• 한국산학기술학회논문지
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• 제17권8호
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• pp.23-30
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• 2016

본 연구에서는 길이 4.5 m와 7.5 m의 다중관 $CO_2$ 급탕 열교환기의 열전달 및 압력강하 특성을 ${\epsilon}-NTU$ 방법을 사용하여 해석하고 결과를 기존의 실험 데이터와 비교하였다. 급탕 열교환기는 쉘측에 물이 흐르고 8개로 구성된 내부 튜브에 $CO_2$를 흐르게 하였으며 열전달 효율을 최대화하기 위하여 대향류로 설계하였다. 각 노드에 대한 물과 $CO_2$ 냉매의 유동에 대한 에너지 평형 방정식은 단면분할법을 이용하여 해석하였다. 열전달율 계산값은 실험값과 ${\pm}5%$ 범위 내에서 잘 일치하였다. 반면에 물의 출구온도는 물 유량이 증가함에 따라 거의 선형적으로 감소하며 계산값과 실험값은 ${\pm}3%$ 내에서 일치하였다. 결과에서 열전달율은 4.5 m와 7.5 m 급탕 열교환기 모두 물 유량 또는 $CO_2$ 입구온도가 증가함에 따라 거의 선형적으로 증가하였으며, 반면에 물 유량이 증가함에 따라 물의 출구온도는 선형적으로 감소하였다. $CO_2$ 압력강하 계산값과 실험값은 $CO_2$가 고유량일 때 5 % 내에서 잘 일치한 반면에 $CO_2$가 저유량일 때 실험값이 약 20 % 높게 나타났다.

• 멤브레인
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• 제17권3호
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• pp.197-209
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• 2007

본 연구는 LNG를 연료로 사용하는 화력발전소 보일러에서 배출되는 1,000 $Nm^3/day$의 연소 배가스에 포함된 $8{\sim}10%$의 $CO_2$를 대상으로 순도 99%, 회수율 90%로 회수할 수 있는 실증규모의 다단계 막분리 공정에 관한 운전 결과이다. 이를 위해 본 연구팀에서는 가소화 안정성이 우수한 폴리이서설폰 중공사막을 개발하고 $CO_2/N_2$의 분리특성을 연구한바 있으며[1], 소형 모듈을 이용하여 압력 및 $CO_2$의 조성 변화에 따른 투과 특성을 실험과 향류 방식의 전산 모사를 통하여 확인하여 막분리에 의한 $CO_2$의 회수 가능성을 확인한 바 있다[2-4]. 이러한 선행 연구결과를 바탕으로 pilot 규모의 다단계 막분리 plant를 설계하여 제작, 설치, 운전하였으며 그 운전 결과를 다단계 공정의 수치 모사 결과와 비교하였다. 전체 공정은 크게 배출되는 배가스 내의 수분을 전단에서 제거하기 위한 제습 공정과 후단에 재순환이 가능한 4단계 막분리 공정으로 구성되어 있다. 4단 분리막 공정에서 배출되는 최종 $CO_2$의 농도는 운전 조건에 따라 $95{\sim}99%$의 $CO_2$가 $0.15{\sim}0.2$ ton/day의 회수율 $70{\sim}95%$회수규모로 얻어졌다. 얻어진 실험 결과는 수치 모사 결과와 비교하였을 때 매우 잘 일치 하는 것을 알 수 있었으며 운전 중 전체 공정은 안정적으로 작동하는 것을 확인할 수 있었다. 본 연구를 통해 다단계 막분리 공정을 통한 배가스에서 $CO_2$를 성공적으로 분리할 수 있었다.

• 자원리싸이클링
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• 제33권1호
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• pp.31-36
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• 2024

폐산화은 전지의 질산 침출액으로부터 Ag(산화상태)와 Zn(산화상태)의 분리를 위해 cyanex272를 추출제로 사용하여 용매추출 실험을 수행했다. Ag와 Zn의 추출은 질산과 추출제의 농도에 영향을 받았다. Cyanex272는 HNO₃ 농도가 0.1 mol/L보다 낮을 때 Ag보다 Zn을 선택적으로 추출되었다. 공동 추출된 Ag는 1 mol/L thiourea로 탈거하여 제거했다. Ag를 제거한 후 0.5 mol/L HNO₃를 사용하여 추출 된 Cyanex272에서 Zn을 탈거했다. Cyanex272를 사용한 Zn의 추출, thiourea를 사용한 Ag의 탈거, HNO₃를 사용한 Zn의 탈거에 대한 McCabe-Thiele 다이어그램이 각각 구성되었다. 위 결과는 시뮬레이션 된 계수 전류 추출 및 탈거 실험을 통해 검증되었다. 마지막으로 산화은 전지에서 Ag와 Zn을 분리하는 공정이 제안되었다.

• Membrane and Water Treatment
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• 제13권5호
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• pp.235-243
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• 2022

The paper presents the effect of operating temperatures and flow rates on the distillate flux that can be obtained from a hydrophobic membrane having the characteristics: pore size of 0.15 ㎛; thickness of 130 ㎛; and 85% porosity. That membrane in the present investigation could be the direct contact (DCMD) or the air-gap membrane distillation (AGMD). To model numerically the membrane distillation processes, the two-dimensional computational fluid dynamic (CFD) is used for the DCMD and AGMD cases here. In this work, DCMD and AGMD models have been validated with the experimental data using different flows (Parallel and Counter-current flows) in non-steady-state situations. A good agreement is obtained between the present results and those of the experimental data in the literature. The new approach in the present numerical modeling has allowed examining effects of the nature of materials (Polyvinylidene fluoride (PVDF) polymers, copolymers, and blends) used on thermal properties. Moreover, the effect of the area surface of the membrane (0.021 to 3.15 ㎡) is investigated to explore both the laminar and the turbulent flow regimes. The obtained results found that copolymer P(VDF-TrFE) (80/20) is more effective than the other materials of membrane distillation (MD). The mass flux and thermal efficiency reach 193.5 (g/㎡s), and 83.29 % using turbulent flow and an effective area of 3.1 ㎡, respectively. The increase of feed inlet temperatures and its flow rate, with the reduction of cold temperatures and its flow rate are very effective for increasing distillate water flow in MD applications.

• Membrane and Water Treatment
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• 제1권3호
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• pp.171-179
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• 2010

The transport of selected salts of sulphuric acid (cobalt, copper, iron(II), manganese, nickel and zinc sulphate) through an anion-exchange membrane Neosepta-AFN was investigated in a counter-current continuous dialyzer at various salt concentrations and volumetric liquid flow rates. The basic transport characteristics - the rejection coefficient of salt and the permeability of the membrane - were calculated from measurements at steady state. The salt concentration in model mixtures was changed in the limits from 0.1 to 1.0 kmol $m^{-3}$ and the volumetric liquid flow rate of the inlet streams was in the limits from $8{\times}10^{-9}$ to $24{\times}10^{-9}m^3\;s^{-1}$. Under the experimental conditions given, the rejection coefficient of salts tested was in the range from 65% to 94%. The lowest values were obtained for iron(II) sulphate, while the highest for copper sulphate. The maximum rejection of salt was reached at the highest volumetric liquid flow rate and the highest salt concentration in the feed. The permeability ($P_A$) of the Neosepta-AFN membrane for the individual salts was in the range from $0.49{\times}10^{-7}m\;s^{-1}$ to $1.8{\times}10^{-7}m\;s^{-1}$ and it can be described by the following series: $P_{FeSO_4}$ < $P_{NiSO_4}$ < $P_{ZnSO_4}$ < $P_{CoSO_4}$ < $P_{MnSO_4}$ < $P_{CuSO_4}$. The permeability of the membrane was strongly affected by the salt concentration in the feed - it decreased with an increasing salt concentration.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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• pp.89.1-89.1
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• 2010

Since Gratzel and co-workers developed a new type of solar cell based on the nanocrystalline $TiO_2$ electrode, dye-sensitized solar cells (DSSCs) have attracted considerable attention on account of their high solar energy-to-conversion efficiencies (11%), their easy manufacturing process with low cost production compared to conventional p-n junction solar cells. The mechanism of DSSC is based on the injection of electrons from the photoexcited dye into the conduction band of nanocrystalline $TiO_2$. The oxidized dye is reduced by the hole injection process from either the hole counter or electrolyte. Thus, the electronic structures, such as HOMO, LUMO, and HOMO-LUMO gap, of dye molecule in DSSC are deeply related to the electron transfer by photoexcitation and redox potential. To date, high performance and good stability of DSSC based on Ru-dyes as a photosensitizer had been widely addressed in the literatures. DSSC with Ru-bipyridyl complexes (N3 and N719), and the black ruthenium dye have achieved power conversion efficiencies up to 11.2% and 10.4%, respectively. However, the Ru-dyes are facing the problem of manufacturing costs and environmental issues. In order to obtain even cheaper photosensitizers for DSSC, metal-free organic photosensitizers are strongly desired. Metal-free organic dyes offer superior molar extinction coefficients, low cost, and a diversity of molecular structures, compared to conventional Ru-dyes. Recently, novel photosensitizers such as coumarin, merocyanine, cyanine, indoline, hemicyanine, triphenylamine, dialkylaniline, bis(dimethylfluorenyl)-aminophenyl, phenothiazine, tetrahydroquinoline, and carbazole based dyes have achieved solar-to-electrical power conversion efficiencies up to 5-9%. On the other hand, organic dye molecules have large ${\pi}$-conjugated planner structures which would bring out strong molecular stacking in their solid-state and poor solubility in their media. It was well known that the molecular stacking of organic dyes could reduce the electron transfer pathway in opto-electronic devices, significantly. In this paper, we have studied on synthesis and characterization of dendritic organic dyes with different number of electron acceptor/anchoring moieties in the end of dendrimer. The photovoltaic performances and the incident photon-to-current (IPCE) of these dyes were measured to evaluate the effects of the dendritic strucuture on the open-circuit voltage and the short-circuit current.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2011년도 춘계학술대회 초록집
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• pp.117.2-117.2
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• 2011

Since Gratzel and co-workers developed a new type of solar cell based on the nanocrystalline TiO2 electrode, dye-sensitized solar cells (DSSCs) have attracted considerable attention on account of their high solar energy-to-conversion efficiencies (11%), their easy manufacturing process with low cost production compared to conventional p-n junction solar cells. The mechanism of DSSC is based on the injection of electrons from the photoexcited dye into the conduction band of nanocrystalline TiO2. The oxidized dye is reduced by the hole injection process from either the hole counter or electrolyte. Thus, the electronic structures, such as HOMO, LUMO, and HOMO-LUMO gap, of dye molecule in DSSC are deeply related to the electron transfer by photoexcitation and redox potential. To date, high performance and good stability of DSSC based on Ru-dyes as a photosensitizer had been widely addressed in the literatures. DSSC with Ru-bipyridyl complexes (N3 and N719), and the black ruthenium dye have achieved power conversion efficiencies up to 11.2% and 10.4%, respectively. However, the Ru-dyes are facing the problem of manufacturing costs and environmental issues. In order to obtain even cheaper photosensitizers for DSSC, metal-free organic photosensitizers are strongly desired. Metal-free organic dyes offer superior molar extinction coefficients, low cost, and a diversity of molecular structures, compared to conventional Ru-dyes. Recently, novel photosensitizers such as coumarin, merocyanine, cyanine, indoline, hemicyanine, triphenylamine, dialkylaniline, bis(dimethylfluorenyl)-aminophenyl, phenothiazine, tetrahydroquinoline, and carbazole based dyes have achieved solar-to-electrical power conversion efficiencies up to 5-9%. On the other hand, organic dye molecules have large ${\pi}$-conjugated planner structures which would bring out strong molecular stacking in their solid-state and poor solubility in their media. It was well known that the molecular stacking of organic dyes could reduce the electron transfer pathway in opto-electronic devices, significantly. In this paper, we have studied on synthesis and characterization of dendritic organic dyes with different number of electron acceptor/anchoring moieties in the end of dendrimer. The photovoltaic performances and the incident photon-to-current (IPCE) of these dyes were measured to evaluate the effects of the dendritic strucuture on the open-circuit voltage and the short-circuit current.

• Journal of Chest Surgery
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• 제16권2호
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• pp.213-220
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• 1983

Pulmonary function is the determinant of blood gas tension. However, Acid-Base disturbances can also alter partial pressures of oxygen and carbon dioxide in arterial blood. During respiratory acidosis $PO_2$ will be lowered and reverse changes will be produced during respiratory alkalosis. On the other hand, in metabolic acidosis $PO_2$ will be elevated and $PCO_2$ will be lowered by the respiratory compensation, and reverse response will be induced in metabolic alkalosis. Urinary gas tension has many influencing factors than arterial blood and difficult to estimate the tendency of its alterations. Urinary $PO_2$ and $PCO_2$ are not always identical level as venous blood. It is to be altered by blood gas tension, flow rate of urine, metabolic rate of kidney, and Acid-Base status of blood. Particularly countercurrent exchange of oxygen and carbon dioxide in the renal medulla will make larger alteration of gas tension than venous blood. After induction of Acid-Base disturbances [disturbances] arterial and urinary $PCO_2$, $PO_2$, urinary volume, and osmolarity were determined in dogs, and the relationships between arterial and urinary $PCO_2$ , $PO_2$ Acid-Base disturbances, urinary volume, and osmolarity were investigated. 1. During the acute Metabolic and Respiratory disturbances urinary pH did not respond on respiratory origin. However, there were immediate urinary response in pH on metabolic origin. 2. Urinary $PO_2$, $PCO_2$, did not always follow arterial or venous gas tension and Acid-Base disturbance. Urinary $PCO_2$, correlate well with the urinary volume. The larger the urinary volume, $PCO_2$ lowered to the venous level. The smaller the urinary volume, urinary $PCO_2$ tends to be higher. However urinary $PO_2$ did not have any particular correlation with urinary volume. 3. Correlation between urinary $PCO_2$ and $PO_2$ were inversely proportional to arterial blood. Differences of $PCO_2$ between arterial blood and urine also did not have any particular correlation with urinary volume. This may suggest that changes on blood gas tensions can influence on urinary $PCO_2$. 4. There were eminent clear inverse correlation between urinary $PCO_2$ and osmolar concentrations of urine. Above results strongly suggest that partial pressure of gas in urine primarily depend upon counter-current exchanges in renal medullary tissues.

• Bulletin of the Korean Chemical Society
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• 제14권6호
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• pp.687-691
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• 1993

Complexation of $Cd^{2+},\;Pb^{2+}\;and\;Hg^{2+}$ ions with four cryptands were studied by potentiometry and solution calorimetry in various weight percent methanol-aqueous solvent at 25${\circ}$C under $CO_2$free nitrogen atmosphere. The stabilities of the complexes were dependent on the cavity size of macrocycles. The $Hg^{2+}$ ion stability constants are higher than those of $Cd^{2+}\;and\;Pb^{2+}$ ion. All the cryptands formed complexes having 1 : 1 (metal to ligand) mole-ratio except for $Hg^{2+}-L_1$ (cryptand 1,2b: 3,5-benzo-9,14,17-trioxa-1,7-diazabicyclo-(8,5,5) heptadecane) and $Cd^{2+}-L_2$ (cryptand 2,2b: 3,5-benzo-10,13,18,21-tetraoxa-1,7-diazabicyclo (8,5,5) eicosane) complexes. $Hg^{2+}-L_1$ complex was a sandwitch type, and the $Cd^{2+}-L_2$ complex showed two stepwise reactions. Thermodynamic parameters of the $Cd^{2+}-L_2$ complex were $6.08(log\;K_1)$, -7.28 Kcal/mol $({\Delta}H_1)$, and $4.78\;(log\;K_2)$, -4.62 Kcal/mol $({\Delta}H_2)$, respectively, for 1 : 1 and 2: 1 mole-ratio. The sequences of the selectivity were increased in the order of $Hg^{2+}\;>Pb^{2+}\;>Cd^{2+}$ ion for $L_3\;and\;L_4$ macrocycles, and the $L_2$-macrocycle has a selectivity for $Cd^{2+}$ ion relative to $Zn^{2+},\;Ni^{2+},\;Pb^{2+}\;and\;Hg^{2+}$ ions. Thus, it is expected that the $L_2$ can be used as carrier for seperation of the post transition metals by macrocycles-mediated liquid membrane because $L_2$ is not soluble in water, and the difference of stability constants of the metal complexes with $L_2$ are large as compared with the other transition metal complexes. The $^1H\;and\;^{13}C-NMR studies indicated that the nitrogen atoms of cryptands have greater affinity to the post transition metal ions than the oxygen atoms, and that the planarities of the macrocycles were lost by complexation with the metal ions because of the perturbation of ring current of benzene molecule attached to macrocycles and counter-anions.

• 디지털융복합연구
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• 제19권9호
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• pp.189-199
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• 2021

국내 제로에너지건축물 의무화를 대응하기 위해서 신재생에너지 자립률을 높이려면 고층 건물일수록 대지면적에 한계가 있고 옥상에 PV모듈을 설치하는 것만으로는 부족하다. 따라서 제로에너지건축물을 실현할 수 있는 핵심 에너지원으로 BIPV(Building Integrated PhotoVoltaic, 이하 BIPV)는 가장 주목받는 산업이다. 이에 본 연구는 BIPV 산업의 올바른 방향 제시와 활성화룰 위해 설계자, 시공자, 제품 제조자, 유지관리자 등 경력 10년 이상 전문가를 대상으로 BIPV 산업의 문제점을 자율 토론 방식으로 설문 조사를 시행하였다. BIPV 적용의 산업적 문제점으로는 제품 인증을 위한 표준 및 인증기준의 범위 확대, 다품종 소량 생산의 현황을 고려한 인증범위 개선, 컬러 모듈과 루버 모듈 및 지붕형 제품을 수용할 수 있는 표준 개정 필요성, 인증제품 의무화를 통한 외산 모듈의 국내 유입 차단의 필요성, BIPV 제품 정보 획득의 어려움, BIPV의 건축 적용 부위 등에 대한 정확한 가이드라인으로 참여자간의 혼란 야기 방지 필요, BIPV 정의의 명확한 정립과 지원 정책이나 제도가 부족하다는 문제들을 도출하였다. 이에 본 연구는 산업계에서 바라보는 시장 변화와 영향을 주고 있는 요소, 경쟁력 강화를 위한 필요한 개선 사항을 바탕으로 대응 방안과 방향성을 제시하고 제안하는데 그 목적이 있다.