JPS63162770A - Water-base covering composition for cement base plate - Google Patents
Water-base covering composition for cement base plateInfo
- Publication number
- JPS63162770A JPS63162770A JP31523686A JP31523686A JPS63162770A JP S63162770 A JPS63162770 A JP S63162770A JP 31523686 A JP31523686 A JP 31523686A JP 31523686 A JP31523686 A JP 31523686A JP S63162770 A JPS63162770 A JP S63162770A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- cement
- resin
- water
- emulsion 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.)
- Granted
Links
- 239000004568 cement Substances 0.000 title claims abstract description 31
- 239000000203 mixture Substances 0.000 title claims abstract description 18
- 229920005989 resin Polymers 0.000 claims abstract description 37
- 239000011347 resin Substances 0.000 claims abstract description 37
- 239000000839 emulsion Substances 0.000 claims abstract description 29
- 239000007787 solid Substances 0.000 claims abstract description 13
- 239000000843 powder Substances 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920001577 copolymer Polymers 0.000 claims abstract description 10
- 239000000049 pigment Substances 0.000 claims abstract description 9
- 239000004593 Epoxy Substances 0.000 claims abstract description 8
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000002245 particle Substances 0.000 claims abstract description 7
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 6
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 229920006122 polyamide resin Polymers 0.000 claims abstract description 5
- 239000000654 additive Substances 0.000 claims abstract description 4
- 239000000945 filler Substances 0.000 claims abstract description 4
- 229920000768 polyamine Polymers 0.000 claims abstract description 4
- 229930185605 Bisphenol Natural products 0.000 claims abstract description 3
- 239000008199 coating composition Substances 0.000 claims description 19
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 16
- 239000000758 substrate Substances 0.000 claims description 14
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 238000004040 coloring Methods 0.000 claims description 4
- 238000005336 cracking Methods 0.000 abstract description 9
- 238000007665 sagging Methods 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 4
- 239000003995 emulsifying agent Substances 0.000 abstract description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract description 2
- 125000003118 aryl group Chemical group 0.000 abstract description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract description 2
- 230000000996 additive effect Effects 0.000 abstract 1
- 239000010408 film Substances 0.000 description 37
- 238000000576 coating method Methods 0.000 description 33
- 239000011248 coating agent Substances 0.000 description 31
- 239000003973 paint Substances 0.000 description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- 230000005856 abnormality Effects 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
- 238000010998 test method Methods 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 125000005907 alkyl ester group Chemical group 0.000 description 5
- 238000006253 efflorescence Methods 0.000 description 5
- 239000003822 epoxy resin Substances 0.000 description 5
- 229920000647 polyepoxide Polymers 0.000 description 5
- 206010037844 rash Diseases 0.000 description 5
- -1 2 -Ethylhexyl Chemical group 0.000 description 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004566 building material Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000010454 slate Substances 0.000 description 3
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 229920000178 Acrylic resin Polymers 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
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910000323 aluminium silicate Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229920006026 co-polymeric resin Polymers 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000000463 material Substances 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- 239000004953 Aliphatic polyamide Substances 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229920003231 aliphatic polyamide Polymers 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000011400 blast furnace cement 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
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical class [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 229910003471 inorganic composite material Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は凹凸表面を有するセメント基板用のタレ、ワレ
等の生じにくい水性被覆組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to an aqueous coating composition for cement substrates having uneven surfaces that is less likely to cause sagging or cracking.
〈従来技術及び問題点〉
モルタル、コンクリート、スレート等のセメント:M品
基板を使用した建材が外装材、ブロック塀等に多く利用
されている。<Prior art and problems> Mortar, concrete, cement such as slate: Building materials using M-grade substrates are often used for exterior materials, block walls, etc.
建築物の寿命が延びるに従い、これら建材には耐久性の
高い仕上げが要求されてきており、さらに建材の量産化
に伴い塗装仕上げのスピード化が要求されてきているが
、従来このような要求を満す被覆組成物はいまだ開発さ
れていない。すなわち従来、例えば未養生セメント製品
への塗装は1〜2週間放置後、セメント製品の表面のp
H及び含水率を調整し、その後被覆組成物を塗装しない
とハクリ、変色等の塗膜欠陥が生じたりする欠点があっ
た。また、従来の被覆組成物、例えばアクリルエマルジ
ョン樹脂とセメントとを主成分とする被覆組成物を塗布
し、さらに耐候性の優れた溶剤型塗料を上塗塗装すると
、下塗塗膜に耐溶剤性がないため、光沢が低下したり塗
膜にシワが生じたりする欠点があった。また最近では、
セメント製品基板にファツション性をもたせるため基板
表面に波形状あるいはランダムな凹凸模様を形成させた
ものが広く採用されるようになってきた。As the lifespan of buildings increases, these building materials are required to have highly durable finishes, and with the mass production of building materials, speedy painting finishing is also required. A coating composition that satisfies this requirement has not yet been developed. In other words, conventionally, for example, when painting an uncured cement product, after leaving it for 1 to 2 weeks, the surface of the cement product was coated.
Unless the coating composition is applied after adjusting the hydrogen content and water content, coating film defects such as peeling and discoloration may occur. Furthermore, if a conventional coating composition, such as a coating composition containing acrylic emulsion resin and cement as the main components, is applied and then a topcoat is applied with a solvent-based paint with excellent weather resistance, the undercoat film lacks solvent resistance. Therefore, there were drawbacks such as reduced gloss and wrinkles in the coating film. Also recently,
In order to impart fashionability to cement product substrates, substrates with wavy or random uneven patterns formed on the surface of the substrate have become widely used.
このような凹凸表面を有するセメント基板に塗料を厚膜
塗装すると塗料がタレを生じ、凹部に塗料がたまり、必
要以上の厚膜となり、逆に凸部が薄膜となり、均一塗膜
の形成が困難であり、さらに塗膜にワレが生じる等の欠
点があった。If a thick film of paint is applied to a cement substrate with such an uneven surface, the paint will sag, and the paint will accumulate in the recesses, resulting in a thicker film than necessary.Conversely, the convex parts will become a thin film, making it difficult to form a uniform paint film. Furthermore, there were other drawbacks such as cracking in the coating film.
本発明は上記の如き従来技術に鑑み、上記欠点のない優
れた性能の被覆組成物を提供することを目的とするもの
である。SUMMARY OF THE INVENTION In view of the above-mentioned prior art, it is an object of the present invention to provide a coating composition with excellent performance that does not have the above-mentioned drawbacks.
〈問題点を解決するための手段〉
このような目的は、
(a) (i ) アクリル酸又はメタクリル酸アル
キルエステルの共重合エマルジョン樹脂(アルキル基は
炭素数1〜8を有する)固形分
……2〜15重量%
(ii) ビスフェノール型エポキシエマルジョン樹
脂固形分 ……1〜5重量%(iii )
平均粒径30〜300μの中空状無機物物粉末
……10〜40重量%(iv) セメント
……20〜60重量%(v) 着色顔料
…… 1〜5重量%(Vl)前記エポキシエマルジョン
l脂の0.8〜1.2当量のポリアミド樹脂又は脂肪族
多価アミン硬化剤、及びさらに必要に応じ各種添加剤少
量からなり、かつ((i)+(ii)) /(iv)の
重盪比が(0,15〜0.28 >の範囲である混合物
100重量部
混合物100重量部
ならびに
ら)水 15〜70重量部
かるなる粘度50〜500ポイズの水性被覆組成物によ
り達成される。<Means for solving the problem> These objectives are as follows: (a) (i) Copolymer emulsion resin of acrylic acid or methacrylic acid alkyl ester (alkyl group has 1 to 8 carbon atoms) solid content... 2 to 15% by weight (ii) Bisphenol type epoxy emulsion resin solid content...1 to 5% by weight (iii)
Hollow inorganic powder with average particle size of 30-300μ
...10-40% by weight (iv) cement
...20-60% by weight (v) Coloring pigment
... 1 to 5% by weight (Vl) of a polyamide resin or aliphatic polyvalent amine curing agent in an amount of 0.8 to 1.2 equivalents of the epoxy emulsion l fat, and further a small amount of various additives as necessary, and ( (i) + (ii)) / (iv) 100 parts by weight of a mixture having a gravimetric ratio of (0.15 to 0.28) and 100 parts by weight of a mixture and 15 to 70 parts by weight of water. This is achieved with a 50-500 poise aqueous coating composition.
本発明の被覆組成物は、凹凸表面を有する硬化セメント
基板はもちろん未養生のセメント基板にもただちに塗装
出来るため施工期間が短縮出来、また常温もしくは強制
乾燥でタレ、ワレ等を生ずることなく厚膜塗膜が可能で
あるため、現地塗装だけでなく工場ライン塗装も可能で
あり、さらに有機と無機の特定複合材を特定割合で配合
しているので長期耐久性、密着性、耐アルカリ性の優れ
た塗膜が得られ、また上塗塗料として水系あるいは溶剤
型塗料を塗り重ねても、前述の如き塗膜欠陥のない塗膜
を得ることが可能である。The coating composition of the present invention can be applied immediately not only to hardened cement substrates with uneven surfaces but also to uncured cement substrates, so the construction period can be shortened, and the coating composition can form a thick film without causing sagging or cracking when dried at room temperature or by forced drying. Since it can be painted, it can be applied not only on-site but also on a factory line.Furthermore, because it contains a specific proportion of organic and inorganic composite materials, it has excellent long-term durability, adhesion, and alkali resistance. A coating film is obtained, and even if a water-based or solvent-based paint is repeatedly applied as a top coat, it is possible to obtain a coating film without the above-mentioned coating film defects.
本発明において用いられるアクリル酸又はメタクリル酸
アルキルエステルの共重合エマルジョン樹脂を構成する
成分であるアクリル酸の炭素数1〜8のアルキルエステ
ルモノマー、メタクリル酸(7)炭素11〜8のアルキ
ルエステルモノマーのアルキル基としてはメチル、エチ
ル、n−ブチル、イソブチル、ターシャリ−ブチル、2
−エチルヘキシル、ベンジル、プロピル、イソプロピル
、5eC−ブチル等が代表的なものとして用いられる。Alkyl ester monomers of acrylic acid having 1 to 8 carbon atoms, methacrylic acid (7) alkyl ester monomers having 11 to 8 carbon atoms, which are components of the copolymerized emulsion resin of acrylic acid or methacrylic acid alkyl ester used in the present invention. Alkyl groups include methyl, ethyl, n-butyl, isobutyl, tert-butyl, 2
-Ethylhexyl, benzyl, propyl, isopropyl, 5eC-butyl, etc. are typically used.
炭素数9以上のアルキル基は乳化重合時にゲル物が発生
したり、エマルジョン粒子の疎水性が高くなり、セメン
ト混和用エマルジョン樹脂の合成には不適である。又、
これらのアクリル酸(又はメタクリル酸)アルキルエス
テルにスチレンを30重攬%まで含めた共重合エマルジ
ョン樹脂も用いられる。ただし、スチレンを30重量%
以上用いると、出来たエマルジョン塗膜の耐候性が著し
く低下するため耐久性の必要な屋外用エマルジョン樹脂
としては好ましくない。Alkyl groups having 9 or more carbon atoms may generate a gel during emulsion polymerization or make emulsion particles highly hydrophobic, making them unsuitable for the synthesis of emulsion resins for cement admixture. or,
A copolymer emulsion resin containing up to 30% by weight of styrene in these acrylic acid (or methacrylic acid) alkyl esters may also be used. However, 30% by weight of styrene
If this is used, the weather resistance of the resulting emulsion coating film will be significantly reduced, making it undesirable for use as an outdoor emulsion resin that requires durability.
特に好ましいアクリル酸又はメタクリル酸アルキルエス
テルとしてはメタクリル酸メチル、アクリル酸エチル、
アクリル酸ブチル、アクリル酸2−エチルヘキシルであ
り、またスチレンを使用する場合は20重量%以下が特
に好ましい。また、必要ならばアクリル酸、メタクリル
酸、メタクリル酸2−ヒドロキシエチル等の官能基モノ
マーを数重1%共重合することも可能である。本発明に
用いられるアクリル酸(又はメタクリル酸)アルキルエ
ステルの共重合エマルジョン樹脂はセメントと混和され
るため、耐アルカリ性を有し、セメント混和安定性に優
れているものがよく、そのためには乳化重合時の乳化剤
としてノニオン界面活性剤が好適である。これらアクリ
ルエマルジョン樹脂の分子量は5万〜30万、好ましく
は10万〜20万であるのが有利である。また最低造膜
温度は5℃以下が好ましい。それ以上になると成膜時に
ワレが生じやすくなるからである。またアクリルエマル
ジョン樹脂は固形分40重量%の時の粘度が10 Qc
ps以下が好ましい。それ以上になると水の量を多くし
粘度を下げる必要があり、そのため固形分が低下し塗膜
乾燥時のヤセによりワレが生じやすくなる。Particularly preferred acrylic acid or methacrylic acid alkyl esters include methyl methacrylate, ethyl acrylate,
Butyl acrylate, 2-ethylhexyl acrylate, and when styrene is used, 20% by weight or less is particularly preferred. Furthermore, if necessary, it is also possible to copolymerize several 1% functional group monomers such as acrylic acid, methacrylic acid, and 2-hydroxyethyl methacrylate. Since the copolymerized emulsion resin of acrylic acid (or methacrylic acid) alkyl ester used in the present invention is mixed with cement, it is preferable to have alkali resistance and excellent cement mixing stability. Nonionic surfactants are suitable as emulsifiers. Advantageously, these acrylic emulsion resins have a molecular weight of 50,000 to 300,000, preferably 100,000 to 200,000. Further, the minimum film forming temperature is preferably 5° C. or lower. This is because if it exceeds this range, cracks are likely to occur during film formation. Also, acrylic emulsion resin has a viscosity of 10 Qc when the solid content is 40% by weight.
ps or less is preferable. If it exceeds that range, it is necessary to increase the amount of water to lower the viscosity, which lowers the solids content and makes the coating film more likely to crack due to fading during drying.
これらの樹脂は上記混合物(a)中において固形分2〜
15重徂%の割合で配合される。樹脂が2重塁%未満で
あると塗膜の初期硬度、耐候性が低下し、エフロレッセ
ンスが生じ易くなる。一方樹脂が15重量%を越えると
厚膜塗装(約0.5〜10碓)が出来ず、ワレが生じ易
くなる。These resins have a solid content of 2 to 2 in the mixture (a).
It is blended at a ratio of 15% by weight. If the resin content is less than 2%, the initial hardness and weather resistance of the coating film will decrease, and efflorescence will likely occur. On the other hand, if the resin content exceeds 15% by weight, thick film coating (approximately 0.5 to 10% by weight) cannot be achieved and cracks are likely to occur.
本発明において用いられるビスフェノール型エポキシエ
マルジョン樹脂としては、ビスフェノールAとエピクロ
ルヒドリンから得られる芳香族ジグリシジルエーテル類
で平均分子量350〜1000の樹脂を乳化剤に用いて
、水分散型にしたものであり、樹脂固形分として、上記
混合物(a)中に1〜5重量%が用いられる。樹脂が1
重量%未満であると、素地との密着性が低下し、5重量
%を越えると、形成された塗膜の耐候性が著しく低下す
る。The bisphenol-type epoxy emulsion resin used in the present invention is made into a water-dispersible type by using an aromatic diglycidyl ether obtained from bisphenol A and epichlorohydrin and having an average molecular weight of 350 to 1000 as an emulsifier. The solid content used in the mixture (a) is 1 to 5% by weight. 1 resin
If it is less than 5% by weight, the adhesion to the substrate will be reduced, and if it exceeds 5% by weight, the weather resistance of the formed coating will be significantly reduced.
本発明において用いられる中空状無機物粉末は、内部が
完全に中空でその中空部が殻で完全に閉ざされている粉
末、あるいは軽石の如く内部に隔壁のある独立もしくは
連続気泡状の粉末であり、その平均粒径は、30〜30
0μ程度のものが適当である。なお平均粒径が30μ以
下であるとワレが生じやすく、また塗膜強度が低下し3
00μを越えるとタレやすく、また塗膜の平滑性を欠き
、美観が低下する。The hollow inorganic powder used in the present invention is a powder that is completely hollow inside and the hollow part is completely closed by a shell, or a powder that is in the form of independent or open cells with partition walls inside, such as pumice, Its average particle size is 30-30
A value of approximately 0μ is appropriate. If the average particle size is less than 30μ, cracking tends to occur, and the strength of the coating film decreases.
If it exceeds 00μ, it tends to sag, and the coating film lacks smoothness, resulting in poor appearance.
中空状無機物粉末としては、ガラスバルーン、シラスバ
ルーン、アルミノシリケートバルーン、シリカバルーン
、アルミナバルーン、ジルコニアバルーン、カーボンバ
ルーン等が代表的なものとして例示出来る。特に塗膜強
度の点から50%破壊静水圧が10kg/ci以上のも
のが望ましく、具体例として、ガラスバルーン、アルミ
ノシリケートバルーン、アルミナバルーン、ジルコニア
バルーンが挙げられる。この中空状無機物粉末は厚膜塗
膜においてもタレ、ワレのない塗膜を得、またもろさの
改良、増量のため配合されるものであり、さらに被覆組
成物の比重を小さくし、塗装作業性をよくする効果をも
有する。なお、通常の体質顔料、骨材等の充填剤のみで
は凹凸表面を有するセメント基板に厚膜塗装した場合、
タレ、ワレが防止出来ない。中空状無機物粉末は、上記
混合物(a)中において10〜40の割合で配合され、
この範囲において前記効果が得られる。Representative examples of the hollow inorganic powder include glass balloons, glass balloons, aluminosilicate balloons, silica balloons, alumina balloons, zirconia balloons, and carbon balloons. In particular, from the viewpoint of coating film strength, it is desirable to have a 50% breaking hydrostatic pressure of 10 kg/ci or more, and specific examples include glass balloons, aluminosilicate balloons, alumina balloons, and zirconia balloons. This hollow inorganic powder is blended to obtain coatings without sagging or cracking even in thick coatings, to improve brittleness, and to increase the coating composition.Furthermore, it reduces the specific gravity of the coating composition and improves coating workability. It also has the effect of improving. In addition, when applying a thick film to a cement substrate with an uneven surface using only ordinary fillers such as extender pigments and aggregates,
Sauces and cracks cannot be prevented. The hollow inorganic powder is blended in the mixture (a) at a ratio of 10 to 40,
The above effects can be obtained within this range.
本発明において用いられるセメントとしてはポルトラン
ドセメント、高炉セメント、シリカセメント、アルミナ
セメント等が例示できるが、その種類は特に制限はない
。セメントは本発明においては上記の混合物(a)中に
おいて20〜60重滑%の割合で配合される。セメント
が20重量96 未満だと厚膜時ワレが生じやすくな
り、また密着性が低下する。一方、60重量%を越える
と塗膜がもろくなり、またエフロレッセンスが生じやす
くなる。Examples of the cement used in the present invention include Portland cement, blast furnace cement, silica cement, and alumina cement, but the type thereof is not particularly limited. In the present invention, cement is blended in the above-mentioned mixture (a) at a ratio of 20 to 60% by weight. If the weight of the cement is less than 20% by weight, cracking is likely to occur when the film is thick, and adhesion is reduced. On the other hand, if it exceeds 60% by weight, the coating film becomes brittle and efflorescence is likely to occur.
本発明において用いられる着色顔料としては一般の無機
質顔料が代表的であるが、色によっては、耐アルカリ性
及び耐候性を有する有機顔料でもよい。たとえば黒く着
色する場合には、カーボンブランク、酸化鉄等、赤の場
合には弁柄等、緑の場合には酸化クロム等、青の場合に
はシアニンブルー等、白の場合には二酸化チタン等が例
示できる。The colored pigment used in the present invention is typically a general inorganic pigment, but depending on the color, an organic pigment having alkali resistance and weather resistance may also be used. For example, to color black, use carbon blank, iron oxide, etc., for red, use Bengara, etc., for green, use chromium oxide, for blue, use cyanine blue, etc. For white, use titanium dioxide, etc. can be exemplified.
着色顔料は上記の混合物(a)中において1〜5重景重
量割合で配合され、この範囲内での配合により充分に着
色する事が出来る。The coloring pigment is blended in the above mixture (a) in a ratio of 1 to 5 by weight, and by blending within this range, sufficient coloring can be achieved.
本発明に用いられるエポキシ樹脂用硬化剤としては、ジ
アミン又はジアミン透導体等と二塩基酸又は二塩基酸誘
導体等の重縮合によって得られるポリアミド樹脂あるい
はエチレンジアミン、ジエチレントリアミン、トリエチ
レンテトラミン等の脂肪族多価アミンあるいはフェノー
ル樹脂、エポキシ樹脂等で変性した脂肪族多価アミンが
適当である。硬化剤の使用量はエポキシ樹脂のエポキシ
基の0.8〜1.2当量になる様に使用する必要がある
。0.8当量未満及び1.2当量を越えると本来のエポ
キシ樹脂の特性、例えば密着性、可撓性が著しく低下し
その他耐久性等の性能も低下するので好ましくない。As the curing agent for epoxy resins used in the present invention, polyamide resins obtained by polycondensation of diamines or diamine transparent conductors with dibasic acids or dibasic acid derivatives, or aliphatic polyamide resins such as ethylenediamine, diethylenetriamine, triethylenetetramine, etc. Polyvalent amines or aliphatic polyamines modified with phenolic resins, epoxy resins, etc. are suitable. It is necessary to use the curing agent in an amount of 0.8 to 1.2 equivalents based on the epoxy group of the epoxy resin. If the amount is less than 0.8 equivalents or more than 1.2 equivalents, the original properties of the epoxy resin, such as adhesion and flexibility, will be significantly reduced, and other performances such as durability will also be deteriorated, which is not preferable.
本発明において用いられる添加剤としては、たとえば顔
料分散性、塗装作業性及び保存性等を良好なものとする
ための分散剤、消泡剤、増粘剤、防腐剤、防カビ剤、ま
た塗膜の成膜性をよくするための成膜助剤等が例示でき
る。Examples of additives used in the present invention include dispersants, antifoaming agents, thickeners, preservatives, antifungal agents, and coating agents to improve pigment dispersibility, coating workability, and storage stability. Examples include film-forming aids for improving the film-forming properties of the film.
なお、本発明において塗膜のもろさの改良、増量のため
炭酸カルシウム、硫酸バリウム、タルク、クレー等の体
質顔料;珪砂等の粒径300μ以下の骨材などの充填剤
を上記の混合物(a)中に40重量%以下の範囲にて配
合することも可能である。In addition, in the present invention, in order to improve the brittleness of the coating film and increase its weight, extender pigments such as calcium carbonate, barium sulfate, talc, and clay; and fillers such as aggregates with a particle size of 300 μm or less such as silica sand are added to the above mixture (a). It is also possible to incorporate it within the range of 40% by weight or less.
上記混合物(a)中(i)アクリル酸く又はメタクリル
酸)アルキルエステルの共重合エマルジョン樹脂の固形
分と(ii)エポキシエマルジョン樹脂の固形分との和
と、(iv)セメントとの重量比は〔(i)+(ii)
3 /<iv) −0,15〜0.28である。この上
ヒ率が0.15より小さい場合には、塗膜の初期硬度が
出ずエフロレッセンスが発生し、塗膜性能の良い状態で
の厚膜を形成することが出来ず、一方この比率が0.2
8より大きい場合には厚膜時、ワレが生じやすくなる。The weight ratio of (i) the solid content of copolymerized emulsion resin of alkyl ester of acrylic acid or methacrylic acid, (ii) the solid content of epoxy emulsion resin, and (iv) cement in the above mixture (a) is [(i)+(ii)
3/<iv) -0.15 to 0.28. If this ratio is smaller than 0.15, the initial hardness of the coating film will not be achieved and efflorescence will occur, making it impossible to form a thick film with good coating performance. 0.2
When it is larger than 8, cracks tend to occur when the film is thick.
前記((ii) +(vi)) / [(i)+(ii
)+(vi))の重量比は特に0.2〜0.45が好ま
しく、この比率が0,2より小さい場合は密着性が低下
し、一方この比率が0.45より大きい場合には耐候性
が低下する。The above ((ii) + (vi)) / [(i) + (ii)
The weight ratio of ) + (vi)) is particularly preferably 0.2 to 0.45; if this ratio is smaller than 0.2, the adhesion will be reduced, while if this ratio is larger than 0.45, the weather resistance will be reduced. Sexuality decreases.
本発明の水性被覆組成物は、上記混合物(a) 100
重塁部に対して水15〜70重量部を配合し組成物粘度
50〜500ポイズにしたものである。この範囲内であ
ればセメントの硬化性及び塗装作業性が良好であるから
である。なあ、水の量が15重量部未満だとセメント混
和時にアクリルエマルジョンが凝集しやすくなり、一方
、70重量部を越えると固形分が低下し乾燥時にヤセを
生じワレが生じやすくなる。The aqueous coating composition of the present invention comprises the above mixture (a) 100
15 to 70 parts by weight of water is added to the heavy base portion to give the composition a viscosity of 50 to 500 poise. This is because, within this range, cement hardenability and painting workability are good. If the amount of water is less than 15 parts by weight, the acrylic emulsion will tend to aggregate when mixed with cement, while if it exceeds 70 parts by weight, the solid content will decrease and it will become loose and crack when drying.
なお、本発明者等はエマルジョン樹脂として酢酸ビニル
樹脂、酢酸ビニル−アクリル樹脂、エチレン−酢酸ビニ
ル樹脂等の酢酸ビ斗ル系エマルジョン樹脂あるいはスチ
レン−ブタジェン系エマルジョン樹脂等、塗料業界にお
いて代表的に使用されているエマルジョン樹脂について
も検討したが、例えば前者にふいては耐候性、耐アルカ
リ性が劣り、さらに長期耐久性に欠け、また後者におい
ては耐候性等が劣り、本発明においては適当でないこと
が判明した。The present inventors have used vinyl acetate-based emulsion resins such as vinyl acetate resin, vinyl acetate-acrylic resin, and ethylene-vinyl acetate resin, or styrene-butadiene-based emulsion resins, which are typically used in the paint industry, as emulsion resins. We have also investigated emulsion resins that have been used in the past, but for example, the former has poor weather resistance, alkali resistance, and lacks long-term durability, and the latter has poor weather resistance and is not suitable for the present invention. found.
以上の如き本発明の水性被覆組成物は通常の塗装方法た
とえば吹付塗装、ローラー塗装、流し塗等によりセメン
ト基材表面等に塗布される。本発明の水性被覆組成物は
0.5〜10mm程度の厚膜でも良好な被覆を施すこと
が出来、常温あるいは100℃以下の温度で強制乾燥さ
せる。また、得られた塗膜に更に上塗塗料を良好に塗布
することができる。この上塗塗料として使用されるもの
は、例えばアクリル酸エステル系共重合樹脂、スチレン
−アクリル酸エステル共重合体等のスチレン系、酢酸ビ
ニル−アクリル酸エステル共重合体等の酢酸ビニル系及
ヒ塩化ビニルーアクリル酸エステル共重合体等の塩化ビ
ニル系の溶液重合より得られるもの及びアクリル酸エス
テル系のアクリルウレタン、スチレン−アクリル酸エス
テル系のアクリルウレタン樹脂、フルオロオレフィンと
ビニルエーテルを必須成分とし、かつ架橋部位を有する
含フツ素共重合樹脂をベースとする溶剤型塗料、アクリ
ル酸エステル系、スチレン−アクリル酸エステル共重合
体等のスチレン系、酢酸ビニル−アクリル酸エステル共
重合体等の酢酸ビニル系等のエマルジョン樹脂をベース
とする水系塗料、不飽和ポリエステル、ポリエステル(
メタ)アクリレート、ウレタン(メタ)アクリレート、
−エポキシ(メタ)アクリレート、アクリル(メタ)ア
クリレート樹脂タイプの紫外線硬化型塗料が例示できる
。The aqueous coating composition of the present invention as described above is applied to the surface of a cement substrate by a conventional coating method such as spray coating, roller coating, flow coating, etc. The aqueous coating composition of the present invention can provide a good coating even in a thick film of about 0.5 to 10 mm, and is force-dried at room temperature or at a temperature of 100° C. or lower. Moreover, a top coat can be further applied satisfactorily to the obtained coating film. The materials used as this top coat include, for example, acrylic ester copolymer resins, styrene-based resins such as styrene-acrylic ester copolymers, vinyl acetate-based resins such as vinyl acetate-acrylic ester copolymers, and vinyl chloride resins. Polymers obtained by solution polymerization of vinyl chloride, such as polyacrylic acid ester copolymer, acrylic urethane based on acrylic ester, acrylic urethane resin based on styrene-acrylic ester, fluoroolefin and vinyl ether as essential components, and crosslinked. solvent-based paints based on fluorine-containing copolymer resins, acrylic ester-based paints, styrene-based paints such as styrene-acrylic ester copolymers, vinyl acetate-based paints such as vinyl acetate-acrylic ester copolymers, etc. water-based paints based on emulsion resins, unsaturated polyesters, polyesters (
meth)acrylate, urethane(meth)acrylate,
- Examples include epoxy (meth)acrylate and acrylic (meth)acrylate resin type UV-curable paints.
〈発明の効果〉
本発明の被覆組成物は、凹凸表面を有するセメント基板
に塗装してもタレがなく、均一膜厚の塗膜が得られ、か
つワレ等を生ずることなく厚膜塗装が可能である。<Effects of the Invention> The coating composition of the present invention does not sag even when applied to a cement substrate having an uneven surface, provides a coating film with a uniform thickness, and can be coated in a thick film without causing cracks or the like. It is.
さらに未養生のセメント基材にも塗装出来るため施工期
間が短縮出来、また長期耐久中、密着生、耐アルカリ性
に優れ、上塗り特性も優れている。Furthermore, since it can be applied to uncured cement substrates, the construction period can be shortened, and it also has long-term durability, excellent adhesion, alkali resistance, and excellent topcoat properties.
以下実施例により本発明を更に詳しく説明する。The present invention will be explained in more detail with reference to Examples below.
なお、実施例、比較例中の組成物の配合割合は重量部で
示す。The blending ratios of the compositions in Examples and Comparative Examples are shown in parts by weight.
実施例1〜3及び比較例1〜5
第1表に示す配合の水性被覆組成物を平均高低差約7
mmの表面が波形の凹凸石綿スレート板表面に乾燥膜要
約2.0 mmになるように吹付塗布し、常温で7日間
放置することにより塗膜を硬化せしめた。Examples 1 to 3 and Comparative Examples 1 to 5 The aqueous coating compositions having the formulations shown in Table 1 were coated with an average height difference of about 7.
The coating was applied by spraying onto the surface of a corrugated asbestos slate board with a wavy surface to give a total dry film thickness of 2.0 mm, and the coating was left at room temperature for 7 days to harden.
得られた着色石綿スレート板の密着性、エフロレッセン
ス促進試験、凍結融解サイクル試験、促進耐候性試験、
塗膜外観の各試験結果を第1表の下段に示した。なお試
験方法及び評価は下記の通り行なった。Adhesion of the obtained colored asbestos slate board, accelerated efflorescence test, freeze-thaw cycle test, accelerated weather resistance test,
The results of each test on the appearance of the coating film are shown in the lower part of Table 1. The test method and evaluation were performed as follows.
(1)密着性
試験方法:塗膜の2 mmゴバン目セロファンテープハ
クリ試験
評 価 :◎・・・5 015 0、○・・・49
150〜26150、×・・・25150
以下
(2)エフロレッセンス促進試験
試験方法:飽和消石灰雰囲気にて
〔5℃×16時間→
20℃×8時間〕20サイクル
評 価:◎・・・全く異常なし、○・・・極く一部異
常あり、X・・・全面異常あり
(3)凍結融解サイクル試験
試験方法:(−20℃X16時間凍結→室温×8時間〕
35サイクル
評 価:◎・・・全く異常なし、○・・・極く一部異
常あり、×・・・全面異常あり
(ワレ有)
(4)促進耐候性試験
試験方法:サンシャインカーボン
2000時間照射
評 価:◎・・・全く異常なし、○・・・極く一部異
常あり、×・・全面異常あり
(チョーキング有)
(5)塗膜外観
試験方法二目視判定
評 価二〇・・・均一塗膜形成
○・・・極く一部タレ、ワレ発生
X・・・多くタレ、ワレ発生
第1表より明らかの如く本発明の水性被覆組成物は優れ
た塗膜性能を有していたが、セメントを過剰に添加した
比較例1、中空状無機物粉末を含まない比較例2、エポ
キシ樹脂を含まない比較例3、アクリル樹脂を含まない
比較例4、酢酸ビニル樹脂を使用した比較例5は、いず
れも塗膜性能が劣っていた。(1) Adhesion test method: 2 mm cellophane tape peeling test of coating film Evaluation: ◎...5 015 0, ○...49
150-26150, ×...25150 or less (2) Efflorescence acceleration test Test method: 20 cycles evaluation in saturated slaked lime atmosphere [5°C x 16 hours → 20°C x 8 hours] Evaluation: ◎...No abnormality at all , ○...There is a very small abnormality, X...There is a complete abnormality (3) Freeze-thaw cycle test Test method: (-20℃ x 16 hours freezing → room temperature x 8 hours)
35 cycle evaluation: ◎... No abnormality at all, ○... Very few abnormalities, ×... Fully abnormal (with cracks) (4) Accelerated weathering test test method: Sunshine carbon irradiation for 2000 hours Evaluation: ◎... No abnormalities at all, ○... Very few abnormalities, ×... Fully abnormalities (with chalking) (5) Paint film appearance test method, second sight judgment evaluation: 20... Uniform coating film formation ○...Very little sagging and cracking X...Many sagging and cracking As is clear from Table 1, the aqueous coating composition of the present invention had excellent coating performance. However, Comparative Example 1 in which excessive cement was added, Comparative Example 2 without hollow inorganic powder, Comparative Example 3 without epoxy resin, Comparative Example 4 without acrylic resin, and Comparative Example 5 using vinyl acetate resin. All had poor coating film performance.
Claims (2)
ルエステルの共重合エマルジョン樹脂(前記ア ルキル基は炭素数1〜8を有する)固形分 ……2〜15重量% (ii)ビスフェノール型エポキシエマルジョン樹脂固
形分……1〜5重量% (iii)平均粒径30〜300μの中空状無機物物粉
末……10〜40重量% (iv)セメント……20〜60重量% (v)着色顔料……1〜5重量% (vi)前記エポキシエマルジョン樹脂の0.8〜1.
2当量のポリアミド樹脂又は脂肪族多価アミン硬化剤、
及びさらに必要に応じ充填 剤、添加剤からなり、 かつ〔(i)+(ii)〕/(iv)の重量比が0.1
5〜0.28の範囲である混合物100重量部 ならびに (b)水15〜70重量部 からなる粘度50〜500ポイズの、凹凸表面を有する
セメント基板用水性被覆組成物。(1) (a) (i) Copolymer emulsion resin of acrylic acid or methacrylic acid alkyl ester (the alkyl group has 1 to 8 carbon atoms) Solid content...2 to 15% by weight (ii) Bisphenol type epoxy emulsion Resin solid content...1 to 5% by weight (iii) Hollow inorganic powder with an average particle size of 30 to 300μ...10 to 40% by weight (iv) Cement...20 to 60% by weight (v) Coloring pigment... 1 to 5% by weight (vi) 0.8 to 1% of the epoxy emulsion resin.
2 equivalents of polyamide resin or aliphatic polyamine curing agent,
and further comprises fillers and additives as necessary, and the weight ratio of [(i)+(ii)]/(iv) is 0.1
An aqueous coating composition for a cement substrate having a textured surface and having a viscosity of 50 to 500 poise, comprising 100 parts by weight of a mixture in the range of 5 to 0.28 and (b) 15 to 70 parts by weight of water.
造膜温度が5℃以下であることを特徴とする、特許請求
の範囲第(1)項記載の水性被覆組成物。(2) The aqueous coating composition according to claim (1), wherein the copolymer emulsion resin (a)(i) has a minimum film forming temperature of 5°C or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31523686A JPS63162770A (en) | 1986-12-25 | 1986-12-25 | Water-base covering composition for cement base plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31523686A JPS63162770A (en) | 1986-12-25 | 1986-12-25 | Water-base covering composition for cement base plate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63162770A true JPS63162770A (en) | 1988-07-06 |
JPH0116872B2 JPH0116872B2 (en) | 1989-03-28 |
Family
ID=18063017
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31523686A Granted JPS63162770A (en) | 1986-12-25 | 1986-12-25 | Water-base covering composition for cement base plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63162770A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0527480A2 (en) * | 1991-08-12 | 1993-02-17 | Cosmo Research Institute | Vibration damping thick-film coating composition and method of forming the coated film |
JP2008222956A (en) * | 2007-03-15 | 2008-09-25 | Toa Doro Kogyo Co Ltd | Coating material composition |
JP2010261166A (en) * | 2009-04-30 | 2010-11-18 | Dainippon Toryo Co Ltd | Manufacturing method for heat shielding and insulating tile |
PT106591A (en) * | 2012-10-22 | 2014-04-22 | Secil S A Companhia Geral De Cal E Cimento S A | WHITE OR COLORED CIMENTAL COATING WITH HYDROCHROMIC PROPERTIES |
CN103740214A (en) * | 2013-11-04 | 2014-04-23 | 安庆菱湖涂料有限公司 | High-strength high-temperature resistant anti-cracking elastic waterproof coating and preparation method thereof |
-
1986
- 1986-12-25 JP JP31523686A patent/JPS63162770A/en active Granted
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0527480A2 (en) * | 1991-08-12 | 1993-02-17 | Cosmo Research Institute | Vibration damping thick-film coating composition and method of forming the coated film |
JP2008222956A (en) * | 2007-03-15 | 2008-09-25 | Toa Doro Kogyo Co Ltd | Coating material composition |
JP2010261166A (en) * | 2009-04-30 | 2010-11-18 | Dainippon Toryo Co Ltd | Manufacturing method for heat shielding and insulating tile |
PT106591A (en) * | 2012-10-22 | 2014-04-22 | Secil S A Companhia Geral De Cal E Cimento S A | WHITE OR COLORED CIMENTAL COATING WITH HYDROCHROMIC PROPERTIES |
PT106591B (en) * | 2012-10-22 | 2014-11-10 | Secil S A Companhia Geral De Cal E Cimento S A | WHITE OR COLORED CIMENTAL COATING WITH HYDROCHROMIC PROPERTIES |
CN103740214A (en) * | 2013-11-04 | 2014-04-23 | 安庆菱湖涂料有限公司 | High-strength high-temperature resistant anti-cracking elastic waterproof coating and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0116872B2 (en) | 1989-03-28 |
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