• Journal of Chest Surgery
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• 제3권2호
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• pp.73-90
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• 1970

Clinical perfusion data on 16 cases of cardiopulmonary bypass using Sigmamotor pump and RyggKyvsgaard Oxygenator which performed at Seoul National University Hospital during the period of Aug. 1968 to Aug. 1970 was analized. AIl cases were hemodiluted and the perfusion was carried out under the normothermic condition. The age of the patients ranged between 6 and 43 years. The b:dy weight varied between 18.3 and 54.0 kg and the body surface area between 0.78 and 1. 59$M^2$. The priming solution was consiste:I with fresh ACD blood. Hartmann solution and Mannitol. The average amount of priming was approximately 2242 ml. The average hemodilution rate was 17%. The flow rate ranged from 1.7L to 3.5L/Min/$M^2$ and averaged 2.4L/Min/$M^2$ or 78mI/Min/kg. The duration of perfusion varied from 22 to 110 min with average of 56.9 minutes. Some hemodynamic responses were observed. The arterial pressure dropped immediately after the initiation of partial perfusion and was more marked after the total perfusion foIlowed by gradual increase to the safety level. The central venous pressure reflected the reduced blood volume especially in the cases of prolonged perfusion which lasted over 60 min. In most of the cases, red blood cell count decreased and white blood ceIl count increased after the perfusion. Hemoglobin level was decreased, averaging of 12.5mg%, Hct 3.3% and platelets count of 18% postoperatively. Plasma hemoglobin increased mildly, from pre-perfusion average value of 4. 06mg% to postperfusion value of 22.5mg%. Serum potassium was 4.4mEq/L pre-operatively and was decreased to 3.7mEq/L postoperatively. Five cases showed definite hypopotassemia immediately after the operation. Sodium and chloride decreased mildly. These electrolyte changes are thought to be related with hemodilution. diuretics and reduced blood volume during and after the perfusion. Arterial blood pH value revealed minimal to moderate elevation from preperfusion average value of 7.376 to 7.461 during perfusion and then 7.365 after perfusion. The pC02 and hicarbonate showed minimal to moderately lowered values. The total CO2 was decreased. Buffer base decreased during perfusion (Av. 42.6mEq/L) and further decreased after the perfusion (Av. 40.8mEq/L). These arterial blood acid base changes suggested that the metabolic acidosis was accompanied by respiratory alkalosis during and immediately after the perfusion. Authors belived that the acidosis could more effectively be corrected with the more additional dose of bicarbonate than we used by this study. The chest tune drainage during the first 24 hours following operation was 1158 ml in average. One case (Case No. 15) showd definite bleeding tendency and it was believed that the cause might be due to the defect of heparin and protamine titration. The average urinary out put during 24 hours post-perfusion was 1291ml. One case (Case No. ]) showed definite post perfusion oliguria. As conclusion hemodilution using fresh ACD blood. Hartmann and Mannitol solution added with Bivon and high flow rate unler normothermia. was thought to amelioratc the severity of mctabolic acidosis during and after perfusion with relatively satisfactory effect on the diuresis and bleeding tendency.

• 전기화학회지
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• 제9권3호
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• pp.124-131
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• 2006

기존의 용융탄산염 연료전지용 연료극인 Ni-Cr전극은 제조과정이 복잡하며, 운전조건에서 전극의 소결과 creep현상으로 인하여 전극의 기공률과 두께가 감소하는 문제점이 있어 상용화에 걸림돌이 되고 있다. 이에 본 연구에서는 Ni-Cr계 전극보다 creep저항성이 우수하다고 알려져 있는 Ni-Al계 합금을 사용하였다. 또한 공정의 단순화로 비용을 절감시키기 위해, 소성과정을 제외하고 tape casting과 건조과정을 거친 green sheet를 단위전지에 장착하여 전처리 과정 중에 소결시키는 in-situ 소결법에 대해 연구하였다. 그러나 기존의 전처리 방법을 이용한 단위전지 평가에서 Ni-Al 합금의 상분리 현상으로 인해 기대하였던 creep저항성 향상을 확인하지 못했고, 운전중 Ni-Al합금 연료극에 단위전지의 구성요소인 matrix 기공크기보다 작은 기공(${\leq}0.4{\mu}m$)이 다량 생성되어 전해질 재분배를 일으켜 성능이 하락하는 문제점이 나타났다. 따라서 이러한 문제점을 해결하고자 전처리 조건을 변화시키며 실험을 수행하였다. 그 결과, 비활성 기체인 질소를 일정한 구간에 사용함으로써 기존 전처리에서 발생하였던 Ni-Al 합금의 상분리 현상을 억제할 수 있었으며 이로 인해 creep저항성 또한 향상시킬 수 있었다. 그러나 운전 중 생성되는 matrix기공크기보다 작은 기공(${\leq}0.4{\mu}m$) 형성비율은 억제할 수 없었다. 위의 전처리 조건을 가지고 단위전지 운전실험을 하였고, 전해질 함침비율을 조절함에 따라 성능을 향상시킬 수 있었으며 2000시간 동안 일정하게 유지함을 확인하였다. 이로부터 기존의 소성전극과 비교하여 많은 장점을 가지고 있는 in-situ 소결법의 가능성을 확인할 수 있었다.

• 대한핵의학회지
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• 제34권4호
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• pp.336-343
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• 2000

목적: $[^{201}Tl]$TICI주사액의 제조과정에서 안정동위원소인 $^{201}Tl$ 및 Cu, Pb의 중금속을 함유할 가능성이 있어 이러한 이물질을 확인하기 위한 방법으로 방사성 물질의 대기오염을 일으키지 않는 폴라로그래피의 분석 조건을 설정하고자 하였다. 대상 및 방법: 원자력병원에서 생산하고 있는 $[^{201}Tl]$-TlCl 주사액에 포함될 수 있는 중금속을 대상으로 하였다. 극미량의 중금속을 측정하기 위한 방법으로 BAS-50W 폴라로그래피를 이용하였고, 여기에 사용된 3 전극계는 작업전극인 DME, 기준전극인 Ag/AgCl 그리고 보조전극인 백금선을 이용하였다. 신속하고 재현성있는 분석을 위한 조건으로 기기의 분석 모드, 각 모드에 적합한 전극, 지지전해질, 석출시간 등의 치적 조건을 설정하였다. 결과: 폴라로그래피의 모드는 OSWSV 방법이 재현성과 감도면에서 가장 우수하였고, 작업전극은 DME와 Au 전극을 비교 실험한 결과 재현성 면에서 DME가 보다 좋은 결과를 보였다. 지지전해질은 염기성인 0.50 M KOH 용액, 산성인 1.0 M $HNO_3$, 용액, 중 성인 pH 7 phosphate 완충용액을 비교 실험하여 pH 7 phosphate 완충용액이 $Tl^+$과 $Cu^{2+}$를 분석하는데 가장 적합함을 확인하였다. 이를 바탕으로 중금속을 측정한 결과 $Tl^+$은 -450 mV, $Cu^{2+}$는 -50 mV에서 각각의 피크가 나타났고, 석출시간을 45초로 하였을 때 $Tl^+$의 경우 y=2.05E-$9{\chi}$+5.66E-9이고 $Cu^{2+}$의 경우는 y=1.23E-$8{\chi}$+1.23E-6의 선형 관계식을 얻었다. 결론: 이 방법에 의한 Tl과 Cu의 검출한계는 약 0.05 ppm이다. 이 방법을 현재 원자력병원에서 생산하고 있는 $[^{201}Tl]$TICl 주사액의 정도관리에 도입하여 중금속을 측정한 결과 약전에서 규정하고 있는 2 ppm 미만임을 확인하였고, 그 결과는 재현성, 정확도, 감도 및 간편성에서 모두 만족할 수 있었다. 이 방법은 $[^{201}Tl]$TlCl 주사액 뿐만 아니라 $^{67}Ga$ 주사액 및 기타 방사성의약품과 중금속 분석에도 응용할 수 있다.

• Journal of Electrochemical Science and Technology
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• 제11권2호
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• pp.172-179
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• 2020

The impact of effective parameters on the electrodeposition rate optimization of Au-Cu alloy at high thicknesses on the silver substrate was investigated in the present study. After ensuring the formation of gold alloy deposits with the desired and standard percentage of gold with the cartage of 18K and other standard karats that should be observed in the manufacturing of the gold and jewelry artifacts, comparing the rate of gold-copper deposition by direct and pulsed current was done. The rate of deposition with pulse current was significantly higher than direct current. In this process, the duty cycle parameter was effectively optimized by the "one factor at a time" method to achieve maximum deposition rate. Particular parameters in this work were direct and pulse current densities, bath temperature, concentration of gold and cyanide ions in electrolyte, pH, agitation and wetting agent additive. Scanning electron microscopy (SEM) and surface chemical analysis system (EDS) were used to study the effect of deposition on the cross-sections of the formed layers. The results revealed that the Au-Cu alloy layer formed with concentrations of 6gr·L^-1 Au, 55gr·L^-1 Cu, 24 gr·L^-1 KCN and 1 ml·L^-1 Lauryl dimethyl amine oxide (LDAO) in the 0.6 mA·cm^-2 average current density and 30% duty cycle, had 0.841 ㎛·min^-1 Which was the highest deposition rate. The use of electrodeposition of pure and alloy gold thick layers as a production method can reduce the use of gold metal in the production of hallow gold artifacts, create sophisticated and unique models, and diversify production by maintaining standard karats, hardness, thickness and mechanical strength. This will not only make the process economical, it will also provide significant added value to the gold artifacts. By pulsating of currents and increasing the duty cycle means reducing the pulse off-time, and if the pulse off-time becomes too short, the electric double layer would not have sufficient growth time, and its thickness decreases. These results show the effect of pulsed current on increasing the electrodeposition rate of Au-Cu alloy confirming the previous studies on the effect of pulsed current on increasing the deposition rate of Au-Cu alloy.

• 한국결정성장학회지
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• 제1권2호
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• pp.79-93
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• 1991

초 고집적 회로의 시대로 접어들면서 지금까지의 금속선 형성 기술 및 배선 재료에 많은 문제점들이 나타나고 있다. 알루미늄의 대체 재료로서 검토되고 있는 구리를, 전기 화학적 방법에 의해 미세 접촉창에 선택적으로 충전함으로써 새로운 금속선 형성 기술을 제시하고자 하였다. 0.75M의 황산구리 수용액을 전해액으로 사용하여 p형 (100) 규소 박판위에 구리 전착막을 형성한 후 Alpha Step, 주사 전자 현미경, 4-탐침법을 사용하여 막의 두께, 입자 크기, 비저항을 측정함으로써 전착 시간, 전류 밀도, 첨가물로 사용한 젤라틴 농도가 전착막의 성질에 미치는 영향에 대해 조사하였다. 평균 전착 속도는 전류 밀도가 $ 2A/dm^2$일 때 0.5-0.6\mu\textrm{m}$/min 였고 구리 입자의 크기는 전류밀도 증가에 따라 증가하였다. 입자 크기 $4000{\AA}$이상에서 얻어진 비저항값은 3-6 Ω.cm였다. 젤라틴을 첨가하여 입자의 크기를 $0.1\mu\textrm{m}$이하로 감소시킴으로써 크기 $1\mu\textrm{m}$이하의 접촉장에 구리를 선택적으로 충전시키는데 성공하였다.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2017년도 춘계학술대회 논문집
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• pp.77-77
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• 2017

Titanium and its alloys offer attractive properties in a variety of applications. These are widely used for the field of biomedical implants because of its good biocompatibility and high corrosion resistance. Titanium anodizing is often used in the metal finishing of products, especially those can be used in the medical devices with dense oxide surface. Based on SAE/AMS (Society of Automotive Engineers/Aerospace Material Specification) 2488D, it has the specification for industrial titanium anodizing that have three different types of titanium anodization as following: Type I is used as a coating for elevated temperature forming; Type II is used as an anti-galling coating without additional lubrication or as a pre-treatment for improving adherence of film lubricants; Type III is used as a treatment to produce a spectrum of surface colours on titanium. In this study, we have focused on Type II anodization for the medical (dental and orthopedic) application, the anodized surface was modified with gray color under alkaline electrolyte. The surface characteristics were analyzed with Focused Ion Beam (FIB), Scanning Electron Microscopy (SEM), surface roughness, Vickers hardness, three point bending test, biocompatibility, and corrosion (potentiodynamic) test. The Ti-6Al-4V alloy was used for specimen, the anodizing procedure was conducted in alkaline solution (NaOH based, pH>13). Applied voltage was range between 20 V to 40 V until the ampere to be zero. As results, the surface characteristics of anodic oxide layer were analyzed with SEM, the dissecting layer was fabricated with FIB method prior to analyze surface. The surface roughness was measured by arithmetic mean deviation of the roughness profile (Ra). The Vickers hardness was obtained with Vickers hardness tester, indentation was repeated for 5 times on each sample, and the three point bending property was verified by yield load values. In order to determine the corrosion resistance for the corrosion rate, the potentiodynamic test was performed for each specimen. The biological safety assessment was analyzed by cytotoxic and pyrogen test. Through FIB feature of anodic surfaces, the thickness of oxide layer was 1.1 um. The surface roughness, Vickers hardness, bending yield, and corrosion resistance of the anodized specimen were shown higher value than those of non-treated specimen. Also we could verify that there was no significant issues from cytotoxicity and pyrogen test.

• 한국수소및신에너지학회논문집
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• 제13권3호
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• pp.181-189
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• 2002

A series of multicomponent $Zr_{0.8}Ti_{0.2}Mn_{0.4}V_{0.6}Ni_{1-x}Fe_{x}$ (x=0.00, 0.08, 0.15, 0.22, and 0.30) alloys are prepared and their oystal structure and P-C-T curves are examined. The electrochemical properties of these allqys such as activation conditions, discharge capacity, cycling performance are also investigated. $Zr_{0.8}Ti_{0.2}Mn_{0.4}V_{0.6}Ni_{1-x}Fe_{x}$ (x=0.00, 0.08, 0.15, 0.22 and 0.30) have the C14 Laves phase hexagonal structure. The electrode was activated by the hot-charging treatment. The best activation conditions were the current density 120 mA/g and the hot-charging time 12h at $80^{\circ}C$ in the case of the alloy with x=0.00. The discharge capacity increased rapidly until the fourth cycle and then decreased. The discharge capacity increased again from the 13th cycle, arriving at 234 mAh/g at the 50th cycle. The discharge capacily just after activation decreases with the increase in the amount of the substituted Fe but the cycling performance is improved. The discharge capacity after activation of the alloy with x=0.00 is 157 mAh/g at the current density 120 mA/g. $Zr_{0.8}Ti_{0.2}Mn_{0.4}V_{0.6}Ni_{0.85}Fe_{0.15}$ is a good composition with a medium quantity of discharge capacities and a good cycling performance. The ICP analysis of the electrolyte for these electrodes after 50 charge-discharge cycles shows that the concentrations of V and Zr are relatively high. Another series of multicomponent $Zr_{0.8}Ti_{0.2}Mn_{0.4}V_{0.6}Ni_{0.85}M_{0.15}$ (M = Fe, Co, Cu, Mo and Al) alloys are prepared. They also have the C14 Laves phase hexagonal structure. The alloys with M = Co and Fe have relatively larger hydrogen storage capacities. The discharge capacities just after activation are relatively large in the case of the alloys with M = Al and Cu. They are 212 and 170 mAh/g, respectivety, at the current density 120mA/g. The $Zr_{0.8}Ti_{0.2}Mn_{0.4}V_{0.6}Ni_{0.85}Co_{0.15}$ alloy is the best one with a relatively large discharge capacity and a good cycling performance.

• 동국한의학연구소논문집
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• 제8권2호
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• pp.83-96
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• 2000

이 실험의 목적은 탄수화물 부하식이요법시의 삼출건비방 투여가 달리기 선수의 뇨중 대사성분변화에 미치는 영향에 대해 관찰 연구한 것이다. 탄수화물 부하식이시 삼출건비탕(蔘朮健脾湯) 투여는 전해질대사 관련 변인에 있어서 $Na^+$, $Cl^-$, $K^+$, $Ca^{+ +}$에 유의성 있는 영향을 미쳤으며, 이는 세포막 투과성의 변화를 의미하는 것으로 $Na^+$-$K^+$ pump의 활성도가 증가하여 운동수행능력을 향상시킬 것으로 기대되나 추후 전해질 대사와 관련하여 renin, aldosterone 등의 호르몬 분비 기전에 관해서도 지속적인 연구가 진행되어야 할 것으로 사려된다.

• Restorative Dentistry and Endodontics
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• 제12권1호
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• pp.39-49
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• 1986

The purpose of this study was to observe characteristic properties through the polarization curves and SEM images from 4 different types of amalgam obtained by using the potentiostats (Princeton EG & G) & SEM (Jeol/35), and to investigate the degree of corrosion on the oxidation peak of the each phase of amalgam. After each amalgam alloy and Hg was triturated as the direction of the manufacturer by means of the mechanical amalgamator (Shofu Co.), the triturated mass was inserted into the cylindrical metal mold which was 12mm in diameter and 10.0mm in height and was condensed by using routine manner. The specimen was removed from the mold and stored at room temperature for about 24 hours. The standard surface preparation was routinely carried out. Anodic polarization measurement was employed to confirm the corrosion behaviour of the amalgams in a 0.9% saline solution (P.H: 6.8-7.0) at $37^{\circ}C$. The initial rest potential (corrosion potential) was determined after 30 minutes of immersion of specimen in electrolyte, and the potential scan was begun at the point of 100mV cathodic from the corrosion potential. The scan rate was 0.17mV/sec. in the study to observe the degree of corrosion of each phase. SEI and EPMA images on the determined oxidation peaks of each amalgam were observed. The results were as follows: 1. In the four anodic polarization curves, low copper amalgams have three oxidation peaks and high copper amalgams have two oxidation peaks, -270mV, +26mV and +179mV(SEC) in the low copper lathe cut, and -300mV, +39mV and +163mV(SEC) in the low copper spherical. -4mV and +154mV(SEC) in the Dispersalloy, and +17mV and +180mV(SEC) in the Tytin as high copper amalgams. 2. ${\gamma}_2$ phase in the low copper amalgam and ${\eta}$ phase in the high copper amalgam were the most corrodible phases and Ag-Cu eutectic in high copper amalgam was the most slowly corroded phase. 3. Low copper amalgam was more susceptible in corrosion than high copper amalgam.

• Restorative Dentistry and Endodontics
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• 제16권1호
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• pp.6-15
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• 1991

The purpose of this study was to observe in vitro chloride corrosion behavior from 5 kinds of amalgam (Caulk spheracal, Amalcap, Dispersalloy, Tytin, Sybralloy) as a function of time after tritruration by using potentiostat. After each amalgam alloy and Hg was triturated as the direction of the manufacturer by the mechanical amalgamator, the triturated mass was inserted the cyrindrical matal mold ($12{\times}10mm$) and was condensed by using routine manner. The specimen was removed from the mold and was stored at room temperature for 1 week, 1 month and 3 months, and standard surface preparation was routine carried out. The 0.9% saline solution was used as electrolyte in pH 6.8~7.0 at $30{\pm}0.5.^{\circ}C$. The open circuit potential was determined after 30 minutes' immersion of 1 week, 1 month and 3 month old specimens. The scan rate was 1 mV/sec and the surface area of amalgam exposed to the solution was $0.65\;Cm^2$ for each specimen. All potentials reported are with respect to a silver / silver chloride electrode (SSE). The following result was obtained. 1. All amalgam specimens became more noble corrosion potentials which represent the improved corrosion resistance as the time elapsed. 2. Three kinds of high copper amalgam always exhibited more noble potential than low copper amalgam at 1 week, 1 month and 3 months. 3. Two kinds of low copper amalgam had the similar polarization curve pattern with 3 current peaks at each time period and current densities associated with these peaks were decreased as aging especially in caulk spherical amalgam. 4. All kinds of high copper amalgam had the similar polarization curve pattern with absence of prominent current peak at each time period, but the polarization curve of D amalgam had one apparent current peak at 1 week.