Please use this identifier to cite or link to this item: http://dspace.chitkarauniversity.edu.in/xmlui/handle/123456789/409
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dc.contributor.authorCaldera-Villalobos, M.-
dc.contributor.authorLeal-Acevedo, B.-
dc.contributor.authorVelazquez-Aguilar, V. M.-
dc.contributor.authorCarreon-Castro, M. D. P.-
dc.date.accessioned2022-04-26T04:25:23Z-
dc.date.available2022-04-26T04:25:23Z-
dc.date.issued2020-02-28-
dc.identifier.issn2321-8649-
dc.identifier.issn2321-9289-
dc.identifier.urihttp://dspace.chitkarauniversity.edu.in/xmlui/handle/123456789/409-
dc.description.abstractGraft polymerization induced by ionizing radiation is a powerful tool in materials science to modifying the physical properties of polymers. Chitosan is a biocompatible, biodegradable, antibacterial, and highly hydrophilic polysaccharide. In this work, we report the obtaining of amphiphilic polymers through graft polymerization of acrylic monomers (methyl acrylate, t-butyl acrylate, and hexyl acrylate) onto chitosan. The polymerization reaction was carried out by simultaneous irradiation of monomers and chitosan using a gamma radiation source of 60Co. The formation of Langmuir films of amphiphilic polymers was studied at the air-water interface through surface pressure versus main molecular area isotherms (Π-A) and hysteresis cycles of compression and decompression. Finally, it was analyzed the transferring of Langmuir films towards solid substrates to obtaining Langmuir-Blodgett films with potential application as an antibacterial coating. The microstructure of the Langmuir-Blodgett films was characterized by AFM microscopy observing a regular topography with roughness ranging between 0.53 and 0.6 μm.en_US
dc.language.isoenen_US
dc.relation.ispartofseries;CHAENG/2013/51628-
dc.subjectBiobased polymersen_US
dc.subjectPolymer coatingsen_US
dc.titleGraft-Copolymerization of Acrylate Monomers onto Chitosan Induced by Gamma Radiation: Amphiphilic Polymers and Their Behavior at The Air-Water Interfaceen_US
dc.typeArticleen_US
Appears in Collections:Vol. 7 No. 2 (2020): Special Issue

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