The effect of binding strength of counterions with the polyelectrolyte chain to the swelling of polyelectrolyte brushes is studied, by investigating the swelling of both the polycation and polyanion in response to the variation of the salt concentration under the change of counterion's identity. Two polyelectrolyte brushes grafted on solid substrates are adopted: the cationic poly [2-(methacryloyloxy)ethyltrimethyl ammonium] (PMETA-X, X = F, Cl, Br, and I) and the anionic polystyrene sulfonate (M-PSS, M = Li, Na, K, and Cs). The swelling change with the salt concentration is investigated by ellipsometry, quartz crystal microbalance with dissipation, and dielectric spectroscopy. It is discovered that although the thickness of PMETA-X brushes is larger than that of M-PSS brushes of similar grafting density, the former has much less solvent incorporated than the latter. Such a difference is attributed to the weaker interaction between the PMETA chain and its halide counterions than that between the PSS chain and its alkali counterions, discovered by dielectric spectroscopy. This makes the original charges on the PMETA-X chain less neutralized and therefore have a higher charge density, compared with the M-PSS chain. The results demonstrate that the stronger binding of the counterions to the polyelectrolytes makes the main chains less charged, resulting in the weaker inter-chain electrostatic repulsion and less swelling of the brushes. Investigations into the effect of ion identity show the following order of binding strength: for the cationic PMETA chain, F < Cl < Br < I and for the anionic PSS chain, Li < Na < K < Cs.
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http://dx.doi.org/10.1021/acs.langmuir.1c00309 | DOI Listing |
Biomacromolecules
March 2025
State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, P.R. China.
Understanding how zwitterionic spherical polyelectrolyte brushes (SPB) fulfill their antifouling functions requires knowledge of their interactions with exogenous nanoparticles, such as proteins. In this study, zwitterionic SPB were synthesized by grafting 3-[(2-(methacryloyloxy)ethyl)dimethylammonio]propanoate (CBMA) and [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl) ammonium hydroxide (SBMA) onto a polystyrene core via photoemulsion polymerization. Small-angle X-ray scattering was employed to elucidate the interactions and protein adsorption behaviors of the zwitterionic SPB and proteins.
View Article and Find Full Text PDFMacromol Rapid Commun
February 2025
Department of Chemistry, University of Tennessee, Knoxville, TN, 37996, USA.
Radioactive pertechnetate (TcO ) from the nuclear fuel cycle presents a severe risk to the environment due to its large solubility in water and non-complexing nature. By utilizing the chaotropic properties of TcO and its nonradioactive surrogate perrhenate (ReO ) and the principle of chaotropic interactions, a series of quaternary ammonium-containing polyelectrolyte brush-grafted silica particles are designed and applied to remove ReO from water. These cationic hairy particles (HPs) are synthesized by surface-initiated atom transfer radical polymerization of 2-(N,N-dimethylamino)ethyl methacrylate and subsequent quaternization with various halogen compounds.
View Article and Find Full Text PDFPhys Rev E
January 2025
Keck Graduate Institute, Henry E. Riggs School of Applied Life Sciences, Claremont, California 91711, USA.
Polyelectrolyte brushes consist of a set of charged linear macromolecules, each tethered at one end to a surface. An example is the glycocalyx which refers to hair-like negatively charged sugar molecules that coat the outside membrane of all cells. We consider the transport and equilibrium distribution of ions and the resulting electrical potential when such a brush is immersed in a salt buffer containing monovalent cations (sodium and/or potassium).
View Article and Find Full Text PDFMacromolecules
February 2025
Department of Molecules and Materials, MESA+ Institute, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands.
Polyelectrolyte brushes are functional surface coatings that react to external stimuli. The response of these brushes in electric fields is nearly immediate as the field acts directly on the charges in the polyion, while the response to bulk stimuli such as temperature, acidity, and ionic composition is intrinsically capped by transport limitations. However, the response of fully charged brushes is limited because large field strengths are required to achieve a response.
View Article and Find Full Text PDFPhys Rev Lett
January 2025
University of California, Department of Chemical and Biomolecular Engineering, Berkeley, California 94720, USA.
Modeling ion correlations in inhomogeneous polymers and soft matters with spatially varying ionic strength or dielectric permittivity remains a great challenge. Here, we develop a new theory that systematically incorporates electrostatic fluctuations into the self-consistent field theory for polymers. The theory is applied to polyelectrolyte brushes to explain abnormal phenomena observed in recent experiments.
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