GB826962A - Process for recovering deuterium - Google Patents

Process for recovering deuterium

Info

Publication number
GB826962A
GB826962A GB7610/56A GB761056A GB826962A GB 826962 A GB826962 A GB 826962A GB 7610/56 A GB7610/56 A GB 7610/56A GB 761056 A GB761056 A GB 761056A GB 826962 A GB826962 A GB 826962A
Authority
GB
United Kingdom
Prior art keywords
hydrogen
contaminants
deuterium
heat regenerator
distilled
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
GB7610/56A
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.)
Stamicarbon BV
Original Assignee
Stamicarbon BV
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 Stamicarbon BV filed Critical Stamicarbon BV
Publication of GB826962A publication Critical patent/GB826962A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B4/00Hydrogen isotopes; Inorganic compounds thereof prepared by isotope exchange, e.g. NH3 + D2 → NH2D + HD

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Separation By Low-Temperature Treatments (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

<PICT:0826962/III/1> Technical hydrogen, which has its content of contaminating gases reduced to a proportion such that these contaminants are entirely precipitated in the solid state on cooling to distillation temperature, is cooled in a reversible heat regenerator to deposit the solidified contaminants, and distilled to recover deuterium. The distilled deuterium-poor hydrogen is passed back through the heat regenerator to take up the solidified contaminants, and is contacted with water to effect catalytic exchange of deuterium therewith. The resulting deuteriumenriched hydrogen is separated from the water, cooled in a reversible heat regenerator to deposit solidified contaminants, distilled to recover deuterium, and the deuterium-poor hydrogen is passed back through the heat regenerator to take up the solidified contaminants. Technical hydrogen may be fed into hydrogen passing in a closed cycle catalytic exchange process just before it enters a reversible heat regenerator, when the distillation of the technical hydrogen and of the hydrogen enriched with deuterium from water, and the solidification of contaminants from both, are effected simultaneously in the same distillation column and heat regenerator, respectively, and excess hydrogen is withdrawn from the circuit after the heat regenerator. Alternatively, technical hydrogen may be distilled in a separate distillation column, and passed wholly or in part into a catalyst exchange process either to be withdrawn from the heat regenerator, or retained as make-up in a closed cycle. The gas from a plant 1, which may be an ammonia synthesis gas plant, or a plant producing hydrogen from coal, oxygen and steam, after being freed from water and CO2 is cooled in heat exchanger 13, when the proportion of contaminants above that desired collects as liquid in tank 14. The cooled gas is passed back through heat exchanger 13 and fed at 18 into a closed circuit catalytic exchange system, where it joins circulating hydrogen, which has been saturated with water vapour in washer column 2, passed through catalyst bed 4, and has had water vapour separated in washer column 5 and absorber 6. The mixture of hydrogen is passed through heat exchanger 7, which cools the gas to just above the solidification point of the contaminants, and heat exchanger 8, where contaminants solidify, to distillation column 9, whence a deuterium concentrate is withdrawn at 10. The distilled hydrogen leaving at 11 passed back through exchangers 8, 7 taking up contaminants. The hydrogen is recycled through 3, while excess is withdrawn at 19 and returned to the synthesis plant after reintroduction through pump 22 of the liquid contaminants in tank 14, which are evaporated to recover cold. Exchangers 13 and 7 may be combined, when liquid is removed at 23. In alternative apparatus (Fig. 2, not shown) a separate distillation column is provided and the distilled hydrogen is fed into a catalytic exchange process which may be operated as a closed cycle or a once-through system. Specifications 799,351, 801,691, [both in Group XXVIII], and 815,098 are referred to.
GB7610/56A 1955-03-12 1956-03-12 Process for recovering deuterium Expired GB826962A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL826962X 1955-03-12

Publications (1)

Publication Number Publication Date
GB826962A true GB826962A (en) 1960-01-27

Family

ID=19841072

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7610/56A Expired GB826962A (en) 1955-03-12 1956-03-12 Process for recovering deuterium

Country Status (3)

Country Link
BE (1) BE545933A (en)
DE (1) DE1066554B (en)
GB (1) GB826962A (en)

Also Published As

Publication number Publication date
DE1066554B (en) 1959-10-08
BE545933A (en)

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