Interest in the development of lignin-containing polymeric materials h
as been upheld more or less continuously for the past 20 years. Tenden
cies toward high moduli and poorly defined thermal transitions have be
en regarded as imposing inevitable limitations upon the use of lignin
derivatives for such purposes. Incorporation of more than 25-40% (w/w)
lignin had usually resulted in materials that were brittle and weak.
For the first time, however, from homogeneous blends containing 85% (w
/w) underivatized industrial kraft lignin with poly(vinyl acetate) and
two plasticizers, a series of thermoplastics has been fabricated with
promising mechanical properties. The tensile behavior of these new po
lymeric materials depends directly upon the degree of association betw
een the intrinsic kraft lignin components. In extending to values abou
t 25 MPa and 1.5 GPa, respectively, the tensile strengths and Young's
moduli vary linearly with the effective M-V(w) for the kraft lignin sp
ecies, under conditions where the proportions of the individual molecu
lar components, both associated and discrete, do not change. Moreover,
melt-flow index measurements indicate that these polymeric materials
are amenable to thermal processing by extrusion molding. Thus a signif
icant step has been taken toward developing a new generation of thermo
plastics that are lignin-based in a very fundamental way. (C) 1997 Joh
n Wiley & Sons, Inc.