A zero-mean flow fan-stirred chamber is used to gather data on suspended fuel droplet evaporation at turbulence intensities, q1/2, approaching 4.30 m/s. This research is driven by the oft-cited but unconfirmed belief that the droplet evaporation rate, K, eventually plateaus with increasing turbulence kinetic energy. Further motivation comes from numerous real-world examples, including combustion systems, where droplets are exposed to turbulence intensities far beyond the experimental capabilities reported in the literature to date. Decane, ethanol, and heptane fuels are selected and grouped into two categories based on the similarity of their vapor pressures, Pv, and mass diffusivity coefficients, DAB, in an effort to discern which thermophysical properties are important to vaporization enhancement, or lack thereof, in high turbulence. Individual droplets with constant initial diameters, d0, of 500 µm are placed in the central region of a highly homogeneous and isotropic turbulent flow field using a novel multi-fiber intersection technique. Neither alkane fuel exhibits any sign of reduced effect of turbulence, as K/K0 remains a strongly linear function of turbulence intensity throughout the test conditions. Conversely, the normalized evaporation rate of ethanol begins to plateau at the higher levels of intensity. Although equalizing the vapor pressures of ethanol and heptane was sufficient to match K/K0 values at low intensity, their divergence as q1/2 increases implies that the thermodynamically-predicted vapor quantity at the droplet surface does not enforce an upper limit on turbulence effectiveness at moderately elevated temperatures. This is confirmed by decane, which has the lowest volatility and yet experiences the greatest improvement in evaporation rate at the highest levels of turbulence.