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Viscosity and Scaling of Semiflexible Polyelectrolyte NaCMC in Aqueous Salt Solutions
Author(s) -
Carlos G. Lopez,
Ralph H. Colby,
P.M. Graham,
João T. Cabral
Publication year - 2016
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.6b02261
Subject(s) - polyelectrolyte , aqueous solution , scaling , crossover , chemistry , thermodynamics , polymer , viscosity , degree of polymerization , intrinsic viscosity , salt (chemistry) , chemical physics , polymerization , physics , organic chemistry , mathematics , geometry , computer science , artificial intelligence
We investigate the viscosity dependence on concentration and molecular weight of semiflexible polyelectrolyte sodium carboxymethylcellulose (NaCMC) in aqueous salt-free and NaCl solutions. Combining new measurements and extensive literature data, we establish relevant power laws and crossovers over a wide range of degree of polymerization (N) as well as polymer (c) and salt (cs) concentrations. In salt-free solution, the overlap concentration shows the expected c* ∝ N–2 dependence, and the entanglement crossover scales as ce ∝ N–0.6±0.3, in strong disagreement with scaling theory for which ce ∝ c* is expected, but matching the behavior found for flexible polyelectrolytes. A second crossover, to a steep concentration dependence for specific viscosity (ηsp ∝ c3.5±0.2), commonly assigned to the concentrated regime, is shown to follow c** ∝ N–0.6±0.2 (with c**/ce ≃ 6) which thus suggests instead a dynamic crossover, possibly related to entanglement. The scaling of c* and ce in 0.01 and 0.1 M NaCl shows neutral polymer in good solvent behavior, characteristic of highly screened polyelectrolyte solutions. This unified scaling picture enables the estimation of viscosity of ubiquitous NaCMC solutions as a function of N, c, and cs and establishes the behavior expected for a range of semiflexible polyelectrolyte solutions

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