A mussel-inspired mechanism was used to solve the problem of filler aggregation in rubber composites. This research aims to improve carbon black (CB) dispersion in epoxidized natural rubber (ENR) composites through π−π stacking and cation−π interactions by adding dopamine (D). In this study, various aromatic interactions (π−π stacking and cation−π interactions) between the D-functionalized ENR molecules and the surface of the CB were observed by Fourier transform infrared (FTIR) and Raman spectroscopy. Notably, the small and wideangle X-ray scattering (SAXS/WAXS) analyses supported our inference from the rubber processing analysis (RPA) and transmission electron microscopy (TEM) results that the aromatic interactions enhanced the CB dispersion in ENR composites. This phenomenon improved the tensile strength (138%), Young’s modulus (93%), and energy-saving properties (50%). Finally, this research provided an alternative strategy using mussel-inspired material to solve the CB aggregation problem in rubber products, yielding ENR composites with superior performance properties.
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This content will become publicly available on September 1, 2026
Investigating Biomimetic Chemoresponsive Cation–π Interactions Using Raman Spectroscopy
ABSTRACT Biomimetic designs are inspired by the complex and unique behavior of naturally occurring materials, and can be applied to many systems, including polymers. ZIPer polymers (Zwitter arene‐ion like polymer) are inspired by byssal threads found on mussels, and their physical state is highly sensitive to various environmental conditions. Specifically, the ZIPer polymer undergoes chemospecific phase transitions, exhibiting potential for its use as an ionic responsive technology. Though this phenomenon has been observed with Raman spectroscopy, little is known about how salt identity or concentration affect polymer inter‐ and intra‐chain interactions. Previous studies have used Raman spectroscopy to analyze ZIPer polymer behavior in the presence of salt; however, the effect is typically only observed with sodium chloride and often only compares spectra at two concentrations. Additionally, studies have mainly focused on the spectral evidence of cation–π interactions, significantly narrowing their spectral range. In order to develop a more predictive framework for ZIPer polymer behavior, a range of salt identities and concentrations need to be tested. This study uses Raman spectroscopy to investigate ZIPer polymer behavior in the presence of a series of salts, namely NaCl, NaOTFA, NaBr, NaBF4, and NaPF6, each at 0.1 M, 0.5 M, 1.0 M, and 1.5 M concentrations. Moreover, we observe spectral changes in a range from 550 to 2000 cm−1. Spectral evidence suggests that the cation–π interactions previously hypothesized to be the driver of ZIPer polymer behavior are not the only mechanism determining the chemoresponsive phase transitions. We hypothesize that cation–π interactions and dispersion forces are competing mechanisms controlling ZIPer polymer behavior. Furthermore, we suggest that at certain concentrations the dominating mechanism transitions, and this inflection point is salt identity dependent.
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- Award ID(s):
- 2429239
- PAR ID:
- 10640436
- Publisher / Repository:
- John Wiley & Sons Ltd.
- Date Published:
- Journal Name:
- Journal of Raman Spectroscopy
- Volume:
- 56
- Issue:
- 9
- ISSN:
- 0377-0486
- Page Range / eLocation ID:
- 808 to 816
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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