• 한국재료학회지
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• 제9권5호
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• pp.452-459
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• 1999

고연소도 핵연료피복관용 신합금 재료를 개발하기 위한 연구로 Zr-0.8Sn-xNb(x = 0.2,0.4,0.8, 1.0) 계 합금을 제조하여 Nb 첨가량이 Zr 합금의 미세구조 및 부식특성에 미치는 영향을 조사하였다. 미세조직 관찰결과 Nb첨가량이 증가함에 따라 결정립의 크기는 강소하였고 석출물의 량은 증가하였다. $360^{\circ}C$ 물 분위기에서 부식시험 한 결과 Nb 함량이 적을수록 부식저항성이 증가하는 경향을 나타냈으며며, Zr-0.8Sn-0.2Nb 합금이 가장 우수한 부식저항성을 보였다. 동얼 두께의 산화막에 대하여 XRD 분석한 결과, 내식성이 우수한 0.2 wt.% Nb 합금에서는 산화막내 tetra-$ZrO_2$의 분율이 높게 관찰되었다. 합금설계 관점에서 Zr-O.8Sn-xNb 합금계에 Nb올 첨가할때 Nb은 고용도 이하로 첨가되어야 한다고 사료된다.

• Corrosion Science and Technology
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• 제2권2호
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• pp.68-74
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• 2003

The effects of Niobium on the structure and properties(especially electric properties) of passive film of Zirconium alloys in pH 8.5 buffer solution are examined by the photo-electrochemical analysis. For Zr-xNb alloys (x = 0, 0.45, 1.5, 2.5 wt%), photocurrent began to increase at the incident energy of 3.5 ~ 3.7 eV and exhibited the $1^{st}$ peak at 4.3 eV and the $2^{nd}$ peak at 5.7 eV. From $(i_{ph}hv)^{1/2}$ vs. hv plot, indirect band gap energies $E_g{^1}$= 3.01~3.47 eV, $E_g{^2}$= 4.44~4.91 eV were obtained. With increasing Nb content, the relative photocurrent intensity of $1^{st}$ peak significantly increased. Compared with photocurrent spectrum of thermal oxide of Zr-2.5Nb, It was revealed that $1^{st}$ peak in photocurrent spectrum for the passive film formed on Zr-Nb alloy was generated by two types of electron transitions; the one caused by hydrous $ZrO_2$ and the other created by Nb. Two electron transition sources were overlapped over the same range of incident photon energy. In the photocurrent spectrum for passive film formed on Zr-2.5Nb alloy in which Nb is dissolved into matrix by quenching, the relative photocurrent intensity of $1^{st}$ peak increased, which implies that dissolved Nb act as another electron transition source.

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 1999년도 춘계학술발표회요약집
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• pp.231-231
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• 1999

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 1999년도 춘계학술발표회요약집
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• pp.226-226
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• 1999

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 1999년도 추계학술발표회요약집
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• pp.272-272
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• 1999

• 한국재료학회지
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• 제11권5호
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• pp.405-412
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• 2001

본 연구에서는 $360^{\circ}C$ 물 및 $360^{\circ}C$, 70ppm LiOH 수용액 분위기의 static autoclave를 이용하여 새롭게 개발한 Zr 신합금 (Zr-0.4Nb-0.8Sn-xFeCrMn, Zr-0.2Nb-1.1Sn-xFeCrMn, Zr-1.0Nb-xFeCu) 의 부식 특성을 평가하였다. 합금의 미세구조를 광학현미경과 TEM을 이용하여 관찰하였고, 부식시험 중에 생성된 산화막은 SEM과 XRD를 이용하여 단면 및 결정구조를 조사하였다. 부식시험 결과, 3종의 합금 모두 $360^{\circ}C$ 물 분위기보다 $360^{\circ}C$, 70ppm LiOH 수용액 분위기에서의 부식저항성이 감소하였으며 특히, High Nb 합금의 경우 급격한 가속 부식현상을 나타내었다. 합금원소 첨가량과 관련하여 Nb의 함량을 고용도 이내로 줄이고 Sn을 적절히 첨가한 조성의 합금이 Sn을 첨가하지 않고 고용도 이상의 Nb을 가진 합금보다 우수한 부식저항성을 나타내었다. 또한 최종열처리가 부식에 미치는 영향의 경우에, 완전재결정 조직의 합금이 부분재결정 조직을 가진 합금보다 부식저항성이 감소되었는데 이는 기지조직에서 석출하늘 제 2상의 크기 및 분포에 의한 영향으로 사료된다.

• 한국재료학회지
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• 제14권10호
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• pp.713-718
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• 2004

To study the dynamic strain aging behavior of Zr-0.4Sn-1.5Nb-0.2Fe sample tube for nuclear fuel cladding in the range of pressurized water reactor (PWR) operation temperature, the tensile tests of the tube specimens, which had been finally heat-treated at $470^{\circ}C\;and\;510^{\circ}C$, had been carried out with the strain rate $1.67{\times}10^{-2}/s\;and\;8.33{\times}10^{-5}/s$ at the various temperatures from room temperature to $500^{\circ}C$. It was observed that the elongation of the specimens got shortened as the temperature increased from $200^{\circ}C\;to\;340^{\circ}C$. The specimens that were finally heat-treated at $470^{\circ}C$ showed a plateau more remarkably on the plot of yield strength-temperature than those heat-treated at $510^{\circ}C$. In the range of $310\sim400^{\circ}C$, the strain rate sensitivity of the specimens finally heat-treated at $510^{\circ}C$ was $30.4\%\sim33.7\%$ lower but the work hardening exponent index of the specimens was a little higher than that without dynamic strain aging effect.

• 한국재료학회지
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• 제21권11호
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• pp.617-622
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• 2011

The effect of oxygen on the shape memory characteristics in Ti-18Nb-6Zr-XO (X = 0-1.5 at%) biomedical alloys was investigated by tensile tests. The alloys were fabricated by an arc melting method at Ar atmosphere. The ingots were cold-rolled to 0.45 mm with a reduction up to 95% in thickness. After severe cold-rolling, the plate was solution-treated at 1173 K for 1.8 ks. The fracture stress of the solution-treated specimens increased from 450 Mpa to 880 MPa with an increasing oxygen content up to 1.5%. The fracture stress increased by 287MPa with 1 at% increase of oxygen content. The critical stress for slip increased from 430 MPa to 695 MPa with an increasing oxygen content up to 1.5 at%. The maximum recovery strain of 4.1% was obtained in the Ti-18Nb-6Zr-0.5O (at%) alloy. The martensitic transformation temperature decreased by 140 K with a 1.0 at% increase in O content, which is lower than that of Ti-22Nb-(0-2.0)O (at%) by 20 K. This may have been caused by the effect of the addition of Zr. This study confirmed that addition of oxygen to the Ti-Nb-Zr alloy increases the critical stress for slip due to solid solution hardening without being detrimental to the maximum recovery strain.

• 한국해양공학회지
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• 제23권2호
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• pp.69-73
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• 2009

The objective of this study was to obtain a better understanding of the delayed hydride cracking (DHC) of Zr-2.5Nb alloy. The DHC model has some defects: first, it cannot explain why the DHC velocity (DHCV) becomes constant regardless of an applied stress intensity factor, even though the stress gradient is affected by the applied stress intensity factor at the notch tip. Second, it cannot explain why the DHCV has a strong dependence on the method of approaching the test temperature by a cool-down or a heating-up, even under the same stress gradient, and third, it cannot predict any hydride size effect on the DHC velocity. The DHC tests were conducted on Zr-2.5Nb compact tension specimens with the test temperatures reached by a heating-up method and a cool-down method. Crack velocities were measured in hydrided specimens, which were cooled from solution-treatment temperatures at different rates by being furnace-cooled, water-quenched, and liquid nitrogen-quenched. The resulting hydride size, morphology, and distributions were examined by optical metallography. It was found that fast cooling rates, which produce very finely dispersed hydrides, result in higher crack growth rates. This different DHC behavior of the Zr-2.5Nb tube with the cooling rate after a homogenization treatment is due to the precipitation of the $\gamma$-hydrides only in the water-quenched Zr-2.5Nb tube. This experiment will provide supporting evidence that the terminal solid solubility of a dissolution (TSSD) of $\gamma$-hydrides is higher than that of $\delta$-hydrides.

• 열처리공학회지
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• 제17권5호
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• pp.271-277
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• 2004

Zr-xNb alloys (x = 0.2, 0.8, 1.5 wt.%) were prepared to study the characteristics of the phase transformation in Zr-Nb system. The samples were heat treated at ${\beta}$-temperature ($1020^{\circ}C$) for 20 min and then cooled with different cooling rate. The microstructures of the specimens having the same compositions were changed with cooling rate and Nb content. The Widmanst$\ddot{a}$tten structure was observed on the furnace-cooled sample. The relationship between ${\alpha}$-Widmanst$\ddot{a}$tten and ${\beta}$-phase was the {0001}${\alpha}$//{110}${\beta}$, <11$\bar{2}$0>//<111>. The ${\beta}$-phase in Widmanst$\ddot{a}$tten structure of Zr-Nb alloys containing Nb more than solubility limit was identified as ${\beta}_{Zr}$ phase which was a stable phase at high temperature. In the water quenched samples, two kinds of martensite structures were observed depending on the Nb-concentration. The lath martensite was formed in Zr-0.2, 0.8 wt.% Nb alloys and the plate martensite having twins was formed in Zr-1.5 wt.% Nb alloy.