TY - JOUR
T1 - A characterization of Ln-Pd/SiO2 (Ln=La, Ce, Sm, Eu, Gd and Yb)
T2 - Correlation of surface chemistry with hydrogenolysis activity
AU - Jujjuri, Satyakrishna
AU - Ding, Errun
AU - Shore, Sheldon G.
AU - Keane, Mark A.
PY - 2007/7/2
Y1 - 2007/7/2
N2 - The gas phase hydrodechlorination (HDC) of chlorobenzene (CB), 1,2-dichlorobenzene (1,2-DCB) and 1,3-dichlorobenzene (1,3-DCB) has been investigated over Pd/SiO2 and a series of Ln-Pd/SiO2 prepared from the organometallic precursor{(DMF)10Ln2[Pd(CN)4]3}8 where Ln = La, Ce, Sm, Eu, Gd and Yb; Pd loading = 5%, w/w. Under identical reaction conditions, the following overall sequence of increasing initial fractional dechlorination has been established: Pd/SiO2 < Yb-Pd/SiO2 ˜ Sm-Pd/SiO2 < Gd-Pd/SiO2 < La-Pd/SiO2 ˜ Ce-Pd/SiO2 < Eu-Pd/SiO2; reaction over Ln/SiO2 resulted in a negligible conversion. HDC activity declined with time-on-stream but the Ln-Pd/SiO2 catalysts maintained a significantly higher fractional HDC than Pd/SiO2; loss of activity is attributed to deleterious HCl/surface interactions. The pre- and post- reaction catalyst samples have been characterized in terms of BET area, TPR, TEM, H2 chemisorption/TPD, XRD and XPS analyses. When compared with Pd/SiO2, Pd is present in the Ln-Pd/SiO2 samples as much smaller particles, while the lanthanide component is finely dispersed over the surface, i.e. Ln is in intimate contact with Pd. The promotional effect of Ln in Ln-Pd/SiO2 is attributed to a surface Pd/Ln synergism resulting in an enhancement of surface reactive hydrogen and a more effective C{single bond}Cl bond activation for hydrogenolytic attack. HDC performance is discussed in terms of surface composition, Pd particle size, Ln electronic structure and H2 uptake/release dynamics. © 2007 Elsevier B.V. All rights reserved.
AB - The gas phase hydrodechlorination (HDC) of chlorobenzene (CB), 1,2-dichlorobenzene (1,2-DCB) and 1,3-dichlorobenzene (1,3-DCB) has been investigated over Pd/SiO2 and a series of Ln-Pd/SiO2 prepared from the organometallic precursor{(DMF)10Ln2[Pd(CN)4]3}8 where Ln = La, Ce, Sm, Eu, Gd and Yb; Pd loading = 5%, w/w. Under identical reaction conditions, the following overall sequence of increasing initial fractional dechlorination has been established: Pd/SiO2 < Yb-Pd/SiO2 ˜ Sm-Pd/SiO2 < Gd-Pd/SiO2 < La-Pd/SiO2 ˜ Ce-Pd/SiO2 < Eu-Pd/SiO2; reaction over Ln/SiO2 resulted in a negligible conversion. HDC activity declined with time-on-stream but the Ln-Pd/SiO2 catalysts maintained a significantly higher fractional HDC than Pd/SiO2; loss of activity is attributed to deleterious HCl/surface interactions. The pre- and post- reaction catalyst samples have been characterized in terms of BET area, TPR, TEM, H2 chemisorption/TPD, XRD and XPS analyses. When compared with Pd/SiO2, Pd is present in the Ln-Pd/SiO2 samples as much smaller particles, while the lanthanide component is finely dispersed over the surface, i.e. Ln is in intimate contact with Pd. The promotional effect of Ln in Ln-Pd/SiO2 is attributed to a surface Pd/Ln synergism resulting in an enhancement of surface reactive hydrogen and a more effective C{single bond}Cl bond activation for hydrogenolytic attack. HDC performance is discussed in terms of surface composition, Pd particle size, Ln electronic structure and H2 uptake/release dynamics. © 2007 Elsevier B.V. All rights reserved.
KW - Catalyst deactivation
KW - Chlorobenzene(s)
KW - Hydrodechlorination
KW - Lanthanide hydrides
KW - Ln-Pd/SiO 2
KW - Pd/SiO 2
UR - http://www.scopus.com/inward/record.url?scp=34249289720&partnerID=8YFLogxK
U2 - 10.1016/j.molcata.2007.03.008
DO - 10.1016/j.molcata.2007.03.008
M3 - Article
SN - 1381-1169
VL - 272
SP - 96
EP - 107
JO - Journal of Molecular Catalysis A: Chemical
JF - Journal of Molecular Catalysis A: Chemical
IS - 1-2
ER -