JPH0755540B2 - Method for manufacturing open cell sponge body - Google Patents
Method for manufacturing open cell sponge bodyInfo
- Publication number
- JPH0755540B2 JPH0755540B2 JP33468087A JP33468087A JPH0755540B2 JP H0755540 B2 JPH0755540 B2 JP H0755540B2 JP 33468087 A JP33468087 A JP 33468087A JP 33468087 A JP33468087 A JP 33468087A JP H0755540 B2 JPH0755540 B2 JP H0755540B2
- Authority
- JP
- Japan
- Prior art keywords
- sponge body
- sintered body
- rubber
- solvent
- sponge
- 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
Links
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、連続気泡スポンジ体の製造方法に関する。TECHNICAL FIELD The present invention relates to a method for producing an open-cell sponge body.
[従来の技術とその問題点] 従来、連続気泡で、かつ、気泡の大きさが5〜10μm位
の所謂ミクロスポンジであり、気孔率の安定したスポン
ジ体の製造方法として、溶出法、焼結法が行われてい
る。溶出法は、製造工程が多くなり、また溶出された溶
出物の処理に多くの費用を要する欠点がある。また、溶
出させるべき溶質を完全に除去するのに非常に労力を費
やし、完全に除去できないと製品中に残った溶質が使用
中に機械等を汚したりする問題があった。一方、焼結法
によるものでは、連泡性が良く、微細なセルを気孔率を
安定させて製造できるが、熱可塑性樹脂を使用するため
温度による硬度変化が大きく、耐圧縮性歪みが大きい欠
点がある。このため適用できる用途範囲が極めて狭い。[Conventional technology and its problems] Conventionally, a so-called micro sponge, which is an open cell and has a cell size of about 5 to 10 μm, is used as a method for producing a sponge body having a stable porosity. The law is taking place. The elution method has the drawbacks that the number of manufacturing steps is large and that processing of the eluted eluate is expensive. Further, it takes much labor to completely remove the solute to be eluted, and if it is not completely removed, there is a problem that the solute remaining in the product stains a machine or the like during use. On the other hand, by the sintering method, open cells have good open cell properties, and it is possible to manufacture fine cells with stable porosity, but since a thermoplastic resin is used, the hardness changes greatly with temperature and the compression strain is large. There is. Therefore, the applicable range of application is extremely narrow.
本発明は、かかる点に鑑みてなされたものであり、温度
による硬度変化が小さくて耐圧縮性歪みが小さく、しか
も、連泡性が良く、微細なセルを気孔率を安定させて容
易に製造できる連続気泡スポンジ体の製造方法を提供す
るものである。The present invention has been made in view of such a point, hardness change due to temperature is small, compression resistance strain is small, moreover, open cell property is good, fine cells can be easily manufactured with stable porosity. The present invention provides a method for producing an open cell sponge body.
[問題点を解決するための手段] 本発明は、加硫ゴム粉末又は熱可塑性樹脂粉末を熱可塑
性樹脂で混合・焼結して焼結体を得る工程と、該焼結体
に、架橋剤を混合したラテックス、溶剤で希釈した液状
ゴムと架橋剤の混合溶液、或は、ゴム配合物を溶剤で溶
液にしたゴム溶液のいずれかを含浸させる工程と、前記
焼結体の含浸物から水または溶剤を乾燥させて加熱・架
橋させてスポンジ体を形成する工程とを具備することを
特徴とする連続気泡スポンジ体の製造方法である。[Means for Solving Problems] The present invention relates to a step of mixing a vulcanized rubber powder or a thermoplastic resin powder with a thermoplastic resin and sintering the mixture to obtain a sintered body, and a crosslinking agent for the sintered body. A mixed latex of rubber, a mixed solution of a liquid rubber diluted with a solvent and a cross-linking agent, or a rubber solution prepared by dissolving a rubber compound in a solvent, and a step of impregnating the sintered body with water. Or a step of forming a sponge body by drying the solvent and heating / crosslinking the solvent to form a sponge body.
[作用] 本発明にかかる連続気泡スポンジ体の製造方法によれ
ば、予め加硫ゴム粉末又は熱可塑性樹脂粉末を熱可塑性
樹脂で混合・焼結して焼結体を形成しておきこれに、架
橋剤を混合したラテックス等を含浸させて加熱・架橋に
よってスポンジ体を形成するので、温度による硬度変化
が小さくて耐圧縮性歪みが小さく、しかも、連泡性が良
く、微細なセルを気孔率を安定させて容易に製造できる
ものである。[Operation] According to the method for producing an open-cell sponge body of the present invention, a vulcanized rubber powder or a thermoplastic resin powder is mixed and sintered with a thermoplastic resin in advance to form a sintered body. Since a sponge body is formed by impregnating latex mixed with a cross-linking agent and heating / cross-linking, hardness change with temperature is small and compression resistance strain is small. Is stable and can be easily manufactured.
[実施例] 以下、本発明の実施例について説明する。[Examples] Examples of the present invention will be described below.
実施例1 NBR(アクリロニトリルブタジエンゴム)配合物からな
る加硫されたゴム粉末100重量部に対して0.5〜5μmの
ポリ塩化ビニル(PVC)樹脂を20重量部と可塑剤DBP(ジ
ブチルフタレート)10重量部を混合・撹拌し、均一に混
合した粉末体を作る。次ぎにこの粉末を大きさが200x20
0mm、深さ3mmのメス型に充填し、1.5mmのオス型で蓋を
して押し込み、熱プレスによって10分間加圧した。これ
を離型して厚さ1.5mm、大きさ200x200mmの連続気泡の焼
結体を得た。Example 1 20 parts by weight of polyvinyl chloride (PVC) resin of 0.5 to 5 μm and 10 parts by weight of a plasticizer DBP (dibutyl phthalate) per 100 parts by weight of a vulcanized rubber powder composed of NBR (acrylonitrile butadiene rubber) compound. The parts are mixed and stirred to form a uniformly mixed powder. Then add this powder to a size of 200x20
It was filled in a female mold of 0 mm and a depth of 3 mm, and was capped with a male mold of 1.5 mm and pushed in, and pressed by a hot press for 10 minutes. This was released from the mold to obtain an open-cell sintered body having a thickness of 1.5 mm and a size of 200 × 200 mm.
次ぎにこの焼結体をシート状とし、これにNBRラテック
ス及びその架橋剤としてコロイド硫黄、亜鉛華1号、加
硫促進剤BZを混合・撹拌して含浸させ、然る後、室温ま
たは80℃のオーブンで乾燥後更に150℃のオーブンで30
分間加熱してラテックスを加硫させ、気孔率が45%のス
ポンジ体を製造した。Next, this sintered body is formed into a sheet, and NBR latex and colloidal sulfur as its cross-linking agent, zinc white No. 1 and vulcanization accelerator BZ are mixed and stirred to be impregnated, and then at room temperature or 80 ° C. After drying in the oven of 30
The latex was vulcanized by heating for a minute to produce a sponge body having a porosity of 45%.
得られたスポンジ体について50%圧縮を4日間行い圧縮
永久歪みテストを行なったところ、テスト後の肉厚減少
は5〜7%であったが、ラテックスを含浸させていない
焼結体の場合は20〜25%の肉厚減少が見られ、実施例1
のものでは十分に圧縮永久歪み特性が改善されているこ
とが分った。また、物理的強度も20〜30倍向上してお
り、更に低温・高温特性についても十分に改善されてい
ることが分った。A 50% compression of the obtained sponge body was carried out for 4 days and a compression set test was carried out. The reduction in wall thickness after the test was 5 to 7%, but in the case of a sintered body not impregnated with latex, A 20-25% reduction in wall thickness was observed, and Example 1
It was found that the material of No. 1 had sufficiently improved compression set characteristics. It was also found that the physical strength was improved 20 to 30 times, and the low temperature and high temperature characteristics were also sufficiently improved.
実施例2 実施例1で得た焼結体に、NBR原料ゴムと加硫剤を配合
したコンパンドにトルエンを混合・撹拌して溶液とした
ものを含浸させ、次いでこれからトルエンを除去した
後、150℃のオーブンで30分間加熱して加硫を行い連続
気泡のスポンジ体を得た。Example 2 The sintered body obtained in Example 1 was impregnated with a compound obtained by mixing NBR raw rubber and a vulcanizing agent with toluene and stirring the mixture to obtain a solution. Vulcanization was performed by heating in an oven at ℃ for 30 minutes to obtain a sponge body having open cells.
得られたスポンジ体について実施例1と同様に圧縮永久
歪み特性、物理的強度、低温・高温特性について調べた
ところ、いずれもNBR原料等を含浸していない焼結体の
ものに比べて遥かに改善されていることが分った。The compression set characteristics, physical strength, and low temperature / high temperature characteristics of the obtained sponge body were examined in the same manner as in Example 1. As a result, the sponge body was far better than the sintered body not impregnated with NBR raw material. I found that it was improved.
実施例3 実施例1で得た焼結体に、液状ポリウレタンゴムと架橋
剤を混合・撹拌してトルエンで希釈した溶液を含浸さ
せ、次いでこれからトルエンを除去した後、120℃のオ
ーブンで60分間加熱して加硫を行い連続気泡のスポンジ
体を得た。Example 3 The sintered body obtained in Example 1 was impregnated with a solution prepared by mixing and stirring liquid polyurethane rubber and a cross-linking agent and diluting with toluene, and then removing toluene from the solution, followed by 60 minutes in an oven at 120 ° C. It was heated and vulcanized to obtain a sponge body having open cells.
得られたスポンジ体について実施例1と同様に圧縮永久
歪み特性、物理的強度、低温・高温特性について調べた
ところ、いずれも液状ポリウレタンゴム等を含浸してい
ない焼結体のものに比べて遥かに改善されていることが
分った。The obtained sponge body was examined for compression set characteristics, physical strength, low temperature and high temperature characteristics in the same manner as in Example 1, and it was found that the sponge bodies were far superior to those of the sintered body not impregnated with liquid polyurethane rubber or the like. I found that it has been improved.
実施例4 NR(天然ゴム)を使用して実施例1と同様にして得た焼
結体に、NRラテックスとその架橋剤を混合・撹拌したも
のを含浸させた後、これから水分を乾燥除去し、150℃
のオーブンで30分間加熱して加硫を行い連続気泡のスポ
ンジ体を得た。Example 4 A sintered body obtained by using NR (natural rubber) in the same manner as in Example 1 was impregnated with a mixture of NR latex and its cross-linking agent and stirring, and then water was removed by drying. , 150 ℃
This was heated in the oven for 30 minutes for vulcanization to obtain an open-cell sponge body.
得られたスポンジ体について実施例1と同様に圧縮永久
歪み特性、物理的強度、低温・高温特性について調べた
ところ、いずれも天然ゴム原料等を含浸していない焼結
体のものに比べて遥かに改善されていることが分った。The obtained sponge body was examined for compression set characteristics, physical strength, low temperature and high temperature characteristics in the same manner as in Example 1, and it was found that they were far better than those of the sintered body not impregnated with natural rubber raw material. I found that it has been improved.
実施例5 フッ素ゴム配合物を使用して実施例1と同様にして得た
焼結体に、フッ素ゴムのラテックスとその架橋剤を混合
・撹拌したものを含浸させた後、これから水分を乾燥除
去し、150℃のオーブンで30分間加熱して加硫を行い連
続気泡のスポンジ体を得た。Example 5 A sintered body obtained by using a fluororubber compound in the same manner as in Example 1 was impregnated with a mixture of fluororubber latex and a crosslinking agent thereof and stirring, and then moisture was removed by drying. Then, it was heated in an oven at 150 ° C. for 30 minutes for vulcanization to obtain an open-cell sponge body.
得られたスポンジ体について実施例1と同様に圧縮永久
歪み特性、物理的強度、低温・高温特性について調べた
ところ、いずれもフッ素ゴムの配合物等を含浸していな
い焼結体のものに比べて遥かに改善されていることが分
った。The resulting sponge body was examined for compression set characteristics, physical strength, low temperature and high temperature characteristics in the same manner as in Example 1. As a result, in comparison with a sintered body not impregnated with a fluororubber compound, etc. I found that it has been improved much.
[発明の効果] 以上説明した如く、本発明にかかる連続気泡スポンジ体
の製造方法によれば、温度による硬化変化が小さくて耐
圧縮性歪みが小さく、しかも、連泡性が良く、微細なセ
ルを気孔率を安定させて容易に製造できるものである。[Effects of the Invention] As described above, according to the method for producing an open-cell sponge body of the present invention, the change in curing due to temperature is small, the compression strain is small, the open-cell property is good, and the fine cells are fine. Can be easily manufactured with stable porosity.
Claims (1)
塑性樹脂で混合・焼結して焼結体を得る工程と、該焼結
体に、架橋剤を混合したラテックス、溶剤で希釈した液
状ゴムと架橋剤の混合溶液、或は、ゴム配合物を溶剤で
溶液にしたゴム溶液のいずれかを含浸させる工程と、前
記焼結体の含浸物から水または溶剤を乾燥させて加熱・
架橋させてスポンジ体を形成する工程とを具備すること
を特徴とする連続気泡スポンジ体の製造方法。1. A step of mixing and sintering a vulcanized rubber powder or a thermoplastic resin powder with a thermoplastic resin to obtain a sintered body, and diluting the sintered body with a latex containing a crosslinking agent and a solvent. A step of impregnating either a mixed solution of liquid rubber and a cross-linking agent or a rubber solution obtained by making a rubber compound into a solution with a solvent, and drying water or a solvent from the impregnated material of the sintered body and heating.
And a step of forming a sponge body by crosslinking the sponge body.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP33468087A JPH0755540B2 (en) | 1987-12-28 | 1987-12-28 | Method for manufacturing open cell sponge body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP33468087A JPH0755540B2 (en) | 1987-12-28 | 1987-12-28 | Method for manufacturing open cell sponge body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01171930A JPH01171930A (en) | 1989-07-06 |
| JPH0755540B2 true JPH0755540B2 (en) | 1995-06-14 |
Family
ID=18280037
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP33468087A Expired - Fee Related JPH0755540B2 (en) | 1987-12-28 | 1987-12-28 | Method for manufacturing open cell sponge body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0755540B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8141717B2 (en) | 2006-08-18 | 2012-03-27 | Porex Corporation | Sintered polymeric materials and applications thereof |
-
1987
- 1987-12-28 JP JP33468087A patent/JPH0755540B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01171930A (en) | 1989-07-06 |
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