Evaporative technology for lithium
mining from salt-lakes
exacerbates
freshwater scarcity and wetland destruction, and suffers from protracted
production cycles. Electrodialysis (ED) offers an environmentally
benign alternative for continuous lithium extraction and is amenable
to renewable energy usage. Salt-lake brines, however, are hypersaline
multicomponent mixtures, and the impact of the complex brine–membrane
interactions remains poorly understood. Here, we quantify the influence
of the solution composition, salinity, and acidity on the counterion
selectivity and thermodynamic efficiency of electrodialysis, leveraging
1250 original measurements with salt-lake brines that span four feed
salinities, three pH levels, and five current densities. Our experiments
reveal that commonly used binary cation solutions, which neglect Na+ and K+ transport, may overestimate the Li+/Mg2+ selectivity by 250% and underpredict the
specific energy consumption (SEC) by a factor of 54.8. As a result
of the hypersaline conditions, exposure to salt-lake brine weakens
the efficacy of Donnan exclusion, amplifying Mg2+ leakage.
Higher current densities enhance the Donnan potential across the solution-membrane
interface and ameliorate the selectivity degradation with hypersaline
brines. However, a steep trade-off between counterion selectivity
and thermodynamic efficiency governs ED’s performance: a 6.25
times enhancement in Li+/Mg2+ selectivity is
accompanied by a 71.6% increase in the SEC. Lastly, our analysis suggests
that an industrial-scale ED module can meet existing salt-lake production
capacities, while being powered by a photovoltaic farm that utilizes
<1% of the salt-flat area.