JPS6363516B2 - - Google Patents
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- Publication number
- JPS6363516B2 JPS6363516B2 JP56095632A JP9563281A JPS6363516B2 JP S6363516 B2 JPS6363516 B2 JP S6363516B2 JP 56095632 A JP56095632 A JP 56095632A JP 9563281 A JP9563281 A JP 9563281A JP S6363516 B2 JPS6363516 B2 JP S6363516B2
- Authority
- JP
- Japan
- Prior art keywords
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- weight
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- iii
- Prior art date
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- 239000011490 mineral wool Substances 0.000 claims description 15
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 239000004568 cement Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- 235000021317 phosphate Nutrition 0.000 claims description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 3
- 239000011787 zinc oxide Substances 0.000 claims description 3
- 150000001642 boronic acid derivatives Chemical class 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 210000000988 bone and bone Anatomy 0.000 claims 1
- 239000000463 material Substances 0.000 description 10
- 239000011247 coating layer Substances 0.000 description 8
- 239000000835 fiber Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 238000009413 insulation Methods 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 238000010276 construction Methods 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000009970 fire resistant effect Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000010455 vermiculite Substances 0.000 description 2
- 229910052902 vermiculite Inorganic materials 0.000 description 2
- 235000019354 vermiculite Nutrition 0.000 description 2
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 229910000676 Si alloy Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 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
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- -1 expanded shale Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- CPSYWNLKRDURMG-UHFFFAOYSA-L hydron;manganese(2+);phosphate Chemical compound [Mn+2].OP([O-])([O-])=O CPSYWNLKRDURMG-UHFFFAOYSA-L 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000005304 joining Methods 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
- 229910052745 lead Inorganic materials 0.000 description 1
- ZPPSOOVFTBGHBI-UHFFFAOYSA-N lead(2+);oxido(oxo)borane Chemical compound [Pb+2].[O-]B=O.[O-]B=O ZPPSOOVFTBGHBI-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 229940063002 magnesium palmitate Drugs 0.000 description 1
- ABSWXCXMXIZDSN-UHFFFAOYSA-L magnesium;hexadecanoate Chemical compound [Mg+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O ABSWXCXMXIZDSN-UHFFFAOYSA-L 0.000 description 1
- JESHZQPNPCJVNG-UHFFFAOYSA-L magnesium;sulfite Chemical compound [Mg+2].[O-]S([O-])=O JESHZQPNPCJVNG-UHFFFAOYSA-L 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- NFMWFGXCDDYTEG-UHFFFAOYSA-N trimagnesium;diborate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]B([O-])[O-].[O-]B([O-])[O-] NFMWFGXCDDYTEG-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- HSYFJDYGOJKZCL-UHFFFAOYSA-L zinc;sulfite Chemical compound [Zn+2].[O-]S([O-])=O HSYFJDYGOJKZCL-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
- Ceramic Products (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Paints Or Removers (AREA)
Description
本発明は、耐火被覆性能の優れた作業性の良い
組成物に関する。
鉄骨などの構造材に建築用耐火被覆材として岩
綿繊維を接合材を介して吹付被覆する方法や硅酸
カルシウム板を貼付被覆する方法が広くなされて
いる。しかしながら、前者の場合は基材構造材へ
の密着性が悪く吹付公害が多く発生し、しかも吹
付作業に多くの手間を要しており、又後者の場合
は板材を所定の基材に被覆するに際して基材への
取付作業が煩雑で、しかも形状の複雑な部位への
施工に際しては相当高度な接合技術を要するため
必ずしも完成した板の耐火被覆性能が一様ではな
いという欠点があつた。
本発明者らは、係る鉄骨などの基材を被覆する
に際し、先に無機質繊維と特定の湿性複合接合材
を用いて係る改良を完成したが、続いて先願発明
の無機質繊維の中でも殊に粒状に加工された岩綿
を選択して使用することによつて断熱性、作業性
の一層の向上などを確認し、よつて上記欠点を解
決し、これに成功したものである。即ち、本発明
は、(a) 水可溶性アルカリ硅酸塩、(b)(i) セメン
ト、酸化亜鉛、シリカダスト、(ii) 高級脂肪酸の
二価以上の金属塩、カルボキシル基を有する水溶
性高分子物質の二価以上の金属塩、酸性金属酸化
物、リン酸塩、二価金属の亜硫酸塩、ホウ酸塩、
及び(iii) 金属粉末から選ばれる少くとも1種の上
記(a)成分の硬化性成分、(c) 無機質軽量骨材、(d)
粒状岩綿、並びに(e) 水から成り、且つ配合比
率は、(a)成分の固形分100重量部に対して、(b)成
分の(i)の場合は5〜250重量部、(ii)の場合は5〜
30重量部、(iii)の場合は10〜200重量部及び(i)〜(iii)
の併用の場合は5〜250重量部、(c)成分30〜200重
量部、及び(d)成分20〜300重量部であることを特
徴とする耐火被覆用組成物に係り、これに水を必
須成分として混配合し、下記に詳述する施工方法
に従つて操作することにより、鉄骨、構造木材等
の基材に極めて容易な操作を通じて無機質の耐火
断熱性の高い被覆層が得られるのである。
次に本発明耐火被覆用組成物の各必須成分につ
いて簡単に述べる。本発明において(a)成分として
は、水可溶性のアルカリ硅酸塩を用い、これによ
り初めて所期の組成物を収得できる。この(a)成分
を構成するアルカリ成分としては、例えばLi、
Na、K、Pb等のアルカリ金属及び第4級アンモ
ニウムを例示でき、その1種を単独で又は2種以
上を併用して、粉末の状態でも又水溶液の形態で
も有利に用い得るが、ペースト調整の容易性を考
慮し、施工直前での固形分濃度を10〜60%程度と
するのが好ましい。また、(b)成分とする水可溶性
アルカリ硅酸塩の硬化性成分は、ポルトランドセ
メント、アルミナセメント、石灰、高硫酸塩セメ
ント等のセメント、酸化亜鉛電熱や金法によつて
硅素や硅素合金を製造する際に副生されるシリカ
ダストを第(i)グループとし、ステアリン酸亜鉛、
ステアリン酸カリウム、パルミチン酸マグネシウ
ム等の高級脂肪酸の二価以上の金属塩、アルギン
酸アルミニウム、ポリアクリル酸バリウム等のカ
ルボキシル基を有する水溶性高分子物質の二価以
上の金属塩、Cr2O3、Mn3O4、PbO等の酸性金属
酸化物、リン酸アルミニウム、リン酸カルシウ
ム、リン酸マンガン等のリン酸塩、亜硫酸マグネ
シウム、亜硫酸亜鉛等の二価金属の亜硫酸塩、ホ
ウ酸鉛、ホウ酸マグネシウム等のホウ酸塩を第(ii)
グループとし、更にTi、Zr、V、Al、Si、Ge、
Zn等の金属粉末を第(iii)グループとし、これら(i)
〜(iii)グループの硬化性成分は粉末状として用いる
のが好ましく、これらの1種を単独で又は2種以
上を併用して供し得る。更に、(c)成分とする無機
質軽量骨材としてはヒル石、膨脹頁岩、パーライ
ト、発泡シリカ、シリカバルーンなどを例示でき
る。更に又、(d)成分とする粒状岩綿とは、岩綿繊
維を主に機械的な操作によつて岩綿繊維を単独で
又は他種短繊維や粉体を添加し若しくは極く少量
の結合性物質を介して粒状に加工したもので、係
る粒状加工された岩綿は本発明組成物中に繊維の
形状で分散されないために岩綿単独での耐火性や
断熱性をかなり保持するものと推定され、且つ粒
状を保つために分散が容易で、粒子の大きさは直
径約2〜20mmのものが好ましい。これらの必須成
分の他、ゼオライト、タルク、マイカ、パリゴル
スカイト等の分散安定性充てん材、モルタル用起
泡剤、カオリン、ベントナイト、ホワイトカーボ
ン等の無機質膨潤性物質、並びに耐火性に左程支
障のない程度で水溶性樹脂、有機質粒状発泡体等
を配合できる。
係る本発明耐火断熱用組成物は、概ね次の配合
比率を基準とする。即ち、(a)成分の固形分100重
量部に対して、(b)成分、即ち(a)成分の硬化性成分
が(i)〜(iii)の何れのものにせよ少なすぎると該組成
物の流動性が低下してボタ落ちや硬化未進行の弊
害、耐火被覆層の耐水性低下、密着性不良などが
生じ易く、逆にこれが過剰に配合されると硬化反
応に寄与しない余剰成分が硬化後の系内に残存
し、耐火被覆層の耐火性、耐水性などの機能を低
下する傾向がでる。次に(c)成分は該組成物によつ
て得られる被覆層を比重を小さくし以て常温ない
し高温下での断熱性向上に寄与するが、配合量が
少ないと当然係る機能をなし得ず、又逆に多過ぎ
るとペーストの流動性が悪く、密着性不良、耐火
性低下などを生ずる更に(d)成分は該組成物の機械
的強度、とりわけ被覆層の乾燥時収縮を防止し密
着性向上などに効果を発揮する他、殊に各成分の
複合化された状態での断熱性、耐火性等の向上に
著しく重要な役割を果たしており、これが少ない
時には耐火性、断熱性の低下と共に作業性が良く
なく、一方過剰に配合されると流動性、耐水性の
低下、被覆層の不均一化などが生ずる傾向となり
好ましくなくなる。
このようにして調整される本発明耐火被覆用組
成物は、その実際の配合比率、配合方法、施工方
法等によつて多少異なるが、実質的に被覆施工し
て乾燥した後のかさ比重が0.3〜1.0程度になるよ
うにすることにより、耐火性、断熱性、機械的強
度等が本発明目的に好ましい形態となる。このこ
とは、単にかさ比重のみの問題ではなく、含水
率、密着性能、熱伝導経路などから調度適度の複
合体を形成するからであろうと推定される。
本発明組成物を用いて鉄骨、金属板、木質構造
材などに耐火被覆層を形成するに際し、該組成物
を瞬時にもしくは通常のミキサー混合によつて一
たんペースト状となし、もちろん該組成物は水性
であるため水希釈が可能で、適度の粘性調整を添
加剤で予めしておいたり、施工時に水を加えたり
した後、コテ付け、ヘラ付け、吹付け、注入など
によつて所定の基材に被覆する。
以下実施例及び比較例により本発明を具体的に
述べる。
実施例
第1表の配合物質及び配合量に従つて本発明被
覆用組成物を調整し、これらに水を加えて粘性調
整し迅速にコテを用いて乾燥後の被覆層厚が約20
mmになるようにして3.2mm厚の鉄板上に塗付けた。
(試料No.1〜8)なお、予め岩綿繊維にタルク及
び石こう、CMCを配合し、これをモルタルミキ
サーに入れて撹拌し粒状岩綿を得た。これらの乾
燥後の供試体を用い、以下に述べる試験方法によ
り性能試験を行つたところ、第1表下段に示すよ
うな結果が得られた。
(イ) コテ作業性……コテさばき性及び1回のコテ
塗りで塗付できる厚さ(厚い程良好)により比
較判定。◎>〇>△>×により評価。
(ロ) 吹付作業性……硬化後10mm厚になるように吹
付けた時のボタ落ちの有無により判定。◎>〇
>△>×により評価。
(ハ) 耐水性……96時間水中浸漬後の変色、割れ、
はがれ等の変化をみる。
(ニ) 密着性……JIS A6909 5.5による(単位:Kg
f/cm2)
(ホ) 浸水後の密着性……48時間水中浸漬後の密着
性(単位:Kgf/cm2)
(ヘ) 加熱後の裏面温度……ISO834に準じて90分
間加熱後の供試体の裏面温度(単位:℃)
比較例
実施例中試料No.1の粒状岩綿を除いたもの(試
料No.9)、試料No.4のヒル石を除いたもの(試料
No.10)及び試料No.2の粒状岩綿をガラス繊維スト
ランドに変えたもの(試料No.11)について実施例
と同じ試験を行つたところ、第1表に示す結果が
得られた。
The present invention relates to a composition with excellent fireproof coating performance and good workability. BACKGROUND OF THE INVENTION As fireproof coating materials for buildings such as steel frames, spray coating of rock wool fibers via a bonding material and coating of calcium silicate plates are widely used. However, in the former case, the adhesion to the base structural material is poor and a lot of spraying pollution occurs, and the spraying work requires a lot of effort. The disadvantage is that the installation work to the base material is complicated, and in addition, a fairly sophisticated joining technique is required when installing on parts with complex shapes, so the fireproof coating performance of the completed board is not always uniform. The present inventors first completed the improvement by using inorganic fibers and a specific wet composite bonding material when covering base materials such as steel frames. By selecting and using rock wool processed into granules, it was confirmed that the heat insulation properties and workability were further improved, and the above-mentioned drawbacks were solved and succeeded. That is, the present invention provides (a) water-soluble alkali silicates, (b) (i) cement, zinc oxide, silica dust, (ii) divalent or higher metal salts of higher fatty acids, and water-soluble high Bivalent or higher valent metal salts of molecular substances, acidic metal oxides, phosphates, divalent metal sulfites, borates,
and (iii) at least one hardening component of component (a) above selected from metal powders, (c) inorganic lightweight aggregate, (d)
It consists of granular rock wool and (e) water, and the blending ratio is 5 to 250 parts by weight in the case of (i) of component (b) to 100 parts by weight of solid content of component (a), (ii) ) in case of 5~
30 parts by weight, 10 to 200 parts by weight in case of (iii) and (i) to (iii)
In the case of a combination of 5 to 250 parts by weight, component (c) is 30 to 200 parts by weight, and component (d) is 20 to 300 parts by weight, By mixing it as an essential component and operating it according to the construction method detailed below, it is possible to obtain an inorganic, highly fire-resistant and heat-insulating coating layer on base materials such as steel frames and structural wood through extremely easy operations. . Next, each essential component of the fireproof coating composition of the present invention will be briefly described. In the present invention, a water-soluble alkali silicate is used as the component (a), and only then can the desired composition be obtained. Examples of alkaline components constituting component (a) include Li,
Alkali metals such as Na, K, Pb and quaternary ammonium can be exemplified, and they can be advantageously used alone or in combination of two or more in the form of powder or aqueous solution, but paste preparation Considering the ease of construction, it is preferable to set the solid content concentration immediately before construction to about 10 to 60%. In addition, the hardening component of the water-soluble alkali silicate (component (b)) can be hardened by cement such as Portland cement, alumina cement, lime, high sulfate cement, silicon or silicon alloy by zinc oxide electric heating or metal method. Group (i) refers to silica dust that is produced as a by-product during manufacturing, and includes zinc stearate,
Divalent or higher valent metal salts of higher fatty acids such as potassium stearate and magnesium palmitate, divalent or higher valent metal salts of water-soluble polymer substances having carboxyl groups such as aluminum alginate and barium polyacrylate, Cr 2 O 3 , Acidic metal oxides such as Mn 3 O 4 and PbO, phosphates such as aluminum phosphate, calcium phosphate, and manganese phosphate, sulfites of divalent metals such as magnesium sulfite and zinc sulfite, lead borate, magnesium borate, etc. The borate of (ii)
as a group, and further Ti, Zr, V, Al, Si, Ge,
Metal powders such as Zn are classified as group (iii), and these (i)
It is preferable to use the curable components in groups (iii) in the form of powder, and one type of these can be used alone or two or more types can be used in combination. Furthermore, examples of the inorganic lightweight aggregate used as component (c) include vermiculite, expanded shale, perlite, expanded silica, and silica balloons. Furthermore, the granular rock wool used as component (d) refers to rock wool fibers that are mainly mechanically processed by adding rock wool fibers alone or other types of short fibers or powder, or by adding a very small amount of rock wool fibers. Rock wool that has been processed into granules via a binding substance, and the rock wool that has been processed into granules is not dispersed in the form of fibers in the composition of the present invention, so it retains a considerable amount of the fire resistance and heat insulation properties of rock wool alone. It is estimated that the particle size is preferably about 2 to 20 mm in diameter, and it is easy to disperse in order to maintain a granular shape. In addition to these essential ingredients, dispersion-stable fillers such as zeolite, talc, mica, and palygorskite, foaming agents for mortar, inorganic swelling substances such as kaolin, bentonite, and white carbon, and materials that do not significantly affect fire resistance. Water-soluble resins, organic granular foams, etc. can be blended to a certain degree. The fireproof and heat insulating composition of the present invention is generally based on the following blending ratio. That is, if the amount of component (b), that is, the curable component of component (a), is too small relative to 100 parts by weight of the solid content of component (a), regardless of whether it is any of (i) to (iii), the composition The fluidity of the compound decreases, which tends to cause problems such as drop-off and uncured, decreased water resistance of the fireproof coating layer, and poor adhesion.On the other hand, if it is added in excess, excess components that do not contribute to the curing reaction will harden. It tends to remain in the subsequent system and deteriorate the fire resistance, water resistance, and other functions of the fire-resistant coating layer. Next, component (c) reduces the specific gravity of the coating layer obtained by the composition and contributes to improving the heat insulation properties at room temperature or high temperature, but if the amount blended is small, it will naturally not be able to achieve this function. On the other hand, if the amount is too large, the fluidity of the paste will be poor, resulting in poor adhesion and reduced fire resistance.Furthermore, component (d) improves the mechanical strength of the composition, especially preventing shrinkage of the coating layer during drying and improving adhesion. It plays an extremely important role in improving heat insulation, fire resistance, etc., especially in the composite state of each component, and when it is low, fire resistance and heat insulation properties decrease and work On the other hand, if excessively blended, fluidity and water resistance tend to decrease, and the coating layer becomes non-uniform, which is undesirable. The composition for fireproof coating of the present invention prepared in this manner varies somewhat depending on the actual blending ratio, blending method, construction method, etc., but substantially has a bulk specific gravity of 0.3 after coating and drying. By setting the value to about 1.0, fire resistance, heat insulation, mechanical strength, etc. become preferable for the purposes of the present invention. It is presumed that this is not simply a matter of bulk specific gravity, but is due to the formation of a properly prepared composite from the moisture content, adhesion performance, heat conduction path, etc. When forming a fireproof coating layer on steel frames, metal plates, wooden structural materials, etc. using the composition of the present invention, the composition can be made into a paste form instantly or by mixing with a conventional mixer, and of course, the composition can be made into a paste form. Since it is water-based, it can be diluted with water, and after adjusting the viscosity with additives or adding water at the time of construction, it can be applied to the specified area by troweling, spatula, spraying, injection, etc. Coat the base material. The present invention will be specifically described below with reference to Examples and Comparative Examples. Example A coating composition of the present invention was prepared according to the ingredients and amounts listed in Table 1, water was added to the composition to adjust the viscosity, and the composition was quickly dried using a trowel so that the coating layer thickness after drying was approximately 20.
It was applied onto a 3.2 mm thick iron plate so that the thickness was 3.2 mm.
(Samples Nos. 1 to 8) Incidentally, talc, gypsum, and CMC were blended in advance with rock wool fibers, and this was placed in a mortar mixer and stirred to obtain granular rock wool. Using these dried specimens, a performance test was conducted according to the test method described below, and the results shown in the lower row of Table 1 were obtained. (a) Trowel workability: Comparative judgment based on trowel handling properties and the thickness that can be applied with one trowel application (the thicker the better). Evaluation by ◎>〇>△>×. (b) Spraying workability: Judging by whether or not there are any droplets when sprayed to a thickness of 10 mm after curing. Evaluation by ◎>〇>△>×. (c) Water resistance...Discoloration, cracking, etc. after immersion in water for 96 hours.
Check for changes such as peeling. (d) Adhesion...according to JIS A6909 5.5 (Unit: Kg
f/cm 2 ) (E) Adhesion after immersion in water...Adhesion after immersion in water for 48 hours (unit: Kgf/cm 2 ) (F) Back side temperature after heating...After heating for 90 minutes according to ISO834 Temperature on the back surface of the specimen (unit: °C) Comparative example Sample No. 1 in the example with the granular rock wool removed (sample No. 9), sample No. 4 with the vermiculite removed (sample
When the same test as in Example was conducted on Sample No. 10) and Sample No. 2 in which the granular rock wool was replaced with glass fiber strands (Sample No. 11), the results shown in Table 1 were obtained.
【表】【table】
Claims (1)
シル基を有する水溶性高分子物質の二価以上
の金属塩、酸性金属酸化物、リン酸塩、二価
金属の亜硫酸塩、ホウ酸塩、及び (iii) 金属粉末 から選ばれる少くとも一種、 (c) 無機質軽量骨材、 (d) 粒状岩綿 (e) 水 から成り、且つ配合率は、(a)成分の固形分100重
量部に対して、(b)成分の(i)の場合は5〜250重量
部、(ii)の場合は5〜30重量部、(iii)の場合は10〜
200重量部及び(i)〜(iii)の併用の場合は5〜250重量
部、(c)成分30〜200重量部及び(d)成分20〜300重量
部であることを特徴とする耐火被覆用組成物。[Scope of Claims] 1 (a) water-soluble alkali silicate, (b)(i) cement, zinc oxide, silica dust, (ii) divalent or higher valent metal salt of higher fatty acid, water-soluble having a carboxyl group At least one selected from divalent or higher valent metal salts of polymeric substances, acidic metal oxides, phosphates, sulfites and borates of divalent metals, and (iii) metal powder; (c) inorganic lightweight bone. (d) granular rock wool (e) water, and the blending ratio is 5 to 250 parts by weight for component (b) (i) based on 100 parts by weight of the solid content of component (a). , 5 to 30 parts by weight in case of (ii), 10 to 30 parts by weight in case of (iii)
200 parts by weight, 5 to 250 parts by weight if (i) to (iii) are used in combination, 30 to 200 parts by weight of component (c) and 20 to 300 parts by weight of component (d). Composition for use.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56095632A JPS57209874A (en) | 1981-06-19 | 1981-06-19 | Refractory coating composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56095632A JPS57209874A (en) | 1981-06-19 | 1981-06-19 | Refractory coating composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57209874A JPS57209874A (en) | 1982-12-23 |
JPS6363516B2 true JPS6363516B2 (en) | 1988-12-07 |
Family
ID=14142892
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56095632A Granted JPS57209874A (en) | 1981-06-19 | 1981-06-19 | Refractory coating composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57209874A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0444409U (en) * | 1990-08-13 | 1992-04-15 | ||
JPH04153513A (en) * | 1990-10-13 | 1992-05-27 | Kubota Corp | Oil pan for engine |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04336144A (en) * | 1991-05-14 | 1992-11-24 | Nitto Boseki Co Ltd | Manufacture of fire resistant backup material and coating thread used therefore |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4874525A (en) * | 1972-01-07 | 1973-10-08 | ||
JPS5129050B2 (en) * | 1973-05-26 | 1976-08-23 | ||
JPS55167183A (en) * | 1979-06-14 | 1980-12-26 | Nissei Ltd | Lining material for industrial ceramic oven |
-
1981
- 1981-06-19 JP JP56095632A patent/JPS57209874A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0444409U (en) * | 1990-08-13 | 1992-04-15 | ||
JPH04153513A (en) * | 1990-10-13 | 1992-05-27 | Kubota Corp | Oil pan for engine |
Also Published As
Publication number | Publication date |
---|---|
JPS57209874A (en) | 1982-12-23 |
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