• 대한치과보철학회지
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• 제18권1호
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• pp.49-57
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• 1980

The adhesive mechanisms on the metal-ceramic restorations have been reported to be mechanical interlocking, chemical bonding, compressive force, and Van der Waal's force, etc. Of these, the mechanical interlocking and chemical bonding forces are thought to affect the adhesive force between Ni-Cr alloy and porcelain. This study investigates the adhesion of Ni-Cr alloy to porcelain according to surface treatment. For this purpose, the following experiments were made; The compositions of Ni-Cr alloy as cast by emission spectrograph, and the oxides produced on Ni-Cr alloy during degassing at $1850^{\circ}F$ for 30 minutes in air and in vacuum were analyzed by X-ray diffractograph. The metal phases of Ni-Cr alloy were observed according to porcelain-baking cyclic heat treatment by photo microscope and the distribution and the shift of elements of Ni-Cr alloy and porcelain and the failure phases between Ni-Cr alloy and porcelain by scanning electron microscope. The adhesive force between Ni-Cr alloy and porcelain was measured according to surface treatment with oxidization and roughening by Instron Universal Testing Machine. Results were as follows; 1. The metal phases of Ni-Cr alloy as cast and degassing state showed the enlarged and fused core, but when subjected to porcelain-baking cyclic heat treatment, showed a dendrite growing. 2. The kinds of metal oxides produced on Ni-Cr alloy during degassing were found to be NiO and $Cr_2O_3$. 3. The distribution of elements at the interface of Ni-Cr alloy and porcelain in degassing state showed demarcation line, but in roughening state, showed mechanical interlocking phase. 4. The shift of elements at the interface occurred in both states, but the shift amount was found to be larger in roughening than in degassing. 5. The adhesive force between Ni-Cr alloy and porcelain was found to be $3.45{\pm}0.93kg/mm^2$, in degassing and $3.82{\pm}0.99kg/mm^2$, in roughening. 6. The failure phase between Ni-Cr alloy and porcelain showed the mixed type failure.

• 한국지하수토양환경학회지:지하수토양환경
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• 제24권3호
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• pp.24-35
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• 2019

It is known that ${\delta}^{13}C_{DIC}$ (carbon-13 isotope of dissolved inorganic carbonate (DIC) ions) of water increases when dissolved $CO_2$ degases. However, ${\delta}^{13}C_{DIC}$ could decrease when the pH of water is lower than 5.5 at the early stage of degassing. Laboratory experiments were performed to observe the changes of ${\delta}^{13}C_{DIC}$ as $CO_2$ degassed from three different artificial $CO_2$-rich waters (ACWs) in which the initial pH was 4.9, 5.4, and 6.4, respectively. The pH, alkalinity and ${\delta}^{13}C_{DIC}$ were measured until 240 hours after degassing began and those data were compared with kinetic isotope fractionation calculations. Furthermore, same experiment was conducted with the natural $CO_2$-rich water (pH 4.9) from Daepyeong, Sejong City. As a result of experiments, we could observe the decrease of DIC and increase of pH as the degassing progressed. ACW with an initial pH of 6.4, ${\delta}^{13}C_{DIC}$ kept increasing but, in cases where the initial pH was lower than 5.5, ${\delta}^{13}C_{DIC}$ decreased until 6 hours. After 6 hours ${\delta}^{13}C_{DIC}$ increased within all cases because the $CO_2$ degassing caused pH increase and subsequently the ratio of $HCO_3{^-}$ in solution. In the early stage of $CO_2$ degassing, the laboratory measurements were well matched with the calculations, but after about 48 hours, the experiment results were deviated from the calculations, probably due to the equilibrium interaction with the atmosphere and precipitation of carbonates. The result of this study may be not applicable to all natural environments because the pressure and $CO_2$ concentration in headspace of reaction vessels was not maintained constant as well as the temperature. Nevertheless, this study provides fundamental knowledge on the ${\delta}^{13}C_{DIC}$ evolution during $CO_2$ degassing, and therefore it can be utilized in the studies about carbonated water with low pH and the monitoring of geologic carbon sequestration.

• 분석과학
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• 제21권6호
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• pp.487-494
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• 2008

극미량 우라늄시료에 대한 열이온화 질량분석기를 이용하여 우라늄 동위원소 비 측정 및 정량과 관련하여 고순도(zone refined) 레늄필라멘트와 일반 레늄필라멘트로부터 오는 바탕값(background) 특성을 비교하였다. 두 종류 필라멘트에서 가벼운 알칼리금속원소들의 클러스터(cluster)인 $(^{39}K_6)^+$, $(^{39}K_5+^{41}K)^+$ 및 금속산화물($PbO_2$)로 추측되는 우라늄 동중원소영향(isobaric effect)을 확인하였다. 고순도 레늄필라멘트를 < $10^{-7}$ torr에서 약 $2000^{\circ}C$로 1.5 시간 이상 degassing 함으로 불순물들을 완전히 제거할 수 있었으나 일반 레늄필라멘트의 경우 5시간 이상 degassing을 하여도 약 3 pg-U이 남아있었다. 일반 레늄필라멘트에 대한 불순물 제거(degassing) 실험결과 5 A, 30 분이 불순물제거의 최소조건이었다. U-233을 spike로 사용, 동위원소희석 질량분석법으로 일반 레늄필라멘트 중 불순물로 포함된 우라늄 양을 측정한 결과 degassing을 하지 않은 필라멘트에서는 0.31 ng-U이 측정되었고, degassing (5.5 A, 1 hr.)을 한 것은 약 3 pg-U 이 측정되었다. 즉, 일반필라멘트의 경우, degassing을 하더라도 1 ng-U 시료에 대하여 0.3% 오차를 근본적으로 갖는 것을 알 수 있었다. 따라서 환경급 극미량 우라늄시료 측정에는 고순도 필라멘트를 degassing하여 사용해야 함을 알 수 있었다. 우라늄 측정 시 필라멘트 전류를 5.5 A로 하였을 때보다 6.0 A로 했을 때 불순물 우라늄 량이 1.5 배 더 크게 나타났다. 따라서 필라멘트 전류를 5.5 A 이상 올리지 않는 것이 바탕값 영향이 작음을 알 수 있었다. 우라늄 표준물질(KRISS 표준물질/NIST U-005, 030)을 사용하여 우라늄 동위원소 함량을 측정한 후 인증 값과 비교한 결과 U-235 는 0.04%, U-234, U-236는 2% 이내에서 각각 일치하였다.

• 한국정밀공학회:학술대회논문집
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• 한국정밀공학회 2012년도 춘계학술대회 논문집
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• pp.851-852
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• 2012

• 대한기계학회:학술대회논문집
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• 대한기계학회 2007년도 춘계학술대회B
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• pp.2648-2653
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• 2007

Recently, increasing demand on not only lighter but also extremely mobile battery make micro fuel cell device very attractive alternative. By reducing the size of fuel cell, surface tension becomes dominant factor with minor gravitational effect. Therefore, it is very difficult to detach the $CO_2$ bubble generating on a cathode side in ${\mu}DMFC$ (micro direct methanol fuel cell). The degassing of a $CO_2$ bubble has drawn quite attention especially for ${\mu}DMFC$ due to its considerable effect on overall machine performance. Our attention has been paid to the dynamic behavior of immiscible bubble attached to the one side of the wall on 2D rectangular channel subject to external shear flow. We use Level Contour Reconstruction Method (LCRM) which is simplified version of front tracking method to track the bubble interface motion. Effects of Reynolds number, Weber number, advancing/receding contact angle and property ratio on bubble detachment characteristic has been numerically identified.

• 한국산학기술학회논문지
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• 제16권2호
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• pp.1364-1369
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• 2015

반도체 칩의 고집적화로 과거 와이어 본딩 공정에서 BUMP 공정으로 전환되면서 반도체칩과 외부 기기로 이어지는 통신선도 더욱 미세해짐으로 인해 보다 정밀한 작업이 필요한 실정이지만 PSPI의 고점도 특성상 정량제어가 어렵고 버블유입에 따른 수율의 저하가 계속되고 있는 실정이다. 따라서 본 논문에서는 반도체 BUMP 공정에서 고점도 감광성 폴리이미드(PSPI : Photosensitive Polyimide)의 도포(coating)시 발생하는 기포(gas)를 제거하여 공급하는 D&P(Degassing and Pumping) 시스템을 개발하였다.

• 대한치과보철학회지
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• 제27권1호
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• pp.143-179
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• 1989

To observe the bonding behavior of palladium-based alloys to porcelain; 1. Pd-Co binary alloy with the higher cobalt content, 2. Pd-Co binary alloy with the lower cobalt content, 3. Pd-Ag-Sn ternary alloy, 4. Pd-Ag binary alloy, 5. Pd-Cu-Au ternary alloy and 6. Pd-Cu binary alloy were made as 6 groups of experimental alloys. Each group of alloy was divided into 4 sub-groups such as one sub-group that was not degassed and three sub-groups that degassed for 5 minutes, 10 minutes and 15 minutes. On each specimen, weight changes after degassing, morphological changes of oxide layer by changing the degassing time, compositional changes at metal-ceramic interface and bond strength of metal-ceramic measured with planar shear test were observed and compared. The results of the present study allow the following conclusions to be drawn: 1. The alloy showing the greatest bond strength was Pd-Cu alloy without gold and bond strength was decreased by alloying gold to them. 2. Although Pd-Co alloy showed the most prominent oxidation behavior, bond strength of them to porcelain was not greatly high by the formation of porosities at metal-ceramic interfaces. 3. Likewise tin, cobalt formed the peaks on line profiles at metal-ceramic interface, however copper did not exhibit such peaks on line profiles. 4. Mainly, oxide layer on Pd-Co alloy was composed with cobalt, and for Pd-Co alloy with higher cobalt content the rise of bond strength was not significant by increased degassing time. 5. On Pd-Ag alloy not containing tin, during degassing for 15 minutes silver content was increased at metal-ceramic interface. 6. As an oxidized element, tin formed the oxide layers that widen their area by increasing the degassing time, while cobalt and copper showed the morphological changes of particle or crystal on oxide layer.

• 대한치과재료학회지
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• 제43권4호
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• pp.317-322
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• 2016

The effect of ice-quenching after degassing on the hardness change during simulated porcelain firing in a metal-ceramic Pd-Au-Ag alloy was investigated by means of hardness test, field emission scanning electron microscopic observations, and X-ray diffraction analysis. The hardness decreased by ice-quenching after degassing, which was induced by the homogenization of the ice-quenched specimen. The decreased hardness by ice-quenching after degassing was recovered from the 1st opaque stage which was the first stage of the remaining firing process for bonding porcelain. The microstructural change showed that the increase in hardness during the remaining firing process was caused by precipitation. The ice-quenching after degassing did not affect the hardness change during the subsequent porcelain firing process.

• 한국주조공학회지
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• 제23권2호
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• pp.69-76
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• 2003

The present work was undertaken to investigate the mutual effect of the individual melt treatment commonly applied in aluminum foundries such as grain refining, modification, degassing and filtration on the microstructures and the mechanical properties. A357 alloys were fabricated through various melt treatments such as degassing by gas bubbling filtration, modification via the addition of Al-Sr master alloy, grain refining through the addition of Al-Ti-B master alloy and filtration before pouring of the melt. Each melt treatment was performed at its optimum condition reported in the literatures. The effects of each melt treatment and their interactions on the microstructures and mechanical properties of A357 alloy were examined.

• 한국산학기술학회논문지
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• 제16권7호
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• pp.4357-4363
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• 2015

본 연구는 베릴륨 함유하지 않은 Ni-Cr계 도재용 금속에 전용도재를 도포, 소성된 시편을 3점 굴곡 시험으로 결합강도를 측정하고, SAM/EDS로 표면성분관찰 실험한 AVOVA와 Tukey HSAD 사후검정을 실시한 결과는 다음과 같은 결론을 얻었다. 첫째. 모든 군에서 ISO 9693의 치과용 금속-도재 시편의 최소 결합강도의 최소치인 25 MPa의 전단결합강도를 상위하며 안정적인 결과값을 나타냈다. 둘째. 결합 강도는 대조군 V1은 $32.37{\pm}1.91MPa$으로 나타났고, 실험군 V2 $38.25{\pm}1.38MPa$, 실험군 V3 $46.43{\pm}2.14MPa$, 그리고 실험군 V4 $47.21{\pm}1.72MPa$, 순으로 나타났으며 통계적으로 유의한 차이를 보였다. 사후 검정 (Tukey's HSD test) 결과, 결합강도 실험결과 실험군 V4는, 대조군 V1보다 높게 나타났다. 셋째. 금속-도재의 결합에서 산화처리를 시행한 군보다 시행하지 않고 불투명 도재를 도포하고 소성한 군이 높게 나타났으며, paste불투명 도재보다 분말 불투명도재의 사용에 따른 결합강도가 더 높게 나타났다. 넷째. 실험군 V4는 금속과 도재의 결합강도 비교에서 가장 높게 나타났다.