JPH06182291A - Method of coating resin composition - Google Patents
Method of coating resin compositionInfo
- Publication number
- JPH06182291A JPH06182291A JP4335992A JP33599292A JPH06182291A JP H06182291 A JPH06182291 A JP H06182291A JP 4335992 A JP4335992 A JP 4335992A JP 33599292 A JP33599292 A JP 33599292A JP H06182291 A JPH06182291 A JP H06182291A
- Authority
- JP
- Japan
- Prior art keywords
- viscosity
- curing agent
- cps
- resin composition
- spraying
- 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
- 238000000576 coating method Methods 0.000 title claims description 24
- 239000011342 resin composition Substances 0.000 title claims description 14
- 238000000034 method Methods 0.000 title abstract description 5
- 239000011248 coating agent Substances 0.000 title description 12
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 46
- 239000000203 mixture Substances 0.000 claims abstract description 32
- 238000005507 spraying Methods 0.000 claims abstract description 20
- 229920005862 polyol Polymers 0.000 claims description 20
- 150000003077 polyols Chemical class 0.000 claims description 19
- 239000007921 spray Substances 0.000 claims description 17
- 239000005002 finish coating Substances 0.000 claims description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 3
- 239000003973 paint Substances 0.000 claims description 3
- 230000003068 static effect Effects 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 abstract description 10
- 239000010454 slate Substances 0.000 abstract description 8
- 238000010422 painting Methods 0.000 abstract description 5
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 3
- 229920001451 polypropylene glycol Polymers 0.000 abstract description 3
- 230000002265 prevention Effects 0.000 abstract description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000007788 liquid Substances 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- -1 isocyanate compound Chemical class 0.000 description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 4
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 4
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 4
- 229930195725 Mannitol Natural products 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 150000002009 diols Chemical class 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 239000000594 mannitol Substances 0.000 description 4
- 235000010355 mannitol Nutrition 0.000 description 4
- 229920005906 polyester polyol Polymers 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 239000000600 sorbitol Substances 0.000 description 4
- 235000010356 sorbitol Nutrition 0.000 description 4
- PISLZQACAJMAIO-UHFFFAOYSA-N 2,4-diethyl-6-methylbenzene-1,3-diamine Chemical compound CCC1=CC(C)=C(N)C(CC)=C1N PISLZQACAJMAIO-UHFFFAOYSA-N 0.000 description 3
- 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 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000004049 embossing Methods 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 239000005056 polyisocyanate Substances 0.000 description 3
- 229920001228 polyisocyanate Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- HOVAGTYPODGVJG-UVSYOFPXSA-N (3s,5r)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol Chemical compound COC1OC(CO)[C@@H](O)C(O)[C@H]1O HOVAGTYPODGVJG-UVSYOFPXSA-N 0.000 description 2
- ICVIFRMLTBUBGF-UHFFFAOYSA-N 2,2,6,6-tetrakis(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1(CO)CCCC(CO)(CO)C1O ICVIFRMLTBUBGF-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- RTWAGNSZDMDWRF-UHFFFAOYSA-N [1,2,2-tris(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1(CO)CO RTWAGNSZDMDWRF-UHFFFAOYSA-N 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- HOVAGTYPODGVJG-UHFFFAOYSA-N methyl beta-galactoside Natural products COC1OC(CO)C(O)C(O)C1O HOVAGTYPODGVJG-UHFFFAOYSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001610 polycaprolactone Polymers 0.000 description 2
- 239000004632 polycaprolactone Substances 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- VOZKAJLKRJDJLL-UHFFFAOYSA-N tolylenediamine group Chemical group CC1=C(C=C(C=C1)N)N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 1
- JUXXCHAGQCBNTI-UHFFFAOYSA-N 1-n,1-n,2-n,2-n-tetramethylpropane-1,2-diamine Chemical compound CN(C)C(C)CN(C)C JUXXCHAGQCBNTI-UHFFFAOYSA-N 0.000 description 1
- QZWKEPYTBWZJJA-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine-4,4'-diisocyanate Chemical compound C1=C(N=C=O)C(OC)=CC(C=2C=C(OC)C(N=C=O)=CC=2)=C1 QZWKEPYTBWZJJA-UHFFFAOYSA-N 0.000 description 1
- IBOFVQJTBBUKMU-UHFFFAOYSA-N 4,4'-methylene-bis-(2-chloroaniline) Chemical compound C1=C(Cl)C(N)=CC=C1CC1=CC=C(N)C(Cl)=C1 IBOFVQJTBBUKMU-UHFFFAOYSA-N 0.000 description 1
- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 230000000386 athletic effect Effects 0.000 description 1
- YBGHFLPNIGPGHX-UHFFFAOYSA-N calcium;octan-1-olate Chemical compound [Ca+2].CCCCCCCC[O-].CCCCCCCC[O-] YBGHFLPNIGPGHX-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- KUDPGZONDFORKU-UHFFFAOYSA-N n-chloroaniline Chemical compound ClNC1=CC=CC=C1 KUDPGZONDFORKU-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920003226 polyurethane urea Polymers 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 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
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
(57)【要約】
【目的】ポリウレタン形成性の主剤及び硬化剤を加熱す
る加熱装置やそのための防災対策を必要とすることな
く、容易に構造物に明瞭な凹凸(エンボス)模様の表面
を形成できる塗装方法を得る。
【構成】硬化剤としてポリプロピレングリコール/ジフ
ェニルメタンジアミン混合液(粘度1500cps/2
5℃以上)を、主剤としてウレタンプレポリマー(粘度
2600cps/25℃)を用い、これをフラットチャ
ンバー(NO.2)+チップ(043−25)を取り付
けてあるプロブラーガンに導入して混合の後、この混合
物の吹付圧を170brとなる様に雨滴状態で、直ちに
スレート板上に吹き付けた(実施例1)。
【効果】加熱装置やその防災対策を必要とせずに、ノン
スリップ性を有する、明瞭なエンボス模様表面が形成で
きた。(57) [Summary] [Purpose] Easily form a clear embossed surface on a structure without the need for a heating device that heats a polyurethane-forming main agent and curing agent, and disaster prevention measures therefor. Get a possible painting method. [Structure] Polypropylene glycol / diphenylmethanediamine mixed liquid as a curing agent (viscosity 1500 cps / 2
Urethane prepolymer (viscosity 2600 cps / 25 ° C.) as a main component was introduced into a flat chamber (NO. 2) + tip (043-25) -attached probler gun for mixing. After that, the mixture was immediately sprayed on a slate plate in a raindrop state so that the spraying pressure was 170 br (Example 1). [Effect] A clear embossed pattern surface having non-slip properties could be formed without the need for a heating device and its disaster prevention measures.
Description
【0001】[0001]
【産業上の利用分野】本願発明は、常温硬化性樹脂組成
物の構造物への塗装方法に関し、特に防水塗装、床面塗
装、及び舗装面に適したノンスリップ面を得るエンボス
仕上げ塗装方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for coating a room temperature curable resin composition on a structure, and more particularly to a waterproof coating, a floor coating, and an emboss finish coating method for obtaining a non-slip surface suitable for paving. Is.
【0002】[0002]
【従来の技術】従来、常温硬化性樹脂組成物を構造物に
塗布するに当たり、表面を平滑に仕上げるため、希釈剤
の多用による低粘化、昇温による低粘化、吹き付けガン
口金径の細小化等が行われて来た。特に近年の超高反応
性ポリウレタン・ポリウレア樹脂の吹付け工法にあって
は、その作業時間の短縮化ができるので、多用されてい
る。2. Description of the Related Art Conventionally, when a room temperature curable resin composition is applied to a structure, the surface is made smooth, so that the viscosity of the spray gun is reduced by virtue of the use of a large amount of diluent, the viscosity of the spray gun is reduced. Have been done. In particular, in recent years, the method of spraying ultra-highly reactive polyurethane / polyurea resin is widely used because the working time can be shortened.
【0003】しかしながら、かかる工法の実施にあたっ
ては使用する機器の吹き付け圧力に上限があり、この
為、材料の低粘化のための昇温用の電源の確保、あるい
は高温による火傷の危険性、材料の保温のために吐出ホ
ースの保温の確保等の施工作業に伴う多大なメンテ素材
が必要であり、塗装時に要する消費エネルギーが極めて
多くなるという欠点がある。しかも塗装に当たっての注
意事項が多く、塗装作業は、高等な熟練が要求されてお
り、非常に煩雑であるとともに人件費等も高額となる。However, in carrying out such a construction method, there is an upper limit to the spraying pressure of the equipment used, and therefore, there is secured a power source for raising the temperature for lowering the viscosity of the material, or the risk of burns due to high temperature, and the material. In order to keep the heat of the discharge hose, a large amount of maintenance material is required for the construction work such as keeping the heat of the discharge hose, and there is a drawback that the energy consumption required for coating becomes extremely large. Moreover, there are many precautions to be taken in painting, and a high level of skill is required for painting work, which is very complicated and labor costs are high.
【0004】また、かかる状態のものによる構造物への
塗布による吹き付け等で、表面の形状をエンボス状に仕
上げるときには、材料が既施工面に付着するまでに飛行
距離を長くと採るように上方に吹き付けたり、吐出量を
絞る等の塗装方法もあるが、作業者の熟練度に依存する
ものが多く、塗装状態の普遍性に欠ける傾向が大きい。When the surface is finished in an embossed shape by spraying a structure in such a state by spraying or the like, it is necessary to increase the flight distance so that the flight distance is long before the material adheres to the existing surface. Although there are coating methods such as spraying and reducing the discharge amount, many methods depend on the skill of the operator, and the generality of the coating state tends to be lacking.
【0005】[0005]
【発明が解決しようとする課題】従来の塗装方法は、い
ずれにせよ、塗装すべき材料を暖めたり保温しておく装
置が必要だし、それに伴う災害への対処策等を必ず予め
講じておく必要があり、塗装作業性もあまりよくない。In any case, the conventional coating method requires a device for heating or keeping the material to be coated warm, and it is necessary to take measures against disasters accompanying it in advance. And the workability of painting is not so good.
【0006】[0006]
【課題を解決するための手段】本発明者らは、上記課題
を解決するため鋭意研究の結果、主剤と硬化剤とを混合
した、硬化性に優れた二液型のポリウレタン樹脂形成性
樹脂組成物を構造物に塗布硬化させて、エンボス塗膜を
形成するに当たって、特定の粘度を有する主剤と硬化剤
からポリウレタン形成性樹脂組成物を得、直ちにそれを
構造物に吹き付けて硬化させるという塗装方法を採用す
れば、特段の加熱装置を必要とせず、しかもわざわざ吹
き付け角度の設定、防災対策等の点で特段の配慮なし
に、極めて容易にエンボス塗装面が得られることを見い
出し、本発明を完成するに至った。Means for Solving the Problems As a result of intensive studies to solve the above-mentioned problems, the present inventors have found that a two-component polyurethane resin-forming resin composition excellent in curability in which a main agent and a curing agent are mixed. A coating method in which a polyurethane-forming resin composition is obtained from a main agent having a specific viscosity and a curing agent when the composition is applied to the structure and cured to form an embossed coating film, and the composition is immediately sprayed and cured on the structure. The present invention has been completed by discovering that the use of a specially designed heating device makes it possible to obtain an embossed coated surface very easily without the need for special settings such as setting the spraying angle and disaster prevention measures. Came to do.
【0007】即ち本発明は、末端にイソシアネート基を
有するプレポリマーを含む粘度1500cps以上の主
剤と、ポリオールを含む粘度1500cps以上の硬化
剤とを混合して常温硬化性樹脂組成物を調製するととも
に、直ちにそれを基材に吹き付け硬化させることを特徴
とするエンボス仕上げ塗装法を提供するものである。That is, the present invention prepares a room temperature curable resin composition by mixing a main agent having a prepolymer having an isocyanate group at a terminal and a viscosity of 1500 cps or more with a curing agent containing a polyol and having a viscosity of 1500 cps or more. The present invention provides an embossing finish coating method characterized by immediately spraying and curing it onto a substrate.
【0008】[0008]
【構成】本発明において使用する構造物としては、例え
ば家屋、ビル、橋、道路、陸上競技上、テニスコート、
等の構築物の屋根面、壁面、床面等が挙げられる。[Structure] Examples of structures used in the present invention include houses, buildings, bridges, roads, athletics, tennis courts,
The roof surface, wall surface, floor surface, etc. of the building such as
【0009】本発明では、特定粘度の主剤と特定粘度の
硬化剤とを混合して、その混合物が完全に硬化しないう
ちに、直ちに構造物に吹き付け塗布する点に特徴があ
り、主剤や硬化剤そのものの組成は、本質的には重要で
はない。The present invention is characterized in that a main agent having a specific viscosity and a curing agent having a specific viscosity are mixed, and before the mixture is not completely cured, the composition is immediately sprayed and applied to the structure. Its composition is essentially unimportant.
【0010】本発明で用いる主剤は粘度1500cps
を越えるものであり、それと組み合わせて用いる一方の
硬化剤は、粘度1500cps以上のものである。The base material used in the present invention has a viscosity of 1500 cps.
One of the curing agents to be used in combination with it has a viscosity of 1500 cps or more.
【0011】本発明で用いる、末端にイソシアネート基
有するプレポリマーを含む粘度1500cpsを越える
主剤としては、有機イソシアネート化合物、例えば2,
4−トリレンジイソシアネ−ト(以下、TDIと略
す)、65/35−TDI、80/20−TDI、4,
4´−ジフェニルメタンジイソシアネ−ト(以下、MD
Iと略す)、ジアニシジンジイソシアネ−ト、トリデン
ジイソシアネ−ト、メタキシリレンジイソシアネート、
ヘキサメチレンジイソシアネート、フェニレンジイソシ
アネート、1,5−ナフタレンジイソシアネート、ポリ
メチレンポリフェニルポリイソシアネート、イソホロン
ジイソシアネート、水添化MDI、水添化TDIなどの
如き芳香族ジイソシアネート類、脂環族ジイソシアネー
ト類の中より選ばれた有機ポリイソシアネート化合物が
挙げられる。The main agent used in the present invention containing a prepolymer having an isocyanate group at the terminal and having a viscosity of more than 1500 cps is an organic isocyanate compound such as 2,
4-tolylene diisocyanate (hereinafter abbreviated as TDI), 65 / 35-TDI, 80 / 20-TDI, 4,
4'-diphenylmethane diisocyanate (hereinafter, MD
Abbreviated as I), dianisidine diisocyanate, tridene diisocyanate, metaxylylene diisocyanate,
Hexamethylene diisocyanate, phenylene diisocyanate, 1,5-naphthalene diisocyanate, polymethylene polyphenyl polyisocyanate, isophorone diisocyanate, hydrogenated MDI, hydrogenated TDI, etc., selected from aromatic diisocyanates and alicyclic diisocyanates. The organic polyisocyanate compound is used.
【0012】もしくは、上記したこれらの単独あるいは
これらの混合物にポリオール化合物、例えば、ポリエス
テルポリオール類、ポリエーテルポリオール類、ポリエ
ステルポリアミドポリオール類、ポリカーボネートポリ
オール類、ポリカプロラクトンポリエステルポリオール
類、ポリブタジエンポリオール類、ポリペンタジエンポ
リオール類、ひまし油系ポリオール、低分子量ジオール
類、トリメチロールプロパン、グリセリン、ソルビトー
ル、マンニトール、ズルシトールなどより選ばれたもの
である。Alternatively, a polyol compound such as polyester polyols, polyether polyols, polyester polyamide polyols, polycarbonate polyols, polycaprolactone polyester polyols, polybutadiene polyols, polypentadiene may be used alone or in a mixture thereof. It is selected from polyols, castor oil-based polyols, low molecular weight diols, trimethylolpropane, glycerin, sorbitol, mannitol, dulcitol and the like.
【0013】好ましくは、ポリエーテルポリオール類で
あって分子量200〜10000程度のもので低分子量
ジオール、グリセリン、トリメチロールプロパン、ヘキ
サントリオール、トリエタノールアミン、ペンタエリス
リトール、エチレンジアミン、トリレンジアミン、ジフ
ェニルメタンジアミン、テトラメチロールシクロヘキサ
ン、メチルグルコシド、2,2,6,6-テトラキス(ヒドロキ
シルメチル)シクロヘキサノール、ジエチレントリアミ
ン、ソルビトール、マンニトール、シュクロース等を出
発物質としてアルキレンオキサイド例えば、エチレンオ
キサイド、プロピレンオキサイド等を付加せしめたもの
で、好ましくはNCO/OH当量比1.5以上、より好ま
しくは1.5〜20の比率で反応させたNCO基含有プレポ
リマーの単独あるいは混合物よりなるもの及び/又は可
塑剤や溶剤に溶解させた溶液系のものから選ばれたもの
が、任意に使用出来る。Preferably, the polyether polyols have a molecular weight of about 200 to 10,000, and have a low molecular weight diol, glycerin, trimethylolpropane, hexanetriol, triethanolamine, pentaerythritol, ethylenediamine, tolylenediamine, diphenylmethanediamine, Tetramethylol cyclohexane, methyl glucoside, 2,2,6,6-tetrakis (hydroxylmethyl) cyclohexanol, diethylenetriamine, sorbitol, mannitol, sucrose, etc. were used as starting materials, and alkylene oxides such as ethylene oxide and propylene oxide were added. And preferably an NCO / OH equivalent ratio of 1.5 or more, more preferably 1.5 to 20 reacted NCO group-containing prepolymer alone or as a mixture. Any material selected from the group consisting of materials and / or a solution system in which a plasticizer or a solvent is dissolved may be used.
【0014】本発明において使用するポリオールを含む
粘度1500cps以上の硬化剤とは、例えば、ポリエ
ステルポリオール類、ポリエーテルポリオール類、ポリ
エステルポリアミドポリオール類、ポリカーボネートポ
リオール類、ポリカプロラクトンポリエステルポリオー
ル類、ポリブタジエンポリオール類、ポリペンタジエン
ポリオール類、ひまし油系ポリオール、低分子量ジオー
ル類、トリメチロールプロパン、グリセリン、ソルビト
ール、マンニトール、ズルシトールなどより選ばれたも
のである。The curing agent having a viscosity of 1500 cps or more containing the polyol used in the present invention includes, for example, polyester polyols, polyether polyols, polyester polyamide polyols, polycarbonate polyols, polycaprolactone polyester polyols, polybutadiene polyols, It is selected from polypentadiene polyols, castor oil-based polyols, low molecular weight diols, trimethylolpropane, glycerin, sorbitol, mannitol, dulcitol and the like.
【0015】好ましくは、ポリエーテルポリオール類で
あって分子量200〜10000程度のもので低分子量
ジオール、グリセリン、トリメチロールプロパン、ヘキ
サントリオール、トリエタノールアミン、ペンタエリス
リトール、エチレンジアミン、トリレンジアミン、ジフ
ェニルメタンジアミン、テトラメチロールシクロヘキサ
ン、メチルグルコシド、2,2,6,6-テトラキス(ヒドロキ
シルメチル)シクロヘキサノール、ジエチレントリアミ
ン、ソルビトール、マンニトール、シュクロース等を出
発物質としてアルキレンオキサイド例えば、エチレンオ
キサイド、プロピレンオキサイド等を付加せしめたもの
で、好ましくは分子量200〜10000程度のもので
ある。Preferably, polyether polyols having a molecular weight of about 200 to 10,000, low molecular weight diols, glycerin, trimethylolpropane, hexanetriol, triethanolamine, pentaerythritol, ethylenediamine, tolylenediamine, diphenylmethanediamine, Tetramethylol cyclohexane, methyl glucoside, 2,2,6,6-tetrakis (hydroxylmethyl) cyclohexanol, diethylenetriamine, sorbitol, mannitol, sucrose, etc. were used as starting materials, and alkylene oxides such as ethylene oxide and propylene oxide were added. Those having a molecular weight of about 200 to 10,000 are preferable.
【0016】本発明において使用するポリオールを含む
粘度1500cps以上の硬化剤には、さらに硬化を促
進させるために、ポリウレタン樹脂用及びエポキシ樹脂
用硬化剤又は硬化促進剤が使用できる。As the curing agent containing the polyol used in the present invention and having a viscosity of 1500 cps or more, a curing agent or curing accelerator for polyurethane resin and epoxy resin can be used to further accelerate the curing.
【0017】この様なものとしては、例えば3,3’−
ジクロロ−4,4’−ジアミノジフェニルメタン、2−
クロロアニリンとホルムアルデヒドの縮合物、ジエチル
トルエンジアミン、MDA、TDA、エチレンジアミ
ン、トリオキシプロピレンジアミン等が挙げられ、その
単独および混合物よりなるものがいずれのものも使用で
きる。As such a thing, for example, 3,3'-
Dichloro-4,4'-diaminodiphenylmethane, 2-
Examples thereof include condensates of chloroaniline and formaldehyde, diethyltoluenediamine, MDA, TDA, ethylenediamine, trioxypropylenediamine, and the like, and any of these alone or as a mixture can be used.
【0018】また硬化触媒としては公知のものがいずれ
も使用できるが、例えばトリメチルアミン、トリエチル
アミン、トリブチルアミン、N−ジメチルラウリルアミ
ン、N−ジエチルラウリルアミン、N,N′−メチルピペ
ラジン、N,N′−ジメチルベンジルアミン、N−メチル
モルホリン、N−エチルモルホリン、トリエチレンジア
ミン、N−ペンタメチルエチレントリアミン、N,N,N',N'
−テトラメチルプロピレンジアミン、N−ポリメチルポ
リエチレンポリアミンなどの第三級アミン類や、例えば
オクチル酸カルシウム、オクチル酸鉛、ジブチルチンジ
ラウレート、スタンナスオクテートなどの有機金属塩類
などが挙げられ、その単独および混合物よりなるもの
が、いずれのものも使用できる。Any known curing catalyst can be used. For example, trimethylamine, triethylamine, tributylamine, N-dimethyllaurylamine, N-diethyllaurylamine, N, N'-methylpiperazine, N, N '. -Dimethylbenzylamine, N-methylmorpholine, N-ethylmorpholine, triethylenediamine, N-pentamethylethylenetriamine, N, N, N ', N'
-Tetramethyl propylene diamine, tertiary amines such as N-polymethyl polyethylene polyamine, and organic metal salts such as calcium octylate, lead octylate, dibutyltin dilaurate, stanna octate, etc., and the like alone. And any mixture can be used.
【0019】これらの硬化触媒の使用量は、好ましくは
有機ポリイソシアネート化合物100重量部に対して
0.01〜1.0重量部、より好ましくは0.05〜
0.50重量部使用するものであるThe amount of these curing catalysts used is preferably 0.01 to 1.0 part by weight, more preferably 0.05 to 1.0 part by weight, based on 100 parts by weight of the organic polyisocyanate compound.
0.50 parts by weight is used
【0020】主剤と硬化剤とを混合した際のゲル化時間
(換言すれば、ポリウレタン形成性樹脂組成物の硬化時
間)は、その吹き付け圧力とも関連があり、限定されな
いが、通常、容易にエンボス模様を構造物表面に形成す
る際には、室温(25℃)において、3〜30秒とする
のが適当である。The gelling time (in other words, the curing time of the polyurethane-forming resin composition) when the main agent and the curing agent are mixed is related to the spraying pressure and is not limited, but it is usually easily embossed. When the pattern is formed on the surface of the structure, it is appropriate that the time is 3 to 30 seconds at room temperature (25 ° C.).
【0021】本発明の塗装方法では、上記主剤と硬化剤
とを混合した組成物をそれが硬化する以前に、構造物に
吹き付けて硬化してやればよい。この際の吹き付け塗布
には、従来の高圧吹き付け発泡機がいずれも使用でき
る。In the coating method of the present invention, the composition obtained by mixing the main component and the curing agent may be sprayed and cured on the structure before it is cured. For the spray coating at this time, any conventional high-pressure spray foaming machine can be used.
【0022】本発明では、高圧吹き付け発泡機から吐出
される混合物を、そのまま構造物に吹き付け塗布しても
よいが、本発明では従来に比べて高粘度の主剤と硬化剤
を併用するので、より均一に混合されたポリウレタン形
成性樹脂組成物を、より短時間で調製するために、狭
い断口から流体を噴出させ、その部分の圧力の減少によ
り、前記流体と、周囲に存在する前記流体とは別種の流
体と混合する機構を有する混合器、又は可動部のない
複数の混合要素が内部に固定されている管状混合器をさ
らに併用して吹き付け塗布を行うことが好ましい。In the present invention, the mixture discharged from the high-pressure blowing foaming machine may be spray-coated on the structure as it is. However, in the present invention, since the main component having a higher viscosity than the conventional one and the curing agent are used together, In order to prepare a uniformly mixed polyurethane-forming resin composition in a shorter time, a fluid is ejected from a narrow opening, and the pressure of that portion is reduced, whereby the fluid and the fluid existing in the surrounding area are separated from each other. It is preferable to perform spray application by additionally using a mixer having a mechanism for mixing with another type of fluid or a tubular mixer having a plurality of mixing elements without moving parts fixed therein.
【0023】上記〜の混合器はいずれも吐出孔部に
駆動部分が無く、主剤と硬化剤の流動そのものによりそ
れらが混合されるもので、例えばスタッチックミキサ
ー、吸引混合ヘッド、衝突混合ヘッド等を有する混合器
が挙げられる。In all of the above mixers (1) to (5), there is no driving part in the discharge hole, and they are mixed by the flow of the main agent and the curing agent itself. For example, a stouch mixer, a suction mixing head, a collision mixing head, etc. are used. The mixer which has is mentioned.
【0024】本発明の塗装方法において、混合物の吐出
状態は特に制限がなく、噴霧状態又は雨滴状態にて吐出
すればよいが、エンボス模様を形成するに当たっては、
雨滴状態で構造物に塗布されることが好ましい。噴霧状
態で構造物上に主剤と硬化剤との混合物が吹き付けられ
る場合、その混合物がレベリングしやすく、エンボス模
様が鮮明に発現しないことがある。In the coating method of the present invention, the discharge state of the mixture is not particularly limited, and it may be discharged in a spray state or a raindrop state. In forming an embossed pattern,
It is preferably applied to the structure in the form of raindrops. When the mixture of the main agent and the curing agent is sprayed onto the structure in the sprayed state, the mixture is likely to be leveled, and the embossed pattern may not be clearly expressed.
【0025】本発明では、高粘度の主剤と硬化剤とを用
いているので、雨滴状態で吐出やすく、上記〜の混
合器を使用した際には、その相乗効果も相俟って、より
良好な鮮明なエンボス模様が得られる。In the present invention, since a high-viscosity base material and a curing agent are used, it is easy to discharge in the state of raindrops, and when the mixers (1) to (3) are used, the synergistic effects thereof are combined, and it is better. A clear embossed pattern can be obtained.
【0026】主剤と硬化剤とを混合したポリウレタン形
成性樹脂組成物を塗装する際の、混合物の吹き付け圧力
は、特に制限されるものではないが、通常140Br以
上である。本発明で用いる主剤と硬化剤は、それぞれ高
粘度であるので、前記した圧力で構造物に吹き付けるの
が、鮮明なエンボス模様を得るうえでも好ましい。The spraying pressure of the mixture for coating the polyurethane-forming resin composition in which the main agent and the curing agent are mixed is not particularly limited, but is usually 140 Br or more. Since the main agent and the curing agent used in the present invention have high viscosities respectively, it is preferable to spray them onto the structure with the above-mentioned pressure in order to obtain a clear embossed pattern.
【0027】140br以上の圧力で混合物を吹付装置
としては、例えばプランジャーの往復動作にて吐出され
るものでエアー圧力駆動、オイル圧力駆動、エンジン直
列駆動等の駆動部分を有するものがいずれも使用でき
る。好ましくはスプレーガン自体のオン・オフ動作に順
応して吐出駆動が制御される高圧吹付発泡装置がよく、
特に好ましくは、吐出圧力が常温においても140br
以上の吹き付け圧力となる様に装置は使用される。As the spraying device for spraying the mixture at a pressure of 140 br or more, for example, a device which is discharged by the reciprocating motion of a plunger and has a driving portion such as air pressure driving, oil pressure driving, engine series driving, etc. is used. it can. Preferably, a high-pressure blowing foaming device in which the discharge drive is controlled in accordance with the on / off operation of the spray gun itself,
Particularly preferably, the discharge pressure is 140 br even at room temperature.
The device is used so that the above spraying pressure is obtained.
【0028】本発明の混合物(ポリウレタン形成性樹脂
組成物)を構成する主剤、硬化剤には、本発明の効果を
損なわない範囲で、必要に応じて、例えば可塑剤、プロ
セスオイル、安定剤、紫外線吸収剤等を添加併用でき
る。The main component and curing agent constituting the mixture (polyurethane-forming resin composition) of the present invention may contain, for example, a plasticizer, a process oil, a stabilizer, if necessary, within a range not impairing the effects of the present invention. An ultraviolet absorber or the like can be added and used in combination.
【0029】それにより、従来の方法で採られている使
用プレポリマーのNCO基濃度を高くしてフリーのイソ
シアネート化合物を多くして低粘度にする、材料を高温
に昇温して低粘度にする、使用機器の温度を高温にして
低粘度にする、吐出ホースをヒーテイングして低粘度を
保つ等の、煩雑で、より多くのエネルギーを消費する塗
装方法を採用する必要がなくなった。As a result, the NCO group concentration of the prepolymer used in the conventional method is increased to increase the amount of free isocyanate compound to reduce the viscosity, and the material is heated to a high temperature to reduce the viscosity. , It is no longer necessary to adopt a complicated and more energy-consuming coating method such as increasing the temperature of the equipment used to lower the viscosity and heating the discharge hose to maintain the low viscosity.
【0030】このため加熱のための設備、ヒーテイング
ホース等を使用せずに、エンボス塗装面を熟練を要する
こと無く得ることが出来るようになり、非常に塗装作業
が効率的となり、施工時のエネルギーも削減でき経済性
も高くなった。Therefore, it becomes possible to obtain an embossed coating surface without requiring skill, without using equipment for heating, a heating hose, etc., which makes the coating work very efficient, and Energy can be reduced and economic efficiency is improved.
【0031】[0031]
【実施例】本発明を実施例にて詳細に説明する。本発明
はこれら実施例のみに限定されるものではない。又、文
中「部」、「%」は、断わりのない限り重量基準であ
る。EXAMPLES The present invention will be described in detail with reference to Examples. The invention is not limited to these examples only. Also, "part" and "%" in the text are based on weight unless otherwise specified.
【0032】実施例1 塗料圧送吐出用タンク〔旭ハナック(株)タイルマン〕
に、硬化剤として分子量1500のポリプロピレングリ
コール/ジフェニルメタンジアミン=80/20wtの
混合液(粘度1500cps/25℃以上)を70リッ
トル秤量する。次に別の塗料圧送吐出用タンク(同上社
製同品)に、主剤としてプレポリマー(ジフェニルメタ
ンジイソシナアネート=100%、未反応NCO基6.
8%、固形分100%、粘度2600cps/25℃)
70リットル秤量する。Example 1 Paint pressure delivery tank [Asahi Hanac Co., Ltd. Tileman]
Then, 70 liters of a mixed liquid (viscosity 1500 cps / 25 ° C. or higher) of polypropylene glycol / diphenylmethanediamine = 80/20 wt having a molecular weight of 1500 is weighed as a curing agent. Next, a prepolymer (diphenylmethane diisocyanananate = 100%) as a main component and another unreacted NCO group were added to another paint pressure-feeding and discharging tank (the same product manufactured by the same company).
8%, solid content 100%, viscosity 2600 cps / 25 ° C)
Weigh 70 liters.
【0033】両吐出機のラインをそれぞれ導入できる様
に、プロブラーガンにとりつけた。このガンには、フラ
ットチャンバー(NO.2)+チップ(043−25)
を取り付けて使用した。吹付装置の主剤と硬化剤との混
合物の吹付圧を170brとなる様、稼働させて、上記
各タンク内の主剤と硬化剤を混合し、直ちにこの混合物
をスレート板上に吹き付けたところ、上記混合物は雨滴
状に板上に吐出された。It was attached to a probler gun so that the lines of both dispensers could be introduced respectively. This gun has a flat chamber (NO.2) + tip (043-25)
Was attached and used. When the spraying device was operated so that the spraying pressure of the mixture of the main agent and the curing agent was 170 br, the main agent and the curing agent in each of the tanks were mixed, and immediately this mixture was sprayed onto a slate plate. Was discharged onto the board in the form of raindrops.
【0034】吐出終了20秒後には、表面が微細な凹凸
(エンボス)で覆われたフラットなノンスリップ性の構
造物表面を得ることが出来た。20 seconds after the end of discharge, a flat non-slip structure surface whose surface was covered with fine irregularities (embossing) could be obtained.
【0035】実施例2 ミニプロブラースプレーガンの口金部分にスターッチク
ミキサーを取付、次にエアーラインに7brのエアー圧
送タンクのラインを予め接続しておく。次に、塗装機
〔旭ハナック(株)APW−5000〕のAタンクに、
主剤のプレポリマー(MDI=100%、未反応NCO
基9%、固形分100%、粘度3000cps/25
℃)を仕込む。一方、Bタンクに硬化剤として分子量2
000のポリプロピレングリコール/ジエチルトルエン
ジアミン=85/15wt混合物(粘度1500cps
以上)を仕込む。Example 2 A Startsch mixer was attached to the mouthpiece of a mini-probler spray gun, and then a line of an air pressure feeding tank of 7 br was connected in advance to the air line. Next, in the A tank of the coating machine [Asahi Hanac Co. APW-5000],
Main polymer prepolymer (MDI = 100%, unreacted NCO
Base 9%, solid content 100%, viscosity 3000 cps / 25
℃) is charged. On the other hand, the B tank has a molecular weight of 2 as a curing agent.
000 polypropylene glycol / diethyltoluenediamine = 85/15 wt mixture (viscosity 1500 cps
Above).
【0036】両吐出ラインのそれぞれをミニプロブラー
スプレーガンに取り付けて、両ラインの吐出圧がガンの
吹付圧力が200brとなる様に稼働させて、主剤と硬
化剤との混合物を直ちにスレート板上に吹き付けたとこ
ろ、その混合物は雨滴状に板上に吐出された。Each of the two discharge lines was attached to a mini-probler spray gun and operated so that the discharge pressure of both lines became a spray pressure of the gun of 200 br, and the mixture of the main agent and the curing agent was immediately put on a slate plate. When sprayed, the mixture was delivered in the form of raindrops onto the plate.
【0037】吐出後40秒には、表面が微細な凹凸(エ
ンボス)で覆われた構造物表面を得ることが出来た。こ
の表面は5分後には通行のできるフラットなノンスリッ
プ性の表面であった。40 seconds after the ejection, a structure surface whose surface was covered with fine irregularities (embossing) could be obtained. This surface was a flat, non-slip surface that was passable after 5 minutes.
【0038】実施例3 塗装機〔旭ハナック(株)APW−5000〕のAタン
クに、主剤としてプレポリマー(MDI=100%、未
反応NCO基6%、固形分100%、粘度1500cp
sを越える/25℃)を仕込む。Bタンクに分子量60
0のポリエチレングリコール/ジエチルトルエンジアミ
ン=80/20wt混合物(粘度8000cps/25
℃)を仕込む。両吐出ラインをプロブラースプレーガン
に取り付けて両ラインの吐出圧がガンの吹付圧で200
brとなる様に稼働させて、その混合物をスレート板上
に吹き付けたところ、この混合物は、噴霧状〜雨滴状態
D吐出された。Example 3 A pre-polymer (MDI = 100%, unreacted NCO group 6%, solid content 100%, viscosity 1500 cp) was used as a main component in an A tank of a coating machine [Asahi Hanac Co., Ltd. APW-5000].
s / 25 ° C). Molecular weight of 60 in B tank
0/20 polyethylene glycol / diethyltoluenediamine = 80/20 wt mixture (viscosity 8000 cps / 25
℃) is charged. Both discharge lines are attached to the Probler spray gun, and the discharge pressure of both lines is 200 by the gun spray pressure.
When the mixture was sprayed onto a slate plate by operating so as to produce br, the mixture was discharged in a spray state to a raindrop state D.
【0039】吐出後20秒には表面が微細な凹凸で覆わ
れた構造物表面を得ることが出来た。この表面は3分後
には通行のできるフラットなノンスリップ性の表面であ
った。Twenty seconds after the ejection, a structure surface whose surface was covered with fine irregularities could be obtained. This surface was a flat, non-slip surface that could pass after 3 minutes.
【0040】比較例1 吐出圧を100brにした以外は実施例1と同様の条件
でスレート板上に混合物を吹き付けたところ、スポレー
ガンの口金部より糸状に吐出されるのみであった。ま
た、このものはエンボス模様を形成せず、スレート板上
においてはうねり状の凹凸状表面を形成するだけであっ
た。しかもこの構造物表面はノンスリップ性を有してい
るものではなかった。Comparative Example 1 When the mixture was sprayed onto the slate plate under the same conditions as in Example 1 except that the discharge pressure was 100 br, it was only discharged in filament form from the mouthpiece of the spray gun. Further, this product does not form an embossed pattern, but only forms a wavy uneven surface on the slate plate. Moreover, the surface of this structure was not non-slip.
【0041】比較例2 混合物温度を70℃に昇温した以外は実施例2と同様の
条件でスレート板上に混合物を吹き付けたところ、スプ
レーガンの口金部分より霧状に吐出された。10秒後に
は微細な凹凸のない、単に表面が光沢を有したフラット
な構造物表面が得られたに過ぎなかった。しかも加熱の
ためのエネルギーが余分に必要であった。Comparative Example 2 When the mixture was sprayed onto the slate plate under the same conditions as in Example 2 except that the temperature of the mixture was raised to 70 ° C., it was discharged in a mist form from the mouth part of the spray gun. After 10 seconds, a flat structure surface without fine irregularities and having a glossy surface was merely obtained. Moreover, extra energy was required for heating.
【0042】しかも、この表面は5分後には通行のでき
るノンスリップ性をも有していない構造物表面に過ぎな
かった。Moreover, this surface was nothing but a non-slip structure surface which could pass after 5 minutes.
【0043】比較例3 実施例3の吐出圧を100brにて稼働させて、スレー
ト板上に吹き付けたところ、吐出物は糸状に吐出され
た。吐出後20秒に形成された表面は、大きなうねり状
の凹凸を有する表面であった。Comparative Example 3 When the discharge pressure of Example 3 was operated at 100 br and sprayed onto the slate plate, the discharge product was discharged in the form of threads. The surface formed 20 seconds after the ejection was a surface having large wavy irregularities.
【0044】この表面は3分後には通行できたが、凹凸
が激しく、フラット性が無く、通行時に靴が引っかかり
スムーズな歩行が困難であった。Although the surface was able to pass after 3 minutes, it had rough irregularities and had no flatness, and it was difficult to walk smoothly because the shoe was caught when passing.
【0045】以上の結果から、本発明の塗装方法によれ
ば、特にノンスリップ性のエンボス表面を得るに当た
り、高粘度な主剤と硬化剤を混合し、直ちに構造物に吹
き付け硬化させることにより、特段の加熱装置を用いる
こと無く、容易にエンボス仕上げ面を得ることが出来る
ものであることが確認された。From the above results, according to the coating method of the present invention, in order to obtain a non-slip embossed surface, a highly viscous base material and a curing agent are mixed and immediately sprayed on the structure to be cured. It was confirmed that the embossed surface can be easily obtained without using a heating device.
【0046】[0046]
【発明の効果】本発明はウレタンプレポリマーからなる
主剤とポリオールからなる硬化剤とを混合し常温硬化性
樹脂組成物を調製し、直ちにその混合物を構造物に吹き
付けて硬化させてエンボス状表面を構造物上に形成させ
るにあたり、高粘度の主剤と硬化剤とを用いて塗装を行
うので、施工作業を加熱装置を必要とすることなく、常
温で行え、災害への対処策等を必ず予め講じておく必要
がなくなるという格別顕著な効果を奏する。Industrial Applicability According to the present invention, a room temperature curable resin composition is prepared by mixing a base material composed of a urethane prepolymer and a curing agent composed of a polyol, and the mixture is immediately sprayed on the structure to be cured to form an embossed surface. When forming on a structure, painting is performed using a high-viscosity main agent and a curing agent, so construction work can be performed at room temperature without the need for a heating device, and measures to deal with disasters must be taken in advance. There is a particularly remarkable effect that there is no need to keep it.
Claims (4)
マーを含む粘度1500cpsを越える主剤と、ポリオ
ールを含む粘度1500cps以上の硬化剤とを混合し
て常温硬化性樹脂組成物を調製するとともに、直ちにそ
れを構造物に吹き付け硬化させることを特徴とするエン
ボス仕上げ塗装方法。1. A room temperature curable resin composition is prepared by mixing a main agent containing a prepolymer having an isocyanate group at a terminal and a viscosity exceeding 1500 cps with a curing agent containing a polyol and having a viscosity of 1500 cps or more. An embossed finish coating method characterized by spraying and curing the structure.
て混合し、単一吐出孔から構造物に雨滴状として吹き付
け塗布する請求項1記載の塗装方法。2. The coating method according to claim 1, wherein the main agent and the curing agent are mixed through a static mixing device and sprayed as raindrops onto the structure from a single discharge hole.
る際の機械吹付け装置の吹き付け圧力を140br以上
で行う請求項1記載の塗装方法。3. The coating method according to claim 1, wherein the spraying pressure of the mechanical spraying device when spraying the room temperature curable resin composition onto the structure is 140 br or higher.
ル化時間が5〜30秒である組成物を用い、かつそれを
140br以上の吹き付け圧力で構造物に吹き付け硬化
させる請求項1記載の塗装方法。4. The room temperature curable resin composition, wherein a composition having a gelling time of 5 to 30 seconds at room temperature is used, and the composition is spray-cured at a spray pressure of 140 br or more to cure the structure. How to paint.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4335992A JPH06182291A (en) | 1992-12-16 | 1992-12-16 | Method of coating resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4335992A JPH06182291A (en) | 1992-12-16 | 1992-12-16 | Method of coating resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06182291A true JPH06182291A (en) | 1994-07-05 |
Family
ID=18294586
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4335992A Pending JPH06182291A (en) | 1992-12-16 | 1992-12-16 | Method of coating resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06182291A (en) |
-
1992
- 1992-12-16 JP JP4335992A patent/JPH06182291A/en active Pending
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