GB791657A - Improvements in or relating to the preparation of titanium dioxide - Google Patents
Improvements in or relating to the preparation of titanium dioxideInfo
- Publication number
- GB791657A GB791657A GB1173655A GB1173655A GB791657A GB 791657 A GB791657 A GB 791657A GB 1173655 A GB1173655 A GB 1173655A GB 1173655 A GB1173655 A GB 1173655A GB 791657 A GB791657 A GB 791657A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxygen
- titanium tetrachloride
- reaction chamber
- reaction
- ports
- 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
Links
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
- C01G23/07—Producing by vapour phase processes, e.g. halide oxidation
Abstract
In the production of rutile titanium dioxide pigment by reacting titanium tetrachloride vapour and oxygen or oxygen containing gases in a reaction chamber, the molar proportion of titanium tetrachloride and oxygen is from 1 : 1 to 1:6, one or both of these being pre-heated to produce when mixed and irrespective of the heat of reaction, a temperature not below 300 DEG C. The reaction gases are passed in two separate streams in the same direction in the reaction chamber, the titanium tetrachloride stream being within the oxygen stream and the ports for the titanium tetrachloride have a perimeter per unit cross-section area greater than 26 cm.-1. The velocity ratio of oxygen to titanium tetrachloride is less than unity and the velocity of each gas is maintained so that the Reynolds flow number does not exceed 1800 and 500 respectively for the titanium tetrachloride and oxygen in the feed ports immediately prior to admission to the reactor. The oxygen may contain 0 to 5 per cent water vapour and the titanium tetrachloride may contain 0 to 25 per cent of silicon tetrachloride. It is preferred that the titanium tetrachloride feed ports are retracted relative to the oxygen feed ports and the ratio of the velocity of oxygen to titanium tetrachloride is preferably from 0.1 to 0.2: 1. The reaction gases are preferably admitted to the reactor through parallel and preferably concentric ducting, such ducting being straight sided and parallel for a length at least 20 times the hydraulic radius when the gas velocities are associated with a Reynolds flow number of 1800. Shorter lengths of straightsided and parallel ducting may be tolerated for lower gas velocities. The reaction chamber may be constructed of silica alumina refractory concrete or fired steatite. The latter may be advantageously employed for the construction of the burner ports by shaping it in its raw mineral state. The reaction chamber is preferably such that a ratio of at least 10 to 1 between the diameter of the reaction chamber and the external diameter of the feed ports is obtained. Liquid cooling devices may be employed around the burner tips. A number of examples and comparative examples are provided.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1173655A GB791657A (en) | 1955-04-22 | 1955-04-22 | Improvements in or relating to the preparation of titanium dioxide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1173655A GB791657A (en) | 1955-04-22 | 1955-04-22 | Improvements in or relating to the preparation of titanium dioxide |
Publications (1)
Publication Number | Publication Date |
---|---|
GB791657A true GB791657A (en) | 1958-03-05 |
Family
ID=9991727
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1173655A Expired GB791657A (en) | 1955-04-22 | 1955-04-22 | Improvements in or relating to the preparation of titanium dioxide |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB791657A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1142830A1 (en) * | 2000-04-03 | 2001-10-10 | Degussa AG | Nano-sized pyrogenic oxides, process for their preparation and their use |
WO2002066378A2 (en) * | 2001-02-20 | 2002-08-29 | Millennium Inorganic Chemicals, Inc. | Methods of producing substantially anatase-free titanium dioxide with silicon halide addition |
EP1752215A1 (en) * | 2005-08-09 | 2007-02-14 | Degussa GmbH | Photocatalyst |
EP1752216A1 (en) * | 2005-08-09 | 2007-02-14 | Degussa AG | Use of a titanium dioxide - mixed oxide as a photocatalyst |
US7465431B2 (en) | 2001-08-06 | 2008-12-16 | Degussa Ag | Nanoscalar pyrogenically produced yttrium-zirconium mixed oxide |
EP2471744A4 (en) * | 2009-08-24 | 2015-07-01 | Univ Hokkaido Nat Univ Corp | Metal oxide particle production method and production device |
-
1955
- 1955-04-22 GB GB1173655A patent/GB791657A/en not_active Expired
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1142830A1 (en) * | 2000-04-03 | 2001-10-10 | Degussa AG | Nano-sized pyrogenic oxides, process for their preparation and their use |
JP2001342011A (en) * | 2000-04-03 | 2001-12-11 | Degussa Ag | Nano size oxide and/or oxide composition obtained through thermo-decomposition of metal and/or metalloid, its manufacturing method, and usage of the oxide and/or oxide composition |
WO2002066378A2 (en) * | 2001-02-20 | 2002-08-29 | Millennium Inorganic Chemicals, Inc. | Methods of producing substantially anatase-free titanium dioxide with silicon halide addition |
WO2002066378A3 (en) * | 2001-02-20 | 2003-03-27 | Millennium Inorganic Chem | Methods of producing substantially anatase-free titanium dioxide with silicon halide addition |
US7465431B2 (en) | 2001-08-06 | 2008-12-16 | Degussa Ag | Nanoscalar pyrogenically produced yttrium-zirconium mixed oxide |
WO2007017326A3 (en) * | 2005-08-09 | 2007-05-31 | Degussa | Photocatalyst |
WO2007017326A2 (en) * | 2005-08-09 | 2007-02-15 | Evonik Degussa Gmbh | Photocatalyst |
WO2007017327A2 (en) * | 2005-08-09 | 2007-02-15 | Evonik Degussa Gmbh | Use of titanium dioxide mixed oxide as a photocatalyst |
EP1752216A1 (en) * | 2005-08-09 | 2007-02-14 | Degussa AG | Use of a titanium dioxide - mixed oxide as a photocatalyst |
WO2007017327A3 (en) * | 2005-08-09 | 2007-06-14 | Degussa | Use of titanium dioxide mixed oxide as a photocatalyst |
EP1752215A1 (en) * | 2005-08-09 | 2007-02-14 | Degussa GmbH | Photocatalyst |
JP2009504367A (en) * | 2005-08-09 | 2009-02-05 | エボニック デグサ ゲーエムベーハー | photocatalyst |
JP2009504368A (en) * | 2005-08-09 | 2009-02-05 | エボニック デグサ ゲーエムベーハー | Use of titanium dioxide mixed oxide as photocatalyst |
US7910515B2 (en) | 2005-08-09 | 2011-03-22 | Evonik Degussa Gmbh | Photocatalyst |
JP4843674B2 (en) * | 2005-08-09 | 2011-12-21 | エボニック デグサ ゲーエムベーハー | photocatalyst |
CN101242894B (en) * | 2005-08-09 | 2012-03-21 | 赢创德固赛有限责任公司 | Photocatalyst |
EP2471744A4 (en) * | 2009-08-24 | 2015-07-01 | Univ Hokkaido Nat Univ Corp | Metal oxide particle production method and production device |
US9617166B2 (en) | 2009-08-24 | 2017-04-11 | National University Corporation Hokkaido University | Metal oxide particle production method and production device |
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