“…Throughout the literature, most reports on dry dechlorination adsorbents have been explored at a high temperature, and the reaction rates of alkaline earth oxides with HCl are strongly dependent upon the reaction temperature. − Yan et al indicated that the utilization rate of calcium hydroxide was less than 15% when the experimental temperature was reduced to 170 °C, which was mainly due to the poor reaction activity and low porosity of the active component. In the past decade, with the extensive research of porous materials, such as activated carbon, molecular sieve, activated alumina, etc., mesoporous substrate-supported active components has been recognized as the most potential candidate for acid gas adsorption and separation. − Moreover, to further improve the structural properties and low-temperature reactivity, transition metal oxides were employed as the main active components in some studies. − However, as a result of the lower solubility product constant ( K sp ) of metal sulfides, H 2 S tends to combine with these transition metal ions first, resulting in the poisoning deactivation of the adsorbent. − In addition, the dense acid species salts formed by carbonation and sulfurization also increase the mass transfer and diffusion resistance of HCl. In view of the above, as a result of poor HCl adsorption selectivity and high cost, these sorbents are far away from industrial practice application. , Up to now, there is a lack of research on high-efficiency selective dechlorination under a low-temperature and complex gas environment …”