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Structure of Cationic Starch (CS)/Anionic Surfactant Complexes Studied by Small-Angle X-ray Scattering (SAXS)
The structure of lyotropic liquid crystalline or gellike phases formed in cationic starch (CS)/anionic surfactant/water systems in the temperature range 25−80 °C has been investigated by small-angle X-ray scattering. The surfactants were sodium dodecyl sulfate (SDS), sodium decanoate (NaDe), sodium...
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Published in: | Macromolecules 2001-04, Vol.34 (9), p.2937-2946 |
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container_issue | 9 |
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container_title | Macromolecules |
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creator | Merta, Juha Torkkeli, Mika Ikonen, Teemu Serimaa, Ritva Stenius, Per |
description | The structure of lyotropic liquid crystalline or gellike phases formed in cationic starch (CS)/anionic surfactant/water systems in the temperature range 25−80 °C has been investigated by small-angle X-ray scattering. The surfactants were sodium dodecyl sulfate (SDS), sodium decanoate (NaDe), sodium dodecanoate (NaDod), sodium palmitate (NaPal), sodium oleate (NaOl), and sodium erucate (NaEr). The phases were in equilibrium with aqueous solutions at 60 °C and contained 15−25 wt % of CS and 10−30 wt % of surfactant, depending on the charge density of the CS and the chain length of the surfactant. The phases consist of CS/surfactant aggregates arranged in long-range structures similar to lyotropic mesophases formed by the pure surfactants alone, but they separate from aqueous solutions at much lower surfactant concentrations. When the charge density of the CS is low or the surfactant hydrocarbon chain is short, cubic or hexagonal phases are formed. As expected, the formation of lamellar phase is promoted by increasing these parameters. Temperature affects the stability of the phases and their structure. At high temperatures the long-range order breaks down, and the phases are akin to concentrated micellar CS/surfactant solutions. |
doi_str_mv | 10.1021/ma001793c |
format | article |
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The surfactants were sodium dodecyl sulfate (SDS), sodium decanoate (NaDe), sodium dodecanoate (NaDod), sodium palmitate (NaPal), sodium oleate (NaOl), and sodium erucate (NaEr). The phases were in equilibrium with aqueous solutions at 60 °C and contained 15−25 wt % of CS and 10−30 wt % of surfactant, depending on the charge density of the CS and the chain length of the surfactant. The phases consist of CS/surfactant aggregates arranged in long-range structures similar to lyotropic mesophases formed by the pure surfactants alone, but they separate from aqueous solutions at much lower surfactant concentrations. When the charge density of the CS is low or the surfactant hydrocarbon chain is short, cubic or hexagonal phases are formed. As expected, the formation of lamellar phase is promoted by increasing these parameters. Temperature affects the stability of the phases and their structure. At high temperatures the long-range order breaks down, and the phases are akin to concentrated micellar CS/surfactant solutions.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma001793c</doi><tpages>10</tpages></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Applied sciences Exact sciences and technology Natural polymers Physicochemistry of polymers Starch and polysaccharides |
title | Structure of Cationic Starch (CS)/Anionic Surfactant Complexes Studied by Small-Angle X-ray Scattering (SAXS) |
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