• Title/Summary/Keyword: $UO_3$

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Fabrication of Carbon-dispersed $UO_3$ Microspheres by an Internal Gelation

  • Lee, Jung-Won;Lee, Young-Woo;Shigeru Yamagishi;Akinori Itoh;Toru Ogawa
    • Proceedings of the Korean Nuclear Society Conference
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    • 1995.05a
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    • pp.662-667
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    • 1995
  • An internal gelation process was adopted for the fabrication of carbon-dispersed UO$_3$ microspheres which will be fed to the fabrication for uranium nitride microsphere fuels by the carbothermic reduction. For investigating the proper process conditions, a composition range of feed solution for preparing good UO$_3$ gel spheres was firstly defined by observing the gelation behavior. Within the defined solution compositions, carbon-dispersed microspheres were prepared and carbon distribution in microspheres were observed by SEM. The results showed that production of good carbon-dispersed microspheres was possible, and the most of carbon were evenly distributed in the microspheres although large carbon-rich aggregates were sparsely existent.

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The Stability Constant of 1, 7, 10, 16-Tetraoxa-4, 13-Diazacyclooctadecane-Uranium (Ⅵ) Complex in Aqueous Solution

  • Suh, Moo-Yul;Eom, Tae-Yoon;Kim, Si-Joong
    • Bulletin of the Korean Chemical Society
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    • v.4 no.5
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    • pp.231-234
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    • 1983
  • The stability constant for the complex of $UO_2^{2+}$ with a macrocyclic aminoether ligand, 1,7,10,16-tetraoxa-4,13-diazacyclooctadecane, has determined in aqueous solution. The conductivity and pH metric measurements suggest that the ligand forms a stable 1:1 complex with $UO_2^{2+}$ ion, and the complex is an ionic form, $UO_2L^{2+}$, in aqueous solution. The fact that the ligand does not form a complex with lanthanides, such as $Ce^{3+}$, $Sm^{3+}$, and $Nd^{3+}$ ions, in aqueous solution suggests a possibility of separation of the lanthanide elements from uranium matrix using the macrocyclic aminoether ligand.

Preparation of an Intermediate and Particle Characteristics for HTGR Nuclear Fuel (고온가스로 핵연료 중간물질 제조와 분말특성)

  • Jeong, Kyung-Chai;Kim, Yeon-Ku;Oh, Seung-Chul;Lee, Young-Woo
    • Journal of the Korean Ceramic Society
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    • v.44 no.2 s.297
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    • pp.124-131
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    • 2007
  • In this study, first the ADU gel particle, an intermediate for final $UO_2$ kernel of a HTGR nuclear fuel, was prepared from sol-gel method using the broth solution which was made by mixing of the uranyl nitrate, poly vinyl alcohol and tetra-hydrofurfuryl alcohol. The prepared dried-ADU gel particles were converted to the $UO_2\;via\;UO_3$ from thermal treatment with the 4% $H_2$ atmosphere. The sizes of the spherical liquid droplets appeared $1900{\sim}2100{\mu}m$, and the harmony between the flow rate of the broth solution and the frequency and the amplitude of a vibrating system are important factors for the spherical ADU gel particles via the mono size spherical droplets. From the XRD and FT-IR analyses, the prepared ADU gel particles were judged to be a $UO_3{\cdot}xNH_3{\cdot}yH_2O$ form, and the most important factor during the thermal treatment of the dried-ADU gel particle must be avoided a rapidly heating rate in the range of $180{\sim}400^{\circ}C$, and the heating rate should be kept below $5^{\circ}C/min$.

Sintering of a Mixture of $UO_2$ and $Gd_2 O_3$ Powders Doped With $Cr_2 O_3-SiO_2$

  • Kim, Keon-Sik;Song, Kun-Woo;Kang, Ki-Won;Yang, Jae-Ho;Kim, Jong-Hun
    • Nuclear Engineering and Technology
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    • v.33 no.4
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    • pp.386-396
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    • 2001
  • Mixtures Of AUC-UO$_2$and Gd$_2$O$_3$ Powders doped With Cr$_2$O$_3$ or Cr$_2$O$_3$-SiO$_2$ were Pressed and sintered at 1730 t in hydrogen gas witk various water-vapor contents. The density of UO$_2$- 6wt% Gd$_2$O$_3$ pellets can be increased from 91% TD to 94.5% TD in 1 vol% $H_2O$-H$_2$ gases by the addition of 0.02wt% Cr$_2$O$_3$-(0.01~0.04) wt% SiO$_2$. The magnitude of density increase is much larger in (1~3 vol%) $H_2O$-H$_2$ gases than in 0.05 vol% $H_2O$-H$_2$ gas. The densification of U0$_2$- Gd$_2$O$_3$ compact is significantly delayed in the temperature range between 1300 and 1500 t , but that of compacts with Cr$_2$O$_3$-SiO$_2$ is not. The role of Cr$_2$O$_3$ and SiO$_2$ in densification is discussed.

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Effect of a Li2O Additive on the Sintering Behavior of UO2 in the H2 and CO2 Atmospheres

  • Kim, Si-Hyung;Joung, Chang-Young;Kim, Yeon-Gu;Lee, Soo-Chul;Kim, Ban-Soo;Na, Sang-Ho;Lee, Young-Woo;Suhr, Dong-Soo
    • Journal of the Korean Ceramic Society
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    • v.41 no.8
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    • pp.567-572
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    • 2004
  • The variation of the sintered density and grain size of UO$_2$ as a function of the Li$_2$O amount and sintering atmosphere was observed. Li$_2$O enhanced the grain growth of the UO$_2$ pellet in H$_2$, but rather hindered it in $CO_2$ atmosphere. Grain size of the UO$_2$ and UO$_2$-0.1 wt%Li$_2$O pellets was, respectively, 8 $\mu$m and 100 $\mu$m at 168$0^{\circ}C$ in the H$_2$ atmosphere, and that of each pellet was, respectively, 24 $\mu$m and 17 $\mu$m at the same temperature in the $CO_2$ atmosphere. As-received Li$_2$O powder, which had been composed of Li$_2$O and LiOH, was converted to the Li$_2$CO$_3$ phase after heating to 80$0^{\circ}C$ in $CO_2$. On the other hand, the Li$_2$O and LiOH phases remained unchanged in H$_2$ atmosphere. In the H$_2$, the as-received Li$_2$O powder began to evaporate at about 105$0^{\circ}C$ and then about 20 wt% residue was left at 150$0^{\circ}C$. But, most of the Li elements evaporated at 150$0^{\circ}C$ in the $CO_2$ atmosphere.

Synthesis and Characterization of UO2(VI), Th(IV), ZrO(IV) and VO(IV) Complexes with Schiff-Base Octaazamacrocyclic Ligands (Schiff-염기인 옥타아자-거대고리 리간드의 UO2(VI), Th(IV), ZrO(IV) 및 VO(IV) 착물 합성 및 특성)

  • Mohapatra, Ranjan Kumar;Dash, Dhruba Charan
    • Journal of the Korean Chemical Society
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    • v.54 no.4
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    • pp.395-401
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    • 2010
  • A series of macrocyclic complexes of the type [M(L/L')$(NO_3)_n$].$mH_2O$ and [VO(L/L')($SO_4$)].$2H_2O$, where L/L' is a Schiff base "3,4,10,11-tetraphenyl/tetramethyl-1,2,5,6,8,9,12,13-octaaza cyclotetradeca-2,4,9,11-tetraene-7,14-dithione" derived from thiocarbohydrazide (TCH), benzilmonohydrazone (BMH)/diacetylmonohydrazone (DMH) and carbon disulphide, M = $UO_2$ (VI), Th(IV) and ZrO(IV), n = 2, 4, m = 2, 3, have been synthesized via metal ion template methods. The complexes are characterized on the basis of elemental analysis, thermal analysis, molar conductivity, magnetic moment, electronic, infrared and $^1H$-NMR spectral studies. The ESR and cyclic voltammetry studies of the vanadyl complexes have been carried out. The results indicate that the VO(IV) ion is penta-coordinated yielding paramagnetic complexes; $UO_2$(VI) and ZrO(IV) ions are hexacoordinated where as Th(IV) ion is octa-coordinated yielding diamagnetic complexes of above composition.

산소농도 측정을 위한 $UO_{2}$ 펠릿 공기산화로 장치의 갈바닉 센서와 지르코니움 센서의 특성 연구

  • Kim, Yeong-Hwan;Jeong, Jae-Hu;Lee, Hyo-Jik;Park, Byeong-Seok;Yun, Ji-Seop
    • Proceedings of the Korean Radioactive Waste Society Conference
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    • 2007.05a
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    • pp.151-152
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    • 2007
  • ACP(Advanced Spent Fuel Conditioning Process)의 금속전환로에 $U_{3}O_{8}$을 공급하기 위하여 20 kgHM/batch의 $UO_{2}$ 펠릿(pellets)을 처리할 수 있는 공기산화로가 개발되고 있다. 그림 1은 산소농도 조절이 가능한 공기산화로이다. 공기산화로 이전의 공정인 슬리팅 장치에서 탈피복된 $UO_{2}$ 펠릿은 공기산화로로 운반되고, $500^{\circ}C$온도에서 공기를 공급하여 일정한 입도범위의 균질한 $U_{3}O_{8}$을 만든다. 그리고 다음공정의 금속전환장치로 이동된다. 본 논문에서는 모의연료의 산화에 대한 정확한 산소농도를 측정하고자 한다. 이를 위해서 갈바닉 센서와 지르코니움 센서가 사용되었고, 그 특성이 비교되었다. 14종의 금속 산화물이 혼합된 모의연료를 제조하여 산화실험이 수행되었으며, 시간변화에 따라 산소농도가 측정되었다. 산소농도 컨트롤러와 산소 센서를 사용한 공기산화로는 산소조절기에 의해 산소농도 100%까지 측정될 수 있다. 그림 2는 공기산화로의 산소농도를 조절할 수 있는 산소농도 측정시스템이다. 유량조절기(Mass Flow Controller)를 사용하여 질소와 산소의 혼합비를 변화시킬 수 있다. 또한 산소농도 측정시스템은 측정된 산소농도 값을 이용하여 $UO_{2}$의 산화시간을 계산하기 위하여 제작하였다. 산화시간 계산방법은 다음과 같다. 산소와 질소의 가스는 각각 40 L의 압력 봄베에 의해서 산소농도를 조절할 수 있는 공기산화로의 산소농도 측정시스템 안으로 유입된다. 유입된 산소와 질소의 배합은 컨트롤시스템 안에 있는 산소 유량조절기와 질소 유량 조절기를 사용하여 조절하며, 일정하게 혼합된 산소농도는 장치의 입구와 출구에서 산소 센서에 의해서 측정된다. 투입된 $UO_{2}$ 펠릿이 $500^{\circ}C$에서 반응하면서 공기산화로의 내부에 있는 산소농도가 감소된다. 이때 초기에 같았던 입력과 출력 농도가 시간의 흐름에 따라 감소되며, 펠릿이 완전히 산화됨과 동시에 출력 산소농도가 입력농도와 다시 같아질 때까지 소요된 구간이 산화시간이 된다.

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Thermophysical Properties of $UO_2$ Fuel Materials

  • Lee, Hung-Joo;Kim, Chul-Whan
    • Nuclear Engineering and Technology
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    • v.8 no.2
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    • pp.81-88
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    • 1976
  • A flash method for measuring the unknown thermal property (the density, specific heat, or thermal diffusivity could be chosen as unknown) is described. The thermal diffusivity of UO$_2$ fuel samples is obtained from room temperature (300 K) to high temperature (1400 K). The specific heat is measured using a commercially available differential scanning calorimeter from room temperature to 500 K. The thermal conductivity of UO$_2$ fuel samples is calculated from the density, thermal diffusivity, and specific heat at constant pressure. The present results are in complete agreement with the usual trends for the thermal conductivity of dielectric materials, in which impurity levels are very important at low temperatures but become relatively unimportant at high temperatures. In addition, the thermal diffusivity values at room temperature are reexamined by measuring the thermal diffusivity of several UO$_2$ fuel samples with same level of doped Gd$_2$O$_3$.

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