Dataset Information

Salt Water-Triggered Ionic Cross-Linking of Polymer Composites by Controlled Release of Functional Ions.

ABSTRACT: A composite that undergoes ionic cross-linking in the presence of salt water is presented as a viable strategy for the development of chemically responsive materials. The permeation of salt water through the composite activates embedded inorganic fillers, resulting in the release of functional ions and subsequent cross-linking with the functional groups of the polymer matrix. The release of a cross-linking agent from the inorganic filler and composite is evaluated along with the impact of the cross-linking on composite properties. The new methodology is then coupled with a dopamine-functionalized polymer in order to evaluate the potential of this approach for environmentally triggered self-healing materials.

SUBMITTER: Mosby BM

PROVIDER: S-EPMC6643778 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Salt Water-Triggered Ionic Cross-Linking of Polymer Composites by Controlled Release of Functional Ions.

Mosby Brian M BM Shah Sachit S Braun Paul V PV

ACS omega 20181128 11

A composite that undergoes ionic cross-linking in the presence of salt water is presented as a viable strategy for the development of chemically responsive materials. The permeation of salt water through the composite activates embedded inorganic fillers, resulting in the release of functional ions and subsequent cross-linking with the functional groups of the polymer matrix. The release of a cross-linking agent from the inorganic filler and composite is evaluated along with the impact of the cr ...[more]

PMID: 31458249

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Project description:Embedding nanomaterials into polymer hydrogels enables the design of functional materials with tailored chemical, mechanical, and optical properties. Nanocapsules that protect interior cargo and disperse readily through a polymeric matrix have drawn particular interest for their ability to integrate chemically incompatible systems and to further expand the parameter space for polymer nanocomposite hydrogels. The properties of polymer nanocomposite hydrogels depend on the material composition and processing route, which were explored systematically in this work. The gelation kinetics of network-forming polymer solutions with and without silica-coated nanocapsules bearing polyethylene glycol (PEG) surface ligands were investigated using in situ dynamic rheology measurements. Network-forming polymers comprised either 4-arm or 8-arm star PEG with terminal anthracene groups, which dimerize upon irradiation with ultraviolet (UV) light. The PEG-anthracene solutions exhibited rapid gel formation upon UV exposure (365 nm); gel formation was observed as a crossover from liquid-like to solid-like behavior during in situ small-amplitude oscillatory shear rheology. This crossover time was non-monotonic with polymer concentration. Far below the overlap concentration (c/c* ≪ 1), spatially separated PEG-anthracene molecules were subject to forming intramolecular loops over intermolecular cross-links, thereby slowing the gelation process. Near the polymer overlap concentration (c/c* ∼ 1), rapid gelation was attributed to the ideal proximity of anthracene end groups from neighboring polymer molecules. Above the overlap concentration (c/c* > 1), increased solution viscosities hindered molecular diffusion, thereby reducing the frequency of dimerization reactions. Adding nanocapsules to PEG-anthracene solutions resulted in faster gelation than nanocapsule-free PEG-anthracene solutions with equivalent effective polymer concentrations. The final elastic modulus of nanocomposite hydrogels increased with nanocapsule volume fraction, signifying synergistic mechanical reinforcement by nanocapsules despite not being cross-linked into the polymer network. Overall, these findings quantify the impact of nanocapsule addition on the gelation kinetics and mechanical properties of polymer nanocomposite hydrogels, which are promising materials for applications in optoelectronics, biotechnology, and additive manufacturing.

Dataset Information

Salt Water-Triggered Ionic Cross-Linking of Polymer Composites by Controlled Release of Functional Ions.

Publications

Salt Water-Triggered Ionic Cross-Linking of Polymer Composites by Controlled Release of Functional Ions.

Similar Datasets

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