There is booming interest in the
application of nanoparticles for
enhanced oil recovery. In this work, a polymer nanoparticle that is
generated by cross-linking a high-molecular weight partially hydrolyzed
polyacrylamide with aluminum(III) and known as linked polymer solution
(LPS) has been studied. The size and conformational state of LPS particles
are influenced by the concentration of Al(III). To the best our knowledge,
there is no current established method for determining the conformational
state, i.e., single coiled particle, coil aggregates, or gel, for
a polymer solution with a high molecular weight (>10 × 106 Da) and a low concentration (<1000 ppm). In this work,
therefore, the phase transition of LPS is investigated by employing
two-dimensional 1H–1H nuclear magnetic
resonance (nuclear Overhauser effect spectroscopy and diffusion ordered
spectroscopy), UV–visible spectroscopy, and oscillatory rheological
methods. Each method is limited to determining the conformational
state; however, the combined methods provided a consistent tool for
mapping various interactions regarding the conformational changes
of LPS as a function of Al(III) concentration. The results of our
study revealed that the phase transition is a stepwise process; the
transition from a random polymer coil to structured coils (intramolecular
cross-linking) was observed by reduction of the hydrodynamic radius
and an increase in the rate of diffusion, followed by coil aggregates
as a function of Al3+ concentration. Ultimately, networked
weak gels are formed by coil aggregates (intermolecular cross-linking)
above the threshold concentration.