TY - JOUR
T1 - The Payne Effect in Nanofilled Cross-Linked Polyisoprene
AU - Dhara, Deboleena
AU - Rahman, Md Anisur
AU - Ruzicka, Eric
AU - Benicewicz, Brian
AU - Vlassopoulos, Dimitris
AU - Kumar, Sanat K.
N1 - Publisher Copyright:
© 2025 American Chemical Society
PY - 2025/10/14
Y1 - 2025/10/14
N2 - We present a systematic study of the Payne effect, i.e., the difference between the small- and large-amplitude oscillatory shear response of filled elastomers, which is relevant to the performance of tires under dynamic driving conditions. The elastomers consist of 14-nm-diameter spherical silica nanoparticles (NPs) grafted with polyisoprene chains, mixed with polyisoprene matrices, and subsequently cross-linked into the gel state. By changing the grafting density and the ratio of the graft-to-matrix chain length, we vary the NP assembly state and examine its response to large-amplitude oscillations. We find that the Payne effect is present at all filler contents but becomes more pronounced at higher NP loadings and for the connected sheet morphology, with the well-dispersed NP state showing the smallest effect. The key concept that apparently controls the strength of the Payne effect is that the core–core contacts are stronger but more fragile compared to interdigitated grafts. Therefore, to achieve increased modulus but reduced Payne effect, a compromise between enhanced NP core interactions and the interdigitation of grafts with other grafts and with the matrix chains is needed. This compromise is best achieved for a morphology intermediate between these two extremes, i.e., a connected network morphology.
AB - We present a systematic study of the Payne effect, i.e., the difference between the small- and large-amplitude oscillatory shear response of filled elastomers, which is relevant to the performance of tires under dynamic driving conditions. The elastomers consist of 14-nm-diameter spherical silica nanoparticles (NPs) grafted with polyisoprene chains, mixed with polyisoprene matrices, and subsequently cross-linked into the gel state. By changing the grafting density and the ratio of the graft-to-matrix chain length, we vary the NP assembly state and examine its response to large-amplitude oscillations. We find that the Payne effect is present at all filler contents but becomes more pronounced at higher NP loadings and for the connected sheet morphology, with the well-dispersed NP state showing the smallest effect. The key concept that apparently controls the strength of the Payne effect is that the core–core contacts are stronger but more fragile compared to interdigitated grafts. Therefore, to achieve increased modulus but reduced Payne effect, a compromise between enhanced NP core interactions and the interdigitation of grafts with other grafts and with the matrix chains is needed. This compromise is best achieved for a morphology intermediate between these two extremes, i.e., a connected network morphology.
UR - https://www.scopus.com/pages/publications/105018574340
U2 - 10.1021/acs.macromol.5c01384
DO - 10.1021/acs.macromol.5c01384
M3 - Article
AN - SCOPUS:105018574340
SN - 0024-9297
VL - 58
SP - 10559
EP - 10566
JO - Macromolecules
JF - Macromolecules
IS - 19
ER -