JPS61192757A - Vinyl chloride resin composition having improved thermal stability - Google Patents

Vinyl chloride resin composition having improved thermal stability

Info

Publication number
JPS61192757A
JPS61192757A JP3384585A JP3384585A JPS61192757A JP S61192757 A JPS61192757 A JP S61192757A JP 3384585 A JP3384585 A JP 3384585A JP 3384585 A JP3384585 A JP 3384585A JP S61192757 A JPS61192757 A JP S61192757A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
thermal stability
carboxyl group
resin composition
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
JP3384585A
Other languages
Japanese (ja)
Inventor
Toshiaki Kobayashi
俊昭 小林
Tatsuo Nakayama
中山 達夫
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.)
Zeon Corp
Original Assignee
Nippon Zeon 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 Nippon Zeon Co Ltd filed Critical Nippon Zeon Co Ltd
Priority to JP3384585A priority Critical patent/JPS61192757A/en
Publication of JPS61192757A publication Critical patent/JPS61192757A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide the titled resin compsn. which has greatly improved durable thermal stability and is freed from the problem of initial discoloration, by incorporating predetermined quantities of hydrotalcite and an organotin compd. in a vinyl chloride resin. CONSTITUTION:0.1-20pts.wt. mixture obtd. by blending 10-1pt.wt. organotin compd. [e.g. poly(dibutyltin maleate)] or lead, zinc or Cd salt of an org. acid (e.g. stearic acid) with 1-20pts.wt. hydrous or anhydrous hydrotalcite composed of a double salt of Mg and Al is blended with 100pts.wt. vinyl chloride resin contg. 0.05-20wt% carboxyl group obtd, by copolymerizing vinyl chloride and a carboxyl group-contg. comonomer to obtain the desired vinyl chloride resin compsn.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は熱安定性の改良された塩化ビニル樹脂組成物に
関し、さらに詳しくは、カルボキシル基含有塩化ビニル
樹脂にハイドロタルサイト及び他の特定の金属化合物を
含有せしめたことを特徴とする初期着色及び持続熱安定
性を大幅に改良した塩化ビニル樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a vinyl chloride resin composition with improved thermal stability, and more particularly, to a carboxyl group-containing vinyl chloride resin containing hydrotalcite and other specific The present invention relates to a vinyl chloride resin composition that contains a metal compound and has significantly improved initial coloring and sustained heat stability.

(従来の技術) 従来、塩化ビニル樹脂の成形加工には、熱分解を抑制す
る為に硬質、軟質を問わず必ず熱安定剤が必要とされる
ことは良く知られている。
(Prior Art) It is well known that in the molding process of vinyl chloride resin, a heat stabilizer is always required, regardless of whether it is hard or soft, in order to suppress thermal decomposition.

一方、塩化ビニル樹脂はバランスの取れた物性。On the other hand, vinyl chloride resin has well-balanced physical properties.

コスト面から最も広範囲に使われている合成樹脂の一つ
であり、要求機能の拡大に伴い、多数の変性塩化ビニル
樹脂も開発上布されている。その変性塩化ビニル樹脂の
一つであるカルボキシル基を含有した塩化ビニル樹脂は
、含有する酸基の為に熱安定性が劣り、従来一般に使わ
れている熱安定剤(例えば鉛、錫、金属石けん系等)で
は成形加工時の熱分解を抑制する事が困難であり、又、
無理に熱安定性を保持しようとすると一般の塩化ビニル
樹脂に比べ数倍の安定剤が必要となりコストが大幅にア
ップするという問題があった。
It is one of the most widely used synthetic resins due to its cost, and as the required functions expand, many modified vinyl chloride resins are also being developed and applied. Vinyl chloride resin containing carboxyl groups, which is one of the modified vinyl chloride resins, has poor thermal stability due to the acid groups it contains. etc.), it is difficult to suppress thermal decomposition during molding, and
If you try to forcefully maintain thermal stability, you will need several times more stabilizers than ordinary vinyl chloride resins, resulting in a significant increase in cost.

(発明が解決しようとする問題点) 本発明者は前記欠点を解決すべく鋭意研究の結果、カル
ボキシル基含有塩化ビニル樹脂にノ・イドロタルサイト
及び他の特定の金属化合物を添加することによって、塩
化ビニル単独重合体と遜色な廊 い初着色調、持続熱安定性を保持することを見出し、こ
の知見に基づいて本発明を完成するに到った。
(Problems to be Solved by the Invention) As a result of intensive research in order to solve the above-mentioned drawbacks, the present inventors have found that by adding no-hydrotalcite and other specific metal compounds to carboxyl group-containing vinyl chloride resin, It was discovered that the initial color tone and sustained thermal stability are comparable to those of vinyl chloride homopolymer, and based on this knowledge, the present invention was completed.

(問題点を解決するための手段) かくして本発明によれば、カルボキシル基含有塩化ビニ
ル樹脂100重量部当たり、(!)ハイドロタルサイト
及び(2)有機錫化合物又は有機酸の鉛。
(Means for Solving the Problems) Thus, according to the present invention, per 100 parts by weight of carboxyl group-containing vinyl chloride resin, (!) hydrotalcite and (2) lead as an organotin compound or an organic acid.

亜鉛若しくはカドミウム塩を(1)及び(2)の合計量
として0.1〜20重量部含有することを特徴とする熱
安定性の改良された塩化ビニル樹脂組成物が提供される
There is provided a vinyl chloride resin composition with improved thermal stability, which contains a zinc or cadmium salt in a total amount of 0.1 to 20 parts by weight of (1) and (2).

(発明の効果) 本発明において用いられるカルボキシル基含有塩化ビニ
ル樹脂としては、塩化ビニルと、これと共重合可能なカ
ルボン酸含有共単量体との共重合体、塩化ビニルとカル
ボン酸エステルとを共重合させた後加水分解した重合体
、又は塩化ビニル重合体製造後、カルボン酸含有化合物
を付加反応させたものなどが挙げられる。カルボキシル
基の含有量は通常O,OS〜20重量%である。
(Effects of the Invention) The carboxyl group-containing vinyl chloride resin used in the present invention includes a copolymer of vinyl chloride and a carboxylic acid-containing comonomer copolymerizable therewith, and a copolymer of vinyl chloride and a carboxylic acid ester. Examples include a polymer obtained by copolymerizing and then hydrolyzing, or a vinyl chloride polymer prepared by addition reaction with a carboxylic acid-containing compound. The content of carboxyl groups is usually O, OS to 20% by weight.

又、(1)のハイドロタルサイトとはMgとAJとの複
塩のことであって、水和物であっても無水物であっても
よい。
Further, the hydrotalcite in (1) is a double salt of Mg and AJ, and may be a hydrate or an anhydride.

(2)の有機錫化合物としては、ポリ(ジプチル錫マレ
ート)、ジブチル錫ビス(アルキルマレート)。
Examples of the organic tin compound (2) include poly(diptyltin malate) and dibutyltin bis(alkyl maleate).

ジオクチル錫ビス(アルキルマレート)、ジブチル錫ビ
ス(アルキルラウレート)、ジブチル錫ビス(アルキル
メルカプタイド)、ジメチル錫ビス(アルキルメルカプ
タイド)、ジオクチル錫ビス(アルキルメルカプタイド
)等のアルキル錫マレート、ラウレート、メルカプタイ
ドの他にアルキル錫メルカプト酸エステル塩、アルキル
エステル錫マレート等が挙げられる。
Alkyl such as dioctyltin bis(alkyl maleate), dibutyltin bis(alkyl laurate), dibutyltin bis(alkyl mercaptide), dimethyltin bis(alkyl mercaptide), dioctyltin bis(alkyl mercaptide), etc. In addition to tin malate, laurate, and mercaptide, alkyl tin mercapto acid ester salts, alkyl ester tin malate, and the like can be mentioned.

(2)の有機酸の鉛、亜鉛若しくはカドミウム塩として
は、ステアリン酸、ラウリル酸、オクチル酸。
(2) The organic acid lead, zinc or cadmium salts include stearic acid, lauric acid, and octylic acid.

パルミチン酸等の飽和又は不飽和脂肪酸の鉛、亜鉛、カ
ドミウム金属塩が挙げられる。
Examples include lead, zinc, and cadmium metal salts of saturated or unsaturated fatty acids such as palmitic acid.

これらの(2)の有機錫化合物、有機酸の鉛、亜鉛、カ
ドミウム塩はそれぞれ単独又は2種以上の化合物の混合
物であっても良い。
These (2) organic tin compounds and organic acid lead, zinc, and cadmium salts may be used alone or in a mixture of two or more kinds of compounds.

ハイドロタルサイトと(2)の金属化合物との使用割合
は1:10〜20:1.より好ましい割合は1:5〜1
0:1である。
The ratio of hydrotalcite to metal compound (2) is 1:10 to 20:1. A more preferable ratio is 1:5-1
The ratio is 0:1.

カルボキシル基含有塩化ビニル樹脂1oo重量部に対す
るハイドロタルサイト及び(2)の金属化合物の合計添
加量はo、 i〜20重量部、好ましくは0.2〜10
重量部である。0.1重量部未満では初期 帯色調及び持続熱安定性の改良効果が小さく、20重量
部を越えて添加してもコストアップになるだけで、添加
量に比例した改良効果は期待できない。
The total amount of hydrotalcite and the metal compound (2) added to 10 parts by weight of the carboxyl group-containing vinyl chloride resin is o, i to 20 parts by weight, preferably 0.2 to 10 parts by weight.
Parts by weight. If it is less than 0.1 part by weight, the effect of improving initial color tone and sustained thermal stability will be small, and if it is added in excess of 20 parts by weight, it will only increase the cost and no improvement effect proportional to the amount added can be expected.

カルボキシル基含有塩化ビニル樹脂と(1)のハイドロ
タルサイト及び(2)の金属化合物との混合方法は特に
限定されず、塩化ビニルの重合途中あるいは終了段階で
(1)及び(2)を添加してもよいし、また通常の添加
剤の混合法と同様、三者を粉末ブレンドしても良い。
The method of mixing the carboxyl group-containing vinyl chloride resin with the hydrotalcite (1) and the metal compound (2) is not particularly limited, and (1) and (2) may be added during or at the end of the polymerization of vinyl chloride. Alternatively, the three materials may be powder blended in the same manner as in the usual method of mixing additives.

本発明における塩化ビニル樹脂組成物の製造に際しては
、一般の塩化ビニル樹脂におけると同様、可塑剤、他の
安定剤、滑剤、充填剤、酸化防止剤、紫外線吸収剤、加
工助剤1発泡剤、顔料、難燃剤。
When producing the vinyl chloride resin composition of the present invention, as in the case of general vinyl chloride resin, plasticizers, other stabilizers, lubricants, fillers, antioxidants, ultraviolet absorbers, processing aids, blowing agents, Pigments, flame retardants.

耐衝撃助剤等の各種添加剤を必要に応じ添加することが
できる。又、他のゴム、プラスチック等の重合体を混合
しても良い。
Various additives such as impact resistance aids can be added as necessary. Further, other polymers such as rubber and plastic may be mixed.

さらに、カルボキシル基含有塩化ビニル樹脂のカルボン
酸を中和する目的で金属化合物又は塩基性化合物を添加
しても良い。
Furthermore, a metal compound or a basic compound may be added for the purpose of neutralizing the carboxylic acid of the carboxyl group-containing vinyl chloride resin.

(実施例) 以下に実施例を挙げて本発明をさらに具体的に説明する
。なお、実施例中の部及びチはとくに断りのないかぎり
重量基準である。
(Example) The present invention will be described in more detail with reference to Examples below. In addition, parts and parts in the examples are based on weight unless otherwise specified.

実施例1 塩化ビニル及びアクリル酸を懸濁共重合してアクリル酸
が1%共重合された。平均重合度1.050のカルボキ
シル基含有塩化ビニル樹脂(A3100部に対し、ブチ
ルステアレート0.3部、エポキシ化大豆油3部及び第
1表に示す量のハイドロタルサイト(協和化学社製アル
カマイザー1)と他の安定剤とを添加した塩化ビニル樹
脂組成物を170℃の熱ロールで3分間混練しシートを
得た。祷られたシートの初期着色を判定し、又、このシ
ートを190℃ギヤーオーブンで熱老化させ、分解黒化
までの時間を測定した。
Example 1 Vinyl chloride and acrylic acid were suspension copolymerized to obtain 1% acrylic acid. Carboxyl group-containing vinyl chloride resin with an average degree of polymerization of 1.050 (to 100 parts of A3, 0.3 parts of butyl stearate, 3 parts of epoxidized soybean oil, and the amount of hydrotalcite (manufactured by Kyowa Kagaku Co., Ltd.) shown in Table 1) A sheet was obtained by kneading a vinyl chloride resin composition to which Miser 1) and other stabilizers were added using a heated roll at 170°C for 3 minutes.The desired initial coloring of the sheet was determined, and this sheet was It was heat aged in a °C gear oven and the time until decomposition blackening was measured.

一方、比較例として、カルボキシル基含有塩化ビニル樹
脂の代りに塩化ビニル単独重合体樹脂(日本ゼオン(株
)製ゼオンIQ3EP、平均重合度1,050)を使用
したものを使用し、同様の実験を行った。結果を第1表
に示す。
On the other hand, as a comparative example, a similar experiment was carried out using a vinyl chloride homopolymer resin (Zeon IQ3EP manufactured by Nippon Zeon Co., Ltd., average degree of polymerization 1,050) instead of the carboxyl group-containing vinyl chloride resin. went. The results are shown in Table 1.

第1表より、カルボキシル基含有重合体であっても1本
発明における二種の安定剤を併用添加した場合には、塩
化ビニル単独重合体に匹敵する初期及び持続熱安定性を
示すことがわかる。
From Table 1, it can be seen that even a carboxyl group-containing polymer exhibits initial and sustained thermal stability comparable to vinyl chloride homopolymer when the two types of stabilizers of the present invention are added together. .

実施例2 可塑剤としてジー2−エチルへキシルフタレートを10
0部さらに添加し、熱ロール温度を150℃とした他は
実施例1と同様の実験を行った。結果を第2表に示す。
Example 2 Di-2-ethylhexyl phthalate as a plasticizer
The same experiment as in Example 1 was conducted, except that 0 part of the solution was further added and the hot roll temperature was set at 150°C. The results are shown in Table 2.

Claims (1)

【特許請求の範囲】[Claims] カルボキシル基含有塩化ビニル樹脂100重量部当たり
、(1)ハイドロタルサイト及び(2)有機錫化合物、
又は有機酸の鉛、亜鉛若しくはカドミウム塩を(1)及
び(2)の合計量として0.1〜20重量部含有するこ
とを特徴とする熱安定性の改良された塩化ビニル樹脂組
成物。
Per 100 parts by weight of carboxyl group-containing vinyl chloride resin, (1) hydrotalcite and (2) organotin compound,
Or a vinyl chloride resin composition with improved thermal stability, characterized in that it contains 0.1 to 20 parts by weight of lead, zinc or cadmium salts of organic acids as the total amount of (1) and (2).
JP3384585A 1985-02-22 1985-02-22 Vinyl chloride resin composition having improved thermal stability Pending JPS61192757A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3384585A JPS61192757A (en) 1985-02-22 1985-02-22 Vinyl chloride resin composition having improved thermal stability

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3384585A JPS61192757A (en) 1985-02-22 1985-02-22 Vinyl chloride resin composition having improved thermal stability

Publications (1)

Publication Number Publication Date
JPS61192757A true JPS61192757A (en) 1986-08-27

Family

ID=12397831

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3384585A Pending JPS61192757A (en) 1985-02-22 1985-02-22 Vinyl chloride resin composition having improved thermal stability

Country Status (1)

Country Link
JP (1) JPS61192757A (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57209943A (en) * 1981-06-18 1982-12-23 Adeka Argus Chem Co Ltd Stabilized halogen-containing resin composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57209943A (en) * 1981-06-18 1982-12-23 Adeka Argus Chem Co Ltd Stabilized halogen-containing resin composition

Similar Documents

Publication Publication Date Title
JP2965773B2 (en) Heat stabilized halogen-containing resin composition having antistatic ability
JPS638137B2 (en)
JP3321755B2 (en) Vinyl chloride polymer composition with improved meltability
JPS61192757A (en) Vinyl chloride resin composition having improved thermal stability
JPS61192756A (en) Thermally stable vinyl chloride resin composition
JP2008081749A (en) Composition of pvc and carbon monoxide-modified ethylene-vinyl ester copolymer having improved color stability
JPS62138546A (en) Vinyl chloride based resin composition
JPH02196845A (en) Vinyl chloride-based resin composition
JPH07188488A (en) Polyvinyl chloride resin composition
JPS6249902B2 (en)
JP2001207003A (en) Vinyl chloride-based resin composition and outdoor building material using the same
JPS62283143A (en) Vinyl chloride resin composition
JP2527752B2 (en) Vinyl chloride resin composition
JPS61213252A (en) Vinyl chloride resin composition
JPH05140404A (en) Chlorinated vinyl chloride resin composition
JPH051195A (en) Flexible vinyl chloride-based resin composition for extrusion molding
JPH051193A (en) Flexible vinyl chloride-based resin composition for extrusion molding
JPS6392663A (en) Novel polyvinyl chloride composition
JPH021855B2 (en)
JPS60149644A (en) Flame-retardant resin composition
JPS5996150A (en) Highly filled halogen-containing resin composition
JPS6156243B2 (en)
JPH05222261A (en) Chlorinated vinyl chloride resin composition
JPS63191851A (en) Flame-retardant resin composition
JPS60120738A (en) Vinyl chloride copolymer composition