Only three types of specimens can be applied for calibration in TXRF,
namely pure particle-, film- or bulk-type samples. In this study ''dro
plet'' standards, as a representative of the particle type, and ''spin
-drying'' standards, for film-type samples were examined and compared
with a pure metal standard (bulk-type). A test procedure is described
which makes it possible to detect faulty calibration samples. An itera
tive data processing technique is presented which extracts layer chara
cteristics and-to a certain extent-depth profiles from TXRF data as a
function of the incident angle. Two selected examples are considered,
a Fe-Ti-Fe thin-layer system and an implantation profile of Ni-atoms i
n silicon. Based on these samples, the capability and limitations of T
XRF for depth profiling are discussed.