Wet samples of Th(IV) sorbed on colloidal amorphous silica particles (Aerosil OX 200) have been studied with extended X-ray absorption fine structure spectroscopy (EXAFS) at the Th L-III edge (16.3 keV), The samples were collected with sample surface coverages ranging from 3.8 to 230%. No fundamental changes in the structural environment of Th in terms of the types and distances of nearest neighbors with increasing surface loading were detected, but the results indicate an increasing degree of structural disorder with increasing surface coverage, The O shell around Th shows a distorted configuration with two O atoms at 2.33 Angstrom distance and four to six O atoms at 2.55 Angstrom. Only one Si shell is observed, with two Si atoms at a distance of 3.8-3.9 Angstrom. These results have been interpreted with a double corner-sharing surface complex of Th on silica, where the Th atom shares one O atom with each of two coordinated SiO4 tetrahedra, accounting for the first O coordination shell detected as well as the Th-Si distances. The longer Th-O distances result from coordinated water molecules from solution, No Th-Th interactions could be detected in the EXAFS spectra.