• Title/Summary/Keyword: carbon adsorbent

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Study on the Adsorption of Carbon Dioxide in Passenger Cabin Using $Al_2O_3$ Adsorbent ($Al_2O_3$ 흡착제를 이용한 객실용 이산화탄소 흡착연구)

  • Cho, Young-Min;Choi, Jin-Sik;Lee, Ji-Yun;Kwon, Soon-Bark;Park, Duck-Shin
    • Proceedings of the KSR Conference
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    • 2011.10a
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    • pp.138-141
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    • 2011
  • Carbon dioxide concentration of railroad passenger cabin is obliged to be kept lower than guideline values of 'Indoor air quality guideline for public transportations', but actual carbon dioxide concentration frequently exceeds this guideline value during the morning and evening rush hours. For improving comfortability and satisfaction of passengers, concentration control method using $Al_2O_3$ adsorbents was presented. The adsorbent is made from $Al_2O_3$ and LiOH. $Al_2O_3$ perform as a frame and LiOH as a chemical adsorbent. The adsorbent performance experiment was carried out by measuring concentration change of Carbon dioxide in terms of flow, initial concentration and amount of adsorbent. It is expexted that the obtained results will be used to lower carbon dioxide concentration of railroad passenger cabin.

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INVESTIGATION OF ACTIVATED CARBON ADSORBENT ELECTRODE FOR ELECTROSORPTION-BASED URANIUM EXTRACTION FROM SEAWATER

  • ISMAIL, AZNAN FAZLI;YIM, MAN-SUNG
    • Nuclear Engineering and Technology
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    • v.47 no.5
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    • pp.579-587
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    • 2015
  • To support the use of nuclear power as a sustainable electric energy generating technology, long-term supply of uranium is very important. The objective of this research is to investigate the use of new adsorbent material for cost effective uranium extraction from seawater. An activated carbon-based adsorbent material is developed and tested through an electrosorption technique in this research. Adsorption of uranium from seawater by activated carbon electrodes was investigated through electrosorption experiments up to 300 minutes by changing positive potentials from +0.2V to +0.8V (vs. Ag/AgCl). Uranium adsorption by the activated carbon electrode developed in this research reached up to 3.4 g-U/kg-adsorbent material, which is comparable with the performance of amidoxime-based adsorbent materials. Electrosorption of uranium ions from seawater was found to be most favorable at +0.4V (vs. Ag/AgCl). The cost of chemicals and materials in the present research was compared with that of the amidoxime-based approach as part of the engineering feasibility examination.

Evaluation of acetaldehyde removal performance of a hybrid adsorbent consisting of organic and inorganic materials (유무기 융복합 흡착제의 아세트알데하이드 제거 성능 평가)

  • Ahn, Hae Young;Lee, Yoon Kyoung;Song, JiHyeon
    • Journal of odor and indoor environment
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    • v.17 no.4
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    • pp.372-380
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    • 2018
  • To abate the problem of odor from restaurants, a hybrid adsorbent consisting of organic and inorganic materials was developed and evaluated using acetaldehyde as a model compound was deveioped and evaluated. Powders of activated carbon, bentonite, and calcium hydroxide were mixed and calcinated to form adsorbent structure. The surface area of the hybrid adsorbent was smaller than that of high-quality activated carbon, but its microscopic image showed that contours and pores were developed on its surface. To determine its adsorption capacity, both batch isotherm and continuous flow column experiments were performed, and these results were compared with those using commercially available activated carbon. The isotherm tests showed that the hybrid adsorbent had a capacity 40 times higher than that of the activated carbon. In addition, the column experiments revealed that breakthrough time of the hybrid adsorbent was 2.5 times longer than that of the activated carbon. These experimental results were fitted to numerical simulations by using a homogeneous surface diffusion model (HSDM); the model estimated that the hybrid adsorbent might be able to remove acetaldehyde at a concentration of 40 ppm for a 5-month period. Since various odor compounds are commonly emitted as a mixture when meat is barbecued, it is necessary to conduct a series of experiments and HSDM simulations under various conditions to obtain design parameters for a full-scale device using the hybrid adsorbent.

Removal of arsenic from aqueous phase using magnetized activated carbon and magnetic separation

  • Kwon, H.W.;Shin, T.C.;Kim, J.J.;Ha, D.W.;Kim, Min Gyu;Kim, Young-Hun
    • Progress in Superconductivity and Cryogenics
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    • v.20 no.2
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    • pp.1-5
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    • 2018
  • Arsenic (As) is one of the elements having most harmful impact on the human health. Arsenic is a known carcinogen and arsenic contamination of drinking water is affecting on humans in many regions of the world. Adsorption has been proved most preferable technique for the removal of arsenic. Many researchers have studied various types of solid materials as arsenic adsorbent, and iron oxide and its modified forms are considered as the most effective adsorbent in terms of adsorption capacity, recovery, and economics. However, most of all iron oxides have small surface area in comparing with common adsorbents in environmental application such as activated carbon but the activated carbon has weak sorption affinity for arsenic. We have used an activated carbon as base adsorbent and iron oxide coating on the activated carbon as high affinity sorption sites and giving magnetic attraction ability. In this study, adsorption properties of arsenic and magnetic separation efficiency of the magnetized activated carbon (MAC) were evaluated with variable iron oxide content. As the iron oxide content of the MAC increased, adsorption capacity has also gradually increased up to a point where clogging by iron oxide in the pore of activated carbon compensate the increased sorption capacity. The increase of iron oxide content of the MAC also affected magnetic properties, which resulted in greater magnetic separation efficiency. Current results show that magnetically modified common adsorbent can be an efficiency improved adsorbent and a feasible environmental process if it is combined with the magnetic separation.

Comparison of Adsorption Performance of Ammonia and Formaldehyde Gas Using Adsorbents Prepared from Water Treatment Sludge and Impregnated Activated Carbon (정수슬러지 유래 흡착제와 첨착활성탄의 암모니아 및 포름알데히드 기체 흡착 성능 비교)

  • Lee, Choul Ho;Park, Nayoung;Kim, Goun;Jeon, Jong-Ki
    • Applied Chemistry for Engineering
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    • v.27 no.1
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    • pp.62-67
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    • 2016
  • In this study, a pellet-type adsorbent was prepared by using the water-treatment sludge as a raw material, and its physical and chemical properties were analyzed through $N_2$-adsorption, XRD, XRF, and $NH_3$-TPD measurements. Adsorption performance for gaseous ammonia and formaldehyde was compared between the pellet-type adsorbents prepared from water-treatment sludge and the impregnated activated carbon. Although the surface area and pore volume of the pellet-type adsorbent produced from water-treatment sludge were much smaller than those of the impregnated activated carbon, the pellet-type adsorbent produced from water-treatment sludge could adsorb ammonia gas even more than that of using the impregnated activated carbon. The pellet-type adsorbent prepared from water-treatment sludge showed a superior adsorption capacity for ammonia which can be explained by chemical adsorption ascribed to the higher amount of acid sites on the pellet-type adsorbent prepared from water-treatment sludge. In the case of formaldehyde adsorption, the impregnated activated carbon was far superior to the adsorbent made from the water-treatment sludge, which can be attributed to the increased surface area of the impregnated activated carbon.

A Study on Adsorption of Volatile Organic Compound by Activated Carbon Fiber Coated with Dielectric Heating Element and Desorption by Applying Microwave (유전가열물질을 코팅한 활성탄소섬유의 휘발성 유기화합물 흡착 및 마이크로파 인가에 의한 탈착 연구)

  • Kim, Sang-Guk;Chang, Ye-Rim
    • Journal of Korean Society for Atmospheric Environment
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    • v.25 no.2
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    • pp.122-132
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    • 2009
  • Adsorption of toluene by activated carbon fiber (ACF) coated with dielectric heating element and desorption by applying microwave were investigated. In order to prepare adsorbent so that VOC can be desorbed by microwave heating, fine dielectric heating element with nano size was coated on the surface of the ACF using hybrid binder. Eight adsorbents (ACF-DHE, Activated Carbon Fiber coated with Dielectric Heating Element) were prepared with different amount of dielectric heating element, kinds of hybrid binder, and solvent. In order to investigate adsorption characteristics, BET surface area, pore volume, and average pore size were measured for each adsorbent including ACF. Breakthrough experiments with toluene concentration, flow rate, bed length using fixed bed reactor were performed to investigate adsorbality of adsorbent, and results were compared with that of the ACF. Desorption reactor was constructed with modified microwave oven to investigate heating effect on ACF-DHE by applying microwave power. Each adsorbent saturated with toluene were put into desorption reactor. Composition of desorbed gas generated by applying controlled microwave power to reactor was measured. Up to now, hot air desorption method has been used. Experimental results showed that desorption method with new adsorbent prepared by coating dielectric heating element on ACF can be used for industrial application.

A study on recycling of cast as adsorbent (흡착제로서 분변토 재활용에 관한 연구)

  • 손희정;전성균;하상안
    • Journal of environmental and Sanitary engineering
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    • v.15 no.3
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    • pp.44-49
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    • 2000
  • The purpose of this research is to evaluate the adsorption capacity of casts for heavy metals. The casts were excreted by earthworm, Lumbricus rubellus, after having eaten the paper sludge. Various batch experiments on adsorption were performed to compare cast and activated carbon. The pH increase in solution due to extractives from cast was 1.3 and the cation exchange capacity which implies adsorption capacity for solubles is greater on activated carbon than on cast. According to the results of batch experiment, the removal rates of Pb, Cu, Cr, Zn using the activated carbon and casts as adsorbent were 98%, 93%, 94%, 89%, 82% and 95%, 90%, 88%,80%, 66%, respectivity, and this removal were achived less than 90 minutes. It can be said that casts is so good adsorbent as activated carbon is, although adsorption carbon was found to be some large than those of casts through Freundlich isotherm applied for adsorption of soluble. As a result on the experiment of isothermic adsorption from the mixed component solution in the batch, the order of preferable elements in heavy metal adsorption was found to be Pb>Cd>Cu>Cr>Zn on activated carbon, respectively.

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Study on the Removal of Carbon Dioxide in the Subway Cabin Using Zeolite Type Carbon Dioxide Adsorbent (제올라이트계 이산화탄소 흡착제를 사용한 지하철 객실 내부의 이산화탄소 제거에 관한 연구)

  • Cho, Young-Min;Park, Duck-Shin;Kwon, Soon-Bark;Lee, Ju-Yeol;Hwang, Yun-Ho
    • Journal of the Korean Society for Railway
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    • v.14 no.1
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    • pp.1-5
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    • 2011
  • High concentration of carbon dioxide at subway cabin is one of the serious environmental concerns because carbon dioxide causes drowsiness, headache, and nervelessness of passengers. Ministry of Environment set a guideline for indoor carbon dioxide levels in train or subway in 2007. In this study, a carbon dioxide removal system for subway cabin was developed and tested using a test subway cabin. Various types of modified zeolites were used as the adsorbent of carbon dioxide. The tested zeolites were applied to the subway cabin, and showed high potential to lower the indoor $CO_2$ level.

Kinetics of In-situ Degradation of Nerve Agent Simulants and Sarin on Carbon with and without Impregnants

  • Saxena, Amit;Sharma, Abha;Singh, Beer;Suryanarayana, Malladi Venkata Satya;Mahato, Timir Haran;Sharma, Mamta;Semwal, Rajendra Prasad;Gupta, Arvind Kumar;Sekhar, Krishnamurthy
    • Carbon letters
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    • v.6 no.3
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    • pp.158-165
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    • 2005
  • Room temperature kinetics of degradation of nerve agent simulants and sarin, an actual nerve agent at the surface of different carbon based adsorbent materials such as active carbon grade 80 CTC, modified whetlerite containing 2.0 and 4.0 % NaOH, active carbon with 4.0 % NaOH, active carbon with 10.0 % Cu (II) ethylenediamine and active carbon with 10.0 % Cu (II) 1,1,1,5,5,5-hexafluoroacetylacetonate were studied. The used adsorbent materials were characterized for surface area and micropore volume by $N_2$ BET. For degradation studies solution of simulants of nerve agent such as dimethyl methylphosphonate (DMMP), diethyl chlorophosphate (DEClP), diethyl cyanophosphate (DECnP) and nerve agent, i.e., sarin in chloroform were prepared and used for the uniform adsorption on the adsorbent systems using their incipient volume at room temperature. Degradation kinetics was monitored by GC/FID and was found to be following pseudo first order reaction. Kinetics parameters such as rate constant and half life were calculated. Half life of degradation with modified whetlerite (MWh/NaOH) system having 4.0 % NaOH was found to be 1.5, 7.9, 1206 and 20 minutes for DECnP, DEClP, DMMP and sarin respectively. MWh/NaOH system showed maximum degradation of simulants of nerve agents and sarin to their hydrolysis products. The reaction products were characterized using NMR technique. MWh/NaOH adsorbent was also found to be active against sulphur mustard.

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Dimerization of tert-Butylmercaptan over the Surface of Aerosil? Impregnated with Copper and Manganese

  • Park, Dong Geon;Park, Seon Hui;Lee, Su Jin
    • Bulletin of the Korean Chemical Society
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    • v.21 no.7
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    • pp.715-719
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    • 2000
  • A ceramic powder of destructive adsorbent was synthesized by impregnating copper and manganese on the surface of silica aerosil@. In-site FTIR measurements on pulses of malodorant tert-butylmercaptan injected over the powder showed that rert-butylmercaptan dimerized into di-tert-hutyldisulfide on the surface of the adsorbent in an ambient condition. GC/MS measurement on the gas over the adsorbent showed no tert-butylmercaptan remaining, and showed only the dimerization product of di-tert-butyldisulfide. Most of the dimerization product, di-tert-butyldisulfide,remained on the surface of the adsorbent as physisorbed condense, and apparently Iowered the destruction efficiency by blocking the surface from the access by tert-butylmercaptan. Upon being heated above $100^{\circ}C$ it was observed that the physisorbed di-tert-butyldisulfide dissociated back into tert-butylmercaptan. tert-butylmercaptan physisorbed on the activated carbon, thereby no dimerization was occurring on the surface of the activated carbon. In an argn environment, the dimerization reaction was practically not occurring even on the surface of the adsorbent, indicating the free oxygen in air was also participating in the dimerization reaction. Water was identified as a by-product of the dimerization reaction. Possible reactions on the surface of the adsorbent were proposed.