GB990419A - Improvements in the preparation of titanium dioxide pigments - Google Patents

Improvements in the preparation of titanium dioxide pigments

Info

Publication number
GB990419A
GB990419A GB2995161A GB2995161A GB990419A GB 990419 A GB990419 A GB 990419A GB 2995161 A GB2995161 A GB 2995161A GB 2995161 A GB2995161 A GB 2995161A GB 990419 A GB990419 A GB 990419A
Authority
GB
United Kingdom
Prior art keywords
titanium dioxide
rutile
seeds
calcination
hydrolysis
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
GB2995161A
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.)
THANN FAB PROD CHEM
Fabriques de Produits Chimiques de Thann et de Mulhouse
Original Assignee
THANN FAB PROD CHEM
Fabriques de Produits Chimiques de Thann et de Mulhouse
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 THANN FAB PROD CHEM, Fabriques de Produits Chimiques de Thann et de Mulhouse filed Critical THANN FAB PROD CHEM
Publication of GB990419A publication Critical patent/GB990419A/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
    • C01G23/04Oxides; Hydroxides
    • C01G23/047Titanium dioxide
    • C01G23/053Producing by wet processes, e.g. hydrolysing titanium salts
    • C01G23/0532Producing by wet processes, e.g. hydrolysing titanium salts by hydrolysing sulfate-containing salts
    • C01G23/0534Producing by wet processes, e.g. hydrolysing titanium salts by hydrolysing sulfate-containing salts in the presence of seeds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

Rutile is prepared by calcination at or above about 1000 DEG C., of a hydrous titanium dioxide containing prior to calcination, rutile seeds, (in addition to those used in the initial hydrolysis) a water-soluble aluminium salt, a water-soluble phosphate and a basic potassium salt. The calcination is continued until the titanium dioxide is substantially completely converted into the rutile form. Ordinarily, the calcination is effected in the presence of 1-6% rutile seeds, 0.3-2.5% of a water-soluble aluminium salt (calculated as Al2O3) 0.1-0.5% of a watersolubl phosphate (calculated as P2O5) and 0.1-1.0% of a basic potassium salt (calculated as K2O) based by weight on the titanium dioxide. However, if the ore from which the titanium sulphate solution is obtained contains phosphorus, then the addition of extra phosphorus compounds may not be required. The seeds added before hydrolysis can be those obtained according to Example 1 of Specification 513,867, by halide hydrolysis in caustic soda and the seeds added after hydrolysis and before calcination, can be obtained by boiling washed hydrous titanium dioxide in a caustic soda solution for 4 hours, washing the precipitate, resuspending it in HCl solution and heating the suspension for 3 hours. In Example II, the rutile seeds are obtained by treating TiCl4 solution with a solution of caustic soda, neutralizing the suspension obtained, and then washing out 75% of the soluble salts present. The suspension thus obtained is added to titanium sulphate solution prior to hydrolysis to obtain hydrous titanium dioxide. The product is separated, washed and reslurried in water, to which is added rutile seeds as prepared in Specification 513,867, and an aluminium sulphate, mono-ammonium phosphate and potassium carbonate. The resulting mixture is dried and calcined at or above about 1000 DEG C.
GB2995161A 1960-08-31 1961-08-18 Improvements in the preparation of titanium dioxide pigments Expired GB990419A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR837375A FR1273440A (en) 1960-08-31 1960-08-31 Improvements in the preparation of shiny titanium pigments and products obtained

Publications (1)

Publication Number Publication Date
GB990419A true GB990419A (en) 1965-04-28

Family

ID=8738229

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2995161A Expired GB990419A (en) 1960-08-31 1961-08-18 Improvements in the preparation of titanium dioxide pigments

Country Status (5)

Country Link
BE (1) BE606147A (en)
ES (1) ES269964A1 (en)
FR (1) FR1273440A (en)
GB (1) GB990419A (en)
SE (1) SE305499B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0779243A1 (en) * 1995-12-15 1997-06-18 Tioxide Group Services Limited Rutile titanium dioxide
WO2003006559A1 (en) * 2001-07-07 2003-01-23 Kronos Titan Gmbh & Co. Ohg Photostable rutile titanium dioxide
JP2004256341A (en) * 2003-02-25 2004-09-16 Ishihara Sangyo Kaisha Ltd Production method of rutile-type, rod-shaped titanium dioxide

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0779243A1 (en) * 1995-12-15 1997-06-18 Tioxide Group Services Limited Rutile titanium dioxide
WO2003006559A1 (en) * 2001-07-07 2003-01-23 Kronos Titan Gmbh & Co. Ohg Photostable rutile titanium dioxide
JP2004256341A (en) * 2003-02-25 2004-09-16 Ishihara Sangyo Kaisha Ltd Production method of rutile-type, rod-shaped titanium dioxide

Also Published As

Publication number Publication date
ES269964A1 (en) 1962-03-01
BE606147A (en) 1961-11-03
FR1273440A (en) 1961-10-13
SE305499B (en) 1968-10-28

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