JPH0820698A - Vinyl chloride resin composition - Google Patents

Vinyl chloride resin composition

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Publication number
JPH0820698A
JPH0820698A JP15604494A JP15604494A JPH0820698A JP H0820698 A JPH0820698 A JP H0820698A JP 15604494 A JP15604494 A JP 15604494A JP 15604494 A JP15604494 A JP 15604494A JP H0820698 A JPH0820698 A JP H0820698A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
weight
rubber
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
JP15604494A
Other languages
Japanese (ja)
Inventor
Fusao Abe
房男 阿部
Kazuo Tanaka
一雄 田中
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.)
Bando Chemical Industries Ltd
Original Assignee
Bando Chemical Industries 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 Bando Chemical Industries Ltd filed Critical Bando Chemical Industries Ltd
Priority to JP15604494A priority Critical patent/JPH0820698A/en
Publication of JPH0820698A publication Critical patent/JPH0820698A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a vinyl chloride resin composition, excellent in thermal stability and processability and capable of effectively preventing the plateout phenomenon from occurring. CONSTITUTION:This vinyl chloride resin composition is obtained by blending 100 pts.wt. vinyl chloride resin containing 15-120 pts.wt. polyester-based plasticizer with 0.1-10 pts.wt. polybutadiene copolymer containing a butadiene-based rubber as a rubber component or an acrylic rubber copolymer containing an acrylic rubber as the rubber component. A vinyl chloride resin containing 0.5-10 pts.wt. dibasic lead phosphite or 1-20 pts.wt. ethylene-vinyl acetate-based resin with 55-70wt.% vinyl acetate content may be used in place of the polyester-based plasticizer.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は塩化ビニル樹脂組成物に
関し、特に塩化ビニル樹脂を成形加工する際に、安定剤
や着色剤等の塩化ビニル樹脂組成物の一部がカレンダー
ロール、テイクオフロール、エンボスロール、ゴムロー
ル、クーラーロールなどの金属表面に分離付着する現
象、いわゆる『プレートアウト』を防止しうる塩化ビニ
ル樹脂組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a vinyl chloride resin composition, and particularly when a vinyl chloride resin is molded and processed, a part of the vinyl chloride resin composition such as a stabilizer and a coloring agent is calender roll, take-off roll, The present invention relates to a vinyl chloride resin composition capable of preventing the phenomenon of so-called "plate-out", which is the phenomenon of separation and adhesion to metal surfaces such as embossing rolls, rubber rolls, and cooler rolls.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】塩化
ビニル樹脂組成物は、可塑剤との相溶性を活かして、透
明性・柔軟性・強度・耐候性・耐寒性・耐熱性およびカ
レンダー加工性ならびに押出し加工性等に優れており、
農業用フィルム・シート、医療用フィルム・シート、マ
ーキングならびにステッカー用フィルム・シート、マス
キングならびにプロテクト用フィルム・シート、車両用
の耐油性ならびに耐溶剤性シート、電気絶縁テープ用フ
ィルム・シート、電線用フィルム・シート、合板用化粧
フィルム・シート、鋼板用化粧フィルム・シート、半硬
質ならびに硬質フィルム・シート等のフィルム、シート
を始めとして、板、パイプ、成型品等あらゆる分野に広
く使用されている。
BACKGROUND OF THE INVENTION Vinyl chloride resin compositions utilize transparency and flexibility, strength, weather resistance, cold resistance, heat resistance and calender processability by taking advantage of compatibility with plasticizers. And excellent in extrudability,
Agricultural film sheets, medical film sheets, marking and sticker film sheets, masking and protection film sheets, vehicle oil and solvent resistant sheets, electrical insulating tape film sheets, electric wire films -Widely used in all fields such as sheets, decorative films / sheets for plywood, decorative films / sheets for steel plates, semi-rigid and hard films / sheets, and plates, pipes, molded products.

【0003】ところが、上記したように、塩化ビニル樹
脂をカレンダー加工する際には、プレートアウトという
現象が生じる可能性があるので、特公平3−45745
号公報および特公平3−45746号公報には、塩化ビ
ニル樹脂にエポキシ樹脂またはエポキシ化植物油を配合
した場合のプレートアウトを防止する目的で、液状ポリ
ブタジエン又はその変性品を添加したものが開示されて
いるが、プレートアウト防止効果は必ずしも十分ではな
い。
However, as described above, when a vinyl chloride resin is calendered, a phenomenon of plate-out may occur, and therefore, Japanese Patent Publication No. 3-45745.
Japanese Patent Publication No. 3-45746 and Japanese Patent Publication No. 3-45746 disclose that liquid polybutadiene or a modified product thereof is added for the purpose of preventing plate-out when a vinyl chloride resin is mixed with an epoxy resin or an epoxidized vegetable oil. However, the plate-out prevention effect is not always sufficient.

【0004】また、一般に、高級脂肪酸、高級脂肪酸エ
ステル、芳香族アルコール脂肪酸エステル、シリカ等は
プレートアウトを抑制するものとして知られている(以
下「従来のプレートアウト防止剤」という)。
Further, higher fatty acids, higher fatty acid esters, aromatic alcohol fatty acid esters, silica and the like are generally known to suppress plate-out (hereinafter referred to as "conventional plate-out inhibitors").

【0005】しかし、従来のプレートアウト防止剤に
は、添加することにより多少のプレートアウト抑制効果
は見られるが、十分ではなく、以下のような欠点を有し
ている。
However, although the conventional plate-out inhibitor has some effect of suppressing plate-out when added, it is not sufficient and has the following drawbacks.

【0006】高級脂肪酸系のものは、塩化ビニル樹脂組
成物のゲル化性を遅らせ、透明性を低下し、加工中に変
色しやすくさせる。高級脂肪酸エステル系、芳香族アル
コール脂肪酸エステル系のものは、塩化ビニル樹脂組成
物の熱安定性を阻害し、加工中に変色しやすくさせる。
シリカは塩化ビニル樹脂組成物の熱安定性を低下し、加
工中に変色しやすくさせ、多量に配合すると透明性が低
下する。
Higher fatty acid-based compounds delay the gelation property of the vinyl chloride resin composition, reduce the transparency, and cause discoloration during processing. The higher fatty acid ester type and aromatic alcohol fatty acid ester type ones impede the thermal stability of the vinyl chloride resin composition and make it easily discolored during processing.
Silica lowers the thermal stability of the vinyl chloride resin composition, makes it easily discolored during processing, and reduces the transparency when incorporated in a large amount.

【0007】さらに、ポリエステル系可塑剤、二塩基性
亜燐酸鉛またはエチレン−酢酸ビニル系樹脂を含む塩化
ビニル樹脂組成物をカレンダー加工した場合、特にカレ
ンダーロール表面、テイクオフロール表面、エンボスロ
ール表面、ゴムロール表面に塩化ビニル樹脂組成物の一
部が吹き出し、各ロール表面が汚染されることにより、
塩化ビニル製品(フィルム・シート)の厚み精度が低下
したり、正常な絞付けができず、製品表面の艶・粗さ・
透明性等の外観性能が低下する。また、各ロール表面の
汚染物を除去しなければならず、生産性が極度に低下す
る。ところが、従来のプレートアウト防止剤では、係る
『吹き出し』の防止効果が十分でないばかりか、それに
伴って上記したような問題を誘発するのである。
Further, when a vinyl chloride resin composition containing a polyester-based plasticizer, a dibasic lead phosphite or an ethylene-vinyl acetate resin is calendered, especially, a calender roll surface, a take-off roll surface, an embossing roll surface, a rubber roll is used. By blowing a part of the vinyl chloride resin composition on the surface and contaminating the surface of each roll,
The thickness accuracy of vinyl chloride products (films / sheets) decreases, and normal tightening cannot be performed, resulting in gloss and roughness of the product surface.
Appearance performance such as transparency decreases. Moreover, the contaminants on the surface of each roll must be removed, resulting in extremely low productivity. However, the conventional plate-out preventing agent not only does not have a sufficient effect of preventing such "blowing", but also causes the above-mentioned problems.

【0008】本発明は従来の技術の有するこのような問
題点に鑑みてなされたものであって、その目的は、熱安
定性および加工性に優れ且つプレートアウト現象を効果
的に防止しうる塩化ビニル樹脂組成物を提供することに
ある。
The present invention has been made in view of the above problems of the prior art, and its object is to provide chloride having excellent thermal stability and processability and capable of effectively preventing the plate-out phenomenon. It is to provide a vinyl resin composition.

【0009】[0009]

【課題を解決するための手段】上記目的を達成するため
に本発明は、ポリエステル系可塑剤を15〜120重量
部含有する塩化ビニル樹脂100重量部に、ブタジエン
系ゴムをゴム成分とするポリブタジエン共重合体または
アクリルゴムをゴム成分とするアクリルゴム共重合体を
0.1〜10重量部配合してなる塩化ビニル樹脂組成物
を第一の発明とし、二塩基性亜燐酸鉛を0.5〜10重
量部含有する塩化ビニル樹脂100重量部に、ブタジエ
ン系ゴムをゴム成分とするポリブタジエン共重合体また
はアクリルゴムをゴム成分とするアクリルゴム共重合体
を0.1〜10重量部配合してなる塩化ビニル樹脂組成
物を第二の発明とし、酢酸ビニル含量が55〜70重量
%のエチレン−酢酸ビニル系樹脂を1〜20重量部含有
する塩化ビニル樹脂100重量部に、ブタジエン系ゴム
をゴム成分とするポリブタジエン共重合体またはアクリ
ルゴムをゴム成分とするアクリルゴム共重合体を0.1
〜10重量部配合してなる塩化ビニル樹脂組成物を第三
の発明とする。
In order to achieve the above object, the present invention is based on 100 parts by weight of a vinyl chloride resin containing 15 to 120 parts by weight of a polyester plasticizer and polybutadiene copolymer containing butadiene rubber as a rubber component. A vinyl chloride resin composition comprising 0.1 to 10 parts by weight of a polymer or an acrylic rubber copolymer containing acrylic rubber as a rubber component is a first invention, and a dibasic lead phosphite is 0.5 to 0.1 to 10 parts by weight of a polybutadiene copolymer containing butadiene rubber as a rubber component or an acrylic rubber copolymer containing acrylic rubber as a rubber component is mixed with 100 parts by weight of vinyl chloride resin containing 10 parts by weight. A vinyl chloride resin composition as a second invention, containing 1 to 20 parts by weight of an ethylene-vinyl acetate resin having a vinyl acetate content of 55 to 70% by weight. To 100 parts by weight, the acrylic rubber copolymer polybutadiene copolymer or an acrylic rubber to butadiene rubber and the rubber component and the rubber component 0.1
A vinyl chloride resin composition prepared by mixing 10 to 10 parts by weight is defined as a third invention.

【0010】塩化ビニル樹脂としては、塩化ビニルホモ
ポリマー、塩化ビニル−酢酸ビニル共重合体および塩化
ビニル−エチレン酢酸ビニル共重合体等の塩化ビニル系
共重合体を使用することができる。
As the vinyl chloride resin, vinyl chloride homopolymers, vinyl chloride-vinyl acetate copolymers and vinyl chloride-ethylene vinyl acetate copolymers can be used.

【0011】第一の発明においては、可塑剤としては、
アジピン酸系ポリエステル可塑剤、フタル酸系ポリエス
テル可塑剤等を使用することができる。また、安定剤と
しては、Pb系、Sn系を除く、Cd−Ba系、Ba−
Zn系、Ca−Zn系等の安定剤を用いることができ
る。Pb系およびSn系安定剤は一般にポリエステル系
可塑剤を分解しやすく、ブリード等の欠陥を発生させる
ので、好ましくない。
In the first invention, as the plasticizer,
Adipic acid type polyester plasticizers, phthalic acid type polyester plasticizers and the like can be used. In addition, as the stabilizer, Pd-based, Sn-based, except for Cd-Ba-based, Ba-
A Zn-based stabilizer, a Ca-Zn-based stabilizer, or the like can be used. Pb-based and Sn-based stabilizers are generally not preferable because they tend to decompose polyester plasticizers and cause defects such as bleeding.

【0012】第二の発明においては、可塑剤としては、
フタル酸エステル系、アジピン酸エステル系、燐酸エス
テル系、トリメリット酸エステル系等の通常塩化ビニル
樹脂の可塑剤として用いられているものを使用すること
ができる。また、安定剤としては、耐候性、耐熱性、電
気絶縁性の向上を目的として、鉛系金属化合物の中で
は、特に二塩基性亜燐酸鉛に限定して用いる。
In the second invention, as the plasticizer,
It is possible to use phthalic acid ester-based, adipic acid ester-based, phosphoric acid ester-based, trimellitic acid ester-based resins and the like which are usually used as plasticizers for vinyl chloride resins. Further, as the stabilizer, among the lead-based metal compounds, dibasic lead phosphite is particularly limited for the purpose of improving weather resistance, heat resistance and electric insulation.

【0013】第三の発明においては、可塑剤としては、
フタル酸エステル系、アジピン酸エステル系、燐酸エス
テル系、ポリエステル系等の通常塩化ビニル樹脂の可塑
剤として用いられているものを使用することができる。
また、安定剤としては、Cd−Ba系、Ba−Zn系、
Ca−Zn系、Pb系、Sn系等の通常塩化ビニル樹脂
に用いられる安定剤を使用することができる。
In the third invention, as the plasticizer,
It is possible to use phthalic acid ester-based, adipic acid ester-based, phosphoric acid ester-based, polyester-based, or other materials that are commonly used as plasticizers for vinyl chloride resins.
Further, as the stabilizer, Cd-Ba type, Ba-Zn type,
It is possible to use stabilizers which are usually used for vinyl chloride resins, such as Ca-Zn type, Pb type and Sn type.

【0014】その他、必要に応じて顔料、充填剤、紫外
線吸収剤、加工助剤、耐熱助剤、耐候性向上剤等を添加
することができる。
In addition, pigments, fillers, UV absorbers, processing aids, heat resistance aids, weather resistance improvers and the like can be added as required.

【0015】[0015]

【作用】第一の発明において、ポリエステル系可塑剤が
15重量部未満では溶融粘度が高く、一方、120重量
部を超えると、溶融粘度が低く、加工が非常に困難にな
る。第二の発明において、二塩基性亜燐酸鉛が0.5重
量部未満では熱安定性が悪く、加工できない。一方、1
0重量部を超えると、滑性が強く、加工性がよくない。
第三の発明において、酢酸ビニル含量が55重量%未満
のエチレン−酢酸ビニル系樹脂は透明性を阻害し、ゲル
化性を低下させ、一方、同含量が70重量%を超えるエ
チレン−酢酸ビニル系樹脂は、耐衝撃性を向上させる効
果が少ない。また、酢酸ビニル含量が55〜70重量%
のエチレン−酢酸ビニル系樹脂が1重量部未満では、耐
衝撃性とゲル化性の向上効果が少ない。一方、同樹脂が
20重量部を超えると、塩化ビニル樹脂との相溶性が悪
くなり、カレンダー加工において、フローマーク等の厚
みムラの欠点を発生させる。塩化ビニル樹脂100重量
部に対して、ブタジエン系ゴムをゴム成分とするポリブ
タジエン共重合体またはアクリルゴムをゴム成分とする
アクリルゴム共重合体が0.1重量部未満では、プレー
トアウトの防止効果が期待できず、一方、10重量部を
超えると、カレンダー加工性が低下する。
In the first invention, when the polyester plasticizer is less than 15 parts by weight, the melt viscosity is high, while when it exceeds 120 parts by weight, the melt viscosity is low and the processing becomes very difficult. In the second invention, if the dibasic lead phosphite is less than 0.5 parts by weight, the thermal stability is poor and it cannot be processed. On the other hand, 1
When it exceeds 0 parts by weight, the slipperiness is strong and the workability is poor.
In the third invention, an ethylene-vinyl acetate resin having a vinyl acetate content of less than 55% by weight hinders transparency and lowers gelation property, while an ethylene-vinyl acetate resin having the same content of more than 70% by weight is used. Resin has little effect of improving impact resistance. Also, the vinyl acetate content is 55 to 70% by weight.
When the amount of the ethylene-vinyl acetate resin is less than 1 part by weight, the effect of improving impact resistance and gelation property is small. On the other hand, when the amount of the resin exceeds 20 parts by weight, the compatibility with the vinyl chloride resin deteriorates, and defects such as flow marks in thickness unevenness occur during calendar processing. If the polybutadiene copolymer containing butadiene rubber as a rubber component or the acrylic rubber copolymer containing acrylic rubber as a rubber component is less than 0.1 parts by weight with respect to 100 parts by weight of the vinyl chloride resin, the effect of preventing plate-out is exerted. It cannot be expected. On the other hand, when it exceeds 10 parts by weight, the calendering workability is deteriorated.

【0016】[0016]

【実施例】以下に本発明の実施例1〜9を対応する比較
例1〜9と対比しながら説明する。
EXAMPLES Examples 1 to 9 of the present invention will be described below in comparison with corresponding Comparative Examples 1 to 9.

【0017】〔1〕実施例1〜3、比較例1〜3 (実施例1、比較例1)次の表1のように配合した塩化
ビニル樹脂組成物を、6インチの2本ロールにて、ロー
ル温度180℃、シート厚み0.2mmで混練し、混練時
間15分後におけるロール表面を観察し、汚れを評価し
た。また、混練時間5分と20分で適当な大きさのシー
トを採取し、色差計で色調を測定し、熱安定性を評価し
た。それらの結果を表1に記載する。なお、汚れの評価
は5段階で行い、5は最も悪く、ロール表面に油膜等
(または粉状のもの)が厚く形成されたもの、4はロー
ル表面に明らかに油膜等(または粉状のもの)が認めら
れたもの、3はロール表面に少し油膜等(または粉状の
もの)が認められたもの、2はロール表面にかすかに油
膜等(または粉状のもの)が認められたもの、1はロー
ル表面に全く油膜等(または粉状のもの)が認められな
かったものを示す。また、色差計は日本電色工業(株)
製のSZ−Σ80を用い、混練時間20分後のシートを
混練時間5分後のシートを標準として色調を測定し、色
差を表示した。
[1] Examples 1 to 3, Comparative Examples 1 to 3 (Example 1, Comparative Example 1) A vinyl chloride resin composition compounded as shown in Table 1 below was placed on a 6-inch two-roll mill. Kneading was performed at a roll temperature of 180 ° C. and a sheet thickness of 0.2 mm, and the roll surface was observed 15 minutes after the kneading time, and the stain was evaluated. Also, a sheet having an appropriate size was sampled at a kneading time of 5 minutes and 20 minutes, the color tone was measured by a color difference meter, and the thermal stability was evaluated. The results are shown in Table 1. In addition, the evaluation of dirt is performed in 5 stages, 5 is the worst, and a thick oil film (or powder) is formed on the roll surface, 4 is clearly an oil film (or powder) on the roll surface ) Was observed, 3 was a little oil film (or powder) on the roll surface, 2 was a slight oil film (or powder) on the roll surface, No. 1 indicates that no oil film or the like (or powdery matter) was observed on the roll surface. The color difference meter is Nippon Denshoku Industries Co., Ltd.
Using SZ-Σ80 manufactured by K.K., the color tone was measured using the sheet after 20 minutes of kneading time as the standard, and the color difference was displayed.

【0018】(実施例2、比較例2)次の表2のように
配合した塩化ビニル樹脂組成物について、実施例1と同
様の方法で混練を行い、ロール表面の汚れと製品の熱安
定性を評価した。その結果を表2に記載する。 (実施例3、比較例3)次の表3のように配合した塩化
ビニル樹脂組成物について、実施例1と同様の方法で混
練を行い、ロール表面の汚れと製品の熱安定性を評価し
た。その結果を表3に記載する。なお、表1〜3および
以下の表4〜9の配合量は重量部を示す。
(Example 2, Comparative Example 2) The vinyl chloride resin composition blended as shown in Table 2 below was kneaded in the same manner as in Example 1 to stain the roll surface and to stabilize the heat of the product. Was evaluated. The results are shown in Table 2. (Example 3, Comparative Example 3) The vinyl chloride resin composition blended as shown in Table 3 below was kneaded in the same manner as in Example 1 to evaluate the stain on the roll surface and the thermal stability of the product. . The results are shown in Table 3. In addition, the compounding quantity of Tables 1-3 and the following Tables 4-9 shows a weight part.

【0019】[0019]

【表1】 [Table 1]

【0020】[0020]

【表2】 [Table 2]

【0021】[0021]

【表3】 [Table 3]

【0022】表1〜3に明らかなように、本実施例1〜
3に係るものには、プレートアウト防止効果があり、且
つ加工中の変色も少ない(熱安定性に優れている)。し
かし、表1に明らかなように、従来のプレートアウト防
止剤を配合した比較例1においては多少のプレートアウ
ト抑制効果は見られるが、十分ではなく、かつ加工中の
変色が大である。また、表2の比較例2のように、本実
施例と同じプレートアウト防止剤を添加しても、その添
加量が0.05重量部と少なければ、プレートアウト防
止効果は少ない。さらに、表3の比較例3のように、本
実施例と同じプレートアウト防止剤を添加しても、その
添加量が15重量部と多ければ、プレートアウト防止効
果は有しても、変色がやや大きくなる。
As is apparent from Tables 1 to 3, the present Examples 1 to 1
The material of No. 3 has a plate-out prevention effect and has little discoloration during processing (excellent thermal stability). However, as is clear from Table 1, in Comparative Example 1 in which the conventional plate-out inhibitor was blended, some plate-out suppressing effect was observed, but it was not sufficient and discoloration during processing was large. Further, even if the same plate-out preventing agent as in this example is added as in Comparative Example 2 in Table 2, the plate-out preventing effect is small if the added amount is as small as 0.05 parts by weight. Further, as in Comparative Example 3 in Table 3, even if the same plate-out preventing agent as in this example was added, if the addition amount was as large as 15 parts by weight, the plate-out preventing effect was exhibited, but discoloration occurred. It gets a little bigger.

【0023】〔2〕実施例4〜6、比較例4〜6 (実施例4、比較例4)次の表4のように配合した塩化
ビニル樹脂組成物について、実施例1と同様の方法で混
練を行い、ロール表面の汚れを評価した。その結果を表
4に記載する。
[2] Examples 4 to 6 and Comparative Examples 4 to 6 (Example 4, Comparative Example 4) Vinyl chloride resin compositions formulated as shown in Table 4 below were prepared in the same manner as in Example 1. Kneading was performed and the stain on the roll surface was evaluated. The results are shown in Table 4.

【0024】(実施例5、比較例5)次の表5のように
配合した塩化ビニル樹脂組成物について、実施例1と同
様の方法で混練を行い、ロール表面の汚れを評価した。
その結果を表5に記載する。
(Example 5, Comparative Example 5) The vinyl chloride resin composition blended as shown in Table 5 below was kneaded in the same manner as in Example 1 to evaluate the stain on the roll surface.
The results are shown in Table 5.

【0025】(実施例6、比較例6)次の表6のように
配合した塩化ビニル樹脂組成物について、実施例1と同
様の方法で混練を行い、ロール表面の汚れと製品の熱安
定性を評価した。その結果を表6に記載する。
(Example 6, Comparative Example 6) The vinyl chloride resin composition blended as shown in the following Table 6 was kneaded in the same manner as in Example 1 to stain the roll surface and heat stability of the product. Was evaluated. The results are shown in Table 6.

【0026】[0026]

【表4】 [Table 4]

【0027】[0027]

【表5】 [Table 5]

【0028】[0028]

【表6】 [Table 6]

【0029】表4〜6に明らかなように、本実施例4〜
6に係るものには、プレートアウト防止効果があり、且
つ表6に見られるように、加工中の変色も少ない(熱安
定性に優れている)。しかし、表4に明らかなように、
従来のプレートアウト防止剤を配合した比較例4にはプ
レートアウト防止効果は見られない。また、表5の比較
例5のように、本実施例と同じプレートアウト防止剤を
添加しても、その添加量が0.05重量部と少なけれ
ば、プレートアウト防止効果は見られない。さらに、表
6の比較例6のように、本実施例と同じプレートアウト
防止剤を添加しても、その添加量が15重量部と多けれ
ば、プレートアウト防止効果は有しても、変色が大きく
なる。
As is apparent from Tables 4 to 6, the present Example 4 to
No. 6 has an effect of preventing plate-out, and as shown in Table 6, there is little discoloration during processing (excellent thermal stability). However, as can be seen in Table 4,
Comparative Example 4 containing a conventional plate-out preventing agent does not show a plate-out preventing effect. Further, even if the same plate-out preventing agent as in the present example is added as in Comparative Example 5 in Table 5, the effect of preventing plate-out is not observed unless the added amount is as small as 0.05 parts by weight. Further, as in Comparative Example 6 in Table 6, even if the same plate-out preventing agent as in the present example was added and the addition amount was as large as 15 parts by weight, the plate-out preventing effect was exhibited, but discoloration occurred. growing.

【0030】〔3〕実施例7〜9、比較例7〜9 (実施例7、比較例7)次の表7のように配合した塩化
ビニル樹脂組成物について、実施例1と同様の方法で混
練を行い、ロール表面の汚れと製品の熱安定性を評価し
た。その結果を表7に記載する。 (実施例8、比較例8)次の表8のように配合した塩化
ビニル樹脂組成物について、実施例1と同様の方法で混
練を行い、ロール表面の汚れと製品の熱安定性を評価し
た。その結果を表8に記載する。 (実施例9、比較例9)次の表9のように配合した塩化
ビニル樹脂組成物について、実施例1と同様の方法で混
練を行い、ロール表面の汚れと製品の熱安定性を評価し
た。その結果を表9に記載する。
[3] Examples 7-9, Comparative Examples 7-9 (Example 7, Comparative Example 7) Vinyl chloride resin compositions formulated as shown in Table 7 below were prepared in the same manner as in Example 1. Kneading was performed to evaluate the stain on the roll surface and the thermal stability of the product. The results are shown in Table 7. (Example 8, Comparative Example 8) A vinyl chloride resin composition blended as shown in Table 8 below was kneaded in the same manner as in Example 1 to evaluate the stain on the roll surface and the thermal stability of the product. . The results are shown in Table 8. (Example 9, Comparative Example 9) A vinyl chloride resin composition blended as shown in Table 9 below was kneaded in the same manner as in Example 1 to evaluate the stain on the roll surface and the thermal stability of the product. . The results are shown in Table 9.

【0031】[0031]

【表7】 [Table 7]

【0032】[0032]

【表8】 [Table 8]

【0033】[0033]

【表9】 [Table 9]

【0034】表7〜9に明らかなように、本実施例7〜
9に係るものには、プレートアウト防止効果があり、且
つ加工中の変色も少ない(熱安定性に優れている)。し
かし、表7に明らかなように、従来のプレートアウト防
止剤を配合した比較例7においては多少のプレートアウ
ト抑制効果は見られるが、十分ではなく、かつ加工中の
変色が大である。また、表8の比較例8のように、本実
施例と同じプレートアウト防止剤を添加しても、その添
加量が0.05重量部と少なければ、プレートアウト防
止効果は少ない。さらに、表9の比較例9のように、本
実施例と同じプレートアウト防止剤を添加しても、その
添加量が15重量部と多ければ、プレートアウト防止効
果は有しても、変色が大きくなる。
As is apparent from Tables 7-9, the present Example 7-
The material of No. 9 has the effect of preventing plate-out, and has little discoloration during processing (excellent thermal stability). However, as is clear from Table 7, in Comparative Example 7 containing the conventional plate-out inhibitor, some plate-out suppressing effect is observed, but it is not sufficient and discoloration during processing is large. Moreover, even if the same plate-out preventing agent as in the present example is added as in Comparative Example 8 in Table 8, the plate-out preventing effect is small if the addition amount is as small as 0.05 parts by weight. Furthermore, as in Comparative Example 9 in Table 9, even if the same plate-out preventing agent as in the present example was added and the addition amount was as large as 15 parts by weight, the plate-out preventing effect was exhibited, but discoloration occurred. growing.

【0035】[0035]

【発明の効果】本発明による塩化ビニル樹脂組成物によ
れば、プレートアウト防止効果が大きく、フィルム・シ
ートの厚み精度が低下することなく、製品表面の艶・粗
さ等の外観性能は良好である。また、各ロール表面の汚
染物を除去する作業は不要であるから、生産性が低下す
ることもない。また、熱安定性がよく、加工中の変色も
ない。さらに、押出成形における『目やに現象』を防止
しうる効果が期待できる
According to the vinyl chloride resin composition of the present invention, the plate-out prevention effect is great, the film / sheet thickness accuracy is not deteriorated, and the appearance performance such as gloss and roughness of the product surface is good. is there. Further, since the work of removing the contaminants on the surface of each roll is unnecessary, the productivity does not decrease. It also has good thermal stability and does not discolor during processing. In addition, the effect that can prevent "eye phenomenon" in extrusion molding can be expected.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C08L 33:08 31:04) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display area C08L 33:08 31:04)

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ポリエステル系可塑剤を15〜120重
量部含有する塩化ビニル樹脂100重量部に、ブタジエ
ン系ゴムをゴム成分とするポリブタジエン共重合体また
はアクリルゴムをゴム成分とするアクリルゴム共重合体
を0.1〜10重量部配合してなる塩化ビニル樹脂組成
物。
1. A polybutadiene copolymer containing butadiene rubber as a rubber component or an acrylic rubber copolymer containing acrylic rubber as a rubber component in 100 parts by weight of a vinyl chloride resin containing 15 to 120 parts by weight of a polyester plasticizer. 0.1 to 10 parts by weight of a vinyl chloride resin composition.
【請求項2】 二塩基性亜燐酸鉛を0.5〜10重量部
含有する塩化ビニル樹脂100重量部に、ブタジエン系
ゴムをゴム成分とするポリブタジエン共重合体またはア
クリルゴムをゴム成分とするアクリルゴム共重合体を
0.1〜10重量部配合してなる塩化ビニル樹脂組成
物。
2. A polybutadiene copolymer containing butadiene rubber as a rubber component or an acrylic rubber containing a rubber component as a rubber component in 100 parts by weight of a vinyl chloride resin containing 0.5 to 10 parts by weight of dibasic lead phosphite. A vinyl chloride resin composition comprising 0.1 to 10 parts by weight of a rubber copolymer.
【請求項3】 酢酸ビニル含量が55〜70重量%のエ
チレン−酢酸ビニル系樹脂を1〜20重量部含有する塩
化ビニル樹脂100重量部に、ブタジエン系ゴムをゴム
成分とするポリブタジエン共重合体またはアクリルゴム
をゴム成分とするアクリルゴム共重合体を0.1〜10
重量部配合してなる塩化ビニル樹脂組成物。
3. A polybutadiene copolymer having a butadiene rubber as a rubber component in 100 parts by weight of a vinyl chloride resin containing 1 to 20 parts by weight of an ethylene-vinyl acetate resin having a vinyl acetate content of 55 to 70% by weight, or An acrylic rubber copolymer containing acrylic rubber as a rubber component is used in an amount of 0.1 to 10
A vinyl chloride resin composition containing 1 part by weight.
JP15604494A 1994-07-07 1994-07-07 Vinyl chloride resin composition Pending JPH0820698A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15604494A JPH0820698A (en) 1994-07-07 1994-07-07 Vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15604494A JPH0820698A (en) 1994-07-07 1994-07-07 Vinyl chloride resin composition

Publications (1)

Publication Number Publication Date
JPH0820698A true JPH0820698A (en) 1996-01-23

Family

ID=15619099

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15604494A Pending JPH0820698A (en) 1994-07-07 1994-07-07 Vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPH0820698A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007060914A1 (en) * 2005-11-22 2007-05-31 Sekisui Chemical Co., Ltd. Optical transmitter
JP2007171894A (en) * 2005-11-22 2007-07-05 Sekisui Chem Co Ltd Optical transmitter
CN103275423A (en) * 2013-05-31 2013-09-04 常熟市弘基无纺制品有限公司 Preparation method of toughened polyvinyl chloride composite material
CN105482318A (en) * 2016-01-05 2016-04-13 合肥瑞瑶环保建材科技有限公司 Compression-resisting type rainwater collecting die block and processing technology thereof
US20210017372A1 (en) * 2018-04-09 2021-01-21 Dow Global Technologies Llc Pvc-based composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007060914A1 (en) * 2005-11-22 2007-05-31 Sekisui Chemical Co., Ltd. Optical transmitter
JP2007171894A (en) * 2005-11-22 2007-07-05 Sekisui Chem Co Ltd Optical transmitter
JP4589890B2 (en) * 2005-11-22 2010-12-01 積水化学工業株式会社 Optical transmission
CN103275423A (en) * 2013-05-31 2013-09-04 常熟市弘基无纺制品有限公司 Preparation method of toughened polyvinyl chloride composite material
CN105482318A (en) * 2016-01-05 2016-04-13 合肥瑞瑶环保建材科技有限公司 Compression-resisting type rainwater collecting die block and processing technology thereof
US20210017372A1 (en) * 2018-04-09 2021-01-21 Dow Global Technologies Llc Pvc-based composition

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