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.Center for Frontier Research & Technology, Hangzhou Zhongce Rubber Company, Hangzhou 310018, China
qqgu@mail.ustc.edu.cn (Q.Q.G.)
zysun@ciac.ac.cn (Z.Y.S.)
收稿:2025-04-12,
修回:2025-05-14,
录用:2025-05-29,
网络首发:2025-08-01,
纸质出版:2025-10-05
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Wang, Y. G.; Guan, J. L.; Chen, S. Y.; Yin, Y.; Sun, H. G.; Zheng, Y. F.; Gu, Q. Q.; Sun, Z. Y. Static flocculation in carbon black-filled rubber: from constrained filler motion to polymer-driven interfacial reinforcement. Chinese J. Polym. Sci. 2025, 43, 1917–1928
Yu-Ge Wang, Jun-Lei Guan, Si-Yuan Chen, et al. Static Flocculation in Carbon Black-filled Rubber: From Constrained Filler Motion to Polymer-driven Interfacial Reinforcement[J]. Chinese Journal of Polymer Science, 2025, 43(10): 1917-1928.
Wang, Y. G.; Guan, J. L.; Chen, S. Y.; Yin, Y.; Sun, H. G.; Zheng, Y. F.; Gu, Q. Q.; Sun, Z. Y. Static flocculation in carbon black-filled rubber: from constrained filler motion to polymer-driven interfacial reinforcement. Chinese J. Polym. Sci. 2025, 43, 1917–1928 DOI: 10.1007/s10118-025-3391-x.
Yu-Ge Wang, Jun-Lei Guan, Si-Yuan Chen, et al. Static Flocculation in Carbon Black-filled Rubber: From Constrained Filler Motion to Polymer-driven Interfacial Reinforcement[J]. Chinese Journal of Polymer Science, 2025, 43(10): 1917-1928. DOI: 10.1007/s10118-025-3391-x.
Mechanistic and rheological distinction between dynamic and static flocculation: Dynamic flocculation involves strain-induced rearrangement of filler networks through particle motion
whereas static flocculation arises from polymer-mediated interfacial enhancement through chain reorganization.
The flocculation behavior of carbon black (CB)-filled isoprene rubber (IR) nanocomposites was systematically investigated under both dynamic and static conditions to unravel the distinct mechanisms governing filler network evolution. Under dynamic conditions
small oscillatory shear strains (0.1%) significantly enhanced filler particle motion
leading to pronounced agglomeration and a flocculation degree of about 4.3 MPa at 145 °C. In contrast
static flocculation exhibited a fundamentally different mechanism dominated by polymer chain dynamics
which is driven mainly by thermal activation. Radial distribution function (RDF) analysis of transmission electron microscopy (TEM) images revealed a slight decrease (2 nm) in the interparticle distance peak after static annealing at 100 °C for 7 h
indicating localized motion of CB particles. However
the overall filler network remained stable
with no significant agglomeration observed. The increase in bound rubber content from about 23% to 28% with rising temperature further confirmed the dominant role of polymer chain adsorption and interfacial reinforcement in static flocculation. These findings highlight the critical influence of external strain on filler network formation and provide new insights into the polymer-dominated mechanism of static flocculation. The results offer practical guidance for optimizing the storage and processing of rubber nanocomposites
particularly in applications where static flocculation during prolonged storage is a concern.
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