The invention discloses a method for synthesizing bisphenol A diglycidyl ethers through halogen-free epoxidation, which is characterized by comprising the following steps of: adding bisphenol A diallyl ethers, a solvent I and a phosphotungstic acid quaternary ammonium salt catalyst into a reactor, adding a hydrogen peroxide solution into the reactor while stirring, raising the temperature of a reactant to 30-80 DEG C, and reacting the obtained object for 5-24 hours at a temperature of 30-80 DEG C so as to obtain a reacted material; cooling the reacted material to room temperature, separating an organic phase, after the separated organic phase is subjected to distillation recycling so as to obtain an organic solvent, uniformly stirring and mixing the rest material and ethyl acetate, carrying out filtering on the obtained product, and after filter liquor is subjected to distillation recycling so as to obtain ethyl acetate, obtaining a coarse product; and carrying out column chromatography on the coarse product by using a solvent III so as to obtain bisphenol A diglycidyl ethers. After the method disclosed by the invention is adopted, no organic chlorine ion contains in the process of synthesis, a synthesized target product not only has no organochlorine heterogeneous client base, but also is low in product viscosity, good in performance, simple in process, easy to operate, high in safety, low in pollution and strong in practicability.