GB780564A - Production of zirconium sulphates - Google Patents

Production of zirconium sulphates

Info

Publication number
GB780564A
GB780564A GB471/56A GB47156A GB780564A GB 780564 A GB780564 A GB 780564A GB 471/56 A GB471/56 A GB 471/56A GB 47156 A GB47156 A GB 47156A GB 780564 A GB780564 A GB 780564A
Authority
GB
United Kingdom
Prior art keywords
sulphuric acid
sulphate
zirconium
zro2
examples
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
GB471/56A
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.)
NAT LEAD CO
NL Industries Inc
Original Assignee
NAT LEAD CO
NL Industries Inc
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 NAT LEAD CO, NL Industries Inc filed Critical NAT LEAD CO
Publication of GB780564A publication Critical patent/GB780564A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G25/00Compounds of zirconium
    • C01G25/06Sulfates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

A soluble basic zirconium sulphate is produced by heating under superatmospheric pressure zirconium dioxide, sulphuric acid and water, the molar ratio of said mixture being from 2:3:0.7 to 2:3:3. By adding sulphuric acid to dissolve said sulphate and make the resulting solution strongly acid, and allowing the solution to stand, Zr(SO4)2.4H2O operates as a crystalline precipitate. The reaction of the oxide with sulphuric acid preferably is carried out at 300-380 DEG C. and the autogeneous pressure is normally employed, in examples by the use of a bomb. Pressures of 2-80 ats. are mentioned. After treatment of the basic product with concentrated sulphuric acid and separation of the hydrated sulphate, the resulting liquid can be diluted and reused to form more of the basic salt and thus avoid loss of zirconium material. Unconverted ZrO2 can be recovered by refurnacing. Examples of the invention are given, and a comparative example discloses the use of a ZrO2:H2SO4:H2O rati of 1:2:2.
GB471/56A 1955-01-24 1956-01-05 Production of zirconium sulphates Expired GB780564A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US780564XA 1955-01-24 1955-01-24

Publications (1)

Publication Number Publication Date
GB780564A true GB780564A (en) 1957-08-07

Family

ID=22141654

Family Applications (1)

Application Number Title Priority Date Filing Date
GB471/56A Expired GB780564A (en) 1955-01-24 1956-01-05 Production of zirconium sulphates

Country Status (1)

Country Link
GB (1) GB780564A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0253818A1 (en) * 1985-05-02 1988-01-27 Ici Australia Limited Purification of zirconium compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0253818A1 (en) * 1985-05-02 1988-01-27 Ici Australia Limited Purification of zirconium compounds
EP0253818A4 (en) * 1985-05-02 1988-04-18 Ici Australia Ltd Purification of zirconium compounds.

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