JPH0243464A - Manufacture of surface reinforce concrete-form plywood - Google Patents
Manufacture of surface reinforce concrete-form plywoodInfo
- Publication number
- JPH0243464A JPH0243464A JP32604688A JP32604688A JPH0243464A JP H0243464 A JPH0243464 A JP H0243464A JP 32604688 A JP32604688 A JP 32604688A JP 32604688 A JP32604688 A JP 32604688A JP H0243464 A JPH0243464 A JP H0243464A
- Authority
- JP
- Japan
- Prior art keywords
- plywood
- paint
- cured
- coating
- resin
- 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
- 239000011120 plywood Substances 0.000 title claims abstract description 43
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 229920005989 resin Polymers 0.000 claims abstract description 25
- 239000011347 resin Substances 0.000 claims abstract description 25
- 239000000945 filler Substances 0.000 claims abstract description 22
- 239000003973 paint Substances 0.000 claims description 52
- 239000011150 reinforced concrete Substances 0.000 claims description 18
- 238000009415 formwork Methods 0.000 claims description 10
- 239000004567 concrete Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 239000000565 sealant Substances 0.000 claims description 9
- 239000000839 emulsion Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 238000003848 UV Light-Curing Methods 0.000 claims 1
- 238000000576 coating method Methods 0.000 abstract description 11
- 238000001035 drying Methods 0.000 abstract description 9
- 239000011248 coating agent Substances 0.000 abstract description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 6
- 239000002987 primer (paints) Substances 0.000 abstract description 5
- 239000004593 Epoxy Substances 0.000 abstract description 4
- 238000010526 radical polymerization reaction Methods 0.000 abstract description 3
- 238000010538 cationic polymerization reaction Methods 0.000 abstract description 2
- 230000001678 irradiating effect Effects 0.000 abstract description 2
- 150000004291 polyenes Chemical class 0.000 abstract description 2
- 229920006295 polythiol Polymers 0.000 abstract description 2
- 238000007342 radical addition reaction Methods 0.000 abstract description 2
- 229920006305 unsaturated polyester Polymers 0.000 abstract description 2
- 239000005002 finish coating Substances 0.000 abstract 1
- 239000004925 Acrylic resin Substances 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 239000003999 initiator Substances 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 6
- 239000003822 epoxy resin Substances 0.000 description 5
- 229920000647 polyepoxide Polymers 0.000 description 5
- 239000000049 pigment Substances 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000012752 auxiliary agent Substances 0.000 description 3
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 3
- 239000012965 benzophenone Substances 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-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
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- NLGDWWCZQDIASO-UHFFFAOYSA-N 2-hydroxy-1-(7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-yl)-2-phenylethanone Chemical compound OC(C(=O)c1cccc2Oc12)c1ccccc1 NLGDWWCZQDIASO-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 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
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 201000001880 Sexual dysfunction Diseases 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000008360 acrylonitriles Chemical class 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 229920006271 aliphatic hydrocarbon resin Polymers 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920005792 styrene-acrylic resin Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Forms Removed On Construction Sites Or Auxiliary Members Thereof (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Finished Plywoods (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、塗料で合板表面を強化したコンクリート型枠
合板の製造方法に間するものであり、さらに詳しくは、
合板表面に目止剤及び/又は下塗塗料を塗布後、上塗塗
料を塗布して表面強化コンクリート型枠合板を製造する
方法に於いて、乾燥工程を省略できる上、クラック発生
の起こり難い表面強化コンクリート型枠合板の製造方法
に関するものである。[Detailed Description of the Invention] <Industrial Application Field> The present invention relates to a method for manufacturing concrete form plywood whose surface is reinforced with paint.
In the method of manufacturing surface-reinforced concrete form plywood by applying a filler and/or undercoat to the plywood surface and then applying a topcoat, the drying process can be omitted and surface-reinforced concrete is less prone to cracking. This invention relates to a method for manufacturing formwork plywood.
〈従来の技術〉
コンクリート型枠合板として合板表面にウレタン樹脂塗
料やアクリル樹脂塗料を塗装したり、ポリエチレンフィ
ルム等のフィルムを貼った所謂る表面強化合板は、型枠
としての転用回数の増加、木材より溶出するセメントの
硬化阻害成分の影響防止、コンクリート仕上り表面性の
向上等の面より広く使用されている。特に最近は、合板
用原木の質の低下が大きく表面強化合板が多く用いられ
るようになってきた。<Conventional technology> So-called surface-reinforced plywood, which is used as concrete formwork plywood by coating the plywood surface with urethane resin paint or acrylic resin paint or pasting a film such as polyethylene film, has been used as formwork plywood for an increased number of times. It is widely used because it prevents the effects of cement hardening inhibiting components that are leached out and improves the surface quality of concrete. Particularly recently, the quality of raw wood for plywood has declined significantly, and surface-reinforced plywood has come into widespread use.
合板表面を塗装して強化合板を製造する場合、通常先ず
目止剤で目止めをした後、下塗塗料を塗布して乾燥後サ
ンダー懸けし、上m塗料を塗装して再び乾燥して製品と
している。When manufacturing reinforced plywood by painting the plywood surface, it is usually first sealed with a sealant, then an undercoat is applied, dried and sanded, then a top coat is applied and dried again to produce the product. There is.
目止剤としては、酢酸ビニル樹脂、エチレン−酢酸ビニ
ル共縮合樹脂等の各種樹脂の水性エマルジョンに砥粉等
の充填剤と顔料を配合したものや油性塗料に充填剤と顔
料を配合したものが多く用いられ、下塗・上塗塗料とし
ては、溶剤型ウレタン樹脂塗料や溶剤型アクリル樹脂塗
料が多く用いられている。Many fillers are made by blending fillers such as abrasive powder and pigments with aqueous emulsions of various resins such as vinyl acetate resin and ethylene-vinyl acetate co-condensed resin, and by blending fillers and pigments into oil-based paints. Solvent-based urethane resin paints and solvent-based acrylic resin paints are often used as undercoats and topcoats.
この場合、塗装面の発泡を防止するため塗料の乾燥を風
乾で行うのが普通であり、乾燥工程の短縮・簡略化が強
く望まれている。また、溶剤型塗料を使用するため乾燥
時に溶剤が揮散して作業場の空気を汚染するので労働安
全衛生面からも溶剤の揮散のない塗装方法の出現が強く
望まれている。In this case, the paint is usually dried by air drying to prevent foaming on the painted surface, and there is a strong desire to shorten and simplify the drying process. Furthermore, since a solvent-based paint is used, the solvent evaporates during drying and contaminates the air in the workplace, so there is a strong desire for a coating method that does not volatilize the solvent from the standpoint of occupational safety and health.
乾燥工程の短縮のため上塗塗料として紫外線硬化型塗料
を利用することも検討され出したが、下塗塗料との密着
性の問題やクラック発生の問題があり実用化に至ってい
ない。The use of UV-curable paints as top coats has been considered in order to shorten the drying process, but this has not been put to practical use due to problems with adhesion with base coats and cracks.
〈発明が解決しようとする課題〉
本発明者らは、乾燥工程を中心とした製造工程を簡略化
した塗装方法により表面塗装強化コンクリート型枠合板
を製造する方法を鋭意研究した結果、上塗塗料として紫
外線硬化型塗料を用いて乾燥工程の短縮化を図るととも
に、従来欠点とされている密着性の問題やクラック発生
の問題を、下塗塗料若しくは目止剤が、硬化/未硬化若
しくは乾燥/未乾燥時に上塗塗料用紫外線硬化型塗料を
塗装することにより解決できることを見出し本発明に至
ったものである。<Problems to be Solved by the Invention> As a result of intensive research into a method for manufacturing surface-coated reinforced concrete form plywood using a coating method that simplifies the manufacturing process centered on the drying process, the present inventors have developed a method for producing surface-coated reinforced concrete form plywood. In addition to shortening the drying process by using ultraviolet curable paints, we have also solved the problems of adhesion and cracking, which have traditionally been considered drawbacks, by making it possible for the primer paint or filler to be cured/uncured or dry/undried. The inventors discovered that the problem could sometimes be solved by applying an ultraviolet curable paint for the top coat, leading to the present invention.
く課題を解決するための手段〉
本発明において、上塗塗料として紫外線硬化型塗料を用
い、下塗塗料若しくは目止め剤が硬化/未硬化若しくは
乾燥/未乾燥時に紫外線硬化型塗料を塗装することによ
り密着性の問題やクラック発生の問題を解決できること
ができたものである。Means for Solving the Problems> In the present invention, an ultraviolet curable paint is used as the top coat, and the UV curable paint is applied when the undercoat or filler is cured/uncured or dry/undried to achieve close contact. It was possible to solve the problem of sexual problems and the problem of crack generation.
本発明に用いることができる紫外線硬化型塗料としては
、次のようなものがある。Examples of ultraviolet curable paints that can be used in the present invention include the following.
(りラジカル重合型アクリレート系樹脂塗料エポキシ−
アクリレート、ウレタン−アクリレート、ポリエステル
−アクリレート、アルキッド−アクリレート、シリコン
−アクリレート等のアクリルオリゴマーに単官能性又は
多官能性アクリレートモノマーとベンゾインエーテル類
、ベンゾフェノン、アセトフェノン類、チオキサントン
系等の光反応開始剤、及び必要に応じてアミン系助剤や
溶剤を主成分とする塗料。(Radical polymerization type acrylate resin paint epoxy)
Acrylic oligomers such as acrylate, urethane acrylate, polyester acrylate, alkyd acrylate, and silicone acrylate, monofunctional or polyfunctional acrylate monomers, and photoreaction initiators such as benzoin ethers, benzophenone, acetophenones, and thioxanthone, and paints whose main ingredients are amine-based auxiliaries and solvents, if necessary.
(2)ラジカル重合型不飽和ポリエステル系樹脂塗料
不飽和二塩基酸とグライコール類を重合して得られる不
飽和ポリエステルオリゴマーに、スチレンモノマーとベ
ンゾインエーテル類等の光反応開始剤、及び必要に応じ
て助剤や溶剤を主成分とする塗料。(2) Radical polymerizable unsaturated polyester resin paint An unsaturated polyester oligomer obtained by polymerizing an unsaturated dibasic acid and a glycol, a styrene monomer, a photoreaction initiator such as benzoin ether, and as necessary. Paints whose main ingredients are auxiliary agents and solvents.
(3)ラジカル付加型ポリチオール−ポリエン系樹脂塗
料
オレフィン系不飽和樹脂(ポリエン)とポリチオールに
ベンゾフェノン類等の光反応開始剤、及び必要に応じて
助剤や溶剤を主成分とする塗料。(3) Radical addition type polythiol-polyene resin paint A paint whose main components are an olefinically unsaturated resin (polyene), a polythiol, a photoreaction initiator such as benzophenone, and if necessary, an auxiliary agent or a solvent.
(4)カチオン重合型エポキシ樹脂塗料エポキシオリゴ
マーにルイス酸塩類を光反応開始剤、及び必要に応じて
助剤や溶剤を主成分とする塗料。(4) Cationic polymerization type epoxy resin paint A paint whose main components are an epoxy oligomer, a Lewis acid salt as a photoreaction initiator, and, if necessary, an auxiliary agent and a solvent.
勿論、これらの樹脂を各種変性剤で変性して使用しても
良い。Of course, these resins may be used after being modified with various modifiers.
コンクリート型枠用材料には耐アルカリ性が要求される
ので、耐アルカリ性に優れたウレタン−アクリレート樹
脂やエポキシ−アクリレート樹脂を用いるのが望ましい
。Since materials for concrete formwork are required to have alkali resistance, it is desirable to use urethane-acrylate resins or epoxy-acrylate resins that have excellent alkali resistance.
下塗塗料としては、酢酸ビニル、エチレン、スチレン、
ブタジェン、アクリルニトリル類等の二重結合を有する
モノマーの1種又は2種以上を水系中でエマルジョン重
合させて得られる各種水性エマルジョン樹脂やアクリル
樹脂、ウレタン樹脂、エポキシ樹脂、アルキッド樹脂、
アミノ樹脂等を塗料化したものを用いることができる。As an undercoat, vinyl acetate, ethylene, styrene,
Various aqueous emulsion resins, acrylic resins, urethane resins, epoxy resins, alkyd resins obtained by emulsion polymerization of one or more monomers having double bonds such as butadiene and acrylonitriles in an aqueous system,
A paint made of amino resin or the like can be used.
製品の外観を向上させるため顔料や充填剤が通常添加さ
れる。Pigments and fillers are usually added to improve the appearance of the product.
目止剤としては、微粉、クレー、微粉シリカ、珪藻土、
炭酸石灰、ゴム粉、パライト、アルミナ、木粉等の充填
剤を水や粘結剤で練り合わせたものや下塗塗料として用
いることができる各種樹脂にこれらの充填剤と顔料およ
び水または溶剤を配合したもの等が用いられる。As a filler, fine powder, clay, fine silica, diatomaceous earth,
Fillers such as carbonated lime, rubber powder, pallite, alumina, and wood flour are mixed with water and a binder, and these fillers, pigments, and water or solvent are blended with various resins that can be used as an undercoat. things etc. are used.
本発明の塗装方法としては、
(1)台板合板を目上剤で目止め後、紫外線硬化樹脂塗
料を塗装して紫外線を照射して硬化させる方法・
(2)台板合板を目止剤で目止め後、下塗塗料を塗装し
、紫外線硬化樹脂塗料を塗装して紫外線により硬化させ
る方法、
の二つの方法がある。The coating method of the present invention is as follows: (1) After sealing the base plywood with a sealant, applying an ultraviolet curable resin paint and curing it by irradiating it with ultraviolet rays; (2) Applying the sealant to the base plywood There are two methods: after sealing the surface, apply an undercoat, and then apply an ultraviolet curing resin coating and cure it using ultraviolet light.
く作用〉
本発明の特長は、目止剤及び/または下塗塗料を塗装後
、乾燥/未乾燥若しくは硬化/未硬化状態で、紫外線硬
化樹脂塗料を塗装し、紫外線を照射させ硬化することに
より乾燥時間を大幅に短縮、生産性を向上させるところ
にある。A feature of the present invention is that after applying the sealant and/or undercoat paint, the UV-curable resin paint is applied in a dry/undried or hardened/uncured state, and the UV-curable resin paint is irradiated with ultraviolet rays to cure. It significantly reduces time and improves productivity.
さらに、目止剤、若しくは下塗塗料が乾燥する前に紫外
線硬化樹脂塗料を塗装することにより従来必要とした乾
燥工程を省略するなら紫外線硬化樹脂塗料の塗膜の応力
による亀裂発生を防止できる。Furthermore, if the conventionally required drying step is omitted by applying the UV-curable resin paint before the filler or undercoat dries, cracking due to stress in the UV-curable resin paint film can be prevented.
目上剤若しくは下I:!に塗料が未乾燥状態である上に
紫外線硬化樹脂塗料を塗装した場合、界面で互いの樹脂
が溶解し合うため密着性が向上するので、従来必要とし
ていた乾燥とサンダー懸は工程を省略でき、大幅な合理
化となる。又、紫外線硬化樹脂塗料は紫外線照射により
急速に硬化するため塗膜に応力が発生して亀裂を起こし
易いが、本発明の方法によると紫外線硬化樹脂塗料が硬
化後、下塗塗料又は目上剤が徐々に硬化するため、この
層で応力が緩和され製品の亀裂が発生しにくくなる。Eye cream or lower I:! When UV-curable resin paint is applied to an undried paint, the adhesion improves as the resins dissolve at the interface, so the drying and sanding processes that were previously required can be omitted. This will result in significant rationalization. Furthermore, since UV-curable resin paints are rapidly cured by UV irradiation, stress is generated in the coating film, which tends to cause cracks; however, according to the method of the present invention, after the UV-curable resin paints are cured, the undercoat or eye cream is applied. Because it hardens gradually, this layer relieves stress and makes the product less likely to crack.
なお、目止剤、若しくは下塗塗料に−NCO基を含有す
る成分を添加しておくと密着性をさらに向上させること
ができる。Note that adhesion can be further improved by adding a component containing an -NCO group to the filler or undercoat.
〈実施例〉 以下、実施例について説明する。<Example> Examples will be described below.
実施例−1
(1−1)目止剤の準備
ビスフェノールA型エポキシ樹脂 100部(エポキ
シ価190.粘度6000CPS/25°C)ポリアミ
ン硬化剤 50部(油化シェルエポ
キシ社1lB−002,アミン価327)微粉
150部トルエン
20部を擢潰機で練り合せてペ
ースト状に調合した。Example-1 (1-1) Preparation of filler Bisphenol A epoxy resin 100 parts (epoxy value 190, viscosity 6000 CPS/25°C) Polyamine curing agent 50 parts (Yuka Shell Epoxy Co., Ltd. 11B-002, amine value 327) Fine powder
150 parts toluene
20 parts were kneaded using a grinder to form a paste.
(1−2)紫外線硬化型ウレタン−アクリレート樹脂の
準備
1.3−ブチレングリコール135.2gr(1,5モ
ル)、1゜6−ヘキサンジオール17?、3gr(1,
5tl)及びアジピン酸277.73r(1,9モル)
を反応させて得たポリエステルポリオール(当量:26
2.5)とトリレンジイソシアネー) 383.2gr
及び、β−ヒドロキシエチルアクリレート278.4g
rを反応させてウレタン−アクリレート樹脂を得た。(1-2) Preparation of UV-curable urethane-acrylate resin 1.3-butylene glycol 135.2 gr (1.5 mol), 1°6-hexanediol 17? ,3gr(1,
5tl) and adipic acid 277.73r (1.9 mol)
Polyester polyol obtained by reacting (equivalent weight: 26
2.5) and tolylene diisocyanate) 383.2gr
and β-hydroxyethyl acrylate 278.4g
A urethane-acrylate resin was obtained by reacting r.
この樹脂700grにトリメチロールプロパントリアク
リレート(T M P T A )300gr、光反応
開始剤としてベンゾフェノン40g「と2,5−ジメチ
ルアミノエタノール35grを配合して紫外線硬化型ウ
レタン−アクリレート樹脂塗料(塗料−八)を得た。700g of this resin, 300g of trimethylolpropane triacrylate (TMPTA), 40g of benzophenone as a photoreaction initiator, and 35g of 2,5-dimethylaminoethanol were blended to create an ultraviolet curable urethane-acrylate resin paint (paint). 8) obtained.
(1−3)表面強化コンクリート型枠合板の作成12a
+s厚さのJAS−類合板に(1−1)で準備した目止
剤100gr/&を塗布後、(1−2)で準備した紫外
線硬化型ウレタン−アクリレート樹脂塗料(塗料−A)
を40gr/vrr塗布し、80ワツト/cぜの紫外線
ランプを2灯設置した連続紫外線硬化装置(装置−1)
内を5−/1n、の速度で通過させて硬化させた。(1-3) Creation of surface reinforced concrete formwork plywood 12a
After applying 100 gr/& of the sealant prepared in (1-1) to +s thick JAS-type plywood, apply the UV-curable urethane-acrylate resin paint (Paint-A) prepared in (1-2).
Continuous ultraviolet curing equipment (equipment-1) that applied 40 gr/vrr and installed two 80 watt/c UV lamps.
It was cured by passing through the inside at a speed of 5-/1n.
硬化後の粘着性は無く、積み重ねても問題無かった。There was no stickiness after curing, and there was no problem when stacking them.
得られた表面強化コンクリート型枠合板を室温でlO日
間養生した。The obtained surface-reinforced concrete form plywood was cured at room temperature for 10 days.
実施例−2
(2−1)目止剤の準備
スチレン−アクリル樹脂エマルジョン 100部(高圧
ガス工業製、ベガールvL−204、粘度5160CP
S/30°C5樹脂分53z)PVA10%水溶液
50部(鹸化度99x5重合度17
00)
クルードMDI 10
部(住友バイエルウレタン製、スミジュール44V−1
0)微粉 150部
水
8o部を摺潰機で練り合せてペースト状に
調合した。Example-2 (2-1) Preparation of filler Styrene-acrylic resin emulsion 100 parts (manufactured by Kosatsu Gas Kogyo, Begar vL-204, viscosity 5160CP
S/30°C5 resin content 53z) PVA 10% aqueous solution
50 parts (saponification degree 99x5 polymerization degree 17
00) Crude MDI 10
(manufactured by Sumitomo Bayer Urethane, Sumidur 44V-1
0) Fine powder 150 parts water
80 parts were kneaded using a grinder to form a paste.
(2−2)表面強化コンクリート型枠合板の作成12a
+n+厚さのJAS−類合板に(2−1)で準備した目
止剤120gr/v/を塗布後1.(1−2)で準備し
た紫外線硬化型ウレタン−アクリレート樹脂塗料(塗料
−A)を503r/Trr塗布し、実施例−1と同様に
連続紫外線硬化装置(装置−1)内を5m/sin、の
速度で通過させて硬化させた。(2-2) Creation of surface reinforced concrete formwork plywood 12a
1. After applying 120 gr/v/ of sealant prepared in (2-1) to JAS-type plywood of +n+ thickness. The ultraviolet curable urethane-acrylate resin paint (paint-A) prepared in (1-2) was applied at 503 r/Trr, and the inside of the continuous ultraviolet curing apparatus (apparatus-1) was heated at 5 m/sin in the same manner as in Example-1. It was cured by passing it at a speed of .
硬化後の粘着性は無く、積み重ねても問題無かった。There was no stickiness after curing, and there was no problem when stacking them.
得られた表面強化コンクリート型枠合板を室温で5日間
養生した。The obtained surface-reinforced concrete form plywood was cured at room temperature for 5 days.
実施例−3
(3−1)目止剤の準備
ウレタン樹脂塗料 100部(住友
バイエルウレタン社製、樹脂分70%、ポリオール07
0410部とイソシアネー) 07025部の混合物)
微粉 150部トルエ
ン 150部を撞潰
機で練り合せてペースト状に調合した。Example 3 (3-1) Preparation of sealant 100 parts of urethane resin paint (manufactured by Sumitomo Bayer Urethane Co., Ltd., resin content 70%, polyol 07
A mixture of 0.410 parts of isocyanate and 0.7025 parts of isocyanate) 150 parts of fine powder and 150 parts of toluene were kneaded in a crusher to form a paste.
(3−2)下塗塗料の準備
ポリエーテルポリオール 100部(住友
バイエルウレタン社製、デス上フェン1915U1水酸
基含量1.1χ)
ポリイソシアネー) 21部(住
友バイエルウレタン社製、デスモジュールし−75、イ
ソシアネート基含量13X)
を混合して無溶剤塗料を調合した。(3-2) Preparation of undercoat 100 parts of polyether polyol (manufactured by Sumitomo Bayer Urethane Co., Ltd., desmodule 1915U1 hydroxyl group content 1.1χ) 21 parts (manufactured by Sumitomo Bayer Urethane Co., Ltd., Desmodur Shi-75, isocyanate group content 13X) to prepare a solvent-free paint.
(3−3)紫外線硬化型エポキシ樹脂の準備光反応開始
剤としてルイス酸塩類を使用した紫外線硬化型エポキシ
樹脂塗料として、旭電化■製アデカオブトマーKR−4
00(塗料−B)を準備した。(3-3) Preparation of UV-curable epoxy resin Adeka Obtomer KR-4 manufactured by Asahi Denka ■ is used as a UV-curable epoxy resin paint using Lewis acid salts as a photoreaction initiator.
00 (Paint-B) was prepared.
(3−4)表面強化コンクリート型枠合板の作成12m
m厚さのJAS−類合板に(1−1)で準備した目上剤
80gr/−を塗布後、(3−2)で準備したウレタン
樹脂下塗塗料を70gr/v/塗布し、さらにその上へ
、(3−3)で準備した紫外線硬化型エポキシ樹脂塗料
(塗料−B)を353r/TIi″塗布し、実施例−1
と同様に連続紫外線硬化装置(装置−1)内を5m/m
i n 、の速度で通過させて硬化させた。(3-4) Creation of surface reinforced concrete formwork plywood 12m
After applying 80g/- of the eye polish prepared in (1-1) to JAS type plywood with a thickness of m, apply 70g/v/- of the urethane resin primer paint prepared in (3-2), and then apply Then, 353r/TIi'' of the ultraviolet curable epoxy resin paint (Paint-B) prepared in (3-3) was applied, and Example-1
5m/m inside the continuous ultraviolet curing equipment (device-1)
It was passed through and cured at a speed of i n .
硬化後の粘着性は無く、積み重ねても問題無かった。There was no stickiness after curing, and there was no problem when stacking them.
得られた表面強化コンクリート型枠合板を室温で10日
間養生した。The obtained surface-reinforced concrete form plywood was cured at room temperature for 10 days.
実施例−4
(トl)表面強化コンクリート型枠合板の作成12■■
厚さのJAS−類合板に(2−1)で準備した目止剤8
0gr//を塗布後、(3−2)で準備したウレタン樹
脂下塗塗料を40gr/ぜ塗布し、さらにその上へ、(
1−2)で準備した紫外線硬化型ウレタン−アクリレー
ト樹脂塗料(塗料−入)を40gr/Wr塗布す、実施
例−1と同様に連続紫外線硬化装置(装ff1−1)内
を5a+/win、の速度で通過させて硬化させた。Example-4 (l) Creation of surface-reinforced concrete formwork plywood 12■■
Filler 8 prepared in (2-1) on thick JAS-type plywood
After applying 0gr//, apply 40gr// of the urethane resin undercoat prepared in (3-2), and then apply (
Apply 40gr/Wr of the ultraviolet curable urethane-acrylate resin paint (paint-containing) prepared in 1-2), and apply 5a+/win in the continuous ultraviolet curing apparatus (equipment ff1-1) in the same manner as in Example-1. It was cured by passing it at a speed of .
硬化後の粘着性は無く、積み重ねても問題無かったφ
得られた表面強化コンクリート型枠合板を室温で10日
間養生した。There was no stickiness after curing, and there was no problem when stacking φ.The obtained surface-reinforced concrete form plywood was cured at room temperature for 10 days.
実施例−5
(5−1)目止剤の準備
スチレン−ブタジェン樹脂エマルジョン 80部(三井
東圧化学製、合成ゴム系ラテックス)PVA10%水溶
液 20部(鹸化度99z1重合
度1700)
クルードMDI 5部
(住友バイエルウレタン製、スミジュール44V−10
)炭酸カルシウム 100部水
200部を摺潰機で練り合せてペースト状に調
合した。Example-5 (5-1) Preparation of filler Styrene-butadiene resin emulsion 80 parts (manufactured by Mitsui Toatsu Chemical, synthetic rubber latex) PVA 10% aqueous solution 20 parts (saponification degree 99z1 polymerization degree 1700) Crude MDI 5 parts (Manufactured by Sumitomo Bayer Urethane, Sumidur 44V-10
) Calcium carbonate 100 parts water
200 parts were kneaded using a grinder to form a paste.
(5−2)表面強化コンクリート型枠合板の作成121
II11厚さのJAS−類合板に(5−1)で準備した
目止剤150gr/−を塗布後、(1−2)で準備した
紫外線硬化型ウレタン−アクリレート樹脂塗料(塗料−
A)を503r/Wr塗布し、実施例−1と同様に連続
紫外線硬化装置(装置t−1)内を5m/ll1in、
の速度で通過させて硬化させた。(5-2) Creation of surface reinforced concrete formwork plywood 121
After applying 150 gr/- of the filler prepared in (5-1) to JAS type plywood with a thickness of II11, apply the UV-curable urethane-acrylate resin paint (paint) prepared in (1-2).
A) was applied at 503r/Wr, and the inside of the continuous ultraviolet curing device (apparatus t-1) was heated at 5m/ll1in in the same manner as in Example-1.
It was cured by passing it at a speed of .
硬化後の粘着性は無く、積み重ねても問題無かった。There was no stickiness after curing, and there was no problem when stacking them.
得られた表面強化コンクリート型枠合板を室温で5日間
養生した。The obtained surface-reinforced concrete form plywood was cured at room temperature for 5 days.
列、横10列入れ、その上にセロハンテープを貼りつけ
て引きはがし、剥離状態をみる。Insert 10 rows and 10 rows, stick cellophane tape on top of it, peel it off, and check how it peels off.
(0)耐アルカリ性
10%苛性ソーダ水溶液中に1週間浸漬(ハ)寒熱繰り
返し試験
一20℃(2Hrs) −+ 60℃(2Hrs)の熱
サイクルを6回
繰り返し。(0) Alkali resistance Soaked in 10% caustic soda aqueous solution for one week (c) Repeated cold/heat test - 20°C (2Hrs) - + Repeated heat cycle of 60°C (2Hrs) 6 times.
(ニ)コンクリート離型性
JIS R−5201rセメントの物理試験方法」の供
試体
の作り方で調合したモルタルを表面上で2日間硬化を5
回繰り返した。(d) Concrete releasability JIS R-5201r Physical test method for cement" Mortar prepared according to the method of preparing the specimen was cured on the surface for 2 days.
Repeated times.
この結果を第1表に示す。The results are shown in Table 1.
以上の各実施例で得られた表面強化コンクリート型枠合
板について下記の特性を測定した。The following characteristics were measured for the surface-reinforced concrete form plywood obtained in each of the above examples.
(イ)基盤目テスト
ナイフで21111x2−一の基盤目状に切り傷を縦1
0第 1
表
第 2
表
一方、比較のため市販の表面塗装強化コンクリート型枠
合板を同一の試験条件で試験した。結果を第2表に示す
。(b) Using a base grain test knife, make a vertical cut in the shape of a 21111x2-1 base grain.
Table 0 Table 1 Table 2 On the other hand, for comparison, commercially available surface-coated reinforced concrete form plywood was tested under the same test conditions. The results are shown in Table 2.
〈発明の効果〉
以上のとおり、本発明により得られた表面強化コンクリ
ート型枠合板は下塗材との接着性に優れ、種々の条件下
においてもクラックの発生がない上、コンクリートから
の離型性も優れている。<Effects of the Invention> As described above, the surface-reinforced concrete form plywood obtained by the present invention has excellent adhesion with the base coating material, does not generate cracks even under various conditions, and has excellent releasability from concrete. is also excellent.
さらに、 製造工程が簡略化でき、 塗料から溶剤 の揮散も殆どない。moreover, The manufacturing process can be simplified, paint to solvent There is almost no volatilization.
Claims (3)
上塗塗料を塗布して表面強化コンクリート型枠合板を製
造する方法に於いて、該目止剤又は塗料が硬化/未硬化
若しくは乾燥/未乾燥状態で、紫外線硬化樹脂塗料を塗
布することを特徴とするコンクリート型枠合板の製造方
法。(1) After applying sealant and/or primer paint to the plywood surface,
A method for manufacturing surface-reinforced concrete form plywood by applying a top coat, characterized in that the UV curing resin paint is applied while the filler or paint is in a cured/uncured or dry/undried state. A method for manufacturing concrete formwork plywood.
ン樹脂を用いることを特徴とする請求項1記載のコンク
リート型枠合板の製造方法。(2) The method for producing concrete form plywood according to claim 1, characterized in that a water-based emulsion resin is used as a sealant and/or an undercoat.
た塗料を用いることを特徴とする請求項1または2記載
のコンクリート型枠合板の製造方法。(3) The method for producing concrete form plywood according to claim 1 or 2, characterized in that a paint containing an -NCO group is used as the filler and/or the undercoat.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32604688A JPH0243464A (en) | 1988-04-14 | 1988-12-26 | Manufacture of surface reinforce concrete-form plywood |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63-90302 | 1988-04-14 | ||
| JP9030288 | 1988-04-14 | ||
| JP32604688A JPH0243464A (en) | 1988-04-14 | 1988-12-26 | Manufacture of surface reinforce concrete-form plywood |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0243464A true JPH0243464A (en) | 1990-02-14 |
Family
ID=26431799
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP32604688A Pending JPH0243464A (en) | 1988-04-14 | 1988-12-26 | Manufacture of surface reinforce concrete-form plywood |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0243464A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02204572A (en) * | 1989-02-01 | 1990-08-14 | Sumitomo Ringyo Kk | Wooden plywood for concrete form and method for treating surface thereof |
| JPH03159702A (en) * | 1989-11-20 | 1991-07-09 | Mitsui Toatsu Chem Inc | Manufacture of surface-treated plywood or concrete form plywood |
| US6935606B2 (en) | 2001-08-31 | 2005-08-30 | Wai Wing Chan | Formwork |
| JP2016005873A (en) * | 2014-06-20 | 2016-01-14 | 株式会社ユニソン | Absorptive base material in which image is formed on outer surface and method for producing the same |
-
1988
- 1988-12-26 JP JP32604688A patent/JPH0243464A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02204572A (en) * | 1989-02-01 | 1990-08-14 | Sumitomo Ringyo Kk | Wooden plywood for concrete form and method for treating surface thereof |
| JPH03159702A (en) * | 1989-11-20 | 1991-07-09 | Mitsui Toatsu Chem Inc | Manufacture of surface-treated plywood or concrete form plywood |
| US6935606B2 (en) | 2001-08-31 | 2005-08-30 | Wai Wing Chan | Formwork |
| JP2016005873A (en) * | 2014-06-20 | 2016-01-14 | 株式会社ユニソン | Absorptive base material in which image is formed on outer surface and method for producing the same |
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