KR100572277B1 - Chemical adsorbent and preparation method thereof - Google Patents

Chemical adsorbent and preparation method thereof Download PDF

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KR100572277B1
KR100572277B1 KR1020040009938A KR20040009938A KR100572277B1 KR 100572277 B1 KR100572277 B1 KR 100572277B1 KR 1020040009938 A KR1020040009938 A KR 1020040009938A KR 20040009938 A KR20040009938 A KR 20040009938A KR 100572277 B1 KR100572277 B1 KR 100572277B1
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chemical adsorbent
chemical
polymer
support
adsorbent
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KR20050081606A (en
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최용석
오석원
이재광
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최용석
오석원
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/32Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3202Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the carrier, support or substrate used for impregnation or coating
    • B01J20/3206Organic carriers, supports or substrates
    • B01J20/3208Polymeric carriers, supports or substrates
    • B01J20/3212Polymeric carriers, supports or substrates consisting of a polymer obtained by reactions otherwise than involving only carbon to carbon unsaturated bonds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/3078Thermal treatment, e.g. calcining or pyrolizing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/30Processes for preparing, regenerating, or reactivating
    • B01J20/32Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3231Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
    • B01J20/3234Inorganic material layers
    • B01J20/3236Inorganic material layers containing metal, other than zeolites, e.g. oxides, hydroxides, sulphides or salts

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Abstract

본 발명은 폴리스티렌과 디비닐벤젠의 가교 중합체 고분자 수지를 탄화 활성화하여 얻은 지지체에 알카리금속류, 전이금속류, 할로겐족 원소 및 산을 함침하여 가정 및 산업현장에 발생하는 악취 및 유해가스를 제거하는 데 효과적인 화학흡착제 및 이의 제조방법에 관한 것으로, 본 발명에 의해 제공되는 화학흡착제는 형상이 구형이고, 높은 강도와 마모성이 우수하며, 가루날림이 없고, 악취 및 유해가스 제거가 뛰어난 흡착성능을 갖는 화학흡착제를 제공하는 것을 특징으로 한다.The present invention is effective in removing odors and harmful gases generated in homes and industrial sites by impregnating alkali metals, transition metals, halogenated elements and acids in a support obtained by carbonizing and activating a crosslinked polymer polymer resin of polystyrene and divinylbenzene. The present invention relates to an adsorbent and a method for manufacturing the same, wherein the chemical adsorbent provided by the present invention is spherical in shape, has high strength and wearability, has no powdering, and has excellent adsorption performance with excellent odor and toxic gas removal. It is characterized by providing.

고분자 수지, 지지체, 화학흡착제 Polymer resin, support, chemical adsorbent

Description

화학흡착제 및 이의 제조방법{CHEMICAL FILTER AND MAKING A PROCESS}Chemical adsorber and its manufacturing method {CHEMICAL FILTER AND MAKING A PROCESS}

도 1은 본 발명에 따른 화학흡착제의 제조방법을 도시한 공정도.1 is a process chart showing a manufacturing method of a chemical adsorbent according to the present invention.

본 발명은 폴리스티렌과 디비닐벤젠의 가교 중합체 고분자 수지를 탄화공정과 활성화공정을 거쳐 얻은 지지체에, 알카리금속류, 전이금속류, 할로겐족 원소 및 산을 함침하여 가정 및 산업현장에 발생하는 황화수소, 메캅탄, SOx의 황화합물, NOx, 암모니아, 아민의 질소화합물, 포름알데히드, 아세트알데히드, 노레인의 알데히드화합물, 벤젠, 툴루엔, 스티렌의 방향족화합물 그리고 CO, CO2, 피디린과 같은 유기화합물의 악취 및 유해가스를 제거하는데 효과적이고, 높은 강도와 마모성이 우수하며, 가루날림이 없는 우수한 구형의 화학흡착제 및 이의 제조 방법에 관한 것이다.The present invention is a hydrogen sulfide, mecaptan, which occurs in home and industrial sites by impregnating alkali metals, transition metals, halogenated elements and acids on a support obtained by carbonizing and activating a crosslinked polymer polymer resin of polystyrene and divinylbenzene. Odors and harmful odors of sulfur compounds of SOx, NOx, ammonia, amine nitrogen, formaldehyde, acetaldehyde, aldehyde compounds of noraine, aromatic compounds of benzene, toluene, styrene and organic compounds such as CO, CO 2 , and pyridin The present invention relates to an excellent spherical chemisorption agent which is effective for removing gas, has excellent high strength and wearability, and is free of dust, and a method for producing the same.

일반적으로 유해가스를 제거하기 위해서 목재 야자각, 석탄, 피치, 셀룰로오스 섬유 및 화학섬유를 원료로 불활성가스로 처리하여 제조되는 일반활성탄에 화학약품을 첨착한 활성탄을 주로 사용하고 있는 데, 이에 관한 특허들이 많이 보고되 어 있는 실정이다. In general, activated carbon obtained by adding chemicals to general activated carbon manufactured by treating wood coconut shell, coal, pitch, cellulose fiber and chemical fiber with inert gas as a raw material is used to remove harmful gas. Many have been reported.

그러나, 이들 특허에 사용되고 있는 활성탄은 비교적 넓은 비표면적이 미세 세공이 잘 발달되어 있어 화학흡착제의 지지체로 사용하기에는 적절하지만 그 형상이 분말상, 파쇄상, 원통형, 판상의 형태를 이루고 있어 효율적으로 충진하거나 필터의 기재에 바인더를 사용함에 있어 붙이는데 용이하지 않게 되고, 또한 낮은 강도와 마찰에 의한 마모가 심하여 가루날림 현상이 심각한 문제점이 발생되었다.However, the activated carbon used in these patents has a relatively large specific surface area and fine pores, so that it is suitable for use as a support for a chemical adsorbent, but its shape is in the form of powder, crushed, cylindrical, or plate, so that it can be filled efficiently. In the use of the binder in the base material of the filter is not easy to stick, and the low strength and severe abrasion due to friction caused a serious problem of powder blowing.

본 발명은 이와 같은 종래의 문제점을 해결하기 위하여 안출된 것으로, 본 발명은 폴리스티렌과 디비닐벤젠의 가교 중합체 고분자 수지를 탄화 및 활성화한 지지체에 화학약품을 첨착하여 화학흡착제를 제조하여 종래의 문제점을 해결하고, 악취 및 유해가스를 제거하는데 우수하며, 악취 및 유해가스 제거 및 필터여재로 사용하기 적합한 화학흡착제 및 이의 제조방법을 제공하는 데 그 목적이 있다.The present invention has been made in order to solve such a conventional problem, the present invention is prepared by adhering a chemical to a support obtained by carbonizing and activating a crosslinked polymer polymer resin of polystyrene and divinylbenzene to produce a chemical adsorbent to solve the conventional problems. It is an object of the present invention to provide a chemical adsorbent and a method for preparing the same, which are excellent in solving, removing odors and harmful gases, and suitable for removing odors and harmful gases and filter media.

이와 같은 본 발명은 0.01mm~5mm 크기의 구형 폴리스티렌과 디비닐벤젠의 가교 중합체인 고분자 수지를 탄화공정, 활성화공정을 거쳐 얻은 지지체에, 화학약품을 처리하고, 건조하여 제조됨을 특징으로 한다.The present invention is characterized in that the polymeric resin, which is a crosslinked polymer of spherical polystyrene and divinylbenzene having a size of 0.01 mm to 5 mm, is obtained by treating and drying a chemical agent on a support obtained through a carbonization process and an activation process.

그리고, 0.01mm~5mm 크기의 구형 폴리스티렌과 디비닐벤젠의 가교 중합체인 고분자 수지를 승온온도를 섭씨 5~50도/분으로 조작하여 온도범위 섭씨 700~900도에서 1~5시간동안 탄화공정 및 활성화공정을 거쳐 얻은 지지체에, 함침공정에서 화학약품을 첨착한 다음, 이를 건조공정에서 섭씨 25~150도로 건조하여 제조됨을 특징으로 한다.In addition, the carbonization process was performed for 1 to 5 hours at a temperature range of 700 to 900 degrees Celsius by operating a polymer resin, which is a crosslinked polymer of 0.01 mm to 5 mm spherical polystyrene and divinyl benzene, at a temperature of 5 to 50 degrees Celsius. The support obtained through the activation process, the chemicals are impregnated in the impregnation process, it is characterized in that it is manufactured by drying at 25 ~ 150 degrees Celsius in the drying process.

이하에서는 상기한 문제점을 해결하기 위하여 화학흡착제의 지지체로 사용하던 활성탄을 대신하여 폴리스티렌과 디비닐벤젠의 가교 중합체 고분자 수지를 탄화하여 지지체로 사용하였다. 폴리스티렌과 디비닐벤젠의 가교 중합체 고분자 수지중 이온교환수지는 산업용으로 생산되어 사용되고 있으며, 사용후 폐기물로 발생함으로 이를 수거하여 이용하면 쉽게 값싸고 질 좋은 담체를 얻을 수 있게 된다. Hereinafter, in order to solve the above problems, the crosslinked polymer polymer resin of polystyrene and divinylbenzene was used as a support in place of the activated carbon used as the support for the chemical adsorbent. Ion-exchange resin in the crosslinked polymer polymer resin of polystyrene and divinylbenzene is produced and used for industrial use. Since it is generated as a waste after use, it can be easily used to obtain a cheap and high quality carrier.

이러한 폴리스티렌과 디비닐벤젠의 가교 중합체 고분자 수지를 탄화하여 얻은 지지체의 특징은 탄화 및 활성공정을 거친 후에도 탄화전의 성상을 그대로 유지하는 데 0.01mm~5mm 크기의 구형(球形)이며, 500-1500m2/g의 넓은 비표면적과 우수한 강도 및 마찰에 의한 가루날림 현상이 없게 된다.The characteristic of the support obtained by carbonizing the crosslinked polymer polymer resin of polystyrene and divinylbenzene is spherical shape of 0.01mm ~ 5mm, even after carbonization and activation process, and is 500-1500m 2. It has a large specific surface area of / g, excellent strength, and no powder blowing due to friction.

이러한 지지체는 형상이 구형이므로 충진하여 사용하거나 메쉬, 허니컴, 우레탄폼 등에 부착 또는 충진하여 사용하는 데 적합하게 된다.Since the support is spherical in shape, it is suitable for use by filling or by attaching or filling to a mesh, honeycomb, urethane foam, or the like.

상기한 지지체를 얻기 위한 공정을 도 1을 참조하여 상세히 설명하면 다음과 같다.The process for obtaining the above support will be described in detail with reference to FIG. 1 as follows.

1단계: 고분자 수지를 섭씨 25~150도 범위에서 건조하여 수분을 제거하게 되는 건조공정; 2단계: 건조공정에서 건조된 고분자 수지를 불활성 기체 분위기에서 섭씨 700~900도 범위내에 1~2시간 탄화시키는 탄화공정; 3단계: 탄화공정을 거쳐 얻어진 지지체를 기체활성법을 이용하여 섭씨 700~900도 범위에서 1~5시간 활성화시키는 활성화공정으로 이루어진다.Step 1: drying the polymer resin to remove moisture by drying in the range of 25 ~ 150 degrees Celsius; Step 2: carbonizing the polymer resin dried in the drying step in a range of 700 to 900 degrees Celsius in an inert gas atmosphere for 1 to 2 hours; Step 3: Activate the support obtained through the carbonization process using a gas activation method for 1 to 5 hours in the range of 700 ~ 900 degrees Celsius.

상기 1단계의 건조공정에서 수분을 제거하지 않으면 탄화공정에서 완전탄화 가 발생되어 발명의 특성중 하나인 구형의 형상을 갖지 못하게 됨으로써 반드시 수분을 제거하여야 한다.If moisture is not removed in the drying step of the first step, complete carbonization occurs in the carbonization process so that it does not have a spherical shape, which is one of the characteristics of the invention, and thus water must be removed.

상기 2단계인 탄화공정의 온도조건은 보다 적절하게는 섭씨 700~800도이다. 탄화공정 수행시 탄소 수율의 손실이 많이 발생되는 온도범위인 섭씨 350~550도에서는 최대한 빨리 통과하는 것이 바람직하다. 탄화공정의 승온온도는 섭씨 5~50도/분 범위가 적절하다. 승온온도가 섭씨 5도 이하인 경우에는 많은 시간과 비용이 소요됨으로 인해 생산성이 저하되어 바람직하지 못하게 된다.The temperature condition of the carbonization process, which is the second step, is more suitably 700 to 800 degrees Celsius. In the carbonization process, it is desirable to pass as quickly as possible at a temperature range of 350 to 550 degrees Celsius, which is a temperature range where a lot of carbon yield is lost. The temperature rise temperature of the carbonization process is appropriate in the range of 5 to 50 degrees Celsius / min. If the elevated temperature is less than 5 degrees Celsius, it takes a lot of time and money, the productivity is undesirably undesirable.

상기 3단계인 활성화공정은 이산화탄소, 수증기, 산소를 이용하여 마이크로 및 메조세공을 발달시키고, 비표면적과 세공의 크기를 넓히는 단계이며, 섭씨 700~900도로 1~5시간 정도의 기체 활성화 공정을 거치게 된다.The three-step activation process is to develop micro and mesopores using carbon dioxide, water vapor, and oxygen, and to expand the specific surface area and pore size, and to undergo a gas activation process of about 700 to 900 degrees Celsius for 1 to 5 hours. do.

이때, 활성화공정에서 기체활성화법을 사용하는 이유는 화학흡착제 또는 촉매 제조를 위한 지지체는 화학약품 첨착을 통해 특수한 목적으로 사용하기 때문에 약품활성화법을 사용하게 되면 활성화 후 존재하는 금속등에 영향을 주어 화학흡착제와 촉매의 성능이 저하될 수 있게 된다.In this case, the reason for using the gas activation method in the activation process is that the chemical adsorbent or the support for the catalyst is used for a special purpose through the addition of chemicals, if the chemical activation method is used to affect the metal present after activation The performance of the adsorbents and catalysts can be reduced.

한편, 제 1 내지 제 3단계만을 거친 지지체 만으로도 흡착제로 사용이 가능하지만, 가정 및 산업현장에서 발생하는 황화수소, 메캅탄, SOx의 황화합물 NOx, 암모니아, 아민의 질소화합물, 포름알데히드, 아세트알데히드, 노레인의 알데히드화합물 그리고 벤젠, 톨루엔, 스티렌의 방향족화합물과 같은 유해가스를 제거하기 위해 4단계인 함침공정에서 화학약품을 처리하여 화학결합력을 높여 흡착성능을 향상시켰다.On the other hand, it is possible to use as an adsorbent with only the first to third stage support, but hydrogen sulfide, mecaptan, SOx sulfur compound NOx, ammonia, amine nitrogen compound, formaldehyde, acetaldehyde, furnace In order to remove harmful gases such as aldehyde compounds of lanes and aromatic compounds of benzene, toluene, and styrene, chemicals were treated in the four-step impregnation process to increase the chemical bonding power to improve adsorption performance.

이러한 화학흡착제는 지지체에 화학약품을 처리하여 제조하는 데, SOx, CH3SH, H2S의 황화합물과 NO, N2O, NO2의 질소산화물을 제거하기에 적합한 화학약품은 KOH, NaOH, KI, NaI중에 선택된 알카리 금속화합물과 브롬, 요오드의 할로겐족 원소로 이루어져 화학약품이 적절하고 아민과 암모니아를 제거하는데는 구연산, 황산, 질산, 인산중에 선택된 화학약품을 처리하는 것이 적절하고, HCHO, CH3CHO, 노레인의 알데히드화합물을 제거하는데는 Cu, Mn, Ni, Co의 전이금속이나 알카리금속을 처리하고 아민기를 가진 화학약품을 처리하게 된다. 벤젠, 톨루엔, 스티렌의 방향족화합물은 전이금속과 알카리금속을 처리하여 제거하게 된다. Such chemical adsorbents are prepared by treating chemicals on a support, and chemicals suitable for removing sulfur compounds of SOx, CH 3 SH, H 2 S and nitrogen oxides of NO, N 2 O, and NO 2 include KOH, NaOH, It is composed of alkali metal compound selected from KI and NaI and halogen group element of bromine and iodine, and the chemical is appropriate. To remove amine and ammonia, it is appropriate to treat chemical selected from citric acid, sulfuric acid, nitric acid and phosphoric acid. 3 To remove the aldehyde compounds of CHO and nolane, the transition metal or alkali metal of Cu, Mn, Ni, Co is treated and chemicals with amine groups are treated. Aromatic compounds of benzene, toluene and styrene are removed by treating transition metals and alkali metals.

고분자 수지를 탄화하여 얻은 지지체에 상기 언급한 화학약품을 처리하여 흡착성능 평가장치에서 일산화질소, 암모니아, 톨루엔의 흡착성능을 평가하였다.The above-mentioned chemicals were treated on the support obtained by carbonizing the polymer resin to evaluate the adsorption performance of nitrogen monoxide, ammonia and toluene in the adsorption performance evaluation apparatus.

이하에서는 본 발명에 따른 구체적인 실시예를 기술하였으며, 본 발명의 범위가 실시예에 한정하는 것은 아니다.Hereinafter, specific embodiments according to the present invention have been described, but the scope of the present invention is not limited to the embodiments.

실시예 1) Example 1

지지체의 제조Preparation of the Support

폴리스티렌과 디비닐벤젠의 가교 중합체 고분자 수지인 양이온교환수지를 1단계인 건조공정에서 실온에서 건조하여 수분을 제거한 다음, 2단계인 탄화공정에서는 전기로에 넣고, 질소를 분당 10cc 불어넣어서 불활성기체 분위기하에서 섭씨 10도/분으로 섭씨 750도까지 승온하여 섭씨 750도에서 1시간 유지한 후 상온으로 자연냉각후에 3단계인 활성화공정으로 질소를 분당 10cc 불어넣어 불할성기체 분위기하에서 섭씨 10도/분으로 섭씨 750도까지 승온하고 섭씨 750도에서 수분을 함유한 증기를 넣어 5시간 유지하면서 활성화를시킨 다음, 냉각하여 화학흡착 및 촉매 담체용 소재를 얻게 된다.The cation exchange resin, which is a crosslinked polymer polymer resin of polystyrene and divinylbenzene, is dried at room temperature in a first stage drying process to remove moisture, and then, in a second stage carbonization process, placed in an electric furnace and blown with nitrogen at 10 cc / min in an inert gas atmosphere. After heating up to 750 degrees Celsius at 10 degrees Celsius / minute and maintaining it at 750 degrees Celsius for 1 hour, natural cooling to room temperature and 3 steps of activation process followed by nitrogen injecting 10cc per minute in an inert gas atmosphere at 10 degrees Celsius / min. The temperature is raised to 750 degrees and the moisture containing steam at 750 degrees Celsius is added and maintained for 5 hours, followed by cooling to obtain a material for chemisorption and catalyst carrier.

실시예 2)Example 2)

일산화질소 화학흡착제Nitric Oxide Chemical Adsorbent

실시예 1)에 의해 제조된 지지체를 요오드화칼륨 수용액에 약 1시간 정도 함침시킨 후 섭씨 120~150도에서 건조하여 화학흡착제를 제조하였다. 요오드화칼륨의 담지된 양은 지지체 중량의 0.1~10wt% 범위이다. 성능을 평가하기 위해서는 고정층 반응기에 일산화질소 화학흡착제를 충진하고 일산화가스를 흘려서 일산화질소의 흡착성능을 측정하였다.(그림 1참조)The support prepared in Example 1) was impregnated with an aqueous potassium iodide solution for about 1 hour and then dried at 120 to 150 degrees Celsius to prepare a chemical adsorbent. The supported amount of potassium iodide ranges from 0.1 to 10 wt% of the weight of the support. In order to evaluate the performance, the nitrogen monoxide adsorbent was packed in a fixed-bed reactor and nitrogen monoxide was flowed to measure the adsorption performance of nitrogen monoxide (see Figure 1).

그림 1) 일산화질소 흡착곡선Figure 1) Nitric Oxide Adsorption Curve

Figure 112004006248828-pat00001
Figure 112004006248828-pat00001

실시예 3) 암모니아 화학흡착제Example 3) Ammonia Chemistry

실시예 1)에 의해 제조된 지지체를 인산수용액으로 약 30분 정도 함침시킨 후 섭씨 40~60도에서 건조하여 화학흡착제를 제조하였다. 인산의 담지된 양은 지지체 중량의 0.1~30wt% 범위이다. 성능을 평가하기 위해서는 고정층 반응기에 암모니아 화학흡착제를 충진하고 암모니아 가스를 흘려서 암모니아의 흡착성능을 측정하였다.(그림 2참조)The support prepared in Example 1) was impregnated with an aqueous phosphate solution for about 30 minutes and then dried at 40 to 60 degrees Celsius to prepare a chemical adsorbent. The supported amount of phosphoric acid ranges from 0.1 to 30 wt% of the weight of the support. To evaluate the performance, the ammonia chemisorption was packed into a fixed bed reactor and ammonia gas was flowed to measure the adsorption performance of ammonia (see Figure 2).

그림 2) 암모니아 흡착곡선Figure 2) Ammonia adsorption curve

Figure 112004006248828-pat00002
Figure 112004006248828-pat00002

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실시예 4)Example 4

톨루엔 화학흡착제Toluene Chemical Adsorbent

실시예 1)에 의해 제조된 지지체에 요오드화구리 용액으로 1시간에서 24시간 정도 함침시킨 후 건조기에서 섭씨 110도로 건조하여 화학흡착제를 제조하였다. 성능을 평가하기 위해서는 고정층 반응기에 톨루엔 화학흡착제를 충진하고 톨루엔 가스를 흘려서 톨루엔 흡착성능을 측정하였다.(그림 3참조)The support prepared in Example 1) was impregnated with a copper iodide solution for 1 hour to 24 hours, and then dried in a dryer at 110 degrees Celsius to prepare a chemical adsorbent. To evaluate the performance, toluene adsorption performance was measured by filling a toluene chemisorbent in a fixed bed reactor and flowing toluene gas (see Figure 3).

그림 3) 톨루엔 흡착곡선Figure 3) Toluene Adsorption Curve

Figure 112004006248828-pat00004
Figure 112004006248828-pat00004

이와 같이 본 발명에 의해 제조된 화학흡착제는 악취 및 유해가스의 제거에 뛰어난 성능을 보이게 되고, 그 형상이 구형이며, 높은 강도와 마모성이 우수하여 가루날림의 현상이 없는 특성을 가지고 있어 대기 및 수질오염을 제어할 수 있는 필터나 흡착제의 제품 생산이 용이한 효과가 제공된다.As described above, the chemical adsorbent prepared by the present invention exhibits excellent performance in removing odors and harmful gases, has a spherical shape, and has a high strength and abrasion property, and has no property of dust blowing. It is easy to produce a filter or adsorbent that can control contamination.

Claims (6)

0.01mm~5mm 크기의 구형 폴리스티렌과 디비닐벤젠의 가교 중합체인 고분자 수지를 탄화공정, 활성화공정을 거쳐 얻은 지지체에, 화학약품을 처리하고, 건조하여 제조된 것을 특징으로 하는 화학흡착제.A chemical adsorbent prepared by treating a polymer obtained by carbonizing and activating a polymer resin, which is a crosslinked polymer of 0.01 mm to 5 mm of spherical polystyrene and divinyl benzene, through a carbonization process and an activation process. 0.01mm~5mm 크기의 구형 폴리스티렌과 디비닐벤젠의 가교 중합체인 고분자 수지를 승온온도 섭씨 5~50도/분으로 조작하여 온도범위 섭씨 700~900도에서 1~5시간동안 탄화공정 및 활성화공정을 거쳐 얻은 지지체에, 함침공정에서 화학약품을 첨착한 다음, 이를 건조공정에서 섭씨 25~150도로 건조하여 제조된 것을 특징으로 하는 화학흡착제 제조방법.Polymerization, which is a cross-linked polymer of 0.01mm ~ 5mm spherical polystyrene and divinylbenzene, is operated at a temperature of 5 ~ 50 ° C for 1 ~ 5 hours at 700 ~ 900 ° C. After adhering the chemicals in the impregnation process to the support obtained through, and then drying them at 25 to 150 degrees Celsius in the drying process, the method for producing a chemical adsorbent. 제 2항에 있어서, The method of claim 2, 상기 구형의 폴리스티렌과 디비닐벤젠의 가교 중합체인 고분자 수지는 이온교환수지를 포함하게 되는 것을 특징으로 하는 화학흡착제 제조방법.The polymer resin is a cross-linked polymer of the spherical polystyrene and divinyl benzene, characterized in that it comprises an ion exchange resin. 제 2항에 있어서, 상기 활성화공정에서 사용되는 활성기체는 이산화탄소, 산소 및 수증기인 것을 특징으로 하는 화학흡착제 제조방법.The method according to claim 2, wherein the active gas used in the activation process is carbon dioxide, oxygen and water vapor. 제 2항에 있어서, 상기 화학약품은 KOH, NaOH, KI, NaI 중에 선택된 알칼리 금속화합물, 구연산, 황산, 질산, 인산 중에 선택된 화합물이고, 브롬, 요오드의 할로겐족을 포함한 Cu, Mn, Ni, Co 중에 선택된 전이금속화합물인 것을 특징으로 하는 화학흡착제 제조방법.The method of claim 2, wherein the chemical agent is a compound selected from alkali metal compounds selected from KOH, NaOH, KI, NaI, citric acid, sulfuric acid, nitric acid, phosphoric acid, Cu, Mn, Ni, Co containing a halogen group of bromine, iodine Method for producing a chemical adsorbent, characterized in that the selected transition metal compound. 삭제delete
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