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Brett P. Fors

Publications and source records attributed to Brett P. Fors.

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Dispersion Polymerization in an Elastomeric Solvent

Polymerization-induced phase separation (PIPS) provides a powerful route to generate structured polymeric materials by coupling chemical conversion with thermodynamic demixing. PIPS in liquid-state systems underlies dispersion polymerization, serving as a cornerstone technique for microparticle production, yet is constrained by solvent compatibility and limited range of morphologies. Here, we establish an elastically mediated PIPS regime that bridges these two limits by conducting controlled polymerization within a deformable elastomeric network. This approach, termed Dispersion Polymerization in an Elastomeric Solvent (DiPolES), serves as a solid-state analogue of dispersion polymerization in which an elastomeric network simultaneously serves as solvent and physical stabilizer. Using photoiniferter-mediated polymerization of methyl methacrylate (MMA) within poly(dimethyl siloxane) (PDMS) elastomeric solvent, DiPolES enables robust fabrication of elastomeric composites containing uniform PMMA microparticles with tunable size (0.85 to 3 μm) and shape (spheroidal and ellipsoidal). The strategy is generalizable beyond the PDMS/MMA system and is applicable to diverse monomers, such as acrylonitrile and 2-vinyl pyridine, which can be extracted from the elastomeric solvent, enabling high-yield production of microparticles. Real-time imaging and compositional analysis reveal that particle formation proceeds through rapid nucleation at low monomer conversion, followed by growth accompanied by cavitation of the surrounding network. Monomer loading governs the particle size, while solvent elasticity modulates the transition from isolated uniform spheroids to heterogeneous clusters. Interestingly, applying uniaxial strain during DiPolES enables production of ellipsoidal particles without any post-processing.

cond-mat.soft

Elucidating the impact of microstructure on mechanical properties of phase-segregated polyurea: Finite element modeling of molecular dynamics derived microstructures

Phase-segregated polyureas (PU) have received considerable interest due to their use as tough, impact-resistant coatings. Polyureas are favored for these applications due to their mechanical strain rate sensitivity and energy dissipation. Predicting and tailoring the mechanical response of PU remains challenging due to the complex interaction between its elastomeric and glassy phases. To elucidate the role of PU microstructure on its mechanical properties, we developed a finite element modeling framework in which each phase is represented by a volume fraction within a representative volume element (RVE). Critically, we used separate constitutive models to describe the elastomeric and glassy phases. We developed a plasticity-driven breakdown process in which we model the glassy phase disaggregating into a new phase. The overall contribution of each phase at a material point is determined by their respective volume fractions within the RVE. We applied our modeling methods to two compositions of PU with differing elastomeric segment lengths derived from oligoether diamines, Versalink P650 and P1000. Our simulations show that a combination of microstructural differences and elastomeric phase properties accounts for the difference in mechanical response between P650 and P1000. We show our model's ability to predict PU behavior in various loading conditions, including low-rate cyclic loading and monotonic loading over a wide range of strain rates. Our model produces microstructure transformations that mirror those indicated by small-angle X-ray scattering (SAXS) experiments. Fourier transform analysis of our RVEs reveals glassy phase fibrillation due to deformation, a finding consistent with SAXS experiments.

cond-mat.mtrl-sci