CN106590301A - Antiaging, flame-retardant, expansible-graphite, waterborne and ultrathin steel-structure fireproof coating and preparation method thereof - Google Patents
Antiaging, flame-retardant, expansible-graphite, waterborne and ultrathin steel-structure fireproof coating and preparation method thereof Download PDFInfo
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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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
- C09D133/12—Homopolymers or copolymers of methyl methacrylate
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
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- 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
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1656—Antifouling paints; Underwater paints characterised by the film-forming substance
- C09D5/1662—Synthetic film-forming substance
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- 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
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1687—Use of special additives
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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
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
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- C08L2201/08—Stabilised against heat, light or radiation or oxydation
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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Abstract
The invention discloses antiaging, flame-retardant, expansible-graphite, waterborne and ultrathin steel-structure fireproof coating. The antiaging, flame-retardant, expansible-graphite, waterborne and ultrathin steel-structure fireproof coating is prepared by, by weight, 20-22 parts of ammonium polyphosphate, 7-8 parts of pentaerythritol, 7-8 parts of melamine, 4-5 parts of expansible graphite, 3-3.5 parts of chlorinated paraffin, 23-25 parts of 0.1Mol/L zinc nitrate aqueous solution, 23-25 parts of 0.1Mol/L hexamethylene tetramine aqueous solution, 0.8-1 part of tetraethyl orthosilicate, 1.6-1.8 parts of lithium silicate, an appropriate amount of water, 2.3-2.6 parts of diphenyl dihydroxy silane, 3-4 parts of tetrabutyl titanate, 3-4 parts of potassium fluotitanate and 1.2-1.5 parts of amino silicone. The antiaging, flame-retardant, expansible-graphite, waterborne and ultrathin steel-structure fireproof coating has the advantages that the diphenyl dihydroxy silane and the tetrabutyl titanate are used to perform reaction to tightly combine with the potassium fluotitanate and the amino silicone, the products react and combine with the coating, and accordingly the flame retardance and thermal stability of the coating are increased, the coating is easy to spray and even and compact in coating film, and the anti-aging performance of the coating is also increased.
Description
Technical field
The present invention relates to fireproof coating technical field, more particularly to a kind of aging-resistant flame-proof expansible graphite water super-thin
Fire-resistant coating for steel structure and preparation method thereof.
Background technology
Solvent-borne type super-thin steel structure fireproof coating contains substantial amounts of volatile organic matter(VOC), which is applied and is increasingly subject to
Limit, or even disabled by developed country.Water super-thin steel structure fire-proof paint is reduced using waterborne polymeric as film forming matter
The discharge capacity of VOC, reduces the coating harm to human body and pollution to environment in the links such as production, construction, application, symbol
Energy-saving and emission-reduction, the development trend of environmental protection are closed, is the emphasis of fireproof coating research.This paper is directed to water super-thin steel structure
The fire protecting performance of fireproof coating is poor, expansion multiplying power is low, low expanding layer structural strength, poor water resistance the problems such as deeply ground
Study carefully, and to film forming matter(The tertiary polymer of vinegar)Thermal decomposition process and charcoal forming machine reason, APP to the thermal decomposition of vinegar tertiary polymer
The impact of process is discussed;Nano zirconium dioxide and aqueouss phosphorous polymer are have studied exploratoryly in fireproof coating
Using.Main research work is as follows:(1)Film forming be have studied from the angle of thermal decomposition characteristic, Dynamic Rheological Properties and compound viscosity
Impact of the material to fireproof coating expansible fireproof performance.Result of study shows:Pure third and the storage modulu of cinepazid polymer melt
(G ')More than loss moduluses(G "), based on elasticity flowing, it is combined viscosity high(>1000Pa·s);The G " of the tertiary polymer melt of vinegar
More than G ', based on VISCOUS FLOW, viscosity is combined low(33Pa·s).With heat stability is good, char forming ability strong, compound viscosity
The polymer of low, viscous fluid characteristics is suitable as the film forming matter of fireproof coating, is conducive to expansion and the fire protecting performance of coating
Raising.(2)With the tertiary polymer of vinegar(VAc-VeoVa)As film forming matter, APP/tetramethylolmethane/tripolycyanamide/can be swollen
Swollen graphite(APP/PER/MEL/EG)As Intumescent Retardant System(IFR), have studied IFR and its with VAc-VeoVa with comparing
The impact of Properties of Fire-Proofing Coatings.Orthogonal experiment analysis result directly perceived shows that impact of each component to Properties of Fire-Proofing Coatings is suitable in IFR
Sequence is followed successively by:APP > EG > PER > MEL, optimum proportioning is APP:PER:MEL:EG=22:8:8:4.5.When VAc-VeoVa is used
Measure for 30%, IFR consumptions be 40% when, the fire protecting performance of fire resistant coating is optimal(After burning 30min, steel plate back of the body temperature is 262 DEG C).(3)
Have studied impact of the factors such as composition, granular size and the form of inorganic filler to fireproof coating.TG, capillary rheology test,
The results of study such as fire protecting performance test show:With TiO2/SAp/HNTs(8/1/1)As during inorganic filler, fireproof coating it is anti-
Fiery excellent performance(3327s), expansion multiplying power is higher(28.14), expansion Rotating fields are good, intensity is high.Inorganic filler is by being constrained to
Membrane polymer strand lax and rotate, and APP is reduced on the catalytic dehydration efficiency of PER and VAc-VeoVa to affect to prevent
The expansion multiplying power and fire protecting performance of fiery coating.Simultaneously when viscosity is higher, inorganic filler is difficult to move to expanding layer surface aggregation
Inorganic thermal insulation layer is formed, causes the fire protecting performance of fireproof coating to decline.By formulation optimization, the performance of aqueous fire-proof coating is made by oneself
Famous foreign brand is exceeded.(4)Have studied nano zirconium dioxide(nano-ZrO2)Effect in fireproof coating.Research knot
Fruit shows:Silane coupler γ-methacryloxypropyl trimethoxy silane(Z-6030)Modified nano-ZrO2
There is in VAc-VeoVa emulsions good dispersibility.In the halogen-free flameproof coating without EG, nano-ZrO is added2After expand
Layer no longer has continuous fine and close structure, and structural strength is reduced, and fire protecting performance is with nano-ZrO2Under consumption ground increases on the contrary
Drop.There is halogen fireproof coating containing EG, EG is interspersed in expanding layer, play a part of structural support;ZrO2In expanding layer
In play a part of heat-insulated and prevent thermal oxide from decomposing, the fire prevention time reaches 3837s.XRD results are generated in showing expanding layer
Titanium pyrophosphate(TiP2O7), zirconium pyrophosphate(ZrP2O7)With zirconium pyrophosphate magnesium-titanium solid solution(Ti0.8Zr0.2P2O7).(5)Have studied
Impact of the thermal decomposition process and APP of Vac-VeoVa to VAc-VeoVa thermal decomposition processes.Result of study shows:In air atmosphere
The thermal oxide catabolic process of middle VAc-VeoVa is divided into three phases:(1)Removing acetic acid and tertiary carbon acid groups, generate unsaturated carbon
Chain;(2)The oxidative dehydrogenation of unsaturated carbon chains, cyclisation, aromatisation, generate hexagonal crystal system carbon;(3)The thermal oxide of hexagonal crystal system carbon.
In nitrogen atmosphere, VAc-VeoVa thermal decomposition processes are divided into two stages:(1)Removing acetic acid and tertiary carbon acid groups, generate insatiable hunger
And carbochain;(2)The chain rupture or cyclisation of unsaturated carbon chains, aromatisation, generate hexagonal crystal system carbon.Density functional theory(DFT)Meter
Calculate relation of the removing for competition fracture that result shows versatic acid and acetic acid group in VAc-VeoVa molecules.TG and FTIR results
Show, APP reduces the heat decomposition temperature of VAc-VeoVa, accelerate the removing speed of VAc-VeoVa side-chain radicals.Additionally,
The pendant hydroxyl group reaction that the polyphosphoric acid that APP is thermally decomposed to generate is generated after removing ketenes with VAc-VeoVa molecules generates P-O-C
Key.The product generated after ethylenic unsaturation hydrocarbon aromatizing is connected to become cross-linked network shape structure by P-O-C keys, has charcoal residue
More preferable heat stability.(6)The phosphorous cinepazid polymer P of aqueouss is synthesized(MMA/St/BA/MAA/PAM100), and in this, as
Film forming matter, have studied its application in fireproof coating.Result of study shows, vinyl alkoxy phosphate ester(PAM100)Carry
The high heat stability of polymer, belongs to the condensed phase mechanism of action.Fire protecting performance test result shows, using StA-P1.5 as into
The fire protecting performance of fireproof coating prepared by membrane substance is optimal.Flymn-Wall-Ozawa(FWO)Method and Kissinger-
Akahira-Sunose(KAS)Method result of calculation shows that PAM100 considerably increases the thermal degradation activation energy of polymer, but
Activation energy increasing with PAM100 consumptions and reducing.The mechanism function of polymer thermal decomposition is respectively g(α)=-ln(1-α), f(α)
=1- α, order of reaction n=1, rhermal decomposition rate expression formula are ddtAexpE/RT1.
《The preparation of water super-thin steel structure fire-proof paint and fireproofing function study mechanism》The fireproof coating that one text is obtained
Containing substantial amounts of phosphate group, water absorption rate is big, easily causes coating and metal erosion, expansible graphite and organic macromolecule phase
Capacitive is poor, the insufficient strength of coating, needs to improve, in addition it is also necessary to improve aging resistance, the fire resistance of coating.
The content of the invention
The object of the invention is exactly for the defect for making up prior art, there is provided a kind of aging-resistant flame-proof expansible graphite aqueouss
Super-thin steel structure fire-proof paint and preparation method thereof.
The present invention is achieved by the following technical solutions:
A kind of aging-resistant flame-proof expansible graphite water super-thin steel structure fire-proof paint, is prepared by the raw materials in:
APP 20-22, tetramethylolmethane 7-8, tripolycyanamide 7-8, expansible graphite 4-5, chlorinated paraffin 3-3.5,0.1Mol/L nitre
Sour zinc aqueous solution 23-25,0.1Mol/L hexamethylene tetramine aqueous solution 23-25, tetraethyl orthosilicate 0.8-1, Lithium metasilicate 1.6-
1.8th, appropriate amount of water, methyl methacrylate 42-43, styrene 42-43, butyl acrylate 58-60, methacrylic acid 4-5, ethylene
Base alkyl oxy phosphate ester 1.5-1.8, nonyl phenyl polyethoxy ether 0.3-0.4, dodecylbenzene sodium sulfonate 1.1-1.5, carbon
Sour hydrogen sodium 1.3-1.5, potassium peroxydisulfate 1.2-1.5, appropriate ammonia, hexichol dihydroxy silane 2.3-2.6, butyl titanate 3-4, fluorine titanium
Sour potassium 3-4, amodimethicone 1.2-1.5.
The preparation method of the aging-resistant flame-proof expansible graphite water super-thin steel structure fire-proof paint, including following step
Suddenly:
(1)Expansible graphite, dehydrated alcohol and 12-14 weight portions water are mixed, 45-48 DEG C is heated with stirring in a water bath, plus
Enter ammonia to adjust pH is 8-9, continues stirring 10-15min, then is slowly added dropwise tetraethyl orthosilicate, permanent at 45-48 DEG C after completion of dropping
Warm stirring reaction 4-4.5h, is cooled to room temperature, carry out washing, sucking filtration, drying, obtain modified expansible graphite;
(2)By 0.1Mol/L zinc nitrate aqueous solutions, 0.1Mol/L hexamethylene tetramine aqueous solution, ultrasonic disperse 6-
8min, reacts two hours in 94-97 DEG C of water-bath, obtains slurry;
(3)By methyl methacrylate, styrene, butyl acrylate, methacrylic acid mix homogeneously, mix monomer is obtained, will
During dodecylbenzene sodium sulfonate, sodium bicarbonate add the water of 50-52 weight portions, stir, be heated to 80-83 in a water bath
DEG C, 1/3 potassium peroxydisulfate is added under 240-260rmin stirrings, is stirred 20-23 minutes, then the mixing list of Deca 1/3
Body, is incubated 20-23 minutes, then remaining mix monomer, potassium peroxydisulfate is mixed with the water of 50-52 weight portions and the slurry of stating
Uniformly, it is added dropwise in reactant, then by vinyl alkyl epoxide phosphate ester, nonyl phenyl polyethoxy ether mix homogeneously, Deca
Enter in reactant, dropwise operation is completed in 3-3.2 hours, be cooled to less than 50 DEG C, filter, obtain glue;
(4)Hexichol dihydroxy silane, butyl titanate are mixed, 72-76 DEG C is heated to, 20-25 minutes is ground, is added fluotitanic acid
Potassium, amodimethicone continue grinding 15-18 minutes, obtain mixed material;
(5)The water of 7-8 weight portions is mixed with modified expansible graphite, mixed material, tripolycyanamide, is uniformly dispersed, added
The glue of 30-32 weight portions and other residual componentss, are uniformly dispersed, obtain final product.
It is an advantage of the invention that:The present invention uses zinc nitrate and hexamethylene tetramine reaction to generate the oxidation of Herba Taraxaci shape
Zinc, carries out polyreaction with monomer, improves thermostability, non-oxidizability and the antifouling resistance to water of glue, improves the strong of coating
Degree, fire line, prevent cracking, it is aging, extend service life;Expansible graphite is changed by using tetraethyl orthosilicate
Property so that expansible graphite is improved with the interface interaction of glue, is dispersed in coating, improves intensity and the densification of coating
Property, the hole even compact of expanding layer after being heated, fire protecting performance are improved;Entered by using hexichol dihydroxy silane, butyl titanate
Row reaction, is formed and is combined closely with potassium fluotitanate, amodimethicone, then is combined with coating reaction, improve the anti-flammability of coating with
Heat stability, easily sprays, and film even compact also improves the ageing resistace of coating.
Specific embodiment
A kind of aging-resistant flame-proof expansible graphite water super-thin steel structure fire-proof paint, by following weight portion(Kilogram)'s
Raw material is made:APP 20, tetramethylolmethane 7, tripolycyanamide 7, expansible graphite 4, chlorinated paraffin 3,0.1Mol/L zinc nitrates
Aqueous solution 23,0.1Mol/L hexamethylene tetramines aqueous solution 23, tetraethyl orthosilicate 0.8, Lithium metasilicate 1.6, appropriate amount of water, methyl-prop
E pioic acid methyl ester 42, styrene 42, butyl acrylate 58, methacrylic acid 4, vinyl alkyl epoxide phosphate ester 1.5, nonyl phenyl
Polyethoxy ether 0.3, dodecylbenzene sodium sulfonate 1.1, sodium bicarbonate 1.3, potassium peroxydisulfate 1.2, appropriate ammonia, hexichol dihydroxy silicon
Alkane 2.3, butyl titanate 3, potassium fluotitanate 3, amodimethicone 1.2.
The preparation method of the aging-resistant flame-proof expansible graphite water super-thin steel structure fire-proof paint, including following step
Suddenly:
(1)Expansible graphite, dehydrated alcohol and 12 weight portion water are mixed, 45 DEG C are heated with stirring in a water bath, ammonia is added
It is 8 to adjust pH, continues stirring 10min, then is slowly added dropwise tetraethyl orthosilicate, in 45 DEG C of constant temperature stirring reactions 4h after completion of dropping,
Be cooled to room temperature, carry out washing, sucking filtration, drying, obtain modified expansible graphite;
(2)By 0.1Mol/L zinc nitrate aqueous solutions, 0.1Mol/L hexamethylene tetramine aqueous solution, ultrasonic disperse 6min,
Two hours are reacted in 94 DEG C of water-baths, slurry is obtained;
(3)By methyl methacrylate, styrene, butyl acrylate, methacrylic acid mix homogeneously, mix monomer is obtained, will
During dodecylbenzene sodium sulfonate, sodium bicarbonate add the water of 50 weight portions, stir, be heated to 80 DEG C in a water bath,
1/3 potassium peroxydisulfate is added under 240rmin stirrings, is stirred 20 minutes, then the mix monomer of Deca 1/3,20 minutes are incubated,
Again remaining mix monomer, potassium peroxydisulfate are mixed homogeneously with the water of 50 weight portions and the slurry of stating, are added dropwise in reactant,
Again by vinyl alkyl epoxide phosphate ester, nonyl phenyl polyethoxy ether mix homogeneously, it is added dropwise in reactant, dropwise operation exists
Complete in 3 hours, be cooled to less than 50 DEG C, filter, obtain glue;
(4)Hexichol dihydroxy silane, butyl titanate are mixed, 72 DEG C are heated to, is ground 20 minutes, is added potassium fluotitanate, ammonia
Base silicone continues grinding 15 minutes, obtains mixed material;
(5)The water of 7 weight portions is mixed with modified expansible graphite, mixed material, tripolycyanamide, is uniformly dispersed, add 30
The glue of weight portion and other residual componentss, are uniformly dispersed, obtain final product.
Experimental data:
The fireproof coating of embodiment is placed into 24h, is brushed on clean steel plate, was brushed once every 8 hours, coating thickness is
1mm, is dried 20d under aeration-drying environment, and film water absorption rate is 9.5%, and the decomposition temperature in nitrogen atmosphere is 476 DEG C, aobvious
The coating of micro- Microscopic observation Jing high-temperature expansions contains the uniform cell of 3-4 microns.
Claims (2)
1. a kind of aging-resistant flame-proof expansible graphite water super-thin steel structure fire-proof paint, it is characterised in that:By following weight
The raw material of part is made:APP 20-22, tetramethylolmethane 7-8, tripolycyanamide 7-8, expansible graphite 4-5, chlorinated paraffin 3-
3.5th, 0.1Mol/L zinc nitrate aqueous solutions 23-25,0.1Mol/L hexamethylene tetramines aqueous solution 23-25, tetraethyl orthosilicate
0.8-1, Lithium metasilicate 1.6-1.8, appropriate amount of water, methyl methacrylate 42-43, styrene 42-43, butyl acrylate 58-60, first
Base acrylic acid 4-5, vinyl alkyl epoxide phosphate ester 1.5-1.8, nonyl phenyl polyethoxy ether 0.3-0.4, detergent alkylate
Sodium sulfonate 1.1-1.5, sodium bicarbonate 1.3-1.5, potassium peroxydisulfate 1.2-1.5, appropriate ammonia, hexichol dihydroxy silane 2.3-2.6, titanium
Four butyl ester 3-4 of acid, potassium fluotitanate 3-4, amodimethicone 1.2-1.5.
2. the preparation side of aging-resistant flame-proof expansible graphite water super-thin steel structure fire-proof paint according to claim 1
Method, it is characterised in that comprise the following steps:
(1)Expansible graphite, dehydrated alcohol and 12-14 weight portions water are mixed, 45-48 DEG C is heated with stirring in a water bath, plus
Enter ammonia to adjust pH is 8-9, continues stirring 10-15min, then is slowly added dropwise tetraethyl orthosilicate, permanent at 45-48 DEG C after completion of dropping
Warm stirring reaction 4-4.5h, is cooled to room temperature, carry out washing, sucking filtration, drying, obtain modified expansible graphite;
(2)By 0.1Mol/L zinc nitrate aqueous solutions, 0.1Mol/L hexamethylene tetramine aqueous solution, ultrasonic disperse 6-
8min, reacts two hours in 94-97 DEG C of water-bath, obtains slurry;
(3)By methyl methacrylate, styrene, butyl acrylate, methacrylic acid mix homogeneously, mix monomer is obtained, will
During dodecylbenzene sodium sulfonate, sodium bicarbonate add the water of 50-52 weight portions, stir, be heated to 80-83 in a water bath
DEG C, 1/3 potassium peroxydisulfate is added under 240-260rmin stirrings, is stirred 20-23 minutes, then the mixing list of Deca 1/3
Body, is incubated 20-23 minutes, then remaining mix monomer, potassium peroxydisulfate is mixed with the water of 50-52 weight portions and the slurry of stating
Uniformly, it is added dropwise in reactant, then by vinyl alkyl epoxide phosphate ester, nonyl phenyl polyethoxy ether mix homogeneously, Deca
Enter in reactant, dropwise operation is completed in 3-3.2 hours, be cooled to less than 50 DEG C, filter, obtain glue;
(4)Hexichol dihydroxy silane, butyl titanate are mixed, 72-76 DEG C is heated to, 20-25 minutes is ground, is added fluotitanic acid
Potassium, amodimethicone continue grinding 15-18 minutes, obtain mixed material;
(5)The water of 7-8 weight portions is mixed with modified expansible graphite, mixed material, tripolycyanamide, is uniformly dispersed, added
The glue of 30-32 weight portions and other residual componentss, are uniformly dispersed, obtain final product.
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Cited By (4)
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CN108441043A (en) * | 2018-03-12 | 2018-08-24 | 武汉工程大学 | A kind of self-repair type intumescent fire-retardant coating material and the preparation method and application thereof |
CN108951271A (en) * | 2018-08-17 | 2018-12-07 | 枣庄市天龙纸业有限公司 | A kind of novel environment friendly facing paper and preparation method thereof |
CN112500653A (en) * | 2020-11-24 | 2021-03-16 | 台春节能新材料(苏州)有限公司 | Preparation method of high-strength xps extrusion molding insulation board |
CN118127713A (en) * | 2024-05-07 | 2024-06-04 | 金华市华尔汽车饰件有限公司 | Automobile sunshade flame-retardant non-woven fabric and processing method thereof |
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CN118127713A (en) * | 2024-05-07 | 2024-06-04 | 金华市华尔汽车饰件有限公司 | Automobile sunshade flame-retardant non-woven fabric and processing method thereof |
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