KR100755019B1 - Antibiotic composition for fiber and cloth coated with the same - Google Patents
Antibiotic composition for fiber and cloth coated with the same Download PDFInfo
- Publication number
- KR100755019B1 KR100755019B1 KR1020060083009A KR20060083009A KR100755019B1 KR 100755019 B1 KR100755019 B1 KR 100755019B1 KR 1020060083009 A KR1020060083009 A KR 1020060083009A KR 20060083009 A KR20060083009 A KR 20060083009A KR 100755019 B1 KR100755019 B1 KR 100755019B1
- Authority
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- South Korea
- Prior art keywords
- silver
- antimicrobial
- composition
- weight
- fabric
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- 239000004744 fabric Substances 0.000 title claims abstract description 51
- 239000000835 fiber Substances 0.000 title claims abstract description 47
- 239000000203 mixture Substances 0.000 title claims description 52
- 230000003115 biocidal effect Effects 0.000 title abstract 4
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 claims abstract description 43
- 229910052709 silver Inorganic materials 0.000 claims abstract description 34
- 239000004332 silver Substances 0.000 claims abstract description 34
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000000284 extract Substances 0.000 claims abstract description 28
- 239000000243 solution Substances 0.000 claims abstract description 27
- 239000002105 nanoparticle Substances 0.000 claims abstract description 19
- 239000000227 bioadhesive Substances 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000011259 mixed solution Substances 0.000 claims abstract description 11
- 239000011248 coating agent Substances 0.000 claims abstract description 10
- 238000000576 coating method Methods 0.000 claims abstract description 10
- 230000000845 anti-microbial effect Effects 0.000 claims description 62
- 235000003261 Artemisia vulgaris Nutrition 0.000 claims description 44
- 240000006891 Artemisia vulgaris Species 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 23
- 238000001035 drying Methods 0.000 claims description 8
- 239000003292 glue Substances 0.000 claims description 5
- 239000004599 antimicrobial Substances 0.000 claims description 4
- 241001474374 Blennius Species 0.000 claims description 3
- 230000006835 compression Effects 0.000 claims description 2
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- 238000002156 mixing Methods 0.000 abstract description 9
- 239000002131 composite material Substances 0.000 abstract description 7
- 239000002245 particle Substances 0.000 description 13
- 239000004094 surface-active agent Substances 0.000 description 11
- 235000009051 Ambrosia paniculata var. peruviana Nutrition 0.000 description 10
- 235000003097 Artemisia absinthium Nutrition 0.000 description 10
- 240000001851 Artemisia dracunculus Species 0.000 description 10
- 235000017731 Artemisia dracunculus ssp. dracunculus Nutrition 0.000 description 10
- 239000001138 artemisia absinthium Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 10
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 10
- 238000002845 discoloration Methods 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 9
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 9
- 238000001179 sorption measurement Methods 0.000 description 8
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 230000000844 anti-bacterial effect Effects 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- 239000001522 artemisia absinthium l. herb extract Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000003205 fragrance Substances 0.000 description 5
- 239000002923 metal particle Substances 0.000 description 5
- 230000005855 radiation Effects 0.000 description 5
- 229920003002 synthetic resin Polymers 0.000 description 5
- 239000000057 synthetic resin Substances 0.000 description 5
- 229940119569 wormwood extract Drugs 0.000 description 5
- 241000588724 Escherichia coli Species 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 239000010946 fine silver Substances 0.000 description 4
- 229910021645 metal ion Inorganic materials 0.000 description 4
- 150000003378 silver Chemical class 0.000 description 4
- -1 silver ions Chemical class 0.000 description 4
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 4
- 230000001954 sterilising effect Effects 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000002114 nanocomposite Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000010944 silver (metal) Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 101710134784 Agnoprotein Proteins 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241000254173 Coleoptera Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- 208000000112 Myalgia Diseases 0.000 description 2
- 241000191940 Staphylococcus Species 0.000 description 2
- 241000191967 Staphylococcus aureus Species 0.000 description 2
- 230000007815 allergy Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 238000007603 infrared drying Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 208000013465 muscle pain Diseases 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 2
- 229940071536 silver acetate Drugs 0.000 description 2
- 229910001961 silver nitrate Inorganic materials 0.000 description 2
- YPNVIBVEFVRZPJ-UHFFFAOYSA-L silver sulfate Chemical compound [Ag+].[Ag+].[O-]S([O-])(=O)=O YPNVIBVEFVRZPJ-UHFFFAOYSA-L 0.000 description 2
- 229910000367 silver sulfate Inorganic materials 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 230000007480 spreading Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 208000007536 Thrombosis Diseases 0.000 description 1
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000012136 culture method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 210000005260 human cell Anatomy 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 108010059642 isinglass Proteins 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229910052627 muscovite Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 description 1
- 229940124595 oriental medicine Drugs 0.000 description 1
- OTCVAHKKMMUFAY-UHFFFAOYSA-N oxosilver Chemical class [Ag]=O OTCVAHKKMMUFAY-UHFFFAOYSA-N 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000037307 sensitive skin Effects 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- YDHABVNRCBNRNZ-UHFFFAOYSA-M silver perchlorate Chemical compound [Ag+].[O-]Cl(=O)(=O)=O YDHABVNRCBNRNZ-UHFFFAOYSA-M 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- 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
- D06M11/32—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 oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—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 oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
- D06M11/42—Oxides or hydroxides of copper, silver or gold
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
-
- 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
- D06M11/83—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 metals; with metal-generating compounds, e.g. metal carbonyls; Reduction of metal compounds on textiles
-
- 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
- D06M13/005—Compositions containing perfumes; Compositions containing deodorants
-
- 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
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
- D06M14/02—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials on to materials of natural origin
- D06M14/04—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials on to materials of natural origin of vegetal origin, e.g. cellulose or derivatives thereof
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2401/00—Physical properties
- D10B2401/13—Physical properties anti-allergenic or anti-bacterial
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Nanotechnology (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Crystallography & Structural Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Description
본 발명은 항균성 섬유용 조성물과 이를 이용한 직물에 관한 것으로, 더욱 상세하게는 쑥 추출물, 은 나노입자, 황토 및 천연접착제와 같은 환경친화적인 소재를 이용하여 제조한 조성물로 코팅한 섬유 제품으로 항균 효과가 우수한 것을 특징으로 하는 항균성 섬유용 조성물과 이를 코팅한 직물에 관한 것이다. The present invention relates to a composition for antimicrobial fibers and fabrics using the same, and more particularly, to an antimicrobial effect as a fiber product coated with a composition prepared using environmentally friendly materials such as mugwort extract, silver nanoparticles, ocher and natural adhesives. The present invention relates to a composition for antimicrobial fibers and a fabric coated thereon, characterized in that excellent.
옛날부터 쑥은 한방에서 그 약효가 다양하여 체내 질환의 상태에 따라 복용할 뿐만 아니라 부인 질환이 있는 여성들의 경우에는 쑥탕을 이용하여 목욕하거나 또는 쑥 찜질을 함으로서 상당한 효과를 보거나 또는 어혈이나 근육통이 있는 사람은 쑥을 잘 찧어서 어혈이 뭉쳐 있는 곳이나 근육통이 있는 곳에 고루 펴서 바르면 소염 진통에 효과가 있는 것으로 알려져 있다. 이러한 약효를 섬유에 적용시키기 위해 개발한 기술로서, 쑥 혼합물에 합성수지 접착제를 첨가하여 항균용 조성물을 제조하는 방법에 관한 특허가 이미 등록된 바 있다. Since ancient times, wormwood has various effects in the oriental medicine, and according to the condition of the body disease, women with gynecological diseases have a significant effect by taking a bath or wormwood steamed with wormwood or having bleeding or muscle pain. Man is well known for its effectiveness in anti-inflammatory analgesics by spreading the mugwort well and spreading it evenly in places where there is a blood clot or muscle pain. As a technology developed to apply such medicinal effects to fibers, a patent has already been registered for a method for producing an antimicrobial composition by adding a synthetic resin adhesive to the mugwort mixture.
그리고 은 나노입자의 경우 항균성의 효과가 이미 입증된 바 있어 직물에 이를 적용시키기 위한 다양한 방법들이 개발되어 특허들이 출원된 바 있지만 이러한 특허들의 대부분 은 나노입자를 직물에 코팅시키기 위해서 합성수지 접착제를 사용하고 있다. In the case of silver nanoparticles, the antimicrobial effect has already been demonstrated, and various methods for applying it to fabrics have been developed and patents have been filed. However, most of these patents use synthetic resin adhesives to coat silver nanoparticles on fabrics. have.
이와 같이 종래의 기술들의 경우에는 인체에 직접 접촉되는 직물에 항균 기능성을 부여하기 위하여 쑥 추출물 또는 은 나노입자의 성분을 합성수지 접착제와 혼합하여 직물에 코팅시킴으로써, 직물에 항균효과가 발생될 수 있도록 하였지만 기타 다른 인체에 유익한 기능성이 부여되어 있지 아니할 뿐만 아니라 쑥 추출물 또는 은 나노입자를 직물에 코팅시키키 위해 사용하는 합성수지 접착제가 피부에 접촉할 경우 피부가 민감한 사람의 경우 알러지(allergy) 등이 쉽게 유발할 우려가 있다. As described above, in order to provide antimicrobial functionality to a fabric directly contacting the human body, the antibacterial effect is generated by mixing a component of mugwort extract or silver nanoparticles with a synthetic resin and coating the fabric onto the fabric. Not only does it not provide any beneficial functionality to the human body, but the synthetic resin adhesive used to coat mugwort extracts or silver nanoparticles on fabrics can easily cause allergy in sensitive skin. There is concern.
따라서 상기 문제점들을 해결하기 위한 방안으로 본 발명은, 쑥을 물과 혼합한 후 열을 가하여 추출하여 은은한 쑥 향기를 발산하는 쑥 추출물과 항균효과가 뛰어난 은 나노입자를 혼합시킨 용액을 이용하여 직물에 코팅시킴으로써 쑥과 은 나노입자의 항균력의 보완 작용으로 항균력의 상승효과를 가져오고, 그리고 황토를 상기 혼합물에 섞어 사용함에 따라 황토에서 방사되는 원적외선에 의한 건강증진의 효과가 있는 것을 특징으로 하는 항균성 섬유용 조성물과 이를 코팅한 직물을 제공함에 그 목적이 있다. Therefore, in order to solve the above problems, the present invention, after the wormwood is mixed with water and extracted by applying heat to the fabric using a solution mixed with wormwood extract and silver nanoparticles excellent antimicrobial effect to give off the wormwood aroma The antimicrobial fiber is characterized in that the antimicrobial activity of the mugwort and silver nanoparticles by the coating to improve the antimicrobial activity, and by using ocher mixed with the mixture, it has the effect of health promotion by far-infrared radiation emitted from the ocher. It is an object to provide a composition for coating and a fabric coated with the same.
그리고 본 발명은 쑥 추출물, 은 나노입자 및 황토를 직물에 코팅시키기 위한 접착제로서, 합성수지 접착제를 배제하고 아교풀, 부레풀과 같은 천연접착제를 사용함으로서, 직물이 피부가 약한 사람에게 접촉시에도 알러지(allergy) 등이 발생될 우려가 적은 친환경적인 것을 특징으로 하는 항균성 섬유용 조성물과 이를 코팅한 직물을 제공함에 다른 목적이 있다. And the present invention as an adhesive for coating the mugwort extract, silver nanoparticles and ocher on the fabric, by using a natural adhesive such as glue, beetle without the synthetic resin adhesive, even when the fabric is in contact with people with weak skin ( It is another object to provide a composition for antimicrobial fibers and fabrics coated with the same, characterized in that the environmentally friendly environment is less likely to occur.
상기 목적을 달성하기 위한 본 발명에 따른 항균성 섬유용 조성물의 구성은 다음과 같다. The composition of the antimicrobial fiber composition according to the present invention for achieving the above object is as follows.
항균성 섬유용 조성물에 있어서, In the composition for antimicrobial fibers,
탈색시킨 쑥 추출물 50~70 중량부와 은 나노입자 용액 30~50 중량부를 혼합한 혼합 용액을 제조하고, To prepare a mixed solution of 50 to 70 parts by weight of decolorized mugwort extract and 30 to 50 parts by weight of silver nanoparticle solution,
그리고 상기 혼합용액 100 중량부에 대하여 황토 1~5 중량부 및 천연접착제 1~5 중량부를 각각 혼합시킨 것을 특징으로 한다. And it is characterized by mixing 1 to 5 parts by weight of yellow soil and 1 to 5 parts by weight of the natural adhesive with respect to 100 parts by weight of the mixed solution.
본 발명에 따른 은은한 쑥 향기를 발산하는 쑥 추출물은 물을 9~10 ㎏에 건 조된 쑥 1 ㎏을 물로 세척한 후 첨가하여 1~2 kg/㎠의 압력하에서 100~150 ℃의 온도를 가열하여 쑥 추출물을 제조한다. 이때 쑥 추출물은 수분 함량이 20~70 중량%인 것이 바람직하다. 상기에서 제조한 쑥 추출물은 색상이 짙은 녹색의 용액이므로 그대로 이용하거나 또는 녹색의 색상을 없애기 위하여 활성탄을 이용하여 녹색을 탈색하는 공정을 거치기도 한다. 쑥 추출물은 수분 함량이 20 중량% 미만이 되면 수분 함량을 줄이기 위한 농축비용이 상승되고, 수분 함량이 70 중량%를 초과할 경우에는 쑥의 향이 약할 뿐만 아니라 항균성능이 저하될 우려가 있다.Mugwort extract emanating a subtle wormwood fragrance according to the present invention is added to the water after washing 1 kg of dried wormwood with water in 9 ~ 10 kg with water to heat the temperature of 100 ~ 150 ℃ under a pressure of 1 ~ 2 kg / ㎠ Prepare mugwort extract. The mugwort extract is preferably a water content of 20 to 70% by weight. The mugwort extract prepared above is a solution of dark green color, so it may be used as it is or may be subjected to a process of decolorizing green color using activated carbon in order to remove green color. If the moisture content of the mugwort extract is less than 20% by weight, the concentration cost for reducing the moisture content is increased, and if the moisture content is more than 70% by weight, the aroma of the mugwort may be weak as well as the antibacterial performance may be lowered.
그리고 본 발명에 따른 은 나노입자 용액은 물에 1.0~20 nm 크기의 은(Ag) 나노입자가 200~10,000 ppm 함유되는 것이 바람직하다. 은 나노입자 용액에서 은의 직경이 1.0 nm 미만이 될 경우 은 나노입자의 제조비용이 상승되며, 20 nm를 초과할 경우 은 나노입자가 균일하게 분산되지 않아 충분한 항균 효과를 나타내지 못할 우려가 있다. 또한 은 나노입자 용액 중에 은 나노입자의 농도가 200 ppm미만이 될 경우에는 쑥 추출물 대비 은의 농도를 유지하기 위하여 다량의 은 나노입자 용액이 사용되어야 하며, 이로 인하여 섬유의 변색이 유발될 우려가 있고, 은 나노입자의 농도가 10,000 ppm을 초과할 경우 농축에 따른 비용이 증가될 뿐만 아니라 나노화된 은이 반응이나 엉김없이 안정되도록 하기 위해 다량의 안정제를 필요로 하며 이로 인하여 섬유에 적용시 변색이 유발될 우려가 있다. In addition, the silver nanoparticle solution according to the present invention preferably contains 200 to 10,000 ppm of silver (Ag) nanoparticles having a size of 1.0 to 20 nm. If the diameter of silver in the silver nanoparticle solution is less than 1.0 nm, the manufacturing cost of the silver nanoparticles is increased, if the diameter exceeds 20 nm, the silver nanoparticles are not uniformly dispersed there is a fear that it may not exhibit sufficient antibacterial effect. In addition, when the concentration of silver nanoparticles in the silver nanoparticles solution is less than 200 ppm, a large amount of silver nanoparticles solution should be used to maintain the silver concentration compared to the mugwort extract, which may cause discoloration of the fiber. However, when the concentration of silver nanoparticles exceeds 10,000 ppm, not only the cost of concentration increases but also a large amount of stabilizer is required to make the nanonized silver stable without reaction or entanglement, which may cause discoloration when applied to the fiber. There is concern.
본 발명에서 사용되는 은 나노입자의 제조 방법은 은염으로부터 흡착 계면 활성제를 이용하여 은을 미세화시키는 방법(이하 '흡착법'이라 한다)과 은염과 기타 고분자를 이용하여 고분자-은(Ag) 나노 복합체로 제조하는 방법(이하 '복합체법'이라 한다)이 일반적으로 사용된다.The method for producing silver nanoparticles used in the present invention is a method of refining silver from silver salt using an adsorption surfactant (hereinafter referred to as 'adsorption method') and a polymer-silver (Ag) nanocomposite using silver salt and other polymers. The manufacturing method (henceforth a "composite method") is generally used.
상기 흡착법에서 미세한 은 입자는 흡착 계면활성제를 이용하여 은염으로부터 미세한 은 입자로 제조된다. 즉, 흡착법에서는 은염 중 은이온이 은 입자로 환원될 때, 계면활성제에 의해 금속입자의 크기 및 분포가 조절된다. 은염을 이용한 은 입자 제조시 계면활성제 수용액이 첨가되고, 흡착되는 계면활성제 고유의 성질로 인하여 금속입자가 형성되는 용액 중에서 계면활성제가 형성되는 은 입자 핵의 표면에 흡착되어 은 입자 핵 사이의 융합이 방지된다. 따라서, 환원된 금속입자가 다른 금속입자 핵 표면에 결합되는 것이 지연 혹은 차단되어 크기 분포가 균일하고 미세한 금속입자가 제조된다. In the adsorption method, fine silver particles are prepared as fine silver particles from silver salt using an adsorption surfactant. That is, in the adsorption method, when silver ions in the silver salt are reduced to silver particles, the size and distribution of the metal particles are controlled by the surfactant. When preparing silver particles using silver salt, aqueous solution of surfactant is added and due to the inherent nature of the adsorbent, it is adsorbed on the surface of silver particle nucleus in which surfactant is formed in the solution in which metal particles are formed. Is prevented. Therefore, the reduced metal particles are delayed or blocked from binding to other metal particle nucleus surfaces, thereby producing metal particles with uniform size distribution and fine particles.
상기 흡착법에서는 질산염(AgNO3)과 같은 은염 및 계면활성제가 사용되며, 히드라진, 리튬알루미늄보로히드라이드, 소디움보로히드라이드 및 에틸렌옥사이드와 같은 금속이온환원제 등이 또한 첨가된다. 이러한 흡착법에 의한 미세 은 입자 제조방법은 대한민국 등록특허 제375525호에 상세히 기술되어 있다. In the adsorption method, silver salts and surfactants such as nitrates (AgNO 3 ) are used, and metal ion reducing agents such as hydrazine, lithium aluminum borohydride, sodium borohydride and ethylene oxide are also added. The method for producing fine silver particles by such an adsorption method is described in detail in Korean Patent No. 375525.
한편, 복합체법으로 은 입자를 미세화하는 방법에서는 은염과 고분자물질을 이용하여 고분자-은 고분자 나노복합체를 형성함으로써 은 입자가 미세화된다. 구체적으로, 상기 복합체법에서 은 입자는 먼저 은염 또는 은산화물염, 이소프로필알코올, 에탄올 및/또는 에틸렌글리콜 용매와 물 그리고 고분자 안정제를 혼합하고, 이를 정화하고, 침전물을 형성하고, 용매를 제거함으로써 제조된다. On the other hand, in the method of refining silver particles by the composite method, the silver particles are refined by forming a polymer-silver polymer nanocomposite using silver salt and a polymer material. Specifically, in the composite method, silver particles are prepared by first mixing silver or silver oxide salts, isopropyl alcohol, ethanol and / or ethylene glycol solvents with water and a polymer stabilizer, purifying them, forming a precipitate, and removing the solvent. Are manufactured.
은염으로는 질산은(AgNO3), 과염소산은(AgClO4), 황산은(AgSO4) 또는 아세트산은(CH3COOAg)이 그리고 고분자 안정제로는 폴리에틸렌, 폴리아크릴로니트릴, 폴리메틸메타크릴레이트, 폴리우레탄, 폴리아크릴아미드, 폴리에틸렌 글리콜, 폴리옥시에틸렌 스테아레이트등이 사용된다. 더욱이, 상기 은염등의 배합시 폴리옥시에틸렌 소비탄 모노올레이트등의 계면활성제를 사용하여 에멀션을 얻을 수 있다. 상기 복합체법에 의한 은 나노복합체의 제조방법은 대한민국 등록특허 제484506호에 상세히 기술되어 있다. Silver salts include silver nitrate (AgNO 3 ), silver perchlorate (AgClO 4 ), silver sulfate (AgSO 4 ) or silver acetate (CH 3 COOAg) and polyethylene, polyacrylonitrile, polymethylmethacrylate, poly Urethane, polyacrylamide, polyethylene glycol, polyoxyethylene stearate, etc. are used. Furthermore, an emulsion can be obtained using surfactants, such as polyoxyethylene sorbitan monooleate, when mix | blending said silver salt. The manufacturing method of the silver nanocomposite by the complex method is described in detail in Korean Patent No. 484506.
상기 흡착법에서는 은염, 계면활성제 및 금속이온 환원제등이 그리고 복합체법에서는 은염, 고분자안정제, 계면활성제, 용매등이 사용된다. 사용된 은염중 음이온부분, 즉, 질산은의 경우NO3 -, 염화은의 경우Cl-, 황산은의 경우SO4 -, 아세트산은의 경우 CH3COO-등의 염중 음이온 부분, 고분자안정제, 계면활성제, 금속이온환원제, 비수용성 용매등은 미세화 은 입자 형성반응 후, 생성물인 은 나노입자 용액 중에 잔류한다. In the adsorption method, silver salts, surfactants, and metal ion reducing agents are used. In the composite method, silver salts, polymer stabilizers, surfactants, solvents, and the like are used. The anionic portion of the silver salt used, i.e. NO 3 - for silver nitrate, Cl -for silver chloride, SO 4 -for silver sulfate, CH 3 COO -for silver acetate, etc., polymer stabilizers, surfactants, The metal ion reducing agent, the non-aqueous solvent and the like remain in the silver nanoparticle solution as a product after the fine silver particle formation reaction.
본 발명에서 사용하는 은 나노입자 용액은 은(Ag)과 물을 제외한 기타 다른 성분이 함유될 경우 은 나노입자 용액을 쑥 추출물과 황토에 섞어서 섬유에 적용할 경우 은 나노입자 용액 중 은(Ag)과 물을 제외한 기타 다른 성분이 섬유의 특성에 악영향을 미치는 불순물로 작용하므로 제거되어야만 한다. When the silver nanoparticle solution used in the present invention contains silver (Ag) and other components except water, the silver nanoparticle solution is mixed with wormwood extract and loess and applied to fibers. Other ingredients except water and water act as impurities that adversely affect the properties of the fiber and must be removed.
따라서, 본 발명에서는 섬유의 변색과 내구성이 손상되지않도록 은염 중 음이온부분, 계면활성제, 금속이온환원제 및 고분자안정제 등의 불순물 성분이 제거된 은 나노입자 용액이 제공된다. Accordingly, the present invention provides a silver nanoparticle solution from which impurities such as anion portion, surfactant, metal ion reducing agent, and polymer stabilizer are removed from silver salt so as to prevent discoloration and durability of the fiber.
본 발명에서 사용하는 은 나노입자 용액 중에 함유된 안정제 및 염이온 등의 불순물은 이온교환수지를 이용한 방법 혹은 기타의 여러가지 방법으로 제거될 수 있다. Impurities such as stabilizer and salt ions contained in the silver nanoparticle solution used in the present invention can be removed by a method using an ion exchange resin or other various methods.
한편 본 발명에서 사용하는 황토는 쑥 추출물과 은 나노입자 용액의 혼합용액 100 중량부에 대하여 황토 1~5 중량부를 첨가하는 것이 바람직하다. 황토의 함량이 1 중량부 미만이 될 경우에는 장기성 항균 효과가 저하될 우려가 있고 5 중량부를 초과할 경우에는 직물과의 부착성이 저하될 우려가 있다. 본 발명에서 사용하는 황토 입자의 크기는 100 메시 이상인 것이 바람직하다. 황토 입자의 크기가 100 메시 미만일 경우에는 황토 입자의 크기가 크고, 균일하지 못해 직물과의 부착성이 저하될 우려가 있다.On the other hand, the ocher used in the present invention is preferably added 1 to 5 parts by weight of ocher with respect to 100 parts by weight of the mixed solution of mugwort extract and silver nanoparticle solution. If the content of ocher is less than 1 part by weight, there is a fear that the long-term antimicrobial effect is lowered, and if it exceeds 5 parts by weight, the adhesion with the fabric may be reduced. The size of the ocher particles used in the present invention is preferably 100 mesh or more. If the size of the ocher particles is less than 100 mesh, the size of the ocher particles is large and not uniform, which may reduce adhesion to the fabric.
일반적으로 황토는 방출하는 원적외선 발산파장이 9.0 ㎛ 전후로 인체가 발산하는 9.4 ㎛과 유사하며, 원적외선의 파장이 유사할 경우 인체세포를 공명, 공진시켜 몸속 노폐물을 제거하며 신진대사를 활발하게 해주는 것으로 알려져 있다.In general, ocher emits far-infrared wavelengths of around 9.0 μm and is similar to 9.4 μm emitted by the human body, and when the wavelengths of far-infrared rays are similar, it is known to resonate and resonate human cells to remove wastes in the body and to activate metabolism. have.
그리고 본 발명에서 은 나노입자와 황토를 직물에 부착시키기 위한 접착제로서 천연접착제를 쑥 추출물과 은 나노입자 용액의 혼합용액 100 중량부에 대하여 1~5 중량부를 혼합시키는 것이 바람직하다. 천연접착제의 혼합량이 1 중량부 미만이 될 경우에는 천연접착제 혼합량의 부족으로 인해 은 나노입자와 황토가 직물에 잘 부착되지 않을 우려가 있고, 5 중량부를 초과할 경우에는 천연접착제 혼합량의 과다로 인해 직물의 촉감이 상실될 우려가 있다. 본 발명에서 사용가능한 천연접착제는 부레풀, 해초풀 또는 아교풀에서 한 가지를 선택하여 사용하는 것이 바람직하다. 본 발명에서 쑥 추출물과 은 나노입자 용액의 혼합용액에 천연접착제인 부레풀, 해초풀 또는 아교풀을 넣고 가열시키면 혼합용액 내에서 천연접착제가 용해되어 접성성을 갖게 된다.In the present invention, it is preferable to mix 1 to 5 parts by weight of the natural adhesive with 100 parts by weight of the mixed solution of the mugwort extract and the silver nanoparticle solution as an adhesive for attaching the silver nanoparticles and loess to the fabric. If the amount of the natural adhesive is less than 1 part by weight, the silver nanoparticles and the loess may not adhere well to the fabric due to the lack of the amount of the natural adhesive, and if the amount is more than 5 parts by weight, the amount of the natural adhesive is excessive. There is a fear that the feel of the fabric is lost. Natural adhesives usable in the present invention is preferably used to select one from the burr, seaweed or glue. In the present invention, when the mixture of the mugwort extract and the silver nanoparticles solution is put a natural adhesive, beetle, seaweed grass or glue paste and heated, the natural adhesive is dissolved in the mixed solution to have the adhesiveness.
이상에서 상세히 설명한 바와 같이 본 발명에 따른 항균성 섬유용 조성물은 쑥 추출물과 은 나노입자 용액 및 천연접착제 등을 모두 혼합하여 제조하면 조성물 내에 함유되어 있는 은 나노입자의 함량이 대략 50~6000 ppm을 유지하며, 이때 항균작용의 효과도 발휘할 수 있게 된다. As described in detail above, the antimicrobial fiber composition according to the present invention maintains the content of silver nanoparticles contained in the composition of about 50 to 6000 ppm when it is prepared by mixing all the mugwort extract, the silver nanoparticle solution, and the natural adhesive. In this case, the effect of the antimicrobial activity can be exerted.
한편 본 발명에 따른 항균성 섬유용 조성물을 이용하여 코팅한 직물의 구성에 대해 살펴보면 다음과 같다. On the other hand look at the configuration of the fabric coated using the antimicrobial fiber composition according to the present invention.
본 발명에 따른 항균성 섬유용 조성물을 코팅한 직물은 직물 90~95 중량%에 항균성 섬유용 조성물 5~10 중량%를 함침시켜 롤러로 압착시킨 후 가열 건조시킨 것을 특징으로 한다.The fabric coated with the composition for antimicrobial fibers according to the present invention is characterized in that the heat-impregnated with a roller by impregnating 5 to 10% by weight of the composition for antimicrobial fibers in 90 to 95% by weight of the fabric.
본 발명에서 직물에 코팅하는 항균성 섬유용 조성물의 함침량은 직물의 면적보다는 두께를 고려하여 직물의 무게에 비례하여 침지시키는 것이 바람직하다. 본 발명에서 바람직한 항균성 섬유용 조성물의 침지량은 직물 90~95 중량%에 항균성 섬유용 조성물 5~10 중량%를 함침시키는 것이 바람직하다. 항균성 섬유용 조성물의 함량이 5 중량% 미만이 될 경우에는 은 나노입자와 쑥 추출물 및 황토 함량의 부족으로 인해 항균성능 및 원적외선 방사능력이 저하될 우려가 있고, 10 중량%를 초과할 경우에는 은 나노입자와 쑥 추출물 함량의 증가에 비례하여 항균력이 현저히 향상되지는 않고, 은 나노입자의 증가에 따른 경제성이 저하되는 문제점이 발생될 우려가 있다. In the present invention, the impregnation amount of the composition for antimicrobial fibers coated on the fabric is preferably immersed in proportion to the weight of the fabric in consideration of the thickness rather than the area of the fabric. In the present invention, the immersion amount of the composition for antimicrobial fibers is preferably impregnated with 5 to 10% by weight of the composition for antimicrobial fibers in 90 to 95% by weight of the fabric. When the content of the antimicrobial fiber content is less than 5% by weight, the antimicrobial performance and far-infrared radiation ability may be deteriorated due to the lack of silver nanoparticles, mugwort extract, and ocher content. The antimicrobial activity is not significantly improved in proportion to the increase in the content of the nanoparticles and mugwort extract, there is a concern that the economy is lowered due to the increase of the silver nanoparticles.
상기에서 롤러의 압착 조건은 1~3 kg/㎠의 압력으로 롤러를 이용하여 직물을 압착시킨다. 압력이 1 kg/㎠미만이 될 경우에는 항균성 섬유용 조성물이 직물의 미세기공에 깊숙이 침투되지 않아 은 나노입자와 황토가 직물에 부착되지 않을 우려가 있고, 압력이 3 kg/㎠을 초과할 경우에는 직물에 가해지는 과압력에 의해 도리어 항균성 섬유용 조성물이 직물에 침투되지 않고 외부로 흘러나와 직물에 도포되는 은 나노입자와 황토의 함량이 줄어들게 됨에 따라 항균성능과 원적외선의 방사능력이 저하될 우려가 있다. The crimping conditions of the roller in the above is to press the fabric using a roller at a pressure of 1 ~ 3 kg / ㎠. If the pressure is less than 1 kg / ㎠, the composition for the antimicrobial fiber does not penetrate deep into the micropores of the fabric, there is a fear that the silver nanoparticles and loess will not adhere to the fabric, if the pressure exceeds 3 kg / ㎠ Due to the overpressure applied to the fabric, the antimicrobial composition does not penetrate into the fabric and flows out to reduce the content of silver nanoparticles and loess applied to the fabric, thereby degrading antimicrobial performance and far-infrared radiation ability. There is.
그리고 항균성 섬유용 조성물을 코팅시킨 직물은 50~150 ℃의 온도에서 30~60분 동안 건조시킨다. 건조온도가 50 ℃미만이 되거나 또는 건조시간이 30분 미만이 될 경우에는 직물에 코팅된 항균성 섬유용 조성물의 코팅액이 완전 건조되지 않을 우려가 있고, 건조온도가 150 ℃를 초과하거나 또는 건조시간이 60분을 초과할 경우에는 직물에 코팅된 항균성 섬유용 조성물의 코팅액이 충분히 건조되지만 에너지의 소비에 따른 경제성이 저하되는 문제점이 발생될 우려가 있다. 건조방법은 일반적인 열풍건조, 근적외선 건조 또는 원적외선 건조 등과 같이 필요에 따라 적절한 건조방법을 선택할 수 있다. And the fabric coated with the antimicrobial fiber composition is dried for 30 to 60 minutes at a temperature of 50 ~ 150 ℃. If the drying temperature is less than 50 ℃ or the drying time is less than 30 minutes, the coating liquid of the antimicrobial fiber composition coated on the fabric may not be completely dried, the drying temperature exceeds 150 ℃ or drying time When it exceeds 60 minutes, the coating liquid of the composition for antimicrobial fibers coated on the fabric is sufficiently dried, but there is a concern that a problem of economical deterioration due to energy consumption may occur. The drying method may be selected as appropriate drying method, such as general hot air drying, near infrared drying or far infrared drying.
본 발명에 따른 항균성 섬유용 조성물이 코팅된 직물은 쑥 추출물과 은 나노입자에 의해 항균능력이 탁월하고, 황토에 의한 원적외선 방사능력이 우수하므로 피부와 직접 접촉되는 속내의, 브래지어, 생리용품 등의 용도로 사용되어 질 수 있 다.The fabric coated with the antimicrobial fiber composition according to the present invention has excellent antibacterial ability by extracting wormwood and silver nanoparticles, and has excellent far-infrared radiation ability due to ocher, so that it is in direct contact with the skin, such as bras, sanitary products, etc. It can be used for purposes.
이하 본 발명의 구성을 실시예를 통해 상세히 설명하면 다음과 같다. Hereinafter, the configuration of the present invention in detail through the following examples.
1. 항균성 섬유용 조성물의 제조1. Preparation of antimicrobial fiber composition
(실시예 1 내지 5 및 비교예 1 내지 5)(Examples 1 to 5 and Comparative Examples 1 to 5)
건조된 쑥 1 ㎏을 물로 세척하여 용기에 넣고, 물을 10 ㎏을 가하여 상압하에서 100±5 ℃의 온도를 가열하여 수분의 함량이 65 중량%인 쑥 추출물을 얻었다. 그리고 아래 [표 1]의 내용과 같이 쑥 추출물, 은 나노입자가 200 ppm 함유된 용액, 100 메시 이상인 황토 및 부레풀을 첨가하여 항균성 섬유용 조성물을 제조하였다. 1 kg of dried mugwort was washed with water, placed in a container, 10 kg of water was added thereto, and heated to a temperature of 100 ± 5 ° C. under normal pressure to obtain a mugwort extract having a water content of 65% by weight. And as shown in Table 1 below, mugwort extract, a solution containing 200 ppm silver nanoparticles, more than 100 mesh ocher and bead was added to prepare a composition for the antimicrobial fiber.
2. 항균성 섬유용 조성물이 코팅된 직물의 제조2. Preparation of Fabric Coated with Antimicrobial Composition
상기에서 [표 1]의 내용에 따라 제조된 항균성 섬유용 조성물 7 중량%를 동일한 조건으로 직물에 함침처리한 후 2 kg/㎠의 압력으로 롤러를 이용하여 압착처리한 후 100 ℃의 온도에서 30 분 동안 건조시켜 항균성 섬유용 조성물이 코팅된 직물을 제조한다. 7 wt% of the antimicrobial fiber composition prepared according to the contents of [Table 1] above was impregnated in the fabric under the same conditions, followed by compression treatment using a roller at a pressure of 2 kg / cm 2, followed by 30 at a temperature of 100 ° C. Drying for minutes prepares a fabric coated with the composition for antimicrobial fibers.
3. 항균성 섬유용 조성물이 코팅된 직물의 시험3. Testing of Textiles Coated with Antimicrobial Compositions
항균성 섬유용 조성물이 코팅된 직물은 KS K 0465의 법에 의해 40℃의 온도에서 세탁하여 건조시킨 후 항균성, 변색성, 부착성, 향기 등을 측정한 결과는 아래 [표 2]의 내용과 같다. The fabric coated with the composition for antimicrobial fibers was washed and dried at a temperature of 40 ° C. according to the method of KS K 0465, and the results of measuring the antimicrobial, discoloration, adhesion, and fragrance are as shown in the following [Table 2]. .
가. 항균성 평가 (대장균, 포도상 구균)end. Antimicrobial Evaluation (E. coli, Staphylococcus aureus)
35±1 ℃의 일반 배양기에서 대장균(Escherichia coil ATCC 25922) 및 포도상 구균(Staphylococcus aureus ATCC 6538)을 20 시간 배양하고, 이 배양액을 멸균인산 완충액으로 20,000 배로 희석한 다음 상기 항균성 섬유용 조성물이 코팅된 직물의 2×2 ㎝의 시편에 1 ㎖적하하고 25 ℃에서 24시간 보존 후 꺼낸다. 그 후 이를 멸균된 한천배지에 다시 48시간 배양하고 석평판 배양법(35±1 ℃, 2일간 배양)으로 조사하여 생균수를 측정한다. 그 후, 아래 산출식에 따라 멸균율(%)을 계산하였다. 99.9%이상인 경우 ◎, 99%이상인 경우 ○, 80%이상인 경우 △, 그 이하인 경우 ×로 표시하였다. Escherichia coli in normal incubator at 35 ± 1 ℃ coil ATCC 25922 ) and Staphylococcus aureus ATCC 6538 ) is incubated for 20 hours, and the culture solution is diluted 20,000 times with sterile phosphate buffer, and then 1 ml is added to 2 × 2 cm specimens of the fabric coated with the antimicrobial fiber composition and stored at 25 ° C. for 24 hours and then taken out. . After that, the cells were incubated again for 48 hours in sterilized agar medium and irradiated with a lithographic plate culture method (35 ± 1 ℃, 2 days culture) to measure the number of viable cells. Then, the sterilization rate (%) was calculated according to the following formula. In the case of 99.9% or more,?, In the case of 99% or more,?, In the case of 80% or more,?
멸균율(%)=[(희석액 생균수-24시간 보존후 생균수)/희석액 생균수]× 100 Sterilization rate (%) = [(diluent viable count-number of viable cells after preservation for 24 hours) / diluent viable count] × 100
나. 변색성 평가I. Discoloration evaluation
항균성 섬유용 조성물이 코팅된 직물을 10일간 방치 후 분광색차계 JP7200C(Juki사)를 이용하여 로 측정하여 채도를 측정한 결과 초기 색도 대비 1% 이하인 경우 ◎, 5% 이하인 경우 ○, 그 이상인 경우 ×로 하여 평가하였다. After leaving the fabric coated with the antimicrobial composition for 10 days, measuring the saturation using a spectrophotometer JP7200C (Juki) and measuring saturation. It evaluated as x.
다. 부착성 평가All. Adhesion evaluation
투과전자현미경(TEM, Transmission electron microscopy)을 사용하여 표면에 은 나노입자 및 황토의 부착면적을 측정한 결과 은 나노입자 및 황토의 부착면적이 98% 이상인 경우 ◎, 95% 이상인 경우 ○, 그 이하인 경우 ×로 하여 평가하였다 When the adhesion area of silver nanoparticles and ocher was measured on the surface by using transmission electron microscopy (TEM), the adhesion area of silver nanoparticles and ocher was 98% or more, ◎, 95% or more. It evaluated as case X
라. 발향성 평가la. Odor evaluation
향기가 나는 경우 ◎, 향기가 나지 않는 경우 ×로 하여 평가하였다. In the case of scent, ◎, in the case of no scent, evaluated as x.
주 1) 20회 세탁한 시편을 이용함.Note 1) Use 20 washed specimens.
2) 10회 세탁한 시편을 사용함. 2) Use 10 washed specimens.
상기 [표 2]의 내용에 의하면, 항균성능 평가에 있어서 실시예 1 내지 3의 경우에는 대장균 및 포도상구균의 멸균성능이 99.9%이상으로 평가되고, 실시예 4 및 5의 경우 실시예 1 내지 3에 비해 은 나노입자의 함량이 줄어들게 됨에 따라 대장균 및 포도상구균의 멸균성능이 99.0%이상으로 평가된 반면에 은 나노입자가 함유되지 아니한 비교예 2 및 3의 경우에는 대장균 및 포도상구균의 멸균성능이 800%미만으로 평가되었으며, 은 나노입자의 함량이 20 중량부 함유되어 있는 비교예 5의 경우에도 실시예 1 내지 5에 비해 항균성이 떨어지는 것으로 평가되었다.According to the contents of [Table 2], in the case of Examples 1 to 3 in the evaluation of antibacterial performance, the sterilization performance of E. coli and Staphylococcus was evaluated to be 99.9% or more, and Examples 1 to 3 in Examples 4 and 5. As the content of silver nanoparticles decreases, the sterilization performance of Escherichia coli and staphylococcus was evaluated to be 99.0% or more. It was evaluated to be less than 800%, and even in Comparative Example 5 containing 20 parts by weight of the silver nanoparticles was evaluated to be less antimicrobial compared to Examples 1 to 5.
변색성능 평가에 있어서, 실시예 1 내지 5의 경우에는 항균성 섬유용 조성물 에 적정량의 은 나노입자 용액이 혼합됨에 따라 채도를 측정한 결과 초기 색도 대비 1% 이하인 경우에 해당되어 변색성능이 우수한 반면 비교예 1 및 4의 경우에는 항균성 섬유용 조성물 내에 과량의 은 나노입자 용액이 혼합됨에 따라 채도를 측정한 결과 초기 색도 대비 5% 이하인 경우에 해당되어 실시예에 비해 변색성능이 떨어짐을 알 수 있다. In the evaluation of discoloration performance, in Examples 1 to 5, when the silver nanoparticle solution was mixed with the appropriate amount of the antimicrobial fiber composition, the saturation was measured. In Examples 1 and 4, when the silver nanoparticle solution is mixed in the composition for the antimicrobial fiber, the saturation was measured, and the color change performance was lower than that of the example, which corresponds to 5% or less of the initial chromaticity.
부착성능 평가에 있어서, 실시예 1 내지 5의 경우에는 항균성 섬유용 조성물에 적정량의 천연접착제인 부레풀을 사용함에 따라 시편에 은 나노입자 및 황토의 부착면적이 98% 이상인 경우로 평가된 반면 비교예 1의 경우에는 항균성 섬유용 조성물에 부레풀 함량의 부족으로 인해 시편에 은 나노입자 및 황토의 부착면적이 95% 이상인 경우로 평가되어 다른 시편에 비해 부착성능이 다소 떨어지는 것으로 평가되었다.In the evaluation of adhesion performance, in Examples 1 to 5, when the appropriate amount of the natural adhesive agent beepule is used in the composition for the antimicrobial fiber, the adhesion area of the silver nanoparticles and the loess on the specimen was evaluated to be 98% or more. In case 1, the adhesion area of the silver nanoparticles and the loess was more than 95% due to the lack of the content of the beepule in the composition for the antimicrobial fiber, and thus the adhesion performance was slightly lower than that of the other specimens.
발향성능 평가에 있어서, 실시예 1 내지 5의 경우에는 항균성 섬유용 조성물에 적정량의 쑥 추출물이 함유되어 있어 시편을 10회 세탁을 한 후에도 쑥 향기가 발생되는 반면 비교예 1의 경우에는 항균성 섬유용 조성물에 적정량 이하의 쑥 추출물이 함유됨에 따라 초기에는 쑥 향기가 발생되었지만 시편을 10회 세탁 후에는 쑥 향기가 거의 발생되지 않았으며, 비교예 4의 경우에는 쑥 추출물이 함유되지 않음에 따라 쑥 향기가 전혀 발생되지 않았다. In the evaluation of the fragrance performance, Examples 1 to 5 contained the appropriate amount of mugwort extract in the composition for antimicrobial fibers, so that after the sample was washed 10 times, the mugwort aroma is generated, whereas in Comparative Example 1 for the antimicrobial fibers Mugwort aroma was initially generated as the composition contained less than the appropriate amount of mugwort extract, but after washing the specimen ten times, mugwort aroma was hardly generated. In Comparative Example 4, mugwort aroma was not contained. Did not occur at all.
따라서 상기 [표 2]의 성능평가에서 나타난 바와 같이 실시예 1 내지 5의 경우에는 항균성, 변색성, 부착성 및 발향성이 모두 우수한 것으로 나타난 반면에 비교예 1의 경우에는 쑥 추출물과 부레풀 함량의 부족으로 인해 발향성과 부착성능이 다소 떨어지고, 그리고 은 나노입자의 함량과다로 인해 변색성이 다소 떨어짐을 알 수 있다. 그리고 비교예 2 및 3의 경우에는 은 나노입자가 혼합되지 아니하여 항균성능이 떨어지고, 비교예 4의 경우 은 나노입자의 함량 과다로 인해 변색성이 다소 떨어지고, 쑥 추출물이 첨가되지 아니하여 쑥 냄새가 나지 아니하여 발향성능이 떨어짐을 알 수 있고, 비교예 5의 경우에는 은 나노입자의 함량 부족으로 인해 항균성능이 다소 떨어짐을 알 수 있었다.Therefore, in the case of Examples 1 to 5 as shown in the performance evaluation of [Table 2] it was shown that all of the antimicrobial, discoloration, adhesion and odor excellent, whereas in the case of Comparative Example 1 of the mugwort extract and the content of Due to the lack of fragrance and adhesion performance is somewhat reduced, and due to the excessive content of silver nanoparticles can be seen that the color fading is slightly reduced. And in the case of Comparative Examples 2 and 3 is not mixed with silver nanoparticles antibacterial performance, in the case of Comparative Example 4 due to the excessive content of silver nanoparticles discoloration is somewhat reduced, wormwood extract is not added to the wormwood smell It can be seen that the fragrance performance is not lowered, and in the case of Comparative Example 5, the antimicrobial performance was somewhat reduced due to the lack of silver nanoparticles.
상기에서 설명 드린 바와 같이 본 발명은 상기의 실시예를 통해 그 물성의 우수성이 입증되었지만 본 발명은 상기의 실시예에 의해서만 반드시 한정되는 것이 아니고, 본 발명의 기술적 사상을 벗어나지 않는 범위 내에서 여러 가지 치환, 변형 및 변경이 가능하다.As described above, the present invention has proved its superiority through the above embodiments, but the present invention is not necessarily limited only to the above embodiments, and various modifications may be made without departing from the technical spirit of the present invention. Substitutions, modifications and variations are possible.
상기의 구성을 갖는 본 발명은 쑥 추출물과 은 나노입자를 혼합하여 제조한 용액을 직물에 코팅시킴으로써 은은한 쑥의 향기와 함께 은 나노입자의 항균력의 작용으로 항균력의 상승효과를 가져오고, 그리고 황토를 상기 혼합물에 섞어 사용함에 따라 황토에서 방사되는 원적외선에 의한 건강증진의 효과가 있으며, 그리고 쑥 추출물, 은 나노입자 및 황토를 직물에 코팅시키기 위한 접착제로서, 아교풀, 부레풀과 같은 천연접착제를 사용함으로써, 직물이 피부가 약한 사람에게 접촉시에도 알러지 등이 발생될 우려가 없는 친환경적인 장점이 있다. The present invention having the above constitution brings a synergistic effect of antimicrobial activity by the action of antimicrobial activity of silver nanoparticles with a scent of wormwood by coating a solution prepared by mixing the mugwort extract and silver nanoparticles on a fabric, and By mixing with the mixture, there is an effect of health promotion by far-infrared radiation emitted from loess, and by using natural adhesives such as glue and burr as an adhesive for coating wormwood extract, silver nanoparticles and loess on the fabric. In addition, there is an environmentally friendly advantage that there is no fear of allergies, even when the fabric is in contact with people with weak skin.
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KR102526746B1 (en) | 2022-09-20 | 2023-04-28 | 주식회사 일송글로벌 | Manufacturing method of coated fabric with improved antifungal, antibacterial, deodorizing and durability |
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KR102526746B1 (en) | 2022-09-20 | 2023-04-28 | 주식회사 일송글로벌 | Manufacturing method of coated fabric with improved antifungal, antibacterial, deodorizing and durability |
KR20240040003A (en) | 2022-09-20 | 2024-03-27 | 주식회사 일송글로벌 | Fibrous products with anti-microbial, antibacterial, deodorant, and durability and their manufacturing methods |
KR20240040001A (en) | 2022-09-20 | 2024-03-27 | 주식회사 일송글로벌 | Coating fabric and its manufacturing method with enhanced UV protection |
KR20240040002A (en) | 2022-09-20 | 2024-03-27 | 주식회사 일송글로벌 | Coating fabric and its manufacturing method with water repellency |
KR20240040000A (en) | 2022-09-20 | 2024-03-27 | 주식회사 일송글로벌 | Coating fabric and its manufacturing method with enhanced flame retardancy |
KR102509994B1 (en) * | 2022-09-29 | 2023-03-16 | 주식회사 더블유비엔에스 | Manufacturing method of eco-friendly fabric with exhibits biodegradability and antibacterial properties |
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