Rheology and dynamic light scattering of octa-ethyleneglycol-monododecylether/chitosan solutions
•Flow activation enthalpy for surfactant-chitosan solutions varies from 3 to 40kJmol−1.•C12E8 addition of 5wt% induced the occurrence of a second enthalpy of activation.•DLS indicated that addition of C12E8 induced a second mode of relaxation at 10−3μs−1.•Relaxation rate activation-enthalpies were i...
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Published in | Carbohydrate polymers Vol. 98; no. 1; pp. 321 - 330 |
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Format | Journal Article |
Language | English |
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15.10.2013
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Abstract | •Flow activation enthalpy for surfactant-chitosan solutions varies from 3 to 40kJmol−1.•C12E8 addition of 5wt% induced the occurrence of a second enthalpy of activation.•DLS indicated that addition of C12E8 induced a second mode of relaxation at 10−3μs−1.•Relaxation rate activation-enthalpies were in the same range of flow activation ones.•Interactions between CS and wormlike C12E8 structures seemed to cause observed changes.
In this work we used rheometry and DLS to probe relaxation phenomena in solutions of chitosan and octa-ethyleneglycol-monododecylether. The dispersions had a marked pseudoplastic behavior, which became less evident, as surfactant concentration was increased. Arrhenius plots showed that systems with surfactant presented a characteristic temperature at which apparent enthalpy of activation (varying from 3 to 40kJmol−1) changed: this change was correlated to a possible transition of colloidal aggregates to a wormlike configuration. DLS intensity correlation functions were described by KWW equation: pure chitosan solutions had relaxation rate distributions centered at a characteristic relaxation rate around 4.6×10−6μS−1; as surfactant was added, a new component, with a faster characteristic relaxation rate with a magnitude order of 10−3μs−1, appeared. It was shown that the dependence between these relaxation rates and surfactant concentration could be used to describe DLS-related relaxation phenomena as an Arrhenius-activated process, agreeing with results obtained using rheometry. |
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AbstractList | •Flow activation enthalpy for surfactant-chitosan solutions varies from 3 to 40kJmol−1.•C12E8 addition of 5wt% induced the occurrence of a second enthalpy of activation.•DLS indicated that addition of C12E8 induced a second mode of relaxation at 10−3μs−1.•Relaxation rate activation-enthalpies were in the same range of flow activation ones.•Interactions between CS and wormlike C12E8 structures seemed to cause observed changes.
In this work we used rheometry and DLS to probe relaxation phenomena in solutions of chitosan and octa-ethyleneglycol-monododecylether. The dispersions had a marked pseudoplastic behavior, which became less evident, as surfactant concentration was increased. Arrhenius plots showed that systems with surfactant presented a characteristic temperature at which apparent enthalpy of activation (varying from 3 to 40kJmol−1) changed: this change was correlated to a possible transition of colloidal aggregates to a wormlike configuration. DLS intensity correlation functions were described by KWW equation: pure chitosan solutions had relaxation rate distributions centered at a characteristic relaxation rate around 4.6×10−6μS−1; as surfactant was added, a new component, with a faster characteristic relaxation rate with a magnitude order of 10−3μs−1, appeared. It was shown that the dependence between these relaxation rates and surfactant concentration could be used to describe DLS-related relaxation phenomena as an Arrhenius-activated process, agreeing with results obtained using rheometry. In this work we used rheometry and DLS to probe relaxation phenomena in solutions of chitosan and octa-ethyleneglycol-monododecylether. The dispersions had a marked pseudoplastic behavior, which became less evident, as surfactant concentration was increased. Arrhenius plots showed that systems with surfactant presented a characteristic temperature at which apparent enthalpy of activation (varying from 3 to 40 kJ mol(-1)) changed: this change was correlated to a possible transition of colloidal aggregates to a wormlike configuration. DLS intensity correlation functions were described by KWW equation: pure chitosan solutions had relaxation rate distributions centered at a characteristic relaxation rate around 4.6×10(-6) μS(-1); as surfactant was added, a new component, with a faster characteristic relaxation rate with a magnitude order of 10(-3) μs(-1), appeared. It was shown that the dependence between these relaxation rates and surfactant concentration could be used to describe DLS-related relaxation phenomena as an Arrhenius-activated process, agreeing with results obtained using rheometry. In this work we used rheometry and DLS to probe relaxation phenomena in solutions of chitosan and octa-ethyleneglycol-monododecylether. The dispersions had a marked pseudoplastic behavior, which became less evident, as surfactant concentration was increased. Arrhenius plots showed that systems with surfactant presented a characteristic temperature at which apparent enthalpy of activation (varying from 3 to 40kJmol⁻¹) changed: this change was correlated to a possible transition of colloidal aggregates to a wormlike configuration. DLS intensity correlation functions were described by KWW equation: pure chitosan solutions had relaxation rate distributions centered at a characteristic relaxation rate around 4.6×10⁻⁶μS⁻¹; as surfactant was added, a new component, with a faster characteristic relaxation rate with a magnitude order of 10⁻³μs⁻¹, appeared. It was shown that the dependence between these relaxation rates and surfactant concentration could be used to describe DLS-related relaxation phenomena as an Arrhenius-activated process, agreeing with results obtained using rheometry. |
Author | Pereira, M.R. Fonseca, J.L.C. dos Santos, Z.M. |
Author_xml | – sequence: 1 givenname: Z.M. surname: dos Santos fullname: dos Santos, Z.M. – sequence: 2 givenname: M.R. surname: Pereira fullname: Pereira, M.R. – sequence: 3 givenname: J.L.C. surname: Fonseca fullname: Fonseca, J.L.C. email: jlcfonseca.br@gmail.com |
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CitedBy_id | crossref_primary_10_1016_j_colsurfa_2020_124933 crossref_primary_10_1016_j_colsurfa_2014_10_045 crossref_primary_10_1080_21691401_2017_1328687 crossref_primary_10_1007_s00396_017_4099_4 crossref_primary_10_1007_s12033_016_9927_0 crossref_primary_10_1080_21622515_2017_1404138 crossref_primary_10_1016_j_colsurfa_2017_11_010 crossref_primary_10_1016_j_cis_2015_03_003 crossref_primary_10_1016_j_porgcoat_2016_12_024 crossref_primary_10_1080_01932691_2017_1296772 crossref_primary_10_1016_j_colsurfa_2016_03_052 |
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Keywords | Chitosan-surfactant interactions Dynamic light scattering Relaxation rate distribution Rheology Non ionic surfactant Light scattering Shear flow Surfactant polymer Experimental study Oligomer Ethylene oxide polymer Intermolecular interaction Dynamical scattering Oside polymer Chitosan Aqueous solution Activation energy |
Language | English |
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Snippet | •Flow activation enthalpy for surfactant-chitosan solutions varies from 3 to 40kJmol−1.•C12E8 addition of 5wt% induced the occurrence of a second enthalpy of... In this work we used rheometry and DLS to probe relaxation phenomena in solutions of chitosan and octa-ethyleneglycol-monododecylether. The dispersions had a... |
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SubjectTerms | Applied sciences chitosan Chitosan - chemistry Chitosan-surfactant interactions dispersions Dynamic light scattering enthalpy equations Ethylene Glycols - chemistry Exact sciences and technology Light light scattering Natural polymers Physicochemistry of polymers Relaxation rate distribution Rheology rheometry Scattering, Radiation Solutions Starch and polysaccharides Surface-Active Agents - chemistry surfactants Temperature |
Title | Rheology and dynamic light scattering of octa-ethyleneglycol-monododecylether/chitosan solutions |
URI | https://dx.doi.org/10.1016/j.carbpol.2013.05.092 https://www.ncbi.nlm.nih.gov/pubmed/23987351 https://search.proquest.com/docview/1429217596 |
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