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JPH0745605B2 - Vinyl chloride resin composition with improved transparency - Google Patents

Vinyl chloride resin composition with improved transparency

Info

Publication number
JPH0745605B2
JPH0745605B2 JP62068655A JP6865587A JPH0745605B2 JP H0745605 B2 JPH0745605 B2 JP H0745605B2 JP 62068655 A JP62068655 A JP 62068655A JP 6865587 A JP6865587 A JP 6865587A JP H0745605 B2 JPH0745605 B2 JP H0745605B2
Authority
JP
Japan
Prior art keywords
vinyl chloride
acid
chloride resin
resin composition
weight
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.)
Expired - Fee Related
Application number
JP62068655A
Other languages
Japanese (ja)
Other versions
JPS63234053A (en
Inventor
正 天野
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.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical 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 Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP62068655A priority Critical patent/JPH0745605B2/en
Priority to ES8800818A priority patent/ES2006113A6/en
Priority to PT8704788A priority patent/PT87047B/en
Publication of JPS63234053A publication Critical patent/JPS63234053A/en
Publication of JPH0745605B2 publication Critical patent/JPH0745605B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、シート、フイルム、各種成形品などの成形材
料として有用な、成形加工後の透明性の改良された塩化
ビニル系樹脂組成物に関するものである。
TECHNICAL FIELD The present invention relates to a vinyl chloride resin composition having improved transparency after molding, which is useful as a molding material for sheets, films, various molded products, and the like. It is a thing.

(従来の技術とその問題点) 従来、塩化ビニル重合体はその優れた特性により、最終
製品で求められる特性に応じた各種の配合剤が添加され
て成形加工され、広範な用途に使用されている。この配
合剤の内には塩化ビニル樹脂コンパウンドの成形加工工
程における嵩比重の増大、帯電性の防止、粉体流動性の
向上、および押出しスクリュウへの食い込みの改良を目
的として、微粉末状のシリカ、タルク、ハイドロタルサ
イト、炭酸バリウム、水酸化バリウム、カルシウムステ
アレート、バリウムステアレート、ジンクステアレート
などのいわゆるブロック防止剤を用いる場合がある。し
かし、これらのブロック防止剤を用いて透明な成形品を
製造しようとすると、濁度が増加するという欠点があっ
た。
(Conventional technology and its problems) Conventionally, due to its excellent properties, vinyl chloride polymers have been used in a wide range of applications by adding various compounding agents according to the properties required in the final product, molding and processing. There is. Among these compounding agents, finely powdered silica is used for the purpose of increasing the bulk specific gravity in the molding and processing step of the vinyl chloride resin compound, preventing the charging property, improving the powder fluidity, and improving the bite into the extrusion screw. So-called antiblocking agents such as talc, hydrotalcite, barium carbonate, barium hydroxide, calcium stearate, barium stearate and zinc stearate may be used. However, when it is attempted to produce a transparent molded article using these antiblocking agents, there is a drawback that the turbidity increases.

(問題点を解決するための手段) 本発明はこのようなブロック防止剤を併用しても透明性
が低下することのない塩化ビニル系樹脂組成物を提供す
ることを目的とするもので、塩化ビニル系樹脂100重量
部に対して、0.005〜0.3重量部のペンタエリスリトール
及びジペンタエリスリトールの脂肪酸エステルと、0.00
5〜0.3重量部のブロック防止剤としてのシリカとを配合
してなる塩化ビニル系樹脂組成物としたことを要旨とす
るものである。
(Means for Solving Problems) An object of the present invention is to provide a vinyl chloride resin composition in which transparency is not deteriorated even when such an antiblocking agent is used in combination. 0.005-0.3 parts by weight of pentaerythritol and dipentaerythritol fatty acid ester with respect to 100 parts by weight of vinyl resin, and 0.00
The gist of the present invention is to provide a vinyl chloride resin composition obtained by mixing 5 to 0.3 parts by weight of silica as a block inhibitor.

これを説明すると、本発明の塩化ビニル系樹脂組成物に
適用されう塩化ビニル系樹脂としては、塩化ビニルホモ
ポリマーのほか、塩化ビニルを50重量%以上含有する塩
化ビニル共重合体を主成分とするものであって、この塩
化ビニルに共重合されるコモノマーとしては、例えば酢
酸ビニル、プロピオン酸ビニルなどのビニルエステル;
アクリル酸メチル、アクリル酸エチルなどのアクリル酸
エステルもしくはメタアクリル酸エステル;エチレン、
プロピレンなどのオレフィン;無水マレイン酸;アクリ
ロニトリル;スチレン;塩化ビニリデンなどが挙げられ
る。
Explaining this, as the vinyl chloride resin applied to the vinyl chloride resin composition of the present invention, in addition to vinyl chloride homopolymer, a vinyl chloride copolymer containing 50% by weight or more of vinyl chloride as a main component is used. Examples of the comonomer copolymerized with vinyl chloride include vinyl esters such as vinyl acetate and vinyl propionate;
Acrylic ester or methacrylic ester such as methyl acrylate, ethyl acrylate; ethylene,
Examples include olefins such as propylene; maleic anhydride; acrylonitrile; styrene; and vinylidene chloride.

一方、これに配合されるペンタエリスリトール及びジペ
ンタエリスリトールの脂肪酸エステルとしては、ペンタ
エリスリトール及びジペンタエリスリトールの水酸基の
一部または全部を、カプロン酸、ペラルゴン酸、ラウリ
ン酸、2−エチルヘキシル酸、ミリスチン酸、パルミチ
ン酸、ウンデシレン酸、リシノール酸、リノール酸、リ
ノレイン酸、ネオデカン酸、イソステアリン酸、12−ヒ
ドロキシステアリン酸、12−ケトステアリン酸、クロロ
ステアリン酸、フェニルステアリン酸、アラキン酸、ベ
ヘン酸、エルカ酸、ブラシジン酸など、獣脂脂肪酸、や
し油脂肪酸、桐油脂肪酸、大豆油脂肪酸、綿実油脂肪酸
など、安息香酸、トルイル酸、サリチル酸、p−tert−
ブチル安息香酸、5−t−オクチルサリチル酸、ナフテ
ン酸、キシリル酸、エチル安息香酸、イソプロピル安息
香酸、ジ−t−ブチル安息香酸、ブロモ安息香酸、アジ
ピン酸などで例示される脂肪酸でエステル化したもので
ある。
On the other hand, as the fatty acid ester of pentaerythritol and dipentaerythritol blended therein, some or all of the hydroxyl groups of pentaerythritol and dipentaerythritol are replaced with caproic acid, pelargonic acid, lauric acid, 2-ethylhexylic acid, myristic acid. , Palmitic acid, undecylenic acid, ricinoleic acid, linoleic acid, linoleic acid, neodecanoic acid, isostearic acid, 12-hydroxystearic acid, 12-ketostearic acid, chlorostearic acid, phenylstearic acid, arachidic acid, behenic acid, erucic acid , Tallow fatty acid, coconut oil fatty acid, tung oil fatty acid, soybean oil fatty acid, cottonseed oil fatty acid, benzoic acid, toluic acid, salicylic acid, p-tert-
Butyl benzoic acid, 5-t-octyl salicylic acid, naphthenic acid, xylyl acid, ethyl benzoic acid, isopropyl benzoic acid, di-t-butyl benzoic acid, bromobenzoic acid, esterified with fatty acids such as adipic acid Is.

これらのペンタエリスリトール及びジペンタエリスリト
ールの脂肪酸エステルの添加量は、塩化ビニル系樹脂10
0重量部に対して0.005〜0.3重量部が好ましく、これが
0.005重量部未満では透明性改良の効果が発揮されず、
また0.3重量部を超えると添加量の割合に効果が乏しく
経済的でない。
The amount of the fatty acid ester of pentaerythritol and dipentaerythritol added is 10
0.005-0.3 parts by weight is preferable to 0 parts by weight, which is
If it is less than 0.005 parts by weight, the effect of improving transparency is not exhibited,
On the other hand, if it exceeds 0.3 parts by weight, the effect of the addition amount is poor and it is not economical.

また、本発明の樹脂組成物に併用されるブロック防止剤
としてのシリカは塩化ビニル系樹脂100重量部に対して
0.005〜0.3重量部の割合で使用される。
Further, silica as a block inhibitor used in combination with the resin composition of the present invention is based on 100 parts by weight of the vinyl chloride resin.
Used in a proportion of 0.005 to 0.3 parts by weight.

上記したペンタエリスリトール及びジペンタエリスリト
ールの脂肪酸エステルおよびブロック防止剤としてのシ
リカの添加の方法としては、それぞれを同時または個別
に、水または溶媒に溶解する、分散液として仕込む、粉
体または液状で直接仕込むなどいずれの方法でも良く、
さらにこの添加の際に必要に応じて、熱安定性改良剤、
抗酸化剤、可塑剤、滑剤、加工助剤、衝撃改良剤などを
添加することも任意である。
The method of adding the fatty acid ester of pentaerythritol and dipentaerythritol and silica as the block inhibitor mentioned above may be simultaneous or individually dissolved in water or a solvent, charged as a dispersion liquid, directly in powder or liquid form. Any method such as charging,
Further, when necessary, a thermal stability improver,
It is also optional to add antioxidants, plasticizers, lubricants, processing aids, impact modifiers and the like.

(実施例) 以下、本発明の具体的態様を実施例および比較例により
説明するが、本発明はこれに限定されるものではない。
(Examples) Hereinafter, specific embodiments of the present invention will be described with reference to Examples and Comparative Examples, but the present invention is not limited thereto.

実施例1〜4.および比較例1. 塩化ビニル系樹脂TK−1300 (信越化学工業者製) 100重量部 DOP 45 〃 エポキシ化大豆油 5 〃 Ba−Zn系安定剤 AC−186(アデカアーガス社製) 1 〃 Rup−10( 〃 ) 1 〃 に、表に示すブロック防止剤および多価アルコールの脂
肪酸エステルをそれぞれ加え、この配合物をテストロー
ルにより150℃で5分間混練し、厚さ0.5mmのシートを作
成し、これをさらに185℃で6分間プレスして厚さ5mmの
透明な試験片とした。
Examples 1 to 4 and Comparative Example 1. Vinyl chloride resin TK-1300 (manufactured by Shin-Etsu Chemical Co., Ltd.) 100 parts by weight DOP 45 〃 Epoxidized soybean oil 5 〃 Ba-Zn stabilizer AC-186 (Adeka Argus company) Made) 1〃 Rup-10 (〃) 1〃, add the block inhibitor and fatty acid ester of polyhydric alcohol shown in the table respectively, and knead this mixture at 150 ℃ for 5 minutes with a test roll, 0.5mm thickness Sheet was prepared and further pressed at 185 ° C. for 6 minutes to obtain a transparent test piece having a thickness of 5 mm.

これについてデジタル濁度計NDH−20D(日本電色工業社
製)を用いて全透過率および濁度を測定した。また熱安
定性は上記の厚さ0.5mmのシートをギヤー氏オーブン中
に入れ、190℃の温度で完全に黒化するまでの時間
(分)で示した。
About this, the total transmittance and the turbidity were measured using a digital turbidimeter NDH-20D (manufactured by Nippon Denshoku Industries Co., Ltd.). The thermal stability was indicated by the time (minutes) required for completely blackening the sheet at a temperature of 190 ° C. by placing the sheet having a thickness of 0.5 mm in a gear oven.

この結果を下表に示した。なお、表中の多価アルコール
の脂肪酸エステルの欄の略記号は次の通りである。
The results are shown in the table below. The abbreviations in the column of fatty acid ester of polyhydric alcohol in the table are as follows.

I:ペンタエリスリトールモノステアレート II:ジペンタエリスリトールジステアレート III:ペンタエリスリトールモノミリステート IV:ジペンタエリスリトールアジペート また、使用したブロック防止剤は次のものである。I: Pentaerythritol monostearate II: Dipentaerythritol distearate III: Pentaerythritol monomyristate IV: Dipentaerythritol adipate The blocking inhibitors used are as follows.

シリカ:富士デヴィソン化学社製、 サイロイド72 (発明の効果) 本発明によれば、ブロック防止剤を併用しても透明性が
低下することのない塩化ビニル系樹脂組成物が得られ
る。
Silica: Fuji DeVison Chemical Company, Syloid 72 (Effect of the Invention) According to the present invention, a vinyl chloride resin composition can be obtained in which the transparency is not deteriorated even when an antiblocking agent is used in combination.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】塩化ビニル系樹脂100重量部に対して、0.0
05〜0.3重量部のペンタエリスリトール及びジペンタエ
リスリトールの脂肪酸エステルと、0.005〜0.3重量部の
ブロック防止剤としてのシリカとを配合してなる透明性
の改良された塩化ビニル系樹脂組成物。
1. A value of 0.0 based on 100 parts by weight of a vinyl chloride resin.
A vinyl chloride resin composition having improved transparency, which is obtained by blending 05 to 0.3 part by weight of pentaerythritol and dipentaerythritol fatty acid ester and 0.005 to 0.3 part by weight of silica as a block inhibitor.
JP62068655A 1987-03-23 1987-03-23 Vinyl chloride resin composition with improved transparency Expired - Fee Related JPH0745605B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP62068655A JPH0745605B2 (en) 1987-03-23 1987-03-23 Vinyl chloride resin composition with improved transparency
ES8800818A ES2006113A6 (en) 1987-03-23 1988-03-18 Vinyl chloride polymer compound having excellent transparency
PT8704788A PT87047B (en) 1987-03-23 1988-03-22 PREPARATION PROCESS OF A VINYL CHLORIDE TYPE RESIN COMPOSITION WITH GREATER TRANSPARENCY

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62068655A JPH0745605B2 (en) 1987-03-23 1987-03-23 Vinyl chloride resin composition with improved transparency

Publications (2)

Publication Number Publication Date
JPS63234053A JPS63234053A (en) 1988-09-29
JPH0745605B2 true JPH0745605B2 (en) 1995-05-17

Family

ID=13379931

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62068655A Expired - Fee Related JPH0745605B2 (en) 1987-03-23 1987-03-23 Vinyl chloride resin composition with improved transparency

Country Status (3)

Country Link
JP (1) JPH0745605B2 (en)
ES (1) ES2006113A6 (en)
PT (1) PT87047B (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS521743B2 (en) * 1973-03-28 1977-01-18
JPS57151635A (en) * 1981-03-16 1982-09-18 Adeka Argus Chem Co Ltd Halogen-containing resin composition
JPS5827735A (en) * 1981-08-12 1983-02-18 Adeka Argus Chem Co Ltd Stabilized halogen-containing resin composition

Also Published As

Publication number Publication date
PT87047B (en) 1992-07-31
JPS63234053A (en) 1988-09-29
ES2006113A6 (en) 1989-04-01
PT87047A (en) 1988-04-01

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