The electrochemical conversion of CO₂ into high value-added carbon materials by molten salt electrolysis offers a promising solution for reducing carbon dioxide emissions. This study focuses on investigating the influence of molten salt composition on the structure of CO₂ direct electroreduction carbon products in chloride molten salt systems. Using CaO as a CO₂ absorber, the adsorption principle of CO₂ in LiCl-CaCl₂, LiCl-CaCl₂-NaCl and LiCl-CaCl₂-KCl molten salts was discussed, and the reasons for the different morphologies and structures of carbon products were analyzed, and it was found that the electrolytic efficiency of the whole process exceeded 85%. Furthermore, cathode products are analyzed through Scanning Electron Microscope (SEM), X-Ray Diffractometer (XRD), Thermal Gravimetric Analyzer (TGA), Raman Spectra and Fourier Transform Infrared (FTIR) techniques with a focus on the content and morphology of carbon elements. It was observed that the carbon content in the carbon powder produced by molten salt electrochemical method exceeded 99%, with most carbon products obtained from electrolysis in the Li-Ca chloride molten salt system being in the form of carbon nanotubes. In contrast, the Li-Ca-K chloride system yielded carbon nanospheres, while a mixture was found in the Li-Ca-Na chloride system. Therefore, experimental results demonstrate that altering the composition of the system allows for obtaining the desired product size and morphology. This research presents a pathway to convert atmospheric CO₂ into high value-added carbon products.

A series of Cu-ZSM-5 molecular sieve adsorbents were prepared by the impregnation method. The experimental results revealed that the mercury removal efficiency of the 2.5 wt% CuCl₂-ZSM-5 can reach up to 99%. Furthermore, both the crystal type and pore size distribution of the ZSM-5 molecular sieve remain the same after the process of copper-based active materials impregnated modification, and its specific surface area decreases as the load increases. Importantly, the surface of ZSM-5 modified by CuCl₂ equips many more Cu-O functional groups, which are beneficial to the catalytic oxidation of mercury and can even oxidize Hg⁰ to Hg²⁺. The adsorption process strictly follows the Mars–Maessen reaction mechanism.