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Rheological Properties of Associative Polyelectrolytes Synthesized by Solution Polymerization

Published online by Cambridge University Press:  10 February 2014

Areli I. Velazquez
Affiliation:
Centro de investigación en Química Aplicada CIQA, Blvd. Enrique Reyna 140, 25294, Saltillo, México.
Alejandro Coronado
Affiliation:
Facultad de Ciencias Químicas, Universidad Autónoma de Coahuila, Blvd. Venustiano Carranza and C. Ing. José Cárdenas Valdez, 25280, Saltillo, México
Enrique J. Jiménez
Affiliation:
Centro de investigación en Química Aplicada CIQA, Blvd. Enrique Reyna 140, 25294, Saltillo, México.
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Abstract

Water-soluble associative polyelectrolytes of methacrylic acid [MAA] and ethyl acrylate [EA] (1:1 molar ratio), hydrophobically modified with small amounts of stearyl metacrylate [MM18], were synthesized by means of solution polymerization. Polyelectrolytes with two different molecular structures: multisticker, with hydrophobic groups randomly distributed along the hydrophilic chain and combined, with the hydrophobic groups along the chain and as terminal groups of the backbone, were obtained. Steady shear behavior and linear viscoelastic properties were studied as a function of polymer microstructure and hydrophobic group concentrations on salt-free aqueous solution using a cone-and-plate rheometer. Concentration regimes were obtained for each synthetized polymer. Viscoelastic study shows that the maximum thickening effect corresponds to the combined structure followed by multisticker structure. These polyelectrolytes exhibit high thickening power on aqueous solutions due to the synergy between the hydrophobic attractive interactions and coil expansion phenomena.

Type
Articles
Copyright
Copyright © Materials Research Society 2014 

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References

REFERENCES

Candau, F. and Selb, J., Advances in colloid and interface science 79, 149 (1999).CrossRefGoogle Scholar
Jiménez, E. J., Selb, J. and Candau, F., Macromolecules 33, 8720 (2000).CrossRefGoogle Scholar
Jiménez, E. J., Selb, J. and Candau, F., Macromolecules 32, 8580 (1999).Google Scholar
Jiménez, E. J., Cadenas, G., Pérez, M. and Hernández, Y., Polymer 45, 1993 (2004).CrossRefGoogle Scholar
Jiménez, E. J., Cadenas, G., Pérez, M. and Hernández, Y., Macromolecular Research 12, 451 (2004).CrossRefGoogle Scholar
Lara, A. C., Rivera, C. and Jiménez, E. J., Polymer Bulletin 58, 425 (2007).CrossRefGoogle Scholar
Rico, J. C. and Jiménez, E. J., Polymer Bulletin 62, 57 (2009).CrossRefGoogle Scholar
González, V. J. and Jiménez, E. J., Polymer Bulletin 62, 727 (2009).CrossRefGoogle Scholar
Williams, P., Handbook of Industrial Water Soluble Polymers. Primera Edición. UK, Blackwell Publishing Ltd. p.2 (2007).CrossRefGoogle Scholar
Gennes, P. G., Scaling Concepts in Polymer Physics, Cornell University Press: London (1979).Google Scholar
Graessley, W. W., Polymer 21, 258 (1980).CrossRefGoogle Scholar
Colby, R. H., Rubinstein, M. and Daoud, M. J., Phys.II France 4, 1299 (1994).CrossRefGoogle Scholar