Dynamic gelation of shear-induced filamentous domains for cellulose ether assemblies due to polyion complexation
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
32070503
DOI
10.1016/j.carbpol.2020.115880
PII: S0144-8617(20)30054-0
Knihovny.cz E-zdroje
- Klíčová slova
- Alginate, Aqueous two phase system, Gel fiber, Hydroxypropyl cellulose, Polyion complex,
- MeSH
- celulosa chemická syntéza chemie MeSH
- ethery chemická syntéza chemie MeSH
- gely chemická syntéza chemie MeSH
- ionty chemie MeSH
- kyseliny polymethakrylové chemie MeSH
- povrchové vlastnosti MeSH
- termodynamika * MeSH
- velikost částic MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- celulosa MeSH
- ethery MeSH
- gely MeSH
- ionty MeSH
- kyseliny polymethakrylové MeSH
- polymethacrylic acid MeSH Prohlížeč
Assemblies of carbohydrate polymers are important in a number of applications and improved methods for their fabrication are increasingly sought after. Herein, we report that an aqueous two-phase system of alginate (Alg) and hydroxypropyl cellulose with poly(methacrylic acid) graft chains (HPC-PMA) facilitated the assembly of Alg/HPC-PMA in both phases. Dynamically formed filamentous domains in a flow field were gelled by rapid complexation with cationic polyethyleneimine (PEI). The fabricated HPC-PMA gel filament morphologies can be switched between the bundled and dissociated gel filaments using a co-flow microfluidic device in response to the amount of supplied PEI crosslinker. Excess complexation of PEI contributes to the fabrication of cationic gel filaments; this contribution results in a dissociated structure due to electrostatic repulsion. In contrast, an appropriate amount of PEI resulted in a bundle structure. The proposed spinning method avoids the risk of nozzle clogging, and enables the one-step spinning of multiple gel filaments.
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