<?xml version="1.0"?><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xmlns:wgs84_pos="http://www.w3.org/2003/01/geo/wgs84_pos" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:rdaGr2="http://rdvocab.info/ElementsGr2" xmlns:oai="http://www.openarchives.org/OAI/2.0/" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:skos="http://www.w3.org/2004/02/skos/core#" xmlns:dcterms="http://purl.org/dc/terms/"><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-J9F4N68B/ee324194-2e56-4c1f-adea-c8dad7a9177f/HTML"><dcterms:extent>50 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-J9F4N68B/8b6bb3d1-f83b-4929-a2b9-fb8ba9fe60ba/PDF"><dcterms:extent>359 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-J9F4N68B/b1752fa0-6119-430f-a7b2-66a73d85b18f/TEXT"><dcterms:extent>46 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="1998-2025"><edm:begin xml:lang="en">1998</edm:begin><edm:end xml:lang="en">2025</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:DOC-J9F4N68B"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/URN:NBN:SI:spr-KC6O72BG" /><dcterms:issued>2006</dcterms:issued><dc:creator>Jerman, Boštjan</dc:creator><dc:creator>Kogej, Ksenija</dc:creator><dc:format xml:lang="sl">10 strani</dc:format><dc:format xml:lang="sl">številka:3</dc:format><dc:format xml:lang="sl">letnik:53</dc:format><dc:format xml:lang="sl">str. 264-273</dc:format><dc:identifier>ISSN:1318-0207</dc:identifier><dc:identifier>COBISSID:27964677</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-J9F4N68B</dc:identifier><dc:language>en</dc:language><dc:publisher xml:lang="sl">Slovensko kemijsko društvo</dc:publisher><dcterms:isPartOf xml:lang="sl">Acta chimica slovenica</dcterms:isPartOf><dc:subject xml:lang="sl">fizikalna kemija</dc:subject><dc:subject xml:lang="sl">fluorimetrične titracije</dc:subject><dc:subject xml:lang="sl">polielektroliti</dc:subject><dc:subject xml:lang="sl">polimetakrilna kislina</dc:subject><dc:subject xml:lang="sl">potenciometrične titracije</dc:subject><dc:subject xml:lang="sl">površinsko aktivne snovi</dc:subject><dc:subject xml:lang="sl">raztopine</dc:subject><dcterms:temporal rdf:resource="1998-2025" /><dc:title xml:lang="sl">Fluorimetric and potentiometric study of the conformational transition of isotactic and atactic poly(methacrylic acid) in mixed solvents|</dc:title><dc:description xml:lang="sl">Fluorimetric and potentiometric titrations of isotactic (i-PMA) and atactic poly(methacrylic acid) (a-PMA) were performed in methanol-water and in dioxane-water mixtures with varying contents of organic solvent. Fluorimetric investigation of a-PMA confirmed previous reports that the conformational transition of the atactic chain disappears when organic solvent content exceeds 40 and 20 % of methanol and dioxane, respectively. For the i-PMA chain, potentiometric data revealed that the conformational transition occurs in methanol-water mixtures with up to 60 % of methanol in approximately the same region of degree of neutralization (áN) as in water. Besides, the irreversibility of this transition does not disappear. On the other hand, the discontinuity in the potentiometric titration curve in dioxane-water mixtures is no longer detectable in 50% dioxane. Concurrently, i-PMA dissolves in 50% dioxane at N = 0, whereas it is not soluble in unneutralized state in any of the pure solvents. The observed behavior is attributed to high tendency of dioxane for hydrogen bond-formation both with water and with PMA. The nature of the change in chain dimensions upon neutralization for i-PMA in 50% dioxane is discussed. Results are discussed also in view of a high intermolecular association tendency of PMA chains</dc:description><dc:description xml:lang="sl">Izvedli smo fluorimetrične in potenciometrične titracije izotaktične (i-PMA) ni več zaslediti, ko je dioksana okrog 50%. Hkrati s tem se i-PMA v 50% dioksanu raztopi že pri .N = 0, medtem ko v nenevtraliziranem stanju ni topna vnoben in ataktične polimetakrilne kislineem od čistih topil. Opazeno obnašanje lahko pripišemo veliki tendenci, ki jo izkazuje dioksan za tvorbo vodikovih vezi z vodo in s PMA. Podan je možen način spremembe v dimenzijah verige i-PMA, do katerega pride pri nevtralizaciji v 50% dioksanu. Rezultati so interpretirani tudi s stališča velike tendence verig PMA po medmolekulski asociaciji</dc:description><edm:type>TEXT</edm:type><dc:type xml:lang="sl">znanstveno časopisje</dc:type><dc:type xml:lang="en">journals</dc:type><dc:type rdf:resource="http://www.wikidata.org/entity/Q361785" /></edm:ProvidedCHO><ore:Aggregation rdf:about="http://www.dlib.si/?URN=URN:NBN:SI:DOC-J9F4N68B"><edm:aggregatedCHO rdf:resource="URN:NBN:SI:DOC-J9F4N68B" /><edm:isShownBy rdf:resource="http://www.dlib.si/stream/URN:NBN:SI:DOC-J9F4N68B/8b6bb3d1-f83b-4929-a2b9-fb8ba9fe60ba/PDF" /><edm:rights rdf:resource="http://creativecommons.org/licenses/by/4.0/" /><edm:provider>Slovenian National E-content Aggregator</edm:provider><edm:intermediateProvider xml:lang="en">National and University Library of Slovenia</edm:intermediateProvider><edm:dataProvider xml:lang="sl">Slovensko kemijsko društvo</edm:dataProvider><edm:object rdf:resource="http://www.dlib.si/streamdb/URN:NBN:SI:DOC-J9F4N68B/maxi/edm" /><edm:isShownAt rdf:resource="http://www.dlib.si/details/URN:NBN:SI:DOC-J9F4N68B" /></ore:Aggregation></rdf:RDF>