“…For example, "Hard Lewis base" ligands (e.g., salicylic acid, glycine, phosphine ligands) incorporated as self-assembled monolayers on mesoporous supports (SAMMS) are effective for selective removal of "Hard Lewis acid" lanthanides [9,10] and actinides (e.g., Am, Pu, U and Th) [12]; while hydroxypyridinones (HOPO)-SAMMS performed well for the selective sequestration of actinides (Pu, Np, and U) [11]. In addition, there are several functionalized mesoporous silica nanoparticles that have been shown to be effective at binding aqueous U, including aminomodified MCM-41 [13] and SBA-15 [21], dopamine-functionalized SBA-15 [24], amidoxime-modified MCM-41 [23][24][25][26] and quartz [27], dihydroimidazole functionalized SBA-15 [15], monoamide resins with porous silica support [28], phosphonate or phosphine oxide-incorporated MCM-41 [16,23], SBA-V [17], KIT-6 [18] and carboxymethylated polyethyleneimine functionalized MSU-H [29]. However, among these studies, most of the functionalized mesoporous silica nanoparticles were evaluated under near-neutral pH conditions (pH [5][6][7][8] in which aqueous U species tend to precipitate or strongly adsorb onto various sorbents.…”