JP4150467B2 - Rubber-based foam material and foamed body thereof - Google Patents
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- JP4150467B2 JP4150467B2 JP15542899A JP15542899A JP4150467B2 JP 4150467 B2 JP4150467 B2 JP 4150467B2 JP 15542899 A JP15542899 A JP 15542899A JP 15542899 A JP15542899 A JP 15542899A JP 4150467 B2 JP4150467 B2 JP 4150467B2
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Description
【0001】
【発明の技術分野】
本発明は、燃焼遅延性を示すEPDM系発泡体を形成できるゴム系発泡材料に関する。
【0002】
【従来の技術】
EPDM系の発泡体は、その優れたクッション性や圧縮性等に基づいてクッション材やパッド材、気密や止水等のシール材、断熱材や防音材などとして家電等の室内用品や自動車等の屋外用品、住宅等の建築物などの各種の分野で広く使用されており、その用途に応じクッション性や圧縮性等の特性が調節されている。
【0003】
しかしながら従来、前記発泡体の難燃化については、EPDM等のオレフィン系ポリマーは燃焼エネルギーが高いこともあって例えば金属水酸化物やリン系化合物、ハロゲン化物やシリコーン系化合物等の難熱剤を配合する方式が専ら採られてきた。そのため難燃性のみが過剰品質となるなど製品の燃焼のしにくさと他の性能とのバランスを採りにくい難点があった。
【0004】
【発明の技術的課題】
本発明は、一般的に用いられている難燃剤を用いることなく燃焼の遅延化を達成して、各種性能のバランスに優れるEPDM系発泡体を形成できるゴム系発泡材料の開発を課題とする。
【0005】
【課題の解決手段】
本発明は、ムーニー粘度(ML1+4、100℃)が5〜30のEPDMと加硫剤と発泡剤と引火点が200〜350℃の可塑剤オイルと、炭酸カルシウム、炭酸マグネシウム、ケイ酸又はケイ酸塩類とを少なくとも成分とする混和物からなり、前記EPDM100重量部あたり炭酸カルシウム、炭酸マグネシウム、ケイ酸又はケイ酸塩類をそれらの合計量で80〜400重量部、かつ前記可塑剤オイルを15〜40重量部含有することを特徴とするゴム系発泡材料を提供するものである。
【0006】
【発明の効果】
上記したEPDMを用いることにより、燃焼特性を制御しうる難燃剤以外の充填材を多量に配合することが可能となり、EPDM系発泡体のゴム物性を良好に温存しつつそのクッション性や圧縮性等の性能を制御でき、かつ難燃剤を用いないで燃焼遅延性をもたせることができて、引火点の高い可塑剤オイルにより燃焼遅延性を向上させることができる。
【0007】
【発明の実施形態】
本発明によるゴム系発泡材料は、ムーニー粘度(ML1+4、100℃)が5〜30のEPDMと加硫剤と発泡剤と引火点が200〜350℃の可塑剤オイルと、炭酸カルシウム、炭酸マグネシウム、ケイ酸又はケイ酸塩類とを少なくとも成分とする混和物からなり、前記EPDM100重量部あたり炭酸カルシウム、炭酸マグネシウム、ケイ酸又はケイ酸塩類をそれらの合計量で80〜400重量部、かつ前記可塑剤オイルを15〜40重量部含有するものである。
【0008】
EPDMとしては、ムーニー粘度(ML1+4、100℃、以下同じ)5〜30のものを1種又は2種以上用いることができる。当該粘度が前記範囲外のEPDMでは、ゴム物性を残しつつ燃焼遅延性や圧縮性等の性能を調節することが困難である。EPDMの好ましいムーニー粘度は8〜25である。なお当該ムーニー粘度を満足する2種以上のEPDMを用いる場合、前記性能の調節操作性等の点より、そのいずれか1種を95〜5重量部、その他を5〜95重量部の割合で用いることが好ましい。
【0009】
加硫剤としては、1種又は2種以上の適宜なものを用いることができ、特に限定はない。ちなみにその例としては、硫黄や硫黄化合物類、セレンや酸化マグネシウム、一酸化鉛や酸化亜鉛、有機過酸化物類やポリアミン類、P−キノンジオキシムやP,P'-ジベンゾイルキノンジオキシムの如きオキシム類やP−ジニトロソベンジンの如きニトロソ化合物類、アルキルフェノール・ホルムアルデヒド樹脂、メラミン・ホルムアルデヒド縮合物の如き樹脂類や安息香酸アンモニウムの如きアンモニウム塩類などがあげられる。
【0010】
得られる発泡体の加硫性や発泡性による耐久性等の物性などの点よりは、硫黄や硫黄化合物類、特に硫黄が好ましく用いうる。加硫剤の使用量は、その種類に基づく加硫効率などに応じて適宜に決定することができる。ちなみに硫黄系の場合、EPDM100重量部あたり通例、0.1〜10重量部、就中0.5〜5重量部が用いられる。
【0011】
また発泡剤としても1種又は2種以上の適宜なものを用いることができ、特に限定はない。ちなみにその例としては、炭酸アンモニウムや炭酸水素アンモニウム、炭酸水素ナトリウムや亜硝酸アンモニウム、水素化ホウ素ナトリウムやアジド類などの無機系発泡剤があげられる。
【0012】
またトリクロロモノフルオロメタンやジクロロモノフルオロメタンの如きフッ化アルカン、アゾビスイソブチロニトリルやアゾジカルボン酸アミド、バリウムアゾジカルボキシレートの如きアゾ系化合物、パラトルエンスルホニルヒドラジドやジフェニルスルホン−3,3'−ジスルホニルヒドラジド、4,4'−オキシビス(ベンゼンスルホニルヒドラジド)、アリルビス(スルホニルヒドラジド)の如きヒドラジン系化合物等の有機系発泡剤もあげられる。
【0013】
さらにρ−トルイレンスルホニルセミカルバジドや4,4'−オキシビス(ベンゼンスルホニルセミカルバジド)の如きセミカルバジド系化合物、5−モルホリル−1,2,3,4−チアトリアゾールの如きトリアゾール系化合物、N,N'−ジニトロソペンタメチレンテトラミンやN,N'−ジメチル−N,N'−ジニトロソテレフタルアミドの如きN−ニトロソ系化合物などの有機発泡剤もあげられる。用いる発泡剤は、加熱膨脹性の物質がマイクロカプセル内に封入された熱膨脹性微粒子などであってもよい。その熱膨脹性微粒子にはマイクロスフェア(商品名、松本油脂社製)などの市販物もある。
【0014】
発泡剤の使用量は、目的とする発泡体の物性などに応じて適宜に決定することができる。一般には、EPDM100重量部あたり0.1〜100重量部、就中0.5〜50重量部、特に1〜30重量部の発泡剤が用いられる。
【0015】
ゴム系発泡材料には、燃焼遅延性を付与するために炭酸カルシウム、炭酸マグネシウム、ケイ酸又はケイ酸塩類の1種又は2種以上が少なくとも配合される。その配合量は、EPDM100重量部あたり炭酸カルシウム、炭酸マグネシウム、ケイ酸又はケイ酸塩類の合計量に基づいて80〜400重量部とされる。
【0016】
前記の配合量が80重量部未満では、燃焼を遅延させる効果に乏しく、400重量部を超えるとゴム的性質が低下して得られる発泡体の性能を調節しにくくなる。かかる燃焼遅延性の付与効果や発泡体性能の調節性などの点より前記した炭酸カルシウム等の好ましい配合量は、380重量部以下、就中350重量部以下、特に100〜300重量部である。
【0017】
混和物の調製は、少なくともEPDM、加硫剤、発泡剤、引火点が200〜350℃の可塑剤オイル及び前記の炭酸カルシウム等からなる配合成分を、例えばニーダやミキシングロール等の混練機を介して混合する方式などの適宜な方式で混合することにより行うことができる。その際、加硫が進行する程度に温度上昇する混合方式は好ましくない。
【0018】
前記した混和物の調製に際しては、粘度や加硫性の調節、得られる発泡体の強度等の物性の調節などを目的に従来に準じた適宜な配合剤を添加することができる。ちなみに加硫の促進を目的に、例えばグアニジン類やチアゾール類、スルフェンアミド類やチューラム類、ジチオカルバミン酸類やキサントゲン酸類、アルデヒドアンモニア類やアルデヒドアミン類、チオウレア類などからなる1種又は2種以上の加硫促進剤、さらには加硫促進助剤を配合することができる。加硫促進剤の使用量は、EPDM100重量部あたり0.1〜10重量部が適当であるが、これに限定されない。
【0019】
また混和物には、その加工性ないし成形性の調節などを目的に例えば無水フタル酸や安息香酸やサリチル酸の如き有機酸、N−ニトロソ−ジフェニルアミンやN−ニトロソ−フェニル−β−ナフチルアミンの如きアミン類などからなる1種又は2種以上の加硫遅延剤を配合して、上記した加硫促進剤とは反対に加硫を遅らせることもできる。
【0020】
さらに混和物には、成形性の調節などを目的に、例えば塩素化パラフィン等のパラフィン類やワックス類、ナフテン類やアロマ類やアスファルト類、アマニ油等の乾性油類や動植物油類、石油系オイル類や各種の低分量ポリマー類、フタル酸エステル類やリン酸エステル類、ステアリン酸やそのエステル類、アルキルスルホン酸エステル類や粘着付与剤などからなる1種又は2種以上の軟化剤ないし可塑剤を添加することもできる。なおステアリン酸やそのエステル類は、滑剤などとしても有用で、従って各種の滑剤も配合しうる成分の例としてあげられる。
【0021】
混和物の調製に際しては燃焼遅延性を活かす点などより、引火点が200〜350℃、好ましくは220〜330℃のオイル類からなる可塑剤が用いられ、成形性のより向上や得られる発泡体のゴム特性の維持性等を加味した場合には、40℃で30〜500mm2/秒、就中60〜450mm2/秒、100℃で5〜50mm2/秒、就中10〜40mm2/秒の動粘度を示すものが特に好ましい。またかかる点より可塑剤オイルの配合量は、EPDM100重量部あたり15〜40重量部とされ、好ましくは20〜35重量部である。
【0022】
加えて混和物には、尿素系やサリチル酸系や安息香酸系等の発泡助剤、タルクやクレーや雲母粉、亜鉛華やベントナイト、カーボンブラックやシリカ、アルミナやアルミニウムシリケート、アセチレンブラックやアルミニウム粉の如き充填剤や老化防止剤、酸化防止剤や顔料、着色剤や防カビ剤などの従来の難燃剤を除く適宜な配合剤の1種又は2種以上を必要に応じて添加することができる。なお前記の亜鉛華は安定剤として、カーボンブラックは補強剤などとしても有用で、従って各種の安定剤や補強剤も配合しうる成分の例としてあげられる。
【0023】
またさらに混和物には、得られる発泡体の強度等の物性の調節を目的に、非ゴム系ポリマーやEPDM以外のゴム系ポリマーを1種又は2種以上配合することもできる。その非ゴム系ポリマーやゴム系ポリマーについては適宜なものを用いることができ、特に限定はない。
【0024】
ちなみに前記非ゴム系ポリマーの例としては、ポリ(メタ)アクリル酸アルキルエステルの如きアクリル系ポリマーやポリ塩化ビニル、ポリエチレンやポリプロピレン、エチレン・酢酸ビニル共重合体やポリ酢酸ビニル、ポリアミドやポリエステル、塩素化ポリエチレンやウレタン系ポリマー、スチレン系ポリマーやシリコーン系ポリマー、エポキシ系樹脂などがあげられる。その使用量は、発泡体のゴム的性質を維持する点などよりEPDMの50重量%以下、就中30重量%以下、特に15重量%以下が好ましい。
【0025】
一方、前記したEPDM以外のゴム系ポリマーの例としては、ブテン−1の如きα−オレフィン・ジシクロペンタジエンやエチリデンノルボルネンの如き非共役二重結合を有する環状又は非環状のポリエンを成分とするゴム系共重合体やエチレン・プロピレンゴム、エチレン・プロピレンターポリマーやシリコーンゴム、フッ素ゴムやアクリルゴム、ポリウレタン系ゴムやポリアミド系ゴム、天然ゴムやポリイソブチレン、ポリイソプレンやクロロプレンゴム、ブチルゴムやニトリルブチルゴム、スチレン・ブタジエンゴムやスチレン・ブタジエン・スチレンゴム、スチレン・イソプレン・スチレンゴムやスチレン・エチレン・ブタジエンゴム、スチレン・エチレン・ブチレン・スチレンゴムやスチレン・イソプレン・プロピレン・スチレンゴム、クロロスルホン化ポリエチレンなどがあげられる。EPDM以外のゴム系ポリマーの配合量は、前記非ゴム系ポリマーの場合に準じうる。
【0026】
本発明によるゴム系発泡材料を用いた発泡体の形成は、上記した混和物を加熱して加硫発泡処理することにより行いうるが、その形成に際しては必要に応じ混和物を例えばシート等の所定の形態に成形して、その成形体を加熱処理して加硫発泡体とすることもできる。その場合、成形体は、適宜な方式にて任意な形態に成形したものであってよく、その形態について特に限定はない。
【0027】
従って加硫発泡処理の対象物は、混和物を例えばミキシングロールやカレンダーロールや押出成形等による適宜な方式でシート状やその他の形態に成形したものであってもよいし、所定の型を介して射出成形やプレス成形等による適宜な方式で凹凸等を有する所定の形態に成形したものなどであってもよい。
【0028】
前記において、凹凸形状を有する発泡体の形成では、未加硫シートを凹凸を有する型の上に配置して加熱し、その型の凹凸に前記未加硫シートを形成する混和物を流動侵入させて加硫発泡処理する方式なども採ることができる。かかる方式は、ヒダ構造を有する複雑で深い凹凸構造を有する型の場合にもその凹凸形状を精度よく形成できる利点などを有している。
【0029】
よって成形体の寸法は任意であり、目的とする加硫発泡体の形態などに応じて適宜に決定することができる。シート等の場合、その厚さは100mm以下、就中1μm〜80mm、特に10μm〜50mmが一般的である。
【0030】
上記した加硫発泡処理は、用いた加硫剤や発泡剤などによる加硫開始温度や発泡温度などにより従来に準じた適宜な条件で行うことができる。一般的な加硫発泡温度は、450℃以下、就中100〜350℃、特に120〜300℃である。かかる加硫発泡処理で通例、混和物が軟化して発泡剤が膨脹し発泡構造を形成しつつ加硫が進行して目的の加硫発泡体が形成される。
【0031】
前記において発泡処理と加硫処理は、異なる温度条件で行うこともでき、適宜な処理条件を採ることができる。また加硫発泡処理は、発泡倍率の調節などを目的に加圧下に行うこともできる。その加圧条件は、従来に準じることができる。
【0032】
形成する加硫発泡体の発泡倍率(発泡前後の密度比)は、使用目的などに応じて適宜に決定されるが、一般には1.1〜25倍、就中1.5倍以上、特に5〜20倍とされる。その発泡倍率は、上記した発泡剤の配合量や加硫発泡の処理時間や温度などにより制御することができる。また発泡倍率の調節などにより、得られる加硫発泡体の独立や連続、それらの混在等の発泡構造を制御することができる。
【0033】
本発明によるゴム系発泡体は、例えばクッション材やパッド材、気密や防水等の各種目的のシール材、断熱材、防音や制振等の振動低減材などの従来に準じた各種の用途に好ましく用いることができる。
【0034】
【実施例】
実施例1
ムーニー粘度23のEPDM(三井化学社製、EPT4021)100部(重量部、以下同じ)、硫黄1部、加硫促進剤(大内新興化学社製、ノクセラーEZ)3部、発泡剤(永和化成工業社製、ビニフォールAC#LQ)20部、発泡助剤(永和化成工業社製、セルペーストK−5)5部、重質炭酸カルシウム200部、低密度ポリエチレン(三井化学社製、ミラソン67)25部、引火点270℃の可塑剤オイル(出光興産社製、ダイアナプロセスオイルPW−90、パラフィンオイル、動粘度40℃:96mm2/秒、100℃:11mm2/秒)25部、カーボンブラック10部、酸化亜鉛(2種)5部及び粉末ステアリン酸1部を加圧ニーダで混練して混和物を得、それを押出し機で成形して厚さ10mmの未加硫シートを得、それを160℃のオーブン中で30分間加熱して加硫発泡処理し、密度0.12g/cm3の発泡シートを得た。
【0035】
実施例2
可塑剤オイルとして、引火点300℃のもの(出光興産社製、ダイアナプロセスオイルPW−380、パラフィンオイル、動粘度40℃:382mm2/秒、100℃:30mm2/秒)を用いたほかは実施例1に準じて密度0.11g/cm3の発泡シートを得た。
【0036】
実施例3
重質炭酸カルシウムの使用量を300部とし、ダイアナプロセスオイルPW−380(可塑剤オイル)を35部用いたほかは実施例1に準じて、密度0.14g/cm3の発泡シートを得た。
【0037】
比較例1
EPDMとしてムーニー粘度が42のもの(三井化学社製、EPT4045)を用い、発泡剤の使用量を15部としたほかは実施例1に準じて、密度0.35g/cm3の発泡シートを得た。
【0038】
比較例2
発泡剤の使用量を15部とし、重質炭酸カルシウムの使用量を50部としたほかは実施例1に準じて、密度0.13g/cm3の発泡シートを得た。
【0039】
比較例3
可塑剤オイルとして引火点が170℃のもの(日本石油社製、日石ポリブテンオイルHV−15、動粘度40℃:655mm2/秒、100℃:31mm2/秒)を用いたほかは実施例1に準じて、密度0.13g/cm3の発泡シートを得た。
【0040】
評価試験
実施例、比較例で得たゴム系発泡体について、UL94安全規格による発泡プラスチック材料の水平燃焼試験方法に準拠して長さ150mm、幅50mmの所定厚の試験片についてその燃焼性を調べると共に、燃焼遅延性に相当するHBFを調べた。なおHBFレベルの基準は、所定数量全ての試験体が着火起点より25mm標線から125mm標線までの間で燃焼速度が40mm/分以下のとき、又は燃焼が着火起点より125mm標線までの間で終了するときに満足する。
【0041】
前記の結果を次表に示した。
[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to a rubber-based foam material capable of forming an EPDM-based foam exhibiting combustion retardance.
[0002]
[Prior art]
EPDM foam is based on its superior cushioning properties and compressibility, such as cushioning materials and pad materials, sealing materials such as airtight and water-stopping materials, heat insulating materials and soundproofing materials, etc. It is widely used in various fields such as outdoor products and buildings such as houses, and characteristics such as cushioning and compressibility are adjusted according to the application.
[0003]
However, conventionally, regarding the flame retardancy of the foam, an olefin polymer such as EPDM has a high combustion energy, so that a flame retardant such as a metal hydroxide, a phosphorus compound, a halide, or a silicone compound is used. A method of blending has been exclusively adopted. For this reason, there is a difficulty that it is difficult to balance the difficulty of combustion of the product with other performances, such as that only the flame retardancy becomes excessive quality.
[0004]
[Technical Problem of the Invention]
An object of the present invention is to develop a rubber-based foam material capable of forming an EPDM-based foam that achieves a retarded combustion without using a generally used flame retardant and has an excellent balance of various performances.
[0005]
[Means for solving problems]
The present invention relates to EPDM having a Mooney viscosity (ML 1 + 4 , 100 ° C.) of 5 to 30, a vulcanizing agent, a foaming agent, a plasticizer oil having a flash point of 200 to 350 ° C., and calcium carbonate, magnesium carbonate, silicic acid or silica. A mixture comprising at least an acid salt as a component , and 80 parts by weight of the total amount of calcium carbonate, magnesium carbonate, silicic acid or silicates per 100 parts by weight of the EPDM , and 15 to 15 parts of the plasticizer oil. The present invention provides a rubber foam material containing 40 parts by weight .
[0006]
【The invention's effect】
By using the above-mentioned EPDM, it becomes possible to mix a large amount of fillers other than the flame retardant that can control the combustion characteristics, and the cushioning property, compressibility, etc. while preserving the rubber physical properties of the EPDM foam well. performance can be controlled, and be able to have a flame retardant without using a flame retardant, it is possible to improve the flame retardancy by a high flash point plasticizer oils.
[0007]
DETAILED DESCRIPTION OF THE INVENTION
The rubber-based foam material according to the present invention comprises an EPDM having a Mooney viscosity (ML 1 + 4 , 100 ° C.) of 5 to 30, a vulcanizing agent, a foaming agent, a plasticizer oil having a flash point of 200 to 350 ° C. , calcium carbonate and magnesium carbonate. , A mixture containing at least a component of silicic acid or silicate , and the total amount of calcium carbonate, magnesium carbonate, silicic acid or silicate is 80 to 400 parts by weight per 100 parts by weight of the EPDM , and the plastic It contains 15 to 40 parts by weight of agent oil .
[0008]
As EPDM, one having Mooney viscosity (ML 1 + 4 , 100 ° C., hereinafter the same) 5 to 30 can be used alone or in combination. When the viscosity is outside the above range, it is difficult to adjust performance such as combustion retardancy and compressibility while leaving rubber properties. The preferred Mooney viscosity of EPDM is 8-25. When two or more kinds of EPDM satisfying the Mooney viscosity are used, any one of them is used at a ratio of 95 to 5 parts by weight, and the others are used at a ratio of 5 to 95 parts by weight, from the viewpoint of the operability for adjusting the performance. It is preferable.
[0009]
As the vulcanizing agent, one or more suitable ones can be used, and there is no particular limitation. Examples include sulfur and sulfur compounds, selenium and magnesium oxide, lead monoxide and zinc oxide, organic peroxides and polyamines, P-quinonedioxime and P, P'-dibenzoylquinonedioxime. Examples thereof include oximes such as nitroso compounds such as P-dinitrosobenzidine, resins such as alkylphenol / formaldehyde resins and melamine / formaldehyde condensates, and ammonium salts such as ammonium benzoate.
[0010]
Sulfur and sulfur compounds, particularly sulfur, can be preferably used from the viewpoint of physical properties such as vulcanizability and foaming durability of the obtained foam. The amount of the vulcanizing agent used can be appropriately determined according to the vulcanization efficiency based on the type. Incidentally, in the case of a sulfur type, usually 0.1 to 10 parts by weight, especially 0.5 to 5 parts by weight are used per 100 parts by weight of EPDM.
[0011]
Moreover, 1 type, or 2 or more types of suitable foaming agents can be used, and there is no particular limitation. Examples thereof include inorganic foaming agents such as ammonium carbonate, ammonium hydrogen carbonate, sodium hydrogen carbonate, ammonium nitrite, sodium borohydride and azides.
[0012]
Also, fluorinated alkanes such as trichloromonofluoromethane and dichloromonofluoromethane, azo compounds such as azobisisobutyronitrile, azodicarboxylic acid amide and barium azodicarboxylate, paratoluenesulfonyl hydrazide and diphenylsulfone-3,3 Organic foaming agents such as hydrazine-based compounds such as' -disulfonylhydrazide, 4,4'-oxybis (benzenesulfonylhydrazide), and allylbis (sulfonylhydrazide) are also included.
[0013]
Further, semicarbazide compounds such as ρ-toluylenesulfonyl semicarbazide and 4,4′-oxybis (benzenesulfonyl semicarbazide), triazole compounds such as 5-morpholyl-1,2,3,4-thiatriazole, N, N′— Organic foaming agents such as dinitrosopentamethylenetetramine and N-nitroso compounds such as N, N′-dimethyl-N, N′-dinitrosotephthalamide are also included. The foaming agent used may be heat-expandable fine particles in which a heat-expandable substance is enclosed in microcapsules. The thermally expandable fine particles include commercially available products such as microspheres (trade name, manufactured by Matsumoto Yushi Co., Ltd.).
[0014]
The amount of the foaming agent used can be appropriately determined according to the physical properties of the target foam. In general, 0.1 to 100 parts by weight, especially 0.5 to 50 parts by weight, especially 1 to 30 parts by weight, of foaming agent is used per 100 parts by weight of EPDM.
[0015]
The rubber-based foam material is blended with at least one or more of calcium carbonate, magnesium carbonate, silicic acid or silicates in order to impart combustion retardancy. The blending amount is 80 to 400 parts by weight based on the total amount of calcium carbonate, magnesium carbonate, silicic acid or silicate per 100 parts by weight of EPDM.
[0016]
If the blending amount is less than 80 parts by weight, the effect of retarding combustion is poor, and if it exceeds 400 parts by weight, it is difficult to adjust the performance of the foam obtained by reducing the rubbery properties. The preferred blending amount of calcium carbonate and the like is 380 parts by weight or less, especially 350 parts by weight or less, particularly 100 to 300 parts by weight, from the viewpoint of the effect of imparting such a flame retardancy and the ability to adjust foam performance.
[0017]
The admixture is prepared by blending at least a blending component consisting of EPDM, a vulcanizing agent, a foaming agent , a plasticizer oil having a flash point of 200 to 350 ° C. and the above calcium carbonate, through a kneader such as a kneader or a mixing roll. Can be carried out by mixing by an appropriate method such as a mixing method. At that time, a mixing method in which the temperature rises to such an extent that vulcanization proceeds is not preferable.
[0018]
In preparing the admixture described above, an appropriate compounding agent according to the prior art can be added for the purpose of adjusting viscosity and vulcanizability, and adjusting physical properties such as strength of the resulting foam. Incidentally, for the purpose of promoting vulcanization, for example, guanidines and thiazoles, sulfenamides and turums, dithiocarbamic acids and xanthogenic acids, aldehyde ammonias, aldehyde amines, thioureas, etc. Vulcanization accelerators, and further vulcanization acceleration assistants can be blended. The amount of the vulcanization accelerator used is suitably 0.1 to 10 parts by weight per 100 parts by weight of EPDM, but is not limited thereto.
[0019]
The admixture contains organic acids such as phthalic anhydride, benzoic acid, and salicylic acid, and amines such as N-nitroso-diphenylamine and N-nitroso-phenyl-β-naphthylamine for the purpose of controlling processability and moldability. One or two or more kinds of vulcanization retarders composed of a kind or the like can be blended to delay the vulcanization, contrary to the above vulcanization accelerator.
[0020]
For admixtures, for example, paraffins such as chlorinated paraffins and waxes, naphthenes, aromas, asphalts, dry oils such as linseed oil, animal and vegetable oils, petroleum One or more softeners or plastics consisting of oils, various low-volume polymers, phthalates and phosphates, stearic acid and esters thereof, alkyl sulfonates and tackifiers An agent can also be added. Note that stearic acid and its esters are useful as a lubricant and the like, and therefore, examples of components in which various lubricants can be blended.
[0021]
The like that utilize the flame retardant is in the preparation of the blend, flash point 200 to 350 ° C., preferably used are plasticizers consisting of oils of 220-330 ° C., moldability further improves and the resulting foam when considering the maintenance and the like of the rubber characteristics of, 30~500mm 2 / s at 40 ° C., especially 60~450mm 2 / sec, 5 to 50 mm 2 / s at 100 ° C., especially 10 to 40 mm 2 / Those showing a kinematic viscosity in seconds are particularly preferred. The amount of such points by Rika plasticizer oil is 15 to 40 parts by weight per EPDM100 parts by weight, preferably 20 to 35 parts by weight.
[0022]
In addition, the admixtures include foaming aids such as urea, salicylic acid and benzoic acid, talc, clay, mica powder, zinc white, bentonite, carbon black and silica, alumina, aluminum silicate, acetylene black and aluminum powder. One kind or two or more kinds of suitable compounding agents excluding conventional flame retardants such as fillers, antioxidants, antioxidants, pigments, colorants and fungicides can be added as necessary. The zinc white is also useful as a stabilizer, and carbon black is useful as a reinforcing agent. Therefore, examples of components in which various stabilizers and reinforcing agents can be blended are listed.
[0023]
Further, in the admixture, one or more kinds of non-rubber polymers and rubber polymers other than EPDM can be blended for the purpose of adjusting physical properties such as strength of the obtained foam. Any suitable non-rubber polymer or rubber polymer can be used without any particular limitation.
[0024]
Incidentally, examples of the non-rubber polymer include acrylic polymers such as poly (meth) acrylic acid alkyl ester, polyvinyl chloride, polyethylene and polypropylene, ethylene / vinyl acetate copolymer, polyvinyl acetate, polyamide and polyester, chlorine. Polyethylene, urethane polymer, styrene polymer, silicone polymer, epoxy resin and the like. The amount used is preferably not more than 50% by weight of EPDM, more preferably not more than 30% by weight, especially not more than 15% by weight, from the viewpoint of maintaining the rubbery properties of the foam.
[0025]
On the other hand, examples of rubber-based polymers other than the above-mentioned EPDM include rubbers containing as a component a cyclic or non-cyclic polyene having a non-conjugated double bond such as α-olefin dicyclopentadiene such as butene-1 or ethylidene norbornene. Copolymer, ethylene / propylene rubber, ethylene / propylene terpolymer and silicone rubber, fluorine rubber and acrylic rubber, polyurethane rubber and polyamide rubber, natural rubber and polyisobutylene, polyisoprene and chloroprene rubber, butyl rubber and nitrile butyl rubber, Styrene / butadiene rubber, styrene / butadiene / styrene rubber, styrene / isoprene / styrene rubber, styrene / ethylene / butadiene rubber, styrene / ethylene / butylene / styrene rubber, styrene / isoprene / propylene / styrene Beam, such as chlorosulfonated polyethylene. The blending amount of the rubber-based polymer other than EPDM can be based on the non-rubber-based polymer.
[0026]
Formation of the foam using the rubber-based foam material according to the present invention can be performed by heating the above-mentioned admixture and subjecting it to vulcanization and foaming treatment. It is also possible to form a vulcanized foam by heat-treating the molded body. In that case, the molded body may be molded into an arbitrary form by an appropriate method, and the form is not particularly limited.
[0027]
Therefore, the object of vulcanization and foaming treatment may be a mixture obtained by molding the admixture into a sheet or other form by an appropriate method such as a mixing roll, a calender roll, or extrusion molding, or through a predetermined mold. Further, it may be formed into a predetermined form having irregularities by an appropriate method such as injection molding or press molding.
[0028]
In the above, in the formation of a foam having an uneven shape, an unvulcanized sheet is placed on a mold having unevenness and heated, and the mixture forming the unvulcanized sheet flows into the unevenness of the mold to flow in A method of vulcanizing and foaming can also be adopted. Such a method has an advantage that the concavo-convex shape can be accurately formed even in the case of a mold having a complex and deep concavo-convex structure.
[0029]
Therefore, the size of the molded body is arbitrary, and can be appropriately determined according to the form of the target vulcanized foam. In the case of a sheet or the like, the thickness is generally 100 mm or less, in particular, 1 μm to 80 mm, particularly 10 μm to 50 mm.
[0030]
The vulcanization foaming treatment described above can be performed under appropriate conditions according to the prior art depending on the vulcanization start temperature, foaming temperature, and the like using the vulcanizing agent and the foaming agent used. A typical vulcanization foaming temperature is 450 ° C. or lower, especially 100 to 350 ° C., particularly 120 to 300 ° C. In general, the vulcanization and foaming treatment softens the admixture and expands the foaming agent to form a foam structure, and vulcanization proceeds to form the desired vulcanized foam.
[0031]
In the above, the foaming treatment and the vulcanization treatment can be performed under different temperature conditions, and appropriate treatment conditions can be taken. The vulcanization foaming treatment can also be performed under pressure for the purpose of adjusting the foaming ratio. The pressurizing condition can be based on the conventional one.
[0032]
The expansion ratio (density ratio before and after foaming) of the vulcanized foam to be formed is appropriately determined according to the purpose of use, etc., but is generally 1.1 to 25 times, especially 1.5 times or more, especially 5 -20 times. The expansion ratio can be controlled by the blending amount of the foaming agent described above, the processing time and temperature of vulcanization foaming, and the like. In addition, by adjusting the foaming ratio, the foamed structure of the obtained vulcanized foam can be controlled independently, continuously, or a mixture thereof.
[0033]
The rubber-based foam according to the present invention is preferably used in various conventional applications such as cushion materials, pad materials, sealing materials for various purposes such as airtightness and waterproofing, heat insulating materials, vibration reducing materials such as soundproofing and vibration damping. Can be used.
[0034]
【Example】
Example 1
100 parts of EPDM (Mitsui Chemicals, EPT4021) with Mooney viscosity 23, 1 part of sulfur, 1 part of sulfur, 3 parts of vulcanization accelerator (Ouchi Shinsei Chemical Co., Noxeller EZ), foaming agent (Eiwa Chemicals) Industrial parts, VINIFOL AC # LQ 20 parts, foaming aid (manufactured by Eiwa Chemical Industries, Cell Paste K-5), heavy calcium carbonate 200 parts, low density polyethylene (Mitsui Chemicals, Mirason 67) 25 parts, plasticizer oil with a flash point of 270 ° C. (Idemitsu Kosan Co., Ltd., Diana Process Oil PW-90, paraffin oil, kinematic viscosity 40 ° C .: 96 mm 2 / sec, 100 ° C .: 11 mm 2 / sec) 25 parts, carbon black 10 parts, 5 parts of zinc oxide (2 types) and 1 part of powdered stearic acid were kneaded with a pressure kneader to obtain a blend, which was molded with an extruder to obtain a 10 mm thick unvulcanized sheet, 1 It was heated in an oven at 60 ° C. for 30 minutes and vulcanized and foamed to obtain a foamed sheet having a density of 0.12 g / cm 3 .
[0035]
Example 2
As a plasticizer oil, those flash point 300 ° C. (manufactured by Idemitsu Kosan Co., Ltd., Diana Process Oil PW-380, paraffin oil, kinematic viscosity 40 ℃: 382mm 2 / s, 100 ℃: 30mm 2 / s) but using the A foamed sheet having a density of 0.11 g / cm 3 was obtained according to Example 1.
[0036]
Example 3
A foamed sheet having a density of 0.14 g / cm 3 was obtained in the same manner as in Example 1 except that the amount of heavy calcium carbonate used was 300 parts and 35 parts of Diana Process Oil PW-380 (plasticizer oil) was used. .
[0037]
Comparative Example 1
A foamed sheet having a density of 0.35 g / cm 3 was obtained in the same manner as in Example 1 except that an EPDM having a Mooney viscosity of 42 (EPT4045 manufactured by Mitsui Chemicals, Inc.) was used and the amount of foaming agent used was 15 parts. It was.
[0038]
Comparative Example 2
A foamed sheet having a density of 0.13 g / cm 3 was obtained in the same manner as in Example 1 except that the amount of foaming agent used was 15 parts and the amount of heavy calcium carbonate used was 50 parts.
[0039]
Comparative Example 3
Flashpoint those 170 ° C. as plasticizer oils other embodiments using the (Nippon Oil Co., Nisseki polybutene oils HV-15, kinematic viscosity 40 ℃:: 655mm 2 / s, 100 ° C. 31 mm 2 / sec) 1, a foamed sheet having a density of 0.13 g / cm 3 was obtained.
[0040]
For the rubber-based foams obtained in the evaluation test examples and comparative examples, the flammability of a test piece having a predetermined thickness of 150 mm in length and 50 mm in width is examined in accordance with the horizontal combustion test method for foamed plastic materials according to UL94 safety standards. At the same time, HBF corresponding to combustion retardancy was examined. The standard for the HBF level is that when a predetermined number of all specimens are between the 25mm mark and the 125mm mark from the ignition start point and the combustion speed is 40mm / min or less, or the combustion is between the ignition start point and the 125mm mark. Satisfied when ending with.
[0041]
The results are shown in the following table.
Claims (4)
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