Thermal depolymerization etching enables rapid, solvent-free formation of high-surface-area mesoporous polymers by selectively removing methacrylate domains. Etching approaches are used to generate nanoscale porosity in polymers. However, existing methods rely on solution-based processes that suffer from slow transport of etching agents and the degradation products arising from pore formation. These constraints become more significant in bulk materials, where transport limitations reduce efficiency and make it difficult to obtain uniform porous structures. Meanwhile, demand for advanced filtration and separation technologies continues to grow, with the global filtration and separation market estimated at approximately $184.75 USD billion in 2024 and projected to exceed $276 USD billion by 2035, reflecting the increasing need for high-performance materials in this space . Therefore, there is a clear need for fast, scalable etching methods that can reliably produce well-defined mesoporous polymers at commercial volumes.
Researchers at the University of Florida have discovered depolymerization etching of polymerization-induced microphase separations (DEPIMS), a rapid, solvent-free thermal process that enables efficient formation of porous polymer systems. This approach selectively removes polymethacrylate domains while maintaining the overall polystyrene structure, allowing scalable, on-demand fabrication of well-defined, high-surface-area mesoporous materials.
Produces high-surface-area mesoporous polymer materials for separations, adsorption, and purification applications
This etching approach is based on a process called DEPIMS – depolymerization etching of polymerization-induced microphase separation. First, a polymer system is formed through the incorporation of a depolymerizable component into a crosslinked matrix that resists degradation. During formation, the material undergoes simultaneous growth, phase separation, and crosslinking, producing a continuous structure with nanoscale domains. Heating the material to elevated temperatures causes the depolymerizable regions to break down into monomer species that are removed, while the crosslinked framework remains intact. This selective removal process results in a porous material with interconnected nanoscale features that can be further functionalized with chemical moeties promoting selective filtration, adsorption, etc. Because the removed components exit as rapidly diffusing species, the process bypasses the transport limitations associated with liquid-based etching and enables efficient formation of high-surface-area materials.