JPH0420601B2 - - Google Patents

Info

Publication number
JPH0420601B2
JPH0420601B2 JP63130979A JP13097988A JPH0420601B2 JP H0420601 B2 JPH0420601 B2 JP H0420601B2 JP 63130979 A JP63130979 A JP 63130979A JP 13097988 A JP13097988 A JP 13097988A JP H0420601 B2 JPH0420601 B2 JP H0420601B2
Authority
JP
Japan
Prior art keywords
sole
molding material
parts
sole molding
shoe
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.)
Expired - Lifetime
Application number
JP63130979A
Other languages
Japanese (ja)
Other versions
JPH01299502A (en
Inventor
Masanori Harada
Hideki Hayafuchi
Koji Tsukamoto
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.)
Asahi Corp
Original Assignee
Asahi 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 Asahi Corp filed Critical Asahi Corp
Priority to JP63130979A priority Critical patent/JPH01299502A/en
Publication of JPH01299502A publication Critical patent/JPH01299502A/en
Publication of JPH0420601B2 publication Critical patent/JPH0420601B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
  • Reinforced Plastic Materials (AREA)
  • Moulding By Coating Moulds (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) この発明は防滑性靴底の成形法に関するもので
ある。 (従来の技術) 従来、実開昭62−21904号によつて、ガラス繊
維を未加硫ゴムに混合し、これを圧延することに
よつて、ガラス繊維を圧延方向に配向させたもの
を適宜数重ねた後、圧延方向と直行する方向に裁
断した防滑片を、裁断面を接地面となるようにし
て、靴底の接地面に埋込み成形した靴底が提案さ
れている。この靴底において防滑片中に介在され
たガラス繊維が接地面に対して直角に配列されて
いるため、防滑性に優れた靴底が得られるが、防
滑片の成形が煩雑でしかも防滑片を靴底に対して
埋込み成形しなければならなく、コストアツプと
なる欠点があつた。出願人は、塩化ビニル系樹脂
にガラス繊維を配合した靴底成形材で靴底を射出
成形する方法を種々検討したがこのようにして得
られた靴底は0℃以下の低温において急速に硬く
なり、柔軟性を喪失し、滑り易くなる欠点があつ
た。 (発明の解決しようとする問題点) この発明は、0℃以下の低温においても優れた
防滑性を発揮できる靴底を極めて簡単な方法で廉
価に提供しようとするものである。 (問題点を解決するための手段) 以下この発明を実施図面によつて説明すれば、
この発明は塩化ビニル系樹脂100重量部と可塑剤
70〜150重量部と長さが0.1mm〜10mmの硬質繊維5
〜50重量部とアクリル系樹脂2〜20重量部からな
り、メルトインデツクスが20〜50g/10分の靴底
成形材を射出圧600〜1000Kg/cm2で靴底成形キヤ
ビテイに射出することを特徴とする防滑性靴底の
成形法を発明の要旨とするものである。 この発明において、塩化ビニル系樹脂として
は、塩化ビニル樹脂、塩化ビニリデン樹脂、塩化
ビニル・塩化ビニリデン共重合体樹脂、塩化ビニ
ル・酢酸ビニル共重合体樹脂、塩化ビニル・エチ
レン共重合体樹脂、塩化ビニル・無水マレイン酸
共重合体樹脂、塩化ビニル・プロピレン共重合体
樹脂等の1種または2種以上の混合が使用され
る。そして、この発明に使用される可塑剤として
は、通常塩化ビニル樹脂に使用されるものであつ
て、ジオクチルフタレート、ジメチルフタレー
ト、ジエチルフタレート、ジイソブチルフタレー
ト、ジブチルフタレート、ジヘプチルフタレー
ト、ジノニルフタレート、ジイソデシルフタレー
ト、ジトリデシルフタレート、ジシクロヘキシル
フタレート等のフタル酸エステル系の可塑剤、ジ
オクチルアジペート、ジオクチルアゼレート、ジ
オクチルセバケート等の直鎖=塩酸エステル類、
トリクレジルホスフエート、トリキシレニルホス
フエート等のリン酸エステル類、ヒマシ油誘導
体、エポキシ化植物油、ポリエステル系可塑剤等
の可塑剤の単独または2種以上を組み合わせたも
のが使用される。そして可塑剤の配合量を、塩化
ビニル系樹脂100重量部に対して、70〜150重量部
に限定したのは、添加量がそれ以上になれば、成
形された靴底は硬化が低下し、機械的強度が低下
するばかりでなく、高温で以上に軟らかくなり表
面が粘性を帯び、靴底としては不適当となり、ま
た添加量がそれ以下となれば、硬くて柔軟性に欠
け、しかも耐衝撃性が著しく低下して、靴底とし
て不適当になるからである。この発明において硬
質繊維としてはガラス繊維、岩綿、ロツクウー
ル、石英繊維、シリカ繊維、クラストナイト繊
維、セラミツクス繊維等の無機質繊維、金属繊
維、炭素質繊維等の一種または2種以上の混合物
が使用される。そしてこれらの硬質繊維をチタン
系カツプリング剤、シラン系カツプリング剤、脂
肪酸、脂肪酸金属塩、脂肪酸エステルなどで表面
処理しておけば、塩化ビニル系樹脂との接着性並
びに分散性を向上させることができる。この発明
において、硬質繊維の長さを0.1mm〜10mmに限定
し、しかも硬質繊維の配合量を塩化ビニル系樹脂
100重量部に対して、5〜50重量部に限定したの
は、繊維の長さと配合量がそれ以下となれば、射
出成形時における靴底成形キヤビテイでの靴底成
形材の流動性が良くなりすぎ、靴底の接地面に沿
つて平行方向に硬質繊維が配向され、得られる靴
底の防滑性が低下する欠点があり、また繊維の長
さと配合量がそれ以上となれば、射出成形時にお
ける靴底成形キヤビテイでの靴底成形材の流動性
が著しく低下し、靴底成形キヤビテイに対する靴
底成形材の充填不足の原因となり、このようにし
て成形された靴底は、意匠が欠けたり、その表面
にひけやフローマークが形成され、その外観が著
しく低下されるからである。 この発明において、アクリル系樹脂は塩化ビニ
ル系樹脂の改質剤並びに加工性改良剤として使用
されるものであり、アクリル系樹脂としてはメチ
ルメタクリレート、エチルメタクリレート、nプ
チルメタクリレート、2−エチルヘキシルメタク
リレート及びヒドロキシエチルメタクリレートな
どのメタクリル酸エステル、メチルアクリレー
ト、2−エチルヘキシルアクリレート、n−プチ
ルアクリレート及びヒドロキシエチルアクリレー
トなどのアクリル酸エステル、メタクリル酸また
はアクリル酸、n−プトキシメチルメタクリルア
ミド等のアクリルアミド又はメタクリルアミド誘
導体等の単量体からの重合体あるいは共重合体が
用いられる。また共重合成分としては上記の単量
体のほかにジメタクリル酸マレイン、イタコン
酸、α−メチレングルタル酸、アコニツト酸ある
いはこれらの酸のエステル誘導体またはアミド、
スチレン、α−メチルスチレンなどのスチレン誘
導体、アクリロニトリル、メタクリロニトリル、
またはこれらの2種以上を併用したものが使用さ
れる。そしてこの発明において、アクリル系樹脂
の配合量を塩化ビニル系樹脂100重量部に対して、
2〜20重量部に限定したのは、配合量がそれ以下
となれば靴底成形材中に硬質繊維が配合されてい
ることと合いまつて、射出成形時における靴底成
形キヤビテイでの靴底成形材の流動性が著しく低
下し、靴底成形キヤビテイに対する靴底成形材の
充填不足の原因となり、このようにして成形され
た靴底は、意匠が欠けたり、その表面にひけやフ
ローマークが形成されその外観が著しく低下し、
しかも物性的に耐寒性における改質効果がみられ
ず0℃以下において硬くなり、柔軟性が喪失さ
れ、屈曲性が低下し、履心地が悪くなるとともに
滑りやすくなる欠点があり、また配合量がそれ以
上となれば靴底の耐寒性は良くなるが、塩化ビニ
ル系樹脂に対するアクリル系樹脂の分散性が悪く
なり、成形性が悪くなり、しかも成形される靴底
の硬化のばらつきが大きく、均質な製品が得られ
なくなる欠点があるからである。そしてこの発明
における靴底成形材中には必要によつて発泡助
剤、安定剤、充填剤、滑剤、着色剤等が添加され
てもよい。このようにして準備された各成分は、
バンバリーミキサー、ヘンシエルミキサー、ミキ
シングロール、ニーダー等によつて均一に混合し
て、靴底成形材のメルトインデツクスを20〜50
g/10分に調整準備する。 この発明において靴底成形材のメルトインデツ
クスを20〜50g/10分に限定したのは、メルトイ
ンデツクスがそれ以下となれば射出成形時におけ
る靴底成形キヤビテイでの靴底成形材の流動性が
著しく低下し、靴底成形キヤビテイに対する靴底
成形材の充填不足の原因となり、このようにして
成形された靴底は意匠が欠けたり、その表面にひ
けやフローマークが形成されその外観が著しく低
下され、またメルトインデツクスがそれ以上とな
れば射出成形時における靴底成形キヤビテイでの
靴底成形材の流動性が良くなりすぎ、靴底の接地
面に沿つて平行方向に硬質繊維が配向され、得ら
れる靴底の防滑性が低下する欠点があるからであ
る。 このようにして準備された靴底成形材は射出圧
600〜1000Kg/cm2で靴底成形キヤビテイに射出さ
れ靴底が成形されるものであるが、射出圧がそれ
以下となれば射出成形時における靴底成形キヤビ
テイでの靴底成形材の流動性が著しく低下し、靴
底成形キヤビテイに対する靴底成形材の充填不足
の原因となり、このようにして成形された靴底は
意匠が欠けたり、その表面にひけやフローマーク
が形成されその外観が著しく低下され、また射出
圧がそれ以上となれば靴底成形キヤビテイでの靴
底成形材の流れが乱流状態となり、流れ方向が定
まらず、靴底成形材中に配合された硬質繊維の配
向性が定まらず、ばらばらの状態で不規則に靴底
中に散在されることになり、靴底の防滑性は殆ど
期待できないからである。 (発明の作用効果) この発明は以上のように構成されており、この
ようにして成形された靴底は、接地面に対して硬
質繊維がほぼ垂直方向に配向されており、防滑性
に優れたものであつた。しかも0℃以下の低温に
おいても、硬度変化が小さく適度の柔軟性と屈曲
性が保持されるから、防滑性が低下されることが
ない。しかもう射出成形によつて靴底成形と同時
に硬質繊維を靴底の接地面に対してほぼ垂直方向
に配向させることができるので、靴底の成形が極
めて廉価である。この発明において、射出成形時
に硬質繊維が靴底の接地面に対してほぼ垂直に配
向される理由として、靴底成形材の限定された範
囲のメルトインデツクスと射出成形時の限定され
た範囲の射出圧の相互作用によつて、射出成形時
に実施図面に示すように靴底成形材が靴底成形キ
ヤビテイの肉厚方向にら線を描きながら流動して
靴底成形キヤビテイに充填されるため、靴底成形
材の流動方向に沿つて靴底成形材中に配合された
硬質繊維が配向されるためと考えられる。 実施例 第1表上段に示す実施例1〜3による配合の靴
底成形を準備し、これをボトムモールド1とサイ
ドモールド2,2と胛被5を吊込んだラスト3と
によつて形成された靴底成形キヤビテイ4に射出
温度195℃射出圧800Kg/cm2の条件で射出してこれ
を発泡させて得られた靴底と比較例1〜2によつ
て同様にして得られた靴底の防滑性、0℃〜20℃
の硬度差(JISK6301 スプリング式硬さ試験A
型による硬度差)並びに外観を比較して第1表下
段に示す実施例によつて成形された靴底は本発明
所望の効果を奏するものであつた。
(Industrial Application Field) The present invention relates to a method of forming a non-slip shoe sole. (Prior art) Conventionally, according to Utility Model Application Publication No. 62-21904, glass fibers are mixed with unvulcanized rubber and rolled, so that the glass fibers are oriented in the rolling direction. A shoe sole has been proposed in which anti-slip pieces are layered several times and then cut in a direction perpendicular to the rolling direction, and then embedded and molded into the ground contact surface of the sole, with the cut surface serving as the ground contact surface. In this sole, the glass fibers interposed in the anti-slip piece are arranged perpendicularly to the ground surface, resulting in a sole with excellent anti-slip properties, but the forming of the anti-slip piece is complicated. It had to be molded into the sole of the shoe, which had the disadvantage of increasing costs. The applicant has investigated various methods of injection molding shoe soles using a shoe sole molding material that is a mixture of vinyl chloride resin and glass fiber, but the soles obtained in this way quickly harden at low temperatures below 0°C. It has the disadvantage of losing flexibility and becoming slippery. (Problems to be Solved by the Invention) The present invention aims to provide a shoe sole that exhibits excellent anti-slip properties even at low temperatures of 0° C. or lower, by an extremely simple method and at a low cost. (Means for solving the problem) This invention will be explained below with reference to the drawings.
This invention consists of 100 parts by weight of vinyl chloride resin and a plasticizer.
70 to 150 parts by weight and hard fibers with a length of 0.1 mm to 10 mm 5
A shoe sole molding material consisting of ~50 parts by weight and 2 to 20 parts by weight of acrylic resin and having a melt index of 20 to 50 g/10 minutes is injected into a shoe sole molding cavity at an injection pressure of 600 to 1000 kg/cm2. The gist of the invention is a method for molding a characteristic anti-slip shoe sole. In this invention, the vinyl chloride resin includes vinyl chloride resin, vinylidene chloride resin, vinyl chloride/vinylidene chloride copolymer resin, vinyl chloride/vinyl acetate copolymer resin, vinyl chloride/ethylene copolymer resin, and vinyl chloride resin. - One or a mixture of two or more of maleic anhydride copolymer resin, vinyl chloride propylene copolymer resin, etc. is used. The plasticizers used in this invention are those normally used in vinyl chloride resins, such as dioctyl phthalate, dimethyl phthalate, diethyl phthalate, diisobutyl phthalate, dibutyl phthalate, diheptyl phthalate, dinonyl phthalate, and diisodecyl phthalate. Phthalate ester plasticizers such as phthalate, ditridecyl phthalate, and dicyclohexyl phthalate; linear hydrochloric acid esters such as dioctyl adipate, dioctyl azelate, and dioctyl sebacate;
Phosphate esters such as tricresyl phosphate and tricylenyl phosphate, plasticizers such as castor oil derivatives, epoxidized vegetable oils, and polyester plasticizers may be used alone or in combination of two or more. The amount of plasticizer added was limited to 70 to 150 parts by weight per 100 parts by weight of the vinyl chloride resin. Not only does the mechanical strength decrease, but it becomes even softer at high temperatures and the surface becomes viscous, making it unsuitable for shoe soles.Additionally, if the amount added is less than that, it becomes hard, lacks flexibility, and has impact resistance. This is because the properties of the material are significantly reduced, making it unsuitable for use as shoe soles. In this invention, as the hard fiber, one or a mixture of two or more of inorganic fibers such as glass fiber, rock wool, rock wool, quartz fiber, silica fiber, crustonite fiber, and ceramic fiber, metal fiber, and carbonaceous fiber is used. Ru. If these hard fibers are surface-treated with a titanium-based coupling agent, a silane-based coupling agent, a fatty acid, a fatty acid metal salt, a fatty acid ester, etc., their adhesion and dispersibility with vinyl chloride resin can be improved. . In this invention, the length of hard fibers is limited to 0.1 mm to 10 mm, and the amount of hard fibers is
The reason for limiting it to 5 to 50 parts by weight per 100 parts by weight is that if the fiber length and blending amount are less than this, the fluidity of the sole molding material in the sole molding cavity during injection molding will be better. If the length and amount of fibers are too long, the hard fibers will be oriented parallel to the contact surface of the sole, reducing the slip resistance of the resulting shoe sole. At times, the fluidity of the sole molding material in the sole molding cavity is significantly reduced, causing insufficient filling of the sole molding material into the sole molding cavity, and the soles molded in this way lack a design. This is because sink marks and flow marks are formed on the surface of the material, which significantly deteriorates its appearance. In this invention, acrylic resins are used as modifiers and processability improvers for vinyl chloride resins, and examples of acrylic resins include methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, 2-ethylhexyl methacrylate, and hydroxyl methacrylate. Methacrylic acid esters such as ethyl methacrylate, acrylic acid esters such as methyl acrylate, 2-ethylhexyl acrylate, n-butyl acrylate and hydroxyethyl acrylate, methacrylic acid or acrylic acid, acrylamide or methacrylamide derivatives such as n-butoxymethylmethacrylamide Polymers or copolymers made from monomers such as In addition to the above monomers, copolymerization components include maleic dimethacrylate, itaconic acid, α-methylene glutaric acid, aconitic acid, or ester derivatives or amides of these acids.
Styrene, styrene derivatives such as α-methylstyrene, acrylonitrile, methacrylonitrile,
Or a combination of two or more of these may be used. In this invention, the amount of acrylic resin to be blended is based on 100 parts by weight of vinyl chloride resin.
The reason for limiting the amount to 2 to 20 parts by weight is that if the amount is less than that, hard fibers will be included in the sole molding material, and the sole molding material will not be used in the sole molding cavity during injection molding. The fluidity of the molding material decreases significantly, causing insufficient filling of the sole molding material into the sole molding cavity, and the soles molded in this way may lack design or have sink marks or flow marks on the surface. formed and its appearance deteriorates significantly,
Moreover, there is no improvement effect on cold resistance in terms of physical properties, and it becomes hard at temperatures below 0°C, loses flexibility, reduces flexibility, becomes uncomfortable, and becomes slippery. If the temperature is higher than that, the cold resistance of the sole will be improved, but the dispersibility of the acrylic resin in the vinyl chloride resin will be poor, resulting in poor moldability, and the hardening of the molded sole will vary widely, resulting in a uniform This is because there is a drawback that it is not possible to obtain a suitable product. A foaming aid, a stabilizer, a filler, a lubricant, a coloring agent, etc. may be added to the shoe sole molding material of the present invention, if necessary. Each ingredient prepared in this way is
Mix uniformly using a Banbury mixer, Henschel mixer, mixing roll, kneader, etc. to bring the melt index of the shoe sole molding material to 20 to 50.
Prepare to adjust to g/10 minutes. The reason why the melt index of the sole molding material is limited to 20 to 50 g/10 minutes in this invention is that if the melt index is lower than this, the fluidity of the sole molding material in the sole molding cavity during injection molding will be reduced. This results in a significant decrease in the sole molding material, which causes insufficient filling of the sole molding material into the sole molding cavity, and the soles molded in this way may lack design or have sink marks or flow marks formed on the surface, resulting in a significant change in appearance. If the melt index is higher than that, the fluidity of the sole molding material in the sole molding cavity during injection molding will be too good, and the hard fibers will be oriented in parallel directions along the contact surface of the sole. This is because there is a drawback that the anti-slip properties of the resulting shoe sole are reduced. The sole molding material prepared in this way has an injection pressure of
The sole molding material is injected into the sole molding cavity at a pressure of 600 to 1000 kg/ cm2 , but if the injection pressure is lower than that, the fluidity of the sole molding material in the sole molding cavity during injection molding will be affected. This results in a significant decrease in the sole molding material, which causes insufficient filling of the sole molding material into the sole molding cavity, and the soles molded in this way may lack design or have sink marks or flow marks formed on the surface, resulting in a significant change in appearance. If the injection pressure is lowered or exceeded, the flow of the sole molding material in the sole molding cavity will become turbulent, the flow direction will not be fixed, and the orientation of the hard fibers mixed in the sole molding material will be affected. This is because the particles are not fixed and are scattered irregularly throughout the shoe sole, making it difficult to expect the sole to be anti-slip. (Operations and Effects of the Invention) The present invention is constructed as described above, and the sole formed in this manner has hard fibers oriented in a direction substantially perpendicular to the ground contact surface, and has excellent slip resistance. It was warm. Moreover, even at low temperatures of 0° C. or lower, the hardness changes are small and appropriate flexibility and flexibility are maintained, so the anti-slip properties are not reduced. Furthermore, injection molding allows the hard fibers to be oriented substantially perpendicularly to the contact surface of the sole at the same time as the sole is formed, making the sole molding extremely inexpensive. In this invention, the reason why the hard fibers are oriented almost perpendicularly to the contact surface of the sole during injection molding is due to the limited range of melt index of the sole molding material and the limited range of melt index during injection molding. Due to the interaction of the injection pressure, the sole molding material flows in the thickness direction of the sole molding cavity as shown in the drawing during injection molding, and is filled into the sole molding cavity. This is thought to be because the hard fibers blended into the sole molding material are oriented along the flow direction of the sole molding material. Example Shoe sole moldings having the formulations according to Examples 1 to 3 shown in the upper row of Table 1 were prepared, and formed by a bottom mold 1, side molds 2, 2, and a last 3 in which a shoe cover 5 was suspended. Shoe soles obtained by injecting into a molded shoe sole molding cavity 4 at an injection temperature of 195° C. and an injection pressure of 800 kg/cm 2 and foaming the same, and soles obtained in the same manner according to Comparative Examples 1 and 2. Anti-slip property, 0℃~20℃
Hardness difference (JISK6301 Spring type hardness test A
A comparison of the differences in hardness depending on the mold and the appearance revealed that the soles molded according to the examples shown in the lower row of Table 1 exhibited the desired effects of the present invention.

【表】【table】

【表】【table】 【図面の簡単な説明】[Brief explanation of drawings]

図面は、この発明による靴底成形状態を示す要
部断面図である。 符号の説明、1……ボトムモールド、2……サ
イドモールド、3……ラスト、4……靴底成形キ
ヤビテイ、5……胛被。
The drawing is a sectional view of a main part showing a state of molding a shoe sole according to the present invention. Explanation of the symbols: 1...Bottom mold, 2...Side mold, 3...Last, 4...Sole molding cavity, 5...Shoe cover.

Claims (1)

【特許請求の範囲】[Claims] 1 塩化ビニル系樹脂100重量部と可塑剤70〜150
重量部と長さが0.1mm〜10mmの硬質繊維5〜50重
量部とアクリル系樹脂2〜20重量部からなり、メ
ルトインデツクスが20〜50g/10分の靴底成形材
を射出圧600〜1000Kg/cm2で靴底成形キヤビテイ
に射出することを特徴とする防滑性靴底の成形
法。
1 100 parts by weight of vinyl chloride resin and 70 to 150 parts of plasticizer
A shoe sole molding material consisting of 5 to 50 parts by weight of hard fibers with weight parts and lengths of 0.1 mm to 10 mm and 2 to 20 parts by weight of acrylic resin, and a melt index of 20 to 50 g/10 minutes, is injected at 600 to 600 parts. A method for molding anti-slip shoe soles characterized by injecting 1000 kg/cm 2 into a shoe sole molding cavity.
JP63130979A 1988-05-27 1988-05-27 Molding of slide resisting sole Granted JPH01299502A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63130979A JPH01299502A (en) 1988-05-27 1988-05-27 Molding of slide resisting sole

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63130979A JPH01299502A (en) 1988-05-27 1988-05-27 Molding of slide resisting sole

Publications (2)

Publication Number Publication Date
JPH01299502A JPH01299502A (en) 1989-12-04
JPH0420601B2 true JPH0420601B2 (en) 1992-04-03

Family

ID=15047076

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63130979A Granted JPH01299502A (en) 1988-05-27 1988-05-27 Molding of slide resisting sole

Country Status (1)

Country Link
JP (1) JPH01299502A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH048301A (en) * 1990-04-26 1992-01-13 Moon Star Co Sole for polyvinyl chloride antislipping shoe
JPH0630807A (en) * 1992-07-16 1994-02-08 Asahi Corp Molding method of anti-slip sole

Also Published As

Publication number Publication date
JPH01299502A (en) 1989-12-04

Similar Documents

Publication Publication Date Title
KR20090035443A (en) Improved Polymer Composition
KR20130099191A (en) Plastisol for spray-molded plastic articles
CN113785011B (en) Thermoplastic elastomer gel
JPH0461899B2 (en)
KR20130107402A (en) Composition of artificial clay for handicraft
JPH01299502A (en) Molding of slide resisting sole
JPH0630807A (en) Molding method of anti-slip sole
US4229338A (en) Suede-look shoe soles
US2502371A (en) Polyvinyl chloride compositions
JPH0223572B2 (en)
JP2627245B2 (en) Anti-slip soles
JP4068760B2 (en) Method for producing composite resin extrusion
JPS6028307B2 (en) Vinyl chloride resin composition for erasing characters
JPH0346121B2 (en)
JPH04198247A (en) Vinyl chloride resin composition for foamed powder slush molding
JP7092039B2 (en) Vinyl chloride resin composition, vinyl chloride resin molded body and laminate
JPH048301A (en) Sole for polyvinyl chloride antislipping shoe
JPS61247745A (en) Thermoplastic resin composition for sole of footwear
CN109504114A (en) Elastic composition, plastic pad and preparation method thereof
JPS60179446A (en) Vinyl chloride resin composition
JP2656343B2 (en) Trans polyisoprene resin composition
JPH0516462B2 (en)
CN120757989A (en) Environmentally friendly, highly elastic, and wear-resistant PET floor and its production method
JP3597642B2 (en) Method for producing molded article having woody feel
JPH07188488A (en) Polyvinyl chloride resin composition