Preparation method for metallic uranium

A technology for metal uranium and U3O8, which is applied in the field of uranium preparation by molten salt electrochemical technology, which can solve the problems of reduced electrolysis efficiency, insufficient contact with electric current, and low solubility

Active Publication Date: 2019-06-21
HARBIN ENG UNIV +1
View PDF6 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] The existing technology cannot obtain metal uranium quickly and efficiently, because U 3 o 8 If the solubility is too low, it will deposit at the bottom of the molten salt and cannot fully contact with the current, thereby reducing the electrolysis efficiency, and its ionic bond energy is very large, making electrolysis difficult;

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method for metallic uranium
  • Preparation method for metallic uranium
  • Preparation method for metallic uranium

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] A method for preparing uranium metal, comprising the steps of:

[0040] Step 1: Put 5g to 20g of U3O8 into a tube furnace, feed high-purity nitrogen gas for 30-300min, heat U3O8 at 100°C for 1 hour, and then heat U3O8 at 250°C for 1 hour ; The temperature of the debugging water bath is 85 degrees Celsius, the carbon tetrachloride in the heating flask is mixed with carbon tetrachloride gas and high-purity nitrogen, and the mixed gas flow rate is 3cm 3 / min, the mixed gas is passed into the quartz tube, and the temperature of the quartz tube is raised to 400-460 degrees Celsius, and heated for 2-6 hours. After the reaction is completed, the tube furnace is opened to cool down immediately, and the porcelain boat is taken out to obtain the powder product A (A is uranium tetrachloride);

[0041] Step 2: Place 4g to 12g of powdered product A on the bottom of the crucible, pour 100-300g of LiCl and KCl mixed molten salt with a mass content of 99%-99.99%, the mass ratio of LiC...

Embodiment 2

[0044] A method for preparing uranium metal, the present embodiment is basically the same as embodiment 1, the difference is that in step 2, the spectroscopically pure graphite rod is used as an auxiliary electrode, and the molybdenum sheet is used as a working electrode, and the electrolysis temperature is 873K; in step 3, the size 2cm*2cm, molybdenum sheet with a thickness of 0.2cm is used as the cathode, and electrolyzed at 0.1A-1A for 1-40 hours.

Embodiment 3

[0046] A method for preparing uranium metal. This embodiment is basically the same as Embodiment 1, except that in step 2, the electrolysis temperature is 873K.

[0047] Technical Note: By adjusting the temperature parameters and providing additional heat, the electrolysis reaction time will be less than 17.05 hours.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a preparation method for metallic uranium, relates to the field of methods for preparing uranium, and specifically relates to the field of methods for preparing uranium by applying a molten salt electrochemistry technology. The specific technical scheme is as follows: U3O8 is heated to remove water, and CCl4 gas and high-purity nitrogen gas are mixed and charged into a quartz pipe for 2-6h at 400-460 DEG C to obtain UCl4; a product A is mixed with the mixed molten salt of LiCl and KCl, electrification is carried out for 1h to 20h at a current of 0.1A to 1A and at 673-873K, and a material metallic uranium crude product or an electrode made from U-Ga alloy is taken out; and a material B is taken as an anode, a molybdenum sheet is taken as a cathode, and electrolysis is carried out for 1-40h at 0.1A-1A, and high-purity metallic uranium can be separated from B. The embodiments indicate that the preparation method for metallic uranium is capable of greatly increasingthe separation speed for metallic uranium and greatly improving the purity of metallic uranium, and significant to nuclear power construction in China to a certain extent.

Description

technical field [0001] The invention relates to the field of a method for preparing uranium, in particular to the field of a method for preparing uranium by using molten salt electrochemical technology. Background technique [0002] When the prior art prepares metal uranium by electrolysis, U 3 o 8 Direct electrolysis is time-consuming, low yield, and produces a large amount of chlorine gas and waste molten salt. Cui Enyu of the Korea Institute of Atomic Energy et al. 2 O molten salt try to put U 3 o 8 For metallization research, the product was obtained after electrolysis at high temperature for more than 40 hours. At the same time, the constant potential electrolysis method used would decompose a large amount of molten salt and produce chlorine gas as a by-product, which seriously affected the progress of the experiment. [0003] Zhang Yu and others from the Nuclear Technology Support Center of the State Administration of Science, Technology and Industry for National D...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C25C1/22C22B60/02
CPCY02E30/30
Inventor 王君蒋可为张宏森刘琦刘静媛陈蓉蓉于静
Owner HARBIN ENG UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products