JPH08134301A - Vinyl chloride resin composition - Google Patents

Vinyl chloride resin composition

Info

Publication number
JPH08134301A
JPH08134301A JP6298938A JP29893894A JPH08134301A JP H08134301 A JPH08134301 A JP H08134301A JP 6298938 A JP6298938 A JP 6298938A JP 29893894 A JP29893894 A JP 29893894A JP H08134301 A JPH08134301 A JP H08134301A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
pts
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
Application number
JP6298938A
Other languages
Japanese (ja)
Inventor
Hitoshi Murata
仁 村田
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.)
Tsutsunaka Plastic Industry Co Ltd
Original Assignee
Tsutsunaka Plastic Industry Co 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 Tsutsunaka Plastic Industry Co Ltd filed Critical Tsutsunaka Plastic Industry Co Ltd
Priority to JP6298938A priority Critical patent/JPH08134301A/en
Publication of JPH08134301A publication Critical patent/JPH08134301A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: To obtain a vinyl chloride resin composition having good heat resistance and a synergistically excellent smoking-preventing effect even in a high temperature processing condition by adding both a specific molybdenum compound and magnesium hydroxide to a vinyl chloride resin. CONSTITUTION: This composition comprises (A) 100 pts.wt. of a vinyl chloride resin, (B) >=1 pt.wt. of a molybdenum compound selected from molybdenum oxide and ammonium molybdate, and (C) >=1 pt.wt. of magnesium hydroxide, wherein the total amount of the components B and C is <=20 pts.wt. The composition preferably comprises 100 pts.wt. of the component A, 2-8 pts.wt. of molybdenum oxide or ammonium molybdate, and 2-8 pts.wt. of the component C, wherein the total amount of the components B and C is 10-15 pts.wt. The components B and C preferably have an average-particle diameter of 0.5-2μm, respectively.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、航空機・船舶・車両等
の輸送機器用、低建造物用の内外装材、窓枠、間仕切り
等、または家具、事務用具、あるいは家電・電子機器用
ハウジング等に使用される合成樹脂材料に関し、詳しく
は、加工時の耐熱性と火災に対する安全性に関連する低
発煙性を併せもつ硬質塩化ビニール系樹脂組成物に関す
るものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to transportation equipment such as aircrafts, ships and vehicles, interior / exterior materials for low buildings, window frames, partitions, etc., furniture, office equipment, or home appliances / electronic equipment housings. More specifically, the present invention relates to a hard vinyl chloride resin composition having both heat resistance during processing and low smoke generation related to fire safety.

【0002】[0002]

【従来の技術】三酸化モリブデン(MoO3),オクタ
モリブデン酸アンモン((NH44Mo826),モリ
ブデン酸亜鉛(ZnMoO4もしくはZn3Mo29)が
PVCに対して、発煙抑制効果があることは公知である
(ポリマーダイジェスト 1994.2 74〜75
頁)。また、タルクをコア材とする含亜鉛モリブデン化
合物や、水酸化アルミニウムをコア材とするモリブデン
化合物が硬質塩化ビニール処方に発煙抑制剤として供試
されている。
2. Description of the Related Art Molybdenum trioxide (MoO 3 ), ammonium octamolybdate ((NH 4 ) 4 Mo 8 O 26 ), zinc molybdate (ZnMoO 4 or Zn 3 Mo 2 O 9 ) smokes PVC. It is known that it has an inhibitory effect (Polymer Digest 1994.
page). Further, a zinc-containing molybdenum compound having talc as a core material and a molybdenum compound having aluminum hydroxide as a core material have been used as smoke suppressants in hard vinyl chloride formulations.

【0003】[0003]

【本発明が解決しようとする課題】硬質塩化ビニール系
組成物の中には、可塑剤が皆無か、殆ど含まず、その上
粘性の高いMBS系、アクリル系の耐衝撃改良剤等をブ
レンドし、さらに、熱安定性を確保するために、滑性に
乏しいジブチル錫マレートを使用するので、混練り、成
形工程における加工温度が、いわゆる軟質塩化ビニール
系組成物の場合に比べて遥かに高く、しばしば200
以上にも達する時もある。
[Problems to be Solved by the Invention] Hard vinyl chloride type
The composition contains no or almost no plasticizer, and
It is recommended to use high-viscosity MBS and acrylic impact modifiers.
Rend and slippery to ensure thermal stability
Since poor dibutyltin malate is used, kneading and
The processing temperature in the forming process is so-called soft vinyl chloride
Much higher than in the case of the system composition, often 200
There are times when it reaches the above.

【0004】このような高熱条件下では、亜鉛成分は塩
化ビニール系樹脂の熱分解触媒となり、加熱着色をおこ
し易くなり、該組成物のリサイクル利用等がはなはだむ
つかしくなる。また、 長時間に渡る連続生産におい
て、安定的に生産することが難しく、はなはだしい場合
は、PVCの分解による機械の損傷も考えられる。ま
た、水酸化アルミニウムを使用した場合は、高熱加工条
件下では一部分解して発泡をおこし、成形品外観の悪化
や品質の低下を招く場合がある。
Under such a high heat condition, the zinc component becomes a thermal decomposition catalyst of the vinyl chloride resin, and is easily colored by heating, so that the recycling of the composition becomes very difficult. Further, in continuous production over a long period of time, stable production is difficult, and in extreme cases, the machine may be damaged due to the decomposition of PVC. Further, when aluminum hydroxide is used, it may partially decompose and foam under high heat processing conditions, which may lead to deterioration of the appearance of the molded product and deterioration of quality.

【0005】上述したように、従来の知見からは硬質塩
化ビニール系組成物の低発煙性の強化という問題に対応
する適切な発煙抑制配合を想到することは甚だ困難であ
った。本発明者はこの課題に対処して、種々研究を重ね
る間に、全く予期し難い事ながら、単独使用では、発煙
抑制性が比較的小さい二種類の化合物を併用配合するこ
とにより、高熱加工条件下でも、良好な耐熱性を有し、
かつ、発煙抑制性については相剰的に優れた効果を発現
する成果を見出し、本発明に到達した。
As described above, it has been very difficult from the conventional knowledge to come up with a suitable smoke suppressing composition for the problem of enhancing the low smoke generating property of the hard vinyl chloride composition. The present inventors have dealt with this problem, and while conducting various studies, it is quite unexpected, but in single use, by combining two types of compounds having relatively small smoke suppression properties, high heat processing conditions Has good heat resistance even under
In addition, they have found the result of exhibiting a reciprocally excellent effect with respect to smoke suppression, and arrived at the present invention.

【0006】[0006]

【課題を解決するための手段】本発明は、塩化ビニール
系樹脂100重量部に対して、酸化モリブデン、モリブ
デン酸アンモンよりの1または2以上のモリブデン化合
物と水酸化マグネシウムをそれぞれ1重量部以上、か
つ、それらの総和量が20重量部以内配合したことを特
徴とする低発煙性硬質ビニール系樹脂組成物を提示す
る。(望ましくは、酸化モリブデン、モリブデン酸アン
モン2〜8重量部、水酸化マグネシウム2〜8重量部、
総和量10〜15重量部以内。)
According to the present invention, one or more molybdenum compounds selected from molybdenum oxide and ammonium molybdate and 1 part by weight or more of magnesium hydroxide are added to 100 parts by weight of vinyl chloride resin. And, a low smoke-producing hard vinyl resin composition characterized in that the total amount thereof is blended within 20 parts by weight is presented. (Preferably, molybdenum oxide, ammonium molybdate 2 to 8 parts by weight, magnesium hydroxide 2 to 8 parts by weight,
Total amount within 10-15 parts by weight. )

【0007】本発明に使用する塩化ビニール系樹脂は、
平均重合度が700万〜1100万の範囲のストレート
PVCを用いるが、各種コポリマーを用いてももちろん
差し支えない。
The vinyl chloride resin used in the present invention is
Straight PVC having an average degree of polymerization of 7 to 11 million is used, but various copolymers may be used as a matter of course.

【0008】本発明に使用する酸化モリブデンは、平均
粒子径が0.5〜5.0μmの範囲で、望ましくは、
0.5〜2.0μの範囲内である。本発明に使用するモ
リブデン酸アンモンは、平均粒子径が0.5〜5.0μ
mの範囲で、望ましくは、0.5〜2.0μの範囲内で
ある。本発明に使用する水酸化マグネシウムは、平均粒
子径が0.5〜5.0μmの範囲で、望ましくは、0.
5〜2.0μの範囲内である。
The molybdenum oxide used in the present invention has an average particle size of 0.5 to 5.0 μm, preferably
It is within the range of 0.5 to 2.0 μ. Ammonium molybdate used in the present invention has an average particle size of 0.5 to 5.0 μm.
In the range of m, it is preferably in the range of 0.5 to 2.0 μ. The average particle diameter of the magnesium hydroxide used in the present invention is in the range of 0.5 to 5.0 μm, and preferably 0.
It is within the range of 5 to 2.0 μ.

【0009】これらの、添加剤の総量が20重量部以上
になると、最終製品の機械物性、衝撃強度の低下、真空
圧空成形性の低下、押出加工時の安定性の阻害などが発
生する。特に、衝撃強度、真空、圧空成形性を重視する
製品の場合、添加剤の総量は15部以内が望ましい。ま
た、実用上十分な低発煙性を実現するためには、総和量
が10部以上が望ましい。この場合の、実用上十分な低
発煙性とは、後述する連邦航空規制の低発煙性に合格す
るレベルの事である。
If the total amount of these additives is 20 parts by weight or more, the mechanical properties of the final product, the impact strength, the vacuum pressure-air moldability, the stability during extrusion, and the like are impaired. In particular, in the case of products that place importance on impact strength, vacuum, and air-pressure moldability, it is desirable that the total amount of additives be 15 parts or less. Further, in order to realize a smoke emission that is practically sufficient, the total amount is preferably 10 parts or more. In this case, the practically sufficient low smoke emission is a level that passes the low smoke emission of the Federal Aviation Regulation, which will be described later.

【0010】本発明の硬質塩化ビニール系樹脂組成物に
は、上述の配合剤の他に、耐衝撃性改良剤、加工性改良
剤、安定剤、滑剤、着色剤、充填剤、防黴剤等各種の公
知の配合剤を使用することができる。これらのうち代表
的なものの配合量を例示すると、 対衝撃改良剤 アクリル系補強剤 5〜20重量部 加工性改良剤 アクリル系加工助剤 1〜10重量部 安定剤 ジブチル錫マレート(ポリマー) 1〜4重量部 滑剤 脂肪酸エステル系 0.5〜1.5重量部 滑剤 ポリエチレンワックス 0.1〜0.5重量部 着色剤 酸化チタン 0〜5重量部
In the hard vinyl chloride resin composition of the present invention, in addition to the above-mentioned compounding agents, impact resistance improvers, processability improvers, stabilizers, lubricants, colorants, fillers, antifungal agents, etc. Various known compounding agents can be used. Typical examples of the compounding amount among these are impact modifiers acrylic reinforcing agent 5 to 20 parts by weight processability improving agent acrylic processing aid 1 to 10 parts by weight stabilizer dibutyltin malate (polymer) 1 4 parts by weight Lubricants Fatty acid ester type 0.5 to 1.5 parts by weight Lubricants Polyethylene wax 0.1 to 0.5 parts by weight Coloring agent Titanium oxide 0 to 5 parts by weight

【0011】実施例1 表1に示した供試配合を180℃二本ロール混練りした
後、プレス成形し、試験片を作成した。 試験方法と条件 (1)発煙性 NBS・スモーク・チャンバー・テスト
(ASTM E−662−79) 76.2mm×76.2mmの上記試験片を完全に密閉
した箱(例:914.4mm×809.6mm×91
4.4mm)内のフレームに垂直に支持して、試験片の
42.4cm2領域に熱をあてる。このとき発煙燃焼の
条件下で、1cm2当たり2.5ワットの熱量が当たる
ように調整する。上記箱中を通る光線に対して、燃焼に
よって発生した煙による光吸収を標準光度計を使用して
測定する。煙の発生が増加すると光吸収も大きくなる。
この測定値に幾何学的因子を考慮して求めた、比光学密
度によって結果を表わす。今回のテストは、燃焼開始後
4.0分後の結果(Ds4.0)によって比較した。ま
た、テストによる合格判定ラインは、アメリカ合衆国の
連邦航空局(FAA:Federal Aviatio
n Administration)の定める、連邦航
空規制(FAR: Federal Aviation
Regulation)の25.853に定めるDs
4.0が200以下であることとした。
Example 1 Test mixes shown in Table 1 were kneaded with two rolls at 180 ° C. and then press-molded to prepare test pieces. Test Method and Conditions (1) Smoke Emission NBS Smoke Chamber Test (ASTM E-662-79) A box in which the above test piece of 76.2 mm x 76.2 mm was completely sealed (Example: 914.4 mm x 809. 6 mm x 91
Heat is applied to the 42.4 cm 2 area of the test piece, supported vertically on the frame within 4.4 mm). At this time, under the condition of smoke combustion, adjustment is performed so that the heat quantity of 2.5 watts per 1 cm 2 is applied. The light absorption by smoke generated by combustion is measured using a standard photometer for the light rays passing through the box. As smoke generation increases, so does light absorption.
The result is represented by the specific optical density obtained by considering the geometrical factor in this measured value. This test was compared by the result (Ds4.0) 4.0 minutes after the start of combustion. In addition, the acceptance line by the test is the Federal Aviation Administration (FAA: Federal Aviation) of the United States.
Federal Aviation Regulations (FAR: Federal Aviation)
Regs) Ds specified in 25.853
It was decided that 4.0 was 200 or less.

【0012】(2)熱安定性試験 (株)東洋精機製作所製、ラボプラストミルを用い、下
記条件にて熱分解テストを行った。 ジャケット温度条件 200℃ 回転数 30rpm 充填量 ジャケット容量の80% 熱安定性は、樹脂の熱分解が始まり、トルク上昇が起こ
るまでの時間で比較した。
(2) Thermal stability test A thermal decomposition test was conducted under the following conditions using a Labo Plastomill manufactured by Toyo Seiki Seisakusho. Jacket temperature conditions 200 ° C. Rotation speed 30 rpm Filling amount 80% of jacket capacity Thermal stability was compared by the time until the thermal decomposition of the resin starts and the torque rises.

【0013】(3)押出時の安定性試験の内容補充 押出条件 表1に示した供試配合を40mmφ単軸押出機に、コー
トハンガータイプのTダストを取り付けたものを用い下
記条件にて押出テストを行った。
(3) Replenishment of stability test contents during extrusion Extrusion conditions Extrusion under the following conditions was carried out using the test composition shown in Table 1 in a 40 mmφ single screw extruder equipped with a coat hanger type T dust. I did a test.

【0014】実施例2〜3、対照例1〜6 表1に示す配合で実施例1と同様に試験片を作成し、同
様の試験に供した。
Examples 2 to 3 and Controls 1 to 6 Test pieces were prepared in the same manner as in Example 1 with the formulations shown in Table 1 and subjected to the same tests.

【0015】[0015]

【表1】 [Table 1]

【0016】表1より明らかなように本発明の塩化ビニ
ール系樹脂組成物は高熱加工条件下でも、良好な耐熱性
を有し、かつ、発煙抑制性については相剰的に優れた効
果を発現する。
As is clear from Table 1, the vinyl chloride resin composition of the present invention has good heat resistance even under high heat processing conditions, and has a reciprocal excellent effect of suppressing smoke emission. To do.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 塩化ビニール系樹脂100重量部に対し
て、酸化モリブデン、モリブデン酸アンモンよりの1又
は2以上のモリブデン化合物と水酸化マグネシウムを、
それぞれ1重量部以上、かつ、それらの総和量が20重
量部以内配合したことを特徴とする低発煙性、硬質塩化
ビニール系樹脂組成物 。
1. One or more molybdenum compounds selected from molybdenum oxide and ammonium molybdate and magnesium hydroxide per 100 parts by weight of vinyl chloride resin.
A low-smoke-proof, hard vinyl chloride resin composition, characterized in that 1 part by weight or more and a total amount thereof are mixed within 20 parts by weight.
【請求項2】 塩化ビニール系樹脂100重量部に対し
て、酸化モリブデン、モリブデン酸アンモン2〜8重
量、水酸化マグネシウム2〜8重量部、かつそれの総和
量10〜15重量部以内配合した事を特徴とする低発煙
性、塩化ビニール系樹脂組成物 。
2. Molybdenum oxide, ammonium molybdate 2 to 8 parts by weight, magnesium hydroxide 2 to 8 parts by weight, and a total amount of 10 to 15 parts by weight, based on 100 parts by weight of vinyl chloride resin. A vinyl chloride resin composition having low smoke generation, which is characterized by:
JP6298938A 1994-11-07 1994-11-07 Vinyl chloride resin composition Pending JPH08134301A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6298938A JPH08134301A (en) 1994-11-07 1994-11-07 Vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6298938A JPH08134301A (en) 1994-11-07 1994-11-07 Vinyl chloride resin composition

Publications (1)

Publication Number Publication Date
JPH08134301A true JPH08134301A (en) 1996-05-28

Family

ID=17866136

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6298938A Pending JPH08134301A (en) 1994-11-07 1994-11-07 Vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPH08134301A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004041930A1 (en) * 2002-11-05 2004-05-21 Mitsubishi Plastics, Inc. Flame-resistant vinyl chloride based resin composition and formed product therefrom
JP2005105221A (en) * 2003-10-01 2005-04-21 Mitsubishi Plastics Ind Ltd Flame retardant vinyl chloride-based resin composition and flame retardant vinyl chloride-based resin-molded article
CN1315936C (en) * 2002-11-05 2007-05-16 三菱树脂株式会社 Flame-resistant vinyl chloride based resin composition and formed product therefrom

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06248141A (en) * 1993-02-24 1994-09-06 Sekisui Chem Co Ltd Vinyl chloride resin composition
JPH06306232A (en) * 1993-04-22 1994-11-01 Sekisui Chem Co Ltd Vinyl chloride-based resin composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06248141A (en) * 1993-02-24 1994-09-06 Sekisui Chem Co Ltd Vinyl chloride resin composition
JPH06306232A (en) * 1993-04-22 1994-11-01 Sekisui Chem Co Ltd Vinyl chloride-based resin composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004041930A1 (en) * 2002-11-05 2004-05-21 Mitsubishi Plastics, Inc. Flame-resistant vinyl chloride based resin composition and formed product therefrom
CN1315936C (en) * 2002-11-05 2007-05-16 三菱树脂株式会社 Flame-resistant vinyl chloride based resin composition and formed product therefrom
KR101014640B1 (en) * 2002-11-05 2011-02-16 미쓰비시 쥬시 가부시끼가이샤 Flame-resistant vinyl chloride based resin composition and formed product therefrom
JP2005105221A (en) * 2003-10-01 2005-04-21 Mitsubishi Plastics Ind Ltd Flame retardant vinyl chloride-based resin composition and flame retardant vinyl chloride-based resin-molded article

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