GB844407A - Process for the production of ammonium uranate - Google Patents

Process for the production of ammonium uranate

Info

Publication number
GB844407A
GB844407A GB29101/57A GB2910157A GB844407A GB 844407 A GB844407 A GB 844407A GB 29101/57 A GB29101/57 A GB 29101/57A GB 2910157 A GB2910157 A GB 2910157A GB 844407 A GB844407 A GB 844407A
Authority
GB
United Kingdom
Prior art keywords
solution
ammonia
vol
uranium
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB29101/57A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Evonik Operations GmbH
Original Assignee
Degussa GmbH
Deutsche Gold und Silber Scheideanstalt
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Degussa GmbH, Deutsche Gold und Silber Scheideanstalt filed Critical Degussa GmbH
Publication of GB844407A publication Critical patent/GB844407A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G43/00Compounds of uranium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

Ammonium uranate is precipitated from an aqueous solution of a hexavalent uranium salt, e.g. uranyl chloride, fluoride, sulphate, or nitrate, having a pH of less than 6, by passing a gaseous mixture of ammonia and an inert diluent, e.g. air, through the solution with vigorous stirring until a pH of 6-7, preferably 6.5 is reached, the ratio of inert gas to ammonia being at least 1:10. The reaction may be continued by the continuous introduction of gas and solution, the flow of gas or solution being regulated so as to maintain the above pH. The uranium salt solution may be a hydrofluoric acid solution of uranyl fluoride obtained by hydrolysis of uranium hexafluoride, or a solution obtained by acidifying a solution of a complex hexavalent uranium carbonate. A product containing less than 1 X 10-5% of boron (based on uranium) may be obtained from a solution containing 10-2% of boron. Precipitation in the form of needles may be effected at a temperature of above 70 DEG C. and with a volumetric ratio of ammonia to inert gas of 1-5 to 1. Precipitation in the form of spheres may be effected at a temperature of below 70 DEG C., e.g. 20-50 DEG C. According to Example 1, spherical particles having a mean diameter of 6 are obtained by introducing a mixture of 1 vol. ammonia and 3 vol. air with stirring at a rate of 150 1/min. and for a period of 5 hours into a uranyl nitrate solution which contains 90 grm./1. of uranium and a small amount of nitric acid and which is held at a temperature of 50 \sB 5 DEG C. When a pH of 6.5 is reached a mixture of 1 vol. ammonia and 2 vol. air at a rate of 150 1./min. and uranyl nitrate solution at a rate of 2 1./min. are continuously introduced while the temperature is maintained at 50 \sB 5 DEG C. and the pH is maintained at 6.5. According to Example 2, needle-like crystals are obtained by introducing a mixture of 1 vol. ammonia and 2 vol. air with stirring at a rate of 60 1./min. and for a period of 2.5 hours into a hydrofluoric acid solution of uranyl fluoride obtained by the hydrolysis of uranium hexafluoride, the solution being held at a temperature of 80-90 DEG C.
GB29101/57A 1956-09-29 1957-09-16 Process for the production of ammonium uranate Expired GB844407A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE844407X 1956-09-29

Publications (1)

Publication Number Publication Date
GB844407A true GB844407A (en) 1960-08-10

Family

ID=6774491

Family Applications (1)

Application Number Title Priority Date Filing Date
GB29101/57A Expired GB844407A (en) 1956-09-29 1957-09-16 Process for the production of ammonium uranate

Country Status (1)

Country Link
GB (1) GB844407A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3174821A (en) * 1961-10-19 1965-03-23 Rio Algom Mines Ltd Purification of yellow cake
US3394997A (en) * 1965-04-12 1968-07-30 Gen Electric Method of preparing uranium diuranate
US4389341A (en) * 1981-06-15 1983-06-21 General Electric Company Fugitive binder-containing nuclear fuel material and method of production
US4476101A (en) * 1979-05-22 1984-10-09 Produits Chimiques Ugine Kuhlmann Producing ammonium uranate in spherical particulate form

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3174821A (en) * 1961-10-19 1965-03-23 Rio Algom Mines Ltd Purification of yellow cake
US3394997A (en) * 1965-04-12 1968-07-30 Gen Electric Method of preparing uranium diuranate
US4476101A (en) * 1979-05-22 1984-10-09 Produits Chimiques Ugine Kuhlmann Producing ammonium uranate in spherical particulate form
US4389341A (en) * 1981-06-15 1983-06-21 General Electric Company Fugitive binder-containing nuclear fuel material and method of production

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