JP2610085C - - Google Patents
Info
- Publication number
- JP2610085C JP2610085C JP2610085C JP 2610085 C JP2610085 C JP 2610085C JP 2610085 C JP2610085 C JP 2610085C
- Authority
- JP
- Japan
- Prior art keywords
- coating
- coating film
- parts
- paint
- top coat
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000576 coating method Methods 0.000 claims description 59
- 239000011248 coating agent Substances 0.000 claims description 56
- 239000003973 paint Substances 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 14
- 239000000049 pigment Substances 0.000 claims description 13
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 9
- -1 hydrazide compound Chemical class 0.000 claims description 9
- 239000000758 substrate Substances 0.000 claims description 8
- 239000012298 atmosphere Substances 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 7
- 239000006185 dispersion Substances 0.000 claims description 6
- QRXWMOHMRWLFEY-UHFFFAOYSA-N Isoniazid Chemical group NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 description 27
- 239000000839 emulsion Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- ROOXNKNUYICQNP-UHFFFAOYSA-N Ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 10
- 239000004568 cement Substances 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- 239000010410 layer Substances 0.000 description 7
- 229920000178 Acrylic resin Polymers 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000004925 Acrylic resin Substances 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 239000008367 deionised water Substances 0.000 description 5
- OMNKZBIFPJNNIO-UHFFFAOYSA-N N-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 125000004432 carbon atoms Chemical group C* 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical group CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine group Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine hydrate Chemical compound O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 3
- 239000004570 mortar (masonry) Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N 2-methyl-2-propenoic acid methyl ester Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- JMADMUIDBVATJT-UHFFFAOYSA-N 2-methylprop-2-enamide;propan-2-one Chemical compound CC(C)=O.CC(C)=O.CC(=C)C(N)=O JMADMUIDBVATJT-UHFFFAOYSA-N 0.000 description 2
- 229960003563 Calcium Carbonate Drugs 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N Iron(III) oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 210000003491 Skin Anatomy 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000005002 finish coating Substances 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- OYLCUJRJCUXQBQ-UHFFFAOYSA-N 1-hepten-3-one Chemical compound CCCCC(=O)C=C OYLCUJRJCUXQBQ-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N 2-cyanopropene-1 Chemical group CC(=C)C#N GYCMBHHDWRMZGG-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
- CWSZBVAUYPTXTG-UHFFFAOYSA-N 5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol Chemical compound O1C(CO)C(OC)C(O)C(O)C1OCC1C(OC2C(C(O)C(OC)C(CO)O2)OCCO)C(O)C(O)C(OC2C(OC(C)C(O)C2O)CO)O1 CWSZBVAUYPTXTG-UHFFFAOYSA-N 0.000 description 1
- 210000001565 ALC Anatomy 0.000 description 1
- IBVAQQYNSHJXBV-UHFFFAOYSA-N Adipic acid dihydrazide Chemical compound NNC(=O)CCCCC(=O)NN IBVAQQYNSHJXBV-UHFFFAOYSA-N 0.000 description 1
- 240000004307 Citrus medica Species 0.000 description 1
- 239000005977 Ethylene Chemical group 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N Itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229910001294 Reinforcing steel Inorganic materials 0.000 description 1
- 108010039491 Ricin Proteins 0.000 description 1
- 229920002803 Thermoplastic polyurethane Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N TiO Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229920001567 Vinyl ester Polymers 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000001771 impaired Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 230000002045 lasting Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910001562 pearlite Inorganic materials 0.000 description 1
- JLIDVCMBCGBIEY-UHFFFAOYSA-N pent-1-en-3-one Chemical compound CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000011414 polymer cement Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000002335 preservative Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000002987 primer (paints) Substances 0.000 description 1
- 230000007261 regionalization Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229910001929 titanium oxide Inorganic materials 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Description
【発明の詳細な説明】
【0001】
【産業上の利用分野】
本発明は、塗装仕上げ方法に関し、詳しくは良好な仕上り外観、高耐久性を有
する複層塗膜を形成できる特に建築内外装に好適な塗装仕上げ方法に関する。
【0002】
【従来の技術】
従来、建築物壁面等の塗装には、下塗材、主材、上塗材などの塗装材を用いて
装飾性のある凹凸模様などに仕上げる複層仕上げ塗装が一般的に行なわれている
。かかる仕上げ塗装法としては、模様形成を目的とする主材の種類によって、合
成樹脂エマルジョン系複層仕上げ方法や、セメント系又はポリマーセメント系複
層仕上げ方法などが挙げられる。前者は、通常、シーラー、下塗材、主材、上塗
材を用いて4層塗膜を構成するものであり、該シーラーは基材と下塗層との付着
性向上を、下塗材は基材を均一に調整することを目的とし、主材は仕上り面に立
体模様を形成することを、上塗材は美観や耐久性付与を目的として塗装されるも
のである。かかる方法は凹凸の変化の大きい意匠性の高い模様を形成することが
できるという利点があるが、塗装工程が多く、コストや工期の面で問題がある。
【0003】
一方、後者の方法は、通常、シーラー、セメント系主材、上塗材を用いた3層
塗膜を構成するものであり、前者の方法に比べて1工程少ないので有利である。
しかしながら通常のセメント系塗装材は、硬質で弾性に乏しいため、建築物壁面
などの基材面に発生するひびワレに該塗膜が追随できず、ひいては上塗塗膜にも
ひびワレが生じるという問題があった。この様なひびワレを放置すると雨水や炭
酸ガスがこのひびワレから侵入し、建築物の鉄筋の腐食及びそれに伴うコンクリ
ート剥落等が起こる原因となる。またセメントを結合材とする塗装材なので、水
/セメント、合成樹脂エマルジョン/セメントの混合物は1〜4時間で固まるた
め、必要な量をその度調合する必要があり、材料管理の面でも非常に手間がかか
る。また、液/粉を混合する時のセメントの飛散及び混合物中に「まま粉」等が
出易く、作業上も多くの問題点がある。さらに該塗装材では、セメント粉中に大
きな粒子があるため形成する塗膜の肌がザラザラとなり、上塗りを該面上に塗布
してもかかるザラザラ感をひろって滑らかな模様塗面とならず、最終の仕上り外
観が劣るという問題点があった。
【0004】
【発明が解決しようとする課題】
本発明は、従来の塗装工程をさらに簡略化して2層構成とし、しかも良好な仕
上り外観を有し、基材面のひびワレ等にも追随しうる高耐久性塗膜を形成できる
塗装仕上げ方法の提供を目的とするものである。
【0005】
【課題を解決するための手段】
本発明者らは上記目的を達成すべく鋭意検討した結果、特定の組成を有し且つ
微弾性を有せしめた塗料を塗装した後、上塗塗装することにより良好な仕上り外
観を有する高耐久性塗膜が得られることを見出し本発明を完成するに至った。
【0006】
すなわち本発明は、基材面に、カルボニル基含有共重合体水分散液(A)、架
橋剤として1分子当たり少なくとも2個以上のヒドラジド基を含有するヒドラジ
ド化合物(B)及び顔料(C)を含有し、該混合物中における顔料体積濃度が4
0〜55%であって、かつ形成塗膜の伸び率が20℃雰囲気で30〜150%で
ある弾性ベース用塗料を塗布した後、該塗面上に形成塗膜の伸び率が20℃雰囲
気で150%以下である上塗塗料を塗布する塗装仕上げ方法を提供するものであ
る。
【0007】
本発明方法は、特定の顔料濃度とし微弾性を有せしめた一液型水性エマルジョ
ン塗料をベース用塗料として使用することにより、基材面のひびワレ等に追随で
きるとともに各種基材及び旧塗膜等との付着性にも優れ且つ強靭で弾性持続力を
有する塗膜層を形成できるので、従来のシーラー塗装+下塗塗装(+模様塗装)
の各工程の有する機能を1つに集約することができ、該ベース塗膜上に上塗塗装
を施すことにより良好な仕上り外観が得られ塗装工程の簡略化を実現できたもの
である。
【0008】
以下、本発明について詳細に説明する。
【0009】
本発明方法に使用する弾性ベース用塗料は、カルボニル基含有共重合体水分散
液(A)、架橋剤として1分子当たり少なくとも2個以上のヒドラジド基を有す
るヒドラジド化合物(B)及び顔料(C)を含有してなる水性エマルジョン塗料
である。
【0010】
上記カルボニル基含有共重合体水分散液(A)としては、(a)1分子中に少
なくとも1個のカルボニル基を有する、重合性のカルボニル基含有単量体を0.
1〜30重量%、(b)3〜5個の炭素原子を有するモノオレフィン性不飽和カ
ルボン酸、同不飽和カルボン酸アミド、同不飽和カルボン酸アミドのN−アルキ
ルおよび/又はN−アルキロール誘導体、モノオレフィン性不飽和カルボン酸よ
りなる群から選ばれた単量体を0〜10重量%、並びに(c)ビニル芳香族化合
物、アクリル酸の炭素数1〜8個のn−アルキルエステル、メタクリル酸の炭素
数1〜8個のn−アルキルエステル、飽和カルボン酸のビニルエステル、1,3
−ジエン、アクリル酸第三級ブチル、ハロゲン化ビニル、エチレン、アクリロニ
トリル、メタクリロニトリルよりなる群から選ばれた単量体を60〜99.9重
量%含有する単量体混合物を、分散剤の存在下で乳化共重合させることにより容
易に得られるものが好適に使用できる。
【0011】
単量体(a)としては、1分子中に少なくとも1個のカルボニル基を有する重
合可能な二重結合を有する単量体が用いられる。単量体(a)の具体例としては
、アグロレイン、ダイアセトンアクリルアミド、ダイアセトンメタアクリルアミ
ド、ホルミルスチロール、4〜7個の炭素原子を有するビニルアルキルケトン(
例えばビニルメチルケトン、ビニルエチルケトン、ビニルブチルケトン)等があ
げられる。特に好ましいのは、ダイアセトンアクリルアミド、ダイアセトンメタ
アクリルアミドである。
【0012】
上記架橋剤として使用する1分子当たり少なくとも2個以上のヒドラジン残基
を有するヒドラジド化合物(B)としては、(d)下記一般式で示されるジヒド
ラジド化合物、
H2 N−NH−CO−(CH2 )n −CO−NH−NH2 (n≦8)
および/又は(e)カルボン酸エステル基を有する重合体をヒドラジン又はヒド
ラジン水化物(すなわちヒドラジンヒドラード)と反応させることにより製造さ
れるジヒドラジド化合物が挙げられる(特公昭52−22878号公報参照)。
【0013】
上記カルボン酸エステル基を有する重合体は、アクリル酸、メタクリル酸、イ
タコン酸等の不飽和カルボン酸と低級アルコールとのエステルに、スチレン、ジ
ビニルベンゼン、イソブチレン等の不飽和単量体を共重合させることにより得ら
れるものが適当である。
【0014】
上記カルボニル基含有共重合体水分散液(A)とヒドラジド化合物(B)の使
用割合は、該共重合体水分散液(A)中に含まれる共重合体のカルボニル基1モ
ルに対してヒドラジド化合物中のヒドラジド残基が、0.02〜3モル、好まし
くは0.1〜2モルになる割合であることが好適である。
【0015】
さらに弾性ベース用塗料に使用される顔料(C)としては、例えば酸化チタン
、カーボンブラック、ベンガラなどの着色顔料、炭酸カルシウム、タルク、マイ
カ、クレー、ケイ藻土、ケイ砂、パライトなどの体質顔料や骨材等が挙げられ、
適宜選択して使用できる。
【0016】
上記顔料(C)は、前記(A)、(B)成分との混合物中における顔料体積濃
度(以下、「PVC」と略称することがある)が40〜55%となるよう配合さ
れる必要がある。ここで「顔料体積濃度(PVC)」は該混合物固形分に占める
顔料分の体積割合であり、次式から得られるものである。
☆【数1】 【0017】
上記PVCが40%未満では、得られる弾性ベース用塗膜の肉持ち感が乏しく
なり下地調整能が低下し、一方PVCが55%を越えると得られる弾性ベース用
塗膜の緻密性が低下し上塗りを塗り重ねた際に上塗塗料の吸いこみムラが発生し
やすく良好な仕上り外観が得られず、またベース用塗膜自体の膜物性も低下する
ので好ましくない。
【0018】
また本発明においては、上記弾性ベース用塗料による形成塗膜の伸び率が20
℃雰囲気で30〜150%、好ましくは40〜140%であることが必要である
。ここで塗膜の伸び率は、恒温槽付万能引張試験機(島津製作所製、オートグラ
フAG2000B型)を用い、20℃において引張速度200mm/分で測定した
ときの値であり、測定に使用する試料はJIS−A−6910に従って作成した
ものである。
【0019】
上記伸び率が30%未満では、得られる弾性ベース用塗膜が基材面のひびワレ
などに十分追随できず、一方150%を越えると該塗膜上に塗り重ねる上塗塗料
の種類によっては上塗塗膜にワレが生じる場合があるので好ましくない。
【0020】
上記弾性ベース用塗料には、さらに必要に応じて界面活性剤、分散剤、消泡剤
、増粘剤、造膜助剤、防腐剤、凍結防止剤、有機溶剤などの塗料用添加剤を配合
することができる。
【0021】
本発明方法に使用する上塗塗料は、形成塗膜の伸び率が20℃雰囲気で150
%以下、好ましくは5〜100%であれば、特に制限なく従来公知の仕上り面の
着色や光沢の付与、また耐候性、防水性などを付与しうる水系または有機溶剤系
の塗料が適用できる。かかる上塗塗料としては、例えばアクリル樹脂、アクリル
・ウレタン樹脂、ポリウレタン樹脂、フッ素樹脂、シリコン・アクリル樹脂など
を主成分とするものが挙げられる。
【0022】
該上塗塗料において、上記伸び率が150%を越える場合には、上塗塗面の耐
汚染性が低下し外観の美粧性を損なうことになるので好ましくない。
【0023】
本発明の塗装仕上げ方法は、適宜な基材面に、前記弾性ベース用塗料をローラ
ー、エアスプレー、エアレススプレー、リシンガン、万能ガン、ハケなどの公知
の塗装器具を用いて塗装してベース塗膜層を形成し、次いで該塗面上に上記上塗
塗料を上記と同様の塗装器具で塗装して上塗塗膜層を形成することからなる。
【0024】
適用できる基材としては、特に制限されるものではないが、例えばコンクリー
ト面、モルタル面、ストレート板、PC板 ALC板、コンクリートブロック面
、木材、石材、プラスチック、金属などが挙げられ、これらはそれぞれ適宜素地
調整を行なっておくことが好ましい。
【0025】
本発明方法において、弾性ベース用塗料による塗装膜厚は、塗布量に基づいて
0.3〜1.5kg/m2、好ましくは0.5〜1.3kg/m2が適当である。該塗料の
塗装は基材面の全面にわたって平滑面もしくは滑らかな凹凸面(ゆず肌状、クレ
ーター状などの模様)などとなるように行なわれるのが好ましい。また上塗塗料
の塗布量は、0.1〜0.5kg/m2程度が適当である。
【0026】
【発明の効果】
本発明の塗装仕上げ方法によれば、1工程目に塗装する弾性ベース用塗料が基
材面との付着性に優れ、形成される微弾性塗膜自体が非常に強靭で基材面のワレ
などに十分追随するので従来の塗装工程を簡略化でき、また該ベース塗膜が基材
と上塗塗膜との間の緩衝材としての機能を有するので、伸びの少ない硬質なタイ
プの上塗塗料を使用しても上塗塗膜にワレが発生することなく良好な仕上り外観
を有する塗膜が得られる。
【0027】
【実施例】
以下、本発明を実施例により、更に詳細に説明する。特にことわらない限り、
すべての部は重量部を示す。
【0028】
水性エマルジョンの製造例
製造例1
2リットルの4つ口フラスコに脱イオン水312部、Newcol 707S
F(日本乳化剤製、固形分30%)2.3部を加え、窒素置換後、80℃に保っ
。下記組成のプレエマルジョンを滴下する直前に0.7部の過硫酸アンモニウム
を加え、プレエマルジョンを3時間にわたって滴下した。
脱イオン水 338部
ダイアセトンアクリルアミド 32部
アクリル酸 3.2部
スチレン 97部
メチルメタクリレート 260部
2−エチルヘキシアクリレート 100部
n−ブチルアクリレート 150部
Newcol 707SF 62部
過硫酸アンモニウム 1.2部
滴下終了後30分より、30分間0.7部の過硫酸アンモニウムを7部の脱イ
オン水に溶かした溶液を滴下し、さらに2時間80℃に保持し、その後約40〜
60℃に降温した後、アンモニア水でpHを8〜9に調整し、エマルジョン(A
)−1を得た。
【0029】
製造例2
滴下するプレエマルジョンを下記組成とする以外は製造例1と同様の方法でエ
マルジョン(A)−2を得た。
脱イオン水 315部
ダイアセトンアクリルアミド 74部
アクリル酸 3.9部
スチレン 105部
メチルメタクリレート 269部
2−エチルヘキシルアクリレート 105部
n−ブチルアクリレート 176部
ヒドロキシエチルアクリレート 15部
Newcol 707SF 49部
過硫酸アンモニウム 1.5部
なお、反応終了後加えた過硫酸アンモニウムは、0.8部を脱イオン水8部に
溶かした溶液とした。
【0030】
上記製造例1〜2で得られたエマルジョン(A)−1、(A)−2の性状値を
表1に示した。
【0031】
☆【表1】
【0032】
(注1)固形分は試料を150℃30分間加熱し、残量を測定して算出した。
【0033】
弾性ベース用塗料の作成
上記製造例で得たエマルジョンに、アジピン酸ジヒドラジドなどの成分を表2
に示す組合せ及び配合量で添加し、撹拌混合して各弾性ベース用塗料〜を得
た。各塗料の特性値を表2に示す。
【0034】
なお、表2中における(注2)〜(注6)は下記のとおりである。
(注2)体質顔料:比重2.7の炭酸カルシウムを使用
(注3)増粘剤:2.5%ヒドロキシエチルセルロース
(注4)消泡剤:「SNデホーマーA63」(サンノプコ社製品)
(注5)分散剤:「ノプコサントK」(サンノプコ社製品)
【0035】
(注6)形成塗膜の伸び率(%):JIS−A−6910に準じて試験片を作成
、該乾燥塗膜の伸び率を、引張試験機オートグラフAG2000B型(島津製作
所製)を用い、20℃雰囲気で引張速度200mm/minにて測定した。
【0036】
☆【表2】
【0037】
実施例及び比較例
上記の如く作成した各弾性ベース用塗料を水で塗装適性粘度に調整した後、エ
アレススプレーでモルタル板(90×300×20mm)に塗布量が約0.9kg/m
2になるよう塗装し、20℃、75RH%で1日乾燥させた。次に各ベース塗膜
上に各種上塗塗料を表3に示す組合せで、エアレススプレーにより塗布量が約0
.2kg/m2になるよう塗装し、20℃、75RH%で7日間乾燥させて塗装仕上
げ板を得た。これらの塗装板の性能試験結果を表3に示す。
【0038】
なお、表3における(*1)〜(*6)の上塗塗料は下記のとおりである。
(*1)アレスレタン白:ポリウレタン樹脂系溶剤型上塗塗料、関西ペイント社
製品、伸び率40%(20℃)
(*2)アレスタイルトップS白:アクリル樹脂系溶剤型上塗塗料、関西ペイン
ト社製品、伸び率15%(20℃)
【0039】
(:3)アレスフロン白:フッ素樹脂系溶剤型上塗塗料、関西ペイント社製品、
伸び率50%(20℃)
(*4)アレスシリコン白:アクリルシリコン樹脂系溶剤型塗料、関西ペイント
社製品、伸び率15%(20℃)
【0040】
(:5)アレスタイルトップE白:アクリル樹脂系水性塗料、関西ペイント社製
品、伸び率20%(20℃)
(*6)アレスゴムテックス白:アクリル樹脂系水性塗料、関西ペイント社製品
、伸び率400%(20℃)
【0041】
☆【表3】
【0042】
表3における性能試験は下記のとおりである。
(注7)仕上り外観:300×300×50mmのモルタル板に実施例及び比較例
の方法で形成した塗膜表面の仕上り外観を目視で評価した。均一にムラなく滑ら
かに仕上っているものを○とし、素地面をひろったりムラが発生して均一に仕上
っていないものを×とした。
(注8)温冷繰返し作用に対する抵抗性:JIS−A−6910に準じて、塗装
板を20℃の水中に18時間浸潰した後、直ちに−20℃の恒温槽中で3時間冷
却し、次いで50℃の恒温槽中で3時間加温する。この24時間を1サイクルと
した操作を10回繰返した後の塗装面を目視観察し、下記基準で評価した。
○:ハガレ、ひびワレ、フクレなどが全くなく、かつ著しい変色及び光沢低下
もない。
×:上記欠陥が1つでもある。
(注9)耐候性:屋外に12ケ月暴露し、塗面を水洗した後の塗面状態や耐汚染
性を目視観察し、下記基準で評価した。試験塗板は底面垂直となるよう設置した
。
(塗面状態)
○:ハガレ、ひびワレ、フクレなどが全くなく、かつ著しい変色及び光沢低下
もない。
×:上記欠陥が1つでもある。
(耐汚染性)
○:ほとんど汚れが認められない。
△:汚れは認められるが目立たない。
×:汚れが著しい。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a coating and finishing method, and more particularly to a coating and finishing method capable of forming a multilayer coating film having a good finished appearance and high durability. It relates to a suitable paint finishing method. 2. Description of the Related Art Conventionally, a multi-layer finish coating for finishing a decorative uneven pattern using a coating material such as an undercoat material, a main material, and a topcoat material is generally used for painting a building wall or the like. It is being done. Examples of such a finish coating method include a synthetic resin emulsion-based multilayer finishing method and a cement-based or polymer cement-based multilayer finishing method, depending on the type of the main material for pattern formation. The former usually comprises a four-layer coating film using a sealer, an undercoat material, a main material, and a topcoat material. The sealer improves the adhesion between the base material and the undercoat layer. The main material is to form a three-dimensional pattern on the finished surface, and the top coating material is to be coated for the purpose of providing aesthetics and durability. Such a method has an advantage that a highly designable pattern having a large change in unevenness can be formed. However, there are many coating steps, and there are problems in terms of cost and construction period. [0003] On the other hand, the latter method is usually used to form a three-layer coating film using a sealer, a cement-based main material, and a topcoat material, and is advantageous because it requires one step less than the former method. However, since ordinary cement-based coating materials are hard and have poor elasticity, the coating film cannot follow cracks generated on a base material surface such as a building wall surface, and thus, a crack occurs in a top coating film. was there. If such cracks are left, rainwater or carbon dioxide gas will enter from the cracks, causing corrosion of the reinforcing steel of the building and accompanying concrete peeling. In addition, since it is a coating material using cement as a binder, a mixture of water / cement and a synthetic resin emulsion / cement hardens in 1 to 4 hours, so it is necessary to prepare a necessary amount each time, which is very difficult in terms of material management. It takes time and effort. Further, when mixing the liquid / powder, the cement is easily scattered and "as powder" is liable to appear in the mixture, so that there are many problems in operation. Further, in the coating material, the skin of the coating film formed due to the presence of large particles in the cement powder is rough, and even when the top coat is applied on the surface, the rough surface is not spread and the pattern does not have a smooth pattern, There is a problem that the final finished appearance is inferior. SUMMARY OF THE INVENTION [0004] The present invention further simplifies the conventional coating process to form a two-layer structure, has a good finished appearance, and follows cracks on the substrate surface. It is an object of the present invention to provide a paint finishing method capable of forming a highly durable coating film. Means for Solving the Problems The inventors of the present invention have conducted intensive studies to achieve the above object, and as a result, after applying a paint having a specific composition and a fine elasticity, a top coat is applied. As a result, it was found that a highly durable coating film having a good finished appearance was obtained, and the present invention was completed. That is, the present invention provides an aqueous dispersion of a carbonyl group-containing copolymer (A), a hydrazide compound (B) containing at least two or more hydrazide groups per molecule as a crosslinking agent, and a pigment ( C), and the pigment has a volume concentration of 4 in the mixture.
After applying a coating material for an elastic base having an elongation percentage of 0 to 55% and a formed coating film having an elongation percentage of 30 to 150% in a 20 ° C atmosphere, the elongation percentage of the formed coating film is set to 20 ° C atmosphere The present invention provides a paint finishing method for applying a top coat of not more than 150%. The method of the present invention can use a one-pack type aqueous emulsion paint having a specific pigment concentration and microelasticity as a base paint, so that it can follow cracks and the like on the base material surface, Conventional sealer coating + primer coating (+ pattern coating) because it can form a coating layer with excellent adhesion to old coatings, etc., and toughness and elastic lasting power.
The functions of each step can be integrated into one, and by applying a top coat on the base coating film, a good finished appearance can be obtained and the coating step can be simplified. Hereinafter, the present invention will be described in detail. The coating material for elastic base used in the method of the present invention comprises an aqueous dispersion of a carbonyl group-containing copolymer (A), a hydrazide compound having at least two or more hydrazide groups per molecule as a crosslinking agent (B), and a pigment. An aqueous emulsion paint containing (C). The aqueous carbonyl group-containing copolymer aqueous dispersion (A) comprises (a) a polymerizable carbonyl group-containing monomer having at least one carbonyl group in one molecule.
1 to 30% by weight, (b) monoolefinically unsaturated carboxylic acid having 3 to 5 carbon atoms, unsaturated carboxylic acid amide, N-alkyl and / or N-alkylol of the same unsaturated carboxylic acid amide 0 to 10% by weight of a monomer selected from the group consisting of a derivative and a monoolefinically unsaturated carboxylic acid, and (c) a vinyl aromatic compound, an n-alkyl ester of acrylic acid having 1 to 8 carbon atoms, Methacrylic acid n-alkyl esters having 1 to 8 carbon atoms, vinyl esters of saturated carboxylic acids, 1,3
A monomer mixture containing 60 to 99.9% by weight of a monomer selected from the group consisting of diene, tertiary butyl acrylate, vinyl halide, ethylene, acrylonitrile and methacrylonitrile, Those easily obtained by emulsion copolymerization in the presence can be suitably used. As the monomer (a), a monomer having a polymerizable double bond having at least one carbonyl group in one molecule is used. Specific examples of the monomer (a) include agrolein, diacetone acrylamide, diacetone methacrylamide, formylstyrene, and vinyl alkyl ketone having 4 to 7 carbon atoms (
Examples thereof include vinyl methyl ketone, vinyl ethyl ketone, and vinyl butyl ketone). Particularly preferred are diacetone acrylamide and diacetone methacrylamide. The hydrazide compound (B) having at least two or more hydrazine residues per molecule used as the crosslinking agent includes (d) a dihydrazide compound represented by the following general formula, H 2 N—NH—CO— It is produced by reacting a polymer having (CH 2 ) n —CO—NH—NH 2 (n ≦ 8) and / or (e) a carboxylic acid ester group with hydrazine or hydrazine hydrate (that is, hydrazine hydroxide). (See Japanese Patent Publication No. 52-22878). The polymer having a carboxylic acid ester group is obtained by adding an unsaturated monomer such as styrene, divinylbenzene or isobutylene to an ester of an unsaturated carboxylic acid such as acrylic acid, methacrylic acid or itaconic acid with a lower alcohol. Those obtained by copolymerization are suitable. The use ratio of the carbonyl group-containing aqueous copolymer dispersion (A) and the hydrazide compound (B) is based on 1 mol of the carbonyl group of the copolymer contained in the aqueous copolymer dispersion (A). On the other hand, the proportion of the hydrazide residue in the hydrazide compound is preferably 0.02 to 3 mol, preferably 0.1 to 2 mol. Further, as the pigment (C) used in the coating material for the elastic base, for example, coloring pigments such as titanium oxide, carbon black and red iron oxide, calcium carbonate, talc, mica, clay, diatomaceous earth, silica sand, pearlite, etc. Extender pigments and aggregates, etc.,
It can be appropriately selected and used. The pigment (C) is blended so as to have a pigment volume concentration (hereinafter may be abbreviated as “PVC”) in a mixture of the components (A) and (B) of 40 to 55%. Need to be Here, “pigment volume concentration (PVC)” is a volume ratio of the pigment to the solid content of the mixture, and is obtained from the following equation. ☆ [Equation 1] If the above PVC is less than 40%, the resulting elastic base coating film has a poor feeling of holding, resulting in poor base adjustment ability, while if the PVC content exceeds 55%, the resulting elastic base coating film has a high density. When the top coat is overcoated, unevenness of the top coat paint is likely to occur and a good finished appearance is not obtained, and the physical properties of the base coating film itself are also deteriorated. In the present invention, the elongation of the coating film formed by the above-mentioned coating material for elastic base is 20%.
It is necessary to be 30 to 150%, preferably 40 to 140% in an atmosphere of ° C. Here, the elongation percentage of the coating film is a value measured at a stretching speed of 200 mm / min at 20 ° C. using a universal tensile tester with a thermostat (manufactured by Shimadzu Corporation, Autograph AG2000B type). The sample was prepared according to JIS-A-6910. If the elongation percentage is less than 30%, the resulting coating film for the elastic base cannot sufficiently follow cracks on the substrate surface, while if it exceeds 150%, the type of topcoat paint to be applied over the coating film In some cases, cracks may occur in the overcoat film, which is not preferable. The above-mentioned paint for an elastic base may further contain a surfactant, a dispersant, an antifoaming agent, a thickener, a film-forming aid, a preservative, an antifreezing agent, an organic solvent, etc., if necessary. An agent can be compounded. The top coat used in the method of the present invention has an elongation percentage of a formed coating film of 150 ° C. in a 20 ° C. atmosphere.
% Or less, preferably 5 to 100%, without any particular limitation, water-based or organic solvent-based coatings which can impart coloring and gloss to the finished surface, weather resistance, waterproofness and the like can be applied without any particular limitation. Examples of such a top coat include those mainly containing acrylic resin, acrylic / urethane resin, polyurethane resin, fluorine resin, silicon / acrylic resin, and the like. [0022] If the elongation exceeds 150% in the top coat, the stain resistance of the top coat surface is reduced, and the aesthetic appearance is impaired, which is not preferable. [0023] In the coating finishing method of the present invention, an appropriate base material surface is coated with the elastic base coating material using a known coating tool such as a roller, an air spray, an airless spray, a ricin gun, a universal gun, and a brush. A base coat layer is formed, and then the top coat is coated on the coated surface with the same coating equipment as above to form a top coat layer. The substrate that can be used is not particularly limited, and examples thereof include a concrete surface, a mortar surface, a straight plate, a PC plate, an ALC plate, a concrete block surface, wood, stone, plastic, and metal. It is preferable that the bases of these are appropriately adjusted. [0025] In the present invention method, coating thickness of the elastic base paints, 0.3~1.5kg / m 2 based on the coating amount, preferably is 0.5~1.3kg / m 2 suitably . It is preferable that the coating is applied so as to form a smooth surface or a smooth uneven surface (a pattern such as citron skin or crater) over the entire surface of the substrate. The amount of the top coat applied is suitably about 0.1 to 0.5 kg / m 2 . According to the coating finishing method of the present invention, the coating material for the elastic base applied in the first step has excellent adhesion to the substrate surface, and the formed microelastic coating film itself is very small. It is tough enough to follow the cracks on the substrate surface, so that the conventional coating process can be simplified, and since the base coating has a function as a buffer between the substrate and the top coating, it has low elongation. Even if a hard type top coat is used, a coat having a good finished appearance can be obtained without cracking of the top coat. EXAMPLES Hereinafter, the present invention will be described in more detail with reference to Examples. Unless otherwise noted,
All parts are parts by weight. Preparation Example of Aqueous Emulsion Preparation Example 1 312 parts of deionized water and Newcol 707S were placed in a two-liter four-necked flask.
2.3 parts of F (manufactured by Nippon Emulsifier, solid content 30%) was added, and the mixture was replaced with nitrogen and kept at 80 ° C. Immediately before dropping the pre-emulsion having the following composition, 0.7 parts of ammonium persulfate was added, and the pre-emulsion was dropped over 3 hours. Deionized water 338 parts Diacetone acrylamide 32 parts Acrylic acid 3.2 parts Styrene 97 parts Methyl methacrylate 260 parts 2-ethylhexyl acrylate 100 parts n-butyl acrylate 150 parts Newcol 707SF 62 parts Ammonium persulfate 1.2 parts After dropping, From 30 minutes, a solution prepared by dissolving 0.7 part of ammonium persulfate in 7 parts of deionized water for 30 minutes is added dropwise, and the temperature is maintained at 80 ° C. for further 2 hours, and then the temperature is reduced to about 40 to 60 ° C. And adjust the pH to 8-9 with emulsion (A).
) -1 was obtained. Production Example 2 Emulsion (A) -2 was obtained in the same manner as in Production Example 1 except that the pre-emulsion to be dropped had the following composition. Deionized water 315 parts Diacetone acrylamide 74 parts Acrylic acid 3.9 parts Styrene 105 parts Methyl methacrylate 269 parts 2-ethylhexyl acrylate 105 parts n-butyl acrylate 176 parts Hydroxyethyl acrylate 15 parts Newcol 707SF 49 parts Ammonium persulfate 1.5 parts The ammonium persulfate added after the completion of the reaction was a solution in which 0.8 part was dissolved in 8 parts of deionized water. The properties of the emulsions (A) -1 and (A) -2 obtained in Production Examples 1 and 2 are shown in Table 1. [Table 1] (Note 1) The solid content was calculated by heating a sample at 150 ° C. for 30 minutes and measuring the remaining amount. Preparation of Paint for Elastic Base Ingredients such as adipic dihydrazide were added to the emulsion obtained in the above Production Example.
In the combinations and amounts shown in Table 1 and mixed by stirring to obtain each coating material for elastic bases. Table 2 shows the characteristic values of each paint. Note that (Note 2) to (Note 6) in Table 2 are as follows. (Note 2) Extender: using calcium carbonate with a specific gravity of 2.7 (Note 3) Thickener: 2.5% hydroxyethylcellulose (Note 4) Defoamer: "SN Deformer A63" (manufactured by San Nopco) 5) Dispersant: "Nopco Santo K" (manufactured by San Nopco) (Note 6) Elongation percentage (%) of formed coating film: A test piece was prepared according to JIS-A-6910, and the elongation of the dried coating film The rate was measured using a tensile tester Autograph AG2000B type (manufactured by Shimadzu Corporation) in a 20 ° C. atmosphere at a tensile speed of 200 mm / min. [Table 2] Examples and Comparative Examples Each of the elastic base paints prepared as described above was adjusted to an appropriate coating viscosity with water, and then applied to a mortar plate (90 × 300 × 20 mm) with an airless spray at an amount of about 0.9 kg /. m
2 and dried at 20 ° C. and 75 RH% for 1 day. Next, various top coats were applied on each base coat in the combinations shown in Table 3, and the amount of coating was about 0 by airless spray.
. It was coated to 2 kg / m 2 and dried at 20 ° C. and 75 RH% for 7 days to obtain a painted plate. Table 3 shows the performance test results of these coated plates. The top coats (* 1) to (* 6) in Table 3 are as follows. (* 1) Alesletan white: polyurethane resin-based solvent-based topcoat, Kansai Paint Co., Ltd., elongation 40% (20 ° C.) (* 2) Alestyle Top S White: acrylic resin-based solvent-based topcoat, Kansai Paint Co., Ltd. , Elongation 15% (20 ° C.) (3) Alesflon White: Fluororesin-based solvent-type top coating, Kansai Paint Co., Ltd.
Elongation rate 50% (20 ° C) (* 4) Ares silicone white: Acrylic silicone resin-based solvent-based paint, a product of Kansai Paint Co., Ltd., elongation rate 15% (20 ° C) Acrylic resin-based water-based paint, product of Kansai Paint Co., Ltd., elongation 20% (20 ° C.) (* 6) Ares Rubber Tex White: Acrylic resin-based water-based paint, product of Kansai Paint Co., elongation 400% (20 ° C.) ☆ [Table 3] The performance tests in Table 3 are as follows. (Note 7) Finished appearance: The finished appearance of the surface of a coating film formed on a mortar plate of 300 × 300 × 50 mm by the methods of Examples and Comparative Examples was visually evaluated. A sample that was uniformly and smoothly finished without unevenness was rated as “O”, and a sample that was unfinished evenly due to spread of the ground surface or unevenness was evaluated as “X”. (Note 8) Resistance to repeated warming / cooling action: According to JIS-A-6910, the coated plate was immersed in water at 20 ° C for 18 hours, immediately cooled in a constant temperature bath at -20 ° C for 3 hours, Then, the mixture is heated in a thermostat at 50 ° C. for 3 hours. After repeating this operation for 24 hours as one cycle ten times, the coated surface was visually observed and evaluated according to the following criteria. :: No peeling, cracks, blisters, etc., and no significant discoloration and gloss reduction. ×: There is at least one of the above defects (Note 9) Weather resistance: The coated surface was exposed to the outdoors for 12 months, the coated surface was washed with water, and the coating surface condition and stain resistance were visually observed and evaluated according to the following criteria. The test coated plate was installed so as to be perpendicular to the bottom surface. (Painted surface condition) :: No peeling, cracks, blisters, etc., and no significant discoloration and gloss reduction. ×: There is at least one of the above defects. (Stain resistance) ○: Almost no stain is observed. Δ: Stain is observed but not conspicuous. X: Stain is remarkable.
Claims (1)
として1分子当たり少なくとも2個以上のヒドラジド基を含有するヒドラジド化
合物(B)及び顔料(C)を含有し、該混合物中における顔料体積濃度が40〜
55%であって、且つ形成塗膜の伸び率が20℃雰囲気で30〜150%である
弾性ベース用塗料を塗布した後、該塗面上に形成塗膜の伸び率が20℃雰囲気で
150%以下である上塗塗料を塗布することを特徴とする塗装仕上げ方法。Claims: 1. A carbonyl group-containing copolymer aqueous dispersion (A) on a substrate surface, and a hydrazide compound (B) containing at least two or more hydrazide groups per molecule as a crosslinking agent. And the pigment (C), and the volume concentration of the pigment in the mixture is from 40 to
After applying an elastic base paint having an elongation percentage of 55% and an elongation percentage of the formed coating film of 30 to 150% in a 20 ° C atmosphere, the elongation percentage of the formed coating film is 150% in a 20 ° C atmosphere. %, Which is characterized by applying a top coat of not more than 10%.
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