Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/30847
Full metadata record
DC FieldValueLanguage
dc.contributor.authorJoseph, Santosh-
dc.contributor.authorVenkateswaran, G-
dc.contributor.authorMoorthy, P N-
dc.date.accessioned2015-03-12T05:11:26Z-
dc.date.available2015-03-12T05:11:26Z-
dc.date.issued1998-07-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/30847-
dc.description222-226en_US
dc.description.abstractEarlier investigations have shown that the dissolution of moderately sintered haematite in a reductive complexing formulation containing citric acid, EDTA and ascorbic acid (CEA) in the initial concentration ratio of 11:44:4 mol mo3at pH 2.8 is faster than at other concentration ratios when the amount of haematite initially taken corresponded to 22 mol m-3 iron. The dissolution was considered for a system having a surface area to volume ratio of 67 m-1 with oxide thickness of 5 microns, a system volume of~6 m-3 and no regeneration of chelant. In the present work, the dissolution behaviour of iron oxides prepared from ferrous hydroxide heated at different temperatures ranging from 373-1073 K in CEA 11:44:4 mol m-3 was investigated. It was observed that the dissolution of samples prepared at lower temperatures was fast, analogous to the behaviour of haematite sols. The results have been interpreted on the basis of 'Grain model’.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJCT Vol.05(4) [July 1998]en_US
dc.titleInfluence of thermal history of iron oxides on their dissolution behaviour in Citric acid - EDTA - Ascorbic acid mixtureen_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.05(4) [July 1998]

Files in This Item:
File Description SizeFormat 
IJCT 5(4) 222-226.pdf381.6 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.