Because
of the considerable CO2 adsorption capacity,
selectivity, and stability, amine-functionalized materials have been
recently investigated as promising adsorbents for biogas upgrading
to biomethane, which provides the preferred gaseous bioenergy resource.
Nevertheless, the typical impurity in biogas, H2S, has
a potential influence on biogas upgrading, as another acid component
to react with amines besides CO2. After all, even the trace
H2S after biogas desulfurization might have an accumulative
effect, based on previous experience in studying other acid impurities.
Herein, we explored the interference of H2S (5–5000
ppm) on the prepared polyethylenimine-functionalized porous resin
(PEI/HP20), which has exhibited excellent performance for biogas upgrading.
The distinct of adsorption capacity, kinetic behavior, and regeneration
performance between the two reactive components (CO2 and
H2S) in biogas was systemically investigated. It was found
that, in contrast with CO2, the adsorbed H2S
on PEI/HP20 was not comparable through slow single-stage kinetic behavior
and had limited impact, especially in consideration of the practical
biogas upgrading within finite time. Besides, the reversible binding
of H2S, proved by the regeneration performance and chemical
characterization, was also favorable and pivotal for the PEI/HP20.
In addition, the stable operation (capacity loss of 1%) by continuous
adsorption–regeneration cycles under H2S-containing
simulated biogas have finally demonstrated the ignorable interference
of H2S on PEI/HP20, manifesting its strong adaptability
in biogas upgrading.