KR20060014896A - A new silverware manufacture which is omtibacteria used chemicol compound of silver and brom - Google Patents

A new silverware manufacture which is omtibacteria used chemicol compound of silver and brom Download PDF

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KR20060014896A
KR20060014896A KR1020040063627A KR20040063627A KR20060014896A KR 20060014896 A KR20060014896 A KR 20060014896A KR 1020040063627 A KR1020040063627 A KR 1020040063627A KR 20040063627 A KR20040063627 A KR 20040063627A KR 20060014896 A KR20060014896 A KR 20060014896A
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silver
solution
silver salt
coating composition
powder
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KR1020040063627A
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Korean (ko)
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최명부
장인철
김학태
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최명부
장인철
김학태
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • C09D7/62Additives non-macromolecular inorganic modified by treatment with other compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/14Paints containing biocides, e.g. fungicides, insecticides or pesticides
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/20Diluents or solvents
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/63Additives non-macromolecular organic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/80Processes for incorporating ingredients

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Plant Pathology (AREA)
  • Inorganic Chemistry (AREA)
  • Paints Or Removers (AREA)

Abstract

벤조페논, 1-하이드록시사이크로헥실아세토페논, 알파,알파-디메틸-알파하이드록시아세토페논, 아크릴레이티드벤조페논, 벤질케탈로 이루어진 군에서 선택된 하나 이상의 화합물인 광개시제 100g과, 페녹시에틸아크릴레이트, N-비닐-2-피닐리돈, 2-하이드록시프로필아크릴레이트에서 선택된 어느 하나의 화합물아크릴수지 200g, 이소프로필알콜 30g, 톨루엔 10g, 은염용액10g 으로 조성된 유브이(UV)코팅조성물 및 그 제조방법에 관한 것이다.100 g of photoinitiator which is at least one compound selected from the group consisting of benzophenone, 1-hydroxycyclohexyl acetophenone, alpha, alpha-dimethyl-alpha hydroxyacetophenone, acrylated benzophenone, and benzyl ketal; UV coating composition composed of 200 g of isopropyl alcohol, 30 g of isopropyl alcohol, 10 g of toluene, 10 g of silver salt solution, and any one compound selected from the group consisting of latex, N-vinyl-2-pinyridone, 2-hydroxypropyl acrylate, and It relates to a manufacturing method.

유브이(UV)코팅조성물. 광개시제. 은염용액, 이소프로필알콜UV coating composition. Photoinitiator. Silver Salt Solution, Isopropyl Alcohol

Description

유브이코팅조성물 및 그 제조방법{A New Silverware Manufacture Which is Omtibacteria Used Chemicol Compound of Silver and Brom}UV coating composition and its manufacturing method {A New Silverware Manufacture Which is Omtibacteria Used Chemicol Compound of Silver and Brom}

본 발명은 각종 합성수지 제품 표면에 코팅시키고자 은염, 톨루엔, 이소프로필알콜, 아크릴수지 및 기타 첨가제로 조성되어 자외선 차단 효과가 있는 유브이(UV)코팅조성물 및 그 제조방법에 관한 것이다.The present invention relates to a UV coating composition having a UV-blocking effect composed of silver salt, toluene, isopropyl alcohol, acrylic resin, and other additives to be coated on various synthetic resin product surfaces, and a manufacturing method thereof.

일반적으로 합성수지제품중에서 햇빛이나 자외선을 포함하는 인공조명등 자외선 광선하에서 변질되는 것을 방지하기 위하여 자외선을 직접조사되지 않도록 유브이(UV)코팅조성물을 코팅하여 사용하여 왔다.In general, in order to prevent deterioration under ultraviolet light such as artificial lighting including sunlight or ultraviolet rays in synthetic resin products, UV coating composition has been used to prevent direct irradiation with ultraviolet rays.

필름의 경우 강화용이나, 기타 다양한 용도에 따라 코팅조성물로 코팅하여 사용하고 있으며, UV코팅제는 강도가 강해지는 장점이 있어 많이 사용되고 있다.In the case of film reinforcement, it is used by coating with a coating composition according to various other uses, UV coating agent has been used a lot because it has the strength of strength.

예를 들면, 대한민국공개특허공보 공개번호 특2001-0084405호에는 스피로피란계 광호변성화합을 톨루엔/알콜 혼합용매에 용해시킨 용액을 수지 그래늄에 20~50℃에서 0.05~38시간동안 침투시킨 후, 160~300℃로 가열하여 성형된 자외선 차단필름이 기재되어 있으며,For example, Korean Laid-Open Patent Publication No. 2001-0084405 discloses a solution in which a spiropyran-based photochromic compound is dissolved in a toluene / alcohol mixed solvent in a resin granium at 0.05 to 38 hours at 20 to 50 ° C. , UV-blocking film formed by heating to 160 ~ 300 ℃ is described,

동 공보 공개번호 제10-2002-0030474호에는 전기전도성 고분자가 표면에 흡 착된 마이크로겔용액과, 수가용성알코올존재하에 테트라 알콕시 실란과 실릴아크릴레이트를 반응시켜 얻은 콜로이달 실리카용액과 1관능에서 qxj 다관능성인 아크릴계 단량체 또는 비닐에테르계단량체와, 자와서 광개시제를 포함하는 전기전도성 마이크로겔을 함유한 자외선 경화형 하드코팅제 및 이의 용도가 기술되어 있으나,Korean Patent Publication No. 10-2002-0030474 discloses a microgel solution in which an electrically conductive polymer is adsorbed on the surface, a colloidal silica solution obtained by reacting tetraalkoxy silane and silyl acrylate in the presence of a water-soluble alcohol, and qxj in monofunctional. Although UV-curable hard coating agents containing polyfunctional acrylic monomers or vinyl ether monomers and electrically conductive microgels including photoinitiators have been described and their use,

상기와 같은 종래의 기술들은 자외선차단기능이 부적절하고, 너무 빨리 분해되거나, 자외선 차단효과가 균질하지 않으며 항균성이 결여되는 문제점이 있어 왔다.Such conventional techniques have been problematic in that the UV blocking function is inadequate, degrades too quickly, the UV blocking effect is not homogeneous, and lacks antimicrobial properties.

본 발명은 상기한 바와 같은 문제점을 해결하기 위하여 항균제 역할을 하는 은염, 톨루엔, 이소프로필알콜, 아크릴수지 및 기타 첨가제로 조성된 유브이(UV)코팅조성물 및 그 제조방법을 제공하는 것을 본 발명이 이루고자 하는 기술적 과제인 것이다.
The present invention is to provide a UV coating composition composed of silver salt, toluene, isopropyl alcohol, acrylic resin and other additives and a method for producing the same to solve the problems as described above. It is a technical problem.

상기와 같은 목적을 달성하기 위한 본 발명은 벤조페논, 1-하이드록시사이크로헥실아세토페논, 알파,알파-디메틸-알파하이드록시아세토페논, 아크릴레이티드벤조페논, 벤질케탈로 이루어진 군에서 선택된 하나 이상의 화합물인 광개시제 100g과, 페녹시에틸아크릴레이트, N-비닐-2-피닐리돈, 2-하이드록시프로필아크릴레이트에서 선택된 어느 하나의 화합물인 아크릴수지 200g, 이소프로필알콜 30g, 톨루엔 10g, 은염용액10g 으로 조성된 유브이(UV)코팅조성물 및 그 제조방법에 관한 것이다.The present invention for achieving the above object is one selected from the group consisting of benzophenone, 1-hydroxycyclohexyl acetophenone, alpha, alpha-dimethyl-alpha hydroxyacetophenone, acrylated benzophenone, benzyl ketal 100 g of photoinitiators which are the above compounds, 200 g of acrylic resins, 30 g of isopropyl alcohol, 10 g of toluene, silver salt which are any compound selected from phenoxyethyl acrylate, N-vinyl-2-pinyridone and 2-hydroxypropyl acrylate The present invention relates to a UV coating composition composed of 10 g of a solution and a method of manufacturing the same.

광범위한 파장의 자외선을 흡수함으로서 다양한 경화에 대해 반응성이 증가하고 경화속도를 증가시키는 광개시제는 벤조페논, 1-하이드록시사이크로헥실아세토페논, 알파,알파-디메틸-알파하이드록시아세토페논, 아크릴레이티드벤조페논, 벤질케탈로 이루어진 군에서 선택된 하나 또는 둘이상의 혼합물이 바람직하고, 첨가제로 실리콘 아크릴레이트를 포함하는 것이 바람직하다.Photoinitiators increase the reactivity and increase the curing rate for various curing by absorbing ultraviolet light of a wide range of wavelengths, benzophenone, 1-hydroxycyclohexylacetophenone, alpha, alpha-dimethyl-alphahydroxyacetophenone, acrylated One or more mixtures selected from the group consisting of benzophenone and benzyl ketal are preferred, and it is preferable to include silicone acrylate as an additive.

비반응성 용제로 이소프로필알코올과 톨루엔을 1.5~3: 1의 비율로 포함하는 것이 바람직하며, 아크릴수지를 첨가하여 사용하였다.It is preferable to include isopropyl alcohol and toluene in the ratio of 1.5-3: 1 as a non-reactive solvent, and acrylic resin was added and used.

본 발명에서 사용되는 아크릴수지는 페녹시에틸아크릴레이트, N-비닐-2-피닐리돈, 2-하이드록시프로필아크릴레이트에서 선택된 어느 하나의 화합물을 사용하는 것이다.The acrylic resin used in the present invention is to use any one compound selected from phenoxyethyl acrylate, N-vinyl-2-pinyridone, 2-hydroxypropyl acrylate.

은염제조를 살펴볼 것 같으면 분쇄한 은300g을 용해조에 넣고 열을 주면서 질산을 첨가시켜 은을 용해하면 280ml의 질산이 소모된다. 또한 염화제1주석 100g을 염산 100ml에 녹여 상기 은용액에 합성 교반한다. 상기 은용액을 PH를 중성으로 조절하기 위하여 가성소오다용액(PH13) 500ml에 산화아연 150g을 용해하여 상기 은용액과 합성하면서 PH7.5가 되게 하여 수분을 증발시켜 분말파우다의 은염을 얻는다. 상기 은염 300g을 물1000ml에 용해하여 브롬소다 100g을 넣고 교반한 다음 과산화수소 3ml를 넣고 30분동안 교반하면서 과산화수소를 증발시키면서 은용액이 산화탈색되게 하여 유리병에 담아 햇볕에 1시간 노출시키면 적은 갈색의 입자가 침전 되고 연갈색이든 액체가 반투명의 액체의 은항균제가 만들어진다. 상기 은항균제를 물500∼1000배 비율로 희석하여 직물에 침지시켜 항균하거나 무기 소독살균제로 사용하므로 인자에 무해할 뿐 아니라 항균력은 물론 생체독성검사에서 국가공인기관인 한국소비자 과학연구소, 한국원사직물연구소 항균 및 시험검사방법 및 독성검사방법이 또한 본 발명의 무기항균제가 99.9%의 항균력과 생체독성검사에서 인자에 무해한 것이 입증되고 있다.If you look at the production of silver salt, crushed 300g of silver in the dissolving tank, add nitric acid while heating and dissolving silver consumes 280ml of nitric acid. In addition, 100 g of stannous chloride is dissolved in 100 ml of hydrochloric acid, and then synthetically stirred with the silver solution. In order to adjust the silver solution to neutral pH, 150 g of zinc oxide was dissolved in 500 ml of caustic soda solution (PH13) to synthesize PH with silver solution to make PH7.5 to evaporate water to obtain silver salt of powder powder. Dissolve 300 g of the silver salt in 1000 ml of water, add 100 g of bromine soda, stir, add 3 ml of hydrogen peroxide, stir for 30 minutes, evaporate the hydrogen peroxide while oxidizing the silver solution, and put it in a glass bottle for 1 hour in the sun. The particles precipitate and light brown or liquid translucent liquid silver antibacterial agents are formed. The silver antibacterial agent is diluted to 500 ~ 1000 times of water and immersed in the fabric to be used as an antibacterial or inorganic disinfectant, so it is harmless to the factor and also has the antimicrobial power as well as the Korea Consumer Science Institute and the Korea Yarn Textile Research Institute. Antimicrobial and test test methods and toxicity test methods have also demonstrated that the inorganic antimicrobial agent of the present invention is harmless to factors in the antibacterial activity and biotoxicity test of 99.9%.

본 발명을 실시예를 통하여 상세히 설명하기로 한다.The present invention will be described in detail by way of examples.

실시예Example

제1공정1st process

은을 분쇄한 분말 300g을 용해조에 넣고 열을 주면서 서서히 1N 질산 280㎖을 첨가시켜 용해하여 은용액을 제조한 후에, 상기 은용액에 염화제1주석 100g을 염산 100㎖를 용해한 용액을 상기 은용액에 합성 교반 한 다음, 1N가성소오다용액(PH13)500㎖에 산화아연 150g을 용해하여 제1공정 은용액에 혼합하면서 PH7.5가 되게하면서 교반한 하여 100℃온도를 유지하면서 3~5시간 수분을 증발시켜 건조기에 넣고 분말파우다를 제조 한 다음, 상기 분말파우다 300g에 브롬소다 100g을 첨가하여 혼합하여 본 발명의 은염을 제조한 후에, 상기은염 300g을 물1000㎖에 용해하면 옅은 브라운 액체의 은염용액이 되며, 상기 은염용액을 탈색 및 산화시키기 위하여 과산화수소 3㎖를 투입하여 30분간 교반하면서 과산화수소를 증발시켜 투명유리병속에 담아 햇볕에 1시간 노출시켜 생성된 소량의 갈색침전물을 여과하여 반투명의 은염용액을 제조한 다음,300 g of pulverized silver powder was put in a dissolution tank and slowly added 280 ml of 1N nitric acid while heating to prepare a silver solution. 100 g of stannous chloride and 100 ml of hydrochloric acid were synthesized and stirred in the silver solution, followed by dissolving 150 g of zinc oxide in 500 ml of 1N caustic soda solution (PH13) and mixing it with the first step silver solution. While stirring to keep the temperature at 100 ℃ while evaporating the water for 3 to 5 hours in a drier to prepare a powder powder, 300 g of the powder powder is added by mixing 100 g of bromine soda to prepare a silver salt of the present invention After dissolving 300 g of the silver salt in 1000 ml of water, it becomes a silver salt solution of a light brown liquid. In order to decolorize and oxidize the silver salt solution, 3 ml of hydrogen peroxide was added and stirred for 30 minutes to evaporate hydrogen peroxide and put in a transparent glass bottle. A small amount of brown precipitate produced by exposure to 1 hour was filtered to prepare a translucent silver salt solution.

제2공정2nd process

벤조페논 100g과, 이소프로필알콜 30g, 톨루엔 10g, 페녹시에틸아크릴레이트 200g, 실리콘 아크릴레이트5g과, 상기 제1공정에서 제조한 은염용액10g을 교반기에 넣어 50℃로 30분간 가열하면서, 1,500~2,500RPM 의 속도로 교반시켜 UV코팅액을 제조한 후에, 1,500 ~ After stirring at a rate of 2500 RPM to prepare a UV coating

제3공정3rd process

콘베아벨트에 의해 유입되는 필름의 상부에 상기 제2공정에서 제조된 유브이(UV)코팅액이 저장된 유브이(UV)코팅액저장탱크에서 분무하여 필름의 상부에 코팅한 다음 건조실로 이송하여 70℃에서 10~20분간 건조하여 필름의 표면에 유브이(UV)코팅액을 코팅하였다. Sprayed in a UV coating liquid storage tank in which the UV coating liquid prepared in the second process is stored on the upper portion of the film introduced by the conveyor belt, coated on the upper portion of the film, and then transferred to a drying chamber at 10 ° C. to 10 ° C. It dried for 20 minutes and coated the UV coating solution on the surface of the film.

실험예Experimental Example

상기 실시예 1와 종래의 유브이(UV)코팅액을 실내 및 태양광에 노출시켰을 때 변색 속도 및 변색 정도를 관능 검사로 판별하였으며 그 결과는 하기 표 1에 기재하였다. 아울러 일광 견뢰도 측정기를 사용하여 40℃, 상대습도 40%의 조건으로 하고 광원으로는 자외선 램프를 사용하여 자외선 조사 및 조사 시간별 변속 속도 및 변색 정도를 관능 거사로 판별하였으며 그 결과를 하기 표 1에 기재하였다.When Example 1 and the conventional UV coating (UV) coating solution was exposed to room and sunlight, the discoloration rate and the degree of discoloration were determined by the sensory test and the results are shown in Table 1 below. In addition, using a daylight fastness measuring instrument, the conditions of 40 ℃, relative humidity 40% and using a UV lamp as a light source to determine the speed of change and the degree of discoloration by UV irradiation and irradiation time by sensory necrosis and the results are shown in Table 1 It was.

[표1]Table 1

구분division 실시예 1Example 1 종래의 유브이(UV)코팅액Conventional UV coating liquid 건조시간Drying time 3∼4시간3 to 4 hours 6시간이상More than 6 hours 경화시간Curing time 20℃에서 6~7시간6-7 hours at 20 ℃ 20℃에서 22시간22 hours at 20 ℃ 건조온도Drying temperature 75℃∼80℃75 ℃ ~ 80 ℃ 80℃80 ℃ 자외선차단UV protection 97%97% 66%66% 탈색decolorization 양호Good 보통usually

상기와 같은 본 발명은 합성수지 표면에 코팅되어, 고강도의 박막이 형성되며, 유연성이 우수하고 자외선이 차단되는 장점이 있는 것이다.












The present invention as described above is coated on the surface of the synthetic resin, a high-strength thin film is formed, it has the advantage of excellent flexibility and UV protection.












Claims (2)

유브이(UV)코팅조성물의 제조방법에 있어서, In the manufacturing method of UV coating composition, 제1공정1st process 은을 분쇄한 분말 300g을 용해조에 넣고 열을 주면서 서서히 1N 질산 280㎖을 첨가시켜 용해하여 은용액을 제조한 후에, 상기 은용액에 염화제1주석 100g을 염산 100㎖를 용해한 용액을 상기 은용액에 합성 교반 한 다음, 1N가성소오다용액(PH13)500㎖에 산화아연 150g을 용해하여 제1공정 은용액에 혼합하면서 PH7.5가 되게하면서 교반한 하여 100℃온도를 유지하면서 3~5시간 수분을 증발시켜 건조기에 넣고 분말파우다를 제조 한 다음, 상기 분말파우다 300g에 브롬소다 100g을 첨가하여 혼합하여 본 발명의 은염을 제조한 후에, 상기은염 300g을 물1000㎖에 용해하면 옅은 브라운 액체의 은염용액이 되며, 상기 은염용액을 탈색 및 산화시키기 위하여 과산화수소 3㎖를 투입하여 30분간 교반하면서 과산화수소를 증발시켜 투명유리병속에 담아 햇볕에 1시간 노출시켜 생성된 소량의 갈색침전물을 여과하여 반투명의 은염용액을 제조한 다음,300 g of pulverized silver powder was added to a dissolution tank, and 280 ml of 1N nitric acid was gradually added to dissolve while heating to prepare a silver solution. Then, a solution obtained by dissolving 100 g of stannous chloride and 100 ml of hydrochloric acid was dissolved in the silver solution. Synthetic agitation and then dissolve 150 g of zinc oxide in 500 ml of 1N caustic soda solution (PH13) and stir at pH 7.5 while mixing with silver solution in the first step. After evaporating the water and putting it in a drier to prepare a powder powder, 300 g of powder powder is added by mixing 100 g of bromine soda to prepare a silver salt of the present invention. Then, 300 g of the silver salt is dissolved in 1000 ml of water to obtain a pale brown liquid. It becomes a silver salt solution. In order to decolorize and oxidize the silver salt solution, 3 ml of hydrogen peroxide is added and stirred for 30 minutes to evaporate hydrogen peroxide, which is placed in a transparent glass bottle and exposed to the sun for 1 hour. By filtering the small amount of brown precipitate to prepare a silver salt solution, and then the semi-transparent, 제2공정2nd process 벤조페논 100g, 이소프로필알콜 30g, 톨루엔 10g, 페녹시에틸아크릴레이트 200g, 실리콘 아크릴레이트5g과, 상기 제1공정에서 제조한 은염용액10g을 교반기에 넣어 50℃로 30분간 가열하면서, 1,500~2,500RPM 의 속도로 교반시켜 제조함을 특징으로 하는 유브이(UV)코팅조성물의 제조방법. 100 g of benzophenone, 30 g of isopropyl alcohol, 10 g of toluene, 200 g of phenoxyethyl acrylate, 5 g of silicon acrylate, and 10 g of the silver salt solution prepared in the first step were put into a stirrer and heated at 50 ° C. for 30 minutes, 1,500 to 2,500 Method for producing a UV (UV) coating composition characterized in that it is prepared by stirring at a rate of RPM. 유브이(UV)코팅조성물에 있어서,In UV coating composition, 벤조페논, 1-하이드록시사이크로헥실아세토페논, 알파,알파-디메틸-알파하이드록시아세토페논, 아크릴레이티드벤조페논, 벤질케탈로 이루어진 군에서 선택된 하나 이상의 화합물인 광개시제 100g과, 100 g of photoinitiator, which is at least one compound selected from the group consisting of benzophenone, 1-hydroxycyclohexylacetophenone, alpha, alpha-dimethyl-alphahydroxyacetophenone, acrylated benzophenone, and benzyl ketal; 페녹시에틸아크릴레이트, N-비닐-2-피닐리돈, 2-하이드록시프로필아크릴레이트에서 선택된 어느 하나의 화합물인 아크릴수지 200g과 , 200 g of acrylic resin which is any compound selected from phenoxyethyl acrylate, N-vinyl-2-pinyridone and 2-hydroxypropyl acrylate; 실리콘 아크릴레이트5g, 이소프로필알콜 30g, 톨루엔 10g, 은염용액10g 으로 조성되어 있음을 특징으로 하는 유브이(UV)코팅조성물.A UV coating composition comprising 5 g of silicone acrylate, 30 g of isopropyl alcohol, 10 g of toluene, and 10 g of silver salt solution.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101453821B1 (en) * 2013-08-06 2014-10-23 주식회사 대하맨텍 Manufacturing method of ultraviolet curable coating composition comprising tungsten doped vanadium dioxide with phase transfer characteristics
CN104312421A (en) * 2014-10-28 2015-01-28 成都纳硕科技有限公司 Ultraviolet-cured and anti-bacterial coating for metal building material
KR101691973B1 (en) 2016-03-02 2017-01-03 동광산업주식회사 Preparing method of two-component type polyuretane coating agent and two-component type polyuretane coating agent prepared thereby

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101453821B1 (en) * 2013-08-06 2014-10-23 주식회사 대하맨텍 Manufacturing method of ultraviolet curable coating composition comprising tungsten doped vanadium dioxide with phase transfer characteristics
CN104312421A (en) * 2014-10-28 2015-01-28 成都纳硕科技有限公司 Ultraviolet-cured and anti-bacterial coating for metal building material
KR101691973B1 (en) 2016-03-02 2017-01-03 동광산업주식회사 Preparing method of two-component type polyuretane coating agent and two-component type polyuretane coating agent prepared thereby

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