• 제목/요약/키워드: Electrolyte temperature

검색결과 962건 처리시간 0.03초

Hypoadrenocorticism in a 1-Year-Old Korean Shorthair Cat

  • Jung, Hansol;Jeong, Yunho;Kim, Yoonhwan;Choi, Sooyoung;Park, Inchul;Ahn, Jin-Ok
    • 한국임상수의학회지
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    • 제39권3호
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    • pp.144-148
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    • 2022
  • A one-year-old spayed female Korean Shorthair cat presented to Kangwon National University Veterinary Hospital with vomiting, weight loss, lethargy, loss of appetite, and polyuria that lasted for more than two weeks. The body condition score, blood pressure, heart rate, and body temperature were abnormally low, and the physical examination findings were consistent with moderate dehydration. Hematological and biochemical tests demonstrated mild azotemia and a low Na:K ratio. Additional abdominal ultrasound imaging revealed reduced size of both adrenal glands. The adrenocorticotropic hormone (ACTH) stimulation test showed decreased post-ACTH cortisol and aldosterone levels and increased endogenous ACTH levels, confirming a diagnosis of primary hypoadrenocorticism. The cat was treated with subcutaneous injections of desoxycorticosterone pivalate (DOCP) and oral prednisolone supplementation, and subsequent electrolyte analysis showed a normal Na:K ratio. Clinical symptoms were also improved in response to treatment. Hypoadrenocorticism in cats is a very rare disease, but it should not be excluded as a potential diagnosis in favor of kidney diseases or other conditions, especially when the Na:K ratio is low. In addition, the prognosis for the disease and the response to DOCP treatment should be further evaluated in cats.

Effect of LiCoO2-Coated Cathode on Performance of Molten Carbonate Fuel Cell

  • Kim, Dohyeong;Kim, Hyung Tae;Song, Shin Ae;Kim, Kiyoung;Lim, Sung Nam;Woo, Ju Young;Han, Haksoo
    • Journal of Electrochemical Science and Technology
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    • 제13권1호
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    • pp.112-119
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    • 2022
  • Molten carbonate fuel cells (MCFCs) are environmentally friendly, large-capacity power generation devices operated at approximately 650℃. If MCFCs are to be commercialized by improving their competitiveness, their cell life should be increased by operating them at lower temperatures. However, a decrease in the operating temperature causes a reduction in the cell performance because of the reduction in the electrochemical reaction rate. The cell performance can be improved by introducing a coating on the cathode of the cell. A coating with a high surface area expands the triple phase boundaries (TPBs) where the gas and electrolyte meet on the electrode surface. And the expansion of TPBs enhances the oxygen reduction reaction of the cathode. Therefore, the cell performance can be improved by increasing the reaction area, which can be achieved by coating nanosized LiCoO2 particles on the cathode. However, although a coating improves the cell performance, a thick coating makes gas difficult to diffuse into the pore of the coating and thus reduces the cell performance. In addition, LiCoO2-coated cathode cell exhibits stable cell performance because the coating layer maintains a uniform thickness under MCFC operating conditions. Therefore, the performance and stability of MCFCs can be improved by applying a LiCoO2 coating with an appropriate thickness on the cathode.

수전해 시스템에 적용하기 위한 상용 음이온교환막의 특성평가 (Evaluation of Commercial Anion Exchange Membrane for the application to Water Electrolysis)

  • 박준호;임광섭;남상용
    • 멤브레인
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    • 제32권6호
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    • pp.496-513
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    • 2022
  • 본 연구에서는 음이온 교환막 수전해 시스템에 적용가능성을 확인하고자 상용 음이온 교환막인 FAA-3-50, Neosepta-ASE, Sustainion grade T, Fujifilm type 10의 관련 물성을 평가하였다. 음이온교환막을 이용하는 특성상 음이온교환기의 확인을 위하여 SEM/EDX를 이용하여 상용막의 모폴로지와 표면의 원소를 분석하여 상용막이 포함하고 있는 작용기의 분포를 확인하였다. 또한, UTM과 TGA를 이용하여 기계적 강도 및 열분해온도를 측정하여 수전해의 구동조건을 만족하는지 확인하였다. 음이온 교환막으로서의 성능을 파악하기 위하여 중요한 특성인 이온교환용량과 이온전도도를 측정하였으며, 알칼리 환경에서 구동되기 때문에 각각의 상용막의 내알칼리성을 확인하기 위한 내구성 테스트를 진행하여 비교하였다. 최종적으로 막-전극 접합체를 제조하여 수전해 single cell test를 진행하여 60℃, 70℃, 80℃의 온도 조건에서 cell 성능을 확인하였고 장기 cell test로 다른 온도에서 20 cycle 측정하여 수전해 성능을 비교하여 상용막의 음이온 교환막 수전해에 적용가능성을 비교하여 확인하였다.

3D 프린팅을 이용한 Pt/Carbon Nanotube composite 기반 전기화학식 황화수소 가스 센서 제작 (Fabrication of Pt/Carbon Nanotube Composite Based Electrochemical Hydrogen Sulfide Gas Sensor using 3D Printing)

  • 하윤태;권진범;최수지;정대웅
    • 센서학회지
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    • 제32권5호
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    • pp.290-294
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    • 2023
  • Among various types of harmful gases, hydrogen sulfide is a strong toxic gas that is mainly generated during spillage and wastewater treatment at industrial sites. Hydrogen sulfide can irritate the conjunctiva even at low concentrations of less than 10 ppm, cause coughing, paralysis of smell and respiratory failure at a concentration of 100 ppm, and coma and permanent brain loss at concentrations above 1000 ppm. Therefore, rapid detection of hydrogen sulfide among harmful gases is extremely important for our safety, health, and comfortable living environment. Most hydrogen sulfide gas sensors that have been reported are electrical resistive metal oxide-based semiconductor gas sensors that are easy to manufacture and mass-produce and have the advantage of high sensitivity; however, they have low gas selectivity. In contrast, the electrochemical sensor measures the concentration of hydrogen sulfide using an electrochemical reaction between hydrogen sulfide, an electrode, and an electrolyte. Electrochemical sensors have various advantages, including sensitivity, selectivity, fast response time, and the ability to measure room temperature. However, most electrochemical hydrogen sulfide gas sensors depend on imports. Although domestic technologies and products exist, more research is required on their long-term stability and reliability. Therefore, this study includes the processes from electrode material synthesis to sensor fabrication and characteristic evaluation, and introduces the sensor structure design and material selection to improve the sensitivity and selectivity of the sensor. A sensor case was fabricated using a 3D printer, and an Ag reference electrode, and a Pt counter electrode were deposited and applied to a Polytetrafluoroethylene (PTFE) filter using PVD. The working electrode was also deposited on a PTFE filter using vacuum filtration, and an electrochemical hydrogen sulfide gas sensor capable of measuring concentrations as low as 0.6 ppm was developed.

RuO2/Ti, PtO2/Ti, IrO2/Ti 및 흑연전극을 이용한 염료폐수의 전기화학적 처리 (Electrochemical Treatment of Dye Wastewater Using Fe, RuO2/Ti, PtO2/Ti, IrO2/Ti and Graphite Electrodes)

  • 김아람;박현정;원용선;이태윤;이제근;임준혁
    • 청정기술
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    • 제22권1호
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    • pp.16-28
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    • 2016
  • 섬유산업은 염색폐수의 농도가 높고 방출량이 많아 고도의 공해산업으로 알려져 있다. 염색폐수에는 색도물질 뿐만 아니라 다량의 유기화합물과 불용성 물질이 섞여 있다. 합성염료 중 아조(azo) 염료는 특히 오염물질의 배출이 많은 것으로 알려져 있다. 전기화학적 폐수처리방법은 전극의 산화·환원반응에 의해 색도와 유기물 등을 처리하는 방법으로 다른 폐수처리방법들에 비해 반응기가 작고 경제적이고 간단하며 오염물제거속도가 빠르다. 본 연구에서는 diazo 화합물인 CI Direct Blue 15 염색 폐수의 전기화학적 분해특성을 연구하였다. 실험은 전극재질과 조업조건을 달리하여 그에 따른 분해효율을 알아보고자 하였으며, 탈색 효율을 향상시킬 수 있는 최적전극 재질과 조업조건을 알아보고자 하였다. 조업조건으로는 전해질 농도, 전류밀도, 반응 온도, 초기 pH의 영향을 검토하였다. 음극은 stainless steel 전극을 사용하였고, 양극은 graphite와 RuO2/Ti, PtO2/Ti, IrO2/Ti를 사용하여 조업조건에 따른 각 전극의 염색폐수 분해성능 실험을 수행하였다. 그 결과 전해질의 농도와 전류밀도 증가에 따라 전기분해 효율은 증가하였다. 양극 재질에 따른 전기분해 효율은 산성 전해질 조건에서 RuO2/Ti > PtO2/Ti > IrO2/Ti > graphite 순이었고 중성과 염기성에서는 RuO2/Ti > IrO2/Ti > PtO2/Ti > graphite의 순으로 나타났다. 따라서 염색 폐수의 전기분해 처리에는 RuO2/Ti와 IrO2/Ti가 가장 효율적인 양극재질이었다.

은나노물질을 포함한 수질시료의 보관조건 (Preservation Conditions of Aqueous Samples Containing silver Nanomaterials)

  • 강문희;박솔;이상우;김현아;이병태;엄익춘;김순오
    • 대한환경공학회지
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    • 제37권4호
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    • pp.218-227
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    • 2015
  • 나노기술의 이용도가 높아지면서 나노물질 유출로 인한 환경오염 문제가 제기되고 있다. 수질시료 내 나노물질의 분석을 위해서는 시료의 교란을 최소화할 수 있는 보관조건 마련이 선결 요건이지만, 아직까지 적합한 보관조건이 제시되고 있지 않다. 이에 본 연구는 citrate로 코팅된 은 나노물질(cit-AgNP)을 대상으로 금속나노물질을 함유한 수질시료의 보관조건을 제시하고자 수행되었다. 이를 위해 시간분해 동적산란법(time-resolved dynamic light scattering)을 이용하여 pH, 배경용액의 농도, 온도, 나노물질의 농도 등과 같은 환경적인 조건과 시간에 따른 cit-AgNP의 크기 변화를 관찰하였다. 실험을 통한 각 환경조건별 AgNP의 응집특성을 해석하고 이러한 결과를 바탕으로 시료의 보관조건을 제시하였다. 그리고 AgNP의 입자농도와 응집속도의 선형적 관계로부터 구한 doublet time을 이용하여 시료의 보관기간을 산정하였다. 실험결과, pH는 7 이상, 배경 용액($Ca(NO_3)_2$)의 농도는 3 mM 이하, 온도는 냉장($4^{\circ}C$) 상태, 그리고 cit-AgNP의 농도는 2 mg/L 이하에서 응집속도가 0에 가까운 값을 나타내었다. 또한 수질시료 내 존재하는 100 nm cit-AgNP의 농도를 환경에 존재할 수 있는 낮은 수준인 $1{\mu}g/L$로 가정한 후 doublet time를 구한 결과, 가능한 시료의 보관기간은 15.79~17.53일 정도인 것으로 조사되었다. 하지만 pH와 배경 용액의 농도 조절은 시료의 변질과 교란이 우려되기 때문에 보관조건으로 일반화하여 제시하는 것은 적절하지 않고, 나노물질 자체의 농도를 조절하는 것은 수질시료 내 나노물질의 농도 등의 분석을 위한 시료의 보관조건으로 바람직하지 않다. 그러므로 본 연구의 결과로부터 일반화하여 제시할 수 있는 보관조건은 냉장($4^{\circ}C$) 상태에서 2주일 정도인 것으로 판단된다.

고분자 전해질 연료전지용 플라즈마 개질 시스템에서 수소 생산 및 CO 산화반응에 관한 연구 (Study on Hydrogen Production and CO Oxidation Reaction using Plasma Reforming System with PEMFC)

  • 홍석주;임문섭;전영남
    • Korean Chemical Engineering Research
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    • 제45권6호
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    • pp.656-662
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    • 2007
  • 고분자 전해질 연료전지 운전에 필요한 수소 공급 장치로서 플라즈마 개질 방법을 이용한 개질기와 일산화탄소 산화반응을 위한 전이 반응기를 설계 및 제작하였다. GlidArc 방전을 이용한 저온플라즈마 개질기는 Ni 촉매를 동시에 사용하여 $CH_4$ 개질함으로서 $H_2$ 선택도를 증대하였다. 개질기의 변수별 연구로서 촉매 온도, 가스 조성비, 전체 가스유량, 전압변화 그리고 개질 특성 및 최적 수소 생산조건을 연구하였으며, 전이반응기의 변수별 연구로서 선택적 산화반응기(PrOx)에 주입되는 공기량, 전이 반응기에 주입되는 수증기량 그리고 온도에 대하여 연구하였다. 플라즈마 개질기에서 최대 수소 생산 조건은 $O_2/C$ 비가 0.64, 가스유량은 14.2 l/min, 촉매 반응기 온도 $672^{\circ}C$ 그리고 유입전력이 1.1 kJ/L일 때 41.1%로 최대 수소 농도를 나타냈다. 그리고 이때의 $CH_4$ 전환율, $H_2$ 수율 그리고 개질기 에너지 밀도는 각각 88.7%, 54%, 35.2%를 나타냈다. 전이 반응기에서 모사된 개질 가스로부터 최대 CO 전환율을 보이는 조건은 2단으로 구성된 PrOx에 주입되는 $O_2/C$ 비가 0.3, HTS에서 주입되는 수증기 주입량 비가 2.8 그리고 HTS, LTS, PrOx I, PrOx II 반응기 온도가 475, 314, 260, $235^{\circ}C$ 일때 가장 높은 CO 전환율을 나타냈다. 플라즈마를 이용한 반응기는 예열 시간은 30분이 소요되었으며, 전이 반응기에서 나오는 최종 개질 가스의 조성은 $H_2$ 38%, CO<10 ppm, $N_2$ 36%, $CO_2$ 21% 그리고 $CH_4$ 4%로 나타냈다.

토끼에서 저체온증의 유발에 의한 생리학적 및 임상병리학적 변화 (The clinical physiopathological changes by induction of hypothermia in rabbits)

  • 이병한;한진수;정병현
    • 대한수의학회지
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    • 제38권4호
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    • pp.867-881
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    • 1998
  • The studies were carried out to investigate the phygiological changes in deep hypothermia in rabbits. Sixty rabbits were continuously cooled with femoral arterio-venous bypass circulation to rectal temperatures of $34.0{\pm}0.3^{\circ}C$(mild hypothermia), $30.0{\pm}0.3^{\circ}C$(moderate hypothermia), and $25.0{\pm}0.3^{\circ}C$(deep hypothermia). The results obtained in these experiments were summarized as follows : In mild, moderate, and deep hypothermia, MAP, HR, RR, pH, $pCO_2$, $pO_2$, $Na^+$, $K^+$, HCT, PLT, glucose, L-lactate, BUN, and creatinine were analyzed. During hypothermia, a statistically significant decrease of MAP occurred between $30^{\circ}C$ and early $25^{\circ}C$(Start) of rectal temperature while significant increases occurred between baseline($38.7^{\circ}C$) and $30^{\circ}C$. Significant decreases of HR and RR were observed in the rabbits, particularly those changes appeared to similar patterns in proportion to hypothermia. Significant decreases of pH occurred between $34^{\circ}C$ and $25^{\circ}C$, and significant increases of $pO_2$ and $pCO_2$ were observed continuously in the hypothermic rabbits. The hypothermia had no significant effect on blood $Na^+$ and serum creatinine. Blood $K^+$ significantly decreased from $3.1{\pm}0.5$(baseline) to $2.6{\pm}0.6mmol/l$($34^{\circ}C$) with the hypothermia for about 30 minutes, and significantly increased from $2.4{\pm}0.6$($25^{\circ}C$(S)) to $2.7{\pm}0.5mmol/l$($25^{\circ}C$(E)) with the hypothermia for 2 hrs. HCT significantly increased to $34^{\circ}C$, thereafter, continuously increased to $25^{\circ}C$(Start, End). PLT increased to $34^{\circ}C$, thereafter, continuously decreased to $25^{\circ}C$(Start, End). Also PLT decreased significantly from 414.3($30^{\circ}C$) to $308.8{\times}103/mm^3$($25^{\circ}C$, Start). Significant increases of blood glucose and L-lactate occurred between $30^{\circ}C$ and $25^{\circ}C$ (Start, End). Slight increase of serum BUN continuously appeared with the hypothermia. These results, such as characteristic changes of the significant decrease of pH and PLT at $34^{\circ}C$, the significant decrease of MAP at $30^{\circ}C$, and the significant increase of glucose and l-lactate at $30^{\circ}C$, suggest that homeostasis of rabbits to hypothermia rapidly decreases at $34{\sim}30^{\circ}C$ of rectal temperature. Therefore, we suggest that, during the period with the rapidly decreased homeostasis, the very carefully control and treatment need to recover hypothermic animals under the circumstances of the various hypothermic experiments and emergency medicine.

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Si and Mg doped Hydroxyapatite Film Formation by Plasma Electrolytic Oxidation

  • Park, Seon-Yeong;Choe, Han-Cheol
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2016년도 추계학술대회 논문집
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    • pp.195-195
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    • 2016
  • Titanium and its alloys are widely used as implants in orthopedics, dentistry and cardiology due to their outstanding properties, such as high strength, high level of hemocompatibility and enhanced biocompatibility. Hence, recent works showed that the synthesis of new Ti-based alloys for implant application involves more biocompatible metallic alloying element, such as, Nb, Hf, Zr and Mo. In particular, Nb and Hf are one of the most effective Ti ${\beta}-stabilizer$ and reducing the elastic modulus. Plasma electrolyte oxidation (PEO) is known as excellent method in the biocompatibility of biomaterial due to quickly coating time and controlled coating condition. The anodized oxide layer and diameter modulation of Ti alloys can be obtained function of improvement of cell adhesion. Silicon (Si) and magnesium (Mg) has a beneficial effect on bone. Si in particular has been found to be essential for normal bone and cartilage growth and development. In vitro studies have shown that Mg plays very important roles in essential for normal growth and metabolism of skeletal tissue in vertebrates and can be detected as minor constituents in teeth and bone. The aim of this study is to research Si and Mg doped hydroxyapatite film formation by plasma electrolytic oxidation. Ti-29Nb-xHf (x= 0, 3, 7 and 15wt%, mass fraction) alloys were prepared Ti-29Nb-xHf alloys of containing Hf up from 0 wt% to 15 wt% were melted by using a vacuum furnace. Ti-29Nb-xHf alloys were homogenized for 2 hr at $1050^{\circ}C$. Each alloy was anodized in solution containing typically 0.15 M calcium acetate monohydrate + 0.02 M calcium glycerophosphate at room temperature. A direct current power source was used for the process of anodization. Anodized alloys was prepared using 270V~300V anodization voltage at room. A Si and Mg coating was produced by RF-magnetron sputtering system. RF power of 100W was applied to the target for 1h at room temperature. The microstructure, phase and composition of Si and Mg coated oxide surface of Ti-29Nb-xHf alloys were examined by FE-SEM, EDS, and XRD.

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Morphology of RF-sputtered Mn-Coatings for Ti-29Nb-xHf Alloys after Micro-Pore Form by PEO

  • Park, Min-Gyu;Park, Seon-Yeong;Choe, Han-Cheol
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2016년도 추계학술대회 논문집
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    • pp.197-197
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    • 2016
  • Commercially pure titanium (CP Ti) and Ti-6Al-4V alloys have been widely used for biomedical applications. However, the use of the Ti-6Al-4V alloy in biomaterial is then a subject of controversy because aluminum ions and vanadium oxide have potential detrimental influence on the human body due to vanadium and aluminum. Hence, recent works showed that the synthesis of new Ti-based alloys for implant application involves more biocompatible metallic alloying element, such as, Nb, Hf, Zr and Mo. In particular, Nb and Hf are one of the most effective Ti ${\beta}-stabilizer$ and reducing the elastic modulus. Plasma electrolyte oxidation (PEO) is known as excellent method in the biocompatibility of biomaterial due to quickly coating time and controlled coating condition. The anodized oxide layer and diameter modulation of Ti alloys can be obtained function of improvement of cell adhesion. Manganese(Mn) plays very important roles in essential for normal growth and metabolism of skeletal tissue in vertebrates and can be detected as minor constituents in teeth and bone. Radio frequency(RF) magnetron sputtering in the various PVD methods has high deposition rates, high-purity films, extremely high adhesion of films, and excellent uniform layers for depositing a wide range of materials, including metals, alloys and ceramics like a hydroxyapatite. The aim of this study is to research the Mn coatings on the micro-pore formed Ti-29Nb-xHf alloys by RF-magnetron sputtering for dental applications. Ti-29Nb-xHf (x= 0, 3, 7 and 15wt%, mass fraction) alloys were prepared Ti-29Nb-xHf alloys of containing Hf up from 0 wt% to 15 wt% were melted by using a vacuum furnace. Ti-29Nb-xHf alloys were homogenized for 2 hr at $1050^{\circ}C$. Each alloy was anodized in solution containing typically 0.15 M calcium acetate monohydrate + 0.02 M calcium glycerophosphate at room temperature. A direct current power source was used for the process of anodization. Anodized alloys was prepared using 270V~300V anodization voltage at room. Mn coatings was produced by RF-magnetron sputtering system. RF power of 100W was applied to the target for 1h at room temperature. The microstructure, phase and composition of Mn coated oxide surface of Ti-29Nb-xHf alloys were examined by FE-SEM, EDS, and XRD.

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