JPH0395238A - Foam - Google Patents
FoamInfo
- 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
Links
- 239000006260 foam Substances 0.000 title abstract description 10
- 229920001821 foam rubber Polymers 0.000 claims abstract description 24
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 18
- 239000004711 α-olefin Substances 0.000 claims abstract description 13
- 238000001816 cooling Methods 0.000 claims abstract description 8
- 239000004636 vulcanized rubber Substances 0.000 claims description 16
- 229920001971 elastomer Polymers 0.000 abstract description 14
- 239000005060 rubber Substances 0.000 abstract description 14
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 6
- 239000005977 Ethylene Substances 0.000 abstract description 6
- 238000003860 storage Methods 0.000 abstract description 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract description 4
- 229920001577 copolymer Polymers 0.000 abstract description 4
- 229920003244 diene elastomer Polymers 0.000 abstract description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract description 2
- 238000004073 vulcanization Methods 0.000 description 10
- -1 cyclic dienes Chemical class 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 230000005484 gravity Effects 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 238000005187 foaming Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000004604 Blowing Agent Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OJOWICOBYCXEKR-APPZFPTMSA-N (1S,4R)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound CC=C1C[C@@H]2C[C@@H]1C=C2 OJOWICOBYCXEKR-APPZFPTMSA-N 0.000 description 1
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- NOSXUFXBUISMPR-UHFFFAOYSA-N 1-tert-butylperoxyhexane Chemical compound CCCCCCOOC(C)(C)C NOSXUFXBUISMPR-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000002848 norbornenes Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000010060 peroxide vulcanization Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 238000010059 sulfur vulcanization Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Abstract
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)
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.
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.
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)
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 |
-
1989
- 1989-09-07 JP JP23439789A patent/JPH0395238A/en active Pending
Cited By (5)
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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