CN111334111A - Expansion type fireproof and explosion-proof coating and preparation method thereof - Google Patents
Expansion type fireproof and explosion-proof coating and preparation method thereof Download PDFInfo
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- CN111334111A CN111334111A CN202010201261.5A CN202010201261A CN111334111A CN 111334111 A CN111334111 A CN 111334111A CN 202010201261 A CN202010201261 A CN 202010201261A CN 111334111 A CN111334111 A CN 111334111A
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- 238000000576 coating method Methods 0.000 title claims abstract description 51
- 239000011248 coating agent Substances 0.000 title claims abstract description 46
- 238000002360 preparation method Methods 0.000 title claims abstract description 24
- 229920001451 polypropylene glycol Polymers 0.000 claims abstract description 19
- 239000002994 raw material Substances 0.000 claims abstract description 18
- 238000010438 heat treatment Methods 0.000 claims abstract description 17
- 239000004970 Chain extender Substances 0.000 claims abstract description 15
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 15
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 14
- 239000006254 rheological additive Substances 0.000 claims abstract description 13
- 239000003063 flame retardant Substances 0.000 claims abstract description 11
- 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 10
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 9
- 239000012948 isocyanate Substances 0.000 claims abstract description 9
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 9
- 238000003756 stirring Methods 0.000 claims description 51
- 238000006243 chemical reaction Methods 0.000 claims description 35
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 28
- 229920001276 ammonium polyphosphate Polymers 0.000 claims description 25
- 239000004114 Ammonium polyphosphate Substances 0.000 claims description 23
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 238000001816 cooling Methods 0.000 claims description 12
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical group C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 11
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 10
- 238000007599 discharging Methods 0.000 claims description 10
- 229920000570 polyether Polymers 0.000 claims description 10
- 238000004880 explosion Methods 0.000 claims description 8
- 230000018044 dehydration Effects 0.000 claims description 6
- 238000006297 dehydration reaction Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- PISLZQACAJMAIO-UHFFFAOYSA-N 2,4-diethyl-6-methylbenzene-1,3-diamine Chemical compound CCC1=CC(C)=C(N)C(CC)=C1N PISLZQACAJMAIO-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- YZZTZUHVGICSCS-UHFFFAOYSA-N n-butan-2-yl-4-[[4-(butan-2-ylamino)phenyl]methyl]aniline Chemical compound C1=CC(NC(C)CC)=CC=C1CC1=CC=C(NC(C)CC)C=C1 YZZTZUHVGICSCS-UHFFFAOYSA-N 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- VIOMIGLBMQVNLY-UHFFFAOYSA-N 4-[(4-amino-2-chloro-3,5-diethylphenyl)methyl]-3-chloro-2,6-diethylaniline Chemical compound CCC1=C(N)C(CC)=CC(CC=2C(=C(CC)C(N)=C(CC)C=2)Cl)=C1Cl VIOMIGLBMQVNLY-UHFFFAOYSA-N 0.000 claims 1
- BXQLKGJCLJZZOP-UHFFFAOYSA-N methylsulfanylmethane;toluene Chemical compound CSC.CC1=CC=CC=C1 BXQLKGJCLJZZOP-UHFFFAOYSA-N 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 abstract description 4
- 239000006261 foam material Substances 0.000 abstract description 3
- 238000005507 spraying Methods 0.000 description 12
- 239000004148 curcumin Substances 0.000 description 8
- 229920002396 Polyurea Polymers 0.000 description 7
- 235000019504 cigarettes Nutrition 0.000 description 7
- 230000006378 damage Effects 0.000 description 5
- 238000001514 detection method Methods 0.000 description 4
- 238000011049 filling Methods 0.000 description 4
- GUSFEBGYPWJUSS-UHFFFAOYSA-N pentaazanium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O GUSFEBGYPWJUSS-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000013530 defoamer Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229920000137 polyphosphoric acid Polymers 0.000 description 2
- AOFIWCXMXPVSAZ-UHFFFAOYSA-N 4-methyl-2,6-bis(methylsulfanyl)benzene-1,3-diamine Chemical compound CSC1=CC(C)=C(N)C(SC)=C1N AOFIWCXMXPVSAZ-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000012824 chemical production Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- -1 lipid compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Classifications
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- 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
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3225—Polyamines
- C08G18/3237—Polyamines aromatic
- C08G18/324—Polyamines aromatic containing only one aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3802—Low-molecular-weight compounds having heteroatoms other than oxygen having halogens
- C08G18/3814—Polyamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3855—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur
- C08G18/3863—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing groups having sulfur atoms between two carbon atoms, the sulfur atoms being directly linked to carbon atoms or other sulfur atoms
- C08G18/3865—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing groups having sulfur atoms between two carbon atoms, the sulfur atoms being directly linked to carbon atoms or other sulfur atoms containing groups having one sulfur atom between two carbon atoms
- C08G18/3868—Low-molecular-weight compounds having heteroatoms other than oxygen having sulfur containing groups having sulfur atoms between two carbon atoms, the sulfur atoms being directly linked to carbon atoms or other sulfur atoms containing groups having one sulfur atom between two carbon atoms the sulfur atom belonging to a sulfide group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/482—Mixtures of polyethers containing at least one polyether containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4825—Polyethers containing two hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5024—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6681—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38
- C08G18/6685—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3225 or polyamines of C08G18/38
-
- 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/08—Polyurethanes from polyethers
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
Abstract
The invention belongs to the technical field of fireproof coatings, and particularly discloses an intumescent fireproof and explosion-proof coating and a preparation method thereof, wherein the coating comprises a component A and a component B, wherein the component A comprises the following raw materials in percentage by weight: 40-60% of isocyanate, 30-55% of polypropylene glycol, 1-3% of rheological additive and 1-7% of flame retardant; the component B comprises the following raw materials in percentage by weight: 10-35% of curing agent, 3-10% of chain extender, 45-90% of polyetheramine, 1-6% of defoaming agent and 1-5% of viscosity reducer. The coating made of the coating has high extension, high tearing and flame retardant performance on the premise that the strength of the coating is not reduced, and the flame retardant is decomposed by heating in the continuous combustion process to form a foam material.
Description
Technical Field
The invention relates to the technical field of fireproof coatings, in particular to an expansion type fireproof and explosion-proof coating and a preparation method thereof.
Background
In petrochemical industry, refining and chemical production enterprises, buildings such as machine cabinet rooms, control rooms, monitoring rooms and the like in the area adjacent to a production device face the damage of explosion hidden danger (60-150 kpa of anti-explosion impact load), in order to avoid the damage of explosion to the buildings and prevent the injury of personnel, safety assessment needs to be carried out on the buildings, then the frames of the buildings are strengthened, and anti-explosion coatings are sprayed on the wall surfaces of the buildings, so that the aims of preventing the damage of the explosion hidden danger and protecting the safety of the personnel are fulfilled. In the prior art, the fireproof and explosion-proof coating taking polyurea as a main component has excellent tear resistance and impact resistance; however, polyurea has the problem of insufficient temperature resistance, so that the fireproof and explosion-proof coating made of the polyurea cannot resist the high-temperature environment of continuous combustion, and cannot effectively protect bearing parts such as concrete, steel and the like in a factory building for a long time.
Disclosure of Invention
In view of the defects of the prior art, the invention aims to provide an intumescent fire-proof and explosion-proof coating and a preparation method thereof, which are used for solving the problems of insufficient high-temperature resistance and flame retardance of the fire-proof and explosion-proof coating in the prior art.
In order to achieve the above objects and other related objects, a first aspect of the present invention provides an intumescent fire and explosion protection coating, which comprises a component a and a component B, wherein the component a comprises the following raw materials by weight: 40-60% of isocyanate, 30-55% of polypropylene glycol, 1-3% of rheological additive and 1-7% of flame retardant; the component B comprises the following raw materials in percentage by weight: 10-35% of curing agent, 3-10% of chain extender, 45-90% of polyetheramine, 1-6% of defoaming agent and 1-5% of viscosity reducer.
Further, when in use, the component A and the component B are uniformly mixed according to the proportion of 1:1 and then are sprayed to prepare a coating.
Optionally, the polyetheramine is selected from at least one of polyetheramine D2000 and polyetheramine T5000; preferably, the polyetheramine comprises polyetheramine D2000 and polyetheramine T5000, and the component B comprises polyetheramine D200040-70% and polyetheramine T50005-20% in percentage by weight.
Optionally, the isocyanate is diphenylmethane diisocyanate selected from at least one of MDI-50 and MDI-100.
Optionally, the polypropylene glycol is selected from at least one of PPG200, PPG600, PPG1000, PPG2000, PPG 4000.
Optionally, the flame retardant is ammonium polyphosphate, and the ammonium polyphosphate is selected from at least one of APP I and APP II. Ammonium polyphosphate is decomposed under heating to generate polyphosphoric acid, the polyphosphoric acid reacts with polyether amine to generate polyphosphoester, then partial lipid compounds are decomposed to form carbide, and carbonaceous foam is formed in the decomposition process to cover the substrate, so that the aim of isolating flame is fulfilled. Wherein APP I initiates decomposition reaction at 150 ℃; APP II initiates decomposition reaction at 250 ℃. And calculating and checking the specific addition proportion according to the design.
Optionally, the curing agent is selected from at least one of diethyltoluenediamine, dimethylthiotoluenediamine.
Optionally, the chain extender is at least one of 4,4 '-bis (sec-butylamino) -diphenylmethane, 4' -methylene-bis (3-chloro-2, 6-diethylaniline).
Optionally, the viscosity reducer is selected from at least one of a high molecular polymer and a polyurethane compound.
The second aspect of the invention provides a preparation method of the intumescent fire-proof and explosion-proof coating, which comprises the following steps:
(1) the preparation method of the component A comprises the following steps: adding polypropylene glycol into a nitrogen-protected reaction kettle according to the raw material ratio, stirring under a vacuum condition, heating for dehydration, then removing vacuum, cooling to below 60 ℃, adding isocyanate, heating and stirring for reaction, after the reaction is completed, cooling to below 60 ℃, adding a rheological additive, stirring uniformly, adding ammonium polyphosphate, stirring uniformly, and discharging to obtain a component A;
(2) the preparation method of the component B comprises the following steps: adding the polyether amine, the curing agent and the chain extender into a reaction kettle according to the raw material ratio, charging nitrogen for protection, uniformly stirring, controlling the temperature in the kettle to be less than 40 ℃, reducing the stirring speed to 150-.
Optionally, in the step (1), the vacuum degree is controlled to be-0.095 MPa to-0.06 MPa.
Alternatively, in the step (1), the temperature of stirring, heating and dehydrating the polypropylene glycol in the reaction kettle is controlled to be 90-110 ℃.
Optionally, in the step (1), isocyanate is added into the reaction kettle, stirred uniformly, and heated to 70-90 ℃ for reaction for 1-3 hours.
As mentioned above, the intumescent fire-proof and explosion-proof coating and the preparation method thereof have the following beneficial effects:
the invention provides a fire-proof and explosion-proof formula for adding an intumescent flame retardant into a coating, and the coating prepared from the coating can have high extension, high tearing and flame retardant properties on the premise of ensuring that the strength of the coating is not reduced; in the continuous combustion process, the flame retardant in the components is heated and decomposed to form a foam material, and the foam material has low thermal conductivity and can effectively isolate the base material, so that the damage to buildings or bearing steel caused by continuous high-temperature combustion and explosion impact is avoided.
Detailed Description
The embodiments of the present invention are described below with reference to specific embodiments, and other advantages and effects of the present invention will be easily understood by those skilled in the art from the disclosure of the present specification. The invention is capable of other and different embodiments and of being practiced or of being carried out in various ways, and its several details are capable of modification in various respects, all without departing from the spirit and scope of the present invention.
Example 1
The formula of the intumescent fire-proof and explosion-proof coating of the embodiment is as follows:
the component A comprises:
raw materials and model | In percentage by weight | Manufacturer of the product |
Diphenylmethane diisocyanate MDI-50 | 40 | Wanhua cigarette holder |
Polypropylene glycol PPG-1000 | 52 | Dongda blue star |
Modified polyurea rheological additive W3420 | 3 | Shi shou material |
Ammonium polyphosphate APP 428 | 5 | Kelaien |
And B component:
raw material | In percentage by weight | Manufacturer of the product |
Curing agent E100 | 25 | American jabao |
Chain extender W6200 | 8 | Wanhua cigarette holder |
Polyetheramine D2000 | 48 | Hensmei food |
Polyether amine T5000 | 17 | Hensmei food |
Water-based antifoaming agent W107 | 1 | Shi shou material |
Viscosity reducer 9860 | 1 | Shi shou material |
The preparation method comprises the following steps:
1. the preparation method of the component A comprises the following steps: adding 40 parts of polypropylene glycol PPG-1000 into a reaction kettle with nitrogen protection, stirring at the vacuum degree of-0.095 MPa at the stirring speed of 600 rpm, and heating at 90 ℃ for dehydration; and then removing vacuum, filling nitrogen for protection, cooling to below 60 ℃, adding 40 parts of diphenylmethane diisocyanate MDI-50, uniformly stirring, heating to 90 ℃ for reaction for 1 hour, cooling to below 60 ℃ after complete reaction, adding 3 parts of rheological additive W3420, uniformly stirring, adding 5 parts of ammonium polyphosphate APP 428, uniformly stirring, and discharging to obtain the component A.
2. The preparation method of the component B comprises the following steps: sequentially adding 17 parts of polyetheramine T5000 and 48 parts of polyetheramine D2000 into a reaction kettle, uniformly stirring, adding 25 parts of curing agent E100 and 8 parts of chain extender W6200, introducing nitrogen for protection while stirring, and reducing the stirring speed to 300 revolutions per minute after the temperature in the kettle is controlled to be less than 40 ℃; and then uniformly mixing 1 part of the water-based defoaming agent W107 and 1 part of the viscosity reducer 9860, adding into the reaction kettle, continuously stirring for 30 minutes, and discharging to obtain the component B.
Spraying by using a Kyowa Pick brand JHPK-BPT1 spraying device according to the proportion of A to B to 1, and spraying to prepare a coating. Through detection, the tensile strength of the coating with the thickness of 2mm is 17 MPa; tear strength 96N/mm.
Example 2
The formula of the intumescent fire-proof and explosion-proof coating of the embodiment is as follows:
the component A comprises:
raw materials and model | In percentage by weight | Manufacturer of the product |
Diphenylmethane diisocyanate MDI-50 | 50 | Wanhua cigarette holder |
Polypropylene glycol PPG-6000 | 40 | Dongda blue star |
Modified polyurea rheological additive W3420 | 3 | Shi shou material |
Ammonium polyphosphate APP 422 | 7 | Kelaien |
And B component:
raw material | In percentage by weight | Manufacturer of the product |
Curing agent E100 | 25 | American jabao |
Chain extender W6200 | 8 | Wanhua cigarette holder |
Polyetheramine D2000 | 42 | Hensmei food |
Polyether amine T5000 | 20 | Hensmei food |
Aqueous defoamer W108 | 3 | Shi shou material |
Viscosity reducer 9870 | 2 | Shi shou material |
The preparation method comprises the following steps:
1. the preparation method of the component A comprises the following steps: adding 40 parts of polypropylene glycol PPG-1000 into a reaction kettle with nitrogen protection, stirring at the vacuum degree of-0.095 MPa at the stirring speed of 600 rpm, and heating at 90 ℃ for dehydration; and then removing vacuum, filling nitrogen for protection, cooling to below 60 ℃, adding 50 parts of diphenylmethane diisocyanate (MDI-50), uniformly stirring, heating to 90 ℃ for reaction for 1 hour, cooling to below 60 ℃ after complete reaction, adding 3 parts of rheological additive W3420, uniformly stirring, adding 7 parts of ammonium polyphosphate (APP) 422, uniformly stirring, and discharging to obtain the component A.
2. The preparation method of the component B comprises the following steps: sequentially adding 20 parts of polyetheramine T5000 and 42 parts of polyetheramine D2000 into a reaction kettle, uniformly stirring, adding 25 parts of curing agent E100 and 8 parts of chain extender W6200, introducing nitrogen for protection while stirring, and reducing the stirring speed to 300 revolutions per minute after the temperature in the kettle is controlled to be less than 40 ℃; and then uniformly mixing 3 parts of water-based defoaming agent W108 and 2 parts of viscosity reducer 9870, adding into the reaction kettle, continuously stirring for 30 minutes, and discharging to obtain the component B.
Spraying by using a Kyowa Pick brand JHPK-BPT1 spraying device according to the proportion of A to B to 1, and spraying to prepare a coating. Through detection, the tensile strength of the coating with the thickness of 2mm is 20 MPa; tear strength 101N/mm.
Example 3
The formula of the intumescent fire-proof and explosion-proof coating of the embodiment is as follows:
the component A comprises:
raw materials and model | In percentage by weight | Manufacturer of the product |
Diphenylmethane diisocyanate MDI-50 | 60 | Wanhua cigarette holder |
Polypropylene glycol PPG-6000 | 30 | Dongda blue star |
Modified polyurea rheological additive W3420 | 3 | Shi shou material |
Ammonium polyphosphate APP 422 | 7 | Kelaien |
And B component:
raw material | In percentage by weight | Manufacturer of the product |
Curing agent E100 | 10 | American jabao |
Chain extender MCDEA | 3 | Zhang hong Yarui chemical industry |
Polyetheramine D2000 | 70 | Hensmei food |
Polyether amine T5000 | 7 | Hensmei food |
Aqueous defoamer W108 | 5 | Shi shou material |
Viscosity reducer 9870 | 5 | Shi shou material |
The preparation method comprises the following steps:
1. the preparation method of the component A comprises the following steps: adding 30 parts of polypropylene glycol PPG-1000 into a reaction kettle with nitrogen protection, stirring at the vacuum degree of-0.095 MPa at the stirring speed of 600 rpm, and heating at 100 ℃ for dehydration; and then removing vacuum, filling nitrogen for protection, cooling to below 60 ℃, adding 70 parts of diphenylmethane diisocyanate MDI-50, uniformly stirring, heating to 80 ℃ for reaction for 2 hours, cooling to below 60 ℃ after complete reaction, adding 3 parts of rheological additive W3420, uniformly stirring, adding 7 parts of ammonium polyphosphate APP 422, uniformly stirring, and discharging to obtain the component A.
2. The preparation method of the component B comprises the following steps: sequentially adding 7 parts of polyetheramine T5000 and 70 parts of polyetheramine D2000 into a reaction kettle, uniformly stirring, adding 10 parts of curing agent E100 and 3 parts of chain extender MCDEA, introducing nitrogen for protection while stirring, and reducing the stirring speed to 200 revolutions per minute after the temperature in the kettle is controlled to be less than 40 ℃; and then, uniformly mixing 5 parts of the aqueous defoaming agent W108 and 5 parts of the viscosity reducer 9870, adding into the reaction kettle, continuously stirring for 30 minutes, and discharging to obtain the component B.
Spraying by using a Kyowa Pick brand JHPK-BPT1 spraying device according to the proportion of A to B to 1, and spraying to prepare a coating. Through detection, the tensile strength of the coating with the thickness of 2mm is 18 MPa; tear strength 100N/mm.
Example 4
The formula of the intumescent fire-proof and explosion-proof coating of the embodiment is as follows:
the component A comprises:
raw materials and model | In percentage by weight | Manufacturer of the product |
Diphenylmethane diisocyanate MDI-50 | 40 | Wanhua cigarette holder |
Polypropylene glycol PPG-6000 | 55 | Dongda blue star |
Modified polyurea rheological additive W3420 | 1 | Shi shou material |
Ammonium polyphosphate APP 428 | 4 | Kelaien |
And B component:
raw material | In percentage by weight | Manufacturer of the product |
Curing agent E100 | 35 | American jabao |
Chain extender W6200 | 10 | Wanhua cigarette holder |
Polyetheramine D2000 | 40 | Hensmei food |
Polyether amine T5000 | 10 | Hensmei food |
Aqueous defoamer W108 | 2 | Shi shou material |
Viscosity reducer 9870 | 3 | Shi shou material |
The preparation method comprises the following steps:
1. the preparation method of the component A comprises the following steps: adding 55 parts of polypropylene glycol PPG-1000 into a reaction kettle with nitrogen protection, stirring at the vacuum degree of-0.095 MPa at the stirring speed of 600 rpm, and heating at 100 ℃ for dehydration; and then removing vacuum, filling nitrogen for protection, cooling to below 60 ℃, adding 40 parts of diphenylmethane diisocyanate MDI-50, uniformly stirring, heating to 70 ℃ for reaction for 3 hours, cooling to below 60 ℃ after complete reaction, adding 1 part of rheological additive W3420, uniformly stirring, adding 4 parts of ammonium polyphosphate APP 422, uniformly stirring, and discharging to obtain the component A.
2. The preparation method of the component B comprises the following steps: sequentially adding 10 parts of polyetheramine T5000 and 40 parts of polyetheramine D2000 into a reaction kettle, uniformly stirring, adding 35 parts of curing agent E100 and 10 parts of chain extender MCDEA, introducing nitrogen for protection while stirring, and reducing the stirring speed to 150 revolutions per minute after the temperature in the kettle is controlled to be less than 40 ℃; then 2 parts of water-based defoaming agent W108 and 3 parts of viscosity reducer 9870 are uniformly mixed and then added into the reaction kettle, and the mixture is continuously stirred for 40 minutes and then discharged, thus obtaining the component B.
Spraying by using a Kyowa Pick brand JHPK-BPT1 spraying device according to the proportion of A to B to 1, and spraying to prepare a coating. Through detection, the tensile strength of the coating with the thickness of 2mm is 20 MPa; tear strength 101N/mm.
Comparative example 1
Compared with the common organic ultrathin type expansion fireproof coating CN100432167C, the coating prepared in the embodiments 1 and 3 of the invention has the following performance comparison under the identical experimental conditions (refer to GB14907-2018 Steel structure fireproof coating):
comparative example 2
Compared with the inorganic intumescent fire-retardant coating CN107216693A, the coatings prepared in the examples 2 and 4 of the invention have the following performance comparisons under the same experimental conditions:
as can be seen from the above examples and comparative examples, the tensile strength, tear strength and fire resistance of the coating of the present invention are superior to those of the existing intumescent coatings.
The foregoing embodiments are merely illustrative of the principles and utilities of the present invention and are not intended to limit the invention. Any person skilled in the art can modify or change the above-mentioned embodiments without departing from the spirit and scope of the present invention. Accordingly, it is intended that all equivalent modifications or changes which can be made by those skilled in the art without departing from the spirit and technical spirit of the present invention be covered by the claims of the present invention.
Claims (10)
1. The intumescent fire-proof and explosion-proof coating is characterized by comprising a component A and a component B, wherein the component A comprises the following raw materials in percentage by weight: 40-60% of isocyanate, 30-55% of polypropylene glycol, 1-3% of rheological additive and 1-7% of flame retardant; the component B comprises the following raw materials in percentage by weight: 10-35% of curing agent, 3-10% of chain extender, 45-90% of polyetheramine, 1-6% of defoaming agent and 1-5% of viscosity reducer.
2. The coating of claim 1, wherein: when in use, the component A and the component B are uniformly mixed according to the proportion of 1:1 and then are sprayed to prepare the coating.
3. The coating of claim 1, wherein: the polyether amine is at least one selected from polyether amine D2000 and polyether amine T5000; preferably, the polyetheramine comprises polyetheramine D2000 and polyetheramine T5000, and the component B comprises polyetheramine D200040-70% and polyetheramine T50005-20% in percentage by weight.
4. The coating of claim 1, wherein: the isocyanate is diphenylmethane diisocyanate, and the diphenylmethane diisocyanate is at least one selected from MDI-50 and MDI-100.
5. The coating of claim 1, wherein: the polypropylene glycol is at least one selected from PPG200, PPG600, PPG1000, PPG2000 and PPG 4000.
6. The coating of claim 1, wherein: the flame retardant is ammonium polyphosphate, and the ammonium polyphosphate is selected from at least one of APP I and APP II.
7. The intumescent coating of claim 1, characterized in that: the curing agent is at least one of diethyl toluene diamine and dimethyl sulfur toluene diamine;
and/or the chain extender is at least one of 4,4 '-bis (sec-butylamino) -diphenylmethane and 4,4' -methylene-bis (3-chloro-2, 6-diethylaniline);
and/or the viscosity reducer is selected from at least one of high molecular polymer and polyurethane compound.
8. A process for the preparation of an intumescent fire and explosion protection coating as claimed in any of claims 1 to 7, characterized in that: the method comprises the following steps:
(1) the preparation method for preparing the component A comprises the following steps: adding polypropylene glycol into a nitrogen-protected reaction kettle according to the raw material ratio, stirring under a vacuum condition, heating for dehydration, then removing vacuum, cooling to below 60 ℃, adding isocyanate, heating and stirring for reaction, after the reaction is completed, cooling to below 60 ℃, adding a rheological additive, stirring uniformly, adding ammonium polyphosphate, stirring uniformly, and discharging to obtain a component A;
(2) the preparation method for preparing the component B comprises the following steps: adding the polyether amine, the curing agent and the chain extender into a reaction kettle according to the raw material ratio, charging nitrogen for protection, uniformly stirring, controlling the temperature in the kettle to be less than 40 ℃, reducing the stirring speed to 150 plus materials for 300 r/min, then adding the defoaming agent and the viscosity reducer into the reaction kettle, continuously stirring for 30 min, uniformly discharging, and obtaining the component B.
9. The method of claim 8, wherein: in the step (1), the vacuum degree is controlled between-0.095 MPa and-0.06 MPa.
10. The method of claim 8, wherein: in the step (1), the temperature of stirring, heating and dehydrating the polypropylene glycol in a reaction kettle is controlled to be 90-100 ℃;
and/or in the step (1), adding isocyanate into the reaction kettle, uniformly stirring, and heating to 70-90 ℃ for reaction for 1-3 hours.
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