US2009324487A1PendingUtilityA1

Method for preparing iron oxides

Assignee: SUED CHEMIE MT SRLPriority: Mar 18, 2002Filed: Jul 11, 2008Published: Dec 31, 2009
Est. expiryMar 18, 2022(expired)· nominal 20-yr term from priority
B41F 1/08B01J 23/745B01J 37/086B01J 37/12B41F 1/50C01G 49/02C01G 49/06C01P 2006/12C01P 2006/13C09C 1/24B01J 35/60B01J 35/613B01J 35/615
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Claims

Abstract

Highly pure iron oxides are prepared by reaction of metallic iron, in the form of microspheroidal particles or of scraps or cuttings, with an agitated aqueous solution of a mono- or polycarboxylic acid with a pKa of 0.5 to 6 relative to the first carboxyl and capable of decomposing, by heating in air at 200 to 350° C., to carbon dioxide and water, using 0.03 to 1.5 moles of acid per g-atoms of iron, a water/iron weight ration of 1 to 20, and by oxidation of the ferrous carboxilate to ferric salt, with an agent selected from oxygen, mixtures containing oxygen, hydrogen peroxide, organic peroxides and hydroperoxides.

Claims

exact text as granted — not AI-modified
1 - 9 . (canceled) 
   
   
       10 . A precursor of a catalyst or a pigment comprising the FeOOH oxides having specific surface area of 1 to 300 m 2 /g, said oxides being free of alkali and/or alkaline earth ions and/or ammonium ions and of sulfate and chloride anions. 
   
   
       11 . A precursor of a catalyst or pigment comprising maghemite (FeO 3 ) having specific surface area of 1-15 m 2 /g, said maghemite being free of alkali and/or alkaline earth ions and/or ammonium ions and of sulfate and chloride anions.

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