JPH093231A - Resin composition for low foaming - Google Patents

Resin composition for low foaming

Info

Publication number
JPH093231A
JPH093231A JP7148760A JP14876095A JPH093231A JP H093231 A JPH093231 A JP H093231A JP 7148760 A JP7148760 A JP 7148760A JP 14876095 A JP14876095 A JP 14876095A JP H093231 A JPH093231 A JP H093231A
Authority
JP
Japan
Prior art keywords
resin
low
resin composition
polyvinyl chloride
foaming
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
JP7148760A
Other languages
Japanese (ja)
Other versions
JP3514551B2 (en
Inventor
Onori Nakabayashi
大典 中林
Masakazu Shimada
昌和 島田
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.)
Kurabo Industries Ltd
Kurashiki Spinning Co Ltd
Original Assignee
Kurabo Industries Ltd
Kurashiki Spinning 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 Kurabo Industries Ltd, Kurashiki Spinning Co Ltd filed Critical Kurabo Industries Ltd
Priority to JP14876095A priority Critical patent/JP3514551B2/en
Publication of JPH093231A publication Critical patent/JPH093231A/en
Application granted granted Critical
Publication of JP3514551B2 publication Critical patent/JP3514551B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE: To obtain a polyvinyl chloride/ABS blended resin for low foaming having improved processability without deteriorating its excellent physical property, especially impact resistance. CONSTITUTION: In a resin composition for low foaming composed 10-90 pts.wt. of a polyvinyl chloride resin and 90-10 pts.wt. of ABS (acrylonitrile-butadiene- styrene copolymer) and containing a foaming agent, an inorganic filler and a lubricant, this resin composition for low foaming contains one species or a mixture of more than two species of a polyethylene wax, an acid-modified polyethylene wax, a styrene-modified polyethylene wax or a polytetrafluoroethylene wax as the lubricant, and a low foaming molded material obtained by foaming extrusion molding the resin composition. Furthermore, the surface of the low foaming molded material is covered with a poly(methyl methacrylate) resin to obtain a double-layered structural molded material.

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、ポリ塩化ビニル樹脂と
ABS樹脂のブレンド物を主成分とする低発泡成形用樹
脂組成物およびこの組成物を押出成形して得られる低発
泡成形体に関する。更に、上記低発泡成形用樹脂組成物
とPMMA樹脂を共押出して得られる2層構造成形体に
関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition for low-foam molding containing a blend of a polyvinyl chloride resin and an ABS resin as a main component, and a low-foam molded article obtained by extruding this composition. Further, the present invention relates to a two-layer structure molded body obtained by co-extruding the low foam molding resin composition and a PMMA resin.

【0002】[0002]

【従来の技術】ポリ塩化ビニル樹脂はその優れた加工性
とバランスのとれた性能のために成形用樹脂として広く
用いられている。特に適度の、且つ十分な剛性と耐候性
および優れた難燃性を有するため、その成形体は屋内、
屋外の建材等としても好適なものとして広く採用されて
いる。このように優れた特性をもつポリ塩化ビニルにと
って大きな欠点であった耐衝撃性と熱安定性について
も、ABS樹脂のような耐衝撃性樹脂とのブレンドおよ
び優れた熱安定剤の発見により、これらを配合して上記
欠点を著しく改良したポリ塩化ビニル組成物がコンパウ
ンドとして供給され、一層広範囲に利用されるようにな
ってきた。またABS樹脂を配合することにより耐熱性
の向上も計られている。
2. Description of the Related Art Polyvinyl chloride resin is widely used as a molding resin because of its excellent workability and balanced performance. Since the molded body has a particularly appropriate and sufficient rigidity, weather resistance and excellent flame retardancy, the molded body is
It is widely used as a suitable outdoor building material. As for impact resistance and thermal stability, which were major drawbacks for polyvinyl chloride having such excellent properties, the blending with impact-resistant resins such as ABS resin and the discovery of excellent heat stabilizers have contributed to these. A polyvinyl chloride composition in which the above-mentioned drawbacks have been remarkably improved by being blended with is supplied as a compound and has come to be used in a wider range. In addition, heat resistance has been improved by blending ABS resin.

【0003】しかし、ポリ塩化ビニル樹脂は熱による分
解のため成形温度を低く保つことが必要であり、必然的
に溶融粘度の高い領域での成形加工を余儀なくされてき
た。したがって、ポリ塩化ビニル樹脂にABS樹脂を配
合した組成物は、耐熱性は向上するものの、一方では成
形加工性が著しく低下し、実質上あまり使用されていな
い。またこの問題の解決のために種々の対策、例えば
低重合度のポリ塩化ビニルを用いる、ABS樹脂とし
て溶融粘度の低いものを用いる、混合組成物中のゴム
分を少なくする、添加剤として脂肪酸多価アルコール
を使用する、等がある。しかし、上記またはの方法
では、加工性は改善されても機械強度が低下する。の
方法では耐衝撃性が低下し、の方法では成形性の改良
は不十分である。特に、低発泡押出成形においては、溶
融状態にある樹脂と押出金型面との摺動性(滑り)が悪
くなるため、樹脂が金型内に付着、滞留し、熱安定性の
乏しいポリ塩化ビニル樹脂が熱分解して著しい着色や分
解ガスが発生し、成形性が著しく低下する。そのため上
記ポリ塩化ビニル樹脂とABS樹脂との配合物は低発泡
押出成形にはほとんど使用されていないのが現状であ
る。
However, since the polyvinyl chloride resin is decomposed by heat, it is necessary to keep the molding temperature low, and thus the molding process is inevitably inevitable in the region where the melt viscosity is high. Therefore, the composition in which the ABS resin is mixed with the polyvinyl chloride resin has improved heat resistance, but on the other hand, the molding processability is remarkably reduced, and thus it has not been used much in practice. In order to solve this problem, various measures are taken, for example, polyvinyl chloride having a low degree of polymerization is used, an ABS resin having a low melt viscosity is used, a rubber content in the mixed composition is reduced, and a fatty acid is used as an additive. For example, use a polyhydric alcohol. However, according to the above method or method, the mechanical strength is reduced although the workability is improved. The method (1) reduces the impact resistance, and the method (2) does not sufficiently improve the moldability. Particularly in low-foam extrusion molding, the slidability (sliding) between the resin in the molten state and the extrusion die surface deteriorates, and the resin adheres and stays in the die, resulting in polychlorination with poor thermal stability. The vinyl resin is thermally decomposed to generate remarkable coloring and decomposed gas, resulting in a marked decrease in moldability. Therefore, at present, the compound of the polyvinyl chloride resin and the ABS resin is hardly used for low foaming extrusion molding.

【0004】[0004]

【発明が解決しようとする課題】本発明の目的はその優
れた物性、特に耐衝撃性を低下することなく、加工成形
性の改良された低発泡成形用のポリ塩化ビニル/ABS
ブレンド樹脂組成物を提供することにある。
SUMMARY OF THE INVENTION The object of the present invention is to improve polyvinyl chloride / ABS for low-foam molding, which has improved processability without lowering its excellent physical properties, especially impact resistance.
It is to provide a blended resin composition.

【0005】[0005]

【課題を解決するための手段】本発明は、ポリ塩化ビニ
ル樹脂の10〜90重量部およびABS(アクリロニト
リル−ブタジエン−スチレン共重合体)樹脂の90〜1
0重量部に発泡剤、無機質充填剤および滑剤を含んでな
る低発泡成形用樹脂組成物に於いて、滑剤がポリエチレ
ンワックス、酸変性ポリエチレンワックス、スチレン変
性ポリエチレンワックスまたはポリテトラフルオロエチ
レンワックスのいずれか一種または二種以上の混合物で
あることを特徴とする低発泡成形用樹脂組成物に関す
る。また本発明は、上記の低発泡成形用樹脂組成物を発
泡押出成形した低発泡成形体に関するものである。更に
また本発明は滑剤がスチレン変性ポリエチレンワックス
である低発泡成形用樹脂組成物を押出機により押出発泡
成形するに当たり、PMMA樹脂を共押出することによ
り、この樹脂組成物の低発泡成形体の表面をPMMAで
被覆した2層構造成形体に関するものである。
SUMMARY OF THE INVENTION The present invention comprises 10 to 90 parts by weight of polyvinyl chloride resin and 90 to 1 of ABS (acrylonitrile-butadiene-styrene copolymer) resin.
A low-foaming resin composition containing 0 part by weight of a foaming agent, an inorganic filler and a lubricant, wherein the lubricant is polyethylene wax, acid-modified polyethylene wax, styrene-modified polyethylene wax or polytetrafluoroethylene wax. It relates to a resin composition for low-foam molding, which is one kind or a mixture of two or more kinds. The present invention also relates to a low-foam molded article obtained by foam-extruding the above-mentioned low-foam molding resin composition. Furthermore, according to the present invention, when a low-foam molding resin composition whose lubricant is styrene-modified polyethylene wax is extrusion-foam-molded by an extruder, by co-extruding a PMMA resin, the surface of the low-foam molded article of this resin composition is The present invention relates to a two-layer structure molded body having PMMA coated with PMMA.

【0006】本発明は、従来低発泡押出成形の場合、溶
融した樹脂と金型との間に付着が生じて安定した成形が
できなかったポリ塩化ビニル/ABS樹脂系組成物に、
滑剤を選択配合することにより、上記問題を解決したも
のである。本発明は滑剤としてポリエチレンワックス、
酸変性ポリエチレンワックス、スチレン変性ポリエチレ
ンワックスまたはポリテトラフルオロエチレンワックス
のいずれか一種または二種以上の混合物を用いるところ
に特徴がある。また本発明では、ポリ塩化ビニル樹脂、
ABS樹脂および滑剤の他に発泡剤および無機充填剤を
含む。
The present invention relates to a polyvinyl chloride / ABS resin composition, which has hitherto been unable to be stably molded due to adhesion between a molten resin and a mold in the case of low foaming extrusion molding.
The above problem is solved by selectively blending a lubricant. The present invention uses polyethylene wax as a lubricant,
It is characterized in that one or a mixture of two or more of acid-modified polyethylene wax, styrene-modified polyethylene wax and polytetrafluoroethylene wax is used. Further, in the present invention, polyvinyl chloride resin,
In addition to ABS resin and lubricant, it contains a foaming agent and an inorganic filler.

【0007】本発明のポリ塩化ビニルは特に限定される
ものではなく、通常の成形用樹脂として用いられるすべ
てのポリ塩化ビニル樹脂を用いることができ、分子量5
00〜1400のもの、好ましくは600〜700のも
のを用いることができる。また一般には直鎖構造のもの
が用いられるが、ポリ塩化ビニル本来の物性を損なわな
い程度にある程度の分岐があってもよい。
The polyvinyl chloride of the present invention is not particularly limited, and any polyvinyl chloride resin used as a usual molding resin can be used and has a molecular weight of 5
The thing of 00-1400, preferably 600-700 can be used. In addition, a linear structure is generally used, but it may have a certain degree of branching to the extent that the original physical properties of polyvinyl chloride are not impaired.

【0008】本発明のABS樹脂は汎用のものでもよい
が、ポリ塩化ビニルとブレンドした際に、優れた透明
性、混和性及び耐衝撃性が得られるように、屈折率、グ
ラフト率、ゴム粒径を調整して製造されたポリ塩化ビニ
ルブレンドタイプが好ましい。ポリ塩化ビニルとABS
樹脂は10:90〜90:10の割合(重量比)で用い
る。ABS樹脂が10重量部より少ないとポリ塩化ビニ
ルに対する耐衝撃性、耐熱性改良の効果がほとんど得ら
れず、ポリ塩化ビニルが10重量部より少ないと成形
性、難燃性、加工性等のポリ塩化ビニル樹脂本来の特徴
が失われる。
Although the ABS resin of the present invention may be a general-purpose resin, it has a refractive index, a graft ratio, and rubber particles so as to obtain excellent transparency, miscibility and impact resistance when blended with polyvinyl chloride. A polyvinyl chloride blend type manufactured by adjusting the diameter is preferable. Polyvinyl chloride and ABS
The resin is used in a ratio (weight ratio) of 10:90 to 90:10. If the amount of the ABS resin is less than 10 parts by weight, the effect of improving impact resistance and heat resistance to polyvinyl chloride is hardly obtained, and if the amount of polyvinyl chloride is less than 10 parts by weight, the moldability, flame retardancy, processability, etc. The original characteristics of vinyl chloride resin are lost.

【0009】上記滑剤は、ポリ塩化ビニルおよびABS
樹脂の合計100重量部を基準にして0.1〜5.0重量
部、好ましくは1.0〜3.0重量部用いられる。ポリエ
チレンワックスは、分子量1000〜4000のもの、
好ましくは1200〜2100のものが用いれらる。酸
変性ポリエチレンワックスは、ポリエチレンワックスに
無水マレイン酸等がグラフトされたもの、スチレン変性
ポリエチレンワックスはポリエチレンワックスにスチレ
ン等がグラフトされたものが使用される。ポリテトラフ
ルオロエチレンワックスは、粒子径0.1μm〜0.5μ
m、融点320℃〜330℃の粉末状のものが好ましく
使用される。
The above lubricants are polyvinyl chloride and ABS.
It is used in an amount of 0.1 to 5.0 parts by weight, preferably 1.0 to 3.0 parts by weight, based on 100 parts by weight of the resin. Polyethylene wax has a molecular weight of 1000 to 4000,
The thing of 1200-2100 is preferably used. As the acid-modified polyethylene wax, polyethylene wax grafted with maleic anhydride or the like is used, and as the styrene-modified polyethylene wax, polyethylene wax grafted with styrene or the like is used. Polytetrafluoroethylene wax has a particle size of 0.1 μm to 0.5 μm.
A powdery substance having a m and a melting point of 320 ° C. to 330 ° C. is preferably used.

【0010】発泡剤としては、押出成形温度で熱分解し
てガスを発生する化合物またはポリ塩化ビニルの軟化点
以下で気化する低沸点物質のような、プラスチックスの
発泡成形用として一般に用いられる発泡剤を用いること
ができる。これらの発泡剤の具体例としては、前者の分
解型のものとして、アゾジカルボンアミド、ジニトロソ
ペンタメチレンテトラミン、OBSH(p,p'-オキシ
ビス(ベンゼンスルホニルヒドラジド))、重炭酸ナトリ
ウム、炭酸アンモニウムまた低沸点物質としてn-ブタ
ン、n-ヘプタン等を例示することができるが、これに
限定されるものではない。好ましくは重炭酸ナトリウ
ム、アゾジカルボンアミド、OBSHである。発泡剤の
含有量はポリ塩化ビニルおよびABS樹脂の合計100
重量部を基準にして0.01〜10.0重量部、好ましく
は0.5〜2.5重量部である。
As the foaming agent, a foaming agent generally used for foam molding of plastics such as a compound which thermally decomposes to generate a gas at an extrusion molding temperature or a low boiling point substance which vaporizes below the softening point of polyvinyl chloride. Agents can be used. Specific examples of these foaming agents include azodicarbonamide, dinitrosopentamethylenetetramine, OBSH (p, p'-oxybis (benzenesulfonylhydrazide)), sodium bicarbonate, ammonium carbonate, and the former decomposition type. Examples of the low boiling point substance include n-butane and n-heptane, but the low boiling point substance is not limited thereto. Preferred are sodium bicarbonate, azodicarbonamide and OBSH. The total content of foaming agents is 100 for polyvinyl chloride and ABS resin.
The amount is 0.01 to 10.0 parts by weight, preferably 0.5 to 2.5 parts by weight, based on parts by weight.

【0011】無機充填剤としては、炭酸カルシウム、タ
ルク、シリカ、マイカ類、アルミナ、カオリン、炭酸マ
グネシウム等を用いることができるが、特に好ましいの
は炭酸カルシウム、タルク、マイカである。これらの無
機充填剤の含有量はポリ塩化ビニルおよびABS樹脂の
合計100重量部を基準にして1.0〜20.0重量部、
好ましくは5.0〜15.0重量部である。
As the inorganic filler, calcium carbonate, talc, silica, mica, alumina, kaolin, magnesium carbonate and the like can be used, but calcium carbonate, talc and mica are particularly preferable. The content of these inorganic fillers is 1.0 to 20.0 parts by weight based on 100 parts by weight of polyvinyl chloride and ABS resin.
It is preferably 5.0 to 15.0 parts by weight.

【0012】本発明の樹脂組成物には、ポリ塩化ビニル
の熱分解を防止するために、安定剤を併用することが好
ましい。使用する安定剤は通常のポリ塩化ビニル用の安
定剤である、2,6-ジ-tert-ブチル-p-クレゾー
ル、2,2'-メチレン-ビス-(4-メチル-6-tert-ブ
チルフェノール)等のフェノール系酸化防止剤、トリフ
ェニルホスファイト、トリス(ノニルフェニル)ホスフ
ァイトのようなリン系酸化防止剤、ジラウリルチオジプ
ロピオネートのような硫黄系酸化防止剤、ジ-ブチルス
ズマレエート等の有機スズ系安定剤、二塩基性ステアリ
ン酸鉛等の鉛系酸化防止剤、を単独または併用して用い
ることができる。
The resin composition of the present invention preferably contains a stabilizer in order to prevent thermal decomposition of polyvinyl chloride. The stabilizer used is the usual stabilizer for polyvinyl chloride, 2,6-di-tert-butyl-p-cresol, 2,2'-methylene-bis- (4-methyl-6-tert-butylphenol). ) And other phenolic antioxidants, phosphorus-based antioxidants such as triphenyl phosphite and tris (nonylphenyl) phosphite, sulfur-based antioxidants such as dilauryl thiodipropionate, di-butyltin maleate An organic tin-based stabilizer such as, and a lead-based antioxidant such as dibasic lead stearate can be used alone or in combination.

【0013】上記の必須成分の他、必要に応じて、ガラ
ス微小中空球、発泡パーライト、バーミキュライト等の
軽量化充填剤、顔料、紫外線吸収剤、難燃剤、メチルセ
ルロースのような有機質添加剤、炭素繊維、アラミド繊
維等のような補強用繊維等を、加工成形性および成形体
の物性を損なわない範囲で任意に加えてもよい。場合に
よっては金属石鹸等の上記した特定滑剤以外の一般に使
用される滑剤や可塑剤を少量加えることもできる。
In addition to the above essential components, if necessary, lightweight fillers such as glass micro hollow spheres, expanded perlite and vermiculite, pigments, ultraviolet absorbers, flame retardants, organic additives such as methyl cellulose, carbon fibers, etc. Reinforcing fibers such as aramid fibers and the like may be optionally added as long as the processability and the physical properties of the molded article are not impaired. In some cases, small amounts of commonly used lubricants and plasticizers other than the above-mentioned specific lubricants such as metal soaps can be added.

【0014】ポリ塩化ビニルは本来耐候性の比較的優れ
た樹脂であるが、更に耐候性を向上させるために硬質の
アクリル樹脂、特にPMMA樹脂でポリ塩化ビニル樹脂
成形体を被覆することが好ましい。しかし、ポリ塩化ビ
ニルの場合、添加している滑剤が成形体表面に移行して
くるため、滑剤の種類、添加量によっては、被覆層とポ
リ塩化ビニルとの接着性が低くなり、アクリル樹脂で被
覆されたポリ塩化ビニル成形体を成形することが困難と
なる場合が生ずる。また、辛うじて成形できたとしても
使用中に剥離が発生することも有り得る。本発明は良好
な接着強度をもって積層されたPMMA被覆ポリ塩化ビ
ニル成形体を得ることにも成功したものである。即ち、
本発明の他のひとつの態様は滑剤としてスチレン変性ポ
リエチレンワックスを用いた本発明の低発泡成形体をP
MMAで被覆した2層構造成形体である。詳しくは、低
発泡成形用樹脂組成物を押出機により発泡押出成形する
に当たり、PMMA樹脂を共押出することにより、上記
のポリ塩化ビニル/ABS樹脂組成物の低発泡成形体の
表面を未発泡のPMMA樹脂が被覆した2層構造成形体
である。滑剤としてスチレン変性ポリエチレンワックス
を用いることにより、PMMAの剥離を生じることな
く、よく一体化したPMMA被覆ポリ塩化ビニル2層構
造成形体を可能にした。
Polyvinyl chloride is originally a resin having relatively excellent weather resistance, but in order to further improve weather resistance, it is preferable to coat the polyvinyl chloride resin molding with a hard acrylic resin, particularly PMMA resin. However, in the case of polyvinyl chloride, the added lubricant migrates to the surface of the molded product, so the adhesiveness between the coating layer and polyvinyl chloride will decrease depending on the type of lubricant and the amount added, and the In some cases, it may be difficult to mold the coated polyvinyl chloride molding. Further, even if it can be barely molded, peeling may occur during use. The present invention has also succeeded in obtaining a laminated PMMA-coated polyvinyl chloride molded product with good adhesive strength. That is,
According to another embodiment of the present invention, the low-foaming molded article of the present invention containing styrene-modified polyethylene wax as a lubricant is used.
It is a two-layer structure molded body coated with MMA. Specifically, in foam-extruding the resin composition for low-foam molding with an extruder, by co-extruding a PMMA resin, the surface of the low-foam molded article of the above polyvinyl chloride / ABS resin composition is unfoamed. It is a two-layer structure molded body coated with PMMA resin. By using styrene-modified polyethylene wax as a lubricant, a PMMA-coated polyvinyl chloride two-layer structure molded body which is well integrated without peeling of PMMA was made possible.

【0015】上記PMMA被覆ポリ塩化ビニル2層構造
成形体は通常の共押出成形機、例えば図1に示すような
ダイスを備えた共押出成形機を用いて成形することがで
きる。即ち、図1の矢印Aの方向からは、本発明の低発
泡成形用樹脂組成物を供給すると共に、矢印Bの方向か
らは被覆用のPMMA樹脂を供給し、押し出され成形体
は、通常はサイザーを用いて冷却する。これにより共押
出成形は非常に円滑に行われる。被覆層の厚さは特に限
定するものではないが、通常は50〜1000μmであ
る。
The above-mentioned PMMA-coated polyvinyl chloride two-layer structure molded body can be molded using a conventional coextrusion molding machine, for example, a coextrusion molding machine equipped with a die as shown in FIG. That is, the low foam molding resin composition of the present invention is supplied from the direction of arrow A in FIG. 1, the PMMA resin for coating is supplied from the direction of arrow B, and the extruded molded product is usually Cool using a sizer. This makes coextrusion very smooth. The thickness of the coating layer is not particularly limited, but is usually 50 to 1000 μm.

【0016】以下、実施例により具体的に本発明を説明
する。
The present invention will be specifically described below with reference to examples.

【実施例】実施例 1 ポリ塩化ビニル樹脂(信越化学株式会社製:重合度60
0)、ABS樹脂(三菱レーヨン株式会社製)、発泡剤
(重炭酸ナトリウム)、無機充填剤(タルク)、滑剤を
加えて十分に混合した(滑剤の種類および各配合成分の
量比は表1に示した)。得られたコンパウンドを押出温
度180℃に設定した2軸押出機(45mmφ)にかけ
て製品断面寸法8mm×80mmの平板を連続的に押出
成形した。成形性、生産性および成形品外観はいずれも
問題なく良好であった。
EXAMPLES Example 1 Polyvinyl chloride resin (manufactured by Shin-Etsu Chemical Co., Ltd .: degree of polymerization: 60)
0), ABS resin (manufactured by Mitsubishi Rayon Co., Ltd.), a foaming agent (sodium bicarbonate), an inorganic filler (talc), and a lubricant were thoroughly mixed (the kind of lubricant and the amount ratio of each compounding component are shown in Table 1). Pointing out toungue). The obtained compound was applied to a twin-screw extruder (45 mmφ ) set at an extrusion temperature of 180 ° C. to continuously extrude a flat plate having a product cross-sectional dimension of 8 mm × 80 mm. The moldability, productivity, and appearance of the molded product were all good without problems.

【0017】[0017]

【表1】 [Table 1]

【0018】実施例 2〜4 滑剤種および配合成分の量比を表1に記載のように使用
した以外は、実施例1と同様にしてコンパウンドを調製
し、押出成形した。成形性、生産性および成形品外観は
いずれも問題なく良好であった。
Examples 2 to 4 Compounds were prepared and extruded in the same manner as in Example 1 except that the lubricant species and the blending components were used as shown in Table 1. The moldability, productivity, and appearance of the molded product were all good without problems.

【0019】実施例 5 図1に示すダイスを備えた共押出成形機を用いて、図2
に示す断面形状を有する2層構造成形体を成形した。即
ち、図1の矢印Aの方向からは実施例1と同じ樹脂組成
物を供給すると共に、矢印Bの方向からはPMMA樹脂
(三菱レーヨン株式会社製)を供給し、押し出された成
形体をサイザーを用いて急冷した後、冷却ボックス内に
入れて更に冷却することによって、図2に示す横断面を
有する2層構造成形体を得た。図2において(1)は被
覆PMMA層を示し、(2)は低発泡成形体を示す。
Example 5 Using a coextrusion molding machine equipped with the die shown in FIG.
A two-layer structure molded body having the cross-sectional shape shown in was molded. That is, the same resin composition as in Example 1 was supplied from the direction of arrow A in FIG. 1, and PMMA resin (manufactured by Mitsubishi Rayon Co., Ltd.) was supplied from the direction of arrow B, and the extruded molded body was sized. After being rapidly cooled using, the mixture was placed in a cooling box and further cooled to obtain a two-layer structure molded body having a cross section shown in FIG. In FIG. 2, (1) shows a coated PMMA layer and (2) shows a low-foam molded article.

【0020】比較例 1 滑剤を加えず、表1に記載の配合成分を用いて、実施例
1と同様にしてコンパウンドを調製し、押出成形した。
樹脂と金型との滑りが悪いため、成形時に樹脂とサイザ
ーとの間に“びびり現象”が生じ、得られた成形体の表
面は“サメ肌”状態であった。また樹脂の金型内への付
着が著しく、5時間以上の運転は困難であった。
Comparative Example 1 A compound was prepared in the same manner as in Example 1 except that the lubricant was not used, and the compounding components shown in Table 1 were used. The compound was extruded.
Due to poor slippage between the resin and the mold, a "chattering phenomenon" occurred between the resin and the sizer during molding, and the surface of the obtained molded product was in a "shark skin" state. Further, the resin was remarkably adhered to the mold, and it was difficult to operate for 5 hours or more.

【0021】比較例 2 表1に記載したように、滑剤としてステアリン酸アマイ
ド用いた配合処方にて、実施例1と同様にコンパウンド
を調製し、これを押出成形した。滑剤作用が適正でな
く、成形体にはやはり肌荒れが生じ、また10時間の連
続運転が限界であった。
Comparative Example 2 As shown in Table 1, a compound was prepared in the same manner as in Example 1 except that stearic acid amide was used as a lubricant, and the compound was extruded. The action of the lubricant was not proper, the molded body was still roughened, and the continuous operation for 10 hours was the limit.

【0022】[0022]

【発明の効果】以上に示したように本発明の組成物は、
従来の低発泡成型用ポリ塩化ビニル/ABSブレンド樹
脂組成物と異なり、加工成形性が良好であり、長時間安
定に連続成形ができ、得られた成形品は均一な気泡をも
つ低発泡成形品であり、耐熱性を初めとする物性も良好
であった。
As described above, the composition of the present invention is
Unlike conventional low-foaming polyvinyl chloride / ABS blend resin compositions for molding, it has good processability and can be continuously molded stably for a long time. The resulting molded product is a low-foaming molded product with uniform cells. The physical properties including heat resistance were also good.

【図面の簡単な説明】[Brief description of drawings]

【図1】 共押出成形用ダイスの模式的縦断面図であ
る。
FIG. 1 is a schematic vertical sectional view of a coextrusion molding die.

【図2】 2層構造成形体の模式的横断面図である。FIG. 2 is a schematic cross-sectional view of a two-layer structure molded body.

【符号の説明】[Explanation of symbols]

A: 本発明の低発泡成形用組成物の供給方向 B: PMMA樹脂の供給方向 1: PMMA被覆層 2: 本発明の低発泡成形体。 A: Supply direction of the low-foam molding composition of the present invention B: Supply direction of the PMMA resin 1: PMMA coating layer 2: Low-foam molded product of the present invention.

───────────────────────────────────────────────────── 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 55/02 LME C08L 55/02 LME //(C08L 27/06 55:02 23:00 27:18) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display location C08L 55/02 LME C08L 55/02 LME // (C08L 27/06 55:02 23:00 27: 18)

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 ポリ塩化ビニル樹脂の10〜90重量部
およびABS(アクリロニトリル-ブタジエン-スチレン
共重合体)樹脂の90〜10重量部に発泡剤、無機質充
填剤および滑剤を含んでなる低発泡成形用樹脂組成物に
於いて、滑剤がポリエチレンワックス、酸変性ポリエチ
レンワックス、スチレン変性ポリエチレンワックスまた
はポリテトラフルオロエチレンワックスのいずれか一種
または二種以上の混合物であることを特徴とする低発泡
成形用樹脂組成物。
1. A low foaming molding comprising a foaming agent, an inorganic filler and a lubricant in 10 to 90 parts by weight of a polyvinyl chloride resin and 90 to 10 parts by weight of an ABS (acrylonitrile-butadiene-styrene copolymer) resin. A resin composition for use in low-foaming molding, wherein the lubricant is any one of polyethylene wax, acid-modified polyethylene wax, styrene-modified polyethylene wax, and polytetrafluoroethylene wax, or a mixture of two or more thereof. Composition.
【請求項2】 滑剤がスチレン変性ポリエチレンワック
スである請求項1に記載の低発泡成形用樹脂組成物。
2. The low foam molding resin composition according to claim 1, wherein the lubricant is a styrene-modified polyethylene wax.
【請求項3】 ポリ塩化ビニル樹脂およびABS樹脂の
合計100重量部を基準にして、発泡剤が0.01〜1
0.0重量部、無機質充填剤が1.0〜20.0重量部お
よび滑剤が0.1〜5.0重量部である請求項1または2
に記載の低発泡成形用樹脂組成物。
3. A foaming agent of 0.01 to 1 based on 100 parts by weight of polyvinyl chloride resin and ABS resin in total.
0.0 parts by weight, the inorganic filler is 1.0-20.0 parts by weight, and the lubricant is 0.1-5.0 parts by weight.
The resin composition for low-foam molding according to 1.
【請求項4】 請求項1、2または3のいずれかに記載
の低発泡成形用樹脂組成物を押出成形機により発泡押出
成形した低発泡成形体。
4. A low-foam molded article obtained by foam-extrusion molding the resin composition for low-foam molding according to claim 1, by an extrusion molding machine.
【請求項5】 請求項2に記載の低発泡成形用樹脂組成
物を押出機により発泡押出成形するに当たり、PMMA
(ポリメチルメタクリレート)樹脂を共押出することに
より、請求項2に記載の樹脂組成物の低発泡成形体の表
面をPMMA樹脂が被覆した2層構造成形体。
5. PMMA is used for foaming extrusion molding of the resin composition for low foaming molding according to claim 2 by an extruder.
A two-layer structure molded product obtained by coating the surface of a low-foam molded product of the resin composition according to claim 2 with a PMMA resin by co-extruding a (polymethylmethacrylate) resin.
JP14876095A 1995-06-15 1995-06-15 Low foam molding resin composition Expired - Fee Related JP3514551B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14876095A JP3514551B2 (en) 1995-06-15 1995-06-15 Low foam molding resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14876095A JP3514551B2 (en) 1995-06-15 1995-06-15 Low foam molding resin composition

Publications (2)

Publication Number Publication Date
JPH093231A true JPH093231A (en) 1997-01-07
JP3514551B2 JP3514551B2 (en) 2004-03-31

Family

ID=15460036

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14876095A Expired - Fee Related JP3514551B2 (en) 1995-06-15 1995-06-15 Low foam molding resin composition

Country Status (1)

Country Link
JP (1) JP3514551B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10231377A (en) * 1997-02-18 1998-09-02 Asahi Chem Ind Co Ltd Abs resin composition for extrusion and foaming, and foamed molded product
EP0988965A3 (en) * 1998-09-26 2000-11-22 Premark RWP Holdings, Inc. Polymeric foam compositions and method of making substrates made from such compositions and method of making products made from such substrates and method of making
CN101875748A (en) * 2010-03-31 2010-11-03 深圳市科聚新材料有限公司 Heat-resistance ABS/PVC alloy and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10231377A (en) * 1997-02-18 1998-09-02 Asahi Chem Ind Co Ltd Abs resin composition for extrusion and foaming, and foamed molded product
EP0988965A3 (en) * 1998-09-26 2000-11-22 Premark RWP Holdings, Inc. Polymeric foam compositions and method of making substrates made from such compositions and method of making products made from such substrates and method of making
CN101875748A (en) * 2010-03-31 2010-11-03 深圳市科聚新材料有限公司 Heat-resistance ABS/PVC alloy and preparation method thereof

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