JP4569936B2 - Foam fireproof paint - Google Patents
Foam fireproof paint Download PDFInfo
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- JP4569936B2 JP4569936B2 JP16254396A JP16254396A JP4569936B2 JP 4569936 B2 JP4569936 B2 JP 4569936B2 JP 16254396 A JP16254396 A JP 16254396A JP 16254396 A JP16254396 A JP 16254396A JP 4569936 B2 JP4569936 B2 JP 4569936B2
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- 239000003973 paint Substances 0.000 title claims description 15
- 239000006260 foam Substances 0.000 title description 10
- 238000000576 coating method Methods 0.000 claims description 20
- 239000011248 coating agent Substances 0.000 claims description 19
- 239000003063 flame retardant Substances 0.000 claims description 12
- 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 claims description 11
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- 229920000877 Melamine resin Polymers 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000004088 foaming agent Substances 0.000 claims description 7
- 239000004114 Ammonium polyphosphate Substances 0.000 claims description 6
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims description 6
- 229920001276 ammonium polyphosphate Polymers 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 6
- 239000012188 paraffin wax Substances 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 5
- 229920005792 styrene-acrylic resin Polymers 0.000 claims description 4
- BHYQWBKCXBXPKM-UHFFFAOYSA-N tris[3-bromo-2,2-bis(bromomethyl)propyl] phosphate Chemical compound BrCC(CBr)(CBr)COP(=O)(OCC(CBr)(CBr)CBr)OCC(CBr)(CBr)CBr BHYQWBKCXBXPKM-UHFFFAOYSA-N 0.000 claims description 3
- 238000004079 fireproofing Methods 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 description 11
- 239000010959 steel Substances 0.000 description 11
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 9
- 229910052794 bromium Inorganic materials 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 239000010408 film Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 230000009970 fire resistant effect Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 238000005187 foaming Methods 0.000 description 4
- -1 for example Substances 0.000 description 4
- 238000007665 sagging Methods 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 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 1
- PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical compound BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 125000005604 azodicarboxylate group Chemical group 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は、建造物の鉄骨やコンクリ−トなどに塗装される耐火塗料に関し、詳しくは、火災発生時の加熱下で均一に発泡層を形成するだけでなく、該発泡層中に良好に炭化層を保持して効果的に断熱し得る発泡形耐火塗料に関する。
【0002】
【従来技術及びその課題】
建造物の鉄骨は、不燃建材であるが、火災発生時の加熱下ではその強度が著しく低下し、建造物全体の倒壊につながる恐れがあるため、従来より、該鉄骨表面を耐火被覆材などによって保護し急激な強度低下を防止してきた。
【0003】
この耐火被覆材としては、従来、セメント系の無機バインダ−にスラグウ−ル等の軽量骨材を混合し水と混練してペ−スト状とした吹付材が使用されていた。
しかしながら該被覆材では、鉄骨に対し30mm以上の厚付けを要するため、工法上制約があるだけでなく、被覆面の凹凸が激しく、鉄骨自体のデザインを活かした美観を要求される部位には不適当であった。
【0004】
そこで、美観を要求される部位に好適な耐火被覆材として、有機バインダ−に発泡剤や炭素生成材などを混合した発泡性耐火塗料が種々提案されている(例えば、特開昭49−132821号、特開平5−86310号公報など)。該塗料による塗膜は、火災時の熱により分解し不燃ガスを発生して発泡し、多孔質の炭化層を形成する。これが断熱層となり鉄骨の温度上昇を抑制するものである。該塗料によれば鉄骨表面に薄膜形成が可能で意匠面で有利である。
【0005】
しかしながら従来の塗料では、加熱時の発泡形状が不均一であり、この中に占める炭化層の割合が低いために、断熱効果が不十分であったり、さらに、加熱が進むと炭化層の下地との付着性が悪くなり炭化層自体が脱落・崩壊して素地が露出し断熱層としての機能が発揮できないことがあった。
【0006】
【課題を解決するための手段】
本発明者らは、上記問題を解決すべく鋭意検討した結果、特定の難燃剤を含有せしめることにより、発泡層中に良好に炭化層を保持して効果的に断熱し得ることを見出だし本発明に到達した。
【0007】
即ち本発明は、樹脂固形分100重量部に対して、発泡剤150〜1100重量部、炭素供給剤25〜300重量部、無機粉末20〜200重量部、及び難燃剤5〜100重量部を含む塗料であって、該樹脂としてスチレンアクリル樹脂を用い、難燃剤としてトリス(トリブロモネオペンチル)ホスフェート及び/又はこの縮合物を用いることを特徴とする発泡形耐火塗料を提供するものである。
【0008】
以下、本発明について詳細に説明する。
【0009】
本発明に用いる樹脂は、塗膜形成成分であり、例えば、アクリル樹脂、オレフィンアクリル樹脂、アルキド樹脂、メラミン樹脂、エポキシ樹脂などが挙げられ、このうちスチレンアクリル樹脂が塗装作業性、顔料分散性等の点から好適である。
【0010】
本発明に用いる発泡剤としては、例えばジシアンジアミド、アゾジカルボンアミド;メラミン、尿素、グアニジン;ポリリン酸アンモニウムなどのリン酸塩;ポリオ−ル、塩素化パラフィン、炭酸水素カリウム、ジニトロソペンタメチレンテトラミン、バリウムアゾジカルボキシレ−トなどが挙げられ、これらは1種又は2種以上混合して使用できる。このうちポリリン酸アンモニウムなどのリン酸塩、メラミン、及び塩素化パラフィンを併用するのが発泡倍率と発泡層の強度等のバランスの点から好適である。
【0011】
該発泡剤の含有量は、上記樹脂固形分100重量部に対して、150〜1100重量部、好ましくは300〜800重量部の範囲内が適当である。特に、樹脂固形分100重量部に対して、ポリリン酸アンモニウムを100〜500重量部、好ましくは200〜400重量部、メラミンを25〜300重量部、好ましくは50〜200重量部、及び塩素化パラフィンを25〜300重量部、好ましくは50〜200重量部の範囲内で含有させるのが好適である。該ポリリン酸アンモニウムの含有量が100重量部未満では発泡倍率が低くなり炭化層が形成しにくくなり、一方500重量部を越えると発泡層の気泡が粗大となり下地との付着性が低下するので望ましくない。またメラミンの含有量が25重量部未満では発泡層が柔らかく崩壊しやすくなり、一方300重量部を越えると発泡倍率が低くなるので望ましくない。さらに塩素化パラフィンの含有量が25重量部未満では発泡倍率が低くなり、一方300重量部を越えると発泡層の気泡が粗大となり空洞化して崩壊しやすくなるので望ましくない。
【0012】
炭素供給剤としては、例えば多糖類、多価アルコ−ル、グラファイトなどが使用できるが、モノ、ジ、トリペンタエリスリト−ルなどの多価アルコ−ルが好適である。
【0013】
該炭素供給剤の含有量は、上記樹脂固形分100重量部に対して、25〜300重量部、好ましくは50〜200重量部の範囲内が適当である。該炭素供給剤の含有量が25重量部未満では発泡倍率が低くなり炭化層が形成しにくくなり、一方300重量部を越えると発泡層の気泡が粗大となり発泡層自体のタレやワレが生じやすくなるので望ましくない。
【0014】
無機粉末としては、例えば、酸化チタン、酸化アルミニウム、マイカ、シリカ、クレ−、粘土、ケイ酸塩、炭酸塩などが挙げられ、これらは1種又は2種以上混合して使用できる。
【0015】
該無機粉末の含有量は、上記樹脂固形分100重量部に対して、20〜200重量部、好ましくは30〜150重量部の範囲内が適当である。該無機粉末の含有量が20重量部未満では発泡層の気泡が不均一となり下地との付着性が低下し、一方200重量部を越えると塗装作業性に悪影響を及ぼし塗膜にワレが生じる恐れがあるので望ましくない。
【0016】
本発明では難燃剤として、融点150℃以上、好ましくは170〜250℃で、臭素含有率が50重量%以上、好ましくは50〜80重量%の含臭素リン酸エステル及び/又はこの縮合物を用いる。該難燃剤の融点が150℃未満では、前記発泡剤より早く分解してしまうため、発泡層中に炭化層の形成に効果が得られず、また臭素含有率が50重量%未満でも、炭化層の形成に効果が得られないので好ましくない。
【0017】
該含臭素リン酸エステルとしては、例えば炭素数5以上の分岐アルキル基を有するトリス(トリブロモアルキル)ホスフェ−ト及びこれらの縮合物等が挙げられ、このうちトリス(トリブロモネオペンチル)ホスフェ−ト及び/又はこの縮合物が好適である。
【0018】
該難燃剤の含有量は、樹脂固形分100重量部に対して、5〜100重量部、好ましくは20〜80重量部の範囲内が適当である。該難燃剤の含有量が5重量部未満では、炭化層の形成に効果が得られず、一方100重量部を越えると経時で塗膜にワレが生じる恐れがあるので望ましくない。
【0019】
本発明塗料には、上記成分以外にさらに必要に応じて、劣化防止剤、着色剤、分散剤、有機溶剤や水などの通常の塗料用添加剤を配合してもよい。
【0020】
本発明塗料は、ハケ、スプレ−など通常の塗装方法により、鉄骨、コンクリ−トなどの各種基材に塗布することができる。
【0021】
特に鉄骨に対しては、ブラスト処理などで除錆後、ショッププライマ−や下塗り塗料により下塗り塗装した上に本発明塗料を塗装するのが望ましい。形成される耐火塗膜面には、さらに必要に応じて中塗り塗装、上塗り塗装を順次行うことができる。
【0022】
【実施例】
以下、実施例を挙げて本発明をさらに詳細に説明する。
【0023】
実施例及び比較例
表1に示す配合量で各配合成分を混合し、各発泡形耐火塗料を作成した。表中の(*1)〜(*7)は下記の通りである。
【0024】
(*1)樹脂:「プリオライト」、グッドイヤ−社製、スチレンアクリル樹脂、固形分100%
(*2)トリス(トリブロモネオペンチル)ホスフェ−ト:融点約181℃、臭素含有率70重量%
(*3)テトラブロモフタレ−トエステル:液体、臭素含有率45重量%
(*4)テトラブロモビスフェノ−ルA:融点約180℃、臭素含有率59重量%(*5)ドデカンブロモジフェニ−ルオキサイド:融点約300℃、臭素含有率83重量%
(*6)トリス(ジブロモプロピル)ホスフェ−ト:液体、臭素含有率69重量%
(*7)希釈剤:ミネラルスピリットとキシレンの混合物
性能試験
グリットブラスト処理した300×300×3.2mmの鋼板を基材とし、この上に上記で得た各発泡形耐火塗料をスプレ−塗装により乾燥膜厚で約2mmの膜厚になるように塗装し、約2週間養生して各試験塗板を作成した。
【0025】
得られた試験塗板を電気炉に設置し、JIS−A−1304に示される標準加熱曲線に沿うように経過時間に対し所定温度に加熱する耐火試験に供した。1時間後、加熱温度925℃に到達した時点で試験を終了し、試験塗板の耐火塗膜の発泡状態を下記項目について観察し夫々評価した。評価結果を表1に示す。
【0026】
(発泡層の均一性)
○:全面が均一に発泡し良好
△:一部に不均一な部分があり、やや不良
×:全面が不均一で不良
(発泡層の垂れ割れ)
○:全く垂れ割れがなく良好
△:一部垂れ割れがあり、やや不良
×:全面に垂れ割れがあり不良
(発泡層の空洞)
発泡層を切り取り、その断面を観察した。
【0027】
○:全く空洞がなく良好
△:小さな空洞がみられ、やや不良
×:大きな空洞がみられ不良
(発泡倍率)
塗装膜厚に対する発泡層の厚みから発泡倍率を調べた。
【0028】
○:35倍以上
△:25倍以上〜35倍未満
×:25倍未満
このうち発泡層に占める炭化層の割合を調べた。
【0029】
○:80%以上
△:50〜80%
×:50%未満
(発泡層の強度)
発泡層を上から指で押して圧迫し、その硬さや靭性を調べた。
【0030】
○:硬さがあり簡単には壊れず、良好
△:硬さ、靭性ともやや不良
×:もろくてすぐに壊れ、不良
(基材との付着性)
発泡層を切り取る際に基材との付着性を調べた。
【0031】
○:良好
△:基材と付着はしているが、簡単に剥離できる
×:空洞があるため基材と付着していないところがある
【0032】
【発明の効果】
本発明の発泡形耐火塗料は、特定の難燃剤を含有することにより、該難燃剤が炭素供給剤の脱水〜炭化を促進するとともに塗膜表面に浮き酸素の遮断及び発泡剤の分解から発生するアンモニアや塩素ガスなどの不燃ガスの揮散を抑制するため、発泡層中に良好に炭化層を保持して効果的に断熱でき優れた耐火性能が得られるものである。
【0033】
【表1】
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a fire-resistant paint applied to a steel frame or concrete of a building, and more specifically, not only forms a foamed layer uniformly under heating in the event of a fire but also carbonizes well in the foamed layer. The present invention relates to a foam-type refractory paint capable of effectively insulating by holding a layer.
[0002]
[Prior art and its problems]
The steel frame of a building is a non-combustible building material. However, the strength of the steel frame is significantly reduced under heating in the event of a fire and may lead to the collapse of the entire building. Protected and prevented sudden drop in strength.
[0003]
As this fireproof covering material, conventionally, a spray material in which a lightweight aggregate such as slag wool is mixed with a cement-based inorganic binder and kneaded with water has been used.
However, since the coating material requires a thickness of 30 mm or more for the steel frame, there are not only restrictions on the construction method but also the unevenness of the coating surface is severe, and it is not suitable for parts that require an aesthetic appearance utilizing the design of the steel frame itself. It was appropriate.
[0004]
Accordingly, various fire-resistant fire-resistant paints in which an organic binder is mixed with a foaming agent, a carbon generating material, or the like have been proposed as fire-resistant coating materials suitable for parts requiring aesthetic appearance (for example, Japanese Patent Application Laid-Open No. 49-132821). JP-A-5-86310). The paint film is decomposed by heat in the event of a fire, generates non-combustible gas, and foams to form a porous carbonized layer. This becomes a heat insulation layer and suppresses the temperature rise of a steel frame. According to the paint, a thin film can be formed on the surface of the steel frame, which is advantageous in terms of design.
[0005]
However, in the conventional paint, the foamed shape at the time of heating is non-uniform, and since the ratio of the carbonized layer occupying this is low, the heat insulating effect is insufficient, and further, when the heating proceeds, In some cases, the adhesion of the steel layer deteriorates, and the carbonized layer itself falls off and collapses, exposing the substrate, and cannot function as a heat insulating layer.
[0006]
[Means for Solving the Problems]
As a result of intensive studies to solve the above problems, the present inventors have found that by containing a specific flame retardant, the carbonized layer can be well retained in the foamed layer and effectively insulated. The invention has been reached.
[0007]
That is, the present invention includes a foaming agent of 150 to 1100 parts by weight, a carbon supply agent of 25 to 300 parts by weight, an inorganic powder of 20 to 200 parts by weight, and a flame retardant of 5 to 100 parts by weight with respect to 100 parts by weight of resin solids. The present invention provides a foam-type fireproof paint characterized by using a styrene acrylic resin as the resin and using tris (tribromoneopentyl) phosphate and / or a condensate thereof as a flame retardant .
[0008]
Hereinafter, the present invention will be described in detail.
[0009]
The resin used in the present invention is a coating film forming component, and examples thereof include acrylic resins, olefin acrylic resins, alkyd resins, melamine resins, and epoxy resins. Among these, styrene acrylic resins are coating workability, pigment dispersibility, etc. From the point of view, it is preferable.
[0010]
Examples of the blowing agent used in the present invention include dicyandiamide, azodicarbonamide; melamine, urea, guanidine; phosphates such as ammonium polyphosphate; polyol, chlorinated paraffin, potassium hydrogen carbonate, dinitrosopentamethylenetetramine, barium. An azodicarboxylate etc. are mentioned, These can be used 1 type or in mixture of 2 or more types. Of these, the combined use of phosphates such as ammonium polyphosphate, melamine, and chlorinated paraffin is preferable from the viewpoint of balance between the expansion ratio and the strength of the foam layer.
[0011]
The content of the foaming agent is suitably in the range of 150 to 1100 parts by weight, preferably 300 to 800 parts by weight with respect to 100 parts by weight of the resin solid content. Particularly, 100 to 500 parts by weight of ammonium polyphosphate, preferably 200 to 400 parts by weight, 25 to 300 parts by weight of melamine, preferably 50 to 200 parts by weight, and chlorinated paraffin with respect to 100 parts by weight of resin solids. Is preferably contained in the range of 25 to 300 parts by weight, preferably 50 to 200 parts by weight. If the content of the ammonium polyphosphate is less than 100 parts by weight, the foaming ratio is low and it is difficult to form a carbonized layer. On the other hand, if it exceeds 500 parts by weight, bubbles in the foamed layer are coarsened and adhesion to the base is reduced. Absent. On the other hand, if the melamine content is less than 25 parts by weight, the foamed layer is soft and easily collapsed. On the other hand, if it exceeds 300 parts by weight, the expansion ratio is undesirably low. Further, when the content of chlorinated paraffin is less than 25 parts by weight, the foaming ratio is low. On the other hand, when it exceeds 300 parts by weight, the bubbles in the foamed layer are coarsened and become hollow and easily collapse, which is not desirable.
[0012]
As the carbon supply agent, for example, polysaccharides, polyhydric alcohols, graphite and the like can be used, but polyhydric alcohols such as mono, di and tripentaerythritol are suitable.
[0013]
The content of the carbon supply agent is suitably in the range of 25 to 300 parts by weight, preferably 50 to 200 parts by weight with respect to 100 parts by weight of the resin solid content. When the content of the carbon supply agent is less than 25 parts by weight, the expansion ratio is low and it is difficult to form a carbonized layer. On the other hand, when the content exceeds 300 parts by weight, the foamed cells are coarse, and the foamed layer itself tends to sag and crack. This is not desirable.
[0014]
Examples of the inorganic powder include titanium oxide, aluminum oxide, mica, silica, clay, clay, silicate, carbonate and the like, and these can be used alone or in combination.
[0015]
The content of the inorganic powder is suitably in the range of 20 to 200 parts by weight, preferably 30 to 150 parts by weight with respect to 100 parts by weight of the resin solid content. If the content of the inorganic powder is less than 20 parts by weight, bubbles in the foamed layer are not uniform and adhesion to the base is lowered. On the other hand, if it exceeds 200 parts by weight, the coating workability is adversely affected and the coating film may be cracked. This is not desirable.
[0016]
In the present invention, a bromine-containing phosphate ester having a melting point of 150 ° C. or higher, preferably 170 to 250 ° C. and a bromine content of 50 wt% or higher, preferably 50 to 80 wt%, and / or a condensate thereof are used as flame retardants. . If the melting point of the flame retardant is less than 150 ° C., the flame retardant decomposes faster than the foaming agent, so that no effect can be obtained in forming a carbonized layer in the foamed layer, and even if the bromine content is less than 50% by weight, the carbonized layer Since an effect is not acquired in formation of this, it is not preferable.
[0017]
Examples of the bromine-containing phosphate ester include tris (tribromoalkyl) phosphate having a branched alkyl group having 5 or more carbon atoms and condensates thereof. Among these, tris (tribromoneopentyl) phosphate- And / or condensates thereof are preferred.
[0018]
The content of the flame retardant is suitably in the range of 5 to 100 parts by weight, preferably 20 to 80 parts by weight with respect to 100 parts by weight of the resin solid content. If the content of the flame retardant is less than 5 parts by weight, the effect of forming the carbonized layer cannot be obtained. On the other hand, if it exceeds 100 parts by weight, the coating film may be cracked over time, which is not desirable.
[0019]
In addition to the above-described components, the paint of the present invention may further contain usual paint additives such as deterioration inhibitors, colorants, dispersants, organic solvents and water.
[0020]
The coating composition of the present invention can be applied to various base materials such as steel frames and concrete by an ordinary coating method such as brush or spray.
[0021]
Particularly for steel frames, it is desirable that the paint of the present invention is applied after being rusted by blasting or the like and then undercoated with a shop primer or undercoat. The fireproof coating surface to be formed can be further subjected to intermediate coating and top coating as necessary.
[0022]
【Example】
Hereinafter, the present invention will be described in more detail with reference to examples.
[0023]
Examples and comparative examples Each blending component was mixed in the blending amounts shown in Table 1 to prepare each foam-type fireproof paint. (* 1) to (* 7) in the table are as follows.
[0024]
(* 1) Resin: “Priolite”, manufactured by Goodyear, styrene acrylic resin, solid content 100%
(* 2) Tris (tribromoneopentyl) phosphate: melting point about 181 ° C., bromine content 70% by weight
(* 3) Tetrabromophthalate ester: liquid, bromine content 45% by weight
(* 4) Tetrabromobisphenol A: Melting point: about 180 ° C., bromine content: 59 wt% (* 5) Dodecane bromodiphenyl oxide: Melting point: about 300 ° C., bromine content: 83 wt%
(* 6) Tris (dibromopropyl) phosphate: liquid, bromine content 69% by weight
(* 7) Diluent: A mixture of mineral spirits and xylene
Performance test Grit blasted 300 × 300 × 3.2 mm steel sheet as a base material, and each foamed fireproof paint obtained above is spray-coated on this to a thickness of about 2 mm in dry film thickness. Each test coating plate was prepared by curing for about 2 weeks.
[0025]
The obtained test coating plate was installed in an electric furnace and subjected to a fire resistance test in which the test coating plate was heated to a predetermined temperature with respect to the elapsed time so as to follow the standard heating curve shown in JIS-A-1304. One hour later, when the heating temperature reached 925 ° C., the test was terminated, and the foaming state of the fireproof coating film on the test coating plate was observed and evaluated for the following items. The evaluation results are shown in Table 1.
[0026]
(Uniformity of foam layer)
○: The entire surface is uniformly foamed and good △: There is a non-uniform portion in part and is slightly defective ×: The entire surface is uneven and defective (sagging of the foam layer)
○: Good with no sagging cracks △: Some sagging cracks, somewhat poor ×: Sagging cracks on the entire surface, bad (foam of the foam layer)
The foam layer was cut out and the cross section was observed.
[0027]
○: Good with no cavities △: Small cavities are seen, slightly poor ×: Large cavities are seen, poor (foaming ratio)
The expansion ratio was examined from the thickness of the foam layer relative to the coating film thickness.
[0028]
○: 35 times or more Δ: 25 times or more to less than 35 times x: less than 25 times Among these, the ratio of the carbonized layer in the foamed layer was examined.
[0029]
○: 80% or more Δ: 50-80%
X: Less than 50% (strength of foam layer)
The foamed layer was pressed from above with a finger and pressed to examine its hardness and toughness.
[0030]
○: Hard and does not break easily, good △: Somewhat poor hardness and toughness ×: It is fragile and breaks immediately, poor (adhesion with substrate)
When the foamed layer was cut out, the adhesion with the substrate was examined.
[0031]
○: Good △: Adhered to the base material, but can be easily peeled ×: There is a portion that is not attached to the base material due to a cavity [0032]
【The invention's effect】
The foam-type fire-resistant paint of the present invention contains a specific flame retardant, so that the flame retardant promotes dehydration to carbonization of the carbon supply agent, and floats on the surface of the coating film and is generated from blocking of the blowing agent and decomposition of the foaming agent. In order to suppress the volatilization of nonflammable gases such as ammonia and chlorine gas, the carbonized layer can be held well in the foamed layer to effectively insulate, and excellent fire resistance can be obtained.
[0033]
[Table 1]
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16254396A JP4569936B2 (en) | 1996-06-24 | 1996-06-24 | Foam fireproof paint |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16254396A JP4569936B2 (en) | 1996-06-24 | 1996-06-24 | Foam fireproof paint |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH107947A JPH107947A (en) | 1998-01-13 |
| JP4569936B2 true JP4569936B2 (en) | 2010-10-27 |
Family
ID=15756607
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16254396A Expired - Fee Related JP4569936B2 (en) | 1996-06-24 | 1996-06-24 | Foam fireproof paint |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4569936B2 (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10221222A1 (en) * | 2002-05-13 | 2003-11-27 | Basf Ag | Flame retardant finishing of objects containing organic latent heat storage materials |
| DE10243231B4 (en) * | 2002-09-17 | 2004-10-28 | Clariant Gmbh | Fire protection coating |
| JP5078814B2 (en) * | 2008-09-11 | 2012-11-21 | 鹿島建設株式会社 | Foam fireproof paint |
| JP6988466B2 (en) * | 2017-12-27 | 2022-01-05 | Agc株式会社 | Foaming refractory paint |
| CN109082182A (en) * | 2018-07-10 | 2018-12-25 | 石家庄市油漆厂 | A kind of Water-borne inflation type refractory coating and preparation method thereof |
| CN115353792A (en) * | 2022-08-15 | 2022-11-18 | 中南大学 | An antibacterial and weather-resistant multifunctional integrated intumescent transparent fireproof coating and its preparation method |
-
1996
- 1996-06-24 JP JP16254396A patent/JP4569936B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH107947A (en) | 1998-01-13 |
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