“…During catalyst preparation, drying and calcination are known to be the important steps that strongly affect the textural properties of a catalyst (in such terms as surface area, pore size, and pore volume); distribution of the active metal on a support , and interaction between active sites and a support are also known to be affected by these two preparation steps . While hot air drying has traditionally been used for catalyst preparation, alternative drying techniques such as freeze drying and microwave drying have also been studied. ,− Different drying techniques and conditions have noted to differently affect the pore size, Brunauer–Emmett–Teller (BET) surface area, dispersion of metal on a support, and hence the performance of a catalyst. , Albretsen et al, for example, reported that an iron-based catalyst dried at 130 °C had larger pore volume, surface area, extent of reduction, and Fischer–Tropsch synthesis rate but lower methane selectivity compared to identical catalysts dried at higher or lower temperatures. Villegas et al found that metal dispersions, especially in the case of Ni, were strongly influenced by the applied drying method; Ni dispersion was more homogenous upon microwave drying or ambient-temperature drying than in the case of oven drying.…”