A series of silica supported Pd (Pd/SiO
2
) catalysts
were prepared in various HCl concentrations (
C
HCl
) of the impregnation solution with different electrostatic
interactions between Pd precursor and support, and their catalytic
properties were evaluated by the selective hydrogenation of nitrile
butadiene rubber (NBR). The results show that with the
C
HCl
increasing from 0.1 to 5 M, the particle size of Pd
nanoparticles dramatically decreases from 24.2 to 5.1 nm and stabilizes
at ∼5 nm when
C
HCl
is higher than
2 M. Using the catalysts prepared with a high
C
HCl
(>2 M), an excellent hydrogenation degree (HD) of ∼94%
with 100% selectivity to C=C can be acquired under mild conditions.
Interestingly, the HD could be remarkably increased from 65 to 92%
by increasing only
C
Cl
–
from 0.1 to 2 M with the addition of NaCl while keeping
C
H
+
at 0.1 M. This is because
PdCl
4
2–
is the predominant existing form
of precursor at high
C
Cl
–
, which has a strong electrostatic attraction with the positively
charged support favorable for the formation of small-sized Pd nanoparticles
over silica. Notably, Pd leaching behavior during the hydrogenation
reaction is closely related to
C
H
+
, and the higher the
C
H
+
, the less Pd residues are detected in the
hydrogenated NBR. Our contribution is to provide a facile strategy
to synthesize effective and stable Pd/SiO
2
catalysts via
adjusting the electrostatic interaction, which exhibits a high activity
and selectivity for NBR hydrogenation.