Co-combustion is a crucial route for the high-efficiency utilization and clean conversion of different carbonaceous feedstocks (biomass, coal, petroleum coke, etc.). The migration and transformation of alkali and alkaline earth metals (AAEMs) are not only related to ash-related issues in actual application, but also directly affect the reaction behavior of binary particles during co-conversion. This review paper summarizes research progress in the detection methods (online and offline) and influencing factors (feedstock type, feedstock blending ratio, reaction temperature, reaction time) of AAEMs migration and transformation during the co-combustion of carbonaceous feedstocks. Furthermore, it provides a detailed summary of research progress on factors (feedstock blending ratio, heating rate, etc.) influencing the co-combustion reactivity of carbonaceous feedstocks, synergy behavior, and its mechanisms. The influence of feedstock type on AAEMs migration and transformation during co-combustion is mainly related to the composition categories, chemical forms and contents of intrinsic mineral in binary feedstocks. The increase in the combustion temperature will intensify the release of inherent AAEMs in carbonaceous feedstocks, and promote AAEM deactivation. For high K and Cl-containing biomass, a higher biomass proportion in blends would result in more AAEMs release during the co-combustion process. Conversely, an increase in coal proportion in blends will directly favor the reduction or inhibition of AAEMs release. Synergy behavior during co-pyrolysis and subsequent char co-combustion is usually presented as an inhibition effect and an synergistic effect, respectively. The synergistic mechanisms of carbonaceous feedstock co-combustion reactions can be divided into two categories: non-catalytic synergistic mechanisms related to the excitation and migration of biomass-based free radicals and catalytic synergistic mechanisms related to biomass-based AAEMs catalysis. Additionally, future research prospects are also proposed based on the systematic review.

The rapid growth of energy storage technologies has led to a surge in spent battery waste, presenting both environmental challenges and opportunities for resource recovery. Emerging research highlights the potential of repurposing battery-derived components into functional materials for wastewater remediation. This review presents a comprehensive overview of recent advances in synthesizing catalysts and adsorbents from spent batteries, with a particular focus on their application in advanced oxidation processes (AOPs) and pollutant adsorption. Key synthesis methods, catalytic mechanisms, and the roles of material properties—such as surface area, defect structures, and heteroatom doping—are critically examined. By bridging materials science and environmental engineering, this work underscores the potential of battery waste valorization and provides guidance for scaling these technologies toward real-world wastewater treatment applications.