JP4060957B2 - Shoe sole material - Google Patents

Shoe sole material Download PDF

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Publication number
JP4060957B2
JP4060957B2 JP23949498A JP23949498A JP4060957B2 JP 4060957 B2 JP4060957 B2 JP 4060957B2 JP 23949498 A JP23949498 A JP 23949498A JP 23949498 A JP23949498 A JP 23949498A JP 4060957 B2 JP4060957 B2 JP 4060957B2
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Prior art keywords
weight
carbon black
shoe sole
added
polymer
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Expired - Lifetime
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JP23949498A
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Japanese (ja)
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JP2000050905A (en
Inventor
仁宏 薮下
健一 原野
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Asics Corp
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Asics Corp
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  • Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【0001】
【発明の属する技術分野】
本発明は靴底材に関し、より詳しくは、アウターソール(接地底)に関するものである。
【0002】
【従来の技術】
スポーツシューズなどの靴のアウターソールを構成する靴底材には、クッション性やグリップ性、耐摩耗性の他に軽量性が要求される。かかる軽量性という観点からは、発泡体からなる靴底材は非発泡体よりも優れている。
【0003】
【発明が解決しようとする課題】
しかし、発泡体は非発泡体に比べ、強度、特に耐摩耗性に劣る。
したがって、本発明の目的は、発泡体からなる靴底材の軽量性および耐摩耗性を向上させることである。
【0004】
【課題を解決するための手段】
前記目的を達成するために、本発明は、樹脂および/またはゴムを発泡硬化させてなると共に接地底を構成する靴底材であって、ポリマー100 重量部に対して、カーボンブラックが10〜50重量部添加され、該カーボンブラックの平均粒子径が11〜30nmに設定され、ポリマー全体に対し、シス1,4 ポリブタジエンが60 80 重量%ブレンドされ、かつ、スチレン系樹脂(以下、「スチレンレジン」という)および/またはシンジオタクチック1,2 ポリブダジエンが総量で5 〜25重量%ブレンドされていることを特徴とする。
【0005】
まず、本発明においては、耐摩耗性を向上させるために、メインポリマーとして、BR(シス1 ,4 ポリブダジエン)を用いている
【0006】
一般に、カーボンブラックを添加することにより、靴底材の耐摩耗性が向上する。しかし、通常、靴底材に用いるジエン系ゴムにカーボンブラックを添加すると、ポリマーとカーボンブラックとの相互作用が強いため、発泡性が低下し、そのため、靴底材の軽量化が図れない。そこで、本発明では、発泡加工性を向上させるために、スチレンレジンおよび/またはRB(シンジオタクチック1,2 ポリブダジエン) を添加することにより、発泡性を向上させている。これらの樹脂は、ゴムに比べ、高温化における流動性が高く、つまり粘度が低下するため、発泡性が向上し、十分な軽量化を図ることができる。
【0007】
スチレンレジンおよび/またはRBのブレンド比は全ポリマーの5重量%以上に設定する。これらの樹脂のブレンド比が5重量%未満であると、発泡性を十分に向上させることができないからである。
【0008】
一方、これらの樹脂のブレンド比は全ポリマーの25重量%以下に設定する。これらの樹脂のブレンド比が25重量%以上であると、発泡体の硬度が大きくなりすぎて、クッション性やグリップ性などの機能が低下するからである。
【0009】
なお、本発明において、前記樹脂のブレンド比は10〜20重量%に設定するのが好ましい。また、前記樹脂としては、RBよりもスチレンレジンの方が汎用的で入手し易いという利点がある。
【0010】
カーボンブラックの添加量を50重量部以下とした理由は、添加量が50重量部を超えると、前記発泡性が低下すると共に材料自体の比重も大きくなり、十分に軽量化を図り得ないからである。
一方、カーボンブラックの添加量を10重量部以上とした理由は、添加量が10重量部よりも少ないと、耐摩耗性が十分に向上しないからである。
なお、カーボンブラックの添加量はポリマー100 重量部に対して10〜35重量部とするのが好ましい。
【0011】
また、カーボンブラックの平均粒子径を11〜30nmとした理由は、この粒子径のカーボンブラックが高い耐摩耗性を発揮すると同時に発泡を低下させる度合いが小さいからである。
【0012】
なお、本発明においては、前記メインポリマー(BR)や前記樹脂の他に、IR,NBRなどのジエン系ゴムやEPDM,EPMなどの合成ゴム、あるいは、EVA(エチレン−酢酸ビニル共重合体)などの樹脂を適宣配合(ブレンド)してもよい。
【0013】
【実施例】
以下、本発明の効果を明瞭にするため、本発明の実施例を示す。
実施例1〜5
図1のゴム配合で、カーボンブラックを添加して発泡体を得た。なお、添加剤は図2に示す。
比較例1〜8
図1のゴム配合で、カーボンブラックを添加して発泡体を得た。なお、添加剤の配合は実施例と同一に設定した。
【0014】
荷重を26.5Nとし、アクロン摩耗試験法(JISK6264)に準じて、1,000 回転当たりの摩耗した体積を測定した。その体積比を、前記図1に示す。
【0015】
比較例1,2より、カーボンブラックの添加量が少ないと、耐摩耗性が小さくなることが分かる。
また、比較例4,5より、添加するカーボンブラックの粒子径が大きすぎると、耐摩耗性が著しく低下することが分かる。
【0016】
比較例3より、メインポリマーであるBRのブレンド比が少なすぎると、耐摩耗性が小さくなることが分かる。
【0017】
これらに対し、実施例1〜5の靴底材は軽量で、かつ、耐摩耗性に優れていることが分かる。
なお、前記各実施例1〜5では、全てハイスチレンレジンをブレンドしているが、ハイスチレンレジンをブレンドせずに、RBのみをブレンドしても同等の結果が得られる。これは、RBもハイスチレンレジンと同様に発泡性に優れており、しかも、メインポリマーであるBRとの親和性が良いからである。
【0018】
なお、ハイスチレンレジンおよびRBを全く配合しなかった比較例6では、プレス生地の流動性が悪くなって、発泡が不均一となった。
また、ハイスチレンレジンおよびRBをポリマー全体に対し総量で40重量%以上添加した比較例7では、硬度が大きくなりすぎ(SRIS−C硬度で82°となった)、クッション性やグリップ性が低下することが分かった。
また、粒子径11〜30nmのカーボンブラックを60重量%添加した比較例8では、発泡性が著しく低下し、そのため、比重が著しく大きくなることが分かった。
【0019】
【発明の効果】
以上説明したように、本発明によれば、スチレンレジンおよび/またはRBをポリマー全体に対して適量添加したので、小さな粒子径のカーボンブラックを添加しても、プレス時の材料の流動性が高くなるため、つまり、粘度が低下するため、発泡性が向上し、均一な発泡が起きると共に、十分に発泡するので、靴底材の軽量化を図ることができる。また、小さな粒子径のカーボンブラックを添加できるから、発泡体の耐摩耗性が向上する。
【図面の簡単な説明】
【図1】本発明の実施形態のポリマーのブレンド比およびカーボンブラックの添加量等を示す図表である。
【図2】実施形態の添加剤の添加量を示す図表である。
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a shoe sole material, and more particularly to an outer sole (a ground contact sole).
[0002]
[Prior art]
In addition to cushioning properties, grip properties, and wear resistance, shoe sole materials that constitute the outer soles of shoes such as sports shoes are required to be lightweight. From the viewpoint of such light weight, a shoe sole material made of a foam is superior to a non-foam.
[0003]
[Problems to be solved by the invention]
However, the foam is inferior in strength, particularly wear resistance, compared to the non-foam.
Accordingly, an object of the present invention is to improve the lightness and wear resistance of a shoe sole made of foam.
[0004]
[Means for Solving the Problems]
To achieve the above object, the present invention provides a shoe sole material comprising a resin and / or rubber foam-cured and constituting a grounded bottom, wherein 10 to 50 carbon blacks per 100 parts by weight of polymer. is added parts by weight, an average particle diameter of the carbon black is set to 11~30Nm, relative to the total polymer, cis-1,4-polybutadiene is 60 to 80 wt% Bed trend, and styrene-based resin (hereinafter, "styrene Resin) and / or syndiotactic 1,2 polybudadiene is blended in a total amount of 5 to 25% by weight.
[0005]
First, in the present invention, BR (cis 1,4 polybutadiene) is used as the main polymer in order to improve the wear resistance .
[0006]
In general, by adding carbon black, the wear resistance of the shoe sole material is improved. However, usually, when carbon black is added to the diene rubber used for the shoe sole material, the interaction between the polymer and the carbon black is strong and the foaming property is lowered, so that the weight of the shoe sole material cannot be reduced. Therefore, in the present invention, in order to improve the foaming processability, the foamability is improved by adding styrene resin and / or RB (syndiotactic 1,2 polybudadiene). These resins have higher fluidity at higher temperatures than rubber, that is, their viscosity decreases, so that foamability is improved and sufficient weight reduction can be achieved.
[0007]
The blend ratio of styrene resin and / or RB is set to 5% by weight or more of the total polymer. This is because the foamability cannot be sufficiently improved when the blend ratio of these resins is less than 5% by weight.
[0008]
On the other hand, the blend ratio of these resins is set to 25% by weight or less of the total polymer. This is because when the blend ratio of these resins is 25% by weight or more, the hardness of the foam becomes too high, and functions such as cushioning and gripping properties are deteriorated.
[0009]
In the present invention, the blend ratio of the resin is preferably set to 10 to 20% by weight. As the resin, styrene resin is more versatile and easily available than RB.
[0010]
The reason why the amount of carbon black added is 50 parts by weight or less is that when the amount added exceeds 50 parts by weight, the foaming properties are reduced and the specific gravity of the material itself is increased, and the weight cannot be reduced sufficiently. is there.
On the other hand, the reason why the amount of carbon black added is 10 parts by weight or more is that if the amount added is less than 10 parts by weight, the wear resistance is not sufficiently improved.
The amount of carbon black added is preferably 10 to 35 parts by weight with respect to 100 parts by weight of the polymer.
[0011]
The reason why the average particle size of carbon black is 11 to 30 nm is that carbon black having this particle size exhibits high wear resistance and at the same time has a small degree of reduction in foaming.
[0012]
In the present invention, in addition to the main polymer (BR) and the resin, diene rubbers such as IR and NBR, synthetic rubbers such as EPDM and EPM, EVA (ethylene-vinyl acetate copolymer), etc. These resins may be properly blended (blended).
[0013]
【Example】
Examples of the present invention will be described below in order to clarify the effects of the present invention.
Examples 1-5
A foam was obtained by adding carbon black in the rubber composition of FIG. The additive is shown in FIG.
Comparative Examples 1-8
A foam was obtained by adding carbon black in the rubber composition of FIG. In addition, the mixing | blending of the additive was set the same as the Example.
[0014]
The load was set to 26.5 N, and the worn volume per 1,000 revolutions was measured according to the Akron abrasion test method (JISK6264). The volume ratio is shown in FIG.
[0015]
From Comparative Examples 1 and 2, it can be seen that the wear resistance decreases when the amount of carbon black added is small.
In addition, it can be seen from Comparative Examples 4 and 5 that if the particle size of the carbon black to be added is too large, the wear resistance is significantly reduced.
[0016]
From Comparative Example 3, it can be seen that if the blend ratio of BR as the main polymer is too small, the wear resistance is reduced.
[0017]
On the other hand, it can be seen that the shoe sole materials of Examples 1 to 5 are lightweight and have excellent wear resistance.
In each of Examples 1 to 5, the high styrene resin is blended, but the same result can be obtained by blending only RB without blending the high styrene resin. This is because RB is also excellent in foamability like high styrene resin, and has good affinity with BR as the main polymer.
[0018]
In Comparative Example 6 in which no high styrene resin and RB were blended, the fluidity of the press dough deteriorated and foaming became non-uniform.
Further, in Comparative Example 7 in which high styrene resin and RB were added in a total amount of 40% by weight or more based on the entire polymer, the hardness was too high (SRIS-C hardness was 82 °), and the cushioning property and gripping property were lowered. I found out that
Further, it was found that in Comparative Example 8 in which 60% by weight of carbon black having a particle size of 11 to 30 nm was added, the foamability was remarkably reduced, and the specific gravity was remarkably increased.
[0019]
【The invention's effect】
As described above, according to the present invention, since an appropriate amount of styrene resin and / or RB is added to the whole polymer, even if carbon black having a small particle diameter is added, the fluidity of the material during pressing is high. In other words, since the viscosity is lowered, foamability is improved, uniform foaming occurs, and foaming is sufficiently performed, so that the weight of the shoe sole material can be reduced. Further, since carbon black having a small particle diameter can be added, the abrasion resistance of the foam is improved.
[Brief description of the drawings]
FIG. 1 is a chart showing a polymer blend ratio, an amount of carbon black added, and the like according to an embodiment of the present invention.
FIG. 2 is a chart showing the amount of additive added according to the embodiment.

Claims (2)

樹脂および/またはゴムを発泡硬化させてなると共に接地底を構成する靴底材であって、
ポリマー100 重量部に対して、カーボンブラックが10〜50重量部添加され、該カーボンブラックの平均粒子径が11〜30nmに設定され、
シス1,4 ポリブタジエンがポリマー全体に対し60 80 重量%ブレンドされ、かつ、スチレン系樹脂および/またはシンジオタクチック1,2 ポリブダジエンが総量でポリマー全体に対し5 〜25重量%ブレンドされていることを特徴とする靴底材。
A shoe sole material formed by foaming and curing resin and / or rubber and constituting a grounding bottom,
10 to 50 parts by weight of carbon black is added to 100 parts by weight of the polymer, and the average particle size of the carbon black is set to 11 to 30 nm.
Cis-1,4-polybutadiene is 60 to 80 wt% Bed trend with respect to the total polymer, and styrene-based resins and / or syndiotactic 1,2 poly butadiene is 5-25 wt% blend with respect to the total polymer in total Sole material characterized by
請求項1において、
比重が0.5 〜0.8 に設定されている靴底材。
In claim 1,
Shoe sole with specific gravity set to 0.5-0.8.
JP23949498A 1998-08-10 1998-08-10 Shoe sole material Expired - Lifetime JP4060957B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23949498A JP4060957B2 (en) 1998-08-10 1998-08-10 Shoe sole material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23949498A JP4060957B2 (en) 1998-08-10 1998-08-10 Shoe sole material

Publications (2)

Publication Number Publication Date
JP2000050905A JP2000050905A (en) 2000-02-22
JP4060957B2 true JP4060957B2 (en) 2008-03-12

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Country Status (1)

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