JPH0566254B2 - - Google Patents
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- Publication number
- JPH0566254B2 JPH0566254B2 JP6999086A JP6999086A JPH0566254B2 JP H0566254 B2 JPH0566254 B2 JP H0566254B2 JP 6999086 A JP6999086 A JP 6999086A JP 6999086 A JP6999086 A JP 6999086A JP H0566254 B2 JPH0566254 B2 JP H0566254B2
- Authority
- JP
- Japan
- Prior art keywords
- powder
- rubber
- heat
- porous
- vulcanized rubber
- 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 - Fee Related
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- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は多孔性ゴム弾性体の製造方法に関す
る。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for manufacturing a porous rubber elastic body.
(従来の技術)
多孔性ゴム弾性体の製造方法としては例えば次
のものが知られている。(Prior Art) For example, the following method is known as a method for manufacturing a porous rubber elastic body.
(イ) 塩、でん粉等の可溶性物質をゴムに混合し、
加硫成形後にこの可溶性物質を溶解抽出する方
法(特開昭49−53256号公報、特開昭49−53257
号公報参照)。(b) Mix soluble substances such as salt and starch with rubber,
A method of dissolving and extracting this soluble substance after vulcanization molding (JP-A-49-53256, JP-A-49-53257)
(see publication).
(ロ) ゴム粉末とPVC(ポリ塩化ビニル)粉末と可
塑剤とを混合し焼結する方法(特開昭57−
64537号公報参照)。(b) A method of mixing and sintering rubber powder, PVC (polyvinyl chloride) powder, and plasticizer (Unexamined Japanese Patent Publication No. 1983-
(See Publication No. 64537).
(発明が解決しようとする問題点)
従来の技術(イ)の方法では、ゴムと可溶性物質と
の混合、加硫、抽出、乾燥というように多孔体を
得るにあたつての工程数が多く、また、抽出によ
つて生ずる排水に可溶性物質が含まれるから、そ
の排水処理が難しくなる。(Problems to be Solved by the Invention) The method of conventional technology (a) requires a large number of steps to obtain a porous body, such as mixing rubber and a soluble substance, vulcanization, extraction, and drying. Furthermore, since the wastewater generated by extraction contains soluble substances, it becomes difficult to treat the wastewater.
従来の技術(ロ)の方法では、得られる多孔体は、
ゴム粉末同志がPVC粉末を介して結合されたも
のとなるため、ゴム粉末とPVC粉末との接触点
の多少により、あるいは各ゴム粉末の周囲に
PVC粉末が適当に分散されているか否かにより、
この多孔体の強度が左右されてくる。従つて、強
度が高く且つ均質な多孔体を得るには、ゴム粉末
とPVC粉末とを均一な分散状態とする必要があ
るが、実際にはこれらの粉末は粒径その他の性状
が異なることもあつて均一な分散状態を得るのが
難しい。 In the method of conventional technology (b), the porous body obtained is
Since the rubber powders are bonded together via the PVC powder, depending on the number of contact points between the rubber powder and the PVC powder, or around each rubber powder.
Depending on whether the PVC powder is properly dispersed or not,
This depends on the strength of this porous body. Therefore, in order to obtain a porous body with high strength and homogeneity, it is necessary to uniformly disperse rubber powder and PVC powder, but in reality, these powders may differ in particle size and other properties. It is difficult to obtain a uniformly dispersed state.
(問題点を解決するための手段および作用)
本発明は上記従来の問題点を解決する手段とし
て、発泡した加硫ゴム粉末または無発泡の加硫ゴ
ム粉末の少なくとも一方と熱融解性粒子を含有す
るラテツクスとを混合した後、乾燥させる工程を
経て熱融解性皮膜を有する2層構造の粉体を形成
し、この粉体を焼結することによつて多孔性ゴム
弾性体を得るようにした製造方法を提供するもの
である。(Means and effects for solving the problems) The present invention, as a means to solve the above-mentioned conventional problems, contains at least one of foamed vulcanized rubber powder or non-foamed vulcanized rubber powder and heat-fusible particles. A porous rubber elastic body was obtained by mixing the powder with latex and drying it to form a powder with a two-layer structure having a heat-melting film, and by sintering this powder. A manufacturing method is provided.
上記無発泡の加硫ゴム粉末は、天然ゴム、イソ
プレンゴム、スチレンブタジエンゴム、ニトリル
ゴム、クロロプレンゴム、ブチルゴム、エチレン
プロピレンゴム、ウレタンゴムなどのベースゴム
に、加硫剤、加硫促進剤、加硫助剤、充填剤、補
強剤、軟化剤、有機あるいは無機の顔料などの各
種配合物を製造すべき多孔性ゴム弾性体の用途に
応じて適宜配合し、混合加硫したものを微粉砕し
て、あるいは高温で乳化重合したゴムをスプレイ
ドライにより粉末化して得ることができる。ま
た、発泡加硫ゴム粉末は、発泡安定剤を利用し機
械的に発泡させゲル化して得た多孔性ゴムを加硫
後に微粉砕して得ることができる。 The above non-foamed vulcanized rubber powder is prepared by adding a vulcanizing agent, a vulcanization accelerator, and a base rubber such as natural rubber, isoprene rubber, styrene-butadiene rubber, nitrile rubber, chloroprene rubber, butyl rubber, ethylene propylene rubber, or urethane rubber. Various compounds such as sulfur aids, fillers, reinforcing agents, softeners, and organic or inorganic pigments are mixed as appropriate depending on the use of the porous rubber elastic body to be manufactured, and the mixed and vulcanized mixture is finely pulverized. Alternatively, it can be obtained by powdering rubber emulsion polymerized at high temperature by spray drying. Further, the foamed vulcanized rubber powder can be obtained by pulverizing porous rubber obtained by mechanically foaming and gelling using a foaming stabilizer, after vulcanization.
また、上記ラテツクスとしては、PVC、酢酸
ビニル、ビニルピリジン樹脂、カルボキシ変性ア
クリル樹脂、グリシジル変性アクリル樹脂、アミ
ン変性アクリル樹脂、酢酸ビニルケン化物などの
熱可塑性樹脂を水に分散したラテツクスや、カル
ボキシ変性アクリロニトリル・ブタジエン系ラテ
ツクスなどを用いることができる。このラテツク
ス中の上記熱可塑性ないしは熱硬化性の樹脂ある
いはゴムなどの熱融解性粒子は均一な皮膜形成の
ためその粒子径を5μ以下とするのが望ましい。 In addition, the above-mentioned latexes include latexes prepared by dispersing thermoplastic resins such as PVC, vinyl acetate, vinylpyridine resin, carboxy-modified acrylic resin, glycidyl-modified acrylic resin, amine-modified acrylic resin, saponified vinyl acetate in water, and carboxy-modified acrylonitrile.・Butadiene latex etc. can be used. The heat-melting particles of the thermoplastic or thermosetting resin or rubber in this latex preferably have a particle diameter of 5 μm or less in order to form a uniform film.
また、上記製造方法において、可塑剤を使用す
る場合、上記乾燥工程の後にこの可塑剤を添加
し、そして焼結を行なうことになる。この可塑剤
としては、例えば、フタル酸エステル類、燐酸エ
ステル類、エポキシ化植物油類、ポリエステル系
可塑剤、アジピン酸系ポリエステル類、液状
NBR、塩化パラフイン類等を利用することがで
きる。 Furthermore, in the above manufacturing method, when a plasticizer is used, the plasticizer is added after the drying step and sintering is performed. Examples of the plasticizer include phthalate esters, phosphate esters, epoxidized vegetable oils, polyester plasticizers, adipic acid polyesters, and liquid
NBR, chlorinated paraffins, etc. can be used.
しかして、上記製造方法によれば、ラテツクス
中の熱融解性粒子が乾燥によつて加硫ゴム粉末の
表面に熱融解性皮膜を形成し、加硫ゴム粉末同志
は熱融解性皮膜同志の溶着により結合することに
なる。この場合、加硫ゴム粉末はラテツクスとの
混合により全表面が簡単に濡れた状態となるた
め、熱融解性皮膜を各加硫ゴム粉末の全表面にわ
たつて、例えば1〜10μ程度の厚さで確実に形成
することができる。そして、各加硫ゴム粉末がそ
れぞれ熱融解性皮膜をもつため、分散不良等の問
題なく、均一な焼結強度をもつ多孔体を得ること
ができる。 According to the above manufacturing method, the heat-fusible particles in the latex form a heat-fusible film on the surface of the vulcanized rubber powder by drying, and the vulcanized rubber powders are welded together to form a heat-fusible film on the surface of the vulcanized rubber powder. This will result in a combination. In this case, the entire surface of the vulcanized rubber powder becomes easily wetted by mixing with the latex, so a heat-melting film is applied over the entire surface of each vulcanized rubber powder to a thickness of, for example, 1 to 10 μm. can be reliably formed. Since each vulcanized rubber powder has a heat-fusible film, a porous body having uniform sintering strength can be obtained without problems such as poor dispersion.
また、加硫ゴム粉末は加熱によつても高い弾性
を維持し且つ熱収縮も少ないことから、多孔体成
形(焼結)時の寸法安定性が良く、従つて、低密
度の多孔体についても粉体の量を変えるだけでヒ
ケを生ずることなく高い強度をもつように成形す
ることができる。 In addition, vulcanized rubber powder maintains high elasticity even when heated and has little thermal shrinkage, so it has good dimensional stability when forming (sintering) porous bodies, and therefore can be used for low-density porous bodies. By simply changing the amount of powder, it can be molded to have high strength without causing sink marks.
(発明の効果)
従つて、本発明によれば、個々の加硫ゴム粉末
に熱融解性皮膜が形成されるため、比較的少ない
工程数で且つ分散不良等の問題を生ずることな
く、上記熱融解性皮膜どうしが溶着してなる均一
な強度をもつ多孔性ゴム弾性体を得ることがで
き、また成形時の寸法安定性もよく、品質ないし
は生産性の向上が図れる。(Effect of the invention) Therefore, according to the present invention, since a heat-melting film is formed on each individual vulcanized rubber powder, the above-mentioned heat-melting film can be formed with a relatively small number of steps and without causing problems such as poor dispersion. A porous rubber elastic body having uniform strength can be obtained by welding the meltable films together, and also has good dimensional stability during molding, improving quality and productivity.
(実施例) 以下、本発明の実施例を説明する。(Example) Examples of the present invention will be described below.
実施例 1
本例においては、加硫ゴム粉末として第1図に
顕微鏡写真(80倍)に示す如く平均粒子径100μ
のNBR(アクリロニトリルブタジエンゴム:ポリ
サー社製クライナツク1411)を用い、ラテツクス
としては粒子系0.1〜0.3μのPVCラテツクス(日
本ゼオン社製G150X−15)を用い、以下の工程
を順に行なつて多孔性ゴム弾性体を得た。Example 1 In this example, the average particle size of the vulcanized rubber powder was 100μ as shown in the micrograph (80x magnification) in Figure 1.
NBR (acrylonitrile butadiene rubber: Kleinak 1411 manufactured by Polycer) was used, and PVC latex with a particle size of 0.1 to 0.3μ (G150X-15 manufactured by Nippon Zeon Co., Ltd.) was used as the latex, and the following steps were performed in order to make it porous. A rubber elastic body was obtained.
混合工程
上記加硫ゴム粉末80重量部に撹拌しながら、
PVCラテツクス20重量部(固形分)を少量ずつ
添加していくことにより、この加硫ゴム粉末と
PVCラテツクスとを混合する。Mixing process Add 80 parts by weight of the above vulcanized rubber powder while stirring.
By adding 20 parts by weight (solid content) of PVC latex little by little, this vulcanized rubber powder and
Mix with PVC latex.
乾燥工程
混合工程で得た混合物を60℃のオーブン中で1
時間放置し、乾燥する(ラテツクスの水分を飛ば
す)。Drying process: Heat the mixture obtained in the mixing process in an oven at 60°C.
Leave it for a while to dry (wick away the moisture from the latex).
可塑剤添加工程
乾燥工程で得たものを撹拌しながら、これに可
塑剤としてDOA(ジオクチルアジペート)の20重
量部を80℃の雰囲気温度で少量ずつ添加し、
DOAが完全に吸収されるまで撹拌を続け、熱融
解性皮膜を有する粉体を得る。この粉体の外観は
第2図に顕微鏡写真(80倍)で示すとおり表面に
微小凹凸ができたものであり、この粉体は断面を
第3図に顕微鏡写真(6000倍)で示すように加硫
ゴム粉体(中央の黒い部分)の表面に熱融解性皮
膜(周辺の白い部分)が形成された2層構造であ
り、かつ内部に熱融解性粒子(PVC粒子)が含
浸により介在したものとなつている。また、第4
図に上記粉体の断面のCl−Kイメージの顕微鏡写
真(6000倍)を示すようにCl(塩素)が感応して
ドーナツ状に表われており、第3図の白い部分は
PVCによる熱融解性皮膜であることがわかる。Plasticizer addition step While stirring the material obtained in the drying step, 20 parts by weight of DOA (dioctyl adipate) as a plasticizer was added little by little at an ambient temperature of 80°C.
Stirring is continued until the DOA is completely absorbed to obtain a powder with a heat-meltable film. The appearance of this powder is as shown in the micrograph (80x magnification) in Figure 2, with minute irregularities on the surface, and the cross section of this powder is as shown in the micrograph (6000x magnification) in Figure 3. It has a two-layer structure in which a heat-melting film (white part around it) is formed on the surface of vulcanized rubber powder (black part in the center), and heat-melting particles (PVC particles) are interposed inside by impregnation. It has become a thing. Also, the fourth
As shown in the figure, a micrograph (6000x) of the Cl-K image of the cross section of the above powder, Cl (chlorine) is sensitive and appears in a donut shape, and the white part in Figure 3 is
It can be seen that it is a heat-melting film made of PVC.
焼結工程
上記可塑剤を添加した粉体を容積率300%で型
に充填し、加圧加熱用プレスを用いて150℃で5
分間保持し、多孔性ゴム弾性体を得る。Sintering process: Fill a mold with the above plasticizer-added powder at a volume ratio of 300%, and heat it at 150℃ using a press for pressure and heating.
Hold for a minute to obtain a porous rubber elastic body.
この多孔性ゴム弾性体は、180度に曲げても破
断しない弾性(強度)を有し、また硬度は高分子
計器社製のアスカー硬度計タイプCでは50であつ
た。また、この多孔性ゴム弾性体にインクを含浸
し、インクロールとして使用したところ20万印字
以上においても鮮明な印影が得られた。 This porous rubber elastic body had elasticity (strength) that would not break even when bent at 180 degrees, and its hardness was 50 on the Asker hardness tester type C manufactured by Kobunshi Keiki Co., Ltd. Furthermore, when this porous rubber elastic body was impregnated with ink and used as an ink roll, clear impressions were obtained even after 200,000 prints or more.
実施例 2
本例は、発泡した加硫ゴム粉末を用いた例であ
る。この加硫ゴム粉末は次の配合により混合した
ものをオークスミキサーにより発泡倍率300%で
発泡させ、これをケイフツ化ソーダでゲル化して
得た多孔性ゴムを加硫後に微粉砕して得たもので
ある。Example 2 This example uses foamed vulcanized rubber powder. This vulcanized rubber powder is obtained by foaming a mixture according to the following formulation at a foaming ratio of 300% using an oak mixer, gelling this with soda silica, and pulverizing the porous rubber after vulcanization. It is.
配合剤 重量部
ゴムラテツクス 115
加硫剤 5.5
発泡安定剤 1.8
老化防止剤(SP-10) 0.5
ZnO 0.5
計123.3
なお、ゴムラテツクスは日本ゼオン社製のニポ
ールLate×531とニポールLate×2507からなり、
加硫剤は日本ゼオン社製FDS−100とイオウから
なる。また、発泡安定剤は白石カルシウム社製の
トリメンベースFR−14である。 Compounding ingredients Parts by weight Rubber latex 115 Vulcanizing agent 5.5 Foam stabilizer 1.8 Anti-aging agent (SP-10) 0.5 ZnO 0.5 Total 123.3 The rubber latex consists of Nipole Latex531 and Nipole Latex2507 manufactured by Nippon Zeon Co., Ltd.
The vulcanizing agent consists of FDS-100 manufactured by Nippon Zeon Co., Ltd. and sulfur. The foaming stabilizer is Trimenbase FR-14 manufactured by Shiraishi Calcium Co., Ltd.
多孔性ゴム弾性体の製造にあたつては、上記発
泡加硫ゴム粉末に撹拌しながらカルボキシ変性の
NBRラテツクス(日本合成ゴム社製JSR−0911)
の10重量部(固形分)を少量ずつ添加して混合し
た後、乾燥して得られた粉体を容積率300%で型
に充填し、160℃で8分間の加圧保持を行なつて
焼結をなす。 When producing a porous rubber elastic body, carboxy-modified rubber is added to the foamed vulcanized rubber powder while stirring.
NBR latex (JSR-0911 manufactured by Japan Synthetic Rubber Co., Ltd.)
After adding and mixing 10 parts by weight (solid content) little by little, the powder obtained by drying was filled into a mold at a volume ratio of 300% and held under pressure at 160°C for 8 minutes. Make sintering.
得られた多孔性ゴム弾性体は、180度に曲げて
も破断せず、また硬度はアスカー硬度計タイプC
で43であつた。また、この多孔性ゴム弾性体をイ
ンクロールとして使用したところ、実施例1と同
様の良好な結果が得られた。 The obtained porous rubber elastic body did not break even when bent at 180 degrees, and its hardness was measured as Asker hardness tester type C.
It was 43. Further, when this porous rubber elastic body was used as an ink roll, good results similar to those in Example 1 were obtained.
なお、上記各実施例は、無発泡の加硫ゴム粉末
か発泡した加硫ゴム粉末のいずれか一方のみを用
いたものであるが、この無発泡の加硫ゴム粉末と
発泡した加硫ゴム粉末の両者を混合して用いても
よい。 In addition, each of the above examples uses only either non-foamed vulcanized rubber powder or foamed vulcanized rubber powder, but this non-foamed vulcanized rubber powder and foamed vulcanized rubber powder You may use a mixture of both.
また、上記実施例では多孔性ゴム弾性体をイン
クロールに適用したが、印材、事務機用ロール、
電子機器用ロール、各種のマツト材など種々の製
品として利用できることはもちろんである。 In addition, in the above example, the porous rubber elastic body was applied to the ink roll, but it can also be used for printing materials, rolls for office machines, etc.
Of course, it can be used for various products such as rolls for electronic devices and various pine materials.
第1図は加硫ゴム粉末の粒子構造を示す顕微鏡
写真、第2図は熱融解性皮膜を有する粉体の粒子
構造を示す顕微鏡写真、第3図は上記粉体の断面
構造を示す顕微鏡写真、第4図は上記粉体におけ
る塩素の分布状態を示す顕微鏡写真である。
Figure 1 is a micrograph showing the particle structure of the vulcanized rubber powder, Figure 2 is a microscope picture showing the particle structure of the powder with a heat-melting film, and Figure 3 is a microscope picture showing the cross-sectional structure of the powder. , FIG. 4 is a micrograph showing the distribution of chlorine in the powder.
Claims (1)
ム粉末の少なくとも一方と熱融解性粒子を含有す
るラテツクスとを混合した後、乾燥させる工程を
経て熱融解性皮膜を有する2層構造の粉体を形成
し、この粉体を焼結することを特徴とする多孔性
ゴム弾性体の製造方法。 2 ラテツクス中の熱融解性粒子は、その粒子径
が5μ以下である特許請求の範囲第1項に記載の
多孔性ゴム弾性体の製造方法。[Scope of Claims] 1. A method of mixing at least one of foamed vulcanized rubber powder or non-foamed vulcanized rubber powder with latex containing heat-melting particles and then drying the mixture to form a heat-melting film. A method for producing a porous rubber elastic body, which comprises forming a powder having a two-layer structure and sintering the powder. 2. The method for producing a porous rubber elastic body according to claim 1, wherein the heat-melting particles in the latex have a particle size of 5 μm or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6999086A JPS62225325A (en) | 1986-03-27 | 1986-03-27 | Manufacture of porous rubber elastic body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6999086A JPS62225325A (en) | 1986-03-27 | 1986-03-27 | Manufacture of porous rubber elastic body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62225325A JPS62225325A (en) | 1987-10-03 |
| JPH0566254B2 true JPH0566254B2 (en) | 1993-09-21 |
Family
ID=13418616
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6999086A Granted JPS62225325A (en) | 1986-03-27 | 1986-03-27 | Manufacture of porous rubber elastic body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62225325A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8141717B2 (en) | 2006-08-18 | 2012-03-27 | Porex Corporation | Sintered polymeric materials and applications thereof |
| EP2721103A1 (en) | 2011-06-15 | 2014-04-23 | Porex Corporation | Sintered porous plastic liquid barrier media and applications thereof |
| EP4034296A1 (en) | 2019-09-23 | 2022-08-03 | Porex Corporation | Sintered porous elastomeric material and application of the same |
-
1986
- 1986-03-27 JP JP6999086A patent/JPS62225325A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62225325A (en) | 1987-10-03 |
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