JPS6211787A - Gasket - Google Patents

Gasket

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Publication number
JPS6211787A
JPS6211787A JP15004185A JP15004185A JPS6211787A JP S6211787 A JPS6211787 A JP S6211787A JP 15004185 A JP15004185 A JP 15004185A JP 15004185 A JP15004185 A JP 15004185A JP S6211787 A JPS6211787 A JP S6211787A
Authority
JP
Japan
Prior art keywords
resin
vinyl chloride
gasket
weight
hard
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
JP15004185A
Other languages
Japanese (ja)
Other versions
JPH0482034B2 (en
Inventor
Katsuo Horigome
勝夫 堀込
Yasuo Harigai
保夫 針谷
Akio Adakawa
昭夫 渾川
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.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
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 Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP15004185A priority Critical patent/JPS6211787A/en
Publication of JPS6211787A publication Critical patent/JPS6211787A/en
Publication of JPH0482034B2 publication Critical patent/JPH0482034B2/ja
Granted legal-status Critical Current

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  • Gasket Seals (AREA)
  • Laminated Bodies (AREA)
  • Sealing Material Composition (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:A co-extruded and molded gasket having improved molding properties, deformation resistance of appearance, sealing and closing effects, comprising a rigid PVC resin, etc., a specific high-molecular weight substance and a plasticizer. CONSTITUTION:The aimed gasket consisting of (A) (i) a rigid PVC resin or ABS resin and (ii) 100pts.wt. high-molecular weight substance consisting of 30-80wt% vinyl chloride resin and 70-20wt% partially crosslinked acrylonitrile- butadiene copolymer and (B) 20-200pts.wt. plasticizer. Trimellitic ester, polyes ter, etc., may be cited as the preferable example of the component B.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は成形性、外観耐変形性に優れた合成樹脂共押出
成形ガスケットに関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a synthetic resin coextrusion molded gasket that has excellent moldability and resistance to deformation in appearance.

〔従、米の技術〕[Second, rice technology]

従来、建築、及び自動車、厨房器具等戸当りパツキン又
はガスケット(以下ガスケットと称する)には、軟質塩
化ビニル樹脂等の軟質合成樹脂または架橋ゴム材料が使
用されている。
Conventionally, soft synthetic resins such as soft vinyl chloride resin or crosslinked rubber materials have been used for door stoppers or gaskets (hereinafter referred to as gaskets) for buildings, automobiles, kitchen appliances, etc.

軟質合成樹脂又はゴム材料が単独で押出成形、射出成型
された製品として使用される場合や建築材料、自動車、
厨房器具への接続を容易にする目的で、硬質合成樹脂材
料又は金属と共押出又は接着製造されたガスケットが使
用される場合がある。
When soft synthetic resin or rubber materials are used alone as extrusion molded or injection molded products, construction materials, automobiles,
Gaskets co-extruded or bonded with hard synthetic resin materials or metals may be used to facilitate connection to kitchen appliances.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

ところが硬質合成樹脂と軟質材料として軟質塩化ビニル
樹脂を同一金型(以下グイと称する)内で溶融一体化(
以下共押出と称する)する場合硬質合成樹脂と軟質塩化
ビニル樹脂との適正成形温度差は通常40−100°C
にも達し、硬質合成樹脂に適正なダイ温度羨保つと、軟
質塩化ビ=・・樹脂が熱分解して製品とならないか又は
表面が平滑性不良、波うち現象発生等極めて外観の不良
な製品となる。逆に軟質塩化ビニル樹脂に適正なダイ温
度を保った場合には軟質塩化ビニル部分は良好な外観を
得られるが硬質合成樹脂は成形温度不足により成形不良
又は融着不良さらに、外観が著しく不良となり、共押出
製品として極めて外観及び物理的強度に劣った製品とな
る。
However, it is difficult to melt and integrate hard synthetic resin and soft vinyl chloride resin in the same mold (hereinafter referred to as Gui).
(hereinafter referred to as coextrusion), the appropriate molding temperature difference between hard synthetic resin and soft vinyl chloride resin is usually 40-100°C.
If the die temperature is maintained at an appropriate temperature for hard synthetic resin, soft vinyl chloride =... The resin will thermally decompose and the product will not form, or the product will have an extremely poor appearance such as poor surface smoothness and waving. becomes. Conversely, if the appropriate die temperature is maintained for soft vinyl chloride resin, the soft vinyl chloride part will have a good appearance, but the hard synthetic resin will have poor molding or poor fusion due to insufficient molding temperature, and the appearance will be extremely poor. As a coextruded product, the product has extremely poor appearance and physical strength.

更に得られた共押出ガスケット製品は使用時の押圧、圧
縮時による変形が太き(、シーリング、密閉効果が使用
途中で減少し良好なシール性能を有するガスケット製品
は得られない。
Furthermore, the resulting coextruded gasket product is highly deformed by pressure and compression during use (the sealing effect decreases during use, making it impossible to obtain a gasket product with good sealing performance).

家 一方軟質材料として加橋ゴム材料を使用する場合、耐変
形性に優れ、シール性能は良好な製品の得られる場合が
多いが、ゴム材料との成形温度の差異及びゴム部分の架
橋処理の為製品加熱等が必要なことから硬質部分に合成
樹脂を使用した合成樹脂との共押出製品は殆んど製品と
なり得ない。
On the other hand, when using cross-linked rubber materials as soft materials, products with excellent deformation resistance and good sealing performance can often be obtained, but due to the difference in molding temperature with the rubber material and the cross-linking treatment of the rubber part. Because the product requires heating, etc., coextrusion products with synthetic resins that use synthetic resins for hard parts are almost impossible to produce.

本発明の目的は、これらの欠点を解決し、良好な外観及
び耐変形性をもち、シーリング、密閉効果の優れた共押
出ガスケットを提供することにある。
An object of the present invention is to solve these drawbacks and provide a coextruded gasket that has good appearance and deformation resistance, and has excellent sealing and sealing effects.

〔問題点を解決するための手段〕[Means for solving problems]

本発明は硬質塩化ビニル樹脂又はABS樹脂と、塩化ビ
ニル樹脂30−80重量%を部分架橋アクリロニトリル
−ブタジエン共重合体70−20重量%とからなる高分
子量体100重量部及び可塑剤20−200重量部より
なる樹脂組成物の共押出ガスケットである。
The present invention consists of hard vinyl chloride resin or ABS resin, 100 parts by weight of a polymer consisting of 30-80% by weight of vinyl chloride resin and 70-20% by weight of partially crosslinked acrylonitrile-butadiene copolymer, and 20-200 parts by weight of a plasticizer. This is a coextruded gasket made of a resin composition consisting of parts.

ここで用いられる塩化ビニル樹脂はポリ塩化ビニル及び
少量の酢酸ビニル、エチレン−酢酸ビニル樹脂等を共重
合又はグラフト重合した塩化ビニル樹脂であれば、特に
制限されないがJIS K−6721で測定される平均
重合度が2000以上であることが共押出成形を行なっ
た場合、特に硬質合成樹脂材料との成形温度差を小さく
し、良好なガスケット製品を得る本発明の目的に合致し
望ましい。
The vinyl chloride resin used here is not particularly limited as long as it is a vinyl chloride resin obtained by copolymerizing or graft polymerizing polyvinyl chloride and a small amount of vinyl acetate, ethylene-vinyl acetate resin, etc., but the average value measured according to JIS K-6721 is not particularly limited. When coextrusion molding is performed, it is desirable that the degree of polymerization is 2000 or more, as this meets the objective of the present invention, which is to reduce the molding temperature difference with the hard synthetic resin material and obtain a good gasket product.

本発明に用いられる部分架橋アクリロニトリル−ブタジ
エン共重合体は、メチルエチルケトンに不溶な架橋アク
リロニトリループタゾエン共重合体を含むものであれば
、その製法を制限するものではなく、ジビニルベンゼン
や、エチレングリコールジメータクリレートなどの多官
能性単量体との共i合で得る方法、または、メチルエチ
ルケトンに不溶な架橋アクリロニトリル−ブタジエン共
重合体が生成するまで反応′率を高める方法、または、
少量の架橋剤を使用して、未加硫アクリロニトリル−ブ
タジエン共重合体を架橋させて得る方法などいずれの製
法でも差し支えない。一般に、入手できる部分架橋アク
リロニトリル−ブタジエン共重合体としては、ケミガム
P83(グツドイヤー社製商品)、JSRN201 (
日本合成ゴム社製商品)、Hycar 1422 (B
、F、グツ−リッチ社製商品)などが挙げられる。  
    − さらに前記塩化ビニル樹脂と部分架橋アクリロニトリル
−ブタジエン共重合体は重量比で30−80重量%/7
O−201t%の範囲にあることが望ましい。塩化ビニ
ル樹脂が60重量%に満たない場合、押出成形時、製品
外観不良等の不良現象が発生する例が大きく、部分架橋
アクリロニトリル−ブタジエン共重合体が20重it%
に満たない場合は、共押出成形時、硬質合成樹脂材料と
の適正成形温度差が大きくなり、製品の外観不良が発生
することから、本発明の目的に合致しない。
The production method of the partially crosslinked acrylonitrile-butadiene copolymer used in the present invention is not limited as long as it contains a crosslinked acrylonitrile-butadiene copolymer that is insoluble in methyl ethyl ketone; A method of obtaining a copolymer with a polyfunctional monomer such as dimeter acrylate, or a method of increasing the reaction rate until a crosslinked acrylonitrile-butadiene copolymer insoluble in methyl ethyl ketone is produced, or
Any production method may be used, such as a method in which unvulcanized acrylonitrile-butadiene copolymer is crosslinked using a small amount of crosslinking agent. In general, partially crosslinked acrylonitrile-butadiene copolymers that are available include Chemi Gum P83 (product manufactured by Gutdeyer), JSRN201 (
Product manufactured by Japan Synthetic Rubber Co., Ltd.), Hycar 1422 (B
, F, products manufactured by Gutsrich), and the like.
- Further, the vinyl chloride resin and the partially crosslinked acrylonitrile-butadiene copolymer are contained in a weight ratio of 30-80% by weight/7.
It is desirable that the content be in the range of O-201t%. If the vinyl chloride resin content is less than 60% by weight, defects such as poor product appearance often occur during extrusion molding.
If the temperature is less than 1, the difference in proper molding temperature with the hard synthetic resin material during coextrusion molding becomes large, resulting in poor appearance of the product, which does not meet the purpose of the present invention.

使用される可塑剤は一般に塩化ビニル樹脂等に使用され
る可塑剤が使用されるが、望ましくは、トリメリット酸
エステル、ポリエステル等いわゆる高分子量可塑剤が硬
質材料との共押出成形時の成形性が良好となり適当であ
るが、その使用量は樹脂100重量部に対して20−2
00重量部の範囲にあることが必要で20重量部に満た
ない場合は押出成形時の成形性不良、ガスケット部の外
観不良を米し200重量部をこえる場合は硬質樹脂材料
との適正押出温度差が大きくなり、ガスケット部の外観
不良および強度不足等の不具合も発生する。
The plasticizer used is generally a plasticizer used for vinyl chloride resin, etc., but preferably a so-called high molecular weight plasticizer such as trimellitic acid ester or polyester is used to improve moldability during coextrusion molding with hard materials. is good and suitable, but the amount used is 20-2 parts by weight per 100 parts by weight of resin.
If it is less than 20 parts by weight, it may cause poor moldability during extrusion molding or poor appearance of the gasket part, and if it exceeds 200 parts by weight, it should be at the appropriate extrusion temperature with the hard resin material. The difference becomes large, and problems such as poor appearance and insufficient strength of the gasket part occur.

硬質材料として使用される硬質塩化ビニル樹脂は通常平
均重合度500〜1500のポリ塩化ビニル又は少:i
!:(特に規定しないが10%以下)酢酸ビニル又はエ
チレス酢酸ビニル樹脂を共重合又はグラフト重合した塩
化ビニル樹脂に所要の安定剤、滑剤、加工助剤及び/又
はABS%MBS樹脂等を適量含む押出成形用硬質塩化
ビニルであっても十分本発明の目的を達する。更にAB
S樹脂についても一般にABS樹脂として成形用に供さ
れているアクリロニトリル−ブタジエン−スチレンを主
要三成分とする樹脂であって、特に個々の成分について
は規制されないが、スチレン成分としてα−メチルスチ
レン、p−メチルスチレン等軟化温度の高い成分を含有
するいわゆる耐熱ABS樹脂を十分使用される。
Hard vinyl chloride resin used as a hard material is usually polyvinyl chloride with an average degree of polymerization of 500 to 1,500 or less than i.
! : (Not specified, but 10% or less) Extrusion containing appropriate amounts of necessary stabilizers, lubricants, processing aids, and/or ABS% MBS resin, etc. to vinyl chloride resin copolymerized or graft polymerized with vinyl acetate or ethylene vinyl acetate resin. Even moldable hard vinyl chloride can sufficiently achieve the purpose of the present invention. Furthermore AB
S resin is also a resin whose main three components are acrylonitrile-butadiene-styrene, which is generally used for molding as ABS resin, and although there are no particular restrictions on the individual components, the styrene component is α-methylstyrene, p - So-called heat-resistant ABS resin containing components with a high softening temperature such as methylstyrene is sufficiently used.

共押出装置については特に規定しないが通常第1=薗呻
ヒ示噂1U六硬質合成樹脂の混練押出装置の軟質樹脂材
料を混練する装置■を同一の金型Cで接合一体化して、
共押出製品0を得る方法か られており、個々の押出装
置■■の大きさ、単軸、二軸等及び模型、竪型装置等の
選定は、使用される材料及び共押出製品の形状、寸法に
より適宜選定されつるものである。
The co-extrusion device is not particularly specified, but usually the device (1) for kneading the soft resin material of the 1U6 hard synthetic resin kneading and extrusion device is joined and integrated with the same mold C.
The method for obtaining a coextruded product is determined, and the size of the individual extrusion equipment, single-screw, twin-screw, etc., model, vertical equipment, etc., is determined by the materials used, the shape of the coextruded product, They are appropriately selected depending on the dimensions.

以下本発明を実施例により説明する。The present invention will be explained below with reference to Examples.

〔実施例〕〔Example〕

実施例1〜5 表に示す樹脂組成の材料を751ヘンシエルミキサーで
攪拌混合後90 m1m単軸押出機(池貝鉄工((社)
製)にて混練ペレット化を行ないペレット各15kgを
得た。
Examples 1 to 5 Materials having the resin composition shown in the table were stirred and mixed using a 751 Henschel mixer, and then mixed using a 90 ml single screw extruder (Ikegai Iron Works Co., Ltd.).
The mixture was kneaded and made into pellets using a commercial machine (manufactured by Kogyo Co., Ltd.) to obtain 15 kg of pellets each.

これを次の押出機にて共押出試験を行なった。A coextrusion test was conducted using the following extruder.

押出機の 65 m1m単軸押出機(池貝鉄工(株)製
) 押出機■ 4 Q m/m竪型単軸押出機((株)fラ
スチツク工業研究所製) 硬質樹脂材料と軟質材料の構成となるよう設計されたダ
イを使用した。
Extruder: 65 m/m single screw extruder (manufactured by Ikegai Tekko Co., Ltd.) Extruder ■ 4 Q m/m vertical single screw extruder (manufactured by F Rustik Industrial Research Institute Co., Ltd.) Composition of hard resin material and soft material A die designed to

実施例1〜乙については硬質材料として硬質塩化ビニル
樹脂成形材料(デンカビニコンR−2001電気化学工
業(株))を使用し、ダイ温度190’Cで共押出成形
を行ない、実施例4S5についてはABS樹脂デンカA
BS GTR−40:電気化学工業((社))を使用し
、ダイ温度200℃で共押出試験を実施した。得られた
共押出製品について軟質部分(以下ガスケット部分と称
する)について、外観の評価を行なうと共にガスケット
部分の高さくH)を測定した。更に得られた共押出製品
を10cIrLの長さに切断し60℃に保たれた恒温槽
中にて6009の荷重をかけ4時間加熱した。
For Examples 1 to B, a hard vinyl chloride resin molding material (Denka Nikon R-2001 Denki Kagaku Kogyo Co., Ltd.) was used as the hard material, and coextrusion molding was performed at a die temperature of 190'C, and for Example 4S5. ABS resin Denka A
A coextrusion test was conducted using BS GTR-40: Denki Kagaku Kogyo (Company) at a die temperature of 200°C. The appearance of the soft portion (hereinafter referred to as gasket portion) of the obtained coextruded product was evaluated, and the height (H) of the gasket portion was measured. Furthermore, the obtained coextruded product was cut into a length of 10 cIrL and heated for 4 hours under a load of 6009 in a constant temperature bath kept at 60°C.

取出し後2Hr室温で放置後ガスケット部の高さHlを
測定し、最初に測定した高さくH)で除比較例1〜4 表に示す樹脂組成の材料を実施例に示したと同一の方法
で混練、押出しペレットを作成後、実施例と同一の設備
、方法にまり共押出成形を行ない同様に製品の評価、測
定を行なった。
After taking it out and leaving it at room temperature for 2 hours, measure the height Hl of the gasket part and divide by the first measured height H) Comparative Examples 1 to 4 Materials with the resin compositions shown in the table were kneaded in the same manner as shown in the examples. After producing extruded pellets, coextrusion molding was performed using the same equipment and method as in the examples, and the products were evaluated and measured in the same manner.

使用材料 (1)塩化ビニル樹脂 電化ビニール5H250(重合
度2500)  電気化学工業(株)) (2)部分架橋アクリロニトリル−ブタジエン共重合体
 、TSRN201  日本合成ゴム(株)(3) T
OTM  ビニサイデー W−700大日本インキ(株
) (4)安定剤 トリパース ((社)耕正(5)滑 剤
 ステアリン酸恍 花王石ケン(株)(6)硬質塩化ビ
ニル樹脂 デンカビニコレR2001電気化学工業(株
) (7) ABS樹脂 デンカABS、 GTR−40〔
発明の効果〕 表の実施例に示すとおり、本発明のガスケットは製造時
の成形性、外観、耐熱変形性に優れていることが確認さ
れた。
Materials used (1) Vinyl chloride resin Electrified Vinyl 5H250 (degree of polymerization 2500) Denki Kagaku Kogyo Co., Ltd. (2) Partially crosslinked acrylonitrile-butadiene copolymer, TSRN201 Japan Synthetic Rubber Co., Ltd. (3) T
OTM Vinicide W-700 Dainippon Ink Co., Ltd. (4) Stabilizer Tripase (Kosei Co., Ltd.) (5) Lubricant Stearic acid Kao Sekiken Co., Ltd. (6) Hard vinyl chloride resin Denkabi Nicole R2001 Denki Kagaku Kogyo ( (7) ABS resin Denka ABS, GTR-40 [
Effects of the Invention] As shown in the Examples in the table, it was confirmed that the gasket of the present invention was excellent in moldability during manufacture, appearance, and heat deformation resistance.

Claims (1)

【特許請求の範囲】[Claims] 1、硬質塩化ビニル樹脂又はABS樹脂と、塩化ビニル
樹脂30−80重量%と部分架橋アクリロニトリル−ブ
タジエン共重合体70−20重量%とからなる高分子量
体100重量部及び可塑剤20−200重量部よりなる
樹脂組成物の共押出ガスケット。
1. Hard vinyl chloride resin or ABS resin, 100 parts by weight of a polymer consisting of 30-80% by weight of vinyl chloride resin and 70-20% by weight of partially crosslinked acrylonitrile-butadiene copolymer, and 20-200 parts by weight of plasticizer. A coextruded gasket made of a resin composition.
JP15004185A 1985-07-10 1985-07-10 Gasket Granted JPS6211787A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15004185A JPS6211787A (en) 1985-07-10 1985-07-10 Gasket

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15004185A JPS6211787A (en) 1985-07-10 1985-07-10 Gasket

Publications (2)

Publication Number Publication Date
JPS6211787A true JPS6211787A (en) 1987-01-20
JPH0482034B2 JPH0482034B2 (en) 1992-12-25

Family

ID=15488209

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15004185A Granted JPS6211787A (en) 1985-07-10 1985-07-10 Gasket

Country Status (1)

Country Link
JP (1) JPS6211787A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03130134A (en) * 1989-05-01 1991-06-03 Gencorp Inc Thermally moldable hard decorative lamina for transport vehicle interior
EP0694383A1 (en) * 1994-07-25 1996-01-31 Denki Kagaku Kogyo Kabushiki Kaisha Extruded product
US5709956A (en) * 1994-07-25 1998-01-20 Denki Kagaku Kogyo Kabushiki Kaisha Co-extruded multilayer laminate
WO2005005538A1 (en) * 2003-07-10 2005-01-20 Denki Kagaku Kogyo Kabushiki Kaisha Polyvinyl chloride-base thermoplastic elastomer composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57187341A (en) * 1981-05-15 1982-11-18 Sumitomo Bakelite Co Ltd Vinyl chloride resin composition
JPS58108122A (en) * 1981-12-22 1983-06-28 Sumitomo Bakelite Co Ltd Manufacture of weather strip

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57187341A (en) * 1981-05-15 1982-11-18 Sumitomo Bakelite Co Ltd Vinyl chloride resin composition
JPS58108122A (en) * 1981-12-22 1983-06-28 Sumitomo Bakelite Co Ltd Manufacture of weather strip

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03130134A (en) * 1989-05-01 1991-06-03 Gencorp Inc Thermally moldable hard decorative lamina for transport vehicle interior
EP0694383A1 (en) * 1994-07-25 1996-01-31 Denki Kagaku Kogyo Kabushiki Kaisha Extruded product
US5709956A (en) * 1994-07-25 1998-01-20 Denki Kagaku Kogyo Kabushiki Kaisha Co-extruded multilayer laminate
WO2005005538A1 (en) * 2003-07-10 2005-01-20 Denki Kagaku Kogyo Kabushiki Kaisha Polyvinyl chloride-base thermoplastic elastomer composition

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JPH0482034B2 (en) 1992-12-25

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