2019
DOI: 10.1016/j.carbpol.2019.115008
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Benzoxazine enhanced amino cellulose-based composite films: Preparation, proposed mechanism, and improved performance

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Cited by 27 publications
(14 citation statements)
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“…From these spectra, it is indicated that the amines have been substituted on the Microcrystalline Cellulose backbone. FTIR spectra of aminated Cellulose derivatives were in accordance with already reported data as described by [ 38 ].…”
Section: Resultssupporting
confidence: 86%
“…From these spectra, it is indicated that the amines have been substituted on the Microcrystalline Cellulose backbone. FTIR spectra of aminated Cellulose derivatives were in accordance with already reported data as described by [ 38 ].…”
Section: Resultssupporting
confidence: 86%
“…A controlled nanoscale microphase separation is observed in a co-L. As shift in Tm value of PCL in blend to higher temperature sugof physical crosslinks between the two, which hinders the transfer of e region of PCL [368]. PCL/PBz blends revealed a single Tg which of the two in the melt state as shown in Figure 57a [359][360][361][362], amino-cellulos [363] and polyurethane [364][365][366][367]. Although, the effect of OH groups on the polymeriza tion of -OH or -NH2 containing benzoxazine monomers, non-benzoxazine monomers and polymers is not explicitly stated.…”
Section: Othersmentioning
confidence: 96%
“…Figure 57b shows a segregation of PCL spherulitic morphologies and an effect on its growth rate is observed which confirms a reduction in their chain mobility and dilution of PCL domains due to the interpenetrating PBz framework [369]. The polymer blends appeared to be homogeneous at the 40-70 nm scale but heterogeneous at the 2-4 nm scale as supported by 13 The H-bonding between the hydroxyl groups of polybenzoxazine influences physical crosslinks due to extension of intermolecular H-bonding with the polar functionalities (carbonyl, ether, amine, hydroxyl) present in other polymers such as poly(ɛ-caprolactone) (PCL) [354][355][356], poly(ethylene oxide), [357,358] chitosan (CS) [359][360][361][362], amino-cellulose [363] and polyurethane [364][365][366][367]. Although, the effect of OH groups on the polymerization of -OH or -NH2 containing benzoxazine monomers, non-benzoxazine monomers and polymers is not explicitly stated.…”
Section: Abbreviationsmentioning
confidence: 99%
“…The introduction of the new functionalities to the backbone of the biopolymers such as cellulose has been achieved through various reactions. For example, cellulose modification is accomplished through the modification of the hydroxyl group along the cellulose chain [6,10,144,147]. Such modifications can be accomplished through cationization, phosphorylation [6,8], (2,2,6,6-tetramethyl-piperidin-1-yl)oxyl (TEMPO) oxidation [6,8,148], The introduction of the new functionalities to the backbone of the biopolymers such as cellulose has been achieved through various reactions.…”
Section: Progress In the Preparation And Functionalisation Of Biopolymers For Water Treatmentmentioning
confidence: 99%
“…Such modifications can be accomplished through cationization, phosphorylation [6,8], (2,2,6,6-tetramethyl-piperidin-1-yl)oxyl (TEMPO) oxidation [6,8,148], The introduction of the new functionalities to the backbone of the biopolymers such as cellulose has been achieved through various reactions. For example, cellulose modification is accomplished through the modification of the hydroxyl group along the cellulose chain [6,10,144,147]. Such modifications can be accomplished through cationization, phosphorylation [6,8], (2,2,6,6-tetramethyl-piperidin-1-yl)oxyl (TEMPO) oxidation [6,8,148], etherification, grafting, halogenation, carboxymethylation, sulfoethylation, sulfonation, aminoguanidine, ozonation, thiolation [6], esterification [6,10], acetylation [10], and amination [6,143,144,149].…”
Section: Progress In the Preparation And Functionalisation Of Biopolymers For Water Treatmentmentioning
confidence: 99%