Search

Lithium recovery is imperative to accommodate the increase in lithium demand. Salt lake brine contains a large amount of lithium and is one of the most important sources of lithium metal. In this study, Li2CO3, MnO2, and TiO2 particles were mixed, and the precursor of a manganese–titanium mixed ion sieve (M-T-LIS) was prepared by a high-temperature solid-phase method. M-T-LISs were obtained by DL-malic acid pickling. The adsorption experiment results noted single-layer chemical adsorption and maximum lithium adsorption of 32.32 mg/g. From the Brunauer–Emmett–Teller and scanning electron microscopy results, the M-T-LIS provided adsorption sites after DL-malic acid pickling. In addition, X-ray photoelectron spectroscopy and Fourier transform infrared results showed the ion exchange mechanism of the M-T-LIS adsorption. From the results of the Li+ desorption experiment and recoverability experiment, DL-malic acid was used to desorb Li+ from the M-T-LIS with a desorption rate of more than 90%. During the fifth cycle, the Li+ adsorption capacity of the M-T-LIS was more than 20 mg/g (25.90 mg/g), and the recovery efficiency was higher than 80% (81.42%). According to the selectivity experiment, the M-T-LIS had good selectivity for Li+ (adsorption capacity of 25.85 mg/g in the artificial salt lake brine), which indicates its good application potential.

Activated carbon has been used to treat organic dyes in water systems; however, the adsorption capacity of the samples studied was limited by the specific surface area and influenced by the pH of the aqueous solution. In this study, a hybrid adsorbent consisting of a mixture (MCS) of activated chestnut shell biochar (CN) and pyrolyzed snail shell material (SS) was developed to solve this problem, with the waste snail shell samples being processed by pyrolysis and the chestnut shell samples chemically pretreated and then pyrolyzed. The BET and SEM results revealed that the SS had a mesoporous fluffy structure with a higher specific surface (1705 m2/g) and an average pore diameter of about 4.07 nm, providing a large number of sites for adsorption. In addition, XPS and FTIR results showed that the main component of SS was calcium oxide, and it also contained a certain amount of calcium carbonate, which not only provided an alkaline environment for the adsorption of biochar but also degradation and photocatalytic capabilities. The results showed that the MCS3-1 sample, obtained when CN and SS were mixed in the ratio of 3:1, had good capacity for adsorption for methylene blue (MB), with 1145 mg/g at an initial concentration of 1300 mg/L (92% removal rate). The adsorption behaviors were fitted with the pseudo-second-order kinetic model and Freundlich isotherm model, which indicated that the adsorption was multilayer chemisorption with a saturated adsorption capacity of 1635 mg/g. The photocatalytic capacity from the SS composition was about 89 mg/g, and the sorption of MB dye onto the sorbent reached equilibrium after 300 min. The results suggested that MCS3-1 has enormous potential for removing MB from wastewater.

The aim of this review is to provide a survey of the recent advances and the main remaining challenges related to the ultrananocrystalline diamond (UNCD) nanowires and other nanostructures which exhibit excellent capability as the core components for many diverse novel sensing devices, due to the unique material properties and geometry advantages. The boron or nitrogen doping introduced in the gas phase during deposition promotes p-type or n-type conductivity. With the establishment of the UNCD nanofabrication techniques, more and more nanostructure-based devices are being explored in measuring basic physical and chemical parameters via classic and quantum methods, as exemplified by gas sensors, ultraviolet photodetectors, piezoresistance effect-based devices, biological applications and biosensors, and nitrogen-vacancy color center-based magnetic field quantum sensors. Highlighted finally are some of the remaining challenges and the future outlook in this area.