The kinetic theory for rigid-rod molecules has been successful in describin
g a variety of experimental observations. from extremely dilute concentrati
ons to the liquid crystalline limit. The theory is formulated in terms of a
n orientation distribution function, whose tensorial moments can be related
to measurable properties. We introduce here a general relation from which
evolution equations for moments of arbitrary order can easily be derived. T
he relation incorporates the effects of flow, magnetic and electric fields
(permanent and induced dipoles), as well as "nematic" interactions necessar
y to describe liquid crystalline transitions. Relevant features of the equa
tion(s) with regard to possible closure strategies are briefly discussed. (
C) 1999 The Society of Rheology. [S0148-6055(99)01706-X].