GB778706A - Apparatus for the production of metal oxides - Google Patents

Apparatus for the production of metal oxides

Info

Publication number
GB778706A
GB778706A GB12789/56A GB1278956A GB778706A GB 778706 A GB778706 A GB 778706A GB 12789/56 A GB12789/56 A GB 12789/56A GB 1278956 A GB1278956 A GB 1278956A GB 778706 A GB778706 A GB 778706A
Authority
GB
United Kingdom
Prior art keywords
mixture
halide
chamber
injected
reaction chamber
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
GB12789/56A
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.)
Godfrey L Cabot Inc
Original Assignee
Godfrey L Cabot 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 Godfrey L Cabot Inc filed Critical Godfrey L Cabot Inc
Publication of GB778706A publication Critical patent/GB778706A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G31/00Compounds of vanadium
    • C01G31/02Oxides
    • 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
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • C01P2004/61Micrometer sized, i.e. from 1-100 micrometer
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/12Surface area

Abstract

An apparatus for the production of oxide pigments by halide hydrolysis according to the process described and claimed in Specification 778,705 consists of a primary cylindrical reaction chamber having a diameter greater than its length, and in axial <PICT:0778706/III/1> <PICT:0778706/III/2> alignment therewith, a secondary reaction chamber having a diameter less than that of the primary chamber and the length greater than its own diameter. The halide to e hydrolysed is injected axially into the first reaction chamber and provision is made for the introduction of a mixture of a combustible gas containing hydrogen, and oxygen into the primary reaction chamber in a direction tangential to the walls thereof which mixture burns to form the water for the hydrolysis. In addition means are provided to inject an auxiliary mixture of combustible gas and air downstream from the point of introduction of the hydrogen/xyogen mixture. As shown in the Figure (Fig. 2), a heat insulated cylindrical reaction chamber 56 is formed in a refractory material 50 and is provided with a manifold 70 and pipes 60 whereby a gas mixture may be injected tangentially into chamber 56. A second chamber 58 is in axial alignment with chamber 56 and at the downstream end it is provided with a further manifold 76 and tangential injection pipes 72. The halide to be hydrolysed is introduced through a nozzle 54 from a pipe 62. If desired supplemental air may be introduced into the reaction chamber to flow around the halide injector nozzle 54 as a smooth flowing or whirling stream or such air may be injected outwardly around the periphery of the nozzle. In operation a halide is injected through pipe 62 under its own vapour pressure and the manifold 70 is supplied with a mixture of combustible hydrogen-containing gas and air which burns as a turbulent rapidly whirling flame into which the metal halides are injected and react with the water produced in the flame. At the same time a mixture of combustible gas and air is introduced into the second manifold 76, and when injected into the downstream end of the chamber 58 such mixture burns to maintain the temperature of the reactant gases above 600 DEG C. thereby diminishing absorption of acid gases produced. The product is recovered in a cyclone and ceramic filters as shown in Fig. 1 where 10 indicates a metal halide reservoir which is heated to force the halide under its own vapour pressure into the reactor 16 where it is hydrolysed to the oxide. An insulated flue 18 leads to a cyclone separator 20 and a ceramic filter 22 from which the product oxide is recovered and the gases then pass to a spray cooler 24 and a scrubber 28 to leave at 40. Suitable spraying liquids are water or a lime slurry and the spraying liquids are collected in a sump 32 from which excess liquid is withdrawn at 42 and the remainder, after the addition of the necessary neutralizing agent is re-cycled through line 36 to scrubber 28. The apparatus is suitable for the production of oxides of Al, Si, Ti, Zn, Sb, Cr, Be, Zr, Co, Ni, B, Cd, Mo and V.
GB12789/56A 1952-11-28 1953-11-27 Apparatus for the production of metal oxides Expired GB778706A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US778705XA 1952-11-28 1952-11-28

Publications (1)

Publication Number Publication Date
GB778706A true GB778706A (en) 1957-07-10

Family

ID=22140531

Family Applications (2)

Application Number Title Priority Date Filing Date
GB12789/56A Expired GB778706A (en) 1952-11-28 1953-11-27 Apparatus for the production of metal oxides
GB32930/53A Expired GB778705A (en) 1952-11-28 1953-11-27 Production of metal oxides

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB32930/53A Expired GB778705A (en) 1952-11-28 1953-11-27 Production of metal oxides

Country Status (2)

Country Link
FR (1) FR1094567A (en)
GB (2) GB778706A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0455324A (en) * 1990-06-25 1992-02-24 Toda Kogyo Corp Cobalt titanate powder and its production

Also Published As

Publication number Publication date
FR1094567A (en) 1955-05-23
GB778705A (en) 1957-07-10

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