• 제목/요약/키워드: Balance adsorption

검색결과 34건 처리시간 0.023초

실리카겔을 이용한 흡착식 담수화 시스템의 기초연구 (Development of Adsorption Desalination System Utilizing Silica-gel)

  • 현준호;김영민;정진호;이윤준;천원기
    • 한국태양에너지학회:학술대회논문집
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    • 한국태양에너지학회 2011년도 춘계학술발표대회 논문집
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    • pp.204-209
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    • 2011
  • According to the environment report of UN, korea was classified as potable water shortage countries. Approximately 71% of the Earth's surface is covered by ocean. However, it is difficult to use for industry of residential purpose without a certain processing. The development of solar and waste-heat used absorption desalination technology have been examined as a viable option for supplying clean energy. In this study, the modelling of the main devices for solar and waste-heat used and adsorption desalination system was introduced. The design is divided into three parts. First, the evaporator for the vaporization of the top water is designed, and then the reactor for the adsorption and release of the steam is designed, followed by the condenser for the condensation of the fresh water is designed. In addition, new features based on the energy balance are also included to design absorption desalination system. In this basicresearch, One-bed(reactor) adsorption desalination plant that employ a low-temperature solar and waste energy was proposed and experimentally studied. The specific water yield is measured experimentally with respect to the time controlling parameters such as heat source temperatures, coolant temperatures, system switching and half-cycle operational times.

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Experimental Investigation and Quantum Chemical Calculations of Some (Chlorophenyl Isoxazol-5-yl) Methanol Derivatives as Inhibitors for Corrosion of Mild Steel in 1 M HCl Solution

  • Sadeghzadeh, Rogayeh;Ejlali, Ladan;Eshaghi, Moosa;Basharnavaz, Hadi;Seyyedi, Kambiz
    • Corrosion Science and Technology
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    • 제18권5호
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    • pp.155-167
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    • 2019
  • In this study, two novel Schiff base compounds including (3-(4-Chlorophenyl isoxazole-5-yl) methanol and (3-(2,4 dichlorophenol isoxazole-5-yl) methanol as corrosion inhibitors for mild steel in 1 M hydrochloric acid solution were investigated by potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and density functional theory (DFT) computations. The results showed that the corrosion inhibition efficiency (IE) is remarkably enhanced with the growing concentration of the Schiff base inhibitors. The results from Tafel polarization and EIS methods showed that IE decreases with gradual increments of temperature. This process can be attributed to the displacement of the adsorption/desorption balance and hence to the diminution of the level of a surface coating. Also, the adsorption of two inhibitors over mild steel followed the Langmuir adsorption isotherm. Too, the results of the scanning electron microscope (SEM) images showed that the Schiff base inhibitors form an excellent protective film over mild steel and verified the results by electrochemical techniques. Additionally, the results from the experimental and those from DFT computations are in excellent accordance.

메탄가스 분리용 탄소분자체 특성 연구 (Characterization of Carbon Molecular Sieve for Separating CH4 Gas)

  • 이범석;김택남;김윤종
    • 한국재료학회지
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    • 제14권2호
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    • pp.157-162
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    • 2004
  • The object of this research is to develop a carbon molecular sieve(below CMS) which can separate selectively to convert mixture gases spout at waste landfill into fuel. And this research is meaningful from the viewpoint of a quality improvement of CH$_4$ gas and an utilization of by-product. CMS was prepared using coconut shell powder as starting material and the effects of activators, temperature and modifier on the reaction were investigated in this research. Also, pore diameter, surface area of CMS and adsorption rate were measured and studied by cahn balance and ASAP2010. Its specific surface area and pore distribution were controlled easily at 800^{\circ}C and adsorption rate was very good. The CMS prepared in this research is shown to be able to separate landfill gases very effectively.

미생물 활성토탄을 이용한 암모니아 제거에 관한 연구 (A Study on the Removal of Ammonia by Using Peat Biofilter)

  • 정연규;안준성
    • 대한토목학회논문집
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    • 제14권3호
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    • pp.655-668
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    • 1994
  • 기존의 토양상 및 퇴비상을 이용한 악취제거가 주로 흡착에 의존한 나머지 탈취상이 쉽게 탈취능의 한계에 이른다. 따라서, 본 연구에서는 미생물 활성 탈취상의 조건인 높은 유기물함량, 보수성, 통기성 및 낮은 정압 등을 고르게 갖추고 있는 토탄에 활성슬러지를 식종하여 분뇨처리장, 하수처리장 등에서 발생빈도 및 취기강도가 큰 무기성악취 중 암모니아의 제거실험을 수행하였다. 실험결과, 자연 토탄상에서는 암모니아의 토탄수분에 의한 이온화에 따라서 pH가 상승하여 암모니아의 자연 유출 현상이 관찰되었다. 암모니아 제거 기작은 주로 음이론 콜로이드에 의한 흡착에 의존하였다. 미생물 활성 토탄상에서는 미생물 활동에 따른 pH의 완만한 상승으로 이론적 암모늄 이온의 비율이 자연토탄상보다 높았으나, 실제로 토탄상에 축적된 암모니아성 질소의 값은 질산균의 질산화에 의해 자연 토탄상보다 적었다. 암모니아의 제거기작은 반응조 운영 초기에는 흡착이 우세하였으며, 중반이후에는 질산화가 두드러졌다. 실험으로 얻은 암모니아 유입부하량, 암모니아 유출부하량, $NH_4{^+}$-N, $NO_x$-N, Org-N을 이용하여 질소에 대한 물질수지(Mass Balance)를 산정하고, 실험결과로 얻은 미생물 활성 탈취상의 최대 활성 시점인 비정상상태의 임계시간과 회귀분석에 의해 구한 암모니아의 흡착곡선을 이용하여 미생물 활성 토탄상에서 흡착능 포화의 연장시간을 산정하였다.

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고도 정수처리장에서의 과불화합물 거동 (Behavior of perfluorinated compounds in advanced water treatment plant)

  • 임채승;김형준;한개희;김호;황윤빈;김극태
    • 상하수도학회지
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    • 제34권5호
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    • pp.323-334
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    • 2020
  • Adsorption by granule activated carbon(GAC) is recognized as an efficient method for the removal of perfluorinated compounds(PFCs) in water, while the poor regeneration and exchange cycles of granule active carbon make it difficult to sustain adsorption capacity for PFCs. In this study, the behavior of PFCs in the effluent of wastewater treatment plant (S), the raw water and the effluents of drinking water treatment plants (M1 and M2) located in Nakdong river waegwan watershed was monitored. Optimal regeneration and exchange cycles was also investigated in drinking water treatment plants and lab-scale adsorption tower for stable PFCs removal. The mean effluent concentration of PFCs was 0.044 0.04 PFHxS g/L, 0.000 0.00 PFOS g/L, 0.037 0.011 PFOA g/L, for S wastewater treatment plant, 0.023 0.073 PFHxS g/L, 0.000 0.00 PFOS g/L, 0.013 0.008 PFOA g/L for M1 drinking water treatment plant and 0.023 0.073 PFHxS g/L, 0.000 0.01 PFOS g/L, 0.011 0.009 PFOA g/L for M2 drinking water treatment plant. The adsorption breakthrough behaviors of PFCs in GAC of drinking water treatment plant and lab-scale adsorption tower indicated that reactivating carbon 3 times per year suggested to achieve and maintain good removal of PFASs. Considering the results of mass balance, the adsorption amount of PFCs was improved by using GAC with high-specific surface area (2,500㎡/g), so that the regeneration cycle might be increased from 4 months to 10 months even if powdered activated carbon(PAC) could be alternatives. This study provides useful insights into the removal of PFCs in drinking water treatment plant.

Dynamics of Hydrogen on Si (100)

  • Boland, John J.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2000년도 제18회 학술발표회 논문개요집
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    • pp.25-25
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    • 2000
  • In this talk we discuss the dynamics of hydrogen on the Si(100)-2xl surface. At room temperature the sticking coefficient for molecular hydrogen on this surface is less than 10sup-12. However, hydrogen molecules desorbing from the surface do not have an excess of energy, suggesting at best a small barrier on the exit channel. These observations have led to speculation about the validity of detailed balance in this system. Here we show that this discrepancy can be explained by considering both the surface-molecule co-ordinate and that associated with the Si-Si dimer bond tiltangle. By preparing the surface dimers with a specific tiltangle we demonstrate that the barrier to adsorption is a function of this angle and that the sticking coefficient dramatically increase for certain angles. The adsorption-desopption dynamics can then be described in terms of a common potential energy hypersurface involving both of these co-ordinates. The implications of these observations are also discussed. The dynamics of adsorbed hydrogen atoms on the Si(100) surface is also described. Paired dangling bonds produced following recombinative hydrogen desorption are mobile at elevated temperatures. Pairs of dangling bonds are observed to dissociate, diffuse, and ultimately recombine. At sufficiently elevated temperatures dangling bond exchange reactions are observed. These data are analyzed in terms of an attractive zone and an effective binding interaction between dangling bonds. Insights that this provides into the nature of surface defects and the localized chemistry that occurs on this surface, are also discussed.

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화학축냉용 무기염들의 수화반응 및 열 및 물질전달 향상방안 (Study of Hydration Reaction Characteristics of Inorganic Salts for Chemical Cold Storage and Method of Enhancement of Heat and Mass Transfer)

  • 김상욱;한종훈;황용준;이건홍
    • 한국에너지공학회:학술대회논문집
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    • 한국에너지공학회 1999년도 춘계 학술발표회 논문집
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    • pp.185-191
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    • 1999
  • An air-conditioning system based on the chemical heat storage principle was considered. $H_2O$ was chosen as the reaction gas and the working fluid as well. Na$_2$S, CaCl$_2$, MnCl$_2$, BaCl$_2$, MgCl$_2$, Fe$_2$(SO$_4$)$_3$ and MnSO$_4$ were tested as the solid reactants by using Cahn pressure balance. Na$_2$S was superior to other salts in respect of high capability of absorption of water gas, 5 moles of $H_2O$ per unit mole of Na$_2$S, and adequate temperature of adsorption, $65^{\circ}C$ at 7torr, and of desorption, 13$0^{\circ}C$ at 76torr. Clausius-Clapeyron diagram of Na$_2$S was obtained via adsorption experiments at several vapor pressures of water gas. To enhance heat and mass transfer characteristics, usually below 1W/m K, of the reactor bed of general adsorption systems, expanded graphite block was adapted as the support of Na$_2$S salt. Expanded graphite blocks had thermal conductivity values of 20~80W/mK with respect to 100~400kg/㎥ of block bulk density. Permeability values of expanded graphite blocks were 10$^{-13}$ ~ 10$^{-14}$ $m^2$ with respect to 100~300kg/㎥ of block bulk density showing highly decreasing values of permeability, below 10$^{-l4}$$m^2$, in the range of above 150kg/㎥ of block bulk density.y.

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석탄가스의 초정밀 정제를 위한 변형된 활성탄의 흡착특성 연구 (The Adsorption of COS with a Modified-Activated Carbon for Ultra-Cleanup of Coal Gas)

  • 이유진;박노국;이태진
    • 청정기술
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    • 제13권4호
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    • pp.266-273
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    • 2007
  • 본 연구에서는 석탄가스화 복합발전시스템용 고온건식탈황공정에 포함된 직접황회수공정의 $SO_2$ 촉매환원 반응에서 발생되는 COS의 효과적인 제거를 위한 활성탄계 흡착제의 흡착특성이 연구되었다. $SO_2$의 촉매적 환원을 위하여 전이금속 담지촉매와 복합금속산화물 촉매가 사용되었으며, 이들 촉매의 반응기구에 따라 COS 생성과정과 반응온도에 따른 유출량이 조사되었다. 생성된 저농도의 COS를 효과적으로 제거하기 위하여 상용활성탄과 활성탄의 COS흡착특성을 개선하기 위하여 알칼리금속 수용액(KOH)으로 담지시킨 활성탄이 이용되었다. TGA를 이용하여 온도에 따른 COS 흡착량과 흡착속도를 알 수 있었고, GC-PFPD가 장착된 고정층 흡착시스템을 이용하여 COS 흡착실험을 수행한 결과, 높은 BET 표면적을 지니는 KOH로 처리된 활성탄의 COS 파과시간이 상용활성탄에 비해 장시간 유지되었다. 이와 같은 결과로부터 활성탄 흡착시스템으로 $SO_2$ 환원으로부터 생성되는 COS를 효과적으로 제거할 수 있으며, 알칼리성 금속을 담지할 경우 흡착특성이 향상됨을 확인할 수 있었다.

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한국 성인 여자의 칼슘과 인 평형에 관한 연구 (A Study on Ca and P Balance in Koran Adult Women)

  • 유춘희;김희선;이정숙;김정윤
    • Journal of Nutrition and Health
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    • 제34권1호
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    • pp.54-61
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    • 2001
  • The Ca and P balance studies were carried out with two different diets varying Ca levels : the current Korean RDA level(normal Ca diet) and the high level (High Ca diet) which was determined by adding 2SD to mean Ca intake of all subjects. The subjects were sever healthy adult woman, aged from 25 to 32 years old. The metabolic studies were conducted for two weeks with a days recess in between : during the fist week with normal Ca diet and during the second week with high Ca diet. The composition of nutrients excepting Ca of both diets was similar to subjects usual intake. The result were summarized as follows: Mean daily Ca intake was 728.8mg from norma Ca diet and 945.5mg from high Ca diet. Fecal excretion of Ca increased significantly(p<0.05) on high Ca diet, but urinary excretion of Ca did not show any differences between the two diet periods. There were also no significant differences in Ca retention between the two diet periods but it tended to be greater during high Ca diet period: 112.1mg/day during normal Ca diet period vs 208.2mg/day during high Ca diet period. Mean apparent Ca absorption was 41.2% on normal Ca diet and 42.1% on high Ca diet, indicating it was not affected by high Ca intake level used in this study. On the contrary, P retention was significantly increased up to 109.4mg/day with high Ca diet as compared to- 41mg/day with normal Ca diet. There were no significant differences in fecal and urinary excretion of P but those to be lower during high Ca diet period. The above results showed that higher Ca intake more than current RDA(700mg/day), in the level of 945.5mg/day, could increase Ca retention through Ca absorption comparable to the rate appeared on RDA level intake. P retention was also improved by high Ca intake. Therefore, higher Ca intake than the current RDA level seemed to produce favorable effects on bone health in adult women. However, the current RDA level seemed to be relatively appropriate, considering the results that all the subjects but one maintained positive Ca balance with normal Ca diet. (Korean J Nutrition 34(1):54-61, 2001)

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컴팩트 타입 실리카막 공정을 이용한 수소 분리 (Hydrogen Separation by Compact-type Silica Membrane Process)

  • 문종호;배지한;이상진;정종태;이창하
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2006년도 추계학술대회
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    • pp.336-339
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    • 2006
  • With the steady depletion off fossil fuel reserves, hydrogen based energy sources become increasingly attractive. Therefore hydrogen production or separation technologies, such as Bas separation membrane based on adsorption technology, have received enormous attention in the industrial and academic fields. In this study, the transport mechanisms of the MTES (methyltriethoxysilane) templating silica/a-alumina composite membrane were evaluated by using unary, binary and quaternary hydrogen gas mixtures permeation experiments at unsteady- and steady-states. Since the permeation flux in the MTES membrane, through the experimental and theoretical study, was affected by molecular sieving effects as well as surface diffusion properties, the kinetic and equilibrium separation should be considered simultaneously in the membrane according to molecular properties. In order to depict the transient multi-component permeation on the templating silica membrane, the GMS (generalized Maxwell-Stefan) and DGM (dust Bas model) were adapted to unsteady-state material balance

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