JP4269384B2 - Olefin resin foam - Google Patents

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Publication number
JP4269384B2
JP4269384B2 JP970899A JP970899A JP4269384B2 JP 4269384 B2 JP4269384 B2 JP 4269384B2 JP 970899 A JP970899 A JP 970899A JP 970899 A JP970899 A JP 970899A JP 4269384 B2 JP4269384 B2 JP 4269384B2
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Japan
Prior art keywords
foam
olefin resin
weight
resin foam
resin
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JP970899A
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JP2000204187A (en
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宗暁 塚田
英雄 小林
史朗 今井
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Toray Industries Inc
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Toray Industries Inc
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Description

【0001】
【発明の属する技術分野】
本発明は広幅シート状の発泡体を多数の細幅にスプリットする時のカット性、或いは、融断刃を用いて各種形状にカットしたり、発泡体表面に各種形状の凹みを作成する時の作業性や加工走行時の滑り性を改良した発泡体に関するものである。また、建造物の壁画、天井、床等の内外面や、道路、通路等の路面などの表面に各種の目地模様等の凹凸模様を形成するために用いられる型部材として好ましく使用され得る発泡体に関するものである。更にまた、表面が平滑性で高温下での保管時等においてブロッキングしやすい発泡体のブロッキング性を改良した発泡体に関するものである。
【0002】
【従来の技術】
オレフィン系樹脂発泡体は、優れたクッション性、緩衝性、耐水性、化学的性質を有することから、クーラー等家電製品の断熱材、高級製品の包装緩衝材、容器のパッキン、粘着テープ、或いは長尺屋根用断熱材、或いは、パイプ形状に加工して温調機器の配管断熱材等幅広く使用されてきた。これら多岐に渡る分野においては、種々の加工が施され製品化されるが、一例として、フレキシブル断熱ホースとして発泡体が用いられる場合、広幅のシート状発泡体を一度に多数の細幅にスプリット加工し、該細幅スプリット品を接続・連続化して用い、フレキシブル断熱ホースに成形される工法がある。かかるスプリット加工が施される際、シート搬送上滑り性が悪く、張力によりシート状発泡体や細幅スプリット品が伸びたり、スプリット刃に粘着したりする問題があった。
【0003】
また、床暖房断熱用として発泡体が用いられる場合、温水通液配管を埋設するための凹みを発泡体に設ける加工が施される場合があるが、かかる加工に際し、融断刃を用いて発泡体表面に凹み加工すると、発泡体が熱で刃に融着しやすく、加工性が悪くなりやすいといった問題点があった。
【0004】
更にまた、建造物の壁面、天井、床等の内外面、道路、通路等の路面などの表面に各種の目地模様等の凹凸模様を形成する方法として、近年、目地模様等に打ち抜いたプラスチックや厚紙または発泡体等の型部材を壁面等に貼り付けた上から、吹付け材或いは塗布材を吹付けまたは塗布し、該吹付け材または塗布材が乾燥固化した後、該型部材を剥離して、目地模様を形成する工法が実施されているが、該吹付け材または塗布材が乾燥固化する際、該型部材と接合し、型部材が剥離困難となり容易に除去できないといった問題点があった。
【0005】
【発明が解決しようとする課題】
本発明は、かかる発泡体の滑り性を改良し、スプリット加工時の走行性、スプリット性や、融断カット性においても何等問題なく加工できる発泡体の提供を主たる目的とする。
また、建造物の壁面、天井、床等の内外面、道路、道路等の路面などの表面に目地模様等の凹凸模様を形成するために使用する型部材として、容易に型部材が除去でき、極めて簡単かつ確実に表面に凹凸模様を形成することができる発泡体の提供を別の目的とする。
【0006】
【課題を解決するための手段】
本発明は、前記課題を達成するため、独立気泡を有するオレフィン系樹脂架橋発泡体であって、ステアリン酸、ステアリン酸金属塩及びステアリン酸アミドのうちの1種以上を0.2〜2.0重量%含有し、かつ、ジメチルポリシロキサンを0.01〜1.0重量%含有してなるオレフィン系樹脂発泡体からなる。
また、本発明は、独立気泡を有するオレフィン系樹脂架橋発泡体であって、ステアリン酸マグネシウムを0.2〜2.0重量%含有し、かつ、オルガノポリシロキサンを0.01〜1.0重量%含有してなるオレフィン系樹脂発泡体からなる。
【0007】
【発明の実施の形態】
以下に本発明の詳細を説明する。
本発明のオレフィン系樹脂発泡体をなすオレフィン系樹脂としては、ポリエチレン樹脂単独、ポリエチレン樹脂に酢酸ビニルやエチレン・エチルアクリレート等を共重合してなるポリエチレン系樹脂、もしくはそれらの混合ポリエチレン系樹脂、または、ポリプロピレン樹脂単独、ポリプロピレン樹脂にエチレン等を共重合してなるポリプロピレン系樹脂、もしくはそれらの混合ポリプロピレン系樹脂が用いられる。
【0008】
ポリエチレン系樹脂としては、低圧法、中圧法または高圧法により製造された密度0.900〜0.965g/cm3 のポリエチレン樹脂、エチレンにブテン、ペンテン、ヘキセン、オクテン、4−メチルペンテン等のαオレフィンが共重合された直鎖状ポリエチレン系樹脂、線状超低密度ポリエチレン系樹脂、エチレン−酢酸ビニル共重合体、エチレンーエチルアクリレート共重合体等を例示することができる。これらのポリエチレン系樹脂はそれぞれ単独で用いてもよいし2種類以上混合して用いてもよい。
ポリプロピレン系樹脂としては、プロピレンの単独重合体、プロピレンにエチレンやブテン等のαオレフィンを共重合させたブロック共重合体、ランダム共重合体、ランダム−ブロック共重合体等を例示することができる。これらのポリプロピレン系樹脂はそれぞれ単独で用いてもよいし2種類以上混合して用いてもよい。
【0009】
本発明に用いられるオレフィン系樹脂の好適な例としては、特に耐寒性が良好なことから、前記ポリエチレン系樹脂からなる発泡体が好ましい。
上記樹脂以外に、耐熱性や発泡安定性を目的に、無機化合物、特に周期律表のII族、III 族、IV族から選ばれた無機化合物を添加してもよい。また、安定剤、着色剤等、通常の発泡体用組成物に添加される添加剤を添加してもよい。
【0010】
本発明のオレフィン系樹脂発泡体には、滑り性改良のために、炭素数8〜22の脂肪酸、脂肪酸該金属塩及び脂肪酸アミド(以下、脂肪酸類と総称する)のうちの1種以上、及び/又は、オルガノポリシロキサンを所定量含有させることが必要である。この脂肪酸としては、炭素数8のオクタン酸(またはカプリル酸)から炭素数22のベヘン酸までの飽和直鎖脂肪酸が例示される。また、不飽和脂肪酸として炭素数12のリンデル酸、炭素数18のオレイン酸、炭素数22の鯨油酸等が例示される。その脂肪酸金属塩としては、上記脂肪酸のアルミニウム塩、カルシウム塩、マグネシウム塩、亜鉛塩等が例示される。また、その脂肪酸アミドとしては、炭素数8のカプリル酸アミドから炭素数22のドコセン酸アミドまでが例示される。
中でも好ましい代表例としては、炭素数18のステアリン酸、その金属塩及びそのアミドが例示される。特に、ステアリン酸マグネシウムで代表されるステアリン酸金属塩が押出時の樹脂の剪断発熱による発泡剤の初期分解が起こりにくい点で好ましい。
【0011】
また、オルガノポリシロキサンとしては、例えばジメチルジクロロシランとトリメチルクロロシランの加水分解、重縮合により製造されるジメチルポリシロキサンをはじめ、メチルフェニルポリシロキサン、メチルハイドロジエンポリシロキサン、ポリオキシアルキレンジメチルポリシロキサン等のシリコーンオイル、アルキル変性、アミノ変性、カルボキシル変性、アルキルアラルキル変性、エポキシ変性等の変性シリコーンオイル等を例示することができる。中でも、ジメチルポリシロキサンが安全性等の観点から特に好ましい。
【0012】
かかる脂肪酸類の発泡体中の含有量は、オレフィン系樹脂発泡体に対し0.2〜2.0重量%である。0.2重量%未満と少な過ぎると本発明の所期の目的達成が困難である。また、2.0重量%を越えると発泡体製造時にサージング現象やプレートアウト現象が発生しやすく、均一な押出シートが得られにくくなったり、製造工程中の各種ロールに転写し、汚れ欠点等を生じやすくなる。また、本発明の発泡体に粘着層を設ける場合は、その粘着層との接着強度が十分に保てない場合も起こり得る。特に好ましい範囲は、0.2〜1.5重量%である。
また、オルガノポリシロキサンの発泡体中の含有量は、オレフィン系樹脂発泡体に対し0.01〜1.0重量%である。0.01重量%未満と少な過ぎると本発明の所期の目的達成が困難である。逆に、1.0重量%を越えると発泡体製造時に上記同様プレートアウト現象が起こりやすく、製造工程中の各種ロールに転写し、汚れ欠点等を生じやすくなる。特に好ましくは、0.05〜0.5重量%の範囲である。
かかる脂肪酸類、特に脂肪酸金属塩、とオルガノポリシロキサンとを併用して用いると、本発明の効果が最も顕著に発現するので、特に好ましい。
【0013】
本発明のオレフィン系樹脂発泡体は、上記樹脂に発泡剤、安定剤、着色剤等の添加剤に加え、さらに上記脂肪酸類及び/またはオルガノポリシロキサンを所定量混合し、押出機でシート状に押出し、電子線で架橋した後、前記組成物を発泡させることにより製造することができる。発泡剤としては、例えばアゾジカルボンアミド等の熱分解型発泡剤を用いることができる。
なお、発泡に先立って、或いは発泡と同時に、オレフィン系樹脂を電離性放射線架橋法やジクミルパーオキサイド等の過酸化物を用いた化学架橋法、または、ビニルメトキシシラン等を用いシラノール縮合させるいわゆるシラン架橋法、或いは、紫外線照射による紫外線架橋等の手段により架橋させることができるが、電子線照射による架橋法が工程管理の容易さの点などから望ましい。なお、架橋に際して、適宜、ジビニルベンゼン、ジアリルフタレート、ヒドロキノンジメタクリレート等を架橋助剤として使用してもよい。
【0014】
本発明のオレフィン系樹脂発泡体の見掛け密度は、使用目的に合わせ、0.02〜0.35g/cm3 の範囲で適宜選択することができるが、粘着テープや目地模様等の作成のための型部材として用いる場合には、特に0.06〜0.35g/cm3 の範囲が強度面、取扱い上の点で好ましい。見掛け密度が上記範囲より小さい場合には、発泡体の強度が小さくなり、かかる目的とする用途には使い勝手の点で好ましくない。目的とする用途に応じた引張強度や剪断強度等をも考慮して、密度、言い換えれば、発泡倍率を選定すればよい。
なお、発泡体の厚みとしては、0.1〜5mmの範囲のものが好ましく用いられるが、特に限定されたものではなく、使用態様に応じ適宜設定すればよい。
本発明のオレフィン系樹脂発泡体の気泡構造は、高い剪断強度が得られることから独立気泡構造である。特に、型部材として用いる場合などでは、吹付け材や塗布剤の発泡体断面から内部への浸透を防止するためにも独立気泡構造であることを要する。かかる独立気泡構造を有する発泡体は、熱分解型発泡剤を用いる上述の方法で製造することができる。
【0015】
【実施例】
以下実施例によって本発明を詳細に説明する。
なお、オレフィン系樹脂発泡体の特性はJIS K6767に準拠して測定したものである。
【0016】
[実施例1]
樹脂密度0.92g/cm3 の低密度ポリエチレン樹脂80重量部、ブチレンを共重合した直鎖状ポリエチレン系樹脂20重量部に対し、発泡剤としてアゾジカルボンアミドを2.5重量部、熱安定剤としてIrganox1010を0.2重量部添加し、さらにジメチルポリシロキサンオイル(東レ・ダウコーニング・シリコーン(株)製SH200)を低密度ポリエチレンに高濃度に混入したシリコーンコンセントレート(シリコーン含有量50%)を0.13重量部(ポリオルガノシロキサンとして0.065重量部)及びステアリン酸マグネシウムを0.25重量部を添加して発泡体用組成物を作成した。
得られた発泡体用組成物を、ヘンシェルミキサーにて混合した後、押出機を用いてT‐ダイ法により押出し、厚み1.4mmのシート状物を得た。このシート状物に電子線を照射し、あらかじめ樹脂に架橋を施した後、300℃の熱風発泡炉内で発泡させ、シート状の発泡体を製造した。得られた発泡体は、独立気泡構造を有する架橋発泡体であり、厚みは2.0mmで、見掛け密度は0.14g/cm3 であった。
【0017】
次に、該発泡体の片面に粘着層及び剥離紙を設けた後、目地模様を形成するため、所定の型枠に打ち抜き、型部材を作成した。しかる後、該型部材から剥離紙を除去し、目地模様を形成する壁面に設置したが、かかる発泡体と粘着層との接着強度は十分な強度を有するものであり、該壁面から型部材が剥がれたり、位置がずれたりすることはなかった。しかる後、アクリル系樹脂エマルジョンを主成分とする吹付け材を吹付け、該吹付け材が乾燥固化した後、該型部材を壁面から剥離・除去した。この際、吹付け材と型部材の側面とは十分な剥離性を有しており、容易に型部材を剥離することができた。
【0018】
[実施例2]
樹脂密度0.93g/cm3 の低密度ポリエチレン樹脂100重量部に対し、実施例1と同一のシリコーンコンセントレート(含有量50%)を0.5重量部(ポリオルガノシロキサンとして0.25重量部)及びステアリン酸マグネシウムを1.0重量部添加する以外は実施例1と同様にして発泡体用組成物を作成した後、電子線照射にて架橋を施した後、発泡体を作成した。得られた発泡体は、独立気泡構造を有する、厚み2.1mm、見掛け密度0.15g/cm3 のものであった。
かかる発泡体の断面とアクリル系樹脂エマルジョンを主成分とする吹付け材との剥離性を実施例1と同様に調べたが良好なものであった。
【0019】
[比較例1]
シリコーンコンセントレートとステアリン酸マグネシウムを添加しない以外は実施例1と全く同様にしてシート状の発泡体を製造し、型に打ち抜き、型部材を作成した。
得られた比較例1の発泡体からなる型部材の断面とアクリル系樹脂エマルジョンを主成分とする吹付け材との剥離性を実施例1と同様に調べたが、比較例の発泡体からなる型部材は、吹付け剤と接合しており、容易に剥離できないばかりか、強い力で剥がそうとしたところ、型部材が切れてしまった。
【0020】
[実施例3]
樹脂密度0.92g/cm3 の低密度ホリエチレン樹脂80重量部、ブチレンを共重合した直鎖状ポリエチレン系樹脂20重量部に対し、発泡剤としてアゾジカルボンアミドを11重量部、熱安定剤としてIrganox1010を0.4重量部添加に加え、シリコーンコンセントレート(ジメチルポリシロキサン含有量50%)を0.5重量部(ポリオルガノシロキサンとして0.25重量部)及びステアリン酸マグネシウムを1.1重量部添加して発泡体用組成物を作成した。
得られた発泡体用組成物を、ヘンシェルミキサーにて混合した後、押出機を用いてT−ダイ法により押出し、厚み1.3mmのシート状物を得た。このシート状物に電子線を照射し、あらかじめ樹脂に架橋を施した後、300℃の熱風発泡炉内で発泡させ、50cm幅のシート状の発泡体を製造した。得られた発泡体は、独立気泡構造を有する架橋発泡体であり、厚みは3.0mmで、見掛け密度は0.035g/cm3 であった。
【0021】
ついで、該シート状の発泡体を幅1cmの細幅テープ状に一度に多数の金属刃を用いてスプリット加工を施したところ、加工走行時のシート状発泡体の滑り性も問題なく、連続カット性も良好で、5,000mの連続加工も問題なく加工でき、かつ、綺麗な細幅テープ状物を得ることができた。
【0022】
[比較例2]
シリコーンコンセントレートとステアリン酸マグネシウムを添加しない以外は実施例3と全く同様にしてシート状の発泡体を製造した。
かかる比較例2のシート状発泡体は、実施例と同様、多数の金属刃を用いてスプリット加工を施したところ、刃に発泡体が融着し、1,000m程度連続加工した時点で刃の切れ味が悪く、綺麗にスプリット加工できなくなった。また、シート状発泡体の加工走行時の状態もシート受け台との抵抗が大きく滑り性に問題があった。
【0023】
【発明の効果】
本発明のオレフィン系樹脂発泡体は以下の効果を有するものである。
(1)広幅シート状の発泡体から同時にかつ連続的に多数の細幅にスプリット加工する際に於いても、連続カット性に優れるものであり、かつ、綺麗な細幅スプリット品を容易に得ることができる。
(2)また受け台やガイドロールとの抵抗も少なく、過度な張力がかかることなく、均一な細幅スプリット品を得ることができる。
(3)融断刃を用いて各種形状にカットしたり、各種形状の凹みを作成する際の作業性にも優れる。
(4)壁面や路面等の表面に各種の目地模様等の凹凸模様を形成するために用いられる型部材として、吹付け材との剥離が容易に行えることから好ましく使用できる。
(5)平面が平滑で、特にエチレン−酢酸ビニル共重合体等を含有した柔軟な発泡体において、高温下での保管時や、接着性を増大するためにコロナ放電処理などを施した場合においても、従来の発泡体ではブロッキングしやすい欠点を有するものであったが、かかるブロッキング性も大幅に改善できる。
[0001]
BACKGROUND OF THE INVENTION
The present invention has a cutting property when a wide sheet-like foam is split into a plurality of narrow widths, or cut into various shapes using a fusing blade, or when creating various shapes of dents on the foam surface. The present invention relates to a foam having improved workability and slippage during processing. Moreover, the foam which can be preferably used as a mold member used to form uneven patterns such as various joint patterns on the inner and outer surfaces of buildings such as murals, ceilings and floors, and road surfaces such as roads and passages It is about. Furthermore, the present invention relates to a foam having an improved blocking property of a foam which has a smooth surface and is easily blocked during storage at high temperatures.
[0002]
[Prior art]
Olefin-based resin foams have excellent cushioning properties, cushioning properties, water resistance, and chemical properties. Therefore, heat insulation materials for home appliances such as coolers, packaging cushioning materials for high-end products, packing for containers, adhesive tapes, or long It has been widely used as a heat insulating material for a lengthy roof, or a pipe heat insulating material processed into a pipe shape for temperature control. In these diverse fields, various processes are applied to produce products. As an example, when foam is used as a flexible heat-insulating hose, a wide sheet-like foam is split into many narrow pieces at once. In addition, there is a construction method in which the narrow split product is connected and continuous to be molded into a flexible heat insulating hose. When such split processing is performed, there is a problem in that the sheet-sliding property is poor and the sheet-like foam or the narrow split product is stretched or sticks to the split blade due to the tension.
[0003]
In addition, when a foam is used for heat insulation for floor heating, there is a case where a process for providing a recess for embedding a hot water flow pipe is provided in the foam, but in such a process, foaming is performed using a fusing blade. If the surface of the body is dented, there is a problem that the foam is likely to be fused to the blades by heat, and the workability tends to deteriorate.
[0004]
Furthermore, as a method of forming uneven patterns such as various joint patterns on the surfaces of buildings such as walls, ceilings and floors, road surfaces such as roads and passages, in recent years, After a mold member such as cardboard or foam is attached to a wall surface or the like, the spray material or coating material is sprayed or applied, and after the spray material or coating material is dried and solidified, the mold member is peeled off. However, there is a problem that when the spraying material or coating material is dried and solidified, it is joined to the mold member, and the mold member becomes difficult to peel off and cannot be easily removed. It was.
[0005]
[Problems to be solved by the invention]
The main object of the present invention is to provide a foam that can improve the slipperiness of such a foam and can be processed without any problems in terms of running performance during split processing, split performance, and fusing cutability.
In addition, as a mold member used to form an uneven pattern such as a joint pattern on the surface of a building such as a wall surface, a ceiling, a floor or the like, a road, a road surface such as a road, the mold member can be easily removed, Another object is to provide a foam capable of forming a concavo-convex pattern on the surface very easily and reliably.
[0006]
[Means for Solving the Problems]
In order to achieve the above object, the present invention provides an olefin-based resin-crosslinked foam having closed cells , wherein one or more of stearic acid, metal stearate and stearamide are 0.2 to 2.0. It consists of an olefin-based resin foam containing 1% by weight and containing 0.01 to 1.0% by weight of dimethylpolysiloxane .
Further, the present invention is an olefin resin cross-linked foam having closed cells, containing 0.2 to 2.0% by weight of magnesium stearate and 0.01 to 1.0% by weight of organopolysiloxane. % Olefin resin foam .
[0007]
DETAILED DESCRIPTION OF THE INVENTION
Details of the present invention will be described below.
As the olefin resin forming the olefin resin foam of the present invention, polyethylene resin alone, polyethylene resin obtained by copolymerizing polyethylene acetate with vinyl acetate, ethylene / ethyl acrylate, or the like, or a mixed polyethylene resin thereof, or Polypropylene resin alone, polypropylene resin obtained by copolymerizing polypropylene resin with ethylene or the like, or mixed polypropylene resin thereof is used.
[0008]
Examples of the polyethylene resin include polyethylene resins having a density of 0.900 to 0.965 g / cm 3 manufactured by a low pressure method, a medium pressure method, or a high pressure method, ethylene, butene, pentene, hexene, octene, 4-methylpentene, and the like. Examples thereof include linear polyethylene resins copolymerized with olefins, linear ultra-low density polyethylene resins, ethylene-vinyl acetate copolymers, ethylene-ethyl acrylate copolymers, and the like. These polyethylene resins may be used alone or in combination of two or more.
Examples of polypropylene resins include propylene homopolymers, block copolymers obtained by copolymerizing propylene with α-olefins such as ethylene and butene, random copolymers, and random-block copolymers. These polypropylene resins may be used alone or in combination of two or more.
[0009]
As a suitable example of the olefin resin used in the present invention, a foam made of the polyethylene resin is preferable because of particularly good cold resistance.
In addition to the above resins, inorganic compounds, particularly inorganic compounds selected from Group II, Group III, and Group IV of the periodic table may be added for the purpose of heat resistance and foaming stability. Moreover, you may add the additive added to the composition for normal foams, such as a stabilizer and a coloring agent.
[0010]
The olefin-based resin foam of the present invention includes one or more of fatty acids having 8 to 22 carbon atoms, fatty acid metal salts and fatty acid amides (hereinafter collectively referred to as fatty acids) for improving slipperiness, and It is necessary to contain a predetermined amount of organopolysiloxane. Examples of the fatty acid include saturated linear fatty acids from octanoic acid (or caprylic acid) having 8 carbon atoms to behenic acid having 22 carbon atoms. Further, examples of unsaturated fatty acids include C12 Lindellic acid, C18 oleic acid, C22 whale oil, and the like. Examples of the fatty acid metal salt include aluminum salts, calcium salts, magnesium salts and zinc salts of the above fatty acids. Examples of the fatty acid amide include those having 8 carbon atoms to caprylic acid amides having 22 carbon atoms.
Among these, preferable representative examples include stearic acid having 18 carbon atoms, a metal salt thereof and an amide thereof. In particular, a metal stearate represented by magnesium stearate is preferable in that the initial decomposition of the foaming agent due to shear heat generation of the resin during extrusion hardly occurs.
[0011]
Examples of the organopolysiloxane include dimethylpolysiloxane produced by hydrolysis and polycondensation of dimethyldichlorosilane and trimethylchlorosilane, methylphenylpolysiloxane, methylhydrogenpolysiloxane, polyoxyalkylenedimethylpolysiloxane, and the like. Examples thereof include silicone oil, modified silicone oil such as alkyl modification, amino modification, carboxyl modification, alkylaralkyl modification, and epoxy modification. Among these, dimethylpolysiloxane is particularly preferable from the viewpoint of safety and the like.
[0012]
The content of the fatty acid in the foam is 0.2 to 2.0% by weight with respect to the olefin resin foam. If the amount is less than 0.2% by weight, it is difficult to achieve the intended object of the present invention. On the other hand, if it exceeds 2.0% by weight, surging phenomenon and plate-out phenomenon are likely to occur during foam production, and it becomes difficult to obtain a uniform extruded sheet, or it is transferred to various rolls during the production process, causing stain defects, etc. It tends to occur. Moreover, when providing the adhesion layer in the foam of this invention, the case where adhesive strength with the adhesion layer cannot fully be maintained may occur. A particularly preferable range is 0.2 to 1.5% by weight.
Moreover, content in the foam of organopolysiloxane is 0.01 to 1.0 weight% with respect to the olefin resin foam. If the amount is less than 0.01% by weight, it is difficult to achieve the intended object of the present invention. On the other hand, if it exceeds 1.0% by weight, the plate-out phenomenon is likely to occur at the time of foam production, and it is easily transferred to various rolls during the production process, and stain defects are likely to occur. Particularly preferably, it is in the range of 0.05 to 0.5% by weight.
Use of such fatty acids, particularly fatty acid metal salts, and organopolysiloxane in combination is particularly preferred because the effects of the present invention are most remarkably exhibited.
[0013]
The olefin-based resin foam of the present invention is mixed with a predetermined amount of the above fatty acids and / or organopolysiloxane in addition to additives such as a foaming agent, a stabilizer, and a coloring agent, and is formed into a sheet with an extruder. After extrusion and crosslinking with an electron beam, the composition can be produced by foaming. As the foaming agent, for example, a thermally decomposable foaming agent such as azodicarbonamide can be used.
Prior to foaming or simultaneously with foaming, an olefin resin is subjected to silanol condensation using an ionizing radiation crosslinking method, a chemical crosslinking method using a peroxide such as dicumyl peroxide, or vinylmethoxysilane. Crosslinking can be carried out by means such as silane crosslinking or ultraviolet crosslinking by ultraviolet irradiation, but crosslinking by electron beam irradiation is desirable from the viewpoint of ease of process control. In the crosslinking, divinylbenzene, diallyl phthalate, hydroquinone dimethacrylate, or the like may be appropriately used as a crosslinking aid.
[0014]
The apparent density of the olefin resin foam of the present invention can be appropriately selected in the range of 0.02 to 0.35 g / cm 3 according to the purpose of use, but for the production of adhesive tapes, joint patterns and the like. When used as a mold member, a range of 0.06 to 0.35 g / cm 3 is particularly preferable in terms of strength and handling. When the apparent density is smaller than the above range, the strength of the foam becomes small, which is not preferable in terms of ease of use for the intended purpose. The density, in other words, the expansion ratio may be selected in consideration of the tensile strength and shear strength according to the intended application.
In addition, as a thickness of a foam, the thing of the range of 0.1-5 mm is used preferably, However It does not specifically limit and should just set suitably according to a use aspect.
The cell structure of the olefin resin foam of the present invention is a closed cell structure because high shear strength is obtained. In particular, when used as a mold member, it is necessary to have a closed cell structure in order to prevent penetration of the spray material or coating agent from the cross section of the foam. The foam having such a closed cell structure can be produced by the above-described method using a pyrolytic foaming agent.
[0015]
【Example】
Hereinafter, the present invention will be described in detail by way of examples.
In addition, the characteristic of an olefin resin foam is measured based on JISK6767.
[0016]
[Example 1]
80 parts by weight of low density polyethylene resin having a resin density of 0.92 g / cm 3 and 20 parts by weight of linear polyethylene resin copolymerized with butylene, 2.5 parts by weight of azodicarbonamide as a foaming agent, heat stabilizer A silicone concentrate (silicone content 50%) in which 0.2 parts by weight of Irganox 1010 was added and dimethylpolysiloxane oil (SH200 manufactured by Toray Dow Corning Silicone Co., Ltd.) was mixed in high density in low density polyethylene. A foam composition was prepared by adding 0.13 parts by weight (0.065 parts by weight as a polyorganosiloxane) and 0.25 parts by weight of magnesium stearate.
The obtained foam composition was mixed with a Henschel mixer and then extruded by a T-die method using an extruder to obtain a sheet-like product having a thickness of 1.4 mm. This sheet-like material was irradiated with an electron beam, and the resin was previously crosslinked, and then foamed in a 300 ° C. hot air foaming furnace to produce a sheet-like foam. The obtained foam was a crosslinked foam having a closed cell structure, and had a thickness of 2.0 mm and an apparent density of 0.14 g / cm 3 .
[0017]
Next, after providing an adhesive layer and release paper on one side of the foam, in order to form a joint pattern, the foam was punched into a predetermined mold to create a mold member. After that, the release paper was removed from the mold member and placed on the wall surface forming the joint pattern. However, the adhesive strength between the foam and the adhesive layer has sufficient strength, and the mold member was removed from the wall surface. There was no peeling or misalignment. Thereafter, a spray material mainly composed of an acrylic resin emulsion was sprayed. After the spray material was dried and solidified, the mold member was peeled off and removed from the wall surface. At this time, the spray material and the side surface of the mold member had sufficient peelability, and the mold member could be easily peeled off.
[0018]
[Example 2]
0.5 parts by weight of the same silicone concentrate (content 50%) as in Example 1 (0.25 parts by weight as polyorganosiloxane) per 100 parts by weight of low density polyethylene resin having a resin density of 0.93 g / cm 3 ) And magnesium stearate were added in the same manner as in Example 1 except that 1.0 part by weight of magnesium stearate was added, and then crosslinked by electron beam irradiation, and then a foam was prepared. The obtained foam had a closed cell structure and had a thickness of 2.1 mm and an apparent density of 0.15 g / cm 3 .
The peelability between the cross section of the foam and the spraying material containing an acrylic resin emulsion as a main component was examined in the same manner as in Example 1 and was satisfactory.
[0019]
[Comparative Example 1]
A sheet-like foam was produced in the same manner as in Example 1 except that the silicone concentrate and magnesium stearate were not added, and punched into a mold to prepare a mold member.
The peelability of the cross section of the obtained mold member made of the foam of Comparative Example 1 and the spraying material mainly composed of an acrylic resin emulsion was examined in the same manner as in Example 1, but the foam of the Comparative Example was made. The mold member was joined to the spraying agent and not only could be easily peeled off, but the mold member was cut when it was attempted to peel off with a strong force.
[0020]
[Example 3]
80 parts by weight of a low density polyethylene resin having a resin density of 0.92 g / cm 3 and 20 parts by weight of a linear polyethylene resin copolymerized with butylene, 11 parts by weight of azodicarbonamide as a foaming agent, and as a heat stabilizer Irganox 1010 is added to 0.4 parts by weight, 0.5 parts by weight of silicone concentrate (dimethylpolysiloxane content 50%) (0.25 parts by weight as polyorganosiloxane) and 1.1 parts by weight of magnesium stearate. The composition for foams was created by adding.
After mixing the obtained composition for foams with a Henschel mixer, it was extruded by a T-die method using an extruder to obtain a sheet-like product having a thickness of 1.3 mm. This sheet-like product was irradiated with an electron beam, and the resin was previously crosslinked, and then foamed in a 300 ° C. hot-air foaming furnace to produce a sheet-like foam having a width of 50 cm. The obtained foam was a crosslinked foam having a closed cell structure, and had a thickness of 3.0 mm and an apparent density of 0.035 g / cm 3 .
[0021]
Next, when the sheet-like foam was split into a thin tape with a width of 1 cm using a large number of metal blades at once, there was no problem with the sliding property of the sheet-like foam during processing, and continuous cutting was performed. In addition, the continuous processing of 5,000 m could be processed without any problem, and a beautiful narrow tape-like product could be obtained.
[0022]
[Comparative Example 2]
A sheet-like foam was produced in the same manner as in Example 3 except that the silicone concentrate and magnesium stearate were not added.
The sheet-like foam of Comparative Example 2 was subjected to split processing using a large number of metal blades as in the examples. When the foam was fused to the blades and continuously processed for about 1,000 m, The sharpness was bad and it became impossible to cleanly split. In addition, the state of the sheet-like foam during processing and running has a problem of slipperiness due to a large resistance with the sheet cradle.
[0023]
【The invention's effect】
The olefin resin foam of the present invention has the following effects.
(1) Even when a wide sheet-like foam is simultaneously and continuously split into a large number of narrow widths, it is excellent in continuous cutability and easily obtains a beautiful narrow width split product. be able to.
(2) Further, there is little resistance to the cradle and the guide roll, and a uniform narrow split product can be obtained without applying excessive tension.
(3) It is excellent in workability at the time of cutting into various shapes using a fusing blade or creating dents of various shapes.
(4) As a mold member used for forming uneven patterns such as various joint patterns on the surface such as a wall surface or a road surface, it can be preferably used because it can be easily separated from the spraying material.
(5) In the case of a smooth foam, especially a flexible foam containing an ethylene-vinyl acetate copolymer, etc., when stored at high temperatures or when subjected to corona discharge treatment to increase adhesion. However, the conventional foams have the drawback of being easily blocked, but such blocking properties can be greatly improved.

Claims (5)

独立気泡を有するオレフィン系樹脂架橋発泡体であって、
ステアリン酸、ステアリン酸金属塩及びステアリン酸アミドのうちの1種以上を0.2〜2.0重量%含有し、かつジメチルポリシロキサンを0.01〜1.0重量%含有してなるオレフィン系樹脂発泡体。
An olefin resin cross-linked foam having closed cells,
Stearate, olefins or one of metal stearates and stearic acid amide containing 0.2-2.0 wt%, and comprising a dimethylpolysiloxane 0.01-1.0 wt% Resin foam.
独立気泡を有するオレフィン系樹脂架橋発泡体であって、
ステアリン酸マグネシウムを0.2〜2.0重量%含有し、かつ、オルガノポリシロキサンを0.01〜1.0重量%含有してなるオレフィン系樹脂発泡体。
An olefin resin cross-linked foam having closed cells,
An olefin resin foam comprising 0.2 to 2.0% by weight of magnesium stearate and 0.01 to 1.0% by weight of organopolysiloxane.
オルガノポリシロキサンがジメチルポリシロキサンである請求項2に記載のオレフィン系樹脂発泡体。The olefin resin foam according to claim 2 , wherein the organopolysiloxane is dimethylpolysiloxane. オレフィン系樹脂発泡体の見掛け密度が0.02〜0.35g/cm3 である請求項1〜3いずれかに記載のオレフィン系樹脂発泡体。The olefin resin foam according to any one of claims 1 to 3 , wherein the apparent density of the olefin resin foam is 0.02 to 0.35 g / cm 3 . オレフィン系樹脂発泡体の見掛け密度が0.06〜0.35g/cm3 であり、かつ、オレフィン系樹脂発泡体の少なくとも片面に粘着層が形成されてなる請求項1〜4いずれかに記載のオレフィン系樹脂発泡体。Apparent density of the olefin resin foam is 0.06~0.35g / cm 3, and, according to any one of claims 1 to 4 at least one side to the adhesive layer of an olefin resin foam is formed Olefin resin foam.
JP970899A 1999-01-18 1999-01-18 Olefin resin foam Expired - Lifetime JP4269384B2 (en)

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AR033668A1 (en) * 2000-03-27 2004-01-07 Du Pont ADDITIVES SYSTEM FOR POLYESTER POLYMERS, METHOD TO REDUCE THE EFFECT OF STATIC FRICTION BETWEEN MOLDED ARTICLES OF HOMOPOLIMEROS AND COPOLIMEROS OF PET, METHOD FOR PRODUCING A MOLDED PET ARTICLE AND MOLDED ARTICLE OBTAINED.

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