The　development　of　efficient　and　stable　catalysts　is　of　great　importance　for　the　elimination　of　volatile　organic　pollutants　(VOCs).　In　this　work,　AuPdx　nanoparticles　(NPs)　were　loaded　on　TiO2　through　the　electrostatic　adsorption　approach　to　generate　the　yAuPd(x)/TiO2　(i.e.,　0.35AuPd(0.46)/TiO2,　0.34AuPd(2.09)/TiO2,　and　0.37AuPd(2.72)/TiO2;　x　and　y　are　Pd/Au　molar　ratio　and　AuPdx　loading,　respectively;　x　=　0.46-2.72;　and　y　=　0.34-0.37　wt%)　catalysts,　and　their　catalytic　activities　for　the　oxidation　of　ethyl　acetate　were　determined.　The　results　showed　that　the　0.37AuPd(2.72)/TiO2　sample　exhibited　the　best　activity　(T-50%　=　217　degrees　C　and　T-90%　=　239　degrees　C　at　SV　=　40,000　mL/(g　h),　E-a　=　37　kJ/mol,　specific　reaction　rate　at　220　degrees　C　=　113.8　mu　mol/(g(Pd)　s),　and　turnover　frequency　(TOFNoble　metal)　at　220　degrees　C　=　109.7　x　10(-3)　s(-1)).　The　high　catalytic　performance　of　the　0.37AuPd(2.72)/TiO2　sample　was　attributed　to　the　good　dispersion　of　AuPd2.72　NPs,　the　strong　redox　ability,　the　large　ethyl　acetate　adsorption　capacity,　and　the　strong　interaction　between　AuPdx　and　TiO2.　Acetaldehyde,　ethanol,　and　acetic　acid　are　the　main　intermediates　in　the　oxidation　of　ethyl　acetate,　and　the　loading　of　AuPdx　NPs　effectively　reduces　the　formation　of　the　toxic　by-product　acetaldehyde.　The　oxidation　of　ethyl　acetate　over　the　0.34AuPd(2.09)/TiO2　sample　might　occur　via　the　pathway　of　ethyl　acetate　-＞　ethanol　-＞　acetic　acid　-＞　acetate　-＞　CO2　and　H2O.　We　believe　that　the　obtained　results　may　provide　a　useful　idea　for　the　design　of　bimetallic　catalysts　under　industrial　conditions　and　for　understanding　the　VOCs　oxidation　mechanisms.