The purpose of performed X-ray examinations was to understand the changes i
n the structures of coke during the blast-furnace process. Prolonged (many-
hour) heating of coke (at a temperature of about 2000 degreesC) in a reduci
ng atmosphere and under high pressures prevailing in the blast furnace may
cause slightly different changes in the structure that typical graphitizati
on. Experimental tests were carried out on three groups of coke samples: th
e so called burden coke (delivered from the coking plant, and designated by
KN), the coke taken from the tuyere level of the blast furnace (DWP), and
cokes subjected to laboratory tests reproducing, to a certain extent, the c
onditions prevailing in the blast furnace (TS) and (KB). The X-ray measurem
ents made by the X-ray diffraction (XRD) method and the small-angle X-ray s
cattering (SAXS) method have enabled the description of the following param
eters characterizing the structure: the interplanar distance, d(oo2); the c
rystallite size, L-e; the crystallinity factor, W-k; and the pore fractal d
imension, D-p, and the boundaris of the fractality range (a, xi). The coke
samples were characterized by some volumetric inhomogeneity, therefore part
icle cross-sections and powder specimens were prepared. In the analysis of
examination results, the average values of the measured parameters were pre
sented for particular groups of cokes, which confirmed the presumption that
an intensive development of the coke crystalline structure and transformat
ions of the type of porosity occurred during the blast-furnace process. The
se changes are probably the more extensive the greater is the degree of cry
stallinity of burden coke loaded to the blast furnace. Thus, there is a pos
sibility of controlling the changes in the structure of coke, and thereby i
ts properties, which can be utilized for reducing the coke consumption in t
he blast-furnace process.