Volatile　organic　compounds　(VOCs)　cause　damage　to　atmospheric　environment　and　human　health.　Supported　noble　metal　catalysts　are　widely　used　to　control　VOCs　emissions.　The　high　cost,　and　low　H2O-,　CO2-,　and　SO2-resistance　of　such　catalysts　are　worthy　to　be　improved.　Herein　we　fabricated　Ce-,　V-,　or　W-doped　TiO2　supported　ultralow　loading　Pt　catalysts　via　the　in-situ　molten　salt　method,　and　evaluated　their　catalytic　performance　for　acetone　(major　pollutants　in　pharmaceutical　industry)　removal.　Under　the　present　reaction　conditions,　all　the　catalysts　exhibited　high　catalytic　activity　and　stability　for　acetone　oxidation,　with　the　temperature　required　90%　acetone　conversion　being　of　245　degrees　C　over　0.57　wt%　CeO2-0.05　wt%　Pt/TiO2.　The　doping　of　Ce,　V,　or　W　enhanced　the　H2O-,　CO2-,　and　SO2-tolerance　ability　of　0.05　wt%　Pt/TiO2.　More　than　85　%85%,　70%,　or　60%　of　acetone　could　be　removed　even　in　the　presence　of　20　vol%　water　vapor,　10　vol%　CO2,　or　100　ppm　SO2,　respectively.　The　improvement　in　SO2-tolerance　ability　was　due　to　the　inhibition　of　SO2　adsorption　and　oxidation　activity　as　well　as　Ti(SO4)(2)　or　TiOSO4　formation.　Acetone　complete　oxidation　over　0.57　wt%　CeO2-0.05　wt%　Pt/TiO2　would　follow　the　pathway:　adsorbed　acetone　molecules　-＞　acetic　acid　and　formic　acid　-＞　carbonate　species　-＞　CO2　and　H2O.　The　present　supported　Pt　catalysts　might　be　suitable　for　oxygenated　VOCs　removal.