WO2022098196A1 - Mousse phénolique et procédé pour la fabrication de celle-ci - Google Patents
Mousse phénolique et procédé pour la fabrication de celle-ci Download PDFInfo
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- WO2022098196A1 WO2022098196A1 PCT/KR2021/016168 KR2021016168W WO2022098196A1 WO 2022098196 A1 WO2022098196 A1 WO 2022098196A1 KR 2021016168 W KR2021016168 W KR 2021016168W WO 2022098196 A1 WO2022098196 A1 WO 2022098196A1
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- Prior art keywords
- foam
- closed cell
- surface layer
- cell ratio
- thickness
- Prior art date
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- 239000006260 foam Substances 0.000 title claims abstract description 217
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 title claims abstract description 97
- 238000004519 manufacturing process Methods 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 17
- 239000002344 surface layer Substances 0.000 claims abstract description 94
- 238000005187 foaming Methods 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 36
- 239000000463 material Substances 0.000 claims description 26
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- 239000004088 foaming agent Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 238000007599 discharging Methods 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 2
- 210000004027 cell Anatomy 0.000 description 81
- 230000000704 physical effect Effects 0.000 description 32
- 239000012634 fragment Substances 0.000 description 15
- 238000009413 insulation Methods 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 12
- 238000009826 distribution Methods 0.000 description 9
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000010586 diagram Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 230000007774 longterm Effects 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000011900 installation process Methods 0.000 description 5
- 239000005011 phenolic resin Substances 0.000 description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000012212 insulator Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920003987 resole Polymers 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
- CZHLPWNZCJEPJB-UHFFFAOYSA-N 1-chloro-3-methylbutane Chemical compound CC(C)CCCl CZHLPWNZCJEPJB-UHFFFAOYSA-N 0.000 description 2
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 2
- SQCZQTSHSZLZIQ-UHFFFAOYSA-N 1-chloropentane Chemical compound CCCCCCl SQCZQTSHSZLZIQ-UHFFFAOYSA-N 0.000 description 2
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 239000001282 iso-butane Substances 0.000 description 2
- QTBFPMKWQKYFLR-UHFFFAOYSA-N isobutyl chloride Chemical compound CC(C)CCl QTBFPMKWQKYFLR-UHFFFAOYSA-N 0.000 description 2
- ULYZAYCEDJDHCC-UHFFFAOYSA-N isopropyl chloride Chemical compound CC(C)Cl ULYZAYCEDJDHCC-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- SNMVRZFUUCLYTO-UHFFFAOYSA-N n-propyl chloride Chemical compound CCCCl SNMVRZFUUCLYTO-UHFFFAOYSA-N 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- JIRHAGAOHOYLNO-UHFFFAOYSA-N (3-cyclopentyloxy-4-methoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC1CCCC1 JIRHAGAOHOYLNO-UHFFFAOYSA-N 0.000 description 1
- SXKNYNUXUHCUHX-UHFFFAOYSA-N 1,1,2,3,3,4-hexafluorobut-1-ene Chemical compound FCC(F)(F)C(F)=C(F)F SXKNYNUXUHCUHX-UHFFFAOYSA-N 0.000 description 1
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 description 1
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 description 1
- OQISUJXQFPPARX-UHFFFAOYSA-N 2-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C(Cl)=C OQISUJXQFPPARX-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 description 1
- BRIXOPDYGQCZFO-UHFFFAOYSA-N 4-ethylphenylsulfonic acid Chemical compound CCC1=CC=C(S(O)(=O)=O)C=C1 BRIXOPDYGQCZFO-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 239000011489 building insulation material Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Images
Classifications
-
- 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
- C08J2361/00—Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
- C08J2361/04—Condensation polymers of aldehydes or ketones with phenols only
Definitions
- the present invention relates to a phenolic foam and a method for preparing the same.
- Insulation is an essential item used to prevent energy loss in buildings. As the importance of green growth continues to be emphasized worldwide due to global warming, insulation is becoming more important to minimize energy loss.
- An object of the present invention is to provide a high-thickness phenolic foam that increases production efficiency by controlling the distribution of the closed cell ratio of the high-thickness foam and exhibits economically superior physical properties.
- the cell ratio is lower than the closed cell ratio of the second surface layer part (NN), and the section (Nmin) having the minimum closed cell ratio among the N slices is located between the first surface layer part (N1) and the middle section (Nc).
- a phenolic foam can be provided.
- the phenolic foam according to the present invention is a high-thickness foam, and it more economically prevents damage in the installation process of the foam, and exhibits excellent thermal insulation and compressive strength, etc. occurrence can be prevented.
- the method for producing a phenol foam according to the present invention can provide a phenol foam having the above properties more economically by increasing production efficiency.
- FIG. 2 is a schematic view of a discharge port of a nozzle for discharging a foaming composition according to an embodiment of the present invention.
- FIG 3 is a schematic diagram schematically showing the arrangement of a plurality of outlets on the lower plate on the conveyor according to another embodiment of the present invention.
- Figure 4 is a schematic diagram briefly showing a method for measuring the degree of warpage of the phenolic foam according to another embodiment of the present invention.
- FIG. 5 is a schematic diagram briefly showing a method for measuring the dimensional stability of a phenolic foam according to another embodiment of the present invention.
- One embodiment of the present invention is a phenolic foam having a thickness of 90 mm or more, and when divided into N (odd number of N ⁇ 7) slices in the thickness direction from any one surface of the foam to the surface, the first surface layer portion (N 1 ) is lower than the closed cell ratio of the second surface layer part (N N ), and the intercept (N min ) having the minimum closed cell ratio among the N slices is the first surface layer part (N 1 ) and the middle section ( N c ) located between the phenolic foams.
- the thickness of the foam increases, it may be easier to secure thermal insulation.
- the thickness of the foam exceeds a certain level or more, internal heat generation increases due to the curing reaction of the central portion in the thickness direction of the foam, and heat is not easily dissipated to the outside, and the internal temperature of the foam composition is excessively increased.
- the physical properties of the foam may be significantly changed depending on the location in the thickness direction of the foam, such as rupture of the bubble near the center of the foam, and the foam may be easily damaged and warp may occur.
- warpage occurs in the foam, there is a high possibility of poor appearance and poor construction, and problems such as product shrinkage over a long period of time occur. And, despite the increased thickness, thermal conductivity may be rather reduced.
- the impact received by a portion having weak physical properties may be significantly different.
- insulators for example, for ceilings or floors, are arbitrarily positioned by workers during an installation process, stepped on, poured cement, etc., and then aged for a certain period of time. Therefore, even if it is a foam that exhibits excellent physical properties during manufacture, the parts with weak properties of the foam are greatly damaged during the installation process. can be lowered
- the phenolic foam has a thickness of about 90 mm or more, has an asymmetric structure with respect to the center portion in the thickness direction of the foam, and adjusts the position having the minimum closed cell ratio in the foam, so that the insulation properties and compressive strength of the foam as a whole It exhibits excellent physical properties, such as, and can prevent warpage. And, even if an impact is applied to either surface of both surfaces of the phenolic foam during the installation process, it is possible to similarly and similarly lower the impact received by a vulnerable part of the foam. Accordingly, the phenolic foam can exhibit excellent physical properties for a long period of time even after the construction process.
- the phenolic foam may have a thickness of about 110 mm or more, about 150 mm or more, and about 180 mm or more to 300 mm.
- the phenolic foam is When divided into N (odd number of N ⁇ 7) slices from the surface of the foam to the thickness direction along the surface, the closed cell ratio of the first surface layer part (N 1 ) is higher than the closed cell ratio of the second surface layer part (N N )
- a fragment (N min ) which is low and has a minimum closed cell ratio among the N fragments is located between the first surface layer portion (N 1 ) and the middle fragment (N c ).
- the thickness refers to the direction in which the foam composition on the face material grows (Z direction), and the surface perpendicular to the thickness direction is the surface, and it means the side to which the face material is attached when the foam is manufactured.
- the foam if there is a face material, the face material is removed, and both surfaces of the foam to which the face material is attached are cut by 5 mm for accurate measurement of the closed cell ratio.
- N an odd number of N ⁇ 7 slices from the surface of the foam body along the surface in the thickness direction. Then, the percentage of closed cells in each section is measured.
- N may be an integer including an even number, N is preferably an odd number in order to more clearly confirm whether physical properties are symmetrical with respect to the center of the thickness direction in the foam.
- Each segment may have a thickness of from about 10 mm to about 30 mm.
- the phenolic foam includes a first surface and a second surface, the first surface layer includes a first surface, and the second surface layer means a segment including the second surface.
- the section with a low closed cell ratio is N 1 (first surface layer)
- the remaining section is N N (second surface layer)
- sequentially from N 1 , N 2 , N 3 , N 4 , N 5 , ... and N N represent each intercept.
- a fragment located in the middle is denoted as a middle fragment (Nc). That is, the middle section Nc refers to a section located at a 1/2 point in the thickness direction of the first surface layer part N 1 and the second surface layer part N N .
- the phenol foam forms an asymmetric structure in which the closed cell ratio of the first surface layer portion (N 1 ) is lower than the closed cell ratio of the second surface layer portion (N N ), and at this time, the segment (N) having the minimum closed cell ratio among the N fragments min ) is located between the first surface layer portion (N 1 ) and the middle section (N c ). Accordingly, even if an impact is applied to any one surface of the first surface layer part and the second surface layer part, the impact received by the fragment (N min ) having the minimum closed cell ratio is similarly lowered, and physical properties such as excellent thermal insulation properties in the entire foam You can prevent warping together.
- the phenolic foam has an asymmetric structure in which the closed cell ratio of the first surface layer part (N 1 ) is lower than the closed cell ratio of the second surface layer part (N N ) to produce a foam more economically, while having a minimum closed cell ratio
- the intercept (N min ) is located between the first surface layer portion (N 1 ) and the middle section (N c ) having a lower closed cell ratio than the closed cell ratio of the second surface layer portion (N N ) to achieve the desired effect can
- the foam having the minimum closed cell ratio (N min ) is located between the middle section (N c ) and the second surface layer portion (N N ) having a high closed cell ratio
- the first surface layer portion (N 1 ) This may not be a problem if an impact is applied to the
- the second surface layer portion (N N ) a large amount of warpage appears in the direction of the intercept (N min ) having the minimum closed cell ratio, and the foam is greatly damaged and the physical properties may be significantly reduced
- the difference between the closed cell ratio of the first surface layer part (N 1 ) and the closed cell ratio of the second surface layer part (N N ) may be from about 0.05% to about 5%. For example, it can be from about 0.1% to about 5% or from about 0.1% to about 3%.
- the difference between the closed cell ratio of the first surface layer part (N 1 ) and the second surface layer part (N N ) is less than the above range, the cost increases, the production efficiency is low, and it is uneconomical, and when it exceeds the above range, the entire foam There is a limit to having excellent physical properties.
- the closed cell ratio of the first surface layer part (N 1 ) and the closed cell ratio of the second surface layer part (N N ) may each be about 85% or more. For example, from about 85% to about 100%.
- the first surface layer portion (N 1 ) and the second surface layer portion (N N ) by having a closed cell ratio in the above range, together with excellent initial thermal conductivity, prevent replacement of the foam and air, the amount of change over time of the insulation performance It can be lowered to exhibit excellent thermal insulation properties.
- the second surface layer portion (N N ) has the maximum closed cell ratio
- the second surface layer portion (N N ) and the intercept (N min ) having the minimum closed cell ratio difference ( ⁇ C2)
- ) may be about 1 to about 20%. For example, it can be from about 1% to about 15% or from about 1% to about 7%.
- the foam may be easily and greatly warped.
- the difference between the closed cell ratio of the first surface layer part (N 1 ) and the intercept (N min ) having the minimum closed cell ratio ( ⁇ C1
- ) may be about 0.1 to about 20%. For example, it may be about 0.1 to about 10%.
- the intercept (N min ) having the minimum closed cell ratio may have a closed cell ratio of about 70% or more. For example, it may be about 70% to about 89%.
- the phenolic foam may control the closed cell ratio of the segment (N min ) within the above range to maintain low thermal conductivity over a long period of time, prevent warpage, and improve dimensional stability. For example, when it is less than the above range, the replacement rate of the foaming agent and air in the bubble increases, so that the change in thermal conductivity over time may be large.
- a ratio of d1 and d2 to the total thickness of the foam may be from about 0.2:0.8 to about 0.45:0.55.
- the overall thickness of the foam means the thickness of the foam after cutting each 5 mm of both surfaces of the foam to which the face material was attached.
- d1 and d2 are from the upper surface of the first surface layer part or the lower surface of the second surface layer part to the 1/2 point in the thickness direction of the intercept Nmin having the minimum closed cell ratio. It means the ratio of the vertical distance.
- the intercept (N min ) having the minimum closed cell ratio is located at the point in the relationship between the first surface layer part (N 1 ) and the second surface layer part (N N ), and is located on any one surface of the first surface layer part and the second surface layer part Even if an impact is applied, it is possible to similarly lower the impact received by the fragment (N min ) having the minimum closed cell ratio, thereby preventing warpage along with physical properties such as excellent thermal insulation properties in the entire foam.
- the intercept (N min ) having the minimum closed cell ratio is outside the above range and is located closer to the first surface layer part (N 1 )
- the physical properties of the first surface layer part (N 1 ) side are significantly reduced and , it is difficult to uniform the physical properties of the entire foam beyond a certain level, the shrinkage of the first surface layer part (N1) including the face material appears as an appearance, and the product warps in the direction of the first surface layer part (N1), and the compressive strength is low
- problems such as degradation.
- the phenolic foam has the difference ( ⁇ C1, ⁇ C2) of the closed cell ratio between each surface layer part (N 1 , N N ) and the intercept (N min ) having the minimum closed cell ratio with each surface layer part and the minimum closed cell ratio.
- a value Y divided by the distance ratio to the intercept (d 1 , d 2 ) may be (
- ) about 0.1 to about 9. For example, it may be from about 0.1 to about 6.5 or from about 0.1 to about 5.
- the Y value exceeds the above range, there may be a problem in that the impact received at a specific position in the thickness direction is increased, or the physical properties of the entire foam are lowered, and warpage occurs.
- the phenolic foam can exhibit excellent physical properties in the entire foam by having the closed cell ratio distribution as described above, and can maintain excellent thermal conductivity despite long-term use.
- the phenolic foam may have a compressive strength of about 100 kPa to about 200 kPa according to KS M ISO 844. For example, it may be from about 115 kPa to about 200 kPa.
- Compressive strength refers to the pressure at which the foam breaks.
- the phenol foam has a compressive strength in the above range, and thus maintains an excellent balance between physical properties, and can exhibit excellent long-term durability even after distribution and construction.
- the phenolic foam may have a dimensional change of from about 0% to about 2.0%.
- the phenolic foam can have a dimensional change of from about 0% to about 1.0% or from about 0% to about 0.7%.
- the dimensional change rate can be measured by the method described in Experimental Example 4.
- the foam as shown in Figure 4, when 7 days elapsed at 25 ° C. and 60% relative humidity, the surface of the foam is bent concavely toward the floor (I), or the surface of the foam is curved convexly toward the ceiling Case (II) may occur.
- the change of the corner portions (P1 to P4), and, in the case of (II), the maximum separation distance (R1, R2) between the two sides in the longitudinal direction of the foam and the bottom surface ) may affect the damage to which the foam is subjected to external impact and the overall deformation of the foam.
- the phenolic foam may have an average warpage of from about 0 cm to about 1.5 cm, respectively, in the case of (I) above, and/or in the case of (II) above. or from about 0.1 cm to about 0.7 cm or from about 0.1 cm to about 0.5 cm, respectively.
- the phenolic foam may have a thermal conductivity of about 0.017 W/m ⁇ K to about 0.020 W/m ⁇ K measured at an average temperature of 20° C. according to KS L 9016.
- the phenolic foam has a thermal conductivity of about 0.018 W/m K to about 0.022 W/ It may be m ⁇ K.
- the phenolic foam includes the closed cell ratio in the same distribution as above, and exhibits excellent properties such as compressive strength, prevents warpage, and may exhibit a change with time of about 10% or less in long-term thermal conductivity.
- Another embodiment of the present invention comprises the steps of discharging a foaming composition comprising a phenol-based resin, a foaming agent and a curing agent onto the face material using a nozzle; and foaming and curing the discharged foaming composition, wherein the nozzle provides a method for producing a phenolic foam having a discharge port having a shape of 1 or more and 2 or less in length (L)/width (W).
- a phenolic foam having a specific closed cell ratio distribution and excellent physical properties in the entire foam can be more economically produced.
- the phenolic foam manufactured by the above manufacturing method has the same and similarly lowered the impact received by the fragment (N min ) having the minimum closed cell ratio even if an impact is applied to any one surface of the first surface layer part and the second surface layer part , it is possible to prevent warping along with physical properties such as excellent thermal insulation and compressive strength throughout the foam.
- the above-mentioned matters such as the thickness of the phenol foam and the closed cell ratio are the same as those described above, except for those specifically described below.
- the foaming composition is continuously discharged on the first face member using one nozzle, and then molded into a plate shape between conveyors in a curing furnace.
- the curing reaction is carried out, and the heat of reaction generated during the reaction is easily radiated through the face material, so it is not difficult to have uniform physical properties throughout the thickness.
- internal heat generation is increased due to a curing reaction in the central portion in the thickness direction of the foam, and heat is not easily dissipated to the outside, so that the internal temperature of the foaming composition is excessively increased.
- the method for manufacturing the phenol foam includes discharging a foaming composition including a phenol-based resin, a foaming agent and a curing agent onto the face member 3 using a nozzle.
- the discharge port 10 which is the inlet of the nozzle, may have a shape in which the length (L)/width (W) is 1 or more and 2 or less.
- the length L may have an elliptical shape longer than the width W, and the length L/width W may be greater than 1 or less than 2 .
- the discharge port means an inlet through which the composition is discharged.
- the length (L) means the length of the major axis in the ellipse
- the width (W) means the length of the minor axis.
- the length (L) direction of the discharge port is parallel to the thickness direction (Z direction) of the foam
- the width (W) direction of the discharge port is in a direction parallel to the width direction (Y direction) of the foam can be located
- the discharge port of the nozzle may have a length (L)/width (W) (aspect ratio) of 1 or more and 2 or less.
- the discharge port of the nozzle may have an elliptical discharge port of more than 1 and 2 or less. Accordingly, it prevents the cells being cured from collapsing due to the movement of the foaming composition, and prevents problems such as excessive foaming and expansion of the foaming composition in the vicinity of the face material (eg, the lower face material) from which the foaming composition is discharged.
- the outlet of the nozzle has a rectangular structure rather than an ellipse, there may be a problem in that a cured product is accumulated near the corner of the outlet.
- the discharge port has a circular or elliptical shape, but the length (L) / width (W) is less than the above range, excessive foaming and expansion occurs near the lower face material from which the foaming composition is discharged, so that the bubbles are easily broken. There may be a problem.
- the ratio of length (L) / width (W) exceeds the above range, the amount of expansion of the foam composition in the width direction (Y direction, direction orthogonal to the discharge direction of the foam composition) of the foam increases while curing by heating The bubbles are broken by the movement of the foaming composition, the foaming and expansion rate in the thickness direction (Z direction) of the foam becomes slower, and the time and amount of the foaming composition staying near the lower face material increases. There may be problems such as
- the outlet may have a length L of about 10 mm to about 100 mm.
- L which is the long axis of the discharge port
- the pressure generated during nozzle discharge may increase, and if it exceeds the above range, the pressure may be lowered and proper foaming may not be performed.
- the foaming composition may be discharged at about 30 kg/min to about 100 kg/min.
- the viscosity of the foaming composition at the time of the discharge may be from about 5,000 cps to about 40,000 cps at 25°C.
- the foaming composition may be discharged in a slurry state suitable for foaming and curing by having a viscosity within the above range.
- the temperature of the foaming composition may be about 0 °C to about 40 °C. If the temperature range is less than the above range, there may be a problem in that the discharge viscosity is excessively increased and thus discharge is difficult.
- the method for producing the phenol foam is arranged along a direction (Y-axis direction, width direction of the foam) orthogonal to the flow direction of the foam composition (X-axis, that is, the running direction of the face material 3)
- a plurality of nozzles having the discharge port 10 may be provided. Specifically, the number of nozzles may be about 4 to about 12. The nozzles may be arranged in parallel at equal intervals.
- the foam composition grows in the direction (Z-axis direction, the thickness direction of the foam) as well as in the flow direction of the foam composition ( Uniform expansion can be induced in the direction (Y-axis direction, width direction of the foam) orthogonal to the X-axis, that is, the running direction of the face material. Accordingly, the growth and distribution of bubbles can be appropriately controlled.
- the foaming composition includes a phenol-based resin, a foaming agent, and a curing agent.
- the phenol-based resin may be obtained by reacting phenol and formaldehyde, and may include, for example, a resol-based phenol resin (hereinafter, 'resol resin').
- the phenolic resin may be included in the phenolic foam in an amount of about 30 wt% to about 90 wt%, or about 50 wt% to about 90 wt%, or about 55 wt% to about 90 wt%.
- the phenol foam may stably form a small-sized foam cell by including the phenol-based resin in an amount within the above range, and may implement excellent thermal conductivity.
- the phenolic foam may include a blowing agent.
- the blowing agent may include one selected from the group consisting of a hydrofluoroolefin (HFO)-based compound, a hydrocarbon-based compound, and combinations thereof.
- the hydrofluoroolefin-based compound is, for example, monochlorotrifluoropropene, trifluoropropene, tetrafluoropropene, pentafluoropropene, hexafluorobutene, and combinations thereof. It may include at least one selected from the group consisting of.
- the hydrocarbon-based compound may include a hydrocarbon having 1 to 8 carbon atoms.
- the hydrocarbon-based compound is dichloroethane, propyl chloride, isopropyl chloride, butyl chloride, isobutyl chloride, pentyl chloride, isopentyl chloride, n-butane, isobutane, n- pentane, isopentane, cyclopentane, It may include at least one selected from the group consisting of hexane, heptane, cyclopentane, and combinations thereof.
- the hydrocarbon-based compound is a hydrocarbon having 1 to 5 carbon atoms, dichloroethane, propyl chloride, isopropyl chloride, butyl chloride, isobutyl chloride, pentyl chloride, isopentyl chloride, n-butane, isobutane, n-pentane, By including at least one selected from the group consisting of isopentane, cyclopentane, and combinations thereof, it may exhibit excellent thermal insulation properties along with eco-friendliness.
- the blowing agent may be included in an amount of about 6 parts by weight to about 13 parts by weight based on about 100 parts by weight of the phenol foam.
- the phenolic foam includes a curing agent.
- the curing agent is an acid curing agent, and may include one acid curing agent selected from the group consisting of toluene sulfonic acid, xylene sulfonic acid, benzenesulfonic acid, phenol sulfonic acid, ethylbenzene sulfonic acid, styrene sulfonic acid, naphthalene sulfonic acid, and combinations thereof.
- the acid curing agent may be included in an amount of about 9 parts by weight to about 20 parts by weight, based on 100 parts by weight of the phenol foam.
- the phenol foam may exhibit appropriate crosslinking, curing and foaming properties by including the curing agent in an amount within the above range.
- the manufacturing method of the phenol foam includes foaming and curing the discharged foam composition.
- the phenolic foam may be foamed and cured in a plate shape between conveyors in a curing furnace. For example, it may be foamed and cured under a temperature condition of about 40 °C to about 90 °C.
- the foaming and curing may be performed for a time of about 2 minutes to about 20 minutes, but is not limited thereto, and may appropriately vary depending on the purpose and use of the invention.
- Another embodiment of the present invention provides an insulating material comprising the phenol foam.
- the phenol foam satisfies excellent compressive strength, warpage prevention and excellent thermal insulation properties at the same time, and can be used as a building insulation material.
- the building insulation may further include a face material on one or both surfaces of the phenolic foam, for example, and may further improve flame retardancy by including aluminum as the face material.
- a foaming composition (25° C., 20,000 cps) comprising 18 parts by weight of toluenesulfonic acid as a curing agent, 10 parts by weight of cyclopentane as a foaming agent and a surfactant was prepared.
- each section is indicated as N 2 , N 3 , N 4 , N 5 , N 6 , N 7 , N 8 , and N 9 . Accordingly, the middle intercept Nc becomes N 5 .
- the closed cell rate of each section is measured using the closed cell rate measuring device (Quantachrome, ULTRAPYC 1200e) by the KS M ISO 4590 measurement method, and the result is It is described in Table 1 below.
- the overall thickness of the foam means the thickness of the foam after cutting each 5 mm of both surfaces of the foam to which the face material was attached.
- the thickness of N1 to Nmin and the thickness of N9 to Nmin are the intercept (Nmin) having the minimum closed cell ratio from the upper surface of the first surface layer part or the lower surface of the second surface layer part, as shown in FIG. 1 . It means the vertical distance to 1/2 of the thickness direction. That is, d1 is the thickness/total thickness of the foam from the upper surface of the first surface layer portion (N 1 ) to the 1/2 point of the intercept (Nmin) having the minimum closed cell ratio, d2 is the lower surface of the second surface layer portion (N 1 ) It means the thickness/full thickness of the foam from 1/2 of the intercept (Nmin) having the minimum closed cell ratio.
- the phenolic foam of Examples and Comparative Examples was prepared as a specimen with the thickness of the foam containing 150 mm (L) ⁇ 150 mm (W) ⁇ face material, and the specimen was placed between the wide plates of Lloyd Instrument's LF Plus universal testing machine (Universal Testing Machine). In the UTM equipment, it was set at a rate of 10% mm/min of the thickness of the specimen, and the compressive strength test was started, and the strength at the first compressive yield point that appeared while the thickness was decreased was recorded. Compressive strength was measured by the method of KS M ISO 844 standard, and the results are shown in Table 2 below.
- FIG 4 is a schematic view briefly showing a method for measuring the degree of warpage of the phenolic foam containing the face material according to the present invention.
- the surface of the phenolic foam including the face material of Examples and Comparative Examples was placed on a flat floor so that the surface was in contact with the floor surface.
- 4 corners (vertices) of the surface of the phenol foam in contact with the bottom surface and the distances (p1, p2, p3, p4) from the bottom surface were measured.
- the maximum separation distance (r1, r2) of the gap between the two sides in the longitudinal direction of the phenol foam and the bottom surface was measured. At this time, when the foam is in close contact with the bottom surface, each interval becomes "0".
- the phenol foam was left to stand for 7 days under conditions of 25° C. and 60% relative humidity, and then the degree of warpage of the phenol foam was measured.
- the surface of the foam is bent toward the bottom (I)
- the four corners (vertices) and the spacing from the bottom (P1, P2, P3, P 4) are measured in the same way as above, and the following Table 2 shows the degree of warpage occurring in the phenol foam according to Formula 1.
- the maximum separation distance (R1, R2) of the gap between the two sides in the longitudinal direction of the phenol foam and the bottom surface is measured, and by the following formula 2 Table 2 shows the extent to which warpage occurred in the phenol foam.
- Figure 4 is a schematic diagram briefly showing a method for measuring the dimensional stability of the phenolic foam of the present invention.
- Dimensional change rate (%) (
- Equation 3 the initial length (a) is the length of each line of n equal points in the length (L) and width (W) directions of the foam, and the later length (a') is the foam at 70° C. It means the later length (a') of each line at each point after standing in the oven for 48 hours.
- n may be 2 to 5.
- the phenolic resin foams of Examples and Comparative Examples were cut to be 50 mm from one surface, cut to a size of 300 mm ⁇ 300 mm to prepare a specimen, and the specimen was dried at 70° C. for 12 hours and pre-treated. And, according to the measurement conditions of KS L 9016 (Method for measuring plate heat flow metering method) for the specimen, the thermal conductivity was measured using a HC-074-300 (EKO company) thermal conductivity instrument at an average temperature of 20° C., and the results are shown in the table below 2 was described.
- KS L 9016 Method for measuring plate heat flow metering method
- the phenolic resin foams of Examples and Comparative Examples were cut to be 50 mm from any one surface, and a specimen was prepared by cutting to a size of 300 mm ⁇ 300 mm, and the specimen was dried at 70° C. for 7 days according to EN13823. After drying at 110° C. for 14 days, thermal conductivity was measured at an average temperature of 20° C. using a thermal conductivity instrument HC-074-300 (EKO), and the results are shown in Table 2 below.
- Example 1 Example 2 Comparative Example 1 Comparative Example 2 Compressive strength (kPa) 139 125 95 83 Warp (cm) 0.3 1.1 1.8 2.3 Dimensional stability (%) 0.5 0.4 1.1 1.4
- Initial thermal conductivity (W/m ⁇ K) 0.0192 0.0193 0.0190 0.0193
- Long-term thermal conductivity (W/m ⁇ K) 0.0205 0.0212 0.0216 0.0230 change in thermal conductivity 0.0013 0.0019 0.0026 0.0037
- the phenolic foam of Examples has excellent compressive strength, suppresses the degree of warpage well, and exhibits excellent thermal conductivity.
- the present invention has been described with reference to the illustrated drawings, but the present invention is not limited by the embodiments and drawings disclosed in this specification, and a variety of It is obvious that variations can be made.
- the effect of the configuration of the present invention is not explicitly described and described while describing the embodiment of the present invention, it is natural that the effect predictable by the configuration should also be recognized.
- d2 the thickness from the second surface layer portion (NN) to the intercept (Nmin) having the minimum closed cell ratio with respect to the total thickness of the foam
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Abstract
L'invention concerne une mousse phénolique ayant une épaisseur supérieure ou égale à 90 mm. Si on divise de manière égale la mousse phénolique en N (un nombre impair ≥ 7) tranches à partir d'une surface de la mousse et le long de la surface dans la direction de l'épaisseur, la proportion d'alvéoles fermées d'une première partie de couche de surface (N1) est inférieure à la proportion d'alvéoles fermées d'une seconde partie de couche de surface (NN) et la tranche (Nmin) ayant la plus petite proportion d'alvéoles fermées parmi les N tranches est positionnée entre la première partie de couche de surface (N1) et une tranche intermédiaire (Nc).
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Citations (5)
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KR20120094030A (ko) * | 2009-12-18 | 2012-08-23 | 아사히 가세이 겐자이 가부시키가이샤 | 페놀 수지 발포판 및 그 제조 방법 |
JP2018095870A (ja) * | 2016-12-10 | 2018-06-21 | 積水化学工業株式会社 | フェノール樹脂発泡板及びその製造方法 |
KR20180083962A (ko) * | 2013-02-26 | 2018-07-23 | 아사히 가세이 겐자이 가부시키가이샤 | 페놀 수지 발포판 및 그 제조 방법 |
KR20190031181A (ko) * | 2017-09-15 | 2019-03-25 | (주)엘지하우시스 | 페놀 발포체 및 그 제조방법 |
KR20200118101A (ko) * | 2018-04-27 | 2020-10-14 | 아사히 가세이 겐자이 가부시키가이샤 | 난연성 페놀 수지 발포체 |
-
2021
- 2021-11-08 WO PCT/KR2021/016168 patent/WO2022098196A1/fr active Application Filing
- 2021-11-08 KR KR1020210152181A patent/KR20220063102A/ko not_active Application Discontinuation
- 2021-11-08 JP JP2023526006A patent/JP2023548687A/ja active Pending
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KR20120094030A (ko) * | 2009-12-18 | 2012-08-23 | 아사히 가세이 겐자이 가부시키가이샤 | 페놀 수지 발포판 및 그 제조 방법 |
KR20180083962A (ko) * | 2013-02-26 | 2018-07-23 | 아사히 가세이 겐자이 가부시키가이샤 | 페놀 수지 발포판 및 그 제조 방법 |
JP2018095870A (ja) * | 2016-12-10 | 2018-06-21 | 積水化学工業株式会社 | フェノール樹脂発泡板及びその製造方法 |
KR20190031181A (ko) * | 2017-09-15 | 2019-03-25 | (주)엘지하우시스 | 페놀 발포체 및 그 제조방법 |
KR20200118101A (ko) * | 2018-04-27 | 2020-10-14 | 아사히 가세이 겐자이 가부시키가이샤 | 난연성 페놀 수지 발포체 |
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