Abstract

Using dynamic light scattering and small angle neutron scattering techniques we investigate the interrelation between the dynamic and static correlation lengths in liquid and supercritical polymer solutions in the poor solvent domain Θ ≥T≥Tc, where Θ is the theta temperature and Tc is the critical temperature of phase demixing. We observe the crossover between the hydrodynamic (T∼Θ) and critical non-diffusive (T∼Tc) regimes and demonstrate that the dynamic correlation length ξd* for polymers in liquid and supercritical polymer solvents is described by the universal function ξd*/ξd*(Θ)=F*(τ′) in terms of the de Genne’s scaling temperature variable τ′≡(T−Tc)/(Θ−Tc).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.