型し厚さ3II
III+のシート状サンプルとした。次いで該サンプル
をJI8  K7201に従って難燃性評価のための限
界酸素指数(LOI)測定用の試料片としたのち上記方
法に準じてLOIを測定した。また発煙性の試験は上記
で得られた(LOI値+0.5)ポイントの酸素濃度に
てJIS  D  12Q1に示される方法に基づいて
最少光1.透過率チを求めたのち次式に基づき最大減光
係数(C%max )を算出した。
Examples 1 to 8, Comparative Examples 1 to 4 Polyvinyl chloride (manufactured by Mitsubishi Monsanto Chemicals; Vinica 57H) was used as the resin base material, and the compositions of the Examples and Comparative Examples shown in Table 1 were milled at 120°C. After uniformly mixing for 20 minutes, press molding at 170°C to a thickness of 3II.
A sheet sample of III+ was prepared. Next, the sample was used as a sample piece for measuring the limiting oxygen index (LOI) for flame retardancy evaluation according to JI8 K7201, and the LOI was measured according to the above method. In addition, the smoke generation test was conducted based on the method shown in JIS D 12Q1 at the oxygen concentration at the (LOI value + 0.5) point obtained above, with a minimum light intensity of 1. After determining the transmittance, the maximum attenuation coefficient (C%max) was calculated based on the following formula.

Ommax=(2,303/L)gof!(10口/ 
Tm i n )(式中りは光起点−0,5w、Tm1
nは最少透過率チを示す)。
Ommax=(2,303/L)gof! (10 bites/
Tm i n ) (in the formula, light origin -0.5w, Tm1
n indicates the minimum transmittance.)

得られた結果を表1に示す。The results obtained are shown in Table 1.

Claims (1)

【特許請求の範囲】 I ポリ塩化ビニル樹脂と該樹脂100部(重量部、以
下同じ)当り30〜80部の4水酸化アルミニウム、1
〜15部のホウ酸亜鉛、3〜50部の三醒化アンチモン
および20〜100部の可塑剤とからなることを特徴と
する低発煙性軟質ポリ塩化ビニル組成物。 ■ 上記可塑剤がトリメリット酸エステlしおよび/ま
たは粘度が150 CF2 B上のアジピン酸ポリエス
テルである特許請求の範囲第一項の低発煙性軟質ポリ塩
化ビニル組成物。
[Scope of Claims] I polyvinyl chloride resin and 30 to 80 parts of aluminum tetrahydroxide per 100 parts (parts by weight, same hereinafter) of the resin, 1
A low-smoking flexible polyvinyl chloride composition comprising ~15 parts of zinc borate, 3-50 parts of antimony trichloride, and 20-100 parts of a plasticizer. (2) The low-smoke flexible polyvinyl chloride composition according to claim 1, wherein the plasticizer is a trimellitic acid ester and/or an adipic acid polyester having a viscosity of 150 CF2B.
JP13490181A 1981-08-27 1981-08-27 Low-smoking flexible polyvinyl chloride composition Granted JPS5837039A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13490181A JPS5837039A (en) 1981-08-27 1981-08-27 Low-smoking flexible polyvinyl chloride composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13490181A JPS5837039A (en) 1981-08-27 1981-08-27 Low-smoking flexible polyvinyl chloride composition

Publications (2)

Publication Number Publication Date
JPS5837039A true JPS5837039A (en) 1983-03-04
JPH0155295B2 JPH0155295B2 (en) 1989-11-24

Family

ID=15139163

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13490181A Granted JPS5837039A (en) 1981-08-27 1981-08-27 Low-smoking flexible polyvinyl chloride composition

Country Status (1)

Country Link
JP (1) JPS5837039A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58168696A (en) * 1982-03-30 1983-10-05 味の素株式会社 Surfactant
JPS59213748A (en) * 1983-05-20 1984-12-03 Fujikura Ltd Vinyl chloride based resin mixture
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
EP1669405A1 (en) * 2003-09-30 2006-06-14 Asahi Denka Co., Ltd. Vinyl chloride based resin composition for vehicle
JP2013189607A (en) * 2012-03-15 2013-09-26 Lonseal Corp Low smoke polyvinyl chloride-based sheet

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58168696A (en) * 1982-03-30 1983-10-05 味の素株式会社 Surfactant
JPS59213748A (en) * 1983-05-20 1984-12-03 Fujikura Ltd Vinyl chloride based resin mixture
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
EP1669405A1 (en) * 2003-09-30 2006-06-14 Asahi Denka Co., Ltd. Vinyl chloride based resin composition for vehicle
EP1669405A4 (en) * 2003-09-30 2007-11-21 Adeka Corp Vinyl chloride based resin composition for vehicle
US7361704B2 (en) 2003-09-30 2008-04-22 Adeka Corporation Vinyl chloride resin composition for vehicles
JP2013189607A (en) * 2012-03-15 2013-09-26 Lonseal Corp Low smoke polyvinyl chloride-based sheet

Also Published As

Publication number Publication date
JPH0155295B2 (en) 1989-11-24

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