JPS6079051A - Vinyl chloride resin composition - Google Patents

Vinyl chloride resin composition

Info

Publication number
JPS6079051A
JPS6079051A JP58187106A JP18710683A JPS6079051A JP S6079051 A JPS6079051 A JP S6079051A JP 58187106 A JP58187106 A JP 58187106A JP 18710683 A JP18710683 A JP 18710683A JP S6079051 A JPS6079051 A JP S6079051A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
tetrahydrofuran
polyester polyol
drawdown
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
JP58187106A
Other languages
Japanese (ja)
Other versions
JPS6241978B2 (en
Inventor
Kazuhiko Fujiwara
一彦 藤原
Giichi Kawashima
川島 義一
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite 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 Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP58187106A priority Critical patent/JPS6079051A/en
Publication of JPS6079051A publication Critical patent/JPS6079051A/en
Publication of JPS6241978B2 publication Critical patent/JPS6241978B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain a resin compsn. which is excellent in discoloration resistance and adhesion to polyurethane foam and suffers less drawdown, by blending Ba, Zn and Mg salts and a polyester polyol with a specified vinyl chloride resin. CONSTITUTION:1-15pts.wt. Ba, Zn and Mg salts and 1-10pts.wt. polyester polyol having an OH value of 5-30 are blended with 100pts.wt. vinyl chloride resin composed of 5-90wt% tetrahydrofuran-insoluble polyvinyl chloride gel component and the balance of tetrahydrofuran-soluble matter. Further, filler, plasticizer, stabilizer, lubricant, processing aid, pigment, etc. may be added. Since the resin compsn. suffers less drawdown in blow molding, moldings having high dimensional accuracy can be obtd. and even articles having large parison weights can be molded.

Description

【発明の詳細な説明】 本発明は発泡ポリウレタンとの接着性が良好でかつ発泡
ポリウレタンにより起る変色が少なく、プロー成形時に
おけるドローダウン性の小さい塩化ビニル系樹脂組成物
に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a vinyl chloride resin composition that has good adhesion to polyurethane foam, less discoloration caused by polyurethane foam, and less drawdown during blow molding.

近年、塩化ビニル樹脂の射出成形品、プロー成形品に発
泡のポリウレタンを注入して了−ムレスト、ベンドレス
トなどの自動車内装部品が多く作られているが、従来よ
シ問題となっていることに塩ビ表皮層と発泡ポリウレタ
ンとの接着方法、発泡ポリウレタンとの接触により起る
塩ビ表皮層の変色(以後ウレタン汚染と名づける)、及
びプロー成形の場合のドローダウン現象()やリンノが
自重で垂れ下が9肉厚、外径が看しく変化する現象)が
大きくパリンン重奮が大きφ成形品はもちろんのこと、
ノ4リソン重蓋が小さi物でも均一な肉厚の表皮層を成
形する事が困難である事などであった。現在は、塩ビ表
皮層に接着剤を塗布する事で発泡ポリウレタンとの接着
力を向上させたり、目ゼリウレタンとの接触汚染につい
ては、汚染の比較的少ない発泡ポリウレタンを選択し表
皮層の色を濃色にして変色をめだたなくさせるなどの方
法が取られているが、十分なものとは言えない。またブ
ロー成形におけるドローダウンについては平均重合度の
高い塩化ビニル樹脂を使用する事でドローダウンを小さ
くする方法が用いられているが、ノクリソン重量の大き
い成形品などには効果が小さく十分なものとは言えなか
った。本発明者らはこのような状況をかんがみ、鋭意検
討を行った結果テトラヒドロ7ランに不溶なポリ塩化ビ
ニルグル分5〜90重量係及び残部がテトラヒドロフラ
ン可溶分からなる塩化ビニル樹脂100恵量部にBa 
、Zn 。
In recent years, many automobile interior parts such as wrap rests and bend rests have been made by injecting polyurethane foam into injection molded and blow molded products made of vinyl chloride resin. The adhesion method between the skin layer and foamed polyurethane, the discoloration of the PVC skin layer caused by contact with foamed polyurethane (hereinafter referred to as urethane contamination), the drawdown phenomenon () in the case of blow molding, and the sagging of linden due to its own weight. 9) The phenomenon in which the wall thickness and outer diameter change appreciably) is large, and the palin is very heavy, not to mention φ molded products.
Even if the heavy lid was small, it was difficult to form a skin layer with uniform thickness. Currently, we are applying an adhesive to the PVC skin layer to improve the adhesion with foam polyurethane, and to prevent contact contamination with jelly urethane, we are choosing foam polyurethane, which is relatively less contaminated, and deepening the color of the skin layer. Methods have been taken to make the discoloration less noticeable, but these methods are not sufficient. Regarding drawdown in blow molding, a method is used to reduce the drawdown by using vinyl chloride resin with a high average degree of polymerization, but the effect is small and is not sufficient for molded products with a large weight of Nocrisone. I couldn't say it. In view of this situation, the present inventors conducted intensive studies and found that 100 parts by weight of a polyvinyl chloride resin consisting of 5 to 90 parts by weight of polyvinyl chloride which is insoluble in tetrahydrofuran and the remainder soluble in tetrahydrofuran contains Ba.
,Zn.

Mノ の金槁塩を1〜15重量部及びOH価5〜30で
あるポリエステルポリオール1〜10!m部よシなる、
りろ泡ポリウレタンとの接着性が良好でかつ発泡ポリウ
レタンによる起る変色が少なく、プロー成形時における
ドローダウン性の小さいポリ塩化ビニル系樹脂組成物を
発明したのである。
A polyester polyol containing 1 to 15 parts by weight of M-golden salt and an OH value of 5 to 30! It's m part,
They have invented a polyvinyl chloride resin composition that has good adhesion to Rirofoam polyurethane, has little discoloration caused by foamed polyurethane, and has low drawdown properties during blow molding.

本発明により塩ビ表皮層と発泡i?ポリレタンとを接着
させるための接着剤塗布の必要がなくなり、大巾なコス
トダウンと行程の合理化をもたらす事ができる。またウ
レタン汚染が少ないため、博9色物の成形品にも適応が
可能となった。またプロー成形においてもドローダウン
が少ないために寸法精度のよい成形品が得られ、ノ母す
ソン重蓋の大きい物でも成形できるようになったのであ
る。
According to the present invention, the PVC skin layer and the foamed i? There is no need to apply adhesive to bond polyurethane, leading to significant cost reductions and streamlining of processes. In addition, because there is little urethane contamination, it can be applied to molded products of nine colors. Also, in plow molding, because drawdown is small, molded products with good dimensional accuracy can be obtained, and it has become possible to mold even products with large lids.

本発明においてBa 、 Zn 、 Mf金属塩の添加
量は1重量部以下ではウレタン汚染防止への効果が少な
く、また熱安定性も患いものとなり、1〜15重量部が
適当である。またポリエステルポリオールは添加量が1
重量部以下あるいはOH価が5以下のものは、発泡ポリ
ウレタンと表皮層の接着への効果が極めて少なく、添加
量を10獣蓋部以上あるいは、OH価が30以上とした
ものは成形品表面にブルーミング現象を起す時がある事
から種々検討の結果OH価が5〜3t)のポリエステル
ポリオールを使用し、かつ添加量を1重量部からlθ重
址部の範囲に入るものが望ましい。本発明の、1? I
J塩化ビニル糸工業調査会発行の塩化ビニル材料便覧に
記載されているものであればなんら限定するものではな
い。
In the present invention, if the amount of Ba, Zn, or Mf metal salt added is less than 1 part by weight, the effect on preventing urethane staining will be small and the thermal stability will be poor, so 1 to 15 parts by weight is suitable. In addition, the amount of polyester polyol added is 1
If the additive amount is less than 10 parts by weight or the OH value is 5 or less, the effect on the adhesion between polyurethane foam and the skin layer is extremely small, and if the amount added is more than 10 parts by weight or the OH value is 30 or more, it will not affect the surface of the molded product. Since blooming phenomenon sometimes occurs, various studies have revealed that it is desirable to use a polyester polyol with an OH value of 5 to 3 tons, and to add an amount within the range of 1 part by weight to 1 part by weight. 1 of the present invention? I
There is no limitation as long as it is listed in the vinyl chloride material handbook published by the J Vinyl Chloride Yarn Industry Research Group.

以下本発明の技術的内容を実施例により説明する。The technical content of the present invention will be explained below using examples.

実施例1 第1表に示す各配合をスーパーミキサーにて混合し、5
0鬼押出機で混練債粒した。これを75%の押出機でノ
ぐリソン径200 tar 、 =リソン肉厚2胴の2
tの了キュムレーターを持つブロー成形機でノ+リソン
を下ろし、ドローダウン性の評価を行った。
Example 1 Each formulation shown in Table 1 was mixed in a super mixer, and 5
The bond was kneaded into grains using a zero extruder. This is extruded using a 75% extruder with a diameter of 200 tar, = 2 of the 2 cylinders with a thickness of 2
The molding material was unloaded using a blow molding machine with a 300 mm accumulator, and the drawdown properties were evaluated.

実施例2 第2表に示す各配合をスーパーミキサーにて混合し5〇
九御出機で混練造粒した。これを75%の押出機でパリ
ソン径200I+III+1パリンン肉厚2圓の2tの
アキュムレーターを持つブロー成形機で成形を行い、そ
の後発泡ポリウレタンを注入し、接着性、ウレタン汚染
性の評価を行った。
Example 2 Each of the formulations shown in Table 2 was mixed in a super mixer and kneaded and granulated in a 509 oder machine. This was molded using a 75% extruder with a blow molding machine equipped with a 2t accumulator with a parison diameter of 200I+III+1 parison wall thickness of 2mm, and then foamed polyurethane was injected and the adhesiveness and urethane staining properties were evaluated.

以上実施例からも本発明による効果が大きいことがわか
る。
It can be seen from the above examples that the effects of the present invention are significant.

Claims (1)

【特許請求の範囲】[Claims] テトラヒドロフランに不溶なポリ塩化ビニルグル外5〜
90 徂i %及び残部がテトラヒドロフラン可m分か
らなる塩化ビニル系樹脂100重址部にBa 、 Zn
 、 Mf の金属塩を1〜15重量部及びOH価が5
〜30−(:あるポリエステルポリオール1〜lo 恵
M部よシなることを特徴とする塩化ビニル系樹脂組成物
Polyvinyl chloride insoluble in tetrahydrofuran
Ba and Zn are added to 100 parts of vinyl chloride resin with 90% and the remainder being tetrahydrofuran.
, 1 to 15 parts by weight of a metal salt of Mf and an OH value of 5
~30-(: A vinyl chloride resin composition characterized by comprising a certain polyester polyol 1~lo).
JP58187106A 1983-10-07 1983-10-07 Vinyl chloride resin composition Granted JPS6079051A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58187106A JPS6079051A (en) 1983-10-07 1983-10-07 Vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58187106A JPS6079051A (en) 1983-10-07 1983-10-07 Vinyl chloride resin composition

Publications (2)

Publication Number Publication Date
JPS6079051A true JPS6079051A (en) 1985-05-04
JPS6241978B2 JPS6241978B2 (en) 1987-09-05

Family

ID=16200203

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58187106A Granted JPS6079051A (en) 1983-10-07 1983-10-07 Vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPS6079051A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01311153A (en) * 1988-06-08 1989-12-15 Sumitomo Bakelite Co Ltd Vinyl chloride-based resin composition
JP2009115168A (en) * 2007-11-05 2009-05-28 Denso Corp Power transmission device
JPWO2016098344A1 (en) * 2014-12-17 2017-09-28 日本ゼオン株式会社 Vinyl chloride resin composition and method for producing the same, vinyl chloride resin molded article and method for producing the same, and laminate

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01311153A (en) * 1988-06-08 1989-12-15 Sumitomo Bakelite Co Ltd Vinyl chloride-based resin composition
JPH0555550B2 (en) * 1988-06-08 1993-08-17 Sumitomo Bakelite Co
JP2009115168A (en) * 2007-11-05 2009-05-28 Denso Corp Power transmission device
JPWO2016098344A1 (en) * 2014-12-17 2017-09-28 日本ゼオン株式会社 Vinyl chloride resin composition and method for producing the same, vinyl chloride resin molded article and method for producing the same, and laminate

Also Published As

Publication number Publication date
JPS6241978B2 (en) 1987-09-05

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