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GB456058A - Improvements in or relating to the forming of titanium products - Google Patents

Improvements in or relating to the forming of titanium products

Info

Publication number
GB456058A
GB456058A GB664835A GB664835A GB456058A GB 456058 A GB456058 A GB 456058A GB 664835 A GB664835 A GB 664835A GB 664835 A GB664835 A GB 664835A GB 456058 A GB456058 A GB 456058A
Authority
GB
United Kingdom
Prior art keywords
ammonium fluoride
titanium
ammonium
solution
silica
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
GB664835A
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.)
CF Burgess Laboratories Inc
Original Assignee
CF Burgess Laboratories 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 CF Burgess Laboratories Inc filed Critical CF Burgess Laboratories Inc
Priority to GB664835A priority Critical patent/GB456058A/en
Publication of GB456058A publication Critical patent/GB456058A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G23/00Compounds of titanium
    • C01G23/002Compounds containing titanium, with or without oxygen or hydrogen, and containing two or more other elements
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G23/00Compounds of titanium
    • C01G23/02Halides of titanium
    • C01G23/028Titanium fluoride
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B34/00Obtaining refractory metals
    • C22B34/10Obtaining titanium, zirconium or hafnium
    • C22B34/12Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08
    • C22B34/1236Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08 obtaining titanium or titanium compounds from ores or scrap by wet processes, e.g. by leaching
    • C22B34/124Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08 obtaining titanium or titanium compounds from ores or scrap by wet processes, e.g. by leaching using acidic solutions or liquors
    • C22B34/1245Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08 obtaining titanium or titanium compounds from ores or scrap by wet processes, e.g. by leaching using acidic solutions or liquors containing a halogen ion as active agent
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/01Particle morphology depicted by an image
    • C01P2004/02Particle morphology depicted by an image obtained by optical microscopy
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/30Particle morphology extending in three dimensions
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/60Optical properties, e.g. expressed in CIELAB-values
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Geology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

Titaniferous materials, such as ilmenite or rutile, are heated with ammonium fluoride or a reaction mixture yielding it, the ammonium fluoride being substantially in excess of the amount required to convert the reactive constituents of the ore to simple fluorides, and the ammonium titanium fluorine compounds formed are recovered as a solution either directly or by leaching the reaction product, or by volatilization. At least six mols of ammonium fluoride may be present for each mol of titanium oxide, and when rutile is used, it may be preheated to 1040 DEG C., and rapidly cooled to render it reactive. The ore may be mixed with the solid fluoride or a concentrated solution thereof, and the mixture be first heated, say to 150 DEG C., till ammonia ceases to be evolved, then to 250 DEG C., until ammonium fluoride ceases to be evolved, and then above 300 DEG C., and it may be up to 500--550 DEG C., to volatilize a mixture of titanium-diaminotetrafluoride and ammonium titanofluoride. By treating the volatilized compounds with an ammoniacal aqueous solution or an ammoniacal solution of ammonium fluoride, for instance at a temperature below 34 DEG C., titanium hydrate may be obtained, but preferably the volatilized products are dissolved in water or a neutral or acid solution of ammonium fluoride, the solution purified from iron as described in Specification 456,314, and the solution treated with ammonia, when, according to the conditions, either titanium hydrate or octohedral crystals of the formula TiF4.2NH3.NH4F are obtained. The crystals, if formed, may be converted to the hydrate by treatment with water and ammonia, preferably in sequence. If the initial material contains silicon, this may be separately volatilized with the ammonium fluoride as silicon diammino fluoride at temperatures below 300 DEG C., or be volatilized together with the titanium compounds. In the first case treatment with water or ammonium fluoride solution precipitates a part of the silica, and yields ammonium silicofluoride, from which the remaining silica may be precipitated by ammonia below 34 DEG C. to give a product adapted for admixture with titanium dioxide to form a composite pigment. In the second case, the further treatment of the mixed titanium and silicon compounds gives a mixed silica-titanium oxide pigment. Alternatively the separately volatilized compounds are mixed, preferably after re-sublimation, and after treatment with water, &c., to remove a part of the silica, are treated with ammonia, &c., to precipitate a mixture of silica and titanium oxide, which has a very high tinting strength when it contains 10--12 per cent silica. The residue from the reaction with ammonium fluoride, comprising ferrous ammonium fluoride, may be heated with ammonium sulphate at 300--350 DEG C. to recover ammonium fluoride and obtain ferrous sulphate, or be heated with steam and oxygen at 400--550 DEG C. to recover ammonium bifluoride and obtain a black iron oxide, the latter being converted to a red pigment, if desired, by treating at 500--550 DEG C. with moist air.
GB664835A 1935-03-02 1935-03-02 Improvements in or relating to the forming of titanium products Expired GB456058A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB664835A GB456058A (en) 1935-03-02 1935-03-02 Improvements in or relating to the forming of titanium products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB664835A GB456058A (en) 1935-03-02 1935-03-02 Improvements in or relating to the forming of titanium products

Publications (1)

Publication Number Publication Date
GB456058A true GB456058A (en) 1936-11-02

Family

ID=9818255

Family Applications (1)

Application Number Title Priority Date Filing Date
GB664835A Expired GB456058A (en) 1935-03-02 1935-03-02 Improvements in or relating to the forming of titanium products

Country Status (1)

Country Link
GB (1) GB456058A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2724646A (en) * 1954-07-12 1955-11-22 Bruce Williams Method for beneficiating manganese-containing materials

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2724646A (en) * 1954-07-12 1955-11-22 Bruce Williams Method for beneficiating manganese-containing materials

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