Evolution of structure in a comb copolymer-surfactant coacervate

Kód výsledku v IS VaVaI

RIV/61389013:_____/19:00507871 - isvavai.cz

Nalezeny alternativní kódy

RIV/00216208:11310/19:10403676

Výsledek na webu

https://pubs.acs.org/doi/10.1021/acs.macromol.9b00332

DOI - Digital Object Identifier

10.1021/acs.macromol.9b00332

Jazyk výsledku

angličtina

Název v původním jazyce

Evolution of structure in a comb copolymer-surfactant coacervate

Popis výsledku v původním jazyce

The interaction between a double-hydrophilic comb copolymer with the polyanionic backbone poly[methacrylic acid-stat-poly(ethylene glycol) methyl ether methacrylate] (PMAA–PEGMA) and the cationic surfactant N-dodecylpyridinium chloride (DPCl) was studied in alkaline aqueous solutions by using a combination of light and X-ray scattering techniques, covering 5 orders of magnitude in space (the q vector range from 10–5 to 5 nm–1) and time (from milliseconds to several hours). The results showed that the polyelectrolyte–surfactant (PE–S) complex of PMAA–PEGMA and DPCl forms micrometer-sized coacervate particles containing collapsed PMAA–PEGMA chains with attached and densely packed DPCl micelles. Time-resolved SAXS measurements coupled with a stopped-flow apparatus revealed that the phase separation of the PE–S complex into a coacervate phase occurred in <25 ms after mixing the polyelectrolyte and the surfactant. Thus, microphase separation was faster than the self-assembly of DPCl into densely packed micelles. The terminal stages of polyelectrolyte–surfactant coacervation were dictated by the Ostwald ripening of the droplets in the time range of hours.

Název v anglickém jazyce

Evolution of structure in a comb copolymer-surfactant coacervate

Popis výsledku anglicky

The interaction between a double-hydrophilic comb copolymer with the polyanionic backbone poly[methacrylic acid-stat-poly(ethylene glycol) methyl ether methacrylate] (PMAA–PEGMA) and the cationic surfactant N-dodecylpyridinium chloride (DPCl) was studied in alkaline aqueous solutions by using a combination of light and X-ray scattering techniques, covering 5 orders of magnitude in space (the q vector range from 10–5 to 5 nm–1) and time (from milliseconds to several hours). The results showed that the polyelectrolyte–surfactant (PE–S) complex of PMAA–PEGMA and DPCl forms micrometer-sized coacervate particles containing collapsed PMAA–PEGMA chains with attached and densely packed DPCl micelles. Time-resolved SAXS measurements coupled with a stopped-flow apparatus revealed that the phase separation of the PE–S complex into a coacervate phase occurred in <25 ms after mixing the polyelectrolyte and the surfactant. Thus, microphase separation was faster than the self-assembly of DPCl into densely packed micelles. The terminal stages of polyelectrolyte–surfactant coacervation were dictated by the Ostwald ripening of the droplets in the time range of hours.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10404 - Polymer science

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2019

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Macromolecules

ISSN

0024-9297

e-ISSN

—

Svazek periodika

52

Číslo periodika v rámci svazku

16

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

8

Strana od-do

6303-6310

Kód UT WoS článku

000483437500028

EID výsledku v databázi Scopus

2-s2.0-85071655824