Nanostructured
MgO sorbents show promise for intermediate-temperature
CO2 capture from post-combustion flue gas stream. However,
their CO2 capture behaviors can be affected by the magnesium
precursors applied for sorbent synthesis. To screen potential precursors
for fabricating excellent CO2 trappers, MgO nanoparticles
(NPs) were synthesized by calcining several organometallic precursors,
including magnesium ethoxide, magnesium acetate tetrahydrate, magnesium
oxalate dehydrate, magnesium lactate dihydrate, magnesium citrate
nonahydrate, and magnesium gluconate hydrate. The precursors and MgO
NPs were characterized by thermogravimetric analysis, X-ray diffraction,
N2 adsorption–desorption, field emission scanning
electron microscopy, and CO2 temperature-programmed desorption.
A fixed-bed reactor was used to evaluate the CO2 capture
performances of the MgO NPs in a simulated flue gas stream. The effect
of organometallic precursors on CO2 capture behaviors of
the sorbents was further demonstrated. Results indicated that the
different precursors would yield MgO NPs with distinct textural and
surface properties, and these could further affect their CO2 capture behaviors. MgO NPs derived from magnesium oxalate dehydrate
exhibited the highest CO2 uptake of 4.41 mmol of CO2/g. The excellent CO2 uptake was mainly attributed
to its superlative textural properties, uniform surface morphology,
and abundant base sites.