Phase Behavior and Conformational Asymmetry near the Comb-to-Bottlebrush Transition in Linear-Brush Block Copolymers.

This study explores how conformational asymmetry influences the bulk phase behavior of linear-brush block copolymers. We synthesized 60 diblock copolymers composed of poly(trifluoroethyl methacrylate) as the linear block and poly[oligo(ethylene glycol) methyl ether methacrylate] as the brush block, varying the molecular weight, composition, and side-chain length to introduce different degrees of conformational asymmetry. Using small-angle X-ray scattering, we determined the morphology and phase diagrams for three different side-chain length systems, mainly observing lamellar and cylindrical phases. Increasing the side-chain length of the brush block from three to nine ethylene oxide units introduces sufficient asymmetry between the blocks to alter the phase behavior, shifting the lamellar-to-cylindrical transitions toward lower brush block compositions and transitioning the brush block from the dense comb-like regime to the bottlebrush regime. Coarse-grained simulations support our experimental observations and provide a mapping between the composition and conformational asymmetry. A comparison of our findings to strong stretching theory across multiple phase boundary predictions confirms the transition between the dense comb-like regime and the bottlebrush regime.

Community Resource for Innovation in Polymer Technology (CRIPT): A Scalable Polymer Material Data Structure.

The Community Resource for Innovation in Polymer Technology (CRIPT) data model is designed to address the high complexity in defining a polymer structure and the intricacies involved with characterizing material properties.

Diffusion of surfactant from a micellar solution to a bare interface. 1. Absorbing boundary.

We analyze dynamic adsorption of surfactant from a micellar solution to a rapidly created surface that acts as an absorbing boundary for surfactant monomers (single molecules), along which the monomer concentration vanishes, with no direct micelle adsorption. This somewhat idealized situation is analyzed as a prototype for situations in which strong suppression of monomer concentration accelerates micelle dissociation, and will be used as a starting point for analysis of more realistic boundary conditions in subsequent work. We present scaling arguments and approximate models for particular time and parameter regimes and compare the resulting predictions to numerical simulations of the reaction-diffusion equations for a polydisperse system containing surfactant monomers and clusters of arbitrary aggregation number. The model considered here exhibits an initial period of rapid shrinkage and ultimate dissociation of micelles within a narrow region near the interface. This opens a micelle-free region near the interface after some time τe, the width of which increases as t1/2 at times t≫τe. In systems that exhibit disparate fast and slow bulk relaxation times τ1 and τ2 in response to small perturbations, τe is usually comparable to or greater than τ1 but much less than τ2. Such systems exhibit a wide intermediate time regime τe

Nonlinear dynamics in micellar surfactant solutions. II. Diffusion.

We discuss diffusion in micellar surfactant solutions in a form appropriate for analyzing experiments that involve large deviations from equilibrium. A general nonlinear dynamical model for inhomogeneous systems is developed that describes the effects of diffusion and micelle kinetics as a set of coupled partial differential equations for unimer concentration, micelle number concentration, average micelle aggregation number, and, optionally, the variance of the micelle aggregation number. More specialized models are developed to describe slow dynamics in situations in which the system stays in a state of partial local equilibrium or full local equilibrium. As an illustrative example of a nonlinear transport phenomenon, we discuss a simple model of diffusion from an initially homogeneous micellar solution to a rapidly created absorbing interface with fast unimer adsorption.

Nonlinear dynamics in micellar surfactant solutions. I. Kinetics.

This is the first of a pair of articles that present the theory of kinetic and transport phenomena in micelle-forming surfactant solutions in a form that facilitates discussion of large deviations from equilibrium. Our goal is to construct approximate but robust reduced models for both homogeneous and inhomogeneous systems as differential equations for unimer concentration c_{1}, micelle number concentration c_{m}, average micelle aggregation number q and (optionally) aggregation number variance σ_{m}^{2}. This first article discusses kinetics in homogeneous solutions. We focus particularly on developing models that can describe both weakly perturbed states and states in which c_{1} is suppressed significantly below the critical micelle concentration, which leads to rapid shrinkage and dissociation of any remaining micelles. This focus is motivated by the strong local suppression of c_{1} that is predicted to occur near interfaces during some adsorption processes that are considered in the second article. Toward this end, we develop a general nonlinear theory of fast stepwise processes for systems that may be subjected to large changes in q and c_{1}. This is combined with the existing nonlinear theory of slow association and dissociation processes to construct a general model for systems governed by stepwise reaction kinetics. We also consider situations in which the slow process of micelle creation and destruction instead occurs primarily by micelle fission and fusion, and analyze the dependencies of micelle lifetime and the slow relaxation time upon surfactant concentration in systems controlled by either association-dissociation or fission-fusion mechanisms.

Simulation of diblock copolymer surfactants. III. Equilibrium interfacial adsorption.

Monte Carlo simulations are used to study adsorption of highly asymmetric diblock copolymers to a polymer-polymer interface, and the results compared to self-consistent field theory (SCFT) predictions. The simulation model used here is a bead-spring model that has been used previously to study equilibrium and kinetic properties of spherical micelles [J. A. Mysona et al., Phys. Rev. E 100, 012602 (2019)2470-004510.1103/PhysRevE.100.012602; Phys. Rev. E 100, 012603 (2019)10.1103/PhysRevE.100.012603; Phys. Rev. Lett. 123, 038003 (2019)10.1103/PhysRevLett.123.038003]. Interfacial copolymer concentration Γ and interfacial tension γ are measured as functions of bulk copolymer concentration at concentrations up to the critical micelle concentration over a range of values of the Flory-Huggins χ parameter. The dependence of interfacial pressure Π = γ_{0}-γ on Γ (where γ_{0} is the interfacial tension in the absence of copolymer) is found to be almost independent of χ and to be accurately predicted by SCFT. The bare interfacial tension γ_{0} and total interfacial tension γ(Γ) can also be accurately predicted by SCFT using an estimate of χ obtained from independent analysis of properties of symmetric diblock copolymer melts. SCFT predictions obtained with this estimate of χ do not, however, adequately describe the thermodynamics of the coexisting bulk copolymer solution, as a result of contraction of the strongly interacting core block of dissolved copolymers. Accurate predictions of the relationship between bulk and interfacial properties can thus only be obtained for this system by combining SCFT predictions of the interfacial equation of state with a fit to the measured equation of state for the bulk solution.

Simulation of diblock copolymer surfactants. II. Micelle kinetics.

Molecular dynamics (MD) simulations are used to measure dynamical properties of a simple bead-spring model of A-B diblock copolymer molecules, and to characterize rates and mechanisms of several dynamical processes. Dynamical properties are analyzed within the context of a kinetic population model that allows for both stepwise insertion and expulsion of individual free molecules and occasional fission and fusion of micelles. Kinetic coefficients for stepwise processes and micelle fission have been extracted from MD simulations of individual micelles. Insertion of a free surfactant molecule into a preexisting micelle is shown to be a completely diffusion-controlled process for the model studied here. Estimates are given for rates of rare events that create and destroy entire micelles by competing mechanisms involving stepwise association and dissociation or fission and fusion. Both mechanisms are shown to be relevant over the range of parameters studied here, with association and dissociation dominating in systems with more soluble surfactants and fission and fusion dominating in systems with less soluble surfactants.

Simulation of diblock copolymer surfactants. I. Micelle free energies.

Semigrand hybrid Monte Carlo simulations are used to measure equilibrium properties of micelles formed in a simple bead-spring model of asymmetric A-B diblock copolymer surfactant molecules in an A homopolymer solvent, over a range of values of surfactant solubility. Simulations are used to accurately measure the free energy of formation of micellar clusters as a function of aggregation number over a wide range of values, and to characterize the crossover from spherical to rodlike micelle shape with increasing aggregation number. Dynamical properties of the same model are considered in an accompanying paper [Phys. Rev. E 100, 012603 (2019)10.1103/PhysRevE.100.012603].

Mechanism of Micelle Birth and Death.

In micellar surfactant solutions, changes in the total number of micelles are rare events that can occur by either of two mechanisms-by stepwise association and dissociation via insertion and expulsion of individual molecules or by fission and fusion of entire micelles. Molecular dynamics simulations are used here to estimate rates of these competing mechanisms in a simple model of block copolymer micelles in homopolymer solvent. This model exhibits a crossover with increasing degree of repulsion between solvent and micelle core components, from a regime dominated by association and dissociation to a regime dominated by fission and fusion.

Formation of defect-free latex films on porous fiber supports.

We present here the creation of a defect-free polyvinylidene chloride barrier layer on the lumen-side of a hollow fiber sorbent. Hollow fiber sorbents have previously been shown to be promising materials for enabling low-cost CO(2) capture, provided a defect-free lumen-side barrier layer can be created. Film experiments examined the effect of drying rate, latex age, substrate porosity (porous vs nonporous), and substrate hydrophobicity/hydrophilicity. Film studies show that in ideal conditions (i.e., slow drying, fresh latex, and smooth nonporous substrate), a defect-free film can be formed, whereas the other permutations of the variables investigated led to defective films. These results were extended to hollow fiber sorbents, and despite using fresh latex and relatively slow drying conditions, a defective lumen-side layer resulted. XRD and DSC indicate that polyvinylidene chloride latex develops crystallinity over time, thereby inhibiting proper film formation as confirmed by SEM and gas permeation. This and other key additional challenges associated with the porous hollow fiber substrate vs the nonporous flat substrate were overcome. By employing a toluene-vapor saturated drying gas (a swelling solvent for polyvinylidene chloride) a defect-free lumen-side barrier layer was created, as investigated by gas and water vapor permeation.