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ON THE REACTIVITY OF URANOURANIC OXIDE. VI. ON THE CHANGES AMONG URANIUM TRIOXIDE AND THEIR HYDRATES (in Japanese)

Journal Article · · J. At. Energy Soc. Japan
DOI:https://doi.org/10.3327/jaesj.3.260· OSTI ID:4054192
Using a thermal balance and an x-ray diffractometer, hydration and dehydration are studied for uranium trioxide UO/sub 3/ which is prepared from uranyl nitrate, ammonium diuranate, and uranium peroxide before decomposing to uranouranic oxide. The crystal system of UO/sub 3/ I may be monoclinic, UO/sub 3/ II also may be of a new crystal system, and UO/sub 3/ III is amorphous. These oxides are changed into hydrate by exposing them in air at room temperature for several days or a few months. UO/sub 3/ I converts into monoclinic UO/sub 3/ 2H/ sub 2/O or orthorhombic UO/sub 3/ H/sub 2/O, and UO/sub 3/ II and III both into monoclinic UO/sub 3/ 2H/sub 2/O. Dehydration of UO/sub 3/ 2H/sub 2/O leads through the orthorhombic UO/sub 3/ H/sub 2/O to monoclinic UO/sub 3/ and then to anhydrous amorphous UO/sub 3/. Further, high temperature x-ray study shows that the orthorhombic UO/sub 3/ - H/sub 2/O begins to decompose at 320 deg C, converts into amorphous UO/sub 3/ at 350 deg C and then to anhydrous monoclinic UO/sub 3/ at 415 deg to 420 deg C. (auth)
Research Organization:
Osaka Metal Ind. Co., Yodogawa Works, Japan
Sponsoring Organization:
USDOE
NSA Number:
NSA-15-020708
OSTI ID:
4054192
Journal Information:
J. At. Energy Soc. Japan, Journal Name: J. At. Energy Soc. Japan Vol. Vol: 3
Country of Publication:
Country unknown/Code not available
Language:
Japanese

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