WO2019054795A1 - Mousse de phénol et procédé de fabrication associé - Google Patents

Mousse de phénol et procédé de fabrication associé Download PDF

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Publication number
WO2019054795A1
WO2019054795A1 PCT/KR2018/010839 KR2018010839W WO2019054795A1 WO 2019054795 A1 WO2019054795 A1 WO 2019054795A1 KR 2018010839 W KR2018010839 W KR 2018010839W WO 2019054795 A1 WO2019054795 A1 WO 2019054795A1
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WIPO (PCT)
Prior art keywords
flame retardant
weight
foam
tank
surfactant
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PCT/KR2018/010839
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English (en)
Korean (ko)
Inventor
박건표
강길호
김명희
지승욱
박인성
배성재
하혜민
김도훈
Original Assignee
주식회사 엘지하우시스
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Application filed by 주식회사 엘지하우시스 filed Critical 주식회사 엘지하우시스
Priority to JP2020515194A priority Critical patent/JP6957745B2/ja
Priority to CN201880057392.1A priority patent/CN111051406B/zh
Publication of WO2019054795A1 publication Critical patent/WO2019054795A1/fr

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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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34—Auxiliary operations
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34—Auxiliary operations
    • B29C44/3442—Mixing, kneading or conveying the foamable material
    • 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
    • C08J3/20—Compounding polymers with additives, e.g. colouring
    • C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
    • 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
    • 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
    • C08J9/0014—Use of organic additives
    • C08J9/0038—Use of organic additives containing phosphorus
    • 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
    • C08J9/22—After-treatment of expandable particles; Forming foamed products
    • 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
    • C08K5/00—Use of organic ingredients
    • C08K5/49—Phosphorus-containing compounds

Definitions

  • the present invention relates to a phenol foam and a method for producing the same, and more particularly, to a phenol foam and a phenol foam which are capable of simultaneously achieving a heat insulating property and a flame retardancy which are mutually correlated with each other by uniformly distributing flame retardant in the phenol foam, And a manufacturing method thereof.
  • Insulation is an essential material used to prevent energy loss in buildings. Since the importance of green growth is being emphasized all over the world due to global warming, insulation is becoming important to minimize energy loss.
  • the method of building insulation is changing from insulation to external insulation, and the thickness of insulation also continues to increase.
  • thermosetting foam insulator expanded polystyrene foam (EPS) insulator, extruded polystyrene foam (XPS) insulator, and vacuum insulator are conventionally used as a heat insulator.
  • EPS expanded polystyrene foam
  • XPS extruded polystyrene foam
  • vacuum insulator vacuum insulator
  • thermosetting foam insulation is widely used because it has the most excellent heat insulation property except for the vacuum insulation material in existing materials.
  • Korean Patent Publication No. 10-2013-0063903 discloses an environment- Form. ≪ / RTI >
  • the above-mentioned phenol foam is an organic material and has a problem of flame retardancy.
  • the relevant regulations concerning flame retardancy of the heat insulating material have been strengthened and the thickness of the heat insulating material has been continuously increased. Therefore, there is a growing need for a heat insulating material having excellent flame retardancy.
  • Patent Document 1 KR 10-2013-0063903 A (2013.6.17)
  • the present invention provides a phenolic foam having a thermal conductivity of less than 0.021 W / mK and a heat release of 10.0 MJ / m 2 (5 minutes) or less.
  • the present invention also provides a process for producing the phenolic foam, comprising the steps of: (1) preparing a subject tank, a hardener tank, a liquid composite flame retardant tank and a blowing agent tank; (2) feeding the subject, the curing agent, the liquid composite flame retardant and the foaming agent from the subject tank, the curing agent tank, the liquid composite flame retardant tank and the foaming agent tank to a high-speed stirrer through a pipe; (3) injecting the foamed phenolic foam composition into a mold and performing foam molding; and (3) subjecting the foamed phenol foam composition to a phenol foam having a thermal conductivity of less than 0.021 W / mK and a heat release of 10.0 MJ / m 2 Of the present invention.
  • the phenol foam of the present invention has the effect of uniformly distributing the flame retardant in the phenol foam and improving the quality stability of the heat insulating property and the flame resistance, so that the heat insulating property and the flame resistance which are mutually related to each other can be realized.
  • the liquid composite flame retardant obtained by liquefying the composite flame retardant is mixed with the subject in a high-speed stirrer without mixing the composite flame retardant with the subject in advance, This has the effect of preventing the clogging of the pipe when the mixture of the high viscosity flame retardant and the flame retardant is transferred to the high-speed stirrer.
  • FIG. 1 is a schematic view of an apparatus for preparing a phenolic foam of the present invention.
  • FIG. 2 is a schematic view of a conventional manufacturing facility for a phenolic foam.
  • the present invention relates to a phenolic foam having a thermal conductivity of less than 0.021 W / mK and a heat release of less than 10.0 MJ / m 2 (5 minutes).
  • the phenolic foam may be a phenol resin, a surfactant, a polyol compound, an inorganic flame retardant, and an organic flame retardant.
  • the phenolic foam may comprise 50-70 wt% of a phenolic resin, 1-10 wt% of a surfactant, 0.1-10 wt% of a polyol compound, 1-20 wt% of an inorganic flame retardant, and 0.1-10 wt% of an organic flame retardant.
  • the phenolic resin may be a resol type phenol resin (hereinafter referred to as "resol resin") synthesized by catalysis of an alkali metal hydroxide or an alkaline earth metal hydroxide, or a novolak type phenol resin synthesized by an acid catalyst, Benzyl ether type phenol resin synthesized by resin, lead naphthenate or the like.
  • an additive such as urea may be added during the polymerization of the phenolic resin, if necessary.
  • the components may be mixed in an amount of 1-10 parts by weight, or 2-7 parts by weight, based on 100 parts by weight of the phenol resin.
  • the phenolic resin may be contained in the phenol foam in an amount of 50-70% by weight or 55-65% by weight. By including the phenolic resin in the above range, the phenolic foam can realize excellent physical properties.
  • the surfactant may be a positive, cationic, anionic or nonionic surfactant.
  • amphoteric surfactant for example, alanine, dodecyldi (aminoethyl) glycine, di (octylaminoethyl) glycine, N-alkyl-N, N-dimethylammonium betaine and the like can be used.
  • cationic surfactant examples include amine salt type surfactants such as alkylamine salts, aminoalcohol fatty acid derivatives, polyamine fatty acid derivatives and imidazoline, alkyltrimethylammonium salts, dialkyldimethylammonium salts, alkyne dimethylbenzylammonium salts, Quaternary ammonium salt type surfactants such as benzyltrimethylammonium chloride, benzyltrimethylammonium chloride, benzyltrimethylammonium chloride, benzyltrimethylammonium bromide, and the like.
  • amine salt type surfactants such as alkylamine salts, aminoalcohol fatty acid derivatives, polyamine fatty acid derivatives and imidazoline, alkyltrimethylammonium salts, dialkyldimethylammonium salts, alkyne dimethylbenzylammonium salts, Quaternary ammonium salt type surfactants such as benzyltrimethylammonium
  • anionic surfactant examples include alkyl benzene sulfonate, a-olefin sulfonate, polyoxyethylene alkyl ether acetate salt surfactant, and phosphoric acid ester.
  • nonionic surfactant examples include a polyoxyethylene alkyl ether surfactant, a polyoxyethylene alkyl phenyl ether surfactant, and an acetylene glycol surfactant.
  • nonionic surfactants are preferred because they have excellent defoaming performance.
  • Particularly preferred nonionic surfactants include SURFYNOL series having an acetylenic ethoxylated diol structure, TERGITOL series having a polyethylene oxide or polypropylene oxide structure, polyoxyethylene sorbitan fatty acid ester acid ester) structure and the like can be used.
  • the surfactant may be contained in the phenol foam in an amount of 1-10% by weight or 3-7% by weight.
  • the polyol compound may use at least one selected from a polyester polyol, a polyether polyol and a polymer-dispersed polyol.
  • the polyester polyol is a compound having a terminal hydroxyl group obtained by polycondensation of a polyfunctional carboxylic acid and a polyfunctional hydroxy compound.
  • a polyfunctional carboxylic acid adipic acid, phthalic acid, succinic acid, azelaic acid, sebacic acid, etc.
  • the multifunctional hydroxy compound include glycols such as ethylene glycol, propylene glycol, butanediol, diethylene glycol and the like; Polyhydric alcohols such as glycerin, trimethylol propane, pentaerythritol and the like can be used.
  • the polyether polyol is a polyether polyol obtained by adding an alkylene oxide such as ethylene oxide, propylene oxide or the like to a glycol such as ethylene glycol, propylene glycol or the like; Triols such as glycerin, trimethylol propane and the like; Polyfunctional polyols such as pentaerythritol, sorbitol, sucrose and the like; Ammonia, triethanolamine, ethylenediamine, diethylenetriamine, aminoethylpiperazine, aniline, and the like.
  • the polymer-dispersed polyol may be obtained by mixing a polyether polyol and an ethylenically unsaturated monomer, optionally adding a chain transfer agent, a dispersion stabilizer, and the like, and subjecting the ethylenically unsaturated monomer to radical polymerization in the presence of a radical initiator.
  • ethylenically unsaturated monomers include monomers containing cyano groups such as acrylonitrile, methacrylonitrile and the like; Acrylates such as methyl (meth) acrylate, butyl (meth) acrylate, stearyl (meth) acrylate, hydroxyalkyl (meth) acrylates such as hydroxyethyl (meth) acrylate, (Meth) acrylate, dimethylaminopropyl (meth) acrylate and the like; Monomers containing carboxyl groups such as acrylic acid, methacrylic acid, itaconic acid, maleic acid, fumaric acid and the like; Monomers containing acid anhydrides such as maleic anhydride, itaconic anhydride and the like; Hydrocarbon compounds such as butadiene, isoprene, 1,4-pentadiene and the like; Aromatic hydrocarbon compounds such as styrene, a-methylstyrene, phenyls
  • the polyol compound may be contained in the phenol foam in an amount of 0.1-10 wt% or 0.1-5 wt%. When the polyol compound is contained in the above range, the flame retardant can be uniformly distributed in the phenol foam.
  • the inorganic flame retardant may be at least one selected from metal hydroxide flame retardants, boron flame retardants, antimony oxide flame retardants, and other inorganic materials.
  • the metal hydroxide-based flame retardant may be at least one selected from magnesium hydroxide, aluminum hydroxide, barium hydroxide, and calcium hydroxide.
  • the boron-based flame retardant may be at least one selected from calcium borate and zinc borate.
  • the antimony oxide flame retardant may be at least one selected from antimony trioxide and antimony pentoxide.
  • the other inorganic material may be at least one selected from talc, mica, vollastonite, titanium dioxide, barium sulfate, expanded graphite, and calcium carbonate.
  • the inorganic flame retardant may be a metal hydroxide which has a small amount of fuming during combustion and emits water (H 2 O) at a high temperature.
  • the inorganic flame retardant may be contained in the phenol foam in an amount of 1-20 wt% or 5-15 wt%.
  • the phenol foam of the present invention can simultaneously realize the heat insulating property and the flame retardancy which are mutually related to each other.
  • the organic flame retardant may be at least one selected from a halogen-based flame retardant, a phosphorus-based flame retardant, and a melamine-based flame retardant.
  • halogen-based flame retardant at least one selected from decabromodiphenyloxide and octabromodiphenyloxide may be used.
  • the phosphorus flame retardant may be selected from the group consisting of trimethyl phosphate (TMP), triethyl phosphate (TEP), triphenyl phosphate (TPP), trisylenyl phosphate (TXP), tributyl Phosphoric acid esters such as tributyl phosphate (TBP), tricresyl phosphate (TCP), and cresyl diphenyl phosphate (CDP), tris- (2-chloroethyl) chloroethyl phosphate, TCEP, Tris- (1-chloro-2-propyl) phosphate, TCPP, Tris (1,3-dichloro-2-propyl) phosphate Phosphoric acid-based, polyunsaturated phosphoric acid based ones such as polychlorophosphonate and ammonium polyphosphate (APP), and the like, and halogen-containing organophosphoric acid based ones such as - (1, 3-dichloro
  • the melamine flame retardant may be at least one selected from melamine cyanurate, melamine phosphate, melamine polyphosphate, melamine borate and melamine sulfate.
  • the organic flame retardant may be, for example, a phosphorus-based flame retardant that forms a char upon combustion.
  • the organic flame retardant may be contained in the phenol foam in an amount of 0.1-10 wt% or 0.1-5 wt%. Since the organic flame retardant is included in the above range, the phenol foam of the present invention can simultaneously realize the heat insulating property and the flame resistance which are in conflict with each other.
  • the weight ratio of the inorganic flame retardant to the organic flame retardant in the phenolic foam of the present invention may be 4-7: 1.
  • the cost of the organic flame retardant is relatively high and the cost is increased.
  • the inorganic flame retarder is used in excess of the above range, the heat insulating property and the flame retardancy which are in conflict with each other can not be simultaneously realized. .
  • the phenolic foam may further contain a curing agent.
  • the curing agent may be at least one selected from the group consisting of inorganic acids such as phosphoric acid and sulfuric acid, and organic acids such as benzenesulfonic acid, ethylbenzenesulfonic acid, para toluenesulfonic acid, xylenesulfonic acid, naphtholsulfonic acid and phenolsulfonic acid, and the content thereof is not limited.
  • the foaming agent may further contain a foaming agent.
  • the blowing agent is inexpensive and is a hydrocarbon blowing agent and may be one kind selected from pentane, isopentane and cyclopentane, but the content thereof is not limited.
  • Thermal conductivity of the phenolic foam of the present invention can be up to less than 0.021W / mk or 0.020W / mk, heat radiation amount can be less than or equal to 10.0 MJ / m 2 (5 min) or less, or 9.8MJ / m 2 (5 minutes).
  • the compressive strength of the phenolic foam of the present invention may be 140-190 kPa or 150-180 kPa.
  • the oxygen index (LOI) of the phenolic foam of the present invention may be 35% or more or 38% or more, the density may be 38-50 kg / m 3 or 42-45 kg / m 3 , and the closed cell ratio may be 80% Or 87% or more.
  • the present invention also relates to a process for producing the phenolic foam.
  • the process for preparing the phenolic foam of the present invention comprises
  • FIG. 1 is a schematic view of a production facility for a phenol foam having a thermal conductivity of less than 0.021 W / mK and a heat release of 10.0 MJ / m 2 (5 minutes) or less.
  • the subject included in the subject tank 10 may include a phenol resin and a surfactant.
  • the content of the surfactant contained in the subject tank 10 may be 0.5-10 parts by weight and 1-5 parts by weight with respect to 100 parts by weight of the phenol resin.
  • the amount is less than the above range, the compatibility between the materials is lowered, the bubbles of the foamed cells are large and the closed cell ratio is low, and when the above range is exceeded, the hardness of the phenol foam is lowered and the physical properties are lowered.
  • the subject may further comprise a nucleating agent or neutralizing agent.
  • the nucleating agent is used for controlling the surface tension and suppressing an increase in thermal conductivity due to the addition of the flame retardant, and a silane-based compound or a siloxane-based compound can be used.
  • the nucleating agent may be contained in an amount of 1-5 parts by weight based on 100 parts by weight of the subject. When the amount is less than the above range, the effect of the use of the nucleating agent is insignificant, and when the above range is exceeded, the durability such as the compressive strength of the foam is lowered.
  • the neutralizing agent may be at least one selected from the group consisting of metal hydrates, metal oxides, and metal carbonates for adjusting the pH of the phenol foam.
  • the neutralizing agent may be included in an amount of 1-10 parts by weight based on 100 parts by weight of the subject. If the amount is less than the above range, the effect of neutralization is insignificant, and when the above range is exceeded, the physical properties of the foam are lowered.
  • the curing agent contained in the curing agent tank 20 is the same as the curing agent contained in the phenol foam described above, and repeated description is omitted.
  • the liquid composite flame retardant contained in the liquid composite flame retardant tank 30 may include 100-400 parts by weight or 200-300 parts by weight of a composite flame retardant composed of an inorganic flame retardant and an organic flame retardant, based on 100 parts by weight of a solution containing a surfactant and a polyol compound can do.
  • a composite flame retardant composed of an inorganic flame retardant and an organic flame retardant, based on 100 parts by weight of a solution containing a surfactant and a polyol compound can do.
  • the amount of the composite flame retardant is less than 100 parts by weight, the flame retardant effect is insufficient.
  • the amount exceeds 400 parts by weight the viscosity of the solution increases, and when the mixture is mixed with a subject, the dispersibility of the flame retardant decreases, It is preferable that the pipe for conveying the liquid composite flame retardant is clogged, and the pipe is included within the above range.
  • the surfactant may include 50-70 wt% or 60-65 wt% of the surfactant, and 30-50 wt% or 35-40 wt% of the polyol compound.
  • the surfactant and the polyol compound should be contained within the above range within the above-mentioned range, so that the viscosity of the composite flame retardant is minimized while mixing with the composite flame retardant agent, so that the solid composite flame retardant agent is not precipitated during long-term storage.
  • the viscosity of the surfactant may be 200-1000 cps or 500-800 cps at 25 ° C.
  • the viscosity of the surfactant may be in the range described above.
  • the viscosity may be measured with a Brookfield viscometer (Brookfield, DV3T Rheometer, # 63 spindle).
  • the hydroxyl value of the polyol compound may be about 250 to 350 mg KOH / g.
  • the viscosity of the polyol compound may also be 1500-3000 cps or 1800-2500 cps at 25 ⁇ ⁇ .
  • the hydroxyl value and viscosity of the above range are preferable because the flame retardant can be uniformly distributed in the phenol foam.
  • the viscosity may be measured with a Brookfield viscometer (Brookfield, DV3T Rheometer, # 63 spindle).
  • the viscosity of the liquid composite flame retardant of the present invention may be 10,000-40,000 cps or 15,000-30,000 cps at 20 ° C.
  • the viscosity may be measured with a Brookfield viscometer (Brookfield, DV3T Rheometer, # 63 spindle).
  • the specific gravity of the liquid phase composite flame retardant of the present invention may be 1.42-2.0. When the specific gravity is less than the above range, the flame retardant effect is lowered. When the specific gravity exceeds the above range, the flame retardant is precipitated and the transfer pipe may be clogged.
  • the foaming agent contained in the foaming agent tank 40 is the same as the foaming agent contained in the phenol foam described above, and repeated description is omitted.
  • the step of supplying the phenol foam to the high-speed agitator 50 in the method of producing the phenol foam according to the present invention may be carried out from the subject tank 10, the hardener tank 20, the liquid composite flame retarder tank 30 and the blowing agent tank 40,
  • the liquid cured composite flame retardant and the foaming agent are supplied to the high-speed agitator 50 through a pipe, the amount of the curing agent supplied to the high-speed agitator 50 is 5 to 30 parts by weight, 10 to 25 parts by weight.
  • the amount is less than the above range, the curing reaction time is prolonged or the curing reaction does not sufficiently take place.
  • the amount exceeds the above range the unreacted curing agent becomes an impurity and the physical properties of the foam are lowered.
  • the amount of the liquid mixed flame retardant supplied to the high-speed stirrer 50 may be 10-40 parts by weight, or 20-30 parts by weight, based on 100 parts by weight of the resin. When the amount is less than the above range, the flame retardancy is lowered, and when the above range is exceeded, the heat insulating property is lowered.
  • the amount of the blowing agent supplied to the high-speed stirrer 50 may be 5 to 30 parts by weight, or 10 to 25 parts by weight, based on 100 parts by weight of the resin.
  • the amount is less than the above range, the foaming cell is poorly formed and the heat insulating property is deteriorated.
  • the above range is exceeded, excessive foaming cells are produced and durability such as compressive strength of the foam is lowered.
  • the foam molding is a step of injecting the phenol foam composition stirred in the high-speed stirrer 50 into a mold 60 and performing a foaming molding.
  • the phenol foam composition is extruded at 3,000- Stirring the mixture at 7,000 rpm, and then introducing the mixture into the mold 60 at 55-70 ° C or 60-65 ° C for foam molding.
  • the phenol foam of the present invention has the effect of uniformly distributing the flame retardant in the phenol foam and improving the quality stability of the heat insulating property and the flame resistance, so that the heat insulating property and the flame resistance which are mutually related to each other can be realized.
  • a liquid flame-retardant agent in which a composite flame retardant agent is liquefied is mixed with a subject in a high-speed stirrer without mixing the composite flame retardant agent with the subject first, so that there is an effect of preventing the problem of clogging of the pipe when the mixture of the high viscosity base and the flame retardant is transferred to the high-speed stirrer.
  • the phenol foam of the present invention is excellent in heat insulation and flame retardancy, and can be applied to a fireproof door core material, a refractory structural core material, and the like.
  • a main tank, a hardener tank, a liquid composite flame retardant tank and a blowing agent tank were prepared.
  • the liquid composite flame retardant was prepared by mixing 18 parts by weight of the composite flame retarding agent 1, 18 parts by weight of the composite flame retarding agent 2, and 10 parts by weight of the flame retarding agent 1 in each of four liquid solution tanks containing 8 parts by weight of the liquid solution consisting of 5 parts by weight of the nonionic surfactant and 3 parts by weight of the polyester polyol. 21 parts by weight of the composite flame retarding agent 3, 21 parts by weight of the composite flame retarding agent 3, and 21 parts by weight of the composite flame retarding agent 4 were mixed and stirred for 20 minutes at a low speed of 500 rpm and at a high speed of 3,000 rpm for 10 minutes so as to homogeneously mix the composite flame- To 1 to 4, respectively. At this time, the composite flame retardants 1 to 4 were mixed as shown in Table 1, and the viscosity and specific gravity of the liquid phase composite flame retardants 1 to 4 were as shown in Table 2 below.
  • Composite flame retardant 1 Composite Flame Retardant 2 Composite Flame Retardant 3 Composite flame retardant 4
  • Liquid composite flame retardant 1 Liquid composite flame retardant 2
  • Liquid composite flame retardant 3 Liquid composite flame retardant 4
  • Viscosity Brookfield viscometer (Brookfield, DV3T Rheometer, # 63 spindle)
  • the subject, the curing agent, the foaming agent and the liquid composite flame retardant were introduced into the high-speed stirrer from the above-mentioned main tank, the hardener tank, the blowing agent tank and the liquid composite flame-retardant tank through a pipe and stirred at 5,000 rpm for 10 seconds at room temperature.
  • Example 1 Example 2
  • Example 3 Example 4 subject 23.23 22.79 23.23 22.79 Hardener 3.33 3.27 3.33 3.27 blowing agent 2.89 2.84 2.89 2.84 Liquid composite flame retardant 1 5.78 - - - Liquid composite flame retardant 2 - 6.33 - - Liquid composite flame retardant 3 - - 5.78 - Liquid composite flame retardant 4 - - - 6.33
  • Example 1 Example 2
  • Example 3 Example 4
  • Polyester polyol 1.90 1.86 1.90 1.86
  • Aluminum hydroxide 9.47 9.28 5.68 5.57
  • Expanded graphite 0 0 3.79 3.71
  • Calcium borate 0 1.86 0 1.86
  • Phosphorous flame retardant (TCPP) 1.90 1.86 1.90 1.86 Para toluenesulfonic acid 9.46 9.28 9.46 9.28 Pentane 8.20 8.05 8.20 8.05
  • the viscosity and specific gravity of the composite flame retarding agents 1 to 4 after charging were as shown in Table 5 below.
  • the viscosity of the subject ie, resole resin, urea, and surfactant
  • specific gravity was 1.20.
  • Theme and composite flame retardant 1 Theme and compound flame retardant 2
  • Theme and compound flame retardant 3 Thematic and Composite Flame Retardants 4 Viscosity (20 °C) 67,420 cps 75,480 cps 46,810 cps 49,740 cps importance 1.38 1.41 1.28 1.30
  • Viscosity Brookfield viscometer (Brookfield, DV3T Rheometer, # 63 spindle)
  • the mixture of the main and composite flame retardants, the curing agent, and the foaming agent were put into a high-speed stirrer through piping from the main tank, the hardener (paratoluene sulfonic acid) tank and the foaming agent (pentane) tank, and stirred at 5,000 rpm for 10 seconds at room temperature.
  • a phenol foam of Comparative Example 1 was prepared in the same manner as in Reference Example 1-4, except that no flame retardant was added.
  • the phenol resin in the phenol foam of Comparative Example 1 contained 75.47% by weight, 1.51% by weight of urea, 1.89% by weight of surfactant, 11.32% by weight of paratoluene sulfonic acid and 9.81% by weight of pentane.
  • the thermal conductivity (W / mk) was measured using a thermal conductivity meter (EKO, HC-074) as a KS L ISO 8301 measurement method.
  • the temperature average was measured under the condition of 20 ⁇ (upper plate 10 ⁇ , lower plate 30 ⁇ ).
  • the oxygen index (LOI) was measured by the KS M ISO 4589-2 measurement method commissioned by an accredited testing laboratory (Korea Institute of Construction & Living Environment Test).
  • the density was calculated by measuring the weight, width, length, and thickness of the sample using the KS M ISO 845 measurement method.
  • the free foaming rate was measured using a KS M ISO 4590 measuring method using a Quantachrome (ULTRAPYC 1200e) instrument.
  • Example 1 Example 2 Example 3
  • Thermal conductivity (W / mk) 0.020 0.020 0.019 0.019 0.022 0.023 0.021 0.022 0.019
  • Compressive strength (kPa) 159 154 174 169 114 124 134 131 163 Heat release (5 min, MJ / m 2 ) 9.4 8.4 9.7 8.7 10.8 10.6 11.4 11.0 13.8
  • the foams of Examples 1-4 and Reference Examples 1-4 include an inorganic flame retardant and an organic flame retardant, the flame retardant such as heat emission and oxygen index And the heat conductivity can be maintained at the same level.
  • the flame retardant such as heat emission and oxygen index
  • the heat conductivity can be maintained at the same level.
  • the phenol foam of Examples 1 to 4 of the present invention had better dispersibility of the flame retardant even if the contents of the flame retardant contained in the foam were similar to those of Reference Examples 1 to 4, improved heat insulation such as thermal conductivity, The flame retardancy can be further improved, and the adiabatic property and the flame retardancy, which are in conflict with each other, can be simultaneously realized.
  • the heat release amount (5 min, MJ / m 2 ) must come within 10 by the flame retardancy test method according to KS F ISO 5660-1. All of the foams can be confirmed to have flame retardancy applicable to the heat insulation material as a core material of the fire door, with a heat release amount (5 minutes, MJ / m 2 ) of not more than 10.
  • the fire resistance door is manufactured by manufacturing the insulation material with the core material having the flame resistance
  • the performance of the fire resistance test can be secured for 1 hour (within 10 seconds of continuous flame generation from the backside of the heating surface for 1 hour)
  • the phenolic foam of the present invention can be applied to a fire-proof door core and a refractory structural core material in which only conventional inorganic insulation materials are used.
  • the method of producing a phenol foam having a thermal conductivity of less than 0.021 W / mK and a heat release of 10.0 MJ / m 2 (5 minutes) or less according to the present invention can be carried out by mixing the liquid phase composite flame- It is possible to prevent the viscosity of the subject from rising sharply, thereby preventing the problem of clogging of the pipeline when the mixture of the conventionally high viscosity flame retardant and the flame retardant is transferred to the agitator.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Casting Or Compression Moulding Of Plastics Or The Like (AREA)
  • Molding Of Porous Articles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

La présente invention concerne une mousse de phénol et un procédé de fabrication associé et plus particulièrement une mousse de phénol et un procédé de fabrication associé, la mousse de phénol présentant un agent ignifuge distribué uniformément en son sein, présentant ainsi une stabilité de qualité accrue dans les propriétés isolantes et ignifuges, et permettant ainsi la réalisation de propriétés à la fois isolantes et ignifuges qui sont dans une relation de compromis entre elles. [Figure représentative] FIG. 1
PCT/KR2018/010839 2017-09-15 2018-09-14 Mousse de phénol et procédé de fabrication associé WO2019054795A1 (fr)

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JP2020515194A JP6957745B2 (ja) 2017-09-15 2018-09-14 フェノール発泡体及びその製造方法
CN201880057392.1A CN111051406B (zh) 2017-09-15 2018-09-14 酚醛发泡体及其制备方法

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KR102326998B1 (ko) * 2017-09-15 2021-11-16 (주)엘엑스하우시스 페놀 발포체 및 그 제조방법
KR102478779B1 (ko) * 2020-02-11 2022-12-19 (주)엘엑스하우시스 열경화성 발포체 및 이의 제조방법
CN112297321B (zh) * 2020-10-12 2021-07-20 广东华瑞环保材料有限公司 一种保温板发泡设备及保温板生产线和生产工艺
WO2022098196A1 (fr) * 2020-11-09 2022-05-12 (주)엘엑스하우시스 Mousse phénolique et procédé pour la fabrication de celle-ci
WO2022255292A1 (fr) * 2021-05-31 2022-12-08 旭有機材株式会社 Composition de résine pour mousse de phénol et mousse

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KR20140017301A (ko) * 2012-07-31 2014-02-11 한국스미더스 오아시스 주식회사 페놀수지를 이용한 난연성 발포폼 단열재의 제조장치 및 제조방법
KR20170007396A (ko) * 2014-06-18 2017-01-18 아사히 가세이 겐자이 가부시키가이샤 페놀 수지 발포체 및 그 제조 방법

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JP2002241529A (ja) * 2001-02-20 2002-08-28 Nisshin Steel Co Ltd フェノール樹脂発泡体の製造方法
JP2007070504A (ja) * 2005-09-08 2007-03-22 Nitto Boseki Co Ltd フェノール樹脂発泡体
KR20130063903A (ko) 2011-12-07 2013-06-17 (주)엘지하우시스 단열 성능이 향상된 친환경 페놀 폼 수지 조성물 및 이를 이용한 페놀 폼
KR101515265B1 (ko) * 2012-01-19 2015-05-06 (주)엘지하우시스 페놀 폼을 이용한 ｈｖａｃ 덕트 및 그 제조 방법
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JP2003311758A (ja) * 2002-04-19 2003-11-05 Nisshin Steel Co Ltd 防火パネルの製造方法及び発泡性樹脂調整装置
JP2005074681A (ja) * 2003-08-28 2005-03-24 Nisshin Steel Co Ltd 金属パネル又はボードの製造方法
KR20130005747A (ko) * 2011-07-07 2013-01-16 (주)엘지하우시스 페놀 수지 경화 발포체를 이용한 불연 알루미늄 복합 판넬 및 그 제조 방법
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KR102438949B1 (ko) 2022-09-01
CN111051406B (zh) 2022-10-25
KR20210135972A (ko) 2021-11-16
JP6957745B2 (ja) 2021-11-02
JP2020533470A (ja) 2020-11-19
KR102326998B1 (ko) 2021-11-16
CN111051406A (zh) 2020-04-21

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