Characteristics of the intrinsic modulus as applied to particulate composites with both soft and hard particulates utilizing the generalized viscosity/modulus equation
Rd. Sudduth et R. Seyfarth, Characteristics of the intrinsic modulus as applied to particulate composites with both soft and hard particulates utilizing the generalized viscosity/modulus equation, J APPL POLY, 77(9), 2000, pp. 1954-1963
Recently, four significantly different particulate composite modulus deriva
tions from the literature were found to yield the same theoretical "intrins
ic modulus" for a particulate composite. In this article, this new intrinsi
c modulus was successfully combined with the generalized viscosity/modulus
equation to yield a good fit of the shear modulus-particulate concentration
data of both Smallwood and Nielsen using a variable intrinsic modulus. Som
e fillers yielded an intrinsic modulus that was close to the Einstein limit
ing value ([G] = [eta] = 2.5), while other fillers yielded intrinsic moduli
that were either somewhat larger or somewhat smaller than this value. The
intrinsic modulus for carbon black in rubber was much larger than was Einst
ein's predicted value. However, intrinsic modulus values for Nielsen's data
for particulate composites were smaller than were Einstein's prediction at
temperatures below the glass transition temperature of the matrix. The exp
lanation for this phenomenon can easily be understood from a review of the
properties of the intrinsic modulus. Likewise, the generalized viscosity/mo
dulus equation was also successfully applied to available modulus literatur
e for ceramics where voids were the particulate phase. When applied to Wang
's data, the intrinsic modulus was found to be negative when describing the
compaction of voids in the hot isostatic pressing of a ceramic. For this a
pplication, the modulus of a particulate composite as a function of the vol
ume fraction of particles was modified to describe the modulus as a functio
n of porosity. For the sets of data analyzed, values of the interaction coe
fficient and the packing fraction were not necessarily unique if the data s
ets were limited to the lower particulate volume fractions. For application
s where a minimum amount of data was found to be available, a new approach
was introduced to address a relative measure of the compatibility of the pa
rticle and the matrix using a new definition for Kraemer's constant. (C) 20
00 John Wiley & Sons, Inc. J Appl Polym Sci 77: 1954-1963, 2000.