Edith Cerbelaud
Rhône-Poulenc
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Industrial chemistry library | 1996
Edith Cerbelaud; Marie-Claude Bontoux; Florence Foray; Didier Faucher; Sophie Levy-Schil; Denis Thibaut; Fabienne Soubrier; Joel Crouzet; Dominique Petre
Publisher Summary An industrial process must be economic and safe for the environment. The chemical hydrolysis of nitrile in acid is well known. Nearly all nitriles react with either basic or acid catalysts, but considerable quantities of inorganic salts are always produced as by-products. The only way to suppress these by-products is to produce the ammonium carboxylate under neutral pH and then to recover the ammonia by dissociation of the salt between the weak base and acid. It is possible to design an excellent catalyst for a bulk product such as caprolactam. The first advantage of the biocatalysis in this route is able to carry out this reaction at neutral pH. The second is to selectively obtain the α,ω-cyanoacid starting from the α,ω-dinitrile. No other type of catalysis can do this.
Archive | 1989
Edith Cerbelaud; Dominique Petre
Archive | 1990
Dominique Petre; Edith Cerbelaud; Jean-François Mayaux; Patrice Yeh
Archive | 1995
Edith Cerbelaud; Sophie Levy-Schil; Dominique Petre; Fabienne Soubrier
Archive | 1993
Dominique Petre; Edith Cerbelaud; Sophie Levy-Schil; Joel Crouzet
Archive | 1989
Edith Cerbelaud; Dominique Petre
Archive | 1989
Edith Cerbelaud; Dominique Petre
Archive | 1993
Dominique Petre; Edith Cerbelaud; Sophie Levy-Schil; Joel Crouzet
Archive | 1995
Dominique Petre; Edith Cerbelaud; Jean-fran Cedilla Ois Mayaux; Patrice Yeh
Archive | 1991
Patrice Yeh; Jean-François Mayaux; Edith Cerbelaud; Dominique Petre