CN108219180A - A kind of preparation method of fire-fighting foam battenboard - Google Patents
A kind of preparation method of fire-fighting foam battenboard Download PDFInfo
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- CN108219180A CN108219180A CN201711245721.9A CN201711245721A CN108219180A CN 108219180 A CN108219180 A CN 108219180A CN 201711245721 A CN201711245721 A CN 201711245721A CN 108219180 A CN108219180 A CN 108219180A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/02—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by the reacting monomers or modifying agents during the preparation or modification of macromolecules
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/08—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the cooling method
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/10—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the pressing technique, e.g. using action of vacuum or fluid pressure
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/12—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by using adhesives
- B32B37/1284—Application of adhesive
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- 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
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/10—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
- C08J3/247—Heating methods
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0066—Use of inorganic compounding ingredients
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/30—Properties of the layers or laminate having particular thermal properties
- B32B2307/304—Insulating
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/30—Properties of the layers or laminate having particular thermal properties
- B32B2307/306—Resistant to heat
- B32B2307/3065—Flame resistant or retardant, fire resistant or retardant
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2397/00—Characterised by the use of lignin-containing materials
- C08J2397/02—Lignocellulosic material, e.g. wood, straw or bagasse
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2433/00—Characterised by the use of homopolymers or 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 of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2433/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2461/00—Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
- C08J2461/04—Condensation polymers of aldehydes or ketones with phenols only
- C08J2461/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2471/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2471/02—Polyalkylene oxides
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- 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
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- Polymers & Plastics (AREA)
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- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
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- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
Abstract
The invention discloses a kind of preparation methods of fire-fighting foam battenboard, belong to building material technical field.The present invention reacts wood powder, phenol, polyethylene glycol and sulfuric acid heating stirring, then adds in formalin, paraformaldehyde, emulsifier, silane coupling agent and the reaction of carbomer heating stirring, adds demulsifier, after being stirred, adjusts pH, obtain wood powder liquefied resin;The nitrogen containing trimethyl aluminium is passed through into wood powder liquefied resin, obtains wood powder liquefied resin foam;From top to bottom according to the adhesive wood powder liquefied resin adhesive surface lining sequence assembly of adhesive non-woven fabrics 1 of foam 2 of adhesive non-woven fabrics 2 of surface lining 1, blank is obtained;Blank is cold-pressed, is divided to get fire-fighting foam battenboard.Fire-fighting foam battenboard provided by the invention has excellent mechanical property, heat-insulating property and flame retardant property.
Description
Technical field
The invention discloses a kind of preparation methods of fire-fighting foam battenboard, belong to building material technical field.
Background technology
Foamed material prepared by lignocellulose liquefied resin has the characteristics that recyclable regenerative, light, specific strength is high,
It can be applied to the building structural materials field of heat-insulated, sound insulation, heat preservation.With the pressure implementation of energy-saving and emission-reduction and building energy-saving standard
Raising, Poplar Powder is prepared into the foamed material of high-strength light for liquid substance by solid liquefaction, it is high-quality, low for developing
The green building of cost is of great significance with light wall material.
The organic foam wall New Building Materials being presently used in building mainly have polyurethane foam, phenol formaldehyde foam, gather
Styrenic foams etc..Wherein, polystyrene foam is a kind of light weight, and the internal foamed material for carrying cavity hole-closing structure,
It is widely used in building as energy-saving wall insulation material, but since polystyrene flame retardant property is poor, limit it
Development and application.Polyurethane foam material is that thermal conductivity factor is minimum in current all building materials, the highest thermal insulation material of thermal resistance value, but
It is also required to can be only achieved the fire protection requirement of construction material by certain flame retardant treatment.Phenol formaldehyde foam has excellent heat preservation and prevents
Fiery performance, and with low cigarette, nontoxic characteristic, it is referred to as " the emerging thermal insulation material of the third generation ", the quilt in many architectural designs
As heat-insulating heat-preserving material.Inorganic light wall material includes foam concrete, plasterboard, fiber cement board etc., wherein, stone
The proportion that cream plate occupies in light wall material is larger, various in style.
Construction material single varieties on the market at present, be largely by the materials such as color steel sheet, stainless steel plate, aluminium sheet with
Phenol formaldehyde foam is combined.But at present traditional foam battenboard also there are heat-insulating property, mechanical property and flame retardant property not
The problem of good, therefore also need to study it.
Invention content
The present invention solves the technical problem of:For conventional foam battenboard heat-insulating property, mechanical property and fire-retardant
The problem of performance is bad provides a kind of preparation method of fire-fighting foam battenboard.
In order to solve the above-mentioned technical problem, the technical solution adopted in the present invention is:
A kind of preparation method of fire-fighting foam battenboard, specific preparation process are as follows:
(1)It counts in parts by weight, takes 30~50 parts of wood powders, 20~30 parts of phenol, 20~30 parts of polyethylene glycol, 5~6 parts of sulfuric acid,
15~20 parts of formalins, 15~20 parts of paraformaldehydes, 8~10 parts of emulsifiers, 5~6 parts of silane coupling agents, 8~10 parts of card waves
Nurse, 5~6 parts of demulsifiers;
(2)By wood powder, phenol, polyethylene glycol and the reaction of sulfuric acid heating stirring, formalin, paraformaldehyde, emulsification are then added in
Agent, silane coupling agent and the reaction of carbomer heating stirring, add demulsifier, after being stirred, adjust pH, obtain wood powder liquefaction tree
Fat;
(3)The nitrogen containing trimethyl aluminium is passed through into wood powder liquefied resin, obtains wood powder liquefied resin foam;
(4)From top to bottom according to-No. 1 adhesive of surface lining-adhesive of non-woven fabrics-2-wood powder liquefied resin-No. 2 glue of foam
Glutinous agent-adhesive of non-woven fabrics-1-surface lining sequence assembly, obtains blank;
(5)Blank is cold-pressed, is cut to get fire-fighting foam battenboard.
Step(1)The wood powder is pine powder, ash powder, any one in birch powder or joss powder.
Step(1)The emulsifier is emulsifier op-10, neopelex, is appointed in Tween-60 or Si Pan -80
Meaning is a kind of.
Step(1)The carbomer is CARBOPOL 971, any one in CARBOPOL 974P or carbomer940.
Step(2)The silane coupling agent is silane resin acceptor kh-550, silane coupling agent KH-560 or silane coupling agent
Any one in KH-570.
Step(2)The demulsifier is benzene sulfonic acid, benzene sulfonic acid sodium salt, fourth sulfonic acid, fourth sodium sulfonate, oxalic acid, sodium oxalate or lemon
Any one in acid.
Step(3)The volume content for being passed through trimethyl aluminium in the nitrogen containing trimethyl aluminium is 5~8%.
Step(4)The surface lining is wood-plastic board, any one in polyvinyl chloride buckle or medium density fibre board (MDF).
Step(4)No. 1 adhesive is wood moulding glue, any one in white glue with vinyl or E-44 epoxide-resin glues.
Step(4)No. 2 adhesives are all-purpose adhesive, any one in acrylic based emulsion or YH-T806 special gelatins.
The beneficial effects of the invention are as follows:
Technical solution of the present invention, first, phenol are mixed with polyethylene glycol, are liquefied through sulfuric acid catalysis, so with formalin and more
Polyformaldehyde reaction generation phenolic resin, the phenolic resin of generation form water-in-oil emulsion so that generation through emulsifier
Phenolic resin is dispersed in system, adds in demulsifier afterwards so that and the phenolic resin after demulsification is preferably penetrated into wood powder,
Secondly, by the stifling of the nitrogen containing trimethyl aluminium, trimethyl aluminium reacts generation methane and aluminium hydroxide with the water in system, and
A large amount of heat is released, the methane gas of generation plays good foaming effect, promotes the hole in wood powder liquefied resin foam
Gap rate, promotes the heat-insulating property and sound insulation value of system, in addition, being added to carbomer in system, contains in carbomer molecular structure
There are a large amount of carboxyls, the aluminium hydroxide of part generation can be reacted with carbomer, make part carboxylic ions in carbomer, another part
Aluminium hydroxide is thermally decomposed to generate aluminium oxide, and the aluminium oxide of generation is adsorbed by the carboxyl of unionization in carbomer, due to card wave
Part carboxylic ions in nurse molecular structure generate negative electrical charge, and repulsive interaction causes carbomer molecule between negative electrical charge
Structure good dispersion in system is unfolded, so that the aluminium oxide of generation is uniformly dispersed being filled in system, reinforcement
It is mechanical property, meanwhile, the flame retardant property of system is promoted, furthermore, a large amount of heat of trimethyl aluminium and water reaction generation can promote
Make the further crosslinking curing of phenolic resin, further enhance the mechanical property of system.
Specific embodiment
It counts in parts by weight, takes 30~50 parts of wood powders, 20~30 parts of phenol, 20~30 parts of polyethylene glycol, 5~6 parts of quality
Score be 60~70% sulfuric acid, 15~20 parts of formalins, 15~20 parts of paraformaldehydes, 8~10 parts of emulsifiers, 5~6 parts of silicon
Alkane coupling agent, 8~10 parts of carbomers, 5~6 parts of demulsifiers;By wood powder, phenol, polyethylene glycol and mass fraction are 60~70%
Sulfuric acid is placed in three-necked flask, and three-necked flask then is placed in digital display tests the speed in constant temperature blender with magnetic force, in temperature be 75~85
DEG C, under the conditions of rotating speed is 300~400r/min, heating stirring reacts 1~2h, and it is 20 to add in mass fraction then to three-necked flask
~35% formalin, paraformaldehyde, emulsifier, silane coupling agent and carbomer, in temperature be 75~85 DEG C, 500~
Under the conditions of 600r/min, heating stirring reacts 1~2h, then adds in demulsifier to three-necked flask, is 75~85 DEG C in temperature, turns
Speed is under the conditions of 700~800r/min, heating stirring mixes 30~50min, is then added dropwise with rubber head dropper into three-necked flask
The ammonium hydroxide that mass fraction is 20~30% adjusts pH to 5.2~5.5, obtains wood powder liquefied resin;Then wood powder liquefied resin is placed in
In fluidized-bed reactor, and the nitrogen containing trimethyl aluminium is passed through as 60~80mL/min into reactor using rate, be continually fed into
After 30~50min, wood powder liquefied resin foam is obtained;From top to bottom according to-No. 1 adhesive of surface lining-gluing of non-woven fabrics -2
Agent-- No. 2 adhesives of wood powder liquefied resin foam-adhesive of non-woven fabrics-1-surface lining sequence assembly, obtains blank;And by base
Material is placed in cold press, is 0.1~0.2MPa in pressure, is cold-pressed 5~6h, cuts to get fire-fighting foam battenboard.The wood powder
For pine powder, ash powder, any one in birch powder or joss powder.The emulsifier be emulsifier op-10, detergent alkylate
Any one in sodium sulfonate, Tween-60 or Si Pan -80.The carbomer is CARBOPOL 971, CARBOPOL 974P or carbomer
Any one in 934P.The silane coupling agent be silane resin acceptor kh-550, silane coupling agent KH-560 or silane coupled
Any one in agent KH-570.The demulsifier be benzene sulfonic acid, benzene sulfonic acid sodium salt, fourth sulfonic acid, fourth sodium sulfonate, oxalic acid, sodium oxalate
Or any one in citric acid.The surface lining is wood-plastic board, arbitrary in polyvinyl chloride buckle or medium density fibre board (MDF)
It is a kind of.No. 2 adhesives are all-purpose adhesive, any one in acrylic based emulsion or YH-T806 special gelatins.It is described to contain trimethyl
Trimethyl aluminium volume content is 5~8% in the nitrogen of aluminium.
Example 1
It counts in parts by weight, takes 50 parts of wood powders, 30 parts of phenol, 30 parts of polyethylene glycol, the sulfuric acid that 6 parts of mass fractions are 70%, 20 parts
Formalin, 20 parts of paraformaldehydes, 10 parts of emulsifiers, 6 parts of silane coupling agents, 10 parts of carbomers, 6 parts of demulsifiers;By wood powder, benzene
The sulfuric acid that phenol, polyethylene glycol and mass fraction are 70% is placed in three-necked flask, and three-necked flask then is placed in digital display tests the speed constant temperature
It it is 85 DEG C in temperature, under the conditions of rotating speed is 400r/min, heating stirring reacts 2h, then to three-necked flask in magnetic stirring apparatus
Add in the formalin that mass fraction is 35%, paraformaldehyde, emulsifier, silane coupling agent and carbomer, in temperature be 85 DEG C,
Under the conditions of 600r/min, heating stirring reaction 2h then adds in demulsifier to three-necked flask, is 85 DEG C in temperature, rotating speed is
Under the conditions of 800r/min, heating stirring mixing 50min, it is 30% that mass fraction is then added dropwise into three-necked flask with rubber head dropper
Ammonium hydroxide adjust pH to 5.5, obtain wood powder liquefied resin;Then wood powder liquefied resin is placed in fluidized-bed reactor, and with speed
Rate is passed through the nitrogen containing trimethyl aluminium into reactor for 80mL/min, after being continually fed into 50min, obtains wood powder liquefied resin bubble
Foam;From top to bottom according to-No. 1 adhesive of surface lining-adhesive of non-woven fabrics-2-wood powder liquefied resin-No. 2 gluings of foam
Agent-the adhesive of non-woven fabrics-1-surface lining sequence assembly, obtains blank;And blank is placed in cold press, it is in pressure
0.2MPa is cold-pressed 6h, cuts to get fire-fighting foam battenboard.The wood powder is pine powder.The emulsifier for polyoxyethylene nonylphenol ether-
10.The carbomer is CARBOPOL 971.The silane coupling agent is silane resin acceptor kh-550.The demulsifier is benzene sulphur
Acid.The surface lining is wood-plastic board.No. 2 adhesives are all-purpose adhesive.Trimethyl aluminium in the nitrogen containing trimethyl aluminium
Volume content is 8%.
Example 2
It counts in parts by weight, takes 50 parts of wood powders, 30 parts of phenol, 30 parts of polyethylene glycol, the sulfuric acid that 6 parts of mass fractions are 70%, 20 parts
Formalin, 20 parts of paraformaldehydes, 10 parts of emulsifiers, 6 parts of silane coupling agents, 6 parts of demulsifiers;By wood powder, phenol, polyethylene glycol
It is placed in three-necked flask with sulfuric acid that mass fraction is 70%, three-necked flask then is placed in digital display tests the speed constant temperature blender with magnetic force
In, it is 85 DEG C in temperature, under the conditions of rotating speed is 400r/min, heating stirring reaction 2h adds in quality point then to three-necked flask
Number for 35% formalin, paraformaldehyde, emulsifier, silane coupling agent, in temperature be 85 DEG C, under the conditions of 600r/min, heating
2h is stirred to react, then adds in demulsifier to three-necked flask, is 85 DEG C in temperature, under the conditions of rotating speed is 800r/min, heating is stirred
Mixing 50min is mixed, the ammonium hydroxide that mass fraction is 30% is then added dropwise into three-necked flask with rubber head dropper adjusts pH to 5.5, obtains wooden
Powder liquefied resin;Then wood powder liquefied resin is placed in fluidized-bed reactor, and is 80mL/min into reactor using rate
The nitrogen containing trimethyl aluminium is passed through, after being continually fed into 50min, obtains wood powder liquefied resin foam;From top to bottom according to surface lining-
No. 1 adhesive-adhesive of non-woven fabrics-2-- No. 2 adhesives of the wood powder liquefied resin foam-adhesive of non-woven fabrics-1-veneer material
Material sequence assembly, obtains blank;And blank is placed in cold press, it is 0.2MPa in pressure, is cold-pressed 6h, cuts and steeped to get fire prevention
Foam battenboard.The wood powder is pine powder.The emulsifier is emulsifier op-10.The silane coupling agent is silane coupling agent
KH-550.The demulsifier is benzene sulfonic acid.The surface lining is wood-plastic board.No. 2 adhesives are all-purpose adhesive.It is described to contain three
Trimethyl aluminium volume content is 8% in the nitrogen of aluminium methyl.
Example 3
It counts in parts by weight, takes 50 parts of wood powders, 30 parts of phenol, 30 parts of polyethylene glycol, the sulfuric acid that 6 parts of mass fractions are 70%, 20 parts
Formalin, 20 parts of paraformaldehydes, 10 parts of emulsifiers, 6 parts of silane coupling agents, 10 parts of carbomers, 6 parts of demulsifiers;By wood powder, benzene
The sulfuric acid that phenol, polyethylene glycol and mass fraction are 70% is placed in three-necked flask, and three-necked flask then is placed in digital display tests the speed constant temperature
It it is 85 DEG C in temperature, under the conditions of rotating speed is 400r/min, heating stirring reacts 2h, then to three-necked flask in magnetic stirring apparatus
Add in the formalin that mass fraction is 35%, paraformaldehyde, emulsifier, silane coupling agent and carbomer, in temperature be 85 DEG C,
Under the conditions of 600r/min, heating stirring reaction 2h then adds in demulsifier to three-necked flask, is 85 DEG C in temperature, rotating speed is
Under the conditions of 800r/min, heating stirring mixing 50min, it is 30% that mass fraction is then added dropwise into three-necked flask with rubber head dropper
Ammonium hydroxide adjust pH to 5.5, obtain wood powder liquefied resin;Then wood powder liquefied resin is placed in fluidized-bed reactor, obtains wood powder
Liquefied resin foam;It is steeped from top to bottom according to-No. 1 adhesive of surface lining-adhesive of non-woven fabrics-2-wood powder liquefied resin
- No. 2 adhesives of the foam-adhesive of non-woven fabrics-1-surface lining sequence assembly, obtain blank;And blank is placed in cold press, in
Pressure is 0.2MPa, is cold-pressed 6h, cuts to get fire-fighting foam battenboard.The wood powder is pine powder.The emulsifier is emulsification
Agent OP-10.The carbomer is CARBOPOL 971.The silane coupling agent is silane resin acceptor kh-550.The demulsifier is
Benzene sulfonic acid.The surface lining is wood-plastic board.No. 2 adhesives are all-purpose adhesive.
Comparative example:The foam battenboard of Changzhou Engineering Co., Ltd production.
1 to 3 gained foam battenboard of example and comparative example product are subjected to performance detection, specific detection method is as follows:
Using the omnipotent mechanics machine of UTM-5000 microcomputer controlled electronics, mechanical property is measured with reference to GB/T8813 and GB/T8812
Energy;Using T322 type thermal conductivity measuring apparatus, thermal conductivity factor is measured with reference to GB/T10294;With reference to GB/T2406 determination limit oxygen
Index.Specific testing result is as shown in table 1:
Table 1
Detection content | Example 1 | Example 2 | Example 3 | Comparative example |
Compressive strength/MPa | 0.70 | 0.63 | 0.67 | 0.55 |
Bending strength/MPa | 14.3 | 9.8 | 8.7 | 6.4 |
Thermal conductivity factor/W/(m·K) | 0.030 | 0.059 | 0.063 | 0.140 |
Limit oxygen index/% | 43.5 | 36.2 | 37.1 | 26.8 |
By 1 testing result of table it is found that present invention gained fire-fighting foam battenboard has excellent mechanical property, heat-insulating property and resistance
Fire performance.
Claims (10)
1. a kind of preparation method of fire-fighting foam battenboard, it is characterised in that:Specific preparation process is as follows:
(1)It counts in parts by weight, takes 30~50 parts of wood powders, 20~30 parts of phenol, 20~30 parts of polyethylene glycol, 5~6 parts of sulfuric acid,
15~20 parts of formalins, 15~20 parts of paraformaldehydes, 8~10 parts of emulsifiers, 5~6 parts of silane coupling agents, 8~10 parts of card waves
Nurse, 5~6 parts of demulsifiers;
(2)By wood powder, phenol, polyethylene glycol and the reaction of sulfuric acid heating stirring, formalin, paraformaldehyde, emulsification are then added in
Agent, silane coupling agent and the reaction of carbomer heating stirring, add demulsifier, after being stirred, adjust pH, obtain wood powder liquefaction tree
Fat;
(3)The nitrogen containing trimethyl aluminium is passed through into wood powder liquefied resin, obtains wood powder liquefied resin foam;
(4)From top to bottom according to-No. 1 adhesive of surface lining-adhesive of non-woven fabrics-2-wood powder liquefied resin-No. 2 glue of foam
Glutinous agent-adhesive of non-woven fabrics-1-surface lining sequence assembly, obtains blank;
(5)Blank is cold-pressed, is cut to get fire-fighting foam battenboard.
2. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(1)The wood
Powder is pine powder, ash powder, any one in birch powder or joss powder.
3. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(1)The breast
Agent is emulsifier op-10, neopelex, any one in Tween-60 or Si Pan -80.
4. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(1)The card
Wave nurse is CARBOPOL 971, any one in CARBOPOL 974P or carbomer940.
5. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(2)The silicon
Alkane coupling agent is silane resin acceptor kh-550, any one in silane coupling agent KH-560 or Silane coupling reagent KH-570.
6. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(2)It is described broken
Emulsion is benzene sulfonic acid, benzene sulfonic acid sodium salt, fourth sulfonic acid, fourth sodium sulfonate, oxalic acid, any one in sodium oxalate or citric acid.
7. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(3)It is described logical
The volume content for entering trimethyl aluminium in the nitrogen containing trimethyl aluminium is 5~8%.
8. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(4)The patch
Plane materiel material is wood-plastic board, any one in polyvinyl chloride buckle or medium density fibre board (MDF).
9. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(4)Described No. 1
Adhesive is wood moulding glue, any one in white glue with vinyl or E-44 epoxide-resin glues.
10. a kind of preparation method of fire-fighting foam battenboard according to claim 1, it is characterised in that:Step(4)Described 2
Number adhesive is all-purpose adhesive, any one in acrylic based emulsion or YH-T806 special gelatins.
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CN201711245721.9A CN108219180A (en) | 2017-12-01 | 2017-12-01 | A kind of preparation method of fire-fighting foam battenboard |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN113736277A (en) * | 2021-08-30 | 2021-12-03 | 上海纤苏新材料科技有限公司 | Fiber-plastic sandwich board and preparation method thereof |
CN116905124A (en) * | 2023-07-05 | 2023-10-20 | 南京林业大学 | Preparation method of bio-based liquefied resin nano composite fiber membrane material |
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Publication number | Priority date | Publication date | Assignee | Title |
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WO2010018142A1 (en) * | 2008-08-15 | 2010-02-18 | Basf Se | Lightweight wood materials with good mechanical properties |
CN104211885A (en) * | 2013-05-31 | 2014-12-17 | 常州市乾翔新材料科技有限公司 | Low-temperature expandable phenolic resin and method of employing same to prepare phenolic foam |
CN105462163A (en) * | 2015-12-28 | 2016-04-06 | 南京林业大学 | Preparation method of composite sandwiched biomass foam partition wall material |
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2017
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2010018142A1 (en) * | 2008-08-15 | 2010-02-18 | Basf Se | Lightweight wood materials with good mechanical properties |
CN104211885A (en) * | 2013-05-31 | 2014-12-17 | 常州市乾翔新材料科技有限公司 | Low-temperature expandable phenolic resin and method of employing same to prepare phenolic foam |
CN105462163A (en) * | 2015-12-28 | 2016-04-06 | 南京林业大学 | Preparation method of composite sandwiched biomass foam partition wall material |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113736277A (en) * | 2021-08-30 | 2021-12-03 | 上海纤苏新材料科技有限公司 | Fiber-plastic sandwich board and preparation method thereof |
CN116905124A (en) * | 2023-07-05 | 2023-10-20 | 南京林业大学 | Preparation method of bio-based liquefied resin nano composite fiber membrane material |
CN116905124B (en) * | 2023-07-05 | 2024-02-27 | 南京林业大学 | Preparation method of bio-based liquefied resin nano composite fiber membrane material |
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Application publication date: 20180629 |