Formation of the structure in a copper-zinc catalyst for methanol synt
hesis is analyzed at each step of its preparation including hydrogen a
ctivation at which catalytically active species are formed. The necess
ary interaction of the catalyst components in fresh precipitates is pr
ovided by formation of mixed copper-zinc hydroxocarbonates. On low-tem
perature calcination, the interaction is preserved due to the formatio
n of mixed copper-zinc oxides modified by OH- and CO32- anions with co
pper ions distributed as clusters in a zinc oxide-type structure. The
activation with hydrogen results in formation of a proton-stabilized s
ystem of zinc oxide with epitaxially bound metallic copper. Both the c
hemical bond cleavage and spatial phase segregation at any step of the
catalyst preparation result in the loss of its catalytic activity.