Journal
ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 1, Pages 691-698Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b16463
Keywords
CO2 capture; lithium zirconate; sorption kinetics; morphology-controllable synthesis; double-exponential model
Funding
- National Natural Science Foundation of China [51773106, 21371105]
- Key Research and Development Program of Shandong Province [2017GSF17124]
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It was reported that the main obstacle of Li2ZrO3 as high-temperature CO2 absorbents is the very slow CO2 sorption kinetics, which are ascribed to the gradual formation of compact zirconia and carbonate shells along with inner unreacted lithium zirconate cores; accordingly, the sticky Li+ and O2- ions have to travel a long distance through the solid shells by diffusion. We report here that three-dimensional interconnected nanoporous Li2ZrO3 exhibiting ultrafast kinetics is promising for CO2 sorption. Specifically, nanoporous Li2ZrO3 (LZ-NP) exhibited a rapid sorption rate of 10.28 wt %/min with an uptake of 27 wt % of CO2. Typically, the k(1) values of LZ-NP (kinetic parameters extracted from sorption kinetics) were nearly 1 order of magnitude higher than the previously reported conventional Li2ZrO3 reaction systems. Its sorption capacity of 25 wt % within similar to 4 min is 2 orders of magnitude faster than those obtained using spherical Li2ZrO3 powders. Furthermore, nanoporous Li2ZrO3 exhibited good stability over 60 absorption-desorption cycles, showing its potential for practical CO2 capture applications. CO2 adsorption isotherms for Li2ZrO3 absorbents were successfully modeled using a double-exponential equation at various CO2 partial pressures.
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