“…[79] The direct CO 2 hydrogenation has been quite well investigated. [149,150] Iron-based [104,130] small zeolite crystal size reduced extent of deactivation attributable to better diffusion [53,104] large supercages (zeolites LTL, Y) and pores increased reducibility, formation of large Fe particles, better diffusion, and consequently, higher C 5+ selectivity [114] zeolites with low Si/Al ratios (e.g., mordenite, beta, or ZSM-5) composition significantly different from classical straight-chain FTS products mediated by distinct zeolite topologies [130,135] zeolites with low Al content oligomerization and cyclization of light olefins [121] C 2 -C 4 olefins and low molar mass hydrocarbons high Si/Al ratios (low Al content) less acidic zeolites do not promote consecutive oligomerization, cyclization, and dehydrogenation reactions [104] high density of weak acid sites increased olefin selectivity ( % 40 %) [85,130] large zeolite crystal size increases the O/(O+P) ratio [104] impregnation rather than a physical mixture different Fe dispersion [130] promotion with Ti, V, Mn, Cs, K, or Pd see Table 5 -catalysts are active in both the rWGS and FT reaction, which makes this metal an ideal candidate for FTS of CO 2 -containing syngas feeds. [49,56] For CO 2 hydrogenation, the operating temperature must be rather high because of the equilibrium constraints for the rWGS reaction.…”