JPH01174744A - Outside wall joint structure - Google Patents
Outside wall joint structureInfo
- Publication number
- JPH01174744A JPH01174744A JP33500787A JP33500787A JPH01174744A JP H01174744 A JPH01174744 A JP H01174744A JP 33500787 A JP33500787 A JP 33500787A JP 33500787 A JP33500787 A JP 33500787A JP H01174744 A JPH01174744 A JP H01174744A
- Authority
- JP
- Japan
- Prior art keywords
- fire
- paint
- layer
- foamed
- joint
- 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 claims abstract description 44
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 9
- 239000000049 pigment Substances 0.000 claims abstract description 9
- 239000000839 emulsion Substances 0.000 claims abstract description 8
- 239000003054 catalyst Substances 0.000 claims abstract description 5
- 238000004079 fireproofing Methods 0.000 claims description 9
- 230000002265 prevention Effects 0.000 claims description 8
- 238000005187 foaming Methods 0.000 claims description 4
- 230000018044 dehydration Effects 0.000 claims description 3
- 238000006297 dehydration reaction Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 abstract description 13
- 206010000369 Accident Diseases 0.000 abstract 2
- 238000012360 testing method Methods 0.000 description 22
- 239000003063 flame retardant Substances 0.000 description 18
- 239000000463 material Substances 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 11
- 239000000565 sealant Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 8
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 6
- 238000002485 combustion reaction Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000010425 asbestos Substances 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- -1 pallite Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229910052895 riebeckite Inorganic materials 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000002518 antifoaming agent Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000011810 insulating material Substances 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000000779 smoke Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 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
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-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
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000011162 core material Substances 0.000 description 2
- 239000011094 fiberboard Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000003566 sealing material Substances 0.000 description 2
- 239000010454 slate Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 235000010215 titanium dioxide Nutrition 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 241001536352 Fraxinus americana Species 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 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
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- GUSFEBGYPWJUSS-UHFFFAOYSA-N pentaazanium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O GUSFEBGYPWJUSS-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002984 plastic foam Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000004590 silicone sealant Substances 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 239000010959 steel Substances 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
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Fireproofing Substances (AREA)
- Building Environments (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は、防火性能が付与された外壁パネルの目地構
造に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a joint structure of an exterior wall panel that is provided with fireproof performance.
防火性能を有する大型外壁パネルの商品展開に伴い、実
際の火災時における延焼を防止するため、外壁パネル間
の目地部における防火性が見直されている。With the development of large exterior wall panels with fire-retardant properties, the fire-retardant properties of joints between exterior wall panels are being reconsidered in order to prevent the spread of fire in the event of an actual fire.
従来、こうした目地部に防火性を付与し、目地部からの
延焼を防止するため、発泡石綿体(商品名:リトフレッ
クス、ニチアス側製等)を目地部底部に挿入し、その上
からコーキング仕上げをする、という方法が採用されて
きた。Conventionally, in order to impart fireproofing properties to these joints and prevent the spread of fire from the joints, foamed asbestos (product name: Litoflex, manufactured by Nichias, etc.) was inserted into the bottom of the joints, and caulking was applied over the top. The method of doing this has been adopted.
しかしながら、目地幅は、製造時に生じる±2鶴程度の
誤差を有するため、それに応じて、上記方法においては
、幅寸法の異なる2〜3種類のリドフレックスを用意し
なければならない。さらに、それらが若干でも目地幅よ
り大きめである場合は、目地部への挿入が困難である、
等の問題点も有している。However, since the joint width has an error of about ±2 mm that occurs during manufacturing, in the above method, two to three types of Lidoflex with different width dimensions must be prepared accordingly. Furthermore, if they are even slightly larger than the joint width, it may be difficult to insert them into the joint.
It also has the following problems.
したがって、この発明は、このような手間のかかる面倒
な作業を必要とせず、工程数を減らして作業性を高め、
効率よく、かつ、防火性能に優れた外壁目地構造を提供
することを課題とする。Therefore, this invention eliminates the need for such time-consuming and troublesome work, reduces the number of steps, increases workability, and
The objective is to provide an exterior wall joint structure that is efficient and has excellent fire prevention performance.
上記課題を解決するために、この発明では、目地部に発
泡性、すなわち、加熱により発泡する性質の防火塗料を
通用している。つまり、この発明は、外壁パネル間の目
地部の構造であって、加熱により発泡断熱層となる発泡
型防火塗料層が設けられていることを特徴とする外壁目
地構造である以下に、この発明を、図面を参照しつつ詳
しく説明する。In order to solve the above-mentioned problems, the present invention uses a fireproofing paint that is foamable, that is, has the property of foaming when heated, for the joint portion. In other words, the present invention relates to a joint structure between exterior wall panels, which is characterized by being provided with a foamed fire protection paint layer that becomes a foamed heat insulating layer when heated. will be explained in detail with reference to the drawings.
第1図は、外壁パネルおよびその目地部の断面を模式的
に示し、■は下地材(基材)、2はパネルを支える芯材
、3は断熱材、4は外装材、5は外装材4の目地部、6
はその目地部5に挿入された発泡型防火塗料層、7は防
水層をそれぞれあられしている。Figure 1 schematically shows a cross section of an exterior wall panel and its joints, where ■ is a base material (base material), 2 is a core material that supports the panel, 3 is a heat insulating material, 4 is an exterior material, and 5 is an exterior material. Joint part of 4, 6
7 is a foamed fireproofing paint layer inserted into the joint portion 5, and 7 is a waterproof layer.
下地材1としては、防火性を有するものとして石膏ボー
ド等が使用されるが、これに限定されることはなく、合
板、パーティクルボード、石綿スレート、硬質繊維板(
商品名ニハードボード)。As the base material 1, a fire-retardant material such as gypsum board is used, but it is not limited to this, and plywood, particle board, asbestos slate, hard fiberboard (
Product name Nihard Board).
軟質繊維板(−船名:インシュレーションボード)等の
一般的基材も使用される。Common base materials such as soft fiberboard (-ship name: insulation board) are also used.
主として外壁パネル全体に強度を付与し、パネルを支え
る働きをする芯材2は、木枠をはじめとして鉄枠9合成
木材(プラスチックの加工・成形品)等、特に限定はさ
れず、また、その枠組み法等も、通常の大型壁構造、鉄
骨ラーメン構造等、任意に選択されうる。The core material 2, which mainly serves to provide strength to the entire exterior wall panel and support the panel, is not particularly limited to wooden frames, iron frames 9, synthetic wood (plastic processed/molded products), etc. The framework method etc. can also be arbitrarily selected, such as a normal large wall structure, a steel rigid frame structure, etc.
断熱材3としても特に限定はされず、ロックウール、グ
ラスウール、プラスチック発泡体(発泡スチロール)等
が使用される。The heat insulating material 3 is not particularly limited, and rock wool, glass wool, plastic foam (styrene foam), etc. can be used.
外装材4としては、石綿スレート、石綿セメント珪酸カ
ルシウム板、ALC(オートクレーブ養住軽量気泡コン
クリート)等が使用されるが、難燃性(防火性)を有す
るものであればこれらに限定されることはない。これら
は任意の方式により、上記断熱材3上に貼着され、縦目
地(合わせ目地)、横目地(重ね目地)等の目地部5が
形成される。As the exterior material 4, asbestos slate, asbestos cement calcium silicate board, ALC (autoclaved lightweight aerated concrete), etc. are used, but it is limited to these as long as it has flame retardancy (fire retardant). There isn't. These are pasted on the heat insulating material 3 by any method to form joint portions 5 such as vertical joints (joint joints) and horizontal joints (overlap joints).
この目地部5に挿入、形成される発泡型防火塗料層6を
構成する防火塗料は、加熱により発泡して断熱層(炭化
層)を形成しうるちのであって、特に限定はされないが
、少なくとも炭化膨張剤。The fire-retardant paint that constitutes the foam-type fire-retardant paint layer 6 inserted into and formed in this joint portion 5 can be foamed by heating to form a heat insulating layer (carbonized layer), and is not particularly limited, but at least Carbonized expansion agent.
説水触媒、顔料およびエマルジョン型展色剤を含んでい
るものが優れた性能を有している。さらに、作業性を考
慮すると、目地部5に圧送方式により自動的に挿入でき
るよう、その粘度は、1万〜10万cpsに調整されて
いることが好ましい。Those containing a hydrocatalyst, a pigment, and an emulsion type vehicle have excellent performance. Furthermore, in consideration of workability, the viscosity is preferably adjusted to 10,000 to 100,000 cps so that it can be automatically inserted into the joint portion 5 by a pressure feeding method.
この防火塗料にあって、炭化膨張剤は、加熱により炭化
して発泡層を形成し、この発泡層が熱を遮断する断熱層
として作用するものである。たとえば、ジペンタエリス
リトール、ペンタエリスリトール等を使用することが好
ましいが、これらに限定されることはない。In this fire protection paint, the carbonized expansion agent carbonizes when heated to form a foam layer, and this foam layer acts as a heat insulating layer that blocks heat. For example, it is preferable to use dipentaerythritol, pentaerythritol, etc., but the present invention is not limited thereto.
脱水触媒は、上記炭化層を形成する物質に脱水作用を起
こさせて炭化させるものであって、それと同時に、不燃
性の無機質リン酸膜を形成する役割を果たす無機リン酸
塩(アンモニウム塩等)系のものなどが使用できるが、
これらに限定されることはない。さらに具体的には、第
一リン酸塩。The dehydration catalyst is a substance that dehydrates and carbonizes the substance that forms the carbonized layer, and at the same time, it is an inorganic phosphate (ammonium salt, etc.) that plays the role of forming a nonflammable inorganic phosphoric acid film. You can use things like
It is not limited to these. More specifically, primary phosphates.
第二リン酸塩、第三すン酸塩、低縮合ポリリン酸塩等が
例示できる。Examples include dibasic phosphates, tertiary phosphates, and low condensation polyphosphates.
顔料としては、難燃性を有する無機系のものなどが適宜
選択され、たとえば、チタン白、カーボンブラック等の
着色顔料やタルク、炭酸カルシウム、パライト、マイカ
、カオリン、珪砂粉等の体質顔料等が挙げられる。As the pigment, inorganic pigments having flame retardancy are appropriately selected, and examples include coloring pigments such as titanium white and carbon black, and extender pigments such as talc, calcium carbonate, pallite, mica, kaolin, and silica sand powder. Can be mentioned.
防火塗料のビヒクル(展色剤)として、被塗物に付着し
て連続した皮膜を形成するとともに上記顔料を結着する
作用を営むエマルジョン型展色剤としては、特に限定は
されないが、上記炭化膨張剤の発泡性を阻害せず、かつ
、被塗物に対する密着性、可撓性等の緒特性に優れたも
のを使用することが好ましい。そのような展色剤として
は、たとえば、アクリル樹脂系エマルジョン、酢酸ビニ
ル樹脂系エマルジョン、ゴム系ラテックス等が挙げられ
る。前記アクリル樹脂系のものとしては、(メタ)アク
リル酸、(メタ)アクリル酸のメチル、エチル、ブチル
、2−エチルヘキシル等の各エステル、(メタ)アクリ
ルアミド、(メタ)アクリロニトリル等の各単量体の重
合体あるいは共重合体、または、これらの(メタ)アク
リル系単量体とスチレン、エチレン、塩化ビニル、酢酸
ビニル、無水マレイン酸等との共重合体などが例示でき
る。後記ゴム系ラテックスとしては、スチレン−ブタジ
ェンゴム系、変性スチレン−ブタジェンゴム系、クロロ
プレンゴム系、天然ゴム系等が例示される。As a vehicle (color vehicle) for fire protection paints, the emulsion type color vehicle adheres to the object to be coated to form a continuous film and acts to bind the pigments, but is not particularly limited. It is preferable to use an expanding agent that does not inhibit the foaming properties of the expanding agent and has excellent properties such as adhesion to the object to be coated and flexibility. Examples of such color vehicles include acrylic resin emulsions, vinyl acetate resin emulsions, and rubber latexes. The acrylic resins include (meth)acrylic acid, esters of (meth)acrylic acid such as methyl, ethyl, butyl, and 2-ethylhexyl, and monomers such as (meth)acrylamide and (meth)acrylonitrile. Examples include polymers or copolymers of these (meth)acrylic monomers and copolymers of styrene, ethylene, vinyl chloride, vinyl acetate, maleic anhydride, and the like. Examples of the rubber latex mentioned below include styrene-butadiene rubber, modified styrene-butadiene rubber, chloroprene rubber, and natural rubber.
以上の各成分は、それぞれ単独で使用されてもよいし、
複数種が併用されてもよいことは言うまでもなく、また
、それらの配合量は、特に限定はされないが、防火塗料
の発泡性および塗膜性能等の種々のバランスを鑑み、
炭化膨張剤 10〜25%説水触媒
20〜30%顔料
5〜15%エマルジョン型展色剤 25〜45
%(ただし、%は重量%を示す)
のような配合割合であることが好ましい。さらに、水等
により希釈されて、前記のように塗料粘度が1万〜10
万cps程度に調整されていることが好ましい。このよ
うに粘度調整することで、下記に述べるような塗料の自
動送入が可能となり、塗装効率を大幅に向上できるので
ある。Each of the above components may be used alone, or
It goes without saying that multiple types may be used in combination, and their blending amounts are not particularly limited, but in consideration of various balances such as foamability and coating performance of the fire prevention paint, carbonized expansion agents 10 to 25 %Hydrothermia catalyst
20-30% pigment
5-15% emulsion type vehicle 25-45
% (where % indicates weight %) is preferable. Furthermore, it is diluted with water, etc., and the viscosity of the paint is 10,000 to 10,000 as described above.
It is preferable that it is adjusted to about 10,000 cps. By adjusting the viscosity in this way, it is possible to automatically feed the paint as described below, and the coating efficiency can be greatly improved.
上記発泡型防火塗料は、以上のような成分の他に、その
他の成分として、消泡剤、増粘剤1分散剤、防腐・防か
び剤、さび止め剤等の各種添加剤を含んでいてもよい。In addition to the above-mentioned components, the above-mentioned foam-type fireproofing paint contains various additives such as an antifoaming agent, a thickener, a dispersant, a preservative/mold inhibitor, and a rust inhibitor. Good too.
これらの添加剤は、特に限定はされないが、消泡剤とし
てはシリコーンオイル系、高級アルコール系等、増粘剤
としてはメチルセルロース、カルボキシメチルセルロー
ス、各種アクリルエマルジョン系等、分散剤としてはア
ルキルベンゼンスルホン酸ナトリウム、ポリビニルアル
コール、ヒドロキシエチルセルロース、ポリオキシエチ
レンアルキルエステル、脂肪酸エステル系等の有機系の
ものやリン酸ナトリウム、ケイ酸ナトリウム等の無機系
のもの、可塑剤としてはポリエステル系、エポキシ系等
のポリメリック型のものやフタル酸エステル系等のモノ
メリック型のもの、防腐・防かび剤としてはホルマリン
。These additives are not particularly limited, but antifoaming agents include silicone oils and higher alcohols, thickeners include methylcellulose, carboxymethylcellulose, and various acrylic emulsions, and dispersants include sodium alkylbenzenesulfonate. , organic types such as polyvinyl alcohol, hydroxyethyl cellulose, polyoxyethylene alkyl esters, fatty acid esters, inorganic types such as sodium phosphate and sodium silicate, and polymeric types such as polyester and epoxy as plasticizers. Monomeric products such as phthalate esters and formalin are used as preservatives and fungicides.
ホウ酸等が、それぞれ例示でき、いずれも、この塗料に
おける効果を妨げない量の範囲内で適宜配合される。Examples include boric acid and the like, and all are appropriately blended within the range of amounts that do not impede the effects of the paint.
このような発泡型防火塗料層6の形成方法、すなわち、
目地部5への防火塗料の挿入方法としては特に限定はさ
れず、通常のはけ塗り、スプレー塗装等により実施でき
るが、作業性や効率といった面から、圧送方式等を採用
して自動的に送入することが好ましい。たとえば、圧送
式スプレーガンを使用すれば、広い面積に連続的に厚い
塗膜を形成でき、かつ、塗料の飛び散りが少ない塗装も
可能である。A method of forming such a foamed fire protection paint layer 6, that is,
There are no particular limitations on the method of inserting the fire prevention paint into the joints 5, and it can be done by normal brushing, spray painting, etc. However, from the standpoint of workability and efficiency, it can be done automatically by adopting a pressure-feeding method, etc. Preferably, it is delivered. For example, if a pressure-feed spray gun is used, it is possible to continuously form a thick coating film over a wide area, and it is also possible to paint with less paint scattering.
形成される防火塗料N6の厚みについては、充分な防火
性能を発揮できるように、はぼ1鰭以上であることが好
ましい。一方、外装材4の厚みや、その上にさらに、以
下に述べるコーキング材層7等の防水層などを重ねる可
能性などを鑑み、10鶴程度以内であることが適当であ
る。The thickness of the formed fire protection paint N6 is preferably one fin or more so as to exhibit sufficient fire protection performance. On the other hand, in consideration of the thickness of the exterior material 4 and the possibility of further layering a waterproof layer such as the caulking material layer 7 described below, etc., it is appropriate that the thickness be within about 10 mm.
一般に、発泡性の防火塗料は耐水性、耐候性に乏しいと
いう欠点を有するものが多いため、上記発泡型防火塗料
層6上に、防水層7が形成され、こうした欠点がカバー
されるようになっていてもよい。防水層7を形成するも
のとしては、特に限定はされないが、シリコーン系コー
キング材(シーリング材)等、難燃性を備えたものを使
用することが好ましい。あるいは、上塗り用の難燃性防
火塗料を使用してもよ(、これは、塗膜自体が難燃性を
有するものであって、たとえば、塩化ビニル樹脂、塩化
ゴム等の含塩素樹脂あるいは含ブロム樹脂等をビヒクル
とする有機系のものや、アルカリ金属塩やリン酸塩のシ
リケートからなる無機系のものが挙げられる。In general, many foamable fireproofing paints have the drawback of poor water resistance and weather resistance, so a waterproof layer 7 is formed on the foamable fireproofing paint layer 6 to cover these drawbacks. You can leave it there. The material forming the waterproof layer 7 is not particularly limited, but it is preferable to use a flame-retardant material such as a silicone caulking material (sealing material). Alternatively, you may use a flame-retardant fire-prevention paint for topcoating (this is a coating film itself that is flame-retardant, such as a chlorine-containing resin such as vinyl chloride resin or chlorinated rubber) or a flame-retardant paint. Examples include organic types using bromine resin as a vehicle, and inorganic types consisting of silicates of alkali metal salts and phosphates.
なお、この発明にかかる外壁目地構造は、上記実施例に
限定されることはなく、たとえば、発泡型防火塗料M6
以外にも、耐火パテ、耐火セメントあるいは無機質粉粒
を含んだ組成物等からなる耐火組成物層等が設けられて
いてもよい。また、外壁パネルは、断熱材3を含まない
ものであっても、あるいは、断熱以外の防音等の効果が
付与されたものであってもよく、要するに、目地部を有
する外壁パネルであれば、この発明における効果が得ら
れるのである。Note that the exterior wall joint structure according to the present invention is not limited to the above-mentioned embodiments, and for example, foam type fire prevention paint M6
In addition, a refractory composition layer made of a refractory putty, a refractory cement, a composition containing inorganic powder, or the like may be provided. Further, the exterior wall panel may not include the heat insulating material 3, or may have an effect other than heat insulation such as soundproofing.In short, as long as the exterior wall panel has joints, The effects of this invention can be obtained.
つぎに、この発明の実施例および比較例について、図面
を参照しつつ説明する。Next, examples and comparative examples of the present invention will be described with reference to the drawings.
■ ゛ ・ ゛の″
下記の各成分を配合し、発泡型防火塗料(ノンフレーム
■型)を調製した。(数字は重量%を示す)
炭化膨張剤として
ジペンタエリスリトール 16.0脱水触
媒として
第三リン酸アンモニウム 17.0顔料とし
て
チタン白 10.0工マル
ジヨン型展色剤として
酢酸ビニル−エチレン−塩化ビニル共fi合体(ヘキス
ト合成■製モビニール117E) 38.0消泡剤と
して
サンノプコ8034L (サンノプコ■製)0.5分散
剤として
トリポリリン酸ナトリウム 0.5増粘剤
として
ポリビニルアルコール 1.0希釈溶剤
として
水 17
.0得られた防火塗料の粘度は、16000cpsであ
り、固形分は67±3%であった。■ ゛・゛の'' A foaming type fireproofing paint (non-flame ■ type) was prepared by blending the following components. (The numbers indicate weight%) Dipentaerythritol as a carbonization expansion agent 16.0 No. 1 as a dehydration catalyst Ammonium triphosphate 17.0 Titanium white as a pigment 10.0 Vinyl acetate-ethylene-vinyl chloride cofi combination as a co-mulsion type vehicle (Movinyl 117E manufactured by Hoechst Synthesis) 38.0 Sannopco 8034L as an antifoaming agent (Sannopco 8034L) as an antifoaming agent 0.5 Sodium tripolyphosphate as a dispersant 0.5 Polyvinyl alcohol as a thickener 1.0 Water as a diluting solvent 17
.. The viscosity of the obtained fire protection paint was 16,000 cps, and the solid content was 67±3%.
(実施例1〜4)
第2図に示したように、パーティクルボード10と2枚
のフライアッシュスラグセメント系(NFC:ノン石綿
)外装板40とを貼り合わせ、4か所をねじ8により固
定して試験板を作製した。(Examples 1 to 4) As shown in FIG. 2, a particle board 10 and two fly ash slag cement type (NFC: non-asbestos) exterior boards 40 are pasted together and fixed at four locations with screws 8. A test plate was prepared.
図において、パーティクルボード1oの長さし。In the figure, the length of particle board 1o.
幅Wlはともに150m、厚みDlは12鶴であり、外
装板40の長さは144鶴1幅W、は65龍、厚みD2
は12N@であって、目地の幅w3は8mmである。な
お、試験板の中心裏側には直径8鶴の温度計差し込み穴
9を設けて目地部裏面温度が測定できるようにした。The width Wl is 150 m, the thickness Dl is 12 m, the length of the exterior plate 40 is 144 m, the width W is 65 m, and the thickness D2 is
is 12 N@, and the joint width w3 is 8 mm. A thermometer insertion hole 9 with a diameter of 8 mm was provided on the back side of the center of the test plate so that the temperature on the back side of the joint could be measured.
第3図(alにみるように、第1表に示した厚さで目地
部50に上記得られた防火塗料ノンフレーム■型を、圧
送式タンク(旭大隈産業側製NP1844SV)により
注入し、室内で5日間の乾燥を行って、防火、塗料層6
0を形成した。As shown in FIG. 3 (al), the obtained fireproof paint non-frame ■ type was injected into the joint portion 50 with the thickness shown in Table 1 using a pressure-feeding tank (NP1844SV manufactured by Asahi Okuma Sangyo Co., Ltd.). After drying indoors for 5 days, fire protection and paint layer 6
0 was formed.
(実施例5〜8)
上記実施例と同様にして、第3図山)にみるように防火
塗料を注入後、乾燥器内で120℃/1分間の乾燥を行
って防火塗料層60を形成し、ついで、−液湿気硬化型
変性シリコーン系シーリング材(ナショナル住宅産業■
製パナホームシーラント)を注入して室内で5日間乾燥
させて、防水層70を形成した。(Examples 5 to 8) In the same manner as in the above examples, after injecting the fire prevention paint as shown in Fig. 3, the fire prevention paint layer 60 is formed by drying at 120°C/1 minute in a dryer. Next, - Liquid moisture curing modified silicone sealant (National Housing Industry ■
A waterproof layer 70 was formed by injecting Panahome Sealant) and drying it indoors for 5 days.
(比較例1)
上記実施例と同様の試験板の目地部50に、第3図(C
1にみるように、上記シーリング材のみを厚さ120で
注入し、室内で5日間乾燥させて防水層70を形成した
。(Comparative Example 1) The joint portion 50 of the test board similar to the above example was
1, the above sealing material alone was injected to a thickness of 120 mm and dried indoors for 5 days to form a waterproof layer 70.
(比較例2)
実施例と同様の試験板の目地部50に、第3図(d)に
みるように何も注入せず、無塗装のままこれを試験体と
した。(Comparative Example 2) As shown in FIG. 3(d), nothing was injected into the joint portion 50 of a test board similar to that of the example, and this was used as a test piece without coating.
(ロ) −および
上記実施例および比較例で得られた試験体の温度針差し
込み穴9に、裏面から1200℃まで測定可能な温度計
を差し込んだ。(b) - A thermometer capable of measuring up to 1200° C. was inserted from the back side into the temperature needle insertion hole 9 of the test specimens obtained in the above Examples and Comparative Examples.
試験体の燃焼面が900℃になるように、プロパンガス
バーナーの炎を調節し、これを試験体目地部中央付近に
垂直に当て、30分間および50分間の加熱をそれぞれ
行った。The flame of the propane gas burner was adjusted so that the temperature of the burning surface of the test piece was 900° C., and the flame was applied vertically to the center of the joint of the test piece, and heating was performed for 30 minutes and 50 minutes, respectively.
目地部裏面温度の測定結果を、第4図〜第6図に示す。The measurement results of the joint back surface temperature are shown in FIGS. 4 to 6.
防火塗料のみを注入した実施例1〜4については、第4
図にみるように、塗膜が厚い程(第4図および第5図に
おいて各記号は、それぞれ以下の乾燥前の防火塗料膜厚
をあられしている;白抜き○:2+n、Δ:3m、黒○
: 4m、 X : 5mm)、裏面温度の上昇が少
なく、また、加熱中の炎も少なく、その発生時間も短い
。30分経過して加熱を中止した後の煙の発生はほとん
どない。For Examples 1 to 4 in which only fire prevention paint was injected, the fourth
As shown in the figure, the thicker the paint film (in Figures 4 and 5, each symbol represents the following fire protection paint film thickness before drying; white circle: 2 + n, Δ: 3 m, Black○
: 4m, X: 5mm), there is little rise in temperature on the back side, there are few flames during heating, and the time for their generation is short. Almost no smoke is generated after heating is stopped after 30 minutes.
防火塗料およびシーリング材を注入した実施例5〜8に
ついては、第5図にみるように、塗料の膜厚にほとんど
影響されずに、いずれも温度の上昇は抑えられたものと
なっている。加熱により、シーリング材が燃焼して炎が
発生するが、途中からそれもおさまり、加熱30分後の
煙の発生もほとんど無かった。第4図との比較で明らか
なように、防火塗料はシーリング材と組み合わせた方が
裏面温度の上昇が少なく、防火性能は良好である。これ
は、シーリング材の燃焼後の灰も、断熱効果を発揮して
いるためと考察される。As shown in FIG. 5, in Examples 5 to 8 in which fireproof paint and sealant were injected, the temperature increase was suppressed in all cases, almost unaffected by the film thickness of the paint. When heated, the sealant burns and a flame is generated, but the flame subsides midway through, and almost no smoke is generated after 30 minutes of heating. As is clear from the comparison with FIG. 4, when the fire-retardant paint is combined with a sealant, the rise in back surface temperature is smaller and the fire-retardant performance is better. This is considered to be because the ash after combustion of the sealant also exerts a heat insulating effect.
第6図において破線によりあられされている、シーリン
グ材のみが注入された比較例1の試験体では、加熱30
分経過後の温度は192℃と比較的低いが、試験体は炎
を出して燃焼し、30分後に加熱を中止した後も、この
炎を伴う燃焼は11!続された。また、炎を吹き消して
も、煙が15分以上にわたって発生し、くすぶりの状態
が長時間続いた。30分加熱後のシーリング材は、全て
白い灰となった。一方、50分間加熱した場合では、裏
面の試験板中心部に、パーティクルボードが燃焼した事
実が認められた。よって、バナホームシーラントのみが
目地部に挿入されていても、シーラント自身す燃焼後、
際限なく木材の燃焼が継続すると考えられる。In the test specimen of Comparative Example 1 in which only the sealant was injected, which is indicated by the broken line in FIG.
After 30 minutes, the temperature was relatively low at 192°C, but the test specimen emitted flames and burned, and even after heating was stopped after 30 minutes, the combustion with flames remained at 11! continued. In addition, even after the flames were blown out, smoke remained for more than 15 minutes and the smoldering state continued for a long time. The sealant after heating for 30 minutes turned into white ash. On the other hand, in the case of heating for 50 minutes, it was observed that the particle board had burned in the center of the test plate on the back side. Therefore, even if only Vanahome sealant is inserted into the joint, after the sealant itself burns,
It is thought that wood burning will continue indefinitely.
同じく第6図において、実線があられす比較例2の目地
部無塗装の試験体では、加熱により燃え出し、燃えなが
ら温度が急速に上昇して21分の時点で300℃に達し
たため、そこで温度測定を中止した。30分加熱後の試
験体の目地部は、深部まで炭化されていた。Similarly, in Fig. 6, the test piece of Comparative Example 2 with unpainted joints, where the solid line is drawn, started to burn due to heating, and the temperature rose rapidly while burning, reaching 300°C in 21 minutes, so the temperature dropped. Measurement was canceled. After heating for 30 minutes, the joints of the test specimen were deeply carbonized.
なお、加熱試験後の試験体のパーティクルボードの状態
を観察した結果、比較例2の目地部無塗装の試験体での
み、燃焼状態が板金体に広がらず、中央目地部を中心に
黒化された状態となっていた。これは、他の試験体では
、目地部に注入された難燃性のシーリング材および/ま
たは防火塗料に阻害されて炎が横に広がり、したがって
、試験体全体が燃焼した状態になったことに比べ、比較
例2のものでは、炎が当たった目地部1点に集中して燃
焼が進行し、木部内に炭化層が広がっていったためであ
る。In addition, as a result of observing the state of the particle board of the test piece after the heating test, it was found that only in the test piece of Comparative Example 2 with unpainted joints, the combustion state did not spread to the sheet metal body, and blackening occurred mainly at the central joint. The situation was as follows. This is because in other test specimens, the flame spread horizontally due to the flame retardant sealant and/or fireproof paint injected into the joints, and the entire specimen was in a state of combustion. In contrast, in Comparative Example 2, combustion proceeded concentrated at one joint area where the flame hit, and a charred layer spread within the wood.
以上の結果を、第1表にまとめて示す。The above results are summarized in Table 1.
・第1表にみるように、目地部に発泡型防火塗料が挿入
された実施例の試験体では、裏面の温度上昇が抑えられ
て、炎および煙の発生も少なく、防火性能が良好である
ことが判明した。また、この防火塗料は、難燃性のシー
リング材等と併用されると、−層優れた効果を発揮する
ことが明らかとなった。・As shown in Table 1, the test specimen of the example in which the foamed fire-retardant paint was inserted into the joints suppressed the temperature rise on the back side, produced less flame and smoke, and had good fire-retardant performance. It has been found. It has also been revealed that this fireproofing paint exhibits excellent effects when used in combination with flame-retardant sealants and the like.
この発明にかかる外壁目地構造は、以上のようであり、
火災時に発泡断熱層を形成する発泡型防火塗料層が設け
られていることを特徴とするため、目地部からの延焼が
防止され、防火性能に優れた外壁の実現を可能とさせる
。The exterior wall joint structure according to the present invention is as described above,
It is characterized by a foam-type fire-retardant paint layer that forms a foam heat-insulating layer in the event of a fire, which prevents the spread of fire from the joints, making it possible to create an exterior wall with excellent fire-retardant performance.
第1図はこの発明にかかる外壁目地構造の一実施例をあ
られす断面模式図、第2図はこの発明の実施例および比
較例における試験板の斜視図、第3図(al〜(d)は
同じ〈実施例および比較例における試験体目地部の断面
模式図、第4図〜第6図は同じ〈実施例および比較例の
一燃焼試験結果(試験体裏面温度変化)をあられすグラ
フである。
1・・・下地材 4・・・外装材 5・・・目地部 6
・・・防火塗料層
代理人 弁理士 松 本 武 彦
第3
(a)
(c)
(b)
(d)Fig. 1 is a schematic cross-sectional view of an example of an external wall joint structure according to the present invention, Fig. 2 is a perspective view of a test plate in an example of the invention and a comparative example, and Fig. 3 (al to (d)). are the same〈Schematic cross-sectional diagram of the joint part of the test specimen in the example and comparative example, Figures 4 to 6 are the same〈One combustion test result (temperature change on the back side of the test specimen) of the example and comparative example is shown in a graph. Yes. 1... Base material 4... Exterior material 5... Joint area 6
... Fire protection paint layer agent Patent attorney Takehiko Matsumoto 3rd (a) (c) (b) (d)
Claims (2)
り発泡断熱層となる発泡型防火塗料層が設けられている
ことを特徴とする外壁目地構造。(1) An exterior wall joint structure characterized in that the joint between exterior wall panels is provided with a foamed fire prevention paint layer that becomes a foamed heat insulating layer when heated.
触媒、顔料およびエマルジョン型展色剤を含み、粘度が
1万〜10万cpsに調整されているものである特許請
求の範囲第1項記載の外壁目地構造。(2) Claim 1, wherein the foaming type fireproofing paint contains at least a carbonized expansion agent, a dehydration catalyst, a pigment, and an emulsion type color vehicle, and has a viscosity adjusted to 10,000 to 100,000 cps. Exterior wall joint structure described.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33500787A JPH01174744A (en) | 1987-12-28 | 1987-12-28 | Outside wall joint structure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33500787A JPH01174744A (en) | 1987-12-28 | 1987-12-28 | Outside wall joint structure |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01174744A true JPH01174744A (en) | 1989-07-11 |
Family
ID=18283696
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP33500787A Pending JPH01174744A (en) | 1987-12-28 | 1987-12-28 | Outside wall joint structure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01174744A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2023032951A (en) * | 2021-08-27 | 2023-03-09 | デンカ株式会社 | Heat-expandable paste composition |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54113922A (en) * | 1978-02-25 | 1979-09-05 | Nat Jutaku Kenzai | Panel joint portion fireeproof structure |
JPS552936B1 (en) * | 1966-11-25 | 1980-01-23 | ||
JPS60215091A (en) * | 1984-04-11 | 1985-10-28 | Hayakawa Rubber Co Ltd | Sealing material |
-
1987
- 1987-12-28 JP JP33500787A patent/JPH01174744A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS552936B1 (en) * | 1966-11-25 | 1980-01-23 | ||
JPS54113922A (en) * | 1978-02-25 | 1979-09-05 | Nat Jutaku Kenzai | Panel joint portion fireeproof structure |
JPS60215091A (en) * | 1984-04-11 | 1985-10-28 | Hayakawa Rubber Co Ltd | Sealing material |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2023032951A (en) * | 2021-08-27 | 2023-03-09 | デンカ株式会社 | Heat-expandable paste composition |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU2645538C2 (en) | Fire-resistant composition and fire-resistant thermal insulating plate | |
US6207085B1 (en) | Heat expandable compositions | |
CA1097455A (en) | Thermal barrier compositions | |
CN104311113B (en) | A kind of fire-resistant door core sheet material and preparation method thereof | |
CN104774509A (en) | Fireproof paint | |
US6340645B1 (en) | Intumescent laminates with high heat transfer resistance | |
HU206739B (en) | Latexbinded anti-burning materials and layered materials against burning | |
KR20180117511A (en) | Method for fabricating of noncombustible styrofoam panel | |
JP3218359B2 (en) | Foamed refractory laminate and method of forming the same | |
JPH09256506A (en) | Wood fire-resistive covering method and fire-resistive covered wood | |
JP2000230287A (en) | Foam fire-resistant laminated body and its formation | |
KR101489583B1 (en) | Non-Flammable composite for expanded polystyrene foam and manufacturing method thereof | |
JPH01174744A (en) | Outside wall joint structure | |
US4671040A (en) | Method for flameproofing shingled surfaces | |
KR0182661B1 (en) | Aqueous intumescent coating composition and the fire-proofing protection agent | |
KR0181365B1 (en) | Intamescent fire-proofing coating composition and fire-proofing coating agents | |
JPS5911377A (en) | Fire-resistant coating composition | |
JP2008214463A (en) | Low-temperature foaming fireproof coating material | |
JP3163414B2 (en) | Composite refractory coating composition, composite refractory coating layer and method of forming the same | |
JP3551808B2 (en) | Method for forming heat-insulating laminate having fire protection | |
JP2000192570A (en) | Foamed fire resisting sheet composition and foamed fire resisting sheet | |
KR20200010721A (en) | Environmentally friendly water-based refractory paint composition having improved water resistance | |
CN215211650U (en) | Novel energy-saving building fireproof board | |
JPH01156378A (en) | Intumescent fireproof coating composition | |
JP2003342517A (en) | Nonflammable coating for building and building material |