JPH0730595B2 - Composite flexible sheet fireproof coating and fireproof coating method - Google Patents
Composite flexible sheet fireproof coating and fireproof coating methodInfo
- Publication number
- JPH0730595B2 JPH0730595B2 JP63144399A JP14439988A JPH0730595B2 JP H0730595 B2 JPH0730595 B2 JP H0730595B2 JP 63144399 A JP63144399 A JP 63144399A JP 14439988 A JP14439988 A JP 14439988A JP H0730595 B2 JPH0730595 B2 JP H0730595B2
- Authority
- JP
- Japan
- Prior art keywords
- fire
- fireproof coating
- resistant
- coating material
- adhesive
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000000576 coating method Methods 0.000 title claims description 56
- 239000011248 coating agent Substances 0.000 title claims description 51
- 239000002131 composite material Substances 0.000 title claims description 8
- 239000000463 material Substances 0.000 claims description 68
- 239000000853 adhesive Substances 0.000 claims description 43
- 230000001070 adhesive effect Effects 0.000 claims description 43
- 230000009970 fire resistant effect Effects 0.000 claims description 35
- 229910052751 metal Inorganic materials 0.000 claims description 27
- 239000002184 metal Substances 0.000 claims description 27
- 229910000831 Steel Inorganic materials 0.000 claims description 26
- 239000010959 steel Substances 0.000 claims description 26
- 239000011888 foil Substances 0.000 claims description 24
- 239000011810 insulating material Substances 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 238000010276 construction Methods 0.000 claims description 8
- 238000009413 insulation Methods 0.000 claims description 8
- 150000002484 inorganic compounds Chemical class 0.000 claims description 7
- 229910010272 inorganic material Inorganic materials 0.000 claims description 7
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 3
- 239000004327 boric acid Substances 0.000 claims description 3
- -1 nitrous acid compound Chemical class 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000002557 mineral fiber Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 3
- 239000011707 mineral Substances 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 2
- 239000000843 powder Substances 0.000 claims 1
- 229910001220 stainless steel Inorganic materials 0.000 description 17
- 239000010935 stainless steel Substances 0.000 description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 239000000377 silicon dioxide Substances 0.000 description 8
- 239000000945 filler Substances 0.000 description 7
- 229910052742 iron Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 239000004567 concrete Substances 0.000 description 5
- 239000005909 Kieselgur Substances 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000011490 mineral wool Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 238000004455 differential thermal analysis Methods 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 235000019353 potassium silicate Nutrition 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 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 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 238000004886 process control Methods 0.000 description 2
- 238000003908 quality control method Methods 0.000 description 2
- 230000008439 repair process Effects 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
- HFGHRUCCKVYFKL-UHFFFAOYSA-N 4-ethoxy-2-piperazin-1-yl-7-pyridin-4-yl-5h-pyrimido[5,4-b]indole Chemical compound C1=C2NC=3C(OCC)=NC(N4CCNCC4)=NC=3C2=CC=C1C1=CC=NC=C1 HFGHRUCCKVYFKL-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229910000746 Structural steel Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910000963 austenitic stainless steel Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000002659 electrodeposit Substances 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 239000013072 incoming material Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 238000009417 prefabrication Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910021487 silica fume Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Building Environments (AREA)
- Laminated Bodies (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 高層建築物の構造鉄骨である柱、梁は、JIS A 1304に定
められた防火防災用の耐火被覆する事が義務づけられて
いる。実用的には、岩綿吹付法は安価で簡易に施工でき
るので重用されているが、現場の汚染防止や規定厚みの
品質管理に問題がある事、更には空気酸化の劣化を生
じ、特に吹抜け部位に長期耐久性確保が困難視されてい
る事は周知の事実である。又、超高層建築の工程管理
上、耐火被覆した鉄骨をプリファブ化すれば、工程短縮
と品質管理に多大のメリットを生ずるものと考えられ
る。更に鉄骨被覆が現れている駐車場は、劣化が早く、
美観上有機塗装するほかなかった。耐火被覆材をシート
化すれば、以上の問題点を解決して、長期耐久材とな
り、美観があり、プリファブ化でき、利用分野は大き
い。DETAILED DESCRIPTION OF THE INVENTION (Industrial field of application) The columns and beams that are structural steel frames of high-rise buildings are obliged to have a fireproof coating for fire prevention and disaster prevention specified in JIS A 1304. In practice, the rock wool spraying method is used heavily because it is cheap and easy to construct, but there are problems in preventing pollution at the site and quality control of the specified thickness, and further deterioration of air oxidation causes It is a well-known fact that it is difficult to secure long-term durability of a part. In addition, in terms of process control of super high-rise buildings, prefabricating the fire-resistant coated steel frame is thought to bring about great advantages in process shortening and quality control. Furthermore, the parking lot where the steel frame coating appears appears to deteriorate quickly,
There was no choice but to paint organically. If the fire-resistant coating material is made into a sheet, the above problems can be solved, and it becomes a long-term durable material, has an aesthetic appearance, can be prefabricated, and has a wide range of applications.
(従来の技術) 論理的に、耐火被覆をプリファブ化すれば工程管理が容
易となる事は、相当以前から検討されてきたが、最大の
難点は、運搬時の破損と補修法にあり実現できなかっ
た。即ち運搬耐久強度のある材料がなかった為である。(Prior art) Logically, it has been considered for a long time that process control can be facilitated by prefabricating the refractory coating, but the biggest difficulty is the damage during transportation and the repair method, which can be realized. There wasn't. That is, there was no material having a durable strength for transportation.
従来の岩綿吹付法のバインダーはセメントであるが、耐
火断熱性を生ずる軽量化や、鉄骨付着力のある様に軽量
化が必要で、空気量が多くなっている。従って空気流入
による炭酸化を促進するのは理の当然といって良い。仮
に経年補修を考えても事実上できない部位がある。岩綿
吹付法が安価である理由で重用されているが、その施工
費と受注者が供与する足場費や養生費を加えれば、必要
な費用はその積算価格となり必ずしも安価とはいえな
い。又、経年劣化を生じ、特に吹抜け部位は劣化が促進
され、環境衛生上公害を生ずるおそれがある。何より
も、災害時に劣化していて対応できない事があれば由々
しい事である。The binder used in the conventional rock wool spraying method is cement, but it is necessary to reduce the weight to produce fire insulation and to reduce the weight so that the steel frame has adhesiveness, and the amount of air is large. Therefore, it is logical to promote carbonation by air inflow. Even if we consider aging repair, there are some parts that are virtually impossible. Although the rock wool spraying method is often used because it is cheap, if the construction cost and the scaffolding and curing costs provided by the contractor are added, the necessary cost is not the same as the integrated price. In addition, deterioration over time may occur, and particularly in the blow-through portion, the deterioration is promoted, which may cause environmental pollution. Above all, if there is something that can not be dealt with due to deterioration at the time of a disaster, it is a terrible thing.
(発明が解決しようとする課題) 先づ、耐火被覆のプリファブ化解決の方法として、剛性
材料は衝撃により破損しやすいので、復元性の高いクッ
ション性のある材料がよい。軽量断熱材は、強度が弱い
ので補強しなければならないが、耐衝撃一耐摩耗性を増
強するには金属がよく、金属は軽量フレキシブルな耐蝕
性の良いステンレス金属箔が良い。然しながら、之を複
合化する接着材は、3時間の耐火性を有する必要がある
ので、この観点から有機接着材は使用できない。例えば
水ガラス系でも、800℃以下ならば薄膜状でクラックを
生じない耐火接着材をする事ができるが、常態でフレキ
シブルとするには難があり1000℃以上ではクラックなく
保持する事が難しい。水ガラスに、水酸化アルミニウム
や水酸化マグネシウムの様に、耐火時に多量の結晶水を
放出するフィラーを混入する方法もあるが、フレキシブ
ルにはならない問題点がある。(Problems to be Solved by the Invention) First, as a method of solving the prefabrication of the fireproof coating, a rigid material is easily damaged by an impact, and therefore a material having a high restoring property and a cushioning property is preferable. Since the light weight heat insulating material has low strength, it must be reinforced, but a metal is preferable to enhance impact resistance and abrasion resistance, and a light weight flexible stainless metal foil having good corrosion resistance is preferable. However, since the adhesive compounded with each other needs to have fire resistance for 3 hours, the organic adhesive cannot be used from this viewpoint. For example, even with water glass, it is possible to make a fireproof adhesive that is thin and does not cause cracks at 800 ° C or lower, but it is difficult to make it flexible in the normal state and it is difficult to hold it without cracks at 1000 ° C or higher. There is also a method of mixing a filler such as aluminum hydroxide or magnesium hydroxide, which releases a large amount of water of crystallization at the time of fire resistance, but there is a problem that it does not become flexible.
本発明は、先に本発明者が提案した、水性造膜性無機化
合物を接着材とする事により、金属との、特に防蝕性あ
るステンレスとの接着が良く、非晶質フィラーを混入し
て肉盛り性と保存性を改善し、可撓性を与えて、前記諸
問題点を解決する事ができた。The present invention, previously proposed by the present inventor, by using an aqueous film-forming inorganic compound as an adhesive material, good adhesion to metal, particularly corrosion-resistant stainless steel, mixed with an amorphous filler. It was possible to solve the above problems by improving the build-up property and the storability and imparting flexibility.
(課題を解決するための手段) 本発明に使用する金属とアルカリ金属の濃厚溶液反応
に、水和して解離した弗酸か硼酸を添加して、PH7〜9
か、PH11〜12.6の水溶性造膜性無機化合物を得た。その
化学組成は、 [AaBb]rCcDd または[Aa、BbCcDd]sCpDq 但A…Al、Si B…FH,H,BH3,B2O3 C…Na,K,Li D…H2O,OH a,b,c,d,p,q,r,s…各モル数 と推定される,水性造膜性無機化合物である。(Means for Solving the Problems) PH7 to PH9 are obtained by adding hydrated and dissociated hydrofluoric acid or boric acid to a concentrated solution reaction of a metal and an alkali metal used in the present invention.
Or, a water-soluble film-forming inorganic compound having a pH of 11 to 12.6 was obtained. Its chemical composition is [AaBb] rCcDd or [Aa, BbCcDd] sCpDq where A ... Al, Si B ... FH, H, BH 3 , B 2 O 3 C ... Na, K, Li D ... H 2 O, OH a , b, c, d, p, q, r, s ... It is an aqueous film-forming inorganic compound estimated to have a number of moles.
その一品種である, A…Si(金属シリコン),B…FH,C…Na,D…OH又はH2Oの
略称P−Si−F−Nの43%固形分液の示差熱分析を第一
図に示す。Differential thermal analysis of 43% solids of A ... Si (metal silicon), B ... FH, C ... Na, D ... OH or H 2 O, which is one of the varieties, is abbreviated as P-Si-F-N. Shown in the figure.
170℃〜80℃に余剰水脱水があり、470℃,580℃,650℃近
辺に結晶水脱水があるが、250℃移行800℃以上に至る
迄、重量の変化が少く、クラックの生じ難い事を示して
いる。前記物品に、一例としてフィラーにカオリン15
部、非晶質ポゾラン35部、硅藻土5部、計55部を加える
と、400cpsが1400cpsとなり粘度を生じた。本発明の配
合は前記例に限定されない。前記接着材を、30μステン
レス箔に塗り、又アルミナシリカブランケット(イソラ
イト製8p)12.5m/mに塗り、更に前記ステンレスとブラ
ンケットを同様の接着材で接着して得た、10cm×10cmの
供試体を電気炉に入れ、1200℃で3時間保持したが、何
れも剥離又はクラックを生じなかった。前記本発明の接
着材と同様に3号水ガラスに同種フィラーを加えて、同
様の試験したが、一部にクラックと剥離を生じた。また
無機繊維状断熱材の中で、1000℃以上の耐熱性があるの
はアルミナ・アルミナシリカ系である。然しながら、第
二図の「温度と熱伝導率」(建築材料ハンドブック 岸
谷幸一編 P.461)によれば、軽量断熱材は高温領域に
おける熱伝導率を上昇し断熱性を低下する傾向のある事
を示す。又、「含水率と熱伝導率」(前記と同じP.46
0)において、水分の存在は軽量断熱材の熱伝導の増
加、即ち断熱性の低下をもたらすとしている。前記示差
熱分析に示した様に、本発明の耐火接着材は、結晶水脱
水の二ピークがあるが(第1図)、本発明の複合化した
耐火接着材は、中高温域において、上記ブランケット単
独の断熱性より表1の様に、すぐれた結果を示してい
る。There is excess water dehydration at 170 ℃ ~ 80 ℃, and crystal water dehydration near 470 ℃, 580 ℃, 650 ℃, but there is little change in weight until 250 ℃ transition to 800 ℃ or more, and it is difficult for cracks to occur. Is shown. Kaolin 15 as a filler, for example, in the article
Parts, 35 parts of amorphous pozzolan, 5 parts of diatomaceous earth, totaling 55 parts, the viscosity became 400 cps to 1400 cps. The formulation of the present invention is not limited to the above examples. A sample of 10 cm x 10 cm obtained by applying the adhesive material to a 30 μ stainless steel foil, applying it to an alumina silica blanket (Isolite 8p) 12.5 m / m, and further adhering the stainless steel and blanket with the same adhesive material. Was placed in an electric furnace and kept at 1200 ° C. for 3 hours, but neither peeled nor cracked. Similar to the adhesive material of the present invention, the same kind of filler was added to No. 3 water glass and the same test was conducted, but cracks and peeling were partially generated. Among the inorganic fibrous heat insulating materials, it is the alumina / alumina-silica type that has a heat resistance of 1000 ° C or higher. However, according to "Temperature and Thermal Conductivity" in Fig. 2 (Building Materials Handbook, Koichi Kishitani, P.461), lightweight insulation materials tend to increase their thermal conductivity in the high temperature region and decrease their thermal insulation. Indicates. Also, "moisture content and thermal conductivity" (see the same P.46 as above)
In 0), the presence of water causes an increase in heat conduction of the lightweight heat insulating material, that is, a decrease in heat insulating property. As shown in the differential thermal analysis, the fire-resistant adhesive material of the present invention has two peaks of dehydration of water of crystallization (FIG. 1). As shown in Table 1, the heat insulation of the blanket alone shows excellent results.
更に本発明の特質を説明する。複合した本発明の耐火被
覆材の25m/m(8P)は、これを構成するブランケット45
〜50m/mに相当するすぐれた性能を示す。断熱性能は、
固体熱伝導、対流熱伝導、輻射熱伝導の複合により定ま
るが、本発明の耐火被覆材が、中高温における断熱性能
が良いのは、表面材の金属箔と、接着材塗膜性能に基づ
いている。表面の金属箔が加熱フレームにより破壊され
れば、ブランケット単独性能に近いが、金属箔の耐熱性
能が保持されていると、輻射熱反射効果を生じて、対流
熱伝導が制御されている。以下の実施例によりことを立
証する事ができる。 Further features of the present invention will be described. 25 m / m (8P) of the composite fireproof coating material of the present invention is composed of the blanket 45
It shows excellent performance equivalent to ~ 50m / m. Insulation performance is
Solid heat conduction, convection heat conduction, radiant heat conduction is determined by a composite, but the fireproof coating material of the present invention has good heat insulation performance at medium and high temperatures based on the metal foil of the surface material and the adhesive coating performance. . If the metal foil on the surface is destroyed by the heating frame, it is close to the performance of the blanket alone, but if the heat resistance of the metal foil is maintained, the radiation heat reflection effect is generated and convection heat conduction is controlled. This can be proved by the following examples.
本発明の耐火被覆材は、可撓性シートであるから、つき
つけたジョイントの処理が必要である。本発明は、耐熱
1000℃以上を有する0.5m/m〜5m/mのアルミナシリカペー
パーと50μステンレスとを、本発明の接着材で複合し、
可撓性薄膜シート(テープ)を作成した。前記ジョイン
ト目地を隠蔽するに足る広巾の、前記耐火被覆テープ
を、ジョイント目地部に本発明の接着材ではりつけ、耐
火被覆材を一体化する事により前記問題点を解決した。Since the fireproof coating material of the present invention is a flexible sheet, it is necessary to treat the attached joint. The present invention is heat resistant
0.5 m / m-5 m / m alumina silica paper having a temperature of 1000 ° C. or higher and 50 μ stainless steel are compounded by the adhesive of the present invention,
A flexible thin film sheet (tape) was prepared. The above-mentioned problems were solved by gluing the fireproof coating tape having a wide width enough to conceal the joint joint to the joint joint portion with the adhesive of the present invention and integrating the fireproof coating material.
本発明の耐火被覆材は複合化しても30m/m厚で、6kg/m2
(<D=0.2、但しDは比重)以内である。本発明の耐
火接着材は、接着時の粘着力(剪断剥離強度)は28g/cm
2であるが、テープで仮止めしておくと、ブランケット
に吸水されて1時間後の粘着力は3.2kg/cm2以上とな
り、団子状(4cm×4cm)の点接着を数点つければ、安全
な接着強度を示し、接着4週間後には30kg/cm2に増強す
る。20cm2の接着点が4点あれば接着強度を生ずる。然
し乍ら、更に長期の安全性を求めるには、ノリ釘併用の
方法と同様に、スダッドを電着して固着化した方がよ
い。このスタッドには公知の各種の方法があるが、本発
明品は薄いので、前記の様にテープで仮止めして、表面
から鉄骨まで貫通して電着するTピン方法が作業性上有
利である。予めスタッドをたて、串差しする方法もあ
り、スタッドの形状、長さ、固着の方法はどれを採用し
てもよい。従って接着、スタッドの各々の単独工法でも
可能であるが、安全上併用が望ましい。The fire-resistant coating material of the present invention has a thickness of 30 m / m even when compounded, and has a pressure of 6 kg / m 2
(<D = 0.2, where D is the specific gravity). The fire-resistant adhesive material of the present invention has an adhesive force (shear peel strength) of 28 g / cm at the time of adhesion.
It is 2 , but when temporarily fixed with tape, the blanket absorbs water and the adhesive strength after 1 hour becomes 3.2 kg / cm 2 or more, and if you attach several points of dumpling (4 cm × 4 cm), It shows a safe adhesive strength and increases to 30 kg / cm 2 after 4 weeks of adhesion. Adhesive strength occurs when there are four 20 cm 2 adhesive points. However, in order to seek further long-term safety, it is better to electrodeposit the sudad and fix it, as in the case of using a glue joint. There are various known methods for this stud, but since the product of the present invention is thin, the T-pin method of temporarily fixing with tape and penetrating from the surface to the steel frame for electrodeposition as described above is advantageous in terms of workability. is there. There is also a method of setting up the stud in advance and inserting the stud, and any shape, length, and fixing method of the stud may be adopted. Therefore, the bonding and the stud can be used individually, but it is preferable to use them together for safety.
本発明の使用材料について述べる。金属箔は如何なる金
属をも使用できるが、耐蝕性能上ステンレス箔がよく、
その耐火性能上ら、フェエライト系よりもステアライト
系がよく、可撓性があり耐火性能を保持するには20〜10
0μが適当である。無機繊維状断熱材は、実用的にはウ
ールまたはフェルト・ブランケットがよく、ジョイント
被覆材は、ペーパー品が良く、アルミナ、アルミナシリ
カ、ボロン、窒化硅素製品の様に、耐熱1000℃〜1200℃
の性能のある製品が望ましい。前記無機繊維状断熱材の
厚さは経済的には耐火時間により10〜40m/mの中の選択
になるが、ニードルパンチしたアルミナシリカブランケ
ットまたはフェルトが適当である。接着材は、表2の本
発明の水性造膜性無機化合物中四種、又はその中間製品
の何れでもよく、フィラーの配合は、前記の初期粘着力
を生じ、クラック、剥離なく硬化し、耐火性を生ずる必
要があり、前記水性造膜性無機化合物の10%〜100%を
配合した製品が望ましい。次に本発明の実施例を説明す
る。Materials used in the present invention will be described. As the metal foil, any metal can be used, but stainless steel foil is preferable for corrosion resistance,
In terms of its fire resistance, stearite is better than ferrite, and it has flexibility of 20 to 10 to maintain fire resistance.
0μ is suitable. Inorganic fibrous insulation is practically wool or felt blanket, and joint coating is good for paper products, such as alumina, alumina-silica, boron, silicon nitride products, heat resistance 1000 ℃ ~ 1200 ℃
A product with the performance of is desirable. The thickness of the inorganic fibrous heat insulating material is economically selected from 10 to 40 m / m depending on the fire resistance time, but a needle punched alumina-silica blanket or felt is suitable. The adhesive may be any of the four types of the water-based film-forming inorganic compound of the present invention in Table 2 or an intermediate product thereof, and the compounding of the filler causes the above-mentioned initial adhesive force, cures without cracks and peeling, and has fire resistance. It is necessary to produce properties, and a product containing 10% to 100% of the aqueous film-forming inorganic compound is desirable. Next, examples of the present invention will be described.
本発明の接着剤に用いる鉱物繊維としては、マグネシア
とシリカの混合物よりなる繊維があり層上化合物として
は珪藻土・雲母を主材とした材料がある。The mineral fiber used in the adhesive of the present invention is a fiber composed of a mixture of magnesia and silica, and the layer compound is a material containing diatomaceous earth / mica as a main material.
(実施例−1) 表2中にカリオン20部、ポゾラン30部、珪藻土3部、
グリセリン1部を加えて耐火接着材にし、竹内金属箔
(株)のステンレス50μと厚さ10m/m無機繊維断熱材の
各種材料を張り合わせ、1000℃2時間(電気炉)の耐火
試験をした結果、ガラスウール、一次焼成カーボンウー
ル、ロックウールは何れも烈火し、アルミナシリカフェ
ルト、ブランケット、ペーパーは残存した。 (Example-1) In Table 2, 20 parts of carion, 30 parts of pozzolan, 3 parts of diatomaceous earth,
1 part glycerin was added to make a fire-resistant adhesive, and various materials such as stainless steel 50μ of Takeuchi Metal Foil Co., Ltd. and thickness 10m / m inorganic fiber heat insulating material were pasted together, and fireproof test at 1000 ° C for 2 hours (electric furnace) was performed. , Glass wool, primary fired carbon wool, and rock wool all ignited, and alumina silica felt, blanket, and paper remained.
ペーパーはパルプ混入物は何れも劣化した。即ち当然の
事ながら1000℃以上の耐熱材料を複合化組成材としなけ
ればならない。前実施例において、本発明の耐火接着材
に、剥離やクラックを生じなかった。然しながら表2の
各製品の固形分に対し、各フィラーの合計が150%以上
になると可撓性を失つた。All papers were degraded by pulp inclusions. That is, as a matter of course, a heat-resistant material having a temperature of 1000 ° C. or higher must be used as the composite composition material. In the previous example, the fire-resistant adhesive material of the present invention did not cause peeling or cracking. However, when the total amount of each filler was 150% or more based on the solid content of each product in Table 2, flexibility was lost.
比較例として水ガラス(3号)に水酸化アルミニウム、
水酸化マグネシウム、カオリン、シリカヒューム、ポゾ
ラン、パイロフィライト、珪藻土其他各種入れて30μス
テンレス箔に塗り、可撓性を調べたが硬化するとグリセ
リンを配合しても可撓性を生じなかった。1150℃で3時
間加熱し、この温度で、一部接着してもクラックなく接
着したものはなかった。またフィラー混入の割合は5%
から100%に及んだ。As a comparative example, aluminum hydroxide on water glass (No. 3),
Magnesium hydroxide, kaolin, silica fume, pozzolan, pyrophyllite, diatomaceous earth and various other materials were added and coated on a 30μ stainless steel foil, and the flexibility was examined. It was heated at 1150 ° C. for 3 hours, and at this temperature, no part was adhered without cracks even if partly adhered. Also, the proportion of filler mixed is 5%
From 100%.
(実施例−2) 8P25m/m厚のアルミナシリカブランケットをフェライト
系ステンレス(A)とオーステナイト系ステンレス
(B)の厚さ50μ箔に、実施例−1の本発明の耐火接着
材を250g/m2の割合に塗り接着して複合化した(300m/m
×300m/m)。旧JIS A 1302の方法に従い厚さ3.2m/mの鉄
板にはり3時間加熱した。(A)は、2時間経過時には
表面劣化し破損が見受けられ、裏面温度は450℃以上に
なったので止めた。(B)は3時間経過しても裏面鉄板
温度は320℃で取出した表面の金属箔は何の破損もな
く、表面の金属箔と耐火接着材の耐火度が性能を支配し
ていた。前記ブランケットを40m/mとすると裏面温度は2
00℃であった。(Example-2) An alumina-silica blanket having a thickness of 8P25m / m was applied to a ferrite-based stainless steel (A) and an austenitic stainless steel (B) with a thickness of 50 µF, and the fire-resistant adhesive material of the present invention of Example-1 to 250g / m. It was coated and adhered at a ratio of 2 to form a composite (300 m / m
× 300m / m). According to the old JIS A 1302 method, it was placed on a 3.2 m / m thick iron plate and heated for 3 hours. In (A), the surface deteriorated and damage was observed after 2 hours, and the back surface temperature became 450 ° C. or higher, so the test was stopped. In (B), the surface metal foil taken out at 320 ° C. on the back side had no damage even after 3 hours had passed, and the fire resistance of the surface metal foil and the fire-resistant adhesive material controlled the performance. If the blanket is 40 m / m, the backside temperature is 2
It was 00 ° C.
(実施例−3) 前記実施例(B)を二分し、これを10m/m厚鉄板に、前
記実施例−1の接着剤で点接着し、二分したつきつけ面
に、ブランケットを2.5m/m厚ペーパーに替えて本発明の
耐火被覆様テープをつくり、この5cm巾を、同一接着材
で接着し、鉄板を全面被覆した。これを前記実施例−1
と同様の方法で、耐火3時間試験した。裏面温度、鉄板
は310℃で、表面ステンレスの破損はなく、点接着材も
金属箔との接着材も、剥離、クラックは皆無であった。
第3図は炉内各部における標準加熱曲線、第4図は裏面
鉄板温度を示す。(Example-3) The above-mentioned Example (B) was divided into two, and this was spot-bonded to a 10 m / m thick iron plate with the adhesive of the above-mentioned Example-1, and a blanket was 2.5 m / m on the divided attachment surface. The fireproof coating-like tape of the present invention was prepared in place of thick paper, and this 5 cm width was adhered with the same adhesive to cover the entire iron plate. This is the same as in Example-1.
Fire resistance was tested for 3 hours in the same manner as in. The back surface temperature was 310 ° C. for the iron plate, the surface stainless steel was not damaged, and neither the point adhesive material nor the adhesive material with the metal foil was peeled or cracked.
FIG. 3 shows the standard heating curve in each part of the furnace, and FIG. 4 shows the backside iron plate temperature.
(実施例−4) 日本ドライブイット(株)のスタッドウエルダーで、T
ピンを前実施例−1の本発明の耐火被覆材の表面からさ
し電着した。この場合に電着するが、本発明の耐火被覆
材は30m/m厚以下と薄く、施工容易で、同性能を、ブラ
ンケットで施工すると50〜60m/m厚を必要とし、スタッ
ド工法は、本工法より多くのスタッドを必要とする。表
面を後施工でステンレスを接着施工しようとすると、接
着材も工数も多大となる。(Example-4) With a stud welder of Nippon Drive It Co., Ltd., T
The pins were electrodeposited from the surface of the fire-resistant coating material of the present invention of the previous Example-1. In this case, it is electrodeposited, but the fire-resistant coating material of the present invention is thin with a thickness of 30 m / m or less, is easy to install, and has the same performance, and when it is installed with a blanket, it requires a thickness of 50 to 60 m / m. It requires more studs than the construction method. If the surface is post-installed to adhere stainless steel, the amount of adhesive material and man-hours will increase.
(実施例−5) 地上におけるH−350×250×9×14に、予め本発明の接
着材を点接着し、本発明の前記25m/m厚耐火被覆材を、
H鋼に巻き、ところどころを粘着テープで仮止めし、T
ピンを差しこみ電着したが極めて容易で、ジョイント部
位に前記2.5m/m厚耐火被覆テープを接着し、更にTピン
を電着した。外観は美麗で、現場の粉塵は一切生じなか
った。(Example-5) The above-mentioned 25 m / m thick fireproof coating material of the present invention was prepared by spot-adhering the adhesive material of the present invention to H-350 x 250 x 9 x 14 on the ground in advance.
Wrap around H steel and temporarily fix some parts with adhesive tape.
Although the pins were inserted and electrodeposited, it was extremely easy. The 2.5 m / m thick fireproof coating tape was adhered to the joint portion, and T pins were electrodeposited. The appearance was beautiful and no dust was generated on site.
(実施例−6) 布団巻き工法において、前実施例−5のH鋼に下地とし
てステンレス帯鋼を回して締結し、又メッシュを熔接
し、スタッドを電着したがメッシュの細線以外は容易に
施工できた。(Embodiment 6) In the futon winding method, stainless steel strip was ground and fastened to the H steel of the previous Embodiment 5 as the base, and the mesh was welded and the studs were electrodeposited. It was able to be constructed.
又、前記2.5m/m厚の本発明の耐火被覆材テープを巻きつ
けて下地にしたが、容易に電着できた。Further, although the fire-resistant coating material tape of the present invention having a thickness of 2.5 m / m was wound as a base, it could be easily electrodeposited.
何れの下地も、本発明の耐火接着材を塗り、前記25m/m
厚の本発明の耐火被覆材を接着したが容易に粘着した。Both bases, coated with a fire-resistant adhesive of the present invention, the 25m / m
A thick refractory coating of the present invention was adhered, but easily adhered.
(実施例−7) 第5図乃至第8図は施工要領を示した。(Example-7) FIG. 5 to FIG. 8 show the construction procedure.
第6図は耐火被覆材1が鉄骨2に無機質系耐火接着剤3
を介して接着された拡大断面図である。前記耐火接着材
1の固定には、スタッドピン5を併用する。また接着部
分の初期剥れ防止を兼ねて、梁鉄骨下端にも止付ける。
第7図は同じくスラブコンクリートに取合う部分の梁の
鉄骨上端の拡大断面図である。即ち耐火被覆材1の固定
は金属箔(ステンレス厚さ50μ)部分を金属板(厚さ1m
/m)の当板6をスポット溶接により止付ける。4はスラ
ブコンクリートを示す。FIG. 6 shows that the fireproof coating material 1 is the steel frame 2 and the inorganic fireproof adhesive 3
It is an expanded sectional view bonded via. A stud pin 5 is also used to fix the fire-resistant adhesive material 1. Also, to prevent the initial peeling of the bonded part, it is also fixed to the lower end of the beam steel frame.
FIG. 7 is an enlarged cross-sectional view of the upper end of the steel frame of the beam in the portion that also fits the slab concrete. That is, the metal foil (stainless steel thickness 50 μ) is fixed to the metal plate (thickness 1 m
/ m) of the contact plate 6 is fixed by spot welding. 4 shows slab concrete.
第8図は耐火被覆材1の構成を示す。FIG. 8 shows the structure of the fireproof coating material 1.
図中7はセラミック繊維系断熱材、3は無機耐火接着
剤、8は厚さ50μのステンレス箔である。In the figure, 7 is a ceramic fiber type heat insulating material, 3 is an inorganic fire resistant adhesive, and 8 is a stainless steel foil having a thickness of 50 μm.
(発明の効果) 前記のように、耐火被覆材として金属箔と無機繊維状断
熱材を耐火接着材で貼合わせた可撓性のあるシート状耐
火被覆材を用い、前記の被覆工法によれば、下記の効果
が得られる。(Effect of the invention) As described above, a flexible sheet-like fireproof coating material obtained by laminating a metal foil and an inorganic fibrous heat insulating material with a fireproof adhesive material is used as the fireproof coating material, and according to the above coating method, The following effects can be obtained.
前記無機繊維状断熱材と金属箔として厚さ50μのス
テンレス箔を無機耐火接着剤で張合わせた耐火被覆材は
鉄骨の耐火被覆材として、従来のものに比べすぐれた多
機能を具備している。The inorganic fibrous heat insulating material and a metal foil, which is a stainless steel foil having a thickness of 50 μ, are laminated with an inorganic fire resistant adhesive.The fire resistant coating material has a multi-functionality superior to conventional ones as a fire resistant coating material for steel frames. .
前記耐火被覆材は、特殊な切断工具を必要とせず、
ナイフ、鋏なでの簡単な切断工具で切断できる。The refractory coating does not require a special cutting tool,
Can be cut with a simple cutting tool such as a knife or scissors.
前記耐火被覆材は、切断や取付け時に粉塵の発生が
ない為、作業者の健康を害するおそれが全くなく、作業
環境も良好である。Since the above-mentioned fireproof coating material does not generate dust at the time of cutting and mounting, there is no possibility of damaging the health of the worker and the working environment is good.
前記耐火被覆材は、柔軟性と可撓性を持っており、
自由に曲げられる。The fireproof coating material has flexibility and flexibility,
Can be bent freely.
その為、鉄骨のいかなる部分(平部、端部、角部、曲面
部、配管廻等)にも隙間なく一体に止付けることが出来
る。Therefore, it can be integrally fixed to any portion of the steel frame (flat portion, end portion, corner portion, curved surface portion, pipe periphery, etc.) without a gap.
更に、表層の金属箔を利用して、角を出して曲げて止付
けることが出来る。Further, the surface metal foil can be used to bend and fix the corners.
前記耐火被覆材は、表層のステンレス面を利用し
て、耐火被覆を兼ねた仕上材としても有効で化粧施工を
省くことも可能である。The fire-resistant coating material is effective as a finishing material that also serves as a fire-resistant coating by utilizing the surface stainless steel surface, and it is possible to omit makeup work.
又、表層のステンレス箔の為、被覆後の粉塵等の発生も
全くなく、クリーンである。Further, since it is the stainless steel foil on the surface layer, it is clean without any dust and the like after coating.
前記耐火被覆材は、優れた性能から、従来のものに
比べて耐火被覆厚さを半分近くに薄くすることが出来
る。その為、構造上の荷重負担も少なくない。Due to its excellent performance, the refractory coating material can be reduced in thickness to nearly half as compared with the conventional one. Therefore, the structural load is not small.
前記耐火被覆材の使用により、切断取付けが容易
で、かつ被覆厚さが薄く軽量である為、耐火被覆施工の
作業性を今までのシート状耐火被覆材の場合に比べ大巾
に改善向上させることができる。By using the above-mentioned fire-resistant coating material, it is easy to cut and install, and since the coating thickness is thin and lightweight, the workability of the fire-resistant coating construction can be greatly improved and improved compared to the case of the sheet-like fire-resistant coating material up to now. be able to.
又、工場裁断により、搬入材の損失を少なくし、発生残
材を少なくすることが出来る。Further, by cutting the factory, it is possible to reduce the loss of the incoming material and the residual material generated.
前記耐火被覆材は、工場での生産が可能である為、
その品質及び厚さを一定に管理して安定化することが出
来る。Since the fireproof coating material can be produced in the factory,
The quality and thickness can be controlled to be constant and stabilized.
前記耐火被覆材の施工は、鉄骨建方前に限らず、鉄
骨の生産工場においても施工が可能であり、又、鉄骨建
方後においても施工が可能である。The construction of the fire-resistant coating material is not limited to before the steel frame is erected, but can be performed at a steel frame production plant, and also after the steel frame is erected.
又、鉄骨の梁への施工に限定されず、柱への適用も可能
である。Further, it is not limited to the construction of steel frame beams, but can be applied to columns.
又、鉄骨の梁、柱は前記H鋼に限定されず、鋼管やボッ
クス鉄骨、その他の鉄骨にも適用可能である。Further, the beams and columns of the steel frame are not limited to the above H steel, and can be applied to steel pipes, box steel frames, and other steel frames.
火災時に表層の金属箔が耐火被覆材と高温の周辺雰
囲気との遮断効果を持つ為、従来の耐火被覆材に比較し
て高温時優れた性能を示す。その為、耐火被覆材の所要
厚さを従来のものに比べて薄くすることが出来る。In the event of a fire, the surface metal foil has a shielding effect between the fire-resistant coating material and the high-temperature surrounding atmosphere, so it exhibits superior performance at high temperatures compared to conventional fire-resistant coating materials. Therefore, the required thickness of the fireproof coating material can be made thinner than that of the conventional one.
この結果被覆施工時の作業性が大巾に良くなる。As a result, the workability during coating is greatly improved.
表層に被覆した金属箔(ステンレス厚さ50μ)が貼
付時及び火災時の高温時においても、断熱材を支えるに
十分な強度を保持している為、鉄骨への耐火被覆材の止
付けを少ない点で固定する事が出来る。The metal foil (stainless steel thickness: 50μ) coated on the surface layer retains sufficient strength to support the heat insulating material even when applied and at high temperatures in the event of a fire, so there is less attachment of the fire resistant coating material to the steel frame. It can be fixed at points.
止付けとしてスタッド溶接するスタッドピンを数点
固定するだけで、被覆材を止付け固定出来る。The stud can be welded as a fastening. The stud pins can be fixed by simply fixing a few points.
スラブコンクリート等に取合う部分は、金属箔自体を小
片の鉄板を当板としてスポット溶接により固定出来る。In the part that fits slab concrete, etc., the metal foil itself can be fixed by spot welding with a small piece of iron plate as the plate.
この為、止付け作業時の作業性が従来の耐火被覆工法に
比べ、著しく改善向上している。For this reason, the workability at the time of fastening work is significantly improved as compared with the conventional fireproof coating method.
作業が簡単な為、特別な熟練工を必要としない。Since the work is easy, no special skilled worker is required.
本発明により鉄骨にプリファブ化できる耐火被覆材
とその工法が始めて可能となった。INDUSTRIAL APPLICABILITY The present invention enables, for the first time, a fire-resistant coating material that can be prefabricated into a steel frame and a method of manufacturing the same.
第1図は表2中の示差熱分析のグラフ、第2図は普通
の耐火断熱の熱伝導率とかさ比重・温度の関係グラフ、
第3図は加熱時間と炉内温度のグラフ、第4図は加熱時
間と鋼板温度のグラフ、第5図乃至第8図はこの発明の
実施例の施工要領図であって、第5図は一部断面図、第
6図は第5図の鉄骨の縦部の一部断面拡大図、第7図は
スラブコンクリートとの接触部の一部断面拡大図、第8
図は耐火被覆材の一部断面拡大図である。 1…耐火被覆材、2…鉄骨、3…耐火接着材、4…スラ
ブコンクリートFig. 1 is a graph of differential thermal analysis in Table 2, Fig. 2 is a graph of the relationship between thermal conductivity and bulk specific gravity / temperature of ordinary refractory insulation.
FIG. 3 is a graph of heating time and furnace temperature, FIG. 4 is a graph of heating time and steel plate temperature, FIGS. 5 to 8 are construction procedure diagrams of the embodiment of the present invention, and FIG. Partial sectional view, FIG. 6 is an enlarged partial sectional view of the vertical portion of the steel frame in FIG. 5, FIG. 7 is an enlarged partial sectional view of a contact portion with slab concrete, and FIG.
The figure is a partially enlarged cross-sectional view of the fireproof coating material. 1 ... Fireproof coating material, 2 ... Steel frame, 3 ... Fireproof adhesive material, 4 ... Slab concrete
フロントページの続き (56)参考文献 特開 昭62−72846(JP,A) 実開 昭61−40230(JP,U) 実開 昭60−191330(JP,U) 特公 昭63−14146(JP,B2)Continuation of the front page (56) References JP 62-72846 (JP, A) Actual opening 61-40230 (JP, U) Actual opening 60-191330 (JP, U) JP-B 63-14146 (JP) , B2)
Claims (4)
される水性造膜性無機化合物よりなる耐火接着材を介し
て無機繊維状断熱材を層着したことを特徴とする複合化
可撓性シート状耐火被覆材。 (イ)金属と、水に解離して硼酸又は弗酸となる鉱酸化
合物、亜鉱酸化合物とアルカリ金属からなり、 [AaBb]rCcDdまたは[AaBbCcDd]sCpDq 但しA…Al、Si B…FH,H,BH3,B2O3 C…Na,K,Li D…H2O,OH a,b,c,d,p,q,r,s…各モル数1. A composite characterized in that a surface material is a metal foil, and an inorganic fibrous heat insulating material is layered on the metal foil through a fire-resistant adhesive composed of an aqueous film-forming inorganic compound described in (a) below. Flexible sheet-like fireproof coating material. (A) A metal, a mineral acid compound that dissociates into water to form boric acid or hydrofluoric acid, and a nitrous acid compound and an alkali metal. H, BH 3 , B 2 O 3 C ... Na, K, Li D ... H 2 O, OH a, b, c, d, p, q, r, s ... Each number of moles
される水性造膜性無機化合物よりなる耐火接着剤に下記
(ロ)を混合した耐火接着剤を介して無機繊維状断熱材
を層着したことを特徴とする複合化可撓性シート状耐火
被覆材。 (イ)金属と、水に解離して硼酸又は弗酸となる鉱酸化
合物、亜鉱酸化合物とアルカリ金属からなり、 [AaBb]rCcDdまたは[AaBbCcDd]sCpDq 但しA…Al、Si B…FH,H,BH3,B2O3 C…Na,K,L D…H2O,OH a,b,c,d,p,q,r,s…各モル数 (ロ)天然か合成の鉱物粉、鉱物繊維又は層状化合物の
一種以上の配合物。2. An inorganic fibrous heat insulation using a metal foil as a surface material, and a fire-resistant adhesive obtained by mixing the following (b) with a fire-resistant adhesive composed of an aqueous film-forming inorganic compound (a) described below. A composite flexible sheet-like fireproof coating material, which is obtained by layering materials. (A) A metal, a mineral acid compound that dissociates into water to form boric acid or hydrofluoric acid, and a nitrous acid compound and an alkali metal. H, BH 3 , B 2 O 3 C… Na, K, LD… H 2 O, OH a, b, c, d, p, q, r, s… each mole number (b) Natural or synthetic mineral Blends of one or more of powders, mineral fibers or layered compounds.
鉄骨の外壁の全部又は一部に、請求項1又は2に記載し
た耐火接着材を用いて接着固定することを特徴とした耐
火被覆工法。3. The fireproof coating material according to claim 1 or 2,
A fire-resistant coating method characterized in that the fire-resistant adhesive material according to claim 1 or 2 is bonded and fixed to all or part of the outer wall of the steel frame.
材を建築前又は建築後の構造物の外壁の全部又は一部
に、請求項1又は2に記載した耐火接着材を用いて接着
固定することを特徴とした耐火被覆工法。4. The fire-resistant coating material according to claim 1 or 2 is used on all or part of the outer wall of a structure before or after construction using the fire-resistant adhesive material according to claim 1 or 2. Fireproof coating method characterized by adhesive fixing.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63144399A JPH0730595B2 (en) | 1988-06-10 | 1988-06-10 | Composite flexible sheet fireproof coating and fireproof coating method |
| AU36281/89A AU634962B2 (en) | 1988-06-10 | 1989-06-09 | Water-Soluble, film-forming inorganic compounds |
| US07/365,112 US5049316A (en) | 1988-06-10 | 1989-06-12 | Water-soluble, film-forming inorganic compounds, fireproof and fire-resistant composites and fire-resistant, flexible, sheet composite covering materials formed by the use of the compounds, and process for preparing fire-resistant coverings |
| CA000602501A CA1333745C (en) | 1988-06-10 | 1989-06-12 | Water-soluble, film-forming inorganic compounds, fireproof and fire-resistance composites and fire-resistance, flexible, sheet composite covering materials formed by the use of the compounds, and fire-resistance-covering process |
| DE68925756T DE68925756T2 (en) | 1988-06-10 | 1989-06-12 | Water-soluble film-forming inorganic compounds, fire-resistant and fire-resistant composite materials and fire-resistant flexible film composite materials for coatings from these compounds and methods for producing a fire-resistant coating |
| EP89305928A EP0346162B1 (en) | 1988-06-10 | 1989-06-12 | Water-soluble, film-forming inorganic compounds, fireproof and fire-resistance composites and fire-resistance, flexible, sheet composite covering materials formed by the use of the compounds, and fire-resistance-covering process |
| US07/693,480 US5234631A (en) | 1988-06-10 | 1991-04-30 | Fireproof or refractory materials containing fire-resistant, water soluble, film-forming inorganic compounds |
| US08/066,223 US5368950A (en) | 1988-06-10 | 1993-05-25 | Water-soluble, film-forming inorganic compounds, fireproof and fire-resistance composites and fire-resistance, flexible, sheet composite covering materials formed by the use of the compounds, and fire-resistance-covering process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63144399A JPH0730595B2 (en) | 1988-06-10 | 1988-06-10 | Composite flexible sheet fireproof coating and fireproof coating method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0235145A JPH0235145A (en) | 1990-02-05 |
| JPH0730595B2 true JPH0730595B2 (en) | 1995-04-05 |
Family
ID=15361260
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63144399A Expired - Fee Related JPH0730595B2 (en) | 1988-06-10 | 1988-06-10 | Composite flexible sheet fireproof coating and fireproof coating method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0730595B2 (en) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60191330U (en) * | 1984-05-25 | 1985-12-18 | 日本板硝子株式会社 | Insulation mat for flame retardant building materials |
| JPS6140230U (en) * | 1984-08-16 | 1986-03-14 | 日本ゼオン株式会社 | non-combustible insulation |
| JPS6314146A (en) * | 1986-07-04 | 1988-01-21 | Konica Corp | Processing method for silver halide color photographic sensitive material |
| JPS6272846A (en) * | 1986-09-19 | 1987-04-03 | ニチアス株式会社 | How to cover steel frames with fireproofing material |
-
1988
- 1988-06-10 JP JP63144399A patent/JPH0730595B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0235145A (en) | 1990-02-05 |
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