TY - JOUR
T1 - Deformation and flow of matter
T2 - Interrogating the physics of materials using rheological methods
AU - McKenna, Gregory B.
N1 - Funding Information:
The author would, first, like to dedicate the present article to three very important people in his development as a scientist: L.J.Z. who was his “scientific father” and mentored him from his first days at the, then, National Bureau of Standards; D.J.P. who taught him the importance of careful experiments and is a dear friend; A.J.K. who introduced him to the subtleties of the glass transition and physical aging. Acknowledgments go to the National Bureau of Standards/National Institute of Standards and Technology for supporting the work on rubber, physical aging, and torsional dilatometry and to the National Science Foundation under Grant Nos. DMR-0304640: DMR-0804438, and the US Army Research Office under Grant Nos. W911NF-04-1-0207 and W911NF-07-1-0418 each for partial support of the work on rheology of ultrathin polymer films. The author thanks the American Chemical Society PRF under Grant No. ACS-PRF 35695-AC7 and the National Science Foundation under Grant No. DMR-0304640 for the work on torsion and normal force measurements in glasses as a function of molecular structure. Also, the J.R. Bradford Endowment at Texas Tech University made possible much of the work through continuous support of the author’s laboratories since 1999. Thanks, also, to B. Xu for preparing some of the figures. Finally, the number of co-authors in the author’s own referenced works attests to the fact that the work could not have been done alone, and their contributions and creativity are greatly appreciated.
PY - 2012/1
Y1 - 2012/1
N2 - Rheological measurements offer a unique means of interrogating the physics of amorphous solids, including crosslinked rubbers and polymeric glasses. Here, we present several vignettes to demonstrate the ability of both classical and novel rheological experiments to resolve important questions in condensed matter physics. First, results from torque and normal force measurements aimed at understanding the thermodynamics and mechanics of polymer networks in both dry and swollen states are presented. In particular, we examine the validity of the Frenkel-Flory-Rehner theory of rubber network swelling. Torsion and normal force measurements are also described for a series of polymeric glasses that exhibit similar shear moduli but, surprisingly, very different normal force responses, with one set of materials showing extreme deviations from neo-Hookean behavior and the other being close to neo-Hookean. We then describe the use of a novel torsional dilatometer, which allows simultaneous measurement of mechanical properties and volume recovery, to investigate the aging and rejuvenation behaviors of glassy polymers. Also, the temperature dependence of dynamics is probed in glassy polymers that have been aged into equilibrium below the nominal glass transition temperature and evidence is presented that time-scale divergence may not be a true signature of the glass transition itself. Finally, we describe a reduction in scale of the classical membrane inflation test to allow measurement of the biaxial creep compliance of nanometer thick polymeric films using an atomic force microscope. In each instance, emphasis is placed on how the measurements are designed to interrogate the physics of interest in the materials investigatedx.
AB - Rheological measurements offer a unique means of interrogating the physics of amorphous solids, including crosslinked rubbers and polymeric glasses. Here, we present several vignettes to demonstrate the ability of both classical and novel rheological experiments to resolve important questions in condensed matter physics. First, results from torque and normal force measurements aimed at understanding the thermodynamics and mechanics of polymer networks in both dry and swollen states are presented. In particular, we examine the validity of the Frenkel-Flory-Rehner theory of rubber network swelling. Torsion and normal force measurements are also described for a series of polymeric glasses that exhibit similar shear moduli but, surprisingly, very different normal force responses, with one set of materials showing extreme deviations from neo-Hookean behavior and the other being close to neo-Hookean. We then describe the use of a novel torsional dilatometer, which allows simultaneous measurement of mechanical properties and volume recovery, to investigate the aging and rejuvenation behaviors of glassy polymers. Also, the temperature dependence of dynamics is probed in glassy polymers that have been aged into equilibrium below the nominal glass transition temperature and evidence is presented that time-scale divergence may not be a true signature of the glass transition itself. Finally, we describe a reduction in scale of the classical membrane inflation test to allow measurement of the biaxial creep compliance of nanometer thick polymeric films using an atomic force microscope. In each instance, emphasis is placed on how the measurements are designed to interrogate the physics of interest in the materials investigatedx.
UR - http://www.scopus.com/inward/record.url?scp=84855915329&partnerID=8YFLogxK
U2 - 10.1122/1.3671401
DO - 10.1122/1.3671401
M3 - Article
AN - SCOPUS:84855915329
SN - 0148-6055
VL - 56
SP - 113
EP - 158
JO - Journal of Rheology
JF - Journal of Rheology
IS - 1
ER -