“…In natural aqueous environments, selenium can be found under two stable oxidation states: Se(IV), generally as a selenite oxyanion SeO 3 2− or in its protonated forms H 2 SeO 3 and HSeO 3 − (pKa 1 = 2.64 and pKa 2 = 8.4 [3]), and Se(VI) as a selenate oxyanion SeO 4 2− . Numerous studies have investigated the sorption of selenium oxyanions on various mineral surfaces such as iron oxyhydroxides [4][5][6][7][8][9][10][11][12][13][14], aluminium oxy-hydroxides [15][16][17][18][19][20], hydrous titanium [21] or manganese [22] oxides, copper(I) oxides [23,24], cements and clays [3,[25][26][27][28][29], soils or complex media [30][31][32][33][34][35], granite [36,37], hydroxyapatite [38], Mg/Fe carbonated layered double hydroxides [39] and iron sulphides [2,40]. In most of these sorption studies , Se(IV) appeared to be more retained by the solid surface than Se(VI).…”