KR20220121972A - Flame-retardant bead composition and method for producing flame-retardant bead composition - Google Patents
Flame-retardant bead composition and method for producing flame-retardant bead composition Download PDFInfo
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- KR20220121972A KR20220121972A KR1020210025920A KR20210025920A KR20220121972A KR 20220121972 A KR20220121972 A KR 20220121972A KR 1020210025920 A KR1020210025920 A KR 1020210025920A KR 20210025920 A KR20210025920 A KR 20210025920A KR 20220121972 A KR20220121972 A KR 20220121972A
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 68
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 65
- 239000000203 mixture Substances 0.000 title claims abstract description 59
- 239000011324 bead Substances 0.000 title claims abstract description 30
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 15
- 239000000463 material Substances 0.000 claims abstract description 23
- 238000003756 stirring Methods 0.000 claims abstract description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 14
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 13
- 238000002156 mixing Methods 0.000 claims abstract description 12
- 239000004254 Ammonium phosphate Substances 0.000 claims abstract description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910000148 ammonium phosphate Inorganic materials 0.000 claims abstract description 10
- 235000019289 ammonium phosphates Nutrition 0.000 claims abstract description 10
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 10
- 239000010439 graphite Substances 0.000 claims abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910001868 water Inorganic materials 0.000 claims abstract description 8
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000001099 ammonium carbonate Substances 0.000 claims abstract description 7
- 239000007788 liquid Substances 0.000 claims abstract description 7
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 6
- 235000012501 ammonium carbonate Nutrition 0.000 claims abstract description 6
- 239000004202 carbamide Substances 0.000 claims abstract description 6
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 5
- 239000002904 solvent Substances 0.000 claims abstract description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 4
- 239000010452 phosphate Substances 0.000 claims abstract description 4
- 239000000853 adhesive Substances 0.000 claims abstract description 3
- 230000001070 adhesive effect Effects 0.000 claims abstract description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 12
- 229910052698 phosphorus Inorganic materials 0.000 claims description 12
- 239000011574 phosphorus Substances 0.000 claims description 12
- 230000008569 process Effects 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 229910000388 diammonium phosphate Inorganic materials 0.000 claims description 4
- 235000019838 diammonium phosphate Nutrition 0.000 claims description 4
- 239000004114 Ammonium polyphosphate Substances 0.000 claims description 2
- 239000005696 Diammonium phosphate Substances 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims description 2
- 229920001276 ammonium polyphosphate Polymers 0.000 claims description 2
- 238000001704 evaporation Methods 0.000 claims description 2
- 239000004794 expanded polystyrene Substances 0.000 abstract description 32
- 239000007789 gas Substances 0.000 abstract description 9
- 239000002245 particle Substances 0.000 abstract description 8
- 229910052799 carbon Inorganic materials 0.000 abstract description 3
- 239000000843 powder Substances 0.000 abstract description 3
- 239000012795 eco-friendly flame retardant Substances 0.000 abstract description 2
- 239000004014 plasticizer Substances 0.000 abstract description 2
- 238000001035 drying Methods 0.000 abstract 1
- 238000002485 combustion reaction Methods 0.000 description 10
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000001934 delay Effects 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 229920006248 expandable polystyrene Polymers 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 1
- 229920006328 Styrofoam Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 229910021383 artificial graphite Inorganic materials 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012796 inorganic flame retardant Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000008261 styrofoam Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
Classifications
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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
- C08J9/0095—Mixtures of at least two compounding ingredients belonging to different one-dot groups
-
- 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
- C08J9/0028—Use of organic additives containing nitrogen
-
- 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
- C08J9/0066—Use of inorganic compounding ingredients
-
- 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
- C08J9/16—Making expandable particles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/21—Urea; Derivatives thereof, e.g. biuret
-
- 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
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/06—Polystyrene
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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
- C08J2325/00—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 at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
- C08J2325/02—Homopolymers or copolymers of hydrocarbons
- C08J2325/04—Homopolymers or copolymers of styrene
- C08J2325/06—Polystyrene
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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)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
본 발명은 내부에 탄소 및 질소가스를 충진하고 표면에 무기계난연재를 도포하여 난연성을 부여한 발포폴리스틸렌입자의 발포소재인 난연비드조성물 및 난연비드 조성물의 제조방법에 관한 것이다.The present invention relates to a flame-retardant bead composition and a method for producing a flame-retardant bead composition, which is a foaming material of expanded polystyrene particles, which is filled with carbon and nitrogen gas and imparted with flame retardancy by applying an inorganic flame-retardant material to the surface.
발포폴리스티렌(Expandable Polystyrene)은 단열성과 완충성 및 가공성이 우수하므로 산업 전반에 걸쳐 널리사용되고 있으며, 특히 건축용 단열재와 흡음재 및 외부의 충격으로 부터 제품을 보호하는 포장재 등으로 널리 사용되고 있지만 열과 화기에 매우 취약한 특성으로 인해 화재시 그 화력의 확산 매개로 작용하여 대형화재를 일으키는 원인을 제공할 뿐만 아니라, 연소되는 과정에서 인체에 치명적인 유독가스가 발생되어 큰 인명피해를 유발하기도 하는 등 상당한 단점도 가지고 있기 때문에 근래에는 발포폴리스티렌에 난연성을 부여하기 위한 연구·노력이 활발히 진행되고 있으며 일예로 발포폴리스티렌의 원료인 비드에 다공성 광물입자를 단순히 도포한 후 이를 이용해 발포 및 압축 성형을 통해 제조하는 방법(특허 제10-0492199호, 제10-0782311호)Expandable polystyrene is widely used throughout the industry because of its excellent insulation, buffering properties and processability. Due to its characteristics, in case of fire, it acts as a diffusion medium of the thermal power and provides a cause of causing a large fire. Recently, research and efforts to impart flame retardancy to expanded polystyrene are being actively conducted. For example, a method of manufacturing through foaming and compression molding using porous mineral particles by simply applying porous mineral particles to beads, which are raw materials of expanded polystyrene (Patent No. 10). -0492199, 10-0782311)
발포, 압축성형된 발포폴리스티렌의 외면에 별도 제작된 난연성시트 내지 난연제를 추가 도포하여 난연성이 발휘되도록 하는 방법과 완성된 발포폴리스티렌성형물에 주사 바늘로 난연재를 주사하여 난연기능을 갖도록 하는 방법 등이 있다. There is a method of additionally applying a flame retardant sheet or a flame retardant prepared separately to the outer surface of foamed or compression-molded expanded polystyrene to exhibit flame retardancy, and a method of injecting a flame retardant into the finished expanded polystyrene molded product with a needle to have a flame retardant function. .
상기한 종래방법 중 비드의 외측에 다공성 광물입자를 도포하여 발포폴리스티렌을 압축 성형하는 방법은 난연성은 우수하나 발포폴리스티렌의 고유한 성질인 가공성과 단열성 및 성형성을 감소시키게 되고 제조된 발포폴리스티렌이 무겁고 쉽게 부러지는 성질이 있어, 취급이 어려울 뿐만 아니라 생산성이 떨어지게 되고 완성된 제품에 수분이 침투하면 난연제의 융착성이 떨어지는 등의 결점이 있고, 발포폴리스티렌의 외면에 난연성시트 또는 난연재를 도포하는 방법의 경우는 난연재를 발포폴리스티렌의 성형물표면에 도포하고 건조하여야 하므로 작업에 많은 인력과 시간이 소요되어 생산성이 저하되고 대형의 제조장치가 추가되어 제조되는 발포폴리스티렌의 가격이 상승하게 되며 발포폴리스티렌의 내부 및 절단면에는 난연재가 존재하지 않음으로써 화재가 어느정도 진척되면 내부의 발포폴리스티렌이 연소되는 문제점이 있으며,성형된 발포폴리스티렌의 내측으로 난연재를 주사하여 투입하는 것은 성형된 발포폴리스티렌에 다수의 주사바늘 구멍등 외면이 손상되어 발포폴리스티렌 성형물의 강도를 약화할 뿐만 아니라, 그 수많은 바늘구멍을 통해 내부 함침된 난연재가 외부로 유출되어 난연효과가 떨어지게 되는 문제점이 있었다.Among the above conventional methods, the method of compression molding expanded polystyrene by applying porous mineral particles to the outside of the beads has excellent flame retardancy, but reduces processability, thermal insulation and moldability, which are inherent properties of expanded polystyrene, and the manufactured expanded polystyrene is heavy and It has a property of being easily brittle, so it is difficult to handle, and productivity is lowered, and when moisture penetrates into the finished product, there are drawbacks such as poor adhesion of the flame retardant. In this case, the flame retardant material must be applied to the surface of the expanded polystyrene molded product and dried, so it takes a lot of manpower and time to work, lowering productivity, adding a large manufacturing device, and increasing the price of expanded polystyrene. Since there is no flame retardant on the cut surface, there is a problem that the internal expanded polystyrene is burned when the fire progresses to some extent. This damage not only weakens the strength of the expanded polystyrene molding, but also has a problem in that the flame retardant material impregnated inside is leaked out through the numerous needle holes, thereby reducing the flame retardant effect.
본 발명은 상기와 같은 종래와 같은 문제점을 해결하고자 제안한 것으로서 스티로폼의 성형원료가 되는 비드의 내측으로 자기소화성을 갖는 난연재를 투입되도록 하여 발포폴리스티렌의 우수한 특성을 저해하지 않으면서 자기소화성을 갖도록 하여 화염이 전달되거나 유해가스가 발생하지 않도록 하는 난연비드조성물 및 난연발포폴리스티렌의 원료가 되는 난연비드조성물의 제조방법을 제안함에 그 목적이 있다.The present invention has been proposed to solve the same problems as in the prior art, and by injecting a flame retardant having self-extinguishing properties into the inside of a bead, which is a molding raw material of Styrofoam, to have self-extinguishing properties without compromising the excellent properties of expanded polystyrene. An object of the present invention is to propose a flame-retardant bead composition and a method for producing a flame-retardant bead composition which is a raw material of flame-retardant expanded polystyrene to prevent the transmission or harmful gas from being generated.
본 발명에서 난연비드조성물은 점성을 가지는 액상의 제1조성물과 분말형의 제2조성물을 순차로 EPS와 혼합하여 난연비드조성물을 형성하는 것으로 난연비드조성물은 연소하기 쉬운 성질을 가진 비드에 불연성 효과가 큰 물질을 첨가함으로써 발화를 늦춰주고, 연소의 확대를 막아주는 첨가제로 크게 첨가형 난연재와 반응형난연재로 구분할 수 있으며 본 발명은 첨가형 난연제 난연성분의 물질을 비드에 물리적으로 혼합, 첨가, 분산하여 흡열반응 등에 의해서 연소되는 곳의 온도를 떨어뜨리는 냉각 및 열, 가연성기체, 산소등 이동방지을 방지하여 연소반응의 지연하는 보호막의 형성하고 비가연성 물질을 생성하여 가연성분을 희석하여 난연 효과를 얻는 것에 그 특징이 있다.In the present invention, the flame-retardant bead composition is to form a flame-retardant bead composition by sequentially mixing a liquid first composition having viscosity and a powder-type second composition with EPS. It is an additive that slows ignition by adding a large material and prevents the expansion of combustion. It can be largely divided into additive type flame retardant and reactive flame retardant. In order to obtain a flame retardant effect by forming a protective film that delays combustion reaction by preventing cooling and heat, inflammable gas, oxygen, etc., which decrease the temperature of the combustion site by endothermic reaction, etc. It has its characteristics.
이상과 같이되는 본 발명은 점성을 가지는 액상의 난연비드조성물과 분말의 난연비드조성물로 되어 EPS와 순차로 교반하고 건조하여 발포폴리스틸렌입자의 소재인 난연비드를 제조할 수 있으므로 그 제조공정이 간단하여 생산성이 우수하고 친환경적인 난연성발포폴리스티렌을 얻을 수 있는 이점이 있다.The present invention as described above is made of a liquid flame-retardant bead composition having viscosity and a powder flame-retardant bead composition, stirred with EPS in sequence and dried to manufacture flame-retardant beads, a material of expanded polystyrene particles, so the manufacturing process is simple, There is an advantage in that it is possible to obtain an eco-friendly flame-retardant expanded polystyrene with excellent productivity.
본 발명에서 난연비드조성물은 연소하기 쉬운 성질을 가진 비드에 불연성 효과가 큰 물질을 첨가함으로써 발화를 늦춰주고, 연소의 확대를 막아주는 첨가제로 크게 첨가형 난연재와 반응형난연재로 구분할 수 있으며 본 발명은 첨가형 난연제 난연성분의 물질을 비드에 물리적으로 혼합, 첨가, 분산하여 흡열반응 등에 의해서 연소되는 곳의 온도를 떨어뜨리는 냉각 및 열, 가연성기체, 산소등 이동방지을 방지하여 연소반응의 지연하는 보호막의 형성하고 비가연성 물질을 생성하여 가연성분을 희석하여 난연 효과를 얻는 것이다In the present invention, the flame-retardant bead composition is an additive that slows ignition by adding a material having a large non-combustible effect to a bead having a property of being easily combusted and prevents the expansion of combustion. Additive type flame retardant The material of the flame retardant component is physically mixed, added, and dispersed in the bead to reduce the temperature of the combustion site by endothermic reaction, etc., and prevent the movement of heat, combustible gas, oxygen, etc. and to obtain a flame retardant effect by diluting the combustible component by creating a non-combustible material.
본 발명의 난연비드조성물은 점성을 가지는 액상의 제1조성물과 분말형의 제2조성물로 형성된다The flame-retardant bead composition of the present invention is formed of a liquid first composition having viscosity and a powdery second composition
먼저 제1조성물은 폴리졸, 메탄올, 인산암모늄, 탄산암모늄, 요소, 가소재, 팽창흑연, 인계난연재, 물을 혼합하여 구성된다.First, the first composition is composed of a mixture of polysol, methanol, ammonium phosphate, ammonium carbonate, urea, plasticizer, expanded graphite, phosphorus-based flame retardant, and water.
상기에서 난연재로서 인계난연재, 탄산암모늄, 인산암모늄, 요소, 팽창흑연이다In the above flame retardants, phosphorus-based flame retardants, ammonium carbonate, ammonium phosphate, urea, and expanded graphite are
인계난연재의 난연 메커니즘은 열분해에 의해 인산 메타인산과 폴리메타 인산을 생성해, 인산 층에 의한 보호 층의 형성과 폴리메타 인산에 의한 탈수작용으로 생성된 열전도율이 낮은 탄화피막을 형성하므로써는 탄화물에 의한 연소를 방지하는 차단 효과가 주로 작용하여 난연성을 나타낸다.The flame retardant mechanism of phosphorus-based flame retardants produces metaphosphoric acid and polymetaphosphoric acid by thermal decomposition, and forms a carbonized film with low thermal conductivity created by the formation of a protective layer by the phosphoric acid layer and dehydration by polymetaphosphoric acid, thereby protecting the carbide. The blocking effect to prevent combustion by the main action acts as a flame retardant.
또한 본 발명에서 인계난연재는 크게 무기계와 유기계로 분류할 수 있으며, 무기계로는 암모늄 포스페이트, 암모늄 폴리포스페이트 등이 사용될 수 있으며 유기계로서 트리아릴 포스페이트류가 사용될 수있다.In addition, in the present invention, phosphorus-based flame retardants can be largely classified into inorganic and organic types, and ammonium phosphate, ammonium polyphosphate, etc. may be used as inorganic types, and triaryl phosphates may be used as organic types.
인계난연재의 탄화층은 불연성 효과가 큰 물질로 연소반응의 지연하는 보호막의 형성하고 다공성을 가지므로 질소, 이산화탄소등의 비가연성 가스를 함유하므로 가연성기체, 산소등의 이동을 방지하여 난연 효과를 얻는다.The carbonized layer of the phosphorus-based flame retardant is a material with a large non-combustible effect, which forms a protective film to delay the combustion reaction and contains non-combustible gases such as nitrogen and carbon dioxide because it has porosity. .
인계난연재는 본 발명 제1조성물에서 6~9%중량비를 갖는다.The phosphorus-based flame retardant has a weight ratio of 6 to 9% in the first composition of the present invention.
인산암모늄은 제1인산암모늄과 제2인산암모늄 및 제3인산암모늄등이 있으며 본 발명에서는 질소 21%, 인산 53%의 제2인산암모늄이 난연재로 바람직하며 인산암모늄은 가열시에 질소가스를 생성하여 가연성기체, 산소등의 이동을 방지하여 연소반응의 지연하는 보호막의 형성하고 비가연성 물질을 생성하여 가연성분 희석하여 난연 효과를 생성한다.Ammonium phosphate includes ammonium phosphate dibasic, ammonium phosphate dibasic and ammonium tertiary. In the present invention, diammonium phosphate containing 21% nitrogen and 53% phosphate is preferred as a flame retardant, and ammonium phosphate generates nitrogen gas when heated. This prevents the movement of combustible gas, oxygen, etc. to form a protective film that delays the combustion reaction, and creates a non-combustible material to dilute the combustible components to create a flame retardant effect.
인산암모늄은 본 발명 제1조성물에서 15~17%중량비를 갖는다.Ammonium phosphate has a weight ratio of 15 to 17% in the first composition of the present invention.
요소는 무색 주상의 결정으로 물에는 비교적 잘 녹고 가열하면 분해되어 이산화탄소와 암모니아가스로 분해되므로 가연성기체, 산소등의 이동을 방지하여 연소반응의 지연하는 보호막의 형성하고 비가연성 물질을 생성하여 가연성분 희석하여 난연 효과를 생성한다.Urea is a colorless columnar crystal that dissolves relatively well in water and decomposes when heated to carbon dioxide and ammonia gas. It is diluted to produce a flame retardant effect.
요소는 본 발명 제1조성물에서 9~11%중량비를 갖는다.Urea has a weight ratio of 9 to 11% in the first composition of the present invention.
탄산암모늄은 무색의 사방정계의 미세한 결정으로 공기 중에 방치하면 암모니아를 발생하면서 서서히 탄산수소암모늄으로 변화하고 가열하면 암모니아, 물, 이산화탄소로 분해되므로써 가연성기체, 산소등의 이동을 방지하여 연소반응의 지연하는 보호막의 형성하고 비가연성 물질을 생성하여 가연성분 희석하여 난연 효과를 생성한다.Ammonium carbonate is colorless orthorhombic fine crystals that, when left in the air, generate ammonia and gradually change to ammonium bicarbonate. When heated, it decomposes into ammonia, water and carbon dioxide, thereby preventing the movement of combustible gases and oxygen, thereby delaying the combustion reaction. It creates a flame retardant effect by diluting combustible components by forming a protective film that
탄산암모늄은 본 발명 제1조성물에서 15~16%중량비를 갖는다.Ammonium carbonate has a weight ratio of 15 to 16% in the first composition of the present invention.
팽창흑연은 천연흑연 인조흑연을 산으로 함침하여 산화시킨 것으로 180℃ 이상으로 가열되면 팽창을 시작한다. Expanded graphite is oxidized by impregnating natural graphite and artificial graphite with acid, and it starts to expand when heated to 180°C or higher.
팽창흑연분말은 다공성층으로 구성되며 다공층에 질소 ,이산화탄소등의 비가연성가스를 함침하여 가연성기체, 산소등 이동방지을 방지하여 연소반응의 지연하고 비가연성 물질을 생성하여 가연성분 희석한다.Expanded graphite powder is composed of a porous layer, and by impregnating the porous layer with non-combustible gases such as nitrogen and carbon dioxide, it prevents the movement of combustible gas and oxygen, thereby delaying the combustion reaction and producing non-combustible substances to dilute combustible components.
팽창흑연은 그 입자가 작을수록 팽창률과 탄소함유량이 크게 되는 특징이 있다.Expanded graphite is characterized in that the smaller the particle, the greater the expansion rate and carbon content.
팽창흑연은 본 발명 제1조성물에서 16~18%중량비를 갖는다.Expanded graphite has a weight ratio of 16 to 18% in the first composition of the present invention.
본 발명의 제1조성물은 점성을 가진 액상으로 구성되므로 상기 난연재에 더하여 용매재로 메탄롤15~16%중량부와 물9~10%중량부, 접착재로서 폴리졸6~7%중량부, 가소재5~7%중량부를 혼합하여 구성된다.Since the first composition of the present invention is composed of a liquid with viscosity, in addition to the flame retardant, 15 to 16% by weight of methanol and 9 to 10% by weight of water as a solvent, 6 to 7% by weight of polysol as an adhesive, and plasticization It is constituted by mixing 5 to 7% parts by weight of ash.
한편 본 발명의 제2조성물은 분말난연재로서 팽창흑연과 인계난연재를 1.5:1중량비로 혼합하여 형성한다.Meanwhile, the second composition of the present invention is formed by mixing expanded graphite and phosphorus-based flame retardant in a weight ratio of 1.5:1 as a powder flame retardant.
이하 상기 조성물과 EPS를 혼합하여 난연비드를 형성하는 제조공정을 상세히 설명하면 다음과 같다.Hereinafter, a manufacturing process of mixing the composition and EPS to form a flame-retardant bead will be described in detail as follows.
먼저 제조공정을 설명하기에 앞서 후술하는 용어를 정의하면 EPS는 발포폴리스티렌의 소재를 지칭하는 명칭이고 난연비드는 EPS에 제1 및 제2조성물이 코팅된 발포되지 않은 발포폴리스티렌의 소재임을 주지하여야 한다.First, when defining the terms to be described below before describing the manufacturing process, it should be noted that EPS is a name that refers to a material of expanded polystyrene, and flame-retardant beads are a material of non-foamed polystyrene in which the first and second compositions are coated on EPS. .
본 발명의 난연비드제조방법으로서 교반기에4:1중량비로 EPS와 제1조성물을 투입하여 1차로 투입하고 교반하여 EPS의 표면에 점성을 가지는 제1조성물을 도포하는 제1교반공정과,As the flame retardant bead manufacturing method of the present invention, a first stirring step of applying the first composition having viscosity to the surface of the EPS by putting the EPS and the first composition into a stirrer in a 4:1 weight ratio, and stirring,
EPS와 제1조성물의 혼합물에 2차조성물을 5:1중량비로 혼합하여 교반하므로서 제1조성물에 2차조성물이 골고루 접착하게 하는 제2교반공정과, A second stirring process of mixing the secondary composition in a mixture of EPS and the first composition in a 5:1 weight ratio and stirring to uniformly adhere the secondary composition to the first composition;
1차교반공정과 2차교반공정을 통하여 EPS에 1차조성물 및 제2차조성물이 순차로 접착된 결과물이 투입된 교반기에 저압의 압축공기를 공급하며 교반하므로서 제1조성물의 용매재인 메탄올과 물의 증발시켜 접착성을 상실하게 하므로서 각각의 EPS가 1차조성물 및 제2차조성물이 코팅된 난연비드로 구성하는 제3교반공정으로 이루어진다.Evaporation of methanol and water, the solvent material of the first composition, by supplying low-pressure compressed air to the stirrer to which the result of sequentially bonding the primary and secondary compositions to EPS through the primary and secondary stirring processes is supplied and stirring to lose adhesiveness, so that each EPS consists of a third stirring process composed of flame-retardant beads coated with a primary composition and a secondary composition.
상기에서 제1 내지 제3교반공정은 본 발명의 이해를 돕기 위하여 구분하여 설명하였지만 제1 내지 제3교반공정은 동일교반기내에서 순차로 연속하여 이루어진다.In the above, the first to third stirring steps have been separately described to help the understanding of the present invention, but the first to third stirring steps are sequentially and continuously performed in the same stirrer.
Claims (6)
메탄롤15~16%중량부와 물9~10%중량부, 의 용매재와
폴리졸6~7%중량부, 의 접착재와.
가소재5~7%중량부,
를 혼합하여 점성을 가지는 액상의 제1조성물과,
팽창흑연과 인계난연재를 1.5:1중량비로 혼합하여 분말상의 제2조성물,
4:1중량비로 EPS와 제1조성물을 교반하고 EPS와 제1조성물의 혼합물에 2차조성물을 5:1중량비로 혼합교반하여서 되는 것을 특징으로 하는 난연비드 조성물 Ammonium phosphate 15-17% weight ratio, ammonium carbonate 15-16% weight ratio, urea 9-11% weight ratio, expanded graphite 16-18% weight ratio, phosphorus-based flame retardant 6-9% weight ratio,
15 to 16% by weight of methanol and 9 to 10% by weight of water, a solvent of
6-7% by weight of polysol, with an adhesive.
Plastic material 5-7% by weight,
A liquid first composition having viscosity by mixing
A powdery second composition by mixing expanded graphite and phosphorus-based flame retardant in a 1.5:1 weight ratio;
Flame-retardant bead composition, characterized in that by stirring the EPS and the first composition in a 4:1 weight ratio, and mixing and stirring the second composition in a mixture of EPS and the first composition in a 5:1 weight ratio
인계난연재는 암모늄 포스페이트 인 것을 특징으로 하는 난연비드 조성물.The method of claim 1
A flame retardant bead composition, characterized in that the phosphorus-based flame retardant is ammonium phosphate.
인계난연재는 암모늄 폴리포스페이트 인 것을 특징으로 하는 난연비드 조성물.The method of claim 1
A flame retardant bead composition, characterized in that the phosphorus-based flame retardant is ammonium polyphosphate.
인계난연재는 트리아릴 포스페이트인 것을 특징으로 하는 난연비드 조성물.The method of claim 1
The flame retardant bead composition, characterized in that the phosphorus-based flame retardant is triaryl phosphate.
인산암모늄은 질소 21%, 인산 53%의 제2인산암모늄인 것을 특징으로 하는 난연비드 조성물.
The method of claim 1
Ammonium phosphate is a flame retardant bead composition, characterized in that the diammonium phosphate of nitrogen 21%, phosphoric acid 53%.
1차교반공정의 결과물에 2차조성물을 5:1중량비로 혼합하여 교반하는 제2교반공정과,
제2교반공정결과물에 저압의 압축공기를 공급하며 교반하므로서 용매재인 메탄올과 물의 증발시켜 건조하는 제3교반공정으로 이루어지는 난연비드조성물의 제조방법.
A first stirring process of mixing and stirring the EPS and the first composition in a 4:1 weight ratio.
A second stirring step of mixing the second composition with the result of the first stirring step in a 5:1 weight ratio and stirring;
A method for producing a flame-retardant bead composition comprising a third stirring step of evaporating methanol and water as a solvent by supplying low-pressure compressed air to the result of the second stirring process and stirring.
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KR100492199B1 (en) | 1997-05-14 | 2005-06-02 | 바스프 악티엔게젤샤프트 | Method for Producing Expandable Styrene Polymers Containing Graphite Particles |
KR100782311B1 (en) | 2005-11-22 | 2007-12-06 | 금호석유화학 주식회사 | Method for manufacturing expandable polystyrene particles with excellent thermal insulation capability |
KR101513977B1 (en) * | 2015-01-29 | 2015-04-21 | 김영선 | Manufacturing Method of Aqueous Frame Retardant Adhesive for Flame-Retardant Coating Composition using in Expanded Polystyrene Molded Articles, and Manufacturing Method of Flame-Retardant Expanded Polystyrene Molded Articles Thereof |
KR101536645B1 (en) * | 2013-10-01 | 2015-07-14 | 이제훈 | Dry manufactuting method of styrofoam for the improvement of non-flammable |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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KR100492199B1 (en) | 1997-05-14 | 2005-06-02 | 바스프 악티엔게젤샤프트 | Method for Producing Expandable Styrene Polymers Containing Graphite Particles |
KR100782311B1 (en) | 2005-11-22 | 2007-12-06 | 금호석유화학 주식회사 | Method for manufacturing expandable polystyrene particles with excellent thermal insulation capability |
KR101536645B1 (en) * | 2013-10-01 | 2015-07-14 | 이제훈 | Dry manufactuting method of styrofoam for the improvement of non-flammable |
KR101513977B1 (en) * | 2015-01-29 | 2015-04-21 | 김영선 | Manufacturing Method of Aqueous Frame Retardant Adhesive for Flame-Retardant Coating Composition using in Expanded Polystyrene Molded Articles, and Manufacturing Method of Flame-Retardant Expanded Polystyrene Molded Articles Thereof |
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