JPH04277580A - Bonding method - Google Patents
Bonding methodInfo
- Publication number
- JPH04277580A JPH04277580A JP6563391A JP6563391A JPH04277580A JP H04277580 A JPH04277580 A JP H04277580A JP 6563391 A JP6563391 A JP 6563391A JP 6563391 A JP6563391 A JP 6563391A JP H04277580 A JPH04277580 A JP H04277580A
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- gelling agent
- adherend
- water
- emulsion
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 20
- 239000000853 adhesive Substances 0.000 claims abstract description 64
- 230000001070 adhesive effect Effects 0.000 claims abstract description 64
- 239000003349 gelling agent Substances 0.000 claims abstract description 24
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000007864 aqueous solution Substances 0.000 claims abstract description 9
- -1 hydrazine compound Chemical class 0.000 claims abstract description 8
- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 claims abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 239000003595 mist Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 abstract description 14
- 239000000203 mixture Substances 0.000 abstract description 8
- 238000005507 spraying Methods 0.000 abstract description 4
- 239000007921 spray Substances 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000003475 lamination Methods 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 238000001879 gelation Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000001464 adherent effect Effects 0.000 description 2
- IBVAQQYNSHJXBV-UHFFFAOYSA-N adipic acid dihydrazide Chemical compound NNC(=O)CCCCC(=O)NN IBVAQQYNSHJXBV-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000004584 polyacrylic acid Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- ZNGSVRYVWHOWLX-KHFUBBAMSA-N (1r,2s)-2-(methylamino)-1-phenylpropan-1-ol;hydrate Chemical compound O.CN[C@@H](C)[C@H](O)C1=CC=CC=C1.CN[C@@H](C)[C@H](O)C1=CC=CC=C1 ZNGSVRYVWHOWLX-KHFUBBAMSA-N 0.000 description 1
- IOOZKHMFNNJCMG-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)propan-2-yl 3-oxobutanoate Chemical compound CC(=C)C(=O)OCC(C)OC(=O)CC(C)=O IOOZKHMFNNJCMG-UHFFFAOYSA-N 0.000 description 1
- NGZDFOYYIXAAPC-UHFFFAOYSA-N 1-prop-2-enoyloxypropan-2-yl 3-oxobutanoate Chemical compound C=CC(=O)OCC(C)OC(=O)CC(C)=O NGZDFOYYIXAAPC-UHFFFAOYSA-N 0.000 description 1
- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- ZGLJYJVYUYQOHR-UHFFFAOYSA-N 3-oxobutanoyl 4-hydroxy-2-methylidenebutanoate Chemical compound CC(=O)CC(=O)OC(=O)C(=C)CCO ZGLJYJVYUYQOHR-UHFFFAOYSA-N 0.000 description 1
- ALEBYBVYXQTORU-UHFFFAOYSA-N 6-hydrazinyl-6-oxohexanoic acid Chemical compound NNC(=O)CCCCC(O)=O ALEBYBVYXQTORU-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- 229920006328 Styrofoam Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- UTTHLMXOSUFZCQ-UHFFFAOYSA-N benzene-1,3-dicarbohydrazide Chemical compound NNC(=O)C1=CC=CC(C(=O)NN)=C1 UTTHLMXOSUFZCQ-UHFFFAOYSA-N 0.000 description 1
- ALHNLFMSAXZKRC-UHFFFAOYSA-N benzene-1,4-dicarbohydrazide Chemical compound NNC(=O)C1=CC=C(C(=O)NN)C=C1 ALHNLFMSAXZKRC-UHFFFAOYSA-N 0.000 description 1
- HCOMFAYPHBFMKU-UHFFFAOYSA-N butanedihydrazide Chemical compound NNC(=O)CCC(=O)NN HCOMFAYPHBFMKU-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- XEVRDFDBXJMZFG-UHFFFAOYSA-N carbonyl dihydrazine Chemical compound NNC(=O)NN XEVRDFDBXJMZFG-UHFFFAOYSA-N 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- ZWLIYXJBOIDXLL-UHFFFAOYSA-N decanedihydrazide Chemical compound NNC(=O)CCCCCCCCC(=O)NN ZWLIYXJBOIDXLL-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- SWRGUMCEJHQWEE-UHFFFAOYSA-N ethanedihydrazide Chemical compound NNC(=O)C(=O)NN SWRGUMCEJHQWEE-UHFFFAOYSA-N 0.000 description 1
- ZEYMDLYHRCTNEE-UHFFFAOYSA-N ethenyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OC=C ZEYMDLYHRCTNEE-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- DIVHIORLOZUTJI-UHFFFAOYSA-N prop-2-enoyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OC(=O)C=C DIVHIORLOZUTJI-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000008261 styrofoam Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、特定の2液水分散型接
着剤を用いて、初期接着力を瞬間的に発現させる接着方
法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an adhesive method for instantaneously developing initial adhesive strength using a specific two-component water-dispersed adhesive.
【0002】0002
【従来技術】従来、接着剤としては主に有機溶剤を媒体
としたものが用いられているが、引火性や毒性、その他
公害上の問題から、近年、被着体の一方または双方が水
や水蒸気を透過吸収するものの場合にはエマルジョン型
水性接着剤などの水分散型接着剤が広く用いられるよう
になっている。エマルジョン型水性接着剤は、一般に、
水を媒体とした高分子物質のエマルジョンに、適宜、タ
ツキファイヤー、充填剤、可塑剤、着色剤、老化防止剤
などを配合してなる接着剤で、引火性がなく、毒性が小
さく、安全で衛生的であり、不揮発分が多くても低粘度
のため充填効果が大きく、水で稀釈できるなどの種々の
利点を有している。しかし、従来の有機溶剤系接着剤と
比較すると、エマルジョン型水性接着剤は初期接着力の
発現が遅く、充分な接着強度が出るまでに時間がかかる
という大きな欠点を有しており、その使用上、大きな問
題となっている。[Prior Art] Conventionally, adhesives mainly using organic solvents as a medium have been used, but due to flammability, toxicity, and other pollution problems, in recent years, one or both of the adherends has been In the case of materials that permeate and absorb water vapor, water-dispersed adhesives such as emulsion-type water-based adhesives have come to be widely used. Emulsion type water-based adhesives are generally
It is an adhesive made of an emulsion of a polymeric substance in water as a medium, mixed with tackifier, fillers, plasticizers, colorants, anti-aging agents, etc., and is non-flammable, has low toxicity, and is safe. It has various advantages such as being hygienic, having a large filling effect due to its low viscosity even though it has a large nonvolatile content, and being dilutable with water. However, compared to conventional organic solvent-based adhesives, emulsion-type water-based adhesives have a major drawback in that the initial adhesive strength is slow to develop and it takes time to develop sufficient adhesive strength. , has become a big problem.
【0003】そこで、該接着剤の初期接着力を早く発現
させる方法が種々検討され、例えば、接着剤の固形分を
多くして増粘したり、接着剤の塗布前または後に被着体
を加熱して水を蒸発させたりなどする方法が提案されて
いるが、これらの方法では接着剤の貯蔵安定性や塗布作
業性が悪化したり、別途設備を必要としたり、効果があ
まり期待できないなど、未だ充分満足するものは見当ら
ない。Therefore, various methods have been investigated to quickly develop the initial adhesive strength of the adhesive, such as increasing the solid content of the adhesive to increase its viscosity, or heating the adherend before or after applying the adhesive. Methods have been proposed, such as evaporating the water by evaporating the adhesive, but these methods deteriorate the storage stability and application workability of the adhesive, require separate equipment, and are not very effective. I haven't found anything that satisfies me yet.
【0004】また、エマルジョン型水性接着剤をゲル化
剤を別々に被着体へ塗布して、貼合わせる接着方法も検
討されているが、接着界面で両者が各々層を形成し、よ
く混合しないため、初期接着力が充分に初発現しない欠
点があった。[0004]Also, an adhesion method has been considered in which an emulsion-type water-based adhesive and a gelling agent are separately applied to the adherend and bonded together, but the two form separate layers at the adhesive interface and do not mix well. Therefore, there was a drawback that sufficient initial adhesive strength was not developed.
【0005】[0005]
【発明が解決しようとする課題】本発明が解決しようと
する課題は、エマルジョン型水性接着剤などの水分散型
接着剤を用いて、安定した初期接着力を瞬間的に発現さ
せる接着方法を提供することにある。[Problems to be Solved by the Invention] The problem to be solved by the present invention is to provide an adhesive method that instantly develops stable initial adhesive strength using a water-dispersed adhesive such as an emulsion-type water-based adhesive. It's about doing.
【0006】[0006]
【課題を解決するための手段】本発明は、アセトアセチ
ル基を有するエマルジョン型水性接着剤を主成分とする
主剤と、ヒドラジン化合物の水性溶液を主成分とするゲ
ル化剤とからなる2液水分散型接着剤を用いて被着体を
接着するにあたり、主剤とゲル化剤を各々、同時に噴霧
し、霧滴状態で混合して被着体に塗布することを特徴と
する接着方法である。[Means for Solving the Problems] The present invention provides a two-liquid solution consisting of a main component mainly composed of an emulsion type water-based adhesive having an acetoacetyl group, and a gelling agent mainly composed of an aqueous solution of a hydrazine compound. When adhering adherends using a dispersion type adhesive, this is an adhesion method characterized by spraying a base agent and a gelling agent at the same time, mixing them in the form of mist droplets, and applying the mixture to the adherend.
【0007】すなわち、本発明は、エマルジョン型水性
接着剤を用いて被着体を接着するにあたり、該接着剤と
、該接着剤ゲル化させる物質を含有するゲル化剤を、各
々、同時に噴霧し、霧滴状態で混合して被着体に塗布す
ることを特徴とする接着方法を提供するものである。
本発明の方法は従来の方法し比較して初期接着力の発現
がきわめて早く、仮止めが不要で、接着作業性が向上し
、接着剤の貯蔵安定性や塗布作業性が悪化したり、別途
特別な設備を必要としない利点を有する。また、エマル
ジョン型水性接着剤とゲル化剤を別々に被着体へ塗布す
ると接着界面で両者が各々層を形成し、よく混合しない
ため、初期接着力が充分に発現しないが、本発明の方法
によれば、接着剤とゲル化剤が被着体へ塗布される直前
に空中にて霧滴状態でよく混合するのできわめて優れた
初期接着力が発現される。That is, in bonding adherends using an emulsion-type water-based adhesive, the present invention simultaneously sprays the adhesive and a gelling agent containing a substance to gel the adhesive. , provides an adhesion method characterized in that the mixture is mixed in the form of mist droplets and applied to an adherend. Compared to conventional methods, the method of the present invention develops initial adhesive strength extremely quickly, does not require temporary fixing, and improves adhesive workability. It has the advantage of not requiring special equipment. Furthermore, when an emulsion-type water-based adhesive and a gelling agent are applied separately to an adherend, they form separate layers at the adhesive interface and do not mix well, resulting in insufficient initial adhesive strength. However, the method of the present invention According to the method, the adhesive and the gelling agent are well mixed in the air in the form of droplets just before being applied to the adherend, so that extremely excellent initial adhesive strength is developed.
【0008】かくして、本発明の方法においては、エマ
ルジョン型水性接着剤とゲル化剤を、各々同時に、噴霧
域が重なるようにして被着体へ噴霧する。用いる噴霧機
器は特に限定するものではなく、該接着剤とゲル化剤を
同時に噴霧でき、これらの噴霧域が重なるものであれば
いずれでもよく、エアスプレー、エアレススプレーいず
れでもよい。例えば、その噴霧域が重なる様に調節した
2個のスプレーガンを用いたり、二頭スプレーガン(例
えば、米国BINKS MANUFACTURRIN
G COMPANY製、69GM PLURAL
COMPONENTSPRAY GUN)を用いる
ことができる。また、1個のスプレーガンを用い、該接
着剤およびゲル化剤を、各々、そのノズルおよび空気孔
から同時に噴霧することも可能である。[0008] Thus, in the method of the present invention, the emulsion type water-based adhesive and the gelling agent are each simultaneously sprayed onto the adherend so that the spray areas overlap. The spraying equipment used is not particularly limited, and any equipment may be used as long as the adhesive and gelling agent can be sprayed at the same time and their spraying areas overlap, and either air spray or airless spray may be used. For example, two spray guns adjusted so that their spray areas overlap may be used, or a two-headed spray gun (for example, BINKS MANUFACTURRIN in the US) may be used.
Made by G COMPANY, 69GM PLURAL
COMPONENTSPRAY GUN) can be used. It is also possible to use one spray gun and spray the adhesive and gelling agent simultaneously from its nozzle and air hole, respectively.
【0009】本発明で使用するアセトアセチル基を有す
るエマルジョン型水性接着剤としては、分子内にアセト
アセチル基を有する高分子化合物の水性溶液即ちポリビ
ニルアルコール、ヒドロキシアルキルセルロース、殿粉
などの水溶性高分子化合物をアセトアセチル化したアセ
トアセチル化ポリビニルアルコール、アセトアセチル化
、アセトアセチル化殿粉などの水性溶液と例えば、天然
ゴムポリ酢酸ビニル、酢酸ビニル共重合体。ポリアクリ
ル酸エステル、アクリル酸エステル共重合体、エチレン
酢酸ビニル共重合体、ポリオレフィン、スチレンブタジ
エン共重合体、メチルメタアクリル酸エステルブタジエ
ン共重合体、ニトリルブタジエン共重合体、ポリクロロ
ピレン、ポリイソプレン。スチレンイソプレン共重合体
、ポリ塩化ビニル、塩化ビニリデン共重合体、ポリビニ
ルアルキルエーテル、フエノールホルマリン反応性混合
液などを主成分とするエマルジョンをブレンドしたもの
がある。又、アセトアセチル基を含有する単量体、例え
ばアクリルアセトアセテート、ビニルアセトアセテート
、2−アセトアセトキシエチルアクリレート、2−アセ
トアセトキシエチルメタクリレート、2−アセトアセト
キシプロピルアクリレート、2−アセトアセトキシプロ
ピルメタクリレートなどと、α、βエチレン性単量体、
例えば酢酸ビニル、α位で分岐した飽和脂肪族のビニル
エステルなどのビニルエステル、メチルアクリレート又
はメチルメタクリレート[以下、メチル(メタ)アクリ
レートの如く記載する]、エチル(メタ)アクリレート
、ブチル(メタ)アクリレート、2−エチルヘキシル(
メタ)アクリレート、ノニル(メタ)アクリレートなど
の(メタ)アクリレート、スチレン、アクリロニトリル
、エチレン、塩化ビニルなどのモノビニル単量体などと
を乳化共重合することにより、分子内にアセトアセチル
基を有する高分子化合物の水性エマルジョンが適合する
。又、アセトアセチル化ポリビニルアルコールを乳化剤
として乳化重合した重合体水性エマルジョンも含まれる
。The emulsion-type water-based adhesive having an acetoacetyl group used in the present invention is an aqueous solution of a polymer compound having an acetoacetyl group in the molecule, ie, a water-soluble highly water-based adhesive such as polyvinyl alcohol, hydroxyalkylcellulose, starch, etc. Aqueous solutions of acetoacetylated polyvinyl alcohol, acetoacetylated, acetoacetylated starch, etc., which are acetoacetylated molecular compounds, and natural rubber polyvinyl acetate, vinyl acetate copolymer, etc. Polyacrylic acid ester, acrylic acid ester copolymer, ethylene vinyl acetate copolymer, polyolefin, styrene butadiene copolymer, methyl methacrylic acid ester butadiene copolymer, nitrile butadiene copolymer, polychloropyrene, polyisoprene. There are blends of emulsions whose main components are styrene isoprene copolymer, polyvinyl chloride, vinylidene chloride copolymer, polyvinyl alkyl ether, and phenol-formalin reactive mixture. Furthermore, monomers containing an acetoacetyl group, such as acryl acetoacetate, vinyl acetoacetate, 2-acetoacetoxyethyl acrylate, 2-acetoacetoxyethyl methacrylate, 2-acetoacetoxypropyl acrylate, 2-acetoacetoxypropyl methacrylate, etc. , α, β ethylenic monomer,
For example, vinyl esters such as vinyl acetate, saturated aliphatic vinyl esters branched at the α-position, methyl acrylate or methyl methacrylate [hereinafter referred to as methyl (meth)acrylate], ethyl (meth)acrylate, butyl (meth)acrylate , 2-ethylhexyl (
By emulsion copolymerizing with (meth)acrylates such as meth)acrylate and nonyl(meth)acrylate, and monovinyl monomers such as styrene, acrylonitrile, ethylene, and vinyl chloride, polymers with acetoacetyl groups in the molecule are produced. Aqueous emulsions of the compounds are suitable. It also includes an aqueous polymer emulsion obtained by emulsion polymerization using acetoacetylated polyvinyl alcohol as an emulsifier.
【0010】次に該接着剤をゲル化させるヒドラジン化
合物としては、ヒドラジン、ヒドラジンヒドラード、ヒ
ドラジンの塩酸、硫酸、硝酸、亜硝酸、リン酸、チオシ
アン酸、炭酸などの無機塩類および酸、シュウ酸などの
有機塩類、ヒドラジンのメチル、エチル、プロピル、ブ
チル、アリルなどの一置換体、1,1−ジメチル、1,
1−ジエチル、4−n−ブチル−メタルなどの非対称二
置換体、並びに1,2−ジメチル、1,2−ジエチル、
1,2−ジイソプロピルなどの対称二置換体などが挙げ
られる。ことに好適なヒドラジン化合物はカルボジヒド
ラジド、シュウ酸ジヒドラジド、マロン酸ジヒドラジド
、コハク酸ジヒドラジド、アジピン酸ジヒドラジド、セ
バチン酸ジヒドラジド、イソフタール酸ジヒドラジド、
テレフタル酸ジヒドラジド、グリコリック酸ジヒドラジ
ド、ポリアクリル酸ヒドラジンなどである。[0010] Next, the hydrazine compound for gelling the adhesive includes hydrazine, hydrazine hydrade, inorganic salts and acids of hydrazine such as hydrochloric acid, sulfuric acid, nitric acid, nitrous acid, phosphoric acid, thiocyanic acid, carbonic acid, and oxalic acid. organic salts such as hydrazine, monosubstituted hydrazine such as methyl, ethyl, propyl, butyl, allyl, 1,1-dimethyl, 1,
asymmetric disubstituted products such as 1-diethyl, 4-n-butyl-metal, and 1,2-dimethyl, 1,2-diethyl,
Examples include symmetric disubstituted compounds such as 1,2-diisopropyl. Particularly suitable hydrazine compounds are carbodihydrazide, oxalic acid dihydrazide, malonic acid dihydrazide, succinic acid dihydrazide, adipic acid dihydrazide, sebacic acid dihydrazide, isophthalic acid dihydrazide,
These include terephthalic acid dihydrazide, glycolic acid dihydrazide, and polyacrylic acid hydrazine.
【0011】これらの水性溶液の濃度は、通常ヒドラジ
ン化合物が1〜50%が適当で、中でも2〜25%が性
能、コスト面で有効である。The concentration of these aqueous solutions is usually 1 to 50% of the hydrazine compound, with 2 to 25% being effective in terms of performance and cost.
【0012】本発明の該水性接着剤:ゲル化剤の重量比
1:01〜1:5の割合で被着体へ噴霧することが好ま
しく、上記比率よりゲル化剤が少なすぎると、ゲル化能
力が低下し、初期強度不足となり、多すぎると被着体へ
の密着性が低下する。It is preferable to spray the aqueous adhesive of the present invention onto the adherend at a weight ratio of 1:01 to 1:5; if the gelling agent is too small than the above ratio, gelation may occur. The capacity decreases, resulting in insufficient initial strength, and if too much, the adhesion to the adherend decreases.
【0013】なお、本発明の接着剤には、密着性、耐熱
性、耐水性、強靱性、弾性などの向上を目的に合成樹脂
エマルジョンや合成ゴムラテックスを併用することがで
きる。また、炭酸カルシウムなどの充填剤、可塑剤、防
腐剤、着色剤などを適宜併用することができる。Note that a synthetic resin emulsion or synthetic rubber latex may be used in combination with the adhesive of the present invention for the purpose of improving adhesion, heat resistance, water resistance, toughness, elasticity, etc. Further, fillers such as calcium carbonate, plasticizers, preservatives, colorants, etc. can be used in combination as appropriate.
【0014】[0014]
【発明の効果】本発明の方法によれば、接着剤とゲル化
剤が被着体へ塗布される直前に空中にて霧滴状態でよく
混合するので均一なゲル化がおこり、極めて安定した初
期強度を得ることができる。[Effects of the Invention] According to the method of the present invention, the adhesive and gelling agent are well mixed in the air in the form of mist droplets immediately before being applied to the adherend, resulting in uniform gelation and extremely stable gelation. Initial strength can be obtained.
【0015】本発明の2液型水性接着剤は、木材、合板
、パーチクルボード、ハードボードのごとき繊維質材料
、スレート板、珪カル板、モルタルのごとき無機質系材
料、発泡スチロールのごときプラスチツク材料、段ボー
ル、板紙、クラフト紙などの紙質材料などの多孔質から
なる被着体の高速接着に好適である。The two-component water-based adhesive of the present invention can be applied to fibrous materials such as wood, plywood, particle board, and hardboard, inorganic materials such as slate board, silica board, and mortar, plastic materials such as styrofoam, cardboard, It is suitable for high-speed adhesion of porous adherends such as paperboard and kraft paper.
【0016】以下に実施例と比較例をあげて説明するが
、%及び部はそれぞれ重量%及び重量部を示す。[0016] Examples and comparative examples will be described below, where % and parts indicate weight % and parts by weight, respectively.
【0017】[0017]
【実施例】実施例1
アセトアセチル化ポリビニルアルコールのゴーセファイ
マーZ−100(日本合成化学社製)の15%水溶液3
0部とアクリルエマルジョンプライマルN−580(ロ
ーム&ハース社製)70部を混合したものを水性接着剤
とした。また、アジピン酸ジヒドラジドの10%水溶液
をゲル化剤とした。[Example] Example 1 15% aqueous solution 3 of acetoacetylated polyvinyl alcohol Gosefimer Z-100 (manufactured by Nippon Gosei Kagaku Co., Ltd.)
0 parts and 70 parts of acrylic emulsion Primal N-580 (manufactured by Rohm & Haas) to prepare a water-based adhesive. Further, a 10% aqueous solution of adipic acid dihydrazide was used as a gelling agent.
【0018】実施例2
アセトアセチル化変性アクリルエマルジョンRA−10
00(アイカ工業社製)を水性接着剤とした。また、実
施例1のゲル化剤をゲル化剤とした。Example 2 Acetoacetylated modified acrylic emulsion RA-10
00 (manufactured by Aica Kogyo Co., Ltd.) was used as the water-based adhesive. Moreover, the gelling agent of Example 1 was used as a gelling agent.
【0019】[0019]
【比較例】比較例1
実施例1の水性接着剤を水性接着剤とした。ゲル化剤は
なし。[Comparative Example] Comparative Example 1 The water-based adhesive of Example 1 was used as a water-based adhesive. No gelling agent.
【0020】比較例2
アクリルエマルジョンプライマルN−580を水性接着
剤とした。10%アジピン酸ヒドラジド水溶液をゲル化
剤とした。Comparative Example 2 Acrylic emulsion Primal N-580 was used as a water-based adhesive. A 10% adipic acid hydrazide aqueous solution was used as a gelling agent.
【0021】比較例3
実施例と同一(水性接着剤・ゲル化剤)但し、実施例1
〜2、比較例1〜2は本接着方法(空中混合式)比較例
3は被着体へ分別塗布。Comparative Example 3 Same as Example (water-based adhesive/gelling agent) except that Example 1
~2, Comparative Examples 1 and 2 were the main adhesion method (air mixing method), and Comparative Example 3 was separate application to the adherend.
【0022】試験方法の概略は次の如くである。実施例
1〜2、比較例1〜2の接着方法は、
被着体…メラミンアルキッド塗装鋼板×ウレタンフォー
ム。
塗 布…鋼板側に同時に空中で混合する様、噴霧。
水性接着剤:150g/m2
ゲル化剤 : 25g/m2
貼り合わせ…塗布後、直ちに貼り合わせ。
養 生 …1分/室温。
比較例3の接着方法は、
被着体…同上。
塗 布…鋼板側に水性接着剤。ウレタンフォームにゲ
ル化剤を分別塗布する。
水性接着剤:150g/m2
ゲル化剤 : 25g/m2
貼り合わせ…塗布後、直ちに貼り合わせ。
養 生 …1分/室温。The outline of the test method is as follows. The adhesion methods of Examples 1 and 2 and Comparative Examples 1 and 2 were as follows: Adherent: melamine alkyd coated steel plate x urethane foam. Application: Spray on the steel plate side at the same time to mix in the air. Water-based adhesive: 150g/m2 Gelling agent: 25g/m2 Lamination: Lamination immediately after application. Curing...1 minute/room temperature. The adhesion method of Comparative Example 3 was as follows: Adherent: Same as above. Application: Water-based adhesive on the steel plate side. Separately apply gelling agent to urethane foam. Water-based adhesive: 150g/m2 Gelling agent: 25g/m2 Lamination: Lamination immediately after application. Curing...1 minute/room temperature.
【0023】測定方法は、下記の如くである。養生後、
ウレタンを下側にして接着体を水平に保持しウレタンフ
ォームの一端に100gの下向きの荷重をかけて、10
0mm剥離するまでの時間を測定する。(90度剥離保
持力)被着体の測定巾は25mmとし、測定温度は25
℃とする。The measuring method is as follows. After curing,
Hold the adhesive horizontally with the urethane side facing down, apply a downward load of 100 g to one end of the urethane foam, and
Measure the time until 0 mm peels off. (90 degree peel retention force) The measurement width of the adherend is 25 mm, and the measurement temperature is 25 mm.
℃.
【0024】測定結果を表1に示す。The measurement results are shown in Table 1.
【0025】[0025]
【表1】[Table 1]
Claims (1)
ン型水性接着剤を主成分とする主剤と、ヒドラジン化合
物の水性溶液を主成分とするゲル化剤とからなる2液型
水分散型接着剤を用いて被着体を接着するにあたり、主
剤とゲル化剤を各々、同時に噴霧し、霧滴状態で混合し
て被着体に塗布することを特徴とする接着方法。[Claim 1] A two-component water-dispersed adhesive consisting of a main component mainly composed of an emulsion-type water-based adhesive having an acetoacetyl group and a gelling agent mainly composed of an aqueous solution of a hydrazine compound. An adhesion method characterized in that when adhering an adherend, a base agent and a gelling agent are each sprayed simultaneously, mixed in the form of mist droplets, and applied to the adherend.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6563391A JPH04277580A (en) | 1991-03-05 | 1991-03-05 | Bonding method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6563391A JPH04277580A (en) | 1991-03-05 | 1991-03-05 | Bonding method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04277580A true JPH04277580A (en) | 1992-10-02 |
Family
ID=13292624
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6563391A Pending JPH04277580A (en) | 1991-03-05 | 1991-03-05 | Bonding method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04277580A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005121225A1 (en) * | 2003-05-03 | 2005-12-22 | Reckitt Benckiser (Uk) Limited | Composition for sealing pvoh |
-
1991
- 1991-03-05 JP JP6563391A patent/JPH04277580A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005121225A1 (en) * | 2003-05-03 | 2005-12-22 | Reckitt Benckiser (Uk) Limited | Composition for sealing pvoh |
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