ABSTRACT
Salt lake brine has become a promising lithium resource, but it remains challenging to separate Li+ ions from the coexisting ions. We designed a membrane electrode having conductive and hydrophilic bifunctionality based on the H2TiO3 ion sieve (HTO). Reduced graphene oxide (RGO) was combined with the ion sieve to improve electrical conductivity, and tannic acid (TA) was polymerized on the surface of ion sieve to enhance hydrophilicity. These bifunctional modification at the microscopic level improved the electrochemical performance of the electrode and facilitated ion migration and adsorption. Poly(vinyl alcohol) (PVA) was used as a binder to further intensify the macroscopic hydrophilicity of the HTO/RGO-TA electrode. Lithium adsorption capacity of the modified electrode in 2 h reached 25.2 mg g-1, more than double that of HTO (12.0 mg g-1). The modified electrode showed excellent selectivity for Na+/Li+ and Mg2+/Li+ separation and good cycling stability. The adsorption mechanism follows ion exchange, which involves H+/Li+ exchange and Li-O bond formation in the [H] layer and [HTi2] layer of HTO.
ABSTRACT
The photo-driven oxidation of organic molecules into corresponding high-value-added products has become a promising method in chemical synthesis. This strategy can drive thermodynamically non-spontaneous reactions and achieve challenging thermocatalytic processes under ambient conditions. Reactive oxygen species (ROS) are not only significant intermediates for producing target products via photoinduced oxidation reactions but also contribute to the creation of sustainable chemical processes. Here, the latest advances in heterogeneous photo-driven oxidation reactions involving ROS are summarized. The major types of ROS and their generation are introduced, and the behaviors of various ROS involved in photo-driven processes are reviewed in terms of the formation of different bonds. Emphasis is placed on unraveling the reaction mechanisms of ROS and establishing strategies for their regulation, and the remaining challenges and perspectives are summarized and analyzed. This Review is expected to provide an in-depth understanding of the mechanisms of ROS involved in photo-driven oxidation processes as an important foundation for the design of efficient catalysts. Clarifying the role of ROS in oxidation reactions has important scientific significance for improving the atomic and energy efficiency of reactions in practical applications.
ABSTRACT
Lithium extraction from salt lake brine is critical for satisfying the increasing demand of a variety of lithium products. We report lithium recovery from pre-synthesized LiAl-layered double hydroxides (LDHs) via a mild solution reaction. Lithium ions were released from solid LiAl-LDHs to obtain a lithium-bearing solution. The LiAl-LDHs phase was gradually transformed into a predominantly Al(OH)3 phase with lithium recovery to the aqueous solution. The lithium recovery percentage and the concentration of the lithium-bearing solution were dependent on the crystallinity of LiAl-LDHs, the initial concentration of the LiAl-LDHs-1 slurry, the reaction temperature, and the reaction time. Under optimized conditions, the lithium recovery reached 86.2% and the Li+ concentration in the filtrate is 141.6 mg/L. Interestingly, no aluminum ions were detected in the filtrate after solid-liquid separation with high crystallinity LiAl-LDHs, which indicated the complete separation of lithium and aluminum in the liquid and solid phases, respectively. The 27Al NMR spectra of the solid products indicate that lithium recovery from the lattice vacancies of LiAl-LDHs affects the AlO6 coordination in an octahedral configuration of the ordered Al(OH)3 phase. The XPS O 1s spectra show that the Oad peak intensity increased and the OL peak intensity decreased with the increasing lithium recovery, which indicated that the Al-OH bond was gradually formed and the metal-oxygen-metal bond was broken.
