GB979564A - Production of titanium oxide - Google Patents

Production of titanium oxide

Info

Publication number
GB979564A
GB979564A GB1607563A GB1607563A GB979564A GB 979564 A GB979564 A GB 979564A GB 1607563 A GB1607563 A GB 1607563A GB 1607563 A GB1607563 A GB 1607563A GB 979564 A GB979564 A GB 979564A
Authority
GB
United Kingdom
Prior art keywords
stream
oxygen
tix4
reaction zone
ticl4
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
GB1607563A
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.)
PPG Industries Inc
Original Assignee
Pittsburgh Plate Glass 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
Priority claimed from US190140A external-priority patent/US3214284A/en
Application filed by Pittsburgh Plate Glass Co filed Critical Pittsburgh Plate Glass Co
Priority claimed from NL6404704A external-priority patent/NL6404704A/xx
Publication of GB979564A publication Critical patent/GB979564A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B35/00Boron; Compounds thereof
    • C01B35/06Boron halogen compounds
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B13/00Oxygen; Ozone; Oxides or hydroxides in general
    • C01B13/14Methods for preparing oxides or hydroxides in general
    • C01B13/20Methods for preparing oxides or hydroxides in general by oxidation of elements in the gaseous state; by oxidation or hydrolysis of compounds in the gaseous state
    • C01B13/22Methods for preparing oxides or hydroxides in general by oxidation of elements in the gaseous state; by oxidation or hydrolysis of compounds in the gaseous state of halides or oxyhalides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B13/00Oxygen; Ozone; Oxides or hydroxides in general
    • C01B13/14Methods for preparing oxides or hydroxides in general
    • C01B13/20Methods for preparing oxides or hydroxides in general by oxidation of elements in the gaseous state; by oxidation or hydrolysis of compounds in the gaseous state
    • C01B13/22Methods for preparing oxides or hydroxides in general by oxidation of elements in the gaseous state; by oxidation or hydrolysis of compounds in the gaseous state of halides or oxyhalides
    • C01B13/24Methods for preparing oxides or hydroxides in general by oxidation of elements in the gaseous state; by oxidation or hydrolysis of compounds in the gaseous state of halides or oxyhalides in the presence of hot combustion gases
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00Silicon; Compounds thereof
    • C01B33/113Silicon oxides; Hydrates thereof
    • C01B33/12Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/18Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
    • C01B33/181Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by a dry process
    • C01B33/183Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof by a dry process by oxidation or hydrolysis in the vapour phase of silicon compounds such as halides, trichlorosilane, monosilane
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B35/00Boron; Compounds thereof
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B35/00Boron; Compounds thereof
    • C01B35/08Compounds containing boron and nitrogen, phosphorus, oxygen, sulfur, selenium or tellurium
    • C01B35/10Compounds containing boron and oxygen
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G23/00Compounds of titanium
    • C01G23/04Oxides; Hydroxides
    • C01G23/047Titanium dioxide
    • C01G23/07Producing by vapour phase processes, e.g. halide oxidation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

In the production of TiO2 by vapour phase oxidation of titanium tetrahalide TiX4, particularly TiCL4, a stream containing O2 and a stream containing TiX4 vapour are projected into the reaction zone, the linear velocity of the stream containing O2 being greater than that of the stream containing TiX4, and product TiO2 and Cl2 are withdrawn from the reaction zone in the same linear direction as the stream containing oxygen is projected into the reaction zone. If VO is the linear velocity of the oxygen-containing stream, VT is the component of linear velocity of the TiX4 <PICT:0979564/C1/1> <PICT:0979564/C1/2> <PICT:0979564/C1/3> <PICT:0979564/C1/4> stream along the axis of oxygen flow and do is the diameter of the oxygen-containing stream, within 0.5 seconds of contact with the TiX4, the formula <FORM:0979564/C1/1> should have a numerical value greater than 50, preferably greater than 300. An inert gas stream, for example N2, CO2, recycled produce gases, A, or particularly Cl2 may also be projected into the reaction zone having velocity VI such that <FORM:0979564/C1/2> is greater than 50, and preferably such that VI< 1/2 VO. Suitable reactors are illustrated in Figs. 1, 3, 4. Fig. 1 shows a furnace A1 having a burner A fitted in its upper part and an outlet 7 at its base. Burner A consists of concentric tubes 2, 3, 4 through which are introduced TiCl4, Cl2 and O2 respectively at feed rates correlated with the tube diameters to give a positive number between 300 and 20,000 as determined by the above formula. Product TiO2 and Cl2 formed in zone 30 are withdrawn in the direction indicated by the arrow from outlet 7. Fig. 3 depicts burner B constructed of concentric tubes 10, 11, 12 through which are passed TiCl4, Cl2, O2 respectively. The tubes differ in length so that O2 jetting past slot 16 is circumscribed by inert gas, and this stream when passing slot 17 is enveloped by TiCl4, the three streams retaining their identity as they are projected into the reaction zone. The reactant streams may also include an aluminium compound or a zirconium salt, and a silicon halide, particularly AlCl3 or ZrCl4, and SiCl4. Other suitable additives include potassium salts and organo potassium compounds; metals and metal compounds of Groups Ia, Ib, IIa, IIb, particularly Mg, Ca, Cu, Zn in the metallic vapour state, as salts, or as organometallic compounds. Fig. 4 illustrates a suitable reactor for the introduction, in separate streams, of oxygen, chlorine, chlorine + AlCl3, and TiCl4. The oxygen-containing gas stream may be pure oxygen, air, or a mixture of oxygen with the products of combustion of a combustible gas, e.g. CO. In the latter case the gas may be formed in situ before the introduction of TiX4. The temperature of the reaction zone is usually maintained between 750 DEG and 1600 DEG C. The reactants may be preheated and the temperature of the inflowing oxygen stream is the same or greater than that of the TiX4 vapour stream. It is also preferred to pass inert gas along the furnace wall during the reaction.
GB1607563A 1962-04-25 1963-04-24 Production of titanium oxide Expired GB979564A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US190140A US3214284A (en) 1962-04-25 1962-04-25 Production of pigmentary titanium oxide
US25545363A 1963-02-01 1963-02-01
NL6404704A NL6404704A (en) 1963-02-01 1964-04-28
BE648462A BE648462A (en) 1963-02-01 1964-05-27

Publications (1)

Publication Number Publication Date
GB979564A true GB979564A (en) 1965-01-06

Family

ID=27424770

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1607563A Expired GB979564A (en) 1962-04-25 1963-04-24 Production of titanium oxide

Country Status (1)

Country Link
GB (1) GB979564A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1619168A1 (en) * 2004-07-20 2006-01-25 E. I. du Pont de Nemours and Company Apparatus for making metal oxide nanopowder
EP1619169A1 (en) * 2004-07-20 2006-01-25 E. I. du Pont de Nemours and Company Process for making metal oxide nanoparticles

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1619168A1 (en) * 2004-07-20 2006-01-25 E. I. du Pont de Nemours and Company Apparatus for making metal oxide nanopowder
EP1619169A1 (en) * 2004-07-20 2006-01-25 E. I. du Pont de Nemours and Company Process for making metal oxide nanoparticles
US7465430B2 (en) 2004-07-20 2008-12-16 E. I. Du Pont De Nemours And Company Apparatus for making metal oxide nanopowder
US7708975B2 (en) 2004-07-20 2010-05-04 E.I. Du Pont De Nemours And Company Process for making metal oxide nanoparticles
AU2005203124B2 (en) * 2004-07-20 2010-05-20 E.I. Du Pont De Nemours And Company Apparatus for making metal oxide nanopowder

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