This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. analysis, FT-IR spectroscopy, and nitrogen adsorption-desorption, were utilized to investigate the effect of functionalization degrees of absorbents on their chemical composition, surface chemistry, pore structures and phosphate adsorption capacities in detail. In the batch adsorption tests, the functionalized absorbents with increasing loadings of diamino groups possessed markedly enhanced adsorption capacities, although there was a gradual loss of ordered mesostructures accompanied. The adsorption isotherms were represented better by using Langmuir model than Freundlich model, which indicated the presence of monolayer adsorption. In particular, for the resulting absorbent prepared with 0.5:1 molar ratio of AAPTS and TEOS, the maximum phosphate capture capacity calculated from Langmuir model is 20.7 mg P/g. In the kinetic study, the phosphate adsorption followed pseudo-second-order equation well with a correlation coefficient of 0.999, suggesting the adsorption process be chemisorption. The phosphate adsorption efficiency of prepared absorbent was highly pH-dependent and the high removal of phosphate was achieved within the pH between 3.0 and 6.0. The presence of Cl − and NO 3 − exhibited small impacts on the phosphate adsorption by using our synthesized absorbent; whereas, there were significantly negative effects from HCO 3 − and SO 4 2− on the phosphate removal. In 0.010 M NaOH, more than 90% of the absorbed phosphate anions on the spent adsorbent could be desorbed, suggesting the absorbent with a capacity of regeneration.