skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Comprehensive Dynamics in a Polyelectrolyte Complex Coacervate
The linear viscoelastic response, LVR, of a hydrated polyelectrolyte complex coacervate, PEC, was evaluated over a range of frequencies, temperatures, and salt concentrations. The PEC was a nearly-stoichiometric blend of a quaternary ammonium poly([3-(methacrylamido)propyl]trimethylammonium chloride), PMAPTAC, and poly(2-acrylamido-2-methyl-1-propanesulfonic acid sodium salt), PAMPS, an aliphatic sulfonate, selected because they remain fully charged over the conditions of use. Narrow molecular weight distribution polyelectrolytes were prepared using fractionation techniques. A partially deuterated version of PMAPTAC was incorporated to determine the coil radius of gyration, Rg, within PECs using small angle neutron scattering. Chain dimensions were determined to be Gaussian with a Kuhn length of 2.37 nm, which remained constant from 25 to 65 0C. The LVR for a series of matched molecular weight PECs, mostly above the entanglement threshold, exhibited crossovers of modulus versus frequency classically attributed to the reptation time, relaxation between entanglements, and the relaxation of a Kuhn length of units (the “monomer” time). The scaling for zero shear viscosity, η0, versus chain length N, was η0 ~ N3.1, in agreement with “sticky reptation” theory. The lifetime and activation energy, Ep, of a pair between polyanion and polycation repeat units, Pol+Pol-, were determined from diffusion coefficients of salt ions within the PEC. The activation energy for LVR of salt-free PECs was 2Ep, showing that the key mechanism limiting the dynamics of undoped PECs is pair exchange. An FTIR technique was used to distinguish whether SCN- acts as a counterion or a co-ion within PECs. Doping of PECs with NaSCN breaks Pol+Pol- pairing efficiently, which decreases effective crosslinking and decreases viscosity. An equation was derived that quantitatively predicts this effect.  more » « less
Award ID(s):
2103703
PAR ID:
10518766
Author(s) / Creator(s):
; ; ;
Publisher / Repository:
American Chemical Society
Date Published:
Journal Name:
Macromolecules
ISSN:
0024-9297
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    Polymer chain diffusion within a hydrated polyelectrolyte complex, PEC, has been measured using an ultrathin film format prepared by the layer-by-layer method. Isotopically labeled self-exchange of deuterated poly(styrene sulfonate), dPSS, with undeuterated PSS of the same narrow molecular weight distribution permitted reliable estimates of whole-molecule diffusion coefficients, D. Narrow molecular weight distribution poly(diallyldimethylammonium), PDADMA, was used as the polycation for the PEC. Extensive pretreatment of starting films was undertaken to remove residual stress, anisotropy, and layering. PSS/PDADMA “multilayers,” PEMUs, thin enough to provide substantial exchange of polyelectrolyte, even with diffusion coefficients as low as 10–16 cm2 s–1, as a function of salt concentration and temperature were measured for this PEC, which has a glass-transition temperature, Tg, close to room temperature. Two molecular weights of dPSS, about 15 and 100 kDa, presumed to be below and above the entanglement molecular weight, respectively, both diffused faster at higher temperatures with respective activation energies, Ea, of about 21 and 53 kJ mol–1, the latter about the same as Ea for the place exchange between two pairs of PSS:PDADMA. Studies of the linear viscoelastic response of macroscopic PECs showed a difference of about 8 °C in the Tg of the two lengths of PSS complexed with the same PDADMA. Increasing concentrations of NaCl influenced D of 100 kDa PSS but not 15 kDa PSS at room temperature. D was faster in the region of the film near the solution interface, again attributed to a lower Tg caused by greater water content at this interface. 
    more » « less
  2. With the rise of green engineering, there is an increasing need to manufacture materials without relying on organic solvents. Using all-aqueous approaches mitigates the industrial safety and environmental concerns that are associated with volatile organic compounds, while enabling scalable and sustainable fabrication processes. Water-insoluble polyelectrolyte complexes (PECs) arise due to the electrostatic attraction between oppositely charged polyelectrolytes in solution. Notably, when salt is present, these rigid or glassy PECs can be transformed into malleable and liquid states, enabling researchers to process solid materials from the previously deemed unprocessable. The liquid PEC phase, also known as a polyelectrolyte complex coacervate, arises through liquid–liquid phase separation and offers a tunable viscosity to match the needs of the processing method. These coacervates exhibit adjustable rheological properties by varying parameters, including temperature, salt type, ionic strength, polymer ratio, and molecular weight. This tunability makes them attractive for applications ranging from coatings and adhesives to biomedical delivery systems. Notably, the transition between liquid and solid PECs is reversible, as removing salt ions restores the physical cross-links. Additionally, PECs exhibit exceptional stability in various organic solvents and solutions with extreme pH values, without requiring chemical cross-linking. However, the aqueous processing strategies and reversibility of PECs have yet to be fully explored. In this Account, we primarily focus on the well-studied PEC system composed of the strong polyelectrolytes poly(sodium 4-styrenesulfonate) and poly(diallyldimethylammonium chloride). First, we describe how salt concentration is a crucial parameter that enables the aqueous processing of coacervates via electrospinning, spin coating, bar casting, and 3D printing into fibers, coatings, membranes, and 3D structures. We also discuss the impact that processing conditions, like drying and quenching, have on the properties of solid materials, such as their porosity and mechanical strength. Next, we highlight reports that explore how the solubility mismatch between polyelectrolyte pairs and salt ions result in solid and liquid PECs that are nonstoichiometric, thereby exhibiting an overcompensation phenomenon or nonstoichiometry. How the mechanical behavior of a material changes as a function of temperature, i.e., their thermomechanical properties, as well as membrane separation performance are notably influenced by nonstoichiometry, even when the degree of nonstoichiometry is minimal. Interestingly, we are starting to see research reports in the literature on how post-treatment methods, including salt and heat annealing, previously applied to polyelectrolyte multilayer films, offer some transferability to bar-casted separation membranes, which warrants further research. We conclude with a forward-looking discussion that highlights the potential opportunities and challenges related to the future implementation of PEC-based materials. 
    more » « less
  3. The assembly and dynamics of polyelectrolyte complexes (PECs) and polyelectrolyte multilayers (PEMs) are influenced by water content, pH, and salt concentration. However, the influence of divalent salts on the assembly of polyelectrolyte complexes remains unclear. This work showcases that divalent chloride salts directly impact the glass transition temperature and the ion–ion interactions within PECs. Here, poly(diallyldimethylammonium)–poly(styrene sulfonate) (PDADMA–PSS) PECs are assembled in solutions containing MgCl2 and CaCl2 (following the Hofmeister series). These PECs are studied for the cations’ influence on physicochemical properties (glass transition, polymer composition, ion pairing) at varying salt concentrations (0.03 M, 0.10 M, 0.15 M, and 0.20 M). Modulated differential scanning calorimetry (MDSC) experiments demonstrate that PECs assembled with CaCl2 have a significantly higher glass transition temperature when compared to PECs assembled with MgCl2. Neutron activation analysis (NAA) and nuclear magnetic resonance (NMR) spectroscopy demonstrate that this difference is due to strong ion-specific effects influencing the ratio of intrinsic and extrinsic ion pairings in the system. Furthermore, this study demonstrates a universal linear relationship between the thermal transition and the number of water molecules surrounding oppositely charged polyelectrolyte–polyelectrolyte intrinsic ion pairs, even when the salt contains divalent cations. Ion-specific trends have implications on the glass transition and composition of PDADMA–PSS PECs. Divalent salts not only follow the trend of the Hofmeister series but also introduce bridging into the polyelectrolyte complex; however, the structural relaxation of the PEC remains the same. This study offers a bridge between divalent cation behavior on polymer assembly properties and its transition to industrial applications such as controlled drug delivery, sensors, and water purification. 
    more » « less
  4. Branched polymers stress relaxation is at the center to their function as viscosity modifiers, though the fundamentals that underlie the correlation between the polymer topology and their impact on viscosity remains an open question. Here, the stress relaxation of short, branched polyethylene comb polymer melts is studied by molecular dynamics simulations. A coarse-grained model where four methylene groups constitute one bead is used, and the results are transposed to the atomistic level. For arms of length comparable to entanglement length ne of the linear polymer, we show that while increasing the number of branches with the same arm length decreases the plateau modulus, the terminal diffusive time does not change significantly. Increasing the arm length decreases the plateau modulus and increases the terminal time. As arms shorter than ne relax by the entanglement time, both the chain mobility and stress relaxation can be described by reptation of the backbone with an increased tube diameter and an increas 
    more » « less
  5. Abstract. Previous studies utilizing the Global Positioning System(GPS) receivers aboard Jason satellites have performed measurements ofplasmasphere electron content (PEC) by determining the total electroncontent (TEC) above these satellites, which are at altitudes of about 1340 km. This study uses similar methods to determine PEC for the Jason-2receiver for 24 July 2011. These PEC values are compared to previousdeterminations of PEC from a chain of ground-based GPS receivers in Africausing the SCORPION method, with a nominal ionosphere–plasmasphere boundaryat 1000 km. The Jason-2 PECs with elevations greater than 60∘were converted to equivalent vertical PEC and compared to SCORPION verticalPEC determinations. In addition, slant (off-vertical) PECs from Jason-2were compared to a small set of nearly co-aligned ground-based slant PECs.The latter comparison avoids any conversion of Jason-2 slant PEC toequivalent vertical PEC, and it can be considered a more representativecomparison. The mean difference between the vertical PEC (ground-basedminus Jason-2 measurements) values is 0.82 ± 0.28 TEC units (1 TEC unit=1016 electrons m−2). Similarly, the mean differencebetween slant PEC values is 0.168 ± 0.924 TEC units. The Jason-2 slantPEC comparison method may provide a reliable determination for theplasmasphere baseline value for the ground-based receivers, especially ifthe ground stations are confined to only midlatitude or low-latituderegions, which can be affected by a non-negligible PEC baseline. 
    more » « less