The
kinetics of water adsorption in powder sorbent layers are important
to design a scaled-up atmospheric water capture device. Herein, the
adsorption kinetics of three sorbents, a chromium (Cr)-based metal–organic
framework (Cr-MIL-101), a carbon-based material (nanoporous sponges/NPS),
and silica gel, have been tested experimentally, using powder layers
ranging from ∼0 to 7.5 mm in thickness, in a custom-made calibrated
environmental chamber cycling from 5 to 95% RH at 30 °C. A mass
and energy transfer model was applied onto the experimental curves
to better understand the contribution of key parameters (maximum water
uptake, kinetics of single particles, layer open porosity, and particle
size distribution). Open porosity (i.e., the void-to-particle ratio
in the sorbent layer) shows the highest influence to improve the kinetics.
Converting the sorbent kinetics data into a daily yield of captured
water demonstrated (i) the existence of an optimal open porosity for
each sorbent, (ii) that thinner layers with moderate open porosity
performed respectively better than thicker layers with high open porosity,
and (iii) that high maximum water uptake and fast single-particle
kinetics are not necessarily predictive of high daily water yield.