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Dry process fluorination of uranium dioxide using ammonium bifluoride

机译:二氟化铵干法二氧化铀氟化

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摘要

An experimental study was conducted to determine the practicality of various unit operations for fluorination of uranium dioxide. The objective was to prepare ammonium uranium fluoride double salts from uranium dioxide and ammonium bifluoride, then decompose these salts to uranium tetrafluoride through heating to temperatures near 425 °C in either a fluidized bed or a stirred bed. Fluorination in the stirred bed was attempted without pretreatment of the reagents. For the fluidized bed experiments, reagents were ball-milled prior to being heated in the bed. Experiments were conducted in either argon or 4% hydrogen in argon. The ball mill appeared to be an effective technique for fluorinating uranium dioxide with ammonium bifluoride. Samples changed color from brown to bright green, and no oxides could be detected in the x-ray diffraction pattern of the product. It was found that stainless steel is a suitable material of construction for reaction vessels, whereas mild steel parts corroded quickly. Only a small degree of fluidization provided adequate mixing in fluidized beds, but a paddle mixing the stirred beds left an unmixed region around the bed perimeter. Results from the stirred beds showed the initial fluorination reaction completed only when the reagents were heated to 110 °C for at least three hours under argon. Decomposition took place under argon with a temperature ramp up to 425 °C. The product UF4 contained less than 1% oxide as an impurity, and the decomposition appeared to be complete. Fluidized beds were run with both argon and 4% hydrogen in argon as carrier gases. Experiments with 4% hydrogen in argon produced uranium tetrafluoride, with ammonium uranium pentafluoride and uranium dioxide as impurties. Experiments in argon produced uranium tetrafluoride, with uranyl difluoride, ammonium diuranyl pentafluoride and triuranium octoxide as impurities. Minimum temperatures and times needed to decompose the double salt in the fluidized beds were 200 minutes at 115 °C, a 500-minute ramp to 425 °C, and 200 minutes at 425 °C. The intermediate double salt produced at 110 °C appeared to be triammonium uranium septafluoride.
机译:进行了实验研究以确定二氧化铀氟化的各种单元操作的实用性。目的是由二氧化铀和氟化氢铵制备氟化铀氟化铵复盐,然后通过在流化床或搅拌床中加热至接近425°C的温度,将这些盐分解为四氟化铀。尝试在搅拌床中进行氟化而不进行试剂预处理。对于流化床实验,先将试剂球磨,然后在床上加热。实验是在氩气或4%氢气/氩气中进行的。球磨机似乎是一种用氟化氢铵氟化二氧化铀的有效技术。样品的颜色从棕色变为亮绿色,在产品的X射线衍射图中未检测到氧化物。人们发现,不锈钢是反应容器的合适结构材料,而低碳钢零件很快就被腐蚀了。只有很小程度的流化作用在流化床中提供了充分的混合,但是混合搅拌床的桨叶在床周边周围留下了未混合的区域。搅拌床的结果表明,仅在将试剂在氩气下加热至110°C至少三小时时,才完成初始氟化反应。分解在氩气下进行,温度上升至425°C。产物UF4包含少于1%的氧化物作为杂质,并且分解似乎完成。使用氩气和氩气中4%的氢气作为载气运行流化床。用氩气中4%氢进行的实验产生了四氟化铀,五氟化铵铀和二氧化铀是杂质。在氩气中进行的实验生产了四氟化铀,其中有二氟化铀酰,五氟化二铀酰铵和八氧化三铀作为杂质。在流化床中分解双盐所需的最低温度和时间是:在115°C下200分钟,在425°C下500分钟升温,在425°C下200分钟。在110°C时产生的中间复盐似乎是三氟化铀铀七氟化物。

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