As
a new modification method, mechanochemistry features the remarkable
advantages of simple operation process, low energy consumption, easy
chemical modification, and suitability for industrialization. In this
work, the coal-fired byproduct fly ash was modified by a mechanical–chemical
method through omnidirectional planetary ball mill. The effect of
the mechanical–chemical modification process parameters on
the performance of mercury removal and physicochemical properties
of the fly ash and the relationship between the mercury removal efficiency
and the physicochemical properties were studied. The experimental
results showed that, under the condition of single mechanical ball
milling, the mercury removal efficiency of fly ash (FA) was slightly
higher than that of raw FA. After being modified by NaBr, the mercury
removal efficiency of FA increased
considerably with the increase of ball milling time and speed and
decreased with the increase of the size of the grinding ball. However,
it was no longer significantly improved with further increasing the
ball milling time and speed owing to the limited unburned carbon content
in FA. The best modification process parameters were determined from
the ball milling time of 1 h, the ball milling speed of 400 rpm, and
the ball size of 5 mm. The characterization results showed that there
was no big difference in physical properties of FA between various
mechanical–chemical modification processes. However, the content
of carbonyl and carboxyl/ester groups and C–Br covalent groups
on modified FA demonstrated a key role in promoting mercury removal
performance. The contents of carbonyl and carboxyl/ester groups and
C–Br covalent groups were positively proportional to the mercury
removal rate, and they were consumed during mercury adsorption. The
results confirmed that the improvement of mercury removal efficiency
of modified FA was dominated mainly by the surface chemical properties.
Compared with the carbonyl and carboxyl/ester groups, the C–Br
covalent group was the major chemisorption site of Hg0.