Polymer-Solvent Interactions in Modified Starches Pastes–Electrokinetic, Dynamic Light Scattering, Rheological and Low Field Nuclear Magnetic Resonance Approach

cris.virtual.author-orcid0000-0002-2994-4019
cris.virtual.author-orcid0000-0002-1438-1217
cris.virtual.author-orcid0000-0001-8851-912X
cris.virtual.author-orcid0000-0001-6597-0858
cris.virtual.author-orcid0000-0003-3967-112X
cris.virtualsource.author-orcideebce1ab-5f89-41d7-a55b-84a904a0efce
cris.virtualsource.author-orcid1c802429-36ee-40e7-b72f-32f16b32d8de
cris.virtualsource.author-orcidfa773a3b-d0b2-4feb-b51f-0901bb0ce777
cris.virtualsource.author-orcid08c06993-c96b-41bb-a5f9-551434fdd7df
cris.virtualsource.author-orcidb5ea5133-b916-419e-aa87-86a713721710
dc.abstract.enStarch paste is a very complex dispersion that cannot be clearly classified as a solution, colloid or suspension and many factors affects its properties. As these ambiguities constitute a barrier to technological development, the aim of this study was to investigate the interaction of starch macromolecules with water by analysing the results of rheological properties, low field nuclear magnetic resonance (LF NMR), dynamic light scattering (DLS) and ζ potential analyses. Starch pastes with a concentration of 1%, prepared with distilled water and buffered to pH values of 2.5, 7.0 and 9.5 were analysed. It was proved that the pH buffering substantially decreased the values of consistency index but the pH value itself was not significant. LF NMR studies indicated that the dissolution of starch in water resulted in a reduction in spin-lattice as well as spin-spin relaxation times. Moreover, changes in relaxation times followed the patterns observed in rheological studies. Electrokinetic and DLS analyses showed that potential values are primarily influenced by the properties of the starches themselves and, to a lesser extent, by the environmental conditions. The conducted research also showed complementarity and, to some extent, substitutability of the applied research methods as well as exclusion chromatography (a method not used in this work).
dc.affiliationWydział Nauk o Żywności i Żywieniu
dc.affiliation.instituteKatedra Technologii Żywności Pochodzenia Roślinnego
dc.affiliation.instituteKatedra Biochemii i Analizy Żywności
dc.affiliation.instituteKatedra Biotechnologii i Mikrobiologii Żywności
dc.affiliation.instituteKatedra Fizyki i Biofizyki
dc.contributor.authorMakowska, Agnieszka
dc.contributor.authorDwiecki, Krzysztof
dc.contributor.authorKubiak, Piotr
dc.contributor.authorBaranowska, Hanna Maria
dc.contributor.authorLewandowicz, Grażyna
dc.date.access2025-09-16
dc.date.accessioned2025-09-16T07:44:30Z
dc.date.available2025-09-16T07:44:30Z
dc.date.copyright2022-07-22
dc.date.issued2022
dc.description.abstract<jats:p>Starch paste is a very complex dispersion that cannot be clearly classified as a solution, colloid or suspension and many factors affects its properties. As these ambiguities constitute a barrier to technological development, the aim of this study was to investigate the interaction of starch macromolecules with water by analysing the results of rheological properties, low field nuclear magnetic resonance (LF NMR), dynamic light scattering (DLS) and ζ potential analyses. Starch pastes with a concentration of 1%, prepared with distilled water and buffered to pH values of 2.5, 7.0 and 9.5 were analysed. It was proved that the pH buffering substantially decreased the values of consistency index but the pH value itself was not significant. LF NMR studies indicated that the dissolution of starch in water resulted in a reduction in spin-lattice as well as spin-spin relaxation times. Moreover, changes in relaxation times followed the patterns observed in rheological studies. Electrokinetic and DLS analyses showed that potential values are primarily influenced by the properties of the starches themselves and, to a lesser extent, by the environmental conditions. The conducted research also showed complementarity and, to some extent, substitutability of the applied research methods as well as exclusion chromatography (a method not used in this work).</jats:p>
dc.description.accesstimeat_publication
dc.description.bibliographyil., bibliogr.
dc.description.financepublication_nocost
dc.description.financecost0,00
dc.description.if5,0
dc.description.number15
dc.description.points100
dc.description.versionfinal_published
dc.description.volume14
dc.identifier.doi10.3390/polym14152977
dc.identifier.issn2073-4360
dc.identifier.urihttps://sciencerep.up.poznan.pl/handle/item/4806
dc.identifier.weblinkhttps://www.mdpi.com/2073-4360/14/15/2977
dc.languageen
dc.relation.ispartofPolymers
dc.relation.pagesart. 2977
dc.rightsCC-BY
dc.sciencecloudnosend
dc.share.typeOPEN_JOURNAL
dc.subject.enstarch
dc.subject.enpotential
dc.subject.enhydrodynamic diameter
dc.subject.enconsistency index
dc.subject.enflow behaviour index
dc.subject.enspin-lattice relaxation time
dc.subject.enspin-spin relaxation time
dc.subject.enmean correlation time
dc.titlePolymer-Solvent Interactions in Modified Starches Pastes–Electrokinetic, Dynamic Light Scattering, Rheological and Low Field Nuclear Magnetic Resonance Approach
dc.title.volumeSpecial Issue Polysaccharides: From Basic Research to Advanced Applications
dc.typeJournalArticle
dspace.entity.typePublication
oaire.citation.issue15
oaire.citation.volume14