GB719185A - Production of anhydrous zirconium fluoride - Google Patents

Production of anhydrous zirconium fluoride

Info

Publication number
GB719185A
GB719185A GB2502/53A GB250253A GB719185A GB 719185 A GB719185 A GB 719185A GB 2502/53 A GB2502/53 A GB 2502/53A GB 250253 A GB250253 A GB 250253A GB 719185 A GB719185 A GB 719185A
Authority
GB
United Kingdom
Prior art keywords
zirconium
zirconium oxide
hours
production
hydrofluoric acid
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
GB2502/53A
Inventor
Raymond James Anderson
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.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
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 Dow Chemical Co filed Critical Dow Chemical Co
Priority to GB2502/53A priority Critical patent/GB719185A/en
Publication of GB719185A publication Critical patent/GB719185A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F11/00Compounds of calcium, strontium, or barium
    • C01F11/20Halides
    • C01F11/22Fluorides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B7/00Halogens; Halogen acids
    • C01B7/19Fluorine; Hydrogen fluoride
    • C01B7/191Hydrogen fluoride
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B9/00General methods of preparing halides
    • C01B9/08Fluorides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/70Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
    • C01P2002/72Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/12Surface area
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/80Compositional purity

Landscapes

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

Abstract

Anhydrous zirconium tetrafluoride is produced by a process comprising (1) heating an aqueous solution of zirconium fluoride containing hydrofluoric acid at 120-170 DEG C. until it is sensibly dry and (2) calcining the dried product at between 300 DEG C. and its sublimation temperature. In the preferred method zirconium oxide is subjected to the action of sufficient 30-70 per cent. by weight aqueous hydrofluoric acid to provide 4.2-4.4 mols of HF per mol of zirconium oxide at 60-80 DEG C. for 4-6 hours; the resulting products are heated to dryness at 140-160 DEG C. and calcined at 300-350 DEG C. for 4-5 hours. Examples are given in which zirconium oxide and zirconyl chloride are used as sources of zirconium.
GB2502/53A 1953-01-28 1953-01-28 Production of anhydrous zirconium fluoride Expired GB719185A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2502/53A GB719185A (en) 1953-01-28 1953-01-28 Production of anhydrous zirconium fluoride

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2502/53A GB719185A (en) 1953-01-28 1953-01-28 Production of anhydrous zirconium fluoride

Publications (1)

Publication Number Publication Date
GB719185A true GB719185A (en) 1954-11-24

Family

ID=9740695

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2502/53A Expired GB719185A (en) 1953-01-28 1953-01-28 Production of anhydrous zirconium fluoride

Country Status (1)

Country Link
GB (1) GB719185A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3025607A1 (en) * 1980-07-05 1982-01-21 Metallgesellschaft Ag, 6000 Frankfurt METHOD FOR PRODUCING ZIRCONIUM TETRAFLUORIDE
CN112441615A (en) * 2020-12-22 2021-03-05 严永生 Preparation method of high-purity anhydrous zirconium fluoride

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3025607A1 (en) * 1980-07-05 1982-01-21 Metallgesellschaft Ag, 6000 Frankfurt METHOD FOR PRODUCING ZIRCONIUM TETRAFLUORIDE
US4399118A (en) * 1980-07-05 1983-08-16 Metallgesellschaft Aktiengesellschaft Process of recovering anhydrous zirconium tetrafluoride
CN112441615A (en) * 2020-12-22 2021-03-05 严永生 Preparation method of high-purity anhydrous zirconium fluoride

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