GB736459A - Improvements relating to the concentration of isotopes - Google Patents

Improvements relating to the concentration of isotopes

Info

Publication number
GB736459A
GB736459A GB16570/53A GB1657053A GB736459A GB 736459 A GB736459 A GB 736459A GB 16570/53 A GB16570/53 A GB 16570/53A GB 1657053 A GB1657053 A GB 1657053A GB 736459 A GB736459 A GB 736459A
Authority
GB
United Kingdom
Prior art keywords
complex
compound
column
isotopes
phase
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
GB16570/53A
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.)
KARL ERIK HOLMBERG
Original Assignee
KARL ERIK HOLMBERG
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 KARL ERIK HOLMBERG filed Critical KARL ERIK HOLMBERG
Publication of GB736459A publication Critical patent/GB736459A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D59/00Separation of different isotopes of the same chemical element
    • B01D59/28Separation by chemical exchange
    • B01D59/32Separation by chemical exchange by exchange between fluids

Abstract

A compound A is separated into two fractions which are relatively enriched in different isotopes of an element contained in A, by forming a complex compound AB, heating the complex compound to form a vapour phase in which the ratio between the content of the compound A in the form of the complex to the total content of the compound A is different from that in the liquid phase, and creating a countercurrent flow between the vapour phase and the liquid phase in a cascade to effect an isotope exchange between the vapour phase and the liquid phase so that lighter isotopes are concentrated at one end of the cascade and heavy isotopes at the other. In examples (1) the complex of diethyl (or dimethyl) ether and boron trifluoride was distilled at 75 DEG C. in a column of 30 theoretical plates at a pressure of 60 mm. Hg. B10 became concentrated at the bottom of the column; (2) trimethyl amine and acetic acid were distilled at 80 DEG C. and 40 mm. Hg. N15 became concentrated at the bottom of the column. The distillation was carried out with total reflux and a boil up of about 1 g. per minute for 24 hours, using about 50 g. material. The distillation of the complex of boron trifluoride and anisole, the anisole being recirculated from bottom to top of the column, and of the complex of triethylamine and sulphur dioxide (for separation of the sulphur isotopes) are also referred to.ALSO:A compound A is separated into two fractions which are relatively enriched in different isotopes of an element contained in A, by forming a complex compound AB and converting the complex compound, if necessary, to the liquid state by solution or heat, heating the complex compound to form a vapour phase in which the ratio between the content of the compound A in the form of the complex to the total content of the compound A is different from that in the liquid phase, and creating a countercurrent flow between the vapour phase and the liquid phase in a cascade to effect an isotope exchange between the vapour phase and the liquid p phase so that lighter isotopes are concentrated at one end of the cascade and heavy isotopes at the other. In examples: (1) the complex of diethyl (or dimethyl) ether and boron trifluoride was distilled at 75 DEG C. in a column of 30 theoretical plates at a pressure of 60 mm. Hg. B10 became concentrated at the bottom of the column. (2) Trimethylamine and acetic acid were distilled at 80 DEG C. and 40 mm. Hg. N15 became concentrated at the bottom of the column. The distillation was carried with total reflux and a boil-up rate of about 1 g. per minute for 24 hours using about 50 g. material. Other examples referred to are the complex of boron trifluoride and anisole, the anisole being recirculated from bottom to top of the column, ammonia, carbon dioxide and water, the water being recirculated, ammonia, sodium hydrogen and sodium dihydrogen phosphate, the water and phosphates in solution being recirculated, the complex of triethylamine and sulphur dioxide, and sulphur dioxide, phosphoric acid and sodium dihydrogen phosphate. In the last two cases the sulphur isotopes are separated.
GB16570/53A 1952-07-09 1953-06-16 Improvements relating to the concentration of isotopes Expired GB736459A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE736459X 1952-07-09

Publications (1)

Publication Number Publication Date
GB736459A true GB736459A (en) 1955-09-07

Family

ID=20319703

Family Applications (1)

Application Number Title Priority Date Filing Date
GB16570/53A Expired GB736459A (en) 1952-07-09 1953-06-16 Improvements relating to the concentration of isotopes

Country Status (3)

Country Link
DE (1) DE944848C (en)
FR (1) FR1081016A (en)
GB (1) GB736459A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3101256A (en) * 1958-08-28 1963-08-20 Quartz & Silice S A Separation of hydrogen isotopes
US7976708B2 (en) 2008-05-12 2011-07-12 Secretary, Department of Atormic Energy Innovative cut-and-feed operation for enhancing the performance of ion-exchange chromatographic separation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3101256A (en) * 1958-08-28 1963-08-20 Quartz & Silice S A Separation of hydrogen isotopes
US7976708B2 (en) 2008-05-12 2011-07-12 Secretary, Department of Atormic Energy Innovative cut-and-feed operation for enhancing the performance of ion-exchange chromatographic separation

Also Published As

Publication number Publication date
DE944848C (en) 1956-06-28
FR1081016A (en) 1954-12-15

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