• Clean Technology
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• v.23 no.4
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• pp.421-428
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• 2017

In this study, we have investigated the characteristics of adsorption and desorption of toluene, methyl ethyl ketone (MEK) and their binary component using activated carbon. The BET analysis was performed to identify the characteristics of the activated carbon, and the desorption characteristics with temperature were examined to find out an optimum desorption temperature. Ten cyclic experiments of adsorption-desorption were performed, where each adsorption temperature was maintained at room temperature and desorption temperature at upto $120^{\circ}C$. In case of single component cyclic test, the efficiencies of adsorption and desorption decreased as the cycle increased. MEK which has lower affinity with activated carbon than toluene showed lower efficiencies of adsorption and desorption. In case of binary component cyclic test, a typical roll-up phenomenon was observed during adsorption process, where MEK reaches at breakpoint first and then was swept out by toluene.

• Journal of Environmental Science International
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• v.17 no.5
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• pp.493-500
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• 2008

This paper describes the adsorption/desorpton efficiency of a modified activated carbon by irradiated microwave to treat toluene. By employing microwave energy, the regeneration time was considerably shortened compared with conventional thermal heating regeneration. New adsorbent called ACB (Activated Carbon-Bentonite) was prepared from powder activated carbon with mixing bentonite as a binder. Specific surface area, average pore size and total pore volume of ACB were calculated from the nitrogen adsorption/desorption isotherm. The surface of ACB was characterized with scanning electron microscope(SEM). The results showed that the specific surface area, total pore volume, average pore size of ABC was not influenced by regenerating cycle with microwave irradiation. Toluene was adsorbed onto ACB which desorbed by MW irradiation. Absorption capacity of ACB was 0.117 $g_{toluene}/g_{ACB}$. Desorption efficiency of toluene increased as higher microwave output was applied.

• Clean Technology
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• v.12 no.4
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• pp.217-223
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• 2006

The operating variables of a desorption step were experimentally investigated tor the cycle of the process made up of benzene adsorption, steam desorption, and drying step. The effect of adsorbent regeneration depending on existence and nonexistence of drying step was studied by breakthrough curves obtained in the adsorption step of the second cycle. The duration of drying step was determined by the experimental results. In case that the amount of nitrogen gas was fixed, the regeneration efficiency increased with the amount of steam. However, the effect of steam decreased as the amount of nitrogen increased. Therefore, it would be possible to predict the optimum amount of steam comparing the amount of nitrogen gas with amount of steam in economic view.

• Korean Chemical Engineering Research
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• v.43 no.3
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• pp.432-437
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• 2005

An electric swing adsorption (ESA) process for recovering highly pure $CO_2$ from the mixed gases was tested. In this study, activated carbon fibers were used as an adsorbent. The activated carbon fibers showed fast adsorption rate and the high adsorption capacity for $CO_2$ adsorption under the condition of the ambient pressure. Activated carbon fiber with higher specific surface area was suitable to repeated adsorption-desorption cycle process, showing consistent breakthrough curve. Especially, the regeneration method by vacuum combined with ESA improved the performance of desorption process by an additional 17％ regeneration efficiency compared to a vacuum only method, and showed the high regeneration efficiency at comparatively low 7-8 Wh energy.

• Applied Chemistry for Engineering
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• v.29 no.5
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• pp.594-603
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• 2018

The effects of operating conditions such as benzene concentration, nitrogen flow rate, steam flow rate, and bed temperature on TSA process were experimentally investigated as a potential VOC removal technology using two kinds of beds packed with activated carbon and zeolite 13X. The TSA cycle studied was composed of the adsorption step, steam desorption step, and drying and cooling step. At 2% benzene concentration, the total adsorption amounts of zeolite 13X and activated carbon were 4.44 g and 3.65 g, respectively. Since the zeolite 13X has a larger packing density than that of the activated carbon, the larger benzene amount could be adsorbed in a single cycle. Increasing the water vapor flow rate to 75 g/hr at 2% benzene concentration reduced the desorption time from 1 hr to a maximum of 33 min. If the desorption time is shortened, the drying and cooling step period can be relatively increased. Accordingly, the steam removal and bed cooling could be sufficiently performed. The desorption amounts increased with the increase of the bed temperature. However, the energy consumption increased while the desorption amount was almost constant above $150^{\circ}C$. In the continuous cycle process, when the amount of remained benzene at the completion of the regeneration step increased, it might cause a decrease in the working capacity of the adsorbent. The continuous cycle process experiment for zeolite 13X showed that the amount of remained benzene at the end of regeneration step maintained a constant value after the fourth cycle.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.19 no.1
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• pp.39-49
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• 2021

The behaviors of various desorption agents were investigated during the desorption of cesium (Cs) from samples of clay minerals and actual soil. Results showed that polymeric cation exchange agents (polyethyleneimine (PEI)) efficiently desorbed Cs from expandable montmorillonite, whereas acidic desorption solutions containing HCl or PEI removed considerable Cs from hydrobiotite. However, most desorption agents could desorb only 54% of Cs from illite because of Cs's specific adsorption to selective adsorption sites. Cs desorption from an actual soil sample containing Cs-selective clay mineral illite (< 200 ㎛) and extracted from near South Korea's Kori Nuclear Power Plant was also investigated. Considerable adsorbed 137Cs was expected to be located at Cs-selective sites when the 137Cs loading was much lower than the sample's cation exchange capacity. At this low 137Cs loading, the total Cs amount desorbed by repeated washing varied by desorption agent in the order HCl > PEI > NH4+, and the highest Cs desorption amount achieved using HCl was 83%. Unlike other desorption agents with only cation exchange capabilities, HCl can attack minerals and induce dissolution of metallic elements. HCl's ability to both alter minerals and induce H+/Cs+ ion exchange is expected to promote Cs desorption from actual soil samples.

• Korean Journal of Air-Conditioning and Refrigeration Engineering
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• v.9 no.1
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• pp.73-81
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• 1997

In this experimental study, the air cooling radial shape heat exchanger which influences on the COP and the cooling capacity by heat and mass transfer rate in the adsorbent bed was designed and applied to test its performance for adsorption heat pump(AHP). Zeolite-water was used for the adsorbent-adsorbat pair. As a result, the cooling COP and a cycle period of this adsorption heat pump are 0.28 and 2 hours, respectively, on the condition of none heat recovery from the adsorption reactor(absorber). The other results and recommendations are mainly related to improving the heat and mass transfer inside the absorber to reduce a cycle period.

• Proceedings of the SAREK Conference
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• 2006.06a
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• pp.1119-1124
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• 2006

The objectives of this paper are to investigate the performance of silica gel-water adsorption refrigeration system with heat recovery process from the system experiment. This system can be driven by waste heat at near ambient temperature from $60^{\circ}C$ to $90^{\circ}C$. The cooling capacity and coefficient of performance(COP) were measured from various experimental conditions. An experimental results revealed the influence of operating temperatures(hot, cooling and chilled water), water flow rates, and adsorption-desorption cycle times on cooling capacity and COP. Under the standard conditions of $80^{\circ}C$ hot water, $25^{\circ}C$ cooling water, $14^{\circ}C$ chilled water inlet temperatures and 420sec cycle time, a cooling capacity of 1.14kW and a COP for cooling of 0.55 can be achieved.

• Journal of the Korea Organic Resources Recycling Association
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• v.24 no.3
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• pp.15-21
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• 2016

This experiment was conducted to test desorption and recycling characteristics for silver ion adsorbed into waste coffee grounds by using various desorbing agents such as nitric acid, ethylene diamine triacetic acid (EDTA) and nitrilo triacetic acid (NTA). It is appeared that the highest desorption efficiency for silver ions was obtained as about 97.8 % by 1.0 M of nitric acid solution. Also, in the case of less than 1.0 of the ratio of solid and liquid (S/L) (g/L), silver ions adsorbed onto coffee grounds was desorbed as about 98~100 %, and most of desorption process was completed within 60min. In addition, adsorption capacity of reused waste coffee grounds for silver ions was highly maintained as about 43.9 mg/g until the $2^{nd}$ cycle, as compared with the adsorption capacity with 45.9 mg/g of the adsorption capacity for virgin waste coffee grounds.

• Clean Technology
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• v.20 no.2
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• pp.179-188
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• 2014

The effect of desorption pressure on $CO_2/N_2$ breakthrough behaviors for 4 different adsorbents was studied at a fixed bed. Zeolite 3A, 4A, 5A, and 13X pellets were used as adsorbents. Cyclic operations were executed with varying desorption pressure from vacuum (0 bar) to 3 bar while other conditions such as adsorption step pressure (3 bar), temperature (293 K), composition ($CO_2:N_2=10:90$vol%) and flow rate (400 ccm) were fixed at constant values. Each adsorption and desorption step was set as 80 min, which totaled up to 160 min per a cycle. 5 cycles with adsorption and desorption steps were run overall. After the experiment, breakthrough time, saturation time, and adsorption amount were measured and compared in order to find an optimum adsorbent and a proper operating condition for a post combustion $CO_2$ capture process.