TY - JOUR
T1 - Do Very Small POSS Nanoparticles Perturb s-PMMA Chain Conformations?
AU - Jouault, Nicolas
AU - Kumar, Sanat K.
AU - Smalley, Robert J.
AU - Chi, Changzai
AU - Moneta, Robert
AU - Wood, Barbara
AU - Salerno, Holly
AU - Melnichenko, Yuri B.
AU - He, Lilin
AU - Guise, William E.
AU - Hammouda, Boualem
AU - Crawford, Michael K.
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/7/24
Y1 - 2018/7/24
N2 - Small-angle neutron scattering (SANS) measurements of syndiotactic s-PMMA polymers mixed with weakly attractive 1.0 nm diameter polyhedral oligomeric silsesquioxane (POSS) nanoparticles (NPs) show no observable changes in the chain radius of gyration Rg, regardless of the polymer molecular weights, the amount of residual solvent, or the POSS NP loading and dispersion (from 0 to 20 vol %). In retrospect, these results are not surprising since scaling arguments imply that chain size in the concentrated region of the phase diagram of a polymer solution is ideal and independent of the polymer volume fraction ø, and only as the semidilute region is entered with decreasing concentration does the chain size for a good solvent begin to increase due to polymer excluded volume and then scales with concentration as ø-1/8. For typical polymer nanocomposites the NP concentrations are less than 50% v/v, so the polymers are still generally within the concentrated regions of their phase diagrams, where ideal chain conformations are observed for small molecule solvents. By combining the present results with previous results from the literature, we conclude that spherical NPs apparently have little effect on the conformations of polymer chains, especially in typical polymer nanocomposites that only incorporate moderate amounts of NPs.
AB - Small-angle neutron scattering (SANS) measurements of syndiotactic s-PMMA polymers mixed with weakly attractive 1.0 nm diameter polyhedral oligomeric silsesquioxane (POSS) nanoparticles (NPs) show no observable changes in the chain radius of gyration Rg, regardless of the polymer molecular weights, the amount of residual solvent, or the POSS NP loading and dispersion (from 0 to 20 vol %). In retrospect, these results are not surprising since scaling arguments imply that chain size in the concentrated region of the phase diagram of a polymer solution is ideal and independent of the polymer volume fraction ø, and only as the semidilute region is entered with decreasing concentration does the chain size for a good solvent begin to increase due to polymer excluded volume and then scales with concentration as ø-1/8. For typical polymer nanocomposites the NP concentrations are less than 50% v/v, so the polymers are still generally within the concentrated regions of their phase diagrams, where ideal chain conformations are observed for small molecule solvents. By combining the present results with previous results from the literature, we conclude that spherical NPs apparently have little effect on the conformations of polymer chains, especially in typical polymer nanocomposites that only incorporate moderate amounts of NPs.
UR - http://www.scopus.com/inward/record.url?scp=85050684632&partnerID=8YFLogxK
U2 - 10.1021/acs.macromol.8b00432
DO - 10.1021/acs.macromol.8b00432
M3 - Article
AN - SCOPUS:85050684632
SN - 0024-9297
VL - 51
SP - 5278
EP - 5293
JO - Macromolecules
JF - Macromolecules
IS - 14
ER -