JPH03134045A - Vinyl chloride resin composition and molded article thereof - Google Patents

Vinyl chloride resin composition and molded article thereof

Info

Publication number
JPH03134045A
JPH03134045A JP1273017A JP27301789A JPH03134045A JP H03134045 A JPH03134045 A JP H03134045A JP 1273017 A JP1273017 A JP 1273017A JP 27301789 A JP27301789 A JP 27301789A JP H03134045 A JPH03134045 A JP H03134045A
Authority
JP
Japan
Prior art keywords
vinyl chloride
resin
chloride resin
styrene
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
JP1273017A
Other languages
Japanese (ja)
Inventor
Hiroshi Kakei
加計 博志
Yasushi Nakada
泰詩 中田
Kazunori Iwase
岩瀬 和徳
Wataru Aono
青野 渉
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui 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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP1273017A priority Critical patent/JPH03134045A/en
Priority to CA 2027917 priority patent/CA2027917A1/en
Priority to EP19900119986 priority patent/EP0423783A3/en
Publication of JPH03134045A publication Critical patent/JPH03134045A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To prepare the title resin compsn. having excellent thermal stability and thermal flowability and giving a molded article having an excellent flame retardance by compounding a vinyl chloride resin having a specified mean chlorine content with a specific impact modifier and calcium stearate each in a specified amt. CONSTITUTION:40-80 wt.% vinyl chloride resin having a mean chlorine content of 60-70 wt.% is compounded with 5-30 wt.% at least one impact modifier selected from the group consisting of an acrylonitrile-butadiene-styrene resin, a methacrylate-butadiene-styrene resin, a chlorinated polyethylene, and an acrylic rubber and 0-40 wt.% copolymer of a styrenic compd. with a vinyl cyanide compd. (e.g. a styrene-acrylonictile copolymer). Then, 100 pts.wt. resulting compsn. is compounded with 2.5-6 pts.wt. calcium stearate to give the title resin compsn., which is easily injection molded and suitably used for an automotive interior part, a housing of office automation equipment, etc.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は塩化ビニル系樹脂組成物及びそれを射出成形し
て得られた成形体に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a vinyl chloride resin composition and a molded article obtained by injection molding the same.

(従来の技術) 塩化ビニル樹脂は難燃性、耐薬品性、耐候性等の優れた
特性を有しているが、耐熱性が低いため、オフィスオー
トメイション(以下OAという)機器のハウジングや自
動車の内部部品のように高温になる部品に使用するのは
不適当であった。
(Prior art) PVC resin has excellent properties such as flame retardancy, chemical resistance, and weather resistance, but because of its low heat resistance, it is used in housings for office automation (hereinafter referred to as OA) equipment and automobiles. It was unsuitable for use on parts exposed to high temperatures, such as the internal parts of a car.

塩化ビニル樹脂に耐熱性を付与する方法として、ABS
樹脂を添加することが、従来より盛んに研究されている
。例えば、特開昭63−191851号公報には、ポリ
塩化ビニル又はポリ塩化ビニルと共重合可能なモノマー
との共重合体からなる塩化ビニル系樹脂と、ゴム変性熱
可塑性樹脂とからなる難燃性樹脂組成物が提案され、ゴ
ム変性熱可塑性樹脂は、スチレン系化合物とシアン化ビ
ニル化合物のスチレン系共重合体と、共役ジエン系ゴム
とスチレン系化合物とシアン化ビニル化合物とを共重合
したグラフト共重合体からなると記載されている。
ABS is a method of imparting heat resistance to vinyl chloride resin.
The addition of resin has been actively researched. For example, JP-A-63-191851 discloses a flame-retardant resin made of a vinyl chloride resin made of polyvinyl chloride or a copolymer of a monomer copolymerizable with polyvinyl chloride, and a rubber-modified thermoplastic resin. A resin composition has been proposed, and the rubber-modified thermoplastic resin is a graft copolymer made by copolymerizing a styrene copolymer of a styrene compound and a vinyl cyanide compound, and a conjugated diene rubber, a styrene compound, and a vinyl cyanide compound. It is described that it is made of a polymer.

上記組成物は、耐熱性は改善されるが、熱流動性が悪く
、射出成形等の方法で成形加工を行う際には、エチレン
ビスステアリン酸アミド等のビスアミド系滑材、ポリエ
チレンワックス、高級アルコール、ステアリン酸金属塩
等の滑材が添加されている。
Although the above composition has improved heat resistance, it has poor thermal fluidity, and when molded using methods such as injection molding, it is necessary to use bisamide lubricants such as ethylene bisstearamide, polyethylene wax, and higher alcohols. , lubricating agents such as stearic acid metal salts are added.

しかしながら、射出成形する際の熱流動性としてはまだ
不足であり、射出成形時にショートショットし完全な形
状の成形品が得られなかったり、得るために射出速度を
上げると剪断発熱がおこりシルバー(銀条)、ヤケ等の
外観不良が発生するという欠点があった。
However, the thermal fluidity during injection molding is still insufficient, and a molded product with a perfect shape may not be obtained due to short shots during injection molding, or shear heat generation occurs when the injection speed is increased to obtain silver (silver). However, there were disadvantages in that poor appearance such as discoloration occurred.

(発明が解決しようとする課題) 本発明の目的は、上記欠点に鑑み、熱安定性及び熱流動
性に優れ、容易に射出成形することができ、難燃性、耐
薬品性、耐熱性等に優れた成形体を得ることができる塩
化ビニル系樹脂組成物及びそれを射出成形して得られた
成形体を提供することにある。
(Problems to be Solved by the Invention) In view of the above-mentioned drawbacks, the object of the present invention is to have excellent thermal stability and thermal fluidity, be easily injection molded, and have flame retardant, chemical resistant, heat resistant, etc. An object of the present invention is to provide a vinyl chloride resin composition capable of obtaining a molded article having excellent properties, and a molded article obtained by injection molding the same.

(課題を解決するための手段) 本発明で使用される塩化ビニル系樹脂(a)とは、塩化
ビニル樹脂、塩化ビニルと、塩化ビニルと共重合可能な
エチレン、プロピレン等のエチレン性不飽和結合を有す
るモノマーとの共重合体及びこれらの樹脂の後塩素化物
をいう。
(Means for Solving the Problems) The vinyl chloride resin (a) used in the present invention refers to vinyl chloride resin, vinyl chloride, and ethylenically unsaturated bonds such as ethylene and propylene that can be copolymerized with vinyl chloride. This refers to copolymers with monomers having the following and post-chlorinated products of these resins.

塩化ビニル系樹脂(a)の平均重合度は、小さくなると
得られた成形体の耐衝撃性が低下し、大きくなると熱流
動性が低下するので300〜800が好ましい、又、後
塩素化物も平均重合度が300〜800の塩化ビニル系
樹脂が後塩素化されたものが好ましい。そして、平均重
合度が300〜800の塩化ビニル系樹脂と平均重合度
が300〜800の塩化ビビニル系樹脂が後塩素化され
た塩素化塩化ビニル樹脂が併用されるのが好ましい。
The average degree of polymerization of the vinyl chloride resin (a) is preferably from 300 to 800, because if it becomes small, the impact resistance of the obtained molded product will decrease, and if it becomes large, the thermal fluidity will decrease. Preferably, a vinyl chloride resin having a degree of polymerization of 300 to 800 is post-chlorinated. It is preferable to use a vinyl chloride resin having an average degree of polymerization of 300 to 800 and a chlorinated vinyl chloride resin obtained by post-chlorinating the vinyl chloride resin having an average degree of polymerization of 300 to 800.

塩化ビニル系樹脂(a)の平均塩素含有量は、少なくな
ると耐熱性が低下し、逆に多くなると熱流動性が低下し
、射出成形しにくくなるので、60〜70wt%に限定
される。従って、塩化ビニル系樹脂(a)は、塩素含有
量がこの範囲にはいるように単独もしくは二種以上の樹
脂が併用して使用される。
The average chlorine content of the vinyl chloride resin (a) is limited to 60 to 70 wt%, because if it is too low, the heat resistance will be lowered, and if it is too high, the thermal fluidity will be low, making injection molding difficult. Therefore, the vinyl chloride resin (a) is used alone or in combination of two or more resins so that the chlorine content falls within this range.

本発明で使用される衝撃改良剤(ロ)は、ABS系樹脂
、MBS系樹脂、塩素化ポリエチレン及びアクリルゴム
系樹脂よりなる群から選ばれ、一種もしくは二種以上が
併用される。
The impact modifier (b) used in the present invention is selected from the group consisting of ABS resins, MBS resins, chlorinated polyethylenes, and acrylic rubber resins, and one or more of them are used in combination.

上記ABS系樹脂とは、ポリブタジェン、スチレン−ブ
タジェン共重合体等のゴム成分にスチレン、アクリロニ
トリル、メタクリロニトリル等がグラフト重合されたも
のであって、ゴム成分が20〜70w t%含まれるも
のが好ましい。又、その分子量は比粘度で0.5〜0.
8のものが好ましい。尚、比粘度は0.4g/100m
1の濃度のクロロホルム溶液を25゛Cで測定したもの
である。
The above ABS resin is a resin in which styrene, acrylonitrile, methacrylonitrile, etc. is graft-polymerized to a rubber component such as polybutadiene or styrene-butadiene copolymer, and contains 20 to 70 wt% of the rubber component. preferable. Moreover, its molecular weight is 0.5 to 0.0 in terms of specific viscosity.
8 is preferred. In addition, the specific viscosity is 0.4g/100m
A chloroform solution with a concentration of 1 was measured at 25°C.

上記MBS系…脂とは、ポリブタジェン、スチレン−ブ
タジェン系共重合体等のゴム系樹脂に、メチルアクリレ
ート、エチルアクリレート、エチルメタクリレート等の
アクリルモノマー、アクリロニトリル、メタクリロニト
リル等のアクリロニトリル系モノマー、スチレン、α−
メチルスチレン等のスチレン系モノマーなどをグラフト
重合したグラフト重合体であって、ゴム系樹脂成分が4
0〜60wt%のものが好ましく、例えば、4淵化学社
製、カネエース B−23、三菱レーヨン社製、メタプ
レンC−110等があげられる。
The above-mentioned MBS resin refers to rubber resins such as polybutadiene and styrene-butadiene copolymers, acrylic monomers such as methyl acrylate, ethyl acrylate, and ethyl methacrylate, acrylonitrile monomers such as acrylonitrile and methacrylonitrile, styrene, α−
A graft polymer obtained by graft polymerizing styrenic monomers such as methylstyrene, with a rubber resin component of 4
It is preferably 0 to 60 wt%, and examples thereof include Kane Ace B-23 manufactured by Shibuchi Kagaku Co., Ltd. and Metaprene C-110 manufactured by Mitsubishi Rayon Co., Ltd.

上記塩素化ポリエチレンは、塩素化度が大き過ぎても小
さ過ぎても衝撃改良効果が低下するので30〜40w 
t%のものが好ましい。又、平均分子量は10万〜15
万のものが好ましい。
The above-mentioned chlorinated polyethylene has a chlorinated degree of 30 to 40 W, since the impact improvement effect decreases if the degree of chlorination is too high or low.
t% is preferred. Also, the average molecular weight is 100,000 to 15
Ten thousand is preferable.

上記アクリルゴム系樹脂は、メチルアクリレート、エチ
ルアクリレート、ブチルアクリレート、オクチルアクリ
レート等のアクリレートを主体とし、こめアクリレート
と2−クロルエチルビニルエーテル、メチルビニルケト
ン、アクリル酸、アクリロニトリル、ブタジェン等のモ
ノマーとの共重合体であり、例えば4淵化学社製、カネ
エースPM、呉羽化学社製、クレハKM−334等があ
げられる。
The above acrylic rubber resin is mainly composed of acrylates such as methyl acrylate, ethyl acrylate, butyl acrylate, and octyl acrylate, and is a combination of acrylate and monomers such as 2-chloroethyl vinyl ether, methyl vinyl ketone, acrylic acid, acrylonitrile, and butadiene. It is a polymer, and examples thereof include Kane Ace PM manufactured by Shibuchi Kagaku Co., Ltd., and Kureha KM-334 manufactured by Kureha Chemical Co., Ltd.

本発明で使用されるスチレン系共重合体(c)はスチレ
ン系化合物とシアン化ビニル化合物との共重合体である
The styrenic copolymer (c) used in the present invention is a copolymer of a styrene compound and a vinyl cyanide compound.

上記スチレン系化合物としては、例えば、スチレン、α
−メチルスチレン等があげられ、スチレンが熱流動性が
優れているので好ましい。
Examples of the above styrene compounds include styrene, α
-Methylstyrene, etc., and styrene is preferred because it has excellent thermal fluidity.

又、シアン化ビニル化合物としては、例えば、アクリロ
ニトリル、メタクリロニトリル等があげられ、アクリレ
ートリルが塩化ビニル系樹脂との相溶性が優れているの
で好ましい。
Examples of vinyl cyanide compounds include acrylonitrile and methacrylonitrile, with acrylaterile being preferred because it has excellent compatibility with vinyl chloride resins.

スチレン系共重合体は、耐衝撃性及び熱流動性の特性か
ら、スチレン系化合物とシアン化ビニル化合物が60:
40〜80 : 20 (重量比)の割合で共重合され
ているのが好ましく、その重量平均分子量は、小さくな
ると成形体の耐衝撃性が低下し、大きくなると熱流動性
が低下するので3万〜10万が好ましく、アクリロニト
リル−スチレン樹脂が好適に使用される。
The styrenic copolymer contains a styrene compound and a vinyl cyanide compound in a ratio of 60% due to its impact resistance and thermal fluidity properties.
It is preferable that they are copolymerized at a ratio of 40 to 80:20 (weight ratio), and the weight average molecular weight should be 30,000 to 30,000, since the smaller the weight average molecular weight, the lower the impact resistance of the molded product, and the larger it is, the lower the thermal fluidity. ~100,000 is preferred, and acrylonitrile-styrene resin is preferably used.

本発明の樹脂組成物は上記塩化ビニル系樹脂(a)と衝
撃改良剤(b)とスチレン系共重合体(c)よりなるが
、塩化ビニル系樹脂(a)の添加量が少なくなると難燃
性が低下し、衝撃改良剤(b)の添加量が少なくなると
耐衝撃性が低下し、多くなると熱流動性、耐熱性が低下
し、スチレン系共重合体(c)の添加量が、多くなると
耐衝撃性が低下するので、塩化ビニル系樹脂(a)が4
0〜80wt%添加され、衝撃改良剤伽)が5〜30w
t%添加され、スチレン系共重合体(c)が0〜40w
t%添加される。
The resin composition of the present invention is composed of the vinyl chloride resin (a), the impact modifier (b), and the styrene copolymer (c). If the amount of the impact modifier (b) added decreases, the impact resistance decreases, and if it increases, the thermal fluidity and heat resistance decrease, and if the amount of the styrenic copolymer (c) added decreases, the impact resistance decreases. If this happens, the impact resistance will decrease, so if the vinyl chloride resin (a)
0~80wt% added, impact modifier 佽) is added 5~30w
t% added, styrenic copolymer (c) is 0 to 40w
t% is added.

本発明の塩化ビニル系樹脂組成物は上記樹脂組成物10
0重量部とステアリン酸カルシウム2.5〜6重量部か
らなる。従来、ステアリン酸カルシウムの添加量は2重
量部以下であったが、このように少量であると、射出成
形の際にヤケが発生し、外観不良を引き起こしていた。
The vinyl chloride resin composition of the present invention is the above-mentioned resin composition 10.
0 parts by weight and 2.5 to 6 parts by weight of calcium stearate. Conventionally, the amount of calcium stearate added was 2 parts by weight or less, but such a small amount caused discoloration during injection molding and caused poor appearance.

ステアリン酸カルシウムの添加量を2.5重量部以上に
すると、熱安定性、特に長時間加熱された際の安定性が
向上し、射出成形の際にヤケが発生せず、成形品の外観
が良好になると共に、良好な成形品の得られる射出条件
の領域が広くなる。又、6重量部より多くなると、表面
からブリードし易くなり、耐候性が低下し、白化し易く
なると共に耐衝撃性が低下する。
When the amount of calcium stearate added is 2.5 parts by weight or more, thermal stability, especially stability when heated for a long time, is improved, no burning occurs during injection molding, and the appearance of the molded product is good. The range of injection conditions under which good molded products can be obtained becomes wider. If the amount exceeds 6 parts by weight, it tends to bleed from the surface, resulting in decreased weather resistance, whitening, and decreased impact resistance.

本発明の塩化ビニル系樹脂組成物の構成は、上述の通り
であり、更に、塩化ビニル系樹脂の成形性、熱安定性等
を向上させるために一般に使用されているポリエチレン
ワックス、高級アルコール、エステル系滑材などの滑材
、ポリメチルメタクリレート系加工助剤、ジプチル錫マ
レート、ジブチル錫メルカプト、金属石鹸、鉛化合物な
どの熱安定剤、酸化防止剤、紫外線吸収剤、滑剤、炭酸
カルシウム、ガラスファイバーなどの充填剤、酸化チタ
ンなどの顔料、染料等が併用されてもよい。
The composition of the vinyl chloride resin composition of the present invention is as described above, and further includes polyethylene wax, higher alcohol, and ester, which are commonly used to improve moldability, thermal stability, etc. of vinyl chloride resin. lubricants such as polymethyl methacrylate processing aids, diptyltin malate, dibutyltin mercapto, metal soaps, heat stabilizers such as lead compounds, antioxidants, ultraviolet absorbers, lubricants, calcium carbonate, glass fibers. fillers such as, pigments such as titanium oxide, dyes, etc. may be used in combination.

本発明の塩化ビニル系樹脂組成物は、押出成形、カレン
ダー成形、ロール・プレス成形、射出成形等従来公知の
任意の加熱態形法で成形することが可能であるが、射出
成形に適しており、本発明の2番目の発明は、上記塩化
ビニル系樹脂組成物を射出成形して得られた成形体であ
る。
The vinyl chloride resin composition of the present invention can be molded by any conventionally known heating method such as extrusion molding, calendar molding, roll press molding, injection molding, etc., but is suitable for injection molding. The second invention of the present invention is a molded article obtained by injection molding the vinyl chloride resin composition.

上記塩化ビニル系樹脂組成物を射出成形するには、例え
ば、組成物をスーパーミキサーで均一に分散した混合物
又はこの混合物を押出機に供給しベレクイザーで切断し
て得られたペレットを射出成形機に供給して成形すれば
よく、射出条件は一般に、バレル温度170〜190’
C1射出圧力120〜150Kg/cdである。
In order to injection mold the above vinyl chloride resin composition, for example, the composition may be uniformly dispersed using a super mixer, or this mixture may be fed to an extruder and pellets obtained by cutting the composition using a Berekizer may be fed into an injection molding machine. The injection condition is generally a barrel temperature of 170 to 190'.
C1 injection pressure is 120 to 150 Kg/cd.

(実施例) 次に、本発明の詳細な説明する。尚、以下「部」とある
のは「重量部」を意味する。又、物性の測定方法は下記
の通りである。
(Example) Next, the present invention will be explained in detail. Note that "parts" hereinafter mean "parts by weight". In addition, the method for measuring physical properties is as follows.

1、熱変形度−2’ X 12X 90m+の試料を作
成し、一端を固定し、2gの荷重をかけ、85°Cで1
時間放置した後、たわみ距離(L)を測定し、次式から
求めた。
1.Create a sample with thermal deformation degree of -2' x 12 x 90m+, fix one end, apply a load of 2g, and heat at 85°C
After standing for a period of time, the deflection distance (L) was measured and calculated from the following equation.

熱変形度(%)= (L/90)X1002、衝撃強度
(ノツチ付アイゾツト強度)−ASTM  D−256
に準拠し、厚さ 0.125インチの試料を23°Cで
測定した。
Thermal deformation degree (%) = (L/90)X1002, impact strength (notched isot strength) - ASTM D-256
0.125 inch thick samples were measured at 23°C.

実施例1〜3、比較例1.2 第1表に示した所定量の塩化ビニル系樹脂と衝撃改良剤
とスチレン系共重合体との合計量100部、ステアリン
酸カルシウム及びジプチル錫マレート3.0部とジブチ
ル錫メルカプト0.5部をスーパーミキサーに供給し、
よく混合した後、スクリュー径45mmの2軸押出機で
混練押出しペレタイザーでペレタイズしてペレットを得
、得られたペレットを射出成形機(東芝機械社製、l5
−450)に供給しバレル温度185°C1射出圧力1
40Kg/ei!、金型温度40’C及び第1表に示し
た条件で300gの箱型ファックス用ハウジング部品を
射出成形した。射出成形の際の樹脂の充填時間、ノズル
から出た樹脂の温度及び充填率を測定し、第1表に示し
た。又、得られた試料の外観を観察すると共に物性を測
定し、結果を第1表に示した。
Examples 1 to 3, Comparative Example 1.2 A total of 100 parts of the predetermined amounts of vinyl chloride resin, impact modifier, and styrene copolymer shown in Table 1, calcium stearate, and diptyltin malate 3.0 parts. and 0.5 parts of dibutyltin mercapto to a super mixer;
After mixing well, pelletization was performed using a twin-screw extruder with a screw diameter of 45 mm and an extrusion pelletizer to obtain pellets.
-450), barrel temperature 185°C, injection pressure 1
40Kg/ei! A 300 g box-shaped fax housing part was injection molded at a mold temperature of 40'C and the conditions shown in Table 1. The resin filling time, the temperature of the resin discharged from the nozzle, and the filling rate during injection molding were measured and are shown in Table 1. In addition, the appearance of the obtained sample was observed and the physical properties were measured, and the results are shown in Table 1.

(以下余白) 第1表 重合度500、塩素含有率61%  (2)重合度50
0、塩素含有率65%重合度500、塩素含有率67% AN含量24%、St含量31%、ゴム含量45%、比
粘度0.63AN含量24%、St含量76%、重量平
均分子量65,000(発明の効果) 本発明の塩化ビニル系樹脂組成物の構成は上述の通りで
あり、熱安定性及び熱流動性に優れており、焼は等がな
く容易に射出成形することができ、射出成形により得ら
れた成形体は、難燃性、耐薬品性、耐熱性、等に優れて
おり、OA機器のハウジングや自動車の内装部品等に好
適に使用される。
(Left below) Table 1 Degree of polymerization: 500, chlorine content: 61% (2) Degree of polymerization: 50
0, chlorine content 65% polymerization degree 500, chlorine content 67% AN content 24%, St content 31%, rubber content 45%, specific viscosity 0.63 AN content 24%, St content 76%, weight average molecular weight 65, 000 (Effects of the Invention) The structure of the vinyl chloride resin composition of the present invention is as described above, and it has excellent thermal stability and thermal fluidity, and can be easily injection molded without burning etc. The molded product obtained by injection molding has excellent flame retardancy, chemical resistance, heat resistance, etc., and is suitably used for housings of OA equipment, interior parts of automobiles, etc.

Claims (1)

【特許請求の範囲】 1、(a)平均塩素含有量が60〜70wt%の塩化ビ
ニル系樹脂40〜80wt%と、(b)ABS系樹脂、
MBS系樹脂、塩素化ポリエチレン及びアクリルゴム系
樹脂よりなる群から選ばれた一種以上の衝撃改良剤5〜
30wt%と、 (c)スチレン系化合物とシアン化ビニル化合物が共重
合されてなるスチレン系共重合体0〜40wt% よりなる樹脂組成物100重量部と (d)ステアリン酸カルシウム2.5〜6重量部からな
ることを特徴とする塩化ビニル系樹脂組成物。 2、(a)平均塩素含有量が60〜70wt%の塩化ビ
ニル系樹脂40〜80wt%と、(b)ABS系樹脂、
MBS系樹脂、塩素化ポリエチレン及びアクリルゴム系
樹脂よりなる群から選ばれた一種以上の衝撃改良剤5〜
30wt%と、 (c)スチレン系化合物とシアン化ビニル化合物が共重
合されてなるスチレン系共重合体0〜40wt% よりなる樹脂組成物100重量部と (d)ステアリン酸カルシウム2.5〜6重量部からな
る塩化ビニル系樹脂組成物を射出成形することにより得
られた成形体。
[Claims] 1. (a) 40 to 80 wt% of a vinyl chloride resin having an average chlorine content of 60 to 70 wt%; (b) an ABS resin;
One or more impact modifiers selected from the group consisting of MBS resin, chlorinated polyethylene, and acrylic rubber resin5-
(c) 100 parts by weight of a resin composition consisting of 0 to 40 wt% of a styrenic copolymer obtained by copolymerizing a styrene compound and a vinyl cyanide compound; and (d) 2.5 to 6 parts by weight of calcium stearate. A vinyl chloride resin composition comprising: 2. (a) 40 to 80 wt% of vinyl chloride resin with an average chlorine content of 60 to 70 wt%, (b) ABS resin,
One or more impact modifiers selected from the group consisting of MBS resin, chlorinated polyethylene, and acrylic rubber resin5-
(c) 100 parts by weight of a resin composition consisting of 0 to 40 wt% of a styrenic copolymer obtained by copolymerizing a styrene compound and a vinyl cyanide compound; and (d) 2.5 to 6 parts by weight of calcium stearate. A molded article obtained by injection molding a vinyl chloride resin composition comprising:
JP1273017A 1989-10-19 1989-10-19 Vinyl chloride resin composition and molded article thereof Pending JPH03134045A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP1273017A JPH03134045A (en) 1989-10-19 1989-10-19 Vinyl chloride resin composition and molded article thereof
CA 2027917 CA2027917A1 (en) 1989-10-19 1990-10-18 Chlorine-containing resin composition and molded articles therefrom
EP19900119986 EP0423783A3 (en) 1989-10-19 1990-10-18 Chlorine-containing resin composition and molded articles therefrom

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1273017A JPH03134045A (en) 1989-10-19 1989-10-19 Vinyl chloride resin composition and molded article thereof

Publications (1)

Publication Number Publication Date
JPH03134045A true JPH03134045A (en) 1991-06-07

Family

ID=17522002

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1273017A Pending JPH03134045A (en) 1989-10-19 1989-10-19 Vinyl chloride resin composition and molded article thereof

Country Status (1)

Country Link
JP (1) JPH03134045A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05125244A (en) * 1991-02-28 1993-05-21 Shin Etsu Chem Co Ltd Vinyl chloride resin composition
JPH05202257A (en) * 1992-01-24 1993-08-10 Shin Etsu Chem Co Ltd Vinyl chloride resin composition
WO2019065739A1 (en) * 2017-09-27 2019-04-04 積水化学工業株式会社 Resin composition for molding
JP2020158707A (en) * 2019-03-27 2020-10-01 株式会社カネカ Fluidity improving agent for vinyl chloride-based resin composition, vinyl chloride-based resin composition, and vinyl chloride-based resin molded body

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05125244A (en) * 1991-02-28 1993-05-21 Shin Etsu Chem Co Ltd Vinyl chloride resin composition
JPH05202257A (en) * 1992-01-24 1993-08-10 Shin Etsu Chem Co Ltd Vinyl chloride resin composition
WO2019065739A1 (en) * 2017-09-27 2019-04-04 積水化学工業株式会社 Resin composition for molding
JPWO2019065739A1 (en) * 2017-09-27 2020-09-10 積水化学工業株式会社 Resin composition for molding
US11174381B2 (en) 2017-09-27 2021-11-16 Sekisui Chemical Co., Ltd. Resin composition for molding
JP2020158707A (en) * 2019-03-27 2020-10-01 株式会社カネカ Fluidity improving agent for vinyl chloride-based resin composition, vinyl chloride-based resin composition, and vinyl chloride-based resin molded body

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