JPS6072964A - How to paint and finish fire walls of fueling facilities, etc. - Google Patents
How to paint and finish fire walls of fueling facilities, etc.Info
- Publication number
- JPS6072964A JPS6072964A JP18082383A JP18082383A JPS6072964A JP S6072964 A JPS6072964 A JP S6072964A JP 18082383 A JP18082383 A JP 18082383A JP 18082383 A JP18082383 A JP 18082383A JP S6072964 A JPS6072964 A JP S6072964A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- weight
- acrylic
- painting
- paint
- 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
- 239000003973 paint Substances 0.000 title claims description 28
- 239000011347 resin Substances 0.000 claims description 68
- 229920005989 resin Polymers 0.000 claims description 68
- 239000000839 emulsion Substances 0.000 claims description 48
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 39
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 26
- 239000000203 mixture Substances 0.000 claims description 26
- 239000007787 solid Substances 0.000 claims description 24
- 238000010422 painting Methods 0.000 claims description 19
- 239000002320 enamel (paints) Substances 0.000 claims description 17
- 239000004568 cement Substances 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000000654 additive Substances 0.000 claims description 14
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 13
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 11
- 239000004593 Epoxy Substances 0.000 claims description 10
- 239000000049 pigment Substances 0.000 claims description 10
- 239000004925 Acrylic resin Substances 0.000 claims description 9
- 229920000178 Acrylic resin Polymers 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 7
- 239000000945 filler Substances 0.000 claims description 7
- 239000000446 fuel Substances 0.000 claims description 6
- 125000005907 alkyl ester group Chemical group 0.000 claims description 5
- 239000011083 cement mortar Substances 0.000 claims description 5
- 239000000057 synthetic resin Substances 0.000 claims description 5
- 229920003002 synthetic resin Polymers 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000011435 rock Substances 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 238000000576 coating method Methods 0.000 description 28
- 239000011248 coating agent Substances 0.000 description 26
- 239000004570 mortar (masonry) Substances 0.000 description 14
- 238000009472 formulation Methods 0.000 description 12
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 10
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 8
- 239000008199 coating composition Substances 0.000 description 6
- 239000003822 epoxy resin Substances 0.000 description 6
- 229920000647 polyepoxide Polymers 0.000 description 6
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 5
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 4
- 238000006253 efflorescence Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 206010037844 rash Diseases 0.000 description 4
- -1 2-ethylhexyl Chemical group 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 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 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000012360 testing method 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
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000007718 adhesive strength test Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011400 blast furnace cement Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying 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
- 238000005562 fading Methods 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 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
- 239000010410 layer Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 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
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 230000000149 penetrating effect Effects 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
- 239000005011 phenolic resin Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 230000035936 sexual power Effects 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000009864 tensile test Methods 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
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
- Aftertreatments Of Artificial And Natural Stones (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は、給油施設等の防火壁面の塗装仕上げ方法に関
する〇
従来、給油施設等(例えばガソリンスタンド)の周囲に
は隣家への延焼防止等の目的で防火壁が設けられており
、通常この防火壁は内側(店側)と上面が厚さ10〜2
0++w程度のモルタルで覆われたコンクリートブロッ
クで出来ている。該防火壁は装飾、汚れ防止等の目的で
、内側(モルタル金ゴテ面)は塗料により塗装されてい
るのが一般的である。モルタル内部含有水分による塗膜
の7クレ防止や、エフロレッセンス発生防止のため、含
水率10係以下、−10以下が適切な塗装条件であると
云われている。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method of painting and finishing fire walls of fuel supply facilities, etc. Conventionally, fire walls were provided around fuel facilities, etc. (for example, gas stations) for the purpose of preventing the spread of fire to neighboring houses. Normally, this fire wall has a thickness of 10 to 2 mm on the inside (store side) and top surface.
It is made of concrete blocks covered with mortar of about 0++W. The inside (mortar metal trowel surface) of the firewall is generally painted with paint for decoration, stain prevention, and other purposes. It is said that a moisture content of 10 parts or less and -10 parts or less is an appropriate coating condition in order to prevent the paint film from cracking due to the moisture contained in the mortar and to prevent the occurrence of efflorescence.
前記の如き防火壁の毛ルタル金ゴテ面への塗装仕様は、
(1) 塩化ビニル樹脂エナメル仕上げ(塩化ビニル樹
脂シーラー士塩化ビニル樹脂エナメル塗料2回塗り)、
(2) アクリル樹脂エナメル塗料仕上げ(塩化ビニル
樹脂シーラー+アクリル樹脂エナメル塗料2回塗り)1
(3) アクリル−ウレタン樹脂エナメル塗料仕上げ
(エポキシ樹脂下塗り士アクリルーウレタン樹脂エナメ
ル塗料2回塗り)
が最も普通である。The specifications for painting the rutal metal trowel surface of the firewall as described above are: (1) Vinyl chloride resin enamel finish (2 coats of vinyl chloride resin sealer and vinyl chloride resin enamel paint), (2) Acrylic resin enamel paint finish ( (2 coats of vinyl chloride resin sealer + acrylic resin enamel paint) 1 (3) Acrylic-urethane resin enamel paint finish (2 coats of epoxy resin undercoat acrylic-urethane resin enamel paint) is the most common.
しかして、一般に給油施設等の防火壁は、裏面及ヒ側面
はコンクリートブロックがそのまま露出し、又上面は未
塗装のモルタル笠木部分であるため、雨水等の内部侵入
はさけられず、前記の如く塗装時に最適条件を選び又耐
水性等に優れた塗装系を採用したとしても、塗装1年後
位には塗膜に数多くのフクレが発生し、2年目になると
フクレ部分から塗膜が剥離する状態となる。However, in general, fire walls such as fuel supply facilities have concrete blocks exposed on the back and sides, and the top surface is made of unpainted mortar, making it impossible to prevent rainwater from penetrating inside. Even if you select the optimal conditions during painting and use a coating system with excellent water resistance, many blisters will appear on the paint film after one year of painting, and the paint film will peel off from the blistered areas in the second year. It becomes a state where
従って、従来は2〜3年に1回程度の塗シ替えが必要で
あった。Therefore, conventionally, it was necessary to recoat about once every two to three years.
本発明は前記の如き従来技術に鑑みて成されたもので、
従来と同様防火壁のモルタル金ゴテ面のみに塗装するに
もかかわらず、長期間にわたってフクレ、剥離等の塗膜
欠陥の発生しない塗装仕上げ方法を提供しようとするも
のである。The present invention has been made in view of the prior art as described above.
The present invention aims to provide a coating finishing method that does not cause paint film defects such as blistering and peeling over a long period of time, even though the coating is applied only to the mortar metal trowel surface of a firewall as in the past.
即ち、本発明は、コンクリートブロック壁の内面をセメ
ントモルタル仕上げし、ついで塗装仕上げする給油施設
等の防火壁の仕上げ方法において、前記セメントモルタ
ル層上に、まず、
(−)(i) アクリルエマルション樹脂固形分 2〜
15重量覧(11) エポキシエマルジョン樹脂固形分
1〜5重量係、011)充填剤 25〜70重量覧
怜 セメント 20〜60!覧
(ψ 着色顔料 1〜5重量%、
6/l 前記エポキシエマルジョン樹脂に対する硬化剤
及びその他添加剤を必要量からなり1かつC(i) +
(ii) ) /怜=0.15〜0.28(重量比〕
の範囲である混合物 100重量部と、(b) 水 1
5〜70重量部
からなろ水性被覆組成物を下塗りし、ついで合成樹脂塗
料を上塗りすることを特徴とする給油施設等の防火壁の
塗装仕上げ方法に関する◎給油施設等の防火壁は、第1
図に示す如くコンクリートブロック11モルタル笠木部
分2.モルタル金ゴテ面3.塗膜4でり成されることは
前記した通りであるが、本発明の方法においては、まず
モルタル金ゴテ面に、
(a)(1) アクリルエマルション樹脂固形分 2〜
15重量へ(11) 工Iキシエマルジョン樹脂固形分
1〜5重量へ(lii) 充填剤 25−70重量係
、4V) セメント 20〜60重量転
(ロ)着色顔料 1〜5顔覧
IVD 前記エポキシエマルジョン樹脂に対する硬化剤
及びその他添加剤を必要量からなり、カ・つ〔(i)+
(11)〕/4φ=0.15〜0.28(重量比)の範
囲である混合物 100重量部と、(b) 水 15〜
70重量部
からなる水性被覆組成物を下塗りする。That is, the present invention provides a method for finishing a fire prevention wall such as a refueling facility, in which the inner surface of a concrete block wall is finished with cement mortar and then painted. Solid content 2~
15 Weight List (11) Epoxy Emulsion Resin Solid Content 1-5 Weight List, 011) Filler 25-70 Weight List Cement 20-60! Color pigment 1 to 5% by weight, 6/l Contains the necessary amount of curing agent and other additives for the epoxy emulsion resin, and C(i) +
(ii) ) / Rei = 0.15 to 0.28 (weight ratio)
(b) 100 parts by weight of a mixture in the range of (b) 1 part of water;
Relating to a method for painting and finishing fire walls of fuel supply facilities, etc., which comprises undercoating a water-based coating composition of 5 to 70 parts by weight and then topcoating with a synthetic resin paint.
As shown in the figure, concrete block 11 mortar cape part 2. Mortar gold trowel surface 3. As described above, the coating film 4 is formed by coating (a) (1) acrylic emulsion resin solid content 2 to 2 on the mortar metal trowel surface in the method of the present invention.
To 15 weight (11) Engineering I xy emulsion resin solid content 1 to 5 weight (lii) Filler 25-70 weight, 4V) Cement 20 to 60 weight (b) Color pigment 1 to 5 List IVD Said epoxy It consists of the necessary amount of curing agent and other additives for the emulsion resin.
(11)]/4φ=100 parts by weight of a mixture in the range of 0.15 to 0.28 (weight ratio), and (b) water 15 to
Prime with an aqueous coating composition consisting of 70 parts by weight.
本発明の下塗り水性被覆組成物に使用されるアクリルエ
マルジョン樹脂は、通常市販のものが使用可能であるが
、特にアクリル酸又はメタクリル酸アルキルエステル共
重合体(アルキルエステルの炭素数は1〜8)、あるい
は前記アクリル酸又はメタクリル酸アルキルエステルと
スチレンとの共重合体(スチレン含量は30重量%以下
)であるアクリルエマルジョン樹脂が好ましい。The acrylic emulsion resin used in the aqueous undercoat coating composition of the present invention can be commercially available, but especially acrylic acid or methacrylic acid alkyl ester copolymers (alkyl ester has 1 to 8 carbon atoms). Alternatively, an acrylic emulsion resin which is a copolymer of the above-mentioned acrylic acid or methacrylic acid alkyl ester and styrene (styrene content is 30% by weight or less) is preferable.
前記アクリル酸又はメタクリル酸エステル共重合エマル
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、メタクリル酸の炭素
数1〜8のアルキルエステル−T−/マーのアルキルエ
ステルとしてはメチル、エチル、n−ブチル、イソグチ
ル、ターシャリ−ブチル、2−エチルヘキシル、(ンジ
ル、グロビル、イングロビル、1lee−ブチルエステ
ル等が代表的なものとして用いられる。炭素数9以上の
エステルは乳化重合時にダル物が発生したり、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(又はメタクリル酸うエステルとスチレンとの共重合
エマル・ノヨン樹脂も好ましく用いられるが、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
耐候性が低下する傾向がみられる。The carbon number of acrylic acid, which is a component constituting the acrylic acid or methacrylic acid ester copolymer emulsion resin, is 1.
-8 alkyl ester monomers, alkyl esters of C1-8 alkyl esters of methacrylic acid -T-/mer, include methyl, ethyl, n-butyl, isobutyl, tert-butyl, 2-ethylhexyl, (ndyl, globil). , Inglovir, 1lee-butyl ester, etc. are typically used.Esters with carbon numbers of 9 or more may generate dull substances during emulsion polymerization, or the emulsion particles may become highly hydrophobic, making it difficult to synthesize emulsion resins for mixing with cement. In addition, copolymerized emuls and Noyon resins of acrylic acid (or methacrylic acid ester) and styrene are also preferably used, but if styrene is used in an amount of 30% by weight or more, the weather resistance of the resulting emulsion coating film may deteriorate. There is a tendency for sexual performance to decrease.
特に好ましいアクリル酸又はメタクリル酸エステルとし
てはメタクリル酸メチル、アクリル酸エチル、アクリル
醸ブチル、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
量%共重合することも可能である。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
℃以下が好ましく、それ以上になると成膜時にクラック
、ワレが生じやすくなる。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100 cps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
ヤセによりクラック、ワレが生じやすくなる。Particularly preferred acrylic acid or methacrylic esters are methyl methacrylate, ethyl acrylate, butyl acrylate, and 2-ethylhexyl acrylate, and when styrene is used, it is particularly preferably 20% by weight or less. If necessary, it is also possible to copolymerize several weight percent of functional group monomers such as acrylic acid, methacrylic acid, and 2-hydroxyethyl methacrylate. Advantageously, the molecular weight of these acrylic emulsion resins is from 50,000 to 300,000, preferably from 100,000 to 200,000. In addition, the minimum film forming temperature is 5
The temperature is preferably below 0.degree. C., and if it is higher than that, cracks and cracks are likely to occur during film formation. Further, the acrylic emulsion resin preferably has a viscosity of 100 cps or less when the solid content is 40% by weight. 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 it easier for cracks and cracks to occur due to fading during drying of the coating.
これらの樹脂は上記混合物(a)中において固形分2〜
15重量%の割合で配合される。樹脂が2重量%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1〜10 vm )が出来ず、クラック、
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 in a proportion of 15% by weight. If the resin content is less than 2% by weight, 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 1 to 10 vm) will not be possible, and cracks and
Cracks are more likely to occur.
又、本発明の水性被覆組成物に使用されるエポキシエマ
ルジョン樹脂は、好ましくはビスフェノール型工Iキシ
エマル−)!lン樹脂である。該ビスフェ/−yW工I
キシエマルジ、ン4141]WトLH、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
化剤を用いて、水分散型圧したものであり、樹脂固形分
として、上記混合物(、)中に1〜5重量重量用いられ
る。エポキシエマルジョン樹脂が1重119ft、未満
であると、素地との密着性が低下し、4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。Furthermore, the epoxy emulsion resin used in the aqueous coating composition of the present invention is preferably a bisphenol-type emulsion resin! It is a resin. Bisfe/-yW Engineering I
Aromatic diglycidyl ethers obtained from bisphenol A and epichlorohydrin and having an average molecular weight of 350 to 1000 are prepared by water dispersion using an emulsifier, and the solid content of the resin is as follows: 1 to 5% by weight are used in the above mixture (,). If the weight of the epoxy emulsion resin is less than 119 feet per weight, the adhesion to the substrate will be reduced, and if it exceeds 4% by weight, the weather resistance of the formed coating will be significantly reduced.
また本発明において用いられる充填剤は体質顔料として
祉炭酸カルシウム、硫酸バリウム、炭酸マグネシウム、
タルク、クレー等の無機質系粒状物が例示でき、骨材と
しては硼砂等である。この充填剤は、もろさの改良、増
重のため、及び塗布後組成物が未だ流動性を保持してい
る間に比重差により上記樹脂成分を塗膜表面へ浮上させ
るため配合されるものであり、比重の大きい粒径50〜
1000μ好ましくは50〜500μのものを用いる。In addition, the fillers used in the present invention include extender pigments such as calcium carbonate, barium sulfate, magnesium carbonate,
Examples include inorganic particulate materials such as talc and clay, and examples of the aggregate include borax. This filler is blended to improve brittleness and increase weight, and to float the resin component to the surface of the coating film due to the difference in specific gravity while the composition still maintains fluidity after coating. , particle size with large specific gravity 50~
1000μ, preferably 50 to 500μ.
充填剤は、上記混合物(、)中において25〜70重量
%の割合で配合される。これはこの範囲において、厚膜
塗膜においてもクラック、ワレのない塗膜が得られるか
らである。The filler is blended in the above mixture (2) in a proportion of 25 to 70% by weight. This is because within this range, a coating film free of cracks and cracks can be obtained even in thick coating films.
また本発明において用いられるセメントとしてはヂルト
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社上記の混合物(&)
中において20〜60重量%の割合で配合される。セメ
ントが20重量%未満だと厚膜時クラック、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。Further, examples of the cement used in the present invention include siltland cement, blast furnace cement, silica cement, alumina cement, etc., but the type thereof is not particularly limited. In the present invention, cement is the above mixture (&)
It is blended in a proportion of 20 to 60% by weight. If the cement content is less than 20% by weight, cracks and cracks will easily occur when the film is thick, and adhesion will decrease. On the other hand, if it exceeds 60% by weight, the coating film becomes brittle and efflorescence is likely to occur.
また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
リ性及び耐候性含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、IFンブラック、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。着色顔料は上記の混合物(、)中に
おいて1〜5重量重量制合で配合され、この範囲内での
配合により充分に着色する事が出来る。Further, 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, when coloring black, car, IF black, iron oxide, etc., for red, Bengara, etc., for green, chromium oxide, etc., for blue, cyanine blue, etc., for white, etc. Examples include titanium dioxide. The coloring pigment is blended in the above mixture (2) in an amount of 1 to 5% by weight, and by blending within this range, sufficient coloring can be achieved.
また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誘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
るいはエチレンジフミン%ノエチレントリアミン、トリ
エチレンテトラミン飾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、可撓性力2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
。Further, as the curing agent for epoxy resin used in the present invention, polyamide resins obtained by polycondensation of diamines or diamine derivatives, etc. and dibasic acids or dibasic acid derivatives, ethylene dihumine% ethylene triamine, triethylene tetramine decorated or aliphatic polyvalent amines modified with phenol 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.
また本発明において用いられる添加剤として社、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
、あるいは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。Additives used in the present invention include, for example, dispersants, antifoaming agents, thickeners, preservatives, antifungal agents, etc. to improve pigment dispersibility, painting workability, storage stability, etc. Examples include film-forming aids for improving the film-forming properties of the coating film.
さらに、上記混合物(&)中(1)アクリルエマル・ゾ
。Furthermore, (1) acrylic emulsion in the above mixture (&).
ン樹脂の固形分と(11)エポキシエマルジョン樹脂の
固形分との和と、4′J)セメントとの重量比は〔0十
(ii) ) / 4φ=Q、15〜0.28である。The weight ratio of the sum of the solid content of the epoxy emulsion resin and the solid content of the epoxy emulsion resin (11) and the 4'J) cement is [00(ii))/4φ=Q, 15 to 0.28.
この比率が0,15より小さい場合には、塗膜の初期硬
度が出す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
.28より大きい場合には厚膜時、クラツク、ワレが生
じやすくなる。If this ratio is smaller than 0.15, efflorescence will occur due to the initial hardness of the coating film, making it impossible to form a thick film with good coating performance.
.. If it is larger than 28, cracks and cracks are likely to occur when the film is thick.
また前記〔(11)+0−〕/〔(i)+(11)十〇
〕の重量比は特K O,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
。Also, the weight ratio of [(11)+0-]/[(i)+(11)10] is preferably 2 to 0.45, and if this ratio is less than 0.2, the adhesion will be poor. On the other hand, if this ratio is greater than 0.45, the weather resistance decreases.
本発明の方法に使用される水性被覆組成物は、上記混合
物(a) 100重量部に対して水15〜70重量部を
配合し組成物粘度50〜1000.16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及び塗装作
業性が良好であるからである。The aqueous coating composition used in the method of the present invention is prepared by blending 15 to 70 parts by weight of water to 100 parts by weight of the mixture (a) to give a composition viscosity of 50 to 1000.16 viscosity. This is because within this range, cement hardening and painting workability are good.
なお、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クラッ
ク、ワレが生じやすくなる。If the amount of water is less than 15 parts by weight, the acrylic emulsion will tend to coagulate when mixed with cement, while if it exceeds 70 parts by weight, the solid content will decrease and it will become loose during drying, causing cracks and cracks.
一方、本発明の塗装仕上は方法において使用される合成
樹脂上塗り塗料として社通常市販されているものが使用
可能であるが、下塗り塗膜との関連で耐アルカリ性や耐
水性、密着性あるいは耐候性等に優れている、溶剤型ア
クリル−ウレタン樹脂エナメル塗料、溶剤型アクリル樹
脂エナメル塗料、溶剤型塩化ビニル樹脂エナメル塗料あ
るい轄ツヤ有りアクリルエマルジョン樹脂塗料カ)ら選
ばれた塗料を使用することが特に好ましい。On the other hand, for the paint finish of the present invention, commonly commercially available synthetic resin topcoats used in the method can be used, but in relation to the basecoat film, it is necessary to It is possible to use paints selected from solvent-based acrylic-urethane resin enamel paints, solvent-based acrylic resin enamel paints, solvent-based vinyl chloride resin enamel paints, or glossy acrylic emulsion resin paints, which have excellent properties such as: Particularly preferred.
本発明の別の態様としては、前記下塗り塗膜上に中塗9
塗料を塗布した後、上塗り塗料を塗布する方法を包含す
るが、前記中塗り塗料としてはアクリル−ウレタン樹脂
サーフェーサー、塩化ビニル樹脂シーラー、アクリルエ
マルジョン樹脂シーラー等が好ましく使用される。しか
して、該中塗り塗料と上塗り塗料との組合せは、〔アク
リル−ウレタン樹脂サーフェーサーとアクリルーウレタ
7m脂エナメル塗料〕、(塩化ビニルm 脂シー ラー
と塩化ビニル樹脂エナメル塗料)、(塩化ビニル樹脂シ
ーラーとアクリル樹脂エナメル塗料)又は(アクリルエ
マルジョン樹脂シーラーとツヤ有りアクリル樹脂エマル
ジョン樹脂塗料)が特に好ましい。前記中塗り塗料及び
上塗り塗料は、各樹脂に必要により着色顔料2体質顔料
、有機溶剤又は水、その他必要な添加剤を混合すること
により製造することが可能である。In another aspect of the present invention, an intermediate coat 9 is applied on the undercoat film.
The method includes a method of applying a top coat after applying a paint, but as the intermediate coat, an acrylic-urethane resin surfacer, a vinyl chloride resin sealer, an acrylic emulsion resin sealer, etc. are preferably used. Therefore, the combinations of the intermediate coat and top coat are [acrylic-urethane resin surfacer and acrylic-urethane 7m fat enamel paint], (vinyl chloride resin sealer and vinyl chloride resin enamel paint), (vinyl chloride resin sealer and Particularly preferred are acrylic resin enamel paint) or (acrylic emulsion resin sealer and glossy acrylic resin emulsion resin paint). The intermediate coating and top coating can be produced by mixing each resin with a colored pigment, a two-body pigment, an organic solvent or water, and other necessary additives, if necessary.
本発明の塗装仕上は方法においては、まず前記下塗り水
性被覆組成物を通常の塗装方法、例えば吹付塗装、ロー
ラー塗装等により、乾燥膜厚が約100〜500μ程度
になるよう塗布し、常温乾燥せしめ、ついで必要により
中塗り塗料を同様に約25〜100μ程度に塗布、乾燥
させ、最後に上塗り塗料を同様に約25〜100μ程度
に塗布−乾燥させるものである。In the coating finishing method of the present invention, first, the aqueous undercoat coating composition is applied by a conventional coating method, such as spray coating or roller coating, to a dry film thickness of about 100 to 500 μm, and then dried at room temperature. Then, if necessary, an intermediate coat is similarly applied to a thickness of about 25 to 100 μm and dried, and finally a top coat is similarly applied to a thickness of about 25 to 100 μm and dried.
かくして本発明の方法によれば、防火壁の裏面あるいけ
上面から侵入する雨水等による塗膜のフクレ、剥離等が
長期間挿えられるとともに付着強度も優れた塗膜層が形
成される。加えて、被塗物(モルタル金ゴテ面)の含水
率やPH1−全く気にせずに下塗りすることが出来(極
端な場合被塗物面が濡れていてもよい)るという利点が
あり、塗装工程の短縮が可能であるという別の効果も奏
するのである。Thus, according to the method of the present invention, blistering, peeling, etc. of the paint film caused by rainwater entering from the back side or the upper side of the firewall can be prevented for a long period of time, and a paint film layer with excellent adhesion strength is formed. In addition, there is the advantage that undercoating can be applied without worrying about the moisture content or pH1 of the object to be coated (mortar metal trowel surface) (in extreme cases, the surface of the object to be coated may be wet). Another effect is that the process can be shortened.
以下実施例により本発明を説明する。なお実施例中で部
及び俤は重量基準である。The present invention will be explained below with reference to Examples. In the examples, parts and weights are based on weight.
まず実施例に先立って各塗料を以下の配合によシ調整し
た。First, prior to the Examples, each paint was prepared according to the following formulation.
〔配合1〕 下塗り塗料
アクリルエマルジョン樹脂(固形分) 7.0部硫酸バ
リウム 20.0
硅砂(粒径100〜200μ) i5.。[Formulation 1] Undercoat paint acrylic emulsion resin (solid content) 7.0 parts Barium sulfate 20.0 Silica sand (particle size 100-200μ) i5. .
セメント 48.0
酸化チタン 3.5
添加剤 1.5
水 32
前記アクリルエマルジヨン樹脂はメタクリル酸メチル/
アクリル酸ブチル/アクリル酸2−エチルヘキシル/ス
チレン=25/20/2015(重量比)の割合で共重
合させたもので、最低造膜温度−5℃のエマルジョン樹
脂であり、前記エポキシ樹脂社平均分子量600のエマ
ルジョン樹脂である。Cement 48.0 Titanium oxide 3.5 Additive 1.5 Water 32 The acrylic emulsion resin is methyl methacrylate/
It is copolymerized in the ratio of butyl acrylate/2-ethylhexyl acrylate/styrene = 25/20/2015 (weight ratio), and is an emulsion resin with a minimum film forming temperature of -5°C, and has an average molecular weight of 600 emulsion resin.
〔配合2〕 下塗り塗料
アクリルエマルション樹脂(固形分)4.2部硫酸バリ
ウム 40.0
硅砂(配合1と同一3 20.0
セメント 29.0
酸化チタン 2.0
硬化剤(配合1と同一)1.5
添加剤 1.5
水 24
前記アクリルエマルジヨン樹脂は、メタクリル酸メチル
/アクリル酸2−エチルヘキシル=20/22 (重量
比)の割合で共重合させたもので、最低造膜温度4℃の
エマルジョン樹脂である。[Formulation 2] Undercoat paint acrylic emulsion resin (solid content) 4.2 parts Barium sulfate 40.0 Silica sand (same as formulation 1 3 20.0 Cement 29.0 Titanium oxide 2.0 Hardening agent (same as formulation 1) 1 .5 Additives 1.5 Water 24 The acrylic emulsion resin is copolymerized at a ratio of methyl methacrylate/2-ethylhexyl acrylate = 20/22 (weight ratio), and has a minimum film forming temperature of 4°C. It is an emulsion resin.
〔配合3〕 中塗り塗料
塩化ビニル樹脂(固形分) 20部
溶剤 80
〔配合4〕 中塗り塗料
アクリルエマルジョン樹脂(固形分) 25.0部酸化
チタン 15.0
炭酸カルシウム 20.0
消泡剤 0.5
添加剤 4.0
水 35.5
前記アクリルエマルジヨン樹脂はアクリル酸ブチル/メ
タクリル酸メチル/アクリル酸2−エチルヘキシル/ス
チレン= 90/90/20150 (重量比〕の割合
で共重合させたアクリルエマルション樹脂である。[Formulation 3] Intermediate paint vinyl chloride resin (solid content) 20 parts Solvent 80 [Formulation 4] Intermediate paint acrylic emulsion resin (solid content) 25.0 parts Titanium oxide 15.0 Calcium carbonate 20.0 Antifoaming agent 0 .5 Additives 4.0 Water 35.5 The acrylic emulsion resin is acrylic copolymerized in the ratio of butyl acrylate/methyl methacrylate/2-ethylhexyl acrylate/styrene = 90/90/20150 (weight ratio). It is an emulsion resin.
〔配合5〕 中塗り塗料
(主剤)
ビスフェノール型エポキシ樹脂(固形分) 12部酸化
チタン 14
硅酸マグネシウム 24
添加剤 2
溶剤 18
(硬化剤〕
ポリアミド樹脂(固形分)15
溶剤 15
〔配合6〕 上塗り塗料
(主剤)
アクリルポリオール樹脂(固形分) 26.0部酸化チ
タン 24.0
添加剤 0・4
溶剤 29.6
(硬化剤)
Iリイソシアネート 10.0
溶剤 10.0
〔配合7〕 上塗り塗料
塩化ビニル樹脂(固形分) 23部
酸化チタン 22
硫酸バリウム 6
可塑剤 2
添加剤 1
溶剤 46
〔配合8〕 上塗り塗料
アクリル樹脂(固形分) 36.0部
酸化チタン 22,0
硫酸バリウム 8.0
可塑剤 2,0
添加剤 1.5
溶剤 30.5
前記アクリル樹脂はアクリル酸ブチル/メタクリル酸メ
チル/アクリル酸2−エチルヘキシル/スチレン= 1
0/1315/8 (重量比〕の割合で共重合せしめた
樹脂である。[Formulation 5] Intermediate paint (main ingredient) Bisphenol-type epoxy resin (solid content) 12 parts Titanium oxide 14 Magnesium silicate 24 Additives 2 Solvent 18 (Curing agent) Polyamide resin (solid content) 15 Solvent 15 [Formulation 6] Top coat Paint (main ingredient) Acrylic polyol resin (solid content) 26.0 parts Titanium oxide 24.0 Additives 0.4 Solvent 29.6 (Curing agent) I-lysocyanate 10.0 Solvent 10.0 [Formulation 7] Top coat chloride Vinyl resin (solid content) 23 parts Titanium oxide 22 Barium sulfate 6 Plasticizer 2 Additive 1 Solvent 46 [Formulation 8] Top coat acrylic resin (solid content) 36.0 parts Titanium oxide 22.0 Barium sulfate 8.0 Plasticizer 2.0 Additive 1.5 Solvent 30.5 The acrylic resin has butyl acrylate/methyl methacrylate/2-ethylhexyl acrylate/styrene = 1
It is a resin copolymerized at a ratio of 0/1315/8 (weight ratio).
〔配合9〕 上塗り塗料
酸化チタン 25.0
消泡剤 0.5
添加剤 4.0
水 45.5
実施例1〜6及び比較例1〜2
まずコンクリートブロック(300X300X150■
〕の上部と片側表面にモルタルを金ゴテで被覆し、屋外
に一週間放置し、素材を用意した。ついで第1表に示す
塗装系で前記素材のモルタル金ゴテ表面のみ(上面は除
<)t−塗装し、24時間常温乾燥させた後、屋外放置
して比較試験に供した。[Formulation 9] Top coat titanium oxide 25.0 Antifoaming agent 0.5 Additive 4.0 Water 45.5 Examples 1 to 6 and Comparative Examples 1 to 2 First, a concrete block (300 x 300 x 150 cm
] The upper part and one side of the surface were covered with mortar using a metal trowel, and the material was prepared by leaving it outdoors for a week. Then, only the surface of the mortar metal trowel of the above material (excluding the top surface) was coated with the coating system shown in Table 1, and after drying at room temperature for 24 hours, it was left outdoors for a comparative test.
尚、塗装置前の素材の含水率は10チ以上、pHは11
.5であった。In addition, the moisture content of the material before painting is 10 cm or more, and the pH is 11.
.. It was 5.
付着強度:建研式引張り試験機を使用。Adhesive strength: Use Kenken type tensile testing machine.
破断表示、qb:付着強度試験時の破断箇所とその面積
を示す。Fracture display, qb: Indicates the fracture location and its area during the adhesive strength test.
Gは素材(モルタル)の凝集破壊 を示す。G is cohesive failure of material (mortar) shows.
GSは素材と下塗り塗膜の間の界面 破壊を示す。GS is the interface between the material and the base coat. Show destruction.
塗膜状態
フクレ発生の程度 ◎:塗膜表面(300X300m)
Kフクレの数が全く認めら
れない。Paint film condition Degree of blistering ◎: Paint film surface (300 x 300 m)
No number of K blisters was observed.
○:同じくフクレが1〜3個発 生。○: 1 to 3 blisters appear as well Living.
Δ:同じく5〜20個発生。Δ: Similarly, 5 to 20 occurred.
×:同じ<21個以上発生。×: Same <21 or more occurrences.
剥離発生の程度 ◎:塗膜表面(300X300■)中
に剥離が全く認められな
い。Degree of peeling: ◎: No peeling is observed on the coating film surface (300×300■).
○:同じく1俤以内の剥離面積 が認められる。○: Peeling area within 1 yen is recognized.
△:同じく1〜5チの剥離面積 が認められる。△: Peeling area of 1 to 5 inches as well is recognized.
×:同じく6チ以上の剥離面積 が認められる。×: Peeling area of 6 inches or more as well is recognized.
前記比較試験結果より明らカニに、本発明の方法により
得られた塗膜層は、素材の未塗装部分からの雨水侵入に
よるフクレ、剥離に対して長期間にわたる耐久性を示す
が、従来公知の塗装系から得られたものは、−午後には
フクレ、剥離が著しく発生する。It is clear from the above comparative test results that the coating layer obtained by the method of the present invention exhibits long-term durability against blistering and peeling due to rainwater entering from unpainted parts of the material, but compared to conventionally known coatings. The coating obtained from the above coating system causes significant blistering and peeling in the afternoon.
更に、本発明の方法による塗膜層は初期付着強度に比し
て一午後の付着強度の方が大きくなり、しかも2年後も
その強度を維持するとともに下塗り塗膜と素材の付着性
も優れたものであった。Furthermore, the coating layer obtained by the method of the present invention has a greater adhesion strength after one day than the initial adhesion strength, maintains this strength even after two years, and has excellent adhesion between the base coat and the material. It was something like that.
(破断箇所呟常に素材の凝集破壊でありた。)(The fracture location was always a cohesive failure of the material.)
第1図は給油施設等の防火壁の一部金示す。
1:コンクlJ゛−)ブロック、2:モルタル笠木部分
、3:コンクリートブロック防火壁内面モルタル金ゴテ
面、4:塗料塗膜。
手続補正書
昭禾口58翠lO月 5日
特許庁長官 若 杉 和 夫 殿
昭和、58年9月30日提出の特許H1l+2、 発明
の名称
給油施設等の防火壁の塗装仕上げ方法
3、捕iEをする者
事件との関係 特許出願人
名称 (332)大日本塗料株式会社
4、代理人
住所 東京都港区虎ノ門五丁目13番1号虎ノ門4o森
ビル図 面Figure 1 shows some of the fire walls of fueling facilities, etc. 1: Concrete lJ゛-) block, 2: Mortar Kasagi part, 3: Mortar metal trowel surface on inner surface of concrete block firewall, 4: Paint coating film. Procedural Amendments Showaguchi 58 Sui lO Month 5 Director General of the Patent Office Kazuo Wakasugi Tono Showa, Patent H1l+2 filed on September 30, 1958 Title of Invention Method 3 of Painting and Finishing Firewalls of Refueling Facilities etc. Relationship with the case involving a person who does
Claims (9)
ルタル仕上げし、ついで塗装仕上げする給油施設等の防
火壁の仕上げ方法において、前記セメントモルタル層上
に1まず (a)(+) アクリルエマルジョン樹脂固形分 2〜
15重」L(11) エポキシエマルジョン樹脂固形分
1〜5重量%、OiD 充填剤 25〜701t’j
、(ψ セメント 20〜60重量%、 0 着色顔料 1〜5u優、 6/It 前記工d?キシエマルジョン樹脂に対する硬
化剤及びその他添加剤の必要量ふらなり、 九つ〔(i)+(II)〕/(ψ=0.15〜0.28
(重量比)の範囲である混合物 100重量部と、 (b) 水 15〜70重量部 からなる水性被覆組成物を下塗りし、ついで合成樹脂塗
料を上塗りするととf:%徴とする給油施設等の防火壁
の塗装仕上げ方法。(1) Core Creation) In a finishing method for fire walls such as refueling facilities where the inner surface of a 7" rock wall is finished with cement mortar and then painted, first 1 (a) (+) acrylic emulsion resin is applied on the cement mortar layer. Solid content 2~
15" L (11) Epoxy emulsion resin solid content 1-5% by weight, OiD filler 25-701t'j
, (ψ Cement 20-60% by weight, 0 Colored pigment 1-5U, 6/It Required amount of curing agent and other additives for the above-mentioned process d?xy emulsion resin Furanari, Nine [(i) + (II) )]/(ψ=0.15~0.28
(wt ratio) and (b) 15 to 70 parts by weight of water, and then a synthetic resin paint is applied as a topcoat, resulting in an f:% refueling facility, etc. How to finish painting fire walls.
脂は、アクリル酸又祉メタクリル酸アルキルエステル共
重合体(アルキルエステルの炭素数は1〜8)、あるい
は前記アクリル酸又はメタクリル酸アルキルエステルと
スチレンとの共重合体(スチレン含量は30重量%以下
)である特許請求の範囲第(1)項記載の給油施設等の
防火壁の塗装仕上げ方法。(2) The acrylic emulsion resin in the undercoat composition is a copolymer of acrylic acid or methacrylic acid alkyl ester (the alkyl ester has 1 to 8 carbon atoms), or a combination of the acrylic acid or methacrylic acid alkyl ester and styrene. (Styrene content is 30% by weight or less) Copolymer (styrene content: 30% by weight or less) The method of painting and finishing fire walls of fuel supply facilities, etc., according to claim (1).
は5℃以下である特許請求の範囲第(1)項記載の給油
施設等の防火壁の塗装仕上げ方法。(3) The method for painting and finishing fire walls of refueling facilities, etc., according to claim (1), wherein the minimum film forming temperature of the acrylic emulsion resin is 5° C. or lower.
(i) + (ii)十付か〕の重量比が0.2〜0
.45の範囲である特許請求の範囲第(1)項記載の給
油施設等の防火壁の塗装仕上げ方法。(4) Said ((ii) + 6Jil) / [:
(i) + (ii) weight ratio of 0.2 to 0
.. 45. A method for painting and finishing a fire wall of a refueling facility, etc., as set forth in claim (1), which is within the scope of claim 45.
樹脂エナメル塗料、アクリル樹脂エナメル塗料2塩化ビ
ニル樹脂エナメル塗料又はツヤ有りアクリルエマルジョ
ン樹脂塗料から選ばれた塗料である特許請求の範囲第(
1)項記載の給油施設等の防火壁の塗装仕上げ方法。(5) The synthetic resin top coat is a paint selected from acrylic-urethane resin enamel paint, acrylic resin enamel paint, vinyl dichloride resin enamel paint, or glossy acrylic emulsion resin paint.
1) Method of painting and finishing fire walls of refueling facilities, etc. as described in section 1).
タル仕上げし、ついで塗装仕上げする給油施設等の防火
壁の仕上げ方法において、前記セメントモルタル層上に
、まず (−)(i) アクリルエマルジョン樹脂固形分 2〜
15重量係、(11) エポキシエマルジョン樹脂固形
分 1〜5重量転(Iij) 充填剤 25〜70重量
へ4ψ セメント 20〜60重貴チ、 (V) 着色顔料 1〜5重量炊 6Jll 前記エポキシエマルジョン樹脂に対する硬化
剤及びその他添加剤の必要量fJiらなり、 かつC(i)+(ii) ) /4V)= 0.15〜
0.28 (重量比)の範囲である混合物 100重量
部と、 (b) 水 15〜70重量部 ふらなる水性被覆組成物を下塗りし、ついで合成樹脂中
塗り塗料を塗布後上塗り塗料を塗布することを特徴とす
る給油施設等の防火壁の塗装仕上げ方法。(6) In a method for finishing a fire wall in a refueling facility, etc., in which the inner surface of a concrete block wall is finished with cement mortar and then finished with painting, first, on the cement mortar layer, (-)(i) acrylic emulsion resin solid content 2 to
15 weight ratio, (11) Epoxy emulsion resin solid content 1 to 5 weight conversion (Iij) Filler 25 to 70 weight to 4ψ Cement 20 to 60 weight ratio, (V) Color pigment 1 to 5 weight ratio 6Jll The above epoxy emulsion The required amount of curing agent and other additives for the resin is fJi, and C(i)+(ii))/4V)=0.15~
100 parts by weight of a mixture in the range of 0.28 (weight ratio); and (b) 15 to 70 parts by weight of water as an undercoat, and then a synthetic resin intermediate coat is applied, followed by a top coat. A method for painting and finishing fire walls of refueling facilities, etc., characterized by:
脂は、アクリル酸又はメタクリル酸アルキルエステル共
重合体(アルキルエステルの炭素数は1〜B)、あるい
は前記アクリル酸又はメタクリル酸アルキルエステルと
スチレンとの共重合体(スチレン含量は30重景俤以下
)である特許請求の範囲第(6)項記載の給油施設等の
防火壁の塗装仕上げ方法。(7) The acrylic emulsion resin in the undercoat composition is an acrylic acid or methacrylic acid alkyl ester copolymer (the alkyl ester has 1 to B carbon atoms), or a copolymer of the acrylic acid or methacrylic acid alkyl ester and styrene. A method for painting and finishing fire walls of fuel supply facilities, etc., as set forth in claim (6), which is a polymer (styrene content is 30% or less).
は5℃以下である特許請求の範囲第(6)項記載の給油
施設等の防火壁の塗装仕上げ方法。(8) The method for painting and finishing fire walls of refueling facilities, etc., according to claim (6), wherein the minimum film forming temperature of the acrylic emulsion resin is 5° C. or lower.
の重量比が0.2〜0,45の範囲である特許請求の範
囲第(6)項記載の給油施設等の防火壁の塗装仕上げ方
法。 α1 前記中塗り塗料と上塗り塗料の組合せは、(アク
リル−ウレタン樹脂サーフェーサーとアクリルウレタン
樹脂エナメル塗料〕、(塩化ビニル樹脂シーラーと塩化
ビニル樹脂エナメル塗料)。 (塩化ビニル樹脂シーラーとアクリル樹脂エナメル塗料
)又は(アクリルエマル−)ヨン樹脂シーラーとツヤ有
りアクリルエマルジョン樹脂塗料)から選ばれた組合せ
である特許請求の範囲第(6)項記載の給油施設等の防
火壁の塗装仕上げ方法。(9) Said ((ii) + ω) / [core (11) 100]
The method for painting and finishing fire walls of refueling facilities, etc., according to claim (6), wherein the weight ratio of is in the range of 0.2 to 0.45. α1 The combinations of the intermediate coat and top coat are (acrylic-urethane resin surfacer and acrylic urethane resin enamel paint), (vinyl chloride resin sealer and vinyl chloride resin enamel paint). (vinyl chloride resin sealer and acrylic resin enamel paint) or (acrylic emulsion) (acrylic emulsion resin sealer and glossy acrylic emulsion resin paint).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18082383A JPS6072964A (en) | 1983-09-30 | 1983-09-30 | How to paint and finish fire walls of fueling facilities, etc. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18082383A JPS6072964A (en) | 1983-09-30 | 1983-09-30 | How to paint and finish fire walls of fueling facilities, etc. |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6072964A true JPS6072964A (en) | 1985-04-25 |
Family
ID=16089976
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18082383A Pending JPS6072964A (en) | 1983-09-30 | 1983-09-30 | How to paint and finish fire walls of fueling facilities, etc. |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6072964A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62260784A (en) * | 1986-05-06 | 1987-11-13 | 住宅・都市整備公団 | Lamination construction method on cement base surface |
JPS62260785A (en) * | 1986-05-06 | 1987-11-13 | 住宅・都市整備公団 | Lamination of silica base paint |
JPS63222803A (en) * | 1987-03-12 | 1988-09-16 | 積水化学工業株式会社 | Manufacture of fiber-reinforced cement molded form |
JPS63256582A (en) * | 1987-04-15 | 1988-10-24 | 株式会社クボタ | Method of dressing ceramic products |
JPS63309561A (en) * | 1987-06-11 | 1988-12-16 | Mitsui Eng & Shipbuild Co Ltd | Heat-resistant alkali paint |
JPH06121965A (en) * | 1992-07-06 | 1994-05-06 | Kanebo Nsc Ltd | Production of coating film and film forming chemicals used therefor |
JPH08954U (en) * | 1991-07-01 | 1996-06-11 | 株式会社北陸ビコー | Waste storage box for construction sites |
KR20010000356A (en) * | 2000-09-21 | 2001-01-05 | 홍승익 | The manufacturing method of color putty |
KR20010007808A (en) * | 2000-09-27 | 2001-02-05 | 홍승익 | The manufacturing method of mono-fluid type plaster finishings |
KR100341935B1 (en) * | 2000-04-07 | 2002-06-24 | 심명수 | Inorganic compositions for the protection of concrete material |
KR100439743B1 (en) * | 2001-06-09 | 2004-07-12 | 김성수 | Coating material for the protection from the salt attack and the carbonation of concrete structures and coating method thereof |
KR100963107B1 (en) | 2010-02-23 | 2010-06-10 | 하태훈 | Structure formed in the sea having anti-corrosion layer |
JP2022160152A (en) * | 2021-04-06 | 2022-10-19 | 藤倉化成株式会社 | Primer paint, method for producing same, and method for producing substrate with coating |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53132030A (en) * | 1977-04-21 | 1978-11-17 | Sanyo Chemical Ind Ltd | Permeable water proof composition |
-
1983
- 1983-09-30 JP JP18082383A patent/JPS6072964A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53132030A (en) * | 1977-04-21 | 1978-11-17 | Sanyo Chemical Ind Ltd | Permeable water proof composition |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0474309B2 (en) * | 1986-05-06 | 1992-11-25 | ||
JPS62260785A (en) * | 1986-05-06 | 1987-11-13 | 住宅・都市整備公団 | Lamination of silica base paint |
JPS62260784A (en) * | 1986-05-06 | 1987-11-13 | 住宅・都市整備公団 | Lamination construction method on cement base surface |
JPH0571550B2 (en) * | 1986-05-06 | 1993-10-07 | Jutaku Toshi Seibi Kodan | |
JPS63222803A (en) * | 1987-03-12 | 1988-09-16 | 積水化学工業株式会社 | Manufacture of fiber-reinforced cement molded form |
JPS63256582A (en) * | 1987-04-15 | 1988-10-24 | 株式会社クボタ | Method of dressing ceramic products |
JPS63309561A (en) * | 1987-06-11 | 1988-12-16 | Mitsui Eng & Shipbuild Co Ltd | Heat-resistant alkali paint |
JPH08954U (en) * | 1991-07-01 | 1996-06-11 | 株式会社北陸ビコー | Waste storage box for construction sites |
JPH06121965A (en) * | 1992-07-06 | 1994-05-06 | Kanebo Nsc Ltd | Production of coating film and film forming chemicals used therefor |
KR100341935B1 (en) * | 2000-04-07 | 2002-06-24 | 심명수 | Inorganic compositions for the protection of concrete material |
KR20010000356A (en) * | 2000-09-21 | 2001-01-05 | 홍승익 | The manufacturing method of color putty |
KR20010007808A (en) * | 2000-09-27 | 2001-02-05 | 홍승익 | The manufacturing method of mono-fluid type plaster finishings |
KR100439743B1 (en) * | 2001-06-09 | 2004-07-12 | 김성수 | Coating material for the protection from the salt attack and the carbonation of concrete structures and coating method thereof |
KR100963107B1 (en) | 2010-02-23 | 2010-06-10 | 하태훈 | Structure formed in the sea having anti-corrosion layer |
JP2022160152A (en) * | 2021-04-06 | 2022-10-19 | 藤倉化成株式会社 | Primer paint, method for producing same, and method for producing substrate with coating |
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