Issue 33, 2011

Modification of activated carbons based on diazonium ionsin situ produced from aminobenzeneorganic acid without addition of other acid

Abstract

Activated carbon products modified with a benzene sulfonic acid group were prepared based on the spontaneous reduction of diazonium salts in situ generated in water without addition of an external acid. The diazotization reaction assisted by the organic acid substituent, produced at once amine, diazonium and triazene functionalities that maximize the grafting yield by a chemical cooperation effect.

Graphical abstract: Modification of activated carbons based on diazonium ionsin situ produced from aminobenzene organic acid without addition of other acid

Supplementary files

Article information

Article type
Communication
Submitted
11 Apr 2011
Accepted
28 Jun 2011
First published
20 Jul 2011

J. Mater. Chem., 2011,21, 12221-12223

Modification of activated carbons based on diazonium ionsin situ produced from aminobenzene organic acid without addition of other acid

E. Lebègue, L. Madec, T. Brousse, J. Gaubicher, E. Levillain and C. Cougnon, J. Mater. Chem., 2011, 21, 12221 DOI: 10.1039/C1JM11538C

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