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용융염 LiCl-Li_2O-Li_3N에서 316LN SS의 용접부 부식거동
조수행,홍순석,신영준,박성원 한국공업화학회 2003 응용화학 Vol.7 No.1
In the development of the advanced spent fuel management process based on the molten salt technology, it is essential to choose the optimum material for the process equipment handling molten salt. As a part of assessment and application of the strutural material for the molten salt handling system, corrosion behavior of 316LN ss weld in the molten salts was investigated. In a molten salt of LiCI-Li_2O, the oxide scales of LiCrO_2 and Li_4M_0O_5 were formed at the rate of similar linear kinetics. But in the molten salt of lI-Li_2O-Li_3N, the oxide and nitride scales of Li_4M_0O_5 and M_02N were formed at the rate of simliar linear kinetics. The corrosion rate of 316 LN ss in the molten salt of LiCI-Li_2O was lower than that in the molten salt of LiCI-Li_2O-Li_3N.
용융염 LiCl 및 LiCl-$Li_2O$에서 내열합금 More 1과 Super 22H의 부식거동
조수행,박상철,장준선,신영준,박현수,Jo, Su-Haeng,Park, Sang-Cheol,Jang, Jun-Seon,Sin, Yeong-Jun,Park, Hyeon-Su 한국재료학회 1999 한국재료학회지 Vol.9 No.6
The corrosion behavior of heat-resistant alloys, More 1 and Super 22H in molten salts of LiCl and $LiCl-Li_2$O was investigated in the temperature range of $650~850^{\circ}C$. In a molten salt of LiCl, a dense protective oxide scale of $LiCrO_2$ was formed, following growth of oxide scale with parabolic kinetics. But in a mixed molten salt of LiCl, a dense protective oxide scale of $LiCrO_2$ was formed, following growth of oxide scale with parabolic kinetics. But in a mixed molten salt of $LiCl-Li_2$O, a porous non-protective scale of Li\ulcorner(Cr, Ni, Fe)\ulcornerO$_2$was formed, following growth of oxide scale with linear kinetics. The corrosion rate increased slowly with the increase of temperature up to $750^{\circ}C$, but above $750^{\circ}C$ rapid increase in corrosion rate observed. The corrosion behavior of Super 22H alloy was similar to that of More 1 alloy, but Super 22H showed higher corrosion resistance than More 1.
조수행,홍순석,정명수,도재범,박현수,Jo, Su-Haeng,Hong, Sun-Seok,Jeong, Myeong-Su,Do, Jae-Beom,Park, Hyeon-Su Materials Research Society of Korea 1999 한국재료학회지 Vol.9 No.4
Effects of heating time and radiation under high temperature on the properties of thermal, mechanical and shielding ability of modified (KNS-101), hydrogenated bisphenol-A(KNS-201) type epoxy resin and phenol-novolac(KNS-301) type epoxy resin based neutron shielding materials that are used for shipping casks for radioactive material have been investigated. At early stages, the offset temperatures of KNS-101, KNS-201 and KNS-301 increased with the heating time under high temperature, but it was rarely affected by the heating time in the later stages. In addition, the thermal conductivities of KNS-101 and KNS-201 decreased with heating time, but that of KNS-301 increased with the heating time. On the contrary, the thermal expansion coefficients of neutron shielding materials decreased with heating time. At the high temperature, the tensile strength and flexural strength of the shielding materials decreased with heating time. On the contrary, the thermal expansion coefficients of neutron shielding materials decreased with heating time. At the high temperature, the tensile strength and flexural strength of the shielding materials of KNS-101 and KNS-301 increased with heating time, but those of KNS-201 decreased with heating time. The shielding ability of neutron shielding materials slightly increased with the radiation dose, and shielding abilities of shielding materials of KNS-101 and KNS-201 were affected to a more extent than that of KNS-301 by radiation dose under high temperature.
LiCl 및 LiCl-${Li_2}O$ 용융염에서 Fe-Ni-Cr 합금의 부식거동 연구
조수행,장준선,홍순선,신영준,박현수,Jo, Su-Haeng,Jang, Jun-Seon,Hong, Sun-Seon,Sin, Yeong-Jun,Park, Hyeon-Su 한국재료학회 2000 한국재료학회지 Vol.10 No.7
Fe-Ni-Cr 합금의 용융염 부식거동을 $650~850^{\circ}C$ 온도범위에서 조사하였다. 용융염 LiCl에서 Cr을 포함하지 않는 KSA(Kaeri Superalloy)-1 합금은 Fe의 내부산화가 발생하고, Cr을 포함한 KSA-4, Incoloy 800H와 KSA-5는 LiCrO$_2$의 치밀한 보호막이 형성되었다. 혼합용융염 $LiCl-LiO_2$O에서 KSA-1은 Fe의 내부산화, KSA-4는 Cr의 내부산화가 발생하였고, Cr 농도가 높은 Incoloy 800H와 KSA-5는 $LiCrO_2$의 다공성 피 이 형성되었다. 혼합용융염 $LiCl-Li_2$O 에서는 Cr 농도의 증가에 따라 부식속도가 증가하였으며, 부식속도는 시간의존선을 8%Cr 이하의 합금에서는 포물선법칙, 8%Cr 이상의 합금에서는 직선법칙을 나타내었다. 이러한 현상은 Li$_2$O에 의한 보호성 산화물 $Cr_2O_3$의 염기성 용해기구로 설명할 수 있다. Corrosion behavior of Fe-Ni-Cr alloy in molten salts of LiCl and LiCl-$Li_2O was investigated in the tempera-ture range of $650~850^{\circ}C$. In the molten salt of LiCl, and internal oxidation of Fe occurred in the KSA(Kaeri Superalloy)-1 alloy without containing Cr, while a dense protective oxide scale of $LiCrO_2$ was formed in the KSA-4, Incoloy 800H and KSA-5 alloys. In the mixed molten salt of LiCl-$Li_2O$, internal oxidation of Fe and Cr took place in the KSA-1 and KSA-4 alloys, respectively. Non-protective porous oxide scales consisting of $LiCrO_2$ and Ni were formed in the Incoloy 800H and KSA-5. The corrosion rate of the alloys increased with the increase in Cr content and the corrosion rate followed the parabolic law for the alloy containing Cr content less than 8%, and the linear law for the alloy containing Cr content more than 8%. Such a corrosion behavior of the alloy in the mixed molten salt of LiCl-$Li_2O$ was interpreted in terms of the basic fluxing mechanism of protective oxide scale of $Cr_2O_3$.
조수행,임종호,정준호,오승철,서중석,박성원,Cho Soo-Hang,Lim Jong-Ho,Chung Jun-Ho,Oh Seung-Chul,Seo Chung-Seok,Park Seoung-Won 한국재료학회 2004 한국재료학회지 Vol.14 No.11
The electrolytic reduction of spent oxide fuel involves the liberation of oxygen in a molten LiCl electrolyte, which is a chemically aggressive environment that is very corrosive for typical structural materials. So, it is essential to choose the optimum material for the process equipment handling molten salt. In this study, corrosion behavior of Haynes 263, 75, and Inconel X-750, 718 in molten salt of $LiCl-Li_{2}O$ under oxidation atmosphere was investigated at $650^{\circ}C\;for\;72\sim360$ hours. At $3\;wt\%\;of\;Li_{2}O$, Haynes 263 alloy showed the highest corrosion resistance among the examined alloys, and up to $8\;wt\%\;of\;Li_{2}O$, Haynes 75 exhibited the highest corrosion resistance. Corrosion products were formed $Li(Ni,Co)O_2,\;LiNiO_2\;and\;LiTiO_2\;and\;Cr_{2}O_3$ on Haynes 263, $Cr_{2}O_3,\;NiFe_{2}O_4,\;LiNiO_2,\;Li_{2}NiFe_{2}O_4,\;Li_{2}Ni_{8}O_10$ and Ni on Haynes 75, $Cr_{2}O_3,\;(Al,Nb,Ti)O_2,\;NiFe_{2}O_4,\;and\;Li_{2}NiFe_{2}O_4$ on Inconel X-750 and $Cr_{2}O_3,\;NiFe_{2}O_4\;and\;CrNbO_4$ on Inconel 718, respectively. Haynes 263 showed local corrosion behavior and Haynes 75, Inconel X-750, 718 showed uniform corrosion behavior.
알루미나 나노템플레이트의 기공형성에 미치는 2차 양극산화의 영향
조수행,오한준,주은균,유창우,지충수,Cho, S.H.,Oh, H.J.,Joo, E.K.,Yoo, C.W.,Chi, C.S. 한국재료학회 2002 한국재료학회지 Vol.12 No.7
Porous anodic aluminum oxide layer for nano templates was prepared in acidic solutions. In order to investigate effects of 2nd anodization on ordered formation behaviors of the porous oxide layers, electrochemical and microstructural studies were performed, primarily using TEM, FE- SEM, AFM, and Ultramicrotomy. The pore diameter of the anodic oxide layer increased approximately linearly with increasing voltages, and to the contrary, the pore density decreased. It was shown that 2nd anodizing on the cell base after dissolving 1st anodic oxide layer was remarkably effective for forming ordered array of the pores, comparing with the case for 1st anodization only. And for controlling the diameter of pores, widening method by chemical dissolution seemed more practical than by electrochemical methods.
조수행,오한준,김성수,주은균,유창우,지충수,Cho, S.H.,Oh, H.J.,Kim, S.S.,Joo, E.K.,Yoo, C.W.,Chi, C.S. 한국재료학회 2002 한국재료학회지 Vol.12 No.11
To investigate effects of heat treatments including grain size control in substrate aluminum on nanopore arrays in anodic alumina template, aluminum was heat treated at $500^{\circ}C$ for 1h. The heat treated aluminum was anodized by two successive anodization processes in oxalic solution and the nanopore arrays in anodic alumina layer were studied using TEM and FE-SEM. The highly ordered porous alumina templates with 110 nm interpore distance and 40 nm pore diameter have been observed and the pore array of the anodic alumina has a uniform and closely-packed honeycomb structure. In the case of alumina template obtained from heat treated aluminum substrate, the well- ordered nanopore region in anodic alumina increased and became more homogeneous compared with that from non-heattreated one.