“…In the trioctahedral structure, the -OH dipole is perpendicular to the biotite (0 0 1) base so that there is a short distance between H-and K-, which leads to the increase of repulsion, a slack K-bond, and K + is easily released (Bassett, 1960). The location of potassium loss in biotite determines the release pattern of potassium in two ways including (1) exchange interaction, H + or Na + cation exchanges K + from the edge of the (h k 0) and interlayer via kinks or defect sites on the biotite (0 0 1) surface, which will not lead to evident alteration on a biotite structure (Hu et al, 2011); (2) hydrolysis, H + reacts with Al-O-Al and Si-O-Si to break the lattice charge-balancing and release K + , which will destroy the mica crystal structure (Ganor et al, 2009;Munson, 1985). Biotite has abundant K, which is one of the three most essential nutrients for plants (Ren et al, 2013;Samal et al, 2010;Steingrobe and Claassen, 2000).…”