JPH0395238A - Foam - Google Patents

Foam

Info

Publication number
JPH0395238A
JPH0395238A JP23439789A JP23439789A JPH0395238A JP H0395238 A JPH0395238 A JP H0395238A JP 23439789 A JP23439789 A JP 23439789A JP 23439789 A JP23439789 A JP 23439789A JP H0395238 A JPH0395238 A JP H0395238A
Authority
JP
Japan
Prior art keywords
rubber
olefin
ethylene
thermoplastic resin
foam
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
JP23439789A
Other languages
Japanese (ja)
Inventor
Masashi Aoshima
正志 青嶋
Tadashi Jinno
正 神野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP23439789A priority Critical patent/JPH0395238A/en
Publication of JPH0395238A publication Critical patent/JPH0395238A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a thermally expansive foam rubber advantageous in both storage and transportation cost and excellent in workability by compressing a vulcanized foam rubber containing a thermoplastic resin at a specified temperature and then cooling it. CONSTITUTION:A foam obtained by compressing a vulcanized foam rubber containing a thermoplastic resin at a temperature above the softening point of the thermoplastic resin and then cooling it. As the rubber, those generally used can be utilized; however, an ethylene/alpha-olefin rubber is particularly useful in the field of application where heat and weather resistances are required. The ethylene/alpha-olefin rubber to be used is an ethylene/alpha-olefin/nonconjugated diene rubber, preferably comprising a copolymer of ethylene and an alpha-olefin at a weight ratio of (90:1) to (40:60). As the alpha-olefin, propylene, butene-1, etc., may be used.

Description

【発明の詳細な説明】 く産業上の利用分野〉 本発明は、自動車用、建築用、および工業用等の分野に
おいて緩衝、シーリングおよび断熱等の目的に使用され
る発泡体に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a foam used for purposes such as cushioning, sealing, and heat insulation in the fields of automobiles, architecture, and industry.

く従来の技術〉 従来より加硫ゴム発泡体は用途に応じた形状に成形され
て使用場所まで運搬され、装着されて使用されてきた。
BACKGROUND TECHNOLOGY Conventionally, vulcanized rubber foams have been molded into a shape according to their intended use, transported to a place of use, and then installed and used.

すなわち、加硫発泡或形時に小体積に圧縮・加工して、
使用時に元の形状に復帰させる技術は知られていなかっ
た。
In other words, it is compressed and processed into a small volume during vulcanization and foaming,
There was no known technology for restoring it to its original shape during use.

く本発明が解決しようとする課題〉 加硫ゴム発泡体は低比重のため嵩高く、保管や運搬時に
大きなスペースをとるため、保管●運賃コストの面で非
発泡体製品に比較して不利であり、改善が望まれていた
Problems to be Solved by the Present Invention> Vulcanized rubber foam is bulky due to its low specific gravity and takes up a large amount of space during storage and transportation, making it disadvantageous compared to non-foam products in terms of storage and shipping costs. There was a need for improvement.

また、シーリング材等の施工に際して、施工する空間に
対して発泡体の体積が大きく、装着し難い、密着●レー
リング特性が必ずしも十分でない等の課題があり、その
改良が望まれていた。
In addition, when applying sealants, etc., there are problems such as the volume of the foam is large relative to the space to be installed, making it difficult to install, and the adhesion and railing properties are not necessarily sufficient, and improvements have been desired.

〈課題を解決するための手段〉 本発明者らは、上記加硫ゴム発泡体の問題点を解決すべ
く研究の結果、高比重●小容量で保管●運搬し、使用、
装着時に加熱することにより、原形に復帰させることの
出来る熱膨張性の形状記憶加硫ゴム発泡体の開発に至っ
たものである。すなわち、本発明は、保管・運搬コスト
が有利で、作業性に優れた熱膨張性を有するゴム発泡体
に関するものであり、次の発明より成る。
<Means for Solving the Problems> As a result of research to solve the above-mentioned problems with vulcanized rubber foam, the present inventors found that it has a high specific gravity, a small capacity for storage, transportation, use,
This led to the development of a thermally expandable shape memory vulcanized rubber foam that can be returned to its original shape by heating during installation. That is, the present invention relates to a rubber foam that is advantageous in storage and transportation costs, has excellent workability, and has thermal expandability, and comprises the following invention.

(1)  熱可塑性樹脂を含む加硫ゴム発泡体を該熱可
塑性樹脂の軟化点以上の温度において圧縮し、冷却して
得ることを特徴とする熱膨張性ゴム発泡体。
(1) A thermally expandable rubber foam obtained by compressing a vulcanized rubber foam containing a thermoplastic resin at a temperature equal to or higher than the softening point of the thermoplastic resin and cooling.

(2)前記加硫ゴム発泡体が熱可塑性樹脂を含むエチレ
ン−α−オレフィン系加硫ゴム発泡体である熱膨張性ゴ
ム発泡体。
(2) A thermally expandable rubber foam, wherein the vulcanized rubber foam is an ethylene-α-olefin vulcanized rubber foam containing a thermoplastic resin.

本発明に用いられるゴムはとくに限定されず一般に用い
られるゴムが適用可能である.例えば、天然ゴムの他エ
チレン−4−オレフィン系ゴム、ステレンーブタジェン
系ゴム、アクリロニトリルーブタジェン系ゴム、レリコ
ーンゴム、クロロブレシゴム等の合成ゴムあるいはこれ
らのゴムの2種以上のブレンドゴムがあげられる。なか
でも耐熱性や耐候性が求められる分野においてはエチレ
ン−α−オレフィン系ゴムがとくに有用である。
The rubber used in the present invention is not particularly limited, and commonly used rubbers can be used. For example, in addition to natural rubber, synthetic rubbers such as ethylene-4-olefin rubber, sterene-butadiene rubber, acrylonitrile-butadiene rubber, silicone rubber, and chlorobresci rubber, or a blend of two or more of these rubbers can be used. Among these, ethylene-α-olefin rubber is particularly useful in fields where heat resistance and weather resistance are required.

本発明に用いられるエチレン−α−オレフィン系ゴムは
、エチレン−α−オレフィンー非兵役ジエンゴムであり
、エチレンとd−オレフィンが重量比で90:10ない
し40:60で共重合されたものが好まし<s’−オレ
フィンとしてはプロピレン、プテン・1等が用いられる
。非共役ジエンとしてはノルボルネン類、環状ジエン類
、脂肪族ジエン類などが使用されるが、なかでも5−エ
チリデン−2一ノルボルネン、シクロペンタジエン及び
1.4−へキサジエンが代表的なものである。
The ethylene-α-olefin rubber used in the present invention is an ethylene-α-olefin non-military diene rubber, preferably a copolymerization of ethylene and d-olefin in a weight ratio of 90:10 to 40:60. <As the s'-olefin, propylene, butene-1, etc. are used. Examples of non-conjugated dienes used include norbornenes, cyclic dienes, and aliphatic dienes, among which 5-ethylidene-2-norbornene, cyclopentadiene, and 1,4-hexadiene are representative.

本発明に用いられる熱可塑性樹脂は発泡体に、加熱、加
圧冷却後の形状を固定させるために配合されるものであ
り、その種類は必ずしも限定されるものでないが、実用
画から、ビカット軟化点が60〜200℃のものが好ま
しく、ポリエチレン〆エチレンーα−オレフィン共重合
体、エチレンー酢酸ビニル共重合体、エチレン−(メタ
)アクリレート共重合体、各種エチレン共重合体、ボリ
プロビレン、プロピレンーα−オレフィン共重合体、ス
チレンーブタジェンブロック共重合体等があげられる。
The thermoplastic resin used in the present invention is blended into the foam to fix the shape after heating, pressure and cooling, and its type is not necessarily limited, but from practical drawings, Vicat softening Those with a temperature of 60 to 200°C are preferred, and include polyethylene-ethylene-α-olefin copolymers, ethylene-vinyl acetate copolymers, ethylene-(meth)acrylate copolymers, various ethylene copolymers, polypropylene, propylene-α-olefins. Examples include copolymers, styrene-butadiene block copolymers, and the like.

熱可塑樹脂の配合量は、エチレンー(1−オレフィン系
ゴム100重量部に対して5〜100重量部であり、2
0−50重量部が特に好ましい。
The blending amount of the thermoplastic resin is 5 to 100 parts by weight per 100 parts by weight of ethylene (1-olefin rubber,
Particularly preferred is 0-50 parts by weight.

熱可塑樹脂の配合量がこれより少ない場合は、加熱、圧
縮、冷却時の形状固定性能が悪く、又、多い場合は加熱
、発泡時の成形性が劣る等の問題を生じる。
If the amount of thermoplastic resin blended is less than this, the shape fixing performance during heating, compression, and cooling will be poor, and if it is greater than this, problems such as poor moldability during heating and foaming will occur.

本発明に用いられる加硫ゴム発泡体を製造するためには
、発泡剤が用いられる。発泡剤としては、ジニトロペン
タメチレンテトラ竃ン、アゾジカルボンアミド,P,P
オキシビスベンゼンスルホニルヒドラジド等が使用され
、必要に応じ、尿素等の発泡助剤を併用することもでき
る。
A blowing agent is used to produce the vulcanized rubber foam used in the present invention. As a blowing agent, dinitropentamethylene tetrasulfur, azodicarbonamide, P, P
Oxybisbenzenesulfonyl hydrazide and the like are used, and if necessary, a foaming aid such as urea can also be used in combination.

本発明においては、前記エチレンー―−オレフィン系ゴ
ム、熱可塑性樹脂、発泡剤の他に充填剤、軟化剤、加硫
剤、加硫促進剤、活性剤等の配合剤を使用することがで
きる。
In the present invention, in addition to the ethylene-olefin rubber, thermoplastic resin, and blowing agent, compounding agents such as fillers, softeners, vulcanizing agents, vulcanization accelerators, and activators can be used.

充填剤としては、カーボンブラック、炭酸カルシウム、
タルク、クレー、微粉ケイ酸などを用いるここができる
Fillers include carbon black, calcium carbonate,
This can be done using talc, clay, finely powdered silicic acid, etc.

加硫剤としては、硫黄、硫黄化合物等を用いることがで
き、通常加硫促進剤を併用する。加硫促進剤としては、
ジテオカルパミン酸塩類、チウラム類、チアゾール類、
チオエリア類、グアニジン類、キサントゲン酸塩類、ア
ルデヒドアミン類、アルデヒドアンモニア類等があげら
れる。
As the vulcanizing agent, sulfur, sulfur compounds, etc. can be used, and a vulcanization accelerator is usually used in combination. As a vulcanization accelerator,
Diteocarpamates, thiurams, thiazoles,
Examples include thioerias, guanidines, xanthates, aldehyde amines, and aldehyde ammonias.

加硫系としては、硫黄加硫系の他に、キノイド加硫、有
機過酸化物加硫も可能であり、P−ベシゾキノンジオキ
シム,P,P’−ジベンゾキノンジオキシム、ジク竃ル
ペルオキシド、2,5−ジメチル−2.6−ジ(t−プ
チルペルオキシ)ヘキサン、2.5−ジメチル−2.5
−ジ(ペンゾイルペルオキシ)ヘキサン、1.1−ジー
t−フテルペルオキシ−8.8.5−}リメチルジク口
ヘキサンなどを用いることが出来る。
In addition to sulfur vulcanization, quinoid vulcanization and organic peroxide vulcanization are also possible as vulcanization systems, including P-besizoquinone dioxime, P,P'-dibenzoquinone dioxime, and Peroxide, 2,5-dimethyl-2,6-di(t-butylperoxy)hexane, 2,5-dimethyl-2.5
-di(penzoylperoxy)hexane, 1.1-di-t-phtherperoxy-8.8.5-}limethyldimethylhexane, and the like can be used.

活性剤としては、亜鉛華、脂肪酸亜鉛、炭酸亜鉛、ステ
アリン酸などがあげられ、軟化剤としては、各種プロセ
スオイル、潤滑油などが例示される。上記配合剤の他に
、加工助剤、酸化防止剤などを必要に応じて配合するこ
とができる。
Examples of the activator include zinc white, zinc fatty acid, zinc carbonate, and stearic acid, and examples of the softener include various process oils and lubricating oils. In addition to the above-mentioned ingredients, processing aids, antioxidants, and the like can be added as necessary.

次に本発明の加硫ゴム発泡体の製造方法について述べる
。前記エチレン−α−オレフィン系ゴム等のゴム、熱可
塑性樹脂等の混線は、バンバリ一〇キサー、二−ダー等
の密閉式混線機あるいは竃キシングロール等を用いて行
う。発泡剤、加硫剤、加硫促進剤等の混線は、分解やス
コーチを防止するため100℃以下の温度にて行うこと
が好ましい。
Next, the method for producing the vulcanized rubber foam of the present invention will be described. The mixing of rubber such as ethylene-α-olefin rubber, thermoplastic resin, etc. is carried out using a closed-type mixing machine such as Banbury 10xer or 2-der, or a wire mixing roll. Mixing of a blowing agent, vulcanizing agent, vulcanization accelerator, etc. is preferably carried out at a temperature of 100° C. or lower to prevent decomposition and scorch.

混線により得られた配合組成物を、押出機、プレス等に
より成形した後、連続的にあるいはバ,テ式に加熱する
ことにより加硫●発泡し加硫ゴム発泡体を製造する。加
硫●発泡法としては、オーブン、PCM%UHF,LC
M,熱プレス、缶加硫等があげられる。
The blended composition obtained by cross-mixing is molded using an extruder, press, etc., and then vulcanized and foamed by heating continuously or in a vat type to produce a vulcanized rubber foam. Vulcanization ●Foaming methods include oven, PCM%UHF, LC
M, heat press, can vulcanization, etc.

得られた加硫ゴム発泡体を、配合に用いた熱可塑性樹脂
の軟化点以上の温度に加熱し、これを金型、ベルト等を
用いて加圧し小体積に圧縮し、圧縮状態で水等で急冷す
る。冷却された後は金型●ベルト等の圧力を開放した後
も熱可塑性樹脂の剛性により収縮状態の形状を保つ。
The obtained vulcanized rubber foam is heated to a temperature higher than the softening point of the thermoplastic resin used for compounding, compressed into a small volume by pressurizing it using a mold, belt, etc., and in the compressed state, water etc. Cool rapidly. After cooling, the rigidity of the thermoplastic resin maintains its contracted shape even after the pressure of the mold and belt is released.

前記した方法によって製造された本発明の加硫ゴム発泡
体は、使用される場所に運搬され設備に装着された後、
用いられた熱可塑性樹脂の軟化点以上の温度に加熱する
ことにより元の形状に復元する。
After the vulcanized rubber foam of the present invention produced by the method described above is transported to the place where it will be used and installed in equipment,
It is restored to its original shape by heating to a temperature above the softening point of the thermoplastic resin used.

本発明の熱膨張性加硫ゴム発泡体を用いることにより、
保管●運搬コストを低減することができるとともに設備
への装着の作業性を改善し、シーリングにおいてはシー
ル特性を向上させることができる。
By using the thermally expandable vulcanized rubber foam of the present invention,
It can reduce storage and transportation costs, improve the workability of installing it on equipment, and improve sealing properties.

以下に実施例により本発明を具体的に説明するが、これ
らは例示的なものであり、本発明はこれらによって限定
されるものではない。
The present invention will be specifically explained below with reference to Examples, but these are merely illustrative and the present invention is not limited thereto.

く実施例〉 実施例1,同2および比較例 表1に記した配合物を、1.71バンバリ一〇キサー及
び10インチQキレングロールを用いて混練した。次い
でこれらの配合組成物を45mφ押出機を用いて%81
XIIX801l1のリボンダイスにより押出し、続い
て連続加硫槽に導びき200℃にて発泡、加硫を行った
Examples> Examples 1, 2 and Comparative Examples The formulations shown in Table 1 were kneaded using a 1.71 Banbury 10 xer and a 10 inch Q Killengrol. Then, these blended compositions were mixed using a 45 mφ extruder to
It was extruded using a XIIX801l1 ribbon die, and then introduced into a continuous vulcanization tank where it was foamed and vulcanized at 200°C.

得られた発泡体を120℃に加熱し、金型にて8分の1
の厚みに圧縮し、この状態で20℃の水に浸漬し、急冷
した。除圧前後の発泡体の比重を表2に示す。さらに、
この発泡体を120℃の熱空気で加熱した後の、発泡体
の比重を表2に示す。
The obtained foam was heated to 120°C and molded into 1/8
The material was compressed to a thickness of 1, and in this state was immersed in water at 20° C. to rapidly cool it. Table 2 shows the specific gravity of the foam before and after pressure removal. moreover,
Table 2 shows the specific gravity of the foam after it was heated with hot air at 120°C.

熱可塑性樹脂を含んだ実施例1.2の発泡体は、加熱、
圧縮、冷却の処理により、高比重、小体積となり、さら
に加熱により、元の比重、体積に回復することがわかる
The foam of Example 1.2 containing a thermoplastic resin was heated,
It can be seen that compression and cooling processes result in high specific gravity and small volume, and further heating restores the original specific gravity and volume.

表1 配合     (u部) (注)1)エスプレン505 住友化学工業(製)EPDM 2)シーストSO 東海カーボン(製)カーボンブラック 8)スミカセンG806 住友化学工業(製)低密度ボリエチレ ヤ ン:ビ〆ット軟化点79℃ 4)エバテートH20 1 1 住友化学工業(製)エチレンー酢酸ビ ニル共重合体:ビ〆ット軟化点82℃ 5)セルyイクA 三協化或(製)発泡剤DPT 6)々ルトンNP 三協化成(製)尿素系発泡助剤Table 1 Mixture (part u) (Note) 1) Esplen 505 Sumitomo Chemical Industries (manufactured) EPDM 2) Seast SO Tokai Carbon (manufactured) carbon black 8) Sumikasen G806 Sumitomo Chemical Industries (manufactured) low-density polyethylene Ya N: Bit softening point 79℃ 4) Evatate H20 1 1 Sumitomo Chemical Co., Ltd. Ethylene-vinyl acetate Nil copolymer: Bit softening point 82℃ 5) Cell y Iku A Foaming agent DPT manufactured by Sankyo Kaoru 6) Zuruton NP Sankyo Kasei (manufactured) urea-based foaming aid

Claims (2)

【特許請求の範囲】[Claims] (1)熱可塑性樹脂を含む加硫ゴム発泡体を該熱可塑性
樹脂の軟化点以上の温度において圧縮し、冷却して得る
ことを特徴とする熱膨張性ゴム発泡体。
(1) A thermally expandable rubber foam obtained by compressing a vulcanized rubber foam containing a thermoplastic resin at a temperature equal to or higher than the softening point of the thermoplastic resin and cooling.
(2)前記加硫ゴム発泡体が熱可塑性樹脂を含むエチレ
ン−α−オレフィン系加硫ゴム発泡体である請求項1の
熱膨張性ゴム発泡体。
(2) The thermally expandable rubber foam according to claim 1, wherein the vulcanized rubber foam is an ethylene-α-olefin vulcanized rubber foam containing a thermoplastic resin.
JP23439789A 1989-09-07 1989-09-07 Foam Pending JPH0395238A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23439789A JPH0395238A (en) 1989-09-07 1989-09-07 Foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23439789A JPH0395238A (en) 1989-09-07 1989-09-07 Foam

Publications (1)

Publication Number Publication Date
JPH0395238A true JPH0395238A (en) 1991-04-19

Family

ID=16970360

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23439789A Pending JPH0395238A (en) 1989-09-07 1989-09-07 Foam

Country Status (1)

Country Link
JP (1) JPH0395238A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011007788A1 (en) * 2009-07-14 2011-01-20 株式会社ブリヂストン Sealing material
WO2013105150A1 (en) 2012-01-11 2013-07-18 パナソニック株式会社 Switching power supply circuit

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011007788A1 (en) * 2009-07-14 2011-01-20 株式会社ブリヂストン Sealing material
JP5746622B2 (en) * 2009-07-14 2015-07-08 株式会社ブリヂストン Sealing material
US9403957B2 (en) 2009-07-14 2016-08-02 Bridgestone Corporation Sealing material
WO2013105150A1 (en) 2012-01-11 2013-07-18 パナソニック株式会社 Switching power supply circuit
US8923020B2 (en) 2012-01-11 2014-12-30 Panasonic Intellectual Property Management Co., Ltd. Switching power supply circuit having shunt regulator with switchable gain

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