• Title/Summary/Keyword: electric adsorption

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Adsorption/desorption of CO2 on Activated Carbon Fibers Using Electric Swing Adsorption (활성탄소섬유상에서 전기변동법을 이용한 CO2의 흡/탈착)

  • Shim, JaeWoon;Moon, SeungHyun
    • 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.

Study on the Adsorption and Desorption Enhance Effect of Oyster Shell Using Peltier Element (페르체소자를 이용한 굴패각의 흡착 및 탈착촉진효과에 관한 연구)

  • Kim, Myoung-Jun
    • Journal of Power System Engineering
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    • v.17 no.1
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    • pp.71-76
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    • 2013
  • This study is experimentally performed for using the oyster shell as a desiccant in the batch type system. The peltier element(thermoelectric device) is used for absorbing and releasing the adsorption and desorption heat generation. The cooling and heating effects of peltier element exist in this experiment and these effects are generally known phenomena among some references. The increase in electric current induced into peltier element is effectively release the heat generation of adsorption and desorption. Consequently, the non-dimensional adsorption and desorption amount would increase with increase in electric current. However, in the case of adsorption, the increase of induced current into peltier element, the heat of cold side can not release sufficiently. So the heat of hot side of peltier is transferred into the cold side.

An Estimation of Breakthrough Curve of Activated Carbon Adsorption Column (활성탄 흡착칼럼의 농도변화곡선 추정)

  • Yang, Ho-Yeon;Park, Chong-Mook;Song, Myung-Jae;Oh, Chang-Yong;Han, Neung-Won
    • Journal of Korean Society of Environmental Engineers
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    • v.22 no.2
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    • pp.217-229
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    • 2000
  • Adsorption equilibrium experiments for the phenol on granular activated carbon(16~25 mesh) and powder activated carbon(325 mesh) were carried out at $25{\pm}1^{\circ}C$ and the results were expressed with Freundlich isotherm. Adsorption rate experiments were executed in batch adsorption system under the condition that can be neglecting mass transfer resistance at the external surface of the particle. The results were analysed with the Miller's method to evaluate the linear driving force(LDF) adsorption rate constant. Fixed bed adsorption experiments were performed by adopting different flow rates in the activated carbon-phenol system at $25{\pm}1^{\circ}C$. The theoretical breakthrough curves were estimated with the simple constant pattern solution. The adsorption rate constant of LDF model was not a fixed value but variable with adsorption amount. The experimental results were better agreed with the estimation of breakthrough curve using the variable adsorption rate constant than the results estimated using the average fixed adsorption rate constant.

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Analysis of Siloxane Adsorption Characteristics Using Response Surface Methodology

  • Park, Jin-Kyu;Lee, Gyeung-Mi;Lee, Chae-Young;Hur, Kwang-Beom;Lee, Nam-Hoon
    • Environmental Engineering Research
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    • v.17 no.2
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    • pp.117-122
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    • 2012
  • A central composite design and response surface methodology were applied to investigate the optimum conditions for maximum adsorption capacity in activated alumina as an adsorbent. The optimized conditions were determined for adsorption capacity using variables of flow rate and temperature. It was found that flow rate and temperature greatly influenced the adsorption capacity, as determined by analysis of variance analysis of these variables. Statistical checks indicated that second order polynomial equations were adequate for representing the experimental values. The optimum conditions for adsorption capacity were $0^{\circ}C$ and 2,718 mL/min, with the estimated maximum adsorption capacity of 17.82%. The experimental adsorption capacity was 17.75% under these optimum conditions, which was in agreement with the predicted value of 17.82%.

Rh-doped carbon nanotubes as a superior media for the adsorption of O2 and O3 molecules: a density functional theory study

  • Cui, Hao;Zhang, Xiaoxing;Yao, Qiang;Miao, Yulong;Tang, Ju
    • Carbon letters
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    • v.28
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    • pp.55-59
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    • 2018
  • Transition-metal-embedded carbon nanotubes (CNTs) have been accepted as a novel type of sensing material due to the combined advantage of the transition metal, which possesses good catalytic behavior for gas interaction, and CNTs, with large effective surface areas that present good adsorption ability towards gas molecules. In this work, we simulate the adsorption of $O_2$ and $O_3$ onto Rh-doped CNT in an effort to understand the adsorbing behavior of such a surface. Results indicate that the proposed material presents good adsorbing ability and capacities for these two gases, especially $O_3$ molecules, as a result of the relatively large conductivity changes. The frontier molecular orbital theory reveals that the conductivity of Rh-CNT would undergo a decrease after the adsorption of two such oxidizing gases due to the lower electron activity and density of this media. Our calculations are meaningful as they can supply experimentalists with potential sensing material prospects with which to exploit chemical sensors.

Comparison between BSCCO Thin Films Fabricated by Co-Deposition and Layer-by-Layer Deposition

  • Lee, Hee-Kab;Park, Yong-Pil;Lee, Joon-Ung
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2000.07a
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    • pp.230-234
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    • 2000
  • Bi$_2$Sr$_2$Ca$_{n}$Cu$_{n+1}$ O$_{y}$(n$\geq$0; BSCCO)thin film is fabricated via two different processes using an ion beam sputtering method i.e. co-deposition and layer-by-layer deposition. A single phase of Bi2212 can be fabricated via the co-deposition process. While it cannot be obtained by the layer-by-layer process. Ultra-law growth rate in our ion beam sputtering system brings out the difference in Bi element adsorption between the two processes and results in only 30% adsorption against total incident Bi amount by layer-by-layer deposition, in contrast to enough Bi adsorption by co-deposition.on.n.

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Removal of Toxic Pollutants from Aqueous Solutions by Adsorption onto Organo-kaolin

  • Sayed Ahmed, S.A.
    • Carbon letters
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    • v.10 no.4
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    • pp.305-313
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    • 2009
  • In this study, the adsorption of toxic pollutants onto cetyltrimethylammonium kaolin (CTAB-Kaolin) is investigated. The organo-kaolin is synthesized by exchanging cetyltrimethylammonium cations (CTAB) with inorganic ions on the surface of kaolin. The chemical analysis, the structural and textural properties of kaolin and CTAB-kaolin were investigated using elemental analysis, FTIR, SEM and adsorption of nitrogen at $-196^{\circ}C$. The kinetic adsorption and adsorption capacity of the organo-kaolin towards o-xylene, phenol and Cu(II) ion from aqueous solution was investigated. The kinetic adsorption data of o-xylene, phenol and Cu(II) are in agreement with a second order model. The equilibrium adsorption data were found to fit Langmuir equation. The uptake of o-xylene and phenol from their aqueous solution by kaolin, CTAB-kaolin and activated carbon proceed via physisorption. The removal of Cu(II) ion from water depends on the surface properties of the adsorbent. Onto kaolin, the Cu(II) ions are adsorbed through cation exchange with $Na^+$. For CTAB-kaolin, Cu(II) ions are mainly adsorbed via electrostatic attraction with the counter ions in the electric double layer ($Br^-$), via ion pairing, Cu(II) ions removal by the activated carbon is probably related to the carbon-oxygen groups particularly those of acid type. The adsorption capacities of CTAB-kaolin for the investigated adsorbates are considerably higher compared with those of unmodified kaolin. However, the adsorption capacities of the activated carbons are by far higher than those determined for CTAB-kaolin.

The Adsorption of Phosphate Son Using Hydroxyapatite synthesized by Wastewater Sludge of Semiconductor Fabrication Process (반도체 제조공정의 폐수슬러지로 합성된 Hydroxyapatite를 이용한 인산이온의 흡착)

  • 강전택;정기호;신학기
    • Journal of Environmental Science International
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    • v.11 no.3
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    • pp.257-262
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    • 2002
  • The hydroxyapatite(HAp) for the present study was prepared with the wastewater sludge from semiconductor fabrication process and it was crystallized in an electric furnace for 30 min at 90$0^{\circ}C$. The adsorption characteristics of HAp for phosphate ion in aqueous solution has been investigated. The adsorbed ratio of phosphate ion for HAp were investigated according to the reaction time, amount of HAp, concentration of standard solution, pH of solution, and influence of concomitant ions. The amount of adsorbed phosphate ion decreased with the increase of pH due to the mutual electrostatic repulsion between adsorbed phosphate ions and competitive adsorption between phosphate ion and OH- ion in aqueous solution. The maxium amount of the adsorption equilibrium for phosphate ion was about 24 mg/g of HAp. The HAp would likely to be a possible adsorbent for the removal of phosphate ion in the waste water.

Adsorption Thermodynamics of Polyamidoamide Epichlorohydrin Polymer in an Aqueous Fibrous Suspension (섬유 현탁액내 PAE 고분자 흡착의 열역학적 고찰)

  • Sung-Hoon Yoon;Kwang-Suk Joo;Tae-Won Lee;Kun-Han Kim;Byung-Bin Park
    • Journal of the Korean Chemical Society
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    • v.47 no.3
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    • pp.220-228
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    • 2003
  • This study was to examine the thermodynamic features of polyelecrolytic adsorption of polyamidoamine-epichlorohydrin(PAE) in a papermaking wet-end. The PAE adsorption experiments were conducted in a stirred jar containing an aqueous fibrous suspension and evaluated in terms of Langmuir and Freundlich parameters. The electrokinetic property of a stock was examined by measuring the zeta potential of each colloidal suspension. The polyelectrolytic PCD titration was employed to determine the adsorbed amounts of PAE polymer. The zeta potential of a stock, being varied significantly depending upon the addition of PAE polymer, showed initially a sharp increase and later an exponential decay as a function of time . The PAE adsorption exhibited a pseudo-Langmuir adsorption behavior at$20^{\circ}C$ , whereas its Freundlich power(v) increased in a proportional way at an elevated temperature. The train numbers calculated on the basis of adsorption thermodynamics were 7 to 8. The length of the extended loop of PAE was calculated as 215 nm at $20^{\circ}C$ and increased at a rate of 9% at every $10^{\circ}C$ rise in temperature. The PAE adsorption was proven to be an exothermic physisorption with the estimated adsorption enthalpy of -27 to -29 kJ/mol.

Adsorption Characteristics of Ni, Co and Ag Ions on The Cation Exchange Resin of Demineralization Process in Primary Coolant System of PWR (원자로 일차 냉각제 계통내 탈염공정의 양이온 교환수지상에서 니켈(Ni), 코발트(Co) 및 은(Ag) 이온의 흡착 특성)

  • Yang, Hyun S.;Kim, Young H.;Kang, Duck W.;Sung, Ki B.
    • Applied Chemistry for Engineering
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    • v.10 no.1
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    • pp.51-57
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    • 1999
  • Adsorption characteristics of Ni(II), Co(II) and Ag(I) ions on the Amberite IRN 77 cation exchange resin have been studied to suggest the guide-line for the optimum operation of demineralization process in primary coolant system during the shut-down period of pressurized water reactor(PWR). The adsorption mechanism of each metal ion, Ni(II), Co(II) or Ag(I) ion, on a cation exchange resin was well coincided with Langmuir isotherm. The adsorption and treatment capacities of $H^+$-form resin were higher than those of $Li^+$-form resin. In the continuous ion exchange process for the solution of multi-component system, the selectivity of the resin was in increasing order of Ni(II)${\approx}$Co(II)>Ag(I). In addition, the increase of the flow rate decreased the treatment capacity of the resin as well as the slope of the breakthrough curve.

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