• 생태와환경
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• 제54권2호
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• pp.120-124
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• 2021

In order to understand the vegetative role of Glycine soja, we studied the basic physiological characteristics between Glycine soja and Glycine max. For this study, the light intensity (μmol m^-2 s^-1) on leaf surface, leaf temperature (℃), transpiration rate (mmol m^-2 s^-1), photosynthetic rate (μmol m^-2 s^-1), substomatal CO₂ partial pressure (vpm) of Glycine soja and Glycine max were measured, and the quantum yield, photosynthesis rate per substomatal CO₂ partial pressure were calculated. In the results of simple regression analysis, the increasing quantum yield decreases leaf temperature both of Glycine soja and Glycine max and the increasing leaf temperature decreases transpiration rate in case of Glycine soja. However, in case of Glycine max, the increasing leaf temperature decreases substomatal CO₂ partial pressure, photosynthetic rate, and photosynthetic rate per substomatal CO₂ partial pressure as well as transpiration rate. Also, increasing transpiration rate increases substomatal CO₂ partial pressure while decreases photosynthetic rate per substomatal CO₂ partial pressure. Thus, Glycine soja is relatively more easily adaptable to severe environments with low soil nutrients and high light levels. Compared to Glycine max susceptible to water loss due to a water-poor terrestrial habitat, the physiological traits of Glycine soja has a high average transpiration rate and are less susceptible to water loss will act as a factor that limits the habitat according to soil moisture.

• 한국포장학회지
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• 제6권1호
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• pp.31-36
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• 2000

10개월 숙성된 전통 된장과 고추장을 232 mL의 유리병 용기에 포장조건을 다르게 하여 각각 180g과 150g씩 포장하고, $13^{\circ}C$에서 저장하면서 포장내의 기체조성, 색택, 총산, pH 등의 품질변화를 측정하였다. 포장 처리구로서는 핀홀을 장착시켜서 통기성을 준 경우와 $CO_2$ 흡수제로서 $Ca(OH)_2$를 장착시킨 경우에 대하여 실험하였다. 된장과 고추장 모두에서 대조구 밀봉포장은 저장중 높은 $CO_2$ 분압의 증가를 일으키고 $O_2$ 분압의 감소소멸를 나타내나, 질소분압은 비교적 일정한 수준에서 유지하여 높은 압력을 발생시켰다. 반면에 $Ca(OH)_2$ 함유포장에서는 저장 70일 부근까지 비교적 낮은 $CO_2$ 분압를 유지하여서 큰 압력 발생 없이 저장이 가능하였다. 핀흘을 장착시킨 통기성 포장에서는 $O_2$ 분압과 $N_2$ 분압이 감소하고 $CO_2$ 분압은 계속 상승한 후, 완만히 감소하였다. 이러한 포장내의 기체조성의 변화는 장류의 품질변화에 영향을 미쳐서 핀홀을 가진 포장에서 그 변화의 정도가 상대적으로 약간 작았으나, 된장 포장의 경우 저장 120일 이후에 곰팡이 오염과 성장의 문제점을 가지고 있었다. 저장 70 여일 후에 측정한 미생물 군집의 변화에서는 포장간에 뚜렷한 차이를 발견할 수 없었다. 핀홀 포장은 저장 전기간동안 포장내에 압력 발생 없이 낮은 $O_2$ 농도와 높은 $CO_2$ 농도를 유지하여 상대적으로 작은 품질변화를 얻을 수 있는 것으로 평가되나 냄새유출과 외부로부터의 오염 문제의 해결을 필요로 한다.

• 한국분말재료학회지
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• 제31권2호
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• pp.163-168
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• 2024

As the demand for lithium-ion batteries for electric vehicles is increasing, it is important to recover valuable metals from waste lithium-ion batteries. In this study, the effects of gas flow rate and hydrogen partial pressure on hydrogen reduction of NCM-based lithium-ion battery cathode materials were investigated. As the gas flow rate and hydrogen partial pressure increased, the weight loss rate increased significantly from the beginning of the reaction due to the reduction of NiO and CoO by hydrogen. At 700 ℃ and hydrogen partial pressure above 0.5 atm, Ni and Li₂O were produced by hydrogen reduction. From the reduction product and Li recovery rate, the hydrogen reduction of NCM-based cathode materials was significantly affected by hydrogen partial pressure. The Li compounds recovered from the solution after water leaching of the reduction products were LiOH, LiOH·H₂O, and Li₂CO₃, with about 0.02 wt% Al as an impurity.

• The Korean Journal of Ceramics
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• 제1권1호
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• pp.21-28
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• 1995

Electrical conductivity of $TiO_2$ thin films, deposited on $Al_2O_3$ substrates by metal organic chemical vapor deposition (MOCVD), was measured by four-point probe method in a temperature range from $800^{\circ}C$ to $1025^{\circ}C$ and an oxygen partial pressure range from $2.7{\times}10^{-5}$ atm to 1 atm. In the low oxygen partial pressure region n-type conduction was dominant, but in the high oxygen partial pressure region p-type conduction behavior appeared due to substitution of Ti ions by Al ions, which were diffused from the substrate during post deposition annealing process. Electrical conductivity of the film decreases in the n-type region and increases in the p-type region as the oxygen partial pressure increases. The transition points, which show the minimum conductivity, shifted to the higher oxygen partial pressure region as the measuring temperature increased, but it shifted to lower oxygen partial pressure region with an increase in the post annealing temperature. The results were also discussed with the possible defect models.

• 자원리싸이클링
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• 제14권4호
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• pp.47-52
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• 2005

수용액에서 탄산계 이온종들은 알칼리도, 완충 용량, 생물학적 생산지수 등과 같은 물의 여러 화학적 성질들을 결정하는데 있어 중요한 역할을 하고 있다. 이러한 화학종들은 또한 수계에서 고체, 액체, 그리고 기체 상태 등으로 변화하며 반응을 하는 특성을 지니고 있다. 고체상이 없는 상황에서 탄산계 이온종들의 총량과 각 이온종들의 상대량은 대기에서의 이산화탄소의 분압에 의해 결정되며 이는 또한 수계의 제반 성질에 직접적인 영향을 미치게 된다. 수환경에서 진행되는 정수, 혹은 폐수 처리 공정, 폐기물 처리공정, 그리고 폐기물의 재활용과 관련된 공정들에 있어 공정의 최적화를 위해서는 수환경의 특성을 파악하는 것이 매우 중요하며 이러한 수환경의 특성에 가장 크게 영향을 미치는 요소들 가운데 하나가 탄산계 이온종들이다. 대기에서의 이산화탄소의 분압과 물의 화학적 성질, 특히 pH와의 근본적인 연관성을 이해하기 위해 물과 접촉한 상태의 드라이아이스로부터 발생하는 순수한 이산화탄소의 활성 분압을 수계에서의 평형론에 근거하여 계산하였다. 탄산의 해리와 관련된 평형상수들을 van't Hoff식에 의해 결정하였으며 평형계산의 결과를 입증하기 위해 pH 에 따른 탄산계 이온종들의 분배 곡선을 작성하였다. 계산된 이산화탄소 기체의 활성 분압은 수용액에서의 탄산계 이온종들의 농도의 함수인 것으로 나타났으며 수용액에서 일어나는 반응들의 체계적 이해를 위해서는 수용액과 접해있는 이산화탄소 등과 같은 기체의 활성 분압에 대한 선행 계산이 필요한 것으로 파악되었다.

• 한국세라믹학회지
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• 제37권8호
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• pp.817-823
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• 2000

A solid-state electrochemicall cell for sensing CO2 gas was fabricated using a solid electrolyte of Li2CO3-Li3PO4-Al2O3 mixture and a reference electrode of LiMn2O4. The e.m.f. (electromotive force) of sensor showed a good accordance with theoretical Nernst slope (n=2) for CO2 gas concentration range of 100-10000 ppm above 35$0^{\circ}C$. The e.m.f. of sensor was constant regardless of oxygen partial pressure at the high temperature above 0.1 atm. It was, however, a little depended on oxygen partial pressure as the pressure decreased below 0.1 atm. The oxygen-dependency of our sensor gradually disappeared as the operating temperature increased. The sensing behavior of our CO2 sensor was affected by the presence of water vapor, but its effect was small comparing with other sensors.

• 한국표면공학회지
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• 제37권5호
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• pp.296-300
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• 2004

The defects of partial denture frameworks are mainly shrinkage porosity, inclusions, micro-crack, particles from investment, and dendritic structure. In order to investigate a good casting condition of partial denture frameworks, the three casting alloys and casting methods were used and detected casting defects were analyzed by using electrochemical methods. Three casting alloys (63Co-27Cr-5.5Mo, 63Ni-16Cr, 63Co-30Cr-5Mo) were prepared for fabricating partial denture frameworks with various casting methods; centrifugal casting (Kerr, USA), high frequency induction casting (Jelenko Eagle, USA), vacuum pressure casting (Bego, Germany). The casting temperature was $1,380^{\circ}C$ (63Co-27Cr-5.5Mo and 63Ni-16Cr) and $1,420^{\circ}C$ (63Co-30Cr-5Mo). The casting morphologies were analyzed using FE-SEM and EDX. The corrosion test of the dendritic structure was performed through potentiodynamic method in 0.9% NaCl solutions at $36.5^{\circ}C$ and corrosion surface was observed using SEM. The defects of partial denture frameworks improved in the order of centrifugal casting, high frequency induction casting, and vacuum pressure casting method, especially, pore defects were found at part of clasp in the case of centrifugal casting method. The structure of casting showed dendritic structure for three casting alloys. In the 63Co-27Cr-5.5Mo and 63Co-30Cr-5Mo, $\alpha$-Co and $\varepsilon$-Co phases were identified at matrix and $${\gamma}$-Ni_2$Cr second phase were shown in 63Ni-16Cr. Also, the corrosion resistance of cast structure increased in the order of vacuum pressure casting, high frequency induction casting, and centrifugal casting method.

• 자원리싸이클링
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• 제29권3호
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• pp.3-10
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• 2020

일메나이트의 선택염화를 통해 제조한 합성루타일을 유동층에서 CO와 Cl₂ 혼합가스를 이용하여 염화시켜 TiO₂의 염화반응 속도에 미치는 반응 온도, 시간, CO가스와 Cl₂가스의 분압 비($p_{Cl_2}/p_{CO}$)의 영향에 대하여 조사하였다. $p_{Cl_2}/p_{CO}$가 높을 때 TiCl₄의 전환율은 감소하였으며, 화학양론 계산결과와 실험결과를 비교하였을 때 Cl₂가스 보다 CO가스의 분압이 더 큰 영향을 미친 것으로 판단되었다. 따라서 실험 결과를 입자의 기공을 고려한 모델에 대입하였을 때 합성 루타일의 염화반응은 화학반응율속으로 결정되었고, 활성화에너지는 53.77 kJ/mol로 계산되었다.

• 대한금속재료학회지
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• 제47권2호
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• pp.107-113
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• 2009

Molten iron with 2 mass % carbon content was decarbonized at 1823 K~1923 K by bubbling $Ar+O_2$ gas through a submerged nozzle. The reaction rate was significantly influenced by the oxygen partial pressure and the gas flow rate. Little evolution of CO gas was observed in the initial 5 seconds of the oxidation; however, this was followed by a period of high evolution rate of CO gas. The partial pressure of CO gas decreased with further progress of the decarbonization. The overall reaction is decomposed to two elementary reactions: the decarbonization and the dissolution rate of oxygen. The assumptions were made that these reactions are at equilibrium and that the reaction rates are controlled by mass transfer rates within and around the gas bubble. The time variations of carbon and oxygen contents in the melt and the CO partial pressure in the off-gas under various bubbling conditions were well explained by the mathematical model. Based on the present model, it was explained that the decarbonization rate of molten iron was controlled by gas-phase mass transfer at the first stage of reaction, but the rate controlling step was transferred to liquid-phase mass transfer from one third of reaction time.

• 한국표면공학회지
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• 제45권5호
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• pp.206-211
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• 2012

Process analysis was carried out during deposition of MgO by inductively coupled plasma assisted reactive magnetron sputtering in Ar and $O_2$ ambient. At the initiation of Mg sputtering with bipolar pulsed dc power in Ar ambient, total pressure showed sharp increase and then slow fall. To analyse partial pressure change, QMS was used in downstream region, where the total pressure was maintained as low as $10^{-5}$ Torr during plasma processing, good for ion source and quadrupole operation. At base pressure, the major impurity was $H_2O$ and the second major impurity was $CO/N_2$ about 10%. During sputtering of Mg in Ar, $H_2$ soared up to 10.7% of Ar and remained as the major impurity during all the later process time. When $O_2$ was mixed with Ar, the partial pressure of Ar decreased in proportion to $O_2$ flow rate and that of $H_2$ dropped down to 2%. It was understood as Mg target surface was oxidized to stop $H_2$ emission by Ar ion sputtering. With ICP turned on, the major impurity $H_2$ was converted into $H_2O$ consuming $O_2$ and C was also oxidized to evolve CO and $CO_2$.