KR20100090566A - Fiber by using spray coating and uv stiffening and preparing thereof - Google Patents
Fiber by using spray coating and uv stiffening and preparing thereof Download PDFInfo
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- KR20100090566A KR20100090566A KR1020090009914A KR20090009914A KR20100090566A KR 20100090566 A KR20100090566 A KR 20100090566A KR 1020090009914 A KR1020090009914 A KR 1020090009914A KR 20090009914 A KR20090009914 A KR 20090009914A KR 20100090566 A KR20100090566 A KR 20100090566A
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- flame retardant
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- 238000005507 spraying Methods 0.000 title claims abstract description 36
- 239000000835 fiber Substances 0.000 title description 5
- 239000004744 fabric Substances 0.000 claims abstract description 95
- 238000000034 method Methods 0.000 claims abstract description 49
- 238000006243 chemical reaction Methods 0.000 claims abstract description 24
- 238000004519 manufacturing process Methods 0.000 claims abstract description 24
- 239000002270 dispersing agent Substances 0.000 claims abstract description 22
- 239000003085 diluting agent Substances 0.000 claims abstract description 19
- 238000003848 UV Light-Curing Methods 0.000 claims abstract description 15
- 239000007921 spray Substances 0.000 claims abstract description 6
- 238000002156 mixing Methods 0.000 claims abstract description 5
- 239000003063 flame retardant Substances 0.000 claims description 105
- 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 claims description 104
- 238000001723 curing Methods 0.000 claims description 50
- 239000007788 liquid Substances 0.000 claims description 22
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 20
- 229910052698 phosphorus Inorganic materials 0.000 claims description 20
- 239000011574 phosphorus Substances 0.000 claims description 20
- 230000008569 process Effects 0.000 claims description 19
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 18
- 239000000178 monomer Substances 0.000 claims description 18
- 239000003431 cross linking reagent Substances 0.000 claims description 17
- 238000001035 drying Methods 0.000 claims description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- 229920005906 polyester polyol Polymers 0.000 claims description 8
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 claims description 6
- 235000010290 biphenyl Nutrition 0.000 claims description 6
- 239000004305 biphenyl Substances 0.000 claims description 6
- 125000006267 biphenyl group Chemical group 0.000 claims description 6
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 229920002113 octoxynol Polymers 0.000 claims description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 5
- 150000002829 nitrogen Chemical class 0.000 claims description 4
- 238000012545 processing Methods 0.000 abstract description 18
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 239000003999 initiator Substances 0.000 abstract 2
- 239000004971 Cross linker Substances 0.000 abstract 1
- 238000005406 washing Methods 0.000 description 10
- 238000003763 carbonization Methods 0.000 description 9
- 239000000779 smoke Substances 0.000 description 9
- 239000000758 substrate Substances 0.000 description 9
- 239000012224 working solution Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 5
- 238000003618 dip coating Methods 0.000 description 4
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 4
- 238000003672 processing method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 230000009977 dual effect Effects 0.000 description 3
- 238000013007 heat curing Methods 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910001507 metal halide Inorganic materials 0.000 description 3
- 150000005309 metal halides Chemical class 0.000 description 3
- MCONGYNHPPCHSD-UHFFFAOYSA-N 3-dimethoxyphosphoryl-n-(hydroxymethyl)propanamide Chemical compound COP(=O)(OC)CCC(=O)NCO MCONGYNHPPCHSD-UHFFFAOYSA-N 0.000 description 2
- 235000010724 Wisteria floribunda Nutrition 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000009501 film coating Methods 0.000 description 2
- 239000007888 film coating Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ARJMTSLMOKRKPM-UHFFFAOYSA-N C(C=C)(=O)O.C(C=C)(=O)O.C(C=C)(=O)O.N=C=O Chemical compound C(C=C)(=O)O.C(C=C)(=O)O.C(C=C)(=O)O.N=C=O ARJMTSLMOKRKPM-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- YACTZEZVNPAVGJ-UHFFFAOYSA-N P.C(=O)(O)C=C.C(=O)(O)C=C.C(=O)(O)C=C Chemical compound P.C(=O)(O)C=C.C(=O)(O)C=C.C(=O)(O)C=C YACTZEZVNPAVGJ-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- JAWMENYCRQKKJY-UHFFFAOYSA-N [3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-ylmethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-en-8-yl]-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]methanone Chemical compound N1N=NC=2CN(CCC=21)CC1=NOC2(C1)CCN(CC2)C(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F JAWMENYCRQKKJY-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- -1 bis-methacryloyl oxyethyl phosphate Chemical compound 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Images
Classifications
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/68—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof
- D06M11/70—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof with oxides of phosphorus; with hypophosphorous, phosphorous or phosphoric acids or their salts
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B1/00—Applying liquids, gases or vapours onto textile materials to effect treatment, e.g. washing, dyeing, bleaching, sizing or impregnating
- D06B1/02—Applying liquids, gases or vapours onto textile materials to effect treatment, e.g. washing, dyeing, bleaching, sizing or impregnating by spraying or projecting
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M10/00—Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements
- D06M10/001—Treatment with visible light, infrared or ultraviolet, X-rays
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/345—Nitriles
- D06M13/348—Nitriles unsaturated, e.g. acrylonitrile
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/347—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated ethers, acetals, hemiacetals, ketones or aldehydes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/30—Flame or heat resistance, fire retardancy properties
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S57/00—Textiles: spinning, twisting, and twining
- Y10S57/904—Flame retardant
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Description
본 발명은 방염직물 및 이의 제조방법에 관한 것으로 보다 상세하게는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물 및 이의 제조방법에 관한 것이다.The present invention relates to a flame retardant fabric and a method for producing the same, and more particularly, to a flame retardant fabric using a spray coating method and an ultraviolet curing method and a method for manufacturing the same.
방염가공은 섬유에 불꽃을 가까이 하면 타기는 하지만 일단 불꽃을 떼면 스스로 불꽃을 내면서 타지 않고 직접 불꽃을 받아 탄화된 면적이상으로 화재를 전파, 확대하지 않도록 섬유를 처리하는 것을 말하는데, 섬유를 방염가공하는 방법으로는 ① 섬유 고분자를 합성할 때 방염성 단량체를 공중합시키는 방법, ② 방사시 방사액에 방염제를 첨가하는 방법, ③ 후가공처리하는 방법이 있는데, 합성섬유는 3가지 방법이 모두 가능하나, 천연섬유는 후가공에 의존할 수 밖에 없다.Flame retardant processing means that the flame is burned when the flame is close to the fiber, but once the flame is removed, the flame is not burned by itself and the flame is directly received and the fiber is treated so as not to spread or spread the fire over the carbonized area. Methods include ① copolymerizing flame retardant monomer when synthesizing fiber polymer, ② adding flame retardant to spinning solution during spinning, and ③ post-treatment treatment. Synthetic fiber is available in three ways, but natural fiber Is forced to rely on post-processing.
방염가공방식에는 기존의 열경화에 의한 방염가공인 피로바텍스(Pyrovatex) CP 방식이 있는데, 이는 시바社의 제품으로 유기인 화합물을 주성분으로 하는 것으 로 멜라민 수지와 촉매로 수지가공과 같은 가공법으로 처리하는 것이므로 가공된 가공포는 저독성이며 내세탁성이 있고, 촉감이 우수한 것이 특징이다. 그러나, 상기 피로바텍스(Pyrovatex) CP 방식은 직물의 방염성을 부여하기 위해서는 여러 가지 문제점을 지니고 있다. 상기 방식은 가공시 가공 조제의 특성상 심한 냄새로 인해 작업장 환경이 문제 될 뿐만 아니라, 가공 후 직물의 물성저하가 초래되는 데 이는 조제액의 pH가 약산성인 pH 3-4 수준으로 직물에는 특히 문제가 많다. 또한, 가공 후 색상차가 심하여 품질관리 면에서도 어려움이 따르는 가공방법이다.Flame-proof processing method is Pyrovatex CP method, which is a conventional flame-resistant processing by heat curing, which is a product of Ciba, which is mainly composed of organophosphorus compound, and it is processed by resin processing with melamine resin and catalyst. Because it is treated, the processed fabric is characterized by low toxicity, washing resistance, and excellent touch. However, the Pyrovatex CP method has various problems in order to impart flame retardancy of the fabric. In the above method, not only the environment of the work environment is affected by the severe smell of the processing aid during processing, but also the degradation of the physical properties of the fabric after the processing, which is a pH 3-4 level of the pH of the preparation liquid is particularly problematic for the fabric. many. In addition, it is a processing method that is difficult in terms of quality control due to severe color difference after processing.
이러한 열경화 방식 방염가공의 문제점으로 인해 열경화 방식이 아닌 다른 방법으로 방염가공을 할 수 있는 방법에 대해서 고민하게 되었고, 이러한 문제점을 해결하면서도 친환경적, 저에너지 소비의 미래지향적 가공법으로 자외선경화방식을 이용한 방염가공에 대해서 생각하게 되었다.Due to the problem of heat curing flame retardant processing, I have been worried about the method of flame retardant processing by a method other than the heat curing method, and using the UV curing method as a future-oriented processing method of eco-friendly and low energy consumption while solving these problems. I came to think about flameproofing.
현재 자외선 경화를 이용한 표면 경화 혹은 표면개질 등은 많은 기술분야에서 다양하게 활용되고 있는데, 목재 및 금속의 표면 코팅, IT 분야 등 자외선 경화가 갖는 미래지향적 가치로 인해 많은 시도들이 행해져 왔으며, 섬유 분야에서도 자외선 경화를 이용한 방염가공 방법에 대한 연구들이 진행되고 있다.Currently, surface hardening or surface modification using UV curing is widely used in many technical fields, and many attempts have been made due to the future-oriented value of UV hardening such as surface coating of wood and metal and IT field. Studies on the flameproof processing method using UV curing are in progress.
자외선을 이용한 직물의 표면경화코팅은 낮은 에너지를 사용하고, 용매(solvent)를 소량 사용하며, 온도 민감 기질체인 종이 또는 플라스틱에도 처리 가능할 뿐만 아니라 경화 속도가 빨라 생산속도를 향상시켜주는 장점을 지녔다. 그러나 UV 경화는 주로 메탈 또는 필름형태의 기질체에 주로 사용되고 있다. The surface hardening coating of the fabric using UV light has the advantages of using low energy, using a small amount of solvent, treating the paper or plastic which is a temperature sensitive substrate, and improving the production speed due to the fast curing speed. However, UV curing is mainly used for substrates in the form of metal or film.
미국 등록특허 제6,420,447호는 수계 코팅 조성물인 분자량 500에서 1,000,000의 폴리우레탄 수지를 이용하여 금속 시트(Metal Sheet) 표면을 UV 경화 처리해 줌으로써 UV경화 잉크 또는 접착제가 잘 접착되도록 해주는 공정을 언급하였다. 그러나 상기 발명에서는 섬유 제품에 대한 공정에 대해서는 언급하지 않았다.US Patent No. 6,420, 447 refers to a process of UV curing the surface of a metal sheet using a polyurethane resin having a molecular weight of 500 to 1,000,000, which is an aqueous coating composition, so that the UV curing ink or adhesive may be adhered well. However, the invention does not mention a process for textile products.
자외선 경화 코팅방식에는 딥 코팅(dip coating), 스프레이 코팅(spray coating), 필름 코팅법(film coating)등이 있다. 기질체를 직물을 이용할 경우 상기 3종류의 코팅방식이 다 적용이 되지만, 딥 코팅(dip coating)의 경우 직물의 두께가 200㎛이상을 지니게 되면 UV가 직물 내부 안까지 깊숙이 침투하여 내부의 경화액이 충분히 경화시키지 못한다. 충분한 경화를 시키기 위해서는 건조 시간을 길게 하거나 건조 온도를 올려야하는 단점이 있다. UV curing coating methods include dip coating, spray coating, film coating, and the like. When the substrate is used as a fabric, all three types of coating methods are applied. However, in the case of dip coating, when the thickness of the fabric is 200 μm or more, UV penetrates deeply into the inside of the fabric and the curing liquid inside It does not cure enough. In order to sufficiently cure, there is a disadvantage in that the drying time is lengthened or the drying temperature is increased.
딥 코팅(dip coating)법 중 하나인 침지방식이 있는 데 이는 직물을 가공액에 침지하여 방염직물 제조하는 것으로써, 최종적으로 제조된 방염직물은 UV가 직물 내부까지 경화되지 못하여 내구성이 약한 단점을 지닌다. There is a dip coating method, which is an immersion method, which manufactures flame retardant fabrics by immersing the fabric in a processing liquid. Finally, the prepared flame retardant fabric has a weak durability due to UV hardening to the inside of the fabric. Have
필름 코팅법(film coating)의 경우는 경화액의 점도가 높아져 가공액의 양이 많아 질 뿐 아니라 직물의 경우 중요한 드레이프(drape)부분에 문제가 발생하기 때문에 직물처리 방법으로는 적합하지 않다.In the case of the film coating method, the viscosity of the curing liquid is increased to increase the amount of the processing liquid, and in the case of the fabric, a problem occurs in an important drape part, which is not suitable as a fabric treatment method.
마직막으로 스프레이 코팅(spray coating)은 직물 표면에 경화액을 충분히 처리해 줌으로써 200㎛이상의 후지의 기질체 내부에 경화되지 못하고 잔류하는 경화액이 존재하지 않아 경화율이 빠르며, 가공액의 손실을 줄일 수 있을 뿐만 아니라, 직물의 드레이프도 유지해주기 때문에 직물을 처리하기에 유용한 코팅방식이 다.Finally, spray coating is enough to treat the curing liquid on the surface of the fabric, which prevents the curing liquid from remaining inside the substrate of Fuji over 200㎛ and there is no remaining curing liquid. In addition to maintaining the drape of the fabric, it is a useful coating method for treating the fabric.
따라서, 방염직물을 제조하는 데 있어 적절한 방염 가공액을 사용하되 스프레이 코팅법의 공정을 통한 내구성이 우수한 방염직물의 제조가 소망되었다.Therefore, it is desired to manufacture a flame retardant fabric having excellent durability through the process of spray coating method while using an appropriate flame retardant processing liquid in the production of flame retardant fabric.
상기와 같은 문제점을 해결하기 위해 본 발명의 목적은 적절한 방염 가공액 및 스프레이 코팅법 공정을 거쳐 방염성이 높은 방염직물을 제공하는 데 있다.In order to solve the above problems, an object of the present invention is to provide a flame retardant high flame retardant fabric through a suitable flame retardant working solution and spray coating process.
또한 본 발명의 다른 목적은 기존의 열 텐터를 사용하지 않아 빠른 경화와 에너지를 절감할 뿐만 아니라, 탄화거리가 적고 경위사 수축율의 변화가 적은 방염직물을 제공하는 데 있다.In addition, another object of the present invention is to provide a flame retardant fabric that does not use a conventional thermal tenter, not only fast curing and energy saving, but also a small carbonization distance and a small change in the warp yarn shrinkage rate.
상기와 같은 목적을 해결하기 위해 본 발명은 방염 직물에 있어서, 방염 가공액은 방염제, 반응 희석제, 가교제, 광개시제, 분산제로 이루어지는데, 상기 방염 가공액 100 중량부에 대하여 자외선 경화형 인계 방염제 20 내지 40 중량부, 반응 희석제 30 내지 70 중량부, 가교제 1 내지 7 중량부, 광개시제 1 내지 5 중량부 및 분산제 0.1 내지 0.5 중량부가 혼합된 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물을 제공한다.In order to solve the above object, the present invention is a flame retardant fabric, the flame retardant working solution consists of a flame retardant, a reaction diluent, a crosslinking agent, a photoinitiator, a dispersant, UV curable phosphorus flame retardant 20 to 40 with respect to 100 parts by weight of the flame retardant working solution. Provided is a flame retardant fabric using a spray coating method and an ultraviolet curing method in which parts by weight, 30 to 70 parts by weight of a reaction diluent, 1 to 7 parts by weight of a crosslinking agent, 1 to 5 parts by weight of a photoinitiator, and 0.1 to 0.5 parts by weight of a dispersant are mixed.
또한 본 발명은 상기 자외선 경화형 인계 방염제가 하이드록시기 2~40개와 인을 포함하는 분자량 200~4000인 폴리에스테르 폴리올(Polyester Polyol) 50 내지 80 중량%와 다관능성 (메타)아크릴레이트 모노머 20 내지 50 중량%의 반응하여 제조된 것을 특징으로 하는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물을 제공한다.In addition, the present invention is the UV-curable phosphorus flame retardant 50 to 80% by weight of a polyester polyol (polyester) polyol having a molecular weight of 200 to 4000 containing 2 to 40 hydroxy groups and phosphorus and 20 to 50 polyfunctional (meth) acrylate monomers It provides a flame retardant fabric using a spray coating method and an ultraviolet curing method, characterized in that prepared by weight% reaction.
또한 본 발명은 상기 반응 희석제가 다관능성 (메타)아크릴레이트 모노머의 형태 및 상기 가교제는 질소계 다관능성 (메타)아크릴레이트 모노머 형태인 것을 특징으로 하는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물을 제공한다.The present invention also provides a flame retardant fabric using a spray coating method and an ultraviolet curing method, wherein the reaction diluent is in the form of a polyfunctional (meth) acrylate monomer and the crosslinking agent is in the form of a nitrogen-based polyfunctional (meth) acrylate monomer. to provide.
또한 본 발명은 상기 광개시제 및 분산제가 각각 1-하이드록시사이클로헥실페닐케톤과 디페닐(2,4,6-트리메틸벤조힐)-포스핀옥사이드를 중량비 4:1로 혼합한 광개시제 및 Triton-X 100을 이용한 분산제인 것을 특징으로 하는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물을 제공한다.In addition, the present invention is the photoinitiator and dispersant photoinitiator and Triton-X 100 mixed 1-hydroxycyclohexylphenyl ketone and diphenyl (2,4,6-trimethylbenzohill) -phosphine oxide in a weight ratio of 4: 1, respectively It provides a flame retardant fabric using a spray coating method and an ultraviolet curing method, characterized in that the dispersant using.
또한 본 발명은 방염직물의 제조방법에 있어서, 방염 가공액 100 중량부에 대하여 자외선 경화형 인계 방염제 20 내지 40 중량부, 반응 희석제 30내지 70 중량부, 가교제 1 내지 7 중량부, 광개시제 1 내지 5 중량부, 분산제 0.1 내지 0.5 중량부를 혼합한 방염 가공액을 제조하는 단계; 상기 방염 가공액을 직물에 코팅하는 스프레이 코팅단계; 상기 스프레이 코팅된 직물을 적외선 램프에 의해 건조하는 건조단계; 및 상기 건조된 직물을 자외선 경화기로 경화시키는 자외선 경화단계를 포함하는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물의 제조방법을 제공한다.In addition, the present invention is a method for producing a flame retardant fabric, 20 to 40 parts by weight of the ultraviolet curable phosphorus flame retardant, 30 to 70 parts by weight of the reaction diluent, 1 to 7 parts by weight of the crosslinking agent, 1 to 5 parts by weight of the flame retardant working solution Part, preparing a flame retardant mixed solution of 0.1 to 0.5 parts by weight of a dispersant; A spray coating step of coating the flame retardant process liquid on a fabric; Drying the spray-coated fabric by an infrared lamp; And it provides a method for producing a flame retardant fabric using a spray coating method and an ultraviolet curing method comprising an ultraviolet curing step of curing the dried fabric with an ultraviolet curing machine.
또한 본 발명은 상기 건조단계에서 적외선 영역 내에서 80 내지 100℃로 1분 내지 2분간 건조하는 것을 특징으로 하는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물의 제조방법을 제공한다.In another aspect, the present invention provides a method for producing a flame retardant fabric using a spray coating method and an ultraviolet curing method characterized in that for 1 minute to 2 minutes to dry at 80 to 100 ℃ in the infrared region in the drying step.
또한 본 발명은 상기 자외선 경화단계에서 중고압식 램프가 일렬로 놓인 경화기로 0.6 내지 2.4 J/㎠의 조사에너지로 경화하는 자외선 경화법을 이용한 방염직물의 제조 방법을 제공한다.In another aspect, the present invention provides a method for producing a flame retardant fabric using an ultraviolet curing method of curing with irradiation energy of 0.6 to 2.4 J / ㎠ in a curing machine in which the high-pressure lamp in a line in the ultraviolet curing step.
또한 본 발명은 상기 자외선 경화형 인계 방염제가 하이드록시기 2~40개와 인을 포함하는 분자량 200~4000인 폴리에스테르 폴리올(Polyester Polyol) 50 내지 80 중량%와 다관능성 (메타)아크릴레이트 모노머 20 내지 50 중량%의 반응하여 제조된 것을 특징으로 하는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물의 제조방법을 제공한다.In addition, the present invention is the UV-curable phosphorus flame retardant 50 to 80% by weight of a polyester polyol (polyester) polyol having a molecular weight of 200 to 4000 containing 2 to 40 hydroxy groups and phosphorus and 20 to 50 polyfunctional (meth) acrylate monomers It provides a method for producing a flame retardant fabric using a spray coating method and an ultraviolet curing method, characterized in that produced by weight% reaction.
또한 본 발명은 상기 반응 희석제가 다관능성 (메타)아크릴레이트 모노머의 형태 및 상기 가교제는 질소계 다관능성 (메타)아크릴레이트 모노머 형태인 것을 특징으로 하는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물의 제조방법을 제공한다.In another aspect, the present invention, the reaction diluent is in the form of a polyfunctional (meth) acrylate monomer and the crosslinking agent is in the form of a nitrogen-based multifunctional (meth) acrylate monomer, characterized in that the spray coating method and ultraviolet curing method It provides a manufacturing method.
또한 본 발명은 상기 광개시제 및 분산제가 각각 1-하이드록시사이클로헥실페닐케톤과 디페닐(2,4,6-트리메틸벤조힐)-포스핀옥사이드를 중량비 4:1로 혼합한 광개시제 및 Triton-X 100을 이용한 분산제인 것을 특징으로 하는 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물의 제조방법을 제공한다.In addition, the present invention is the photoinitiator and dispersant photoinitiator and Triton-X 100 mixed 1-hydroxycyclohexylphenyl ketone and diphenyl (2,4,6-trimethylbenzohill) -phosphine oxide in a weight ratio of 4: 1, respectively It provides a method for producing a flame retardant fabric using a spray coating method and an ultraviolet curing method, characterized in that the dispersant using.
본 발명에 의한 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물은 스프레이법을 통해 직물 상에 처리 후 UV 조사하여 방염층을 형성함으로써 기존의 열 텐터를 사용하지 않아 빠른 경화와 에너지를 절감할 뿐만 아니라, 경위사 수축율이 변화가 적은 방염직물을 제조할 수 있는 효과가 있다.The flame retardant fabric using the spray coating method and the ultraviolet curing method according to the present invention does not use a conventional thermal tenter to form a flame retardant layer by UV irradiation after treatment on the fabric through the spray method, thereby not only fast curing and saving energy. In addition, there is an effect that can produce a flame retardant fabric with a small change in the warp yarn shrinkage.
또한, 스프레이 코팅법 및 자외선 경화법을 이용한 방염직물 및 이의 제조방법은 자외선 경화형 방염제가 폴리올을 통해 제조된 방염제로 내수성이 강할 뿐 아니라 반응성 희석제로 사용되는 인계 다관능 (메타)아크릴레이트 및 질소가 포함된 가교제의 사용으로 방염성이 우수한 탄화거리 20cm이내, 연기밀도 200%이내의 방염직물을 제조할 수 있는 효과가 있다.In addition, a flame retardant fabric using a spray coating method and an ultraviolet curing method, and a method of manufacturing the same, is a flame retardant prepared by using a polyol as an ultraviolet curable flame retardant, which is not only resistant to water resistance but also to phosphorus-based polyfunctional (meth) acrylate and nitrogen used as a reactive diluent. The use of the included crosslinking agent has an effect of producing a flame retardant fabric of less than 20cm in the carbonization distance, excellent smoke density 200%, flame retardant.
이하 본 발명에 첨부된 도면을 참조하여 발명의 실시를 위한 구체적인 내용에서는 본 발명의 바람직한 일실시예를 상세히 설명하기로 한다. 우선, 도면들 중, 동일한 구성요소 또는 부품들은 가능한 한 동일한 참조부호를 나타내고 있음에 유의하여야 한다. 본 발명을 설명함에 있어, 관련된 공지기능 혹은 구성에 대한 구체적인 설명은 본 발명의 요지를 모호하지 않게 하기 위하여 생략한다.DETAILED DESCRIPTION Hereinafter, exemplary embodiments of the present invention will be described in detail with reference to the accompanying drawings. First, it should be noted that in the drawings, the same components or parts denote the same reference numerals as much as possible. In describing the present invention, detailed descriptions of related well-known functions or configurations are omitted in order not to obscure the subject matter of the present invention.
본 명세서에서 사용되는 정도의 용어 “약”, “실질적으로” 등은 언급된 의미에 고유한 제조 및 물질 허용오차가 제시될 때 그 수치에서 또는 그 수치에 근접한 의미로 사용되고, 본 발명의 이해를 돕기 위해 정확하거나 절대적인 수치가 언급된 개시 내용을 비양심적인 침해자가 부당하게 이용하는 것을 방지하기 위해 사용된다.As used herein, the terms “about”, “substantially”, and the like, are used at, or in close proximity to, numerical values when manufacturing and material tolerances inherent in the meanings indicated are intended to aid the understanding of the invention. Accurate or absolute figures are used to assist in the prevention of unfair use of unscrupulous infringers.
본 발명은 인을 포함하는 폴리에스테르 폴리올과 다관능성 (메타)아크릴레이트 모노머의 반응으로 제조된 UV 경화형 인계 (메타)아크릴레이트 올리고머를 이용한 방염 가공액을 제조하여, 침지 방식이 아닌 스프레이 코팅법을 사용함으로써 다량으로 사용되던 물을 사용하지 않아 적외선 램프를 통해 건조가 가능하게 하였으며, UV 조사를 해줌으로써 직물표면에서 경화가 이루어진 방염직물을 제조하는 특징이 있다.The present invention provides a flame retardant process solution using a UV-curable phosphorus-based (meth) acrylate oligomer prepared by the reaction of a polyester polyol containing phosphorus with a polyfunctional (meth) acrylate monomer, and a spray coating method other than the dipping method. By using it, it was possible to dry through infrared lamps without using water that was used in large quantities, and it was characterized by manufacturing a flame-retardant fabric which was cured on the fabric surface by UV irradiation.
본 발명의 방염 가공액은 UV 경화형 인계 방염제, 반응희석제, 가교제, 광개시제, 분산제를 혼합하여 사용하는 것을 특징으로 한다. The flame retardant process liquid of the present invention is characterized by using a UV curable phosphorus flame retardant, a reaction diluent, a crosslinking agent, a photoinitiator, and a dispersant.
본 발명의 UV 경화형 방염제로는 OH기를 다량 함유한 단량체인 경화형 방염제가 아닌 고분자량의 폴리올을 통해 제조된 인계 아크릴레이트 올리고머 방염제를 사용함으로써 종래 방염제에 비하여 세탁 내구성이 강한 장점이 있다. 상기 UV 경화형 인계 방염제는 하이드록시기 2~40개와 인을 포함하는 분자량 200~4000인 폴리에스테르 폴리올(Polyester Polyol) 50 내지 80 중량%와 다관능성 (메타)아크릴레이트 모노머 20 내지 50 중량%의 반응으로 제조된다. 상기 제조된 인계 방염제의 가공액에 혼합되는 양은 상기 방염 가공액 100에 대하여 상기 UV 경화형 인계 방염제 20 내지 40 중량부가 혼합되는 것이 바람직하다. 상기 범위내에서 방염제품으로 좋은 성능을 보이며 직물의 촉감이 좋게 된다.UV-curable flame retardant of the present invention has a strong washing durability compared to the conventional flame retardant by using a phosphorus acrylate oligomer flame retardant prepared through a high molecular weight polyol, not a curable flame retardant is a monomer containing a large amount of OH groups. The UV curable phosphorus flame retardant is a reaction of 50 to 80% by weight of a polyester polyol having a molecular weight of 200 to 4000 containing 2 to 40 hydroxyl groups and phosphorus and 20 to 50% by weight of a polyfunctional (meth) acrylate monomer Is prepared. It is preferable that 20 to 40 parts by weight of the UV-curable phosphorus flame retardant is mixed with the amount of the phosphorus flame retardant prepared in the processed liquid. The flame retardant product within the above range shows good performance and the fabric feels good.
또한 상기 반응희석제는 상기 다관능성 (메타)아크릴레이트 모노머의 형태 및 상기 가교제는 질소계 다관능성 (메타)아크릴레이트 모노머 형태인 것이 바람직 하다. 혼합되는 양은 각각 상기 방염 가공액 100에 대하여 반응 희석제 30 내지 70 중량부, 가교제 1 내지 7 중량부를 사용하는 것이 바람직하다. 상기 범위내에서 상기 반응희석제 및 상기 가교제를 사용함으로써 올리고머 타입의 방염제로 인하여 다소 떨어질 수 있는 방염성을 보완하여 주며 스프레이 코팅법에 적용하기 좋은 점도를 유지할 수 있다.In addition, the reaction diluent is preferably in the form of the polyfunctional (meth) acrylate monomer and the crosslinking agent is in the form of a nitrogen-based polyfunctional (meth) acrylate monomer. It is preferable to use 30-70 weight part of reaction diluents and 1-7 weight part of crosslinking agents with respect to the said flameproof process liquid 100, respectively. By using the reaction diluent and the cross-linking agent within the above range it is possible to compensate for the flame retardant that may fall somewhat due to the oligomer type flame retardant and maintain a good viscosity to apply to the spray coating method.
또한 상기 광개시제는 1-하이드록시사이클로헥실페닐케톤(시바社, Igacure 184) 및 디페닐(2,4,6-트리메틸벤조힐)-포스핀옥사이드(상품명:TPO, 시바社)를 중량비 4:1로 혼합한 것을 사용하는 것이 바람직한데, 상기 광개시제는 종래의 광개시제에 비해 끓는점이 높고, 디페닐(2,4,6-트리메틸벤조힐)-포스핀옥사이드(상품명:TPO, 시바社)로 인하여 장파장에서도 자외선에 의해 경화가 됨으로써 내부까지 깊숙히 경화되는 장점을 지님으로 직물과 같은 후지 상태의 기질체를 용이하게 처리할 수 있다. 상기 광개시제의 혼합량은 방염 가공액 100에 대하여 광개시제 1 내지 5 중량부를 사용하는 것이 바람직하다. 상기 범위내에서 직물의 경화가 잘 일어나며, 광개시제가 1 중량부 미만일 경우에는 경화하는 데 오랜 시간이 소요되며, 5중량부를 초과할 경우에는 오히려 경화효율이 떨어진다.In addition, the photoinitiator 1-hydroxycyclohexylphenyl ketone (Ciba, Igacure 184) and diphenyl (2,4,6-trimethylbenzohill) -phosphine oxide (trade name: TPO, Ciba) 4: 1 weight ratio It is preferable to use a mixture of the photoinitiator, the photoinitiator is higher boiling point than the conventional photoinitiator, and the long wavelength due to diphenyl (2,4,6-trimethylbenzoyl) -phosphine oxide (trade name: TPO, Ciba) In addition, since it is cured by ultraviolet rays, it has the advantage of being deeply cured to the inside, and thus it is possible to easily process the substrate in a fuji state such as fabric. The mixing amount of the photoinitiator is preferably used 1 to 5 parts by weight of the photoinitiator relative to the flame retardant 100. Hardening of the fabric is well within the above range, if the photoinitiator is less than 1 part by weight, it takes a long time to cure, if it exceeds 5 parts by weight, the curing efficiency is rather low.
한편 상기 분산제는 Triton-X 100을 사용하는 것이 바람직한 데, 상기 분산제의 혼합량은 방염 가공액 100에 대하여 0.1 내지 0.5 중량부가 함유된 방염가공액이 바람직하다. 상기 범위내에서 사용할 때 분산제가 방염제를 균일하게 혼합할 수 있다.On the other hand, the dispersant is preferably used Triton-X 100, the mixing amount of the dispersant is preferably a flame retardant solution containing 0.1 to 0.5 parts by weight relative to the flame retardant 100. When used within the above range, the dispersant may mix the flame retardant uniformly.
도 1 및 도 2는 본 발명의 바람직한 일실시예에 따른 직물의 방염가공 처리 단계 및 방염직물을 제조하는 장치로 듀어 큐어(Dual cure)인 열과 UV를 이용하여 경화되는 공정도를 나타낸 것이다.Figures 1 and 2 show the process of curing using heat and UV as a dual cure (dual cure) as an apparatus for producing a flame retardant processing step and a flame retardant fabric of the fabric according to an embodiment of the present invention.
상기 스프레이 코팅단계에서는 상기 언급된 방염 가공액 100에 대하여 자외선 경화형 방염제 20 내지 40 중량부, 반응 희석제 30 내지 70 중량부, 가교제 1 내지 7 중량부, 광개시제 1 내지 5 중량부 및 분산제 0.1 내지 0.5 중량부가 혼합된 가공액을 상온인 25℃에서 30 내지 60분 동안 자석교반기를 이용하여 약 800 rpm으로 충분히 교반(stirring)시켜 방염 가공액을 제조한다. In the spray coating step, 20 to 40 parts by weight of the ultraviolet curable flame retardant, 30 to 70 parts by weight of the reaction diluent, 1 to 7 parts by weight of the crosslinking agent, 1 to 5 parts by weight of the photoinitiator, and 0.1 to 0.5 weight of the dispersant based on the flame retardant 100 mentioned above. The addition-mixed working solution is sufficiently stirred at about 800 rpm using a magnetic stirrer at 25 ° C. at room temperature for 30 to 60 minutes to prepare a flameproof working solution.
상기 방염 가공액을 직물에 코팅하는 스프레이 코팅단계에서는 상기 제조된 방염 가공액을 스프레이 코팅 존(zone)에 있는 스프레이건을 통해 기질체인 직물 표면 위에 스프레이 코팅으로 500 내지 700㎛ 정도로 도포됨으로써 방염층을 형성시킨다.In the spray coating step of coating the flame retardant process liquid on the fabric, the prepared flame retardant process liquid is sprayed on the surface of the substrate with a spray coating on the surface of the substrate through a spray gun in a spray coating zone to obtain a flame retardant layer. Form.
상기 방염층이 형성된 직물은 다음으로 적외선 램프에 의해 건조하는 단계를 거치는 데 도 2의 열건조 존(zone)에서 분당 20 내지 30m로 이송되어 80 내지 100℃의 온도에서 1 내지 2분 정도 건조시키는 것이 바람직하다. 이는 방염 가공액이 직물에 잘 흡착되도록 하기 위함이다. 상기 적외선 램프에 의해 건조가 됨으로써 처리속도가 개선되고 이로 인하여 직물의 수축율에도 영향을 끼쳐 낮은 수축율을 보이게 된다. The fabric having the flame resistant layer is then dried by an infrared lamp to be transferred to 20 to 30 meters per minute in the heat drying zone of FIG. 2 to be dried at a temperature of 80 to 100 ° C. for 1 to 2 minutes. It is preferable. This is to ensure that the flame retardant process liquid is well adsorbed on the fabric. Drying by the infrared lamp improves the processing speed, thereby affecting the shrinkage rate of the fabric and thus exhibiting a low shrinkage rate.
마지막으로 상기 본 발명의 자외선 경화단계에서는 상기 건조된 직물을 자외선 경화기를 이용하여 경화시키는 데, 중고압식 수은램프와 메탈할라이드 램프가 일렬로 놓인 경화기가 장착된 UV 경화 존(zone)에서 0.6 내지 2.4 J/㎠ 의 조사에 너지로 연속적으로 자외선 경화를 시킨다. 상기 범위내의 에너지로 경화시켰을 때 방염 가공액이 직물에 잘 고착되어 제품의 성능이 좋아진다. 자외선 경화시 0.6J/㎠ 미만에서는 경화효율이 떨어지는 문제점이 발생하고, 2.4 J/㎠를 초과하는 경우 방염제의 화학구조가 파괴되어 경화효율이 떨어져 한계산소지수(Limited Oxyzen Index, LOI)값이 떨어지고, 높은 자외선 에너지로 인하여 직물 표면에 황변이 발생하는 문제점이 있다.Finally, in the ultraviolet curing step of the present invention, the dried fabric is cured using an ultraviolet curing machine, which is 0.6 to 2.4 in a UV curing zone equipped with a curing machine in which a high pressure mercury lamp and a metal halide lamp are lined up. Ultraviolet curing is continuously performed with energy of irradiation of J /
상기와 같은 단계를 거쳐 원단 배출 존(zone)에서 얻어진 방염직물은 유연성을 갖게 되며, 상기 방염 직물은 방화도 평가인 수직법을 통해 얻어진 탄화거리 값이 20cm이내 이며, 연기밀도 200% 이내일 뿐만 아니라, 물성저하가 거의 없고 직물의 경사수축율 4% 및 위사 수축률은 2% 이내이다.The flame retardant fabric obtained in the fabric discharge zone through the above steps has flexibility, and the flame retardant fabric has a carbonization distance value of less than 20 cm obtained by the vertical method of evaluating the degree of fire resistance, and has a smoke density of less than 200%. However, there is little physical property deterioration and the warp shrinkage rate of the fabric is 4% and the weft shrinkage is within 2%.
이하, 본 발명의 실시예 및 비교예에 대하여 상세히 설명한다.Hereinafter, the Example and comparative example of this invention are demonstrated in detail.
실시예 1Example 1
방염 가공액으로는 방염 가공액 100에 대하여 자외선 경화형 방염제(폴리네트론 사) 30 중량부, 반응 희석제인 비스-메타아크릴로일 옥시 에틸 포스페이트(폴리네트론 사) 50 중량부, 가교제인 트리 하이드록시 에틸 아이소시아네이트 트리아크릴레이트(폴리네트론 사) 5 중량부, 1-하이드록시사이클로헥실페닐케톤(시바社, Igacure 184)과 디페닐(2,4,6-트리메틸벤조힐)-포스핀옥사이드(상품명:TPO, 시바社)를 4:1로 혼합된 광개시제 3 중량부 그리고 분산제인 Triton-X 100을 0.5 중량부가 혼합된 형태의 가공액을 상온에서 60분 동안 자석 교반기를 이용하여 800rpm 으로 충분히 교반(stirring)시켜 방염 가공액을 제조하였다. 제조된 방염 가공액은 기질체인 직물 표면 위에 스프레이 코팅으로 500 내지 700㎛ 정도로 도포됨으로써 방염층을 형성시킨다. 방염층이 형성된 직물은 분당 30m로 이송되어 적외선 영역에서 2분간 건조시켰다. 건조된 직물은 분당 30m로 연속적으로 이송되어져 중고압식 수은램프와 메탈할라이드 램프를 일렬로 놓인 경화기가 장착된 UV 영역에서 2.4 J/㎠의 조사에너지로 자외선 경화하였다. 상기와 같이 제조한 직물의 방화도를 측정하기 위해서 탄화거리 측정 및 연기 밀도를 측정하였고, 세탁 전 후의 세탁 수축률을 측정하였다. As the flame retardant, 30 parts by weight of an ultraviolet curable flame retardant (polynetron), 50 parts by weight of bis-methacryloyl oxyethyl phosphate (polynetron) as a reaction diluent, and a trihydrate as a crosslinking agent relative to the flame retardant 100 5 parts by weight of oxyethyl isocyanate triacrylate (polynetron), 1-hydroxycyclohexylphenyl ketone (Igacure 184, Ciba) and diphenyl (2,4,6-trimethylbenzohill) -phosphine oxide (Product name: TPO, Ciba, Inc.) A processing liquid in which 3 parts by weight of a photoinitiator mixed with 4: 1 and 0.5 parts by weight of Triton-X 100, a dispersant, was mixed at 800 rpm using a magnetic stirrer at room temperature for 60 minutes. Stirring to prepare a flameproof working solution. The prepared flame retardant solution is applied on the surface of the substrate, which is a substrate, by spray coating to a degree of 500 to 700 µm to form a flame retardant layer. The fabric on which the flame resistant layer was formed was transferred at 30m / min and dried for 2 minutes in the infrared region. The dried fabric was continuously transported at 30m / min and was UV cured with an irradiation energy of 2.4 J /
비교예 1Comparative Example 1
딥 코팅(Dip Coating)법을 이용한 침지 방식의 방염 직물제조에서 방염 가공액 제조는 실시예 1과 동일하게 실시하였으며, 상기 방염 가공액에 60 내지 80%의 픽업율로 직물을 침지시킨 후 120 내지 160℃의 열풍식 텐터에서 1분간 예비 건조를 해준 후, 건조된 직물은 중고압식 수은램프와 메탈할라이드 램프를 일렬로 놓인 경화기가 장착된 UV 영역으로 분당 30m로 연속적으로 이송되어져 0.6 내지 2.4 J/㎠의 조사에너지로 자외선 경화하였다. 제조된 직물은 실시예 1과 같이 탄화거리, 연기 밀도 및 세탁 전 후의 세탁 수축율을 측정하였다. In the production of flame retardant fabric by dipping method using a dip coating method was prepared in the same manner as in Example 1, 120 to 120 after immersing the fabric at a pick-up rate of 60 to 80% in the flame retardant process solution After preliminary drying for 1 minute in a hot air tenter at 160 ° C, the dried fabric was continuously transferred at 30 m / min to a UV zone equipped with a curing machine lined with a medium-pressure mercury lamp and a metal halide lamp, ranging from 0.6 to 2.4 J / UV curing was carried out with an irradiation energy of 2
*측정 방법*How to measure
1. 탄화거리Carbonization distance
방화도를 측정하는 방법으로 KS K 0585에 의거하여 수직법에 의거하여 직물이 화원을 제거 후에도 타들어가는 정도를 평가하는 것. 탄화거리가 짧을수록 방화도가 우수하다.A method of measuring the degree of fire resistance and evaluating the degree to which the fabric burns after removing the flower garden according to the vertical method in accordance with KS K 0585. The shorter the carbonization distance, the better the fire resistance.
2. 연기밀도2. Smoke density
방화도를 측정하는 방법으로 소방법에 의거하여 직물에 화원을 가한 후 제거하였을 때 발생하는 연기의 밀도를 측정하는 것. 연기밀도가 낮을수록 방화도가 우수하다.A method of measuring the degree of fire protection by measuring the density of smoke generated when a fabric is applied to and removed from a fabric in accordance with a fire method. The lower the smoke density, the better the fire resistance.
3. 세탁 수축율3. Washing shrinkage rate
방염 직물의 세탁 전후의 수축률을 측정하는 것으로 KS K 0465에 의거하여 측정. 수축률은 규격상 경사 ± 4(%), 위사 ± 2% 이내.Measured according to KS K 0465 by measuring shrinkage before and after washing of flame retardant fabric. Shrinkage is within ± 4 (%) and weft ± 2% by standard.
division
Smoke density (%)
※ 실험결과※ Experiment result
본 발명에 제조된 방염 직물은 방화도 평가인 수직법을 통해 얻어진 탄화거리 값이 20cm이내로 규격에 적절하며, 연기밀도는 30%로 방화도가 우수하며, 물성저하가 거의 없고 직물의 경사수축률 3%, 위사 수축률 1%로 수축율 규격에 적절함을 알 수 있다.The flame retardant fabric produced in the present invention has a carbonization distance value of 20 cm or less obtained through the vertical method of evaluating the degree of fire resistance, and is suitable for the specification. The smoke density is 30%, and the fire resistance is excellent. %, Weft shrinkage 1%, it can be seen that it is suitable for shrinkage standard.
이상에서 설명한 본 발명은 전술한 실시예 및 첨부된 도면에 의해 한정되는 것은 아니고, 본 발명의 기술적 사상을 벗어나지 않는 범위 내에서 여러 가지 치환, 변형 및 변경이 가능함은 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자에게 있어서 명백할 것이다.The present invention described above is not limited to the above-described embodiment and the accompanying drawings, and various substitutions, modifications, and changes are possible within the scope without departing from the technical spirit of the present invention. It will be evident to those who have knowledge of.
도 1은 본 발명의 바람직한 일실시예에 따른 직물의 방염가공 처리 단계를 나타낸 도면이다.1 is a view showing a flame retardant treatment step of the fabric according to an embodiment of the present invention.
도 2는 본 발명의 일실시예에 따른 스프레이 방식을 이용하여 방염직물을 제조하는 장치로 듀어 큐어 (Dual cure)인 열과 UV를 이용하여 경화되는 공정도를 나타낸 것이다.Figure 2 is a device for manufacturing a flame retardant fabric using a spray method according to an embodiment of the present invention shows a process diagram that is cured using the heat and UV (dual cure).
<도면의 주요부분에 대한 부호의 설명><Description of the symbols for the main parts of the drawings>
1. 원단 투입 존(zone) 1. Fabric input zone
2. 스프레이 코팅 존(zone) 2. Spray coating zone
3. 열 건조 존(zone)3. Thermal drying zone
4. UV 경화 존(zone) 4. UV Curing Zone
5. 원단 배출 존(zone) 5. Fabric discharge zone
Claims (10)
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| KR1020090009914A KR101035112B1 (en) | 2009-02-06 | 2009-02-06 | Fiber by using Spray Coating and UV stiffening and Preparing thereof |
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| Application Number | Priority Date | Filing Date | Title |
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| KR1020090009914A KR101035112B1 (en) | 2009-02-06 | 2009-02-06 | Fiber by using Spray Coating and UV stiffening and Preparing thereof |
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| KR20100090566A true KR20100090566A (en) | 2010-08-16 |
| KR101035112B1 KR101035112B1 (en) | 2011-05-19 |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105615073B (en) * | 2014-12-01 | 2017-07-14 | 嘉兴晟合衬布有限公司 | The production method and dress materials of warp knit inlaid thread stamp compound clothing material |
| CN112921640A (en) * | 2021-02-01 | 2021-06-08 | 石狮锦亮织带有限公司 | Preparation method of flame-retardant woven tape |
| KR102640713B1 (en) * | 2023-10-12 | 2024-02-29 | 주식회사 유진레이블 | Method for manufacturing function mattress and the function mattress maunfactured by the same |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| KR101234044B1 (en) | 2010-09-15 | 2013-02-15 | 웅진케미칼 주식회사 | Ultraviolet-curable type fabric for waterproof and breathable and preparing the same |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH11100419A (en) | 1997-09-26 | 1999-04-13 | Jsr Corp | Radiation-curable resin composition |
| EP1689800A1 (en) | 2003-12-02 | 2006-08-16 | DSM IP Assets B.V. | Flame retardant radiation curable compositions |
| JP4606223B2 (en) | 2005-03-30 | 2011-01-05 | 太陽ホールディングス株式会社 | Ultraviolet curable resin composition and cured coating film thereof |
| KR100938431B1 (en) * | 2007-12-28 | 2010-01-25 | (주)디피아이 홀딩스 | Preparing Method Of Unsaturated Polyester Resins Containing Phosphate And Uv-Curing Flame Retarding Paint |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105615073B (en) * | 2014-12-01 | 2017-07-14 | 嘉兴晟合衬布有限公司 | The production method and dress materials of warp knit inlaid thread stamp compound clothing material |
| CN112921640A (en) * | 2021-02-01 | 2021-06-08 | 石狮锦亮织带有限公司 | Preparation method of flame-retardant woven tape |
| CN112921640B (en) * | 2021-02-01 | 2022-07-29 | 石狮锦亮织带有限公司 | Preparation method of flame-retardant woven tape |
| KR102640713B1 (en) * | 2023-10-12 | 2024-02-29 | 주식회사 유진레이블 | Method for manufacturing function mattress and the function mattress maunfactured by the same |
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| KR101035112B1 (en) | 2011-05-19 |
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