US2125340A - Oxidation of titanous salts - Google Patents

Oxidation of titanous salts Download PDF

Info

Publication number
US2125340A
US2125340A US58256A US5825636A US2125340A US 2125340 A US2125340 A US 2125340A US 58256 A US58256 A US 58256A US 5825636 A US5825636 A US 5825636A US 2125340 A US2125340 A US 2125340A
Authority
US
United States
Prior art keywords
titanium
solution
oxidation
trivalent titanium
trivalent
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 - Lifetime
Application number
US58256A
Inventor
Charles R Hager
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and 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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to US58256A priority Critical patent/US2125340A/en
Application granted granted Critical
Publication of US2125340A publication Critical patent/US2125340A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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

Definitions

  • the present invention relates to the oxidation of dissolved trivalent titanium salts by means of elemental oxygen and a catalyst, the latter being, particularly, copper.
  • Titanous salt solutions such as titanous chloride or particularly titanous sulfate are, under certain conditions, relatively easy to oxidize by means of elemental oxygen or atmospheric air, for example, when the titanium content of such solutions is rela tively very low and when the solutions are neutral or nearly neutral. If, however, the titanium solution is such as is produced under the usual conditions of manufacture the behavior is entirely difierent and the titanium in the titanous state is extremely difficult to oxidize by means of elemental oxygen or atmospheric air.
  • the solutions of titanium salt prior to the hydrolysis step contain from 150 grams to 275 grams of titanium in solution. From 99.5 per cent to 98.0 per cent of such titanium is in the titanic state with from 0.5 per cent to 2.0 per cent in the titanous state. Furthermore, such solutions contain relatively large quantities of free sulfuric acid, from 150 grams to 300 grams of HzSO4 per liter. It is under conditions such as these that the oxidation of trivalent titanium content of such solutions by means of elemental oxygen or atmospheric air is extremely diflicult and too time consuming to be practical on a commercial scale.
  • a process for oxidizing trivalent titanium to tetravalent titanium comprising contacting a trivalent titanium containing acid solution with a gaseous oxidizing medium from the group consisting of oxygen and air in the presence of a slight amount of an added copper salt as a catalyst and maintaining said solution during such contact at a temperature of substantially 45-50 C.
  • a process for oxidizing trivalent titanium to tetravalent titanium comprising adding a slight amount of a copper compound to an acidic titanium salt solution prepared for hydrolysis, and thence subjecting the same to the oxidizing action of air.
  • a process for oxidizing trivalent titanium to tetravalent titanium comprising introducing a gaseous oxidizing medium from the group consisting of oxygen and air into an acidic solution containing trivalent titanium and a small amount of a catalytic copper compound previously added to said solution.
  • a process for oxidizing trivalent titanium to tetravalent titanium comprising introducing a gaseous oxidizing medium from the group consisting of oxygen and air into an acidic solution containing trivalent titanium and a small amount of a catalytic copper salt previously added to said solution.
  • Patent 110 2,125, L 0, August 2, 19

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)
  • Catalysts (AREA)

Description

Patented Aug. 2, 1938 UNITED STATES PATENT OFFICE OXIDATION OF TITANOUS SALTS 'No Drawing. Application January 9, 1936, Serial No. 58,256
'7 Claims.
The present invention relates to the oxidation of dissolved trivalent titanium salts by means of elemental oxygen and a catalyst, the latter being, particularly, copper. Titanous salt solutions such as titanous chloride or particularly titanous sulfate are, under certain conditions, relatively easy to oxidize by means of elemental oxygen or atmospheric air, for example, when the titanium content of such solutions is rela tively very low and when the solutions are neutral or nearly neutral. If, however, the titanium solution is such as is produced under the usual conditions of manufacture the behavior is entirely difierent and the titanium in the titanous state is extremely difficult to oxidize by means of elemental oxygen or atmospheric air.
For example, in titanium oxide manufacture the solutions of titanium salt prior to the hydrolysis step contain from 150 grams to 275 grams of titanium in solution. From 99.5 per cent to 98.0 per cent of such titanium is in the titanic state with from 0.5 per cent to 2.0 per cent in the titanous state. Furthermore, such solutions contain relatively large quantities of free sulfuric acid, from 150 grams to 300 grams of HzSO4 per liter. It is under conditions such as these that the oxidation of trivalent titanium content of such solutions by means of elemental oxygen or atmospheric air is extremely diflicult and too time consuming to be practical on a commercial scale.
I found, however, that if the solution contains small amounts of a copper salt, elemental oxygen will readily oxidize trivalent titanium compounds to tetravalent titanium. I found, for instance, that when atmospheric air is bubbled through strong acid solutions containing trivalent titanium no oxidation of the trivalent titanium takes place, particularly at temperatures below C. If a, copper salt, however is present in the solution air will readily oxidize the trivalent titanium to tetravalent titanium even at room temperature and as the temperature is raised the speed with which oxidation takes place increases tremendously. The amount of copper salt needed as a catalyst in this reaction, is very slight, and it is usually sufilcient to suspend some copper oxide in the acid solution and very little copper is dissolved. For practical use of this reaction I prefer to carry it out at somewhat elevated temperature, as between 45 and 50 C. This type of reaction has many other practical applications in processes where small amounts of trivalent titanium present in a tetravalent titanium salt solution are desired to be oxidized, such as disclosed in an application by Carlton E. Smith, Serial No. 58,257 filed at even date herewith.
I claim:
1. In an acid process of oxidizing trivalent titanium to tetravalent titanium the step of contacting a solution containing trivalent titanium with elemental oxygen in the presence of a small amtount of an added copper compound as a catalys 2. In a process of oxidizing trivalent titanium to tetravalent titanium the step of bubbling air through an aqueous acid solution of trivalent titanium containing a small amount of an added copper compound as a catalyst.
3. In a process of oxidizing the trivalent titanium in an acid solution containing a major proportion of tetravalent titanium and a minor proportion of trivalent titanium, the steps of adding a small amount of a copper compound as a catalyst to said solution and contacting said solution with elemental oxygen.
4. A process for oxidizing trivalent titanium to tetravalent titanium, comprising contacting a trivalent titanium containing acid solution with a gaseous oxidizing medium from the group consisting of oxygen and air in the presence of a slight amount of an added copper salt as a catalyst and maintaining said solution during such contact at a temperature of substantially 45-50 C.
5. A process for oxidizing trivalent titanium to tetravalent titanium, comprising adding a slight amount of a copper compound to an acidic titanium salt solution prepared for hydrolysis, and thence subjecting the same to the oxidizing action of air.
6. A process for oxidizing trivalent titanium to tetravalent titanium, comprising introducing a gaseous oxidizing medium from the group consisting of oxygen and air into an acidic solution containing trivalent titanium and a small amount of a catalytic copper compound previously added to said solution.
'7. A process for oxidizing trivalent titanium to tetravalent titanium, comprising introducing a gaseous oxidizing medium from the group consisting of oxygen and air into an acidic solution containing trivalent titanium and a small amount of a catalytic copper salt previously added to said solution.
CHARLES R. HAGER.
CERTIFICATE OF CORRECTION.
Patent 110., 2,125, L 0, August 2, 19
CHARLES R. HAGER.
It is hereby certified that error appears in the printed specification of, the above numbered patent requiring correction as follows: Page 1, second column, line 6, claim 1,. for the words "an acidprocess read a process; line 8,v same claim, for "a solution" read an acid solution; and that the said Letters Patent shouldbe read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 27th day of September, A, D. 1958.
Henry Van Arsdale (Seal) I Acting Commissioner of Patents. v
US58256A 1936-01-09 1936-01-09 Oxidation of titanous salts Expired - Lifetime US2125340A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US58256A US2125340A (en) 1936-01-09 1936-01-09 Oxidation of titanous salts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US58256A US2125340A (en) 1936-01-09 1936-01-09 Oxidation of titanous salts

Publications (1)

Publication Number Publication Date
US2125340A true US2125340A (en) 1938-08-02

Family

ID=22015657

Family Applications (1)

Application Number Title Priority Date Filing Date
US58256A Expired - Lifetime US2125340A (en) 1936-01-09 1936-01-09 Oxidation of titanous salts

Country Status (1)

Country Link
US (1) US2125340A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2589909A (en) * 1949-03-24 1952-03-18 New Jersey Zinc Co Production of titanium dioxide
US2589910A (en) * 1949-03-24 1952-03-18 New Jersey Zinc Co Production of titanium dioxide
US2980508A (en) * 1955-12-05 1961-04-18 Nat Lead Co Oxidation of trivalent titanium compounds contained in solid titaniferous materials
US2990250A (en) * 1958-11-25 1961-06-27 Nat Lead Co Method for oxidizing trivalent titanium in solid titanium oxide containing materials

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2589909A (en) * 1949-03-24 1952-03-18 New Jersey Zinc Co Production of titanium dioxide
US2589910A (en) * 1949-03-24 1952-03-18 New Jersey Zinc Co Production of titanium dioxide
US2980508A (en) * 1955-12-05 1961-04-18 Nat Lead Co Oxidation of trivalent titanium compounds contained in solid titaniferous materials
US2990250A (en) * 1958-11-25 1961-06-27 Nat Lead Co Method for oxidizing trivalent titanium in solid titanium oxide containing materials

Similar Documents

Publication Publication Date Title
Halfpenny et al. 168. Pernitrous acid. The reaction between hydrogen peroxide and nitrous acid, and the properties of an intermediate product
US2125340A (en) Oxidation of titanous salts
US3399956A (en) Process for converting monovalent thallium compounds to trivalent thallium compounds
Carothers et al. Platinum Oxide as a Catalyst in the Reduction of Organic Compounds. II. Reduction of Aldehydes. Activation of the Catalyst by the Salts of Certain METALS1
US3860479A (en) Catalytic oxidation of alkaline pulping liquor
Vannerberg et al. Reaction between SO2 and wet metal surfaces
GB1463050A (en) Process for the manufacture of bromine
US4320097A (en) Recovery of vanadium from acidic solutions thereof
Lundell et al. The Determination of Titanium by Reduction with Zinc and Titration with PERMANGANATE1
Willard et al. Ceric Sulfate as a Volumetric Oxidizing Agent. Iv. The Determination of Arsenic. V. The Determination of Antimony
ES461935A1 (en) Catalyst for producing methacrylic acid
US2149370A (en) Treatment of titanium liquors
US2259895A (en) Process for manufacture of aliphatic carboxylic acid anhydrides
Furman et al. Applications of Ceric Sulfate in Volumetric Analysis. V. Potentiometric Study of the Reaction Between Ferrocyanide and Ceric Ions
US1856144A (en) Production of phosphoric acid
US1269443A (en) Pickling process and bath.
Walton et al. The catalytic influence of ferric ions on the oxidation of ethanol by hydrogen peroxide
US4526762A (en) Recovery of vanadium from acidic solutions thereof
US3425801A (en) Method of preparing palladium sulfate solution
US1992053A (en) Oxidation of arsenious acid
JPS608980B2 (en) Method for producing iron chloride solution
Satchell claiming failed.
SU414194A1 (en)
Robertson Promoter action in homogeneous catalysis. III. Cobalt salts as promoters in the catalytic decomposition of hydrogen peroxide by potassium dichromate
Mehrotra Kinetic Study of the Oxidation of Lactic and Mandelic Acids by Manganic Acetate in Glacial Acetic Acid