KR101744343B1 - Metal-complex polymer film for air cleaning filter and method for manufacturing same - Google Patents
Metal-complex polymer film for air cleaning filter and method for manufacturing same Download PDFInfo
- Publication number
- KR101744343B1 KR101744343B1 KR1020150067789A KR20150067789A KR101744343B1 KR 101744343 B1 KR101744343 B1 KR 101744343B1 KR 1020150067789 A KR1020150067789 A KR 1020150067789A KR 20150067789 A KR20150067789 A KR 20150067789A KR 101744343 B1 KR101744343 B1 KR 101744343B1
- Authority
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- South Korea
- Prior art keywords
- filter
- metal complex
- polymer membrane
- metal
- complex type
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- 150000004696 coordination complex Chemical class 0.000 title claims abstract description 38
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- 229910052751 metal Inorganic materials 0.000 claims abstract description 17
- 239000002184 metal Substances 0.000 claims abstract description 17
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- 238000001179 sorption measurement Methods 0.000 claims description 24
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- 229920001155 polypropylene Polymers 0.000 claims description 12
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- 238000010559 graft polymerization reaction Methods 0.000 claims description 10
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- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000012528 membrane Substances 0.000 description 6
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 5
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- 229910021607 Silver chloride Inorganic materials 0.000 description 2
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- 230000007423 decrease Effects 0.000 description 2
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- 150000003839 salts Chemical class 0.000 description 2
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 2
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- 238000003756 stirring Methods 0.000 description 2
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- ZXSQEZNORDWBGZ-UHFFFAOYSA-N 1,3-dihydropyrrolo[2,3-b]pyridin-2-one Chemical compound C1=CN=C2NC(=O)CC2=C1 ZXSQEZNORDWBGZ-UHFFFAOYSA-N 0.000 description 1
- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
- KZEVSDGEBAJOTK-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[5-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CC=1OC(=NN=1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O KZEVSDGEBAJOTK-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- JQMFQLVAJGZSQS-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JQMFQLVAJGZSQS-UHFFFAOYSA-N 0.000 description 1
- YJLUBHOZZTYQIP-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=N2 YJLUBHOZZTYQIP-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- ALYNCZNDIQEVRV-PZFLKRBQSA-N 4-amino-3,5-ditritiobenzoic acid Chemical compound [3H]c1cc(cc([3H])c1N)C(O)=O ALYNCZNDIQEVRV-PZFLKRBQSA-N 0.000 description 1
- CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 1
- DFGKGUXTPFWHIX-UHFFFAOYSA-N 6-[2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]acetyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)C1=CC2=C(NC(O2)=O)C=C1 DFGKGUXTPFWHIX-UHFFFAOYSA-N 0.000 description 1
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
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- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
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- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
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- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- LBPGAOJVQOCVLO-UHFFFAOYSA-N benzene ethylbenzene toluene Chemical compound C1=CC=CC=C1.CC1=CC=CC=C1.CCC1=CC=CC=C1 LBPGAOJVQOCVLO-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
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- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003183 carcinogenic agent Substances 0.000 description 1
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- 229940116318 copper carbonate Drugs 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- ZKXWKVVCCTZOLD-UHFFFAOYSA-N copper;4-hydroxypent-3-en-2-one Chemical compound [Cu].CC(O)=CC(C)=O.CC(O)=CC(C)=O ZKXWKVVCCTZOLD-UHFFFAOYSA-N 0.000 description 1
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
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- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- SFMJNHNUOVADRW-UHFFFAOYSA-N n-[5-[9-[4-(methanesulfonamido)phenyl]-2-oxobenzo[h][1,6]naphthyridin-1-yl]-2-methylphenyl]prop-2-enamide Chemical compound C1=C(NC(=O)C=C)C(C)=CC=C1N1C(=O)C=CC2=C1C1=CC(C=3C=CC(NS(C)(=O)=O)=CC=3)=CC=C1N=C2 SFMJNHNUOVADRW-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 230000002572 peristaltic effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000001120 potassium sulphate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011403 purification operation Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 229940071536 silver acetate Drugs 0.000 description 1
- LKZMBDSASOBTPN-UHFFFAOYSA-L silver carbonate Substances [Ag].[O-]C([O-])=O LKZMBDSASOBTPN-UHFFFAOYSA-L 0.000 description 1
- 229910001958 silver carbonate Inorganic materials 0.000 description 1
- YPNVIBVEFVRZPJ-UHFFFAOYSA-L silver sulfate Chemical compound [Ag+].[Ag+].[O-]S([O-])(=O)=O YPNVIBVEFVRZPJ-UHFFFAOYSA-L 0.000 description 1
- 229910000367 silver sulfate Inorganic materials 0.000 description 1
- CHACQUSVOVNARW-LNKPDPKZSA-M silver;(z)-4-oxopent-2-en-2-olate Chemical compound [Ag+].C\C([O-])=C\C(C)=O CHACQUSVOVNARW-LNKPDPKZSA-M 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/14—Other self-supporting filtering material ; Other filtering material
- B01D39/16—Other self-supporting filtering material ; Other filtering material of organic material, e.g. synthetic fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
- B01D53/228—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion characterised by specific membranes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0009—Organic membrane manufacture by phase separation, sol-gel transition, evaporation or solvent quenching
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dispersion Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
본 발명은 공기정화 필터용 금속착물형 고분자막 및 이의 제조방법에 관한 것으로서, 보다 상세하게는 고분자 필터와 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기를 갖는 디아조늄염을 그래프트 중합하여, 필터 표면에 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기가 포함된 고분자 필터를 제조하는 단계; 및 상기 표면에 기능기가 포함된 고분자 필터에 금속을 착물형태로 담지하여 금속착물형 고분자막을 제조하는 단계를 포함함으로써, 단순한 공정으로 휘발성 유기 화합물의 제거효율이 우수하고, 악취에 대한 탈취효과 및 향균성에 대한 효과가 우수한 공기정화 필터용 금속착물형 고분자막 및 이의 제조방법에 관한 것이다. The present invention relates to a metal complex type polymer membrane for an air purification filter and a method of manufacturing the same. More particularly, the present invention relates to a polymer membrane and a diazonium salt having at least one functional group selected from the group consisting of carboxylic acid, sulfonic acid group and phosphoric acid group, Preparing a polymer filter including at least one functional group selected from the group consisting of carboxyl groups, sulfonic groups and phosphoric groups on the surface of the filter; And a step of preparing a metal complex type polymer membrane by supporting a metal in a complex form on a surface of the polymer filter including a functional group on the surface thereof. Thus, the removal efficiency of the volatile organic compound is excellent by a simple process, The present invention relates to a metal complex type polymer membrane for an air purification filter having excellent effects on the property and a method for manufacturing the same.
Description
본 발명은 항균, 흡착성이 우수한 공기정화 필터용 금속착물형 고분자막 및 이의 제조방법에 관한 것이다.
The present invention relates to a metal complex type polymer membrane for an air purification filter having excellent antibacterial and adsorptive properties and a method for producing the same.
일반적으로 반도체 제조 공정이나 건축물 등에는 공기 청정기와 같은 정화 장치가 구비되어 있다. 최근 들어 정화 장치에는 유체가 소정의 속도로 유동되는 상황에서 유체 내에 함유된 여러가지 유해 물질, 예를 들면 산성가스, 알카리성 가스 또는 휘발성 유기화합물 (Volatile Organic Compounds, VOCs)과 같은 유해 가스 성분을 화학적으로 제거하기 위하여 화학 흡착 필터들이 많이 사용되고 있다. BACKGROUND ART [0002] In general, a semiconductor manufacturing process, a building, and the like are equipped with a purifier such as an air purifier. In recent years, in a purification apparatus, a harmful gas component such as an acidic gas, an alkaline gas, or a volatile organic compound (VOCs) is chemically Chemisorption filters are widely used to remove these gases.
이러한 화학 흡착 필터는 성능 및 품질을 결정하는데 중요한 요인인 다음과 같은 조건을 고려하여 제조하게 된다. Such a chemisorption filter is manufactured considering the following conditions, which are important factors for determining performance and quality.
1) 유해 물질의 제거 효율 및 제거 흡착능 확보 여부; 2) 진동 또는 풍속 등과 같은 물리적 충격에 의해 발생되는 필터의 마모 및 분진 입자의 발생 여부; 3) 여과 작용시 화학 흡착 필터를 통과하는 유체의 압력 손실을 최소화할 수 있는지 여부; 4) 여과를 위해 사용된 흡착제에 의한 2차 오염 발생 여부. 대표적인 화학 흡착 필터로는 주로 공기 중에 포함되어 있는 산성 및 알카리성 물질을 제거할 목적으로 활성탄계 첨착 흡착 필터가 많이 사용되고 있다. 첨착 흡착 필터는 표면적과 세공 부피가 큰 입상체나 조립 활성탄에 제거하고자 하는 유해 물질과 반응하는 물질, 예를 들어 인산이나 수산화카륨 또는 과망간산 칼륨 등의 산성 또는 알카리성 물질을 첨착하여 제조하게 된다. 1) Whether to remove harmful substances and to secure removability; 2) Whether the filters are worn or dust particles are generated by physical impact such as vibration or wind speed; 3) whether the pressure loss of the fluid passing through the chemisorption filter during filtration can be minimized; 4) Secondary contamination by adsorbent used for filtration. As a typical chemisorption filter, active carbon impregnated adsorption filters are mainly used for the purpose of removing acidic and alkaline substances contained in the air. The impregnated adsorption filter is manufactured by attaching an acidic or alkaline substance such as phosphoric acid, potassium hydroxide, or potassium permanganate to a particulate material having a large surface area and a large pore volume or reacting with harmful substances to be removed.
하지만 이러한 화학 흡착 필터는 유해 물질을 제거하기 위해 첨착된 물질들이 정화 작용중 산·알카리 중화 반응으로 염을 생성하게 되고 정화 시간이 길어질수록 염의 발생량이 많아져서 화학 흡착 필터의 세공을 막아 버리기 때문에, 유체가 정화를 위해 필터를 통과하는 유체의 압력손실, 즉 유동 압력의 저하를 초래하게 되어 정화 시간이 길어질수록 필터로서의 기능이 떨어지게 되는 문제가 발생하게 되었다. 또한, 첨착된 산성 및 알카리성 물질들은 높은 휘발성을 가지고 있기 때문에 이들 첨착 물질들의 휘발에 의해 2차 오염이 이루어질 가능성이 있어 상당히 높은 청정도를 요구하는 반도체 제조 장비의 클린룸(clean room) 등에는 사용할 수 없는 문제가 발생하게 되었다. However, in such a chemisorption filter, since the impregnated materials generate salts by acid-alkali neutralization reaction during the purification operation, and the longer the purification time becomes, the more salt is generated and the pores of the chemisorption filter are blocked, There has been a problem that the function of the filter becomes deteriorated as the cleaning time becomes longer as the fluid causes pressure loss of the fluid passing through the filter for purification, that is, lowering of the flow pressure. In addition, since the impregnated acidic and alkaline materials have high volatility, secondary contamination may occur due to the volatilization of these impregnated materials, which can be used in a clean room of semiconductor manufacturing equipment requiring a high degree of cleanliness There was no problem.
활성탄을 이용하는 것으로 오존 분해용 화학 흡착 필터가 대한민국등록특허 제10-0358262호에 공개되어 있다. A chemisorption filter for ozone decomposition using activated carbon is disclosed in Korean Patent No. 10-0358262.
상기 오존 분해용 화학 흡착 필터는 활성탄 입자를 폴리에틸렌 또는 알루미늄 망체에 부착하여 저렴하고 효율이 좋은 에어 필터를 제시하고 있다. 그러나, 상기 오존 분해용 화학 흡착 필터 또한 여전히 충격 및 마모에 의한 분진 발생이나 첨착 물질에 의한 2차 오염에 대한 위험성이 있어 청결을 요하는 반도체 장비의 클린룸용으로 적용하는데 어려움이 따르는 문제점이 있다. 이러한 활성탄계를 이용한 종래의 화학 흡착 필터가 갖는 단점인 분진 발생 및 첨착 물질의 휘발에 의한 2차 오염의 위험성을 보완하고자 최근에는 분진 발생 및 흡착 물질의 위험이 적은 새로운 화학 흡착용 필터의 연구가 진행되고 있는 실정이다. The chemical adsorption filter for ozone decomposition has proposed an air filter which is inexpensive and efficient by attaching activated carbon particles to a polyethylene or aluminum net. However, the chemical adsorption filter for ozone decomposition still has a problem of dust generation due to impact and abrasion or secondary contamination due to impregnated material, which makes it difficult to apply it to a clean room of semiconductor equipment requiring cleanliness. In order to compensate for the risk of secondary pollution due to dust generation and volatilization of impregnated material, which is a disadvantage of conventional chemical adsorption filters using activated carbon, recently, a new chemisorption filter having a low risk of dust generation and adsorbed matter It is in progress.
이에, 본 출원인은 한국등록특허 제1,402,604호에 금속착물형 탄소기공막 공기정화용 필터를 제시하였다. 구체적으로 상기 공기정화용 필터는 다공성 탄소 분리막의 표면을 개질하고, 상기 개질된 탄소 분리막에 금속을 착물형태로 담지하여 제조하였다.Accordingly, the present applicant has proposed a filter for air purification of a metal complex type carbon-based membrane in Korean Patent No. 1,402,604. Specifically, the air purification filter was produced by modifying the surface of the porous carbon separation membrane and supporting the reformed carbon separation membrane in the form of a complex in the form of a metal.
상기 금속착물형 탄소기공막 공기정화용 필터는 휘발성 유기 화합물의 제거효율, 악취에 대한 탈취효과 및 항균성은 우수하나, 다공성 탄소 분리막의 제조공정이 매우 복잡하여 제조 시간이 길다는 단점이 있다.
The metal complex type carbon-dioxide air cleaning filter is excellent in the removal efficiency of volatile organic compounds, deodorizing effect against odor, and antibacterial property, but the manufacturing process of the porous carbon separation membrane is complicated and the manufacturing time is long.
이에 본 출원인은 종래와 동등 이상의 휘발성 유기 화합물의 제거효율, 악취에 대한 탈취효과 및 항균성을 유지하면서, 제조공정을 단순화하여 시간 및 비용을 감소시킬 수 있는 공기정화 필터용 금속착물형 고분자막의 제조방법 및 이로부터 얻어진 공기정화 필터용 금속착물형 고분자막을 제공하는 데 그 목적이 있다.
The applicant of the present invention has proposed a method for producing a metal complex type polymer membrane for an air purification filter which can reduce the time and cost by simplifying the manufacturing process while maintaining the removal efficiency of volatile organic compounds equal to or more than the conventional ones, And a metal complex type polymer membrane for an air purification filter obtained therefrom.
상기 목적을 달성하기 위하여, 본 발명은 고분자 필터와 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기를 갖는 디아조늄염을 그래프트 중합하여, 필터 표면에 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기가 포함된 고분자 필터를 제조하는 단계; 및 상기 표면에 기능기가 포함된 고분자 필터에 금속을 착물형태로 담지하여 금속착물형 고분자막을 제조하는 단계를 포함하는 것을 특징으로 하는 공기정화 필터용 금속착물형 고분자막의 제조방법을 제공한다.In order to achieve the above object, the present invention provides a method for producing a polymer electrolyte membrane, comprising graft polymerizing a polymer filter and a diazonium salt having at least one functional group selected from the group consisting of carboxyl, sulfonic acid and phosphoric acid groups, Preparing a polymer filter including at least one functional group selected from the group consisting of a phosphate group and a phosphoric acid group; And forming a metal complex type polymer membrane by supporting a metal in a complex form on a polymer filter including a functional group on the surface thereof.
상기 그래프트 중합은 디아조늄염 1몰에 대하여 황산칼륨 0.01 내지 0.1몰을 사용하여 수행할 수 있다. The graft polymerization may be carried out using 0.01 to 0.1 mole of potassium sulfate per mole of the diazonium salt.
상기 그래프트 중합은 50 내지 80℃에서 1분 내지 24시간 동안 수행할 수 있다. The graft polymerization may be carried out at 50 to 80 DEG C for 1 minute to 24 hours.
상기 금속은 은, 구리, 금, 아연 및 백금을 이루어진 군에서 선택된 1종 이상일 수 있다. The metal may be at least one selected from the group consisting of silver, copper, gold, zinc and platinum.
상기 금속의 크기는 1 내지 100㎚일 수 있다. The size of the metal may be 1 to 100 nm.
상기 고분자 필터는 폴리에틸렌, 폴리프로필렌, 폴리우레탄, 폴리에틸렌테레프탈레이트, 스티렌-부타디엔 고무 및 니트릴-부타디엔 고무로 이루어진 군에서 선택된 1종 이상의 소재일 수 있다. The polymer filter may be at least one material selected from the group consisting of polyethylene, polypropylene, polyurethane, polyethylene terephthalate, styrene-butadiene rubber and nitrile-butadiene rubber.
상기 고분자 필터는 다공율이 1 내지 50%일 수 있다. The polymer filter may have a porosity of 1 to 50%.
상기 고분자 필터는 부직포상일 수 있다. The polymer filter may be a nonwoven fabric.
상기 고분자 필터는 두께가 1 내지 5mm인 것일 수 있다.The polymer filter may have a thickness of 1 to 5 mm.
또한, 본 발명은 상기 제조방법으로 얻어진 금속착물형 고분자막으로, 비표면적이 25 내지 250m2/g이고, 항균효율이 90 내지 99%이고, 휘발성 유기화합물의 흡착효율이 90 내지 99%이며, 휘발성 유기화합물의 탈취효율이 95 내지 99%인 것을 특징으로 하는 공기정화 필터용 금속착물형 고분자막을 제공한다.
Further, the present invention is a metal complex type polymer membrane obtained by the above production method, which has a specific surface area of 25 to 250 m 2 / g, an antibacterial efficiency of 90 to 99%, an adsorption efficiency of a volatile organic compound of 90 to 99% And a deodorization efficiency of the organic compound is 95 to 99%. The present invention also provides a metal complex type polymer membrane for an air purifying filter.
본 발명에 따른 공기정화 필터용 금속착물형 고분자막은 종래의 다공성 탄소 분리막에 비해 제조공정이 단순하여 시간 및 비용을 감소시켜 경제성이 우수한 이점이 있다. The metal complex type polymer membrane for an air purifying filter according to the present invention is advantageous in that the manufacturing process is simpler than that of the conventional porous carbon separation membrane and thus the time and cost are reduced and the economical efficiency is excellent.
또한, 본 발명에 따른 공기정화 필터용 금속착물형 고분자막은 종래의 필터보다 휘발성 유기 화합물의 제거효율이 우수하고, 악취에 대한 탈취효과 및 향균성에 대한 효과가 우수한 이점이 있다.In addition, the metal complex type polymer membrane for an air purifying filter according to the present invention has an excellent removal efficiency of volatile organic compounds and a deodorizing effect against odor and an effect on antibacterial property compared to the conventional filter.
또한, 본 발명에 따른 공기정화 필터용 금속착물형 고분자막은 흡착 제거 방식이므로 2차 부산물이 생성되지 않아 환경 친화적인 이점이 있다.
In addition, since the metal complex type polymer membrane for air purifying filter according to the present invention is an adsorption elimination method, secondary byproducts are not produced, thereby being environmentally friendly.
도 1은 본 발명에 따라 실시예 1에서 제조된 기능기가 포함된 고분자 필터(a)와, 이를 이용하여 제조된 공기정화 필터용 금속착물형 고분자막의 SEM 사진(b)이고,
도 2는 본 발명에 따라 실시예 2-1에서 제조된 기능기가 포함된 고분자 필터(a)와, 이를 이용하여 제조된 공기정화 필터용 금속착물형 고분자막의 SEM 사진(b)이고,
도 3은 휘발성 유기화합물의 흡착성능을 측정하기 위한 흡착 시스템의 구성도이다.1 is an SEM photograph (b) of a polymeric filter (a) including the functional group prepared in Example 1 and a metal complex type polymer membrane for an air purifying filter manufactured using the polymeric filter (a) according to the present invention,
2 is an SEM photograph (b) of a polymeric filter (a) including the functional group prepared in Example 2-1 according to the present invention and a metal complex type polymer membrane for an air purifying filter manufactured using the polymeric filter (a)
3 is a configuration diagram of an adsorption system for measuring the adsorption performance of a volatile organic compound.
본 발명은 휘발성 유기 화합물의 제거효율, 악취에 대한 탈취효과 및 향균성에 대한 효과가 우수한 공기정화 필터용 금속착물형 고분자막과, 이의 제조방법에 관한 것이다. 본 발명에서 상기 휘발성 유기 화합물이란, 증기압이 높아 대기 중으로 쉽게 증발되는 액상 또는 기체상 유기화합물을 의미하는 것으로, 대기오염 뿐만 아니라 발암성 물질로서, 지구온난화의 원인물질로 지적되고 있다. 일예를 들면, 벤젠, 툴루엔, 에틸벤젠, 자일렌, 또는 아세틸렌 등을 의미한다.
TECHNICAL FIELD The present invention relates to a metal complex type polymer membrane for an air purification filter, which is excellent in the removal efficiency of a volatile organic compound, a deodorizing effect on odors, and an antibacterial effect, and a method for producing the same. In the present invention, the volatile organic compound means a liquid or gaseous organic compound that has a high vapor pressure and is easily evaporated into the atmosphere. It is not only air pollution but also a carcinogenic substance, which is pointed out as a cause of global warming. For example, benzene, toluene, ethylbenzene, xylene, acetylene, and the like.
본 발명에 따른 공기정화 필터용 금속착물형 고분자막의 제조방법은 고분자 필터와 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기를 갖는 디아조늄염을 그래프트 중합하여, 필터 표면에 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기가 포함된 고분자 필터를 제조하는 단계; 및 상기 표면에 기능기가 포함된 고분자 필터에 금속을 착물형태로 담지하여 금속착물형 고분자막을 제조하는 단계를 포함한다.
The method for producing a metal complex type polymer membrane for an air purification filter according to the present invention comprises graft polymerizing a polymer filter and a diazonium salt having at least one functional group selected from the group consisting of carboxyl, sulfonic acid and phosphoric acid groups, Preparing a polymer filter including at least one functional group selected from the group consisting of a sulfonic acid group and a phosphoric acid group; And a step of preparing a metal complex type polymer membrane by supporting a metal in a complex form on a polymer filter including a functional group on the surface.
이하, 본 발명에 따른 공기정화 필터용 금속착물형 고분자막의 제조방법을 각 단계별로 구체적으로 설명하면 다음과 같다.Hereinafter, a method for producing a metal complex type polymer membrane for an air filter according to the present invention will be described in detail.
먼저, 필터 표면에 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기가 포함된 고분자 필터를 제조하는 단계이다.First, a polymer filter including at least one functional group selected from the group consisting of carboxyl groups, sulfonic groups, and phosphoric groups is prepared on the filter surface.
상기 기능기가 포함된 고분자 필터는 고분자 필터와 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기를 갖는 디아조늄염을 그래프트 중합한다. 상기 그래프트 중합에 의해 고분자 필터의 표면이 개질되어 후술하는 공정에서 금속과 고분자 필터를 결합하게 된다.The polymer filter including the functional group graft-polymerizes a polymer filter and a diazonium salt having at least one functional group selected from the group consisting of carboxyl, sulfonic acid and phosphoric acid groups. The surface of the polymer filter is modified by the graft polymerization to bind the metal and the polymer filter in the process described below.
고분자 필터는 당 분야에서 일반적으로 사용되는 것으로 고분자를 소재로 하여 필터가 가능한 것이면 특별히 한정하지는 않는다. 구체적으로 상기 고분자 소재는 폴리에틸렌, 폴리프로필렌, 폴리우레탄, 폴리에틸렌테레프탈레이트, 스티렌-부타디엔 고무 및 니트릴-부타디엔 고무로 이루어진 군에서 선택된 1종 이상일 수 있다. 가격경쟁력, 취급 용이성 및 표면상태와 재질 등을 고려하면 폴리에틸렌, 폴리프로필렌이 바람직하다.The polymer filter is generally used in the art and is not particularly limited as long as it is made of a polymer and filterable. Specifically, the polymer material may be at least one selected from the group consisting of polyethylene, polypropylene, polyurethane, polyethylene terephthalate, styrene-butadiene rubber, and nitrile-butadiene rubber. Considering cost competitiveness, ease of handling, and surface condition and materials, polyethylene and polypropylene are preferred.
또한, 상기 고분자 필터는 다공율이 1 내지 50%인 것이 바람직하며, 다공율이 1%미만이면 공기투과율이 떨어지고 50%를 초과하는 경우에는 그래프트율이 떨어지는 단점이 있다. In addition, the polymer filter preferably has a porosity of 1 to 50%. When the porosity is less than 1%, the air permeability decreases. When the porosity exceeds 50%, the graft ratio decreases.
또한, 상기 고분자 필터는 두께가 1 내지 5mm인 것이 바람직하며, 두께가 1mm미만이면 균일한 그래프팅이 어려울 수 있고 5mm을 초과하는 경우에는 작업성이 떨어질 수 있다.The thickness of the polymer filter is preferably 1 to 5 mm. If the thickness is less than 1 mm, uniform grafting may be difficult. If the thickness is more than 5 mm, the workability may be deteriorated.
상기와 같이, 다공율, 두께, 재질, 용도 및 비용 등을 고려하면 상기 고분자 필터는 부직포상인 것이 바람직하다.As described above, it is preferable that the polymer filter is a nonwoven fabric in consideration of porosity, thickness, material, use and cost.
카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기를 갖는 디아조늄염은 당 분야에서 일반적으로 사용되는 방법으로 제조되거나, 시판되는 제품을 이용할 수 있다. 일례로, 카르복실시, 술폰산기 및 인산기로 이루어진 군에서 선택된 1종 이상의 기능기를 갖는 방향족 1차 아민을 아질산으로 디아조화하여 얻을 수 있으나, 이에 한정되지는 않는다.The diazonium salt having at least one functional group selected from the group consisting of a carboxyl group, a sulfonic acid group and a phosphoric acid group may be prepared by a method generally used in the field or a commercially available product may be used. For example, the aromatic primary amine having at least one functional group selected from the group consisting of carboxyl, sulfonic acid group and phosphoric acid group can be obtained by diazotization with nitrous acid, but is not limited thereto.
본 발명의 그래프트 중합을 보다 효율적으로 수행하기 위하여, 황산칼륨, 철, 질산나트륨 등의 촉매를 추가하여 사용할 수 있으며, 최종생산물의 순도을 고려하면 황산칼륨이 바람직하다.In order to more efficiently perform the graft polymerization of the present invention, a catalyst such as potassium sulfate, iron, or sodium nitrate may be added, and potassium sulphate is preferable considering the purity of the final product.
상기 황산칼륨은 디아조늄염 1몰에 대하여 0.01 내지 0.1몰을 사용하며, 0.01몰 미만이면 목적으로 하는 효과 달성이 어려울 수 있고 0.1몰을 초과하면 증점되는 문제가 있다.The potassium sulfate may be used in an amount of 0.01 to 0.1 mol based on 1 mol of the diazonium salt. If it is less than 0.01 mol, it may be difficult to achieve the desired effect.
그래프트 중합은 50 내지 80℃에서 1분 내지 24시간 동안 수행하는 것이 바람직하다. 상기 중합온도가 50℃ 미만이면 반응이 불충분하게 일어날 수 있고 80℃를 초과하는 경우에는 섬유자체가 변형될 수 있는 문제가 있다. 또한 중합시간이 1분 미만이면 그래프트 중합이 미반응될 수 있고 24시간을 초과하는 경우에는 호모 폴리머 중합체가 다량 생성될 수 있는 문제가 있다.
The graft polymerization is preferably carried out at 50 to 80 DEG C for 1 minute to 24 hours. If the polymerization temperature is less than 50 캜, the reaction may occur insufficiently. If the polymerization temperature exceeds 80 캜, the fiber itself may be deformed. If the polymerization time is less than 1 minute, the graft polymerization may be unreacted, and if the polymerization time exceeds 24 hours, homopolymer polymer may be produced in a large amount.
다음으로, 상기 표면에 기능기가 포함된 고분자 필터에 금속을 착물형태로 담지하여 금속착물형 고분자막을 제조하는 단계를 수행한다.Next, a metal complex type polymer membrane is prepared by supporting a metal in complex form on a polymer filter including a functional group on the surface.
금속은 항균성을 나타낼 수 있는 것이면 특별히 한정하지 않으며, 예를 들면 은, 구리, 금, 아연 및 백금을 이루어진 군에서 선택된 1종 이상을 사용할 수 있다. 항균 효율성을 고려하면 은, 구리가 바람직하다.The metal is not particularly limited as long as it can exhibit antimicrobial activity. For example, at least one selected from the group consisting of silver, copper, gold, zinc and platinum can be used. Copper is preferable in view of antibacterial efficiency.
이때, 금속은 전구체를 사용하며, 일례로 은 전구체는 질산은, 황산은, 은아세틸아세토네이트, 은아세테이트, 은카보네이트 및 은클로라이드로 이루어진 군에서 선택된 1종 이상이 사용될 수 있으며, 구리 전구체는 질산구리, 황산구리, 구리아세틸아세토네이트, 구리아세테이트, 구리카보네이트 및 은클로라이드로 이루어진 군에서 선택된 1종 이상이 사용될 수 있다.At this time, the metal is a precursor. For example, the silver precursor may be at least one selected from the group consisting of silver nitrate, silver sulfate, silver acetylacetonate, silver acetate, silver carbonate and silver chloride. , Copper sulfate, copper acetylacetonate, copper acetate, copper carbonate and silver chloride may be used.
상기 금속의 크기는 1-100nm인 것이 바람직하며, 상기의 범위로 금속을 포함하는 것이 착물형태로 고분자 필터의 표면에 결합되기 용이하며, 항균성의 효과를 증대시켜 주기 때문에 바람직하다.
The size of the metal is preferably in the range of 1 to 100 nm, and it is preferable that the metal includes the metal in the above range because it is easy to bind to the surface of the polymer filter in a complex form and increases the antibacterial effect.
이상과 같은 방법으로 제조된 공기정화 필터용 금속착물형 고분자막은 비표면적이 25 내지 250m2/g이고, 항균효율이 90 내지 99%고, 휘발성 유기화합물의 흡착효율이 90 내지 99%이며, 휘발성 유기화합물의 탈취효율이 95 내지 99%일 수 있다.
The metal complex type polymer membrane for an air purifying filter manufactured by the method described above has a specific surface area of 25 to 250 m 2 / g, an antibacterial efficiency of 90 to 99%, an adsorption efficiency of a volatile organic compound of 90 to 99% The deodorization efficiency of the organic compound may be 95 to 99%.
전술한 본 발명의 설명은 예시를 위한 것이며, 본 발명이 속하는 기술분야의 통상의 지식을 가진 자는 본 발명의 기술적 사상이나 필수적인 특징을 변경하지 않고서 다른 구체적인 형태로 쉽게 변형이 가능하다는 것을 이해할 수 있을 것이다. 그러므로 이상에서 기술한 실시예들은 모든 면에서 예시적인 것이며 한정적이 아닌 것으로 이해해야만 한다. 예를 들어, 단일형으로 설명되어 있는 각 구성 요소는 분산되어 실시될 수도 있으며, 마찬가지로 분산된 것으로 설명되어 있는 구성 요소들도 결합된 형태로 실시될 수 있다.It will be understood by those skilled in the art that the foregoing description of the present invention is for illustrative purposes only and that those of ordinary skill in the art can readily understand that various changes and modifications may be made without departing from the spirit or essential characteristics of the present invention. will be. It is therefore to be understood that the above-described embodiments are illustrative in all aspects and not restrictive. For example, each component described as a single entity may be distributed and implemented, and components described as being distributed may also be implemented in a combined form.
본 발명의 범위는 상기 상세한 설명보다는 후술하는 특허청구범위에 의하여 나타내어지며, 특허청구범위의 의미 및 범위 그리고 그 균등 개념으로부터 도출되는 모든 변경 또는 변형된 형태가 본 발명의 범위에 포함되는 것으로 해석되어야 한다.
The scope of the present invention is defined by the appended claims rather than the detailed description and all changes or modifications derived from the meaning and scope of the claims and their equivalents are to be construed as being included within the scope of the present invention do.
실시예Example 1 One
1)One) 카르복시기를Carboxy group 갖는 디아조늄염 제조 Diazonium salt preparation
얼음조(Ice bath)하에서, 2L 반응용기에 0.2M HCl 1L를 넣고 300rpm으로 교반하였다. 여기에 4-Aminobenzoic acid 27.428g을 가한 후, 20mL/min 연동펌프(peristaltic pump)를 이용하여 0.02M NaNO2 250mL를 소량씩 천천히 가하였다. 이후에 300rpm으로 2시간동안 교반하여 카르복시기를 갖는 디아조늄염을 제조하였다.Under an ice bath, 1 L of 0.2 M HCl was added to a 2 L reaction vessel and stirred at 300 rpm. After adding 27.428 g of 4-aminobenzoic acid, 250 mL of 0.02 M NaNO 2 was added slowly by using a 20 mL / min peristaltic pump. Thereafter, the mixture was stirred at 300 rpm for 2 hours to prepare a diazonium salt having a carboxyl group.
2)2) 기능기가Function giga 포함된 고분자 필터 제조 Manufacture of Polymer Filters
5cm×5cm×0.3cm 크기이고 다공율이 20%인 폴리에틸렌 부직포(대산물산, 폴리에틸렌)를 MeOH로 10분 동안 세척한 후, 진공오븐을 사용하여 70℃에서 3시간 동안 건조하였다. 상기 건조된 폴리에틸렌 부직포의 무게를 5회 반복 측정하였다.A polyethylene nonwoven fabric (Taesan, polyethylene) having a size of 5 cm x 5 cm x 0.3 cm and a porosity of 20% was washed with MeOH for 10 minutes and then dried at 70 ° C for 3 hours using a vacuum oven. The weight of the dried polyethylene nonwoven fabric was measured five times repeatedly.
별도로 핫플레이트(Hot plate) 상에 70℃의 항온수조(water bath)를 준비하고, 상기 항온수조(water bath)에 500mL 플라스크를 담근 후 상기에서 제조한 카르복시기를 갖는 디아조늄염 100mL를 가하였다.Separately, a constant temperature water bath at 70 ° C was prepared on a hot plate, and a 500 ml flask was immersed in the water bath. Then 100 ml of the diazonium salt having the carboxyl group prepared above was added.
여기에 상기 건조된 폴리에틸렌 부직포를 추가하여 충분히 적신 후 교반하였다. 이후에 카르복시기를 갖는 디아조늄염 1몰에 대하여 황산칼륨을 0.03몰을 가한 후 500rpm으로 1시간 동안 교반하였다.(그래프트 중합)The dried polyethylene nonwoven fabric was further added thereto, sufficiently wetted, and then stirred. Thereafter, 0.03 mol of potassium sulfate was added to 1 mol of the diazonium salt having a carboxyl group, followed by stirring at 500 rpm for 1 hour. (Graft Polymerization)
상기 교반한 후 부직포를 꺼내 증류수로 세척하고 진공오븐을 사용하여 70℃에서 3시간 동안 건조하였다. 상기 건조된 폴리에틸렌 부직포의 무게를 5회 반복 측정하였다.After the agitation, the nonwoven fabric was taken out, washed with distilled water, and dried in a vacuum oven at 70 ° C for 3 hours. The weight of the dried polyethylene nonwoven fabric was measured five times repeatedly.
3)공기정화 필터용 3) For air purifying filter 금속착물형Metal complex type 고분자막 제조 Polymer Film Manufacturing
넓적 바닥 플라스크(Flat bottom flask)에 0.2mM 질산은 용액 250mL을 가하고, 여기에 상기에서 제조된 기능기가 포함된 폴리에틸렌 부직포를 넣고 1시간 동안 교반하였다. 이후에 상기 기능기가 포함된 폴리에틸렌 부직포를 꺼내 증류수로 세척한 후 진공오븐을 사용하여 70℃에서 3시간 동안 건조하였다.250 mL of 0.2 mM silver nitrate solution was added to a flat bottom flask, and a polyethylene nonwoven fabric containing the above-prepared functional group was added thereto, followed by stirring for 1 hour. Thereafter, the polyethylene nonwoven fabric containing the functional group was taken out, washed with distilled water, and dried at 70 ° C for 3 hours using a vacuum oven.
실시예Example 2 2
상기 실시예 1과 동일하게 실시하되, 폴리에틸렌 부직포(대산물산, 폴리에틸렌 대신에 하기 표 1의 고분자 부직포를 사용하여 공기정화 필터용 금속착물형 고분자막을 제조하였다.A metal complex type polymer membrane for an air filter was prepared in the same manner as in Example 1, except that a polymer nonwoven fabric (a polymer nonwoven fabric of the following Table 1 was used in place of a nonwoven fabric of Daisan Co., polyethylene.
실시예Example 3 3
상기 실시예 1과 동일하게 실시하되, 0.2mM 질산은 용액 250mL 대신에 하기 표 2의 금속의 용액을 사용하여 공기정화 필터용 금속착물형 고분자막을 제조하였다. A metal complex type polymer membrane for an air purification filter was prepared in the same manner as in Example 1 except that a solution of the metal shown in Table 2 was used instead of 250 mL of 0.2 mM silver nitrate solution.
실시예Example 4 4
상기 실시예 1과 동일하게 실시하되, 카르복시기를 갖는 디아조늄염질대신에 하기 표 3의 디아조늄염을 사용하여 공기정화 필터용 금속착물형 고분자막을 제조하였다.Except that the diazonium salt of the following Table 3 was used instead of the diazonium salt having a carboxyl group to prepare a metal complex type polymer membrane for an air filter.
실시예Example 5 5
상기 실시예 1과 동일하게 실시하되, 하기 그래프트 중합조건을 표 4와 같이 수행하여 공기정화 필터용 금속착물형 고분자막을 제조하였다. The procedure of Example 1 was followed except that the following graft polymerization conditions were carried out as shown in Table 4 to prepare a metal complex type polymer membrane for an air filter.
실시예Example 6 6
상기 실시예 1과 동일하게 실시하되, 하기 표 5와 같이 폴리에틸렌 부직포의 두께 및 다공율을 달리하여 공기정화 필터용 금속착물형 고분자막을 제조하였다. A metal complex type polymer membrane for an air filter was prepared in the same manner as in Example 1 except that the thickness and the porosity of the polyethylene nonwoven fabric were changed as shown in Table 5 below.
비교예Comparative Example 1 One
넓적 바닥 플라스크(Flat bottom flask)에 0.2mM 질산은 용액 250mL을 가하고, 여기에 5cm×5cm×0.3cm 크기이고 다공율이 20%인 폴리에틸렌 부직포(대산물산, 폴리에틸렌)를 넣고 1시간 동안 교반하였다. 이후에 상기 폴리에틸렌 부직포를 꺼내 증류수로 세척한 후 진공오븐을 사용하여 70℃에서 3시간 동안 건조하였다.
250 mL of 0.2 mM silver nitrate solution was added to a flat bottom flask, and a polyethylene nonwoven fabric (Taesan product, polyethylene) having a size of 5 cm x 5 cm x 0.3 cm and a porosity of 20% was added thereto and stirred for 1 hour. Thereafter, the polyethylene nonwoven fabric was taken out, washed with distilled water, and then dried in a vacuum oven at 70 ° C for 3 hours.
비교예Comparative Example 2 2
한국등록특허 제1,402,604호의 실시예 1
Example 1 of Korean Patent No. 1,402,604
비교예Comparative Example 3 3
시판되는 공기정화용 필터(유한킴벌리)
Commercial air purification filter (Yuhan-Kimberly)
실험예Experimental Example 1 One
상기 실시예 및 비교예에서 제조된 금속착물형 고분자막의 BET를 측정하여, 비표면적을 표 6에 기재하였다.The BET of the metal complex type polymer membranes prepared in the above Examples and Comparative Examples was measured, and the specific surface area thereof is shown in Table 6.
상기 표 6과 같이, 본 발명의 실시예가 그래프트 중합을 수행하지 않은 비교예 1 및 시판되는 공기정화 필터에 비해 비표면적이 월등히 우수하다는 것을 확인할 수 있었다.
As shown in Table 6, it can be seen that the embodiment of the present invention is much superior to Comparative Example 1 in which graft polymerization is not performed and the commercially available air purifying filter.
실험예Experimental Example 2: 항균활성 2: Antimicrobial activity
상기 실시예 및 비교예에서 제조된 금속착물형 고분자막을 집진필터로 사용하여 항균활성 시험을 실시하였다. 실험과정은 공기 중의 미생물을 집진필터 표면에 채취한 후, 액체배지에 그 집진필터를 넣고 흔들어 꺼낸 다음 그 액체배지를 64시간 동안 배양하여, 액체 배지에 대한 셀카운트(cell count)를 측정하여 미생물의 증식여부를 확인하였다.Antimicrobial activity tests were conducted using the metal complex type polymer membranes prepared in the above Examples and Comparative Examples as dust collecting filters. In the experimental procedure, the microorganisms in the air were collected on the surface of the dust filter, the dust filter was put into the liquid medium, and the liquid medium was shaken out. Then, the liquid medium was cultured for 64 hours and the cell count for the liquid medium was measured. Was confirmed.
상기 표 7과 같이, 본 발명의 실시예가 비교예 1 및 3에 비해 항균활성이 우수하다는 것을 확인할 수 있었다. 다만, 비교예 2는 실시예와 동등한 항균활성을 가지나 필터의 제조공정이 매우 복잡하고 제조 시간이 길어 제조 효율성이 실시예에 비해 현저히 낮다는 단점이 있다.
As shown in Table 7, it can be confirmed that the examples of the present invention are superior in antibacterial activity to those of Comparative Examples 1 and 3. However, Comparative Example 2 has an antibacterial activity equivalent to that of the Example, but has a disadvantage in that the manufacturing process of the filter is very complicated and the manufacturing time is long, so that the manufacturing efficiency is significantly lower than in the Examples.
실험예Experimental Example 3: 휘발성 유기화합물의 흡착성능 측정 3: Measurement of adsorption performance of volatile organic compounds
톨루엔, 벤젠, 에틸벤젠 및 m-, p-, o-자일렌 농도가 각각 800ppb 수준인 시험 가스를 단면유속 0.8m/s 조건으로 상기 실시예 및 비교예에서 제조된 금속착물형 고분자막을 통과시킬 때 지속적으로 흡착되는 시간 및 최종 흡착량을 측정하였다. 상기 측정결과는 표 8에 나타내었다.The test gas having concentrations of toluene, benzene, ethylbenzene and m-, p- and o-xylene of 800 ppb was passed through the metal complex type polymer membrane prepared in the above Examples and Comparative Examples at a cross-sectional flow rate of 0.8 m / The time of continuous adsorption and the amount of final adsorption were measured. The measurement results are shown in Table 8.
이때, 상기 흡착성능은 하기 도 4와 같이 구성된 흡착 시스템을 이용하였다. At this time, the adsorption performance using the adsorption system as shown in FIG. 4 was used.
상기 표 8과 같이, 본 발명에 따른 실시예는 비교예에 비해 톨루엔, 벤젠, 에틸벤젠 및 m-, p-, o-자일렌에 대한 흡착시간이 길고 흡착량이 높다는 것을 확인할 수 있었다.
As shown in Table 8, it can be seen that the examples according to the present invention have a longer adsorption time and a higher adsorption amount to toluene, benzene, ethylbenzene and m-, p- and o-xylene than the comparative examples.
실험예Experimental Example 4: 휘발성 유기화합물의 탈취성능 측정 4: Measurement of deodorization performance of volatile organic compounds
암모니아 계수 측정 장비를 이용하여 상기 실시예 및 비교예에서 제조된 금속착물형 고분자막 공기정화용 필터를 밀폐된 탱크 안에 방치하고, 이 상태에서 NH4OH용액을 첨가하여 탱크안의 암모니아(NH3)의 농도를 가스 검지관을 사용하여 측정하였다. 탱크안에 방치된 시료에 암모니아 용액이 흡착, 분해하는 과정에서 탱크안의 암모니아 농도를 측정시간 1시간, 4시간, 7시간으로 측정하였으며, 측정한 결과를 표 9에 나타내었다.The metal complex type polymer membrane air purification filter prepared in the above Examples and Comparative Examples was left in a sealed tank by using an ammonia coefficient measuring instrument, and NH 4 OH solution was added in this state, and the concentration of ammonia (NH 3 ) Were measured using a gas detection tube. The concentration of ammonia in the tank was measured at 1 hour, 4 hours, and 7 hours, respectively, during the adsorption and decomposition of the ammonia solution in the sample left in the tank. The measurement results are shown in Table 9.
상기 표 9와 같이, 본 발명에 따른 실시예는 비교예 1 및 3의 초기 1시간 흡착력이 50% 내외인 것에 비하여 90%이상으로 우수하고, 최종 탈취율이 98%이상임을 확인할 수 있었다. As shown in Table 9, it can be seen that the examples according to the present invention are superior to those of Comparative Examples 1 and 3 by more than 90%, and that the final deodorization rate is 98% or more, as compared with about 50%
Claims (10)
상기 표면에 카르복실기가 포함된 폴리프로필렌 필터에 금속을 착물형태로 담지하여 금속착물형 고분자막을 제조하는 단계를 포함하고,
상기 금속은 은인 것을 특징으로 하며,
상기 제조된 금속착물형 고분자막은 각각 800ppb 수준인 시험 가스를 단면유속 0.8m/s 조건으로 통과시킬 때 지속적으로 흡착되는 시간 및 최종 흡착량 측정 시,
톨루엔은 53min과 5.69x10-3mg/g이고 벤젠은 57min과 5.90x10-3mg/g이고 에틸벤젠은 55min과 5.36x10-3mg/g이고 m,p-자일렌은 57min과 5.72x10-3mg/g이고 o-자일렌은 56min과 5.85x10-3mg/g인 것을 특징으로 하는 공기정화 필터용 금속착물형 고분자막의 제조방법.
A polypropylene filter containing a carboxyl group on the surface of the filter by graft polymerization at 50 to 80 ° C for 1 minute to 24 hours containing 1 mole of a diazonium salt having a carboxyl group and 0.01 to 0.1 mole of potassium sulfate, Producing; And
And a step of preparing a metal complex type polymer membrane by supporting a metal in a complex form on a polypropylene filter containing a carboxyl group on the surface,
Characterized in that the metal is silver,
The metal complex type polymer membranes prepared above each passed 800 ppb test gas at a cross-sectional flow rate of 0.8 m / s. When measuring the time of continuous adsorption and the final adsorption amount,
Toluene 53min and 5.69x10 -3 mg / g and benzene 57min and 5.90x10 -3 mg / g and ethylbenzene 55min and 5.36x10 -3 mg / g and m, p- xylene was 57min and 5.72x10 -3 mg / g and o- xylene production method of 56min and 5.85x10 -3 mg / g of the metal complex for the air filter, characterized in the polymer membrane type.
[2] The method according to claim 1, wherein the polypropylene filter has a porosity of 1 to 50%.
The method according to claim 1, wherein the polypropylene filter is a non-woven fabric.
The method according to claim 1, wherein the polypropylene filter has a thickness of 1 to 5 mm.
각 800ppb 수준인 시험 가스를 단면유속 0.8m/s 조건으로 통과시킬 때 지속적으로 흡착되는 시간 및 최종 흡착량 측정 시, 톨루엔은 53min과 5.69x10-3mg/g이고 벤젠은 57min과 5.90x10-3mg/g이고 에틸벤젠은 55min과 5.36x10-3mg/g이고 m,p-자일렌은 57min과 5.72x10-3mg/g이고 o-자일렌은 56min과 5.85x10-3mg/g인 것을 특징으로 하는 공기정화 필터용 금속착물형 고분자막.A metal complex type polymer membrane obtained by the production method of any one of claims 1, 7, 8 and 9, which comprises a polypropylene filter having a carboxyl group on its surface,
When the test gas at the level of 800 ppb was passed at a cross-sectional flow rate of 0.8 m / s, the time of continuous adsorption and the amount of final adsorption were measured at 53 min and 5.69 × 10 -3 mg / g of toluene, 57 min and 5.90 × 10 -3 mg / g, the ethylbenzene was 55 min and 5.36 x 10 -3 mg / g, the p-xylene was 57 min and the 5.72 x 10 -3 mg / g, the o-xylene was 56 min and the 5.85 x 10 -3 mg / g Characterized in that the metal complex type polymer membrane for air purifying filter.
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