Common collectors for rare earth mineral (REM) flotation, which include carboxylates and hydrox-amates, face problems such as being non-selective and sensitive to impurity ions. A type of ionic liquid (IL), tetraethylammonium mono-(2-ethylhexyl)2-ethylhexyl phosphonate ([N2222][EHEHP]), has been investigated previously for rare earth elements (REE) solvent extraction, and was proven to be selective and effective. In this work, [N2222][EHEHP] was evaluated as a collector in bastn(a)site (a primary REM source for REE production) flotation for the first time. The results were compared with quartz and he-matite, two common gangue minerals in REM deposits. Zeta potential measurements and Fourier-transform infrared spectroscopy (FT-IR) were completed to investigate the surface chemical properties involved in the flotation of these minerals using this collector. The findings were compared with microflotation results. FT-IR and zeta potential measurements suggest adsorption of the collector's phosphonate group onto bastn(a)site and hematite, likely through chemisorption;whereas for quartz, the minimum microflotation recovery is likely due to no adsorption of IL on its surface. Microflotation results show higher collectability of [N2222][EHEHP] for hematite than bastn(a)site, the latter only shows appre-ciable recovery at pH 5 with elevated dosage of IL (500 g/t). To achieve better separation, a two-stage flotation scheme was designed and evaluated by bench scale flotation on a synthetic mineral mixture. The concentrates and tails were analyzed by magnetic separation, and it is found that bastn(a)site recovery over 90% with maximum upgrade ratio 1.7 can be achieved with elevated collector dosage.