KR102605718B1 - Fabric for radiation protective clothing and its manufacturing method - Google Patents
Fabric for radiation protective clothing and its manufacturing method Download PDFInfo
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- KR102605718B1 KR102605718B1 KR1020230086782A KR20230086782A KR102605718B1 KR 102605718 B1 KR102605718 B1 KR 102605718B1 KR 1020230086782 A KR1020230086782 A KR 1020230086782A KR 20230086782 A KR20230086782 A KR 20230086782A KR 102605718 B1 KR102605718 B1 KR 102605718B1
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- 239000004744 fabric Substances 0.000 title claims abstract description 30
- 230000001681 protective effect Effects 0.000 title claims abstract description 25
- 230000005855 radiation Effects 0.000 title description 18
- 238000004519 manufacturing process Methods 0.000 title description 9
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 32
- 239000004917 carbon fiber Substances 0.000 claims description 32
- 238000010438 heat treatment Methods 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 27
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 claims description 26
- 239000002131 composite material Substances 0.000 claims description 24
- 239000000843 powder Substances 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 19
- 239000000835 fiber Substances 0.000 claims description 18
- -1 polyethylene Polymers 0.000 claims description 12
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 10
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 10
- 239000008188 pellet Substances 0.000 claims description 10
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 10
- 229920000742 Cotton Polymers 0.000 claims description 9
- 239000004698 Polyethylene Substances 0.000 claims description 8
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- 239000004927 clay Substances 0.000 claims description 6
- OKIWLDVQGKRUNR-UHFFFAOYSA-L magnesium;hydrogen phosphate;trihydrate Chemical compound O.O.O.[Mg+2].OP([O-])([O-])=O OKIWLDVQGKRUNR-UHFFFAOYSA-L 0.000 claims description 6
- 229920000609 methyl cellulose Polymers 0.000 claims description 5
- 239000001923 methylcellulose Substances 0.000 claims description 5
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- 238000001035 drying Methods 0.000 claims description 4
- 238000000227 grinding Methods 0.000 claims description 4
- 238000009941 weaving Methods 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 33
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 28
- 229910021389 graphene Inorganic materials 0.000 description 20
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
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- 125000000524 functional group Chemical group 0.000 description 5
- OUHCLAKJJGMPSW-UHFFFAOYSA-L magnesium;hydrogen carbonate;hydroxide Chemical compound O.[Mg+2].[O-]C([O-])=O OUHCLAKJJGMPSW-UHFFFAOYSA-L 0.000 description 5
- 238000009832 plasma treatment Methods 0.000 description 5
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- 238000005809 transesterification reaction Methods 0.000 description 5
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
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- 230000008569 process Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 2
- 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 description 2
- XRKLXLGVJOJYOO-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethanol;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.CC(=C)C(O)=O.OCCOCCO XRKLXLGVJOJYOO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
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- 230000000694 effects Effects 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- UACSZOWTRIJIFU-UHFFFAOYSA-N hydroxymethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCO UACSZOWTRIJIFU-UHFFFAOYSA-N 0.000 description 2
- 150000007517 lewis acids Chemical class 0.000 description 2
- 239000002071 nanotube Substances 0.000 description 2
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- 230000035484 reaction time Effects 0.000 description 2
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- 238000001179 sorption measurement Methods 0.000 description 2
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- 238000005406 washing Methods 0.000 description 2
- BYLSIPUARIZAHZ-UHFFFAOYSA-N 2,4,6-tris(1-phenylethyl)phenol Chemical compound C=1C(C(C)C=2C=CC=CC=2)=C(O)C(C(C)C=2C=CC=CC=2)=CC=1C(C)C1=CC=CC=C1 BYLSIPUARIZAHZ-UHFFFAOYSA-N 0.000 description 1
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- 241000192125 Firmicutes Species 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
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- 239000000443 aerosol Substances 0.000 description 1
- 230000005260 alpha ray Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
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- 239000003124 biologic agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 229910021387 carbon allotrope Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
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- 239000000356 contaminant Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
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- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000012857 radioactive material Substances 0.000 description 1
- 239000003642 reactive oxygen metabolite Substances 0.000 description 1
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- 150000003839 salts Chemical class 0.000 description 1
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- 230000002588 toxic effect Effects 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D11/00—Double or multi-ply fabrics not otherwise provided for
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/18—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from other substances
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
- D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
- D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
- D01F9/14—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments
- D01F9/20—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products
- D01F9/21—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F9/22—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyacrylonitriles
- D01F9/225—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyacrylonitriles from stabilised polyacrylonitriles
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/22—Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
- D02G3/26—Yarns or threads characterised by constructional features, e.g. blending, filament/fibre with characteristics dependent on the amount or direction of twist
- D02G3/28—Doubled, plied, or cabled threads
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D1/00—Woven fabrics designed to make specified articles
- D03D1/0035—Protective fabrics
-
- 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
- D06M10/02—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 ultrasonic or sonic; Corona discharge
- D06M10/025—Corona discharge or low temperature plasma
-
- 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
- D06M10/04—Physical treatment combined with treatment with chemical compounds or elements
- D06M10/06—Inorganic compounds or elements
-
- 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
- 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
- D06M11/77—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 silicon or compounds thereof
- D06M11/79—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 silicon or compounds thereof with silicon dioxide, silicic acids or their salts
-
- 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
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/03—Polysaccharides or derivatives thereof
- D06M15/05—Cellulose or derivatives thereof
Abstract
본 발명은 안감; 상기 안감 상부에 내층; 및 상기 내층 상부에 형성된 겉감;을 포함하는 보호복용 원단을 제공한다.The present invention provides a lining; An inner layer on top of the lining; and an outer layer formed on top of the inner layer. It provides a protective clothing fabric including a.
Description
본 발명은 방사능 보호복용 원단 및 이의 제조방법에 관한 것이다.The present invention relates to a radioactive protective clothing fabric and a method of manufacturing the same.
제1차 세계대전부터 현대사회에 이르기까지 세계 각국의 인류는 화학 작용제, 생물학 작용제 및 방사능의 위험에 노출되어 왔으며, 이를 차단하기 위한 보호용품 소재에 대한 연구는 국방 분야를 비롯하여 화학, 의약, 보건, 위생 등 각종 산업 분야에서 다방면으로 진행되고 있다.From World War I to modern society, humans around the world have been exposed to the dangers of chemical agents, biological agents, and radioactivity, and research on protective material to block these has been conducted in the fields of defense, chemistry, medicine, and health. It is being carried out in various fields such as sanitation, etc.
방사선 방호복은 원자력 발전소의 관리구역을 출입하는 보수요원이나 방사능 물질을 취급하는 실험기술자 등이 착용하는 것으로, 방사선 등과 같은 오염물질로부터 작업자를 보호한다.Radiation protective clothing is worn by maintenance personnel entering the management area of a nuclear power plant or laboratory technicians handling radioactive materials, and protects workers from contaminants such as radiation.
또한, 최근 수년간 전통적 화학작용제 및 비전통적 신종작용제 등을 활용한 테러가 국제사회에 충격을 주고 있으며, 코로나-19의 팬데믹은 생물학적 위협이 군사적 차원을 넘어서 국가적으로 커다란 위협이 될 수 있음을 시사하였다. 이러한 화생방 전장상황 및 테러위협에서 전투원이나 초기대응요원을 보호하는 유일한 수단은 화생방 보호복이다.In addition, in recent years, terrorism using traditional chemical agents and new, non-traditional agents has shocked the international community, and the COVID-19 pandemic suggests that biological threats can go beyond the military and become a major national threat. did. The only means of protecting combatants or first responders in such chemical, biological, and biological battlefield situations and terrorist threats is chemical, biological, and biological protective clothing.
현재, 화생방 보호복은 외피와 내피로 구성되어 있으며, 화생방 보호복 내피로 활성탄 단일 소재가 사용되고 있다. 활성탄 단일 소재의 경우 경제성이 우수한 장점이 있으나, 높은 중량, 제한적인 흡착 성능, 구조적 한계로 인해 무겁고 불편한 소재 특성을 나타내어 복합 기능을 요구하는 미래 화생방 보호의 내피 소재로 발전하기에 어려움이 있다. 또한, 테플론 또는 유기고분자 기반의 선택 투과막으로 구성된 보호복의 경우 에어로졸 입자 방호에 효과적이나, 공기 투과도가 없어 발한에 의한 실질적인 체온 유지가 어려워 제한적으로 사용되고 있다.Currently, chemical, biological and biological protective clothing consists of an outer shell and an inner layer, and a single material, activated carbon, is used as the inner layer of chemical, biological and biological protective clothing. Activated carbon as a single material has the advantage of excellent economic efficiency, but due to its high weight, limited adsorption performance, and structural limitations, it is heavy and uncomfortable, making it difficult to develop into an endothelial material for future chemical, biological and radiological protection that requires complex functions. In addition, protective clothing made of a selectively permeable membrane based on Teflon or organic polymers is effective in protecting against aerosol particles, but its use is limited because it has no air permeability, making it difficult to maintain actual body temperature through sweating.
따라서, 방사능의 위험, 독성 산업물질 또는 미지의 화학물질 위협에 대한 보호 성능이 강화되고 착용감을 향상시킬 수 있는 보호복 기술 개발이 필요하다.Therefore, there is a need to develop protective clothing technology that can enhance protection against radiation hazards, toxic industrial substances, or unknown chemical threats and improve wearing comfort.
본 발명의 목적은 방사능 보호복을 제공하는 것이다.The object of the present invention is to provide radiation protective clothing.
본 발명의 과제는 이상에서 언급한 과제들로 제한되지 않으며, 언급되지 않은 또 다른 과제들은 아래의 기재로부터 당업자에게 명확하게 이해될 수 있을 것이다.The object of the present invention is not limited to the problems mentioned above, and other problems not mentioned will be clearly understood by those skilled in the art from the description below.
상기 목적을 달성하기 위하여 본 발명은In order to achieve the above object, the present invention
안감;lining;
상기 안감 상부에 내층; 및 An inner layer on top of the lining; and
상기 내층 상부에 형성된 겉감;을 포함하는 보호복용 원단 및 이를 이용하여 제조되는 보호복을 제공한다.Provided is a protective clothing fabric including an outer layer formed on the inner layer, and a protective clothing manufactured using the same.
또한, 상기 보호복의 내층은,In addition, the inner layer of the protective suit is,
상기 안감 상부에 형성된 제1층;A first layer formed on the top of the lining;
상기 제1층 상부에 형성된 제2층; 및a second layer formed on top of the first layer; and
상기 제2층 상부에 형성된 제3층;을 포함하고,It includes a third layer formed on top of the second layer,
상기 안감은 사방으로 신축되는 구조의 면스판이고,The lining is a cotton spandex with a structure that expands and contracts in all directions,
상기 겉감은 사방으로 신축되는 구조의 폴리스판이고,The outer fabric is a poly board with a structure that expands and contracts in all directions,
상기 제1층은 알루미늄 실리케이트 복합분말을 포함하고,The first layer includes aluminum silicate composite powder,
상기 알루미늄 실리케이트 복합분말은, The aluminum silicate composite powder,
알루미늄 실리케이트 68-72 중량부, 산성백토 8-12 중량부, 메틸셀룰로오스 8-12 중량부, 인산수소마그네슘 삼수화물(MgHPO4ㆍ3H2O) 3-7 중량부 및 폴리비닐알콜 3-7 중량부를 혼합하여 실리케이트 혼합물을 제조하는 단계; 상기 실리케이트 혼합물을 진공압출성형기로 압출하여 펠렛을 제조하는 단계; 제조된 펠렛을 건조 및 분쇄하는 단계; 건조 및 분쇄한 분쇄물을 120-160℃의 온도에서 2-4시간 동안 1차 열처리하는 단계; 및 1차 열처리한 분쇄물을 480-520℃의 온도에서 3-7분 동안 2차 열처리하는 단계;를 수행하여 제조되고,68-72 parts by weight of aluminum silicate, 8-12 parts by weight of acidic clay, 8-12 parts by weight of methyl cellulose, 3-7 parts by weight of magnesium hydrogen phosphate trihydrate (MgHPO 4 ㆍ3H 2 O), and 3-7 parts by weight of polyvinyl alcohol. mixing the parts to prepare a silicate mixture; Extruding the silicate mixture using a vacuum extruder to produce pellets; Drying and grinding the prepared pellets; Primary heat treatment of the dried and pulverized pulverized material at a temperature of 120-160°C for 2-4 hours; and secondary heat treatment of the primary heat treated pulverized material at a temperature of 480-520°C for 3-7 minutes.
상기 제2층은 스티렌부타디엔고무 및 부틸고무를 포함하고,The second layer includes styrene butadiene rubber and butyl rubber,
상기 제3층은 폴리에틸렌 섬유 및 탄소섬유를 직조하여 형성된 직물층인 것을 특징으로 한다.The third layer is characterized as a fabric layer formed by weaving polyethylene fibers and carbon fibers.
또한, 상기 보호복의 내층은,In addition, the inner layer of the protective suit is,
상기 안감 상부에 형성된 제1층;A first layer formed on the top of the lining;
상기 제1층 상부에 형성된 제2층; 및a second layer formed on top of the first layer; and
상기 제2층 상부에 형성된 제3층;을 포함하고,It includes a third layer formed on top of the second layer,
상기 안감은 사방으로 신축되는 구조의 면스판이고,The lining is a cotton spandex with a structure that expands and contracts in all directions,
상기 겉감은 사방으로 신축되는 구조의 폴리스판이고,The outer fabric is a poly board with a structure that expands and contracts in all directions,
상기 제1층은 아크릴계 고분자 수지 58-62 중량부, 아크릴계 혼합물 5-9 중량부, 알루미늄 실리케이트 복합분말 8-12 중량부, 폴리비닐알콜 3-7 중량부, 탄산칼슘 3-7 중량부, 탄소나노튜브 3-7 중량부, 셀룰로오즈 아세테이트 부틸레이트 1-5 중량부 및 메틸에틸케톤 3-7 중량부를 포함하는 제1층 형성용 조성물로 형성된 것이고,The first layer includes 58-62 parts by weight of acrylic polymer resin, 5-9 parts by weight of acrylic mixture, 8-12 parts by weight of aluminum silicate composite powder, 3-7 parts by weight of polyvinyl alcohol, 3-7 parts by weight of calcium carbonate, and carbon. It is formed of a composition for forming a first layer containing 3-7 parts by weight of nanotubes, 1-5 parts by weight of cellulose acetate butyrate, and 3-7 parts by weight of methyl ethyl ketone,
상기 아크릴계 고분자 수지는 메틸메타크릴레이트 단량체 단위 23-27 중량부, 하이드록시메틸메타크릴레이트 단량체 단위 23-27 중량부, 글리시딜메타크릴레이트 단량체 단위 23-27 중량부 및 2-포스포노옥시에틸 메타크릴레이트(2-(phosphonooxy)ethyl methacrylate) 단량체 단위 23-27 중량부를 포함하는 아크릴레이트계 공중합체이고,The acrylic polymer resin includes 23-27 parts by weight of methyl methacrylate monomer units, 23-27 parts by weight of hydroxymethyl methacrylate monomer units, 23-27 parts by weight of glycidyl methacrylate monomer units, and 2-phosphonooxy It is an acrylate-based copolymer containing 23-27 parts by weight of ethyl methacrylate (2-(phosphonooxy)ethyl methacrylate) monomer units,
상기 아크릴계 혼합물은 하이드록시에틸메타크릴레이트, 글리시딜메타크릴레이트 및 디메타크릴레이트 디에틸렌글리콜이 3:3:4의 중량비율로 혼합된 혼합물이고,The acrylic mixture is a mixture of hydroxyethyl methacrylate, glycidyl methacrylate, and dimethacrylate diethylene glycol in a weight ratio of 3:3:4,
상기 알루미늄 실리케이트 복합분말은, The aluminum silicate composite powder,
알루미늄 실리케이트 68-72 중량부, 산성백토 8-12 중량부, 메틸셀룰로오스 8-12 중량부, 인산수소마그네슘 삼수화물(MgHPO4ㆍ3H2O) 3-7 중량부 및 폴리비닐알콜 3-7 중량부를 혼합하여 실리케이트 혼합물을 제조하는 단계; 상기 실리케이트 혼합물을 진공압출성형기로 압출하여 펠렛을 제조하는 단계; 제조된 펠렛을 건조 및 분쇄하는 단계; 건조 및 분쇄한 분쇄물을 120-160℃의 온도에서 2-4시간 동안 1차 열처리하는 단계; 및 1차 열처리한 분쇄물을 480-520℃의 온도에서 3-7분 동안 2차 열처리하는 단계;를 수행하여 제조되고,68-72 parts by weight of aluminum silicate, 8-12 parts by weight of acidic clay, 8-12 parts by weight of methyl cellulose, 3-7 parts by weight of magnesium hydrogen phosphate trihydrate (MgHPO 4 ㆍ3H 2 O), and 3-7 parts by weight of polyvinyl alcohol. mixing the parts to prepare a silicate mixture; Extruding the silicate mixture using a vacuum extruder to produce pellets; Drying and grinding the prepared pellets; Primary heat treatment of the dried and pulverized pulverized material at a temperature of 120-160°C for 2-4 hours; and secondary heat treatment of the primary heat treated pulverized material at a temperature of 480-520°C for 3-7 minutes.
상기 제2층은 스티렌부타디엔고무 33-37 중량부, 부틸고무 18-22 중량부, 수산화탄산마그네슘 26-30 중량부, 알루미늄 실리케이트 복합분말 2-6 중량부, 이산화티타늄 분말 2-6 중량부, 노화방지제 1-5 중량부, 가소제 1-5 중량부 및 프로세스오일 1-5 중량부를 포함하는 제2층 형성용 조성물로 형성된 것이고,The second layer includes 33-37 parts by weight of styrene butadiene rubber, 18-22 parts by weight of butyl rubber, 26-30 parts by weight of magnesium hydroxide carbonate, 2-6 parts by weight of aluminum silicate composite powder, 2-6 parts by weight of titanium dioxide powder, It is formed of a composition for forming a second layer containing 1-5 parts by weight of an anti-aging agent, 1-5 parts by weight of a plasticizer, and 1-5 parts by weight of a process oil,
상기 제3층은,The third layer is,
폴리아크릴로나이트릴(PAN) 섬유를 질소분위기에서 1-2℃/분의 승온속도로 300-400℃의 온도까지 승온시킨 후 2-4시간 동안 1차 열처리하여 탄소섬유 전구체를 제조하는 단계; 상기 탄소섬유 전구체를 질소분위기에서 4-6℃/분의 승온속도로 700-800℃의 온도까지 승온시킨 후 0.5-2시간 동안 2차 열처리하여 탄소섬유를 제조하는 단계; 상기 탄소섬유를 이용하여 산소플라즈마 처리하는 단계; 카르복시기를 포함하는 그래핀 산화물과 10 중량%의 황산 수용액을 준비하여, 상기 황산 수용액 100 중량부에 대하여 상기 그래핀 산화물을 1 중량부 포함하는 분산액을 제조한 후, 상기 분산액에 산소플라즈마 처리된 탄소섬유를 침지한 후, 40-60℃의 온도에서 6-10시간 동안 반응시켜 산소플라즈마 처리된 탄소섬유를 그래핀 산화물로 코팅하는 단계; 및 그래핀 산화물이 코팅된 탄소섬유를 물 및 에탄올을 1:1의 중량비율로 포함하는 세정제를 이용하여 세척하는 단계;를 포함하는 탄소섬유를 제조하는 단계;Preparing a carbon fiber precursor by heating polyacrylonitrile (PAN) fibers to a temperature of 300-400°C in a nitrogen atmosphere at a temperature increase rate of 1-2°C/min and then performing primary heat treatment for 2-4 hours; Preparing carbon fiber by heating the carbon fiber precursor to a temperature of 700-800°C in a nitrogen atmosphere at a temperature increase rate of 4-6°C/min and then performing secondary heat treatment for 0.5-2 hours; Oxygen plasma treatment using the carbon fiber; Prepare graphene oxide containing a carboxyl group and a 10% by weight aqueous solution of sulfuric acid, prepare a dispersion containing 1 part by weight of the graphene oxide based on 100 parts by weight of the aqueous sulfuric acid solution, and then add oxygen plasma-treated carbon to the dispersion. After immersing the fiber, reacting at a temperature of 40-60°C for 6-10 hours to coat the oxygen plasma-treated carbon fiber with graphene oxide; and washing the graphene oxide-coated carbon fiber using a detergent containing water and ethanol in a weight ratio of 1:1; manufacturing carbon fiber including;
상기 탄소섬유 및 폴리에틸렌 섬유를 5:5의 중량비율로 포함하도록 합사하여 복합사를 제조하는 단계; 및manufacturing a composite yarn by plying the carbon fiber and polyethylene fiber in a weight ratio of 5:5; and
상기 복합사를 경사 및 위사로 포함시켜 직물을 제조하는 단계;를 수행하여 제조되는 직물인 것을 특징으로 한다.It is characterized as a fabric manufactured by performing the step of manufacturing a fabric by including the composite yarn as warp and weft yarns.
본 발명에 따른 보호복은 착용감이 우수하고 방사능, 화생방 보호 기능을 가진다.The protective clothing according to the present invention is comfortable to wear and has radiation, chemical, biological and radiological protection functions.
이하에서는 다양한 실시예를 보다 상세하게 설명한다. 본 명세서에 기재된 실시예는 다양하게 변형될 수 있다. 특정한 실시예가 상세한 설명에서 자세하게 설명될 수 있다. 그러나 개시된 특정한 실시 예는 다양한 실시예를 쉽게 이해하도록 하기 위한 것일 뿐이다. 따라서 개시된 특정 실시예에 의해 기술적 사상이 제한되는 것은 아니며, 발명의 사상 및 기술 범위에 포함되는 모든 균등물 또는 대체물을 포함하는 것으로 이해되어야 한다.Hereinafter, various embodiments will be described in more detail. The embodiments described herein may be modified in various ways. Specific embodiments may be described in detail in the detailed description. However, the specific embodiments disclosed are only intended to facilitate understanding of the various embodiments. Accordingly, the technical idea is not limited to the specific embodiments disclosed, and should be understood to include all equivalents or substitutes included in the spirit and technical scope of the invention.
1차, 2차, 제1, 제2 등과 같이 서수를 포함하는 용어는 다양한 구성요소들을 설명하는데 사용될 수 있지만, 이러한 구성요소들은 상술한 용어에 의해 한정되지는 않는다. 상술한 용어는 하나의 구성요소를 다른 구성요소로부터 구별하는 목적으로만 사용된다.Terms containing ordinal numbers, such as primary, secondary, first, second, etc., may be used to describe various components, but these components are not limited by the above-mentioned terms. The above-mentioned terms are used only for the purpose of distinguishing one component from another.
본 명세서에서, '포함한다' 또는 '가지다' 등의 용어는 명세서상에 기재된 특징, 숫자, 단계, 동작, 구성요소, 부품 또는 이들을 조합한 것이 존재함을 지정하려는 것이지, 하나 또는 그 이상의 다른 특징들이나 숫자, 단계, 동작, 구성요소, 부품 또는 이들을 조합한 것들의 존재 또는 부가 가능성을 미리 배제하지 않는 것으로 이해되어야 한다. 어떤 구성요소가 다른 구성요소에 '연결되어' 있다거나 '접속되어' 있다고 언급된 때에는, 그 다른 구성요소에 직접적으로 연결되어 있거나 또는 접속되어 있을 수도 있지만, 중간에 다른 구성요소가 존재할 수도 있다고 이해되어야 할 것이다. 반면에, 어떤 구성요소가 다른 구성요소에 '직접 연결되어' 있다거나 '직접 접속되어' 있다고 언급된 때에는, 중간에 다른 구성요소가 존재하지 않는 것으로 이해되어야 할 것이다.In this specification, terms such as 'include' or 'have' are intended to designate the presence of features, numbers, steps, operations, components, parts, or combinations thereof described in the specification, but are not intended to indicate the presence of one or more other features. It should be understood that this does not exclude in advance the possibility of the existence or addition of elements, numbers, steps, operations, components, parts, or combinations thereof. When a component is said to be 'connected' or 'connected' to another component, it is understood that it may be directly connected or connected to the other component, but that other components may exist in between. It should be. On the other hand, when a component is mentioned as being 'directly connected' or 'directly connected' to another component, it should be understood that there are no other components in between.
그 밖에도, 본 발명을 설명함에 있어서, 관련된 공지 기능 혹은 구성에 대한 구체적인 설명이 본 발명의 요지를 불필요하게 흐릴 수 있다고 판단되는 경우, 그에 대한 상세한 설명은 축약하거나 생략한다.In addition, when describing the present invention, if it is determined that a detailed description of a related known function or configuration may unnecessarily obscure the gist of the present invention, the detailed description thereof is abbreviated or omitted.
본 발명은This invention
안감;lining;
상기 안감 상부에 내층; 및 An inner layer on top of the lining; and
상기 내층 상부에 형성된 겉감;을 포함하는 보호복용 원단을 제공한다.It provides a protective clothing fabric including; an outer layer formed on top of the inner layer.
이하, 본 발명에 따른 보호복용 원단에 대하여 상세히 설명한다.Hereinafter, the protective clothing fabric according to the present invention will be described in detail.
상기 안감은 사방으로 신축되는 구조의 면스판으로 이루어진다. 상기 안감은 사방으로 신축되도록 격자구조로 편조된 면직물인 면스판으로 이루어진 것이 바람직하다. 본 발명에서는 상기 면스판을 안감으로 적용하여 착용감을 높일 수 있다.The lining is made of cotton spandex with a structure that expands and contracts in all directions. The lining is preferably made of cotton spandex, which is a cotton fabric braided in a lattice structure so that it can expand and contract in all directions. In the present invention, the wearing comfort can be improved by applying the cotton spandex as a lining.
상기 내층은 상기 안감 상부에 형성된 제1층; 상기 제1층 상부에 형성된 제2층; 및 상기 제2층 상부에 형성된 제3층;을 포함하는 것이 바람직하다.The inner layer includes a first layer formed on the top of the lining; a second layer formed on top of the first layer; and a third layer formed on top of the second layer.
상기 제1층은 알루미늄 실리케이트 복합분말을 포함하는 것이 바람직하다.The first layer preferably contains aluminum silicate composite powder.
알루미늄 실리케이트 복합분말은 분말(powder)형태의 물질로 높은 비표면적 측정 결과를 가지고 있어 흡착 능력이 뛰어나다. 본 발명에서는 방사능 차폐 물질로 적용되어 방사능 차폐 성능을 향상시켜준다.Aluminum silicate composite powder is a powder-type material that has a high specific surface area measurement result and has excellent adsorption ability. In the present invention, it is applied as a radiation shielding material to improve radiation shielding performance.
상기 알루미늄 실리케이트 복합분말은, The aluminum silicate composite powder,
알루미늄 실리케이트 68-72 중량부, 산성백토 8-12 중량부, 메틸셀룰로오스 8-12 중량부, 인산수소마그네슘 삼수화물(MgHPO4ㆍ3H2O) 3-7 중량부 및 폴리비닐알콜 3-7 중량부를 혼합하여 실리케이트 혼합물을 제조하는 단계; 상기 실리케이트 혼합물을 진공압출성형기로 압출하여 펠렛을 제조하는 단계; 제조된 펠렛을 건조 및 분쇄하는 단계; 건조 및 분쇄한 분쇄물을 120-160℃의 온도에서 2-4시간 동안 1차 열처리하는 단계; 및 1차 열처리한 분쇄물을 480-520℃의 온도에서 3-7분 동안 2차 열처리하는 단계;를 수행하여 제조되는 것을 사용한다.68-72 parts by weight of aluminum silicate, 8-12 parts by weight of acidic clay, 8-12 parts by weight of methyl cellulose, 3-7 parts by weight of magnesium hydrogen phosphate trihydrate (MgHPO 4 ㆍ3H 2 O), and 3-7 parts by weight of polyvinyl alcohol. mixing the parts to prepare a silicate mixture; Extruding the silicate mixture using a vacuum extruder to produce pellets; Drying and grinding the prepared pellets; Primary heat treatment of the dried and pulverized pulverized material at a temperature of 120-160°C for 2-4 hours; and secondary heat treatment of the pulverized material subjected to the primary heat treatment at a temperature of 480-520° C. for 3-7 minutes.
상기 알루미늄 실리케이트 및 인산수소마그네슘 삼수화물은 방사능 차폐 성능을 발현시킬 수 있으며, 상기 산성백토 등의 성분을 이용하여 표면처리를 함으로써 성능을 극대화시킬 수 있다.The aluminum silicate and magnesium hydrogen phosphate trihydrate can exhibit radiation shielding performance, and the performance can be maximized by surface treatment using components such as acidic clay.
상기 1차 열처리를 통해 각 성분을 결합하여 알루미늄 실리케이트의 차폐 성능을 향상시킬 수 있고, 2차 열처리를 통해 결합제 성분을 제거하여 알루미늄 실리케이트의 차폐 성능을 더욱 향상시킬 수 있다.The shielding performance of aluminum silicate can be improved by combining each component through the first heat treatment, and the shielding performance of aluminum silicate can be further improved by removing the binder component through the second heat treatment.
상기 제1층은 아크릴계 고분자 수지 58-62 중량부, 아크릴계 혼합물 5-9 중량부, 알루미늄 실리케이트 복합분말 8-12 중량부, 폴리비닐알콜 3-7 중량부, 탄산칼슘 3-7 중량부, 탄소나노튜브 3-7 중량부, 셀룰로오즈 아세테이트 부틸레이트 1-5 중량부 및 메틸에틸케톤 3-7 중량부를 포함하는 제1층 형성용 조성물로 형성된 것이 바람직하고, 아크릴계 고분자 수지 59-61 중량부, 아크릴계 혼합물 6-8 중량부, 알루미늄 실리케이트 복합분말 9-11 중량부, 폴리비닐알콜 4-6 중량부, 탄산칼슘 4-6 중량부, 탄소나노튜브 4-6 중량부, 셀룰로오즈 아세테이트 부틸레이트 2-4 중량부 및 메틸에틸케톤 4-6 중량부를 포함하는 제1층 형성용 조성물로 형성된 것이 더욱 바람직하다.The first layer includes 58-62 parts by weight of acrylic polymer resin, 5-9 parts by weight of acrylic mixture, 8-12 parts by weight of aluminum silicate composite powder, 3-7 parts by weight of polyvinyl alcohol, 3-7 parts by weight of calcium carbonate, and carbon. It is preferably formed of a composition for forming the first layer containing 3-7 parts by weight of nanotubes, 1-5 parts by weight of cellulose acetate butyrate, and 3-7 parts by weight of methyl ethyl ketone, 59-61 parts by weight of an acrylic polymer resin, and an acrylic polymer. 6-8 parts by weight of mixture, 9-11 parts by weight of aluminum silicate composite powder, 4-6 parts by weight of polyvinyl alcohol, 4-6 parts by weight of calcium carbonate, 4-6 parts by weight of carbon nanotubes, 2-4 parts by weight of cellulose acetate butyrate It is more preferable that it is formed from a composition for forming the first layer containing 4-6 parts by weight of methyl ethyl ketone.
상기 아크릴계 고분자 수지는 메틸메타크릴레이트 단량체 단위 23-27 중량부, 하이드록시메틸메타크릴레이트 단량체 단위 23-27 중량부, 글리시딜메타크릴레이트 단량체 단위 23-27 중량부 및 2-포스포노옥시에틸 메타크릴레이트(2-(phosphonooxy)ethyl methacrylate) 단량체 단위 23-27 중량부를 포함하는 아크릴레이트계 공중합체인 것이 바람직하다. 상기 아크릴계 고분자 수지를 적용하여 차폐 물질과 혼화성을 높일 수 있을 뿐만 아니라, 난연 및 내열성을 가지는 층을 형성할 수 있다.The acrylic polymer resin includes 23-27 parts by weight of methyl methacrylate monomer units, 23-27 parts by weight of hydroxymethyl methacrylate monomer units, 23-27 parts by weight of glycidyl methacrylate monomer units, and 2-phosphonooxy It is preferable that it is an acrylate-based copolymer containing 23-27 parts by weight of ethyl methacrylate (2-(phosphonooxy)ethyl methacrylate) monomer units. By applying the acrylic polymer resin, not only can compatibility with the shielding material be increased, but a layer having flame retardancy and heat resistance can be formed.
상기 아크릴계 혼합물은 하이드록시에틸메타크릴레이트, 글리시딜메타크릴레이트 및 디메타크릴레이트 디에틸렌글리콜이 3:3:4의 중량비율로 혼합된 혼합물인 것이 바람직하다. 상기 아크릴계 혼합물을 적용하여 안감과의 접착력을 높여주어 우수한 결합력을 가지며, 이에 따라 내구성이 향상된다.The acrylic mixture is preferably a mixture of hydroxyethyl methacrylate, glycidyl methacrylate, and dimethacrylate diethylene glycol in a weight ratio of 3:3:4. By applying the acrylic mixture, the adhesion with the lining is improved, resulting in excellent bonding strength, thereby improving durability.
상기 폴리비닐알콜은 중성자 차폐물질로 적용되어 차폐성능을 향상시켜준다.The polyvinyl alcohol is applied as a neutron shielding material to improve shielding performance.
상기 탄산칼슘은 충전제로 적용되어 인체에 안전하며 방사능 차폐 효과가 우수하고, 보호복용 원단의 내구성을 향상시켜준다.The calcium carbonate is applied as a filler and is safe for the human body, has excellent radiation shielding effect, and improves the durability of the protective clothing fabric.
상기 탄소나노튜브는(CNT)는 6각형으로 배열된 탄소원자들이 튜브 형상의 모양을 하고 있는 탄소동소체 중의 하나로서, 탄소 원자 철망의 시트가 실린더 형으로 말려있는 형상을 하고 있다. 상기 탄소나노튜브는 화학적으로 안정하고 생체친화적인 특성을 가지며 양성자에 대한 차폐 능력이 우수하다. 또한 내열성을 보조하여 주는 첨가제로 적용된다.The carbon nanotube (CNT) is one of the carbon allotropes in which carbon atoms arranged in a hexagon are shaped like a tube, and has a shape in which a sheet of carbon atom wire mesh is rolled into a cylindrical shape. The carbon nanotubes are chemically stable, have biocompatible properties, and have excellent proton-shielding ability. It is also used as an additive to assist heat resistance.
상기 셀룰로오즈 아세테이트 부틸레이트는 각 성분들의 혼화성을 높여주어 층 형성이 용이하도록 도와준다.The cellulose acetate butyrate increases the miscibility of each component and helps facilitate layer formation.
상기 메틸에틸케톤은 용매로 적용되어 혼화성을 높여준다.The methyl ethyl ketone is applied as a solvent to increase miscibility.
상기 제2층은 스티렌부타디엔고무 및 부틸고무를 포함하는 것이 바람직하다. 상기 제2층은 고무로 이루어진 층으로 내구성 향상과 동시에 화생방 보호, 방사능 보호 기능을 가진다.The second layer preferably includes styrene butadiene rubber and butyl rubber. The second layer is a layer made of rubber and has the functions of chemical, biological and radiological protection and radiation protection while improving durability.
상기 제2층은 스티렌부타디엔고무 33-37 중량부, 부틸고무 18-22 중량부, 수산화탄산마그네슘 26-30 중량부, 알루미늄 실리케이트 복합분말 2-6 중량부, 이산화티타늄 분말 2-6 중량부, 노화방지제 1-5 중량부, 가소제 1-5 중량부 및 프로세스오일 1-5 중량부를 포함하는 제2층 형성용 조성물로 형성된 것이 바람직하고, 스티렌부타디엔고무 34-36 중량부, 부틸고무 19-21 중량부, 수산화탄산마그네슘 27-29 중량부, 알루미늄 실리케이트 복합분말 3-5 중량부, 이산화티타늄 분말 3-5 중량부, 노화방지제 2-4 중량부, 가소제 2-4 중량부 및 프로세스오일 2-4 중량부를 포함하는 제2층 형성용 조성물로 형성된 것이 더욱 바람직하다.The second layer includes 33-37 parts by weight of styrene butadiene rubber, 18-22 parts by weight of butyl rubber, 26-30 parts by weight of magnesium hydroxide carbonate, 2-6 parts by weight of aluminum silicate composite powder, 2-6 parts by weight of titanium dioxide powder, It is preferably formed of a composition for forming a second layer containing 1-5 parts by weight of an anti-aging agent, 1-5 parts by weight of a plasticizer, and 1-5 parts by weight of a process oil, 34-36 parts by weight of styrene butadiene rubber, and 19-21 parts by weight of butyl rubber. parts by weight, 27-29 parts by weight of magnesium hydroxide carbonate, 3-5 parts by weight of aluminum silicate composite powder, 3-5 parts by weight of titanium dioxide powder, 2-4 parts by weight of anti-aging agent, 2-4 parts by weight of plasticizer and 2-4 parts by weight of process oil. It is more preferable that it is formed of a composition for forming a second layer containing 4 parts by weight.
상기 스티렌부타디엔고무 및 부틸고무는 천연고무에 비해 기체 투과성이 작아 내가스 투과성이 증가하여 유독 가스로부터 착용자를 보호할 수 있다. 또한, 이 두가지의 고무 성분을 조합하여 착용감을 향상시키고 내마모성, 인장강도 및 경도 등의 물성이 향상되어 안정성이 우수하다.The styrene butadiene rubber and butyl rubber have lower gas permeability than natural rubber and thus increase internal gas permeability, thereby protecting the wearer from toxic gases. In addition, the combination of these two rubber components improves wearing comfort and improves physical properties such as abrasion resistance, tensile strength, and hardness, resulting in excellent stability.
상기 수산화탄산마그네슘은 난연제로 적용되어 난연성을 높여준다.The magnesium hydroxide carbonate is applied as a flame retardant to increase flame retardancy.
상기 이산화티타늄 분말은 학적으로 안정하고 음폐력이 커 거의 모든 용매에 녹지 않으며 생화학적으로 반응을 하지 않아 친환경적이므로 환경과 인체에 무해하다. The titanium dioxide powder is scientifically stable, has a high sine resistance, is insoluble in almost all solvents, and does not react biochemically, making it eco-friendly and harmless to the environment and the human body.
상기 노화 방지제는 주재료인 고무가 산소, 산화성 물질, 오존, 열, 햇빛, 방사능 등과 같은 외적 인자와 가황도, 고무의 종류, 가황제의 종류, 가황 촉진제의 종류 등과 같은 내적 인자로 인해 산화되어 균열 및 경화 현상을 방지하기 위한 것으로서, 예를 들어, 방향족 아민(amine)계 노화 방지제나 스티레네이티드페놀(styrenated phenol), 니켈 디뷰틸 디티오카바메이트(nickel dibutyl dithiocarbamate) 등의 페놀(phenol)계 노화 방지제가 사용될 수 있다.The anti-aging agent prevents rubber, which is the main material, from being oxidized and cracked due to external factors such as oxygen, oxidizing substances, ozone, heat, sunlight, radiation, etc. and internal factors such as vulcanization degree, type of rubber, type of vulcanizing agent, type of vulcanization accelerator, etc. and to prevent hardening, for example, aromatic amine-based anti-aging agents or phenol-based agents such as styrenated phenol and nickel dibutyl dithiocarbamate. Anti-aging agents may be used.
상기 가소제는 고무 성분에 유연성을 부여하고 경도를 저하시켜 가소성을 향상시킨다. 이로 인해, 상기 층 형성에 있어서 성형 및 가공이 좀더 용이하게 행해진다. 상기 가소제는 스테아린산을 사용하는 것이 바람직하다.The plasticizer provides flexibility to the rubber component and reduces hardness to improve plasticity. Because of this, molding and processing in forming the layer are performed more easily. It is preferable to use stearic acid as the plasticizer.
상기 프로세스 오일은 배합 고무의 작업 공정 중에 작업성을 좋게 하기 위해 첨가되는 광유로서, 주로 파라핀(paraffin)계, 나프텐계(naphthen), 방향족(aromatic)계의 것을 사용할 수 있다.The process oil is a mineral oil added to improve workability during the working process of compounded rubber, and can mainly be used as paraffin, naphthene, or aromatic oil.
상기 제3층은 폴리에틸렌 섬유 및 탄소섬유를 직조하여 형성된 직물층인 것이 바람직하다.The third layer is preferably a fabric layer formed by weaving polyethylene fibers and carbon fibers.
상기 제3층은,The third layer is,
폴리아크릴로나이트릴(PAN) 섬유를 질소분위기에서 1-2℃/분의 승온속도로 300-400℃의 온도까지 승온시킨 후 2-4시간 동안 1차 열처리하여 탄소섬유 전구체를 제조하는 단계; 상기 탄소섬유 전구체를 질소분위기에서 4-6℃/분의 승온속도로 700-800℃의 온도까지 승온시킨 후 0.5-2시간 동안 2차 열처리하여 탄소섬유를 제조하는 단계; 상기 탄소섬유를 이용하여 산소플라즈마 처리하는 단계; 카르복시기를 포함하는 그래핀 산화물과 10 중량%의 황산 수용액을 준비하여, 상기 황산 수용액 100 중량부에 대하여 상기 그래핀 산화물을 1 중량부 포함하는 분산액을 제조한 후, 상기 분산액에 산소플라즈마 처리된 탄소섬유를 침지한 후, 40-60℃의 온도에서 6-10시간 동안 반응시켜 산소플라즈마 처리된 탄소섬유를 그래핀 산화물로 코팅하는 단계; 및 그래핀 산화물이 코팅된 탄소섬유를 물 및 에탄올을 1:1의 중량비율로 포함하는 세정제를 이용하여 세척하는 단계;를 포함하는 탄소섬유를 제조하는 단계;Preparing a carbon fiber precursor by heating polyacrylonitrile (PAN) fibers to a temperature of 300-400°C in a nitrogen atmosphere at a temperature increase rate of 1-2°C/min and then performing primary heat treatment for 2-4 hours; Preparing carbon fiber by heating the carbon fiber precursor to a temperature of 700-800°C in a nitrogen atmosphere at a temperature increase rate of 4-6°C/min and then performing secondary heat treatment for 0.5-2 hours; Oxygen plasma treatment using the carbon fiber; Prepare graphene oxide containing a carboxyl group and a 10% by weight aqueous solution of sulfuric acid, prepare a dispersion containing 1 part by weight of the graphene oxide based on 100 parts by weight of the aqueous sulfuric acid solution, and then add oxygen plasma-treated carbon to the dispersion. After immersing the fiber, reacting at a temperature of 40-60°C for 6-10 hours to coat the oxygen plasma-treated carbon fiber with graphene oxide; and washing the graphene oxide-coated carbon fiber using a detergent containing water and ethanol in a weight ratio of 1:1; manufacturing carbon fiber including;
상기 탄소섬유 및 폴리에틸렌 섬유를 5:5의 중량비율로 포함하도록 합사하여 복합사를 제조하는 단계; 및manufacturing a composite yarn by plying the carbon fiber and polyethylene fiber in a weight ratio of 5:5; and
상기 복합사를 경사 및 위사로 포함시켜 직물을 제조하는 단계;를 수행하여 제조되는 직물을 적용한다.The fabric manufactured by performing the step of manufacturing a fabric by including the composite yarn as warp and weft yarns is applied.
먼저, 폴리아크릴로나이트릴(PAN) 섬유를 질소분위기에서 1-2℃/분의 승온속도로 300-400℃의 온도까지 승온시킨 후 2-4시간 동안 1차 열처리하여 탄소섬유 전구체를 제조한다. 바람직하게는 1-2℃/분의 승온속도로 330-370℃의 온도까지 승온시킨 후 2.5-3.5시간 동안 1차 열처리한다.First, polyacrylonitrile (PAN) fibers are heated to a temperature of 300-400°C in a nitrogen atmosphere at a temperature increase rate of 1-2°C/min and then subjected to primary heat treatment for 2-4 hours to produce a carbon fiber precursor. . Preferably, the temperature is raised to 330-370°C at a temperature increase rate of 1-2°C/min and then subjected to primary heat treatment for 2.5-3.5 hours.
다음, 상기 탄소섬유 전구체를 질소분위기에서 4-6℃/분의 승온속도로 700-800℃의 온도까지 승온시킨 후 0.5-2시간 동안 2차 열처리하여 탄소섬유를 제조한다. 바람직하게는 5℃/분의 승온속도로 730-770℃의 온도까지 승온시킨 후 0.8-1.2시간 동안 1차 열처리한다.Next, the carbon fiber precursor is heated to a temperature of 700-800°C in a nitrogen atmosphere at a heating rate of 4-6°C/min and then subjected to secondary heat treatment for 0.5-2 hours to produce carbon fiber. Preferably, the temperature is raised to 730-770°C at a temperature increase rate of 5°C/min and then subjected to primary heat treatment for 0.8-1.2 hours.
다음, 상기 탄소섬유를 이용하여 산소플라즈마 처리한다. 상기 산소플라즈마 처리를 통해 탄소섬유 표면에 균일한 작용기를 도입할 수 있다. 이는 후단에서 그래핀 산화물을 용이하게 코팅하기 위한 전처리 공정이다.Next, oxygen plasma treatment is performed using the carbon fiber. Through the oxygen plasma treatment, uniform functional groups can be introduced to the surface of carbon fiber. This is a pretreatment process to easily coat graphene oxide at the later stage.
다음, 카르복시기를 포함하는 그래핀 산화물과 10 중량%의 황산 수용액을 준비하여, 상기 황산 수용액 100 중량부에 대하여 상기 그래핀 산화물을 1 중량부 포함하는 분산액을 제조한 후, 상기 분산액에 산소플라즈마 처리된 탄소섬유를 침지한 후, 40-60℃의 온도에서 6-10시간 동안 반응시켜 산소플라즈마 처리된 탄소섬유를 그래핀 산화물로 코팅한다.Next, prepare graphene oxide containing a carboxyl group and a 10% by weight aqueous solution of sulfuric acid, prepare a dispersion containing 1 part by weight of the graphene oxide based on 100 parts by weight of the aqueous sulfuric acid solution, and then subject the dispersion to oxygen plasma treatment. After immersing the carbon fiber, it is reacted at a temperature of 40-60°C for 6-10 hours to coat the oxygen plasma-treated carbon fiber with graphene oxide.
산소플라즈마 처리된 탄소섬유는 히드록시기 등의 작용기를 포함하고 있기 때문에, 그래핀 산화물에 포함된 카르복시기와 탈수축합반응하기에 용이하다.Since carbon fiber treated with oxygen plasma contains functional groups such as hydroxy groups, it is easy to undergo a dehydration condensation reaction with carboxyl groups contained in graphene oxide.
또한, 상기 그래핀 산화물에 포함된 카르복시기는 산 촉매 존재 하에서 탄소섬유에 포함되어 있는 히드록시기와 반응하여 새로운 공유결합을 형성할 수 있다.Additionally, the carboxylic group contained in the graphene oxide can react with the hydroxyl group contained in the carbon fiber in the presence of an acid catalyst to form a new covalent bond.
탄소섬유의 표면에 그래핀 산화물이 코팅된 후에도, 그래핀 산화물에 포함된 적어도 일부의 카르복시기는 반응에 참여하지 않은 상태로 남아있게 된다. 또한, 대기 조건에서 상술한 작용기들은 산소분자와 반응하여 쉽사리 라디칼화 되며 활성 산소종을 생성한다. 그 결과, 섬유의 표면에서 그램 음성 세균 혹은 그램 양성 세균이 번식하는 것을 지연시키거나 방지할 수 있다.Even after graphene oxide is coated on the surface of the carbon fiber, at least some of the carboxyl groups contained in the graphene oxide remain without participating in the reaction. In addition, under atmospheric conditions, the above-mentioned functional groups react with oxygen molecules and are easily radicalized to generate reactive oxygen species. As a result, it is possible to delay or prevent the propagation of gram-negative or gram-positive bacteria on the surface of the fiber.
이와 같은 반응은 달리 트랜스-에스테리피케이션(trans-esterification) 반응이라 칭해질 수 있으며, 에스테르기 또는 히드록시기가 교환되는 반응에 해당한다. 따라서, 그래핀 산화물의 코팅은 산 촉매 조건에서 섬유의 표면에 위치한 작용기 및 그래핀 산화물의 작용기 사이의 트랜스-에스테리피케이션(trans-esterification) 반응에 의하여 수행된 것이 바람직하다.This reaction may otherwise be called a trans-esterification reaction, and corresponds to a reaction in which an ester group or a hydroxy group is exchanged. Therefore, the coating of graphene oxide is preferably performed by a trans-esterification reaction between the functional groups located on the surface of the fiber and the functional groups of graphene oxide under acid-catalyzed conditions.
전술한 바와 같은 트랜스-에스테리피케이션은 그래핀 산화물 분산액에 섬유를 침지하고 촉매인 산을 첨가함으로써 수행될 수 있다. 이 때, 산이란 루이스 산(Lewis acid)를 의미한다. 루이스 산은 전자를 공여받을 수 있는 종으로서, 황산, 질산, 염산 외에도 금속염을 포함하는 개념이며, 아연 양이온, 이리듐 양이온 등을 포함한다.Trans-esterification as described above can be performed by immersing the fiber in a graphene oxide dispersion and adding an acid as a catalyst. At this time, acid means Lewis acid. Lewis acids are species that can donate electrons, and include metal salts in addition to sulfuric acid, nitric acid, and hydrochloric acid, and include zinc cations and iridium cations.
또한, 상기 트랜스-에스테리피케이션은 40-60℃의 온도조건에서 6-10시간 동안 수행되는 것이 바람직하다. 온도조건이 40℃ 미만이거나 반응시간이 6시간 미만이 경우에는 트랜스-에스테리피케이션이 충분히 진행되지 아니할 가능성이 상당하고, 온도조건이 60℃를 초과하거나 반응시간이 10시간을 초과하는 경우에는 섬유의 훼손이 문제될 수 있다.Additionally, the trans-esterification is preferably performed for 6-10 hours at a temperature of 40-60°C. If the temperature condition is less than 40℃ or the reaction time is less than 6 hours, there is a significant possibility that trans-esterification will not proceed sufficiently, and if the temperature condition is more than 60℃ or the reaction time is more than 10 hours, the fiber Damage may be a problem.
다음, 그래핀 산화물이 코팅된 탄소섬유를 물 및 에탄올을 1:1의 중량비율로 포함하는 세정제를 이용하여 세척한다.Next, the carbon fiber coated with graphene oxide is washed using a detergent containing water and ethanol in a weight ratio of 1:1.
다음, 상기 탄소섬유 및 폴리에틸렌 섬유를 5:5의 중량비율로 포함하도록 합사하여 복합사를 제조한다. 상기 합사는 일반적인 합사 방법을 이용하여 제조한다. 상기 폴리에틸렌 섬유는 바람직하게 난연 섬유이다.Next, a composite yarn is manufactured by plying the carbon fiber and polyethylene fiber in a weight ratio of 5:5. The ply yarn is manufactured using a general ply yarn method. The polyethylene fiber is preferably a flame retardant fiber.
다음, 상기 복합사를 경사 및 위사로 포함시켜 직물을 제조한다. 상기 직물은 일반적인 공정을 이용하여 제조된다.Next, fabric is manufactured by including the composite yarn as warp and weft yarns. The fabric is manufactured using common processes.
상기 겉감은 사방으로 신축되는 구조의 폴리스판으로 이루어진다. 상기 겉감은 사방으로 신축되는 구조의 폴리스판(polyspan)으로 이루어진 것이 바람직하다. 상기 폴리스판은 충분한 신축성을 갖기 때문에 체중감량용 기능성 의류 또는 착용물로 이용할 경우 신체를 알맞게 압박할 수 있는 소재로, 본 발명에서는 상기 폴리스판을 겉감으로 적용하여 착용감을 높일 수 있다.The outer fabric is made of a poly board with a structure that expands and contracts in all directions. The outer fabric is preferably made of polyspan, which has a structure that expands and contracts in all directions. Since the polyester plate has sufficient elasticity, it is a material that can appropriately compress the body when used as functional clothing or wear for weight loss. In the present invention, the polyester plate can be applied as an outer material to increase wearing comfort.
이하, 본 발명을 하기의 실시예 및 실험예에 의해 보다 상세하게 설명한다.Hereinafter, the present invention will be described in more detail through the following examples and experimental examples.
단, 하기 실시예 및 실험예는 본 발명의 내용을 예시하는 것일 뿐 발명의 범위가 실시예 및 실험예에 의해 한정되는 것은 아니다.However, the following examples and experimental examples only illustrate the content of the present invention and the scope of the invention is not limited by the examples and experimental examples.
<제조예 1> 알루미늄 실리케이트 복합분말의 제조<Preparation Example 1> Preparation of aluminum silicate composite powder
알루미늄 실리케이트 70 중량부, 산성백토 10 중량부, 메틸셀룰로오스 10 중량부, 인산수소마그네슘 삼수화물(MgHPO4ㆍ3H2O) 5 중량부 및 폴리비닐알콜 5 중량부를 혼합하여 실리케이트 혼합물을 제조하고, 상기 실리케이트 혼합물을 진공압출성형기로 압출하여 펠렛을 제조하였다. 이후, 제조된 펠렛을 건조 및 분쇄하고, 분쇄물을 가열로에 넣어 140℃의 온도에서 3시간 동안 1차 열처리하고, 이후 500℃의 온도로 가열하여 5분 동안 2차 열처리하여 알루미늄 실리케이트 복합분말을 제조하였다.A silicate mixture was prepared by mixing 70 parts by weight of aluminum silicate, 10 parts by weight of acidic clay, 10 parts by weight of methylcellulose, 5 parts by weight of magnesium hydrogen phosphate trihydrate (MgHPO 4 3H 2 O), and 5 parts by weight of polyvinyl alcohol, The silicate mixture was extruded using a vacuum extruder to produce pellets. Afterwards, the prepared pellets were dried and ground, the ground product was placed in a heating furnace and subjected to primary heat treatment at 140°C for 3 hours, and then heated to 500°C and secondary heat treatment for 5 minutes to produce aluminum silicate composite powder. was manufactured.
<실시예 1> 보호복용 원단의 제조<Example 1> Manufacturing of protective clothing fabric
면스판을 준비하고, 상기 면스판 상부에 아크릴계 고분자 수지 60 중량부, 아크릴계 혼합물 7 중량부, 상기 제조예 1에서 제조된 알루미늄 실리케이트 복합분말 10 중량부, 폴리비닐알콜 5 중량부, 탄산칼슘 5 중량부, 탄소나노튜브 5 중량부, 셀룰로오즈 아세테이트 부틸레이트 3 중량부 및 메틸에틸케톤 5 중량부를 혼합하여 제조한 제1층 형성용 조성물을 도포하고 가열 및 건조하여 제1층을 형성하였다. 이후, 스티렌부타디엔고무 35 중량부, 부틸고무 20 중량부, 수산화탄산마그네슘 28 중량부, 알루미늄 실리케이트 복합분말 4 중량부, 이산화티타늄 분말 4 중량부, 노화방지제 3 중량부, 가소제 3 중량부 및 프로세스오일 3 중량부를 혼합하여 제조한 제2층 형성용 조성물을 제1층 상에 도포하여 제2층을 형성하고, 폴리에틸렌 섬유 및 탄소섬유를 직조하여 형성된 직물층을 제2층 상에 위치시켜 제3층을 형성하고, 제3층 상부에 폴리스판을 위치시킨 후 압착, 가열 및 건조하여 보호복용 원단을 제조하였다.Prepare a cotton spandex, and on top of the cotton spandex, 60 parts by weight of acrylic polymer resin, 7 parts by weight of acrylic mixture, 10 parts by weight of aluminum silicate composite powder prepared in Preparation Example 1, 5 parts by weight of polyvinyl alcohol, and 5 parts by weight of calcium carbonate. A composition for forming a first layer prepared by mixing 5 parts by weight of carbon nanotubes, 3 parts by weight of cellulose acetate butyrate, and 5 parts by weight of methyl ethyl ketone was applied, heated, and dried to form a first layer. Afterwards, 35 parts by weight of styrene butadiene rubber, 20 parts by weight of butyl rubber, 28 parts by weight of magnesium hydroxide carbonate, 4 parts by weight of aluminum silicate composite powder, 4 parts by weight of titanium dioxide powder, 3 parts by weight of anti-aging agent, 3 parts by weight of plasticizer and process oil. A composition for forming a second layer prepared by mixing 3 parts by weight was applied on the first layer to form a second layer, and a fabric layer formed by weaving polyethylene fibers and carbon fibers was placed on the second layer to form a third layer. was formed, a polyplate was placed on top of the third layer, and then pressed, heated, and dried to produce protective clothing fabric.
<실험예 1> 방사능 보호 효과 분석<Experimental Example 1> Analysis of radiation protection effect
상기 실시예 1에서 제조된 보호복용 원단을 이용하여 선형가속기 실험실에서 방사선 차폐 실험을 실시하였다.A radiation shielding experiment was conducted in a linear accelerator laboratory using the protective clothing fabric prepared in Example 1.
구체적으로, 보호복용 원단을 50×50 cm로 절단한 후 하기 표 1에 기재된 선원과 평균에너지에 따라 방사선 차폐율을 매번 그 위치를 달리하여 10회 측정한 후, 그 평균값과 변동률을 측정하여 아래의 표 1에 나타내었다. 상기 변동률의 의미는 아래에 표시된 수학식과 같다.Specifically, after cutting the protective clothing fabric into 50 It is shown in Table 1. The meaning of the rate of change is the same as the equation shown below.
<수학식><Equation>
변동율(%) = 측정된 최대 방사선 차폐율 - 측정된 최소 방사선 차폐율Percent variation (%) = maximum measured radiation shielding - minimum measured radiation shielding.
상기 표 1에 나타낸 바와 같이, 본 발명에 따른 보호복용 원단은 방사능 보호가 가능한 것임을 확인할 수 있었다.As shown in Table 1 above, it was confirmed that the protective clothing fabric according to the present invention was capable of protecting against radiation.
Claims (3)
상기 안감 상부에 형성된 내층; 및
상기 내층 상부에 형성된 겉감;을 포함하고,
상기 내층은,
상기 안감 상부에 형성된 제1층;
상기 제1층 상부에 형성된 제2층; 및
상기 제2층 상부에 형성된 제3층;을 포함하고,
상기 안감은 사방으로 신축되는 구조의 면스판이고,
상기 겉감은 사방으로 신축되는 구조의 폴리스판이고,
상기 제1층은 알루미늄 실리케이트 복합분말을 포함하고,
상기 알루미늄 실리케이트 복합분말은,
알루미늄 실리케이트 68-72 중량부, 산성백토 8-12 중량부, 메틸셀룰로오스 8-12 중량부, 인산수소마그네슘 삼수화물(MgHPO4ㆍ3H2O) 3-7 중량부 및 폴리비닐알콜 3-7 중량부를 혼합하여 실리케이트 혼합물을 제조하는 단계; 상기 실리케이트 혼합물을 진공압출성형기로 압출하여 펠렛을 제조하는 단계; 제조된 펠렛을 건조 및 분쇄하는 단계; 건조 및 분쇄한 분쇄물을 120-160℃의 온도에서 2-4시간 동안 1차 열처리하는 단계; 및 1차 열처리한 분쇄물을 480-520℃의 온도에서 3-7분 동안 2차 열처리하는 단계;를 수행하여 제조되고,
상기 제2층은 스티렌부타디엔고무 및 부틸고무를 포함하고,
상기 제3층은 폴리에틸렌 섬유 및 탄소섬유를 직조하여 형성된 직물층인 것을 특징으로 하는 보호복용 원단.lining;
An inner layer formed on top of the lining; and
It includes an outer fabric formed on the upper part of the inner layer,
The inner layer is,
A first layer formed on the top of the lining;
a second layer formed on top of the first layer; and
It includes a third layer formed on top of the second layer,
The lining is a cotton spandex with a structure that expands and contracts in all directions,
The outer fabric is a poly board with a structure that expands and contracts in all directions,
The first layer includes aluminum silicate composite powder,
The aluminum silicate composite powder,
68-72 parts by weight of aluminum silicate, 8-12 parts by weight of acidic clay, 8-12 parts by weight of methyl cellulose, 3-7 parts by weight of magnesium hydrogen phosphate trihydrate (MgHPO 4 ㆍ3H 2 O), and 3-7 parts by weight of polyvinyl alcohol. mixing the parts to prepare a silicate mixture; Extruding the silicate mixture using a vacuum extruder to produce pellets; Drying and grinding the prepared pellets; Primary heat treatment of the dried and pulverized pulverized material at a temperature of 120-160°C for 2-4 hours; and secondary heat treatment of the primary heat treated pulverized material at a temperature of 480-520°C for 3-7 minutes.
The second layer includes styrene butadiene rubber and butyl rubber,
The third layer is a protective clothing fabric, characterized in that the third layer is a fabric layer formed by weaving polyethylene fibers and carbon fibers.
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KR102353824B1 (en) | 2021-06-04 | 2022-01-20 | 국방과학연구소 | Multilayer fabric for cbr-protective suit, manufacturing method thereof and cbr-protective suit |
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KR200177044Y1 (en) | 1999-11-01 | 2000-04-15 | 주식회사코넥 | Wearing apparel for protecting radioactive contamination |
JP2002067205A (en) * | 2000-08-28 | 2002-03-05 | Unitica Fibers Ltd | Moisture permeable waterproof laminate cloth having excellent antidewing properties |
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