%0 Journal Article %1 RN46 %A Rios, H.E. %A Gonzalez-Navarrete, J. %A Vargas, V. %A Urzua, M.D. %D 2011 %I 2011 Elsevier B.V. %J Colloids and Surfaces a-Physicochemical and Engineering Aspects %K adsorption adsorption, air/water amphipathic dqcauchile energy, equilibrium, films free interface, polyelectrolytes, polysoaps, rheology, sodium-salts, surface tension, water-interface, %N 1-3 %P 262-267 %R 10.1016/j.colsurfa.2011.03.063 %T Surface Properties of Cationic Polyelectrolytes Hydrophobically Modified %U /brokenurl#<Go to ISI>://WOS:000293035000039 %V 384 %X Poly (N,N-dimethyl-N,N-diallyl ammonium) chloride, a highly hydrophilic polyelectrolyte, was hydrophobically modified and the surface properties of the resulting amphipathic polyelectrolytes were determined. The surface activity increases with the polyelectrolyte side chain length despite the ability of this type of polyelectrolyte to form hydrophobic micro domains in solution. The standard free energy of the adsorption process, Delta G degrees(ads), were a linear function of the number of carbon atoms in the lateral chain as well as their transfer and interfacial contributions to the adsorption process with -1.73 kJ mol(-1) of methylene group to Delta G degrees(ads). From the dependence of the surface tension with the temperature the Delta S degrees(ads) was determined. The latter parameter was always positive regardless the polyelectrolyte side chain length, thus the main driving force to Delta G degrees(ads) arises from the large positive Delta S degrees(ads) values.

@article{RN46, abstract = {Poly (N,N-dimethyl-N,N-diallyl ammonium) chloride, a highly hydrophilic polyelectrolyte, was hydrophobically modified and the surface properties of the resulting amphipathic polyelectrolytes were determined. The surface activity increases with the polyelectrolyte side chain length despite the ability of this type of polyelectrolyte to form hydrophobic micro domains in solution. The standard free energy of the adsorption process, Delta G degrees(ads), were a linear function of the number of carbon atoms in the lateral chain as well as their transfer and interfacial contributions to the adsorption process with -1.73 kJ mol(-1) of methylene group to Delta G degrees(ads). From the dependence of the surface tension with the temperature the Delta S degrees(ads) was determined. The latter parameter was always positive regardless the polyelectrolyte side chain length, thus the main driving force to Delta G degrees(ads) arises from the large positive Delta S degrees(ads) values. }, added-at = {2019-12-04T03:57:35.000+0100}, author = {Rios, H.E. and Gonzalez-Navarrete, J. and Vargas, V. and Urzua, M.D.}, biburl = {https://www.bibsonomy.org/bibtex/26dc345839528548642041ca071d87f5b/dqcauchile}, doi = {10.1016/j.colsurfa.2011.03.063}, interhash = {d3ea35405f0275c2d20c4aa75a08ece9}, intrahash = {6dc345839528548642041ca071d87f5b}, issn = {0927-7757}, journal = {Colloids and Surfaces a-Physicochemical and Engineering Aspects}, keywords = {adsorption adsorption, air/water amphipathic dqcauchile energy, equilibrium, films free interface, polyelectrolytes, polysoaps, rheology, sodium-salts, surface tension, water-interface,}, number = {1-3}, pages = {262-267}, publisher = {2011 Elsevier B.V.}, timestamp = {2019-12-04T03:58:17.000+0100}, title = {Surface Properties of Cationic Polyelectrolytes Hydrophobically Modified}, type = {Journal Article}, url = {/brokenurl#<Go to ISI>://WOS:000293035000039}, volume = 384, year = 2011 }