• Title/Summary/Keyword: 이온당량

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Effect of Nation binder with different equivalent weight on cell performance (이온당량(EW)이 다른 Nafion binder가 고분자 전해질 연료전지의 성능에 미치는 영향)

  • Kim, Kun-Ho;Kim, Hyoung-Juhn;Lim, Tae-Hoon;Lee, Kwan-Young
    • 한국신재생에너지학회:학술대회논문집
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    • 2007.11a
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    • pp.129-132
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    • 2007
  • 고분자 전해질 연료전지의 성능에 영향을 주는 많은 인자들 중에서도 촉매층의 조성과 구조의 최적화는 성능변화에 큰 요인으로 작용 된다. 촉매층내 반응 활성점인 삼상계면을 형성시키기 위해 함침하는 Nafion binder를 anode와 cathode의 두 전극에 이온당량(Equivalent weight, EW)이 동일하게 함침시켜 그 성능을 확인하였다. 그 결과를 토대로 anode와 cathode에 이온당량을 각기 다르게 하여 각각의 전극마다 이온당량이 미치는 영향에 대해서도 살펴보았다. Anode와 cathode의 이온당량을 동일하게 EW1100, EW1000, EW900으로 변화 시켜주었을 경우 이온당량의 물성치가 상대적으로 향상된 EW900의 단위 전지 성능이 가장 우수하였으며, 이온당량이 EW900이었을 때 최적의 Nafion binder 함침량은 EW1100의 Nafion binder 함침량과 동일하였다. Anode와 cathode에 함침하는 Nafion binder의 이온당량을 각각 EW1100과 EW900, EW900과 EW1100으로 MEA를 제조하여 전극에 따라 이용당량이 미치는 영향을 살펴보았다.

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Solvation Number and Selective Solvation of Ions in Water-Methanol Systems (물-메탄올 混合溶媒中에서 이온들의 溶媒和數와 選擇的 溶媒和)

  • Jong-Jae Chung;Hag-Sung Kim
    • Journal of the Korean Chemical Society
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    • v.37 no.3
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    • pp.309-316
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    • 1993
  • The limiting equivalent ionic conductances of Li$^+$, Na$^+$, K$^+$, Cl$^-$, and Br$^-$ ions were obtained with TATB[Tetraphenyl Arsonium Tetraphenyl Borate] method from limiting equivalent conductances of LiCl, NaCl, KCl and KBr measured in water-methanol systems by conductometric method. With those values and viscosity of water-methanol systems, the Stokes radii of corresponding ions have been extracted. The latter values corrected by calibration method of Nightingale and supplemented by the crystallographic radii were utilized to calculate the volume of solvation-shell that surrounds ions. The reasonable solvation numbers (h$_{H_2O}$ + h$_0$) were estimated by comparing the values obtained by the various suggested methods. The selective properties of ion solvation were also discussed.

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Selective Solvation and Reasonable Solvation Number of Some Univalent Ions in Water-Ethanol Systems (물-에탄올 混合溶媒에서 몇가지 1가 이온들의 選擇的 溶媒和와 妥當한 溶媒和數)

  • Kim, Hag-Sung
    • Journal of the Korean Chemical Society
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    • v.39 no.8
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    • pp.589-597
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    • 1995
  • In water-ethanol systems, the limiting equivalent conductances of electrolytes were obtained using conductometric method. Using TATB method, the limiting equivalent ionic conductances of Li+, Na+, K+, Cl-, and Br- ions were also obtained. The effective radii of corresponding ions were determined using Nightingale method. From the volume of the solvation shell, the four solvation numbers were suggested. The reasonable solvation numbers (hH2O+hO) were estimated by comparing the values obtained by from the various suggested methods. The isosolvation point of ion in water-ethanol estimated was found to be larger than that of in water-methanol. This result agree with ET (solvent polarity) values of solvents. From the reasonable solvation numbers of ions in water-ethanol, the selective solvents of corresponding ions in water-ethanol were obtained.

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Precise Control of Nutrient Solution and Analysis of Ionic Contribution to EC Reading (양액의 정밀 제어 및 이온의 EC 기여도 분석)

  • Son, Jung-Eek
    • Horticultural Science & Technology
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    • v.16 no.3
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    • pp.352-354
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    • 1998
  • A soilless culture system with the precise control of nutrient solution was developed and the time changes of ionic contribution to EC reading was analyzed. The measuring device designed was able to wash electrodes cleanly and to measure the pH and EC of nutrient solution stably in the box. The nutrient supply system using metering device was also able to control the EC and pH within ${\pm}0.05mS/cm$ and ${\pm}0.05$, respectively. Under the EC control, activity coefficients of all ions decreased with time as ionic concentrations of $SO_4$, Mg and Ca increased due to the selective nutrient absorption by plants. Time changes of ionic contribution to EC reading could be calculated using equivalent ionic conductivities and activity coefficients obtained by numerical analysis.

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Ion Exchange Modeling with Mass Action Law and Surface Complexation Models (질량작용법칙과 표면착화모델을 이용한 이온교환 모델링)

  • 이인형;안현경;김상대
    • Proceedings of the KAIS Fall Conference
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    • 2003.06a
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    • pp.322-324
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    • 2003
  • 이온교환은 액체상에 존재하는 이온과 고체상에 존재하는 이온이 당량적으로 치환되는 것으로 정의하며, 치환되는 정도는 일반적으로 전하의 크기와 이온이 수화반경에 따라 달라진다. 지금까지의 이온교환 반응에 대한 모델링 연구는 실험식, 질량작용식, 열역학식, 전기이중층이론, 표면착화모델 등을 이용하여 2 성분에 대하여 다양한 시도를 하였다. 본 연구에서는 2, 3, 4성분에 대해 질량작용법칙과 전기이중층이론을 조합한 표면착화모델과 질량작용법칙을 이용한 모델을 수행하였다. 그 결과 표면착화모델이 질량작용법칙을 이용한 것보다 실험치와 일치함을 알 수 있었다.

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Study on Flooding Phenomena at Various Stoichiometries in Transparent PEM Unit Fuel Cell (PEM 단위 연료전지 가시화 셀을 이용한 당량비 변화에 따른 플러딩 현상에 관한 연구)

  • Nam, Ki-Hoon;Byun, Jae-Ki;Choi, Young-Don
    • Transactions of the Korean Society of Mechanical Engineers B
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    • v.36 no.6
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    • pp.625-632
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    • 2012
  • The objective of this paper is to demonstrate the cathode channel flooding effects at different stoichiometries in proton exchange membrane (PEM) fuel cells by using visualization techniques. The phenomena of liquid water formation and removal caused by current variations were also examined experimentally. Tests were conducted at cathode stoichiometries of 1.5 and 2.0, and the anode stoichiometry was fixed at 1.5. It is found that at an air-side stoichiometry of 2.0, liquid water begins to form and the flooding occurs faster than at an air-side stoichiometry of 1.5. Also, when the air-side stoichiometry of 1.5 is maintained, the dry-out phenomena is observed in the dry-out area 7.8 A following the field of flooding. Thus, a stoichiometry of 1.5 produced better performance in terms of membrane electrode assembly (MEA) durability and hydrogen ion conductivity than did a stoichiometry of 2.0, in which dry-out occurs beyond 8A.

The Effects of Iron Powder Agglomeration on the Copper Removal Efficiency during Cementation Process for Treating Mine Drainages (광산배수 처리를 위한 세멘테이션 공정 중 구리제거효율에 대한 철분 응집의 영향)

  • Na, Hyunjin;Eom, Yuik;Hong, Seunggwan;Yoo, Kyoungkeun
    • Resources Recycling
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    • v.28 no.5
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    • pp.74-79
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    • 2019
  • The effects of equivalent of iron powder, particle size, agitation speed on the removal efficiency of copper ion were investigated by adding iron powder as cementation agents to simulated mine drainage solution with 117.15 mg/L Cu ion. The 50 % of Cu was removed at 90 min with 2 equivalent of iron powder while more than 99 % of Cu was removed at 60 min with 16 equivalent at 200 rpm and $20^{\circ}C$. The removal efficiencies of Cu ion were not different using 2 equivalent of $48{\mu}m$ and $150{\mu}m$ iron powder, and the removal efficiency increased rapidly with increasing the agitation speed to more than 400 rpm. This lower removal efficiency resulted from agglomeration of iron powder observed by SEM, which could reduce the effective specific surface area. More than 99 % of copper ion was removed using 2 equivalent of $48{\mu}m$ iron powder at 60 min, 600 rpm and $20^{\circ}C$.

Measurement of Flame Propagation Velocity Using an Ion Current Apparatus Design (이온전류장치 설계에 의한 화염전파속도 측정)

  • 정진도;이충섭;권병철
    • Journal of Energy Engineering
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    • v.3 no.1
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    • pp.62-69
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    • 1994
  • 화염중에 존재하는 이온 및 전자의 전기적 성질을 이용하여 연소실내의 화염전파속도를 파악하기 위해 실린더 헤드에 이온 프로브를 삽입하여 천연가스 및 가솔린의 화염전파속도를 측정하였다. 본 연구에 이용된 이온전류장치 설계에 의한 방법은 광학적 측정 장비에 비해 간단하며 쉽게 측정할 수 있고 가격도 저렴하고 응답성도 우수하였다. 이온 프로브의 제작과 신호처리에 관한 기초적인 지식을 얻었으며 천연가스 및 가솔린의 연소시 연소압력의 상승지점과 이온발생지점이 일관성있게 나타났다. 기관회전수의 증가에 따라서 연소실내의 화염전파속도가 증가했으며 같은 연소조건이라고 할 수 있는 동일 기관회전수, 당량비의 조건에서 점화시간에 대한 화염전파속도를 비교해 보면 메탄의 경우가 이론치보다 6 ms∼9 ms 정도 늦었다. 또한, 메탄가스 및 가솔린에 대해 이온 전류강도 및 화염 도달시간을 측정하였으며 연소실 벽면에서는 열전달에 의한 냉각효과로인해 화염 전파속도 및 이온농도가 감소했다.

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Conductances of 1-1 Electrolytes in Ethylene Carbonate-Acetone Mixtures (탄산에틸렌-아세톤 혼합용액에서의 1-1 전해질의 전기전도도)

  • Si-Joong Kim;Young-kook Shin
    • Journal of the Korean Chemical Society
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    • v.27 no.3
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    • pp.178-182
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    • 1983
  • The conductances of sodium, potassium, ammonium, tetramethylammonium, and tetraethylammonium iodides, picrates(Pic) of sodium and potassium, and tetrabutylammonium tetraphenyl-boride have been measured in ethylene carbonate-acetone mixtures at $25{\circ}C$. The limiting equivalent conductances of the electolytes were computed by Fuoss-Kraus equation and the order was $(C_4H_9)_4NB(ph)_4 at any composition of the mixtures. The dissociation constants of the salts showed that the mixtures are good ionizing solvents for the salts. The order of limiting ionic equivalent conductance, $Na^+, is consistent with exactly the reverse order found for solvation number. Effective solvated radii calibrated by the Nightingale method showed that picrate ion seems to be unsolvated and that iodide ion seems to be solvated to some extent in the mixtures.

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Irrigation Water Qualities along Dong-Jin River Watershed during 1994-1998 (동진강 수계 농업용수 수질평가)

  • Uhm, Mi-Jeong;Choi, Jeong-Sik;Han, Soo-Gon;Kim, Kab-Cheol;Moon, Young-Hun
    • Korean Journal of Environmental Agriculture
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    • v.19 no.2
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    • pp.110-115
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    • 2000
  • This study was conducted to monitor the irrigation water qualities along Dong-Jin river watershed. The water quality was surveyed at 6 sites from April to september during $1994{\sim}1998$. And the results were as follows : In July and August, water quality was better than that of any other months due to dilution with rainwater. Whereas, it became worse in April but it involved lower contents than limitted contents affected to the crop damage. Content of inorganic components was higher at Jeong-up and Won-pyeong stream. The reason for it that Jeong-up stream was deteriorated with sewage water from Jeong-up city, and Won-pyeong stream has narrow width. Water quality in upstream of Dong-Jin river, was evaluated best conditions in all sampling sites. For investigated period, water quality got worse from 1994 to 1995 but it was getting better to 1998 after 1995, especially at Jeong-up stream. The total equivalent of cation and anion was the highest at April through all months and at Jeong-up stream in sampling sites. Equivalent ratio of cation to $anions({\Sigma}C/{\Sigma}A)$ was higher at May than any other months and lower at Won-pyeong streams than any other sites. The value of most inorganic components was highly correlated with those of other components. But the value of $NO_3\;^--N$ was not correlated with that of most components, and $PO_4\;^{3-}-P$ was not correlated with COD, $NH_4\;^+-N$, $NO_3\;^--N$, $SO_4\;^{2-}$.

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