Abstract

A series of perfluoroalkyl end-capped poly(ethylene oxide) (PEO) of molecular weight Mn = 10 000 and 20 000, noted F-HEUR-10K and F-HEUR-20K, with a well-defined structure were synthesized in two reaction steps. The reaction of PEO with a large excess of isophorone diisocyanate (IPDI) leads to an isocyanate-terminated prepolymer which is then reacted with the semifluorinated alcohol [C8F17(CH2)11OH]. Experimental conditions were improved to prevent polycondensation in the first step of the synthesis. The degree of functionalization is controlled by 19F NMR. The influence of the terminal perfluorinated group on the linear viscoelasticity of aqueous solutions has been investigated as a function of the polymer concentration Cpol, PEO chain length, degree of functionalization, surfactant (SDS), and temperature. A steep increase of the static viscosity η0, attributed to the sol−viscoelastic transition with the formation of a multiconnected network, is observed at Cpol ≈ 1 wt %. The stress relaxation function G(t) is best fitted by a stretched exponential G(t) = G0 exp[−(t/τ)α], where G0 is the elastic plateau modulus. The relaxation time τ and static viscosity η0 were found to be temperature-dependent according to the Arrhenius law. The hydrophobic character of the end caps reinforced by the perfluorinated segments leads to larger relaxation times (several hundred seconds) and higher activation energies (≈120 kJ mol-1) compared to those of hydrocarbon HEUR-type associative polymers.

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.