For the increasing number of RME users, a compilation of possible measuring
errors is made. A detailed description of sample preparation is given, sta
rting from granular as well as powdery polymers. The preparation of smooth
surface sample for optical rheometry is also addressed. A large part of the
paper deals with the evaluation of true strain rates by particle tracking.
A discussion of the errors arising from using different strain rate measur
es is made. Data on the elongation of LDPE at <(<epsilon>) over dot> = 0.01
s(-1) is given to show the possibility of increasing the measuring sensiti
vity by repetition and averaging. The surface tension of the LDPE melt is m
easured as an example. The influences of sample thickness and the diameter
of the distance pins on the measured viscosity are shown. The influences ar
e small, and an upper limit of 1.5 mm for the sample thickness is recommend
ed. The possibility of performing stress relaxation and recovery measuremen
ts after cessation of steady elongational flow is mentioned but not support
ed by our own measurements. The same holds for optical rheometry.