Classifications

• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G23/00—Compounds of titanium
  • C01G23/04—Oxides; Hydroxides
  • C01G23/047—Titanium dioxide
  • C01G23/0475—Purification
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G23/00—Compounds of titanium
  • C01G23/04—Oxides; Hydroxides
  • C01G23/047—Titanium dioxide
  • C01G23/053—Producing by wet processes, e.g. hydrolysing titanium salts
  • C01G23/0532—Producing by wet processes, e.g. hydrolysing titanium salts by hydrolysing sulfate-containing salts
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G23/00—Compounds of titanium
  • C01G23/04—Oxides; Hydroxides
  • C01G23/047—Titanium dioxide
  • C01G23/08—Drying; Calcining ; After treatment of titanium oxide
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2006/00—Physical properties of inorganic compounds
  • C01P2006/80—Compositional purity
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2006/00—Physical properties of inorganic compounds
  • C01P2006/80—Compositional purity
  • C01P2006/82—Compositional purity water content

Definitions

• the invention relates to a process for the production of titanium dioxide hydrate with low sulfate content from a hydrolysate which was obtained by hydrolysis of titanyl sulfate as well as particularly pure titanium dioxide hydrate.
• titanium dioxide hydrate hydrolysate which still contains chemically bound sulfate ions after the removal of metal sulfate-containing diluted sulfuric acid, from titanyl sulfate solutions in metal sulfate-containing sulfuric acid, which solutions are obtained by digestion of titanium raw materials with concentrated sulfuric acid.
• This hydrolysate still contains 5 to 10% by weight S0 4 2" ions with respect to Ti0 2 after intensive washing with water or diluted acid and an optional reducing (so-called bleaching) treatment (Ullmanns Encyclopaedia of Technical
• a sulfate-poor hydrate is created by treating a bleached hydrolysate with ammonia, ammonium hydroxide or carbonate and washing out the ammonium sulfate.
• the hydrate obtained in this manner still contains 0.5 to 2.0% sulfate.
• the S-content of the washed hydrate is still at 0.3% by weight corresponding to 0.9% by weight S0 4 2" .
• DE-A 43 21555 describes a process for the production of mixed oxide powders for denitrating catalysts in which the sulfur ion-containing titanium dioxide hydrate suspension is partially neutralized with lye to a pH value between 4.0 and 6.0, filtered and the filter cake is washed intensively.
• the starting material is a preferably bleached titanium dioxide hydrate suspension with 20 to 40% by weight solids. In this manner, a hydrate can be produced with approximately 2.5% S0 4 2 ⁇ and 20 ppm Na 2 0 content.
• the sulfate-containing hydrate suspension is mixed with 0.1 to 2 parts by weight alkali metal hydroxide or carbonate and stirred at 60 to 120°C for 30 to 60 minutes.
• the pH value of the hydrate suspension must be lowered with organic acids to below 6, preferably below 4.5, in order to remove chemically bound alkali metal ions from the hydrate. Residual organic acids are decomposed by calcining.
• the titanium dioxide hydrates created with this very extensive process contained between 110 and 480 ppm S corresponding to 330 and 1440 ppm S0 4 2" as well as up to 293 ppm Na + .
• An object of the present invention is to provide a simple process for the production of titanium dioxide hydrate with low sulfate content from a optionally bleached hydrolysate which was produced by hydrolysis of titanyl sulfate solutions that contain other metal sulfates and optionally free sulfuric acid.
• an object of the invention is to provide a pure titanium dioxide hydrate that contains less than 250 ppm S0 4 2 " ions and less than 50 ppm ammonium or alkali metal ions with respect to Ti0 2 .
• the objects according to the invention could be surprisingly achieved by neutralization of a 2 to 18% by weight titanium dioxide hydrate suspension.
• Subject matter of the invention is process for the production of pure titanium dioxide hydrate with less than 100 ppm S ⁇ 4 2" ions and less than 25 ppm ammonium or alkali metal ions from titanium dioxide hydrate produced by titanyl sulfate hydrolysis, characterized in that an aqueous suspension is produced with the sulfate-containing titanium dioxide hydrate with 2 to 18% by weight, preferably 5 to 15% by weight, solid calculated as Ti0 2 , the sulfate content of the suspension calculated as H 2 S0 4 is determined, 95 to 101.1 mol-% of the stoichiometric amount of ammonia or alkali metal hydroxide required for neutralization of the calculated H 2 S0 4 amount is added under stirring, the suspension is filtered after a stirring time of 5 to 60 minutes, preferably 10 to 30 minutes, and washed with water of low salt content, preferably deionized water, and a diffusion wash with deionized water at a pressure of 3 to 5 bar is then performed.
• the sulfate-containing hydrate is conventionally obtained in that titanium crude materials such as ilmenite or titanium slag are decomposed with concentrated sulfuric acid.
• the metal sulfates obtained thereby are dissolved in water or dilute sulfuric acid.
• the titanyl sulfate is hydrolysed at 90 to 110°C in the presence of hydrolysis nuclei under formation of sulfate- containing titanium dioxide hydrate and sulfuric acid.
• the filter cake can be freed from coloring heavy metal ions such as Fe 3+ , Cr 3+ - V 3+ if required by a reducing treatment in dilute acid (“bleaching") or by dissolving in sulfuric acid and renewed hydrolysis in the presence of Ti 3+ ions.
• coloring heavy metal ions such as Fe 3+ , Cr 3+ - V 3+ if required by a reducing treatment in dilute acid (“bleaching") or by dissolving in sulfuric acid and renewed hydrolysis in the presence of Ti 3+ ions.
• This titanium dioxide hydrate filter cake which contains 5 to 10% by weight S0 4 2* ions with respect to Ti0 2 that is obtained according to the art by hydrolysis of titanyl sulfate represents the starting material for the production of the pure titanium dioxide hydrate according to the invention and the products produced therefrom by drying or calcining.
• an aqueous suspension with 2 to 18% by weight solids calculated as Ti0 2 , preferably with 5 to 15% by weight solids, is produced from the obtained titanium dioxide hydrate filter cake.
• the S0 4 2" ion content, calculated as H 2 S0, of this suspension is determined and 95 to 100.1 mol-%, preferably 99.5 to 100.1 mol-%, most preferably 99.8 to 100.05 mol-% of the stoichiometric amount of ammonium or alkali metal hydroxide required for neutralization of the calculated H 2 S0 4 amount are added under stirring at 20 to 100°C, preferably 30 to 80°C.
• the suspension mixed with hydroxide After the suspension mixed with hydroxide has been stirred for 5 to 60 minutes, preferably 10 to 30 minutes, it is filtered and washed with hot water at 30 to 100°C, preferably 50 to 95°C.
• the wash occurs with low-salt, preferably deionized water.
• filtration and washing with vacuum filters or preferably pressure filters is carried out at pressures up to a maximum of 3 bar. If the conductivity of the filtrate is clearly lowered, preferably to approximately 300 mS/cm, then the removal of the residual sulfates is carried out on a pressure filter by diffusion washing with salt-free water at 30 to 100°C and a pressure of 3 to 5 bar.
• this is washed until the conductivity of the wash filtrate is below 100 ⁇ S/cm. If a membrane filter press is used as the preferred filter aggregate, then the mother liquor is pressed out with a pressure of 3 to 5 bar before the beginning of the diffusion wash.
• a partial removal of water from the filter cake can occur with increased compacting pressure after the completed diffusion wash.
• the filter cake obtained by applying the process according to the invention generally contains less than 1% by weight sulfate ions and less than 100 ppm ammonia and alkali metal ions, each with respect to Ti0 2 .
• the preferred ammonium or alkali metal hydroxide amounts one obtains the pure titanium dioxide hydrate according to the invention which contains less than 250 ppm S0 4 2" ions and less than 50 ppm ammonium and alkali metal ions, especially less than 100 ppm S0 4 2" ions and less than 25 ppm ammonium or alkali metal ions, each with respect to Ti0 2 .
• This titanium dioxide hydrate is distinguished by a particularly large reaction capability, a high absorption capacity for anions and cations and, depending on the degree of removal of water, a high catalytic activity.
• Subject matter of the invention is also a method for the production of titanium dioxide and/or titanium dioxide hydrate of the composition Ti0 2 x nH 2 0 with 1 > n >. 0 which contains less than 250 ppm, preferably less than 100 ppm, sulfate ions and less than 50 ppm, preferably less than 25 ppm, ammonium and alkali metal ions, each with respect to Ti0 2 that is obtainable by drying and/or calcining the titanium dioxide hydrate according to claim 5 at temperatures in a range of 50 to 750°C.
• sulfate-containing titanium dioxide hydrate was produced by hydrolysis of a sulfuric acid, metal sulfate- containing titanyl sulfate solution.
• the washed filter cake was "bleached” by a reducing treatment.
• the washed filter cake of the "bleached” titanium dioxide hydrate was mashed with water.
• the suspension obtained in this manner contained 25.24% by weight titanium dioxide hydrate calculated as Ti0 2 and 2.14% by weight sulfate ions calculated as H 2 S0 4 .
• the suspension served as the starting material for all examples.
• Comparative Example 1 6240 kg of this suspension were mixed with 213 kg 50% by weight NaOH under intensive stirring. The NaOH amount was sufficient for the neutralization of 97.7 mol % of the H 2 S0 4 contained in the suspension such that a residual content of 1950 ppm H 2 S0 4 is to be expected after washing out the Na 2 S0 4 . 30 minutes after the NaOH addition, the suspension was pumped into a membrane filter press. After completed filtration, the mother liquor was pressed off with 4 bar membrane pressure and washed for 180 minutes with deionized water. The conductivity of the filtrate fell off thereby to 122 ⁇ S. The filter cake was suspended in deionized water and a sample was analyzed. The sample contained 3184 ppm H 2 S0 4 and 266 ppm Na 2 0 with respect to Ti0 2 .
• the homogenized titanium dioxide hydrate suspension contained 2030 ppm S0 4 2" and 5 ppm Na + each with respect to Ti0 2 .
• the sulfate-containing suspension was mixed analogously to example 3 and mixed with 706 1 10 % by weight NaOH corresponding to 100.1 mol-% of the amount required for the neutralization of the contained H 2 S0 4 . Filtration and cake washing were carried out analogously to example 1 until the conductivity of the wash filtrate was 83 ⁇ S/cm. In the homogenized titanium dioxide hydrate suspension, no sulfate could be detected such that ⁇ 50 ppm S0 4 2" with respect to Ti0 2 were present. The Na + content was 86 ppm with respect to Ti0 2 .

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• General Life Sciences & Earth Sciences (AREA)
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• Inorganic Chemistry (AREA)
• Inorganic Compounds Of Heavy Metals (AREA)

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• 1998
  • 1998-02-17 DE DE19806471A patent/DE19806471A1/de not_active Ceased
• 1999
  • 1999-02-12 MY MYPI99000511A patent/MY133018A/en unknown
  • 1999-02-16 AU AU22938/99A patent/AU742966B2/en not_active Ceased
  • 1999-02-16 JP JP2000531403A patent/JP2002503620A/ja active Pending
  • 1999-02-16 PL PL99342451A patent/PL342451A1/xx unknown
  • 1999-02-16 WO PCT/IB1999/000272 patent/WO1999041200A1/en not_active Application Discontinuation
  • 1999-02-16 CA CA002321250A patent/CA2321250A1/en not_active Abandoned
  • 1999-02-16 CN CN99803046A patent/CN1291168A/zh active Pending
  • 1999-02-16 KR KR1020007009010A patent/KR20010072550A/ko not_active Application Discontinuation
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  • 1999-02-16 ZA ZA9901226A patent/ZA991226B/xx unknown
  • 1999-02-16 EP EP99902739A patent/EP1060127A1/de not_active Withdrawn
• 2000
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