

FOLLOWUS
a.State Key Laboratory of Polymer Science and Technology, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
b.School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei 230026, China
c.Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Mianyang 621000, China
d.Institute of Polymer Science and Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China
zhwang@ciac.ac.cn (Z.H.W.)
yylu@mail.tsinghua.edu.cn (Y.Y.L.)
Received:07 October 2025,
Accepted:25 November 2025,
Online First:22 January 2026,
Published:05 February 2026
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Wang, X. Y.; Liu, B.; An, L. J.; Wang, Z. H.; Lu, Y. Y. Short-chain length dependence of equilibrium dynamics and nonlinear rheology in unentangled long-chain/short-chain polymer blends. Chinese J. Polym. Sci. 2026, 44, 525–535
Xiao-Yang Wang, Bo Liu, Li-Jia An, et al. Short-chain Length Dependence of Equilibrium Dynamics and Nonlinear Rheology in Unentangled Long-chain/Short-chain Polymer Blends[J]. Chinese Journal of Polymer Science, 2026, 44(2): 525-535.
Wang, X. Y.; Liu, B.; An, L. J.; Wang, Z. H.; Lu, Y. Y. Short-chain length dependence of equilibrium dynamics and nonlinear rheology in unentangled long-chain/short-chain polymer blends. Chinese J. Polym. Sci. 2026, 44, 525–535 DOI: 10.1007/s10118-025-3514-4.
Xiao-Yang Wang, Bo Liu, Li-Jia An, et al. Short-chain Length Dependence of Equilibrium Dynamics and Nonlinear Rheology in Unentangled Long-chain/Short-chain Polymer Blends[J]. Chinese Journal of Polymer Science, 2026, 44(2): 525-535. DOI: 10.1007/s10118-025-3514-4.
Molecular dynamics simulations reveal that the diffusion coefficient
D
and the relaxation time
τ
0
exhibit a strong
non-monotonic
N
S
-dependence
transitioning from monomeric friction dominance at small
N
S
to collective segmental rearrangement at large
N
S
.
The equilibrium dynamics and nonlinear rheology of unentangled polymer blends remain inadequately understood
especially regarding the influence of short-chain matrix length
N
S
on the structure and rhe
ological behavior of dispersed long chains. Using molecular dynamics simulations based on the Kremer-Grest model
we systematically explore the
N
S
-dependence of static conformations
equilibrium dynamics
and nonlinear shear responses in unentangled long-chain/short-chain polymer blends. Our results demonstrate a decoupling between the static and dynamic sensitivity to
N
S
: while the static chain size
R
g
follows Flory theory with slight swelling at small
N
S
due to incomplete excluded volume screening
the diffusion coefficient
D
and the relaxation time
τ
0
exhibit a strong
non-monotonic
N
S
-dependence
transitioning from monomeric friction dominance at small
N
S
to collective segmental rearrangement at large
N
S
. Additionally
we observe partial decoupling between the viscous and normal stress responses: while the zero-shear viscosity
η
is strongly
N
S
-dependent
the first and second normal stress coefficients
Ψ
1
and
Ψ
2
collapse onto universal curves when scaled by the dimensionless shear rate
$$ \dot{\gamma } $$
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τ
0
suggesting a common mechanism of orientation and stretching. Under shear
long chains compress in the vorticity direction
λ
z
~
Wi
−
0.2
which reduces co
llision frequency and contributes to shear thinning
while the scaling of weaker orientation resistance
m
G
~
Wi
0.35
reflects hydrodynamic screening by the short-chain matrix. These findings highlight the limitations of single-chain models and emphasize the necessity of considering
N
S
-dependent matrix dynamics and flow-induced structural changes in understanding the rheology of unentangled polymer blends.
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