Laser light scattering has been used to study the solution behavior in
aqueous NaCl of poly(acrylamide) (PAM), polymerized by using two diff
erent polymerization processes: solution(S) and microemulsion(M). Resu
lts show that poly(acrylamide) samples polymerized from the microemuls
ion polymerization process behave as branched flexible chains, but pol
y(acrylamide) samples synthesized from solution polymerization exhibit
a fairly expanded flexible coil-chain behavior. By combining the stat
ic light scattering results with the characteristic linewidth distribu
tion as determined by a Laplace inversion of the intensity-intensity t
ime correlation function, the molecular weight distribution (MWD) and
the radius of gyration distribution (RGD) could be estimated. The mole
cular weight dependence of the z-average diffusion coefficient (D-z) w
as determined during this conversion, with D-z(0) = (3.05 x 10(-4)) M(
w)(-0.585) cm(2) s(-1) and D-z(0) = (1.52 x 10(-4)) M(w)(-0.518) cm(2)
s(-1) for PAM(S) and PAM(M), respectively, with the weight average mo
lecular weight M(w) expressed in g mol(-1) and D-z(0) in cm(2) s(-1).
The superscript zero denotes the value at infinite dilution. The small
er alpha(D) value of 0.52 for PAM(M) suggests that PAM(M) could have a
fairly compact, but still soluble, flexible coil-chain structure, pos
sibly arising asa result of (apparent) branching. Two different models
, polydisperse branched chains and branched soft spheres, were used to
fit the particle scattering factor obtained from SLS measurements. Th
e results show that the particle scattering factors of:samples PAM(M)
(but not of PAM(S)) could be fitted satisfactorily by either model. Co
ncentration and angular dependence of the mean characteristic linewidt
h, as well as the molecular weight distribution derived by using the C
ONTIN analysis, are presented. The origin of the apparent branching in
the microemulsion prepared poly(acrylamide) is shown to be a noncoval
ent aggregation in 1 M NaCl which is not manifest formamide solutions
of the same polymer.