Reusable, solid acid carbon supported catalysts were generated from biomass by pyrolysis (400-500 degrees C) to generate a soft to hard carbon backbone (i.e., biochar) for addition of acidic functional groups. Acid catalysts were synthesized by sulfonating the biochar and wood derived activated carbon using concentrated H2SO4 at 100, 150 and 200 degrees C (12 h) and gaseous SO3 (23 degrees C). Attenuated Total Reflectance, sulfur, and NH3-TPD analysis of the sulfonated carbons indicated the presence of -SO3H groups on the 100 degrees C sulfonated biochar and activated carbon (AC), with higher active site densities (SO3H density) for the SO3 sulfonated material. The sulfonated carbons were tested for their ability to esterify free fatty acids with methanol in blends with vegetable oil and animal fat (5-15 wt.% FFA). Esterification of the fatty acids was typically complete (similar to 90-100% conversion) within 30-60 min at 55-60 degrees C (large methanol excess), but decreased with lower methanol to oil ratios using the biochar catalysts (e.g., 70%, 6 h, 20:1). Solid acid catalysts derived from wood based activated carbon had significantly higher activity compared to the biochar derived catalysts (e.g., 97%, 6 h, 6:1). Of the synthesized biochar catalysts, 400 degrees C pyrolyzedpine chip biochar, sulfonated at 100 degrees C, resulted in the highest reaction rate and lowest reduction in conversion (or deactivation) when reused multiple times. Drying the biochar catalysts for 1 h at 125 degrees C between uses maintained esterification activity, allowing the catalysts to be reused up to 7 cycles. For the SO3 sulfonated AC catalyst, such a regeneration step was not required, as the fractional conversion of palmitic and stearic acid (5% FFA, 10:1, 3 h) remained >90% after 6 cycles. (C) 2012 Elsevier B.V. All rights reserved.