Gas phase hydrogenation of p-chloronitrobenzene over Pd-Ni/Al2O3

作者：Cardenas Lizana Fernando; Gomez Quero Santiago; Amorim Claudia; Keane Mark A^*

来源：Applied Catalysis A: General , 2014, 473: 41-50.

DOI：10.1016/j.apcata.2014.01.001

• Selective hydrogenation
• Bimetallic catalyst
• p-Chloronitrobenzene
• p-Chloroaniline
• Co-impregnation
• Pd-Ni/Al2O3

The gas phase (1 atm; T = 393 K) hydrogenation of p-chloronitrobenzene (p-CNB) has been examined over alumina supported mono-(Pd or Ni) and bi-metallic (Pd:Ni = 1:3,1:1 and 3:1) catalysts prepared by (co-)impregnation. The catalytic action of physical mixtures (Pd/Al2O3 + Ni/Al2O3) was also considered. The catalysts have been characterised by temperature programmed reduction (TPR), H-2 chemisorption, powder XRD, HRTEM-EDX and XPS measurements. TPR analysis has provided evidence of a more facile reduction of Pd and Ni in Pd-Ni/Al2O3 relative to Pd/Al2O3 and Ni/Al2O3.TEM-EDX and XPS measurements show Pd surface enrichment in Pd-Ni/Al2O3 with evidence of modification to Pd electronic character. Ni/Al2O3 promoted exclusive -NO2 group reduction to generate p-chloroaniline (p-CAN). Pd/Al2O3 delivered a higher specific p-CNB consumption rate, yielding undesired nitrobenzene and aniline via coupled hydrodechlorination and hydrogenation. The Pd/Al2O3 + Ni/Al2O3 combination generated an overall rate and product distribution equivalent to Pd/Al2O3, i.e. the catalytic response was governed by Pd in the physical mixture. In contrast, reaction over Pd-Ni/Al2O3 resulted in exclusive production of the target p-CAN. This is consistent with lower chlorobenzene hydrodechlorination activity recorded for Pd-Ni/Al2O3 (relative to Pd/Al2O3). Reaction rate was sensitive to composition where Pd:Ni = 1:1 delivered the highest p-CAN yield. We attribute the catalytic response observed for Pd-Ni/Al2O3 to bimetallic particle formation as demonstrated by TPR, XRD and XPS analyses.

• 出版日期2014-3-5