Asphaltene association in crude oil in the native condition was studie
d using electron-nuclear double resonance (ENDOR) spectroscopy. Most o
f the asphaltene molecules are associated with each other in the range
from room temperature up to 90 degrees C. The core of the associate i
s a stack of condensed aromatic sheets of characteristic radius simila
r to 10 Angstrom. The effect of dilution by various low-molecular-weig
ht solvents on destruction of the associates was observed. The extent
of associate destruction was not found to correlate with the solvent p
olarity. The outer coordination sphere of a micelle with the asphalten
e associate as a core is assumed to be sufficiently labile to allow th
e low-molecular-weight solvents used to reach the core.