CN117126585A - High-heat-flow-resistant expansion type fireproof coating and preparation method thereof - Google Patents
High-heat-flow-resistant expansion type fireproof coating and preparation method thereof Download PDFInfo
- Publication number
- CN117126585A CN117126585A CN202311216491.9A CN202311216491A CN117126585A CN 117126585 A CN117126585 A CN 117126585A CN 202311216491 A CN202311216491 A CN 202311216491A CN 117126585 A CN117126585 A CN 117126585A
- Authority
- CN
- China
- Prior art keywords
- parts
- coating
- epoxy resin
- heat flow
- high heat
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 105
- 239000011248 coating agent Substances 0.000 title claims abstract description 90
- 238000002360 preparation method Methods 0.000 title abstract description 14
- 239000003063 flame retardant Substances 0.000 claims abstract description 74
- 239000003822 epoxy resin Substances 0.000 claims abstract description 48
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 48
- 239000000835 fiber Substances 0.000 claims abstract description 35
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 33
- 239000000463 material Substances 0.000 claims abstract description 28
- 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 abstract description 25
- 239000003960 organic solvent Substances 0.000 claims abstract description 18
- 239000002987 primer (paints) Substances 0.000 claims abstract description 18
- 239000004088 foaming agent Substances 0.000 claims abstract description 17
- 239000003607 modifier Substances 0.000 claims abstract description 17
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 16
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 16
- 239000011256 inorganic filler Substances 0.000 claims abstract description 16
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 16
- 239000010452 phosphate Substances 0.000 claims abstract description 16
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 16
- 238000010276 construction Methods 0.000 claims abstract description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 20
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 238000010438 heat treatment Methods 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 238000003756 stirring Methods 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 10
- 229910000420 cerium oxide Inorganic materials 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 claims description 9
- 239000003973 paint Substances 0.000 claims description 9
- 238000007873 sieving Methods 0.000 claims description 9
- 229910001868 water Inorganic materials 0.000 claims description 9
- 239000011787 zinc oxide Substances 0.000 claims description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 238000000498 ball milling Methods 0.000 claims description 8
- RGPUVZXXZFNFBF-UHFFFAOYSA-K diphosphonooxyalumanyl dihydrogen phosphate Chemical compound [Al+3].OP(O)([O-])=O.OP(O)([O-])=O.OP(O)([O-])=O RGPUVZXXZFNFBF-UHFFFAOYSA-K 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 8
- -1 polymethylphenylsiloxane Polymers 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- 229910000831 Steel Inorganic materials 0.000 claims description 6
- 239000010959 steel Substances 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 5
- 238000000227 grinding Methods 0.000 claims description 5
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 claims description 5
- 229920002647 polyamide Polymers 0.000 claims description 5
- 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 claims description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- 229920000877 Melamine resin Polymers 0.000 claims description 4
- 239000004113 Sepiolite Substances 0.000 claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 4
- 238000006011 modification reaction Methods 0.000 claims description 4
- 235000011007 phosphoric acid Nutrition 0.000 claims description 4
- 229910052624 sepiolite Inorganic materials 0.000 claims description 4
- 235000019355 sepiolite Nutrition 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 239000004114 Ammonium polyphosphate Substances 0.000 claims description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims description 3
- 229920001276 ammonium polyphosphate Polymers 0.000 claims description 3
- 239000004202 carbamide Substances 0.000 claims description 3
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- 239000010439 graphite Substances 0.000 claims description 3
- 229910002804 graphite Inorganic materials 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 229910052863 mullite Inorganic materials 0.000 claims description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- UXMYUFHUUYBDLL-UHFFFAOYSA-N 2,2-dimethyl-3-(oxiran-2-ylmethoxy)propan-1-ol Chemical compound OCC(C)(C)COCC1CO1 UXMYUFHUUYBDLL-UHFFFAOYSA-N 0.000 claims description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 claims description 2
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 claims description 2
- WHJFNYXPKGDKBB-UHFFFAOYSA-N hafnium;methane Chemical compound C.[Hf] WHJFNYXPKGDKBB-UHFFFAOYSA-N 0.000 claims description 2
- 235000019837 monoammonium phosphate Nutrition 0.000 claims description 2
- 239000010451 perlite Substances 0.000 claims description 2
- 235000019362 perlite Nutrition 0.000 claims description 2
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 claims description 2
- 230000009970 fire resistant effect Effects 0.000 claims 2
- 238000010000 carbonizing Methods 0.000 claims 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 239000006012 monoammonium phosphate Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 10
- 239000000758 substrate Substances 0.000 abstract description 3
- 231100000252 nontoxic Toxicity 0.000 abstract description 2
- 230000003000 nontoxic effect Effects 0.000 abstract description 2
- 238000012360 testing method Methods 0.000 description 26
- 238000009413 insulation Methods 0.000 description 10
- 238000002485 combustion reaction Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- 238000012546 transfer Methods 0.000 description 8
- 229910018557 Si O Inorganic materials 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- 229910021641 deionized water Inorganic materials 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 230000001934 delay Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 239000002341 toxic gas Substances 0.000 description 2
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000003779 hair growth Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000011112 process operation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/002—Priming paints
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/18—Fireproof paints including high temperature resistant paints
- C09D5/185—Intumescent paints
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
- C08K2003/321—Phosphates
- C08K2003/322—Ammonium phosphate
- C08K2003/323—Ammonium polyphosphate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
- C08K2003/329—Phosphorus containing acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/14—Gas barrier composition
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
- C08L2203/206—Applications use in electrical or conductive gadgets use in coating or encapsulating of electronic parts
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
本发明属于涂料制备技术领域,涉及一种耐高热流膨胀型防火涂料及其制备方法。所述耐高热流膨胀型防火涂料由面涂涂料和底涂涂料构成,其中面涂涂料的组份按质量份计包括:环氧树脂50~80份、环氧树脂改性剂20~40份、阻燃剂10~25份、成碳剂25~45份、发泡剂20~40份、耐火纤维10~30份、无机填料10~40份、固化剂5~15份、消泡剂5~10份及有机溶剂;底涂涂料的组份按质量份计包括:磷酸盐基料70~90份。本发明制备得到的膨胀型防火涂料绿色无毒,可常温固化,涂料粘度可调控,施工方式可喷涂可刷涂,所需的涂层厚度薄且与基体粘结强度高,在高热流的使用工况下能够提高优异且稳定的阻燃效果。
The invention belongs to the technical field of coating preparation and relates to a high heat flow-resistant expansion fireproof coating and a preparation method thereof. The high heat flow expansion-resistant fire retardant coating is composed of a top coating and a primer. The components of the top coating include: 50 to 80 parts by mass of epoxy resin and 20 to 40 parts of epoxy resin modifier. , 10 to 25 parts of flame retardant, 25 to 45 parts of carbon-forming agent, 20 to 40 parts of foaming agent, 10 to 30 parts of refractory fiber, 10 to 40 parts of inorganic filler, 5 to 15 parts of curing agent, 5 defoaming agents ~10 parts and organic solvent; the components of the primer coating include: 70~90 parts of phosphate base material in terms of parts by mass. The intumescent fireproof coating prepared by the invention is green and non-toxic, can be cured at room temperature, the viscosity of the coating can be adjusted, and the construction method can be sprayed or brushed. The required coating thickness is thin and the bonding strength with the substrate is high, and it can be used in high heat flow applications. It can improve excellent and stable flame retardant effect under working conditions.
Description
技术领域Technical field
本发明属于涂料制备技术领域,更具体的说是涉及一种耐高热流膨胀型防火涂料及其制备方法。The invention belongs to the technical field of coating preparation, and more specifically relates to a high heat flow expansion resistant fire retardant coating and a preparation method thereof.
背景技术Background technique
防火涂料是一种可以提高建筑物耐火性能的材料,其作用是在建筑表面形成一层防火膜,从而起到防火的效果。目前,防火涂料已经广泛应用于建筑、交通工具、电子设备、化工设备等领域。Fire retardant coating is a material that can improve the fire resistance of buildings. Its function is to form a fire retardant film on the surface of the building, thereby achieving a fire prevention effect. At present, fire retardant coatings have been widely used in construction, transportation, electronic equipment, chemical equipment and other fields.
根据防火原理不同,防火涂料可分为非膨胀型涂料和膨胀型涂料两类。非膨胀型防火涂料防火隔热原理是利用了涂层热导率低,延滞了热量传向被保护基材的速度,同时涂层对钢构件起屏障和防止热辐射作用,避免了火焰和高温直接进攻钢构件,但是为了取得一定的防火隔热效果,非膨胀型的防火涂层需要较厚才能达到一定的防火隔热性能要求。According to different fire protection principles, fire retardant coatings can be divided into two categories: non-intumescent coatings and intumescent coatings. The principle of fire protection and heat insulation of non-expandive fire retardant coating is to take advantage of the low thermal conductivity of the coating, which delays the speed of heat transfer to the protected substrate. At the same time, the coating acts as a barrier and prevents thermal radiation to the steel components, avoiding flames and high temperatures. Directly attack steel components, but in order to achieve a certain fire protection and heat insulation effect, the non-expandive fire protection coating needs to be thicker to achieve certain fire protection and heat insulation performance requirements.
膨胀型防火涂料具有在高温条件下迅速膨胀并形成厚实的绝热层的特性,质地疏松的泡沫层隔绝氧气和延滞热量传递,能够有效地保护被涂物表面免受高温热辐射和火焰的损害。与传统的防火涂料相比,膨胀型防火涂料不仅能够提高防火等级和防火时间,而且还能够增加涂层的绝热性能,阻止热量的传递,从而保证建筑物和其他设施的安全性。Intumescent fire-retardant coatings have the characteristics of rapidly expanding under high temperature conditions and forming a thick thermal insulation layer. The loose foam layer isolates oxygen and delays heat transfer, which can effectively protect the surface of the coated object from damage by high-temperature thermal radiation and flames. Compared with traditional fire retardant coatings, intumescent fire retardant coatings can not only improve the fire protection level and fire protection time, but also increase the thermal insulation performance of the coating and prevent the transfer of heat, thus ensuring the safety of buildings and other facilities.
随着技术的不断进步和应用场景的不断扩大,研究人员着力于对膨胀型防火涂料材料、工艺和应用等方面进行了研究,膨胀型防火涂料正在得到广泛的应用和发展。但是,目前一些膨胀型防火涂料的性能稳定性存在一定的问题,容易受到湿度、温度等环境因素的影响,降低其使用寿命和效果,以及涂层材料组份包括卤族元素,卤族元素在使用过程中会产生有毒气体,不符合绿色环保的需求。此外,由于膨胀型防火涂料具有较高的技术含量和复杂的生产工艺,生产和研发成本相对较高,限制了其在大规模应用中的推广和使用。With the continuous advancement of technology and the expansion of application scenarios, researchers have focused on studying the materials, processes and applications of intumescent fire-retardant coatings. Intumescent fire-retardant coatings are being widely used and developed. However, there are certain problems with the performance stability of some intumescent fire-retardant coatings at present. They are easily affected by environmental factors such as humidity and temperature, reducing their service life and effectiveness. In addition, the coating material components include halogen elements, which are Toxic gases will be produced during use, which does not meet the needs of green environmental protection. In addition, because intumescent fire-retardant coatings have high technical content and complex production processes, production and research and development costs are relatively high, which limits their promotion and use in large-scale applications.
因此,如何提供一种耐高热流膨胀型防火涂料及其制备方法,能够解决现有技术中膨胀型防火涂料生产施工复杂,在高热流工况下防火效果较差的问题,同时具有绿色环保经济、施工方便安全、防火阻燃效果优秀等特点是本领域技术人员亟需解决的问题。Therefore, how to provide a high heat flow resistant expansion type fire retardant coating and its preparation method, which can solve the problems in the existing technology of complex production and construction of intumescent fire retardant coatings and poor fire protection effect under high heat flow conditions, while being green, environmentally friendly and economical , convenient and safe construction, excellent fire prevention and flame retardant effects, etc. are issues that technicians in this field urgently need to solve.
发明内容Contents of the invention
为解决上述技术问题,本发明提供了一种耐高热流膨胀型防火涂料及其制备方法。本发明制备得到的耐高热流膨胀型防火涂料绿色环保,制备方法工艺简单。且在防火涂料施工时采用底涂结合面涂的方式,可常温固化,涂料的粘度可调控,施工方式可采用刷涂方式,也可采用喷涂方式,所需的涂层厚度薄且与基体粘结强度高,在高热流的使用工况下能够提高优异且稳定的阻燃效果。In order to solve the above technical problems, the present invention provides a high heat flow expansion-resistant fire retardant coating and a preparation method thereof. The high heat flow expansion-resistant fire retardant coating prepared by the invention is green and environmentally friendly, and the preparation method is simple. In addition, when constructing fire-retardant coatings, a primer combined with a topcoat is used, which can be cured at room temperature, and the viscosity of the coating can be adjusted. The construction method can be brushing or spraying. The required coating thickness is thin and adheres to the substrate. The knot strength is high, which can improve the excellent and stable flame retardant effect under high heat flow conditions.
为实现上述目的,本发明提供了如下技术方案:In order to achieve the above objects, the present invention provides the following technical solutions:
本发明技术方案之一:提供一种耐高热流膨胀型防火涂料,包括底涂涂料和面涂涂料;One of the technical solutions of the present invention is to provide a high heat flow-resistant expansion type fire retardant coating, including a primer coating and a top coating coating;
按质量份计:所述面涂涂料的组分包括环氧树脂50~80份、环氧树脂改性剂20~40份、阻燃剂10~25份、成碳剂25~45份、发泡剂20~40份、耐火纤维10~30份、无机填料10~40份、固化剂5~15份、消泡剂5~10份和有机溶剂30~50份;所述底涂涂料的组份包括磷酸盐基料70~90份。In terms of parts by mass: the components of the topcoat include 50 to 80 parts of epoxy resin, 20 to 40 parts of epoxy resin modifier, 10 to 25 parts of flame retardant, 25 to 45 parts of carbon-forming agent, and hair growth agent. 20 to 40 parts of foaming agent, 10 to 30 parts of refractory fiber, 10 to 40 parts of inorganic filler, 5 to 15 parts of curing agent, 5 to 10 parts of defoaming agent and 30 to 50 parts of organic solvent; the composition of the primer coating Parts include 70 to 90 parts of phosphate base.
进一步的,所述环氧树脂为F51型未改性环氧树脂。Further, the epoxy resin is F51 type unmodified epoxy resin.
进一步的,所述环氧树脂改性剂为聚甲基苯基硅氧烷(有机硅改性剂)。Further, the epoxy resin modifier is polymethylphenylsiloxane (organic silicone modifier).
本发明所用的环氧树脂改性剂中大量甲基降低了有机硅与环氧树脂的相容性,改性树脂的耐热性及力学性能的提高。利用有机硅活性基团与环氧树脂反应,保留环氧基的同时引入有机硅树脂,适量苯基的存在进一步改善了有机硅与环氧树脂的相容性。The large amount of methyl groups in the epoxy resin modifier used in the present invention reduces the compatibility between silicone and epoxy resin, and improves the heat resistance and mechanical properties of the modified resin. The silicone reactive group is used to react with the epoxy resin, and the silicone resin is introduced while retaining the epoxy group. The presence of an appropriate amount of phenyl groups further improves the compatibility between the silicone and the epoxy resin.
本发明选用的环氧树脂的环氧基含量高,黏度较大,固化后产物交联密度高,耐热性好,经有机硅化学改性后,体系交联密度增加,硅氧键取代部分碳氧键,由于硅氧键的键能高于碳氧键的键能,且Si-O原子电负性差异大,以及Si-O键的极性大,对所连接的基团起到屏蔽作用,从而使得改性环氧树脂的韧性、耐热性都有很大的提高。The epoxy resin selected in the present invention has high epoxy group content and high viscosity. The cured product has high cross-linking density and good heat resistance. After chemical modification with silicone, the cross-linking density of the system increases and the silicon-oxygen bond replaces part of the Carbon-oxygen bond, because the bond energy of silicon-oxygen bond is higher than that of carbon-oxygen bond, and the electronegativity difference of Si-O atoms is large, and the polarity of Si-O bond is large, it acts as a shield for the connected group function, thereby greatly improving the toughness and heat resistance of the modified epoxy resin.
进一步的,所述阻燃剂包括聚磷酸铵、磷酸和磷酸二氢铵中的至少一种。Further, the flame retardant includes at least one of ammonium polyphosphate, phosphoric acid and ammonium dihydrogen phosphate.
进一步的,所述成碳剂包括双季戊四醇、乙二醇和季戊四醇中的一种。Further, the carbon-forming agent includes one of dipentaerythritol, ethylene glycol and pentaerythritol.
本发明中阻燃剂与成碳剂具有协同功效,通过阻燃剂的脱水作用,在受热后能够加速成碳剂脱水在燃烧过程中形成炭层。In the present invention, the flame retardant and the carbon-forming agent have a synergistic effect. Through the dehydration effect of the flame retardant, the dehydration of the carbon-forming agent can be accelerated after being heated to form a char layer during the combustion process.
进一步的,所述发泡剂包括三聚氰胺、三聚氰胺磷酸盐和尿素中的至少一种。Further, the foaming agent includes at least one of melamine, melamine phosphate and urea.
本方发明选用的发泡剂为无卤发泡剂,受热分解时会产生大量的胺类气体或氮气,不会产生有毒气体,一方面促使膨胀炭层形成疏松的泡沫状结构,一方面降低膨胀炭层的导热系数,提高阻燃效果。The foaming agent selected in this invention is a halogen-free foaming agent. When it is thermally decomposed, it will produce a large amount of amine gas or nitrogen, and will not produce toxic gases. On the one hand, it promotes the expanded carbon layer to form a loose foam-like structure, and on the other hand, it reduces The thermal conductivity of the expanded carbon layer improves the flame retardant effect.
进一步的,所述耐火纤维为形成尺寸梯度级配的短切纤维,包括短切高硅氧纤维、短切氧化铝纤维和短切莫来石纤维中的至少一种。Further, the refractory fibers are chopped fibers forming a size gradient gradation, including at least one of chopped high silica fibers, chopped alumina fibers and chopped mullite fibers.
优选的,所述尺寸梯度级配是由长度为6mm、8mm、10mm和12mm的耐火纤维构成,质量比为2:2:3:3。Preferably, the size gradient gradation is composed of refractory fibers with lengths of 6mm, 8mm, 10mm and 12mm, and the mass ratio is 2:2:3:3.
本发明添加的耐火纤维能够协同增强膨胀炭层的稳定性,同时降低热量传递速率,且纤维尺寸形成梯度级配能够保证涂层遇火后的膨胀炭层具有更佳的稳定性。The refractory fibers added in the present invention can synergistically enhance the stability of the expanded carbon layer and simultaneously reduce the heat transfer rate, and the gradient gradation of fiber size can ensure better stability of the expanded carbon layer after the coating encounters fire.
进一步的,所述无机填料包括滑石粉、珍珠岩、膨胀型石墨、氢氧化铝、硼化锆、碳化铪和海泡石中的至少一种。Further, the inorganic filler includes at least one of talc, perlite, expanded graphite, aluminum hydroxide, zirconium boride, hafnium carbide and sepiolite.
本发明中无机填料起到阻燃协效剂的作用,能够协同为涂料提供优秀的防火耐高温性能。In the present invention, the inorganic filler acts as a flame retardant synergist and can synergistically provide excellent fire protection and high temperature resistance for the coating.
进一步的,所述固化剂包括聚酰胺、脂环胺和脂肪胺中的一种。Further, the curing agent includes one of polyamide, alicyclic amine and fatty amine.
进一步的,所述消泡剂为有机硅类消泡剂BYK-065。Furthermore, the defoaming agent is organic silicon defoaming agent BYK-065.
进一步的,所述有机溶剂为无水乙醇、丙酮和新戊二醇缩水甘油醚中的至少一种。Further, the organic solvent is at least one of anhydrous ethanol, acetone and neopentyl glycol glycidyl ether.
本发明中有机溶剂的添加,能够改善环氧树脂和环氧树脂改性剂的溶解程度,调整涂料粘稠度。The addition of organic solvent in the present invention can improve the solubility of epoxy resin and epoxy resin modifier, and adjust the viscosity of the coating.
进一步的,所述磷酸盐基料由磷酸二氢铝、氧化锌、氧化铈和水组成,质量比为3:1:1:1。Further, the phosphate base material is composed of aluminum dihydrogen phosphate, zinc oxide, cerium oxide and water, with a mass ratio of 3:1:1:1.
磷酸盐基料作为粘结性材料进行底涂施工,能够保证涂料突出的粘结性能的同时提供防火性能,氧化锌、氧化铈还能够吸收化学反应过程中产生的水分,以防生成水的溢出,缓释基体的酸度,同时降低固化温度以便常温下大规模施工。The phosphate base material is used as a bonding material for primer construction, which can ensure the outstanding bonding performance of the paint and provide fire protection properties. Zinc oxide and cerium oxide can also absorb moisture generated during chemical reactions to prevent the overflow of generated water. , slow-release the acidity of the matrix, and at the same time reduce the curing temperature to facilitate large-scale construction at room temperature.
本发明技术方案之二:提供一种上述耐高热流膨胀型防火涂料的制备方法,包括:The second technical solution of the present invention is to provide a method for preparing the above-mentioned high heat flow expansion-resistant fire retardant coating, which includes:
将环氧树脂加热熔化后升温至70~100℃,再加入环氧树脂改性剂及有机溶剂总量的1/3,进行改性反应,得到改性环氧树脂;Heat and melt the epoxy resin and then raise the temperature to 70-100°C, then add 1/3 of the total amount of epoxy resin modifier and organic solvent to perform a modification reaction to obtain a modified epoxy resin;
将阻燃剂和成碳剂加热反应后加入发泡剂继续反应,经研磨过筛得到白色固体;Heat the flame retardant and carbon-forming agent to react, add the foaming agent to continue the reaction, and obtain a white solid after grinding and sieving;
在所述改性环氧树脂中加入耐火纤维、无机填料和余量有机溶剂,加热搅拌均匀,经球磨后得到混合物料;Add refractory fiber, inorganic filler and remaining organic solvent to the modified epoxy resin, heat and stir evenly, and obtain a mixed material after ball milling;
将所述混合物料与所述白色固体混合后加入固化剂和消泡剂经球磨分散后得到所述面涂涂料;After mixing the mixed material with the white solid, a curing agent and a defoaming agent are added and dispersed by ball milling to obtain the top coating;
将磷酸盐基料中的磷酸二氢铝、氧化锌和氧化铈经球磨分散后过筛得到固体粉末;Aluminum dihydrogen phosphate, zinc oxide and cerium oxide in the phosphate base material are dispersed by ball milling and then sieved to obtain solid powder;
在水浴加热搅拌条件下,将所述固体粉末和水混合,搅拌反应至凝胶状,即得底涂涂料。Under the conditions of heating and stirring in a water bath, the solid powder and water are mixed, and the reaction is stirred until the mixture becomes gel-like, thereby obtaining a primer coating.
进一步的,所述改性反应的时间为0.5~1h。Further, the modification reaction time is 0.5 to 1 h.
进一步的,所述加热反应的温度为120~170℃。Further, the temperature of the heating reaction is 120-170°C.
进一步的,所述研磨过筛为过100~300目筛。Further, the grinding and sieving is passing through a 100-300 mesh sieve.
进一步的,所述加热搅拌的温度为60~90℃。Further, the temperature of the heating and stirring is 60 to 90°C.
进一步的,所述球磨为在300~600r/min条件下球磨1~3h。Further, the ball milling is performed at 300 to 600 r/min for 1 to 3 hours.
进一步的,所述分散后过筛为过100~300目筛。Further, the sieving after dispersion is 100-300 mesh sieve.
本发明技术方案之三:提供一种上述耐高热流膨胀型防火涂料在建筑钢结构防火及新能源电池防火领域的应用。The third technical solution of the present invention is to provide an application of the above-mentioned high heat flow expansion-resistant fire retardant coating in the fields of building steel structure fire protection and new energy battery fire protection.
本发明技术方案之四:提供一种防火涂层,使用上述耐高热流膨胀型防火涂料涂覆而成。The fourth technical solution of the present invention is to provide a fire-retardant coating, which is coated with the above-mentioned high heat flow-resistant expansion-type fire-retardant coating.
进一步的,所述涂覆为先涂覆底涂涂料,再涂覆面涂涂料。Further, the coating is to apply the base coating first and then the top coating.
优选的,所述底涂涂料的涂覆厚度为900~1000μm。Preferably, the coating thickness of the primer is 900-1000 μm.
优选的,所述面涂涂料的涂覆厚度为500~800μm。Preferably, the coating thickness of the topcoat is 500-800 μm.
经由上述的技术方案可知,与现有技术相比,具有如下有益效果:It can be seen from the above technical solution that compared with the existing technology, it has the following beneficial effects:
1、本发明在进行有机硅改性后的树脂结构中的C-O键被Si-O键替代,提升了体系的交联密度,在受热过程中键能和极性都更大的Si-O键可以对周围的基团起到屏蔽作用,延长材料在受热时热阻塞效应的时间,降低材料内部的热量传递。1. In the present invention, the C-O bonds in the silicone-modified resin structure are replaced by Si-O bonds, which improves the cross-linking density of the system. During the heating process, the Si-O bonds have greater bond energy and polarity. It can shield the surrounding groups, prolong the thermal blocking effect when the material is heated, and reduce the heat transfer inside the material.
2、本发明所用原料中的阻燃剂在遇热后会先于环氧树脂产生热降解,在热降解的过程中大量吸热,同时膨胀型阻燃剂中气源成分产生不可燃气体冲淡燃烧反应中的氧气浓度,而阻燃剂和成碳剂在此时迅速脱水成炭,最终生成了一个能够隔绝火焰和阻挡热量传递的保护炭层,从而达到阻燃的目的。2. The flame retardant in the raw materials used in the present invention will thermally degrade before the epoxy resin when exposed to heat. During the thermal degradation process, it will absorb a large amount of heat. At the same time, the gas source component in the intumescent flame retardant will produce non-combustible gas and dilute it. The oxygen concentration in the combustion reaction, while the flame retardant and carbon-forming agent are rapidly dehydrated into charcoal at this time, ultimately forming a protective charcoal layer that can isolate the flame and block heat transfer, thereby achieving the purpose of flame retardancy.
3、本发明涂料中添加的耐火纤维和无机填料为保护炭层提供力学支撑,降低热量在涂层与被保护集体之间的传递速率,耐火纤维尺寸呈现梯度级配,能够更大程度地保证膨胀炭层的稳定性,使涂层能在高热流工况下正常工作。3. The refractory fibers and inorganic fillers added to the coating of the present invention provide mechanical support for the protective carbon layer, reducing the heat transfer rate between the coating and the protected object. The size of the refractory fibers presents a gradient gradation, which can ensure a greater degree of protection. The stability of the expanded carbon layer enables the coating to work normally under high heat flow conditions.
4、本发明制备得到的耐高热流膨胀型防火涂料,涂层涂覆厚度为1400~1800μm时,即可达到优异隔热防火效果。4. The high heat flow expansion-resistant fire retardant coating prepared by the present invention can achieve excellent heat insulation and fire retardant effects when the coating thickness is 1400-1800 μm.
5、本发明制备得到的膨胀型防火涂料绿色无毒,可常温固化,涂料粘度可调控,施工方式可喷涂可刷涂。5. The intumescent fire-retardant coating prepared by the present invention is green and non-toxic, can be cured at room temperature, the viscosity of the coating can be adjusted, and the construction method can be sprayed or brushed.
附图说明Description of the drawings
构成本申请的一部分的附图用来提供对本申请的进一步理解,本申请的示意性实施例及其说明用于解释本申请,并不构成对本申请的不当限定。在附图中:The drawings that form a part of this application are used to provide a further understanding of this application. The illustrative embodiments and descriptions of this application are used to explain this application and do not constitute an improper limitation of this application. In the attached picture:
图1为涂覆有实施例1-3防火涂料涂层的试验件。Figure 1 is a test piece coated with the fire retardant coating of Examples 1-3.
图2为试验例中燃烧背温测试装置。Figure 2 shows the combustion back temperature test device in the test example.
图3为实施例3的试验件经过燃烧背温测试后的膨胀炭层图片。Figure 3 is a picture of the expanded carbon layer of the test piece in Example 3 after the combustion back temperature test.
具体实施方式Detailed ways
下面将结合本发明实施例中的附图,对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only some of the embodiments of the present invention, rather than all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative efforts fall within the scope of protection of the present invention.
本发明中耐火纤维为形成尺寸梯度级配的短切纤维,尺寸梯度级配是由长度为6mm、8mm、10mm和12mm的耐火纤维构成,质量比为2:2:3:3。The refractory fibers in the present invention are chopped fibers forming a size gradient gradation. The size gradient gradation is composed of refractory fibers with lengths of 6 mm, 8 mm, 10 mm and 12 mm, and the mass ratio is 2:2:3:3.
实施例1Example 1
耐高热流膨胀型防火涂料,按质量份计,包括如下组份:High heat flow expansion resistant fire retardant coating includes the following components in terms of parts by mass:
面涂涂料:环氧树脂70份、环氧树脂改性剂30份、阻燃剂20份、成碳剂20份、发泡剂25份、耐火纤维20份、无机填料25份、固化剂10份、消泡剂5份、有机溶剂40份。Top coating: 70 parts of epoxy resin, 30 parts of epoxy resin modifier, 20 parts of flame retardant, 20 parts of carbon-forming agent, 25 parts of foaming agent, 20 parts of refractory fiber, 25 parts of inorganic filler, 10 parts of curing agent 5 parts of defoaming agent and 40 parts of organic solvent.
底涂涂料:磷酸盐基料80份。Primer coating: 80 parts of phosphate base.
其中,环氧树脂为F51型未改性环氧树脂,环氧树脂改性剂为聚甲基苯基硅氧烷,阻燃剂为磷酸,成碳剂为双季戊四醇,发泡剂为三聚氰胺,耐火纤维为短切高硅氧纤维,无机填料为质量比为1:1的氢氧化铝粉末和硼化锆粉末混合物,固化剂为聚酰胺,消泡剂为BYK-065,有机溶剂为无水乙醇;磷酸盐基料由磷酸二氢铝、氧化锌、氧化铈和去离子水组成,质量比为3:1:1:1。Among them, the epoxy resin is F51 unmodified epoxy resin, the epoxy resin modifier is polymethylphenylsiloxane, the flame retardant is phosphoric acid, the carbon-forming agent is dipentaerythritol, and the foaming agent is melamine. The refractory fiber is chopped high silica fiber, the inorganic filler is a mixture of aluminum hydroxide powder and zirconium boride powder with a mass ratio of 1:1, the curing agent is polyamide, the defoaming agent is BYK-065, and the organic solvent is anhydrous Ethanol; the phosphate base material is composed of aluminum dihydrogen phosphate, zinc oxide, cerium oxide and deionized water, with a mass ratio of 3:1:1:1.
耐高热流膨胀型防火涂料的制备方法:Preparation method of high heat flow expansion-resistant fire retardant coating:
S1、底涂涂料的制备S1. Preparation of primer paint
将磷酸盐基料按比例混合,以无水乙醇作为介质,在300r/min条件下球磨1h充分分散,分散后干燥处理过200目筛,在水浴90℃加热搅拌条件下,将研磨分散过筛后的粉末加入去离子水,搅拌反应至凝胶状,即得底涂涂料。Mix the phosphate base material in proportion, use absolute ethanol as the medium, ball mill at 300r/min for 1 hour to fully disperse, dry and pass through a 200 mesh sieve after dispersion, heat and stir in a water bath at 90°C, grind, disperse and sieve Add deionized water to the final powder, stir and react until it becomes gel-like, and the primer is obtained.
S2、面涂涂料的制备S2. Preparation of topcoat paint
1)将环氧树脂加热融化,升温至80℃后加入环氧树脂改性剂以及有机溶剂总量的1/3,反应1h,冷却至室温,即得改性环氧树脂,备用。1) Heat and melt the epoxy resin, raise the temperature to 80°C, add epoxy resin modifier and 1/3 of the total amount of organic solvent, react for 1 hour, and cool to room temperature to obtain the modified epoxy resin, which is ready for use.
2)将阻燃剂以及成碳剂搅拌均匀后加热至120℃,在120℃条件下反应4h,得到无色透明液体,再将发泡剂加入透明液体中继续反应4h,最后反应结束,经研磨后过200目筛,得到白色固体,备用。2) Stir the flame retardant and carbon-forming agent evenly and heat to 120°C. React at 120°C for 4 hours to obtain a colorless transparent liquid. Then add the foaming agent to the transparent liquid and continue the reaction for 4 hours. Finally, the reaction is completed. After grinding, pass through a 200-mesh sieve to obtain a white solid, which is set aside.
3)将改性环氧树脂与耐火纤维、无机填料、余量有机溶剂混合,升温至80℃搅拌均匀,在300r/min条件下球磨1.5h,得到混合物料备用。3) Mix the modified epoxy resin with refractory fiber, inorganic filler, and remaining organic solvent, raise the temperature to 80°C, stir evenly, and ball-mill at 300 r/min for 1.5 hours to obtain a mixed material for later use.
4)将白色固体与混合物料混合,加入固化剂及消泡剂,经搅拌分散均匀后即得面涂涂料。4) Mix the white solid with the mixed materials, add curing agent and defoaming agent, stir and disperse evenly to obtain the top coating.
实施例2Example 2
耐高热流膨胀型防火涂料,按质量份计,包括如下组份:High heat flow expansion resistant fire retardant coating includes the following components in terms of parts by mass:
面涂涂料:环氧树脂70份、环氧树脂改性剂30份、阻燃剂30份、成碳剂15份、发泡剂15份、耐火纤维20份、无机填料30份、固化剂10份、消泡剂5份、有机溶剂40份。Top coating: 70 parts of epoxy resin, 30 parts of epoxy resin modifier, 30 parts of flame retardant, 15 parts of carbon-forming agent, 15 parts of foaming agent, 20 parts of refractory fiber, 30 parts of inorganic filler, 10 parts of curing agent 5 parts of defoaming agent and 40 parts of organic solvent.
底涂涂料:磷酸盐基料80份。Primer coating: 80 parts of phosphate base.
其中,环氧树脂为F51型未改性环氧树脂,环氧树脂改性剂为聚甲基苯基硅氧烷,阻燃剂为聚磷酸铵,成碳剂为双季戊四醇,发泡剂为尿素,耐火纤维为短切高硅氧纤维,无机填料为海泡石粉末,固化剂为聚酰胺,消泡剂为BYK-065,有机溶剂为无水乙醇;磷酸盐基料由磷酸二氢铝、氧化锌、氧化铈和去离子水组成,质量比为3:1:1:1。Among them, the epoxy resin is F51 unmodified epoxy resin, the epoxy resin modifier is polymethylphenylsiloxane, the flame retardant is ammonium polyphosphate, the carbon forming agent is dipentaerythritol, and the foaming agent is Urea, the refractory fiber is chopped high silica fiber, the inorganic filler is sepiolite powder, the curing agent is polyamide, the defoaming agent is BYK-065, the organic solvent is absolute ethanol; the phosphate base material is aluminum dihydrogen phosphate , zinc oxide, cerium oxide and deionized water, with a mass ratio of 3:1:1:1.
耐高热流膨胀型防火涂料的制备方法:Preparation method of high heat flow expansion-resistant fire retardant coating:
与实施例1相比,不同之处在于面涂涂料的制备时步骤2)中的加热温度为150℃,研磨过300目筛,其余与实施例1相同。Compared with Example 1, the difference lies in that the heating temperature in step 2) during the preparation of the topcoat coating is 150°C, and the mixture is ground through a 300-mesh sieve, and the rest is the same as in Example 1.
实施例3Example 3
耐高热流膨胀型防火涂料,按质量份计,包括如下组份:High heat flow expansion resistant fire retardant coating includes the following components in terms of parts by mass:
面涂涂料:环氧树脂70份、环氧树脂改性剂30份、阻燃剂30份、成碳剂15份、发泡剂20份、耐火纤维25份、无机填料30份、固化剂10份、消泡剂5份及有机溶剂40份。Top coating: 70 parts of epoxy resin, 30 parts of epoxy resin modifier, 30 parts of flame retardant, 15 parts of carbon-forming agent, 20 parts of foaming agent, 25 parts of refractory fiber, 30 parts of inorganic filler, 10 parts of curing agent 5 parts of defoaming agent and 40 parts of organic solvent.
底涂涂料:磷酸盐基料70份。Primer coating: 70 parts of phosphate base.
其中,环氧树脂为F51型未改性环氧树脂,环氧树脂改性剂为聚甲基苯基硅氧烷,阻燃剂为磷酸,成碳剂为季戊四醇,发泡剂为三聚氰胺,耐火纤维为短切莫来石纤维,无机填料为质量比为1:1的海泡石粉末与氢氧化铝粉末混合物,固化剂为聚酰胺,消泡剂为BYK-065,有机溶剂为无水乙醇;磷酸盐基料由磷酸二氢铝、氧化锌、氧化铈和去离子水组成,质量比为3:1:1:1。Among them, the epoxy resin is F51 unmodified epoxy resin, the epoxy resin modifier is polymethylphenylsiloxane, the flame retardant is phosphoric acid, the carbon-forming agent is pentaerythritol, the foaming agent is melamine, and the fire resistance The fiber is chopped mullite fiber, the inorganic filler is a mixture of sepiolite powder and aluminum hydroxide powder with a mass ratio of 1:1, the curing agent is polyamide, the defoaming agent is BYK-065, and the organic solvent is absolute ethanol. ; The phosphate base material is composed of aluminum dihydrogen phosphate, zinc oxide, cerium oxide and deionized water, with a mass ratio of 3:1:1:1.
耐高热流膨胀型防火涂料的制备方法与实施例1相同。The preparation method of the high heat flow expansion-resistant fire retardant coating is the same as in Example 1.
对比例1Comparative example 1
与实施例3相比,不同之处仅在于,使用膨胀石墨代替阻燃剂、成碳剂和发泡剂制备得到的白色固体产物。Compared with Example 3, the only difference lies in the white solid product prepared by using expanded graphite instead of the flame retardant, carbon-forming agent and foaming agent.
试验例Test example
将实施例1~3及对比例1制备得到的底涂涂料分别均匀的涂覆在150mm×70mm的标准试验钢板上,涂层厚度为900μm,常温干燥8h,干燥后再将面涂涂料均匀的涂覆在底涂涂料表面,涂层厚度为500μm,72h后涂料常温固化完全,得到涂有防火涂层的试验件,如图1所示,从左到右依次为涂覆实施例1、实施例2和实施例3涂料的试验件。The primer paints prepared in Examples 1 to 3 and Comparative Example 1 were evenly coated on a 150mm×70mm standard test steel plate with a coating thickness of 900 μm, and dried at room temperature for 8 hours. After drying, the topcoat paint was evenly applied. Coating on the surface of the primer coating, the coating thickness is 500 μm. After 72 hours, the coating is completely cured at room temperature, and a test piece coated with a fire retardant coating is obtained. As shown in Figure 1, from left to right are coating example 1 and implementation. Test pieces of Example 2 and Example 3 coatings.
为考察材料在实际应用下的隔热性能,采用如图2所示的装置进行测试。In order to examine the thermal insulation performance of the material in practical applications, the device shown in Figure 2 was used for testing.
1、燃烧背温测试1. Combustion back temperature test
测试方法:Test Methods:
使用支架将由实施例1~3和对比例1制备得到的试验件分别固定在测试台上,然后在试验件的背面固定用来测量温度的热电偶,使用甲烷喷枪对样件正面进行灼烧,灼烧温度为1200℃,持续10分钟,记录灼烧5分钟和10分钟时,背面温度,记为T1和T2。燃烧背温测试数据如表1所示:The test pieces prepared in Examples 1 to 3 and Comparative Example 1 were fixed on the test bench respectively using brackets, and then a thermocouple for measuring temperature was fixed on the back of the test piece, and a methane spray gun was used to burn the front of the sample. The burning temperature is 1200°C and lasts for 10 minutes. Record the temperature of the backside when burning for 5 minutes and 10 minutes, and record them as T 1 and T 2 . The combustion back temperature test data is shown in Table 1:
表1Table 1
由表1数据可以看出,经1200℃火焰持续灼烧10min后,实施例1~3样品的背面温度均未超过500℃,表现出了较为明显的隔热效果,能够在实际火焰燃烧的情况下保证背面材料不受高温的破坏。It can be seen from the data in Table 1 that after continuous burning with a 1200°C flame for 10 minutes, the back surface temperature of the samples in Examples 1 to 3 did not exceed 500°C, showing a relatively obvious heat insulation effect and being able to burn under actual flame conditions. This ensures that the back material is not damaged by high temperatures.
通过实施例3与对比例1的T1和T2数据对比,可以看出,实施例3中灼烧5分钟的背温温度下降了44.8%,灼烧10分钟的背温温度下降了38.9%,可见本申请制备得到的防火涂料的隔热性能优异。By comparing the T 1 and T 2 data of Example 3 and Comparative Example 1, it can be seen that the back temperature after burning for 5 minutes in Example 3 dropped by 44.8%, and the back temperature after burning for 10 minutes dropped by 38.9%. , it can be seen that the fire retardant coating prepared by this application has excellent heat insulation performance.
2、热稳定性能测试2. Thermal stability performance test
测试方法:采用热重-差热(TG-DSC)分析这种测试方法来进行热分析,速率10℃/min,升温至1200℃对固化后的涂层材料进行测试,分析其受热反应。Test method: Thermogravimetric-differential thermal (TG-DSC) analysis is used to conduct thermal analysis at a rate of 10°C/min. The temperature is raised to 1200°C to test the cured coating material and analyze its thermal response.
记录样品失重10%和50%时的加热温度以及在600℃和1200℃样品的残重率,结果如表2所示。Record the heating temperature when the sample loses 10% and 50% weight and the residual weight rate of the sample at 600°C and 1200°C. The results are shown in Table 2.
表2Table 2
由表2数据的残重率的数值来看,本发明涂层材料在600℃下残重率均在50%以上,1200℃下的残重率均在20%以上,说明本发明制备得到的膨胀型防火涂料在受热过程中具有优异的成炭性能。Judging from the numerical values of the residual weight ratio of the data in Table 2, the residual weight ratios of the coating materials of the present invention are all above 50% at 600°C, and the residual weight ratios at 1200°C are all above 20%, indicating that the coating materials prepared by the present invention are Intumescent fire retardant coatings have excellent char-forming properties during heating.
3、热导率测试3. Thermal conductivity test
激光闪光法:利用激光法在0.3ms的脉冲作用下测试防火涂层在室温下的热导率,测试平均结果如表3所示,可见本发明所制备得到的防火涂层具有良好的隔热性能。Laser flash method: The laser method is used to test the thermal conductivity of the fire-retardant coating at room temperature under the action of a 0.3ms pulse. The average test results are shown in Table 3. It can be seen that the fire-retardant coating prepared by the present invention has good heat insulation. performance.
表3table 3
4、附着力测试4. Adhesion test
测试方法:利用PosiTest附着力测试仪,依据CB/T 5210-2006标准测试实施例1-3防火涂层在钢板上的附着力,如表4所示。Test method: Use the PosiTest adhesion tester to test the adhesion of the fire retardant coating on the steel plate in Example 1-3 according to the CB/T 5210-2006 standard, as shown in Table 4.
表4Table 4
由表4数据可以看出,本发明防火涂层的附着力均大于2.9MPa,说明本发明的防火涂层具有优异的附着力。It can be seen from the data in Table 4 that the adhesion of the fire-retardant coating of the present invention is greater than 2.9MPa, indicating that the fire-retardant coating of the present invention has excellent adhesion.
5、膨胀炭层高度测试5. Expanded carbon layer height test
在燃烧背温测试后随机切开实施例3涂层完好的某一角,测量涂层膨胀炭层的厚度最大值hmax和最低值hmin,测试结果如表5所示。After the combustion back temperature test, a certain corner of the intact coating of Example 3 was randomly cut, and the maximum value h max and the minimum value h min of the thickness of the expanded carbon layer of the coating were measured. The test results are shown in Table 5.
表5table 5
由表5可以看出,本发明实施例1-3在1200℃下分别膨胀2.5~3.2cm、2.3~3.6cm、2.2~3.4cm,可见本发明实例所制备的耐高热流膨胀型防火涂料在遇火之后具有表现优异的膨胀度,厚的膨胀炭层能够理想地抵抗热流阻止火焰蔓延。It can be seen from Table 5 that Examples 1-3 of the present invention expanded by 2.5-3.2cm, 2.3-3.6cm, and 2.2-3.4cm respectively at 1200°C. It can be seen that the high heat flow-resistant expansion type fire retardant coating prepared by the examples of the present invention has It has excellent expansion performance after encountering fire, and the thick expanded carbon layer can ideally resist heat flow and prevent the spread of flames.
图3为膨胀炭层图,是实施例3的试验件经过燃烧背温测试后的实物照片,从图中可以看出,在经过燃烧后涂层生成了明显的膨胀炭层,炭层呈连续分布没有破损,说明涂层能够很好的产生膨胀现象,炭层能够耐受高热流并阻挡热流传递,该涂层具有优秀的耐高热流能力。Figure 3 is a diagram of the expanded carbon layer, which is a physical photo of the test piece of Example 3 after the combustion back temperature test. It can be seen from the picture that after combustion, the coating formed an obvious expanded carbon layer, and the carbon layer was continuous. There is no damage in the distribution, indicating that the coating can produce expansion well, and the carbon layer can withstand high heat flow and block heat flow transfer. The coating has excellent high heat flow resistance.
本说明书中各个实施例采用递进的方式描述,每个实施例重点说明的都是与其他实施例的不同之处,各个实施例之间相同相似部分互相参见即可。此外,本案发明人还参照前述实施例,以本说明书述及的其它原料、工艺操作、工艺条件进行了试验,并均获得了较为理想的结果。Each embodiment in this specification is described in a progressive manner. Each embodiment focuses on its differences from other embodiments. The same and similar parts between the various embodiments can be referred to each other. In addition, the inventor of the present case also conducted experiments with other raw materials, process operations, and process conditions mentioned in this specification with reference to the aforementioned embodiments, and all achieved relatively ideal results.
对所公开的实施例的上述说明,使本领域专业技术人员能够实现或使用本发明。对这些实施例的多种修改对本领域的专业技术人员来说将是显而易见的,本文中所定义的一般原理可以在不脱离本发明的精神或范围的情况下,在其它实施例中实现。因此,本发明将不会被限制于本文所示的这些实施例,而是要符合与本文所公开的原理和新颖特点相一致的最宽的范围。The above description of the disclosed embodiments enables those skilled in the art to make or use the present invention. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be practiced in other embodiments without departing from the spirit or scope of the invention. Thus, the present invention is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202311216491.9A CN117126585A (en) | 2023-09-20 | 2023-09-20 | High-heat-flow-resistant expansion type fireproof coating and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202311216491.9A CN117126585A (en) | 2023-09-20 | 2023-09-20 | High-heat-flow-resistant expansion type fireproof coating and preparation method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN117126585A true CN117126585A (en) | 2023-11-28 |
Family
ID=88860060
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202311216491.9A Pending CN117126585A (en) | 2023-09-20 | 2023-09-20 | High-heat-flow-resistant expansion type fireproof coating and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN117126585A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102781871A (en) * | 2009-12-11 | 2012-11-14 | 18纬度有限公司 | Inorganic phosphate compositions and methods |
CN105238222A (en) * | 2015-11-13 | 2016-01-13 | 海洋化工研究院有限公司 | Environment-friendly epoxy intumescent fire-retardant coating and preparing method thereof |
CN116120814A (en) * | 2023-04-17 | 2023-05-16 | 内蒙古工业大学 | A kind of environment-friendly organosilicon modified intumescent fireproof coating |
-
2023
- 2023-09-20 CN CN202311216491.9A patent/CN117126585A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102781871A (en) * | 2009-12-11 | 2012-11-14 | 18纬度有限公司 | Inorganic phosphate compositions and methods |
CN105238222A (en) * | 2015-11-13 | 2016-01-13 | 海洋化工研究院有限公司 | Environment-friendly epoxy intumescent fire-retardant coating and preparing method thereof |
CN116120814A (en) * | 2023-04-17 | 2023-05-16 | 内蒙古工业大学 | A kind of environment-friendly organosilicon modified intumescent fireproof coating |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105694620B (en) | A kind of high solid content water ultra-thin expansion fireproof coating and preparation method thereof | |
CN109370288B (en) | Intumescent water-based fireproof flame-retardant coating for wood material and preparation method thereof | |
CN101857760A (en) | A water-based ultra-thin intumescent steel structure fireproof and anticorrosion coating and preparation method thereof | |
CN106497339B (en) | A kind of power equipment environment-friendly fireproof material and preparation method thereof | |
CN108676427B (en) | A kind of water-based microencapsulated ultra-thin steel structure fireproof coating and preparation method thereof | |
CN101434760A (en) | Transparent halogen-free fire-retardant coating composition | |
CN105778694B (en) | A kind of expansion type facing fire retardant coating | |
CN111662585A (en) | Fireproof coating with heat insulation and preservation performance | |
CN102993835A (en) | Fireproof and high temperature resistant coating | |
CN101497756B (en) | A radiation-curable intumescent transparent flame-retardant coating and its preparation method | |
Zhang et al. | Enhanced flame‐retardant performance of rigid polyurethane foam by using APTES‐MMT and ATH mixed intumescent coatings | |
CN117126585A (en) | High-heat-flow-resistant expansion type fireproof coating and preparation method thereof | |
CN118344783A (en) | A non-expandable epoxy-based porcelain fire-retardant coating material and a preparation method thereof | |
CN108847469A (en) | A kind of lithium battery painting cloth diaphragm flame retardant type ceramic slurry and preparation method thereof | |
CN106497267A (en) | A kind of expanding fire-proof paint and preparation method thereof | |
CN109401406B (en) | Intumescent smoke-suppressing fire retardant for water-based paint and preparation method thereof | |
CN106833194A (en) | A kind of flame-retardant coating material of cable and preparation method thereof | |
CN108384410B (en) | Environment-friendly fireproof coating and preparation method thereof | |
CN118109102A (en) | Ultra-thin solvent-free heat-insulating fireproof flame-retardant coating for aviation aluminum alloy device | |
CN106833259A (en) | A kind of frosting flame retardant coating and preparation method thereof | |
CN116925611B (en) | Fire retardant coating and preparation method thereof | |
CN118956209B (en) | Intumescent flame retardant heat insulating multilayer coating, heat insulating filler and preparation method | |
CN118406422B (en) | Fireproof flame-retardant composite material plate and preparation method thereof | |
CN118165580A (en) | A bio-based intumescent water-based flame-retardant coating with strong adhesion performance and preparation method thereof | |
CN118652533B (en) | A flame retardant composite material and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |