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Poly(N-isopropylacrylamide)-SiO2 nanocomposites interpenetrated by starch: Stimuli-responsive hydrogels with attractive tensile properties
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SYSNO ASEP 0471497 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Poly(N-isopropylacrylamide)-SiO2 nanocomposites interpenetrated by starch: Stimuli-responsive hydrogels with attractive tensile properties Tvůrce(i) Depa, Katarzyna (UMCH-V)
Strachota, Adam (UMCH-V) RID, ORCID
Šlouf, Miroslav (UMCH-V) RID, ORCID
Brus, Jiří (UMCH-V) RID, ORCIDZdroj.dok. European Polymer Journal. - : Elsevier - ISSN 0014-3057
Roč. 88, March (2017), s. 349-372Poč.str. 24 s. Jazyk dok. eng - angličtina Země vyd. GB - Velká Británie Klíč. slova PNIPAm hydrogel ; starch ; silica Vědní obor RIV CD - Makromolekulární chemie Obor OECD Polymer science CEP LD14010 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy Institucionální podpora UMCH-V - RVO:61389013 UT WOS 000396952500031 EID SCOPUS 85012149780 DOI 10.1016/j.eurpolymj.2017.01.038 Anotace Doubly filled nanocomposite poly(N-isopropylacrylamide)-SiO2-starch hydrogels were prepared via simultaneous polymerization of N-isopropylacrylamide (NIPAm) and tetramethoxysilane hydrolysis, in the presence of colloid amylopectin starch (4–30 wt.% in dry gel). Besides bulk hydrogels, also highly porous ones were prepared, the latter via solvent freezing during synthesis (cryogels). The branched starch molecules, which interpenetrate PNIPAm, appear to enforce less crosslinked but more regular PNIPAm network with a wider mesh, in place of the irregular one, which is normally obtained in divinyl-crosslinked PNIPAm. The hydroxyl groups of starch form efficient hydrogen bonds to the PNIPAm matrix, as well as to the SiO2 nanofiller, which in turn also has strong H-bonds to PNIPAm. In bulk gels, a strong synergy of both fillers is clearly observed, leading to a marked increase in moduli, in spite of the wider network mesh. Very distinct is the improvement of tensile properties if starch is incorporated: the elongation at break increases 2 times in porous gels and 3–6 times in bulk ones. The gels’ toughness is also tremendously improved. The porous PNIPAm-SiO2-starch gels further display an ultra-fast swelling response to temperature jumps, both deswelling and re-swelling. Interestingly, starch-rich bulk PNIPAm-starch and PNIPAm-SiO2-starch gels also display a very fast (and also very extensive) temperature-induced deswelling, while their re-swelling is very slow (as would be expected). This behaviour practically represents a strong ‘one way response’ to temperature jumps. The specific properties of the interface between swollen PNIPAm and starch enable the rapid water escape from the bulk gels, especially if starch-rich domains are present. Pracoviště Ústav makromolekulární chemie Kontakt Eva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358 Rok sběru 2017
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