2014
DOI: 10.1039/c3gc41317a
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Facile preparation of agarose–chitosan hybrid materials and nanocomposite ionogels using an ionic liquid via dissolution, regeneration and sol–gel transition

Abstract: We report simultaneous dissolution of agarose (AG) and chitosan (CH) in varying proportions in an ionic liquid (IL), 1-butyl-3-methylimidazolium chloride [C 4 mim] [Cl]. Composite materials were constructed from AG-CH-IL solutions using the antisolvent methanol, and IL was recovered from the solutions. Composite materials could be uniformly decorated with silver oxide (Ag 2 O) nanoparticles (Ag NPs) to form nanocomposites in a single step by in situ synthesis of Ag NPs in AG-CH-IL sols, wherein the biopolymer… Show more

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Cited by 89 publications
(84 citation statements)
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References 70 publications
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“…This strong interaction can result in the formation of additional cross links which can restrict the entry of water. Our results were in accordance with what has been previously observed [18,38]. The strong water retaining capacity of the synthesized scaffolds could be attributed to their hydrophilicity and a 3-D architecture.…”
Section: Swelling Testsupporting
confidence: 92%
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“…This strong interaction can result in the formation of additional cross links which can restrict the entry of water. Our results were in accordance with what has been previously observed [18,38]. The strong water retaining capacity of the synthesized scaffolds could be attributed to their hydrophilicity and a 3-D architecture.…”
Section: Swelling Testsupporting
confidence: 92%
“…This can be due to the amorphous nature of agarose. XRD pattern for silver nitrate shows distinct diffraction peaks at around 25 , 37 , 45 , 70 and 76 which are characteristics of (110), (111), (200), (220) and (311) planes of Face centred cubic (FCC) silver, respectively [18,34]. Presence of peak at 2h ¼ 20 Figure 2.…”
Section: Synthesis and Characterization Of Ag-chnp Scaffoldsmentioning
confidence: 98%
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“…On the other hand, the characteristic absorption peaks at trueν˜ =1725 cm −1 for the C=O ester, trueν˜ =1234 and 743 cm −1 for the C−N carbamate stretching, and trueν˜ =1603 cm −1 for the phenyl skeleton confirmed the carbanilation of AG. Additionally, the main characteristic IR bands of agarose are also maintained after functionalization, which confirms the stable structure of the functionalized AG samples . The expected conformation changes during the functionalization of AG in the IL were examined by comparing the circular dichroism (CD) spectra of native AG and modified AG.…”
Section: Resultsmentioning
confidence: 59%