Gas-phase dehydration of aqueous propane polyols including glycerol, 1,2- and 1,3-propanediols was investigated over various solid catalysts with a wide range of acid-base properties. Fairly high selectivity (40-75 mol%) for propanal formation from 1,2-propanediol, and acrolein from glycerol was obtained over the catalysts with high fractional acidity in the range of -8.2 < H-0 <= -3.0, in which Bronsted acidity appeared advantageous over Lewis acidity. The dehydration of 1,3-propanediol produced quite scattered products and a clear relationship between its product selectivity and the catalyst acidity could not be established. Mechanistic implications of these observations are discussed, which point to that the dehydration reactions of both 1,2-propanediol and glycerol are initiated by activation of the hydroxyl group bonded with the central carbon atoms. (C) 2014 Elsevier B.V. All rights reserved.