JPS6128693B2 - - Google Patents
Info
- Publication number
- JPS6128693B2 JPS6128693B2 JP12743781A JP12743781A JPS6128693B2 JP S6128693 B2 JPS6128693 B2 JP S6128693B2 JP 12743781 A JP12743781 A JP 12743781A JP 12743781 A JP12743781 A JP 12743781A JP S6128693 B2 JPS6128693 B2 JP S6128693B2
- Authority
- JP
- Japan
- Prior art keywords
- foam
- sealing material
- adhesive
- foamed
- foaming agent
- 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
Links
- 239000006260 foam Substances 0.000 claims description 34
- 239000003566 sealing material Substances 0.000 claims description 22
- 230000001070 adhesive effect Effects 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 14
- 239000004088 foaming agent Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 13
- 239000000853 adhesive Substances 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000011148 porous material Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- 238000001035 drying Methods 0.000 description 8
- 238000005470 impregnation Methods 0.000 description 8
- 238000005187 foaming Methods 0.000 description 7
- 239000011344 liquid material Substances 0.000 description 6
- 239000000565 sealant Substances 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- VJRITMATACIYAF-UHFFFAOYSA-N benzenesulfonohydrazide Chemical compound NNS(=O)(=O)C1=CC=CC=C1 VJRITMATACIYAF-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- -1 heat dry it Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000002832 nitroso derivatives Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Gasket Seals (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
この発明は建築、土木、車輌、弱電関係などの
各種構造物の間隙を埋めるために用いられる発泡
弾性シール材の製造方法に関する。
従来、発泡弾性シール材として、アスフアルト
の如き瀝青物質やポリアクリル酸エステル、ポリ
イソブチレン、エチレン−酢酸ビニル共重合物な
どの合成樹脂、その他スチレン−ブタジエン共重
合ゴム、エチレン−プロピレン共重合ゴムなどの
合成ゴムからなる被膜形成物質を有機溶剤に溶解
させあるいは水に乳化させてなる液状物を調製
し、これをポリウレタン系発泡体やポリ塩化ビニ
ル系発泡体などの連続発泡体に含浸被覆させ、加
熱乾燥してなるものが知られている。上記の被膜
形成物質は連続発泡体の孔壁全体に被膜を形成し
て孔内を適度に充てんし防水性を発揮させるため
のものである。
この種のシール材においては、液状物の含浸量
つまり孔壁に形成される被膜の厚みによつて通気
度が変化し、含浸量を多くすればするほど通気度
が小さくなり防水性の面で好結果が得られる。し
かし、その反面シール材圧縮時比較的高温状態に
おかれたとき含浸されたものが圧力、温度により
連続発泡体から流れ出しやすくなり、構造物や作
業者への汚染性を増す。特にこの傾向は被膜形成
物質が粘着性を有するものである場合に顕著とな
る。
また、シール材自体の重量が重くなつて作業性
や経済性の面で不利となるばかりか、施工箇所が
限られる、本来のシール機能を充分に発揮できな
い、外観に劣るなどの欠点が生じてくる。この理
由は明らかで、含浸量の増加に伴いシール材自体
が硬くなるため、被着体の凹凸面にシール材を良
好に追随密着させにくくなり、またひも状シール
材を曲率面を有する被着体に適用する際にシール
材の内外周面側で曲げ破壊を生じやすく、さらに
圧縮率が限定される結果極端な凹凸を有する被着
体に圧縮充てんしにくいなどの理由による。
一方、かかる問題を解消するために、含浸量を
少なくし被膜厚みを薄くすると、通気度が大とな
り防水性の面で満足できなくなる。
この発明は、上記従来の欠点を回避せんとする
もので、その要旨とするところは、連続発泡体に
感熱発泡剤と粘着性を有する被膜形成物質とを含
ませた液状物を含浸させたのち、加熱により上記
発泡剤をガス化発泡させながら乾燥して、上記発
泡体の孔壁に粘着性発泡被膜を形成することを特
徴とする発泡弾性シール材の製造方法にある。
すなわち、この発明においては、含浸させるべ
き液状物にあらかじめ感熱発泡剤を含ませてお
き、これを連続発泡体に含浸後加熱乾燥する際に
上記発泡剤をガス化発泡させることにより、連続
発泡体の孔壁に粘着性発泡被膜を形成するように
したもので、この発泡被膜は発泡構造であるがた
めにその厚みを相当厚くしてもシール材の重量を
重くしたり硬くする心配が少なく、しかもシール
材の圧縮率を高次に保持させる。
このため、かかる粘着性発泡被膜を設けたこの
発明の発泡弾性シール材によれば、所期するとお
りの防水性能を発揮できるとともに、従来の如き
含浸量過多による流れ出しないし汚染性やその重
量増加に起因した作業性や経済性の面での不利を
きたすことがない。また、シール材自体が柔軟で
かつ高い圧縮率を与え、しかも発泡被膜が粘着性
を有するものであるため、被着体の凹凸面に対し
て良好に追随密着させることができ、また曲率面
への施工に当たつて曲げ破壊を生じさせる心配が
少なく、さらに極端な凹凸を有する被着体に対し
ても良好に圧縮充てんできるなどの利点が得ら
れ、これによつて施工箇所につきとくに限定され
ることなく各種の被着体に対し外観およびシール
機能良好にシールすることができる。
この発明において用いられる連続発泡体は、ウ
レタン系発泡体であつてもその他の発泡体であつ
てもよく、連続気泡性を有するものであれば従来
公知のものを広く適用することができる。代表的
なものとしては、ポリエーテル系ないしポリエス
テル系のウレタン発泡体、ポリ塩化ビニル系発泡
体などがある。
この発泡体に含浸させる液状物のタイプは、有
機溶剤系、水性エマルジヨン系など従来含浸用液
として用いられている各種タイプのものがいずれ
も適用可能である。この液状物に含ませる被膜形
成物質としては、粘着性を有するものであること
が必要で、すでに述べたようなアスフアルトの如
き瀝青物質やポリアクリル酸エステル、ポリイソ
ブチレン、オチレン−酢酸ビニル共重合物などの
各種合成樹脂その他天然ゴム、スチレン−ブタジ
エン共重合ゴム、エチレン−プロピレン共重合ゴ
ムなどの合成ゴムなどを主材としたものの中から
粘着性を有するものが選択使用される。この被膜
形成物質の液状物中に占める割合は、通常30〜70
重量%程度である。
また上記被膜形成物質とともに用いられる感熱
発泡剤としては、形成される粘着性発泡被膜が独
立気泡構造となるものが好ましいが、連続気泡構
造となるものであつてもよい。独立気泡構造を与
える発泡剤としては、たとえばアゾジカルボンア
ミド、アソビスイソブチロニトリルのようなアゾ
化合物、ジニトロソペンタメチレンテトラミンな
どのニトロソ化合物、パラトルエンスルホニルヒ
ドラジツド、4・4′−オキシビスベンゼンスルホ
ニルヒドラジツドなどのスルホニルヒドラジツド
化合物などが挙げられる。また、粘着性発泡被膜
を連続気泡構造とする場合、一般に分解温度の低
いものがよく、上述の如き発泡剤に有機酸や尿素
の如く発泡助剤を加えたものを用いると分解温度
が下がり、連続気泡構造となりやすい。
感熱発泡剤の使用量は、加熱発泡させたときの
発泡倍率が1.1〜10倍、とくに好適には3〜5倍
となるように、粘着性被膜形成物質の種類および
液状物中に占める割合に応じて適宜設定すること
ができる。一般には、粘着性被膜形成物質100重
量部に対して2〜20重量部程度である。
この発明において連続発泡体に上述した液状物
を含浸し加熱乾燥して発泡させる手段は任意でよ
く、また含浸工程と加熱乾燥(発泡)工程とを連
続工程としても非連続工程としてもよい。連続工
程とする場合、たとえば第1図に示される如く、
ロール状に巻回された連続発泡体1を含浸用液状
物2の貯槽3に含浸ロール4,4を介して導き、
含浸調節ロール5,5によつて適量含浸させたの
ち、加熱乾燥室6に導通して発泡と液媒体の乾燥
とを同時に行わせればよい。
含浸量は、連続発泡体の種類や比重、含浸用液
状物の種類や粘度あるいはシール材の用途目的な
どによつてかなり相違するが、一般には連続発泡
体に対し粘着性被膜形成物質を主とする固形分重
量比で0.1〜10倍、とくに好適には0.5〜5倍とす
るのがよい。前述したとおり、この発明では、上
記の含浸量を従来に較べて少なくする一方、含浸
後の発泡によつて形成される被膜厚みを厚くでき
るという特徴を有している。加熱乾燥室での切熱
手段としては熱風吹きつけやその他公知の手段を
とれるが、加熱温度は感熱発泡剤をガス化発泡で
きかつ液媒体を揮散除去できる温度とされる。
第1図において、7は上記の如くして得られる
この発明の発泡弾性シール材をロール状に巻回し
た状態を示したもので、このシール材は前記した
とおりのすぐれた防水機能ないしシール機能を具
備し、建築、土木、車輌、弱電関係などの各種構
造物の間隙を埋めるためのシール材として有効に
利用することができる。
つぎに、この発明の実施例を記載する。
実施例
ポリアクリル酸ブチル100重量部とジニトロソ
ペンタメチレンテトラミン5重量部とを溶解混合
させた固形分30重量%、粘度(20℃)500センチ
ポイズのトルエン溶液を調製し、これを、比重
0.030のポリエーテル系のウレタン発泡体(10mm
×1000mm×2000mm)に、固形分重量比で4倍とな
るように、2本ロールを備えた含浸液槽で含浸さ
せ、その後加熱乾燥室で140℃で10分間加熱して
ガス化発泡させながら溶媒を揮散除去し、この発
明の発泡弾性シール材を得た。このシール材の粘
着性発泡被膜は、3〜4倍の発泡倍率、つまり発
泡剤を含ませないものに較べて3〜4倍の厚みを
有していた。
比較例
含浸用溶液中から発泡剤(ジニトロソペンタメ
チレンテトラミン)を除くとともに、含浸量を多
くして加熱乾燥後の被膜厚みが実施例の粘着性発
泡被膜と同厚となるようにした以外は、実施例と
同様の操作によつて発泡弾性シール材を得た。
上記の実施例および比較例の各シール材の特性
を評価したところ、つぎの表に示されるとおりで
あつた。
The present invention relates to a method for manufacturing a foamed elastic sealing material used to fill gaps in various structures such as buildings, civil engineering, vehicles, and light electrical equipment. Conventionally, as foamed elastic sealing materials, bituminous substances such as asphalt, synthetic resins such as polyacrylic esters, polyisobutylene, ethylene-vinyl acetate copolymers, and other styrene-butadiene copolymer rubbers, ethylene-propylene copolymer rubbers, etc. A liquid substance is prepared by dissolving a film-forming substance made of synthetic rubber in an organic solvent or emulsifying it in water, and this is impregnated and coated on an open foam such as polyurethane foam or polyvinyl chloride foam, and then heated. It is known to be dried. The above-mentioned film-forming substance is used to form a film on the entire pore walls of the open foam to appropriately fill the pores and exhibit waterproof properties. In this type of sealing material, the air permeability changes depending on the amount of liquid impregnated, that is, the thickness of the coating formed on the hole wall. Good results can be obtained. However, on the other hand, when the sealing material is compressed at a relatively high temperature, the impregnated material tends to flow out of the open foam due to pressure and temperature, increasing the risk of contaminating structures and workers. This tendency is particularly noticeable when the film-forming substance has adhesive properties. In addition, the weight of the sealing material itself becomes heavy, which is disadvantageous in terms of workability and economic efficiency, and it also has drawbacks such as limited application areas, inability to fully demonstrate its original sealing function, and poor appearance. come. The reason for this is obvious: as the amount of impregnation increases, the sealant itself becomes harder, making it difficult to properly follow and adhere the sealant to the uneven surface of the adherend. This is because, when applied to a body, bending failure tends to occur on the inner and outer circumferential surfaces of the sealing material, and furthermore, the compressibility is limited, making it difficult to compress and fill adherends with extremely uneven surfaces. On the other hand, in order to solve this problem, if the amount of impregnation is reduced and the thickness of the coating is made thin, the air permeability becomes large and the waterproof property becomes unsatisfactory. This invention aims to avoid the above-mentioned conventional drawbacks, and its gist is that after impregnating an open foam with a liquid material containing a heat-sensitive foaming agent and an adhesive film-forming substance, , a method for producing a foamed elastic sealing material, comprising drying the foaming agent while gasifying and foaming it by heating to form an adhesive foam coating on the pore walls of the foam. That is, in this invention, a heat-sensitive foaming agent is pre-impregnated into the liquid material to be impregnated, and the foaming agent is gasified and foamed when the open foam is impregnated with the heat-sensitive foam and then dried by heating. An adhesive foam coating is formed on the hole walls of the sealant, and since this foam coating has a foam structure, even if the thickness of the foam coating is made considerably thick, there is no need to worry about adding weight or hardness to the sealing material. Moreover, the compressibility of the sealing material is maintained at a high level. Therefore, according to the foamed elastic sealing material of the present invention provided with such an adhesive foamed coating, it is possible to exhibit the desired waterproof performance, and it is also possible to prevent run-off, contamination, and increase in weight due to excessive impregnated amount as in the past. There is no disadvantage in terms of workability or economic efficiency. In addition, since the sealant itself is flexible and has a high compressibility, and the foam coating has adhesive properties, it can adhere well to uneven surfaces of adherends, and can also adhere to curved surfaces. It has the advantage that there is less risk of bending failure during construction, and it can be compressed and filled well even to adherends with extremely uneven surfaces. It is possible to seal various adherends with good appearance and sealing function without any problems. The open foam used in this invention may be a urethane foam or other foam, and a wide range of conventionally known foams can be used as long as they have open cell properties. Typical examples include polyether-based or polyester-based urethane foams and polyvinyl chloride-based foams. The type of liquid to be impregnated into the foam may be any of the various types conventionally used as impregnating liquids, such as organic solvent-based and aqueous emulsion-based liquids. The film-forming substance to be included in this liquid must have adhesive properties, such as bituminous substances such as asphalt as already mentioned, polyacrylic esters, polyisobutylene, and ethylene-vinyl acetate copolymers. Those having adhesive properties are selected from among various synthetic resins such as , natural rubber, styrene-butadiene copolymer rubber, ethylene-propylene copolymer rubber, and other synthetic rubbers as main materials. The proportion of this film-forming substance in the liquid is usually 30 to 70.
It is about % by weight. The heat-sensitive foaming agent used together with the film-forming substance is preferably one that gives the adhesive foamed film a closed-cell structure, but it may also have an open-cell structure. Examples of blowing agents that provide a closed cell structure include azo compounds such as azodicarbonamide and azobisisobutyronitrile, nitroso compounds such as dinitrosopentamethylenetetramine, paratoluenesulfonyl hydrazide, and 4,4'-oxybis Examples include sulfonyl hydrazide compounds such as benzenesulfonyl hydrazide. In addition, when forming an adhesive foam coating into an open-cell structure, it is generally preferable to use a foam with a low decomposition temperature, and using a foaming agent such as the one described above with a foaming aid such as an organic acid or urea lowers the decomposition temperature. It tends to have an open cell structure. The amount of the heat-sensitive foaming agent to be used depends on the type of adhesive film-forming substance and its proportion in the liquid so that the foaming ratio when heated and foamed is 1.1 to 10 times, particularly preferably 3 to 5 times. It can be set as appropriate. Generally, the amount is about 2 to 20 parts by weight per 100 parts by weight of the adhesive film-forming substance. In the present invention, any means may be used to impregnate the open foam with the above-mentioned liquid material, heat dry it, and foam it, and the impregnation step and heat drying (foaming) step may be continuous or discontinuous steps. If it is a continuous process, for example as shown in Figure 1,
The continuous foam 1 wound into a roll is introduced into a storage tank 3 for impregnating liquid material 2 via impregnating rolls 4, 4,
After impregnating an appropriate amount with the impregnation control rolls 5, 5, the heating and drying chamber 6 is connected to perform foaming and drying of the liquid medium at the same time. The amount of impregnation varies considerably depending on the type and specific gravity of the open foam, the type and viscosity of the impregnating liquid, and the intended use of the sealant, but in general, it is The solid content weight ratio is preferably 0.1 to 10 times, particularly preferably 0.5 to 5 times. As described above, the present invention is characterized in that the above-mentioned amount of impregnation can be reduced compared to the conventional method, and the thickness of the coating formed by foaming after impregnation can be increased. As a heating means in the heating drying chamber, blowing hot air or other known means can be used, but the heating temperature is set to a temperature at which the heat-sensitive foaming agent can be gasified and foamed and the liquid medium can be volatilized and removed. In FIG. 1, numeral 7 shows the state in which the foamed elastic sealing material of the present invention obtained as described above is wound into a roll. It can be effectively used as a sealing material to fill gaps in various structures such as architecture, civil engineering, vehicles, and light electrical equipment. Next, examples of this invention will be described. Example A toluene solution with a solid content of 30% by weight and a viscosity (20°C) of 500 centipoise was prepared by dissolving and mixing 100 parts by weight of butyl polyacrylate and 5 parts by weight of dinitrosopentamethylenetetramine.
0.030 polyether urethane foam (10mm
x 1000mm x 2000mm) in an impregnating liquid tank equipped with two rolls so that the solid content is 4 times the weight ratio, and then heated in a heating drying room at 140℃ for 10 minutes to gasify and foam. The solvent was removed by volatilization to obtain a foamed elastic sealing material of the present invention. The adhesive foam coating of this sealing material had a foaming ratio of 3 to 4 times, that is, a thickness of 3 to 4 times that of one not containing a foaming agent. Comparative Example Except that the foaming agent (dinitrosopentamethylenetetramine) was removed from the impregnating solution and the amount of impregnation was increased so that the coating thickness after heat drying was the same as the adhesive foam coating of the example. A foamed elastic sealing material was obtained by the same operation as in the example. The characteristics of each of the sealing materials of the above Examples and Comparative Examples were evaluated and were as shown in the following table.
【表】【table】
【表】
上表から明らかなように、この発明の発泡弾性
シール材は、シール材として好適な特性を有して
いるものであることが判る。[Table] As is clear from the above table, it can be seen that the foamed elastic sealing material of the present invention has suitable characteristics as a sealing material.
第1図はこの発明の発泡弾性シール材の製造例
を説明するための概略図、第2図は発泡弾性シー
ル材の水密性を調べるために用いた装置の形状寸
法を示した断面図である。
1……連続発泡体、2……感熱発泡剤と粘着性
被膜形成物質とを含ませた液状物、3……液状物
の貯槽、6……加熱乾燥室、7……発泡弾性シー
ル材。
FIG. 1 is a schematic diagram for explaining an example of manufacturing the foamed elastic sealing material of the present invention, and FIG. 2 is a sectional view showing the shape and dimensions of an apparatus used to examine the watertightness of the foamed elastic sealing material. . DESCRIPTION OF SYMBOLS 1... Continuous foam, 2... Liquid material containing a heat-sensitive foaming agent and adhesive film forming substance, 3... Liquid material storage tank, 6... Heating drying chamber, 7... Foamed elastic sealing material.
Claims (1)
膜形成物質とを含ませた液状物を含浸させたの
ち、加熱により上記発泡剤をガス化発泡させなが
ら乾燥して、上記発泡体の孔壁に粘着性発泡被膜
を形成することを特徴とする発泡弾性シール材の
製造方法。1. After impregnating an open foam with a liquid containing a heat-sensitive foaming agent and an adhesive film-forming substance, the foaming agent is dried while being gasified and foamed by heating, and the pore walls of the foam are A method for producing a foamed elastic sealing material, the method comprising forming an adhesive foamed film on.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12743781A JPS5829840A (en) | 1981-08-13 | 1981-08-13 | Production of expanded elastic sealing material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12743781A JPS5829840A (en) | 1981-08-13 | 1981-08-13 | Production of expanded elastic sealing material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5829840A JPS5829840A (en) | 1983-02-22 |
JPS6128693B2 true JPS6128693B2 (en) | 1986-07-02 |
Family
ID=14959922
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12743781A Granted JPS5829840A (en) | 1981-08-13 | 1981-08-13 | Production of expanded elastic sealing material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5829840A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63136422A (en) * | 1986-11-26 | 1988-06-08 | 三和工業株式会社 | Manufacture of cable using thermally foaming tape |
JPH039173A (en) * | 1989-06-07 | 1991-01-17 | Nitto Denko Corp | Ventilating packing material |
-
1981
- 1981-08-13 JP JP12743781A patent/JPS5829840A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5829840A (en) | 1983-02-22 |
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