• 한국재료학회지
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• 제12권4호
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• pp.259-263
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• 2002

Three different ribbons of amorphous $Til_{1-x}Be_x$ alloys such as $Ti_{0.59}Be_{0.41},\;Ti_{0.61}Be_{0.39}\;and\;Ti_{0.63}Be_{0.37}$ were made by melt-spinning method to be used as brazing filler metals for joining Zircaloy-4 nuclear fuel cladding tubes, and their crystallization behavior as well as microstructure of the brazed zone were examined. The crystallization behavior was investigated in teams of thermal stability, crystallization temperature and activation energy. The crystallization of the $Ti_{1-x}Be_x$ alloys proceeded in two steps by the formation of ${\alpha}$-Ti at a lower temperature and of TiBe at a higher temperature. The crystallization temperature and activation energy of $Ti_{1-x}Be_x$ alloys were higher and larger than those of $Zr_{1-x}Be_x$ alloys and PVD Be. Those resulted thinner joining layer with $Ti_{1-x}Be_x$ alloys, which kept sound thickness of Zircaloy-4 nuclear fuel cladding tubes after brazing. But in the brazed zones made by $Ti_{1-x}Be_x$ filler metals, a little solid-solution layers composed of Zr and Ti were formed toward the Zr cladding tube and Zr was detected in the brazed zones. Microstructure of brazed zone was changed from globular to dentrite with decreasing Be content in the $Ti_{1-x}Be_x$ filler metal.

• 한국식품과학회지
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• 제34권2호
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• pp.238-243
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• 2002

자색고구마 anthocyanin 색소 용액은 가열에 의해 1차 반응속도식에 따라 색소 함량이 감소하였으며, 이 반응은 색소용액의 농도와 가열온도에 영향을 받았다. 이 반응의 활성화 에너지 값은 색소 용액의 농도에 따라 51.29-73.02 kJ/mol이었으며, 농축하지 않은 색소 추출액을 제외하면 활성화 에너지는 색소의 농도가 증가함에 따라 직선적으로 감소하였다. 자색고구마색소를 첨가한 매실음료의 anthocyanin 색소 역시 저장 중 1차 반응에 따라 색소가 감소하였는데, 저장온도가 낮아질수록 반응속도가 낮아져 저장기간이 증가하여, $5^{\circ}C$에서 저장한 경우는 저장 8개월까지 80%이상의 색소 잔존률을 나타냈다. 매실음료에 함유된 자색고구마 anthocyanin색소 변화에 대한 활성화 에너지는 75.80 kJ/mol이었다.

• 한국재료학회지
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• 제23권10호
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• pp.580-585
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• 2013

To observe the formation of defects at the interface between an oxide semiconductor and $SiO_2$, ZnO was prepared on $SiO_2$ with various oxygen gas flow rates by RF magnetron sputtering deposition. The crystallinity of ZnO depends on the characteristic of the surface of the substrate. The crystallinity of ZnO on a Si wafer increased due to the activation of ionic interactions after an annealing process, whereas that of ZnO on $SiO_2$ changed due to the various types of defects which had formed as a result of the deposition conditions and the annealing process. To observe the chemical shift to understand of defect deformations at the interface between the ZnO and $SiO_2$, the O 1s electron spectra were convoluted into three sub-peaks by a Gaussian fitting. The O 1s electron spectra consisted of three peaks as metal oxygen (at 530.5 eV), $O^{2-}$ ions in an oxygen-deficient region (at 531.66 eV) and OH bonding (at 532.5 eV). In view of the crystallinity from the peak (103) in the XRD pattern, the metal oxygen increased with a decrease in the crystallinity. However, the low FWHM (full width at half maximum) at the (103) plane caused by the high crystallinity depended on the increment of the oxygen vacancies at 531.66 eV due to the generation of $O^{2-}$ ions in the oxygen-deficient region formed by thermal activation energy.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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• pp.323-323
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• 2013

High power light-emitting diodes (LEDs) are widely used in many device applications due to its ability to operate at high power and produce high luminance. However, releasing the heat accumulated in the device during operating time is a serious problem that needs to be resolved to ensure high optical efficiency. Ceramic or Aluminium base metal printed circuit boards are generally used as integral parts of communication and power devices due to its outstanding thermal dissipation capabilities as heat sink or heat spreader. We investigated the characterisation of electroless plating of Ni-B film according to plating bath temperature, ranging from $50^{\circ}C$ to $75^{\circ}C$ on Ag paste/anodised Al ($Al_2O_3$)/Al substrate to be used in metal PCB for high power LED packing systems. X-ray diffraction (XRD), Field-Emission Scanning Electron Microscopy (FE-SEM) and X-ray Photoelectron Spectroscopy (XPS) were used in the film analysis. By XRD result, the structure of the as deposited Ni-B film was amorphous irrespective of bath temperature. The activation energy of electroless Ni-B plating was 59.78 kJ/mol at the temperature region of $50{\sim}75^{\circ}C$. In addition, the Ni-B film grew selectively on the patterned Ag paste surface.

• 대한화학회지
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• 제21권6호
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• pp.427-433
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• 1977

강물 시료속에 함유된 크롬, 철, 란탄, 스칸듐 및 아연의 함량을 방사화 분석법으로 동시정량하는 방법을 확립하였다. 10ml의 강물 시료를 사전 처리없이 석영관 속에 밀봉한 다음 열중성자속이 $1{\times}10^{13}n{\cdot}cm^{-2}{\cdot}sec^{-1}$인 곳에서 1주일간 조사하였다. 약 2일간 냉각시킨 후 시료 속에든 원소들을 0.1M 옥신의 클로로포름용액으로 여러 pH에서 연속적으로 추출하였다. 감마선 분광분석을 위하여 유기층을 800챈널 펄스높이 분석기에 연결된 $″3\;{\times}\;3″$ NaI (T1) 검출기로 계측하였다. 본분석법에 의하여 대부분의 강물 시료에 ppb 농도범위로 함유된 이들 원소들의 정량이 가능하였다. 추적자를 써서 이들 원소의 정량적 분리를 위한 연구를 수행하였다.

• Korean Chemical Engineering Research
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• 제50권3호
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• pp.551-555
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• 2012

활성탄을 이용한 산업체 악취물질 제거 특성을 규명하기 위하여 일반적으로 사용되는 상업용 활성탄의 탈착반응 특성을 조사하였다. 활성탄의 물리 화학적 특성을 조사하기 위해 BET 비표면적을 분석하였으며, 활성탄의 흡착력을 평가하기 위해 요오드가를 측정하였다. 활성탄에 흡착된 악취물질의 탈착반응특성 평가를 위해 열중량분석기(Thermogravimetric Analyzer; TGA)를 사용하였다. 활성탄의 흡 탈착에 따른 반응특성을 알아보기 위해 Friedman 법과 Freeman-Carroll 법을 이용하여 활성화에너지와 반응차수를 계산하였다. 활성탄은 신탄일 때 보다 재생탄일 때 흡착능력이 현저히 떨어졌으며, Friedman 법을 이용하여 활성화 에너지를 계산한 결과 15.9~23.4 kJ/mol, Freeman-Carroll 법을 이용하여 계산한 결과 22.7~33.8 kJ/mol로 나타났다.

• BMB Reports
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• 제29권6호
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• pp.493-499
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• 1996

The biochemical properties of purified D-hydruxyisovalerate dehydrogenase from Fusarium sambucinum was elucidated. D-Hydroxyisovalerate dehydrogenase produced solely D-hydroxyisovalerate from 2-ketoisovalerate. The isoelectric point of the purified enzyme was 7.0. The enzyme was highly specific with 2-ketoisovalerate ($K_{m}=0.188$ mM, $V_{max}=8.814$ mmol/min mg) and 2-keto-3-methyl-n-valerate ($K_{m}=0.4$ mM, $V_{max}=1.851$ mmol/min mg) for the reductive reaction. This was also seen by comparing D-hydroxyisovalerate ($K_{m}=1.667$ mM, $V_{max}=0.407$ mmol/min mg) and D-hydroxy-3-methyl-n-valerate ($K_{m}=6.7$ mM, $V_{max}=0.648$ mmol/min mg) for the oxidative reaction. Thiol blocking reagents, such as iodoacetamide, N-ethylmaleimide and p-chloromecuribenzoate inhibited about 80% of enzyme activity at 0.02 mM, 50 mM and 50 mM, respectively. The enzyme activity was also inhibited by the addition of 0.1 mM of various metal ions, such as $Fe^{2+}$ (67%), $Cu^{2+}$ (88%), $Zn^{2+}$ t (76%) and $Mg^{2+}$ (9%). The enzyme was stable over three months in 50 mM potassium phosphate buffer (pH 5~7) at $-80^{\circ}C$. However the purified enzyme lost 30% of its activity in the same buffer after 24 h at $4^{\circ}C$. The studies about thermal inactivation of D-hydroxyisovalerate dehydrogenase exhibit 209.2 kJ/M of activation enthalpy and 0.35 kJ/mol K of activation entropy.

• 대한전자공학회논문지
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• 제14권3호
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• pp.25-31
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• 1977

Fe O 와 V O 를 적당한 mole비로 혼합하여 H -CO 분위기 중 1,100℃에서 10시간씩 5∼6회 반복소성하여 Fe V O Spinel을 제조하였다. 제조된 시편의 온도에 대한 저항률을 측정하고 이로부터 활성화에너지를 구해서 시편의 도전기구를 고찰하고, x, 주위온도, 시편의 두께 및 인가전압 상승률에 대한 I-V 특성곡선을 얻어서 부성저항 발생기구의 해명을 시도하였다. Fe V -O spinel의 도전은 주로 B자리의 Fe 와 F 사이의 전자 hopping에 기인되며, 부성저항은 filament형의 통전로에 기인되는 열적현상이라 생각된다.

• 대한화학회지
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• 제8권2호
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• pp.88-91
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• 1964

모나자이트中의 스칸디움含量을 더욱 簡便히 決定할 수 있도록 改良한 放射化分析法을 記述하였다. 즉 熱中性子束($10^{12}n/cm^2/sec$)에 照射된 試料에 스칸듐擔體와 黃酸을 넣고 加熱融解한 後 물로 稀釋한 試液에 암모니아水를 加하여 稀土類元素를 沈澱分離하였다. 沈澱을 鹽酸에 녹힌 다음 티오시안酸암모늄을 넣어 스칸듐을 에테르로 抽出하였다. 스칸듐의 化學的 回收率은 스칸듐을 만델린酸으로 沈澱시켜서 重量分析法에 依하여 決定하였다. 本分離法에 依한 스칸듐의 分離能과 共存元素의 放射能의 妨害與否는 이온交換樹脂를 使用하여 스칸듐을 分離한 結果와 比較檢討하였다. 스칸듐의 放射能은 Gamma-scintillation spectrometry 에 依하여 計測하였고 韓國産 모나자이트에는 約 12 p.p.m.의 스칸듐의 含有되어 있음을 알았다.

• 한국전기전자재료학회논문지
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• 제12권1호
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• pp.44-49
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• 1999

In this study, microstructure and electrical conductivity of {(G $d_2$ $O_3$)$_{0.75}$( $Y_2$ $O_3$)$_{0.25}$}$_{x}$ (Ce $O_2$)$_{1-x}$ (0.01$\leq$x$\leq$0.25) was investigated as a function of composition x. GYO addition(x) increased the bulk density and G $d_2$ $O_3$ was found to be monoclinic at x>0.15. From the change of the lattice parameter with the addition(x), GYO solution limit for ceria was exceeded in the range of x=0.05 to 0.09. Thermal expansion coefficient(15~17$\times$10$^{-6}$ $^{\circ}C$) of GYC samples at x=0.01 to 0.07 was higher in value than that of 8YSZ(10.8$\times$10$^{-6}$ $^{\circ}C$). The electrical conductivity of GYC samples at x=0.05 showed the maximum(0.01S/cm) in value at 1073K which was 2 times higher than that of 8YSZ. The activation energy for the electrical conduction was determined to be 0.60eV in the temperature range of 1073K.3K..3K.