JPS59159845A - Vinyl chloride resin composition - Google Patents

Vinyl chloride resin composition

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Publication number
JPS59159845A
JPS59159845A JP3296183A JP3296183A JPS59159845A JP S59159845 A JPS59159845 A JP S59159845A JP 3296183 A JP3296183 A JP 3296183A JP 3296183 A JP3296183 A JP 3296183A JP S59159845 A JPS59159845 A JP S59159845A
Authority
JP
Japan
Prior art keywords
vinyl chloride
resin
weight
parts
copolymer 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
JP3296183A
Other languages
Japanese (ja)
Inventor
Isamu Osada
長田 勇
Koji Sato
佐藤 公司
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.)
Tosoh Corp
Original Assignee
Toyo Soda Manufacturing 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 Toyo Soda Manufacturing Co Ltd filed Critical Toyo Soda Manufacturing Co Ltd
Priority to JP3296183A priority Critical patent/JPS59159845A/en
Publication of JPS59159845A publication Critical patent/JPS59159845A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide a vinyl chloride resin compsn. having excellent resistance to weather and low-temperature impact, consisting of a vinyl chloride resin and a vinyl chloride graft copolymer resin obtd. by copolymerizing vinyl chloride with an ethylene/vinyl acetate copolymer resin. CONSTITUTION:A resin compsn. consists of 10-40pts.wt. vinyl chloride resin having an average degree of polymn. of 600-1,400 and 90-60pts.wt. vinyl chloride graft copolymer resin obtd. by graft copolymerizing 95-80pts.wt. vinyl chloride onto 5-20pts.wt. ethylene/vinyl acetate copolymer resin having a vinyl acetate content of 10-45wt%. Pref. the vinyl acetate content of said copolymer resin is 15-30wt% from the viewpoint of reducing lowering in rigidity. The vinyl chloride resin is one having an average degree of polymn. of 600-1,400 prepd. by suspension polymn., and one having an average degree of polymn. of 700-1,100 is preferred from the viewpoints of flow characteristics and compatibility.

Description

【発明の詳細な説明】 本発明は、耐候性、低温耐衝撃性例優れた塩化ビニル系
樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a vinyl chloride resin composition having excellent weather resistance and low-temperature impact resistance.

更に詳しくは、酢酸ビニル含有量10〜45重量%のエ
チレン酢酸ビニル共重合樹脂の5〜20重景部に対し、
塩化ビニルの95〜80重量部をグラフト共重合させて
得られる塩化ビニル系グラフト共重合樹脂90〜60重
量部と平均重合度600〜1400の塩化ビニ遁系樹脂
10〜40重量部とから成ることを特徴とする樹脂組成
物に関する。
More specifically, for 5 to 20 parts of ethylene vinyl acetate copolymer resin having a vinyl acetate content of 10 to 45% by weight,
Consists of 90 to 60 parts by weight of a vinyl chloride-based graft copolymer resin obtained by graft copolymerizing 95 to 80 parts by weight of vinyl chloride, and 10 to 40 parts by weight of a vinyl chloride-based resin having an average degree of polymerization of 600 to 1,400. The present invention relates to a resin composition characterized by:

塩化ビニル樹脂は、優れた物理的2機械的性質を有して
いるため多くの用途に使用されている。
Vinyl chloride resins have excellent physical and mechanical properties and are therefore used in many applications.

捷た、耐熱性、 −11性の面でも実用上十分な性能を
そなえている。しかし耐衝撃性の面では非常に弱い−と
いう欠点があり、衝撃強化剤を添加しなければならない
。この衝撃強化剤にはMBS、塩素化ポリエチレン、ア
クリルゴム等種々のものが従来公知であるがそのほとん
どが常温での衝撃強度は改善するが、耐熱性、剛性を大
巾に低下さ。せかつ低温における耐衝撃性はほとんど向
上せず、耐候性もよくないという欠点があっただめ低温
での耐衝撃性″、耐候性を要求する建材用途、窓枠用途
では実用上制限があった。
It has sufficient performance for practical use in terms of warpability, heat resistance, and -11 resistance. However, it has the disadvantage that it has very low impact resistance, and an impact strengthener must be added. Various types of impact strengthening agents are known in the art, such as MBS, chlorinated polyethylene, and acrylic rubber, but most of them improve impact strength at room temperature, but greatly reduce heat resistance and rigidity. There was little improvement in impact resistance at low temperatures and poor weather resistance, so there were practical limitations in building materials and window frame applications that required impact resistance and weather resistance at low temperatures. .

本発明者らは上記のような種々の欠点を克服するために
検討を重ねた結果、エチレン酢酸ビニル共重合樹脂と塩
化ビニル樹脂の混合使用により耐候性が良く、低温耐衝
撃性、耐熱性、剛性のバランスのとれた樹脂組成物が得
られるという知見を得て本発明を完成したものである。
As a result of repeated studies by the present inventors to overcome the various drawbacks mentioned above, we found that the use of a mixture of ethylene vinyl acetate copolymer resin and vinyl chloride resin provides good weather resistance, low-temperature impact resistance, heat resistance, The present invention was completed based on the knowledge that a resin composition with well-balanced rigidity can be obtained.

すなわち、本発明は耐候性、低温耐衝撃性に優れた塩化
ビニル系樹脂組成物に関するものであり、特に屋外用建
築部材、寒冷地向外付窓枠に好適な組成物を提供するも
のである。
That is, the present invention relates to a vinyl chloride resin composition with excellent weather resistance and low-temperature impact resistance, and provides a composition particularly suitable for outdoor building components and external window frames for cold regions. .

本発明で使用されるエチレン酢酸ビニル共重合樹脂と塩
化ビニルのグラフト共重合樹脂は、懸濁重合、乳化重合
、膨潤重合、塊状重合などのいずれの方法によって製造
されたものでもよく、またその形状も粉末状1粒状のい
ずれであっても良い。
The graft copolymer resin of ethylene vinyl acetate copolymer resin and vinyl chloride used in the present invention may be produced by any method such as suspension polymerization, emulsion polymerization, swelling polymerization, or bulk polymerization, and its shape It may also be in the form of a powder or a single grain.

後述する様に本発明では懸濁重合塩化ビニル樹脂と混合
使用するのでグラフト共重合樹脂は、懸濁重合法の粉末
状のものが好ましい。
As will be described later, in the present invention, the graft copolymer resin is preferably used in a powder form obtained by the suspension polymerization method, since it is used in combination with the suspension polymerization vinyl chloride resin.

本発明で使用されるグラフト共重合樹脂を構成する成分
のエチレン酢酸ビニル共重合樹脂の酢酸ビニル含有量は
、10〜45重量%の範囲のものが使用できるが剛性の
低下を少なくするため、酢酸ビニル含有量15〜30重
量%のものが好ましい。また、グラフト共重合樹脂は、
塩化ビニル95〜80重量部に対して、エチレン酢酸ビ
ニル共重合樹脂5〜20重量部の範囲のものが使用でき
る。
The vinyl acetate content of the ethylene vinyl acetate copolymer resin, which is a component constituting the graft copolymer resin used in the present invention, can range from 10 to 45% by weight. Preferably, the vinyl content is 15 to 30% by weight. In addition, the graft copolymer resin is
An ethylene vinyl acetate copolymer resin can be used in a range of 5 to 20 parts by weight per 95 to 80 parts by weight of vinyl chloride.

本発明で使用される塩化ビニル系樹脂は懸濁重合法で製
造される平均重合度600〜1400の範囲のものであ
″るが流動性、相溶性の問題から平均重合度700〜1
100の範囲のものが好ましい。
The vinyl chloride resin used in the present invention is produced by a suspension polymerization method and has an average polymerization degree of 600 to 1,400, but due to fluidity and compatibility issues, the average polymerization degree is 700 to 1.
A range of 100 is preferred.

この塩化ビニル系樹脂は、塩化ビニル単独重合樹脂、塩
化ビニル・酢酸ビニル共重合樹脂、塩イトビニル・エチ
レン共重合樹脂のいずれであっても良い。
This vinyl chloride resin may be any of vinyl chloride homopolymer resin, vinyl chloride/vinyl acetate copolymer resin, and vinyl chloride/ethylene copolymer resin.

本発明で用いられるグラフト共重合樹脂と塩化ビニル系
樹脂の混合比率は、グラフト共重合樹脂90〜60重量
部に対して塩化ビニル系樹脂10 ・〜40重量部の比
率であるが、剛性と低温での耐衝撃性のバランスの面か
ら、グラフト共重合樹脂90〜70重量部に対して塩化
ビニル系樹脂10〜30重量部が好ましい。
The mixing ratio of the graft copolymer resin and vinyl chloride resin used in the present invention is 10 to 40 parts by weight of the vinyl chloride resin to 90 to 60 parts by weight of the graft copolymer resin. In view of the balance of impact resistance, it is preferable to use 10 to 30 parts by weight of the vinyl chloride resin based on 90 to 70 parts by weight of the graft copolymer resin.

上記において、グラフト共重合樹脂が90重量部以上の
場合は剛性が不足し、60重量部以下の場合は低温での
耐衝撃性が不足するという欠点が発生する。
In the above, when the graft copolymer resin is 90 parts by weight or more, the rigidity is insufficient, and when it is 60 parts by weight or less, the impact resistance at low temperatures is insufficient.

本発明の組成物には必要に応じて安定剤、滑剤。The composition of the present invention optionally contains stabilizers and lubricants.

充填剤、紫外線吸収剤、酸化防止剤、顔料などを従来公
知の配合割合で任意に添加しても何ら差しつかえない。
There is no problem in adding fillers, ultraviolet absorbers, antioxidants, pigments, etc. in conventionally known proportions.

添加できる安定剤としては1三塩基性硫酸鉛。An example of a stabilizer that can be added is tribasic lead sulfate.

ステアリン酸鉛等の鉛系安定剤、ステアリン酸カルシウ
ム、ステアリン酸亜鉛等の金属石鹸系安定剤、オクチル
錫メルカプタイド、ジプチル錫マレエート等の有機錫系
安定剤があげられ、更に有機面リン酸エステル、2フエ
ニルインドールなどの補助安定剤があげられる。
Examples include lead stabilizers such as lead stearate, metal soap stabilizers such as calcium stearate and zinc stearate, organotin stabilizers such as octyltin mercaptide and diptyltin maleate, and organic surface phosphate esters, Examples include co-stabilizers such as phenylindole.

滑剤としては天然パラフィン、流動パラフィンポリエチ
レンワックス等の炭化水素系滑剤、ステアリン酸等の脂
肪酸系滑剤、ステアリン酸アミド等の脂肪酸アミド系滑
剤、エチレングリコールモノステアレート等のエステル
系滑剤、ラウリン酸カルシウム等の金属石鹸系滑剤があ
げられる。
Examples of lubricants include hydrocarbon lubricants such as natural paraffin and liquid paraffin polyethylene wax, fatty acid lubricants such as stearic acid, fatty acid amide lubricants such as stearamide, ester lubricants such as ethylene glycol monostearate, and calcium laurate. Examples include metal soap-based lubricants.

充填剤としては炭酸カルシウム、カオリン、クレー、石
こう等があげられる。
Examples of fillers include calcium carbonate, kaolin, clay, and gypsum.

紫外線吸収剤としては′2.4−ジヒドロキシベンゾフ
ェノン等のベンゾフェノン系、2−(2’−ヒドロキシ
−5−メチルフェニル)ペンシトリアゾ、ル ー等のベンシト′リアゾール系、サリチル酸フェニル等
のサリチル酸エステル系紫外線吸収剤があげられる。
Examples of ultraviolet absorbers include benzophenone-based UV absorbers such as 2,4-dihydroxybenzophenone, bencitoriazole-based UV absorbers such as 2-(2'-hydroxy-5-methylphenyl)pencitriazo and Ru, and salicylic acid ester-based UV absorbers such as phenyl salicylate. can be given.

酸化防止剤としては2−27−メチレン−ビス−(4メ
チル−6−ターシャリ−ブチルフェノール)等のビスフ
ェノール系、2.6−ジターシャリ−ブチルフェノール
等のモノフェノール系、2.5−ジターシャリ−ブチル
ヒドロキノン等のヒドロキノン系酸化防止剤があげられ
る。
Examples of antioxidants include bisphenols such as 2-27-methylene-bis-(4methyl-6-tert-butylphenol), monophenols such as 2,6-ditertiary-butylphenol, and 2,5-ditertiary-butylhydroquinone. Examples include hydroquinone antioxidants.

顔料としてはカーボンブラック、酸化チタン等があげら
れる。
Examples of pigments include carbon black and titanium oxide.

本発明の樹脂組成物はグラフト共重合樹脂および塩化ビ
ニル系樹脂に各種の添加剤すなわち安定剤、充填剤、滑
剤、顔料等をヘンシェルミキサー。
The resin composition of the present invention is prepared by adding various additives such as stabilizers, fillers, lubricants, pigments, etc. to the graft copolymer resin and vinyl chloride resin in a Henschel mixer.

バンバリーミキサ−などを使用して、従来公知の方法で
均一に混合することによって得られ、該組成物を実際に
使用する場合、従来公知の押出成型法、射出成型法によ
り建築部材、窓枠等が得られる。
It is obtained by uniformly mixing the composition using a conventionally known method using a Banbury mixer, etc. When the composition is actually used, it can be manufactured into building materials, window frames, etc. by conventionally known extrusion molding method or injection molding method. is obtained.

本発明の組成物は低温での耐衝撃性能が高くかつ耐候性
能が優れているため苛酷な使用条件に耐え得る。従って
とくにきびしい低温での耐衝撃性。
The composition of the present invention has high impact resistance at low temperatures and excellent weather resistance, so it can withstand severe usage conditions. Therefore, it is particularly impact resistant at severe low temperatures.

耐候性を要求する、窓枠分野、屋外用建築部材に好適で
ある。
Suitable for window frames and outdoor building materials that require weather resistance.

以下実施例によって本発明を説明する。The present invention will be explained below with reference to Examples.

実施例1 酢酸ビニル含有量20重量−のエチレン酢酸ビニル共重
合樹脂12重量部と塩化ビニル88重量部から成るグラ
フト共重合樹脂75重量部に対し平均重合度820の塩
化ビニル樹脂25重量部を混合して得られた樹脂100
重量部に対し三塩基性硫酸鉛1.5重置部、ステアリン
酸鉛2.0重量部。
Example 1 25 parts by weight of a vinyl chloride resin having an average degree of polymerization of 820 was mixed with 75 parts by weight of a graft copolymer resin consisting of 12 parts by weight of an ethylene vinyl acetate copolymer resin having a vinyl acetate content of 20 parts by weight and 88 parts by weight of vinyl chloride. Resin 100 obtained by
1.5 parts by weight of tribasic lead sulfate and 2.0 parts by weight of lead stearate.

二塩基性ステアリン酸鉛15重量部、炭酸カルシウム5
.0重量部を均一に混合し、これを165°Cの熱ロー
ルで10分間混練し、180°Cの熱プレスで10分間
プレスすることによりシートを作成し、このシートから
採取した試料について物性を測定した。
15 parts by weight of dibasic lead stearate, 5 parts by weight of calcium carbonate
.. 0 parts by weight were uniformly mixed, kneaded for 10 minutes with a hot roll at 165°C, and pressed for 10 minutes with a hot press at 180°C to create a sheet, and the physical properties of samples taken from this sheet were determined. It was measured.

比較例1 平均重合度820の塩化ビニル樹脂100重量部に対し
メタクリル酸メチルーブタジエンースチレングラフトコ
ボリマ−10重量部を混合した樹脂を実施例1の混合し
た樹脂100重量部に置き換えて行った他は実施例1と
同様に行った。
Comparative Example 1 A resin prepared by mixing 100 parts by weight of vinyl chloride resin with an average degree of polymerization of 820 and 10 parts by weight of methyl methacrylate-butadiene-styrene graft cobolimer was substituted for 100 parts by weight of the mixed resin of Example 1. The rest was carried out in the same manner as in Example 1.

物性試験結果をまとめて表1に記した。The physical property test results are summarized in Table 1.

これらの物性の測定に使用した測定方法は、次のとおシ
である。
The measurement methods used to measure these physical properties are as follows.

(1)  熱変形温度試験 JIBK7207記載の方
法(2)  引張試験    J工S K 6745記
載の方法(3)  シーr疼衝眺線1欺J工8に711
1記載の方法(4)  曲げ試験    JよりK72
Q5記載の方法(5)促進耐候性試験 JIsA14?
5記載の方法衣1 表1から熱変形温度を比較すれば実施例1は比較例1よ
り優れており熱的性質の低下が少ないことを示している
(1) Heat distortion temperature test Method described in JIBK 7207 (2) Tensile test Method described in J Engineering S K 6745 (3) Sea r pain view line 1 deception J engineering 8 to 711
Method described in 1 (4) Bending test J to K72
Method described in Q5 (5) Accelerated weathering test JIsA14?
Comparing the heat distortion temperatures from Table 1, Example 1 is superior to Comparative Example 1, indicating that there is less deterioration in thermal properties.

降伏強さ、最大曲げ強さ9曲げ弾性率はほぼ同等の性能
を有しておシ剛性はあまシ低下しないことを示している
The results show that the yield strength, maximum bending strength, and bending modulus are almost the same, and the rigidity is not significantly reduced.

シャルピー衝撃強度を比較すれば実施例1は比較例1よ
り低温域で2倍以上の性能を示し特に優れていることを
示している。
Comparing the Charpy impact strength, Example 1 shows particularly excellent performance in the low temperature range, which is more than double that of Comparative Example 1.

促進耐候性試験後のシャルピー衝撃強度を比較すれば実
施例1は比較例1よシ強度残率が大巾に高く特に優れて
゛いることを示している。
A comparison of the Charpy impact strength after the accelerated weathering test shows that Example 1 has a significantly higher strength retention than Comparative Example 1, and is particularly excellent.

すなわち本発明の樹脂組成物は、高度な低温での耐衝撃
性能及び耐候性能を要求される分野に適しているといえ
る。
That is, the resin composition of the present invention can be said to be suitable for fields that require high impact resistance and weather resistance at low temperatures.

実施例2 酢酸ビニル含有量21重量%のエチレン酢酸ビニル共重
合樹脂15重量部と塩化ビニル85重量部から成るグラ
フト共重合樹脂60重量部に対し平均重合度1050の
塩化ビニル樹脂40重量部を混合して得られた樹脂10
0重量部に対し実施例1と同様の方法で物性評価を行っ
たところ一20℃測定のシャルピー衝撃強度10kg・
す保。
Example 2 40 parts by weight of a vinyl chloride resin having an average degree of polymerization of 1050 was mixed with 60 parts by weight of a graft copolymer resin consisting of 15 parts by weight of an ethylene-vinyl acetate copolymer resin having a vinyl acetate content of 21% by weight and 85 parts by weight of vinyl chloride. Resin 10 obtained by
The physical properties of 0 parts by weight were evaluated in the same manner as in Example 1, and the Charpy impact strength measured at -20°C was 10 kg.
Suho.

促進耐候性試験1000時間後の23.:C測定のシャ
ルピー衝撃強さ16 kg −on/crl (残率7
8チ)であり優れていることを示した。
23. After 1000 hours of accelerated weathering test. :Charpy impact strength measured by C: 16 kg-on/crl (remaining rate: 7
8ch), which showed that it was excellent.

特許出願人  東洋曹達工業株式会社Patent applicant: Toyo Soda Kogyo Co., Ltd.

Claims (1)

【特許請求の範囲】 酢酸ビニル含有量10〜45重置部のエチレン酢酸ピ′
ニル共重合樹脂の5〜20重量部に対し、塩化ビニルの
95〜80重量部をグラフト共重合させて得られる塩化
ビニル系グラフト共重合樹脂90〜60重量部と平均重
合度600〜1400重景 の塩化ビニル系樹脂10〜4agとから成ることを特徴
とする塩化ビニル系樹脂組成物
[Claims] Ethylene acetate with a vinyl acetate content of 10 to 45 parts
90 to 60 parts by weight of a vinyl chloride graft copolymer resin obtained by graft copolymerizing 95 to 80 parts by weight of vinyl chloride to 5 to 20 parts by weight of a vinyl copolymer resin, and an average degree of polymerization of 600 to 1400 parts by weight. A vinyl chloride resin composition comprising 10 to 4 ag of a vinyl chloride resin.
JP3296183A 1983-03-02 1983-03-02 Vinyl chloride resin composition Pending JPS59159845A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3296183A JPS59159845A (en) 1983-03-02 1983-03-02 Vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3296183A JPS59159845A (en) 1983-03-02 1983-03-02 Vinyl chloride resin composition

Publications (1)

Publication Number Publication Date
JPS59159845A true JPS59159845A (en) 1984-09-10

Family

ID=12373512

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3296183A Pending JPS59159845A (en) 1983-03-02 1983-03-02 Vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPS59159845A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0755991A3 (en) * 1995-07-27 1997-08-13 Taisei Corp Dry-type or wet-type sealing material and method of manufacturing them

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS494310A (en) * 1972-05-01 1974-01-16

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS494310A (en) * 1972-05-01 1974-01-16

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0755991A3 (en) * 1995-07-27 1997-08-13 Taisei Corp Dry-type or wet-type sealing material and method of manufacturing them

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