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Control of competing hydrogenation of phenylhydroxylamine to aniline in a single-step hydrogenation of nitrobenzene to p-aminophenol / Jayprakash M. Nadgeri in Industrial & engineering chemistry research, Vol. 50 N° 9 (Mai 2011) 

Public ISBD [article]  in Industrial & engineering chemistry research > Vol. 50 N° 9 (Mai 2011) . - pp. 5478–5484 Titre : Control of competing hydrogenation of phenylhydroxylamine to aniline in a single-step hydrogenation of nitrobenzene to p-aminophenol Type de document : texte imprimé Auteurs : Jayprakash M. Nadgeri, Auteur ; Narayan S. Biradar, Auteur ; Priyanka B. Patil, Auteur Année de publication : 2011 Article en page(s) : pp. 5478–5484 Note générale : Chimie industrielle Langues : Anglais (eng) Mots-clés : Catalytic  hydrogenation  Nitrobenzene Résumé : Two steps involving catalytic hydrogenation of nitrobenzene to phenylhydroxylamine (PHA) in acid medium and its rearrangement to p-aminophenol (PAP) were studied separately in a batch reactor, using a well-characterized 3% Pt/C catalyst. The first step of hydrogenation of nitrobenzene to PHA could be carried out at 303 K and a H2 pressure of 0.69 MPa with complete conversion of nitrobenzene, while the achieved selectivity to PHA was higher than 90% with some formation of aniline, even at lower temperature. The second step of PHA rearrangement to PAP could be achieved under a hydrogen atmosphere at elevated temperature of 353 K to give a maximum selectivity to PAP of 74%. DEWEY : 660 ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie102544a [article] Control of competing hydrogenation of phenylhydroxylamine to aniline in a single-step hydrogenation of nitrobenzene to p-aminophenol [texte imprimé] / Jayprakash M. Nadgeri, Auteur ; Narayan S. Biradar, Auteur ; Priyanka B. Patil, Auteur . - 2011 . - pp. 5478–5484. Chimie industrielle Langues : Anglais (eng) in Industrial & engineering chemistry research > Vol. 50 N° 9 (Mai 2011) . - pp. 5478–5484 Mots-clés : Catalytic  hydrogenation  Nitrobenzene Résumé : Two steps involving catalytic hydrogenation of nitrobenzene to phenylhydroxylamine (PHA) in acid medium and its rearrangement to p-aminophenol (PAP) were studied separately in a batch reactor, using a well-characterized 3% Pt/C catalyst. The first step of hydrogenation of nitrobenzene to PHA could be carried out at 303 K and a H2 pressure of 0.69 MPa with complete conversion of nitrobenzene, while the achieved selectivity to PHA was higher than 90% with some formation of aniline, even at lower temperature. The second step of PHA rearrangement to PAP could be achieved under a hydrogen atmosphere at elevated temperature of 353 K to give a maximum selectivity to PAP of 74%. DEWEY : 660 ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie102544a

Selectivity tuning options in hydrogenation of m-chloronitrobenzene to m-chloroaniline over mono- and bimetallic supported Pt catalysts / Rasika B. Mane in Industrial & engineering chemistry research, Vol. 51 N° 48 (Décembre 2012) 

Public ISBD [article]  in Industrial & engineering chemistry research > Vol. 51 N° 48 (Décembre 2012) . - pp. 15564-15572 Titre : Selectivity tuning options in hydrogenation of m-chloronitrobenzene to m-chloroaniline over mono- and bimetallic supported Pt catalysts Type de document : texte imprimé Auteurs : Rasika B. Mane, Auteur ; Aparna S. Potdar, Auteur ; Jayprakash M. Nadgeri, Auteur Année de publication : 2013 Article en page(s) : pp. 15564-15572 Note générale : Industrial chemistry Langues : Anglais (eng) Mots-clés : Catalyst  Hydrogenation Résumé : Supported monometallic (Pt, Ni,) and bimetallic (Ni―Pt) catalysts were prepared for the selective liquid phase nydrogenation ot m-chlronitrobenzene to m-chloroaniline (m-CAN). It was found that the use of sodium carbonate as an additive substantially reduced the extent of dehydrohalogenation in the case of monometallic, 1% Pt/C catalyst, to give the highest selectivity of 96% to m-CAN. Ni—Pt bimetallic catalyst although showed almost complete selectivity (>99%) to mchloroaniline; its activity was several fold lower than that of 1% Pt/C―Na2CO3 system. However, compared with Ni monometallic catalyst, bimetallic Ni-Pt showed higher activity and selectivity due to the presence of electron rich surface metallic Pt stabilized by Ni having lower ionization potential compared with Pt. ISSN : 0888-5885 En ligne : http://cat.inist.fr/?aModele=afficheN&cpsidt=26710594 [article] Selectivity tuning options in hydrogenation of m-chloronitrobenzene to m-chloroaniline over mono- and bimetallic supported Pt catalysts [texte imprimé] / Rasika B. Mane, Auteur ; Aparna S. Potdar, Auteur ; Jayprakash M. Nadgeri, Auteur . - 2013 . - pp. 15564-15572. Industrial chemistry Langues : Anglais (eng) in Industrial & engineering chemistry research > Vol. 51 N° 48 (Décembre 2012) . - pp. 15564-15572 Mots-clés : Catalyst  Hydrogenation Résumé : Supported monometallic (Pt, Ni,) and bimetallic (Ni―Pt) catalysts were prepared for the selective liquid phase nydrogenation ot m-chlronitrobenzene to m-chloroaniline (m-CAN). It was found that the use of sodium carbonate as an additive substantially reduced the extent of dehydrohalogenation in the case of monometallic, 1% Pt/C catalyst, to give the highest selectivity of 96% to m-CAN. Ni—Pt bimetallic catalyst although showed almost complete selectivity (>99%) to mchloroaniline; its activity was several fold lower than that of 1% Pt/C―Na2CO3 system. However, compared with Ni monometallic catalyst, bimetallic Ni-Pt showed higher activity and selectivity due to the presence of electron rich surface metallic Pt stabilized by Ni having lower ionization potential compared with Pt. ISSN : 0888-5885 En ligne : http://cat.inist.fr/?aModele=afficheN&cpsidt=26710594