Abstract

The sintering of iron ammonia synthesis catalysts (nanocrystalline iron promoted with: Al2O3, CaO and K2O) was studied under a hydrogen atmosphere, in a temperature range of 773 to 973 K to obtain stationary states. The catalysts were characterized by measuring the nitriding reaction rate under an ammonia atmosphere at 748 K to obtain steady states and the measurement of specific surface area. Chemical processes were conducted in a tubular differential reactor enabling thermogravimetric measurements and the chemical composition analysis of a gas phase under conditions allowing experiments to be carried out in the kinetic region of chemical reactions. An extended model of the active surface of the iron ammonia synthesis catalyst was presented, taking into account the influence of the gas phase composition and process temperature. The surface of iron nanocrystallites was wetted using promoters in an exothermic process associated with the formation of the surface Fes-O- bond and the change in the surface energy of iron nanocrystallites. Promoters formed on the surface of iron nanocrystallites with different structures of chemisorbed dipoles, depending on the composition of the gas phase. The occupied sites stabilized the structure, and the free sites were active sites in the process of adsorption of chemical reagents and in sintering. Based on the bonding energy of the promoter oxides and the difference in surface energy between the covered and uncovered surfaces, the wetting abilities of promoters, which can be arranged according to the order K2O > Fe3O4 > Al2O3 > CaO, were estimated. By increasing the temperature in the endothermic sintering process, the degree of surface coverage with dipoles of promoters decreased, and thus the catalyst underwent sintering. The size distribution of nanocrystallites did not change with decreasing temperature. Only the equilibrium between the glass phase and the surface of iron nanocrystallites was then established.

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