JPH11206407A - Molded foam - Google Patents

Molded foam

Info

Publication number
JPH11206407A
JPH11206407A JP3364698A JP3364698A JPH11206407A JP H11206407 A JPH11206407 A JP H11206407A JP 3364698 A JP3364698 A JP 3364698A JP 3364698 A JP3364698 A JP 3364698A JP H11206407 A JPH11206407 A JP H11206407A
Authority
JP
Japan
Prior art keywords
elastomer
raw material
powder
material elastomer
molded foam
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP3364698A
Other languages
Japanese (ja)
Inventor
Hitohiro Yabushita
仁宏 薮下
Osamu Umeno
治 梅野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Asics Corp
Original Assignee
Asics Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Asics Corp filed Critical Asics Corp
Priority to JP3364698A priority Critical patent/JPH11206407A/en
Publication of JPH11206407A publication Critical patent/JPH11206407A/en
Pending legal-status Critical Current

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  • Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

PROBLEM TO BE SOLVED: To uniform the formed state of a raw material elastomer and to reduce deterioration in tearing strength at the time of adding a large quantity of filler by compounding the pulverized powder of a sponge elastomer with a raw material elastomer and also cross-linking the raw material elastomer with a filler. SOLUTION: Since a boundary between the filler 1 of the sponge elastomer and the crosslinked sponge 2 of the raw material elastomer is erosslinked, the both of them 1 and 2 are firmly adhered by an anchor effect owing to the complicated projections/recessions of the interface 3, the occurrence of an interfacial peeling is eliminated because the area of the interface 3 for the adhesion of the members is drastically large. Moreover, a configuration and a structure are made uniform since the sponges are fixed and stress concentration does not occur so that tearing strength, etc., is not deteriorated and also resistance to repeated stress is increased. The addition quantity of filler to the raw material elastomer is preferably 0.5-50 wt.% and, more preferably, 5.0-20 wt.%.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、主として、靴底に
用いられる成型発泡体に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a molded foam used mainly for shoe soles.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】スポ
ーツシューズなどの靴底には、衝撃緩衝材として樹脂や
ゴムの独立発泡の成型発泡体が用いられている。靴底用
の成型発泡体は、一般に、バフ研磨によって所定の形状
に加工され、かかるバフ研磨の際には、いわゆるバフ粉
(研磨粉)が生じる。バフ粉は産業廃棄物として廃棄さ
れるので、資源の有効利用や環境保全上好ましくない
上、廃棄のための費用も発生するから、製造コストが高
くなる。
2. Description of the Related Art In a shoe sole such as a sports shoe, a molded foam of a closed cell made of resin or rubber is used as an impact buffer. Molded foams for shoe soles are generally processed into a predetermined shape by buffing, and so-called buffing powder (polishing powder) is generated during such buffing. Since the buff powder is discarded as industrial waste, it is not preferable from the viewpoint of effective use of resources and environmental conservation, and the cost for disposal is increased, so that the production cost is increased.

【0003】樹脂スポンジやスポンジゴムの廃材を利用
する技術としては、下記のような技術が提案されている
ものの、それぞれ、欠点があり、未だ実用化されていな
い。
The following techniques have been proposed as techniques for using resin sponge and sponge rubber waste, but each has a drawback and has not yet been put to practical use.

【0004】たとえば、靴底板の屑板の破砕片を原料エ
ラストマーに混合して発泡体を得る履物底成型法(特公
昭56−15241号、特開昭52−116343号)
では、混合する破砕片の粒径が大きく、また、配合エラ
ストマーを加熱して型に流し込むので、所定の強度が得
られない。
[0004] For example, a shoe sole molding method in which a crushed piece of a scrap plate of a shoe sole plate is mixed with a raw material elastomer to obtain a foam (JP-B-56-15241, JP-A-52-116343)
In this case, the crushed pieces to be mixed have a large particle size, and since the compounded elastomer is heated and poured into a mold, a predetermined strength cannot be obtained.

【0005】また、前記破砕片ではなく粒径の小さいバ
フ粉を用いた靴底の製造方法も開示されているが(特開
平5−154004号)、該製造方法では、エマルジョ
ンによってバフ粉同士が互いに固着されているので、所
定の強度が得られない。また、加工工程が複雑で、生産
コストが大幅にアップする。
[0005] Also, a method of manufacturing shoe soles using buff powder having a small particle size instead of the crushed pieces has been disclosed (Japanese Patent Application Laid-Open No. 5-154004). Since they are fixed to each other, a predetermined strength cannot be obtained. Further, the processing steps are complicated, and the production cost is greatly increased.

【0006】したがって、本発明の目的は、靴底等のス
ポンジの廃材を有効利用してコストダウンを図り得ると
共に、所定の強度を持つ成型発泡体を提供することであ
る。
SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a molded foam having a predetermined strength, which can effectively reduce waste by effectively using sponge waste such as shoe soles.

【0007】[0007]

【課題を解決するための手段】前記目的を達成するため
に、本発明の成型発泡体は、原料エラストマーに架橋剤
および発泡剤が添加された配合エラストマーを発泡させ
ると共に架橋させた発泡体において、原料エラストマー
に架橋済のスポンジエラストマーの研磨粉が添加されて
いると共に、該研磨粉と原料エラストマーの架橋スポン
ジとの間が架橋されていることを特徴とする。
In order to achieve the above object, a molded foam of the present invention comprises a foamed elastomer obtained by foaming a crosslinked elastomer obtained by adding a crosslinking agent and a foaming agent to a raw elastomer, and crosslinking the foamed elastomer. A cross-linked sponge elastomer polishing powder is added to the raw material elastomer, and a cross-link is formed between the polishing powder and the cross-linked sponge of the raw material elastomer.

【0008】本発明によれば、架橋済のスポンジエラス
トマーの研磨粉(以下、単に「研磨粉」という。)が、
原料エラストマーの架橋時に生成される新たな架橋スポ
ンジと架橋することにより、研磨粉と新たな架橋スポン
ジとの界面が強固に固着する。
According to the present invention, the crosslinked sponge elastomer polishing powder (hereinafter simply referred to as “polishing powder”) is used.
By cross-linking with a new cross-linked sponge generated at the time of cross-linking of the raw material elastomer, the interface between the abrasive powder and the new cross-linked sponge is firmly fixed.

【0009】また、本発明では、図1に示すように、ス
ポンジエラストマーの研磨粉1と、原料エラストマーの
架橋スポンジ2との界面3が架橋しているので、該界面
3の複雑な凹凸によるアンカー効果によって両者1,2
の間が強固に接着されると共に、部材の密度に対する界
面3の面積が極めて大きい。したがって、界面剥離を生
じるおそれもない。
In the present invention, as shown in FIG. 1, since the interface 3 between the abrasive powder 1 of the sponge elastomer and the crosslinked sponge 2 of the raw elastomer is cross-linked, the anchor 3 due to the complex unevenness of the interface 3 is formed. Depending on the effect, both 1, 2
Are strongly bonded, and the area of the interface 3 with respect to the density of the member is extremely large. Therefore, there is no possibility that interface peeling will occur.

【0010】さらに、スポンジ同士が固着されるので、
組成や構造が均一になるから、応力集中の生じるおそれ
がないから、引裂強さなどが低下しにくいうえ、繰り返
し応力にも強い。
[0010] Further, since the sponges are fixed to each other,
Since the composition and the structure are uniform, there is no possibility that stress concentration occurs, so that the tear strength and the like are hardly reduced, and it is also resistant to repeated stress.

【0011】本発明において、「研磨粉」とは、破砕片
ではなく、バフなどの研磨機で研磨ないしは研削されて
生成されるものをいい、その粒径は 5.0mm以下とするの
が好ましい。粒径が 5.0mmよりも大きくなると、発泡状
態が均一でなくなり、エアーホールも発生し易くなっ
て、良好な成型品が得られないからである。かかる観点
から、研磨粉の粒径は、略2mm以下が更に好ましい。な
お、「略2mm以下」とは、網目が2mm以下の篩いを通過
したものをいう。
In the present invention, the "polishing powder" is not crushed pieces, but is produced by polishing or grinding with a polishing machine such as a buff, and the particle size is preferably 5.0 mm or less. If the particle size is larger than 5.0 mm, the foaming state is not uniform, air holes are easily generated, and a good molded product cannot be obtained. From this viewpoint, the particle size of the polishing powder is more preferably about 2 mm or less. Here, “approximately 2 mm or less” means that the mesh has passed through a sieve of 2 mm or less.

【0012】原料エラストマーに対する研磨粉の添加量
は、 0.5〜50重量%とするのが好ましく、 5.0〜30重量
%とするのがより好ましく、 5.0〜20重量%とするのが
更に好ましい。研磨粉の添加量が少なすぎると、研磨粉
を添加する意味がなく、一方、研磨粉の添加量が多すぎ
ると、引裂強さが小さくなるからである。特に、研磨粉
の添加量が50重量%を超えると、ロール練り加工が困難
になるなど加工性が著しく低下して、エアーホールの発
生が急増するので、工業的に生産することはできない。
The amount of the abrasive powder added to the raw material elastomer is preferably 0.5 to 50% by weight, more preferably 5.0 to 30% by weight, and even more preferably 5.0 to 20% by weight. If the amount of the abrasive powder is too small, there is no point in adding the abrasive powder. On the other hand, if the amount of the abrasive powder is too large, the tear strength decreases. In particular, if the added amount of the abrasive powder exceeds 50% by weight, the workability of the roll is extremely reduced, for example, the roll kneading becomes difficult, and the occurrence of air holes increases rapidly, so that industrial production cannot be performed.

【0013】本発明のポリマーの主成分としては、つま
り、原料エラストマーおよび研磨粉のポリマーの主成分
としては、以下のような樹脂またはゴムを用いることが
できるが、同一ないし同種の材料または界面が共架橋し
得る(相溶性の良い)材料同士を選択する必要がある。
同一ないし同種の材料または界面が共架橋し得る材料同
士でないと、原料エラストマーの架橋スポンジと研磨粉
との界面が架橋しないので、十分な引裂強さが得られな
いからである。
As the main component of the polymer of the present invention, that is, the following resin or rubber can be used as the main component of the raw material elastomer and the polymer of the abrasive powder, the same or similar material or interface is used. It is necessary to select materials capable of co-crosslinking (having good compatibility).
This is because if the same or similar materials or materials that can be co-crosslinked at the interface are not the same, the interface between the crosslinked sponge of the raw elastomer and the abrasive powder will not be crosslinked, so that sufficient tear strength cannot be obtained.

【0014】原料エラストマーおよび研磨粉のポリマー
の主成分としては、それぞれ、エチレン−酢酸ビニル共
重合体(EVA)、ポリエチレンまたはシンジオタクチ
ック1,2-ポリブタジエン(RB)のうちの1種または2
種以上を選択して用いることができる。また、同ポリマ
ーの主成分としては、天然ゴム、SBR,BR,IR,
NBRなどのジエン系ゴム、クロロプレンゴムまたはE
PDMのうちの1種または2種以上を選択して用いるこ
とができる。
The main components of the raw material elastomer and the polymer of the abrasive powder are one or two of ethylene-vinyl acetate copolymer (EVA), polyethylene or syndiotactic 1,2-polybutadiene (RB), respectively.
More than one species can be selected and used. The main components of the polymer include natural rubber, SBR, BR, IR,
Diene rubber such as NBR, chloroprene rubber or E
One or more of the PDMs can be selected and used.

【0015】架橋剤としては、ジクミルパーオキサイド
や1,1-ジ-(t-ブチルパーオキシ) -3,3,5- トリメチルシ
クロヘキサンなどの有機過酸化物を用いることができ
る。また、発泡剤としては、アゾジカルボンアミドやジ
ニトロソペンタメチレンテトラミンなどの有機発泡剤を
用いることができる。また、配合剤として、充填剤、軟
化剤、可塑剤、活性剤、着色剤およびその他の添加剤を
適宜混入することができる。さらに、主成分のポリマー
の他に、天然ゴム、合成ゴムおよび熱可塑性エラストマ
ー等を適宣混入することができる。但し、前記特公昭5
6−15241号の非架橋成型不良品の破砕屑は、微細
な粒子にできないから添加しない。
As a crosslinking agent, an organic peroxide such as dicumyl peroxide or 1,1-di- (t-butylperoxy) -3,3,5-trimethylcyclohexane can be used. Further, as the foaming agent, an organic foaming agent such as azodicarbonamide or dinitrosopentamethylenetetramine can be used. As a compounding agent, a filler, a softener, a plasticizer, an activator, a colorant, and other additives can be appropriately mixed. Further, in addition to the main component polymer, a natural rubber, a synthetic rubber, a thermoplastic elastomer, and the like can be appropriately mixed. Provided, however, that
The crushed debris of the non-crosslinked molded product of No. 6-15241 is not added because it cannot be made into fine particles.

【0016】本発明の研磨粉は、EVAやRBなどの樹
脂やゴムの熱可塑性エラストマーの発泡体を、砥石やワ
イヤーブラシなどのバフで研磨した際に発生したバフ粉
を用いることができる。バフ粉は、所定の大きさの網目
の篩いなどを使用して、異物や粒径の大きいバフ粉を除
去することで、強度および仕上がりの良い成型品(成型
発泡体)が得られる。
As the polishing powder of the present invention, buff powder generated when a thermoplastic elastomer foam of resin or rubber such as EVA or RB is polished with a buff such as a grindstone or a wire brush can be used. The buff powder removes foreign substances and buff powder having a large particle size by using a mesh sieve having a predetermined size, thereby obtaining a molded product (molded foam) having good strength and finish.

【0017】研磨粉は、母材である原料エラストマーの
生地の練りや攪拌などのミキシング工程の際に添加す
る。たとえば、EVAの成型発泡体を得るには、EVA
樹脂に配合剤を混練する際に研磨粉を添加した後、プレ
ス成型や射出成型などの方法により発泡成型する。勿
論、母材(ベースポリマー)である原料エラストマーに
配合剤を混練した配合エラストマーに、研磨粉を添加し
てもよい。
The polishing powder is added at the time of a mixing step such as kneading and stirring of the base elastomer raw material dough. For example, to obtain a molded foam of EVA, EVA
After kneading the compounding agent with the resin, the abrasive powder is added, and then foamed by a method such as press molding or injection molding. Of course, abrasive powder may be added to a compounded elastomer obtained by kneading a compounding agent with a raw material elastomer as a base material (base polymer).

【0018】[0018]

【実施例】以下、本発明の効果を明瞭にするために、実
施例および比較例を示す。 比較例10,実施例11〜18:図2(a)の表1に示
すように、EVA90重量部とIR10重量部からなる
原料エラストマーに、配合剤およびEVAバフ粉を添加
した後、プレス成型して成型発泡体を得た。EVAバフ
粉は、1mmの網目の篩いを通過させて粒径を略1mm以下
とし、添加量を変化させた。こうして得られた成型発泡
体は、図2(b)に示すように、EVAバフ粉を添加し
ていない比較例10に比べて、一般に、引裂強さが若干
低下するが、実用には支障がない。
EXAMPLES Examples and comparative examples will be described below to clarify the effects of the present invention. Comparative Example 10, Examples 11 to 18: As shown in Table 1 of FIG. 2 (a), after adding a compounding agent and EVA buff powder to a raw material elastomer composed of 90 parts by weight of EVA and 10 parts by weight of IR, press molding was performed. Thus, a molded foam was obtained. The EVA buff powder was passed through a 1 mm mesh sieve to reduce the particle size to about 1 mm or less, and the amount added was changed. As shown in FIG. 2 (b), the molded foam thus obtained generally has a slightly lower tear strength than Comparative Example 10 in which the EVA buff powder is not added, but does not hinder practical use. Absent.

【0019】また、本発明にかかる成型発泡体は、前記
比較例10の成型発泡体と外観上区別できない程度の仕
上がりが得られた。したがって、商品が本発明にかかる
成型発泡体か否かを肉眼で判別するのは一般に困難であ
るが、以下に説明するように、電子顕微鏡写真を介し
て、本発明にかかる成型発泡体か否かを判別することが
できる。
The molded foam according to the present invention had a finish which was indistinguishable in appearance from the molded foam of Comparative Example 10. Therefore, it is generally difficult to visually determine whether the product is the molded foam according to the present invention or not. However, as described below, whether or not the product is the molded foam according to the present invention is determined by an electron micrograph. Can be determined.

【0020】図3(a)はバフ粉を10重量%添加した
実施例14の成型発泡体の断面を撮影した顕微鏡写真
(倍率50倍)であり、一方、図3(b)はバフ粉を添
加していない比較例10の顕微鏡写真である。これらの
写真におけるセルの壁に注目すると、実施例14の成型
発泡体の方がセルの壁の形状が若干崩れていることが分
かる。つまり、比較例10の成型発泡体の方がセルの壁
の形状が均一で美しいことが分かる。したがって、顕微
鏡写真を介して観察することにより、本発明品か否かを
判別し得る。
FIG. 3A is a photomicrograph (magnification: 50 ×) of a cross section of the molded foam of Example 14 to which 10% by weight of buff powder was added, while FIG. It is a microscope picture of comparative example 10 which does not add. Paying attention to the cell walls in these photographs, it can be seen that the shape of the cell walls of the molded foam of Example 14 is slightly collapsed. In other words, it can be seen that the molded foam of Comparative Example 10 has a more uniform and beautiful cell wall shape. Therefore, by observing through a micrograph, it can be determined whether or not the product of the present invention.

【0021】実施例21〜24:図4(a)の表2に示
すように、EVA90重量部とIR10重量部からなる
原料エラストマーに、配合剤およびEVAバフ粉を添加
した後、プレス成型して成型発泡体を得た。EVAバフ
粉は、2mmまたは4mmの網目の篩いを通過させて粒径を
略2mm以下または略4mm以下としたものを用いた。ま
た、バフ粉の添加量は5重量部または20重量部とし
た。
Examples 21 to 24: As shown in Table 2 of FIG. 4 (a), a compounding agent and EVA buff powder were added to a raw material elastomer composed of 90 parts by weight of EVA and 10 parts by weight of IR, followed by press molding. A molded foam was obtained. EVA buff powder having a particle size of about 2 mm or less or about 4 mm or less passed through a 2 mm or 4 mm mesh sieve was used. The amount of the buff powder was 5 parts by weight or 20 parts by weight.

【0022】こうして得られた実施例21〜24と前述
の比較例10および実施例13および15の成型発泡体
の引裂強さを測定した測定結果を図4(b)に示す。こ
の測定結果から分かるように、バフ粉の粒径が2mmを超
えると、引裂強度が若干低下するものの、実用上は支障
がない範囲である。
FIG. 4 (b) shows the measurement results of the tear strength of the molded foams of Examples 21 to 24, Comparative Example 10 and Examples 13 and 15 obtained as described above. As can be seen from the measurement results, when the particle size of the buff powder exceeds 2 mm, the tear strength is slightly reduced, but is in a range that does not hinder practical use.

【0023】比較例30,実施例31〜33:図5
(a)の表3に示すように、RB70重量部とIR30
重量部からなる原料エラストマーに、配合剤およびEV
Aバフ粉を添加した後に、プレス成型して発泡体を得
た。EVAバフ粉は、4mmの網目の篩いを通過させて粒
径を略4mm以下とし、添加量を変化させた。こうして得
た実施例31〜33の成型発泡体は、図5(b)に示す
ように、十分な引裂強さを有していることが分かる。こ
れは新たに生成されたRBスポンジとEVAバフ粉の界
面が共架橋しているためであると推測される。
Comparative Example 30, Examples 31 to 33: FIG.
As shown in Table 3 of (a), 70 parts by weight of RB and IR30
A raw material elastomer consisting of parts by weight, a compounding agent and EV
After adding the A buff powder, press molding was performed to obtain a foam. The EVA buff powder was passed through a 4 mm mesh sieve to reduce the particle size to about 4 mm or less, and the amount added was changed. It can be seen that the molded foams of Examples 31 to 33 thus obtained have a sufficient tear strength as shown in FIG. This is presumed to be because the interface between the newly generated RB sponge and the EVA buff powder was co-crosslinked.

【0024】比較例40,実施例41、42:図6
(a)の表4に示すように、SBR50重量部、IR1
5重量部およびハイスチレン樹脂35重量部からなる原
料エラストマーに、配合剤およびラバーバフ粉を添加し
た後に、プレス成型して発泡体を得た。ラバーバフ粉
は、前記原料エラストマーに対して相溶性の良いジエン
系ゴム(天然ゴム、SBRおよびBRのブレンド)を主
成分とする一般的な靴底材を研磨して得、4mmの網目の
篩いを通過させて粒径を略4mm以下とし、添加量を変化
させた。こうして得た実施例41、42の成型発泡体
は、図6(b)に示すように、十分な引裂強さを有して
いることが分かる。これは新たに生成されたスポンジと
ラバーバフ粉の界面が共架橋しているためであると推測
される。
Comparative Example 40, Examples 41 and 42: FIG.
As shown in Table 4 of (a), 50 parts by weight of SBR, IR1
After adding a compounding agent and rubber buff powder to a raw material elastomer composed of 5 parts by weight and 35 parts by weight of a high styrene resin, a foam was obtained by press molding. The rubber buff powder is obtained by polishing a general shoe sole material mainly composed of a diene rubber (a blend of natural rubber, SBR and BR) having good compatibility with the raw material elastomer, and sieving a 4 mm mesh sieve. The particle size was reduced to about 4 mm or less by passing through, and the amount of addition was changed. It can be seen that the molded foams of Examples 41 and 42 thus obtained have a sufficient tear strength, as shown in FIG. This is presumed to be due to co-crosslinking of the interface between the newly generated sponge and the rubber buff powder.

【0025】比較例40〜43:図7(a)の表5に示
すように、溶液重合SBR50重量部、IR15重量部
およびハイスチレン樹脂35重量部からなる原料エラス
トマーに配合剤およびEVAバフ粉を添加した後に、プ
レス成型して発泡体を得た。EVAバフ粉は、4mmの網
目の篩いを通過させて粒径を略4mm以下とし、添加量を
変化させた。こうして得た比較例41〜43の成型発泡
体は、図7(b)に示すように、添加量が増加すると、
引裂強さが著しく低下することが分かる。これは、原料
エラストマーの架橋スポンジとバフ粉との界面が共架橋
していないためであると推測される。
Comparative Examples 40 to 43: As shown in Table 5 of FIG. 7 (a), a compounding agent and EVA buff powder were added to a raw material elastomer comprising 50 parts by weight of solution-polymerized SBR, 15 parts by weight of IR and 35 parts by weight of a high styrene resin. After the addition, press molding was performed to obtain a foam. The EVA buff powder was passed through a 4 mm mesh sieve to reduce the particle size to about 4 mm or less, and the amount added was changed. As shown in FIG. 7B, the molded foams of Comparative Examples 41 to 43 obtained as described above showed that
It can be seen that the tear strength is significantly reduced. This is presumably because the interface between the crosslinked sponge of the raw elastomer and the buff powder was not co-crosslinked.

【0026】[0026]

【発明の効果】以上説明したように、本発明によれば、
スポンジの屑板を破砕した破砕片ではなく、粒径の小さ
いスポンジエラストマーの研磨粉を原料エラストマーに
添加(配合)するので、原料エラストマーの発泡状態が
均一になると共に、エアーホールが生じにくく、しか
も、原料エラストマーと研磨粉とが架橋して固着してい
るので、研磨粉を多量に添加しても、引裂強さが差程低
下しない。したがって、靴底等のスポンジの廃材を有効
利用して環境の保全を図り得ると共に、コストダウンを
図りつつ、十分な強度の成型発泡体を得ることができ
る。
As described above, according to the present invention,
A sponge elastomer polishing powder with a small particle size is added (blended) to the raw material elastomer instead of the crushed pieces obtained by crushing the sponge waste plate. Since the raw material elastomer and the abrasive powder are cross-linked and fixed, even if a large amount of the abrasive powder is added, the tear strength does not decrease so much. Accordingly, it is possible to effectively use waste materials of sponges such as shoe soles to protect the environment, and to obtain a molded foam having sufficient strength while reducing costs.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の成型発泡体の拡大断面を示す模式図で
ある。
FIG. 1 is a schematic view showing an enlarged cross section of a molded foam of the present invention.

【図2】(a)は試験に用いた材料を示す図表、(b)
は引裂強さの測定結果を示すグラフである。
FIG. 2 (a) is a chart showing the materials used in the test, and FIG. 2 (b)
Is a graph showing the measurement results of tear strength.

【図3】成型発泡体を示す電子顕微鏡写真である。FIG. 3 is an electron micrograph showing a molded foam.

【図4】(a)は試験に用いた材料を示す図表、(b)
は引裂強さの測定結果を示すグラフである。
FIG. 4 (a) is a chart showing the materials used in the test, and FIG. 4 (b)
Is a graph showing the measurement results of tear strength.

【図5】(a)は試験に用いた材料を示す図表、(b)
は引裂強さの測定結果を示すグラフである。
FIG. 5 (a) is a chart showing the materials used in the test, and (b)
Is a graph showing the measurement results of tear strength.

【図6】(a)は試験に用いた材料を示す図表、(b)
は引裂強さの測定結果を示すグラフである。
FIG. 6 (a) is a chart showing the materials used in the test, and FIG. 6 (b)
Is a graph showing the measurement results of tear strength.

【図7】(a)は試験に用いた材料を示す図表、(b)
は引裂強さの測定結果を示すグラフである。
FIG. 7 (a) is a chart showing materials used in the test, and FIG.
Is a graph showing the measurement results of tear strength.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 原料エラストマーに架橋剤および発泡剤
が添加された配合エラストマーを発泡させると共に架橋
させた発泡体において、 前記原料エラストマーに架橋済のスポンジエラストマー
の研磨粉が添加されていると共に、該研磨粉と前記原料
エラストマーの架橋スポンジとの間が架橋されているこ
とを特徴とする成型発泡体。
1. A foam obtained by foaming and cross-linking a compounded elastomer obtained by adding a cross-linking agent and a foaming agent to a raw material elastomer, wherein a cross-linked sponge elastomer polishing powder is added to the raw material elastomer, and A molded foam, wherein a portion between the abrasive powder and the crosslinked sponge of the raw material elastomer is crosslinked.
【請求項2】 請求項1において、 前記研磨粉の粒径が5mm以下である成型発泡体。2. The molded foam according to claim 1, wherein the particle size of the polishing powder is 5 mm or less. 【請求項3】 請求項2において、 前記研磨粉の添加量が原料エラストマーに対して 0.5〜
50重量%以下に設定されている成型発泡体。
3. The method according to claim 2, wherein the amount of the abrasive powder is 0.5 to 0.5% with respect to the raw material elastomer.
Molded foam set to 50% by weight or less.
【請求項4】 請求項1,2もしくは3において 前記原料エラストマーおよび研磨粉のポリマーの主成分
が、共に、エチレン−酢酸ビニル共重合体、ポリエチレ
ンまたはシンジオタクチック1,2-ポリブタジエンのうち
の1種または2種以上からなる成型発泡体。
4. The raw material elastomer and the polymer of the polishing powder according to claim 1, wherein the main component of the polymer is one of ethylene-vinyl acetate copolymer, polyethylene or syndiotactic 1,2-polybutadiene. Molded foam consisting of seeds or two or more kinds.
【請求項5】 請求項1,2もしくは3において、 前記原料エラストマーおよび研磨粉のポリマーの主成分
が、共に、ジエン系ゴム、クロロプレンゴムまたはEP
DMのうちの1種または2種以上からなる成型発泡体。
5. The rubber composition according to claim 1, wherein the main components of the raw material elastomer and the polymer of the polishing powder are diene rubber, chloroprene rubber or EP.
A molded foam comprising one or more of DM.
JP3364698A 1998-01-29 1998-01-29 Molded foam Pending JPH11206407A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3364698A JPH11206407A (en) 1998-01-29 1998-01-29 Molded foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3364698A JPH11206407A (en) 1998-01-29 1998-01-29 Molded foam

Publications (1)

Publication Number Publication Date
JPH11206407A true JPH11206407A (en) 1999-08-03

Family

ID=12392219

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3364698A Pending JPH11206407A (en) 1998-01-29 1998-01-29 Molded foam

Country Status (1)

Country Link
JP (1) JPH11206407A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100894963B1 (en) 2008-11-24 2009-04-24 임세영 Rubber composition for shoes sole materials and a shoe sole having natural leather material-like feel prepared using the same
WO2016021023A1 (en) * 2014-08-07 2016-02-11 株式会社アシックス Sole for shoes, and shoes

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100894963B1 (en) 2008-11-24 2009-04-24 임세영 Rubber composition for shoes sole materials and a shoe sole having natural leather material-like feel prepared using the same
WO2016021023A1 (en) * 2014-08-07 2016-02-11 株式会社アシックス Sole for shoes, and shoes
JPWO2016021023A1 (en) * 2014-08-07 2017-04-27 株式会社アシックス Sole for shoes and shoes
EP3178340A4 (en) * 2014-08-07 2017-09-20 ASICS Corporation Sole for shoes, and shoes

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