JPS6310745B2 - - Google Patents
Info
- Publication number
- JPS6310745B2 JPS6310745B2 JP55021466A JP2146680A JPS6310745B2 JP S6310745 B2 JPS6310745 B2 JP S6310745B2 JP 55021466 A JP55021466 A JP 55021466A JP 2146680 A JP2146680 A JP 2146680A JP S6310745 B2 JPS6310745 B2 JP S6310745B2
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- propellant
- emulsion
- pressure
- container
- 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
- 239000000853 adhesive Substances 0.000 claims description 81
- 230000001070 adhesive effect Effects 0.000 claims description 81
- 239000003380 propellant Substances 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000006260 foam Substances 0.000 claims description 14
- 239000000839 emulsion Substances 0.000 claims description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 239000001273 butane Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 4
- 239000001294 propane Substances 0.000 claims description 4
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 3
- 239000011118 polyvinyl acetate Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 238000005187 foaming Methods 0.000 description 13
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 239000004570 mortar (masonry) Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 229920005789 ACRONAL® acrylic binder Polymers 0.000 description 4
- 239000012790 adhesive layer Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000011120 plywood Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- HOWJQLVNDUGZBI-UHFFFAOYSA-N butane;propane Chemical compound CCC.CCCC HOWJQLVNDUGZBI-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- -1 chlorofluorocarbons Chemical compound 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000008257 shaving cream Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical group ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Nozzles (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
本発明は、発泡性接着剤の塗布方法に関する。
一般に、接着剤を用いて多孔質表面や凹凸のは
げしい表面、例えば発泡ウレタンや布等を接着さ
せる場合には、接着力が充分に発揮されず、例え
ば、これら被着体の孔部、繊維の間隙、凹部に接
着剤が流入するため、平滑面を接着させる場合の
数倍の塗布量を通常必要とし、また塗り広げにく
いという欠点がある。
そのため、近年に至つては、撹拌容器内で泡立
てミキサーにより接着剤を泡立てて接着剤の吸収
を防止し、かつ塗り広げやすくする技術が提案さ
れているが、必要以上に界面活性剤等の起泡剤を
添加する必要があり、接着性能の低下を来たす。
また、塗布直前に泡立てる必要があり、繰返し撹
拌しなければならない。さらに、発泡した接着剤
は取り扱いにくいにもかかわらず、撹拌容器から
これをすくい取つて塗布しなければならず、塗布
作業は煩雑である。しかも、この種の発泡方法で
は、撹拌容器内で発泡むらが生じやすく、付着む
らが生ずる場合がある。特に、鉛直面に塗布した
場合、撹拌むらがあると垂れ落ちの原因となる。
また、壁面に壁紙を貼着する場合、一般に、接
着剤層を薄くしないと貼着施行後、壁紙の表面が
でこぼこになる。しかし、壁面または壁紙に美麗
な仕上状態になる程度に接着剤を薄く塗布するこ
とは実際の施行ではきわめて困難で、多大の手間
と時間を要する。このため、壁紙の裏面に予め粘
着剤または再湿活性の接着剤を塗布したものが市
販されているが、粘着剤タイプのものは一旦粘着
したら修正が不可能であり、また再湿活性タイプ
のものも一度水に湿めさなければならず煩雑であ
る。
このような事情のもとに、均一な発泡性を示
し、被着面に直接かつ均一に塗布することがで
き、しかも薄塗、厚塗も自由な発泡性接着剤を得
るべく、種々研究した結果、耐圧容器内にエマル
ジヨン型水性接着剤を噴射剤とともに一定割合で
封入し、該噴射剤を接着剤とともに耐圧容器外に
噴出させると、接着剤の均一な発泡が形成される
ことを見い出し、本発明を完成するに至つた。
従来、エアゾル型式の接着剤が知られている
が、いずれも接着剤が霧状にスプレーされるもの
で、特にエマルジヨン型水性接着剤と噴射剤とを
耐圧容器内に封入し、これを噴出させることによ
り均一な発泡性接着剤を得ることは本発明者によ
り初めて見い出されたものである。
本発明の目的は、エマルジヨン型水性接着剤と
噴射剤、好ましくは液化プロパンおよび/または
液化ブタンとを耐圧容器内に封入してなる発泡性
接着剤の塗布方法を提供することである。
かかる発泡性接着剤は、該噴射剤を接着剤とと
もに耐圧容器外にそのノズルを介して噴射させる
ことにより接着剤が発泡するものであるから、被
着面に向けて噴射させれば、直接被着面発泡した
接着剤を塗布することができる。
したがつて、本発明は、エマルジヨン型水性接
着剤を噴射剤とともに一定割合で耐圧容器内に封
入し、該噴射剤とともに上記接着剤を耐圧容器の
ノズルから噴出させて直接被着面に接着剤を泡状
に形成塗布する発泡性接着剤の塗布方法を提供す
るものである。
特に、接着剤と噴射剤との容量配合比は、下記
に例示する種類・粘度等によつても異なるが、通
常使用される接着剤を用いる場合、均一な発泡を
形成するためには、液体状態にある噴射剤を基準
として、とくに90:10〜70:30の範囲が望まし
い。この範囲だと、接着剤がノズルよりひも状ま
たは切れたひも状に発射され、被着体面に付着し
てからさらに発泡する。この場合にはノズルを被
着体に接近させなくても目的の部分にのみ離れた
ところから塗布作業ができるため、壁などの被着
体に対する塗布作業の能率を向上させることがで
きる。なお上記範囲より接着剤成分が多くなる
と、充分な発泡性が得られず、これより少なくな
ると、接着剤が霧状にスプレーされて好ましくな
い。
本発明において用いられる接着剤成分として
は、エマルジヨン型水性接着剤以外に、水溶液型
接着剤の使用が考えられるが、水溶液型接着剤に
比較してエマルジヨン型水性接着剤を配合した方
が、きめ細かい均一な発泡が得やすく、しかも鉛
直面に塗布する場合に垂れ落ちにくい。また、同
粘度ではエマルジヨン型水性接着剤の方が固形分
を多くできるので、吐出量が調節しやすく、塗布
した場合押し広げやすい。これらの点から、エマ
ルジヨン型水性接着剤を配合する方が望ましい。
エマルジヨン型水性接着剤としては、ポリアク
リルエマルジヨンまたはポリ酢酸ビニルエマルジ
ヨンを使用する。
これら水系エマルジヨン型水性接着剤には、所
望により、各種界面活性剤、ロジン、変性フエノ
ール樹脂、テルペン、石油樹脂、クマロンインデ
ン樹脂のようなタツキフアイヤー、炭酸カルシウ
ム、クレー、シリカ、アスベストのような充填
剤、高級アルコール、グリコール、フタル酸エス
テルのような可塑剤、チタン白その他の染顔料の
ような着色剤、酸化防止剤、防カビ剤などを添加
してもよい。通常、これら添加剤を含めて固形分
15〜75%のものが使用される。
本発明で使用される噴射剤としては、プロパ
ン、ブタン、フロン、二酸化炭素、ジメチルエー
テル、窒素またはそれらの混合物等が挙げられる
が、耐圧容器内では噴射剤と接着剤は二層に分離
することがあるため、接着剤を最後まで無駄なく
吐出させるには、接着剤より液化した噴射剤の比
重が軽い方がよく、また接着剤の安定性を保持し
泡の生成を高めるには噴射剤が水に溶け込まない
方が望ましい。この点から、液化プロパン、液化
ブタンもしくは液化フロンまたはこれらの混合物
を使用する。
上記接着剤と噴射剤とを適宜上述した容量配合
比で組合わせて発泡性接着剤を構成することがで
きる。該発泡性接着剤は第1図に示すような耐圧
容器に常法にしたがつて封入される。
第2図は第1図に示す耐圧容器の上部断面図
で、アルミニウム容器1は、かん胴部1aの開口
部にふた体1bが巻締られて形成される。該ふた
体1bの中央部には、噴射用部材2が装着されて
いる。該噴射用部材2は環状のハウジング3の上
端開口にステムラバー4が取付けてあり、該ラバ
ーの中央部孔を通して流路5aを有するステム5
がハウジング3の内に挿入され、ハウジング内側
底部に設けられたスプリング6により上方に付勢
されている。該ステム5の上端には、開放したく
ちばし状のノズル部7aを有する押圧ボタン7が
取付けてある。一方、ハウジング3の底部には開
口があり、容器下方に延びるスタンドパイプ8に
連通している。したがつて、押圧ボタン7を押下
げると、ステム5の流路5aはその入口がステム
ラバー4との当接を解除され、噴射用部材2が開
放状態(第3図参照)となるため、接着剤Aは噴
射剤Bにより発泡されながら、ノズル部7aを介
して外部に噴出されることになる。
被着面に発泡した接着剤を塗布した後、第4図
に示すようにヘラ兼用キヤツプ10を用い、接着
剤層を平担にすることもできる。
該ヘラ兼用キヤツプ10は、キヤツプ部11の
上部にヘラ部12を備え、その上端には広い波形
状端部12aが形成されている。使用の際、キヤ
ツプ部11は把持部として使用できる(第4図参
照)。
第5図は他の態様の耐圧容器による発泡塗布の
状態を示し、押圧ボタン7のノズル部7aは径の
小さいもので、これにより塗布面において接着剤
が発泡するため離れた所から塗布作業が行なえる
利点を有する。
本発明によれば、水系エマルジヨン型接着剤を
噴射剤とともに耐圧容器内に封入して発泡性接着
剤を構成することができるので、従来のように必
要以上の界面活性剤等の起泡剤とともに接着剤を
撹拌容器に入れ、泡立てミキサーにより発泡さ
せ、これをすくい取つて塗布するという煩雑な作
業を要せず、耐圧容器のノズル口を被着面に向
け、単に押圧ボタンを押下げれば、発泡した接着
剤が吐出して被着面に塗布され、塗布作業が極め
て簡単である。また、接着剤が発泡状態で塗布さ
れるので、被着面が多孔質、繊維質、凹凸面に吸
収することがない。また、簡単に押し広げること
ができるので、少量の接着剤で薄く広い接着剤層
を形成することができる。さらに、接着剤が泡状
となるため、乾燥速度を適当に調節でき、しかも
厚塗や厚みにむらのある塗布をしても気泡が体積
のほとんどをしめるため、乾燥後は全く目立たな
くなり、壁紙等広い被着面の接着に適当である。
また塗布の際はみ出た場合でも、発泡体であるた
め、取除き易くまた乾燥すれば目立たなくなる。
さらに、霧状となつて飛散しないので、安全衛生
上の問題もない。また、ノズルの吐出口の大きさ
は吐出量に応じて細いスプレータイプからシエー
ビングクリーム用の広口タイプまで自由に選ぶこ
とができ、耐圧容器内に比較的多量の噴射剤が封
入されるので、従来のエアーゾル型接着剤のよう
にノズルが詰まることはほとんどなくなる等種々
の利点を有する。
以下、本発明を実施例にもとずき、さらに具体
的に説明する。
実施例 1
ポリアクリルエマルジヨン(油化バデイシユ社
製アクロナール80D) 90部(容量)
液化プロパン―ブタン混合物(容量比40:60)
10部
上記成分をそれぞれ同じアルミニウム製耐圧容
器に入れ、5分間よく振盪して発泡性接着剤を得
る。(発泡倍率16倍)
実施例 2
ポリ酢酸ビニルエマルジヨン(大同化成工業社
製ビニゾール#210) 77部
水 13部
液化フロン 10部
上記成分をそれぞれ同じアルミニウム製耐圧容
器に入れ、5分間よく振盪して発泡性接着剤を得
る。(発泡倍率18倍)
実施例 3
合板(100×100×5mm)の片面上に、実施例1
および2の発泡性接着剤を耐圧容器より吐出さ
せ、巾3cmの発泡性接着剤層を一条形成塗布し、
その上からキヤンバス(100×100mm)を押し当
て、そのまま24時間放置してそのキヤンバスの剥
離接着強度を測定した。一方、アクロナール80D
およびビニゾール#210をハケで上記と同一の合
板片側全面に塗布し、その上に上記と同一のキヤ
ンバスを押し当て、そのまま24時間放置してその
キヤンバスの剥離接着強度を測定し、結果を下記
第1表に示す。
The present invention relates to a method of applying a foamable adhesive. In general, when adhesives are used to bond porous or highly uneven surfaces, such as foamed urethane or cloth, the adhesive strength is not sufficiently exerted. Since the adhesive flows into the gaps and recesses, it usually requires several times the amount to be applied than when bonding a smooth surface, and it also has the disadvantage that it is difficult to spread. Therefore, in recent years, a technology has been proposed in which the adhesive is foamed using a foaming mixer in a stirring container to prevent the adhesive from being absorbed and to make it easier to spread. It is necessary to add a foaming agent, which causes a decrease in adhesive performance.
In addition, it is necessary to foam immediately before application, and it must be stirred repeatedly. Furthermore, although the foamed adhesive is difficult to handle, it must be scooped out of the stirring container and applied, making the application process complicated. Moreover, in this type of foaming method, uneven foaming tends to occur within the stirring container, and uneven adhesion may occur. Particularly when applied to a vertical surface, uneven stirring may cause dripping. Furthermore, when pasting wallpaper onto a wall surface, the surface of the wallpaper will generally become uneven after pasting unless the adhesive layer is thinned. However, in actual practice, it is extremely difficult to apply adhesive thinly enough to give a beautiful finish to a wall or wallpaper, and it requires a great deal of effort and time. For this reason, there are commercially available wallpapers with adhesive or rewetting active adhesive applied to the back side of the wallpaper in advance, but once the adhesive type sticks, it cannot be repaired, and the rewetting active type Things also have to be soaked in water once, which is cumbersome. Under these circumstances, we conducted various research in order to obtain a foaming adhesive that exhibits uniform foamability, can be applied directly and uniformly to the adhered surface, and can be applied thinly or thickly. As a result, they discovered that when an emulsion-type water-based adhesive is sealed in a pressure-resistant container together with a propellant at a fixed ratio, and the propellant is jetted out of the pressure-resistant container together with the adhesive, uniform foaming of the adhesive is formed. The present invention has now been completed. Conventionally, aerosol-type adhesives have been known, but in all of them, the adhesive is sprayed in the form of a mist. In particular, an emulsion-type water-based adhesive and a propellant are sealed in a pressure-resistant container and then sprayed out. It was discovered for the first time by the present inventor that a uniform foamable adhesive can be obtained by this method. An object of the present invention is to provide a method for applying a foamable adhesive, which comprises sealing an emulsion-type water-based adhesive and a propellant, preferably liquefied propane and/or liquefied butane, in a pressure-resistant container. Such foamable adhesives are foamed when the propellant is injected with the adhesive into the outside of the pressure container through the nozzle, so if the adhesive is injected toward the surface to be adhered, the adhesive will be directly exposed. A foamed adhesive can be applied to the surface. Therefore, the present invention involves sealing an emulsion-type water-based adhesive together with a propellant in a pressure-resistant container at a fixed ratio, and spraying the adhesive together with the propellant from a nozzle of the pressure-resistant container to directly apply the adhesive to the surface to be adhered. The present invention provides a method for applying a foamable adhesive by forming and applying it in the form of a foam. In particular, the volume ratio of adhesive and propellant varies depending on the type and viscosity as shown below, but when using commonly used adhesives, in order to form uniform foam, it is necessary to Based on the current propellant, a range of 90:10 to 70:30 is particularly desirable. In this range, the adhesive is ejected from the nozzle in the form of a string or broken strings, adheres to the surface of the adherend, and then foams. In this case, the nozzle can be applied from a distance without having to bring the nozzle close to the adherend, so it is possible to improve the efficiency of coating work on adherends such as walls. It should be noted that if the adhesive component exceeds the above range, sufficient foamability cannot be obtained, and if it is less than this, the adhesive will be sprayed in a mist form, which is not preferable. As the adhesive component used in the present invention, it is possible to use an aqueous solution adhesive in addition to an emulsion-type water-based adhesive. It is easy to obtain uniform foaming and does not drip easily when applied to vertical surfaces. Furthermore, with the same viscosity, emulsion-type water-based adhesives can have a higher solids content, making it easier to control the discharge amount and making it easier to spread when applied. From these points of view, it is preferable to use an emulsion type water-based adhesive. As the emulsion type water-based adhesive, polyacrylic emulsion or polyvinyl acetate emulsion is used. These water-based emulsion-type water-based adhesives may optionally contain various surfactants, rosin, modified phenolic resins, terpenes, petroleum resins, tackifiers such as coumaron indene resin, calcium carbonate, clay, silica, and asbestos. fillers, higher alcohols, glycols, plasticizers such as phthalate esters, colorants such as titanium white and other dyes and pigments, antioxidants, antifungal agents, and the like may be added. Usually, solid content including these additives
15-75% is used. Examples of propellants used in the present invention include propane, butane, chlorofluorocarbons, carbon dioxide, dimethyl ether, nitrogen, and mixtures thereof, but the propellant and adhesive can separate into two layers in a pressure-resistant container. Therefore, in order to discharge the adhesive to the end without wasting it, it is better that the specific gravity of the liquefied propellant is lower than that of the adhesive, and in order to maintain the stability of the adhesive and increase bubble generation, the propellant should be water-resistant. It is better not to blend in. From this point on, liquefied propane, liquefied butane or liquefied Freon or mixtures thereof are used. A foamable adhesive can be constructed by appropriately combining the above adhesive and a propellant at the above-mentioned volume mixing ratio. The foamable adhesive is sealed in a pressure-resistant container as shown in FIG. 1 in a conventional manner. FIG. 2 is a top sectional view of the pressure-resistant container shown in FIG. 1. The aluminum container 1 is formed by wrapping a lid 1b around the opening of a barrel 1a. An injection member 2 is attached to the center of the lid 1b. The injection member 2 has a stem rubber 4 attached to the upper end opening of an annular housing 3, and a stem 5 having a flow path 5a through a central hole of the rubber.
is inserted into the housing 3 and urged upward by a spring 6 provided at the inner bottom of the housing. A push button 7 having an open beak-shaped nozzle portion 7a is attached to the upper end of the stem 5. On the other hand, there is an opening at the bottom of the housing 3, which communicates with a stand pipe 8 extending below the container. Therefore, when the push button 7 is pressed down, the inlet of the flow path 5a of the stem 5 is released from contact with the stem rubber 4, and the injection member 2 is placed in an open state (see FIG. 3). The adhesive A is foamed by the propellant B and is sprayed to the outside through the nozzle portion 7a. After applying the foamed adhesive to the surface to be adhered, the adhesive layer can be flattened using a cap 10 that also serves as a spatula, as shown in FIG. The cap 10 which also serves as a spatula includes a spatula section 12 on the upper part of a cap section 11, and a wide wave-shaped end section 12a is formed at the upper end of the spatula section 12. In use, the cap part 11 can be used as a gripping part (see FIG. 4). FIG. 5 shows the state of foam application using another embodiment of the pressure container, in which the nozzle portion 7a of the press button 7 has a small diameter, and this allows the adhesive to foam on the application surface, making it possible to apply from a distance. It has the advantage of being able to According to the present invention, a foaming adhesive can be constructed by sealing a water-based emulsion type adhesive together with a propellant in a pressure-resistant container. There is no need for the complicated work of putting the adhesive in a stirring container, foaming it with a foam mixer, scooping it out, and applying it. Simply point the nozzle of the pressure container toward the surface to be adhered, and press the press button. The foamed adhesive is discharged and applied to the adhered surface, making the application process extremely simple. Furthermore, since the adhesive is applied in a foamed state, it will not absorb into porous, fibrous, or uneven surfaces. Furthermore, since it can be easily spread, a thin and wide adhesive layer can be formed with a small amount of adhesive. Furthermore, since the adhesive forms a foam, the drying speed can be adjusted appropriately, and even if the adhesive is applied thickly or unevenly, the air bubbles will occupy most of the volume, making it completely unnoticeable after drying. Suitable for bonding a wide range of surfaces such as
Furthermore, even if it protrudes during application, since it is a foam, it is easy to remove and becomes unnoticeable once it dries.
Furthermore, since it becomes a mist and does not scatter, there are no health and safety problems. In addition, the size of the nozzle discharge port can be freely selected depending on the discharge amount, from a narrow spray type to a wide-mouth type for shaving cream, and a relatively large amount of propellant is sealed in a pressure-resistant container. It has various advantages, such as almost no nozzle clogging unlike conventional aerosol adhesives. Hereinafter, the present invention will be explained in more detail based on Examples. Example 1 Polyacrylic emulsion (Acronal 80D manufactured by Yuka Vadish Co., Ltd.) 90 parts (volume) Liquefied propane-butane mixture (volume ratio 40:60)
10 parts Each of the above components is placed in the same aluminum pressure container and shaken well for 5 minutes to obtain a foamable adhesive. (Foaming ratio: 16 times) Example 2 Polyvinyl acetate emulsion (Vinizol #210 manufactured by Daido Kasei Kogyo Co., Ltd.) 77 parts Water 13 parts Liquefied Freon 10 parts The above components were placed in the same aluminum pressure-resistant container and shaken well for 5 minutes. to obtain a foamable adhesive. (Foaming ratio: 18 times) Example 3 Example 1 was applied on one side of plywood (100 x 100 x 5 mm).
Discharge the foaming adhesive of 2 from a pressure container, apply a foaming adhesive layer with a width of 3 cm in a single strip,
A canvas (100 x 100 mm) was pressed onto it and left as is for 24 hours, and the peel adhesion strength of the canvas was measured. On the other hand, Acronal 80D
Then apply Vinizol #210 to one side of the same plywood with a brush, press the same canvas as above on top of it, leave it as it is for 24 hours, measure the peel adhesion strength of the canvas, and report the results below. It is shown in Table 1.
【表】
上記結果より、塗布量が同一である場合、発泡
性接着剤の方がおよそ2倍の接着強度を示す。こ
れは繊維間への接着剤の吸収が防止され、接着に
実質的に関与する接着剤量が発泡させない場合よ
り多くなるためである。
実施例 4
モルタル(100×100×10mm)上に、実施例1の
発泡性接着剤を耐圧容器より吐出させて塗布し、
その上から壁紙(100×100mm)を押し当てて実施
例3と同様にして接着させる。一方、同一のモル
タルにハケでアクロナール80Dを塗布し、同一の
壁紙を押し当てて接着させる。両者の剥離接着強
度を測定した。結果を下記第2表に示す。[Table] From the above results, when the coating amount is the same, the foamable adhesive exhibits approximately twice the adhesive strength. This is because absorption of the adhesive between the fibers is prevented, and the amount of adhesive substantially involved in adhesion is greater than when foaming is not performed. Example 4 The foamable adhesive of Example 1 was applied onto mortar (100 x 100 x 10 mm) by discharging it from a pressure container, and
Wallpaper (100 x 100 mm) was pressed onto it and adhered in the same manner as in Example 3. Meanwhile, apply Acronal 80D to the same mortar with a brush and press the same wallpaper to adhere. The peel adhesion strength of both was measured. The results are shown in Table 2 below.
【表】
上記結果から明らかなように、実施例1の発泡
性接着剤の発泡塗布の場合、塗布量の差によつて
接着強度に差はないのに対し、アクロナール80D
のハケ塗布の場合、接着強度は塗布量の増加とと
もに増大するが、塗布量150g/m2でも本発明の
発泡塗布の塗布量100g/m2の接着強度に達しな
い。これはハケ塗布の場合、接着剤がモルタル面
に吸収されて実質的に接着に関与する接着量が減
少するのに対し、発泡塗布の場合、モルタル面に
吸収される量がほとんど減少せず、モルタル面に
薄く効率よく押し広げられて最少の塗布量によつ
て最大の接着強度が得られやすいからである。[Table] As is clear from the above results, in the case of foam application of the foamable adhesive of Example 1, there was no difference in adhesive strength depending on the difference in application amount, whereas Acronal 80D
In the case of brush application, the adhesive strength increases as the application amount increases, but even an application amount of 150 g/m 2 does not reach the adhesive strength of the foam coating of the present invention with an application amount of 100 g/m 2 . This is because in the case of brush application, the adhesive is absorbed into the mortar surface and the amount of adhesive involved in adhesion is substantially reduced, whereas in the case of foam application, the amount absorbed by the mortar surface is hardly reduced. This is because it can be spread thinly and efficiently on the mortar surface, making it easy to obtain maximum adhesive strength with the minimum amount of application.
第1図は本発明で使用する耐圧容器の斜視図、
第2図および第3図は第1図に示す耐圧容器のキ
ヤツプを取つた状態の上部断面図で、第2図は噴
射用部材が閉鎖状態にあり、第3図は開放状態に
ある。第4図は第1図の耐圧容器のヘラ兼用キヤ
ツプの使用状態を示す斜視図である。第5図は他
の態様の耐圧容器による発泡塗布の状態を示す図
である。
1……耐圧容器、2……噴射用部材、7a……
ノズル部、10……ヘラ兼用キヤツプ、A……接
着剤、B……噴射剤。
FIG. 1 is a perspective view of a pressure-resistant container used in the present invention;
2 and 3 are sectional views of the top of the pressure vessel shown in FIG. 1 with the cap removed; FIG. 2 shows the injection member in the closed state, and FIG. 3 shows it in the open state. FIG. 4 is a perspective view showing the state in which the spatula cap of the pressure container shown in FIG. 1 is used. FIG. 5 is a diagram showing a state of foam coating using another embodiment of the pressure container. 1...Pressure container, 2...Injection member, 7a...
Nozzle part, 10... Cap that also serves as a spatula, A... Adhesive, B... Spraying agent.
Claims (1)
ニルエマルジヨンから選ばれるエマルジヨン型水
性接着剤と、液化プロパン、液化ブタンもしくは
液化フロンまたはこれらの混合物から選ばれる噴
射剤を、この容量配合比が液体状態の噴射剤を基
準として90:10〜70:30となるように耐圧容器内
に封入し、該噴射剤とともに上記接着剤を耐圧容
器のノズルから噴出させて接着剤を被着面に直接
泡状に形成塗布することを特徴とする発泡性接着
剤の塗布方法。1. An emulsion-type water-based adhesive selected from polyacrylic emulsion or polyvinyl acetate emulsion and a propellant selected from liquefied propane, liquefied butane, liquefied fluorocarbon, or a mixture thereof, in a volume mixing ratio of a propellant in a liquid state. 90:10 to 70:30 based on the ratio of 90:10 to 70:30, and the adhesive is sprayed from the nozzle of the pressure container together with the propellant to form a foam directly on the surface to be applied. A method for applying a foamable adhesive, characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2146680A JPS56116766A (en) | 1980-02-21 | 1980-02-21 | Foam adhesive and coating method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2146680A JPS56116766A (en) | 1980-02-21 | 1980-02-21 | Foam adhesive and coating method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56116766A JPS56116766A (en) | 1981-09-12 |
JPS6310745B2 true JPS6310745B2 (en) | 1988-03-09 |
Family
ID=12055753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2146680A Granted JPS56116766A (en) | 1980-02-21 | 1980-02-21 | Foam adhesive and coating method thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56116766A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59172569A (en) * | 1983-03-22 | 1984-09-29 | Konishi Kk | Aerosol type spraying adhesive |
JPS62156365U (en) * | 1986-03-24 | 1987-10-05 | ||
JPS63111966U (en) * | 1987-01-12 | 1988-07-19 | ||
HUP0700784A2 (en) | 2007-12-05 | 2009-07-28 | Hungarocoll Kft | Method and apparatus for foaming a waterbase adhesive composition |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS517042A (en) * | 1974-07-09 | 1976-01-21 | Kao Corp | EAZOORUNORISOSEIBUTSU |
JPS557830A (en) * | 1978-07-03 | 1980-01-21 | Nippon Carbide Ind Co Ltd | Aerosol sizing composition |
-
1980
- 1980-02-21 JP JP2146680A patent/JPS56116766A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS517042A (en) * | 1974-07-09 | 1976-01-21 | Kao Corp | EAZOORUNORISOSEIBUTSU |
JPS557830A (en) * | 1978-07-03 | 1980-01-21 | Nippon Carbide Ind Co Ltd | Aerosol sizing composition |
Also Published As
Publication number | Publication date |
---|---|
JPS56116766A (en) | 1981-09-12 |
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