KR100398062B1 - High functional viscose rayon activated carbon and a process of making them - Google Patents
High functional viscose rayon activated carbon and a process of making them Download PDFInfo
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- KR100398062B1 KR100398062B1 KR10-2001-0025920A KR20010025920A KR100398062B1 KR 100398062 B1 KR100398062 B1 KR 100398062B1 KR 20010025920 A KR20010025920 A KR 20010025920A KR 100398062 B1 KR100398062 B1 KR 100398062B1
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/002—Inorganic yarns or filaments
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
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Abstract
본 발명은 고기능성 비스코스레이온계 활성 탄소섬유 및 이의 제조방법에 관한 것으로서, 더욱 상세하게는 비스코스레이온계 섬유 또는 이의 섬유구조물을 인산화 반응과 탄화 반응 및 활성화 반응시킴으로써, 종래에 비해 마이크로기공(micro pore)과 메조기공(meso pore) 등의 미세기공이 발달되어 우수한 흡착효과를 가지는 고기능성 활성 탄소섬유와 그 제조방법에 관한 것이다.The present invention relates to a high-functional viscose rayon activated carbon fiber and a method of manufacturing the same, and more particularly, by the phosphorylation reaction and carbonization reaction and activation reaction of the viscose rayon-based fibers or fiber structure thereof, micro pores (micro pore) The present invention relates to a highly functional activated carbon fiber having excellent adsorption effect due to the development of fine pores such as) and meso pores.
Description
본 발명은 고기능성 비스코스레이온계 활성 탄소섬유 및 이의 제조방법에 관한 것으로서, 더욱 상세하게는 비스코스레이온계 섬유 또는 이의 섬유구조물을 인산화 반응과 탄화 반응 및 활성화 반응시킴으로써, 종래에 비해마이크로기공(micro pore)과 메조기공(meso pore) 등의 미세기공이 발달되어 우수한 흡착효과를 가지는 고기능성 활성 탄소섬유와 그 제조방법에 관한 것이다.The present invention relates to a high-functional viscose rayon activated carbon fiber and a method for manufacturing the same, and more particularly, by the phosphorylation reaction, carbonization reaction and activation reaction of the viscose rayon-based fibers or fiber structure thereof, compared to the micro pores The present invention relates to a highly functional activated carbon fiber having excellent adsorption effect due to the development of fine pores such as) and meso pores.
일반적으로 수돗물의 정수처리 및 산업폐수의 고도처리 등의 수처리정화와 NOx, 폐가스 및 VOC제거, 크린룸 및 실내 공기정화 등의 대기정화를 위해 입상 및 분말상의 활성탄이 광범위하게 사용되고 있으나 비표면적 및 흡착특성의 제한적특성으로 미량의 오염물질을 완전히 제거할 수 없으며 흡착시간이 길고 압력손실이 매우 큰 문제가 있다. 또한 흡착용량이 작으므로 활성탄의 충진량이 많아 설비면적이 증가함에 따른 시설비 및 관리비의 문제점이 대두되고 있으며 또한 사용 후 재생이 어려워 이차 오염원의 문제점이 대두된다.Generally, granular and powdery activated carbon is widely used for water purification such as water treatment of tap water and advanced treatment of industrial wastewater, and for purifying NOx, waste gas and VOC, clean room and indoor air purification, but specific surface area and adsorption characteristics Due to the limited characteristics of, it is not possible to completely remove traces of contaminants. In addition, since the adsorption capacity is small, the amount of activated carbon is increased, so the problems of facility cost and management cost are increased as the facility area is increased.
이러한 종래의 활성탄의 문제점을 해소하기 위해 최근 가는 섬유에 미세기공들이 형성된 활성 탄소섬유의 관심이 고조되면서 흡착능력이 매우 뛰어나고 흡착용량이 매우 크며 또한 사용하기에도 편리하고 재생성이 우수한 새로운 흡착재료인 활성 탄소섬유가 개발되었다.In order to solve the problem of the conventional activated carbon, as the interest of activated carbon fiber in which fine pores are formed in the fine fiber recently, the adsorption capacity is very high, the adsorption capacity is very large, and it is convenient to use and excellent in regeneration. Carbon fibers have been developed.
현재 활성 탄소섬유의 적용기술은 많이 알려져 있으나 이의 정확한 제조기술은 공개되어 있지 않고 있으며 그 원료물질 및 방법에 대해서만 간략하게 알려져 있다. 활성 탄소섬유의 원료로는 셀룰로오스계(미국특허 제3,847,833호, 제3,256,206호), 폴리아크릴니트릴계(독일특허 제2,246,572호), 핏치계(일본특허 제 54-2299호, 미국특허 제5,994,261호) 등의 섬유가 사용되고 있다.Currently, there are many known technologies for applying activated carbon fibers, but their exact manufacturing techniques are not disclosed and only briefly known about their raw materials and methods. The raw materials of activated carbon fiber include cellulose (US Pat. Nos. 3,847,833, 3,256,206), polyacrylonitrile (Germany 2,246,572), and pitch (Japanese Patent No. 54-2299, US Pat. No. 5,994,261). Fibers, such as this, are used.
또한 탄화방법으로는 난연제를 사용하지 않고 온도를 승온시키면서 탄화시키는 방법을 개발 초기에는 주로 사용되었으나, 최근 난연기술이 발달하면서 탄화시간을 줄이고 탄화온도를 낮추기 위해서 난연제를 많이 사용하고 있다.In addition, the carbonization method was mainly used in the early stages of the development of carbonization while increasing the temperature without the use of a flame retardant, but recently flame retardant technology has been used a lot of flame retardants to reduce the carbonization time and lower the carbonization temperature.
활성 탄화방법으로는 고온에서 수증기와 이산화탄소를 넣어주거나, 저온에서 오존을 불어넣어주는 방법이 있는데, 공업적으로는 제조단가 때문에 고온에서 수증기나 이산화탄소를 넣어주는 방법을 주로 사용하고 있으나 특히, 이산화탄소를 이용한 활성탄소방법은 지구온난화의 결정적인 환경문제로 문제시되고 있다.Activated carbonization method involves adding water vapor and carbon dioxide at high temperature or blowing ozone at low temperature. Industrially, due to manufacturing cost, it is mainly used to add water vapor or carbon dioxide at high temperature. The activated carbon method used is problematic as a critical environmental problem of global warming.
한편, 활성 탄소섬유의 흡착특성은 섬유에 형성되는 미세기공에 크게 좌우되며 크게 마이크로 기공(micro pore)과 메조기공(meso pore)으로 분류된다. 마이크로기공의 세공지름은 8 ∼ 30Å 이며 메조기공은 30 ∼ 500Å으로 마이크로기공율이 80% 이상 유지되어야 우수한 흡착특성을 가진다. 그러나, 종래의 활성 탄소섬유는 균일한 마이크로 기공을 유지하지 못하는 문제가 있었다.On the other hand, the adsorption characteristics of activated carbon fibers largely depend on the micropores formed in the fibers and are classified into micro pores and meso pores. The pore diameter of the micropores is 8 to 30Å and the mesopores are 30 to 500Å, which has excellent adsorption characteristics only when the microporosity is maintained at 80% or more. However, the conventional activated carbon fiber has a problem that can not maintain uniform micro pores.
이에, 본 발명자들은 상기 문제를 개선하기 위하여 비스코스레이온계 섬유 또는 이의 섬유구조물을 인산화 반응과 탄화 반응 및 활성화 반응시켜 고기능성 활성 탄소섬유를 제조함으로써 본 발명을 완성하였다.Thus, the present inventors completed the present invention by producing a high functional activated carbon fiber by phosphorylation reaction and carbonization reaction and activation reaction of the viscose rayon-based fiber or its fiber structure in order to improve the problem.
따라서, 본 발명의 목적은 높은 비표면적과 잘 발달된 미세기공을 가져 흡착특성이 우수한 고기능성 비스코스레이온계 활성 탄소섬유와 이의 제조방법을 제공하는데 있다.Accordingly, an object of the present invention is to provide a highly functional viscose rayon-based activated carbon fiber having a high specific surface area and well developed micropores, and having excellent adsorption properties, and a method of manufacturing the same.
도 1은 본 발명의 각 단계별 생성물의 FT-IR 스펙트럼을 나타낸 것이다.Figure 1 shows the FT-IR spectrum of each step product of the present invention.
도 2는 본 발명의 실시예와 종래제품의 기공크기 분포도를 나타낸 그래프이다.Figure 2 is a graph showing the pore size distribution of the embodiment of the present invention and the conventional product.
도 3은 본 발명의 실시예와 종래제품의 조직표면을 전자현미경(×100K) 사진으로 나타낸 것이다.Figure 3 shows the tissue surface of the embodiment of the present invention and the conventional product by an electron microscope (x100K) photograph.
도 4는 본 발명의 실시예와 종래제품의 흡착능력 시험 결과를 나타낸 그래프이다.Figure 4 is a graph showing the adsorption capacity test results of the embodiment of the present invention and the conventional product.
본 발명은 비스코스레이온계 섬유 또는 이의 섬유구조물을 인산화 반응, 탄화 반응, 및 활성화 반응시켜 얻은 것으로 비표면적이 1800 이상이고, 마이크로기공 크기가 1 ∼ 20 Å이고, 메조기공 크기가 30 ∼ 100 Å인 고기능성 활성 탄소섬유를 그 특징으로 한다.The present invention is obtained by phosphorylation, carbonization, and activation of a viscose rayon fiber or a fiber structure thereof, having a specific surface area of 1800 or more, a micropore size of 1 to 20 mm 3, and a mesopore size of 30 to 100 mm 3. It is characterized by high functional activated carbon fibers.
본 발명은 비스코스레이온계 섬유 또는 이의 섬유구조물을 인화합물과 질소화합물을 함유하는 수용액에 함침시켜 건조 후 질소분위기하에서 반응온도 200 ∼ 400 ℃에서 인산화 반응시키는 1 단계; 상기 1 단계의 인산염이 형성된 비스코스레이온계 섬유 또는 이의 섬유구조물을 금속염화물수용액에 함침시켜 건조 후 질소분위기하에서 반응온도 700 ∼ 1000 ℃에서 탄화 반응시키는 2 단계; 상기 2 단계의 탄화섬유 또는 탄화구조물을 700 ∼ 900 ℃의 온도에서 수증기를 주입시켜 활성화 반응시키는 3 단계;를 포함하는 고기능성 활성 탄소섬유의 제조방법을 또 다른 특징으로 한다.The present invention comprises one step of impregnating a viscose rayon-based fiber or a fiber structure thereof in an aqueous solution containing a phosphorus compound and a nitrogen compound and then phosphorylated at a reaction temperature of 200 to 400 ℃ under a nitrogen atmosphere after drying; 2 steps of impregnating the viscose rayon-based fiber or its fibrous structure in which the phosphate of step 1 is formed into an aqueous metal chloride solution, followed by carbonization reaction at a reaction temperature of 700 to 1000 ° C. under a nitrogen atmosphere after drying; It is characterized by another method for producing a high functional activated carbon fiber comprising; three steps of activating reaction by injecting water vapor at a temperature of 700 ~ 900 ℃ the carbon fiber or the carbon structure of the two steps.
이와 같은 본 발명을 더욱 상세히 설명하면 다음과 같다.Referring to the present invention in more detail as follows.
상기 1 단계는 인산화 반응 단계로 비스코스레이온계 섬유 또는 이의 섬유구조물을 0.5 ∼ 3 몰의 인화합물과 0.5 ∼ 3 몰의 질소화합물의 수용액에서 0.1 ∼ 3 시간 함침 건조시킨 후 질소분위기하에서 반응온도 200 ∼ 400 ℃, 반응시간 0.5 ∼ 3 시간 인산화 반응시켜 비스코스레이온 인산염을 제조한다. 상기 인화합물로는 인산, 인산중수소암모늄 또는 나트륨인산염 등을 사용할 수 있으며, 질소화합물로는 요소, 헥사메틸렌디아민 또는 멜라민 등을 사용할 수 있다. 상기 섬유구조물은 부직포, 직포, 섬유사 등의 형태를 가진다.The first step is a phosphorylation step in which the viscose rayon-based fiber or its fibrous structure is impregnated and dried for 0.1 to 3 hours in an aqueous solution of 0.5 to 3 moles of phosphorus compound and 0.5 to 3 moles of nitrogen compound, followed by reaction temperature of 200 to 200 ° C. under nitrogen atmosphere. Viscose rayon phosphate is manufactured by carrying out phosphorylation reaction at 400 degreeC and reaction time 0.5 to 3 hours. As the phosphorus compound, phosphoric acid, ammonium deuterium phosphate or sodium phosphate may be used, and as the nitrogen compound, urea, hexamethylenediamine or melamine may be used. The fiber structure has the form of a nonwoven fabric, a woven fabric, a fiber yarn and the like.
상기 2 단계는 탄화 반응 단계로 인산염이 형성된 비스코스레이온계 섬유 또는 이의 섬유구조물을 0.1 ∼ 3 몰의 금속염화물수용액에 0.1 ∼ 3 시간 함침 건조시킨 후 질소분위기하에서 반응온도 700 ∼ 1000 ℃, 반응시간 1 ∼ 4 시간 탄화 반응시켜 금속인산염을 함유하는 탄화섬유 또는 탄화섬유구조물을 제조한다. 제조된 금속인산염을 함유하는 탄화섬유 또는 탄화섬유구조물은 1 ∼ 3 몰의 염산용액에 0.5 ∼ 4 시간 함침시켜 탄화섬유 또는 탄화섬유구조물에 형성된 금속인산염을 제거한 후 증류수로 세척하여 건조시켜 탄화섬유 또는 탄화섬유구조물을 얻는다. 상기 금속염화물로는 알루미늄, 니켈, 티타늄, 철, 몰리브덴 또는 지르코늄 등을 사용할 수 있다.The second step is a carbonization reaction step of impregnating and drying the phosphate-forming viscose rayon-based fiber or its fibrous structure in 0.1 to 3 moles of metal chloride aqueous solution for 0.1 to 3 hours, under a nitrogen atmosphere, the reaction temperature 700 ~ 1000 ℃, reaction time 1 Carbonization reaction is carried out for 4 hours to produce carbonized fiber or carbonized fiber structure containing metal phosphate. The carbonized fiber or carbonized fiber structure containing the prepared metal phosphate is impregnated with 1 to 3 mol of hydrochloric acid solution for 0.5 to 4 hours to remove the metal phosphate formed on the carbonized fiber or carbonized fiber structure, and then washed with distilled water and dried to obtain carbonized fiber or Obtain a carbide fiber structure. As the metal chloride, aluminum, nickel, titanium, iron, molybdenum or zirconium may be used.
상기 3 단계는 활성화 반응 단계로 금속인산염이 제거된 탄화섬유 또는 탄화섬유구조물을 700 ∼ 900 ℃의 고온하에서 0.5 ∼ 3 시간동안 수증기를 1 ∼ 5 ml/min 속도로 주입시켜 활성화 반응을 시켜 미세기공을 가지는 고기능성 활성 탄소섬유 또는 탄소섬유구조물을 제조한다. 만일 주입속도가 상기 범위를 벗어나면 미세기공이 발달되지 못하는 문제가 있다.The third step is an activation reaction step in which the carbon phosphate-removed carbonized fiber or carbonized fiber structure is injected at a rate of 1 to 5 ml / min at 0.5 to 3 hours at a high temperature of 700 to 900 ° C. for micropores. To prepare a high functional activated carbon fiber or carbon fiber structure having. If the injection speed is out of the above range there is a problem that the micropores do not develop.
상기 단계를 포함하는 본 발명에 따른 활성 탄소섬유의 제조방법을 통해 제조된 고기능성 활성 탄소섬유는 비표면적이 1800 이상이며, 대체로 1500 ∼ 3000을 나타낸다. 그리고, 본 발명에 따른 활성 탄소섬유의 마이크로기공 크기는 1 ∼ 20 Å이고, 메조기공 크기는 30 ∼ 100 Å을 나타낸다.The high functional activated carbon fiber produced by the method for producing an activated carbon fiber according to the present invention comprising the above step has a specific surface area of 1800 or more and generally represents 1500 to 3000. In addition, the micropore size of the activated carbon fiber according to the present invention is 1 to 20 mm 3, and the mesopore size is 30 to 100 mm 3.
이와 같은 본 발명의 활성 탄소섬유는 비표면적이 높고, 미세기공이 잘 발달되어 우수한 흡착특성을 나타내므로 빌딩공조용 대기정화장치, 지하공간 정화용 대기정화장치, 산업체용 유해가스 제거용 대기정화장치, 수처리용 정화장치, 각종 유기용제의 분리 및 회수장치, 악취제거용품, 촉매, 촉매의 담체, Bio-reactor, 자동차용 공기정화 필터, 오일필터 등 광범위하게 응용될 수 있다.Since the activated carbon fiber of the present invention has a high specific surface area, fine pores are well developed, and exhibits excellent adsorption characteristics, the air purification device for building air conditioning, the air purification device for underground space purification, the air purification device for removing harmful gases for industrial use, It can be applied to a wide range of applications such as water purifiers, various organic solvent separation and recovery devices, odor removal products, catalysts, catalyst carriers, bio-reactors, automotive air purification filters and oil filters.
이하, 실시예에 의하여 본 발명을 더욱 상세하게 설명하겠는바, 본 발명이 실시예에 의하여 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited by Examples.
실시예 1Example 1
비스코스레이온 부직포를 인산과 요소가 각각 1M씩 녹아있는 수용액에 1시간 함침시킨 후 90 ℃에서 건조하여 수분을 제거하였다. 그 후 질소분위기가 유지되는 반응로에서 250 ℃의 온도로 1시간 인산화 반응시켜 비스코스레이온 인산염이 형성되는 섬유구조물을 제조하였다. 이것을 0.5몰 NiCl2용액에 2시간 함침시킨 후 건조하여 다시 질소분위기가 유지되는 반응로에서 3시간동안 800 ℃에서 탄화시켜 니켈파이로인산염(Nickel pyrophosphate)이 형성된 탄화구조물을 제조하였다. 탄화후 탄화구조물을 HCl 2M 용액에 2시간 함침시켜 니켈파이로인산염을 제거하고, 탄화구조물을 증류수로 세척하여 건조시켰다. 건조된 탄화구조물은 반응로에서 800 ℃에서 1시간동안 3 ml/min의 속도로 수증기를 주입시키면서 활성화 반응을 행하여 활성 탄소섬유구조물을 제조하였다.The viscose rayon nonwoven fabric was impregnated in an aqueous solution in which 1 M of phosphoric acid and urea were dissolved for 1 hour, and then dried at 90 ° C. to remove moisture. Thereafter, phosphorylation was carried out at a temperature of 250 ° C. for 1 hour in a reactor in which a nitrogen atmosphere was maintained to prepare a fibrous structure in which viscose rayon phosphate was formed. This was impregnated with 0.5 mol NiCl 2 solution for 2 hours, dried and carbonized again at 800 ° C. for 3 hours in a reactor maintained with a nitrogen atmosphere to prepare a carbonized structure in which nickel pyrophosphate was formed. After carbonization, the carbonized structure was impregnated with HCl 2M solution for 2 hours to remove nickel pyrophosphate, and the carbonized structure was washed with distilled water and dried. The dried carbonized structure was activated by injecting water vapor at a rate of 3 ml / min at 800 ° C. for 1 hour in a reactor to prepare an activated carbon fiber structure.
상기 제조된 활성 탄소섬유구조물을 FT-IR 스펙트럼으로 분석한 결과를 도 1에 나타내었다. 도 1에 나타난 바와 같이, 탄화단계에서 NiCl2를 이용한 탄화섬유구조물(도 1의 D)과 NiCl2을 이용하지 않은 탄화섬유구조물(도 1의 E)은 큰 차이를 보이고 있다. 즉, NiCl2를 넣지 않은 경우 탄화섬유구조물에 생성된 인산염이 모두 분해되어, 고리형의 탄소분자가 형성되어, FT-IR에는 피크가 발견되지 않는다(도 1의 E). 그러나 NiCl2를 이용한 탄화공정에서는 니켈파이로인산염(Ni2P2O7)가 형성되어, 1103 cm-1에서 Ni-O 피크와 1287 cm-1에 P=O 피크가 생성되었으며, 이러한 니켈파이로인산염은 염산과 같은 산에 잘 녹는다(도 1의 C). 그리고 활성화 반응 후 1198, 1097, 1074, 980 cm-1에서 peak가 생성되었는데, 이는 탄소고리에 생성된 에테르 피크에 의한 것이다(도 1의 D).The result of analyzing the prepared activated carbon fiber structure by FT-IR spectrum is shown in FIG. 1. As shown in Fig. 1, the carbonized fiber structure (D in Fig. 1) carbonized fiber structure using NiCl 2 in the carbonization step and are not used to NiCl 2 (of Fig. 1 E) has shown a great difference. That is, when NiCl 2 is not added, all of the phosphate produced in the carbon fiber structure is decomposed to form cyclic carbon molecules, and no peak is found in the FT-IR (FIG. 1E). However, in the carbonization process using NiCl 2 , nickel pyrophosphate (Ni 2 P 2 O 7 ) was formed, resulting in a Ni—O peak at 1103 cm −1 and a P═O peak at 1287 cm −1 . Rorophosphate is well soluble in acids such as hydrochloric acid (FIG. 1C). And after the activation reaction peaks were generated at 1198, 1097, 1074, 980 cm -1 , which is due to the ether peak generated in the carbon ring (D in Fig. 1).
시험예 1.Test Example 1.
<활성 탄소섬유의 기공크기에 따른 기공부피분율>Pore volume fraction according to pore size of activated carbon fiber
상기 실시예에 따른 활성 탄소섬유의 기공크기에 따른 기공부피분율(dV/dD)을 확인하기 위하여 BJH식을 이용하여 도 2에 나타내었다.In order to determine the pore volume fraction (dV / dD) according to the pore size of the activated carbon fiber according to the embodiment is shown in Figure 2 using the BJH equation.
상기 실시예의 비교예로서 종래 사용되던 활성탄(칼톤, 미국제품; 비교예 1)과 활성 탄소섬유(비스쿰, 러시아제품; 비교예 2)를 사용하였다.As a comparative example of the above embodiment, activated carbon (Carlton, USA; Comparative Example 1) and activated carbon fiber (Biscum, Russia; Comparative Example 2), which were conventionally used, were used.
도 2에 나타난 바와 같이, 실시예는 마이크로 기공과 메조기공이 잘 발달되어 있으며 특히 마이크로기공이 잘 발달되어 있음을 알 수 있었다. 그러나, 비교예 1은 마이크로기공과 메조기공이 어느정도 발달된 경향을 보여주고 있으며, 비교예 2는 마이크로기공과 메조기공이 어느정도 발달되어 있으나 특히 메조기공이 잘 발달되어 있음을 알 수 있었다.As shown in FIG. 2, the micropore and mesopores were well developed, and in particular, the micropores were well developed. However, Comparative Example 1 shows a tendency of the micropores and mesopores developed to some extent, Comparative Example 2 was found that the micropores and mesopores to some extent, but especially mesopores are well developed.
<활성 탄소섬유의 조직표면 관찰><Tissue surface observation of activated carbon fiber>
상기 도 2의 결과를 뒷받침을 위해 전자현미경(×100K)으로 실시예 및 비교예의 표면조직을 관찰하였으며, 그 결과를 도 3에 나타내었다.In order to support the results of FIG. 2, the surface textures of the examples and the comparative examples were observed using an electron microscope (× 100K), and the results are shown in FIG. 3.
도 3에 나타난 바와 같이, 실시예는 마이크로기공이 많이 존재하는 것을 볼 수 있으며, 비교예 1은 기공은 크게 발견되지 않고 크랙만이 발견되었으며, 비교예 2는 메조기공이 많이 존재하는 것을 관찰할 수 있었다.As shown in Figure 3, the embodiment can see that there are a lot of micropores, Comparative Example 1 was found not only large pores but cracks, Comparative Example 2 to observe that there are many mesopores Could.
본 발명에 따른 활성 탄소섬유는 도 2와 3에 나타난 바와 같이 미세기공, 특히 마이크로 기공이 잘 발달되어 있어 우수한 흡착성능을 가짐을 확인할 수 있었다.Activated carbon fiber according to the present invention was confirmed that the fine pores, in particular the micro pores are well developed as shown in Figure 2 and 3 has excellent adsorption performance.
시험예 2.Test Example 2.
상기 실시예와 비교예의 비표면적(Specific surface area)을 BET로 측정하여 그 결과를 표 1에 나타내었다.Specific surface areas of the Examples and Comparative Examples were measured by BET, and the results are shown in Table 1.
상기 표 1에 나타난 바와 같이, 본 발명에 따른 실시예는 1860으로 종래제품보다 높은 값을 나타내어 흡착능력이 우수함을 확인할 수 있었다.As shown in Table 1, the embodiment according to the present invention showed a higher value than the conventional product to 1860, it was confirmed that the adsorption capacity is excellent.
시험예 3.Test Example 3.
활성 탄소섬유의 흡착능력을 KS M 1082에 의한 메틸렌 블루 흡착실험으로 평가하였으며, 그 결과를 도 4에 나타내었다.Adsorption capacity of activated carbon fibers was evaluated by methylene blue adsorption experiment by KS M 1082, and the results are shown in FIG.
도 4에 나타난 바와 같이, 실시예의 활성 탄소섬유는 약 240 ㎎/g[메틸렌블루/활성 탄소섬유]의 흡착력을 보였으며, 비교예 1은 약 150 ㎎/g[메틸렌블루/활성탄]으로 포화되었으며, 비교예 2는 약 170 mg/g[메틸렌블루/활성 탄소섬유]의 흡착력을 나타내었다. 따라서, 본 발명에 따른 활성 탄소섬유인 실시예가 종래제품보다 우수한 흡착능력을 가짐을 알 수 있었다.As shown in Figure 4, the activated carbon fiber of the Example showed an adsorption capacity of about 240 mg / g [methylene blue / activated carbon fiber], Comparative Example 1 was saturated to about 150 mg / g [methylene blue / activated carbon] , Comparative Example 2 showed an adsorption capacity of about 170 mg / g [methylene blue / activated carbon fiber]. Therefore, it can be seen that the embodiment of the activated carbon fiber according to the present invention has superior adsorption capacity than the conventional product.
상술한 바와 같이, 본 발명에 따른 활성 탄소섬유는 미세기공, 특히 마이크로 기공이 잘 발달되어 있고 표면에는 큰 기공이 고루 분포되어 있으며 비표면적이 매우 높아 흡착특성이 우수하여 빌딩공조용 대기정화장치, 지하공간 정화용 대기정화장치, 산업체용 유해가스 제거용 대기정화장치, 수처리용 정화장치, 각종 유기용제의 분리 및 회수장치, 악취제거용품, 촉매, 촉매의 담체, Bio-reactor, 자동차용 공기정화 필터, 오일필터 등 광범위하게 응용될 수 있다.As described above, the activated carbon fiber according to the present invention is well developed micropores, especially micropores, evenly distributed large pores on the surface and very high specific surface area, the adsorption characteristics of the building air conditioning equipment, Atmospheric purification device for underground space purification, Atmospheric purification device for removing harmful gases for industrial use, Purification device for water treatment, Separation and recovery device for various organic solvents, Odor removal products, Catalyst, Carrier of catalyst, Bio-reactor, Air filter for automobile It can be widely applied to oil filter, etc.
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| KR101329104B1 (en) * | 2013-04-18 | 2013-11-14 | 삼공물산 주식회사 | Manufacturing method of rayon -type activated carbon fiber using potassium permanganate |
| KR101329105B1 (en) * | 2013-04-18 | 2013-11-14 | 삼공물산 주식회사 | Manufacturing method of gask-mask |
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| KR100481737B1 (en) * | 2002-07-10 | 2005-04-08 | 주식회사 동운인터내셔널 | Preparation of mesocellular carbon foam using colloidal silica template |
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| KR102707971B1 (en) | 2024-03-19 | 2024-09-23 | 주식회사 익성 | Method of preparing cellulose needle punching nonwoven carbon fiber fabric, cellulose needle punching nonwoven carbon fiber fabric, method of preparing graphitized fiber fabric and graphitized fiber fabric |
| KR102707973B1 (en) | 2024-03-19 | 2024-09-23 | 주식회사 익성 | Method of preparing cellulose needle punching nonwoven activated carbon fiber fabric and cellulose needle punching nonwoven activated carbon fiber fabric prepared from the same |
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