TY - JOUR
T1 - Linear Viscoelasticity of Spherical SiO 2 Nanoparticle-Tethered Poly(butyl acrylate) Hybrids
AU - Goel, Vivek
AU - Pietrasik, Joanna
AU - Matyjaszewski, Krzysztof
AU - Krishnamoorti, Ramanan
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): KUS-C1-018-02
Acknowledgements: V.G. and R.K. gratefully acknowledge the partial support of the National Science Foundation (CMMI-0708096). This publication is based on work supported in part by Award No. KUS-C1-018-02, made by King Abdullah University of Science and Technology (KAUST). J.P. and K.M. thank the Kosciuszko Foundation, Ministry of Science and Higher Education (Grant No. N508 3820 33) and the National Science Foundation (DMR-09-69301) for financial support.
This publication acknowledges KAUST support, but has no KAUST affiliated authors.
PY - 2010/12
Y1 - 2010/12
N2 - The melt state linear viscoelastic properties of spherical silica nanoparticles with grafted poly(n-butyl acrylate) chains of varying molecular weight were probed using linear small amplitude dynamic oscillatory measurements and complementary linear stress relaxation measurements. While the pure silica-tethered-polymer hybrids with no added homopolymer exhibit solid-like response, addition of matched molecular weight free matrix homopolymer chains to this hybrid, at low concentrations of added homopolymer, maintains the solid-like response with a lowered modulus that can be factored into a silica concentration dependence and a molecular weight dependence. While the silica concentration dependence of the modulus is strong, the dependence on molecular weight is weak. On the other hand, increasing the amount of added homopolymer changes the viscoelastic response to that of a liquid with a relaxation time that scales exponentially with hybrid concentration. © 2010 American Chemical Society.
AB - The melt state linear viscoelastic properties of spherical silica nanoparticles with grafted poly(n-butyl acrylate) chains of varying molecular weight were probed using linear small amplitude dynamic oscillatory measurements and complementary linear stress relaxation measurements. While the pure silica-tethered-polymer hybrids with no added homopolymer exhibit solid-like response, addition of matched molecular weight free matrix homopolymer chains to this hybrid, at low concentrations of added homopolymer, maintains the solid-like response with a lowered modulus that can be factored into a silica concentration dependence and a molecular weight dependence. While the silica concentration dependence of the modulus is strong, the dependence on molecular weight is weak. On the other hand, increasing the amount of added homopolymer changes the viscoelastic response to that of a liquid with a relaxation time that scales exponentially with hybrid concentration. © 2010 American Chemical Society.
UR - http://hdl.handle.net/10754/598721
UR - https://pubs.acs.org/doi/10.1021/ie1007129
UR - http://www.scopus.com/inward/record.url?scp=78649551091&partnerID=8YFLogxK
U2 - 10.1021/ie1007129
DO - 10.1021/ie1007129
M3 - Article
SN - 0888-5885
VL - 49
SP - 11985
EP - 11990
JO - Industrial & Engineering Chemistry Research
JF - Industrial & Engineering Chemistry Research
IS - 23
ER -