A sustainable way to produce plastics made from biomass (biomass to gas) and electricity (power to gas) could be obtained by the direct synthesis of light alkenes. Samples (<= 1 g) of the bulk catalysts Co/Fe, Fe/Na/S and the supported catalysts Fe/Mn vertical bar MgO and Co vertical bar SiO2 are mentioned in the literature to allow the direct synthesis of light alkenes. These materials are studied in extended fixed beds with catalyst amounts between 35 and 70 g and classic syngas (H-2 and CO) in this work in order to prepare a potential scale-up of this technology. The influence of activation conditions (H2 or CO as reduction agent; 350 or 420 degrees C at 1.5 bar) and synthesis temperature (230-500 degrees C) on catalyst activity and product selectivity are pointed out. Selectivities to ethene of up to 11% are found for Fe/Mn vertical bar MgO at T approximate to 440 degrees C and for Fe/Na/S at T approximate to 310 degrees C. The other materials did not produce significant amounts of ethene. CO2 and CH4 were the main products in any case, while C2H6 was the main C-2 product. Applying CO as reduction agent was superior to activation with H2 at low times on stream (< 20 h). This is justified by the fast formation of carbides with CO as reduction agent since they are the most catalytically active species on Fe catalysts. The low selectivities observed for ethene are likely caused by the low GHSV value of 160 h(-1) applied in this study, which facilitates the conversion of primary alkenes in secondary reactions. Recommendations on operational conditions of Fischer-Tropsch to olefins processes are specified.